A community-based lifestyle intervention targeting Type II Diabetes risk factors in an Australian Aboriginal population: a feasibility study

Rankin P, Morton D, Kent L, Mitchell B (2016) A community-based lifestyle intervention targeting Type II Diabetes risk factors in an Australian Aboriginal population: a feasibility study. Australian Indigenous HealthBulletin 16(3). Retrieved [access date] from http://healthbulletin.org.au/articles/a-community-based-lifestyle-intervention-targeting-type-ii-diabetes-risk-factors-in-an-australian-aboriginal-population-a-feasibility-study

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Review of illicit drug use among Aboriginal and Torres Strait Islander people

MacRae A, Hoareau J (2016) Review of illicit drug use among Aboriginal and Torres Strait Islander people. Australian Indigenous HealthInfoNet. Retrieved [access date] from  https://healthbulletin.org.au/articles/review-of-illicit-drug-use-among-aboriginal-and-torres-strait-islander-people

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Introduction

Illicit drug use can harm individuals, communities and society. Australia’s Aboriginal and Torres Strait Islander people are affected by significantly higher levels of substance use than non-Indigenous people, contributing to higher levels of associated health and social harms [1, 2].

Most Aboriginal and Torres Strait Islander people do not use illicit drugs, but the proportion of drug use is higher among Aboriginal and Torres Strait Islander people than among non-Indigenous people [3, 4]. Cannabis is the most commonly used illicit drug among Aboriginal and Torres Strait Islander people; in 2012-2013, 19% of Aboriginal and Torres Strait Islander people aged 15 years and over reported having recently 1 used cannabis [5, 6]. Research suggests high levels of heavy cannabis use in some Aboriginal and Torres Strait Islander communities, which may be associated with dependence and harms to social and emotional wellbeing [7-9]. Illicit drug use is associated with a number of health impacts and social harms that disproportionately affect Aboriginal and Torres Strait Islander people. These harms include increased risk of contracting hepatitis C and human immunodeficiency virus (HIV) from injecting drug use [10]; higher levels of psychological distress [6]; and an increased risk of suicide [11, 12]. Illicit drug use is also linked with social issues, such as harms to children and family, violence, crime and incarceration [6].

Box 1: Illicit drug use

Illicit drug use describes the use of drugs that are illegal to possess (e.g. cannabis, heroin, and cocaine), and those legally available including the use of volatile substances (e.g. petrol, glue, and solvents), and the non-medical use of prescription drugs (e.g. pain killers (analgesics)) [13]. For the purposes of this review, specific information on volatile substance use is not included. Detailed information on volatile substance use is available in the Review of volatile substance use among Aboriginal and Torres Strait Islander people.

For more information on categories and definitions of illicit drugs, refer to the Australian Indigenous Alcohol and Other Drugs Knowledge Centre: background information on illicit drugs.

About this review

The purpose of this review is to provide an overview of the use of illicit drugs among Aboriginal and Torres Strait Islander people in Australia. It provides general information on the context of illicit drug use in Australia and the factors of particular relevance to Aboriginal and Torres Strait Islander people, including the historical context, social context, and other social factors. This review provides detailed information on the extent of illicit drug use among Aboriginal and Torres Strait Islander people, including overall self-reported prevalence and prevalence by type of substance. It outlines the health and social and emotional wellbeing harms associated with substance use, as well as the associated hospitalisations, mortality, and wider social impacts. This review also provides information on policies and strategies addressing illicit drug use among Aboriginal and Torres Strait Islander people, including a number of past policies that provide historical context. This review concludes by describing a number of services that aim to address illicit drug use in Australia, with particular focus on elements of effective service design and delivery and barriers commonly faced by Aboriginal and Torres Strait Islander people when accessing these services.

The Australian Indigenous HealthInfoNet produces a wide range of publications and narrative reviews of specific health topics. In these publications, authors summarise and present data from other sources. It is often difficult to determine whether original sources are referring to Aboriginal people only, Torres Strait Islander people only or to both groups. In these instances the authors are ethically bound to utilise the terms from the original source unless they can obtain clarification from the report authors/copyright holders. Readers may see these terms used interchangeably with the term ‘Indigenous’ in some instances. If they have any concerns they should be advised to contact the HealthInfoNet for further information.

Acknowledgements

Special thanks are extended to:

  • the anonymous peer reviewer whose comments greatly assisted finalisation of this review
  • other staff at the Australian Indigenous HealthInfoNet, particularly Caitlin Gray and Kathy Ride, for their assistance and support
  • the Australian Government Department of Health for their ongoing support of the work of the HealthInfoNet.

Key facts

Extent of illicit drug use among Aboriginal and Torres Strait Islander people

  • Illicit drug use among Aboriginal and Torres Strait Islander people needs to be understood within the social and historical context of colonisation, dispossession of land and culture, and economic exclusion.
  • Surveys consistently show that most Aboriginal and Torres Strait Islander people do not use illicit drugs.
  • In 2012-2013, 22% of Aboriginal and Torres Strait Islander people aged 15 years and older had used an illicit drug in the 12 months prior to the survey.
  • In 2012-2013, cannabis was the most common recently used illicit drug for Aboriginal and Torres Strait Islander people, followed by analgesics and sedatives for non-medical use, and amphetamines.

Health impacts

  • Illicit drug use has been estimated to be responsible for 3.4% of the overall burden of disease among Aboriginal and Torres Strait Islander people and 2.8% of deaths.
  • Cannabis use among Aboriginal and Torres Strait Islander people has been linked with increased risk of anxiety, depression and psychosis; injecting drug use is associated with an increased risk of hepatitis C and HIV infection.
  • In 2012-13, the most common drug-related conditions resulting in hospitalisation were for ‘poisoning’ and ‘mental and behavioural disorders’.
  • Illicit drug use has been identified as a major risk factor for suicide among Aboriginal and Torres Strait Islander people.

Social impacts of drug use among Aboriginal and Torres Strait Islander people

  • Illicit drug use is a significant contributing factor in harms to children and family.
  • The 2008 NATSISS found that Aboriginal and Torres Strait Islander people aged 15 years and older who had used substances in the previous 12 months were twice as likely to have been the victim of physical or threatened violence  than were Aboriginal and Torres Strait Islander people who had not used substances .
  • In 2010, 68% of Aboriginal and Torres Strait Islander prison entrants reported illicit drug use in the previous 12 months.

Policies and strategies

  • The National Aboriginal and Torres Strait Islander peoples’ drug strategy 2014-2019 identifies four priority areas: building the capacity and capability of alcohol and other drug services; increase access to a range of culturally responsive and appropriate programs; strengthen partnerships between Aboriginal and Torres Strait Islander peoples, government, and mainstream service providers; establish meaningful performance measure with effective data collection to support community-led monitoring and evaluation.
  • The National Aboriginal and Torres Strait Islander peoples’ drug strategy 2014-2019 aims to reduce levels of illicit drug use, reduce offending, and reduce the risk of blood-borne viral infections.
  • The National Ice Taskforce, established in 2015, examined the impact of crystal methamphetamine or ‘ice’ on communities including Aboriginal and Torres Strait Islander communities and recommended increased access to integrated, culturally appropriate alcohol and other drug  services for Aboriginal and Torres Strait Islander people.

Programs and services

  • In 2013-14, the Australian Government provided grants to around 269 organisations to fund primary health care and other services, including alcohol and other drugs services, to Aboriginal and Torres Strait Islander people.
  • Elements identified as contributing to effective alcohol and other drug services include: services that are initiated and controlled by communities; culturally appropriate services; strong partnerships between Aboriginal and Torres Strait Islander and mainstream services; good governance and management systems; and provision of skills development and training for staff.
  • Barriers to effective services that have been identified include: lack of cultural sensitivity in mainstream services; uncertain or inadequate funding; lack of follow up care; lack of access in remote areas; and the need for more information on the types of alcohol and other drug services that best serve the needs of Aboriginal and Torres Strait Islander people.

Context of illicit drug use in Australia

The use of licit (legal) drugs, particularly alcohol and tobacco, contributes greatly to the burden of disease and social costs in Australia [14]. Illicit drug use also contributes to ill-health, injuries, violence, criminal behaviour, and social disruption. The National drug strategy household survey (NDSHS) found that 15% of Australians aged 14 years and older had used illicit substances in the previous 12 months, and around 42% had used an illicit substance at least once in their lifetime [3]. These levels are similar to those found in previous surveys [4].

Illicit drug use contributes significantly to ill-health in Australia; it is associated with injury, violence, chronic disease, blood-borne viruses, and lower levels of social and emotional wellbeing [15]. In 2011-2012, there were over 46,000 hospital separations with a principal diagnosis related to illicit drug use, representing about 43% of all hospital separations related to drug use during this time period [16]. Illicit drug use also contributes to deaths in Australia. The most recent study examining the burden of disease in Australia found that 1.3% of deaths in 2003 could be attributed to illicit drug use [17].2 In 2007, there were 976 deaths where the underlying cause of death was related to drugs (excluding alcohol and tobacco); 743 of these deaths were among people aged 15-54 years [18]. The majority of accidental deaths were caused by opioids.

The economic cost of illicit drug use is considerable. The total cost of substance use in 2004-05 was $56 billion, of which $8.2 billion (15%) was for illicit drug use [14]. Of this, $3.8 billion was for law-enforcement and crime-related costs and $1.6 billion was for lost productivity in the workplace. The real cost of illicit drug use increased by 11% (from $7.4 billion to $8.2 billion) between 1998-99 and 2004-05.

Factors contributing to illicit drug use among Aboriginal and Torres Strait Islander people

Illicit drug use among Aboriginal and Torres Strait Islander people, and the harms associated with its use, are ‘socially determined and are both a consequence and a cause of social and economic disadvantage’ [1, p.755]. The historical context and the social factors that operate within contemporary Australian society play a role in Aboriginal and Torres Strait Islander health generally, and in illicit drug use specifically.

Historical factors

The higher level of substance use among Aboriginal and Torres Strait Islander people than that among non-Indigenous people must be ‘understood in the historical context of colonialism and dispossession’ [1, p.757]. European colonisation resulted in the loss of traditional Aboriginal and Torres Strait Islander lands and customs for many Aboriginal and Torres Strait Islander people, and began the long history of dispossession and social and economic exclusion: ‘socioeconomic deprivation is clearly linked to substance misuse among Aboriginal people, continuing feelings of exclusion and hurt exacerbate such behaviour, and many families are enmeshed in an intergenerational cycle in which this is perpetuated’ [1, p.758].

Social context

The perpetuation of disadvantage from historical origins to contemporary society involves the social factors associated with health, including education, employment, and income. Drug use is associated with measures of social disadvantage and ‘is strongest for the illicit drugs versus the licit, and also for more intensely problematic patterns of drug use, including dependence’ [19, p.242].

Education

Educational attainment affects employment opportunities and, in turn, affects an individual’s living standards. Recent surveys indicate that Aboriginal and Torres Strait Islander people experience higher levels of educational disadvantage than non-Indigenous people, including lower educational achievement [20], lower retention rates [21], lower levels of year 12 completion, and leaving school at a younger age [22]. The relationship between illicit drug use and educational outcomes is likely to be complex because of the interrelation with other types of social disadvantage [23].

Associations between low educational attainment and drug use among Aboriginal and Torres Strait Islander people have been examined in a number of studies:

  • A 2003 analysis [24] of a 1997 study of Indigenous children in Albany, Western Australia (WA) [25], found that, among children aged 8-14 years, those who were disengaged from school were 23 times more likely to be poly-drug users than those who were not [24].
  • A 2004 study of Indigenous cannabis users found that cannabis users were less likely to participate in education and training than non-users [8].
  • A 2010 analysis of the 2005 Australian secondary students’ alcohol and drug survey [26] found that illicit drug use was higher for Indigenous students and associated with poorer self-reported academic performance [23].

Employment

Employment directly affects a person’s quality of life. Unemployment ‘may encourage and sustain drug use, and established drug use may discourage the ability or desire to seek and maintain employment’ [27, p.104].

Based on counts3 from the 2011 Census, there was a lower level of employment among Aboriginal and Torres Strait Islander people aged 15 years and older than among non-Indigenous people (42% compared with 61%), and a higher level of unemployment (17% compared with 5.4%) [28]. Age-adjusted comparisons of the 2008 National Aboriginal and Torres Strait Islander social survey (NATSISS) and the 2007-08 National health survey (NHS) found that Aboriginal and Torres Strait Islander people were less likely to be employed than non-Indigenous people (54% compared with 76%), and almost four times as likely to be unemployed as non-Indigenous people (11% compared with 3%) [22].

Drug use and employment among the Aboriginal and Torres Strait Islander population have been examined in a number of studies: a 2010 study found that cannabis use increased during periods of unemployment [29]; and a 2001 study of people who inject drugs in South Australia (SA) reported that 66% of participants were unemployed [30].

Income

Past studies have shown an association between income and health, with the highest rates of ill health experienced by those with the lowest income [19]. In 2012-13, the median equivalised gross weekly household income for Aboriginal and Torres Strait Islander adults was $465 compared with $869 for non-Indigenous adults [6]. Similarly, comparison of the 2008 NATSISS and the 2007-08 NHS found that Aboriginal and Torres Strait Islander people aged 18 years and over had a lower mean equivalised gross household income than their non-Indigenous counterparts ($580 compared with $983) [22].

Family and peers

Strong, healthy familial relationships may decrease the likelihood of a person using illicit drugs and may help some people to overcome drug dependence [7, 31-34]. Previous literature has noted that positive relationships may act as a protective factor for illicit drug use: ‘the best protections against substance misuse are strong families and communities that protect children and young people and encourage them to become educated, provide them with real employment opportunities, access to quality health care and a decent standard of living, and make them feel valued members of Australian society’ [1, p.764]. Family was identified as a key measure of quality of life in a 2012 review of substance use treatment [32] and family support and involvement were seen as key aspects of recovery from drug use for Aboriginal people in a 2011 review of injecting drug use [33]. Changes in social circumstances, including getting married or having a baby, are associated with quitting drug use [7, 34].

Family support may be a protective factor, but existing drug use within the family network may be a risk factor [35]. One study noted that ‘many key informants spoke of the need to break the cycle of injecting drug use in some Aboriginal families’ [33, p.82]. Similarly, initiation of injecting drug use and sharing of injecting equipment is common between sexual partners [36, 37].

Peers also play a role in drug use; a 2009 survey of young people in custody in New South Wales (NSW) found that peer pressure was the most common factor influencing the decision to first try an illicit drug [38]. A higher proportion of Indigenous youths than non-Indigenous youths identified peer pressure as the main factor influencing their decision to try an illicit drug (66% and 57%, respectively). Illicit drug use by peers may also adversely affect a person’s ability to moderate consumption or quit [39].

Community

Community can act as a risk or protective factor: dysfunctional community dynamics have been associated with increased risk of drug use while positive community involvement has been associated with reduced drug use [19, 40, 41]. The Dampier Peninsula prevention project identified ‘recreational opportunities; information and support; community cohesion and cultural leadership’ as ways to address substance use [40, p.118]. Providing community recreational activities can alleviate boredom and provide an alternative to drug use. Prevention programs that reconnect individuals with their culture (including arts programs, or those that provide traditional skills like hunting) can foster a sense of pride and empower individuals, which may protect people from drug use [42-44].

Extent of illicit drug use among Aboriginal and Torres Strait Islander people

Self-reported illicit drug use

Surveys consistently show that most Aboriginal and Torres Strait Islander people do not use illicit drugs. According to the 2012-2013 Australian Aboriginal and Torres Strait Islander health survey (AATSIHS), 52% of Aboriginal and Torres Strait Islander people aged 15 years and older reported never using illicit drugs [45]. Similarly, never using illicit drugs was reported by 57% of Aboriginal and Torres Strait Islander people aged 15 years and older in the 2008 NATSISS, and by 51% in the 2002 NATSISS [46]. Proportions of never using illicit drugs are consistently higher for Aboriginal and Torres Strait Islander females those that for males [45, 46].

While the majority of Aboriginal and Torres Strait Islander people do not use illicit drugs, surveys have consistently reported higher levels of ‘recent’4 illicit drug use among Aboriginal and Torres Strait Islander people than those among non-Indigenous people [3, 45-47]. According to the 2012-2013 AATSIHS, 22% of Aboriginal and Torres Strait Islander people aged 15 years and older had used an illicit drug in the 12 months prior to the survey (there are no non-Indigenous data for comparison) [45]. Similarly, after age-adjustment, the 2013 NDSHS found that 23% of Aboriginal and Torres Strait Islander people aged 14 years and older had ‘recently used’ an illicit drug, compared with 15% of non-Indigenous people [3].5 In the 2008 NATSISS, 23% of Aboriginal and Torres Strait Islander people had ‘recently used’ an illicit drug; and in the 2007 NDSHS, 24% of Aboriginal and Torres Strait Islanders were ‘recent users’ of an illicit drug compared with 13% of non-Indigenous Australians [2, 46, 47].

Box 2: Data sources and limitations

Information about the extent of illicit drug use in Australia relies heavily on self-reported survey data which may under-estimate the true extent of use because of the under-reporting of drugs that are illegal to possess [48].

The main sources of illicit drug use information are the 2012-13 AATSIHS [45]; the 2008 NATSISS [49]; the Overcoming Indigenous disadvantage: key indicators report series; and the Aboriginal and Torres Strait Islander health performance framework report series. Other useful sources of information include the Australian secondary students’ alcohol and drug survey (ASSAD) [50] and the Illicit drug reporting system (IDRS). Specific information on the scope and limitations of each of these sources is outlined in Appendix 1.

The most recent source of information on illicit drug use in the total population is the 2013 NDSHS [3]; unfortunately the small sample size in this survey under-represented Aboriginal and Torres Strait Islander people. Therefore comparisons of data between Aboriginal and Torres Strait Islander people and non-Indigenous people should be viewed with caution. The 2007 NDSHS [47] is also used throughout this review to provide general comparisons between Aboriginal and Torres Strait Islander people and non-Indigenous Australians6 but all comparisons should be viewed with caution because of methodological and statistical differences between the 2007 NDSHS and the 2008 NATSISS (for details on the surveys used in this review, see Appendix 1).

Comparison of the various measures of illicit drug use by Aboriginal and Torres Strait Islander and non-Indigenous people needs to take account of the fact that Aboriginal and Torres Strait Islander population is younger overall than the non-Indigenous population. A procedure known as age-standardisation adjusts health measures (such as prevalence and rates) to minimise the effects of the differences in the age structures of the two populations [51]. Comparisons are normally presented as the ratios of age-standardised (or age-adjusted) prevalence and rates.

Surveys consistently show that higher proportions of Aboriginal and Torres Strait Islander males have used illicit drugs than females. According to the 2012-2013 AATSIHS, 27% of Aboriginal and Torres Strait Islander males and 18% of Aboriginal and Torres Strait Islander females aged 15 years and older had ‘recently used’ an illicit drug [45]. Similar results were found in the 2008 NATSISS, with 28% of Aboriginal and Torres Strait Islander males and 17% of Aboriginal and Torres Strait Islander females aged 15 years and older having ‘recently used’ illicit drugs [46]. When comparing different age cohorts, prevalence of ‘recent use’ in the 2012-2013 AATSIHS was highest for Aboriginal and Torres Strait Islander people in the 15-24 years (28%) and 25-34 years (27%) age-groups but decreased for the 35-54 years age groups (around 21%) and 55 and older age-groups (7%) (Table 1)  [45].

Surveys have reported higher levels of ‘ex use‘7 of illicit drugs among Aboriginal and Torres Strait Islander people than those among non-Indigenous people. The 2012-2013 AATSIHS found that 23% of Aboriginal and Torres Strait Islander people aged 15 years and older had used an illicit drug but not in the last 12 months [45]. The 2013 NDSHS reported that 30% of Aboriginal and Torres Strait Islander people 14 years and older were ex users of an illicit drug compared with 27% of non-Indigenous people [3].8 For ex users of illicit drugs, males had higher proportions than females: 25% compared with 21% in the 2012-2013 AATSIHS [45].

Table 1. Proportions (%) of illicit drug use among Aboriginal and Torres Strait Islander people aged 15 years and older, by age-group and frequency of use, Australia, 2012-2013

Used illicit drug in the previous 12 months Used illicit drug but not in the last 12 months

Age-group (years)

15-24

28

15

25-34

27

30

35-44

23

27

45-54

19

29

55+

7

14

All ages

22

23

Source: ABS, 2013 [45]

Proportions of illicit drug use were higher among Aboriginal and Torres Strait Islander people living in non-remote areas than among those living in remote areas. The 2012-2013 AATSIHS found that 23% of Aboriginal and Torres Strait Islander people aged 15 years and over living in non-remote areas had ‘recently used’, and 24% were ex users of an illicit drug, compared with 19% and 17% respectively of those living in remote locations [5]. The 2008 NATSISS reported a similar proportion (24%) of Aboriginal and Torres Strait Islander people aged 15 years and older living in non-remote areas had ‘recently used’ an illicit drug, compared with 17% of Aboriginal and Torres Strait Islander people living in remote areas [46].

The 2008 Australian secondary students alcohol and drug survey (ASSAD) found that 19% of Indigenous participants aged 12-15 years had used an illicit drug in the previous year and 13% had used an illicit drug in the previous month (compared with 9% and 5% respectively for all respondents) [50]. Indigenous students were nearly twice as likely as all ASSAD respondents to report having ‘ever used’9 an illicit drug (23% compared with 11% respectively).

Self-reported use by type of illicit drug

Levels of illicit drug use differ by type of drug. Cannabis is consistently identified as the most commonly used illicit drug in Australia, for both the Aboriginal and Torres Strait Islander population and the total population [3, 4]. Other illicit drugs used by Aboriginal and Torres Strait Islander people include analgesics (painkillers and sedatives for non-medical use) and amphetamines (Table 2) [5].

Table 2. Proportions (%) of recent illicit drug use among Aboriginal and Torres Strait Islander people aged 15 years and older, by type of illicit drug, Australia, 2012-13

Type of illicit drug

Proportions of ‘recent use’

Cannabis (marijuana/hashish/cannabis resin)

19

Analgesics and sedatives

3.9

Amphetamines

2.3

Kava

1.3

Other

2.8

Source: ABS, 2013 [5]

Notes:

  1. ‘Recent use’ refers to use in the 12 months prior to survey
  2. ‘Other’ includes heroin, cocaine, petrol, LSD/synthetic hallucinogens, ecstasy/designer drugs, methadone and other inhalants

Cannabis

Cannabis is the illicit drug most commonly used by Aboriginal and Torres Strait Islander people. The 2012-2013 AATSIHS found that 19% of Aboriginal and Torres Strait Islander people aged 15 years and older had ‘recently used’ cannabis [5], a slight increase on levels reported in the 2008 NATSISS (17%) [46].

The 2013 NDSHS reported that 10% of the total population had ‘recently used’ cannabis and 35% had used cannabis at least once in their lifetime [3]. After age-adjustment, the proportion of Aboriginal and Torres Strait Islander people who ‘recently used’ cannabis was more than 1.5 times higher than that for non-Indigenous people (13% compared to 8%). Proportions of ex use among Aboriginal and Torres Strait Islander and non-Indigenous were similar (28% and 25%).

According to the 2012-2013 AATSIHS, a higher proportion of Aboriginal and Torres Strait Islander males than females had ‘recently used’ cannabis (24% compared with 14%) [5]. Comparisons of the 2012-2013 AATSIHS the 2008 NATSISS show the proportion of ‘recent use’ among Aboriginal and Torres Strait Islander males remained similar (24% and 23%), but there has been a slight increase in ‘recent use’ among females (from 12% to 14%) [5, 22]. Cannabis use in 2012-2013 was more common in non-remote areas than in remote areas: 19% of Indigenous people aged 15 years and older living in non-remote areas reported ‘recent use’ compared with 17% of their remote-living counterparts [5]. This is a slight increase in proportions reported for 2008 (18% and 14%) [22].

The 2008 ASSAD reported that cannabis was the most commonly used illicit drug for Aboriginal and Torres Strait Islander respondents aged 12-15 years [50]. Around 20% of Aboriginal and Torres Strait Islander respondents aged 12-15 years had ‘ever used’ cannabis; 16% had used it in the previous year; 10% had used it in the previous month; and 8% had used it in the previous week (Table 3). Cannabis use was almost twice as common among Aboriginal and Torres Strait Islander respondents as among all ASSAD respondents. 

Table 3. Proportions (%) of cannabis use among students aged 12-15 years, by Aboriginal and Torres Strait Islander status and frequency of use, Australia, 2008

Frequency of use

Aboriginal and Torres Strait Islander respondents

All ASSAD respondents

Never used

81

91

Ever used

20

9.4

Used in the previous year

16

7.8

Used in the previous month

10

4.3

Used in the previous week

7.6

2.6

Source: Smith G, White V, 2010 [50]

Note: Due to rounding, percentages totals may be higher than 100%

National surveys provide self-reported prevalence of use, but they do not provide information on other aspects of cannabis use by Aboriginal and Torres Strait Islander people, including how often and how much cannabis is used, and the financial costs for individuals and the community. The limited information that is currently available comes from small, community-specific studies. These studies indicate a very high level of heavy cannabis use among Aboriginal and Torres Strait Islander people living in some remote communities with associated social and emotional wellbeing issues. Data is generally not available before the early 1990s because the reporting of cannabis use in remote communities was rare before this date (but it was available for urban areas and rural towns) [52]. The following studies provide data from remote communities:

  • Two studies conducted in 1999 and 2000 in Arnhem Land, Northern Territory (NT), found ‘current’ cannabis use was reported by 31% of Aboriginal males and 8% of Aboriginal females in 1999, rising to 39% of Aboriginal males and 20% of Aboriginal females in 2000 [53]. The median duration of cannabis use was 4 years, and the median age at first use was 25 years, suggesting that cannabis use was ‘a comparatively new practice in this population’ [53, p.353]. The estimated cost of cannabis use was $6,000/month for the community and $42/month per user.
  • A 2001-2002 study of Aboriginal people aged 13-36 years from three remote communities in Arnhem Land found that 67% of males and 22% of females were ‘current users’, and 69% of males and 26% of females had ‘ever used’ cannabis [8]. Among ‘current users’, 44% used cannabis on a daily or almost daily basis, 31% used on a regular weekly basis, and 26% used on an irregular monthly basis. The study estimated that 2.4 to 4.1kg of cannabis was used weekly, resulting in an estimated cost of $19,000 to $32,000/week being spent on cannabis in these communities.
  • A study conducted in several Aboriginal communities in the NT in 2001, with follow-up in 2004, reported lower prevalence of cannabis use in 2004 [11]. The reduction was most pronounced among females and older males. This study found ‘a reduction in cannabis use is supported by the decreased prevalence of adverse psychological symptoms of its use, in particular symptoms of fragmented thought processes, memory disruption, difficulties controlling use, auditory and visual hallucinations reported by cannabis users’ [11, p.702].
  • A study of three remote Aboriginal communities in Arnhem Land with data gathered in three stages (2001, 2004, and 2005-2006) [9, 11, 39] among people aged 13-42 years revealed that 49% of the 106 participants were heavy cannabis users10 (the remaining 51% of participants had never used cannabis, were former users, or were light cannabis users) [9]. The study found a strong association between heavy cannabis use and moderate to severe depressive symptoms among study participants. Data from 2005-2006 collected as part of this study found that among Aboriginal people aged 13-34 years in Arnhem Land, 61% of males and 58% of females were using cannabis on at least a weekly basis [54]. Interviews conducted with 60 cannabis users who were opportunistically recruited revealed daily use among 92% of male users and 78% of female users. Examination of data collected for only the 2001 and 2005-2006 periods revealed that more than half of the cannabis users (57% in 2001 and 55% in 2005-2006) reported heavy cannabis use [39]. Among continuing cannabis users (those who reported use in 2001 and 2005-2006), 88% demonstrated three or more symptoms of cannabis dependence, including persistent desire or unsuccessful efforts to control use, and withdrawal symptoms.
  • A study conducted between July 2010 and March 2011 in one alcohol-restricted community in Cape York, Queensland (Qld), found high levels of cannabis use among participants aged 14-50 years: around 66% of males and 31% of female participants were ‘current users’; 12% of males and 31% of females were ‘former users’; and 22% of males and 39% of females had never used cannabis [7]. Among ‘current users’, 37% used cannabis daily, 34% used cannabis weekly, and 28% used cannabis less than weekly. The mean age of cannabis users was 16 years and the mean duration of use was more than 11 years. Symptoms of dependence were evident in 64% of all users and included ‘stressing out’ when cannabis was not available.

Analgesics (pain killers) and sedatives

The 2012-2013 AATSIHS identified illicit use of analgesics and sedatives for non-medical use11 as the second most common ‘recently used’ illicit drug among Aboriginal and Torres Strait Islander people aged 15 years and older [5]. ‘Recent use’ was reported by 3.9% of respondents, with a slightly higher proportion among females than males (4.1% and 3.6%). Proportions were higher among those living in non-remote areas than those living in remote areas (4.5% and 1.8%).12

In the 2008 NATSISS, analgesics13 were ‘recently used’ by 4.5% of Aboriginal and Torres Strait Islander respondents [46]. Aboriginal and Torres Strait Islander people living in non-remote areas were almost three times more likely to use analgesics than those living in remote areas (5.4% compared to 1.9%).

