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Implementing voluntary assisted dying in New South Wales correctional settings

Diya Ahluwalia and Leigh Haysom
Med J Aust 2025; 223 (2): . || doi: 10.5694/mja2.52688
Published online: 21 July 2025

New South Wales was the last Australian state to pass voluntary assisted dying (VAD) legislation, effective on 28 November 2023.1 The Justice Health and Forensic Mental Health Network (JHNSW) is responsible for the health care of people in contact with the criminal justice system in NSW (www.nsw.gov.au/health/justicehealth/) and was tasked with implementing a VAD pathway for prisoners. A steering committee was formed with the Corrective Services NSW (CSNSW; https://correctiveservices.dcj.nsw.gov.au/), the local health district, the CSNSW Inmate Consumer Referent Group, the Mental Health Review Tribunal (https://mhrt.nsw.gov.au/the‐tribunal/), the JHNSW Clinical Ethics Committee, the Victims Support Scheme and the Aboriginal Health and Medical Research Council of NSW (www.ahmrc.org.au) to create dignified and culturally safe pathways for prisoners to access VAD. The ethical and legal challenges of integrating VAD into the NSW correctional settings are highlighted below, with a hypothetical patient journey demonstrating the pathway.

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Bone health perspectives among Indigenous people: a qualitative study

Troy Walker (Yorta Yorta), Karan P Singh, Vanessa Gan, Brooke Conley (Ngiyampaa), Jessica Bravo, Nigel Smith (Weilwan), April Clarke (Eastern Maar, Kirrae Whurrung, Djap Wurrung), Jackson Baker, Louise J Maple‐Brown, Robin M Daly, Jennifer Browne, Jesse Zanker, Cat Shore‐Lorenti, David Scott, Peter R Ebeling and Ayse Zengin
Med J Aust || doi: 10.5694/mja2.52704
Published online: 7 July 2025

Abstract

Objectives: To explore perspectives and beliefs on bone health among Indigenous adults in Victoria.

Design: Qualitative focus groups with semi‐structured questions. Focus group discussions were analysed for themes and subthemes using an Indigenous research framework based on three concepts: Ways of Knowing, Ways of Being and Ways of Doing.

Setting, participants: Focus groups were conducted at Aboriginal Community‐controlled organisations and Community centres. Men and women aged ≥ 35 years who identified as Indigenous and were able to give informed consent were invited to participate.

Results: Eighty‐two Indigenous people participated in twelve focus groups across ten sites in Victoria. Most participants (64) were women, and the majority lived in metropolitan centres, regional centres and large rural towns (Modified Monash categories 1–3). Five themes were developed around the Indigenous framework proposed by Karen Martin‐Booran Mirraboopa — Ways of Knowing, Ways of Doing and Ways of Being — which guided participants in identifying knowledge of exercise for bone and muscle health; connection to Country; importance of regular preventive health activities; food and nutrients as good medicine for bone health; and healthy futures for Community through education. An overarching theme of holistic health, including the aspect of spirituality and related lifestyle factors pertaining to musculoskeletal health, was highlighted.

Conclusion: Increasing bone health awareness by a co‐created Community education program was valued as it would be beneficial for Indigenous people across the life course. To be effective, incorporating traditional Indigenous ways and knowledge along with present‐day health evidence is required.

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  • 1 Monash University, Melbourne, VIC
  • 2 National Centre for Healthy Ageing, Melbourne, VIC
  • 3 University of Melbourne, Melbourne, VIC
  • 4 Victorian Aboriginal Community Controlled Health Organisation, Melbourne, VIC
  • 5 Murrumbidgee Local Health District, Moama, NSW
  • 6 Gariwerd Dreaming, Melbourne, VIC
  • 7 Njernda Aboriginal Corporation, Echuca, VIC
  • 8 Menzies School of Health Research, Charles Darwin University, Darwin, NT
  • 9 Royal Darwin and Palmerston Hospitals NT Health, Darwin, NT
  • 10 Institute for Physical Activity and Nutrition, Deakin University, Melbourne, VIC
  • 11 Deakin University, Melbourne, VIC
  • 12 Royal Melbourne Hospital, Melbourne, VIC


Correspondence: troy.walker@monash.edu


Open access:

Open access publishing facilitated by Monash University, as part of the Wiley ‐ Monash University agreement via the Council of Australian University Librarians.


Data sharing:

The data for this study will not be shared, as we do not have permission from the participants or ethics approval to do so.


