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Pre‐exposure prophylaxis for HIV prevention during pregnancy and lactation: forget not the women and children

Lisa Horgan, Christopher C Blyth, Asha C Bowen, David A Nolan and Andrew P McLean‐Tooke
Med J Aust 2019; 210 (6): . || doi: 10.5694/mja2.50052
Published online: 1 April 2019

Summary

 

  • Pregnancy is known to be a time of increased susceptibility to acquiring to human immunodeficiency virus (HIV) infection and this increased maternal risk places the unborn child at risk of vertical transmission.
  • Pre‐exposure prophylaxis (PrEP) involves the provision of antiretroviral therapy to an HIV‐negative individual with ongoing risk of HIV exposure to limit the likelihood of HIV transmission.
  • The inclusion of PrEP as part of a comprehensive strategy is recognised as an effective and safe means of reducing HIV infection in serodiscordant couples, thereby reducing the risk of vertical transmission of HIV.
  • Current data suggest that PrEP is safe to continue during pregnancy and breastfeeding in HIV‐negative women who remain vulnerable to acquiring HIV.
  • The recent Pharmaceutical Benefits Scheme subsidisation of PrEP has reduced the financial and practical obstacles of PrEP provision, and a subsequent increase in patient awareness and acceptance of PrEP is expected.
  • The framework for appropriately identifying and managing at‐risk pregnant and lactating women requiring PrEP is poorly defined and warrants further clarification to better support clinicians and this patient group.
  • This review discusses the current recommendations highlighting the gaps in the guidelines and makes some recommendations for future guideline development.

 


  • 1 Perth Children's Hospital, Perth, WA
  • 2 University of Western Australia, Perth, WA
  • 3 Princess Margaret Hospital for Children, Perth, WA
  • 4 Wesfarmers Centre of Vaccines and Infectious Diseases, Telethon Kids Institute, Perth, WA
  • 5 Royal Perth Hospital, Perth, WA
  • 6 PathWest Laboratory Medicine WA, Perth, WA



Competing interests:

No relevant disclosures.

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The Guttmacher–Lancet Commission on sexual and reproductive health and rights: how does Australia measure up?

Deborah J Bateson, Kirsten I Black and Shailendra Sawleshwarkar
Med J Aust 2019; 210 (6): . || doi: 10.5694/mja2.50058
Published online: 1 April 2019

There have been many advances in sexual and reproductive health and rights in Australia but we must also recognise the gaps that affect our most vulnerable populations

Australia is a signatory to the United Nations Sustainable Development Goals, which see sexual and reproductive health and rights as central to achieving progress in health and gender equity by 2030.1 Historically, sexual health and reproductive health have been separate entities but the necessity of integrating them is now recognised. In May 2018, the Guttmacher Institute partnered with The Lancet to create a commission on sexual and reproductive health and rights,2 which proposes a bold vision in which everyone is able to exercise their rights and responsibilities regarding sexual behaviour and reproduction freely and with dignity. And while sexual and reproductive health and rights are universal, some populations have distinct needs (Box 1).

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  • 1 Family Planning NSW, Sydney, NSW
  • 2 University of Sydney, Sydney, NSW
  • 3 Royal Prince Alfred Hospital, Sydney, NSW
  • 4 Westmead Clinical School, University of Sydney, Sydney, NSW
  • 5 Western Sydney Sexual Health Centre, Westmead Hospital, Sydney, NSW


Correspondence: deborahb@fpnsw.org.au

Competing interests:

No relevant disclosures.