The 2013 NDSHS found that 4.7% of the total Australian population aged 14 years and older had ‘recently used’ pharmaceuticals14 for non-medical reasons [3]. After age-adjustment, the proportion of Aboriginal and Torres Strait Islander people who had ‘recently used’ pharmaceuticals was 1.4 times higher than that for non-Indigenous people.15

In the 2008 NATSISS, tranquilisers/sleeping pills were ‘recently used’ by 1.4% of Aboriginal and Torres Strait Islander people aged 15 years and older. Similar to the pattern of use for analgesics, the non-medical use of tranquillisers/sleeping pills was more common for Aboriginal and Torres Strait Islander people living in non-remote areas than for those living in remote areas. The proportion of ‘recent use’ was more than four times higher in non-remote areas (1.7%) than in remote areas (0.4%). The 2007 NDSHS found that 1.4% of the total Australian population aged 14 years and older had recently used tranquillisers/sleeping pills, the same as the proportion for the Aboriginal and Torres Strait Islander population in the 2008 NATSISS [46, 47]16.

Amphetamines

Since 2007 the use of methamphetamine has remained relatively stable for the total Australian population, however, reports show that the more potent and potentially harmful crystal methamphetamine or ice has become the preferred form of methamphetamine, with use of ice more than doubling since 2010 (see also section on hospitalisation for harms associated with amphetamines) [55].

The 2013 NDSHS reported that 2.1% of Australians aged 14 years and older had ‘recently used’, and 7.0% had ‘ever used’, meth/amphetamines [3].17 After age-adjustment, the levels of ‘recently used’ meth/amphetamines among the Aboriginal and Torres Strait Islander population were similar to those among the total Australian population, but the proportion for ex use was around 1.5 times higher for Aboriginal and Torres Strait Islander people than that for non-Indigenous people [3].

The 2012-2013 AATSIHS identified amphetamines18 as the third most common ‘recently used’ illicit drug by Aboriginal and Torres Strait Islander people aged 15 years and older (2.3% of respondents) [5]. Proportions of ‘recent use’ were 1.5 times higher for males than for females (2.9% and 1.8%), and more than three times higher for those living in non-remote areas than for those in remote areas (2.8% and 0.8%)19. Between 2008 to 2012-2013, ‘recent use’ of amphetamines decreased among Aboriginal and Torres Strait Islander people living in both non-remote areas (5.0% to 2.8%) and remote areas (1.0% to 0.8%)20 [5, 22]. In the 2008 NATSISS, amphetamines were identified as the second most common drug ‘ever used’ by Aboriginal and Torres Strait Islander people (11%) [46]. In the 2008 ASSAD, a higher proportion of Aboriginal and Torres Strait Islander respondents had ‘ever used’ amphetamines compared with all ASSAD respondents (8.0% compared with 2.7%) [50]. Similarly, a higher proportion of Aboriginal and Torres Strait Islander respondents than all ASSAD respondents had used amphetamines in the previous year (7.1% compared with 2.2%), and in the previous month (4.7% compared with 1.2%). Proportions of use were slightly higher for Aboriginal and Torres Strait Islander males than for females for both age-groups and for all frequencies of use; males were twice as likely as females to have used in the previous month.

Ecstasy and other designer drugs

The 2013 NDSHS reported that 2.5% of Australians aged 14 years and older had ‘recently used’ ecstasy, and 11% had ‘ever used’ [3]. After age-adjustment, Aboriginal and Torres Strait Islander people were three times less likely to have ‘recently used’ ecstasy (0.8%) than non-Indigenous people (2.4%), but had similar proportions for ‘ex use’ (8.0% and 6.5%, respectively).

In the 2008 NATSISS,21 ‘ecstasy or designer drugs’ were identified as the fourth most common ‘recently used’ illicit drug among Aboriginal and Torres Strait Islander people aged 15 years and older (3.3%), and the third most common ‘ever used’ illicit drug (7.7%) [46]. Proportions of ‘recent use’ were almost twice as high for males than for females (4.4% and 2.3%) and ‘ever used’ was 1.5 higher for males than for females (9.6% and 6.0%). ‘Recent use’ among Aboriginal and Torres Strait Islander people living in non-remote areas was more than twice that of those living in remote areas (3.9% and 1.5%) and proportions of ‘ever used’ were almost four times higher for those living in non-remote than remote areas (9.4% and 2.6%).

In the 2008 ASSAD, 6.1% of Aboriginal and Torres Strait Islander respondents aged 12-15 years reported using ecstasy at least once in their lifetime [50]. This level was more than twice as high as that among all ASSAD respondents (2.6%). The proportions of Aboriginal and Torres Strait Islander respondents who reported using ecstasy in the previous year (5.6%) and previous month (3.6%) were higher than the corresponding proportions among all ASSAD respondents (2.2% and 1.2%, respectively). Use of ecstasy at least once was higher for older Aboriginal and Torres Strait Islander respondents (10%) than for younger respondents (2.5%). Proportions were slightly higher for Aboriginal and Torres Strait Islander males than for females; males were twice as likely as females to have used ecstasy in the previous month.

Kava

In the 2012-2013 AATSIHS, 1.3% of Aboriginal and Torres Strait Islander people aged 15 years and older reported ‘recently using’ kava, with figures higher among males than females (2.0% and 0.6%)22 [5, 22]. Similarly in the 2008 NATSISS, kava was ‘recently used’ by 1.2% and ‘ever used’ by 5.7% of Aboriginal and Torres Strait Islander people aged 15 years and older [46].

In 2008, the proportion of Aboriginal and Torres Strait Islander people aged 18 years and over reporting ‘recent use’ of kava was the same for those living in non-remote and remote areas (1.2%) (Table 4) [2]. There has been a decline in use in very remote areas since 2002 which reflects the impact of restrictions that have been placed on kava during this time [56, 57]. For details, please see the Review of the use of kava among Indigenous people (http://www.aodknowledgecentre.net.au/aodkc/illicit-drug-use/reviews/kava-review).

Table 4. Proportions (%) of recent kava use among Aboriginal and Torres Strait Islander people aged 18 years and older, by area of residence, Australia, 2002 and 2008

Major cities

Inner regional

Outer regional

Total non-remote

Remote

Very remote

Total remote

2002

0.7

1.1

0.4

0.7

0.7

4.3

3.2

2008

1.4

1.8

0.4

1.2

n.p.

1.8

1.2

Source: Steering Committee for the Review of Government Service Provision, 2011 [2]

Notes:

  1. ‘n.p.’ means ‘not provided’
  2. Data for remote areas should be viewed with caution because relative standard errors exceed 25%

Injecting drug use

As is the case for other illicit drugs, the accuracy of studies and surveys about injecting drug use may be affected by the illegal nature of the drugs involved. Additionally, studies on injecting drug use can be affected by ‘the shame and stigma that may be associated with injecting drug use’ [33, p.17].

Very few surveys and studies provide national information on injecting drug use among Aboriginal and Torres Strait Islander people [33]. Among the earliest sources of information was the 1994 Urban Aboriginal and Torres Strait Islander peoples supplement, a supplementary document to the NDSHS, which reported that 3% of Aboriginal and Torres Strait Islander respondents had injected drugs during their lifetime [58]. Among the group of 51 respondents who reported injecting drugs in the 12 months prior to the survey, 81% had injected speed (amphetamines), 20% heroin, 5% cocaine, and 11% other drugs.

A more recent national survey on sexual health among young Aboriginal and Torres Strait Islander people, The goanna surveyem[23], asked questions about risk behaviour such as illicit drugs and injecting drug use [59]. Of the 3,000 survey participants, 3% reported injecting drug(s) in the last year. The most common drugs injected were meth/amphetamine and heroin (37% and 36%), followed by methadone, morphine and cocaine (26%, 19% and 15%). The most common drug injected in regional areas was meth/amphetamine and in urban areas was heroin. Over a third (37%) of those who reported injecting drugs had shared needles.

In the 2012 Illicit drug use reporting system (IDRS), 16% of respondents identified as Aboriginal and/or Torres Strait Islander; the proportions of respondents were highest in NSW (30%) and the NT (28%) (Table 5) [60].24

Table 5. Proportion (%) of Aboriginal and Torres Strait Islander people included in the IDRS, by jurisdiction, Australia, 2012

Jurisdiction

NSW

Vic

Qld

WA

SA

Tas

ACT

NT

Australia

Proportion

30

11

16

1

11

10

15

28

16

Note:       A predetermined quota was set for the sample size of each jurisdiction.

Source: Stafford J, Burns L, 2013 [60]

No detailed information is provided by Aboriginal and/or Torres Strait Islander status for the 2012 IDRS, but the first drug of choice among all IDRS respondents was heroin (54%), followed by methamphetamine (21%) [60]. Heroin was identified as the most recent drug injected by 41% of respondents, followed by methamphetamine (26%), and morphine (15%). Heroin was the drug injected most often by respondents in the month prior to interview (42%), followed by methamphetamine (25%), and morphine (16%). In terms of frequency of use, 35% of respondents injected ‘more than weekly, but less than daily’; 21% of respondents injected ‘two to three times daily’; and 19% of respondents injected ‘once daily’.

According to data from Alcohol and other drug treatment services in Australia 2013-14, 14% of all clients receiving treatment for their own drug use were Aboriginal and Torres Strait Islander people [61]. Amphetamines and heroin (17% and 7% respectively of all closed episodes)25 were the second and third most common principal drugs of concern after cannabis for both Aboriginal and Torres Strait Islander clients and non-Indigenous clients. In 2013-14 injecting was the most common method of use for amphetamines and heroin (44% and 83% respectively).

In a study involving clients of needle and syringe programs (NSPs) across Australia in 1998-2008, around 9% of participants were Aboriginal or Torres Strait Islander people [62]. Aboriginal and Torres Strait Islander participants and non-Indigenous participants were similar ages at first use (17 and 18 years respectively) and they had the same median duration of injecting drug use (10 years). A higher proportion of Aboriginal and Torres Strait Islander participants than non-Indigenous participants reported ‘daily or more’ use in the month prior to the survey (61% compared with 53%) (Table 6). Heroin was the most commonly reported recent drug injected by all participants (38% of Aboriginal and Torres Strait Islander participants and 42% of non-Indigenous participants), followed by amphetamine/methamphetamine (31% for both Aboriginal and Torres Strait Islander participants and non-Indigenous participants).

Table 6. Proportions (%) of injecting drug users attending NSPs, by Aboriginal and Torres Strait Islander status and characteristics, Australia, 1998-2008

Characteristic

Aboriginal and Torres Strait Islander participants Non-Indigenous participants

Duration of injecting

Less than 3 years

13

14

3-8 years

29

31

9-15 years

30

26

16 years+

29

29

Drug last injected

Heroin

38

42

Amphetamine/methamphetamine

31

31

Other opiates

10

11

Cocaine/cocaine and heroin

 6

 4

Methadone/buprenorphine/subuxone

 6

 6

Injecting characteristics (month prior to survey)

Injecting frequency – daily or more

61

53

Injecting location – injected in public

54

49

Source: Ward J, Topp L, Iversen J, Wand H, Akre S, Kaldor J, Maher L, 2011 [62]

A variety of Australian studies provide valuable information about Aboriginal and Torres Strait Islander injecting drug use in specific locations:

  • A 2009 study in Victoria (Vic) found that the average age of Aboriginal and Torres Strait Islander people who inject drugs was 35 years, and most reported having injected drugs for a duration of 5 to 10 years [36]. The most commonly reported injected drugs were amphetamines and heroin.
  • Around 20% of respondents in the 2008 Pharmacy needle and syringe survey in NSW identified as Aboriginal [63]. Of these participants, the average age of injecting was 34 years and the average duration of injecting was 17 years. Around 73% of Aboriginal participants reported they injected daily or more often (compared with 55% of non-Indigenous participants). Aboriginal participants were more likely to have been in prison in the previous year, share ancillary equipment, and have less knowledge about hepatitis C.
  • A 2001 study conducted in SA, involving 307 Aboriginal and Torres Strait Islander people who inject drugs, found that heroin was used by 97% of study participants in the previous six months; 85% of participants used heroin at least once per day [37]. Methamphetamine was used by 68% of participants; it was used daily by 32% of participants and used ‘at least once a week’ by 36% of participants.

Poly-drug use

Poly-drug use refers to use of multiple drugs at the same time (concurrent use) or substituting one drug for another when the preferred one is not available [1, 64]. The 2008 NATSISS reported that 6.4% of Aboriginal and Torres Strait Islander people aged 15 years and older had recently used two or more illicit drugs [46]. Aboriginal and Torres Strait Islander males were more likely than Aboriginal and Torres Strait Islander females to use two or more substances (8.9% compared with 4.0%).

The 2008 ASSAD reported that Aboriginal and Torres Strait Islander participants aged 12-15 years used more than one drug concurrently in similar proportions to that found among all ASSAD participants [50]. The three drugs most commonly used in combination were alcohol, cannabis, and tobacco. Aboriginal and Torres Strait Islander participants reported concurrent use of cannabis with alcohol (58%), and cannabis with tobacco (42%). The combination of cannabis and other illicit drugs also occurred, but less frequently (Table 7).

Table 7. Proportion (%) of ASSAD participants aged 12-15 years who engaged in concurrent substance use in the 12 months prior to interview, by Aboriginal and Torres Strait Islander status and type of substance, Australia, 2008

Type of substance

Concurrent use with cannabis Concurrent use with amphetamines Concurrent use with ecstasy
 

Aboriginal and

Torres Strait

Islander

All ASSAD

Aboriginal and

Torres Strait

Islander

All ASSAD

Aboriginal and

Torres Strait

Islander

All ASSAD

Alcohol

58

58

52

48

55

61

Tobacco

42

43

35

34

36

42

Cannabis

40

32

54

39

Hallucinogens

6.6

4.9

17

10

14

15

Amphetamines

3.6

5.8

24

14

Ecstasy

13

8.8

26

15

Analgesics

12

9.4

19

7.3

10

9.7

No other substances used

29

29

21

29

12

19

Source: Smith G, White V, 2010 [50]

Of the 7.1% of Aboriginal and Torres Strait Islander participants in the 2008 ASSAD who reported use of amphetamines in the past year, 52% also used alcohol, 40% used cannabis, and 35% used tobacco on the same occasion (Table 7) [50]. Of the 5.6% of Aboriginal and Torres Strait Islander participants who reported using ecstasy in the past year, 55% had also used alcohol (55%), cannabis (54%), and tobacco (36%) on the same occasion. Similar proportions were found among all ASSAD respondents, but use of ecstasy and cannabis on the same occasion was more common among Aboriginal and Torres Strait Islander respondents (54% compared with 39%).

There are no detailed national data, but a number of specific studies provide information on poly-drug use among Aboriginal and Torres Strait Islander people:

  • Studies conducted in Arnhem Land suggest a correlation between cannabis use and the use of other substances [8, 9, 39]. In 2005-2006, petrol sniffing was a ‘key predictor of heavy [cannabis] use’ [39, p.627], similar to findings in a 2007-2009 study in the NT [65]. Another study, conducted in 2001 with follow-up in 2004, noted that ‘cannabis use was associated strongly with tobacco use, alcohol use and petrol sniffing at baseline and these same associations held in the sample at follow-up’ [11, p.699]. A 2001-2002 study expressed concern about the concurrent use of cannabis and alcohol and the concurrent use of cannabis and petrol sniffing [8]. The study found that the people who continued petrol sniffing and those who reported using ‘speed’ (likely methamphetamine) were all current cannabis users. In 2001, concurrent substance use was common among heavy cannabis users, with tobacco and alcohol being the most commonly used substances [9].
  • A 2001 study of Aboriginal and Torres Strait Islander injecting drug users in SA found that poly-drug use was very common [37]. Most study participants used four different drugs or drug types during the six months prior to interview, most commonly cannabis and heroin, cannabis and amphetamines, amphetamines and alcohol, heroin and alcohol, and heroin and methadone.

Health impacts of drug use among Aboriginal and Torres Strait Islander people

While some of the various health impacts of illicit drug use result in hospitalisation or death, many do not. Illicit drug use is estimated to be responsible for 3.4% of the overall burden of disease among Aboriginal and Torres Strait Islander people and 2.8% of deaths (compared with 2.0% and 1.3% respectively among the total population) [17, 66].

Harms associated with cannabis

Cannabis use has been linked with a variety of mental health harms among Aboriginal and Torres Strait Islander people, including mild changes of mood, lack of motivation, anxiety, fragmented thought processes, memory disruption, depression, and psychosis [9, 11, 65, 67-70]. Studies suggest that mental health risks increase with increased use of cannabis [65, 69].

Evidence also suggests that cannabis use is implicated in suicidal ideation [71]. A WA study reviewing the State’s coronial records for suicides among people aged 15-24 years in 1986-1998 found that cannabis was the illicit drug most commonly detected during suicide post-mortems, being detected in 20% of males and 11% of females [72].

Harms associated with injecting drug use

There are a number of health harms associated specifically with injecting drug use, particularly infection with hepatitis C and HIV. The increased transmission of these viruses among people who inject drugs is due to the sharing of injecting equipment [73]. Aboriginal and Torres Strait Islander people who inject drugs identified that feelings of shame and discrimination affected their ability to access new injecting equipment from NSPs and other substance use services [33, 36, 74].

A study conducted at NSPs across Australia in 1998-2008 found that a higher proportion of Aboriginal and Torres Strait Islander people who inject drugs than non-Indigenous people who inject drugs reported using a new needle for all injections in the previous month (73% and 70% respectively), but Aboriginal and Torres Strait Islander people who inject drugs were more receptive than their non-Indigenous counterparts to needle sharing (21% and 16%), and the sharing of other injecting drug equipment (38% and 33%) [62].

A NSW study in 2008 involving pharmacy needle and syringe exchanges found that 38% of Aboriginal participants had re-used another person’s needle and 65% had re-used another person’s ancillary injecting equipment in the previous month [63]. Earlier studies show variability in the proportion of Aboriginal and Torres Strait Islander people who inject drugs re-using injecting equipment: 39% of Aboriginal and Torres Strait Islander participants in a 1996 Brisbane study reported sharing equipment in the previous month [75]; 14% of Aboriginal and Torres Strait Islander respondents in a 2001 SA study reported sharing equipment in the last 2-3 months [30]; and 43% of Aboriginal participants in a study conducted in WA in 2001 reported ‘normally’ sharing needles [76].

Hepatitis C

Around 80-90% of Australia’s hepatitis C infections are caused by injecting drug use [62, 77]. Studies found that the prevalence of hepatitis C among injecting drug users remained around 50% between 1996 and 2004 [77]. The prevalence of hepatitis C infections is strongly associated with the duration of injecting drug use; incidence is also related to the type of drug injected (the highest rates for 1999-2005 being for cocaine (83 per 100 person-years), heroin (38), and amphetamine (13)).

Of the 6,317 people diagnosed with hepatitis C in WA, SA, Tas and the NT in the three-year period 2011-2013, 847 (15%) were identified as Aboriginal and Torres Strait Islander [78]. The rate of diagnosis of hepatitis C was significantly higher for Aboriginal and Torres Strait Islander people than that for non-Indigenous people (142 and 41 per 100,000, respectively). In 2013, the rates of diagnosis were much lower for Aboriginal and Torres Strait Islander people living in the NT (41 per 100,000) and Tas (90 per 100,000) than for those living in WA (211 per 100,000) and SA (204 per 100,000). Notification rates of newly diagnosed hepatitis C infections for Aboriginal and Torres Strait Islander people in WA, SA, Tas and the NT increased from 110 per 100,000 in 2009 to 142 per 100,000 in 2013. In contrast, rates for the non-Indigenous population decreased slightly, from 44 per 100,000 in 2009 to 41 per 100,000 in 2013.

Treatment for hepatitis C is currently available, but uptake among people who inject drugs is low [79]. A recent study examining the uptake of treatment among people who inject drugs at Australian NSPs between 1999 and 2011 found that 10% of participants identified as Aboriginal and Torres Strait Islander. During this time, the proportion of all participants currently receiving treatment increased from 1.1% to 2.1%; for those who had ever received treatment, the proportion increased from 3.4% to 8.6%.

HIV

As is the case for hepatitis C, HIV infections can result from the sharing of injecting equipment. During 2004 to 2011, the rate of HIV diagnosis among Aboriginal and Torres Strait Islander people remained relatively stable (3.5 per 100,000). In 2012 and 2013, this figure increased to 4.8 per 100,000 [78].26 Among non-Indigenous people, the rate of HIV diagnosis also remained stable during 2004 to 2011 (3.8 per 100,000), increasing to 4.2 per 100,000 in 2012 and then decreasing to 3.0 per 100,000 in 2013.

HIV transmission through injecting drug use is much more common among Aboriginal and Torres Strait Islander people than among non-Indigenous people [78]. In 2009-2013, 12% of newly diagnosed HIV cases among Aboriginal and Torres Strait Islander people were attributed to injecting drug use, compared with 3% of cases among non-Indigenous people.

Other harms associated with injecting drug use

In addition to hepatitis C and HIV infection, a number of other health harms are associated with injecting drug use. A study conducted in SA in 2001 found that among Aboriginal and Torres Strait Islander people who inject drugs a median of eight health problems were reported by participants [30]. The most commonly reported physical reactions included poor appetite (reported by 82% of participants), hot or cold flushes (80%), and a lack of energy (79%) (Table 8). Several of these symptoms are consistent with withdrawal symptoms, and others are due to intoxication. Participants reported an average of five injecting-related health problems, most commonly track marks (81%), shaking and shivering (66%), and nausea (55%).

Table 8. Proportion (%) of Aboriginal and Torres Strait Islander participants reporting physical reactions and injecting-related health problems from injecting drug use, SA, 2001

Physical reactions

Proportion of participants Injecting-related health problems Proportion of participants

Poor appetite

82

Track marks

81

Hot or cold flushes

80

Shaking or shivering

66

Lack energy

79

Nausea

55

Aching muscles or joints

76

Headache due to hit

54

Headache

69

Vein problems

52

Nausea

65

Hurt self while intoxicated

41

Teeth

51

Dirty hit

27

Breathing problems

49

Virus from injecting

22

Stomach problems

48

Liver problems

39

Skin problems

33

Virus

25

Heart problems

17

Source: Holly C, Shoobridge J, 2004 [30]

Overdose

The 2012 IDRS included information on non-fatal and fatal overdose from several types of illicit drugs that can be administered via injection, but no detailed information is available by Aboriginal and Torres Strait Islander status [60].27 For non-fatal overdose, 41% of respondents had overdosed on heroin at some point in their lifetime, with a median of two overdoses. Of those who had ever overdosed on heroin, 20% had done so during the previous year and 2% during the previous month; of those participants who had overdosed in the previous year, 18% did not receive treatment. During 2008, there were 500 accidental deaths among people aged 15-54 years from all types of opioids. The number of accidental deaths from opioids was highest in Vic (170) and NSW (137). Males accounted for 74% of overdose deaths. The largest proportion of these deaths occurred among people aged 25-34 years.

Impacts on social and emotional wellbeing

Illicit drug use is associated with a number of negative outcomes for social and emotional wellbeing. The 2012-2013 AATSIHS reported that 73% of Aboriginal and Torres Strait Islander people aged 15 years and older had experienced at least one stressor in the previous year; 11% had experienced stressors associated with drug-related problems [80]. The highest proportion of drug-related stressors occurred in the 25-34 years age-group (14%). The 2008 NATSISS found that Aboriginal and Torres Strait Islander people aged 15 years and over who reported high levels of psychological distress were more likely to report they had recently used illicit drugs in the last 12 months compared to those who had never used illicit drugs (40% and 28%, respectively) [22].

A 2007-09 NT study found associations between the use of a variety of drugs (cannabis, inhalants, alcohol, and tobacco) and depression or anxiety [65]. It found that ‘together these results suggest that symptoms of depression or anxiety may be common for individuals seeking treatment for substance misuse’ [65, p.36]. Cannabis use among Aboriginal and Torres Strait Islander people has been linked with anxiety, depression, and psychosis (see section on harms associated with cannabis for details) [9, 11, 67-69]. Injecting drug use among Aboriginal and Torres Strait Islander people also impacts on their social and emotional wellbeing. A 2001 study of Aboriginal and Torres Strait Islander people who inject drugs in SA found a median of nine mental health symptoms was reported by participants, including mood swings (84%), less enjoyment of things (84%), and sleeping problems (84%) [30]. The study also reported a median of five social problems, mostly financial problems and difficulties in relationships with family, friends, and others.

Hospitalisation

Hospitalisation data for illicit drug use relate only to conditions that are directly attributable to drug use; they do not include ‘conditions where drug use may be a contributing factor but where the link is not direct and immediate’ [13, p. 11.15].

The most recent detailed national information on hospital separations related to drug use for Aboriginal and Torres Strait Islander people is available for the period 2012-13 [13]. The most common drug-related conditions resulting in hospitalisation were for ‘poisoning’ and ‘mental and behavioural disorders’. The hospitalisation rate for poisoning for Aboriginal and Torres Strait Islander people was more than twice the rate for non-Indigenous people (284 per 100,000 and 124 per 100,000, respectively) (Table 9). The hospitalisation rate for mental and behavioural disorders for Aboriginal and Torres Strait Islander people was around three times the rate for non-Indigenous people (262 per 100,000 and 85 per 100,000 respectively).

Drug-related hospitalisations for mental/behavioural disorders had the highest rate of separations from the use of amphetamines28 than for any other type of drug for the total population [13]. The rate for Aboriginal and Torres Strait Islander people was three times higher than the rate for non-Indigenous people (76 per 100,000 and 23 per 100,000, respectively) [13]. Analysis of hospital separations for the total population show that, between 2008-09 and 2012-13, hospital separations for psychotic disorders due to methamphetamine use increased by 312% [55]. In 2012-13, hospitalisation of Aboriginal and Torres Strait Islander people for mental/behavioural disorders from the use of cannabinoids (71 per 100,000) was more than four times higher than that for non-Indigenous people (16 per 100,000).

Table 9. Age-standardised hospital separations relating to drug use, by Aboriginal and Torres Strait Islander status and principal diagnosis, Australia 2012-13

Diagnosis group/principal diagnosis

Aboriginal and Torres Strait Islander

Non-Indigenous

Rate ratio

Poisoning 

Antibiotics and hormones

69.0

38.3

1.8

Narcotics including opium, heroin, methadone and cocaine

51.4

15.0

3.4

Antiepileptic, sedative-hypnotic and antiparkinsonism drugs

73.0

31.3

2.3

Psychotropic drugs, includes antidepressants

86.0

38.6

2.2

Toxic effect of organic solvents

4.4

1.1

4.0

Total

283.8

124.3

2.3

Accidental poisoning 

Antidepressants and barbiturates

42.5

15.2

2.8

Narcotics (includes cannabis, cocaine, heroin, methadone, opium) and hallucinogens

32.6

10.3

3.2

Organic solvents, including petroleum derivatives

2.5

0.8

3.3

Unspecified (includes glues and paints)

13.3

7.0

1.9

Total

83.5

30.6

2.7

Mental/behavioural disorders

From use of opioids

42.4

18.6

2.3

From use of cannabinoids

71.1

16.3

4.4

From use of sedatives

11.4

6.6

1.7

From use of cocaine

1.2

1.4

0.8

From use of other stimulants

76.2

22.6

3.4

From use of hallucinogens

1.1

0.6

1.9

From use of volatile solvents

7.1

0.1

48.2

From use of multiple drug and psychoactive substances

51.3

19.0

2.7

Total

261.8

85.4

3.1

Other

Acute hepatitis C

1.5

0.4

3.7

Maternal care for suspected damage to fetus by drugs

0.3

Neonatal withdrawal symptoms from maternal use of drugs of addictions

6.7

1.9

3.5

Total

8.5

2.4

3.6

Source: AIHW, 2014 [13]

Notes:

  1. Rates are per 100,000 population; age-standardised using the Australian 2001 standard population
  2. Rate ratio is the Aboriginal and Torres Strait Islander rate divided by the non-Indigenous rate
  3. Non-Indigenous includes hospitalisations for non-Indigenous people; only for WA does it includes hospitalisations where Aboriginal and Torres Strait Islander status was not recorded
  4. See original source for relevant ICD codes

Aboriginal and Torres Strait Islander people living in major cities were more likely to be hospitalised for drug-related conditions than those living in remote areas (372 per 100,000 and 181 per 100,000) [13].

In NSW, Vic, Qld, WA, SA and the NT, rates for hospital separations due to poisoning for Aboriginal and Torres Strait Islander people increased from 149.2 per 100,000 in 2004-05 to 289.4 per 100,000 in 2012-13 [13]. Compared to other Australians, rate ratios for Aboriginal and Torres Strait Islander people for separations due to poisoning increased from 1.3 to 2.3.

Mortality

In 2008-2012, the age-adjusted death rate for drug-related deaths was 1.5 times higher for Aboriginal and Torres Strait Islander people living in NSW, Qld, WA, SA and the NT than that for their non-Indigenous counterparts (Table 10) [13]. The rates for Aboriginal and Torres Strait Islander people in SA was three times higher than that for the total Aboriginal and Torres Strait Islander population (22 compared with 9.9 per 100,000).

Table 10. Age-standardised rates of drug-related deaths, by Aboriginal and Torres Strait Islander status and jurisdiction, and Aboriginal and Torres Strait Islander:non-Indigenous rate ratios, NSW, Qld, WA, SA, and the NT, 2008-2012

Jurisdiction

Aboriginal and Torres Strait Islander

Non-Indigenous

Rate ratio

NSW

12.6

6.2

2.0

Qld

7.2

6.3

1.1

WA

8.7

7.1

1.2

SA

22.3

6.8

3.3

NT

n.p.

3.8

NSW, Qld, WA, SA and the NT

9.9

6.4

1.5

Source: Steering Committee for the Review of Government Service Provision, 2014 [13]

Notes:

  1. Rates are per 100,000 (indirect method of age-standardisation)
  2. ‘n.p.’ means ‘not provided’

Between 2003-2007, more than one-half (52%) of the 63 drug-related deaths of Aboriginal and Torres Strait Islander people in NSW, Qld, WA, SA and the NT were due to accidental poisoning from narcotics; almost one-in-six (17%) were caused by accidental poisoning from organic solvents [81]. Among their non-Indigenous counterparts, there were 993 drug-related deaths in the same time period, 53% of which were due to accidental poisoning from narcotics and 28% from accidental poisoning from antidepressants.

