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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/26277
Title: Hydroxychloroquine with or without Azithromycin in Mild-to-Moderate Covid-19
Authors: Cavalcanti AB
Zampieri FG
Rosa RG
Azevedo LCP
Veiga VC
Avezum A
Damiani LP
Marcadenti A
Kawano-Dourado L
Lisboa T
Junqueira DLM
de Barros e Silva PGM
Tramujas L
Abreu-Silva EO
Laranjeira LN
Soares AT
Echenique LS
Pereira AJ
Freitas FGR
Gebara OCE
Dantas VCS
Furtado RHM
Milan EP
Golin NA
Cardoso FF
Maia IS
Hoffmann Filho CR
Kormann APM
Amazonas RB
Bocchi de Oliveira MF
Serpa-Neto A
Falavigna M
Lopes RD
Machado FR
Berwanger O
Keywords: Adult;Aged;Aged, 80 and over;Antiviral Agents;Azithromycin;Betacoronavirus;Brazil;COVID-19;Coronavirus Infections;Drug Therapy, Combination;Female;Hospitalization;Humans;Hydroxychloroquine;Male;Middle Aged;Pandemics;Patient Acuity;Pneumonia, Viral;SARS-CoV-2;Treatment Failure
Publication Date: 19-Nov-2020
Publisher: Massachusetts Medical Society
Citation: Cavalcanti, Alexandre B., et al. “Hydroxychloroquine with or without Azithromycin in Mild-to-Moderate Covid-19.” New England Journal of Medicine, vol. 383, no. 21, Massachusetts Medical Society, July 2020, pp. 2041–52, doi:10.1056/NEJMoa2019014.
Abstract: BACKGROUND: Hydroxychloroquine and azithromycin have been used to treat patients with coronavirus disease 2019 (Covid-19). However, evidence on the safety and efficacy of these therapies is limited. METHODS: We conducted a multicenter, randomized, open-label, three-group, controlled trial involving hospitalized patients with suspected or confirmed Covid-19 who were receiving either no supplemental oxygen or a maximum of 4 liters per minute of supplemental oxygen. Patients were randomly assigned in a 1:1:1 ratio to receive standard care, standard care plus hydroxychloroquine at a dose of 400 mg twice daily, or standard care plus hydroxychloroquine at a dose of 400 mg twice daily plus azithromycin at a dose of 500 mg once daily for 7 days. The primary outcome was clinical status at 15 days as assessed with the use of a seven-level ordinal scale (with levels ranging from one to seven and higher scores indicating a worse condition) in the modified intention-to-treat population (patients with a confirmed diagnosis of Covid-19). Safety was also assessed. RESULTS: A total of 667 patients underwent randomization; 504 patients had confirmed Covid-19 and were included in the modified intention-to-treat analysis. As compared with standard care, the proportional odds of having a higher score on the seven-point ordinal scale at 15 days was not affected by either hydroxychloroquine alone (odds ratio, 1.21; 95% confidence interval [CI], 0.69 to 2.11; P = 1.00) or hydroxychloroquine plus azithromycin (odds ratio, 0.99; 95% CI, 0.57 to 1.73; P = 1.00). Prolongation of the corrected QT interval and elevation of liver-enzyme levels were more frequent in patients receiving hydroxychloroquine, alone or with azithromycin, than in those who were not receiving either agent. CONCLUSIONS: Among patients hospitalized with mild-to-moderate Covid-19, the use of hydroxychloroquine, alone or with azithromycin, did not improve clinical status at 15 days as compared with standard care. (Funded by the Coalition Covid-19 Brazil and EMS Pharma; ClinicalTrials.gov number, NCT04322123.).
URI: http://hdl.handle.net/11375/26277
metadata.dc.identifier.doi: https://doi.org/10.1056/nejmoa2019014
ISSN: 0028-4793
1533-4406
Appears in Collections:Faculty Publications (via McMaster Experts)

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