Hydroxychloroquine or Chloroquine for Treatment or Prophylaxis of COVID-19 A Living Systematic Review

被引:156
|
作者
Hernandez, Adrian V. [1 ,2 ,3 ,4 ,6 ]
Roman, Yuani M. [1 ,2 ,6 ]
Pasupuleti, Vinay [5 ,7 ]
Barboza, Joshuan J. [4 ,8 ]
White, C. Michael [1 ,2 ,3 ,6 ]
机构
[1] Univ Connecticut, Hlth Outcomes Policy & Evidence Synth Grp, Hartford, CT 06112 USA
[2] Hartford Hosp, Dept Res Adm, Hartford, CT 06115 USA
[3] Sch Pharm, Storrs, CT USA
[4] Univ San Ignacio de Loyola, Vicerrectorado Invest, Lima, Peru
[5] MedErgy HealthGrp, Yardley, PA USA
[6] Hlth Outcomes Policy & Evidence Synth Grp, 69 North Eagleville Rd,U3092, Storrs, CT 06269 USA
[7] MedErgy HealthGrp Inc, 790 Township Line Rd, Yardley, PA 19067 USA
[8] Univ San Ignacio de Loyola USIL, Vicerrectorado Invest, Ave Fontana 750, Lima 15024, Peru
关键词
D O I
10.7326/M20-2496
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Hydroxychloroquine and chloroquine have antiviral effects in vitro against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Purpose: To summarize evidence about the benefits and harms of hydroxychloroquine or chloroquine for the treatment or prophylaxis of coronavirus disease 2019 (COVID-19). Data Sources: PubMed (via MEDLINE), EMBASE (via Ovid), Scopus, Web of Science, Cochrane Library, bioRxiv, Preprints, ClinicalTrials.gov, World Health Organization International Clinical Trials Registry Platform, and the Chinese Clinical Trials Registry from 1 December 2019 until 8 May 2020. Study Selection: Studies in any language reporting efficacy or safety outcomes from hydroxychloroquine or chloroquine use in any setting in adults or children with suspected COVID-19 or at risk for SARS-CoV-2 infection. Data Extraction: Independent, dually performed data extraction and quality assessments. Data Synthesis: Four randomized controlled trials, 10 cohort studies, and 9 case series assessed treatment effects of the medications, but no studies evaluated prophylaxis. Evidence was conflicting and insufficient regarding the effect of hydroxychloroquine on such outcomes as all-cause mortality, progression to severe disease, clinical symptoms, and upper respiratory viro- logic clearance with antigen testing. Several studies found that patients receiving hydroxychloroquine developed a QTc interval of 500 ms or greater, but the proportion of patients with this finding varied among the studies. Two studies assessed the efficacy of chloroquine; 1 trial, which compared higher-dose (600 mg twice daily for 10 days) with lower-dose (450 mg twice daily on day 1 and once daily for 4 days) therapy, was stopped owing to concern that the higher dose therapy increased lethality and QTc interval prolongation. An observational study that compared adults with COVID-19 receiving chloroquine phosphate, 500 mg once or twice daily, with patients not receiving chloroquine found minor fever resolution and virologic clearance benefits with chloroquine. Limitation: There were few controlled studies, and control for confounding was inadequate in observational studies. Conclusion: Evidence on the benefits and harms of using hydroxychloroquine or chloroquine to treat COVID-19 is very weak and conflicting.
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页码:287 / +
页数:11
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