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Chlamydia among Australian Aboriginal and/or Torres Strait Islander people attending sexual health services, general practices and Aboriginal community controlled health services

Abstract

Background

Chlamydia infections are notified at much higher rates in Aboriginal and/or Torres Strait Islander people compared to non-Indigenous people. The Australian Collaboration Chlamydia Enhanced Sentinel Surveillance System (ACCESS) was established to complement population-based surveillance.

Methods

We describe patient demographics, completeness of recording of Aboriginal and/or Torres Strait Islander (‘Aboriginal’) status, chlamydia testing rates and positivity rates from the Aboriginal Community Controlled Health Service (ACCHSs), General Practice (GP) clinics and Sexual Health Services (SHSs) networks in ACCESS during 2009. Data were extracted from electronic medical records of each participating health service for consultations with patients aged 16–29 years and for chlamydia testing and positivity.

Results

Data were included from 16–29 year olds attending six ACCHSs (n = 4,950); 22 SHSs (n = 20,691) and 25 GP clinics (n = 34,462). Aboriginal status was unknown for 79.3% of patients attending GP clinics, 4.5% attending SHSs and 3.8% of patients attending ACCHSs. Chlamydia testing rates among Aboriginal patients were 19.8% (95%CI:18.6%-21.0%) at ACCHSs, 75.5% (95% CI:72.5%-78.4%) at SHSs and 4.3% (95% CI: 2.6%-6.6%) at GP clinics. Positivity rates were highest in Aboriginal patients tested at SHSs at 22.7% (95% CI:19.5%-26.2%), followed by 15.8% (95% CI:3.8%-43.4%) at GP clinics and 8.6% at ACCHSs (95% CI:7.9%-12.4%). This compared with non-Indigenous patients positivity rates at SHSs of 12.7% (95% CI:12.2-13.2%); 8.6% (7.2%-11.3%) at GP clinics and 11.3% at ACCHSs (95% CI:15.4%-24.9%).

Conclusions

Higher chlamydia positivity in Aboriginal people across a range of clinical services is reflected in national notification data. Targeted efforts are required to improve testing rates in primary care services; to improve identification of Aboriginal patients in mainstream services such as GP clinics; and to better engage with young Aboriginal Australians.

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Background

Chlamydia trachomatis is a sexually transmitted infection that is easily diagnosed and treated, but most infections go undetected since up to 80% are asymptomatic [1, 2]. If left untreated chlamydia can cause pelvic inflammatory disease which in turn can lead to tubal factor infertility and ectopic pregnancy [3, 4]. Chlamydia is the most commonly notified infection in Australia with more than 80,000 cases reported in 2013, a three-fold increase in the last decade [5]. The burden of chlamydia is highest among young Aboriginal and/or Torres Strait Islander people (hereafter ‘Aboriginal’) [68]. Notification rates among Aboriginal people are 24 times higher than among non-Indigenous people [9]; however, notification rates are subject to testing biases [10, 11].

The focus of the Council of Australian Government’s commitment to Closing the Gap in health difference and life expectancy between non-Indigenous and Aboriginal peoples is principally directed towards mortality reduction from chronic disease and improvements to child and maternal health [12], with little focus on sexually transmissible infections (STIs) despite these causing substantial ill health among Aboriginal people. However, included within the Closing the Gap initiative are measures to improve surveillance systems that lead to increased understanding of disease among Aboriginal people and communities.

In this paper we report patient demographics, completeness of recording of patients’ Aboriginal status, chlamydia testing and positivity rates during 2009, within three ACCESS clinical networks providing primary care: sexual health services (SHSs), general practice (GP) clinics and Aboriginal Community Controlled Health Services (ACCHSs).

Methods

Study design

The Australian Collaboration for Chlamydia Enhanced Sentinel Surveillance System (ACCESS) program is an independent initiative that aims to complement and improve interpretation of passive chlamydia surveillance data among priority populations including Aboriginal people [13]. ACCESS aims to supplement notification data by gaining a better understanding of chlamydia testing and positivity rates within a range of health service networks.

The methods of the ACCESS systems have been described in detail elsewhere [13, 14]. ACCESS includes five clinical networks made up of SHSs, family planning clinics, GP clinics, antenatal clinics and ACCHSs; and a laboratory network to collectively monitor the uptake and outcome of chlamydia testing in Australia using patient encounter data. ACCESS is managed by a coordinating committee and each of the six networks is overseen by a steering committee which manages all aspects of the project including development, implementation, interpretation and analysis of data from individual networks.

