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A cluster-randomized trial of hydroxychloroquine for prevention of Covid-19

Authors :
Oriol, Mitjà
Marc, Corbacho-Monné
Maria, Ubals
Andrea, Alemany
Clara, Suñer
Cristian, Tebé
Aurelio, Tobias
Judith, Peñafiel
Ester, Ballana
Carla A, Pérez
Pol, Admella
Núria, Riera-Martí
Pep, Laporte
Jordi, Mitjà
Mireia, Clua
Laia, Bertran
Maria, Sarquella
Sergi, Gavilán
Jordi, Ara
Josep M, Argimon
Gabriel, Cuatrecasas
Paz, Cañadas
Aleix, Elizalde-Torrent
Robert, Fabregat
Magí, Farré
Anna, Forcada
Gemma, Flores-Mateo
Cristina, López
Esteve, Muntada
Núria, Nadal
Silvia, Narejos
Aroa, Nieto
Nuria, Prat
Jordi, Puig
Carles, Quiñones
Ferran, Ramírez-Viaplana
Juliana, Reyes-Urueña
Eva, Riveira-Muñoz
Lidia, Ruiz
Sergi, Sanz
Alexis, Sentís
Alba, Sierra
César, Velasco
Rosa M, Vivanco-Hidalgo
Juani, Zamora
Jordi, Casabona
Martí, Vall-Mayans
Camila, González-Beiras
Bonaventura, Clotet
Esther, Diaz Soler
Source :
The New England Journal of Medicine, Dipòsit Digital de la UB, Universidad de Barcelona, New England Journal of Medicine, r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol, instname
Publication Year :
2021
Publisher :
Massachusetts Medical Society, 2021.

Abstract

BackgroundCurrent strategies for preventing severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection are limited to nonpharmacologic interventions. Hydroxychloroquine has been proposed as a postexposure therapy to prevent coronavirus disease 2019 (Covid-19), but definitive evidence is lacking. MethodsWe conducted an open-label, cluster-randomized trial involving asymptomatic contacts of patients with polymerase-chain-reaction (PCR)-confirmed Covid-19 in Catalonia, Spain. We randomly assigned clusters of contacts to the hydroxychloroquine group (which received the drug at a dose of 800 mg once, followed by 400 mg daily for 6 days) or to the usual-care group (which received no specific therapy). The primary outcome was PCR-confirmed, symptomatic Covid-19 within 14 days. The secondary outcome was SARS-CoV-2 infection, defined by symptoms compatible with Covid-19 or a positive PCR test regardless of symptoms. Adverse events were assessed for up to 28 days. ResultsThe analysis included 2314 healthy contacts of 672 index case patients with Covid-19 who were identified between March 17 and April 28, 2020. A total of 1116 contacts were randomly assigned to receive hydroxychloroquine and 1198 to receive usual care. Results were similar in the hydroxychloroquine and usual-care groups with respect to the incidence of PCR-confirmed, symptomatic Covid-19 (5.7% and 6.2%, respectively; risk ratio, 0.86 [95% confidence interval, 0.52 to 1.42]). In addition, hydroxychloroquine was not associated with a lower incidence of SARS-CoV-2 transmission than usual care (18.7% and 17.8%, respectively). The incidence of adverse events was higher in the hydroxychloroquine group than in the usual-care group (56.1% vs. 5.9%), but no treatment-related serious adverse events were reported. ConclusionsPostexposure therapy with hydroxychloroquine did not prevent SARS-CoV-2 infection or symptomatic Covid-19 in healthy persons exposed to a PCR-positive case patient. (Funded by the crowdfunding campaign YoMeCorono and others; BCN-PEP-CoV2 ClinicalTrials.gov number, NCT04304053.) In a trial involving asymptomatic contacts of patients with PCR-confirmed Covid-19 in Spain, the authors compared the use of hydroxychloroquine with usual care. Postexposure therapy with hydroxychloroquine did not prevent SARS-CoV-2 infection or symptomatic Covid-19 in healthy persons.

Details

Language :
English
ISSN :
00284793
Database :
OpenAIRE
Journal :
The New England Journal of Medicine, Dipòsit Digital de la UB, Universidad de Barcelona, New England Journal of Medicine, r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol, instname
Accession number :
edsair.doi.dedup.....791e4bc67140e052060e45a06d9cfd09