Acknowledgements: 

Thank you to all of the Aboriginal and Torres Strait Islander participants who attended the focus groups and the ACCHOs for hosting the focus groups. This study was funded by was funded by a grant from the National Centre for Healthy Ageing (NCHA) through the Commonwealth Government of Australia, for which Ayse Zengin was the lead investigator. Louise Maple‐Brown was supported by a National Health and Medical Research Council Investigator Grant (11194698).

Open access publishing facilitated by Monash University, as part of the Wiley ‐ Monash University agreement via the Council of Australian University Librarians.

Competing interests:

No relevant disclosures.

Received 2 July 2024, accepted 18 December 2024

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Am I on the list? Clinician‐reported factors for kidney transplantation non‐waitlisting among Aboriginal and Torres Strait Islander people with kidney failure: a cross‐sectional study

Stephen P McDonald AM, Katie Cundale, Christopher E Davies, Kelli Karrikarringka Owen (Kaurna, Nharangga, and Ngarrindjeri), Kerry Dole, Feruza Kholmurodova, Matilda D’Antoine (Paakantyi) and Jaquelyne T Hughes (Wagadagam)
Med J Aust 2025; 223 (1): . || doi: 10.5694/mja2.52698
Published online: 7 July 2025

Abstract

Objectives: To describe clinician‐reported reasons for non‐waitlisting of patients with kidney failure for deceased donor kidney transplantation, and to examine disparities affecting Aboriginal and Torres Strait Islander people.

Design: Retrospective cross‐sectional analysis of data from a national clinical quality registry.

Participants and setting: Patients receiving dialysis in 26 Australian renal units as of 31 December 2020.

Main outcome measures: Rates of active waitlisting for kidney transplantation and clinician‐reported reasons for non‐waitlisting.

Results: Thirty‐six of 1832 Aboriginal and Torres Strait Islander people (2.0%) were actively waitlisted, compared with 512 of 6128 non‐Indigenous people (8.4%). For Aboriginal and Torres Strait Islander patients aged < 65 years, 457 of 1204 (38%) were not waitlisted due to a permanent contraindication, 276 (23%) due to a temporary contraindication, and 232 (19%) due to incomplete work‐up. Among those with a contraindication, cardiovascular disease was reported as the reason for about a quarter of people in both groups. Obesity was cited for 163 Aboriginal and Torres Strait Islander patients aged < 65 years (22%) and 30 Aboriginal and Torres Strait Islander patients aged ≥ 65 years (10%); in the non‐Indigenous group, obesity was cited for 207 (26%) and 163 (9%) patients aged < 65 years and ≥ 65 years, respectively. Cancer was reported for 28 Aboriginal and Torres Strait Islander patients aged < 65 years (4%) and 86 non‐Indigenous patients aged < 65 years (11%). Other reasons for non‐waitlisting, reported as free text, included patient safety, smoking, age and mental health.

Conclusions: Aboriginal and Torres Strait Islander people experience inequities in waitlisting for kidney transplantation across multiple stages of a complex process. Addressing these barriers requires system‐level reform and accountability to improve equity in transplantation access.

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  • 1 Australia and New Zealand Dialysis and Transplant Registry, Adelaide, SA
  • 2 Adelaide EpiCentre, Adelaide, SA
  • 3 National Indigenous Kidney Transplantation Taskforce, Adelaide, SA
  • 4 University of Adelaide, Adelaide, SA
  • 5 AKction Reference Group, Adelaide, SA
  • 6 Northern Territory Department of Health, Alice Springs, NT
  • 7 Flinders University, Darwin, NT
  • 8 Royal Darwin Hospital, Darwin, NT


Correspondence: stephenm@anzdata.org.au


Open access:

Open access publishing facilitated by The University of Adelaide, as part of the Wiley – The University of Adelaide agreement via the Council of Australian University Librarians.


Data Sharing:

ANZDATA has established policies for access to various types of data (including those underlying this manuscript). These policies and associated application procedures are available at https://www.anzdata.org.au/anzdata/data‐requests/request‐procedure.


Acknowledgements: 

The National Indigenous Kidney Transplantation Taskforce is funded by a grant from the Australian Government Department of Health and Aged Care (4‐BIA3J8Y) that is held by the Transplantation Society of Australia and New Zealand. The Australia and New Zealand Dialysis and Transplant Registry (ANZDATA) receives funding from the Australian Organ and Tissue Authority to support its core operations. Neither body had a role in study design, data collection, data analysis or interpretation of findings. The authors recognise Indigenous peoples research leadership and their knowledges contained within the following cited references: 1,2,8,11,12,18,19,20,31,32 and 34,35,36.

