Topics
Health services administration
Towards a best practice framework for eHealth with Aboriginal and Torres Strait Islander peoples — important characteristics of eHealth interventions: a narrative review
Foundational qualities of culturally safe and sustainable eHealth interventions for Aboriginal and Torres Strait Islander people
the eHRCATSIH Group
“Social prescribing” another stolen Indigenous concept?
Uday N Yadav · Rosemary Wyber · Fiona Cornforth (Wuthathi/Maluilgal) · Raymond W Lovett (Wongaibon/Ngiyampaa)
The impact of ageing‐in‐place reforms on the provision of home care packages for older Australians, 2008–21: a repeated cross‐sectional study
Meeting demand for higher care level support will require a larger aged care workforce particularly in regional and remote areas
Johannes Schwabe · Gillian E Caughey · Steve L Wesselingh · Craig Whitehead · Renuka Visvanathan · Keith Evans · Maria C Inacio
Measuring progress toward the Closing the Gap healthy birthweight target for Indigenous babies: an analysis of Queensland perinatal data, 2011–2020
Are we accurately tracking healthy birthweights for Indigenous babies?
M Mamun Huda · James Ward · Abdullah Al Mamun
The rise of direct‐to‐consumer telemedicine services in Australia: implications for primary care and future research
Vishnu Khanal · Deborah J Russell · John Wakerman
Understanding modelled economic evaluations: a reader's guide for clinicians
The role of modelled versus study-based economic evaluations, and an introduction to common modelling approaches
Winnie Chen · Martin Howell · Alan Cass · Gillian Gorham · Kirsten Howard
The resurgence of congenital syphilis in Australia: novel approaches and sustained, effective public health efforts are required
Coordinated antenatal and sexual health care policies, clear guidelines, and broad education programs could reduce the rate
Stephanie Bond · Marcus Y Chen
The Alfred Health post‐COVID‐19 service, Melbourne, 2020–2022: an observational cohort study
To the Editor: Holland and colleagues reported on the Alfred Health post‐COVID‐19 service experience with the health of patients who had previously been hospitalised, or managed in a hospital‐in‐the‐home setting, with COVID‐19.1 Participants responded to an invitation to register for follow‐up, and then completed a questionnaire. The study also included a separate group (13% of the cohort) who were not necessarily admitted to Alfred Health but lived in the Alfred Health catchment — and might have been managed as outpatients or inpatients in another service but were referred by their local doctors to a specialist clinic targeted for patients with symptoms after initial COVID‐19, and subsequently completed the questionnaire. Sixty per cent of respondents had at least one persistent symptom at eight weeks. The study reported apparently high prevalences of other symptoms, such as post‐traumatic stress disorder in 23%. These results are derived from their cohort and may not be generally applicable. The authors caution: “We could not distinguish between new symptoms and those attributable to other health conditions. Our study did not include a contemporary control group”.1 More importantly, there was no control group of patients hospitalised from non‐COVID‐19 viral illness (with sufficient severe illness to lead to almost 5% spending time in an intensive care unit), who were then concentrated by an invitation, and then sufficiently motivated to fill out a questionnaire. Plausibly in such a group, at eight weeks, 60% would report at least one persistent symptom. Interpretation of their results is also obscured by the patients referred from the community, who came from a bigger population of patients with COVID‐19 concentrated to include only those who sought or agreed to a referral to a specialist follow‐up clinic. The authors wisely identified weaknesses and they should be applauded for their review of their experience. More definitive conclusions about higher rates of persisting ill health caused by COVID‐19 (in comparison to similarly severe infectious illness) might be achieved if they can follow this up — as they perhaps recognise — with a prospective analytic design in a cohort of patients presenting with similar severity of viral illness comparing those with and without COVID‐19 over the long term.
Jeremy L Millar
Developing the green operating room: exploring barriers and opportunities to reducing operating room waste
Assessment of the strategies adopted in the operating room to reduce waste and provision of an in-depth analysis of the barriers to scalable waste reduction strategies
Ludmilla Pillay · Kenneth D Winkel · Timothy Kariotis
The Alfred Health post‐COVID‐19 service, Melbourne, 2020–2022: an observational cohort study
In reply: We thank Millar1 for taking the time to respond to our article,2 which details an evaluation of the Alfred Health post‐COVID‐19 clinical service established in June 2020. At that time we, like many health services around the world, faced the challenge of providing ongoing clinical management for patients with persistent and debilitating symptoms following SARS‐CoV‐2 infection, with little evidence to guide service provision or model of care. As there were no data to guide patient selection, we invited all patients with a diagnosis of COVID‐19 who had been managed by our health service (in hospital or in the community) to opt in if they perceived a need for ongoing care. This allowed us to quantify demand, as identified by patients who were affected. Our data confirm that a small proportion (6%) of individuals had persistent symptoms of long COVID that required medical and allied health specialist management. We consider this opt in approach a strength of our report; estimates of ongoing care needs following COVID‐19 vary enormously,3 and our data suggest that demand may be at the lower end of those estimates. As the pandemic progressed and more people with COVID‐19 were managed in the community, we adapted to the clinical needs of our patients by accepting referrals from general practice. We agree that there are limitations to our report, which are inherent in its nature as a service evaluation. We did not aim to provide epidemiological data on the prevalence or characteristics of long COVID; rather, we aimed to document the proportion of our patients following COVID‐19 who identified ongoing care needs, and to describe their characteristics. The recent federal parliamentary inquiry into long COVID4 states that “The role of specific long COVID clinics as a resource for primary health providers is very important to allow adequate services for major complications” and calls for the establishment of multidisciplinary long COVID clinics in selected public hospitals. We hope that our experience might be informative for other health services who are seeking to provide care for this small but important group of patients.
