dc.contributor.author | Saygılı, Emre Sedar | |
dc.contributor.author | Karakılıç, Ersen | |
dc.contributor.author | Mert, Erdal | |
dc.contributor.author | Şener, Alper | |
dc.contributor.author | Mirci, Arzu | |
dc.date.accessioned | 2023-06-05T10:15:20Z | |
dc.date.available | 2023-06-05T10:15:20Z | |
dc.date.issued | 2022 | en_US |
dc.identifier.citation | Saygili, E. S., Karakiliç, E., Mert, E., Şener, A., & Mirci, A. (2022). Preadmission usage of metformin and mortality in COVID-19 patients including the post-discharge period. Irish Journal of Medical Science, 191(2), 569-575. doi:10.1007/s11845-021-02823-9 | en_US |
dc.identifier.issn | 0021-1265 / 1863-4362 | |
dc.identifier.uri | https://doi.org/10.1007/s11845-021-02823-9 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12428/4244 | |
dc.description.abstract | 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. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Springer Science and Business Media Deutschland GmbH | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Coronavirus disease 2019 | en_US |
dc.subject | Metformin | en_US |
dc.subject | Mortality | en_US |
dc.subject | Preadmission | en_US |
dc.subject | Treatment | en_US |
dc.title | Preadmission usage of metformin and mortality in COVID-19 patients including the post-discharge period | en_US |
dc.type | article | en_US |
dc.authorid | 0000-0003-0022-5704 | en_US |
dc.authorid | 0000-0003-3590-2656 | en_US |
dc.authorid | - | en_US |
dc.authorid | - | en_US |
dc.authorid | - | en_US |
dc.relation.ispartof | Irish Journal of Medical Science | en_US |
dc.department | Fakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü | en_US |
dc.identifier.volume | 191 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.startpage | 569 | en_US |
dc.identifier.endpage | 575 | en_US |
dc.institutionauthor | Saygılı, Emre Sedar | |
dc.institutionauthor | Karakılıç, Ersen | |
dc.institutionauthor | Mert, Erdal | |
dc.institutionauthor | Şener, Alper | |
dc.institutionauthor | Mirci, Arzu | |
dc.identifier.doi | 10.1007/s11845-021-02823-9 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.authorwosid | K-8579-2019 | en_US |
dc.authorwosid | AAB-1936-2021 | en_US |
dc.authorwosid | - | en_US |
dc.authorwosid | - | en_US |
dc.authorwosid | - | en_US |
dc.authorscopusid | 57220639037 | en_US |
dc.authorscopusid | 56200500500 | en_US |
dc.authorscopusid | 57226195055 | en_US |
dc.authorscopusid | 23996235800 | en_US |
dc.authorscopusid | 57315547200 | en_US |
dc.identifier.wosquality | Q3 | en_US |
dc.identifier.wos | WOS:000712245600001 | en_US |
dc.identifier.scopus | 2-s2.0-85118131349 | en_US |
dc.identifier.pmid | PMID: 34713419 | en_US |