Data inclusion

We included all consultation and routine chlamydia testing data from 25 GP clinics, 22 SHSs and six ACCHSs within ACCESS for both Aboriginal and non-Indigenous patients. These services nominated to participate in the ACCESS study, and were selected based on their size and geographical location to ensure national representatives [13]. A Memorandum of Understanding between research agencies and the National Aboriginal Community Controlled Health Organisation (NACCHO) supported ACCHSs involvement.

Data from GP clinics and ACCHSs were collected using software called GRHANITE developed by the Rural Clinical School at University of Melbourne [14]. GRHANITE collected client demographic, health service utilisation and testing and positivity data from each service’s electronic medical records. Data from the SHSs were directly extracted from their respective patient management systems. All extracted data was de-identified at the clinical service before sharing.

Data analysis

Data on patient demographics, chlamydia testing and positivity were analysed for patients aged 16–29 years, who attended the services in 2009. We calculated: (i) the number of patients who were identified or identified as Aboriginal for each network; (ii) the proportion of patients tested at least once for chlamydia (testing rate) (iii) the proportion of those tested who had a positive test result (chlamydia positivity) where the result was known. All results were stratified by Aboriginal status, sex, age groups and clinic networks.

Ethics

Ethical approval for the ACCHS network was gained from six Human Research Ethics Committees located at the Alfred Hospital, (Victoria); Aboriginal Health and Medical Research Council (New South Wales); Aboriginal Health Research Ethics Committee (South Australia); Central Australian Human Research Ethics Committee Northern Territory (NT)]; Western Australian (WA) Aboriginal Health Information and Ethics Committee; and the Human Research Ethics Committee of the NT Department of Health and Families and Menzies School of Health Research (NT). Approval for the GP network was granted by the Royal Australian College of General Practitioners (RACGP). Approval for the SHS network was granted by the Human Research Ethics Committees (HRECs) of St Vincent’s Hospital and the University of New South Wales with further ethical approval granted by the separate HRECs overlooking each of the 22 participating SHSs.

Results

Health services

Of the six ACCHS one was located in a metropolitan area and the remaining were in regional/remote areas, whereas the majority of the GP clinics (14 of 25; 56%) and SHSs (13 of 22; 59%) were located in metropolitan areas.

Patient demographics

Within ACCHSs 4,950 unique patients aged 16–29 years attended during 2009. Of these, 60% were female, 33% were aged 16–19 years and 37% were aged 20–24 years. In the 25 GP clinics, 34,462 unique patients aged 16–29 years attended during 2009; 61% were female, 26% were aged 16–19 years and 38% aged 20–24 years. In the same year, 20,691 16–29 year olds attended the 22 SHSs, of these 48.9% were female; 17% were aged 16–19 years and 44% were aged 20–24 years (Table 1).

Table 1 Aboriginal status recording, by ACCESS network, age group, sex and area of residence, among 16–29 year olds

Aboriginal status

The majority of patients (85%) attending ACCHSs were identified as Aboriginal, 11% as non-Indigenous, and in 4% this status was not recorded. Of all patients attending GP clinics, 1.3% were recorded as being Aboriginal, 31.2% as non-Indigenous, and for 67.5% of patients Aboriginal status was not recorded. Aboriginal patients comprised, 4.1% of the total patients seen at SHSs, with 91.5% recorded as non-Indigenous and for 4.3% Aboriginal status was not recorded (Table 1).

Chlamydia testing rates

Chlamydia testing rates in each of the networks among Aboriginal patients were: 19.8% (95% CI:18.6%-21.0%) attending ACCHSs; 4.3% (95% CI:2.6-6.6%) at GP clinics, and 75.5% (95% CI:72.5%-78.4%) at SHSs (p < 0.01) (Table 2). Whereas, in non-Indigenous people, the testing rates were: 8.6% (95% CI:8.0%-9.1%) at ACCHSs, 11.2% (95% CI:8.6%-14.1%) at GP clinics, and 78.3% (95% CI:77.7%-78.9%) at SHSs (p < 0.01). Testing rates were higher in both Aboriginal and non-Indigenous males attending SHSs, 81.7% vs. 79.9% respectively; compared to 71.5% of females (both Aboriginal and non-Indigenous) (p < 0.01 for both). Conversely testing rates were higher for females both Aboriginal and non-Indigenous at ACCHS compared to males (22.5% vs 15.6%, p < 0.01 and 13.7% vs. 7.6%, respectively (p < 0.05 for both). Testing rates were similar between Aboriginal and non-Indigenous patients, both males and females at GP clinics (5.2% vs 2.1%; p = 0.136).