Competing interests:

Jaquelyne Hughes is a Guest Editor for the 2025 NAIDOC Week MJA Special Issue and was not involved in any editorial decision making about this article.


Author contributions:

McDonald SP: Conceptualization; formal analysis; methodology; supervision; writing – original draft; writing – review and editing. Cundale K: Formal analysis; project administration; writing – original draft; writing – review and editing. Davies C: Data curation; formal analysis; visualization; writing – original draft; writing – review and editing. Owen K: Conceptualization; writing – review and editing. Dole K: Conceptualization; supervision; writing – review and editing. Kholmurodova F: Data curation; formal analysis; visualization. D’Antoine M: Project administration; writing – review and editing. Hughes JT: Conceptualization; methodology; supervision; writing – original draft; writing – review and editing. All authors have reviewed and approved the final manuscript and agree to be accountable for their contributions.

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What do Aboriginal people in the Northern Territory value during the operation journey? A qualitative study

Edith B Waugh, Marita Hefler, Sophie Pascoe, Mark Mayo, Matthew JL Hare, David A Story, Neil Wilkshire, Peter Henwood, David Croker and Jampijinpa Ross
Med J Aust 2025; 223 (1): . || doi: 10.5694/mja2.52695
Published online: 7 July 2025

Abstract

Objective: To explore the values of Aboriginal people in the Northern Territory during their perioperative journey.

Design: A community‐based participatory action research approach was used, integrating yarning, deep listening and reflection methods to gather qualitative data in culturally appropriate ways. Data collection involved two yarning circles followed by interpretation and triangulation sessions with co‐researchers.

Setting: Conducted in non‐health care settings in Garramilla (Darwin) between May 2023 and September 2024, the study included participants from urban, regional and remote NT Aboriginal communities.

Participants: Purposive and snowball sampling were used to engage 18 participants with lived experience of surgery, who share expertise in renal health journeys and have kinship ties spanning from Saltwater Country to Desert Country, with diverse age, language and gender representation.

Main outcome measures: Thematic insights into what First Nations peoples in the NT value during the perioperative journey, to inform culturally safe models of care.

Results: Respect emerged as the core principle in the perioperative journey, with family involvement, cultural practices and effective communication identified as key elements. Respect was evident in honouring cultural protocols, integrating traditional healing practices and recognising patient autonomy. Family involvement was highlighted as essential, with kinship ties influencing shared decision‐making processes and support throughout the perioperative experience. Culturally competent communication, including the use of interpreters and clear explanations, played a critical role in bridging cultural differences and ensuring shared understanding. Together, these elements fostered a sense of safety, belonging and empowerment. Ultimately, trust was identified as an overarching outcome that unified these interconnected values, enhancing patient comfort, engagement and overall satisfaction in the perioperative journey.

Conclusion: Respect is integral to Aboriginal people in the perioperative journey, and they value family, culture and communication when navigating surgery. When these values coalesce, trust is generated. These findings highlight the need to integrate culturally informed, patient‐centred care models that prioritise respect and trust building to improve accessibility, experience and surgical outcomes.

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  • 1 Menzies School of Health Research, Charles Darwin University, Darwin, NT
  • 2 Royal Darwin Hospital, Tiwi, NT
  • 3 University of Melbourne, Melbourne, VIC
  • 4 Flinders University, Darwin, NT
  • 5 Austin Health, Melbourne, VIC
  • 6 Purple House, Alice Springs, NT


Correspondence: edith.waugh@menzies.edu.au


Open access:

Open access publishing facilitated by Charles Darwin University, as part of the Wiley – Charles Darwin University agreement via the Council of Australian University Librarians.


Data Sharing:

Data collected and analysed during the study are not publicly available due to privacy issues and ethical considerations. Data may be available from the corresponding author on reasonable request.


Acknowledgements: 

Warning: Aboriginal and Torres Strait Islander readers are advised that this article captures the knowledge and lived experiences of Indigenous people who have passed. With permission from family, we refer to our senior co‐author as “Jampijinpa” Ross. This article is a testament to his contributions to First Nations health. Out of cultural sensitivity, we do not use the names nor images of Indigenous people who participated in this research who have subsequently passed away.