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Medical abortion: it is time to lift restrictions

Caroline M de Costa, Kirsten I Black and Darren B Russell
Med J Aust 2019; 210 (6): . || doi: 10.5694/mja2.50060
Published online: 1 April 2019

Lifting the special drug status applied to medical abortion medications will enable equitable access

In 2016, the Committee on Economic, Social and Cultural Rights (a collection of human rights experts tasked with interpreting these rights), in its groundbreaking interpretation of the right to sexual and reproductive health, asserted that abortion services are an integral part of the right to health.1


  • 1 James Cook University, Cairns, QLD
  • 2 University of Sydney, Sydney, NSW
  • 3 Royal Prince Alfred Hospital, Sydney, NSW
  • 4 Cairns Sexual Health Service, Cairns, QLD


Correspondence: Caroline.DeCosta@jcu.edu.au

Acknowledgements: 

We thank Philip Goldstone for his assistance in the preparation of this article.

Competing interests:

No relevant disclosures.

  • 1. ESCR‐Net, International Network for Economic Social and Cultural Rights. General Comment No. 22 (2016) on the right to sexual and reproductive health (article 12 of the International Covenant on Economic, Social and Cultural Rights). ESCR‐Net, 2016. https://www.escr-net.org/resources/general-comment-no-22-2016-right-sexual-and-reproductive-health (viewed Feb 2019).
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  • 18. Shankar M, Black K, Goldstone P, et al. Access, equity and costs of induced abortion services in Australia: a cross‐sectional study. Aust N Z J Public Health 2017; 41: 309–314.

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Updates in the management of inflammatory bowel disease during pregnancy

Sally J Bell and Emma K Flanagan
Med J Aust 2019; 210 (6): . || doi: 10.5694/mja2.50062
Published online: 25 March 2019

Summary

 

  • The best pregnancy outcomes for women with inflammatory bowel disease (IBD) occur when their disease is in remission at conception and remains in remission throughout pregnancy.
  • Active IBD can lead to adverse pregnancy outcomes, including spontaneous abortion, pre‐term birth and low birthweight.
  • The majority of women with IBD who are taking maintenance medication will require medication throughout the pregnancy to prevent disease relapse.
  • Most IBD medications are considered safe in pregnancy and breastfeeding, except for methotrexate.
  • Pre‐conception counselling should be arranged with the patient's IBD specialist and should include discussions regarding the importance of optimising disease control before and during pregnancy as well as the medication management plan for pregnancy.
  • Patients with IBD should be reassured that their fertility is normal when the disease is quiescent, with the exception of women who have had pelvic surgery.
  • IBD activity should be carefully monitored during pregnancy using non‐invasive techniques, and disease flares during pregnancy should be treated promptly with escalation of therapy in consultation with the patient's IBD specialist.
  • Mode of delivery should be determined by obstetric need; however, caesarean delivery is preferred for women with a history of ileal pouch anal anastomosis surgery or active perianal Crohn's disease.

 


  • St Vincent's Hospital, Melbourne, VIC


Correspondence: Sally.Bell@svhm.org.au

Competing interests:

No relevant disclosures.

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  • 52. Mahadevan U, Vermeire S, Lasch K, et al. Vedolizumab exposure in pregnancy: outcomes from clinical studies in inflammatory bowel disease. Aliment Pharmacol Ther 2017; 45: 941–950.
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  • 54. Foulon A, Dupas JL, Sabbagh C, et al. Defining the most appropriate delivery mode in women with inflammatory bowel disease: a systematic review. Inflamm Bowel Dis 2017; 23: 712–720.

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Evaluating the benefits of a rapid access chest pain clinic in Australia

James Andrew Black, Kevin Cheng, Jo‐Anne Flood, Garry Hamilton, Serena Parker, Anees Enayati, Faisal S Khan and Tom Marwick
Med J Aust 2019; 210 (7): . || doi: 10.5694/mja2.50021
Published online: 25 March 2019

Abstract

Objectives: To compare the outcomes and safety of a rapid access chest pain clinic (RACPC) in Australia with those of a general cardiology clinic.

Design: Prospective comparison of the outcomes for patients attending an RACPC and those of historical controls.

Setting: Royal Hobart Hospital cardiology outpatient department.

