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Multimorbidity and frailty are associated with poorer SARS-CoV-2-related outcomes: systematic review of population-based studies
TT. Makovski, J. Ghattas, S. Monnier-Besnard, L. Cavillot, M. Ambrožová, B. Vašinová, R. Feteira-Santos, P. Bezzegh, FP. Bollmann, J. Cottam, R. Haneef, B. Devleesschauwer, N. Speybroeck, PJ. Nogueira, MJ. Forjaz, J. Coste, L. Carcaillon-Bentata
Jazyk angličtina Země Německo
Typ dokumentu systematický přehled
NLK
ProQuest Central
od 1997-02-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 1997-02-01 do Před 1 rokem
Springer Journals Complete - Open Access
od 2024-12-01
Springer Nature OA/Free Journals
od 2024-12-01
- MeSH
- COVID-19 * epidemiologie MeSH
- Evropská unie MeSH
- křehkost * epidemiologie MeSH
- lidé MeSH
- multimorbidita MeSH
- SARS-CoV-2 MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- systematický přehled MeSH
BACKGROUND: Estimating the risks and impacts of COVID-19 for different health groups at the population level is essential for orienting public health measures. Adopting a population-based approach, we conducted a systematic review to explore: (1) the etiological role of multimorbidity and frailty in developing SARS-CoV-2 infection and COVID-19-related short-term outcomes; and (2) the prognostic role of multimorbidity and frailty in developing short- and long-term outcomes. This review presents the state of the evidence in the early years of the pandemic. It was conducted within the European Union Horizon 2020 program (No: 101018317); Prospero registration: CRD42021249444. METHODS: PubMed, Embase, World Health Organisation COVID-19 Global literature on coronavirus disease, and PsycINFO were searched between January 2020 and 7 April 2021 for multimorbidity and 1 February 2022 for frailty. Quantitative peer-reviewed studies published in English with population-representative samples and validated multimorbidity and frailty tools were considered. RESULTS: Overall, 9,701 records were screened by title/abstract and 267 with full text. Finally, 14 studies were retained for multimorbidity (etiological role, n = 2; prognostic, n = 13) and 5 for frailty (etiological role, n = 2; prognostic, n = 4). Only short-term outcomes, mainly mortality, were identified. An elevated likelihood of poorer outcomes was associated with an increasing number of diseases, a higher Charlson Comorbidity Index, different disease combinations, and an increasing frailty level. DISCUSSION: Future studies, which include the effects of recent virus variants, repeated exposure and vaccination, will be useful for comparing the possible evolution of the associations observed in the earlier waves.
Department of Epidemiology and Public Health Sciensano Brussels Belgium
Directorate for Project Management National Directorate General for Hospitals Budapest Hungary
Institute of Biostatistics and Analyses Faculty of Medicine Masaryk University Brno Czech Republic
Institute of Health and Society Université catholique de Louvain Brussels Belgium
Institute of Tropical Medicine Antwerp Belgium
National Center of Epidemiology Instituto de Salud Carlos 3 RICAPPS Madrid Spain
Citace poskytuje Crossref.org
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