Table 2 Chlamydia testing and positivity rate, by Aboriginal status, ACCESS network, age group, sex and area of residence, among 16–29 year olds

Chlamydia positivity rates

Among Aboriginal patients, chlamydia positivity at ACCHSs was 8.6% (95% CI:6.8%-10.8%) (72 of 833 patients tested), 15.8% (95% CI:3.4%-39.6%) (3/19) at GP clinics, and 22.7% (95% CI:19.5%-26.2%) (145/638) at SHSs (p < 0.01). Among non-Indigenous people, chlamydia positivity at ACCHS was 11.3% (95% CI:4.7%-22.0%) (7/62), 8.2% (95% CI:6.4%-10.1%) (75/920) at GP clinics, and 12.7% (95% CI:12.2%-13.2%) (1887/14851) at SHSs (p < 0.01) (Table 2).

Among Aboriginal females, chlamydia positivity was highest at SHSs; 21.5% (95% CI:17.3%-26.1%), while those tested at ACCHSs had a positivity rate of 9.4% (95% CI:7.2%-12.1%,p < 0.01). Among Aboriginal males chlamydia positivity rates within SHSs was 24.5% (95% CI:19.5%-30.0%) and within ACCHSs 8.1% (95% CI:4.8%-12.5%,p < 0.01) (Table 2).

Discussion

This report adds significantly to our understanding of the health care utilisation by young Aboriginal people and complements STI notification data by informing chlamydia positivity across a range of primary care services- two generalist (GP and ACCHSs) and one specialised (SHSs). The study is the first comprehensive analyses, and certainly the biggest that compares Aboriginal/non-Aboriginal populations using the same recruitment methods for both populations. Previous comparisons have been based virtually entirely on notification data, which is subject to variabililty due to dependence on testing uptake.

Data from three different types of primary care services are represented, covering a period of 12 months with over 60,100 patients. Elsewhere, we reported the representativeness of participating sites according to Australian population distributions [13]. Accordingly, results particularly related to Chlamydia testing and positivity are likely to be generalisable to the Australian population aged 16–29 years.

At the participating services, 4.1% of clients at SHSs were identified as Aboriginal, compared to 1.3% at GP clinics and 85% at ACCHSs. Aboriginal attendances in GPs and ACCHSs from this dataset were consistent with those reported in national audits across all ages, and affirm that young Aboriginal people only make up a small proportion of those attending mainstream encounters the patient identified as sexual health services for STI care and management. Of all patients attending GP clinics in 2011–2012 1.5% were identified as Aboriginal [15] while 78% of patients who attended ACCHS in 2010–2011 were identified as Aboriginal [16]. Given that young Aboriginal people make up 4% of Australia’s total 15–29 year old population [17], further efforts are required to make GP services more accessible to them. It should be noted however that young men accessed SHSs more than the GP clinics and ACCHSs; this is likely for two reasons (i) either they are accessing clinics on their own or (ii) they attend as named contacts. Whatever the case, all services should be encouraged to promote their services to young men.

The Aboriginal status of patients was better recorded at ACCHSs and SHSs compared with GP clinics where only one third of patients status was recorded. Improving data quality on Aboriginal status within GP clinics is a priority of Australian Governments [18] with the Close the Gap Indigenous health incentive payment aiming to improve recording of Aboriginal status [19].

This study confirms that the majority of ACCHSs patients are Aboriginal people and that people aged 16–29 years attend these services for health care, including for STI screening. This concurs with two previous studies, the first, a cross sectional survey of young people aged 16–29 years where 54% reported that they had an STI test in the previous year and did so at an ACCHS [20], and a second study of resilience related to STI and blood borne viruses whereby young people reported positive aspects of attending an ACCHS for STI and BBV screening and management. In the latter study, young Aboriginal people described the comfort and understanding they experienced at the ACCHS; and positive personal relationships especially with Indigenous care providers [21]. Our results support the central role that ACCHSs play in STI service provision for Aboriginal people.

