Evidence map›Paper›PMID 36601684›Full record

SynthesisClinical and translational science2023

Hydroxychloroquine for treatment of non-hospitalized adults with COVID-19: A meta-analysis of individual participant data of randomized trials.

Oriol Mitjà, Gilmar Reis, David R Boulware, Adam M Spivak, Ammar Sarwar, Christine Johnston, Brandon Webb, Michael D Hill, Davey Smith, Peter Kremsner and 17 more

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Clinical and translational science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 4 pooled it
2.5field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 4 syntheses or guidelines pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. One Week of Oral Camostat Versus Placebo in Nonhospitalized Adults With Mild-to-Moderate Coronavirus Disease 2019: A Randomized Controlled Phase 2 Trial.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
    Trial
  7. Article
  8. COVID-19 therapeutics.Clinical microbiology reviews · 2024
    Review
  9. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors at 18 institutions in 7 countries.

Oriol MitjàFight AIDS and Infectious Diseases Foundation, Barcelona, Spain.
Gilmar ReisResearch Division, Cardresearch Cardiologia Assistencial e de Pesquisa, Pontifícia Universidade Católica de Minas Gerais, Bello Horizonte, Brazil.
David R BoulwareDivision of Infectious Diseases and International Medicine, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
Adam M SpivakUniversity of Utah, Salt Lake City, Utah, USA.
Ammar SarwarHarvard Medical School, Boston, Massachusetts, USA.
Christine JohnstonDepartment of Medicine and Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Brandon WebbIntermountain Health Care, University of Utah, Salt Lake City, Utah, USA.
Michael D HillUniversity of Calgary, Calgary, Alberta, Canada.
Davey SmithDivision of Infectious Diseases & Global Public Health, UC San Diego School of Medicine, San Diego, California, USA.
Peter KremsnerUniversity Hospital of Tübingen, Tübingen, Germany.
Marla CurranBill & Melinda Gates Medical Research Institute, Cambridge, Massachusetts, USA.
David CarterMMS Holdings, Canton, Michigan, USA.
Jim AlexanderBill & Melinda Gates Medical Research Institute, Cambridge, Massachusetts, USA.
Marc CorbachoFight AIDS and Infectious Diseases Foundation, Barcelona, Spain.ORCID 0000-0001-8675-2868
Todd C LeeDivision of Infectious Diseases and International Medicine, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
Katherine Huppler HullsiekDivision of Infectious Diseases and International Medicine, Department of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
Emily G McDonaldDivision of General Internal Medicine, McGill University Health Center, Montreal, Quebec, Canada.
Rachel HessUniversity of Utah, Salt Lake City, Utah, USA.ORCID 0000-0003-2545-8504
Michael HughesHarvard Medical School, Boston, Massachusetts, USA.
Jared M BaetenDepartment of Medicine and Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Ilan SchwartzUniversity of Alberta, Edmonton, Canada.
Luanne MetzUniversity of Calgary, Calgary, Alberta, Canada.
Lawrence RicherUniversity of Alberta, Edmonton, Canada.
Kara W ChewDivision of Infectious Diseases, Department of Medicine, David Geffen School of Medicine at University of California, Los Angeles, California, USA.
Eric DaarLundquist Institute at Harbor-UCLA Medical Center, Torrance, California, USA.
David WohlSchool of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Michael DunneBill & Melinda Gates Medical Research Institute, Cambridge, Massachusetts, USA.
Gates Foundation · USUniversity of Minnesota · USHarvard University · USUniversity of Alberta · CAUniversity of Calgary · CAUniversity of Utah · USUniversity of Washington · USCentre de Recherche Médicales de Lambaréné · GAFundació Lluita contra les Infeccions · ESHospital Universitari Germans Trias i Pujol · ESIntermountain Healthcare · USMontreal General Hospital · CAPontifícia Universidade Católica de Minas Gerais · BRTechnology Holding (United States) · USUCLA Medical Center · USUC San Diego Health System · USUniversity of California, Los Angeles · USUniversity of North Carolina at Chapel Hill · US

Funding

Leadership and Operations Center (LOC), AIDS Clinical Trials Group (ACTG); LOC 1/UM1AI068636 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Joseph J Eron, RAJESH T GANDHI · 2011 to 2026
$1073.1M
Statistical and Data Management Center (SDMC), AIDS Clinical Trials Group (ACTG)UM1AI068634 · NIAID · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Marlene Ann Cooper, Michael David Hughes · 2011 to 2026
$246.6M
University of North Carolina Global HIV Prevention and Treatment Clinical Trials Unit 2024 SupplementUM1AI069423 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Joseph J Eron, MINA CHRISTINE HOSSEINIPOUR · 2012 to 2026
$71.8M
UCLA AIDS Prevention and Treatment Clinical Trials UnitUM1AI069424 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Judith S. Currier, RAPHAEL J LANDOVITZ · 2012 to 2026
$51.8M
Utah Center for Clinical and Translational ScienceUL1TR002538 · NCATS · UNIVERSITY OF UTAH · PI HESS, RACHEL, MAJERSIK, JENNIFER JUHL · 2018 to 2022
$26.0M
UCLA AIDS Prevention and Treatment Clinical Trials UnitU01AI069424 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CURRIER, JUDITH S. · 2007 to 2011
$13.9M
NCATS NIH HHS UL1 TR002538NIAID NIH HHS U01 AI069424NIAID NIH HHS UM1 AI068634NIAID NIH HHS UM1 AI068636NIAID NIH HHS UM1 AI069423NIAID NIH HHS UM1 AI069424
6 · The paper itself

Abstract

Hydroxychloroquine (HCQ) was initially promoted as an oral therapy for early treatment of coronavirus disease 2019 (COVID-19). Conventional meta-analyses cannot fully address the heterogeneity of different designs and outcomes of randomized controlled trials (RCTs) assessing the efficacy of HCQ in outpatients with mild COVID-19. We conducted a pooled analysis of individual participant data from RCTs that evaluated the effect of HCQ on hospitalization and viral load reduction in outpatients with confirmed COVID-19. We evaluated the overall treatment group effect by log-likelihood ratio test (-2LL) from a generalized linear mixed model to accommodate correlated longitudinal binary data. The analysis included data from 11 RCTs. The outcome of virological effect, assessed in 1560 participants (N = 795 HCQ, N = 765 control), did not differ significantly between the two treatment groups (-2LL = 7.66; p = 0.18) when adjusting for cohort, duration of symptoms, and comorbidities. The decline in polymerase chain reaction positive tests from day 1 to 7 was 42.0 and 41.6 percentage points in the HCQ and control groups, respectively. Among the 2037 participants evaluable for hospitalization (N = 1058 HCQ, N = 979 control), we found no significant differences in hospitalization rate between participants receiving HCQ and controls (odds ratio 0.995; 95% confidence interval 0.614-1.610; -2LL = 0.0; p = 0.98) when adjusting for cohort, duration of symptoms, and comorbidities. This individual participant data meta-analysis of 11 HCQ trials that evaluated severe acute respiratory syndrome-coronavirus 2 viral clearance and COVID-19 hospitalization did not show a clinical benefit of HCQ. Our meta-analysis provides evidence to support the interruption in the use of HCQ in mild COVID-19 outpatients to reduce progression to severe disease.

Indexed as

COVID-19AdultCOVID-19 Drug TreatmentHumansHydroxychloroquineRandomized Controlled Trials as TopicTreatment OutcomeHydroxychloroquine

Identifiers

PMID36601684
PMCPMC10014689
OpenAlexW4313500418

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.