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Use of eye care services by Indigenous Australian adults

Anna-Lena M R Arnold, Lucy Busija, Jill E Keeffe and Hugh R Taylor
Med J Aust 2011; 194 (10): 537-538. || doi: 10.5694/j.1326-5377.2011.tb03093.x
Published online: 16 May 2011

To the Editor: Indigenous Australians have a higher risk of vision loss from preventable and treatable causes than non-Indigenous Australians1 and have been reported to attend eye care services at a lower rate than non-Indigenous Australians.2 Here, we report results from the National Indigenous Eye Health Survey1 which indicate that many Indigenous Australians with vision problems have accessed eye care services but not as frequently as recommended by the National Aboriginal Community Controlled Health Organisation (NACCHO) and the National Health and Medical Research Council (NHMRC), particularly for high-risk groups of patients with diabetes.3,4

The survey methods have been reported elsewhere.1 Briefly, 1694 Indigenous children and 1189 Indigenous adults from 30 communities across Australia had a standardised eye examination and completed a questionnaire in 2008. Recruitment rates were 84% for children aged 5–15 years and 72% for adults aged ≥ 40 years, and 96% of responses to questionnaire items were complete.

Seventy-nine per cent (936/1189) of Indigenous adults reported vision problems, of whom 83% (778/936) had sought care from an eye care service (Box 1). Similar to previous studies,5 we found use of eye care services increased with increasing age, but being male and having no education were barriers to accessing services. There was a significant association between higher education levels and higher rates of using of eye care services, with the odds for using eye care services being the highest among those with the highest level of education (data not shown). These factors should be considered when designing public health messages on the importance of using eye care services.

As elsewhere in Australia, optometric services were the most frequently used facilities (49%, 378/778) across all regions except very remote inland, where primary health care services had the highest reported usage (33%, 49/149). Participants from very remote coastal and very remote inland regions were twice as likely to consult an ophthalmologist compared with the other regions (Box 2).

Twenty-three per cent (179/769) of participants with vision problems reported that they had last seen someone about their vision problem within the previous year, 67% (519/769) within the previous 3 years, and for 33% (250/769) it had been ≥ 3 years. Only 20% (87/444) of participants with self-reported diabetes had seen someone about their vision problem within the previous year. NACCHO recommends that Indigenous adults aged ≥ 40 years should be screened for reduced visual acuity at least every 2 years,3 and NHMRC guidelines recommend that Indigenous adults with diabetes have their eyes checked every year.4 Our results show that we are far from reaching these targets. As regular eye examinations have the potential to reduce the incidence of vision loss, this is a matter of great concern. The importance of regular eye examinations and follow-up, particularly for high-risk groups, should be emphasised to health care providers and the community.

Reasons given for not seeking eye care were: not enough time (41%, 62/153); condition not severe enough (22%, 33/153); too expensive (17%, 26/153); eye care not available in area (14%, 22/153); decided not to seek care (14%, 22/153); transport or distance issues (10%, 15/153); and waiting time too long (10%, 15/153). The two most common reasons for not seeking care indicate a lack of awareness about the importance of regular eye examinations, possibly because of a lack of culturally appropriate public health messages.

  • Anna-Lena M R Arnold1
  • Lucy Busija1
  • Jill E Keeffe1
  • Hugh R Taylor2

  • 1 Population Health Unit, Centre for Eye Research Australia, Melbourne, VIC.
  • 2 Melbourne School of Population Health, University of Melbourne, Melbourne, VIC.


Correspondence: jillek@unimelb.edu.au

Acknowledgements: 

We particularly acknowledge the contributions to this manuscript of the following staff from the Population Health Unit at the Centre for Eye Research Australia: Nicolas Goujon (International Research Fellow), Sarah Fox (Project Coordinator) and Jing Xie (Senior Biostatistician).

  • 1. Taylor HR, Xie J, Fox S, et al. The prevalence and causes of vision loss in Indigenous Australians: the National Indigenous Eye Health Survey. Med J Aust 2010; 192: 312-318. <MJA full text>
  • 2. Hecker R. A review of eye health services for aboriginal communities in NSW. Office of Aboriginal and Torres Strait Islander Health, Commonwealth Department of Health and Family Services. Canberra: Australian Government Publishing Service, 1998.
  • 3. National Aboriginal Community Controlled Health Organisation. National guide to a preventive health assessment in Aboriginal and Torres Strait Islander peoples. Melbourne: Royal Australian College of General Practitioners, 2005.
  • 4. National Health and Medical Research Council. Clinical guidelines for the management of diabetic retinopathy. Canberra: NHMRC, 2008.
  • 5. Keeffe JE, Weih LM, McCarty CA, Taylor HR. Utilisation of eye care services by urban and rural Australians. Br J Ophthalmol 2002; 86: 24-27.

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