Further efforts are required to improve STI testing rates in primary care. Testing rates among Aboriginal patients attending ACCHSs and GP clinics were quite different with testing rates within ACCHS almost five times greater than that offered by GPs for both Aboriginal and non-Indigenous patients. As expected, testing rates were high among both Aboriginal and non-Indigenous patients attending SHSs. There are two main reasons to test for Chlamydia- to screen those who are asymptomatic or to diagnose symptomatic infection. Thus, chlamydia testing rates of services may reflect their adherence to screening protocols, as well as the burden of disease affecting their populations. With regards to screening, clinical practice guidelines recommend that all sexually active people up to the age of 29 years be offered a chlamydia test at least annually [22, 23]. The lower rates of testing within GPs and ACCHSs compared with SHSs could be due to a number of factors: patients declining testing; patients not being offered testing (staff lacking awareness of screening guidelines, due lack of time and awareness about chlamydia testing amongst clinic staff, or sensitivities regarding sexual health issues); or other clinical priorities [2426]. In order to achieve higher chlamydia testing rates in GP and ACCHS settings, supportive quality improvement strategies are warranted [27, 28] as well as initiatives such as offering a test to all patients prior to the consultation [29] Quality improvement audits are a key feature of the Closing the Gap funding initiatives particularly involving ACCHSs [30] but do not currently explore STI testing patterns.

Mathematical modelling has suggested that increasing rates of chlamydia testing to 40% in males and females aged less than 25 years or to 20% in young people aged less than 30 years could halve the prevalence of chlamydia within ten years; with most of this decline occurring within the first four years [31]. If the intent is to achieve high chlamydia testing rates in the population, health promotion and clinical education and systems within ACCHS and GPs should address the different health care utilisation patterns of Aboriginal females and males; since in most ACCESS sites a higher proportion of females either attended or were tested than males.

A key strength of this study is that the results reflect actual clinical practice in the participating health services. All data were collected retrospectively and thus did not influence the decision to offer a chlamydia test or not. In addition, within each network, study data were collected from services that are geographically dispersed across the country; thus reducing biases introduced when data are reported from one service or region.

A limitation of the study was the poor identification of Aboriginal patients at mainstream GP clinics with more than two thirds of patients having an unknown Aboriginal status. The poor completeness of Aboriginal status in GP clinics means we cannot be confident about the true testing and positivity rates in Aboriginal patients. In addition, the study did not record patients who declined to have a test when offered one. Clinical audits would be needed to measure the extent of decline in any of these primary care facilities. Further, we were not able to identify symptomatic patients from asymptomatic patients making interpretation of positivity results difficult to correlate with community prevalence rates. Only first patient visits involving Chlamydia testing were counted, thus excluding subsequent testing and positivity data. Finally, in view of the small sample size of GP clinics and ACCHSs in the ACCESS network, these findings may not be representative of all such health services because of the small sample size of these clinics in Australia.

Conclusions

In conclusion, this study provides a snapshot of chlamydia testing and positivity among young people attending three types of primary care health services. Improved completeness of recording of Aboriginal status should be a priority in GP clinics, not only to evaluate chlamydia testing and prevention programs but also for other Closing the Gap initiatives that are directed at mainstream general practice [32]. Quality improvement initiatives will play a key role in influencing adherence to clinical practice guideline recommendations for chlamydia testing and are becoming a feature of current funding programs. More research is needed to determine how effective mainstream strategies are at engaging young Aboriginal people to the range of health services available to them.

References

  1. Peipert JF: Genital chlamydial infections. N Engl J Med. 2003, 349 (25): 2424-2430.

    Article  CAS  PubMed  Google Scholar 

  2. Oakeshott P, Kerry S, Aghaizu A, Atherton H, Hay S, Taylor-Robinson D, Simms I, Hay P: Randomised controlled trial of screening for Chlamydia trachomatis to prevent pelvic inflammatory disease: the POPI (prevention of pelvic infection) trial. BMJ. 2010, 340 (apr08 1): c1642.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Haggerty C, Gottlieb S, Taylor B, Low N, Xu F, Ness R: Risk of sequelae after Chlamydia trachomatis genital infection in women. J Infect Dis. 2010, 201 (S2): 134-155.

