Inpatient Omission of Angiotensin-Converting Enzyme Inhibitors and Angiotensin Receptor Blockers Is Associated With Morbidity and Mortality in Coronavirus Disease 2019.


Journal

Clinical therapeutics
ISSN: 1879-114X
Titre abrégé: Clin Ther
Pays: United States
ID NLM: 7706726

Informations de publication

Date de publication:
04 2021
Historique:
received: 15 01 2021
revised: 08 02 2021
accepted: 22 02 2021
pubmed: 14 3 2021
medline: 6 7 2021
entrez: 13 3 2021
Statut: ppublish

Résumé

Due to the affinity of severe acute respiratory syndrome coronavirus 2 for the human angiotensin-converting enzyme 2 (ACE2) receptor, use of ACE inhibitors and angiotensin receptor blockers (ARBs) has been a major concern for clinicians during the 2020 pandemic. Meta-analyses have affirmed that these agents do not worsen clinical outcomes in patients with severe acute respiratory syndrome coronavirus 2 infection. To date, only a limited number of studies have directly evaluated the safety of inpatient prescription of ACE inhibitors/ARBs during acute coronavirus disease 2019 (COVID-19) illness. A retrospective cohort analysis was conducted to investigate the impact of inpatient provision of ACE inhibitors/ARBs on morbidity and mortality in patients admitted to the hospital with COVID-19. Relationships were explored by using linear and logistic regression. A total of 612 adult patients met the inclusion criteria, of whom 151 (24.7%) patients were established on ACE inhibitors/ARBs. Despite correction for known confounders, discontinuation of ACE inhibitors/ARBs was highly predictive of worsened outcomes in COVID-19. The proportion of doses omitted in the hospital was significantly associated with increased mortality (OR, 9.59; 95% CI, 2.55-36.09; P < 0.001), maximum National Early Warning Score 2 (OR, 1.66; 95% CI, 1.27-2.17; P < 0.001), maximum oxygen requirements (OR, 3.00; 95% CI, 1.83-4.91; P < 0.001), and maximum C-reactive protein concentration (OR, 1.83; 95% CI, 1.06-3.17; P = 0.030). Our data show a strong association between missed ACE inhibitor/ARB doses with increased morbidity and mortality. The available evidence supports continuation of currently accepted practice surrounding ACE inhibitor/ARB therapy in acute illness, which is to limit drug omission to established acute contraindications, to actively monitor such decisions, and to restart therapy as soon as it is safe to do so. (Clin Ther. 2021;43:e97-e110) © 2021 Elsevier HS Journals, Inc.

Identifiants

pubmed: 33712270
pii: S0149-2918(21)00101-6
doi: 10.1016/j.clinthera.2021.02.004
pmc: PMC7906507
pii:
doi:

Substances chimiques

Angiotensin Receptor Antagonists 0
Angiotensin-Converting Enzyme Inhibitors 0
C-Reactive Protein 9007-41-4

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e97-e110

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest The authors have indicated that they have no conflicts of interest regarding the content of this article.

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Auteurs

Christopher Oddy (C)

St. Helier Hospital, London, United Kingdom. Electronic address: christopher.oddy1@nhs.net.

Jonathan Allington (J)

St. Helier Hospital, London, United Kingdom.

James McCaul (J)

St. Helier Hospital, London, United Kingdom.

Polly Keeling (P)

St. Helier Hospital, London, United Kingdom.

Dhanuja Senn (D)

St. Helier Hospital, London, United Kingdom.

Neesha Soni (N)

St. Helier Hospital, London, United Kingdom.

Hannah Morrison (H)

St. Helier Hospital, London, United Kingdom.

Ruwani Mawella (R)

St. Helier Hospital, London, United Kingdom.

Thomas Samuel (T)

St. Helier Hospital, London, United Kingdom.

John Dixon (J)

St. Helier Hospital, London, United Kingdom.

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Classifications MeSH