Participants: 1914 patients referred for outpatient evaluation of new onset chest pain (1479 patients seen in the RACPC, 435 patients previously seen in the general cardiology clinic).

Main outcome measures: Service outcomes (review times, number of clinic reviews); adverse events (unplanned emergency department re‐attendances at 30 days and 12 months; major adverse cardiovascular events at 12 months, including unplanned revascularisation, acute coronary syndrome, stroke, cardiac death).

Results: Median time to review was shorter for RACPC than for usual care patients (12 days [IQR, 8–15 days] v 45 days [IQR, 27–89 days]). All patients seen in the RACPC received a diagnosis at the first clinic visit, but only 139 patients in the usual care group (32.0%). There were fewer unplanned emergency department re‐attendances for patients in the RACPC group at 30 days (1.6% v 4.4%) and 12 months (5.7% v 12.9%) than in the control group. Major adverse cardiovascular events were less frequent among patients evaluated in the RACPC (0.2% v 1.4%).

Conclusions: Patients were evaluated more efficiently in the RACPC than in a traditional cardiology clinic, and their subsequent rates of emergency department re‐attendances and adverse cardiovascular events were lower.

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  • 1 Royal Hobart Hospital, Hobart, TAS
  • 2 Austin Health, Melbourne, VIC
  • 3 Baker IDI Heart and Diabetes Institute, Melbourne, VIC


Correspondence: andrew.black@ths.tas.gov.au

Acknowledgements: 

We gratefully acknowledge grants from the Tasmanian Community Fund and the virtual Tasmanian Academic Health Sciences Precinct. We thank the staff and patients of the Royal Hobart Hospital who attended or worked in the RACPC, as well as the National Heart Foundation for their ongoing support. We are grateful to James Sharman for his assistance with the statistical analyses.

Competing interests:

No relevant disclosures.

  • 1. Nawar EW, Niska RW, Xu J. National Hospital Ambulatory Medical Care Survey: 2005 emergency department summary. Adv Data 2007; 386: 1–32.
  • 2. Cullen L, Greenslade J, Merollini K, et al. Cost and outcomes of assessing patients with chest pain in an Australian emergency department. Med J Aust 2015; 202: 427–432. https://www.mja.com.au/journal/2015/202/8/cost-and-outcomes-assessing-patients-chest-pain-australian-emergency-department
  • 3. Acute Coronary Syndrome Guidelines Working Group. Guidelines for the management of acute coronary syndromes. Med J Aust 2006; 184 (8 Suppl): S1–S29. https://www.mja.com.au/journal/2006/184/8/guidelines-management-acute-coronary-syndromes-2006
  • 4. Dougan JP, Mathew TP, Riddell JW, et al. Suspected angina pectoris: a rapid‐access chest pain clinic. Q J Med 2001; 94: 679–686.
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  • 7. Davie AP, Caesar D, Caruana L, et al. Outcome from a rapid‐assessment chest pain clinic. Q J Med 1998; 91: 339–343.
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  • 9. Fox KF, Tenkorang J, Rogers A, et al. Are rapid access cardiology clinics a valued part of a district cardiology service? Int J Cardiol 2009; 137: 42–46.
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  • 14. Chew DP, Scott IA, Cullen L, et al. National Heart Foundation of Australia and Cardiac Society of Australia and New Zealand: Australian clinical guidelines for the management of acute coronary syndromes 2016. Heart Lung Circ 2016; 25: 895–951.
  • 15. Sandoval Y, Smith SW, Shah AS, et al. Rapid rule‐out of acute myocardial injury using a single high‐sensitivity cardiac troponin I measurement. Clin Chem 2017; 63: 369–376.
  • 16. Ashrafi R, Raga S, Abdool A, et al. NICE recommendations for the assessment of stable chest pain: assessing the early economic and service impact in the rapid‐access chest pain service. Postgrad Med J 2013; 89: 251–257.
  • 17. Elford A, Black A, Flood J. Review of the rapid access chest pain assessment clinic at the Royal Hobart Hospital [abstract]. Heart Lung Circ 2016; 25 (Suppl 2): S63.