Suicide

Drug use has been identified as a major risk factor for suicide among Aboriginal and Torres Strait Islander people [11, 12]. Drug use can increase the risk of suicide ‘through the short-term effects of intoxication increasing the likelihood of impulsive suicide, and through the indirect effects of longer-term use and/or dependency resulting in accumulating psychosocial stress triggering, or by exacerbating existing mental health disorders’ [72, p.vii]. Cannabis use, in particular, has been associated with suicidal ideation [71].

The actual extent to which drug use contributes to suicide among Aboriginal and Torres Strait Islander people is not known, but the suicide death rate for Aboriginal and Torres Strait Islander people living in NSW, Qld, WA, SA, and the NT in 2012 was 2.0 times the rate reported for non-Indigenous people [82]. It was the fifth leading specific cause of death among Aboriginal and Torres Strait Islander people.

For the period 2008-2012, deaths from intentional self-harm were much higher for Aboriginal and Torres Strait Islander people living in NSW, Qld, WA, SA, and the NT than for their non-Indigenous counterparts; age-standardised death rates ranged from 14.0 per 100,000 in NSW to 39.1 per 100,000 in WA [82]. In those jurisdictions for which details for females were available, death rates were higher for Aboriginal and Torres Strait Islander males than for females.

In the absence of comprehensive information on the association between drug use and Aboriginal and Torres Strait Islander suicide, specific studies provide some insights into the links between drug use, mental illness, and Aboriginal and Torres Strait Islander suicide (because these studies examine discrete populations, the findings cannot be generalised):

  • A study examining suicide among Western Australians aged 15-24 years during 1986-1998 found that the drugs most commonly associated with suicide were alcohol and cannabis [72]. Cannabis was detected in 20% of male deaths and 11% of female deaths; stimulants were detected in 9% of male and 8% of female deaths; and opiates were detected in 7% and 12% of male and female deaths.29 Illicit drugs were detected among fewer Aboriginal and Torres Strait Islander males who had attempted suicide than among non-Indigenous males (25% and 31%, respectively).30
  • A study investigating suicide trends in the NT from 1981 to 2002 found that, by 2001-2002, Aboriginal and Torres Strait Islander males had the highest age-adjusted suicide rates (66.3 per 100,000 compared with 34.0 per 100,000 for non-Indigenous males) [83]. Aboriginal and Torres Strait Islander females also had higher suicide rates than those for their non-Indigenous counterparts (11.2 per 100,000 and 5.9 per 100,000, respectively). Between 1981 and 2002 there was an 800% increase in suicide rates among Aboriginal and Torres Strait Islander males; for Aboriginal and Torres Strait Islander females the rate rose from 2.2 per 100,000 in 199131 to 11.2 per 100,000 in 2002. The study found that diagnosed mental illness was present in 49% of all suicides among both Aboriginal and Torres Strait Islander people and non-Indigenous people in the Top End of the NT in 2000-2002. Excluding alcohol use, other drug use was involved in 16% of deaths by suicide (overall, 71% of suicides were associated with alcohol and other drug use).
  • Extensive multi-stage research on suicide among Aboriginal and Torres Strait Islander people in the NT during 1996-2007 reported that ‘alcohol and other substance abuse have been found to play a definitive role in co-morbid mental, physical and behavioural disorders implicated in completed suicide in the NT’ [84, p.16]. Cannabis was detected in 19% of suicides among Aboriginal and Torres Strait Islander people in 1996-2006 [85]. Cannabinoids and hallucinogens were detected in 30% of younger and 20% of older Aboriginal and Torres Strait Islander people who died from ‘external causes of death’ [86].
  • A 2000 study that interviewed 25 Aboriginal people who inject drugs in the Lower Murray region of SA found that more than one-half of study participants (13 people) had attempted suicide at least twice [87]. Of these 13 people, 12 (92%) had attempted suicide while intoxicated, noting that intoxication often facilitated the decision. The drugs used when attempting suicide were alcohol (two participants), benzodiazepines (two participants), amphetamines (one participant), or a combination of drugs (four participants).

Social impacts of drug use among Aboriginal and Torres Strait Islander people

As well as health impacts, the use of illicit drugs is associated with a number of social impacts, including domestic violence, assaults, and crime.

Child and family harm

Illicit drug use can negatively affect families, in particular children. Harmful alcohol and other drug use is one of the ‘“key risk factors” for child abuse and neglect’ [88, p.2], contributing to an unsafe and harmful environment for children. Parents who use drugs may be unable to undertake routine household tasks or focus on the needs of their child if they are feeling symptoms of intoxication or withdrawal [89]. Drug use may also cause financial difficulties and parents may favour buying drugs instead of household essentials like food and clothes [90]. Children whose parents use illicit drugs are more likely to witness family violence.

There is a recognised association between family violence and drug use. Drug use can be a contributing factor and/or the result of family violence [90, 91]. Research in the field of drug use and violence indicates that ‘Indigenous family violence is increasingly acknowledged to be interconnected with levels of drug and alcohol misuse’ [90, p.52], and that ‘there is also evidence to show that the use of other substances – particularly cannabis and, to a lesser extent, amphetamines and inhalants – contributes to violent crime, particularly family violence, and conflict within the community’ [91, p.46]. A 2005 study in the NT, Qld, SA, and WA found that the vast majority of urban and non-urban police thought that family violence was affected by cannabis (73% and 76%, respectively) and amphetamines (67% and 46%) [92]. Evidence suggests that children who experience family violence and neglect may be more likely to become perpetrators of violence [93].

Illicit drug use negatively affects families in other ways, including tension within families. A study of Aboriginal and Torres Strait Islander people who inject drugs in Vic found that ‘the biggest concern with the clients interviewed for the project was their family’s negative reaction towards their injecting drug use behaviour’ [36, p.21]. In particular, clients cited fears of shaming and stigma from their family and community, as well as the potential for physical violence, if the family learned of their habit. These fears directly affected how they accessed injecting equipment, with many clients unwilling to collect clean injecting equipment from Aboriginal and Torres Strait Islander community-controlled health services where they may be identified by members of their community, preferring instead to use mainstream services that were more anonymous.

Community harm and violence

Illicit drug use can adversely affect the whole community; one effect is the perception of safety within the community. The 2008 NATSISS found that 36% of Aboriginal and Torres Strait Islander people 15 years and older reported that illegal drugs were a problem in their neighbourhood or community [2, 46]. A 2009-2010 study examining the perception of community safety in Aboriginal and Torres Strait Islander communities in NSW, Qld, WA and the NT found that 62% of respondents thought that illegal drug use was a social problem in their community [94].

Violence, including assault and homicide, is associated with drug use: the 2008 NATSISS found that Aboriginal and Torres Strait Islander people aged 15 years and older who had used substances in the 12 months prior to the survey were twice as likely to have been the victim of physical or threatened violence (40%) than were Aboriginal and Torres Strait Islander people who had not used substances (19%) [49].

From 1999-2000 to 2008-2009, there were 335 Aboriginal and Torres Strait Islander victims of homicide in Australia, almost one-quarter (24%) of which involved drugs [2]. Of all Aboriginal and Torres Strait Islander victims of homicide, 8.4% occurred when both the victim and offender were under the influence of drugs (compared with 7.7% for non-Indigenous victims of homicide); 12% occurred when only the victim was under the influence of drugs (compared with 15% for non-Indigenous victims of homicide); and 3.9% occurred when only the offender was under the influence of drugs (compared with 7.6% of non-Indigenous victims of homicide).

Crime and incarceration

Imprisonment rates for Aboriginal and Torres Strait Islander people are much higher than those for non-Indigenous people; in 2013 rates were 15 times higher for Aboriginal and Torres Strait Islander people than those for non-Indigenous people [95]. Links between crime, incarceration, and illicit drug use are complex. Studies have found that illicit drug use and crime co-exist in the same populations [96-99]. Such links are illustrated in the following surveys:

  • In 2010, 68% of Aboriginal and Torres Strait Islander prison entrants reported illicit drug use in the previous 12 months, a similar proportion as non-Indigenous prison entrants (65%) [100]. Among Aboriginal and Torres Strait Islander prison entrants, the most commonly used illicit drugs were cannabis (54%), meth/amphetamine (19%), and analgesics (17%). Non-Indigenous prison entrants were twice as likely as Aboriginal and Torres Strait Islander prison entrants to have used synthetic drugs (including meth/amphetamines and ecstasy).
  • The 2009-10 Drug use monitoring in Australia (DUMA) survey found that 66% of detainees tested positive for at least one drug [97].32 In this time period, 45% of detainees reported that their current offence related to drug use. Alcohol was more likely to be a contributing factor for violence and drink driving offences, whereas drugs such as heroin and amphetamines were more likely to be related to property and drug offences.
  • A 2009 survey of the health of prison inmates in NSW found that 43% of inmates had used an illicit drug while in prison and 17% had injected drugs while in prison [101]. The survey also found that inmates were at increased risk of contracting hepatitis C and HIV due to a lack of new injecting equipment. Of the 112 participants who reported injecting drug use in prison, only 2.7% had used a new needle. Almost one-half (48%) of inmates reported that obtaining drugs in prison was ‘quite easy’ or ‘very easy’.
  • The 2008 Pharmacy needle and syringe survey in NSW found that a higher proportion of Aboriginal participants than non-Indigenous participants had been to prison in the year prior to the survey (38% compared with 17%) [63]. This study found that ‘Aboriginal respondents had significantly more risk factors for the acquisition of hepatitis C, including being more likely to have been to prison in the previous year’ [63, p.3].

Policies and strategies

National Drug Strategy 2010-2015

Australia’s National drug strategy (NDS) provides a national framework for actions to minimise drug use-related harms in Australia. The aim of the NDS 2010-2015 is to ‘build safe and healthy communities by minimising alcohol, tobacco and other drug-related health, social and economic harms among individuals, families and communities’ [102, p.4]. Since its inception in 1985, the NDS has been guided by the harm minimisation approach. This approach is based on three pillars: demand reduction; supply reduction; and harm reduction.

Demand reduction

Demand reduction strategies aim to prevent and/or delay the use of alcohol and other drugs; and to minimise harms among people who are already using drugs [102, 103]. They also support the recovery of people who are dependent on drugs. Demand reduction ‘embraces a wide range of strategies including health promotion, treatment and ongoing care’ [103, p.5].

Supply reduction

Supply reduction strategies aim to reduce the availability of illegal drugs and control and regulate the supply of legal drugs, such as alcohol and tobacco [102, 103].

Harm reduction

Harm reduction strategies aim to reduce drug-related harms for individuals, families and the community, without necessarily reducing the use of drugs [102, 103].

National Drug Strategy Aboriginal and Torres Strait Islander Peoples Complementary Action Plan 2003-2009

The first National drug strategy Aboriginal and Torres Strait Islander Peoples complementary action plan (CAP) (2003-2006) was prepared in 2003, and later extended to 2003-2009 to bring it into line with the NDS [104, 105]. The CAP was developed ‘in recognition of the need for deliberate action to address the specific needs of Indigenous people affected by alcohol and drugs’ [104, p.3]. The CAP complemented the NDS, providing national direction for communities, non-government organisations, Aboriginal and Torres Strait Islander community-controlled health organisations, and governments to provide appropriate strategies for Aboriginal and Torres Strait Islander people.

The CAP underwent an external review in 2009 and was found to be well regarded and valuable [104]. It provided a useful framework for policy makers and service providers for implementing culturally appropriate approaches to Aboriginal and Torres Strait Islander drug use. However it was also found to have limitations as an ‘action plan’ in that the key result areas do not identify specific actions on how these priority areas should be addressed. The recommendations from this review indicated that the CAP should be retained and updated through a culturally-appropriate consulting process. The revised CAP should be more concise and user-friendly, with streamlined reporting requirements and improved monitoring processes to more effectively measure the outcomes of the key result areas.

National Aboriginal and Torres Strait Islander Peoples Drug Strategy 2014-2019

The National Aboriginal and Torres Strait Islander peoples’ drug strategy 2014-2019 is a sub strategy of the NDS and builds upon the strengths of the CAP to identify four priority areas [106]. For each of the priority areas, the strategy outlines a range of intended outcomes and suggested actions for how these can be achieved:

  • Priority area one – build capacity and capability of the alcohol and other drug service system, particularly Aboriginal and Torres Strait Islander‐controlled services and its workforce, as part of a cross‐sectoral approach with the mainstream alcohol and other drug services to address harmful alcohol and other drug use.
  • Priority area two – increase access to a full range of culturally responsive and appropriate programs, including prevention and interventions aimed at the local needs of individuals, families and communities to address harmful alcohol and other drug use.
  • Priority area three – strengthen partnerships based on respect both within and between Aboriginal and Torres Strait Islander peoples, government and mainstream service providers, including in law enforcement and health organisations, at all levels of planning, delivery and evaluation.
  • Priority area four – establish meaningful performance measures with effective data systems that support community‐led monitoring and evaluation [106].

In relation to illicit drug use, these priorities are directed toward:

  • reducing the levels of illicit and licit drug use
  • reducing offending related to substance use and involvement in the criminal justice system
  • reducing blood-borne viral infections due to injecting drug use [106].

Policies for specific types of illicit drugs

There are a number of national policies that focus on specific types of illicit drugs or their route of administration. These policies generally do not focus specifically on Aboriginal and Torres Strait Islander people, but many include them as a priority population.

Injecting drug use related policies

A number of Australian policy documents include information relevant to injecting drug use and associated blood-borne viruses. These documents include the:

  • Fourth national Aboriginal and Torres Strait Islander blood borne viruses and sexually transmissible infections strategy 2014-2017 [107]
  • National hepatitis B strategy 2010-2013 [108]
  • Fourth national hepatitis C strategy 2014-2017 [109]
  • Sixth national HIV strategy 2010-2013 [110]
  • National needle and syringe programs strategic framework 2010-2014 [111].

All of these policies identify Aboriginal and Torres Strait Islander people as a priority population [107-111]. These policies all advocate for harm reduction through the increased availability of clean injecting equipment, often delivered through NSPs, as well as increased peer education, the reduction of stigma associated with injecting drug use, and integrated health services that can appropriately cater to the needs of Aboriginal and Torres Strait Islander people who inject drugs. The need for improved data collection, which includes Aboriginal and Torres Strait Islander status, is also highlighted.

The Australian National Council on Drugs (ANCD) released a position paper on NSPs in 2013 that outlined 12 recommendations to all Australian governments [112]. These recommendations aimed primarily to increase the provision of safe injecting equipment to people who inject drugs, and secondarily to have NSPs function as additional health and education services, and to provide referrals to people who inject drugs. Two of the recommendations targeted towards Aboriginal and Torres Strait Islander people include: providing NSP staff with culturally appropriate training; and encouraging the employment of Aboriginal and Torres Strait Islander people at NSPs.

Cannabis related policy

The Ministerial Council on Drug Strategy’s National cannabis strategy 2006-2009 aimed to reduce cannabis use and the associated harms [70]. It is consistent with the harm minimisation approach of the NDS and supports the priorities and key results of a number of other national policies. This policy identified Aboriginal and Torres Strait Islander people as a priority population and outlined four priority areas: community cannabis education; preventing the use of cannabis; preventing problems associated with cannabis; and responding to problems associated with cannabis. Each of these areas encompasses supply, demand, and harm reduction strategies. Many of the responses outlined in the policy relate to the creation and use of specific resources for Aboriginal and Torres Strait Islander people, developed in partnership with communities, as well as increasing the workforce capacity of Aboriginal and Torres Strait Islander health workers.

Amphetamine related policy

The National Ice Taskforce was established in April 2015 to develop a National ice action strategy in response to the issues surrounding the drug crystal methamphetamine (ice). As part of the terms of reference, the taskforce examined the impact of ice on individuals and communities, including specific populations such as regional populations and Aboriginal and Torres Strait Islander people [113].

Six areas for action were identified in the interim report:

  • target primary prevention
  • improve access to early intervention, treatment and support services
  • support local communities to respond
  • improve tools for frontline workers
  • focus law enforcement actions
  • improve and consolidate research and data [113].

The final report makes a number of recommendations including that the ‘Commonwealth, state and territory governments, in close consultation with Aboriginal Community Controlled Organisations, should take steps to  improve access to integrated, evidence-based, culturally appropriate services for Indigenous Australians’ [114, p. xi].

Programs and services

Current alcohol and other drug services aim to reduce the harms from drug use in three ways:

  • primary prevention: preventing the uptake of drug use
  • secondary prevention: minimising the harms of short-term/experimental drug use and preventing drug dependency
  • tertiary prevention: reducing the harms from chronic drug use and providing rehabilitation [1].

All three levels of intervention are important in Australia’s harm minimisation policy framework (demand reduction, supply reduction, and harm reduction). The table below (Table 11) demonstrates how services addressing Aboriginal and Torres Strait Islander drug use fit within the three pillars of harm minimisation and the three levels of prevention (note that services addressed in this review are not exhaustive).

Table 11. Services by pillar of harm minimisation and type of prevention

Demand reduction Supply reduction              Harm reduction

Primary prevention

(preventing the uptake of drugs)

  • Addressing social determinants
  • Recreational activities
  • Education
  • Health promotion campaigns
  • Law enforcement

Secondary prevention

(minimising the harms of short-term use; preventing drug dependency)

  • Brief interventions
  • Diversion of offenders
  • Education
  • Health promotion campaigns
  • Primary health care
  • Community-based treatment
  • Counselling and support services
  • Law enforcement
  • Night patrols
  • Sobering-up shelters
  • Needle and syringe programs

Tertiary prevention

(reducing harms from chronic use; rehabilitation)

  • Primary health care
  • Community-based treatment
  • Residential treatment
  • Counselling and support services
  • Sobering-up shelters
  • Needle and syringe programs

Sources: Gray et al, 2008 [1], Gray et al, 2010 [41]

Notes:

  1. List of services is not exhaustive
  2. Services may fit in multiple categories
  3. Services exclude those for alcohol exclusively (notably supply control of alcohol)

Many services address more than one prevention classification, for example, education, health promotion campaigns, and supply-side law enforcement all aim to prevent (primary prevention) or minimise (secondary prevention) the use of harmful drugs.

In 2013-14, the Australian Government provided grants to around 269 organisations to fund primary health care and other services, including alcohol and other drugs services, to Aboriginal and Torres Strait Islander people [115]. Fifty-six organisations providing alcohol and other drug services to Aboriginal and Torres Strait Islander people contributed to the ‘online services report’ (OSR). These services provided treatment to around 43,000 Aboriginal and Torres Strait Islander clients, a 13% decrease from 2012-13.33 Organisations in outer regional areas reported having around 14,000 (32%) clients, while ‘very remote areas’ reporting having around 12,000 (27%) clients. Case management (96%), education (96%), and counselling (93%) were the most common treatment approaches for all of these services. The most common issues reported for illicit drugs related to cannabis (100%), multiple drug use (57%), and amphetamines (45%).

Primary prevention

Primary prevention interventions aim to minimise the risk of harmful drug use by addressing the underlying social determinants and educating the public on the harms associated with drug use in the hope of decreasing and delaying use [1].

Social determinants

It is widely acknowledged that addressing the social determinants across the lifespan may help to reduce harmful drug use and lead to a variety of improvements for individuals and communities [19, 116]. The social determinants of health are the circumstances in which people are born, live and age, which are shaped by wider political, social, and economic forces [117]. Factors such as inadequate housing, lack of education, unemployment, and institutional racism perpetuate disadvantage and contribute to poor health outcomes for individuals and communities, including behaviours associated with harmful drug use [118]. The social determinants of harmful drug use for Aboriginal and Torres Strait Islander people need to be understood not only within the current environment of disadvantage but also within a context of colonisation, dispossession of land, and past practices of forcible removal of children (stolen generations) [116, 119]. This legacy of trauma continues to impact on Aboriginal and Torres Strait Islander people today [120, 121].

Addressing the social determinants is likely to reduce harmful drug use and improve health outcomes. ‘There are additional social benefits beyond reduction of harmful drug use that can be expected to flow from programs that more generally improve the developmental opportunities of children and their community social environments’ [19, p.243]. For example, addressing poor academic outcomes in school may lead to an increase in school completion, increased post-secondary attendance, and better employment opportunities, all of which have the potential to reduce drug use.

Recreational activities

Organised recreational activities may prevent the uptake of drugs by providing alternative entertainment, positive role models and peers, and a safe place for community members [19, 42, 122, 123]. Recreational activities can take a number of forms, including sport, cultural activities, art, and music. In 2007 the Select Committee on Substance Abuse in the Community found that ‘the provision of recreational facilities and services for young people is a major element in demand reduction and a key in “carrot and stick” approaches that allow communities to guide young people away from substance abuse’ [122, p.21].

Evidence suggests that these programs are well received and important but may suffer from lack of resourcing [124, 125]. Further evidence notes that ‘recreational and cultural activities are often provided on an ad hoc basis with one-off funding … to be effective these interventions need to be sustained’ [103, p.5]. The Centre for Remote Health and the Central Australian Youth Link-Up Service undertook a study to explore the enablers and barriers of youth programs, including recreational activities, in remote Central Australian Aboriginal communities [42]. They found that programs need to be:

constant, reliable and regular, offer variety, focus on engagement, and be context–specific, meaning they should focus on the provision of meaningful, culturally relevant, gender and age status appropriate activities. They should incorporate the involvement, guidance, and support from older family members, and employ skilled youth workers who develop ideas and lead activities. It is also crucial that programs have appropriate funding and resources, including infrastructure. A ‘whole of community’ involvement in youth programs was often raised as the ideal. [42, p.7]

In 2011-12, 79% of Commonwealth-funded alcohol and other drug services for Aboriginal and Torres Strait Islander people provided treatment approaches involving group cultural activities like art, hunting, traditional healing, mentoring from Elders, and bush outings [126]. There are a number of examples of specific programs that provide recreational activities that are likely to reduce harmful drug use among Aboriginal and Torres Strait Islander people:

  • Discovering relationships using music, beliefs, emotions, attitudes and thoughts (DRUMBEAT) is an evidence-based therapeutic intervention that uses music to engage participants, teach social skills, and build-self-esteem. Developed by Holyoake, a WA alcohol and other drug service provider, it was designed to address the difficulties in engaging young people, particularly Aboriginal and Torres Strait Islander youth and youth at-risk, using traditional interventions such as cognitive behavioural therapy. Program participants have reported a range of positive outcomes including: enhanced social skills; increased self-esteem; improved school attendance; decrease in classroom behavioural incidents; and greater cooperation [127, 128].
  • The Young men and yarndi program provides information about cannabis use to young Aboriginal and Torres Strait Islander men from NSW through activities in a multi-day camp setting [129]. Feedback from participants indicate that ‘information and knowledge was retained, and there was a willingness to transmit and diffuse this information and knowledge acquired to family members and peers as opportunities arose’ [129, p.10].

Education and health promotion campaigns

Aboriginal and Torres Strait Islander-specific education and health promotion campaigns aim to provide culturally relevant information about drug use to Aboriginal and Torres Strait Islander people, and are some of the most common services provided for drug use [1, 130]. Some health promotion activities are based on the belief that harmful drug use results from a lack of knowledge, which can be ameliorated through education and public awareness campaigns. The effectiveness of education and health promotion campaigns has been shown, however, to be equivocal among the Aboriginal and Torres Strait Islander population [130-133]. Despite the lack of evidence, they remain common ‘because of “common sense” notions of “what works” and their relatively low cost’ [1, p.768].

In 2011-12, almost all (96%) Commonwealth-funded alcohol and other drug services for Aboriginal and Torres Strait Islander people provided information and education about drug use [126]. Around 84% of services provided community education and activities and 54% provided school-based education.

There are a number of education and health promotion campaigns designed for the Aboriginal and Torres Strait Islander population:

  • MAKINGtheLINK: promoting help seeking for drug use and mental health issues among Aboriginal and Torres Strait Islander school students is an educational project that encourages young Aboriginal and Torres Strait Islander people to seek help for problems relating to drug use [134]. The project targets young people in an effort to stop long-term problems resulting from drug use, and aims to be both culturally appropriate and relevant to the target group.
  • The National Cannabis Prevention and Intervention Centre initiated a yearly music competition after Aboriginal and Torres Strait Islander communities identified the need to increase awareness about cannabis use [134]. This competition has successfully raised awareness of cannabis-related harms, helped to provide community-driven health promotion resources, enabled capacity building for Aboriginal and Torres Strait Islander communities, and provided insight into community concerns about cannabis.

Law enforcement

Despite the limited evidence for supply side law enforcement strategies, ‘Australian governments’ expenditure on law enforcement is much greater than their expenditure on treatment services’ (demand and harm reduction) [135, p.404]. In-depth examination of law enforcement expenditure in 2002-03 found that proactive expenditure (law enforcement-related activity) amounted to around $740.4 million (including general policing, trafficking and organised crime, border protection, judicial and legal costs, and corrective services). Reactive expenditure (crime-related consequences) amounted to around $1,653 million (including police services, judicial resources, legal expenses, corrective services, and compensation and victim services). Together, this accounts for around 75% of all governmental spending on illicit drug-related activities in 2002-03.

A more recent analysis of government expenditure on illicit drug policy for 2009-10 found that Australian governments’ direct (proactive) spending on illicit drug policy was approximately $1.7 billion [136]. In 2009-10, approximately 64% of the illicit drug budget was spent on law enforcement, 23% on treatment, 10% on prevention, and 2% on harm reduction. This analysis found that between 2002-03 and 2009-10 there had been little change in the relative balance of spending across the four policy domains (prevention, treatment, harm reduction and law enforcement). Overall spending had increased by a small amount but harm reduction was one domain where spending had reduced.

Evidence suggests that ‘law enforcement should focus its efforts on the dealers and suppliers of illicit drugs, rather than on the users of drugs – who are better managed through education and treatment systems rather than the criminal justice system’ [64, p.37], but consumer arrests in Australia still constituted the vast majority of arrests in 2009-10 (around 80% of all arrests);34 cannabis-related crimes accounted for 67% of arrests [137].

Research on legislative and regulatory interventions suggests that ‘law enforcement, by reinforcing community values against illicit drug use, plays an important role in prevention’ [19, p.195]. Law enforcement aims to reduce the demand through establishing and maintaining ‘anti-drug’ social norms, and reduce supply through deterrent effects like fear of apprehension and punishment.

One example of an Aboriginal and Torres Strait Islander project that involves supply-side law enforcement is the Weed it out program which aims to reduce cannabis in Cape York and the Torres Strait, Qld [134]. This program involves collaboration between James Cook University, the Queensland Police Service, Australian Customs and Border Protection Service, Australian Federal Police, local elected representatives, and leaders of Cape York and Torres Strait communities to police cannabis distribution, production, and importation in this remote part of Australia [138]. Community support of the program has been shown through the dramatic increase in the number of Crime Stoppers and Crime Intelligence reports offered by the community, as well as the high accuracy of the information provided [138, 139].

Secondary prevention

Secondary prevention aims to avert risky or problematic drug use and stop experimental or occasional use from progressing to dependency [1]. Secondary prevention also aims to minimise harms among early users. The minimisation of harms from a single episode of drug use includes harms associated with:

  • the quantity of drug
  • how the drug is used
  • circumstances of use (e.g. location, social setting and related activities)
  • concurrent use of other drugs
  • risky behaviours (e.g. driving under the influence of drugs and risky sexual behaviour).

Brief interventions

Brief intervention describes a range of activities delivered in health care settings (such as a general practitioners’ (GP) offices or community counselling) [140]. Activities relevant to drug use include the use of appropriate screening tools, opportunistic provision of advice, encouragement to consider the consequences of use, and support for reducing use or abstaining [1, 140]. The advice is personalised and may include a referral to a specialist if required.

Brief interventions may be appropriate for staff at Aboriginal community-controlled health services (ACCHS) and GPs. A recent study found that training for ACCHS staff gave them the confidence required to provide brief interventions to Aboriginal and Torres Strait Islander clients, and that workshop materials developed for GPs could successfully be adapted for health care providers in ACCHSs [141]. Brief interventions provided by GPs may provide Aboriginal and Torres Strait Islander patients with forthright advice that is culturally appropriate, particularly if an Aboriginal and Torres Strait Islander Health Worker is involved [142]. Evidence suggests that barriers to the use of brief interventions for drug use include: complex patient needs that need to be addressed in a short period of time; patient resistance; tools that are unwieldy to use; cultural inappropriateness of certain brief intervention techniques; and lack of follow up services for referral [141, 143-145].

One Aboriginal and Torres Strait Islander-specific project that aims to address cannabis use and includes brief intervention is Could it be the gunja?, developed by the National Drug Research Institute (NDRI) in collaboration with six Aboriginal and Torres Strait Islander communities [134]. The project includes screening and brief interventions, a comprehensive implementation plan, and the creation of appropriate resources that reflect community feedback. Implementation of the project increased the proportion of clinic staff talking to clients about cannabis from 20% to around 60%. Project participants reported feeling more comfortable asking clients about cannabis and had gained the skills required to help people using this drug.

Night patrols

Night patrols are ‘community-based intervention initiatives that seek to improve personal and community safety in Aboriginal communities’ [146, p.13]. Night patrols involve teams of local people who patrol communities at night, either in a vehicle or on foot, and assist people who may be at risk of causing harm or being harmed. They originated in the NT in the late 1980s as a response to under-policing in some remote communities [146, 147], but now operate in urban, regional, and remote areas of Australia [148].

