Association of Treatment With Hydroxychloroquine or Azithromycin With In-Hospital Mortality in Patients With COVID-19 in New York State.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
23 06 2020
Historique:
pubmed: 12 5 2020
medline: 2 10 2020
entrez: 12 5 2020
Statut: ppublish

Résumé

Hydroxychloroquine, with or without azithromycin, has been considered as a possible therapeutic agent for patients with coronavirus disease 2019 (COVID-19). However, there are limited data on efficacy and associated adverse events. To describe the association between use of hydroxychloroquine, with or without azithromycin, and clinical outcomes among hospital inpatients diagnosed with COVID-19. Retrospective multicenter cohort study of patients from a random sample of all admitted patients with laboratory-confirmed COVID-19 in 25 hospitals, representing 88.2% of patients with COVID-19 in the New York metropolitan region. Eligible patients were admitted for at least 24 hours between March 15 and 28, 2020. Medications, preexisting conditions, clinical measures on admission, outcomes, and adverse events were abstracted from medical records. The date of final follow-up was April 24, 2020. Receipt of both hydroxychloroquine and azithromycin, hydroxychloroquine alone, azithromycin alone, or neither. Primary outcome was in-hospital mortality. Secondary outcomes were cardiac arrest and abnormal electrocardiogram findings (arrhythmia or QT prolongation). Among 1438 hospitalized patients with a diagnosis of COVID-19 (858 [59.7%] male, median age, 63 years), those receiving hydroxychloroquine, azithromycin, or both were more likely than those not receiving either drug to have diabetes, respiratory rate >22/min, abnormal chest imaging findings, O2 saturation lower than 90%, and aspartate aminotransferase greater than 40 U/L. Overall in-hospital mortality was 20.3% (95% CI, 18.2%-22.4%). The probability of death for patients receiving hydroxychloroquine + azithromycin was 189/735 (25.7% [95% CI, 22.3%-28.9%]), hydroxychloroquine alone, 54/271 (19.9% [95% CI, 15.2%-24.7%]), azithromycin alone, 21/211 (10.0% [95% CI, 5.9%-14.0%]), and neither drug, 28/221 (12.7% [95% CI, 8.3%-17.1%]). In adjusted Cox proportional hazards models, compared with patients receiving neither drug, there were no significant differences in mortality for patients receiving hydroxychloroquine + azithromycin (HR, 1.35 [95% CI, 0.76-2.40]), hydroxychloroquine alone (HR, 1.08 [95% CI, 0.63-1.85]), or azithromycin alone (HR, 0.56 [95% CI, 0.26-1.21]). In logistic models, compared with patients receiving neither drug cardiac arrest was significantly more likely in patients receiving hydroxychloroquine + azithromycin (adjusted OR, 2.13 [95% CI, 1.12-4.05]), but not hydroxychloroquine alone (adjusted OR, 1.91 [95% CI, 0.96-3.81]) or azithromycin alone (adjusted OR, 0.64 [95% CI, 0.27-1.56]), . In adjusted logistic regression models, there were no significant differences in the relative likelihood of abnormal electrocardiogram findings. Among patients hospitalized in metropolitan New York with COVID-19, treatment with hydroxychloroquine, azithromycin, or both, compared with neither treatment, was not significantly associated with differences in in-hospital mortality. However, the interpretation of these findings may be limited by the observational design.

Identifiants

pubmed: 32392282
pii: 2766117
doi: 10.1001/jama.2020.8630
pmc: PMC7215635
doi:

Substances chimiques

Anti-Infective Agents 0
Hydroxychloroquine 4QWG6N8QKH
Azithromycin 83905-01-5

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

2493-2502

Commentaires et corrections

Type : CommentIn
Type : CommentIn

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Auteurs

Eli S Rosenberg (ES)

University at Albany School of Public Health, State University of New York, Rensselaer.

Elizabeth M Dufort (EM)

New York State Department of Health, Albany.

Tomoko Udo (T)

University at Albany School of Public Health, State University of New York, Rensselaer.

Larissa A Wilberschied (LA)

New York State Department of Health, Albany.

Jessica Kumar (J)

New York State Department of Health, Albany.

James Tesoriero (J)

New York State Department of Health, Albany.

Patti Weinberg (P)

IPRO, Lake Success, New York.

James Kirkwood (J)

New York State Department of Health, Albany.

Alison Muse (A)

New York State Department of Health, Albany.

Jack DeHovitz (J)

IPRO, Lake Success, New York.
Downstate Health Sciences University, State University of New York, Brooklyn.

Debra S Blog (DS)

New York State Department of Health, Albany.

Brad Hutton (B)

New York State Department of Health, Albany.

David R Holtgrave (DR)

University at Albany School of Public Health, State University of New York, Rensselaer.

Howard A Zucker (HA)

New York State Department of Health, Albany.

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