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Risk factors for mortality in hemodialysis patients with COVID-19: a systematic review and meta-analysis

BACKGROUND: New evidence from studies on risk factors for mortality in hemodialysis (HD) patients with COVID-19 became available. We aimed to review the clinical risk factors for fatal outcomes in these patients. METHODS: We performed meta-analysis using the PubMed, EMBASE, and Cochrane databases. A...

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Autores principales: Wang, Fengping, Ao, Guangyu, Wang, Yushu, Liu, Fuqiang, Bao, Mulong, Gao, Ming, Zhou, Shulu, Qi, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8510603/
https://www.ncbi.nlm.nih.gov/pubmed/34629011
http://dx.doi.org/10.1080/0886022X.2021.1986408
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author Wang, Fengping
Ao, Guangyu
Wang, Yushu
Liu, Fuqiang
Bao, Mulong
Gao, Ming
Zhou, Shulu
Qi, Xin
author_facet Wang, Fengping
Ao, Guangyu
Wang, Yushu
Liu, Fuqiang
Bao, Mulong
Gao, Ming
Zhou, Shulu
Qi, Xin
author_sort Wang, Fengping
collection PubMed
description BACKGROUND: New evidence from studies on risk factors for mortality in hemodialysis (HD) patients with COVID-19 became available. We aimed to review the clinical risk factors for fatal outcomes in these patients. METHODS: We performed meta-analysis using the PubMed, EMBASE, and Cochrane databases. A fixed- or random-effects model was used for calculating heterogeneity. We used contour-enhanced funnel plot and Egger’s tests to assess potential publication bias. RESULTS: Twenty-one studies were included. The proportion of males was lower in the survivor group than in the non-survivor group (OR = 0.75, 95% CI [0.61, 0.94]). The proportion of respiratory diseases was significantly lower in the survivor group than in the non-survivor group (OR = 0.42, 95% CI [0.29, 0.60]). The proportion of patients with fever, cough, and dyspnea was significantly lower in the survivor group (fever: OR = 0.53, 95% CI [0.31, 0.92]; cough: OR = 0.50, 95% CI [0.38, 0.65]; dyspnea: OR = 0.25, 95% CI [0.14, 0.47]) than in the non-survivor group. Compared with the non-survivor group, the survivor group had higher albumin and platelet levels and lower leucocyte counts. CONCLUSIONS: Male patients might have a higher risk of developing severe COVID-19. Comorbidities, such as respiratory diseases could also greatly influence the clinical prognosis of COVID-19. Clinical features, such as fever, dyspnea, cough, and abnormal platelet, leucocyte, and albumin levels, could imply eventual death. Our findings will help clinicians identify markers for the detection of high mortality risk in HD patients at an early stage of COVID-19.
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spelling pubmed-85106032021-10-13 Risk factors for mortality in hemodialysis patients with COVID-19: a systematic review and meta-analysis Wang, Fengping Ao, Guangyu Wang, Yushu Liu, Fuqiang Bao, Mulong Gao, Ming Zhou, Shulu Qi, Xin Ren Fail Clinical Study BACKGROUND: New evidence from studies on risk factors for mortality in hemodialysis (HD) patients with COVID-19 became available. We aimed to review the clinical risk factors for fatal outcomes in these patients. METHODS: We performed meta-analysis using the PubMed, EMBASE, and Cochrane databases. A fixed- or random-effects model was used for calculating heterogeneity. We used contour-enhanced funnel plot and Egger’s tests to assess potential publication bias. RESULTS: Twenty-one studies were included. The proportion of males was lower in the survivor group than in the non-survivor group (OR = 0.75, 95% CI [0.61, 0.94]). The proportion of respiratory diseases was significantly lower in the survivor group than in the non-survivor group (OR = 0.42, 95% CI [0.29, 0.60]). The proportion of patients with fever, cough, and dyspnea was significantly lower in the survivor group (fever: OR = 0.53, 95% CI [0.31, 0.92]; cough: OR = 0.50, 95% CI [0.38, 0.65]; dyspnea: OR = 0.25, 95% CI [0.14, 0.47]) than in the non-survivor group. Compared with the non-survivor group, the survivor group had higher albumin and platelet levels and lower leucocyte counts. CONCLUSIONS: Male patients might have a higher risk of developing severe COVID-19. Comorbidities, such as respiratory diseases could also greatly influence the clinical prognosis of COVID-19. Clinical features, such as fever, dyspnea, cough, and abnormal platelet, leucocyte, and albumin levels, could imply eventual death. Our findings will help clinicians identify markers for the detection of high mortality risk in HD patients at an early stage of COVID-19. Taylor & Francis 2021-10-11 /pmc/articles/PMC8510603/ /pubmed/34629011 http://dx.doi.org/10.1080/0886022X.2021.1986408 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Wang, Fengping
Ao, Guangyu
Wang, Yushu
Liu, Fuqiang
Bao, Mulong
Gao, Ming
Zhou, Shulu
Qi, Xin
Risk factors for mortality in hemodialysis patients with COVID-19: a systematic review and meta-analysis
title Risk factors for mortality in hemodialysis patients with COVID-19: a systematic review and meta-analysis
title_full Risk factors for mortality in hemodialysis patients with COVID-19: a systematic review and meta-analysis
title_fullStr Risk factors for mortality in hemodialysis patients with COVID-19: a systematic review and meta-analysis
title_full_unstemmed Risk factors for mortality in hemodialysis patients with COVID-19: a systematic review and meta-analysis
title_short Risk factors for mortality in hemodialysis patients with COVID-19: a systematic review and meta-analysis
title_sort risk factors for mortality in hemodialysis patients with covid-19: a systematic review and meta-analysis
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8510603/
https://www.ncbi.nlm.nih.gov/pubmed/34629011
http://dx.doi.org/10.1080/0886022X.2021.1986408
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