Ensitrelvir for Covid-19 postexposure prophylaxis in household contacts (Registro nro. 22902)

000 -Cabecera
Campo de control interno 03207nam a2200301 4500
001 - Número de control
control field ESSALUD
005 - Fecha y hora de la última transacción
Campo de control 20260902160450.0
007 - Tipo material - Descripcion fisica - info general
Tipo material - Descripcion fisica - info general ta
008 - Elementos de Longitud Fija - Información General
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040 ## - Origen de la Catalogación
Origen de la Catalogación BMG
041 ## - Idioma
Idioma eng
100 ## - Autor
Autor Hayden, Frederick G.
9 (RLIN) 54466
245 ## - Titulo
Titulo Ensitrelvir for Covid-19 postexposure prophylaxis in household contacts
300 ## - Páginas
Paginación páginas: 1905-1915
520 ## - Resumen
Resumen Background: Ensitrelvir, an oral inhibitor of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) 3C-like protease, is approved in Japan for the treatment of mild-to-moderate coronavirus disease 2019 (Covid-19). Previously, no antiviral agents were approved for postexposure prophylaxis in household contacts of patients with Covid-19. Methods: In this double-blind, randomized, placebo-controlled trial, we randomly assigned persons who were SARS-CoV-2–negative on local diagnostic testing but were household contacts of a patient with Covid-19 (the index patient) to receive either ensitrelvir (375 mg on day 1 and 125 mg daily on days 2 through 5) or placebo within 72 hours after symptom onset in the index patient. The primary end point was Covid-19 (defined by a central laboratory–confirmed positive reverse-transcriptase–polymerase-chain-reaction assay and the presence of ≥1 of 14 prespecified Covid-19 symptoms lasting ≥48 hours) by day 10 in a household contact in the modified intention-to-treat population (all the participants who underwent randomization, had a central laboratory–confirmed negative RT-PCR test for SARS-CoV-2 at baseline, and received at least one dose of the trial drug or placebo). Results: The modified intention-to-treat population included 1030 participants in the ensitrelvir group and 1011 in the placebo group. The mean age of the participants was 42.4 years; 71.1% had undergone randomization within 48 hours after symptom onset in the index patient, and 37.0% had at least one risk factor for severe Covid-19. The incidence of Covid-19 was lower in the ensitrelvir group than in the placebo group (2.9% vs. 9.0%; risk ratio, 0.33; 95% confidence interval [CI], 0.22 to 0.49; P<0.001). The incidence of adverse events during the trial was similar in the two groups (15.1% in the ensitrelvir group and 15.5% in the placebo group), as was the incidence of serious adverse events (0.2% in each group). No Covid-19–related hospitalizations or deaths were reported. Conclusions: Ensitrelvir administered to household contacts of a patient with Covid-19 within 72 hours after symptom onset in the index patient was effective in preventing Covid-19 in the contacts.
650 ## - Temas - Descriptores
Temas - Descriptores CORONAVIRUS
9 (RLIN) 39659
650 ## - Temas - Descriptores
Temas - Descriptores SALUD GLOBAL
9 (RLIN) 10472
650 ## - Temas - Descriptores
Temas - Descriptores ENFERMEDADES INFECCIOSAS GENERALES
9 (RLIN) 54087
650 ## - Temas - Descriptores
Temas - Descriptores INFECCIONES VIRALES
9 (RLIN) 53766
700 ## - Autor Personal
Autor Personal Shinkai, Masaharu
9 (RLIN) 54467
700 ## - Autor Personal
Autor Personal Clark, Tristan W.
9 (RLIN) 54468
700 ## - Autor Personal
Autor Personal Luetkemeyer, Anne F.
9 (RLIN) 54469
700 ## - Autor Personal
Autor Personal Sax, Paul E.
9 (RLIN) 54470
700 ## - Autor Personal
Autor Personal Hanage, William P.
9 (RLIN) 54471
700 ## - Autor Personal
Autor Personal Gebo, Kelly A.
9 (RLIN) 54472
773 0# - Revista (Relacion con el numero)
Host Biblionumber 22717
Host Itemnumber 22669
Ciudad, Editorial Massachusetts NEJM Group
Codigo barras item/ejemplar NEJM014
Titulo de la Revista The New England Journal of Medicine
Número de control de registro ESSALUD
ISSN 0028-4793
942 ## - Elementos de Koha
Tipo de Documento Artículos
Fecha procesamiento 2026-08-31
Catalogador sqb

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