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Preadmission usage of metformin and mortality in COVID-19 patients including the post-discharge period

BACKGROUND: The effect of preadmission metformin usage (PMU) on the mortality of coronavirus disease-2019 (COVID-19) patients with diabetes is conflicting. Most studies have focused on in-hospital mortality; however, mortality after discharge also increases in COVID-19 patients. AIMS: Examining the...

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Autores principales: Saygili, Emre Sedar, Karakiliç, Ersen, Mert, Erdal, Şener, Alper, Mirci, Arzu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553499/
https://www.ncbi.nlm.nih.gov/pubmed/34713419
http://dx.doi.org/10.1007/s11845-021-02823-9
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author Saygili, Emre Sedar
Karakiliç, Ersen
Mert, Erdal
Şener, Alper
Mirci, Arzu
author_facet Saygili, Emre Sedar
Karakiliç, Ersen
Mert, Erdal
Şener, Alper
Mirci, Arzu
author_sort Saygili, Emre Sedar
collection PubMed
description BACKGROUND: The effect of preadmission metformin usage (PMU) on the mortality of coronavirus disease-2019 (COVID-19) patients with diabetes is conflicting. Most studies have focused on in-hospital mortality; however, mortality after discharge also increases in COVID-19 patients. AIMS: Examining the effect of PMU on all-cause mortality, including the post-discharge period. METHODS: Patients with diabetes who were hospitalised in 2020 due to COVID-19 were included in the study. They were divided into two groups: those with a history of metformin use (MF( +)) and those without such history (MF( −)). Propensity score matching (PSM) was performed at a ratio of 1:1 for age and sex. COX regression analyses were used to demonstrate risk factors for mortality. RESULTS: We investigated 4103 patients hospitalised for COVID-19. After excluding those without diabetes or with chronic liver/kidney disease, we included the remaining 586 patients, constituting 293 women (50%) with an overall mean age of 66 ± 11.9 years. After PSM analysis, the in-hospital and post-discharge mortality rates were higher in the MF( −) group though not significantly different. However, overall mortality was higher in the MF( −) group (51 (42.5%) vs. 35 (29.2%), p = 0.031). For overall mortality, the adjusted HR was 0.585 (95% CI: 0.371 − 0.920, p = 0.020) in the MF( +) group. CONCLUSION: PMU is associated with reducing all-cause mortality. This effect starts from the in-hospital period and becomes more significant with the post-discharge period. The main limitations were the inability to evaluate the compliance with metformin and the effects of other medications due to retrospective nature.
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spelling pubmed-85534992021-10-29 Preadmission usage of metformin and mortality in COVID-19 patients including the post-discharge period Saygili, Emre Sedar Karakiliç, Ersen Mert, Erdal Şener, Alper Mirci, Arzu Ir J Med Sci Original Article BACKGROUND: The effect of preadmission metformin usage (PMU) on the mortality of coronavirus disease-2019 (COVID-19) patients with diabetes is conflicting. Most studies have focused on in-hospital mortality; however, mortality after discharge also increases in COVID-19 patients. AIMS: Examining the effect of PMU on all-cause mortality, including the post-discharge period. METHODS: Patients with diabetes who were hospitalised in 2020 due to COVID-19 were included in the study. They were divided into two groups: those with a history of metformin use (MF( +)) and those without such history (MF( −)). Propensity score matching (PSM) was performed at a ratio of 1:1 for age and sex. COX regression analyses were used to demonstrate risk factors for mortality. RESULTS: We investigated 4103 patients hospitalised for COVID-19. After excluding those without diabetes or with chronic liver/kidney disease, we included the remaining 586 patients, constituting 293 women (50%) with an overall mean age of 66 ± 11.9 years. After PSM analysis, the in-hospital and post-discharge mortality rates were higher in the MF( −) group though not significantly different. However, overall mortality was higher in the MF( −) group (51 (42.5%) vs. 35 (29.2%), p = 0.031). For overall mortality, the adjusted HR was 0.585 (95% CI: 0.371 − 0.920, p = 0.020) in the MF( +) group. CONCLUSION: PMU is associated with reducing all-cause mortality. This effect starts from the in-hospital period and becomes more significant with the post-discharge period. The main limitations were the inability to evaluate the compliance with metformin and the effects of other medications due to retrospective nature. Springer International Publishing 2021-10-29 2022 /pmc/articles/PMC8553499/ /pubmed/34713419 http://dx.doi.org/10.1007/s11845-021-02823-9 Text en © The Author(s), under exclusive licence to Royal Academy of Medicine in Ireland 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
Saygili, Emre Sedar
Karakiliç, Ersen
Mert, Erdal
Şener, Alper
Mirci, Arzu
Preadmission usage of metformin and mortality in COVID-19 patients including the post-discharge period
title Preadmission usage of metformin and mortality in COVID-19 patients including the post-discharge period
title_full Preadmission usage of metformin and mortality in COVID-19 patients including the post-discharge period
title_fullStr Preadmission usage of metformin and mortality in COVID-19 patients including the post-discharge period
title_full_unstemmed Preadmission usage of metformin and mortality in COVID-19 patients including the post-discharge period
title_short Preadmission usage of metformin and mortality in COVID-19 patients including the post-discharge period
title_sort preadmission usage of metformin and mortality in covid-19 patients including the post-discharge period
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553499/
https://www.ncbi.nlm.nih.gov/pubmed/34713419
http://dx.doi.org/10.1007/s11845-021-02823-9
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