Edith Waugh received an ANZCA Foundation (Australian and New Zealand College of Anaesthetists) Health Equity Grant 2022. The funding allowed planning, coordination and completion of focus (yarning) groups; participation and sharing of First Nations knowledge was appropriately reimbursed. Edith Waugh is supported by an Australian Government Research Training Scholarship. Matthew Hare is supported by the National Health and Medical Research Council (grant number 1194698), the Sylvia and Charles Viertel Foundation and an Australian Diabetes Society Skip Martin Fellowship.

The Top End Indigenous Reference Group and research assistant Stephanie Long from the INFERR (INtravenous iron polymaltose for First Nations Australian patients with high FERRitin levels on hemodialysis) study at Menzies School of Health Research were the catalysts leading to this study. This study emerged in response to their feedback about exploring postoperative outcomes for First Nations people in the Northern Territory and the need for this research to incorporate patient values.

Competing interests:

No relevant disclosures.


Author contributions:

Waugh EB: Conceptualization; methodology; investigation (data collection); formal analysis; writing – original draft; writing – review and editing; project administration; funding acquisition. Hefler M: Methodology; formal analysis; writing – review and editing; supervision. Pascoe S: Methodology; investigation (data collection); formal analysis; writing – review and editing; project administration. Mayo M: Conceptualization; writing – review and editing; supervision. Hare MJL: Writing – review and editing; supervision. Story DA: Writing – review and editing; funding acquisition, supervision. Wilkshire N: Writing – methodology; investigation (data collection); formal analysis; review and editing; supervision. Henwood P: Writing – methodology; investigation (data collection); formal analysis; review and editing; supervision. Croker D: Writing – methodology; investigation (data collection); formal analysis; review and editing; supervision. Ross J: Writing – methodology; investigation (data collection); formal analysis; review and editing; supervision.

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Climate and environmental crisis: effects on ear and hearing health in Australia and for Aboriginal and Torres Strait Islander peoples

Georgia M Tongs (Wiradjuri), Isabella Ludbrook, Jennifer H Martin, Robert Eisenberg and Kelvin M Kong (Worimi)
Med J Aust 2025; 223 (1): . || doi: 10.5694/mja2.52689
Published online: 7 July 2025

As a collaborative research team, we acknowledge the diverse perspectives, lived experiences, and cultural knowledges that shape our work. We are united in our commitment to examining health and climate through the lens of Aboriginal and Torres Strait Islander peoples, recognising the profound and disproportionate impacts these intersecting issues have on Indigenous communities globally.

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  • 1 John Hunter Hospital, Newcastle, NSW
  • 2 University of Newcastle, Newcastle, NSW
  • 3 Hunter Medical Research Institute, Newcastle, NSW
  • 4 University of New South Wales, Sydney, NSW
  • 5 Macquarie University, Sydney, NSW



Open access:

Open access publishing facilitated by University of New South Wales, as part of the Wiley – University of New South Wales agreement via the Council of Australian University Librarians.


Competing interests:

Kelvin Kong is a Guest Editor for the 2025 NAIDOC Week MJA Special Issue and was not involved in any editorial decision making about this article.


Author contributions:

Tongs G: Formal analysis, investigation, methodology, resources, visualization, writing – original draft, writing – review and editing. Ludbrook I: Conceptualization, formal analysis, methodology, project administration, resources, supervision, visualization, writing – original draft, writing – review and editing. Martin J: Conceptualization, formal analysis, methodology, project administration, supervision, writing – original draft, writing – review and editing. Eisenberg R: Conceptualization, data curation, formal analysis, investigation, methodology, project administration, supervision, visualization, writing – original draft, writing – review and editing. Kong K: Conceptualization, formal analysis, investigation, methodology, resources, supervision, writing – original draft, writing – review and editing.

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Factors that affect the provision of medical abortion services in Australian primary care: a mixed methods systematic review

Greta Skahill and Mridula Shankar
Med J Aust || doi: 10.5694/mja2.52707
Published online: 30 June 2025

Abstract

Objectives: To synthesise primary research findings about factors that affect medical abortion provision by general practitioners, nurses, midwives, and pharmacists in Australia.

Study design: Mixed methods systematic review of peer‐reviewed primary publications of qualitative, quantitative, and mixed methods studies of the provision of medical abortion in Australian primary care, 1 January 2013 – 18 January 2025.

Data sources: MEDLINE, Scopus, Web of Science, CINAHL (Cumulative Index to Nursing and Allied Health Literature).