Anne Holland · Simone Dal Corso
The time is right to do more to reduce ACL injuries
Phased introduction of an injury prevention program, supported by a national ACL registry, would facilitate best practice
Chris Schilling · Siddharth Rele
Indigenous governance, ethics and data collection in Australian clinical registries
Aboriginal and Torres Strait Islander communities remain invisible in data which is used to inform policy, clinical models of care, health services and initiatives
Courtney Ryder · Sadia Hossain · Leanne Howard · Julia Severin · Rebecca Ivers
Obesity in women giving birth in Victoria, 2010–2019: a retrospective cohort study
The proportion of births to Victorian women with obesity rose during 2010–2019, particularly in regional areas
Yvonne E Baker · Glyn Teale · Vidanka Vasilevski · Alemayehu Mekonnen · Linda Sweet
Outcomes for people admitted to Australian and New Zealand intensive care units with primary, exacerbating, or incidental SARS‐CoV‐2 infections, 2022–23: a retrospective analysis of ANZICS data
SARS-CoV-2 infections are still associated with poorer clinical outcomes for people admitted to ICUs
Alastair Brown · Andrew Udy · Martyn Kirk · Sonya Bennett · Shaila Chavan · Sue Huckson · David Pilcher
The economics of a national anterior cruciate ligament injury prevention program for amateur football players: a Markov model analysis
Investing in a national, evidence-based program for averting ACL injuries in amateur footballers is economically justifiable
Andrew Ross · Joosup Kim · Marnee McKay · Evangelos Pappas · Natalie Hardaker · Matt Whalan · Kerry Peek
Who is bearing the brunt of the increasing cost of cancer care?
Increasing out- of- pocket health care expenses, particularly for people with cancer, are clearly concerning, especially if they compromise the care of those who are unable to pay
Colin Williams · Peter Gibbs
Out‐of‐pocket health care expenses for people with and without cancer, New South Wales, 2020: a cross‐sectional study
High out-of-pocket expenses can restrict access to health care for people with limited financial resources, especially those with cancer
David E Goldsbury · Philip Haywood · Alison Pearce · Louisa G Collins · Deme Karikios · Karen Canfell · Julia Steinberg · Marianne F Weber
Living evidence syntheses: the emerging opportunity to increase evidence‐informed health policy in Australia
Living evidence syntheses are critical for evidence-informed policy; however, their use is not as straightforward as providing policy makers with summarised results from research studies
Samantha P Chakraborty · Alex Collie · Rebecca Hodder · Suman S Majumdar · Kim Sutherland · Bernie Towler · Joshua Vogel · Andrew Wilson · Luke Wolfenden · Sally Green · Tari Turner
Implementing the cultural determinants of health: our knowledges and cultures in a health system that is not free of racism
Systemic racism and its structural biases and institutional impediments must be addressed to implement the cultural determinants of health
Carmen Parter (Murrana, Juru and Darumbal Clans of Birra Gubba Nation with South Sea Islander heritage from Tanna Island of the Republic of Vanuatu) · Donna Murray (Wiradyuri Wonnarua) · Romlie Mokak (Djugun; member of Yawuru people) · Karl Briscoe (Kuku Yalanji) · Richard Weston (Meriam) · Janine Mohamed (Nurungga Kaurna)
Fulfilling cultural safety expectations in specialist medical education and training: considerations for colleges to advance recognition and quality
Colleges must direct efforts to centre the development of critical allyship to support Indigenous peoples
Paul Saunders
“Simply put: systems failed”: lessons from the Coroner's inquest into the rheumatic heart disease Doomadgee cluster
Queensland Health must act on the coronial recommendations to avoid more preventable deaths in Doomadgee
Avelina Tarrago (Wangkamahdla) · Ella Veit‐Prince · Claire E Brolan
Seeking a voice: the inadequacy of the “four principles” and the need for care ethics in the provision of health care to vulnerable populations
The moral and practical justification for Indigenous representation at all levels of health care provision
Kenneth JE Barns · Louis Peachey (Girrimay/Djirribal)
Evaluation of the Cultural, Social and Emotional Wellbeing Program with Aboriginal women in the Boronia Pre‐Release Centre for Women: a mixed methods study
Improving their social and emotional wellbeing could help reduce the number of Aboriginal people in Australian prisons by reducing recidivism
Pat Dudgeon (Bardi) · Ee Pin Chang · Joan Chan · Carolyn Mascall · Gillian King (Noongar) · Jemma R Collova · Angela Ryder (Noongar)
Supporting intersectional mentoring of women in medicine
Women mentorship programs in medicine provide significant benefits, but need more consideration of intersectionality
Pallavi Prathivadi · Naomi MacPherson
Dying of heart failure: how do we improve the experience?
Cardiologists require competency and confidence in managing not only deteriorating but also end of life, heart failure
Dominica Zentner · Vithoosharan Sivanathan · Jennifer Philip · Natasha Smallwood