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Systematic review and meta-analysis of randomized trials of hydroxychloroquine for the prevention of COVID-19.
García-Albéniz, Xabier; Del Amo, Julia; Polo, Rosa; Morales-Asencio, José Miguel; Hernán, Miguel A.
Afiliação
  • García-Albéniz X; RTI Health Solutions, Av. Diagonal, 605, 9-1, 08028, Barcelona, Spain. xgarcia@rti.org.
  • Del Amo J; CAUSALab. Harvard T.H. Chan School of Public Health, Boston, MA, USA. xgarcia@rti.org.
  • Polo R; Division for HIV, STI, Viral Hepatitis and TB Control. Ministry of Health, Madrid, Spain.
  • Morales-Asencio JM; Division for HIV, STI, Viral Hepatitis and TB Control. Ministry of Health, Madrid, Spain.
  • Hernán MA; Department of Nursing and Podiatry, Instituto de Investigacion Biomedica de Malaga, Universidad de Málaga, Málaga, Spain.
Eur J Epidemiol ; 37(8): 789-796, 2022 Aug.
Article em En | MEDLINE | ID: mdl-35943669
BACKGROUND: Recruitment into randomized trials of hydroxychloroquine (HCQ) for prevention of COVID-19 has been adversely affected by a widespread conviction that HCQ is not effective for prevention. In the absence of an updated systematic review, we conducted a meta-analysis of randomized trials that study the effectiveness of HCQ to prevent COVID-19. METHODS: A search of PubMed, medRxiv, and clinicaltrials.gov combined with expert consultation found 11 completed randomized trials: 7 pre-exposure prophylaxis trials and 4 post-exposure prophylaxis trials. We obtained or calculated the risk ratio of COVID-19 diagnosis for assignment to HCQ versus no HCQ (either placebo or usual care) for each trial, and then pooled the risk ratio estimates. RESULTS: The pooled risk ratio estimate of the pre-exposure prophylaxis trials was 0.72 (95% CI: 0.58-0.90) when using either a fixed effect or a standard random effects approach, and 0.72 (95% CI: 0.55-0.95) when using a conservative modification of the Hartung-Knapp random effects approach. The corresponding estimates for the post-exposure prophylaxis trials were 0.91 (95% CI: 0.72-1.16) and 0.91 (95% CI: 0.62-1.35). All trials found a similar rate of serious adverse effects in the HCQ and no HCQ groups. DISCUSSION: A benefit of HCQ as prophylaxis for COVID-19 cannot be ruled out based on the available evidence from randomized trials. However, the "not statistically significant" findings from early prophylaxis trials were widely interpreted as definite evidence of lack of effectiveness of HCQ. This interpretation disrupted the timely completion of the remaining trials and thus the generation of precise estimates for pandemic management before the development of vaccines.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article