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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

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

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

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Indigenous health Perspectives 1 July 2024 Open Access

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)

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