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dc.contributor.authorRECOVERY Collaborative Group
dc.contributor.authorDhasmana, Devesh J
dc.date.accessioned2021-11-01T17:30:09Z
dc.date.available2021-11-01T17:30:09Z
dc.date.issued2020-11-19
dc.identifier275408412
dc.identifier06d36d85-2b9c-427f-a537-8a68e409cd4f
dc.identifier33031652
dc.identifier85096456735
dc.identifier.citationRECOVERY Collaborative Group & Dhasmana , D J 2020 , ' Effect of hydroxychloroquine in hospitalized patients with Covid-19 ' , New England Journal of Medicine , vol. 383 , no. 21 , pp. 2030-2040 . https://doi.org/10.1056/NEJMoa2022926en
dc.identifier.issn0028-4793
dc.identifier.otherPubMedCentral: PMC7556338
dc.identifier.urihttps://hdl.handle.net/10023/24236
dc.descriptionSupported by a grant (MC_PC_19056) to the University of Oxford from UK Research and Innovation and the NIHR and by core funding provided by NIHR Oxford Biomedical Research Centre, Wellcome, the Bill and Melinda Gates Foundation, the Department for International Development, Health Data Research UK, the Medical Research Council Population Health Research Unit, the NIHR Health Protection Unit in Emerging and Zoonotic Infections, and NIHR Clinical Trials Unit Support Funding.en
dc.description.abstractBACKGROUND: Hydroxychloroquine and chloroquine have been proposed as treatments for coronavirus disease 2019 (Covid-19) on the basis of in vitro activity and data from uncontrolled studies and small, randomized trials. METHODS: In this randomized, controlled, open-label platform trial comparing a range of possible treatments with usual care in patients hospitalized with Covid-19, we randomly assigned 1561 patients to receive hydroxychloroquine and 3155 to receive usual care. The primary outcome was 28-day mortality. RESULTS: The enrollment of patients in the hydroxychloroquine group was closed on June 5, 2020, after an interim analysis determined that there was a lack of efficacy. Death within 28 days occurred in 421 patients (27.0%) in the hydroxychloroquine group and in 790 (25.0%) in the usual-care group (rate ratio, 1.09; 95% confidence interval [CI], 0.97 to 1.23; P = 0.15). Consistent results were seen in all prespecified subgroups of patients. The results suggest that patients in the hydroxychloroquine group were less likely to be discharged from the hospital alive within 28 days than those in the usual-care group (59.6% vs. 62.9%; rate ratio, 0.90; 95% CI, 0.83 to 0.98). Among the patients who were not undergoing mechanical ventilation at baseline, those in the hydroxychloroquine group had a higher frequency of invasive mechanical ventilation or death (30.7% vs. 26.9%; risk ratio, 1.14; 95% CI, 1.03 to 1.27). There was a small numerical excess of cardiac deaths (0.4 percentage points) but no difference in the incidence of new major cardiac arrhythmia among the patients who received hydroxychloroquine. CONCLUSIONS: Among patients hospitalized with Covid-19, those who received hydroxychloroquine did not have a lower incidence of death at 28 days than those who received usual care.
dc.format.extent11
dc.format.extent640259
dc.language.isoeng
dc.relation.ispartofNew England Journal of Medicineen
dc.subjectAgeden
dc.subjectAged, 80 and overen
dc.subjectAntiviral Agents/adverse effectsen
dc.subjectBetacoronavirusen
dc.subjectCOVID-19en
dc.subjectCoronavirus infections/drug therapyen
dc.subjectFemaleen
dc.subjectHospitalizationen
dc.subjectHumansen
dc.subjectHydroxychloroquine/adverse effectsen
dc.subjectMaleen
dc.subjectMiddle ageden
dc.subjectPandemicsen
dc.subjectPneumonia, viral/drug therapyen
dc.subjectRespiration, artificialen
dc.subjectSARS-CoV-2en
dc.subjectTreatment failureen
dc.subjectRA0421 Public health. Hygiene. Preventive Medicineen
dc.subjectRM Therapeutics. Pharmacologyen
dc.subject3rd-DASen
dc.subjectSDG 3 - Good Health and Well-beingen
dc.subjectNISen
dc.subject.lccRA0421en
dc.subject.lccRMen
dc.titleEffect of hydroxychloroquine in hospitalized patients with Covid-19en
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.identifier.doihttps://doi.org/10.1056/NEJMoa2022926
dc.description.statusPeer revieweden
dc.date.embargoedUntil2021-05-19


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