The Northern Territory night patrols program runs around 80 night patrols, which are administered by the Attorney-General’s Department as part of the Indigenous Justice Program [147]. Night patrols are now run in almost all states and territories [146], but a 2010 review of alcohol and other drug services for Aboriginal and Torres Strait Islander people noted a lack of night patrols in many parts of Australia [41].

Few evaluations have been conducted, but the Little children are sacred report and the Northern Territory emergency response evaluation report both found that night patrols were highly valued by the community [149, 150] in providing a ‘culturally appropriate mobile service that can respond quickly to problems in the community’ [149, p.191]. The Australian Institute of Health and Welfare (AIHW) and Australian Institute of Family Studies released a paper in 2013 that reviewed community patrols across Australia [148]. They found that ‘the available evidence suggests that they can reduce juvenile crime rates, alcohol-related harm and crime and the number of police lock-ups. They have also been shown to increase perceptions of safety, improve partnerships and cultural understanding between Indigenous and non-Indigenous communities and empower the local community’ [148, p.15].

Sobering-up shelters

Sobering-up shelters provide care for people who are publicly intoxicated and are an alternative to arrest [130, 151]. Sobering-up shelters do not aim to deal with underlying causes of drug use, rather they provide a safe place where people can get sober, avoid harming themselves and others, and avoid police custody. Shelters offer practical care, provide opportunities for brief interventions and referral, and offer basics like food. Sobering-up shelters have been integral to the decriminalisation of public intoxication in Australia. In 2013-14, there were nine Aboriginal and Torres Strait Islander alcohol and other drug services that provided sobering-up, residential respite, and short-term client care to around 5,000 people [115]. A 2010 review of alcohol and other drug services reported 36 sobering-up shelters nationally, but noted a shortage of sobering-up shelters in many part of Australia [41]. Sobering-up shelters have been shown to have strong community and police support [124, 130, 151].

Needle and syringe programs

NSPs provide sterile needles, syringes, and other injecting equipment free of charge, on an exchange basis, or for sale. They also provide information and counselling and referral services for people who inject drugs [111]. NSPs aim to reduce the sharing of injecting equipment and provide education to users, both of which aim to lower the risks associated with injecting drug use. NSPs are delivered at fixed locations (including hospitals, pharmacies, or community health services), via vending machines (providing 24 hour accessibility to sterile injecting equipment), and through outreach and mobile methods (usually in a vehicle or utilising the ‘foot outreach’ model). NSPs form a part of the harm minimisation approach outlined by the NDS, with more than 3,000 programs established across the country [62].

The NSP program has been described as ‘the single most important and cost-effect strategy in reducing drug-related harms’ among people who inject drugs. [111, p.14]. A 2009 evaluation of NSPs in Australia found that they had directly averted around 32,050 HIV infections and 96,667 hepatitis C infections during 2000-2009, provided substantial savings to health care costs, and added substantial gains to the ‘disability adjusted life years’ [152].

The NUHIT (clean needle program), run by Nunkuwarrin Yunti in SA, is a NSP program for Aboriginal and Torres Strait Islander people that provides safe injecting equipment and connects Aboriginal and Torres Strait Islander people with treatment and support [33]. A Victorian study into injecting drug use among Aboriginal and Torres Strait Islander people suggests that the availability of mainstream services in providing NSP for Aboriginal and Torres Strait Islander clients is also important as Aboriginal and Torres Strait Islander clients may feel more comfortable visiting a mainstream NSP or vending machine because of increased anonymity [36].

Diversion

Aboriginal and Torres Strait Islander people are over-represented in the criminal justice system in Australia [153]. One way to reduce this over-representation is through diversion which aims to: avoid the stigma associated with criminal contact; prevent further offending by minimising contact with the criminal justice system; reduce the number of people reaching courts and prisons; and provide appropriate interventions to people in need of treatment or other services [99]. Diversion programs mainly target juvenile and drug-related offenders, and include strategies like cautioning or conferencing. Examples of Aboriginal and Torres Strait Islander diversion programs include: Queensland’s Indigenous alcohol diversion program; the Indigenous diversion program in WA; and the Magistrates early referral into treatment (MERIT) program in NSW [99, 154]. Diversion also includes court programs like Victoria’s Koori court and the Murri court in Qld, which provide a culturally responsive and appropriate alternative to the mainstream court system [99].

The MERIT program has been shown to reduce re-offending and lead to improved health outcomes [154, 155]. A study compared MERIT participant completion (between 2004 and 2005) and recidivism records (for the period 2004 to 2007) [155].35 It found a 30% reduction in risk of re-offending for participants who completed the MERIT program compared to those that did not complete the program. Other studies have found that, although Aboriginal people are referred to the MERIT program in proportion to their rate of appearance before NSW courts, Aboriginal clients were significantly less likely to complete the program [156, 157]. Subsequent research has demonstrated that by identifying barriers to participation in MERIT and changing the way services are provided, Aboriginal clients were more likely to complete the program (33% increase compared to 7% for services that made no changes) [158].

Diversion programs also aim to provide relevant health services for offenders. Establishing NSPs or opioid substitution treatment in prisons are ways to potentially reduce the harms associated with injecting drug use among inmates [159-161].

Tertiary prevention

Tertiary prevention aims to reduce health and social harm among problem users, and help them to reduce or discontinue their drug use [1]. This prevention includes treatment, rehabilitation, and counselling for chronic drug users. Tertiary prevention also seeks to avert harms affecting other people, including family members and the wider community.

Primary health care

Primary health care refers to a patient’s first point of contact with the health care system, typically involving a GP, Aboriginal and Torres Strait Islander Health Worker, or other clinic staff [162]. Many ACCHSs aim to provide comprehensive care (including physical, mental, and social wellbeing) that involves community participation and self-determination as part of the decision making and planning for their services [126, 162]. Many of the services provided by ACCHSs include treatment, rehabilitation, and counselling, all of which fit into tertiary prevention.

In 2013-14, there were 203 Aboriginal and Torres Strait Islander primary health care services that were receiving Commonwealth funding [115]. These services were available in all states and territories and in all remoteness levels across the country (Table 12). Of the 7,108 full-time equivalent staff employed by these services, 53% identified as Aboriginal and Torres Strait Islander.

Table 12. Number and proportion (%) of Aboriginal and Torres Strait Islander primary health care services, by remoteness level, Australia, 2013-14

Major cities

Inner regional

Outer regional

Remote

Very remote

Total

22 (11%)

43 (21%)

45 (22%)

27 (13%)

66 (33)%

203 (100%)

Source: AIHW, 2015 [115]

In 2013-14, primary health care organisations reported that the most common drug use issues were cannabis (88%), amphetamines (41%), and poly drug use (39%) [115]. The most common services offered by these organisations were individual counselling (172 organisations, 85%), community education (158 organisations, 78%), and crisis intervention (127 organisations, 63%) [115].

Community-based treatment

Community-based treatment provides specialised, intensive, and supported drug use services for Aboriginal and Torres Strait Islander people in the community [1]. Such treatments may include an abstinence model (like Alcoholics anonymous), recreational programs, or family therapy, counselling, and case management.

In 2013-14, non-residential services were provided by 95% of Commonwealth-funded alcohol and other drug services for Aboriginal and Torres Strait Islander people [115]. There were around 353,000 episodes of non-residential, follow-up, and after-care reported. On average each client received 11 episodes of care. This is a large increase from 2011-12 when 61,000 episodes of non-residential care (on average three episodes of care per client) were recorded [126].36

According to the 2013-14 AIHW report on alcohol and other drug treatment services in Australia, the three main illicit drugs that both Aboriginal and Torres Strait Islander and non-Indigenous clients sought treatment for were cannabis (24%), amphetamines (17%), and heroin (7%) [61]. The majority of the treatment was received in non-residential settings. In more than half (54%) of closed episodes, the client also reported additional drugs of concern. Of all clients receiving treatment for their own drug use, around one-in-seven (14%) were Aboriginal and Torres Islander people, while 8% of clients receiving support for someone else’s drug use identified as Aboriginal and Torres Strait Islander.

Residential rehabilitation

Residential rehabilitation services provide the same types of services as community-based treatment but are able to distance clients from environments where they may typically use drugs [1]. These therapeutic environments allow for recovery of client health and the opportunity for intensive interventions, which seek to change drug use behaviours. Some services include the involvement of family members. Other residential services, such as sobering up shelters (overnight, or short term (1-7 days) residential care), provide respite but not formal rehabilitation [115].

In 2013-14, nearly half (46%) of Commonwealth funded alcohol and other drug services for Aboriginal and Torres Strait Islander people provided residential treatment, and one-quarter (23%) provided sobering up or short term residential services [115]. Of the 21 organisations providing residential rehabilitation, 2,300 clients were provided services with around 2,400 episodes of care. Three quarters (76%) of these organisations had waiting lists. The nine organisations providing sobering up services or short term residential care provided services to around 5,000 clients, with around 16,000 episodes of care [115]. On average each client received around three episodes of care.

Some studies into the efficacy of residential rehabilitation services for Aboriginal and Torres Strait Islander people have provided inconclusive results [163, 164]. Positive aspects of these services included: the provision of respite so people can recover from drug use; the provision of drug use education; and the opportunity to acquire life-skills. Negative aspects included: the gradual resumption of the problematic drug use for some clients returning to the community; not dealing with the underlying causes of drug use; lack of cultural awareness; poor staff training; lack of follow-up support; and separation from family. Other studies have found that residential rehabilitation is beneficial where evidence-based interventions are adapted to match the therapeutic and cultural needs of the client and where good follow up care is provided [165, 166]. As a treatment option, residential rehabilitation is best suited to those people with moderate to severe levels of dependence and less social stability [166].

Elements of effective service

A number of elements that make alcohol and other drug services for Aboriginal and Torres Strait Islander people effective have been identified in the literature [1, 24, 31, 33, 36, 41, 90, 105, 106, 133, 164, 167-172]. Services that incorporate these elements are more likely to improve outcomes for their Aboriginal and Torres Strait Islander clients, as well as provide them with culturally safe and appropriate environments. Ensuring that Aboriginal and Torres Strait Islander communities are involved during the planning and implementation stages, and that all staff are appropriately trained and supported, will likely lead to better outcomes.

Community originated and controlled services

In theory, Aboriginal and Torres Strait Islander people have access to mainstream alcohol and other drug services, but, in practice, these services are often ‘unaffordable, inaccessible, inappropriate, and unacceptable’ [24, p.172]. Alcohol and other drug services that originate with and are controlled by communities ensure their relevance and appropriateness, leading to better outcomes [33, 41, 133, 167].

Enhancing the capacity of Aboriginal and Torres Strait Islander community-controlled services and its workforce, as part of a cross-sectoral approach with mainstream services is the first priority area of the National Aboriginal and Torres Strait Islander peoples’ drug strategy 2014–2019 [106].

Culturally appropriate

The cultural appropriateness of alcohol and other drug services is consistently identified as a very important factor for effective service provision [41, 90, 167-169]. Services that integrate cultural practices into evidence-based approaches have been shown to be more effective than mainstream services [166]. Increasing the capacity for Aboriginal and Torres Strait Islander organisations to respond to drug use issues in the community, while also expanding the cultural competence of mainstream organisations to build effective partnerships, has been identified as a key component to improving services for Aboriginal and Torres Strait Islander clients [172]. Ensuring that services are culturally appropriate includes: employing local Aboriginal and Torres Strait Islander staff; conducting cultural competence training; delivering services in partnership with ACCHSs; and on-going consultation with members of local communities [41]. Providing greater access to a full range of culturally responsive programs aimed at the local needs of individuals, families, and communities is the second priority area in the National Aboriginal and Torres Strait Islander people’s drug strategy 2014-2019 [106].

Holistic

The provision of holistic services helps to address the multiple problems faced by many Aboriginal and Torres Strait Islander clients (such as drug use and social and emotional wellbeing issues) [23, 41, 169]. Many of these problems cannot be properly addressed in isolation and an organisation’s ability to provide a continuum of services at one location is likely to benefit clients.

Partnerships

Effective partnerships between Aboriginal and Torres Strait Islander and mainstream services may provide a network of care that can address the reality of limited resources [33, 41, 164, 167]. These partnerships allow organisations to best use their own expertise and, when required, refer clients to organisations that are supported, trusted, and respected by the community. Collaboration and the development of partnerships both within and between Aboriginal and Torres Strait Islander peoples, government, and mainstream alcohol and other drug services is the third priority area in the National Aboriginal and Torres Strait Islander people’s drug strategy 2014-2019 [106].

Flexible and innovative

The need for services that are flexible and offer innovative solutions to clients has been identified as important [33, 41, 168, 170]. Service flexibility includes structuring solutions around client needs (such as staff meeting clients in a variety of locations) and taking account of a client’s cultural duties (such as missing appointments because of family business). The ability to respond to individual cases with innovation and flexibility will improve alcohol and other drug services.

Inclusion of family and community

Some of the literature indicates that the appropriate inclusion of family and community may enhance alcohol and other drug services for some Aboriginal and Torres Strait Islander people, especially treatment services [31, 33, 90]. Thus, ‘families have the potential to play a crucial role in the success of an individual’s experience in drug treatment, particularly when family members reinforce positive health behaviours’ [33, p.82].

Confidentiality

Client confidentiality has been identified as an important strategy for effective service [168], especially among people who inject drugs [33, 36].

Workforce development

Good governance and management systems to support staff in alcohol and other drug services for Aboriginal and Torres Strait Islander people are essential elements in ensuring effective delivery of services [169, 171, 173]. Building the capacity for organisations to respond to alcohol and other drug issues requires addressing both the structural factors in delivering services as well as individual training and skills development [172, 174].

A workforce that is well trained and undertakes continuing professional development is more likely to deliver effective services [1, 33, 41, 167]. Studies show that ongoing training increases the confidence of workers who become more willing and able to provide a wider variety of services [141, 143, 175].

Increasing workforce capacity by protecting worker wellbeing from stress and burnout, providing career paths, making sure that work places are culturally safe, providing clinical supervision and good administrative support are some of the ways organisations can ensure that alcohol and other drug workers are adequately supported [176].

Barriers to services

There are a number of factors that are routinely identified as service barriers for Aboriginal and Torres Strait Islander people [33, 41, 103, 105, 143, 163, 164]. These barriers may negatively affect the outcomes for Aboriginal and Torres Strait Islander clients, either by neglecting to provide appropriate services, providing only short-term services because of inadequate funding, or failing to provide ongoing care after rehabilitation, potentially leading to relapse. In addition, services may not be provided to Aboriginal and Torres Strait Islander people where they live, either because of remoteness level, because services are not adequately integrated, or because of a lack of reliable and relevant information. By addressing these barriers, Aboriginal and Torres Strait Islander clients are more likely to receive the quality care they deserve.

Lack of cultural sensitivity

Aboriginal and Torres Strait Islander people may find mainstream alcohol and other drug services culturally inappropriate or insensitive, and some mainstream strategies may not transfer appropriately to the Aboriginal and Torres Strait Islander population [33, 41]. It is important that Aboriginal and Torres Strait Islander communities lead initiatives dealing with drug use in their own communities, and that services are guided by community members. Services should also be flexible enough to deal with the changing needs of the community.

Lack of adequate resources

Access to adequate and ongoing resources is essential in providing appropriate and effective alcohol and other drug services. The lack of adequate and/or recurrent funding was identified as a major barrier for organisations providing alcohol and other drug services to Aboriginal and Torres Strait Islander people [41, 103, 172]. Organisations without adequate and recurrent funding will not be able to attract and retain qualified staff and will not be able to provide integral and holistic services [41].

Lack of ongoing care

There is a need for ongoing care services for Aboriginal and Torres Strait Islander people after they have completed rehabilitation treatment [41, 143, 164]. A 2010 review found only two services were funded to provide ongoing care, and a small number of other organisations provided ongoing care on an ad hoc basis [41].

Geographic and service gaps

Appropriate and integrated alcohol and other drug services should ideally be available across Australia, regardless of remoteness level. A 2010 review of Aboriginal and Torres Strait Islander alcohol and other drug services found that there were large gaps at a regional level, with some regions poorly serviced, and with no integration between services to ensure that regions have a suitable range of services [41]. The provision of services was not found to correlate to population size or level of remoteness.

Lack of reliable information

There is currently a lack of information about what types of alcohol and other drug services and interventions best serve the needs of Aboriginal and Torres Strait Islander people [103, 163]. Without up-to-date and reliable data, information, and knowledge, including formal reviews of services, it is not possible to assess the effectiveness of interventions and determine ‘what works’ in illicit drug use among Aboriginal and Torres Strait Islander people. Developing a robust evidence-base through improved data collection and dissemination is identified as the fourth priority area in the National Aboriginal and Torres Strait Islander people’s drug strategy 2014-2019 [106].

Concluding comments

While more than half of Aboriginal and Torres Strait Islander people do not use illicit drugs, the levels of illicit drug use are substantially higher among Aboriginal and Torres Strait Islander people than non-Indigenous people in Australia [45, 46]. Prevalence of specific types of illicit drug use is consistently higher for Aboriginal and Torres Strait Islander people than those for non-Indigenous people, especially cannabis which is used at very high levels in some remote Aboriginal and Torres Strait Islander communities. The impacts of illicit drug use are greater for Aboriginal and Torres Strait Islander people than they are for non-Indigenous people, including higher levels of social and emotional distress and infection from blood-borne viruses. The most recent data reveals that the drug-related death rate was 1.5 times higher for Aboriginal and Torres Strait Islander people than for non-Indigenous people.

Factors contributing to the higher proportions of illicit drug use and the associated health and social burdens among Aboriginal and Torres Strait Islander people are complex. The higher levels of illicit drug use are directly associated with the social determinants of health; social and economic disadvantage and the legacy of colonisation that perpetuates harmful drug use and compounds the disadvantage suffered by Aboriginal and Torres Strait Islander Australians.

Australia’s drug use policy framework aims to minimise harmful drug use through the pillars of demand reduction, supply reduction, and harm reduction. The National Aboriginal and Torres Strait Islander people’s drug strategy 2014-2019, a sub-strategy of the NDS, is shaped by four priority areas and includes performance measures against which to evaluate progress.

Services that are most likely to effectively address drug use among Aboriginal and Torres Strait Islander people are those that originate within and are controlled by the community, are culturally appropriate, provide holistic services, and create strong partnerships with other organisations in order to provide clients with a complete continuum of care. Other elements of effective service include flexibility and innovation in service delivery, involvement of family and community, high levels of confidentiality with client information, and having a highly trained and supported workforce that is able to access ongoing and relevant professional development. The literature on alcohol and other drug services for Aboriginal and Torres Strait Islander people also highlights the importance of designing services specifically for Aboriginal and Torres Strait Islander people, providing adequate resourcing and funding of services, and the need to collect better information so that ‘best practice’ can be established for Aboriginal and Torres Strait Islander clients.

All levels of government have an obligation to work with Aboriginal and Torres Strait Islander communities and health organisations to address the current levels of illicit drug use among Aboriginal and Torres Strait Islander people. Policies addressing illicit drug use need to provide long-term, culturally appropriate guidance that equally addresses each of the three pillars of harm minimisation. Illicit drug use services need to be adequately resourced and funded in the long-term to be able to provide the holistic quality of care Aboriginal and Torres Strait Islander Australians deserve.

Appendix 1

Data sources and quality

National drug surveys

2013 National drug strategy household survey

The 2013 National drug strategy household survey (NDSHS) is the 11th survey undertaken by the AIHW on behalf of the Department of Health in a series that began in 1985 [3].This survey included people aged 12 and older or 14 and older (depending on the jurisdiction) from all states and territories in Australia and was conducted between July and December 2013. There were 23,855 eligible survey responses that have been included in the 2013 NDSHS. Less than two percent (1.9%) of the respondents identified as Aboriginal and Torres Strait Islander; this sample size under-represented Aboriginal and Torres Strait Islander people (Aboriginal and Torres Strait Islander people comprise about 3% of Australia’s population)[13, 177, 178].

Limitations for this survey include:

  • the small sample size of Aboriginal and Torres Strait Islander people means survey results should be interpreted with caution
  • people who did not speak English as their main language at home were under-represented
  • self-administered questionnaires may not be accurate (since illicit drug use is, by definition, illegal, many people may not accurately report their use of such substances)
  • the 2013 NDSHS is generally not directly comparable with the Aboriginal and Torres Strait Islander-specific surveys (such as the National Aboriginal and Torres Strait Islander social survey and the National Aboriginal and Torres Strait Islander health survey) because of the differences in survey design and questions asked, though it should be noted that many of the relative proportions are consistent with other surveys.
2010 National drug strategy household survey

The 2010 National drug strategy household survey (NDSHS) included people aged 12 and older or 14 and older (depending on the jurisdiction) from all states and territories in Australia and was conducted between April and September 2010 [4]. There were 26,648 eligible survey responses. About 460 (1.7%) of the respondents identified as Aboriginal and Torres Strait Islander.

Limitations for this survey include:

  • the small sample size of Aboriginal and Torres Strait Islander people means survey results should be interpreted with caution
  • the under-representation of Aboriginal and Torres Strait Islander people living in very remote areas; the survey sample of Aboriginal and Torres Strait Islander people living in very remote areas comprised only 4% of the population in those regions compared with 16% of Aboriginal and Torres Strait Islander people living in very remote areas (based on the 2006 Census)
  • the sampling method employed for the survey included responses from only one household member; many Aboriginal and Torres Strait Islander people live in very large households and this method may not be appropriate. This sampling method means that Aboriginal and Torres Strait Islander people were proportionately less likely to be selected and contributed to the under-representation of Aboriginal and Torres Strait Islander people for this survey
  • the data collection for this survey included self-administered questionnaires written in English (no translations were available). The survey design may have excluded Aboriginal and Torres Strait Islander communities and those with low levels of English literacy
  • self-administered questionnaires may not be accurate (since illicit drug use is, by definition, illegal, many people may not accurately report their use of such substances)
  • the 2010 NDSHS is generally not directly comparable with the Aboriginal and Torres Strait Islander-specific surveys (such as the National Aboriginal and Torres Strait Islander social survey and the National Aboriginal and Torres Strait Islander health survey) because of the differences in survey design and questions asked; though it should be noted that many of the relative proportions are consistent with other surveys.
2007 National drug strategy household survey

The 2007 NDSHS was managed by the AIHW on behalf of the Department of Health and conducted between July and November 2007 [179]. A total of 23,356 Australians aged 12 years and older or 14 years and older living in private dwellings from all states and territories participated in this survey. The proportion of Aboriginal and Torres Strait Islander people included in the 2007 NDSHS was only 1.3% [47].

This survey provides the most promising total population data to compare with the Aboriginal and Torres Strait Islander data from the National Aboriginal and Torres Strait Islander social survey (NATSISS), but comparisons should be viewed with caution. There were many methodological and statistical differences between the NDSHS and the NATSISS that make the data not directly comparable, but it has been used throughout this review to estimate comparisons of illicit drug use between the Aboriginal and Torres Strait Islander and non- Indigenous populations.

Limitations for this survey include:

  • the small sample size of Aboriginal and Torres Strait Islander people means that survey results should be interpreted with caution
  • the self-administered questionnaires and telephone responses may inhibit collection of accurate information in some cases
  • the exclusion of non-private dwellings (e.g. hotels, boarding houses) and institutional settings (e.g. hospitals, nursing homes, rehabilitation centres, prisons) may have contributed to the under-representation of Aboriginal and Torres Strait Islander people (the 2006 Census indicated that 4% of Aboriginal and Torres Strait Islander people lived in non-private dwellings [180])
  • it is generally not directly comparable with the Aboriginal and Torres Strait Islander-specific surveys because of the differences in survey design and questions asked.

National social surveys

2008 National Aboriginal and Torres Strait Islander social survey

The 2008 National Aboriginal and Torres Strait Islander social survey (NATSISS) collected data from around 13,300 Aboriginal and Torres Strait Islander people across all states and territories between August 2008 and April 2009 [49]. The data collected was from Aboriginal and Torres Strait Islander people living in private dwellings in remote and non-remote areas, including discrete communities. Information on substance use was collected by self-administered forms in non-remote areas, and asked by interviewers in remote locations.

Limitations of this survey include:

  • information collected from non-remote respondents may be affected by privacy concerns (presence of other household members); respondents may not have felt comfortable responding to some sensitive and personal questions
  • the survey did not include people living in non-private dwellings (the 2006 census indicated that 4% of Indigenous people lived in non-private dwellings [180])
  • self-completed questionnaires and interview responses may not be accurate.
2002 National Aboriginal and Torres Strait Islander social survey

The 2002 NATSISS, conducted by the Australian Bureau of Statistics, was the second national social survey of Aboriginal and Torres Strait Islander people [181]. It collected data from 9,400 Aboriginal and Torres Strait Islander people aged 15 years and older living in private dwellings from all states and territories in Australia. The data were collected between August 2002 and April 2003 in remote and non-remote areas.

Limitations of this survey include:

  • lack of confidentiality about substance use questions in some remote locations: respondents were required to respond verbally to substance use questions in Aboriginal and Torres Strait Islander communities (including any associated out-stations). It is assumed that the very low prevalence of substance use in these areas were a result of this verbal questioning. The substance use data from remote areas were considered unreliable and not released
  • the exclusion of non-private dwellings (the 2001 census indicated that around 4% of the Aboriginal and Torres Strait Islander population resided in non-private dwellings [182]).

National health surveys

2012-13 Aboriginal and Torres Strait Islander health survey

The 2012-13 Aboriginal and Torres Strait Islander health survey (AATSIHS) was conducted from April 2012 to February 2013 across all states and territories in Australia [45]. It collected information from around 13,000 Aboriginal and Torres Strait Islander people in both remote and non-remote parts of Australia. It encompassed information from three Aboriginal and Torres Strait Islander surveys: the National Aboriginal and Torres Strait Islander health survey (NATSIHS); the National Aboriginal and Torres Strait Islander nutrition and physical activity survey (NATSINPAS); and the National Aboriginal and Torres Strait Islander health measures survey (NATSIHMS). The AATSIHS provided prevalence estimates of certain chronic diseases and conditions, selected behavioural risk factors and objective biomedical measures of selected chronic diseases, nutrition status and other risk factors.

The ABS collected substance use information from Aboriginal and Torres Strait Islander people aged 15 years and older. Participants in non-remote areas were encouraged to record their own responses to questions about substance use on a computer without field collectors viewing the screen. Participants in remote areas were personally interviewed.

A limitation of this survey includes:

  • the possible under-estimation of substance use due to the sensitive nature of the topic. Participants may have been unwilling to respond, particularly for remote participants who answered directly to the interviewer [45].
2004-2005 National Aboriginal and Torres Strait Islander health survey

The 2004-2005 National Aboriginal and Torres Strait Islander health survey(NATSIHS) was conducted between August 2004 and July 2005 across all states and territories in Australia. It collected self-reported information from 10,439 Aboriginal and Torres Strait Islander people across Australia living in remote and non-remote locations [183]. Information on substance use was collected from Aboriginal and Torres Strait Islander people aged 15 years and older living in non-remote areas using a voluntary self-administered form [184]. The ABS had intended to conduct this survey every six years.

Limitations of this survey include:

  • information on substance use was not collected for Aboriginal and Torres Strait Islander people in remote locations
  • possible under-estimation of substance use in non-remote locations due to self-reported information.

Other surveys

2008 Australian secondary students alcohol and drug survey

The 2008 Australian secondary students alcohol and drug survey (ASSAD) was conducted during the 2008 academic year in mainstream schools in Vic, Qld, WA, SA and the NT [50]. The 2008 ASSAD also includes 19 rural schools from WA, Qld, SA, and the NT. This survey targeted students in years 7 to 10 (aged 12-15 years), and included responses from about 24,000 students, 1,317 of whom identified themselves as Aboriginal and Torres Strait Islander.

Limitations of this survey include:

  • self-completed questionnaires may not have been accurately completed by students
  • teachers were discouraged from being present during the completion of the study questionnaire, but almost 80% of students had a teacher present during the questionnaire completion: this may have affected the study results (students completing the survey with a teacher present were less likely to report drinking or use of ecstasy than those completing without a teacher present).
Illicit drug use reporting system

The Illicit drug use reporting system (IDRS) has been conducted in all states and territories across Australia since 2000 [60]. This report series aims to provide a coordinated approach to monitoring the use of illicit drugs. It is designed to provide insight on trends throughout time and current national data. The IDRS collects information in three ways: interviews with a group of people who regularly inject drugs in Australia’s capital cities; interviews with professionals in regular contact with illicit drug users; examination of relevant data sources (e.g. opioid overdose data).

Participants for the 2012 IDRS were aged 16 years and older, had injected at least monthly for the six months preceding interview, and were resident in the capital city in which they were interviewed for at least 12 months before the survey. The 2012 IDRS interviewed 924 people who inject drugs in capital cities across Australia between June and August; 16% of participants identified as Aboriginal and Torres Strait Islander.

Limitations of this survey include:

  • the Aboriginal and Torres Strait Islander people sampled may not accurately reflect the wider population of Aboriginal and Torres Strait Islander injecting drug users
  • no detailed information is provided based on Aboriginal and Torres Strait Islander status.

