Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/180762
Title: A cluster-randomized trial of hydroxychloroquine for prevention of Covid-19
Author: Mitjà Villar, Oriol
Corbacho-Monné, Marc
Ubals, Maria
Alemany, Andrea
Suñer Navarro, Clara
Tebé, Cristian
Tobias, Aurelio
Peñafiel, Judith
Ballana, Ester
Pérez, Carla A.
Admella, Pol
Riera-Martí, Núria
Laporte, Pep
Mitjà, Jordi
Clua, Mireia
Bertran, Laia
Sarquella, Maria
Gavilán, Sergi
Ara, Jordi
Argimón Pallás, José M.
Cuatrecasas, Gabriel
Cañadas, Paz
Elizalde Torrent, Aleix
Fabregat, Robert
Farré Albaladejo, Magí
Forcada, Anna
Flores Mateo, Gemma
López, Cristina
Muntada, Esteve
Nadal, Núria
Narejos, Silvia
Nieto, Aroa
Prat, Núria
Puig, Jordi
Quiñones, Carles
Ramírez-Viaplana, Ferran
Reyes Urueña, Juliana Maria
Riveira-Muñoz, Eva
Ruiz, Lidia
Sanz, Sergi
Keywords: Agents antiinfecciosos
Ús terapèutic
COVID-19
Anti-infective agents
Therapeutic use
COVID-19
Issue Date: 4-Feb-2021
Publisher: Massachusetts Medical Society
Abstract: Background: current 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. Methods: we 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. Results: the 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. Conclusions: postexposure 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.).
Note: Reproducció del document publicat a: https://doi.org/10.1056/NEJMoa2021801
It is part of: New England Journal of Medicine, 2021, vol. 384, num. 5, p. 417-427
URI: http://hdl.handle.net/2445/180762
Related resource: https://doi.org/10.1056/NEJMoa2021801
ISSN: 0028-4793
Appears in Collections:Articles publicats en revistes (Ciències Clíniques)

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