Association of Treatment With Hydroxychloroquine or Azithromycin With In-Hospital Mortality in Patients With COVID-19 in New York State.
Adolescent
Adult
Aged
Anti-Infective Agents
/ adverse effects
Arrhythmias, Cardiac
/ chemically induced
Azithromycin
/ adverse effects
Betacoronavirus
COVID-19
Coronavirus Infections
/ drug therapy
Drug Therapy, Combination
Female
Heart Arrest
/ etiology
Hospital Mortality
Hospitalization
Humans
Hydroxychloroquine
/ adverse effects
Logistic Models
Male
Middle Aged
New York
Pandemics
Pneumonia, Viral
/ drug therapy
Proportional Hazards Models
Retrospective Studies
SARS-CoV-2
Young Adult
COVID-19 Drug Treatment
Journal
JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160
Informations de publication
Date de publication:
23 06 2020
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
2493-2502Commentaires et corrections
Type : CommentIn
Type : CommentIn
Références
Lancet. 2020 Feb 15;395(10223):470-473
pubmed: 31986257
Int J Clin Pract. 2018 May;72(5):e13095
pubmed: 29691971
Clin Exp Rheumatol. 2018 Jul-Aug;36(4):545-551
pubmed: 29652656
Cell Discov. 2020 Mar 18;6:16
pubmed: 32194981
N Engl J Med. 2020 Jun 11;382(24):2372-2374
pubmed: 32302078
Med. 2020 Dec 18;1(1):114-127.e3
pubmed: 32838355
JAMA Netw Open. 2020 Apr 24;3(4):e208857
pubmed: 32330277
MMWR Morb Mortal Wkly Rep. 2020 Apr 03;69(13):382-386
pubmed: 32240123
Clin Infect Dis. 2020 Nov 5;71(8):1953-1959
pubmed: 32382743
JAMA. 2020 May 19;323(19):1891-1892
pubmed: 32293639
Ann Intern Med. 2017 Aug 15;167(4):268-274
pubmed: 28693043
J Am Heart Assoc. 2014 Oct 06;3(5):e001339
pubmed: 25288614
Int J Antimicrob Agents. 2020 Jul;56(1):105949
pubmed: 32205204
MMWR Morb Mortal Wkly Rep. 2020 Apr 17;69(15):458-464
pubmed: 32298251
Clin Infect Dis. 2020 Jul 28;71(15):732-739
pubmed: 32150618
JAMA. 2020 May 26;323(20):2052-2059
pubmed: 32320003
Lancet. 2020 Mar 28;395(10229):1054-1062
pubmed: 32171076
Clin Infect Dis. 2020 Apr 27;:
pubmed: 32338708
N Engl J Med. 2020 Jun 18;382(25):2411-2418
pubmed: 32379955
Int J Antimicrob Agents. 2020 Apr;55(4):105932
pubmed: 32145363
Eur Heart J. 2003 Jul;24(13):1204-9
pubmed: 12831814
Nat Med. 2020 Jun;26(6):808-809
pubmed: 32488217