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  176. Roche A, Nicholas N, Trifonoff A, Steenson T (2013) Staying deadly: strategies for preventing stress and burnout among Aboriginal and Torres Strait Islander alcohol and other drug workers. Adelaide: National Centre for Education and Training on Addiction
  177. Australian Bureau of Statistics (2013) Population projections, Australia, 2012 (base) to 2101. (ABS Catalogue no 3222.0) Canberra: Australian Bureau of Statistics
  178. Australian Bureau of Statistics (2014) Estimates and projections, Aboriginal and Torres Strait Islander Australians, 2001 to 2026. (ABS Catalogue no.3238.0) Canberra: Australian Bureau of Statistics
  179. Australian Institute of Health and Welfare (2008) 2007 national drug strategy household survey: first results. (Drug Statistics Series number 20. Cat. no. PHE 98) Canberra: Australian Institute of Health and Welfare
  180. Australian Bureau of Statistics (2010) Population characteristics, Aboriginal and Torres Strait Islander Australians, 2006 (reissue). (ABS Catalogue no 4713.0) Canberra: Australian Bureau of Statistics
  181. Australian Bureau of Statistics (2004) National Aboriginal and Torres Strait Islander Social Survey, 2002. (ABS Catalogue no. 4714.0) Canberra: Australian Bureau of Statistics
  182. Australian Bureau of Statistics (2006) National Aboriginal and Torres Strait Islander Health Survey: Australia, 2004-05. (ABS Catalogue no. 4715.0) Canberra: Australian Bureau of Statistics
  183. Australian Bureau of Statistics (2006) National Aboriginal and Torres Strait Islander Health Survey: expanded confidentialised unit record file; technical manual, Australia, 2004-05. (ABS Catalogue no. 4715.0.55.002) Canberra: Australian Bureau of Statistics
  184. Australian Bureau of Statistics (2006) National Aboriginal and Torres Strait Islander Health Survey: Australia, 2004-05: user’s guide. (ABS Catalogue no. 4715.0.55.004) Canberra: Australian Bureau of Statistics

[1] ‘Recent use’ refers to use in the previous 12 months.

[2] Of the 1,705 deaths attributed to illicit drug use in the study, hepatitis C accounted for 759 deaths, hepatitis B for 329 deaths, heroin and poly-drug use for 263 deaths, and suicide and self-inflicted injuries accounted for 204 deaths.

[3] There is a difference between the Census ‘counts’ and ‘estimates’. Counts do not adjust for a number of factors, and are considered less accurate.

[4] ‘Recent’ refers to use in the 12 months prior to survey.

[5] Because of the small sample size, comparison of data between Aboriginal and Torres Strait Islander people and non-Indigenous people should be viewed with caution.

[6] Comparisons between Aboriginal and Torres Strait Islander people and non-Indigenous people are made wherever possible, but comparisons have also been made between the Aboriginal and Torres Strait Islander and total Australian populations when non-Indigenous data was not available.

[7] ‘Ex use’ refers to the use of an illicit drug, but not in the 12 months prior to survey.

[8] Percentages are age-standardised.

[9] ‘Ever used’ refers to those who indicated any use of a drug, either in their lifetime, the past month, or past week.

[10] Heavy cannabis use was defined as six or more cones daily.

[11] Non-medical use of analgesics and sedatives (including painkillers, tranquilisers, and sleeping pills) is considered illicit.

[12] The proportion has a relative standard error between 25% and 50% and should be used with caution.

[13] Analgesics and tranquilisers are considered separately in the 2008 NATSISS.

[14] For the NDSHS, pharmaceuticals includes paracetamol, over-the-counter and prescription codeine combinations, tranquilisers, steroids, methadone/buprenorphine or other opiates.

[15] Due to the small sample size, comparisons between data for Aboriginal and Torres Strait Islander people and non-Indigenous people should be viewed with caution.

[16] Comparisons between the 2007 NDSHS and 2008 NATSISS should be viewed with caution.

[17] Since 2007 the term ‘meth’ was introduced and in 2010 clarification about non-medical use was added for the NDSHS.

[18] Respondents were asked to choose from a list that included ‘amphetamines and speed’.

[19] The proportion has a relative standard error between 25% and 50% and should be used with caution.

[20] The proportion has a relative standard error between 25% and 50% and should be used with caution.

[21] There is no information specifically about ecstasy/designer drugs available in the 2012-2013 AATSIHS.

[22] The proportion has a relative standard error between 25% and 50% and should be used with caution.

[23] The survey was conducted from 2011-2013.

[24] It should be noted that the high proportion of Aboriginal and Torres Strait Islander people may reflect the recruitment strategy where a substantial proportion of participants were drawn from populations that were currently in treatment.

[25] A closed episode is a period of contact between a client and treatment provider. An episode is closed when treatment is completed or there has been no further contact from the client for three months.

[26] Recent trends in HIV diagnosis among Aboriginal and Torres Strait Islander people are based on small numbers and may reflect localised trends rather than national patterns.

[27] The 2012 IDRIS does not provide separate information about overdose for Aboriginal and Torres Strait Islander people, but 16% of study participants were Indigenous.

[28] ICD code F15 hospitalisation from use of other stimulants includes amphetamine-related disorders and caffeine but not cocaine.

[29] Up to six substances were recorded for each person’s toxicology analysis in this study.

[30] This difference is not statistically significant.

[31] Very few deaths from suicide were reported prior to this time period.

[32] Around 21% of 2009-10 DUMA participants identified as Aboriginal and Torres Strait Islander.

[33] This is mainly due to fewer services reporting data.

[34] The numbers of consumers are much greater than the number of suppliers so these numbers should be taken in context.

[35] A total of 15% or participants identified as Aboriginal and/or Torres Strait Islander (176 of 1160 participants).

[36] This may indicate increases in staffing levels and improvements in data recording in some organisations.

Review of diabetes among Aboriginal and Torres Strait Islander people

Burrow S, Ride K (2016) Review of diabetes among Aboriginal and Torres Strait Islander people. Australian Indigenous HealthInfoNet. Retrieved [access date] from https://healthbulletin.org.au/articles/review-of-diabetes-among-aboriginal-and-torres-strait-islander-people

Survey

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Introduction

Diabetes is the world’s fastest growing chronic disease [1]. Type 2 diabetes in particular, has reached epidemic proportions globally and in Australia, and poses a challenge for public health systems everywhere [2-4]. The greatest burden tends to fall on socially disadvantaged groups and Indigenous peoples [2]. Aboriginal and Torres Strait Islander Australians experience disproportionately high levels of diabetes. They are three times more likely to have diabetes1 than non-Indigenous Australians [5, 6] and Aboriginal and Torres Strait Islander women are almost twice as likely to develop gestational diabetes as non-Indigenous women [7]. There is also evidence that Aboriginal and Torres Strait Islander children2 are eight times more likely to develop type 2 diabetes (traditionally considered an adult disorder [2]) than their non-Indigenous peers [8]. Mortality rates are correspondingly high, and Aboriginal and Torres Strait Islander people are six times more likely to die from diabetes than non-Indigenous Australians [9].

Box 1: Diabetes

Diabetes (diabetes mellitus) is a disease marked by high levels of glucose in the blood [10]. It is caused by the body’s inability to produce and/or use insulin effectively. It is a complex, chronic condition that can lead to morbidity, disability, reduced quality of life and premature death [3, 10, 11]. Diabetes can affect the entire body and typically requires lifelong management [3, 11]. There is currently no known cure [3]. If undiagnosed or poorly managed, diabetes can lead to a range of complications and death [6]. Complications include diseases of the large blood vessels (macrovascular disease), such as heart disease and stroke, and diseases of the small blood vessels (microvascular disease), such as kidney disease, eye disease and nerve disease [12]. Type 2 diabetes is the most common form of diabetes, frequently affecting older people but increasingly occurring in young people and children [2, 3]. Type 1 diabetes and gestational diabetes are the other main types of diabetes [10].

The high level of diabetes among Aboriginal and Torres Strait Islander people reflects a broad range of contributing factors [13, 14]. Addressing these factors should reduce the impact of diabetes on Aboriginal and Torres Strait Islander people; but this will require a range of tailored, culturally appropriate prevention and management programs, and broader action beyond the health service sector [13, 15, 16].

About this review

The purpose of this review is to provide a comprehensive synthesis of key information on diabetes among Aboriginal and Torres Strait Islander people in Australia to: (1) inform those involved or interested in Aboriginal and Torres Strait Islander health; and (2) provide the evidence for those involved in policy, strategy and program development and delivery. The review focuses primarily on type 2 diabetes among Aboriginal and Torres Strait Islander people—which is responsible for the majority of cases of diabetes in this population—but also refers to type 1 diabetes and gestational diabetes where relevant. It provides general information on the historical, social and cultural context of diabetes, and the behavioural and biomedical factors that contribute to diabetes among Aboriginal and Torres Strait Islander people. This review provides detailed information on the extent of diabetes, and its complications and comorbidities among Aboriginal and Torres Strait Islander people, including: incidence and prevalence data; hospitalisations; mortality and burden of disease. This review discusses the issues of prevention and management of diabetes, and provides information on relevant programs, services, policies and strategies that address the health issue of diabetes among Aboriginal and Torres Strait Islander people. This review concludes by discussing possible future directions for combatting the growing epidemic of diabetes in Australia.

This review draws mostly on journal publications, government reports, national data collections and national surveys, the majority of which can be accessed through the HealthInfoNet’s Australian Indigenous HealthBibliography.

When referring to Australia’s Indigenous people, the HealthInfoNet prefers to use the terms Aboriginal, Torres Strait Islander, or Aboriginal and Torres Strait Islander. However, when referencing information from other sources, our authors are ethically bound to utilise the terms from the original source unless they can obtain clarification from the report authors/copyright holders. As a result, readers may see these terms used interchangeably with the term ‘Indigenous’ in some instances. If they have any concerns they are advised to contact the HealthInfoNet for further information.

Acknowledgements

Special thanks are extended to:

  • the anonymous reviewer whose comments greatly assisted finalisation of this review
  • other staff at the Australian Indigenous HealthInfoNet, particularly to Christine Potter, Miranda Poynton and Millie Harford-Mills, for their assistance and support
  • the Australian Government Department of Health for their ongoing support of the work of the HealthInfoNet.

Key facts

The context of Aboriginal and Torres Strait Islander health and diabetes

  • The factors contributing to diabetes among Aboriginal and Torres Strait Islander people reflect a combination of broad historical, social and cultural factors as well as proximal health risk factors.
  • In 2012-2013, after age-adjustment, Aboriginal and Torres Strait Islander people were more likely than non-Indigenous people to: be overweight or obese (1.2 times); have high blood pressure (1.2 times); have abnormal high density lipoprotein cholesterol (1.8 times) and triglycerides (1.9 times); and to smoke (2.6 times). Aboriginal and Torres Strait Islander people were less likely to meet the guidelines for daily fruit intake (0.9 times) or daily vegetable intake (0.8 times) than non-Indigenous people.
  • In 2012-2013, obese Aboriginal and Torres Strait Islander people were nearly five times as likely to have diabetes than those who were of normal weight or underweight (19% compared with 4%).
  • In 2012-2013, Aboriginal and Torres Strait Islander people with high blood pressure were nearly three times as likely as those without high blood pressure to have diabetes(24% compared with 9%).

The extent of diabetes among Aboriginal and Torres Strait Islander people

  • Individual studies provide varying estimates of the prevalence of diabetes in specific Aboriginal and Torres Strait Islander communities—some as low as 4%, others as high as 33%.
  • In 2012-2013, national estimates of the prevalence of diabetes (type 1, type 2 or high sugar levels) among Aboriginal and Torres Strait Islander people ranged from 9% (based on self-reported data) to 11% (based on biomedical data). After age-adjustment, Aboriginal and Torres Strait Islander people were more than 3 times as likely as non-Indigenous people to have diabetes.
  • Between 2006 and 2011, the age-specific incidence rates of type 2 diabetes for young Aboriginal and Torres Strait Islander people were more than eight times higher than those for non-Indigenous 10-14 year olds, and almost four times higher than those for non-Indigenous 15-19 year olds.
  • Between 2005 and 2007, 1.5% of Aboriginal and Torres Strait Islander women who gave birth had pre-existing diabetes and 5.1% had gestational diabetes mellitus (GDM). Aboriginal and Torres Strait Islander women who gave birth were more than three times as likely to have pre-existing diabetes and almost two times as likely to have GDM as their non-Indigenous counterparts.
  • In 2012-13, after age-adjustment, Aboriginal and Torres Strait Islander people were four times more likely to be hospitalised for diabetes than non-Indigenous people. They were nearly two times more likely to be hospitalised for type 1 diabetes and GDM, and four times more likely to be hospitalised for type 2 diabetes, than their non-Indigenous counterparts.
  • In 2013, diabetes (excluding GDM) was the second leading underlying cause of death among Aboriginal and Torres Strait Islander people, with an age-adjusted death rate six times higher than that for non-Indigenous people.

Complications and comorbidities associated with diabetes

  • In 2012-13, age-standardised hospitalisation rates for complications of type 2 diabetes (as a principal diagnosis) were almost six times higher for Aboriginal and Torres Strait Islander people living in all jurisdictions, than those for non-Indigenous people.
  • In 2012-13, hospitalisation rates for renal complications of type 2 diabetes were 10 times higher among Aboriginal and Torres Strait Islander people than those among non-Indigenous people.
  • In 2012-13, Aboriginal and Torres Strait Islander people with diabetes, cardiovascular disease and chronic kidney disease (i.e. all three conditions at the same time) were seven times more likely to be hospitalised than their non-Indigenous counterparts.
  • In 2005-2007, Aboriginal and Torres Strait Islander mothers who had diabetes during pregnancy were more likely than their non-Indigenous counterparts to have complications, including: pre-term delivery, pre-term induction, and a long hospital stay. Their babies were more likely than non-Indigenous babies to have a low Apgar score, high level resuscitation, and a long hospital stay.

Prevention and management of diabetes

  • Evidence suggests that short-term healthy lifestyle programs designed to prevent type 2 diabetes among Aboriginal and Torres Strait Islander people, can have positive health effects for up to two years, and are more likely to be effective if they are initiated by the community.
  • Evidence suggests that structured management strategies used in primary care settings can lead to sustained improvements in diabetes care and health outcomes for Aboriginal and Torres Strait Islander people.

Diabetes programs and services

  • Evidence suggests that competent, culturally appropriate primary health care services can be effective in improving diabetes care and outcomes for Aboriginal and Torres Strait Islander people.
  • Evidence suggests that primary health care services that apply continuous quality improvement (CQI), can experience improvements in both service delivery rates and clinical outcome measures in Aboriginal and Torres Strait Islander patients with diabetes.

Diabetes policies and strategies

  • In 2013, Diabetes Australia developed the Aboriginal and Torres Strait Islanders and diabetes action plan. It provided to government a proposed national plan, the first of its kind, to guide future approaches in Aboriginal and Torres Strait Islander diabetes policy and program development.
  • At the end of 2015, the Federal Government released the Australian national diabetes strategy 2016-2020. This strategy includes a specific goal to reduce the impact of diabetes among Aboriginal and Torres Strait Islander people. Many of the potential areas for action identified in the strategy are consistent with recommendations in the Diabetes Australia Action plan.
  • The Diabetes Australia Action plan and the new National diabetes strategy highlight the need for a coordinated national approach to guide the development of holistic diabetes programs that integrate cultural values and address the health of Aboriginal and Torres Strait Islander people across their lifespan.

The context of Aboriginal and Torres Strait Islander health and diabetes

The risk of developing diabetes is influenced not only by an individual’s behavior, but also by: historical, social, cultural, geographical, economic and community factors; and government health policies and services [16]. Diabetes exists alongside a broad range of historical, social and cultural determinants that influence the health of Aboriginal and Torres Strait Islander people [13, 15].

The broad health disadvantages experienced by Aboriginal and Torres Strait Islander people can be considered historical in origin [17], but they have been perpetuated by the contemporary social and cultural determinants of health that contribute to current Aboriginal and Torres Strait Islander health inequalities [18, 19]. To understand the impact of diabetes on Aboriginal and Torres Strait Islander people it is necessary to understand the historical, social and cultural context of Aboriginal and Torres Strait Islander health.

The historical, social and cultural context

Aboriginal and Torres Strait Islander people maintained a hunter-gatherer lifestyle up until the late 18th century, but the arrival of Europeans in 1788 led to major changes in lifestyle [20, 21]. Traditional activities associated with finding renewable food and resources, maintaining familial and cultural practices, and sustaining the spiritual connection to country changed over time [17, 20-23].

Adverse changes in physical activity and nutrition (key risk factors for diabetes) played an important role in the development of diabetes in Aboriginal and Torres Strait Islander people, particularly in the second half of the 20th century [20, 23]. The first case of diabetes among Aboriginal and Torres Strait Islander people was recorded in Adelaide in 1923 [24]. Records prior to this time showed that Aboriginal and Torres Strait Islander people were fit and lean, and did not suffer from the metabolic conditions characteristic of European populations [25 cited in 26]. The earliest detailed studies investigating the development of diabetes in Aboriginal and Torres Strait Islander populations were not undertaken until the early 1960s [26]. These and subsequent studies found a significant correlation between the development of a ‘westernised’ lifestyle and the levels of diabetes in the Aboriginal and Torres Strait Islander population [26, 27].

In contemporary society, economic opportunity, physical infrastructure and social conditions influence the health of individuals and communities [18, 28, 29]. These factors are apparent in measures of education, employment, income, housing, access to services, connection with land, racism, and incarceration. On all these measures, Aboriginal and Torres Strait Islander people suffer substantial disadvantage in comparison with their non-Indigenous counterparts.

The factors contributing to diabetes among Aboriginal and Torres Strait Islander people reflect a combination of broad historical influences, and social and cultural determinants, as well as proximal health risk factors. It is beyond the scope of this review to discuss the underlying social and cultural determinants that influence the development of diabetes; or emerging evidence regarding the role of epigenetic factors3, the intrauterine environment and other early life factors [2]; but the main health risk factors are discussed below.

Factors contributing to diabetes among Aboriginal and Torres Strait Islander people

Several behavioural and biomedical factors are known to increase the risk of developing diabetes, particularly type 2 diabetes [31]; conversely improvements in these factors can reduce the risk of diabetes and become protective in nature.

Protective factors

Beneficial changes in lifestyle, such as a reduction in obesity, increases in physical activity and improvements in diet, are critical to reducing the risk of type 2 diabetes [16, 31]. There is also evidence that breastfeeding can reduce the risk of maternal type 2 diabetes in later life [32]. An Australian study published in 2010, found an excess risk of diabetes among childbearing women who did not breastfeed, compared with women who did not have children. This risk was substantially reduced by breastfeeding, and the benefit increased with the duration of breastfeeding. Breastfeeding also reduces the risk of babies becoming overweight [13], and reduces the risk of early onset obesity and diabetes in babies born to mothers who have diabetes in pregnancy [15]. According to the 2004-2005 National Aboriginal and Torres Strait Islander health survey, 84% of Aboriginal and Torres Strait Islander mothers aged 18-64 years reported having breastfed their children [33]. In the 2008 National Aboriginal and Torres Strait Islander social survey, 76% of Aboriginal and Torres Strait children aged 0-3 years were reported to have been breastfed [34].

Risk factors

Behavioural and biomedical risk factors known to increase the risk of developing diabetes, particularly type 2 diabetes, include high blood pressure, high blood cholesterol, tobacco smoking, low levels of physical activity, poor diet, and being overweight or obese [31]. Aboriginal and Torres Strait Islander people are more likely to have these risk factors for diabetes than non-Indigenous Australians [5], and many who already have diabetes have multiple risk factors and other related health problems [35-37].

Box 2: Health risk factors for diabetes

Health risk factors refer to the behaviours, characteristics, or exposures that increase the likelihood of a person developing a disease [31]. When people have multiple risk factors, the likelihood of developing the disease is heightened. Risk factors can also increase the severity of the disease and the likelihood of developing complications or other diseases, and can compromise efforts to provide optimal care to people who already have the disease.

The conventional risk factors for diabetes can be divided into two main categories: non-modifiable and modifiable [31, 38]. Non-modifiable risk factors include family history and age. Modifiable risk factors can be categorised as behavioural or biomedical and can be modified by changes in behaviour and lifestyle, or the use of medical interventions. Behavioural risk factors are health-related behaviours and include tobacco smoking, low levels of physical activity and poor nutrition. Biomedical risk factors are often influenced by behavioural risk factors, but refer to factors that are present in the body and include impaired glucose regulation, high blood pressure (hypertension), high blood cholesterol (dyslipidaemia) and obesity. When these risk factors occur together, known collectively as the metabolic syndrome, they greatly increase the risk of type 2 diabetes.

Having more than one risk factor increases the risk of diabetes and having diabetes increases the risk of some other diseases including cardiovascular disease, kidney disease and diabetic retinopathy [31, 39]. Cardiovascular disease is itself a risk factor for diabetes.

Self-reported and biomedical data regarding the prevalence of selected health risk factors among Aboriginal and Torres Strait Islander people is available from the 2012-13 Australian Aboriginal and Torres Strait Islander health survey (AATSIHS) [5, 6]. Although this data is from a national cross-sectional survey, and cause and effect cannot be attributed to risk factors and chronic conditions present at the time of the survey [31], the high prevalence of some risk factors among Aboriginal and Torres Strait Islander people is likely to contribute to the high prevalence of diabetes in this population compared with the non-Indigenous population [16].

Box 3: The 2012-2013 Australian Aboriginal and Torres Strait Islander health survey (AATSIHS)

The 2012–2013 AATSIHS is the latest national Aboriginal and Torres Strait Islander health survey conducted by the Australian Bureau of Statistics (ABS). It collected information from a nationally representative sample of around 12,900 Aboriginal and Torres Strait Islander people [5, 6]. Results from the AATSIHS provide information on health risk factors, long-term health conditions (including diabetes/high sugar levels), use of health services, and biomarkers of chronic disease (including diabetes) and nutrition. The 2012-2013 AATSIHS expands on the information included in previous health surveys via two new components – the National Aboriginal and Torres Strait Islander nutrition and physical activity survey (NATSINPAS) and the National Aboriginal and Torres Strait Islander health measures survey (NATSIHMS).

Included among the health risk factors for which data has been collected in the 2012-13 AATSIHS, are several that are risk factors for diabetes, specifically: overweight and obesity; high blood pressure; abnormal cholesterol and triglycerides; smoking; and inadequate fruit and vegetable intake [5, 6].

Overweight and obesity

Sixty-six percent of Aboriginal and Torres Strait Islander people aged 15 years and over were either overweight (29%) or obese (37%) according to their body mass index (BMI) [40]. The proportion of Torres Strait Islanders4 who were overweight or obese was slightly higher (33% and 40% respectively) than the proportion of Aboriginal people (28% and 37% respectively). The proportion of overweight or obese children aged 2-4 years was smaller in the Aboriginal and Torres Strait Islander population than in the non-Indigenous population (17% compared with 23%) but similar among children aged 5-9 years (24% and 23% respectively) [41]. The proportion of overweight or obese people in all other age groups was significantly greater for Aboriginal and Torres Strait Islander people than for non-Indigenous people [41, 42]. After age-adjustment, Aboriginal and Torres Strait Islander people aged 15 years and over were 1.2 times as likely as non-Indigenous people to be overweight or obese [42].

Obese Aboriginal and Torres Strait Islander people aged 18 years and over were around five times more likely to have diabetes5 than those who were of normal weight or underweight (19% compared with 4%) [36].

High blood pressure

Twenty percent of Aboriginal and Torres Strait Islander adults aged 18 years and over had high blood pressure (≥140/90 mmHg or higher) [43]. After age-adjustment, Aboriginal and Torres Strait Islander adults were more likely to have high blood pressure than non-Indigenous adults (rate ratio 1.2).

Aboriginal and Torres Strait Islander people with high blood pressure were nearly three times as likely as those without high blood pressure to have diabetes(24% compared with 9%) [36].

Abnormal cholesterol and triglycerides

The proportion of Aboriginal and Torres Strait Islander adults aged 18 years and over with abnormal test results for cholesterol or triglycerides was as follows [44]:

  • twenty-five percent had abnormal test results for total cholesterol (≥5.5 mmol/L)
  • twenty-five percent had abnormal test results for low density lipoprotein (LDL) cholesterol (≥3.5 mmol/L)
  • forty percent had abnormal test results for high density lipoprotein (HDL) cholesterol (for males <1.0 mmol/L; for females < 1.3 mmol/L)
  • twenty-five percent had abnormal test results for triglycerides (≥2.0 mmol/L).

After age-adjustment, Aboriginal and Torres Strait Islander adults were more likely to have abnormal HDL cholesterol and triglycerides than non-Indigenous adults (ratios of 1.8 and 1.9 respectively), but were less likely to have abnormal total cholesterol and LDL cholesterol (ratios for both were 0.8) [45].

Aboriginal and Torres Strait Islander adults with diabetes were around twice as likely to have abnormal HDL cholesterol (67% compared with 35%) and triglycerides (44% compared with 22%) than those without diabetes [37].

Smoking

Forty-two percent of Aboriginal and Torres Strait Islander people aged 15 years and over smoked on a daily basis (42% of Aboriginal people and 38% of Torres Strait Islander people) [40]. After age-adjustment, Aboriginal and Torres Strait Islander people aged 15 years and over were 2.6 times as likely as non-Indigenous people to be current daily smokers [46]. Sixty-nine percent of Aboriginal and Torres Strait Islander adults aged 18 years and over were current or ex-smokers (47% and 22% respectively).

Among current and ex-smokers, 11% and 17% (respectively) had diabetes, compared with 12% among those who had never smoked [36].

Inadequate fruit and vegetable intake

Forty-six percent of Aboriginal and Torres Strait Islander people aged 2 years and over had inadequate daily fruit intake and 92% had inadequate daily vegetable intake based on 2013 National Health and Medical Research Council (NHMRC) guidelines [47]. Among Aboriginal and Torres Strait Islander people aged 2 years and over, 93% had inadequate fruit and/or vegetable intake, and the proportion was higher (97%) among Aboriginal and Torres Strait Islander people aged 15 years and over. Torres Strait Islander people aged 15 years and over were less likely to have inadequate daily fruit intake (52%) compared with Aboriginal people (59%), but were similarly likely to have inadequate daily vegetable intake (94% and 95% respectively) [40]. After age-adjustment, Aboriginal and Torres Strait Islander people aged 15 years and over were less likely to meet the guidelines for daily fruit intake or daily vegetable intake than non-Indigenous people (ratios were 0.9 and 0.8 respectively) [5].

Trends in chronic disease risk factors

In a study conducted between 1992 and 2006, Wang and colleagues describe trends in chronic disease risk factors over a 10 to 14-year interval in a high-risk, remote Aboriginal community in the Northern Territory (NT) [48]. Community members aged five years or older participated in two health surveys, the first performed between 1992 and 1997 and the second between 2004 and 2006. Outcomes were compared across age-matched and sex-matched pairs. Results from the two surveys suggest improvements in some risk factors for diabetes over this period, including:

  • a reduction in smoking and rates of elevated blood pressure for males aged 15-24 years
  • a decrease in weight, BMI, systolic blood pressure and triglycerides among males aged 15-44 years
  • higher levels of HDL cholesterol among males aged 15+ years
  • improvements in HDL cholesterol for women aged 15+ years and LDL cholesterol for those aged 45+.

Despite these improvements, and a decrease in the prevalence of diabetes among males aged 45-54 years, the prevalence of other risk factors for diabetes increased (particularly among women) and the prevalence of diabetes remained the same or increased across all other age groups [48]. The prevalence of diabetes was notably higher among males aged 55 years and over and females aged 45 years and over, compared with the same age groups in the preceding survey. Approximately 50% or more of people in these age groups had diabetes at the time of the second survey, and the prevalence of diabetes increased by more than 50% in all females aged 15 years and over. Addressing the factors that increase the risk of diabetes remains critical to the prevention and management of this condition among Aboriginal and Torres Strait Islander people [13].

Extent of diabetes among Aboriginal and Torres Strait Islander people

There are several types of diabetes, of which the most frequently occurring are type 1, type 2 and gestational diabetes (GDM) (see Box 4) [49, 50]. Type 1 diabetes is relatively uncommon in the Aboriginal and Torres Strait Islander population, but Aboriginal and Torres Strait Islander people experience disproportionately high levels of type 2 diabetes [51]. Levels of GDM are also higher among Aboriginal and Torres Strait Islander women than among non-Indigenous women [7, 52].

Box 4: Types of diabetes

Type 1 diabetes (also known as type 1 diabetes mellitus—T1DM) is most frequently diagnosed in childhood and adolescence [7, 35, 53]. It is an autoimmune condition that is characterised by hyperglycaemia (high blood sugar levels) resulting from the body’s inability to produce insulin. Most cases are caused by the destruction of insulin-producing cells in the pancreas by the body’s own immune system. People with type 1 diabetes need insulin replacement for survival.

Type 2 diabetes (also known as type 2 diabetes mellitus—T2DM) usually develops in adulthood, although it is increasingly reported in some child and adolescent populations [7, 53]. It is characterised by hyperglycaemia due to insulin resistance and/or a deficiency in insulin production. This form of diabetes often runs in families, and typically occurs when risk factors such as obesity, poor nutrition, and lack of physical activity are present. Type 2 diabetes can usually be controlled through lifestyle modifications, but may require insulin treatment over time.

Gestational diabetes (also known as gestational diabetes mellitus—GDM) is a form of diabetes that develops during pregnancy in some women [7, 35, 53]. GDM is caused by placental hormones that block the action of insulin, leading to insulin resistance and high blood sugar levels in pregnant women not previously diagnosed with other forms of diabetes [7, 35, 53, 54]. This type of diabetes is short term and usually develops in the second or third trimester of pregnancy, with potentially adverse outcomes for both mother and baby [7, 35]. GDM usually disappears after the baby is born, although it puts the mother at increased risk of developing type 2 diabetes later in life. GDM can recur in later pregnancies.

There are various ways to measure the extent of diabetes in a given population, including prevalence, incidence, health service utilisation, mortality and burden of disease. This review focuses primarily on national data that provide an aggregate picture of the impact of diabetes on Aboriginal and Torres Strait Islander people. Much of the published data pertains to type 2 diabetes, but figures for type 1 diabetes and GDM are reported where available. Separate data for Torres Strait Islanders is limited, but is also provided where available. The various measurements used in this review are defined below (see Box 5). It should be noted however, that:

  • the availability and quality of data varies
  • there are data limitations associated with each of the measures of diabetes
  • statistics about diabetes for Aborignal and Torres Strait Islander people are often underestimated (Appendix 1 provides a brief discussion of limitations associated with data sources used in this review).