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Cultural respect in general practice: a cluster randomised controlled trial

Siaw‐Teng Liaw, Vicki Wade, John S Furler, Iqbal Hasan, Phyllis Lau, Margaret Kelaher, Wei Xuan and Mark F Harris
Med J Aust 2019; 210 (6): . || doi: 10.5694/mja2.50031
Published online: 25 March 2019

Abstract

Objective: To examine whether the Ways of Thinking and Ways of Doing (WoTWoD) cultural respect framework improves clinically appropriate anticipatory care in general practice and the cultural respect levels of medical practice staff.

Design: Mixed methods, cluster randomised controlled trial with a participatory action research approach.

Setting, participants: Fifty‐six general practices in Sydney and Melbourne, 2014–2017.

Intervention: WoTWoD encompasses a toolkit (ten scenarios illustrating cross‐cultural behaviour in clinical practice), one half‐day workshop, cultural mentor support for practices, and a local care partnership between participating Medicare locals/primary health networks and local Aboriginal Community Controlled Health Services for guiding the program and facilitating community engagement. The intervention lasted 12 months at each practice.

Major outcomes: Rates of claims for MBS item 715 (health assessment for Aboriginal and Torres Strait Islander People) and recording of chronic disease risk factors; changes in cultural quotient (CQ) scores of practice staff.

Results: Complete results were available for 28 intervention (135 GPs, 807 Indigenous patients) and 25 control practices (210 GPs, 1554 Indigenous patients). 12‐Month rates of MBS item 715 claims and recording of risk factors for the two groups were not statistically significantly different, nor were mean changes in CQ scores, regardless of staff category and practice attributes.

Conclusion: The WoTWoD program did not increase the rate of Indigenous health checks or improve cultural respect scores in general practice. Conceptual, methodologic, and contextual factors that influence cultural mentorship, culturally respectful clinical practice, and Indigenous health care require further investigation.

Trial registration: Australia New Zealand Clinical Trials Registry ACTRN12614000797673.

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  • 1 UNSW Sydney, Sydney, NSW
  • 2 Centre for Primary Health Care and Equity, UNSW Sydney, Sydney, NSW
  • 3 Menzies School of Health Research, Darwin, NT
  • 4 University of Melbourne, Melbourne, VIC
  • 5 Centre for Health Policy, University of Melbourne, Melbourne, VIC
  • 6 Ingham Institute of Applied Medical Research, Sydney, NSW


Correspondence: siaw@unsw.edu.au

Acknowledgements: 

We acknowledge the contributions of Lisa Jackson‐Pulver and the cultural mentors Phillip Orcher, Faye Daniels, Rhonda McPherson, Aunty Diane Kerr, and Nina Fitzgerald that ensured the cultural appropriateness of the design, implementation and interpretation of our study. The trial was funded by the National Health and Medical Research Council (APP1065491).

Competing interests:

No relevant disclosures.

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Early initiation of antiretroviral therapy for people newly diagnosed with HIV infection in Australia: trends and predictors, 2004–2015

Hamish McManus, Denton Callander, Basil Donovan, Darren B Russell, Catherine C O'Connor, Stephen C Davies, David A Lewis, Margaret E Hellard, Marcus Y Chen, Kathy Petoumenos, Rick Varma, Aaron Cogle, Mark Alastair Boyd, Andrew Grulich, James Pollard, Nick Medland, Christopher K Fairley and Rebecca J Guy
Med J Aust 2019; 210 (6): . || doi: 10.5694/mja2.50006
Published online: 25 March 2019

Abstract

Objectives: To determine trends in and predictors of early treatment for people newly diagnosed with human immunodeficiency virus (HIV) infection in Australia.

