New England Journal of Medicine, volume 386, issue 18, pages 1721-1731
Effect of Early Treatment with Ivermectin among Patients with Covid-19
Gilmar Reis
1
,
Eduardo A.S.M. Silva
1
,
Daniela Nascimento Silva
1
,
Lehana Thabane
1
,
Aline C. Milagres
1
,
Thiago S. Ferreira
1
,
Castilho V.Q. dos Santos
1
,
Vitoria H.S. Campos
1
,
Ana P V Almeida
1
,
Eduardo D. Callegari
1
,
Adhemar D.F. Neto
1
,
Leonardo C.M. Savassi
1
,
Maria I.C. Simplicio
1
,
Luciene B. Ribeiro
1
,
Rosemary Oliveira
1
,
Ofir Harari
1
,
Jamie I. Forrest
1
,
Hinda Ruton
1
,
Sheila Sprague
1
,
Paula McKay
1
,
Christina Guo
1
,
Karen ROWLAND-YEO
1
,
GH Guyatt
1
,
Craig R. Rayner
1
,
E. Mills
1
Publication type: Journal Article
Publication date: 2022-03-30
Journal:
New England Journal of Medicine
scimago Q1
SJR: 20.544
CiteScore: 145.4
Impact factor: 96.2
ISSN: 00284793, 15334406
PubMed ID:
35353979
General Medicine
Abstract
The efficacy of ivermectin in preventing hospitalization or extended observation in an emergency setting among outpatients with acutely symptomatic coronavirus disease 2019 (Covid-19), the disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is unclear.We conducted a double-blind, randomized, placebo-controlled, adaptive platform trial involving symptomatic SARS-CoV-2-positive adults recruited from 12 public health clinics in Brazil. Patients who had had symptoms of Covid-19 for up to 7 days and had at least one risk factor for disease progression were randomly assigned to receive ivermectin (400 μg per kilogram of body weight) once daily for 3 days or placebo. (The trial also involved other interventions that are not reported here.) The primary composite outcome was hospitalization due to Covid-19 within 28 days after randomization or an emergency department visit due to clinical worsening of Covid-19 (defined as the participant remaining under observation for >6 hours) within 28 days after randomization.A total of 3515 patients were randomly assigned to receive ivermectin (679 patients), placebo (679), or another intervention (2157). Overall, 100 patients (14.7%) in the ivermectin group had a primary-outcome event, as compared with 111 (16.3%) in the placebo group (relative risk, 0.90; 95% Bayesian credible interval, 0.70 to 1.16). Of the 211 primary-outcome events, 171 (81.0%) were hospital admissions. Findings were similar to the primary analysis in a modified intention-to-treat analysis that included only patients who received at least one dose of ivermectin or placebo (relative risk, 0.89; 95% Bayesian credible interval, 0.69 to 1.15) and in a per-protocol analysis that included only patients who reported 100% adherence to the assigned regimen (relative risk, 0.94; 95% Bayesian credible interval, 0.67 to 1.35). There were no significant effects of ivermectin use on secondary outcomes or adverse events.Treatment with ivermectin did not result in a lower incidence of medical admission to a hospital due to progression of Covid-19 or of prolonged emergency department observation among outpatients with an early diagnosis of Covid-19. (Funded by FastGrants and the Rainwater Charitable Foundation; TOGETHER ClinicalTrials.gov number, NCT04727424.).
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