Box 5: Measuring diabetes

Incidence is the number of new cases of diabetes that occur during a given period [55].

Prevalence is the number or proportion of cases of diabetes in a population at a given time [55].

Age-standardised rates enable comparisons of rates of diabetes between populations that have different age structures [56]. Age standardisation is often used when comparing Aborignal and Torres Strait Islander people and non-Indigenous people because the Aborignal and Torres Strait Islander population has a younger age structure than the non-Indigenous population.

Rate ratio (RR) is the rate of Aborignal and Torres Strait Islander people affected by diabetes divided by the rate of non-Indigenous people affected by diabetes [56].

Ratio (R) is the proportion of Aborignal and Torres Strait Islander people affected by diabetes divided by the proportion of non-Indigenous people affected by diabetes.

Potentially preventable hospitalisations are hospital admissions for conditions (including diabetes) that may have been avoided through appropriate preventive measures and early disease management, usually delivered in primary care and community-based care settings [56].

Potentially avoidable deaths are deaths among people aged less than 75 years from conditions (including diabetes) considered potentially preventable and treatable [56]. Potentially avoidable deaths can be reduced through lifestyle improvements and appropriate primary prevention, early intervention and medical treatment.

Burden of disease is measured in disability-adjusted life years (DALYs). It provides a combined estimate of years of life lost due to premature mortality caused by diabetes, and years of life lost due to disability or ill health caused by diabetes [57].

Fatal burden is measured in years of life lost (YLLs) and refers to the burden of disease that is caused by premature mortality from diabetes [57].

Prevalence

A systematic review conducted in 2011—of studies published between 1997 and 2010—reported considerable variation in the prevalence of diabetes among Aboriginal and Torres Strait Islander people [58]. Estimates of the prevalence of diabetes ranged from 4% to 33% depending on the communities or groups surveyed. According to the 2012-2013 AATSIHS, national estimates of the prevalence of diabetes (type 1, type 2 or high sugar levels) among Aboriginal and Torres Strait Islander people range from 8.6% (based on self-reported data [5]) to 11.1% (based on biomedical data [6]).

Self-reported data

According to the 2012-2013 AATSIHS, around 8.6% of Aboriginal and Torres Strait Islander people (8.8% of Aboriginal people and 7.0% of Torres Strait Islander people) aged 2 years and over reported that they had type 1 or type 2 diabetes and/or high sugar levels in their blood or urine [5, 40]. After age-adjustment, rates of diabetes and/or high sugar levels were 3.2 times higher among Aboriginal and Torres Strait Islander people than among non-Indigenous people [59]. Diabetes and/or high sugar levels were reported by a higher proportion of Aboriginal and Torres Strait Islander females (9.6%) than males (7.7%) [60].

The prevalence of diabetes and/or high sugar levels increased with age,6 [61] ranging from 1% for Aboriginal and Torres Strait Islander people aged 2-14 years to 40% for those aged 55 years and over (Table 1) [59]. The age-specific levels from 25 years onwards were between three and five times higher than those for non-Indigenous people.

Table 1. Proportions (%)1 of people reporting diabetes/high sugar levels as a long-term health condition, by Indigenous status, and Indigenous:non-Indigenous ratios, Australia, 2012-2013

Age group (years)

Aboriginal and Torres

Strait Islander (%)

Non-Indigenous (%) Ratio2,4
2-14 0.5 NA3 NA3
15-24 1.4 NA3 NA3
25-34 5.3 1.1 4.8
35-44 11 2.8 4.0
45-54 23 5.6 4.2
55+ 40 14 2.9

Notes:

  1. Proportions are expressed as percentages
  2. Ratio is the Indigenous proportion divided by the non-Indigenous proportion
  3. Not available
  4. Rounding may result in inconsistencies in calculated ratios

Source: ABS, 2014 (derived from Table 6.3) [59]

The prevalence of diabetes/high sugar levels was lower among Aboriginal and Torres Strait Islander people living in non-remote areas (7.5%) than among those living in remote areas (12.8%) [59] and varied between states and territories [45]. The prevalence among Aboriginal and Torres Strait Islander people was highest in the Northern Territory (NT) at 12%, and lowest in Tasmania (Tas) at 3.8%, with 10% in Western Australia (WA), 8.9% in South Australia (SA), 8.3% in Queensland (Qld), 8.1% in New South Wales (NSW), 7.6% in the Australian Capital Territory (ACT), and 7.1% in Victoria (Vic).

Biomedical data

Biomedical results broadly confirmed the self-reported results obtained from the AATSIHS. Biomedical data was obtained for a subset of Aboriginal and Torres Strait Islander adults (18 years and over) who provided blood and urine samples [6]. Results for fasting plasma glucose levels revealed that 11% of Aboriginal and Torres Strait Islander adults had diabetes (9.6% had known diabetes and 1.5% were newly diagnosed from their test results) [62]. A further 4.7% of Aboriginal and Torres Strait Islander adults were at high risk of diabetes. After age-adjustment, Aboriginal and Torres Strait Islander adults were 3.3 times as likely as non-Indigenous adults to have diabetes [63]. Biomedical results also revealed that:

  • diabetes prevalence among Aboriginal and Torres Strait Islander adults increased with age, with particularly high rates among those aged 55 years and over (35%) [63]
  • diabetes tended to occur at earlier ages among Aboriginal and Torres Strait Islander adults than among non-Indigenous adults, with Aboriginal and Torres Strait Islander people having diabetes at rates similar to those of non-Indigenous people who were 20 years older [63]
  • Aboriginal and Torres Strait Islander adults in remote areas were twice as likely to have diabetes as those living in non-remote areas (20.8% compared with 9.4%) [64]
  • around half of Aboriginal and Torres Strait Islander adults with diabetes also had signs of chronic kidney disease (53% compared with 11% without diabetes) [37].

Gestational diabetes mellitus

The Australian Institute of Health and Welfare (AIHW) has analysed data from the National perinatal data collection (NPDC) and calculated the prevalence of GDM for the period 2005-2007 [7]. In this period, 6.6% of Aboriginal and Torres Strait Islander women who gave birth in Australia had diabetes during pregnancy: 1.5% had pre-existing diabetes and 5.1% had GDM. Aboriginal and Torres Strait Islander women who gave birth were 3.2 times more likely than their non-Indigenous counterparts to have pre-existing diabetes and 1.6 times more likely to have GDM.

A systematic review investigating GDM prevalence among Aboriginal and Torres Strait Islander women was published in 2015. The meta-analysis of studies conducted between 1980 and 2013, found that the prevalence of GDM among Aboriginal and Torres Strait Islander women was 5.7% [52]. This pooled GDM prevalence is similar to that reported for 2005-2007 [7]; however GDM prevalence varied substantially between studies (1.3% to 18.5%) [52]. The researchers noted that the prevalence of GDM increased fourfold between 1985-1987 and 1989 (from 3% to 12%)—following the introduction of universal screening for Aboriginal women in Central Australia—and concluded that those studies reporting higher screening rates are more likely to reflect the true prevalence.

Incidence

Insulin-treated diabetes

National incidence data for diabetes is based on estimates for insulin-treated diabetes (type 1, type 2 and GDM) and obtained from the National (insulin-treated) diabetes register (NDR) [10] (Appendix 1 provides information regarding the limitations associated with this data).

In 2013, there were 70 new cases of type 1 diabetes among Aboriginal and Torres Strait Islander people, accounting for 3% of all new cases [65]. Between 2005 and 2013, 489 Aboriginal and Torres Strait Islander people were diagnosed with type 1 diabetes. The incidence rate for Aboriginal and Torres Strait Islander people in this period was lower than the rate for non-Indigenous people (7 per 100,000 population compared with 10 per 100,000 population).

In 2011, 62 Aboriginal and Torres Strait Islander people were diagnosed with type 1 diabetes7, 656 began using insulin to treat type 2 diabetes and 118 Aboriginal and Torres Strait Islander females began using insulin to treat GDM8 [10]. Of the new cases of insulin-treated diabetes identified in 2011, Aboriginal and Torres Strait Islander people accounted for 2.6% of cases of type 1 diabetes, 1.8% of cases of type 2 diabetes, and 1.9% of cases of GDM among females aged 15-49. Type 1 diabetes occurred more frequently among Aboriginal and Torres Strait Islander males (60%) than females, and type 2 diabetes (insulin-treated cases only) occurred more frequently among Aboriginal and Torres Strait Islander females (54%) than males.

Aggregated data for the years between 2006 and 2011 revealed that [10]:

  • age-adjusted incidence rates of insulin-treated type 2 diabetes were almost 4 times higher for Aboriginal and Torres Strait Islander people (134 per 100,000) than non-Indigenous people (36 per 100,000)
  • age-adjusted incidence rates of type 1 diabetes were lower for Aboriginal and Torres Strait Islander people (7 per 100,000) than for non-Indigenous people (10 per 100,000)
  • age-adjusted incidence rates of insulin-treated GDM were similar for Aboriginal and Torres Strait Islander females (60 per 100,000) and non-Indigenous females (59 per 100,000).

Type 2 diabetes in Aboriginal and Torres Strait Islander children and adolescents

There is growing concern regarding the emergence of type 2 diabetes in Aboriginal and Torres Strait Islander children and adolescents [2]. Data is limited, but type 2 diabetes accounts for the majority of new cases of diabetes in this population [8]. It occurs more frequently among Aboriginal and Torres Strait Islander adolescents than among their non-Indigenous counterparts [66], and places them at heightened risk of comorbidities, diabetes complications and associated premature mortality [67].

Between 2006 and 2011, 252 new cases of diabetes were reported among Aboriginal and Torres Strait Islander youth aged 10-19 years at diagnosis9 [8]. Of these, 55% were type 2 and 43% were type 1 diabetes. The age-specific rates of type 2 diabetes for young Aboriginal and Torres Strait Islander people were much higher than for their non-Indigenous counterparts (8.3 times as high among 10-14 year olds and 3.6 times as high for 15-19 year olds). After age-adjustment, the incidence rate of type 2 diabetes for Aboriginal and Torres Strait Islander people aged 10-39 years was 3.5 times that of non-Indigenous people.

A population-based study conducted in NSW between 2001 and 2008, found that young Aboriginal and Torres Strait Islander people (aged 10-18 years) experienced a disproportionately high rate of type 2 diabetes10 [68]. The mean annual incidence of type 2 diabetes was 6.9 times higher in Aboriginal and Torres Strait Islander youth than in their non-Indigenous peers. Young Aboriginal and Torres Strait Islander females were more likely to be diagnosed with type 2 diabetes than their male counterparts (55% compared with 45%). Aboriginal and Torres Strait Islander youth were diagnosed with type 2 diabetes at an earlier average age than their non-Indigenous peers (13.5 years compared with 14.8 years) and were more likely to reside in rural areas than urban areas (71% compared with 26%).

Health service utilisation

Measures of health service utilisation cannot provide information about whether the health system is meeting the needs of Aboriginal and Torres Strait Islander people, but they give some indication of the demand for, and access to, health services [69]. Included among these measures are figures for attendance at general practices and hospitals.

General practice attendances

General practitioners (GPs) are usually the initial point of contact for people with diabetes and often play a key role in coordinating the other specialised services and health professionals who are needed to manage the condition [38]. The Bettering the evaluation and care of health (BEACH) survey is a continuous, national, cross-sectional survey of the clinical activity of GPs [70]. The survey provides some evidence of the frequency with which GPs manage diabetes for Aboriginal and Torres Strait Islander patients.

According to survey data for the period April 2008 to March 2013, GPs were twice as likely to manage type 2 diabetes during encounters with Aboriginal and Torres Strait Islander patients compared with encounters with other patients (8.2 per 100 encounters compared with 4.0 per 100 encounters) [71].

Based on survey data for the period April 2006 to March 2011, diabetes was the most common individual problem managed by GPs during encounters with Aboriginal and Torres Strait Islander patients (7.6 per 100 encounters), due mainly to the higher management rate of type 2 diabetes (7.2 per 100 encounters) [72]. After adjusting for age, this was almost three times the rate for non-Indigenous patients. GP encounters with Aboriginal and Torres Strait Islander patients with type 1 diabetes or GDM occurred much less frequently (0.3 and 0.1 per 100 encounters respectively). After adjusting for age, these rates were higher than rates for non-Indigenous patients (1.6 times and 1.5 times respectively) but the differences were not statistically significant.

Hospitalisation

Hospital services are typically required to treat the advanced stages of complications of diabetes or acute episodes of poor glycaemic control [35]. Hospitalisation data therefore usually provides information on the more severe aspects of the disease  and doesn’t necessarily reflect the burden of diabetes in the community [38]. Despite these limitations (Appendix 1 provides further information regarding the limitations associated with this data), hospitalisation data remains the most comprehensive source of information about health service utilisation. The higher levels of diabetes observed among Aboriginal and Torres Strait Islander people are clearly reflected in hospitalisation figures.

In 2012-13 there were 2,749 hospital separations for diabetes (excluding GDM) for Aboriginal and Torres Strait Islander people in all Australian jurisdictions11 [56]. After age-adjustment, Aboriginal and Torres Strait Islander people were four times more likely to be hospitalised for diabetes than non-Indigenous people.

There were similar numbers of hospitalisations for Aboriginal and Torres Strait Islander males and females (1,379 and 1,370 respectively). In comparison, males were 3.5 times more likely to be hospitalised, and females 4.7 times more likely to be hospitalised, than their non-Indigenous counterparts [56].

Hospitalisation rates for Aboriginal and Torres Strait Islander people with diabetes increased with increasing remoteness [56]. Age-standardised hospitalisation rates for Aboriginal and Torres Strait Islander people were highest in remote and very remote areas (11 per 1,000), followed by inner and outer regional areas (6.0 per 1,000), and major cities (4.3 per 1,000). Aboriginal and Torres Strait Islander people were 5.3 times more likely to be hospitalised for diabetes in remote and very remote areas, 3.4 times more likely to be hospitalised in inner and outer regional areas, and 2.8 times more likely to be hospitalised in major cities, than their non-Indigenous counterparts.

Further details are available for hospitalisations for diabetes as the principal and/or an additional diagnosis12. In 2012-13, Aboriginal and Torres Strait Islander people were four times more likely to be hospitalised for diabetes (all types13) as the principal and/or an additional diagnosis than non-Indigenous people [35]. Aboriginal and Torres Strait Islander males and females were both more likely to be hospitalised than their non-Indigenous counterparts (three and five times respectively).

Age-standardised hospitalisation rates for Aboriginal and Torres Strait Islander people with a principal or additional diagnosis of type 2 diabetes (5.5 and 115 per 1,000 respectively) were higher than those with a principal or additional diagnosis of type 1 diabetes (0.8 and 3.4 per 1,000 respectively) [35]. Aboriginal and Torres Strait Islander people were four times more likely to be hospitalised for type 2 diabetes, and 1.7 times more likely to be hospitalised for type 1 diabetes, than non-Indigenous people. Age-standardised hospitalisation rates for Aboriginal and Torres Strait Islander females with a principal or additional diagnosis of GDM were 1.5 and 3.9 per 1,000 respectively. Aboriginal and Torres Strait Islander females were 1.9 times more likely to be hospitalised for GDM than non-Indigenous females. Aboriginal and Torres Strait Islander males and females were more likely to be hospitalised for each type of diabetes than their non-Indigenous counterparts. When principal and additional diagnoses were analysed separately, the disparity was greatest for Aboriginal and Torres Strait Islander females with a principal diagnosis of type 2 diabetes, who were 8.1 times more likely to be hospitalised than non-Indigenous females (Tables 2 and 3).

Table 2: Diabetes hospitalisation rates, as the principal diagnosis, by Indigenous status and sex, 2012-13 (rate per 100,000 population)

Males

Females

Diabetes type

Indigenous Non-Indigenous RR Indigenous Non-Indigenous RR
Type 1 88 61 1.4 78 63 1.2
Type 2 563 129 4.4 529 65 8.1
GDM 150 19 7.9
Notes:

  1. ‘Non-Indigenous’ includes hospitalisations of those for whom Indigenous status was not stated.
  2. Directly age-standardised to the 2001 Australian standard population.

Source: AIHW, 2014 (derived from Tables A6, A7 and A8) [35]

Table 3: Diabetes hospitalisation rates, as an additional diagnosis, by Indigenous status and sex, 2012-13 (rate per 100,000 population)

Males

Females

Diabetes type

Indigenous Non-Indigenous RR Indigenous Non-Indigenous RR
Type 1 328 181 1.8 344 177 1.9
Type 2 10,126 3,258 3.1 12,821 2,200 5.8
GDM 390 266 1.5
Notes:

  1. ‘Non-Indigenous’ includes hospitalisations of those for whom Indigenous status was not stated.
  2. Directly age-standardised to the 2001 Australian standard population.

Source: AIHW, 2014 (derived from Tables A6, A7 and A8) [35]

Hospitalisation figures for 2012-13 do not provide an analysis of hospital separations for diabetes by age and Indigenous status, but these figures are available for the period July 2008 to June 2010 for Aboriginal and Torres Strait Islander people with a principal diagnosis of diabetes (all types excluding GDM) living in NSW, Vic, Qld, WA, SA and the NT14 [72]. In this period, age-specific hospitalisation rates for diabetes increased with age for both Aboriginal and Torres Strait Islander people and non-Indigenous people, but Aboriginal and Torres Strait Islander males and females had much higher hospitalisation rates for diabetes than their non-Indigenous counterparts in all age groups from 15–24 years onwards (Table 4). The greatest rate ratio between Aboriginal and Torres Strait Islander and non-Indigenous hospitalisation rates occurred among males in the 35-44 year age group and females in the 45-54 year age group, for which Indigenous rates were 9.1 and 11.8 times greater than their non-Indigenous counterparts.

Table 4: Age-specific hospitalisation rates for a principal diagnosis of diabetes1, by Indigenous status and sex, NSW, Vic, Qld, WA, SA, and NT2, July 2008 to June 2010 (age-standardised rate per 1,000 population)

Age group

Males

Females

Indigenous

Non-Indigenous

RR3,5

Indigenous

Non-Indigenous

RR3,5

0-4

0.1

0.3

0.4

0.2

0.3

0.5

5-14

1.1

0.9

1.2

1.0

1.0

1.0

15-24

1.6

0.9

1.7

1.9

1.2

1.6

25-34

3.0

0.8

4.0

4.8

0.9

5.5

35-44

11

1.2

9.1

9.8

1.1

9.2

45-54

21

2.5

8.6

20

1.7

11.8

55-64

34

6.6

5.2

36

3.9

9.1

65+

42

20

2.1

44

14

3.1

All ages4

14

4.1

3.4

14

3.0

4.8

Notes:

  1. Based on the ICD-10-AM sixth edition codes E10-E14 (this excludes GDM). Indigenous rates are calculated using population estimates based on the 2006 Census.
  2. Data excludes private hospitals in the NT
  3. RR is the rate ratio Indigenous: non-Indigenous people
  4. Directly age-standardised using the Australian 2001 standard population
  5. Rounding may result in inconsistencies in calculated ratios

Source: AIHW, 2013 (derived from Table 1.09.6) [72]

Age-standardised hospitalisation rates for Aboriginal and Torres Strait Islander people with diabetes were greatest in WA (21 per 1,000), followed by SA (18 per 1,000), the NT (17 per 1,000), Qld (17 per 1,000), NSW (8.7 per 1,000), and Vic (8.1 per 1,000) [72]. The greatest disparities between Aboriginal and Torres Strait Islander and non-Indigenous hospitalisation rates were seen among females in WA and the NT (6.2 and 7.2 times higher respectively).

Potentially preventable hospitalisations

Hospitalisations for various chronic conditions, including complications of diabetes, are considered potentially preventable [56]. In 2012-13, after age-adjustment, Aboriginal and Torres Strait Islander people were hospitalised for potentially preventable chronic conditions at 4.3 times the rate for non-Indigenous people15. Diabetes complications accounted for the largest proportion (67%) of these hospitalisations, resulting in an age-adjusted rate for Aboriginal and Torres Strait Islander people that was 6.1 times greater than the rate for non-Indigenous people.

Age-adjusted hospitalisation rates for diabetes complications were greatest for Aboriginal and Torres Strait Islander people in remote and very remote areas combined, where they were 10.5 times greater than rates for their non-Indigenous counterparts [56]. In comparison, rates in major cities, and inner and outer regional areas (combined), were 5.7 and 4.5 times greater (respectively) for Aboriginal and Torres Strait Islander people.

Mortality

In 201316, diabetes17 was the second leading underlying cause of death for Aboriginal and Torres Strait Islander people, with an age-adjusted death rate six times higher than that for non-Indigenous people [9, 73]. Diabetes was responsible for 7.6% of deaths (202 deaths) among Aboriginal and Torres Strait Islander people living in NSW, Qld, SA, WA and the NT. In comparison, diabetes was responsible for 2.7% of deaths (2,726 deaths) of non-Indigenous people in these jurisdictions.

Diabetes was the leading cause of death among Aboriginal and Torres Strait Islander females in 2013, responsible for 121 deaths (10%). In comparison, there were 81 deaths (5.7%) among Aboriginal and Torres Strait Islander males [73]. After age-standardisation, Aboriginal and Torres Strait Islander females and males were both more likely to die from diabetes than their non-Indigenous counterparts (8.1 and 4.2 times respectively).

Between 2009 and 2013, the number of Aboriginal and Torres Strait Islander females dying from diabetes increased by 15.2%, compared with a 2.1% increase in deaths among non-Indigenous females [9]. In this period, the greatest disparity in Indigenous: non-Indigenous age-specific death rates occurred in the 45-54 year age group [73]. In this age group Aboriginal and Torres Strait Islander people were 17 times more likely to die from diabetes than their non-Indigenous counterparts (rate ratios were 26.5 for females and 12.9 for males). Age-standardised death rates for diabetes for Aboriginal and Torres Strait Islander people were greatest in the NT (180 per 100,000), followed by WA (139 per 100,000), Qld (87 per 100,000), SA (60 per 100,000) and NSW (50 per 100,000). The greatest disparity in Indigenous: non-Indigenous death rates were observed in WA (9.0 times higher among Aboriginal and Torres Strait Islander people), followed by the NT (7.9), Qld (5.6), NSW (3.5) and SA (3.3) [73].

From 2010-2012, diabetes was the underlying cause of death for 564 Aboriginal and Torres Strait Islander people (8% of all Indigenous deaths) in NSW, Qld, SA, WA and the NT [14]. Of these deaths, the underlying cause of death was recorded as: type 1 diabetes (5.0% of deaths); type 2 diabetes (46% of deaths); or the type of diabetes was unspecified (49% of deaths). In this period, diabetes was the underlying or associated cause of death for 1,474 Aboriginal and Torres Strait Islander people (21% of all Indigenous deaths).

For the period 2008-2012, diabetes was the third most common cause of avoidable mortality (after ischaemic heart disease and cancer) among Aboriginal and Torres Strait Islander people, responsible for 734 (10%) potentially avoidable deaths [56]. After age-adjustment, the potentially avoidable mortality rate from diabetes was 12.0 times greater for Aboriginal and Torres Strait Islander people than the rate for non-Indigenous people.

Burden of disease

The latest in a series of reports from the Australian burden of disease study 2011 (ABDS) provides estimates of the fatal burden of disease and injury for Aboriginal and Torres Strait Islander people, and the ‘gap’ in fatal burden between Aboriginal and Torres Strait Islander people and non-Indigenous people for the 2010 reference year18 [57]. Burden of disease estimates from the ABDS 2011 provide evidence regarding the diseases and injuries currently making the greatest contribution to Aboriginal and Torres Strait Islander mortality19.

Endocrine disorders (which include diabetes) were the sixth most common contributor to fatal burden20 (5%) for Aboriginal and Torres Strait Islander people and were in the top five causes of fatal burden for both Aboriginal and Torres Strait Islander men and women in all age groups from 45 years and over [57].

Endocrine disorders were the fourth most common contributor to the gap in fatal burden21 (10%) and had the highest relative disparity in fatal burden, with the rate for Aboriginal and Torres Strait Islander people being 7.9 times higher than the rate for non-Indigenous Australians [57]. The ABDS suggests that reducing Aboriginal and Torres Strait Islander deaths from endocrine disorders has the potential to make major inroads to ‘closing the gap’ in fatal burden between Aboriginal and Torres Strait Islander people and non-Indigenous people.

Complications and comorbidities associated with diabetes

Diabetes can cause many serious health complications [74] and is frequently accompanied by comorbidities, particularly cardiovascular disease (CVD) and chronic kidney disease (CKD) [35].

Complications

Some complications of diabetes may occur soon after diagnosis while others may develop over several years [74]. Short-term health complications include: diabetic ketoacidosis22, hypoglycaemia (low blood glucose level), increased susceptibility to infections and reduced ability to heal [10]. Over the longer term diabetes may progress to diseases of the small blood vessels (microvascular diseases) and diseases of the large blood vessels (macrovascular diseases) [74]. Diabetes can also contribute to feelings of distress, anxiety and depression [8].

Microvascular and macrovascular complications are the major causes of associated morbidity and mortality in people with diabetes [38]. Microvascular complications of diabetes include damage to the kidneys (nephropathy), nerves (neuropathy) and eyes (retinopathy) [53, 74]. Macrovascular complications include coronary heart disease, stroke and peripheral vascular disease.

Common complications of diabetes can be broadly grouped into circulatory, renal, ophthalmic and other complications23 [56] and are described briefly in Box 6. Complications in pregnancy are discussed separately in the following section [10].

Box 6: Common complications of diabetes

Circulatory complications

Circulatory complications of diabetes affect the heart and blood vessels and include coronary heart disease (angina and heart attacks), stroke, and peripheral vascular disease [35, 38].
Angina – temporary pain or discomfort in the chest resulting from inadequate blood supply in the heart at times of extra need, such as during exercise [35].
Heart attack – a life-threatening emergency that occurs when a blood clot suddenly blocks a vessel that supplies blood to the heart muscle [35].
Stroke – a sudden blockage or bleed in an artery supplying blood to the brain. This may cause paralysis of parts of the body, speech problems, or other disabilities [35].
Peripheral vascular disease (PVD) – inadequate blood supply to the extremities, often the legs, characterised by pain in the affected areas [35]. PVD, in association with peripheral neuropathy, increases the risk of developing foot complications, specifically foot ulcers and infections, which can in turn lead to lower limb amputations [38].

Renal complications

Renal complications of diabetes affect the kidneys and include diabetic nephropathy and chronic kidney failure [38]. These occur when high blood sugar levels damage the capillaries in the kidneys, reducing their filtering efficiency. Diabetic nephropathy is often asymptomatic until the disease is well-established, by which time interventions are less effective. Severe cases of diabetic nephropathy may lead to a type of chronic kidney failure called end-stage kidney disease (ESKD) that, if left untreated, is fatal.

Ophthalmic complications

Ophthalmic complications of diabetes affect the eyes and include diabetic retinopathy, cataracts and glaucoma [38]. They can result in vision impairment and blindness if not identified and treated in the early stages.
Diabetic retinopathy (DR) – damage to the blood vessels of the light-sensitive tissue at the back of the eye (retina).
Cataract – clouding of the normally clear lens that leads to a reduction in light entering the eye.
Glaucoma – pressure in the eye pinches the capillaries that carry blood to the retina and optic nerve. Over time this causes damage to these parts of the eye.

Other specified complications

Other specified complications of diabetes include damage to the nerve structure and function (neuropathy) and occur as a result of reduced blood flow to the nerves [38].
Peripheral neuropathy – occurs most frequently in the nerves of the toes, feet and legs, however the hands and arms can also be affected. Some sufferers will require amputation of the affected limbs.
Autonomic neuropathy – affects the nerves that control the heart and blood vessels, digestive system, urinary tract, sex organs, sweat glands and eyes leading to dysfunction in the major organs.

Hospitalisation figures are available for some of the conditions that can result from diabetes. These complications of diabetes are categorised according to the ICD-10-AM24 classification of diseases and refer to specific peripheral circulatory complications, renal complications, ophthalmic complications and other specified complications [56].

In 2012-13, age-standardised hospitalisation rates for complications of type 2 diabetes (as a principal diagnosis) were 5.6 times higher for Aboriginal and Torres Strait Islander people living in all jurisdictions, than those for non-Indigenous people [56]. The disparity in hospitalisation rates between Aboriginal and Torres Strait Islander people and non-Indigenous people was greatest for renal complications of type 2 diabetes (10 times higher). In comparison, hospitalisation rates for circulatory and opthalmic complications were 2.8 and 2.7 times higher (respectively) for Aboriginal and Torres Strait Islander people than for other Australians. The hospitalisation rate for multiple complications of diabetes was 6.5 times higher for Aboriginal and Torres Strait Islander people.

In 2012-13, age-standardised hospitalisation rates for complications of type 2 diabetes were greater for Aboriginal and Torres Strait Islander people than for non-Indigenous people regardless of the areas in which they lived. Disparities in the rates of renal and circulatory complications were greatest in regional areas (10.7 and 3.5 times higher respectively); for ophthalmic complications the disparity was greatest in remote areas (3.1 times higher) (Table 5) [56]. Hospitalisations for multiple complications of type 2 diabetes were 9.7 times more likely to occur among Aboriginal and Torres Strait Islander people in remote areas than among their non- Indigenous counterparts. In comparison, the age-standardised hospitalisation rates for Aboriginal and Torres Strait Islander people with multiple complications in regional areas and major cities were 5.2 and 3.3 times greater (respectively) than for other Australians.