Data synthesis: Twenty‐three publications satisfied our inclusion criteria. We undertook a thematic synthesis of the qualitative study findings to identify barriers and facilitators of medical abortion provision, and assessed the confidence of each review finding using the GRADE‐CERQual approach; we also compared the qualitative synthesis with quantitative study findings. We developed ten review findings grouped under three themes: moral, legal, and regulatory influences on abortion care (three review findings; very low to moderate confidence); the absence of a systems‐based approach to abortion provision (six review findings; moderate to high confidence); and early medical abortion belongs in primary care (one review finding; high confidence). Barriers to providing medical abortion include the absence of a supportive service delivery strategy, insufficient Medicare remuneration, geographic isolation, limited access to training, and colleagues who conscientiously object to abortion. Facilitators of its provision include clinician support networks and personal motivation to improve access to reproductive health care.

Conclusions: A range of individual, service level, and system factors exacerbate the effects of geographic location and financial considerations on the provision of medical abortion in Australian primary care. Our findings indicate that financial and structural support is needed for the geographic decentralisation of medical abortion training and services, the establishment of nurse‐led models of care, and the integration of abortion care into primary care.

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  • 1 The University of Melbourne, Melbourne, VIC
  • 2 Nossal Institute for Global Health, the University of Melbourne, Melbourne, VIC



Open access:

Open access publishing facilitated by the University of Melbourne, as part of the Wiley – the University of Melbourne agreement via the Council of Australian University Librarians.


Acknowledgements: 

We are grateful to Rana Islamiah Zahroh (Nossal Institute for Global Health, the University of Melbourne) for training the authors in applying GRADE‐CERQual to qualitative evidence synthesis findings. We thank Alya Hazfiarini (Nossal Institute for Global Health, the University of Melbourne) for providing input on the quality appraisals. We are grateful to Shelly Makleff (Centre for Health Equity, the University of Melbourne) for her input to our discussion of values clarification workshops for health care providers.

Competing interests:

No relevant disclosures.

Received 30 October 2024, accepted 24 February 2025

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  • 65. Long C. Health specialists say biased Medicare rebates are costing women more [online]. ABC News (Australia), 4 Apr 2024. https://www.abc.net.au/news/2024‐04‐04/medicare‐bias‐costing‐women‐more‐mbs‐schedule/103664726?utm_campaign=abc_news_web&utm_content=link&utm_medium=content_shared&utm_source=abc_news_web (viewed Oct 2024).
  • 66. Cheng HC, de Costa C. Abortion education in Australian medical schools. Aust N Z J Obstet Gynaecol 2021; 61: 793‐797.
  • 67. Millar E. Abortion stigma, abortion exceptionalism, and medical curricula. Health Sociol Rev 2023; 32: 261‐276.
  • 68. Srinivasan S, James SM, Kwek J, et al. What do Australian primary care clinicians need to provide long‐acting reversible contraception and early medical abortion? A content analysis of a virtual community of practice. BMJ Sex Reprod Health 2025; 51: 94‐101.
  • 69. Queensland Health. Termination of pregnancy: action plan 2032. Mar 2024. https://www.health.qld.gov.au/__data/assets/pdf_file/0028/1316467/Termination‐of‐Pregnancy‐Plan_Digital.pdf (viewed Oct 2024).
  • 70. Australian Capital Territory (Legislative Assembly). Health (Improved Abortion Access) Amendment Bill 2024. https://classic.austlii.edu.au/au/legis/act/bill/haaab2024383 (viewed June 2025).
  • 71. Parliament of Western Australia. Abortion Legislation Reform Act 2023. https://www.legislation.wa.gov.au/legislation/statutes.nsf/law_a147399.html (viewed June 2025).
  • 72. Mazza D, Shankar M, Botfield JR, et al. Improving rural and regional access to long‐acting reversible contraception and medical abortion through nurse‐led models of care, task‐sharing and telehealth (ORIENT): a protocol for a stepped‐wedge pragmatic cluster‐randomised controlled trial in Australian general practice. BMJ Open 2023; 13: e065137.
  • 73. Australia Department of Health. National women's health strategy 2020–2030. Updated 31 Oct 2023. https://www.health.gov.au/sites/default/files/documents/2021/05/national‐women‐s‐health‐strategy‐2020‐2030_0.pdf (viewed Oct 2024).
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Ending nuclear weapons, before they end us