Design, setting: Retrospective cohort analysis of routinely collected longitudinal data from 44 sexual health clinics participating in the Australian Collaboration for Coordinated Enhanced Sentinel Surveillance (ACCESS) program.

Participants: Patients diagnosed with HIV infections, January 2004 – June 2015.

Main outcome measures: Commencement of antiretroviral therapy within 6 months of HIV diagnosis (early treatment); demographic, clinical, and risk group characteristics of patients associated with early treatment; trends in early treatment, by CD4+ cell count at diagnosis.

Results: 917 people were diagnosed with HIV infections, their median age was 34 years (interquartile range [IQR]: 27–43 years), and 841 (92%) were men; the median CD4+ cell count at diagnosis was 510 cells/μL (IQR, 350–674 cells/μL). The proportion of patients who received early treatment increased from 17% (15 patients) in 2004–06 to 20% (34 patients) in 2007–09, 34% (95 patients) in 2010–12, and 53% (197 patients) in 2013–15 (trend, P < 0.001). The probability of early treatment, which increased with time, was higher for patients with lower CD4+ cell counts and higher viral loads at diagnosis.

Conclusions: The proportion of people newly diagnosed with HIV in sexual health clinics in Australia who received treatment within 6 months of diagnosis increased from 17% to 53% during 2004–2015, reflecting changes in the CD4+ cell count threshold in treatment guidelines. Nevertheless, further strategies are needed to maximise the benefits of treatment to prevent viral transmission and morbidity.

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  • 1 The Kirby Institute, University of New South Wales, Sydney, NSW
  • 2 Sydney Sexual Health Centre, Sydney Hospital, Sydney, NSW
  • 3 Sexual Health Service Cairns, Cairns, QLD
  • 4 Northern Sydney Sexual Health Service, Royal North Shore Hospital, Sydney, NSW
  • 5 Western Sydney Sexual Health Centre, University of Sydney, Sydney
  • 6 Centre for Population Health, Burnet Institute, Melbourne, VIC
  • 7 Melbourne Sexual Health Centre, Alfred Health, Melbourne, VIC
  • 8 Sydney Sexual Health Centre, South Eastern Sydney Local Health District, Sydney, NSW
  • 9 National Association of People with HIV Australia, Melbourne, NSW
  • 10 University of Adelaide, Adelaide, SA
  • 11 Lyell McEwin Hospital, Adelaide, SA
  • 12 University Hospital, Geelong, VIC
  • 13 Melbourne Sexual Health Centre, Monash University Central Clinical School, Melbourne, VIC


Correspondence: hmcmanus@kirby.unsw.edu.au

Competing interests:

No relevant disclosures.

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Monitoring the missing half: why reporting adolescent births is insufficient

Jennifer L Marino and Susan M Sawyer
Med J Aust 2019; 210 (5): . || doi: 10.5694/mja2.50047
Published online: 18 March 2019

Lack of national abortion data impedes development of sexual and reproductive health care policies and programs for young Australians

Recent data show a steady decrease in adolescent births to a historic low of 10 births per 1000 15–19‐year‐olds.1 Notwithstanding that some adolescent pregnancies are planned or wanted, these data are surely positive, as pregnant adolescents are vulnerable to numerous adversities and delaying pregnancy is healthier for mothers and children.2 However, birth rates reflect access to comprehensive sexuality education, reliable contraception and safe abortion. Specifically, as lower birth rates may reflect higher abortion rates, a complete national picture is required. More broadly, pregnancy and its outcomes reflect various inequities that continue to affect adolescents and their offspring across their lives. Greater understanding of adolescent pregnancy outcomes, including abortion, would help shape a suite of interventions for vulnerable adolescents, including interventions that facilitate access to quality schooling and alleviate poverty.