Table 5. Hospitalisations for type 2 diabetes as a principal diagnosis among Aboriginal and Torres Strait Islander people, by complication, by remoteness, 2012-13 (age  standardised rate per 100,000 population and rate ratio)

Complication1

Major cities2

Inner and outer regional combined2

Remote and very remote combined2

Total

Rate3 Rate ratio4 Rate3 Rate ratio4 Rate3 Rate ratio4 Rate3 Rate ratio4
Circulatory 34 2.8 37 3.5 23 1.3 33 2.8
Renal 15 5.3 31 10.7 52 7.7 30 10.4
Ophthalmic 26 2.8 16 3.0 29 3.1 23 2.7
Other specified 143 3.8 251 6.0 413 8.3 252 6.5
Multiple 94 3.3 153 5.2 412 9.7 192 6.7
No complications 21 4.5 13 3.3 22 4.6 18 4.1
Total5 334 3.5 502 5.3 951 7.3 549 5.8
Notes:

  1. Categories are based on ICD-10-AM classification of diseases (International Statistical Classification of Diseases and Related Health Problems, 10th Revision, Australian Modification).
  2. Disaggregation by remoteness area is based on the ABS’ 2011 Australian Statistical Geography Standard (ASGS) and relates to the patient’s usual residence, not the location of the hospital.
  3. The age standardised rates per 100,000 population are calculated using the ABS Estimated 2012 Resident population by remoteness classification from the 2011 Census. Rates were directly age-standardised to the 2001 Australian population. Results for individual complications may be affected by small numbers and should be interpreted with caution.
  4. Rate ratio is the age standardised Aboriginal and Torres Strait Islander hospitalisation rate divided by the non-Indigenous hospitalisation rate.
  5. The total is not the sum of the individual conditions because diabetes complications overlap other categories.

Source: Derived from Steering Committee for the Review of Government Service Provision, 2014 (based on unpublished data from the National Hospital Morbidity Database (NHMD))

Complications in pregnancy

Diabetes in pregnancy refers to GDM and pre-existing diabetes, all of which can lead to a range of complications for the mother and child (see Box 7) [7].

Box 7: Complications associated with diabetes in pregnancy

Risks for the child include: miscarriage, stillbirth, congenital malformations and respiratory distress. There is also increased risk of obesity, impaired glucose tolerance and type 2 diabetes in early adulthood [7].

Risks for the mother include: miscarriage, pre-eclampsia, induced labour, pre-term birth, caesarean section, and first appearance or progression of complications including those associated with kidney, eye and cardiovascular diseases [7]. For mothers with GDM there is a risk of recurrent GDM in subsequent pregnancies and progression from GDM to type 2 diabetes.

Among Australian women who have diabetes during pregnancy, Aboriginal and Torres Strait Islander mothers and babies are more likely to experience adverse effects during pregnancy, labour and delivery than non-Indigenous mothers and babies [7]. Aboriginal and Torres Strait Islander mothers have higher rates of pre-term delivery, pre-term induction and hypertension than non-Indigenous mothers, and are more likely to have a long hospital stay. Aboriginal and Torres Strait Islander babies have higher rates of pre-term birth, low Apgar score25 and high level resuscitation26, and are more likely to have a long hospital stay. National figures regarding complications of diabetes in pregnancy for Aboriginal and Torres Strait Islander mothers and babies are available for the period 2005-07 (Table 6).

Table 6. Selected maternal and infant complications of diabetes among Aboriginal and Torres Strait Islander women who gave birth, by diabetes in pregnancy status, Australia, 2005-07 (percentage1 and standardised incidence ratio2)

Complication

Pre-existing diabetes

GDM

No diabetes

Maternal %1 Ratio3 %1 Ratio3 %1 Ratio3
Pre-term delivery4 34 7.8 14 17.7 13 7.3
Pre-term induction5 NA6 NA6 107 28 107 28
Long antenatal hospital stay9 13 2.9 5.2 3.4 1.2 1.8
Long postnatal hospital stay10 19 1.9 9.2 2.5 5.0 2.0
Infant11 %1 Ratio12 %1 Ratio12 %1 Ratio12
Pre-term birth13 34 1.4 15 1.4 13 1.7
Low Apgar score14 4.2 1.4* 2.3 1.7 2.2 1.5
High level resuscitation15 21 1.4 12 1.4 9.3 1.2
Long hospital stay16 33 1.6 15 1.7 11 1.7
Notes:

  1. Not age-standardised.
  2. The standardised incidence ratio of actual cases divided by the expected number of cases among the Indigenous population based on the age-specific rate of the non-Indigenous population.
  3. Indirectly age-standardised to the 2005-07 non-Indigenous maternal population, by diabetes in pregnancy status.
  4. Duration of pregnancies from 20-36 weeks (5 pregnancies of less than 20 weeks duration also included).
  5. Labour induced at less than 37 weeks.
  6. Not available due to the small number of inductions among Indigenous women with pre-existing diabetes.
  7. Approximate figure only. Directly age-standardised to the 2005-07 population of Indigenous women with induced labour and without diabetes in pregnancy.
  8. Approximate figure only.
  9. Includes Indigenous women who gave birth in hospital (only) and were in hospital for seven or more days prior to giving birth.
  10. Includes Indigenous women who gave birth in hospital and were discharged home (only) and were in hospital for seven or more days after giving birth.
  11. Includes live born babies only.
  12. Indirectly age-standardised to the 2005-07 population of live born babies of non-Indigenous women, by maternal diabetes in pregnancy status.
  13. Gestational age of live born babies from 20-36 weeks (5 babies of less than 20 weeks gestational age were also included).
  14. Apgar score (at five minutes) of 0-6.
  15. High level resuscitation includes intermittent positive pressure respiration through bag and mask, endotracheal intubation and intermittent positive pressure respiration, and external cardiac massage and ventilation.
  16. Includes live born babies discharged home (only) seven or more days following birth.

* Not significant

Source: Derived from AIHW, 2010 (based on data from the NHMD and NPDC)

Comorbidities

When a person has two or more health problems at the same time it is known as comorbidity [35]. Diabetes, CVD and CKD share complex causal relationships and often occur together in the same individual. The effects of comorbidity may lead to more severe illness and poorer outcomes for people with diabetes. This is apparent in hospitalisation figures for Aboriginal and Torres Strait Islander people.

The disparity in hospitalisation rates seen between Aboriginal and Torres Strait Islander people with diabetes and non-Indigenous people with diabetes, increases with greater comorbidity [35]. In 2012-13, Aboriginal and Torres Strait Islander people with diabetes, CVD and CKD were 7.3 times more likely to be hospitalised than their non-Indigenous counterparts. Aboriginal and Torres Strait Islander males and females aged 25 years and over, with all three diseases, were 5.0 and 10.7 times more likely (respectively) to be hospitalised than non-Indigenous males and females.

Prevention and management of diabetes

The prevention and management of diabetes is vital to the current and future health of Aboriginal and Torres Strait Islander people [15]. It is generally accepted that for diabetes prevention and management programs to be effective they require evidence based health promotion measures, public health interventions and clinical services. It is important that programs for Aboriginal and Torres Strait islander people are delivered sensitively, tailored to community needs, and not perceived as being forced upon communities [13]. It is also recommended that such programs be complimented by broader action that extends beyond the health service sector , and addresses the social determinants of Aboriginal and Torres Strait Islander health such as poverty, culture, racism, employment and education [13, 15].

Formal evaluations of long-term diabetes prevention and management programs for Aboriginal and Torres Strait Islander communities are limited, but the Australian experience suggests that the current high levels of diabetes among Aboriginal and Torres Strait Islander people are potentially preventable [75].

Prevention

There is currently no known way to prevent type 1 diabetes27 [76] or GDM28 [77], but the prevention of type 2 diabetes in high risk individuals is a critical component of diabetes care [78]. Best practice primary prevention can prevent or delay the onset of type 2 diabetes in high risk individuals by :

  • identifying those at high risk through the use of risk assessment tools
  • delivering education programs
  • promoting lifestyle modifications that focus on increased physical activity, dietary change and weight loss.

The Aboriginal and Torres Strait Islanders and diabetes action plan [13], released by Diabetes Australia in 2013, recommends implementing prevention programs that focus on Aboriginal and Torres Strait Islander people across the lifecycle. A predisposition to diabetes starts in utero and it is recommended that prevention programs include a focus on: women prior to and during pregnancy; pre-school and school-aged children; adolescents; and high risk people of all ages. It is also important to prevent complications in people with existing diabetes.

Risk assessment

To deliver evidence based prevention programs to high risk Aboriginal and Torres Strait Islander people they must first be identified through culturally appropriate risk assessment [13]. Systematic risk assessment of Aboriginal and Torres Strait Islander people during initial consultations with health professionals is recommended to ensure high risk individuals are identified.

The Australian type 2 diabetes risk assessment tool (AUSDRISK) has been developed to facilitate identification of high risk individuals. This non-invasive assessment uses basic clinical information including anthropometric measurements, family history, ethnic background, age and gender to calculate the risk of developing diabetes over a 5-year period [78-80]. The tool can be self-administered, it is practical for use in community settings, and its utility has been recognised by all Australian governments.

It is recommended that Aboriginal and Torres Strait Islander people are screened using the AUSDRISK tool from the age of 18 years29 [78]. There are however, some limitations associated with its use in this population:

  • development of the AUSDRISK tool relied on an approach that may not give a true representation of the level of diabetic risk in the Aboriginal and Torres Strait Islander population [81, 82]
  • use of the AUSDRISK tool to assess whether Aboriginal and Torres Strait Islander people should have a blood glucose test is considered controversial as it does not take into account the heterogeneity of this population [83].

In 2015, Adegbija and colleagues published an article describing the development of a new diabetes prediction model and tool based on long-term cohort data from a remote Aboriginal community [82]. The model predicts the 10-year absolute risk of type 2 diabetes for individuals in the community, based on waist circumference (WC) and age. To date this work has not been replicated to assess whether the findings can be generalised to other Aboriginal and Torres Strait Islander communities. The authors recommend that the prediction tool be validated with the inclusion of other risk factors such as family history of diabetes, physical activity and diet.

Education

It is recommended that education in diabetes prevention is tailored for Aboriginal and Torres Strait Islander communities, families and individuals [13]. Education should raise awareness of the risk of diabetes, and the positive steps required to lower that risk. It should also challenge the perception that diabetes is ‘normal’ in Aboriginal and Torres Strait Islander communities.

Early years education and intervention programs, including a systematic approach to improving nutritional status in infants and children [15], is considered critical to preventing risk factors and diabetes in later life [13]. It is suggested that children who are healthy in mind and body develop resilience and self-regulation and are more likely to make healthy choices as young adults. Programs for children and adolescents, including school-based education programs, can play an important part in providing the knowledge necessary for them to make informed decisions about their health in later life.

The Deadly choices program has conducted school-based chronic disease education initiatives for young Aboriginal and Torres Strait Islander students (years 7 to 12) in Brisbane, Qld [84]. The program provided health education and opportunities for participation in physical activity, and made arrangements for health checks. A recent evaluation of the program found that participants demonstrated significant improvements over time in knowledge, attitudes and self-efficacy associated with types of chronic disease, chronic disease risk factors, prevention and health checks. The evaluation also found significant increases in breakfast frequency and physical activity per week, fruit and vegetable consumption per day, and the uptake of health checks among students who participated in the program. The students who took part in the program showed a significant improvement in their knowledge of chronic disease and associated risk factors, and a significant increase in their breakfast frequency compared with a control group.

Lifestyle modifications

Excess weight, poor nutrition and physical inactivity are risk factors that contribute to the disproportionately high levels of diabetes seen in Aboriginal and Torres Strait Islander communities [13]. Internationally, intensive lifestyle programs have reduced the incidence of diabetes among overweight people with pre-diabetes to an extent that is comparable to the use of medication [16]. Whether similar programs would be effective for Aboriginal and Torres Strait Islander people has yet to be established, but culturally appropriate, locally supported, targeted prevention programs are recommended for Aboriginal and Torres Strait Islander people with pre-diabetes [13, 16]. Such programs would provide participants with the life skills, knowledge and support needed to make sustainable lifestyle changes to prevent the onset of type 2 diabetes [13].

A recent review of healthy lifestyle programs addressing physical activity and nutrition among Aboriginal and Torres Strait Islander people found that programs can have positive health effects for up to two years, and are more likely to be effective if they are initiated by the community [16]. However, without adequate long term funding, sustaining healthy lifestyle programs in communities where multiple social and economic problems exist is particularly challenging, and very few healthy lifestyle programs have to date continued to operate beyond five years [13, 16].

The Healthy weight program—later renamed the Living strong program—was initiated in Queensland in 1997 in response to high levels of type 2 diabetes and other chronic diseases among Aboriginal and Torres Strait Islander adults [85-87]. The program offered health screenings and conducted workshops promoting healthy weight, good nutrition and physical activity. Although no longer in operation, an evaluation of the program in 2005 documented weight loss, increased fruit and vegetable intake, and modest gains in physical activity among some participants.

A long-term program that has demonstrated considerable success is the Looma healthy lifestyle project. This project began in a remote WA community in 1993 and was still in operation 18 years after inception [16]. The community-directed project aimed to decrease the incidence of obesity, diabetes and coronary heart disease through strategies to increase physical activity and improve diet, such as promotion of traditional cooking methods, store management policy changes, and nutrition education. Although an initial evaluation found no significant changes in the prevalence of obesity or diabetes in the community [88] a subsequent health assessment, undertaken in 2009, found that the prevalence of diabetes in the community had not increased since 2003 [16].

A lifestyle modification program designed to help people reduce their risk of developing diabetes and cardiovascular disease, is currently funded by the Victorian Government and managed by Diabetes Australia — Victoria [89]. The Life! program offers a course specifically for Aboriginal people and their families called the Road to good health [90]. Run by Aboriginal Health Workers and other health professionals, this course supports participants to make long term, sustainable lifestyle changes, such as adopting a healthier diet and becoming more physically active [13]. A working group, that includes some Aboriginal and/or Torres Strait Islander members and organisations, has ensured that Indigenous values and health promotion practices are embedded in the course. Results suggest the course is culturally relevant and valuable to users, but published evaluations are not yet available.

Various programs have used sport to promote healthy lifestyles among Aboriginal and Torres Strait Islander children and adults, but further studies are required to establish their long-term impact [16]. Evaluation of short-term outcomes have demonstrated some positive results, such as those reported in 12-week exercise programs for Aboriginal and Torres Strait Islander men [91] and women [92].

  • The men’s program was conducted in a regional NSW community. The evaluation of the program found that sport and group-based physical activities reduced clinical risk factors for the development of type 2 diabetes among previously inactive, clinically obese Indigenous men [91]. The program led to improvements in various metabolic, anthropometric and fitness variables, including reduced WC, BMI and waist to hip ratio (WHR), and a decrease in insulin resistance. The observed improvements suggest there is potential for sports-based training programs to reduce the risk of developing type 2 diabetes in high risk Indigenous men.
  • The women’s program provided nutrition education and opportunities for physical activity to urban Aboriginal and Torres Strait Islander women in Adelaide, SA [92]. Modest reductions in weight, BMI and blood pressure were demonstrated at the completion of the program, and further improvements were observed at three-month follow-up. Changes in WC, fasting glucose and insulin, glycated haemoglobin (HbA1c), and other clinical measures were not significant. The positive intervention effects were observed despite low attendance at exercise classes and nutrition workshops. Analysis of the barriers to participation is currently underway and further follow-up is required to assess the longer-term results of the program.

Broader initiatives that extend beyond the immediate scope of the health sector have also been proposed to help reduce the incidence of type 2 diabetes in the Aboriginal and Torres Strait Islander population. They include [13]:

  • increasing availability of and access to healthy foods (e.g. in stores and through community gardens and traditional food projects)
  • limiting advertising and making healthy foods cheaper
  • providing clearer food labelling and education regarding the nutritional value of foods
  • use of taxation levers to reduce intake of sugary drinks (e.g. soft drinks)
  • encouraging physical activity through partnerships with local councils
  • improving housing.

Management

Providing appropriate, effective diabetes management for Aboriginal and Torres Strait Islander people depends on: access to a broad range of health services in a broad range of settings [13]; and coordinated interaction between patients, healthcare providers and the healthcare system [78]. Recent recommendations for improving diabetes management for Aboriginal and Torres Strait Islander people include:

  • earlier detection of undiagnosed diabetes
  • good quality primary health care
  • access to medications
  • self-management education
  • tertiary specialist treatment when complications develop.

The following sections refer mainly to the management of type 2 diabetes for Aboriginal and Torres Strait Islander people. Some information about managing diabetes in pregnancy is also provided.

Early detection

Most primary health care services in Australia play a critical role in the early detection of diabetes [93]. Improvements in the early detection of undiagnosed diabetes in the primary health care setting are recommended to facilitate early intervention and management for Aboriginal and Torres Strait Islander people [13].

Current NHMRC guidelines for diagnosing diabetes involve a fasting plasma glucose test (FPG) or a random blood glucose test (RBG), followed by an oral glucose tolerance test if glucose results are equivocal [83]. It has been suggested that using HbA1c as a diagnostic test could be of particular benefit in rural and remote Aboriginal and Torres Strait Islander communities where the currently recommended testing is not always accepted or practical [13]. There is evidence that point-of-care (POC) capillary HbA1c testing in remote communities is an accurate alternative to laboratory testing [83] and may avoid the substantial delays that often occur when tests must be analysed in urban facilities [94]. The availability of immediate HbA1c results is likely to improve early detection and expedite the initiation of diabetes education and management. Since 1 November, 2014 a Medicare rebate (that can be claimed once every 12 months) has been available for HbA1c testing to diagnose diabetes in high risk patients [95]. It is anticipated that NHMRC guidelines may soon be changed to recommend HbA1c testing for the diagnosis of diabetes [83].

Managing diabetes in the primary health care setting

The Royal Australian College of General Practitioners (RACGP) provides clear guidelines for the management of type 2 diabetes [78], but there are often large gaps between recommended diabetes care and the care patients actually receive [96]. Access to a range of different models of culturally appropriate care [13] and involvement of an Aboriginal and Torres Strait Islander Health Worker, liaison officer, outreach worker or care coordinator [78] is recommended to address the needs of Aboriginal and Torres Strait Islander people. Other recommendations for improved diabetes management for Aboriginal and Torres Strait Islander people include up-skilling GPs to help them manage more complex patients, and providing access to local services that offer specialised treatment (such as renal dialysis for those with diabetes-related complications) [13]. It is proposed that this would reduce travel, ensure patients remain close to their support networks, and facilitate self-management.

Structured approaches to diabetes care are recommended to improve client outcomes [97, 98] and the processes of diabetes care planning, management and self-management in Aboriginal and Torres Strait Islander communities are evolving [99, 100]. The RACGP recommends the use of written plans (see Box 8) to provide a structured approach to the management of diabetes [78].

Box 8: Written plans to manage diabetes

A General practice management plan (GPMP), typically developed by a GP in consultation with the patient, documents the patient’s needs and goals, and the management strategies and resources used [78]. A Team care arrangement (TCA) is an expansion of the GPMP to include multidisciplinary, team-based care from at least two other healthcare professionals (e.g. allied health care workers).

Some chronic condition management strategies implemented in the general population have been successfully tailored to suit Aboriginal settings and clients [101]. In particular, those strategies that include structured and holistic client-centred care plans, point of care pathology testing and coordinated care arrangements—with appropriate supports and training for staff—have produced positive health outcomes.

For clients, the benefits of such strategies have included [101]:

  • improved understanding of chronic conditions and their management
  • greater control and active involvement in managing their own health
  • ability to set and achieve realistic personal goals
  • reassurance and capacity to monitor progress
  • improved health and wellbeing and seeking early intervention for potential complications.

There is evidence from Aboriginal and Torres Strait Islander communities that diabetes care and outcomes can be improved and maintained over an extended period. In a pilot study in three Aboriginal communities in SA, the involvement of Aboriginal people in structured management strategies for chronic conditions led to improvements in their overall health status and health outcomes [100, 101]. In the remote Kimberley region of northern WA, an Aboriginal community controlled health service demonstrated that diabetes care and outcomes can be improved and maintained over a 10 year period [98]. This was achieved despite the challenges associated with the recruitment and retention of health care professionals that are typically experienced by remote services.

As with studies of diabetes care in Aboriginal communities, studies undertaken with Torres Strait Islanders living in remote communities in Far North Queensland (FNQ) have demonstrated improvements in clinical services and some intermediate health outcomes [97, 102, 103]. Between 1999 and 2000, a one year trial of a simple recall system, managed by local Indigenous Health Workers and supported by a specialist outreach service achieved significant improvements in diabetes care and reductions in hospital admissions [97]. The improvements were sustained two years after the initial study [103], but weight gain and glycaemic control have remained a major challenge in the study population [102, 103].

In 2015, Gibson and colleagues published a systematic review that identified factors that support and inhibit the implementation of primary health care interventions for chronic diseases in indigenous populations from Australia, New Zealand, Canada and the United States [104]. They recommended that the following factors be considered when planning and implementing these interventions:

  • intervention design – community engagement, the policy and funding environment, leadership, staff approach to change, and sufficient resourcing
  • workforce issues – recruitment and retention of staff, adequate staff training, dedicated chronic disease positions with clear roles and responsibilities, employing Indigenous Health Workers, and including them in decision making
  • health care provider skills and expertise – understanding, supportive and empowering attitudes towards patients, the capacity to communicate sensitively, and the willingness to allow patients to be partners in their care
  • clinical care pathways – effective electronic support systems and clear referral pathways
  • access issues – the provision of culturally safe, consistent services and coordinated care.

Access to primary health care services

It is generally accepted that inadequate access to primary health care services contributes to the poor health status of Aboriginal and Torres Strait Islander people [105]. Some of the barriers to accessing primary health care services that are experienced by Aboriginal and Torres Strait Islander people, include [106]:

  • costs associated with consultation fees, medicines, transport, lost wages and time taken to access care
  • distance and poor availability of services in remote areas
  • poorer access to community controlled health organisations in metropolitan and regional areas compared to remote areas
  • poor collaboration between different parts of the health system
  • lack of cultural safety in mainstream services
  • cultural misunderstandings, poor communication and experiences of discrimination with mainstream practitioners.

Research indicates that the current model of service delivery in remote communities in the NT has resulted in low rates of primary care use and high rates of hospitalisation for Indigenous people with diabetes [107]. The study concluded that improving access to primary health care services that provide diabetes care in remote communities would result in better health outcomes and be more cost effective.

Access to medicines

To provide the most appropriate diabetes management regime, it is recommended that Aboriginal and Torres Strait Islander people have access to the broadest range of health services and medicines, in the broadest range of settings [13]. However, many Aboriginal and Torres Strait Islander people face difficulties that impact on their capacity to access and adhere to a medication regime [108]. Potential barriers to access and use of medicines by Aboriginal and Torres Strait Islander people include:

  • lack of transport and access to services
  • inability to afford medication and services
  • difficulty interpreting labelling and consumer medicine information
  • client beliefs and behaviour about filling scripts, taking medication, sharing medication and side effects.

Suggested strategies for improving access to and use of medicines for Aboriginal and Torres Strait Islander people include:

  • changes to the Pharmaceutical benefits scheme (PBS) to allow prescriptions to be filled and supplied in hospitals [13]
  • use of Webster packs [109]
  • home medication reviews [109]
  • initiatives to heighten awareness of the subsidised products, and information and support services available through the National diabetes services scheme (NDSS) [110]
  • cultural awareness programs for pharmacists and their staff [108, 109]
  • provision of medicine education programs for Aboriginal and Torres Strait Islander Health Workers (by pharmacists) [108]
  • recruitment, employment and training of Aboriginal and Torres Strait Islander pharmacy staff [108]
  • improved medicine information for consumers [108].

Self-management

Self-management and support for self-management is essential to managing diabetes [78, 93]. The primary health system can support Aboriginal and Torres Strait Islander people with diabetes through improved self-management education, but the success of such programs is dependent on long term funding [13]. There is evidence that culturally appropriate self-management support for Aboriginal and Torres Strait Islander people is most effective when led by Aboriginal and Torres Strait Islander Health Workers [93]. Examples of culturally appropriate self-management support programs include the Aunty Jean’s good health team program [111] and the Wurli-Wurlinjang diabetes day program [112].

Box 9: Self-management

Self-management involves the patient (and any carers they may have) working in partnership with health professionals to [78]:

  • understand diabetes and its treatment options
  • be actively involved in a plan of care
  • undertake activities that protect and promote health
  • monitor and manage the symptoms and signs of diabetes
  • manage the impact of diabetes on the patient’s physical, emotional and social wel l being.

The RACGP recommends that patients (and their carers) receive structured, evidence-based diabetes education [78]. Diabetes education can be delivered in groups or individually, but should be culturally sensitive and tailored to the needs of the recipient. Identifying barriers that impact on an individual’s capacity to self-manage their diabetes is also important. Such barriers include issues around cognition, physical disability, mental health, health literacy, socioeconomic constraints, location and access to services.

Aunty Jean’s good health team was a pilot project to develop a combined model of health promotion, education and self-management to support Aboriginal people with chronic and complex care needs [111]. The program was designed around a strong belief in the community’s capacity to work together, and the importance given to the participation of Aboriginal Elders. It consisted of 12 modules, delivered one day per week for 12 weeks, combined with a self-managed and self-directed home program of activity. Evaluation of the program outcomes provided strong evidence of improvements in: self-management; appropriate and effective working partnerships; culturally acceptable and appropriate information-sharing; levels of physical activity; and self-management strategies. Key factors in the success of the program included: the leadership, commitment and participation of Elders; the strength of existing relationships within the community and between the community and health professionals; the input of specialist knowledge and support; a commitment to developing culturally appropriate health promotion strategies and behaviours; and location of the program within a safe community space.

The Wurli-Wurlinjang diabetes day program, conducted by an Aboriginal community controlled health service in Katherine in the NT [113], has been operating since 2008 [112]. The program operates once a week with the aim of providing a supportive environment and culturally appropriate, comprehensive care that fosters empowerment and promotes self-management among clients with type 2 diabetes. Evaluation of the program outcomes demonstrated: a considerable improvement in social and emotional wellbeing; an overall improvement in the proportion of clients receiving GPMPs, health checks and HbA1c testing; and a small but significant improvement in clinical outcomes, including control of blood sugar, blood pressure, cholesterol levels and weight. Certain system failures—concerning recall, medication and education—were also highlighted and subsequently addressed.

Tertiary care

Tertiary specialist services are required to treat the complications of diabetes, and many Aboriginal and Torres Strait Islander people access diabetes care in hospitals [13]. The Aboriginal and Torres Strait Islanders and diabetes action plan (2013), produced by Diabetes Australia, recognises that effective diabetes management requires high quality primary health care and support for self-management, but also affordable and timely access to tertiary specialist services to treat and manage complications. The Action plan suggests that appropriate access to tertiary and specialist services may be facilitated through investment in telehealth, and recommends models of care that promote integration between the primary and tertiary care settings. More specifically the Action plan recommends:

  • up-skilling GPs to help them manage more complex patients
  • opportunistic risk assessment in hospitals (as well as in primary care settings)
  • the supply of PBS prescriptions in hospitals.

A surgical approach to diabetes management for obese Aboriginal adults has recently been trialled and evaluated in a regional community in Central Victoria [114]. Obese Aboriginal participants (26 females and 4 males) with type 2 diabetes underwent laparoscopic adjustable gastric banding (LAGB) at the regional hospital and were followed for two years. The evaluation found that LAGB led to weight loss and diabetes remission in 20 of the original 30 participants, and that the outcomes were comparable with those observed in metropolitan non-Indigenous Australians who underwent the same treatment program. Rather than having participants attend a program in a metropolitan centre, the regional model of care relied on an initial period of developing trust, sharing information, and learning. This led to close collaboration between the research team, the regional hospital, the local Aboriginal health service and the local Indigenous community. The researchers concluded that a collaborative, regional model of care centred on the LAGB, was feasible and acceptable to obese Indigenous people in this community and an effective approach to diabetes management.

Managing diabetes in pregnancy

The early detection and management of diabetes during pregnancy30 is important to reduce complications in both mothers and babies [13]. Management typically involves advice regarding diet and exercise, blood glucose monitoring, and insulin therapy as required. However, research is underway to explore the various demographic, clinical, biochemical, anthropometric and socioeconomic factors that may contribute to the high level of diabetes among Aboriginal and Torres Strait Islander women and their children [115]. The range of contributing factors suggests the need for comprehensive programs that may address:

  • increasing women’s access to health support before and during their pregnancy [13]
  • improving control of diabetes in pregnancy [15]
  • delivering healthy babies [13]
  • encouraging breastfeeding (to reduce the risk of obesity and diabetes) [15]
  • assisting mothers and families to establish healthy lifestyles [13].

The Northern Territory diabetes in pregnancy partnership project commenced in 2012 to improve the clinical care and outcomes for women with diabetes in pregnancy (including high risk Aboriginal and Torres Strait Islander women) and their babies [116]. It involves a partnership between researchers, health care providers and policy organisations in the NT, to build evidence and improve practice in relation to screening, management and post-partum follow-up [13, 115]. The project has three key elements [116]:

  • a review of current models of care in the NT to improve health service delivery for women with diabetes in pregnancy
  • development of a NT clinical register of referred patients for use by health professionals
  • a detailed research project to assess rates and outcomes of diabetes in pregnancy in the NT (Pregnancy and adverse neonatal outcomes in remote Australia, PANDORA).

The project aims to contribute to the development of policy and planning for the management of diabetes in pregnancy, and the follow-up of mother and baby, in urban, rural and remote regions throughout Australia [115, 116].