Kamran Abbasi, Parveen Ali, Virginia Barbour, Marion Birch, Inga Blum, Peter Doherty, Andy Haines, Ira Helfand, Richard C Horton, Kati Juva, José Florencio F Lapeña, Robert Mash, Olga Mironova, Arun Mitra, Carlos A Monteiro, Elena N Naumova, David Onazi, Tilman A Ruff, Peush Sahni, James Tumwine, Carlos Umaña, Paul Yonga and Chris Zielinski
Med J Aust 2025; 222 (11): . || doi: 10.5694/mja2.52676
Published online: 16 June 2025

In May 2025, the World Health Assembly (WHA) will vote on re‐establishing a mandate for the World Health Organization (WHO) to address the health consequences of nuclear weapons and war.1 Health professionals and their associations should urge their governments to support such a mandate and support the new United Nations (UN) comprehensive study on the effects of nuclear war

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  • 1 The British Medical Journal, London, United Kingdom
  • 2 International Nursing Review, Sheffield, United Kingdom
  • 3 University of Sheffield, Sheffield, United Kingdom
  • 4 Medical Journal of Australia, Sydney, NSW, Australia
  • 5 Medicine, Conflict and Survival, London, United Kingdom
  • 6 International Physicians for the Prevention of Nuclear War, Hamburg, Germany
  • 7 University of Melbourne, Melbourne, VIC, Australia
  • 8 London School of Hygiene and Tropical Medicine, London, United Kingdom
  • 9 International Physicians for the Prevention of Nuclear War, Springfield (OR), United States
  • 10 The Lancet, London, United Kingdom
  • 11 International Physicians for the Prevention of Nuclear War, Helsinki University Central Hospital, Helsinki, Finland
  • 12 University of the Philippines System, Ermita (NCR), Philippines
  • 13 African Journal of Primary Health Care and Family Medicine, Cape Town, South Africa
  • 14 Stellenbosch University, Stellenbosch, South Africa
  • 15 International Physicians for the Prevention of Nuclear War, Russian Cardiology Research and Production Complex, Sechenov University, Moscow, Russian Federation
  • 16 International Physicians for the Prevention of Nuclear War, Ludhiana, India
  • 17 Indian Doctors for Peace and Development, Ludhiana, India
  • 18 Revista de Saúde Pública, São Paulo, Brazil
  • 19 University of São Paulo, São Paulo, Brazil
  • 20 Journal of Public Health Policy, Boston (MA), United States
  • 21 Tufts University, Boston (MA), United States
  • 22 International Physicians for the Prevention of Nuclear War, Society of Nigerian Doctors for the Welfare of Mankind, Abuja, Nigeria
  • 23 Nossal Institute for Global Health, University of Melbourne, Melbourne, VIC, Australia
  • 24 International Physicians for the Prevention of Nuclear War, University of Melbourne, Melbourne, VIC, Australia
  • 25 National Medical Journal of India, New Delhi, India
  • 26 All India Institute of Medical Sciences, New Delhi, India
  • 27 Makerere University, Kampala, Uganda
  • 28 Kabale University, Kabale, Uganda
  • 29 International Physicians for the Prevention of Nuclear War, Costa Rican Ministry of Health, San José, Costa Rica
  • 30 East African Medical Journal, Nairobi, Kenya
  • 31 CA Medlynks, Nairobi, Kenya
  • 32 Centre for Global Health, University of Winchester, Winchester, United Kingdom
  • 33 World Association of Medical Editors, Winchester, United Kingdom


Correspondence: czielinski@ippnw.org


Author contribution statement:

Tillman Ruff and Andy Haines developed the idea of the editorial and led drafting along with Chris Zielinski. All other authors contributed significantly to the editorial content.


Competing interests:

All relevant disclosures are listed in the Supporting Information.

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Fan‐first heat‐health protection

Angie Bone, Federico Tartarini and Ollie Jay
Med J Aust || doi: 10.5694/mja2.52662
Published online: 2 June 2025

Heat‐related illnesses occur when environmental heat stress exceeds the body's physiological limits of heat tolerance. This most often arises when these limits are already constrained by cofactors such as older age, chronic diseases and certain medications.1 Global heat‐related mortality, estimated to be about 489 000 deaths per year,2 is predicted to increase substantially as climate change progresses.3

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  • 1 Monash Sustainable Development Institute, Monash University, Melbourne, VIC
  • 2 Heat and Health Research Centre, University of Sydney, Sydney, NSW
  • 3 University of Sydney, Sydney, NSW


Correspondence: angie.bone@monash.edu


Open access:

Open access publishing facilitated by Monash University, as part of the Wiley ‐ Monash University agreement via the Council of Australian University Librarians.