  • 1 Royal Women's Hospital, Melbourne, VIC
  • 2 University of Melbourne, Melbourne, VIC
  • 3 Murdoch Children's Research Institute, Melbourne, VIC



Acknowledgements: 

Jennifer Marino is supported by National Health and Medical Research Council Centre of Research Excellence in Adolescent Health grant 1134894 and project grant 1161145. We thank Dr Deborah Bateson (Family Planning Victoria), Ms Sarah Gafforini and Dr Philip Goldstone (Marie Stopes Australia), Dr Cedric Manen (Family Planning Tasmania) and Prof Rachel Skinner (University of Sydney and Children's Hospital Westmead) for enlightening conversations about this topic and comments on the manuscript.

Competing interests:

No relevant disclosures.

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The burden of pancreatic cancer in Australia attributable to smoking

Maria E Arriaga, Claire M Vajdic, Robert J MacInnis, Karen Canfell, Dianna J Magliano, Jonathan E Shaw, Julie E Byles, Graham G Giles, Anne W Taylor, Tiffany K Gill, Vasant Hirani, Robert G Cumming, R Paul Mitchell, Emily Banks, Julie Marker, Barbara‐Ann Adelstein and Maarit A Laaksonen
Med J Aust 2019; 210 (5): . || doi: 10.5694/mja2.12108
Published online: 11 March 2019

Abstract

Objective: To estimate the burden of pancreatic cancer in Australia attributable to modifiable exposures, particularly smoking.

Design: Prospective pooled cohort study.

Setting, participants: Seven prospective Australian study cohorts (total sample size, 365 084 adults); participant data linked to national registries to identify cases of pancreatic cancer and deaths.

Main outcome measures: Associations between exposures and incidence of pancreatic cancer, estimated in a proportional hazards model, adjusted for age, sex, study, and other exposures; future burden of pancreatic cancer avoidable by changes in exposure estimated as population attributable fractions (PAFs) for whole population and for specific population subgroups with a method accounting for competing risk of death.

Results: There were 604 incident cases of pancreatic cancer during the first 10 years of follow‐up. Current and recent smoking explained 21.7% (95% CI, 13.8–28.9%) and current smoking alone explained 15.3% (95% CI, 8.6–22.6%) of future pancreatic cancer burden. This proportion of the burden would be avoidable over 25 years were current smokers to quit and there were no new smokers. The burden attributable to current smoking is greater for men (23.9%; 95% CI, 13.3–33.3%) than for women (7.2%; 95% CI, –0.4% to 14.2%; P = 0.007) and for those under 65 (19.0%; 95% CI, 8.1–28.6%) than for older people (6.6%; 95% CI, 1.9–11.1%; P = 0.030). There were no independent relationships between body mass index or alcohol consumption and pancreatic cancer.

Conclusions: Strategies that reduce the uptake of smoking and encourage current smokers to quit could substantially reduce the future incidence of pancreatic cancer in Australia, particularly among men.

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  • 1 Centre for Big Data Research in Health, University of New South Wales, Sydney, NSW
  • 2 Cancer Council Victoria, Melbourne, VIC
  • 3 Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, VIC
  • 4 Cancer Council NSW, Sydney, NSW
  • 5 University of Sydney, Sydney, NSW
  • 6 Prince of Wales Clinical School, University of New South Wales, Sydney, NSW
  • 7 Baker Heart and Diabetes Institute, Melbourne, VIC
  • 8 Research Centre for Gender, Health and Ageing, University of Newcastle, Newcastle, NSW
  • 9 Adelaide Medical School, University of Adelaide, Adelaide, SA
  • 10 Charles Perkins Centre, University of Sydney, Sydney, NSW
  • 11 ANZAC Research Institute, University of Sydney and Concord Hospital, Sydney, NSW
  • 12 Centre for Vision Research, Westmead Institute for Medical Research, University of Sydney, Sydney, NSW
  • 13 Australian National University, Canberra, ACT
  • 14 Cancer Voices South Australia, Adelaide, SA


Correspondence: m.laaksonen@unsw.edu.au

Acknowledgements: 

