AI Article Synopsis

  • Recruitment for trials on hydroxychloroquine (HCQ) for COVID-19 prevention was hindered by widespread skepticism about its effectiveness, prompting a meta-analysis of existing trials to re-evaluate its efficacy.
  • The analysis included 11 randomized trials, with results indicating a 28% reduction in risk of COVID-19 diagnosis for pre-exposure prophylaxis using HCQ, while post-exposure trials showed no significant protective effect.
  • Despite the findings suggesting potential benefits for pre-exposure use, misinterpretations of early trial results hindered the timely completion of ongoing research, affecting pandemic response strategies prior to vaccine availability.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9360718PMC
http://dx.doi.org/10.1007/s10654-022-00891-4DOI Listing

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