Acknowledgements: 

Ollie Jay acknowledges funding from the National Health and Medical Research Council (NHMRC) Investigator Grant (2021/GNT2009507).

Competing interests:

Angie Bone is a Board Member of Doctors for the Environment Australia.

  • 1. Ebi KL, Capon A, Berry P, et al. Hot weather and heat extremes: health risks. Lancet 2021; 398: 698‐708.
  • 2. Zhao Q, Guo Y, Ye T, et al. 2021 Global, regional, and national burden of mortality associated with non‐optimal ambient temperatures from 2000 to 2019: a three‐stage modelling study Lancet Planet Health 2021; 5: e415‐e425.
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  • 16. Jay O, Capon A, Berry P, et al. Reducing the health effects of hot weather and heat extremes: from personal cooling strategies to green cities. Lancet 2021; 398: 709‐724.
  • 17. Suresh Bhuvad S, You R, Chen Q. Evaluation of physiological and thermal comfort effectiveness of ceiling fan and table fan during a heat wave. Energy Build 2024; 322: 114706.
  • 18. Ravanelli NM, Hodder SG, Havenith G, Jay O. Heart rate and body temperature responses to extreme heat and humidity with and without electric fans. JAMA 2015; 313: 724‐725.
  • 19. Morris NB, English T, Hospers L, et al. The effects of electric fan use under differing resting heat index conditions: a clinical trial. Ann Inter Med 2019; 171: 675‐677.
  • 20. Morris NB, Chaseling G, English T, et al. Electric fan use for cooling during hot weather: a biophysical modelling study. Lancet Planet Health 2021; 5: e368‐e377.
  • 21. Chaseling GK, Vargas NT, Hospers L, et al. Simple strategies to reduce cardiac strain in older adults in extreme heat. N Engl J Med 2024; 391: 1754‐1757.
  • 22. O'Connor FK, Meade RD, Wagar KE, et al. Effect of electric fans on body core temperature in older adults exposed to extreme indoor heat. JAMA 2024; 330: 1752‐1754.
  • 23. International Organization for Standardization. ISO 7730: 2005. Ergonomics of the thermal environment. Analytical determination and interpretation of thermal comfort using calculation of the PMV and PPD indices and local thermal comfort criteria. Edition 3. ISO, 2005. https://www.iso.org/standard/39155.html (viewed Sept 2024).
  • 24. Sera F, Hashizume M, Honda Y, et al. Air conditioning and heat‐related mortality: a multi‐country longitudinal study. Epidemiology 2020; 31: 779‐787.
  • 25. Gupta S, Carmichael C, Simpson C, et al. Electric fans for reducing adverse health impacts in heatwaves. Cochrane Database Syst Rev 2012; 7: CD009888.
  • 26. Tartarini F, Jay O. Heatwatch [website]. Sydney: University of Sydney, 2024. https://heatwatch.sydney.edu.au/ (viewed Sept 2024).
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Current gaps in knowledge and future research directions for Aboriginal and Torres Strait Islander children with cancer

Alexandra Truong, Kayla Williams‐Tucker (Ngarluma, Wongutha, Wudjari Noongar), Ahmi Narkle (Whadjuk Goreng Noongar), Eden Slicer (Gundungurra), Jessica‐Elise Chapman (Kamilaroi, Bundjalung), Jessica Lawler, Rishi S Kotecha, Hetal Dholaria, Justine R Clark (Adnyamathanha), Alex Brown (Yuin), Raelene Endersby, Nicholas G Gottardo and Jessica Buck (Kamilaroi)
Med J Aust 2025; 222 (10): . || doi: 10.5694/mja2.52650
Published online: 2 June 2025

Summary

  • Paediatric cancer is the leading cause of disease‐related death in Australian children. Limited research focuses on cancer in Aboriginal and Torres Strait Islander children.
  • Although there appears to be a lower incidence of cancer overall in Aboriginal and Torres Strait Islander children compared with non‐Indigenous children, a high proportion of Aboriginal and Torres Strait Islander children are diagnosed with acute myeloid leukaemia.
  • Five‐year overall survival is lower for many cancer types in Aboriginal and Torres Strait Islander children.
  • There is a need for Indigenous‐specific research focused on molecular and genetic profiles, pharmacogenomics and survivorship, both within Australia and globally.
  • Future research in this space should be co‐designed and led by Aboriginal and Torres Strait Islander communities; alongside clinicians, researchers and services to ensure that the priorities of Aboriginal and Torres Strait Islander people are met.