Programs and services

A range of Australian Government Department of Health programs contribute to the prevention and management of diabetes and other chronic conditions among Aboriginal and Torres Strait Islander people at a national level [117, 118]. These programs include:

  • the Medicare benefits schedule (MBS) – provides subsidies for patient care and includes Medicare items for the planning and management of chronic conditions. GP health assessments are available for Aboriginal and Torres Strait Islander patients (MBS Aboriginal and Torres Strait Islander health assessments), along with follow on care and incentive payments for GPs (Practice incentive payment – Indigenous health incentive). Eligible patients can also be referred by a GP for up to five Medicare subsidised allied health services that are directly related to the treatment of their chronic condition, including diabetes
  • the Pharmaceutical benefits scheme (PBS) – provides subsidies for medicines used in the treatment of diabetes (PBS medicine co-payments)
  • the National diabetes services scheme (NDSS) – provides subsidised diabetes products and services to persons with diagnosed diabetes who are registered with the scheme
  • healthy lifestyle promotion programs including those that tackle smoking
  • a care coordination, outreach and support workforce based in Medicare Locals (Medicare Locals were replaced by Primary Health Networks in 2015) and Aboriginal community controlled health organisations (ACCHOs)
  • GP, specialist and allied health outreach services
  • funding for research into diabetes conditions through the NHMRC
  • funding for AIHW to support national surveillance and monitoring of vascular diseases including diabetes.

Despite government investment in these programs, and broader initiatives such as Closing the gap, disproportionately high levels of diabetes persist in Aboriginal and Torres Strait Islander communities [13]. Diabetes experts are calling for a nationwide, large scale, sustained effort to prevent type 2 diabetes, and the Australian Government‘s recent release of a new national diabetes strategy is considered an encouraging development [119].

Primary health care services

At a local level, most mainstream and community controlled primary health care services in Australia play a critical role in the delivery of diabetes care [93]. To meet the needs of Aboriginal and Torres Strait Islander people, primary health care services need to deliver both competent and culturally appropriate chronic disease care [120].

Culturally appropriate primary health care services

Culture and identity are central to Aboriginal and Torres Strait Islander perceptions of health, which encompass both the physical wellbeing of the individual, and the social, emotional and cultural wellbeing of the community [120]. It is important that services that deliver primary health care to Aboriginal and Torres Strait Islander people are culturally appropriate and recognise the importance of community values such as connection to culture, family and land, and opportunities for self-determination [107].

Culturally appropriate chronic disease services are typically characterised by [120]:

  • a high level of Aboriginal and Torres Strait Islander community engagement and effective communication at all levels
  • local knowledge about what works and what is acceptable
  • strong Aboriginal and Torres Strait Islander leadership
  • partnerships and community engagement that foster shared responsibilities
  • sufficient sustainable resources and effective financial and project management
  • integrated data and information systems to monitor the impacts of the intervention.

The involvement of Aboriginal and Torres Strait Islander Health Workers has been identified by health professionals and patients as an important factor in the delivery of good diabetes care to Aboriginal and Torres Strait Islander people [93, 121]. Aboriginal and Torres Strait Islander Health Workers have been shown to help patients feel comfortable, help break down communication and cultural barriers that may exist between patients and non-Indigenous health staff [93], and provide culturally appropriate self-management support [121].

A cluster randomised controlled trial, conducted between 2011 and 2013, found that an Indigenous Health Worker led case management approach to diabetes care (supported by an Indigenous clinical outreach team) was effective in improving diabetes care and control among Aboriginal and Torres Strait Islander adults in remote FNQ communities [121]. The health workers helped patients make and keep appointments, understand their medications, and learn about nutrition and the effects of smoking. Where appropriate, they also helped families to support the patient in self-management. Home visits and out of clinic care were provided, according to the patients’ preferences.

However, there can be barriers to the involvement of Aboriginal and Torres Strait Islander Health Workers in diabetes care such as: inadequate training; lack of clear role divisions among health care professionals; lack of stable relationships with non-Indigenous staff; and high demands for acute care [122]. Workforce initiatives that have been implemented to address some of the training needs of Aboriginal and Torres Strait Islander Health Workers include: the development of the diabetes education tool ‘Feltman’ (a life-sized felt body showing relevant organs and body parts) [123]; and the delivery of accredited postgraduate diabetes educator courses [124]. However, primary health care services need more Aboriginal and Torres Strait Islander Health Workers (including males) [122] and more diabetes-trained Aboriginal and Torres Strait Islander staff at all levels (health and allied health professionals, and support workers) [13]. This will require greater access to training and mentoring [13], clarification and support for the role of the Health Worker [122], and the identification and promotion of structured career pathways in Aboriginal and Torres Strait Islander chronic disease management [13].

Aboriginal and Torres Strait Islander community controlled primary health care services

Aboriginal and Torres Strait Islander community controlled primary health care services play a major role in delivering essential primary health care services to Aboriginal and Torres Strait Islander people in a culturally secure manner [125]. Health services run by Aboriginal and Torres Strait Islander communities provide holistic care that is relevant to the local community and addresses the physical, social, spiritual and emotional health of the clients [13]. Such services can deliver effective prevention and management programs that enable lifestyle changes that are maintained and supported by the community. In 2011-12, 80% of Aboriginal and Torres Strait Islander primary health care services that received funding from the Federal Government provided early detection activities for diabetes [126].

Box 10: Aboriginal and Torres Strait Islander community controlled primary health care services

Aboriginal and Torres Strait Islander community controlled primary health care services are located in all jurisdictions and funded by the federal, state and territory governments and other sources [126]. They are planned and governed by local Aboriginal and Torres Strait Islander communities and aim to deliver holistic and culturally appropriate health and health-related services. Aboriginal and Torres Strait Islander community controlled primary health care services vary in the primary health care activities they offer. Possible activities include: diagnosis and treatment of illness or disease; management of chronic illness; transportation to medical appointments; outreach clinic services; immunisations; dental services; and dialysis services.

National initiatives to improve diabetes care in Aboriginal and Torres Strait Islander primary care settings

The disproportionately high level of diabetes experienced by Aboriginal and Torres Strait Islander people necessitates an understanding of how primary care services are organised to deliver diabetes care, monitor the quality of diabetes care, and improve systems for better diabetes care [127]. Continuous quality improvement (CQI)31 can assist health services to identify and address poor quality of care [93].

Health services that deliver primary care to Aboriginal and Torres Strait Islander people are at the forefront of applying CQI [129]. In Aboriginal and Torres Strait Islander primary care settings CQI has been shown to improve service delivery rates and clinical outcome measures in patients with diabetes [93].

Over the past decade, the Audit and best practice for chronic disease project (ABCD) (and the subsequent extension project) has operated a wide-scale CQI program in Aboriginal and Torres Strait Islander community controlled and government health centres [130]. The project has, from its inception, included a focus on type 2 diabetes. Health centres participating in the project have shown substantial variations in the delivery of guidelines-scheduled services, medication management, and intermediate health outcomes associated with diabetes care [96]. However, Improvements in systems and processes of care have been demonstrated [127, 130], as have some improvements in intermediate health outcomes [127].

Adding to the body of knowledge regarding CQI and diabetes care, a recent study—conducted in 2011-12 with four ACCHSs in remote northern Western Australia—found that good diabetes care was facilitated by [93]:

  • clearly defined staff roles for diabetes management
  • support and involvement of Aboriginal Health Workers
  • efficient recall systems
  • well-coordinated allied health services.

The Healthy for life program (HfL) is funded by the Federal Government and includes a focus on early detection and management of chronic disease among Aboriginal and Torres Strait Islander people. It commenced data collection and reporting in 2007 and has a strong focus on CQI [131]. The program is available to Aboriginal community controlled health services and other primary health care services that provide health care to Aboriginal and Torres Strait Islander people. Services participating in the program are located in every state and territory, and across urban and remote areas of Australia. The program collects and reports on service activity and health outcome data, including clinical outcomes for diabetes. HfL program data collected from most participating services has been reported for the period between July 2007 and June 2011. In this period there were improvements in various service activities, including:

  • an increase in the proportion of clients who had a health assessment from 12% to 15% for those aged 15-54 years, and from 15% to 21% for those aged 55 and over32
  • an increase in the proportion of clients with type 2 diabetes who had a GPMP from 25% to 32%
  • an increase in the proportion of clients with type 2 diabetes who had a TCA from 16% to 22%
  • an increase in the proportion of clients with type 2 diabetes who had a HbA1c test in the previous 6 months from 46% to 56%
  • an increase in the proportion of clients with type 2 diabetes who had a blood pressure test in the last 6 months from 53% to 62%.

However clinical outcomes for diabetes have not yet shown an improvement [131]:

  • the proportion of clients with type 2 diabetes whose HbA1c was less than or equal to 7% decreased from 34% to 30%
  • the proportion of clients with type 2 diabetes who had a blood pressure result less than or equal to 130/80mmHg remained about the same at 41% and 42% respectively.

As a result of the generally positive findings from the HfL program the Australian Government has recently committed funding to expand the program into an additional 32 Aboriginal and Torres Strait Islander community controlled health services [132].

Policies and strategies

There are few national policies and strategies that focus specifically on diabetes in the Aboriginal and Torres Strait Islander population. However, there are relevant policy developments that pertain to diabetes in the general population, chronic diseases in general, or broader aspects of Aboriginal and Torres Strait Islander health.

The recent national emphasis on addressing diabetes within broader chronic disease policies and strategies reflects the common risk factors and co-existence of chronic diseases (particularly cardiovascular disease, diabetes and kidney disease) [55, 133]. However, diabetes experts are concerned that without a specific emphasis on diabetes prevention and management the seriousness, complexity and challenge of diabetes will be underestimated [133]. Diabetes Australia released the Aboriginal and Torres Strait Islanders and diabetes action plan in 2013 [13], and the Federal Government’s recent release of a new National diabetes strategy is considered an encouraging development by diabetes experts [119].

Figure 1: Selected national policy developments relevant to addressing diabetes among Aboriginal and Torres Strait Islander people

1987

  • National diabetes service scheme (NDSS) is established

1996

  • Diabetes becomes a National health priority area (NHPA)
  • Ministerial Advisory Committee on Diabetes is established

1998

  • National diabetes strategy and implementation plan report is published

1999

  • National (insulin-treated) diabetes register (NDR) is established

2000

  • National diabetes strategy 2000-2004 is signed

2002

  • Australian Health Ministers’ Advisory Council (AHMAC) agreed to the development of a national policy approach to chronic disease prevention and care

2006

  • National service improvement framework for diabetes is released
  • National chronic disease strategy is released
  • Australian better health initiative is announced

2007

  • Diabetes is included in the National reform agenda
  • A national package to prevent type 2 diabetes is announced

2008

  • Australian type 2 diabetes risk assessment tool (AUSDRISK) is introduced
  • New Medicare item introduced to develop a Diabetes risk plan for high risk individuals
  • Close the gap statement of intent is signed
  • National partnership agreement on closing the gap in Indigenous health outcomes is established
  • Indigenous chronic disease package is announced

2010

  • Practice incentives program – Indigenous health incentive receives funding

2011

  • NDSS introduces National development programs that include initiatives for Aboriginal and Torres Strait Islander people

2013

  • Aboriginal and Torres Strait Islanders and diabetes action plan is released
  • National Aboriginal and Torres Strait Islander health plan 2013-2023 is released

2014

  • Indigenous Australians’ health programme is established

2015

  • New National diabetes strategy 2016-2020 is released

Diabetes first became a National health priority area (NHPA) in 1996 [134], however, some national developments addressing diabetes were implemented prior to this. Selected national policy developments relevant to addressing diabetes among Aboriginal and Torres Strait Islander people are described briefly below.

  • The NDSS was established in 1987 [135]. The NDSS is an initiative of the Federal Government administered by Diabetes Australia. It provides diabetes-related products at subsidised prices and offers information and support services to people with diabetes. The latest five year agreement (2011-2016) between the Federal Government and Diabetes Australia provides for the introduction of National development programs that place particular emphasis on increasing access and support for various population groups including Aboriginal and Torres Strait Islander communities [110].
  • In mid-1996, Australian health ministers agreed to the inclusion of diabetes as the fifth NHPA [134]. In doing so they formally recognised the health burden imposed by diabetes, and the significant health gains that can be achieved through appropriate prevention and management [136]. Later that year, a report to the ministers outlined a future work program which included consideration of a national register of insulin-treated diabetes [134].
  • In the same year the Federal Minister for Health and Family Services announced the establishment of the Ministerial Advisory Committee on Diabetes to provide the Government with independent advice on the management of diabetes in Australia [137]. The National diabetes strategy and implementation plan, published in 1998, was an initiative of this committee. It made recommendations for reducing the burden of diabetes in Australia. Aboriginal and Torres Strait Islander people were highlighted among the groups within the Australian population who would require special consideration in the planning, delivery and coordination of diabetes prevention and care services.
  • In 1999, the NDR was established. The NDR aims to record all new cases of people who use insulin to treat diabetes, including type 1, type 2, GDM and other forms of diabetes [10]. While there are various reasons why the NDR may underestimate the number of Aboriginal and Torres Strait Islander people with insulin-treated diabetes (see Appendix 1), it remains one of the main sources of information on the incidence of insulin-treated diabetes in the Aboriginal and Torres Strait Islander population.
  • In the year 2000, all Australian health ministers signed the National diabetes strategy 2000-2004 [133]. It aimed to help reduce the personal and public burden of diabetes in Australia [138]. The Strategy identified five goals and a framework for action. Aboriginal and Torres Strait Islander people were identified as a high-risk population who would require specific attention.
  • In 2002, the Australian Health Ministers’ Advisory Council (AHMAC) agreed to the development of a national policy approach to chronic disease prevention and care [139]. This led to the development of the National service improvement frameworks (one of which is for diabetes) [140], followed by the National chronic disease strategy in 2006 [139]. A blueprint for a national surveillance system was also developed [141]. There was an emphasis on improving access to services for Aboriginal and Torres Strait Islander people in each of these initiatives.
  • In 2007, the Council of Australian Governments (COAG) announced that it would add diabetes to the ‘human capital’ stream of the National reform agenda and the Federal Government provided funding over four years for a national package to prevent type 2 diabetes [142]. This led to the introduction of a new Medicare item for GPs to develop a diabetes risk plan for high risk individuals aged 40-49 years. It also led to the development of a risk assessment tool (the AUSDRISK tool) that predicts the five year risk of type 2 diabetes [143]. Aboriginal and Torres Strait Islander people aged 15-54 years (inclusive) who receive a ‘high’ score on the AUSDRISK tool are eligible for a MBS health assessment [80].
  • In 2007, COAG also agreed to a partnership between all levels of government to work with Aboriginal and Torres Strait Islander communities to ’close the gap’ in Indigenous disadvantage [144]. COAG set targets to address the disadvantage faced by Aboriginal and Torres Strait Islander people : life expectancy, child mortality, education and employment [145]. In 2008, the Government and Opposition signed the Close the gap statement of intent [146],committing to closing the health and life expectancy gap between Aboriginal and Torres Strait Islander people and other Australians by 2030. By the end of 2010, most state and territory governments and oppositions had also signed the Statement [147].
  • In 2009, all Australian governments committed to achieving the Closing the gap targets in the National Indigenous reform agreement (Closing the gap) [148]. COAG also agreed to the National partnership agreement on closing the gap in Indigenous health outcomes [149] which included a commitment to expanded primary health care and targeted prevention activities to reduce the burden of chronic disease. As part of this Agreement, the Federal Government committed funding to the Indigenous chronic disease package (ICDP) [144]. The ICPD aimed to reduce the burden of chronic diseases by: reducing chronic disease risk factors; improving chronic disease management and follow-up care; and increasing the capacity of the primary care workforce through expansion and support [144, 150]. The Federal Government’s Implementation plan [151] was subsequently endorsed by the Australian Health Ministers’ Conference [152].
  • The Practice incentives program Indigenous health incentive commenced in 2010 [153]. Funding was allocated over four years to support primary health care services to provide better health care for Aboriginal and Torres Strait Islander people, including best practice management of chronic disease [150, 153]. The program offers incentives to: identify Aboriginal and Torres Strait Islander patients with chronic disease; undertake and review chronic disease management plans; and provide a targeted level of care.
  • In 2013, Diabetes Australia developed the first national policy document specific to diabetes in the Aboriginal and Torres Strait Islander population. Titled the Aboriginal and Torres Strait Islanders and diabetes action plan [13], it seeks to address the disproportionate burden of mortality and morbidity that Aboriginal and Torres Strait Islander people experience due to diabetes.
  • The National Aboriginal and Torres Strait Islander health plan 2013-2023 (the Health plan) was also released in 2013 [147]. It is the latest evidence-based policy framework developed to guide policies and programs to improve Aboriginal and Torres Strait Islander health [154]. The Health plan [155] makes specific reference to the impact of chronic diseases, including diabetes, on the health of Aboriginal and Torres Strait Islander adults. Recommendations include strategies to review and improve the implementation of the ICDP, and to ensure best practice primary health care services are focused on chronic disease prevention and treatment. In mid-2014, the Federal Government announced it was beginning work on the Implementation plan [147].
  • The Indigenous Australianshealth programme was established in 2014, consolidating four existing Aboriginal and Torres Strait Islander health funding streams including the Aboriginal and Torres Strait Islander chronic disease fund (which replaced the ICDP) [156]. The majority of the original ICDP measures continue to be funded under the new program.
  • The Australian national diabetes strategy 2016-2020 was released at the end of 2015 [157]. It outlines a national response to diabetes that includes a specific goal to reduce the impact of diabetes among Aboriginal and Torres Strait Islander people. The strategy identifies potential areas for action and measures of progress, but notes that further work is required to develop policy options to implement the strategy. Collaboration across all levels of government, the health sector and relevant organisations will be required to develop an implementation plan.

Future directions

In 2013, Diabetes Australia consulted with Aboriginal and Torres Strait Islander community groups, clinicians, peak health organisations and researchers to develop the Aboriginal and Torres Strait Islanders and diabetes action plan for submission to the Federal Government [13]. The Action plan outlined a series of principles to guide future diabetes policy and program development for Aboriginal and Torres Strait Islander people. The principles were:

  • prioritising children, family and community to address health across the lifespan
  • engaging with Aboriginal and Torres Strait Islander communities and building trust
  •  improving health outcomes by focusing on diabetes as an intergenerational issue
  • providing long term funding for interventions
  • building on the effective and innovative Aboriginal and Torres Strait Islander programs that already exist
  • addressing the broader determinants of Aboriginal and Torres Strait Islander health
  • integrating cultural values into policy and program design and implementation.

The Action plan recommended that Australian governments address diabetes in the Aboriginal and Torres Strait Islander population by [13]:

  • broadening access to clinical screening for diabetes and diabetes complications
  • funding a national, high risk prevention program to address pre-diabetes
  • funding a national diabetes self-management program
  • allowing PBS prescriptions to be supplied in hospitals
  • developing the Aboriginal and Torres Strait Islander health workforce
  • funding programs that
    • enhance pre-conception and antenatal health
    • optimise early detection and management of diabetes in pregnancy
    • provide early years education and intervention
    • promote awareness about the seriousness of diabetes and its complications
    • enable early identification of risk factors and high risk individuals
    • improve access to healthy foods
    • offer clearer food labelling and better pricing mechanisms.

Many of the recommendations in the Action plan have been identified as potential areas for action in the recently released Australian national diabetes strategy 2016-2020 [157]. This new strategy prioritises a national response to diabetes and outlines seven high-level goals, one of which is to reduce the impact of diabetes among Aboriginal and Torres Strait Islander people.

Recommendations for specific actions associated with this goal include:

  • developing and implementing community-wide, culturally relevant awareness programs
  • promoting pre-conception, pregnancy and early years programs
  • providing early years education and intervention programs that address the social and environmental determinants of Aboriginal and Torres Strait Islander health
  • developing and implementing community-wide healthy eating interventions
  • promoting access to specialist support services
  • encouraging better identification and management of diabetes in primary care settings
  • supporting diabetes workforce development in primary care settings
  • encouraging use of the My health record among rural and remote health care providers.

Both the Action plan and the National diabetes strategy have identified the need for holistic, culturally appropriate diabetes programs that integrate cultural values and address the health of Aboriginal and Torres Strait Islander people across their lifespan [13]. A study undertaken in 2013 and 2014 has contributed to our understanding of how this can be achieved by investigating ways to deliver culturally appropriate chronic care to Aboriginal and Torres Strait Islander people. The study has developed a Wellbeing framework that seeks to incorporate not just the physical aspects of health and wellbeing, but also the social, emotional, cultural and spiritual aspects [158, 159]. The Framework consists of two core values considered fundamental to the provision of care for Aboriginal and Torres Strait Islander people, and four essential elements that can assist primary health care services to support the wellbeing of Aboriginal and Torres Strait Islander people living with chronic disease.

The core values highlight that wellbeing is supported by [158, 159]:

  • upholding peoples’ identities in connection to culture, spirituality, families, communities and country
  • culturally safe primary health care services.

The four elements recommend that wellbeing be supported by [158, 159]:

  • locally defined, culturally safe primary health care services
  • appropriately skilled and culturally competent health care teams
  • holistic care throughout the lifespan
  • best practice care that addresses the particular needs of a community.

It is anticipated that primary health care services, in consultation with the communities they serve, may be able to use the Wellbeing framework to more effectively address the particular chronic care needs of their communities [158, 159].

Concluding comments

Aboriginal and Torres Strait Islander people are disproportionately affected by the diabetes epidemic [5, 6, 9] and face particular challenges accessing effective chronic care [96, 107]. The high levels of diabetes in many Aboriginal and Torres Strait Islander communities reflect a broad range of historical, social and cultural determinants, and the contribution of lifestyle and other health risk factors [13, 15, 16]. The prevention and management of diabetes is vital for the current and future health of Aboriginal and Torres Strait Islander people, and will require programs that are tailored to community needs and are culturally appropriate [13, 15]. Action beyond the health service sector that addresses the broader historical, social and cultural determinants of health will also be required.

The importance of mitigating the impact of the diabetes epidemic is recognised by experts and Australian governments alike [119], but the high prevalence of type 2 diabetes, and the associated burden of early deaths and serious complications experienced by Aboriginal and Torres Strait Islander people persists [13]. Providing effective diabetes prevention and management for Aboriginal and Torres Strait Islander people will require improved access to both high quality primary health care services and tertiary specialist services. Effective and innovative programs for the prevention and management of diabetes among Aboriginal and Torres Strait Islander people do exist at the local level [16, 101], and much can be learned from the ways in which Aboriginal and Torres Strait Islander community controlled health services provide culturally appropriate care [125], but a coordinated national approach is also required [75, 133]. The release of the new Australian national diabetes strategy 2016-2020 [157] may be an important first step toward this goal. Without a long term commitment to culturally appropriate prevention and management interventions that address diabetes across the lifespan, Aboriginal and Torres Strait Islander people will continue to suffer unacceptably high levels of diabetes.

Appendix 1: data sources, limitations and methods

The statistical information provided in this review draws on data from a number of sources. The various limitations associated with the data are discussed briefly below:

Defining diabetes
Reported statistics on diabetes prevalence, incidence, health service utilisation, mortality and burden of disease may not clearly define which type (or combination of types) of diabetes is being analysed. Care should be taken to avoid assumptions and generalisations.

Prevalence
People who develop diabetes are often unaware they have the condition,  and surveys that do not medically verify self-reported data may underestimate the true prevalence of diabetes [160].

Incidence
The National (insulin-treated) diabetes register (NDR) is a database established in 1999 to collect information on new cases of insulin-treated diabetes [10, 161, 162]. The register is operated by the Australian Institute of Health and Welfare (AIHW), using data from the National diabetes service scheme (NDSS) and the Australasian Paediatric Endocrine Group (APEG). Information is only held for individuals who consent to be included. Cases of type 2 diabetes and GDM that do not require insulin treatment are not included in the register.

The NDR may underestimate the number of Aboriginal and Torres Strait Islander people with insulin-treated diabetes and incidence data should be interpreted with caution. Underestimates may result from non-identification of people of Aboriginal or Torres Strait Islander origin. Underestimates may also be due to low levels of registration with the NDSS, as Aboriginal and Torres Strait Islander people can access diabetes services and products through other programs (this is particularly true in rural and remote areas) [10].

The incidence of type 2 diabetes not requiring insulin treatment cannot be estimated with accuracy due to gaps in currently available data [162].

Hospitalisations
Hospitalisation figures can provide information about the impact of chronic diseases (such as diabetes) on a population, but should be interpreted with caution. Hospitalisation figures are for ‘separations’, and as there can be multiple separations for the same individual, hospital records do not necessarily reflect the prevalence of a disease in the population [56].

The overall quality of data provided for Indigenous status varies between states and territories [163]. For analysis and reporting purposes, Indigenous identification in hospital statistics has been considered adequate in all jurisdictions since 2010-11 [56, 164]. Between 2004-05 and 2009-10, Indigenous identification in hospital statistics was considered adequate for NSW, Vic, Qld, WA, SA and public hospitals in the NT [56].

Mortality
Indigenous status may be under-identified in death data. Death data for Aboriginal and Torres Strait Islander people is typically only available for NSW, Qld, WA, SA and the NT, as these jurisdictions have sufficient levels of identification and sufficient numbers of deaths to support analysis [56, 165].

Death data probably underestimates deaths due to diabetes as the condition is frequently under-reported on death certificates or not recorded as the underlying cause of death [166]. Death data may be aggregated over five year periods to account for the volatility associated with small numbers of deaths [56].

Burden of disease
The Australian burden of disease study uses the underlying cause of death to calculate estimates of fatal burden [57]. Use of the underlying cause of death alone (without consideration of associated causes) cannot reflect more complex situations where more than one disease contributes to death. Diabetes is often associated with other diseases and listed as an associated cause of death; therefore burden of disease estimates may not reflect the total fatal burden of diabetes.

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Endnotes

1. Based on self-reported and biomedical data from a 2012-2013 national survey measuring type 1 diabetes, type 2 diabetes, and/or high sugar levels [5, 6].
2. Aged 10-14 years [8].
3. Epigenetics is the study of heritable changes in our genes that occur without altering the DNA or genetic code [30].
4. Includes people who are of Torres Strait Islander origin only, and those who are of both Aboriginal and Torres Strait Islander origin [40]
5. Diabetes was diagnosed based on glycated haemoglobin (HbA1c) test results [36].
6. Data for age groups less than 25 should be used with caution due to the associated high standard error. Prevalence data for non-Indigenous people aged 2-14 and 15-24 was not reported [59].
7. Year of first insulin use is a proxy for year of diagnosis [10].
8. Results should be interpreted with caution as status (Indigenous/non-Indigenous) was not recorded for: 24% of cases of type 1 diabetes; 54% of cases of type 2 diabetes; and 26% of cases of GDM [10].
9. Based on combined data from the National diabetes services scheme (NDSS) and the Australasian Paediatric Endocrine Group (APEG) [8].
10. Based on data from the APEG diabetes register and the NDR [68].
11. Data is for public and private hospitals in all jurisdictions. Data for all jurisdictions is considered to be of acceptable quality from 2010-11 onwards [56].
12. A principal diagnosis is the diagnosis considered to be chiefly responsible for the patient’s hospitalisation. An additional diagnosis is recorded when another condition affects the patient’s care during hospitalisation [35].
13. ICD-10-AM codes E10-E14 (type 1, type 2, other and unspecified diabetes) and O24.4 (GDM) [35].
14. Data from the NT is for public hospitals only [72].
15. Data is from public and private hospitals in all jurisdictions [56].
16. At the time of writing, cause of death data for 2013 was preliminary and subject to a revision process  [73].
17. Based on the ICD-10-AM sixth edition codes E10-E14 (this excludes GDM) [73].
18. The estimates use the average of deaths data from 2009, 2010 and 2011 [57].
19. Methodological advancements used to calculate burden of disease estimates from the ABDS 2011 preclude direct comparisons with previous burden of disease estimates for Aboriginal and Torres Strait Islander people [57].
20. The five most common contributors to fatal burden for Aboriginal and Torres Strait Islander people of all ages were: injuries, cardiovascular diseases, cancer, infant and congenital conditions and gastrointestinal diseases [57].
21. The three most common contributors to the gap in fatal burden were: CVD, cancer and injuries [57].
22. Diabetic ketoacidosis occurs when the breakdown of fat in the body results in an accumulation of ketones, and an increased acidity in the blood. This condition can be life-threatening if not treated [10].
23. Categories are based on ICD-10-AM classification of diseases [56].
24. The ICD-10-AM (International Statistical Classification of Diseases and Related Health Problems, 10th Revision, Australian Modification) is the classification system used to code diseases and health problems in Australian hospitals [56].
25. The Apgar score is an assessment tool to test a baby’s condition after delivery [7]. A score of 0-6 at 5 minutes after birth indicates the presence of complications and poor outcomes for the baby. A score of 7-10 is normal.
26. The level of resuscitation applied to a baby immediately after birth to promote normal breathing is an indication of a baby’s health and expected outcome [7]. Resuscitation measures vary from none, to suction and oxygen (low level), to ventilation and external cardiac massage (high level).
27. Type 1 diabetes is an autoimmune condition that cannot currently be prevented or cured [76].
28. Although losing excess weight before pregnancy, and adopting healthy eating and exercise habits before and during pregnancy, may reduce the risk of developing GDM and subsequent type 2 diabetes [77].
29. Screening for the general population is recommended from the age of 40 years [78].
30. Diabetes in pregnancy refers to pre-existing diabetes and GDM.
31. CQI is a structured, ongoing process of improvement and evaluation. It involves a systematic approach to collecting and reviewing data to identify opportunities for improving the quality of services [128].
32. There was a slight decrease in the proportion of clients aged 0-14 years who had a health assessment (from 16% to 14%) [131].