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Hospitalisation for cirrhosis in Australia: disparities in presentation and outcomes for Indigenous Australians

BACKGROUND: Indigenous Australians experience greater health disadvantage and have a higher prevalence of many chronic health conditions. Liver diseases leading to cirrhosis are among the most common contributor to the mortality gap between Indigenous and other Australian adults. However, no compara...

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Autores principales: Valery, Patricia C., Clark, Paul J., Pratt, Gregory, Bernardes, Christina M., Hartel, Gunter, Toombs, Maree, Irvine, Katharine M., Powell, Elizabeth E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027067/
https://www.ncbi.nlm.nih.gov/pubmed/32066438
http://dx.doi.org/10.1186/s12939-020-1144-6
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author Valery, Patricia C.
Clark, Paul J.
Pratt, Gregory
Bernardes, Christina M.
Hartel, Gunter
Toombs, Maree
Irvine, Katharine M.
Powell, Elizabeth E.
author_facet Valery, Patricia C.
Clark, Paul J.
Pratt, Gregory
Bernardes, Christina M.
Hartel, Gunter
Toombs, Maree
Irvine, Katharine M.
Powell, Elizabeth E.
author_sort Valery, Patricia C.
collection PubMed
description BACKGROUND: Indigenous Australians experience greater health disadvantage and have a higher prevalence of many chronic health conditions. Liver diseases leading to cirrhosis are among the most common contributor to the mortality gap between Indigenous and other Australian adults. However, no comparative data exist assessing differences in presentation and patient outcomes between Indigenous and non-Indigenous Australians hospitalised with cirrhosis. METHODS: Using data from the Hospital Admitted Patient Data Collection and the Death Registry, this retrospective, population-based, cohort study including all people hospitalised for cirrhosis in the state of Queensland during 2008–2017 examined rate of readmission (Poisson regression), cumulative survival (Kaplan–Meier), and assessed the differences in survival (Multivariable Cox regression) by Indigenous status. Predictor variables included demographic, health service characteristics and clinical data. RESULTS: We studied 779 Indigenous and 10,642 non-Indigenous patients with cirrhosis. A higher proportion of Indigenous patients were younger than 50 years (346 [44%] vs. 2063 [19%] non-Indigenous patients), lived in most disadvantaged areas (395 [51%) vs. 2728 [26%]), had alcohol-related cirrhosis (547 [70%] vs. 5041 [47%]), had ascites (314 [40%] vs. 3555 [33%), and presented to hospital via the Emergency Department (510 [68%] vs. 4790 [47%]). Indigenous patients had 3.04 times the rate of non-cirrhosis readmissions (95%CI 2.98–3.10), 1.35 times the rate of cirrhosis-related readmissions (95%CI 1.29–1.41), and lower overall survival (17% vs. 27%; unadjusted hazard ratio (HR) = 1.16 95%CI 1.06–1.27), compared to non-Indigenous patients. Most of the survival deficit was explained by Emergency Department presentation (adj-HR = 1.03 95%CI 0.93–1.13), and alcohol-related aetiology (adj-HR = 1.08 95%CI 0.99–1.19). The remaining survival deficit was influenced by the other clinico-demographic and health service factors (final adj-HR = 1.08 95%CI 0.96–1.20). CONCLUSIONS: There was evidence of differential presentation, higher rates of readmissions, and poorer survival for Indigenous Australians with cirrhosis, compared to other Australians. The increased prevalence of Emergency Department presentation among Indigenous patients suggests missed opportunities for early intervention to prevent progressive cirrhosis complications and hospital readmissions.
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spelling pubmed-70270672020-02-24 Hospitalisation for cirrhosis in Australia: disparities in presentation and outcomes for Indigenous Australians Valery, Patricia C. Clark, Paul J. Pratt, Gregory Bernardes, Christina M. Hartel, Gunter Toombs, Maree Irvine, Katharine M. Powell, Elizabeth E. Int J Equity Health Research BACKGROUND: Indigenous Australians experience greater health disadvantage and have a higher prevalence of many chronic health conditions. Liver diseases leading to cirrhosis are among the most common contributor to the mortality gap between Indigenous and other Australian adults. However, no comparative data exist assessing differences in presentation and patient outcomes between Indigenous and non-Indigenous Australians hospitalised with cirrhosis. METHODS: Using data from the Hospital Admitted Patient Data Collection and the Death Registry, this retrospective, population-based, cohort study including all people hospitalised for cirrhosis in the state of Queensland during 2008–2017 examined rate of readmission (Poisson regression), cumulative survival (Kaplan–Meier), and assessed the differences in survival (Multivariable Cox regression) by Indigenous status. Predictor variables included demographic, health service characteristics and clinical data. RESULTS: We studied 779 Indigenous and 10,642 non-Indigenous patients with cirrhosis. A higher proportion of Indigenous patients were younger than 50 years (346 [44%] vs. 2063 [19%] non-Indigenous patients), lived in most disadvantaged areas (395 [51%) vs. 2728 [26%]), had alcohol-related cirrhosis (547 [70%] vs. 5041 [47%]), had ascites (314 [40%] vs. 3555 [33%), and presented to hospital via the Emergency Department (510 [68%] vs. 4790 [47%]). Indigenous patients had 3.04 times the rate of non-cirrhosis readmissions (95%CI 2.98–3.10), 1.35 times the rate of cirrhosis-related readmissions (95%CI 1.29–1.41), and lower overall survival (17% vs. 27%; unadjusted hazard ratio (HR) = 1.16 95%CI 1.06–1.27), compared to non-Indigenous patients. Most of the survival deficit was explained by Emergency Department presentation (adj-HR = 1.03 95%CI 0.93–1.13), and alcohol-related aetiology (adj-HR = 1.08 95%CI 0.99–1.19). The remaining survival deficit was influenced by the other clinico-demographic and health service factors (final adj-HR = 1.08 95%CI 0.96–1.20). CONCLUSIONS: There was evidence of differential presentation, higher rates of readmissions, and poorer survival for Indigenous Australians with cirrhosis, compared to other Australians. The increased prevalence of Emergency Department presentation among Indigenous patients suggests missed opportunities for early intervention to prevent progressive cirrhosis complications and hospital readmissions. BioMed Central 2020-02-17 /pmc/articles/PMC7027067/ /pubmed/32066438 http://dx.doi.org/10.1186/s12939-020-1144-6 Text en © The Author(s). 2020 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Valery, Patricia C.
Clark, Paul J.
Pratt, Gregory
Bernardes, Christina M.
Hartel, Gunter
Toombs, Maree
Irvine, Katharine M.
Powell, Elizabeth E.
Hospitalisation for cirrhosis in Australia: disparities in presentation and outcomes for Indigenous Australians
title Hospitalisation for cirrhosis in Australia: disparities in presentation and outcomes for Indigenous Australians
title_full Hospitalisation for cirrhosis in Australia: disparities in presentation and outcomes for Indigenous Australians
title_fullStr Hospitalisation for cirrhosis in Australia: disparities in presentation and outcomes for Indigenous Australians
title_full_unstemmed Hospitalisation for cirrhosis in Australia: disparities in presentation and outcomes for Indigenous Australians
title_short Hospitalisation for cirrhosis in Australia: disparities in presentation and outcomes for Indigenous Australians
title_sort hospitalisation for cirrhosis in australia: disparities in presentation and outcomes for indigenous australians
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027067/
https://www.ncbi.nlm.nih.gov/pubmed/32066438
http://dx.doi.org/10.1186/s12939-020-1144-6
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