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  • 1 WA Kids Cancer Centre, The Kids Research Institute Australia, Perth, WA
  • 2 Centre for Child Health Research, The University of Western Australia, Perth, WA
  • 3 The University of Notre Dame Australia, Fremantle, WA
  • 4 University of New South Wales, Sydney, NSW
  • 5 Perth Children's Hospital, Perth, WA
  • 6 The Kids Research Institute Australia, Adelaide, SA


Correspondence: jessica.buck@thekids.org.au


Open access:

Open access publishing facilitated by The University of Western Australia, as part of the Wiley ‐ The University of Western Australia agreement via the Council of Australian University Librarians.


Acknowledgements: 

We acknowledge the First Nations Childhood Cancer Advisory Group for their advice in preparing this manuscript. We acknowledge our Elders and the communities in which we live and write. We also acknowledge First Nations people living with and passed from cancer, and their families.

Competing interests:

No relevant disclosures.

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Urgent care centres for reducing the demand on emergency departments: a scoping review of published quantitative and qualitative studies

Feby Savira, Madison Frith, Clarissa J Aditya, Sean Randall, Naomi White, Andrew Giddy, Lauren Spark, Jamie Swann and Suzanne Robinson
Med J Aust 2025; 222 (9): . || doi: 10.5694/mja2.52663
Published online: 19 May 2025

Abstract

Objectives: To identify published studies that examined the impact of urgent care centres on the numbers of presentations to emergency departments (EDs), or explored the experiences and views of patients and practitioners regarding urgent care centres as alternative sources of health care and advice.

Study design: Scoping review of qualitative and quantitative studies published to 28 August 2024.

Data sources: MEDLINE, Embase, Cochrane Central Register of Controlled Trials (CENTRAL), PsycINFO, and CINAHL databases; grey literature searches.

Data synthesis: Of 2698 potentially relevant publications, 51 met our inclusion criteria (30 quantitative studies; 21 qualitative studies). Urgent care centres of various types were led by general practitioners in 41 of 51 studies, primarily managed people with non‐urgent conditions or minor illnesses in 34 studies and non‐emergency but urgent conditions in eight, and nine of the 22 studies that discussed funding indicated that access to the centres was free of charge. The effect of urgent care centres on ED presentation numbers was mixed; all seven studies of after‐hours clinics, one of two studies of 24‐hour clinics, and four of five studies of walk‐in centres reported reduced ED visit numbers; in eleven studies that reported effects on hospital admissions from the ED, they were lower in seven (studies of an urgent cancer care centre, four community health centres, and a general practitioner cooperative). Patient satisfaction with urgent care centres is generally as high as with other primary care services; they preferred them to EDs, and preferred personal triage to telephone triage. Reasons for people choosing urgent care centres included easier access and the unavailability of doctors or appointments elsewhere. Clinicians reported increased workload, mixed experiences with the coordination of care, concerns about unregistered or undocumented people using the services, and protocol confusion, particularly with respect to triage. Continuity of care was a concern for both clinicians and patients.

Conclusions: Urgent care centres, especially walk‐in and after‐hours clinics, can help reduce the number of ED presentations and reduce health care costs. Patient satisfaction with such clinics is high, but public health education could guide people to appropriate care for non‐urgent health problems. Training in the management of conditions frequently seen in urgent care centres is needed to ensure consistent, effective care.

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  • 1 Institute for Health Transformation, Deakin University, Melbourne, VIC
  • 2 Western Victoria Primary Health Network, Ballarat, VIC
  • 3 Melbourne, VIC


Correspondence: feby.savira@deakin.edu.au


Open access:

Open access publishing facilitated by Deakin University, as part of the Wiley – Deakin University agreement via the Council of Australian University Librarians.


Acknowledgements: 

The study was funded by Western Victoria Primary Health Network as part of the Priority Primary Care Centre evaluation program. The funders had no role in the planning, writing, or publication of this review. We acknowledge the support received from the Western Victoria Primary Health Network to conduct this study and to ensure evidence‐based research in Victoria and Australia.

Competing interests:

Naomi White, Andrew Giddy, and Jamie Swann are employees of the Western Victoria Primary Health Network.

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