Association between benzodiazepine receptor agonist use and mortality in patients hospitalised for COVID-19: a multicentre observational study
dc.contributor.author | Hoertel, N. | |
dc.contributor.author | Sánchez Rico, M. | |
dc.contributor.author | Gulbins, E. | |
dc.contributor.author | Kornhuber, J. | |
dc.contributor.author | Vernet, R. | |
dc.contributor.author | Beeker, N. | |
dc.contributor.author | Neuraz, A. | |
dc.contributor.author | Blanco, C. | |
dc.contributor.author | Olfson, M. | |
dc.contributor.author | Airagnes, G. | |
dc.contributor.author | Lemogne, C. | |
dc.contributor.author | Alvarado Izquierdo, Jesús María | |
dc.contributor.author | Arnaout, M. | |
dc.contributor.author | Cougoule, C. | |
dc.contributor.author | Meneton, P. | |
dc.contributor.author | Limosin, F. | |
dc.date.accessioned | 2023-06-22T10:44:46Z | |
dc.date.available | 2023-06-22T10:44:46Z | |
dc.date.issued | 2022-03-30 | |
dc.description | CRUE-CSIC (Acuerdos Transformativos 2022) | |
dc.description.abstract | Aims To examine the association between benzodiazepine receptor agonist (BZRA) use and mortality in patients hospitalised for coronavirus disease 2019 (COVID-19). Methods A multicentre observational study was performed at Greater Paris University hospitals. The sample involved 14 381 patients hospitalised for COVID-19. A total of 686 (4.8%) inpatients received a BZRA at hospital admission at a mean daily diazepam-equivalent dose of 19.7 mg (standard deviation (S.D.) = 25.4). The study baseline was the date of admission, and the primary endpoint was death. We compared this endpoint between patients who received BZRAs and those who did not in time-to-event analyses adjusted for sociodemographic characteristics, medical comorbidities and other medications. The primary analysis was a Cox regression model with inverse probability weighting (IPW). Results Over a mean follow-up of 14.5 days (S.D. = 18.1), the primary endpoint occurred in 186 patients (27.1%) who received BZRAs and in 1134 patients (8.3%) who did not. There was a significant association between BZRA use and increased mortality both in the crude analysis (hazard ratio (HR) = 3.20; 95% confidence interval (CI) = 2.74–3.74; p < 0.01) and in the IPW analysis (HR = 1.61; 95% CI = 1.31–1.98, p < 0.01), with a significant dose-dependent relationship (HR = 1.55; 95% CI = 1.08–2.22; p = 0.02). This association remained significant in sensitivity analyses. Exploratory analyses indicate that most BZRAs may be associated with an increased mortality among patients hospitalised for COVID-19, except for diazepam, which may be associated with a reduced mortality compared with any other BZRA treatment. Conclusions BZRA use may be associated with an increased mortality among patients hospitalised for COVID-19, suggesting the potential benefit of decreasing dose or tapering off gradually these medications when possible. | |
dc.description.department | Depto. de Psicobiología y Metodología en Ciencias del Comportamiento | |
dc.description.faculty | Fac. de Psicología | |
dc.description.refereed | TRUE | |
dc.description.status | pub | |
dc.eprint.id | https://eprints.ucm.es/id/eprint/72611 | |
dc.identifier.doi | 10.1017/S2045796021000743 | |
dc.identifier.issn | 2045-7960 | |
dc.identifier.officialurl | https://doi.org/10.1017/S2045796021000743 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14352/71571 | |
dc.journal.title | Epidemiology and Psychiatric Sciences | |
dc.language.iso | eng | |
dc.publisher | Cambridge University Press | |
dc.rights | Atribución 3.0 España | |
dc.rights.accessRights | open access | |
dc.rights.uri | https://creativecommons.org/licenses/by/3.0/es/ | |
dc.subject.keyword | Benzodiazepine | |
dc.subject.keyword | COVID-19 | |
dc.subject.keyword | mortality | |
dc.subject.keyword | SARS-CoV-2 | |
dc.subject.ucm | Inmunología | |
dc.subject.ucm | Salud pública (Medicina) | |
dc.subject.unesco | 2412 Inmunología | |
dc.subject.unesco | 3212 Salud Pública | |
dc.title | Association between benzodiazepine receptor agonist use and mortality in patients hospitalised for COVID-19: a multicentre observational study | |
dc.type | journal article | |
dc.volume.number | 31 | |
dspace.entity.type | Publication | |
relation.isAuthorOfPublication | b19a5f6e-1571-404c-bd21-332c59ade169 | |
relation.isAuthorOfPublication.latestForDiscovery | b19a5f6e-1571-404c-bd21-332c59ade169 |
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