We thank the investigators and participants of the participating cohort studies and surveys for providing the data for the cohort consortium. Our investigation was supported by the National Health and Medical Research Council (NHMRC; 1060991). The NHMRC also supported Maarit Laaksonen (I1053642), Karen Canfell (1082989), Emily Banks (1136128), Jonathan Shaw (1079438) and Dianna Magliano (1118161). Maarit Laaksonen was also supported by the Cancer Institute NSW (13/ECF/1‐07). Maria Arriaga was supported by an Australian Postgraduate Award and a Translational Cancer Research Network PhD Scholarship Top‐up Award.Details of funding and data sources for the 45 and Up Study (www.saxinstitute.org.au/our-work/45-up-study/for-partners) and the Australian Longitudinal Study on Women's Health (www.alswh.org) are available on the study websites. Cohort recruitment for the Melbourne Collaborative Cohort Study was funded by Cancer Council Victoria and the Victorian Health Promotion Foundation (VicHealth); the study was supported by NHMRC grants 209057 and 396414 and by Cancer Council Victoria (infrastructure support). The CHAMP study is funded by the NHMRC (301916) and the Ageing and Alzheimer's Institute, Sydney. We acknowledge the assistance of the Data Linkage Unit at the Australian Institute of Health and Welfare for undertaking the data linkage to the Australian Cancer Database and the National Death Index.

Competing interests:

No relevant disclosures.

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Identifying the cultural heritage of patients during clinical handover and in hospital medical records

David JR Morgan, Tania Harris, Ron Gidgup and Martin Whitely
Med J Aust 2019; 210 (5): . || doi: 10.5694/mja2.12107
Published online: 11 March 2019

Abstract

Objective: To examine the frequency of and rationale for hospital doctors mentioning a patient's cultural heritage (ethnicity, national heritage, religion) during medical handovers and in medical records.

Design: Four‐phase observational study, including the covert observation of clinical handovers in an acute care unit (ACU) and analysis of electronic medical records (EMRs) of ACU patients after their discharge to ward‐based care.

Setting, participants: 1018 patients and the doctors who cared for them at a tertiary hospital in Western Australia, May 2016 – February 2018.

Main outcome measure: References to patients’ cultural heritage by ACU doctors during clinical handover (written or verbal) and by ward‐based doctors in hospital EMRs (written only), by geographic ethnic–national group.

Results: In 2727 ACU clinical handovers of 1018 patients, 142 cultural heritage identifications were made (ethnicity, 84; nationality, 41; religion, 17); the rate was highest for Aboriginal patients (370 [95% CI, 293–460] identifications per 1000 handovers). 14 505 EMR pages were reviewed; 380 cultural heritage identifications (ethnicity, 257; nationality, 119; religion, 4) were recorded. A rationale for identification was documented for 25 of 142 patients (18%) whose ethnic–national background was mentioned during handover or in their EMR. Multivariate analysis (adjusted for demographic, socio‐economic and medical factors) indicated that being an Aboriginal Australian was the most significant factor for identifying ethnic–national background (handovers: adjusted odds ratio [aOR], 21.7; 95% CI, 7.94–59.4; hospital EMRs: aOR, 13.6; 95% CI, 5.03–36.5). 44 of 75 respondents to a post‐study survey (59%) were aware that Aboriginal heritage was mentioned more frequently than other cultural backgrounds.

Conclusions: Explicitly mentioning the cultural heritage of patients is inconsistent and seldom explained. After adjusting for other factors, Aboriginal patients were significantly more likely to be identified than patients with other backgrounds.

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  • 1 South Metroplitan Health Service, Perth, WA
  • 2 Health Consumers’ Council (WA), Perth, WA
  • 3 John Curtin Institute of Public Policy, Curtin University, Perth, WA



Acknowledgements: 

We thank Jenny Thompson for assisting with the collection of the APACHE III data.

Competing interests:

No relevant disclosures.

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