    Article  Google Scholar 

  4. Gray-Swain MR, Peipert JF: Pelvic inflammatory disease in adolescents. Curr Op Obstet Gynecol. 2006, 18 (5): 503-510.

    Article  Google Scholar 

  5. The Kirby Institute: HIV, viral hepatitis and sexually transmissible infections in Australia. Annual surveillance report 2013. 2013, Sydney: Kirby Institute, UNSW

    Google Scholar 

  6. Graham S, Guy RJ, Donovan B, McManus H, Su JY, El-Hayek C, Kwan KS, Dyda A, Wand HC, Ward JS: Epidemiology of chlamydia and gonorrhoea among Indigenous and non-Indigenous Australians, 2000–2009. Med J Aust. 2012, 197 (11): 642-646.

    Article  PubMed  Google Scholar 

  7. Latif A, Smith K: Sexually transmitted infections in Central Australia–time for concerted action. Public Health Bull South Aust. 2006, 4: 32-34.

    Google Scholar 

  8. Huang RL, Torzillo PJ, Hammond VA, Coulter ST, Kirby AC: Epidemiology of sexually transmitted infections on the Anangu Pitjantjatjara Yankunytjatjara Lands: results of a comprehensive control program. Med J Aust. 2008, 189 (8): 442-445.

    PubMed  Google Scholar 

  9. The Kirby Institute: Bloodborne viral and sexually transmitted infections in Aboriginal and Torres Strait Islander people: surveillance and evaluation report 2012. 2013, Sydney: The Kirby Institute, UNSW, 2013

    Google Scholar 

  10. Hocking J, Willis J, Tabrizi S, Fairley C, Garland S, Hellard M: A chlamydia prevalence survey of young women living in Melbourne. Victoria Sex Health. 2006, 3 (4): 235-240.

    Article  PubMed  Google Scholar 

  11. Ali H, Guy RJ, Fairley CK, Wand H, Chen MY, Dickson B, O’Connor CC, Marshall L, Grulich AE, Kaldor JM, Hellard ME, Donovan B: Understanding trends in genital Chlamydia trachomatis can benefit from enhanced surveillance: findings from Australia. Sex Transm Infect. 2012, 88 (7): 552-557.

    Article  PubMed  Google Scholar 

  12. Council of Australian Governments: Closing the gap in Indigenous disadvantage. http://www.coag.gov.au/closing_the_gap_in_indigenous_disadvantage.

  13. Guy RJ, Kong F, Goller J, Franklin N, Bergeri I, Dimech W, Reilly N, Sullivan E, Ward J, Kaldor JM, Hellard M, Donovan B: A new national chlamydia sentinel surveillance system in Australia: evaluation of the first stage of implementation. Comm Dis Intell. 2010, 34 (1): 319.

    Google Scholar 

  14. Boyle DIR, Kong FA: Systematic mechanism for the ethical collection and interpretation of display format pathology test results from Australian Primary Care records. Proceedings of the 17th annual HISA Health Informatics Conference. 2009, Canberra

    Google Scholar 

  15. Britt H, Miller GC, Henderson J, Bayram C, Valenti L, Harrison C, Charles J, Pan Y, Zhang C, Pollack AJ, O’Halloran J: General practice activity in Australia 2012–13 General practice series no.33. 2013, Sydney: Sydney University Press

    Google Scholar 

  16. AIHW: Healthy for Life. ACCHSs Report Card. 2013, Canberra, Cat No AIHW 97

    Google Scholar 

  17. Australian Bureau of Statistics: Estimates of Aboriginal and Torres Strait Islander Australians. http://www.abs.gov.au/ausstats/abs@.nsf/mf/3238.0.55.001.

  18. AIHW: National Advisory Group on Aboriginal and Torres Strait Islander Health Information Strategic Plan 2011–2015. 2011, Canberra: AIHW

    Google Scholar 

  19. Australian Government Department of Health and Ageing: Closing the gap: tackling chronic disease. overview of the Commonwealth Indigenous Chronic disease package. http://www.healthyactive.gov.au/internet/main/publishing.nsf/Content/health-oatsih-ctg-package.

  20. Ward J, Bryant J, Worth H, Hull P, Solar S, Bailey S: Use of health services for sexually transmitted and blood-borne viral infections by young Aboriginal people in New South Wales. 2012, Aust J Prim: Health

    Google Scholar 

  21. Mooney-Somers J, Erick W, Scott R, Akee A, Kaldor J, Maher L: Enhancing Aboriginal and Torres Strait Islander young people’s resilience to blood-borne and sexually transmitted infections: findings from a community-based participatory research project. Health Promot J Austr. 2009, 20 (3): 195-201.

