Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/30172
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSubramaniam, Ashwin-
dc.contributor.authorShekar, Kiran-
dc.contributor.authorAfroz, Afsana-
dc.contributor.authorAshwin, Sushma-
dc.contributor.authorBillah, Baki-
dc.contributor.authorBrown, Hamish-
dc.contributor.authorKundi, Harun-
dc.contributor.authorLim, Zheng Jie-
dc.contributor.authorPonnapa Reddy, Mallikarjuna-
dc.contributor.authorCurtis, J Randall-
dc.date2022-03-21-
dc.date.accessioned2022-06-23T00:26:20Z-
dc.date.available2022-06-23T00:26:20Z-
dc.date.issued2022-05-
dc.identifier.citationInternal medicine journal 2022; 52(5): 724-739en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/30172-
dc.description.abstractObservational data during the pandemic have demonstrated mixed associations between frailty and mortality. To examine associations between frailty and short-term mortality in patients hospitalised with coronavirus disease 2019 (COVID-19). In this systematic review and meta-analysis, we searched PubMed, Embase and the COVID-19 living systematic review from 1 December 2019 to 15 July 2021. Studies reporting mortality and frailty scores in hospitalised patients with COVID-19 (age ≥18 years) were included. Data on patient demographics, short-term mortality (in hospital or within 30 days), intensive care unit (ICU) admission and need for invasive mechanical ventilation (IMV) were extracted. The quality of studies was assessed using the Newcastle-Ottawa Scale. Twenty-five studies reporting 34 628 patients were included. Overall, 26.2% (n = 9061) died. Patients who died were older (76.7 ± 9.6 vs 69.2 ± 13.4), more likely male (risk ratio (RR) = 1.08; 95% confidence interval (CI): 1.06-1.11) and had more comorbidities. Fifty-eight percent of patients were frail. Adjusting for age, there was no difference in short-term mortality between frail and non-frail patients (RR = 1.04; 95% CI: 0.84-1.28). The non-frail patients were commonly admitted to ICU (27.2% (4256/15639) vs 29.1% (3567/12274); P = 0.011) and had a higher mortality risk (RR = 1.63; 95% CI: 1.30-2.03) than frail patients. Among patients receiving IMV, there was no difference in mortality between frail and non-frail (RR = 1.62; 95% CI 0.93-2.77). This systematic review did not demonstrate an independent association between frailty status and short-term mortality in patients with COVID-19. Patients with frailty were less commonly admitted to ICU and non-frail patients were more likely to receive IMV and had higher mortality risk. This finding may be related to allocation decisions for patients with frailty amidst the pandemic.en
dc.language.isoeng
dc.subjectCOVID-19en
dc.subjectfrailtyen
dc.subjecthospital-related mortalityen
dc.subjectmeta-analysisen
dc.subjectolder peopleen
dc.subjectsystematic reviewen
dc.titleFrailty and mortality associations in patients with COVID-19: a systematic review and meta-analysis.en
dc.typeJournal Articleen
dc.identifier.journaltitleInternal medicine journalen
dc.identifier.affiliationAnaesthesia..en
dc.identifier.affiliationQueensland University of Technology, Brisbane, Queensland, Australia..en
dc.identifier.affiliationBond University, Gold Coast, Queensland, Australia..en
dc.identifier.affiliationCentre for Integrated Critical Care, Department of Medicine and Radiology, Melbourne Medical School, Melbourne, Victoria, Australia..en
dc.identifier.affiliationDepartment of Health Economics, School of Health and Social Development, Deakin University, Melbourne, Victoria, Australia..en
dc.identifier.affiliationDepartment of Intensive Care Medicine, Calvary Hospital, Canberra, Australian Capital Territory, Australia..en
dc.identifier.affiliationDepartment of Intensive Care Medicine, Peninsula Health, Melbourne, Victoria, Australia..en
dc.identifier.affiliationPeninsula Clinical School, Monash University, Melbourne, Victoria, Australia..en
dc.identifier.affiliationDepartment of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia..en
dc.identifier.affiliationAdult Intensive Care Services, The Prince Charles Hospital, Brisbane, Queensland, Australia..en
dc.identifier.affiliationUniversity of Queensland, Brisbane, Queensland, Australia..en
dc.identifier.affiliationDepartment of Cardiology, Ankara City Hospital, Ankara, Turkey..en
dc.identifier.affiliationCambia Palliative Care Centre of Excellence, University of Washington, Seattle, Washington, USA.. Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University of Washington, Seattle, Washington, USA..en
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/35066970/en
dc.identifier.doi10.1111/imj.15698en
dc.type.contentTexten
dc.identifier.orcid0000-0002-8292-7357en
dc.identifier.orcid0000-0002-3470-6701en
dc.identifier.orcid0000-0001-8864-4844en
dc.identifier.pubmedid35066970
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
Appears in Collections:Journal articles
Show simple item record

Page view(s)

34
checked on Dec 17, 2024

Google ScholarTM

Check


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.