    PubMed  Google Scholar 

  22. Royal Australian College of General Practitioners: Guidelines for preventive activities in general practice (“The Red Book”). 2012, Melbourne: Royal Australian College of General Practitioners

    Google Scholar 

  23. National Aboriginal Community Controlled Health Organization, Royal Australian College of General Practitioners: National guide to a preventive health assessment for Aboriginal and Torres Strait Islander people. 2012, South Melbourne: The RACGP

    Google Scholar 

  24. McNulty CA, Freeman E, Bowen J, Shefras J, Fenton KA: Barriers to opportunistic chlamydia testing in primary care. Br J Gen Pract. 2004, 54 (504): 508.

    PubMed  PubMed Central  Google Scholar 

  25. Ma R, Clark A: Chlamydia screening in general practice: views of professionals on the key elements of a successful programme. J Fam Plan Rep Health Care. 2005, 31 (4): 302-306.

    Article  Google Scholar 

  26. Temple-Smith M, Kneebone J, Bilardi J, Pirotta M: Chlamydia screening: barriers to a complex intervention in the general practice setting. [Abstract]. General Practice and Primary Health Care Conference. 2009, Melbourne

    Google Scholar 

  27. Merritt TD, Durrheim DN, Hope K, Byron P: General practice intervention to increase opportunistic screening for chlamydia. Sex Health. 2007, 4 (4): 249-251.

    Article  PubMed  Google Scholar 

  28. Shafer MAB, Tebb KP, Pantell RH, Wibbelsman CJ, Neuhaus JM, Tipton AC, Kunin SB, Ko TH, Schweppe DM, Bergman DA: Effect of a clinical practice improvement intervention on Chlamydial screening among adolescent girls. JAMA. 2002, 288 (22): 2846-2852.

    Article  PubMed  Google Scholar 

  29. Guy RJ, Ali H, Liu B, Poznanski S, Ward J, Donovan B, Kaldor J, Hocking JS: Efficacy of interventions to increase the uptake of chlamydia screening in primary care: a systematic review. BMC Infect Dis. 2011, 11 (1): 211.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Council of Australian Governments National Indigenous Reform Agreement: Closing the Gap. http://www.federalfinancialrelations.gov.au/content/npa/health_indigenous/indigenous-reform/national-agreement_sept_12.pdf.

  31. Regan DG, Wilson DP, Hocking JS: Coverage is the key for effective screening of Chlamydia trachomatis in Australia. J Infect Dis. 2008, 198 (3): 349.

    Article  PubMed  Google Scholar 

  32. Council of Australian Governments: Closing the gap: National Urban and Regional Service Delivery Strategy for Indigenous Australians. http://www.coag.gov.au/node/67.

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Acknowledgements

We thank all sentinel sites which provided data for ACCESS.

ACCESS is a collaboration between the Kirby Institute, the Burnet Institute, the National Serology Reference Library, the National Perinatal Statistics Unit, and the National Aboriginal Community Controlled Health organization.

ACCESS was overseen by a coordinating committee from 2007–2010 which included: Basil Donovan, Rebecca Guy, John Kaldor, James Ward, Hammad Ali - the Kirby Institute, Sydney, NSW; Margaret Hellard, Jane Goller, Fabian Kong, Caroline van Gemert - Burnet Institute, Melbourne, VIC; Elizabeth Sullivan - Perinatal and Reproductive Epidemiology Research Unit, Sydney, NSW; Wayne Dimech - National Serology Reference Laboratory, Fitzroy, VIC.

The ACCESS project in 2009 was funded by the Australian Government, Department of Health and Ageing. However the views expressed in this paper are not necessarily the views of the Department of Health and Ageing now known as Department of Health.

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Correspondence to James Ward.

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The authors declare that they have no competing interests.

Authors’ contributions

JW conceptualized the study. JW, JG, HA and AB conducted the analysis. JW drafted the manuscript with assistance from JG, HA, RJG, SC and BD. JW, JMK, MH, RJG and BD are investigators on ACCESS. All authors contributed to the manuscript and read and approved the final version.

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Ward, J., Goller, J., Ali, H. et al. Chlamydia among Australian Aboriginal and/or Torres Strait Islander people attending sexual health services, general practices and Aboriginal community controlled health services. BMC Health Serv Res 14, 285 (2014). https://doi.org/10.1186/1472-6963-14-285

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