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A retrospective cohort study of Paxlovid efficacy depending on treatment time in hospitalized COVID-19 patients.
Du, Zhanwei; Wang, Lin; Bai, Yuan; Liu, Yunhu; Lau, Eric H Y; Galvani, Alison P; Krug, Robert M; Cowling, Benjamin John; Meyers, Lauren A.
Afiliación
  • Du Z; WHO Collaborating Center for Infectious Disease Epidemiology and Control, School of Public Health, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.
  • Wang L; Laboratory of Data Discovery for Health Limited, Hong Kong, China.
  • Bai Y; Department of Genetics, University of Cambridge, Cambridge, United Kingdom.
  • Liu Y; WHO Collaborating Center for Infectious Disease Epidemiology and Control, School of Public Health, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.
  • Lau EHY; Laboratory of Data Discovery for Health Limited, Hong Kong, China.
  • Galvani AP; WHO Collaborating Center for Infectious Disease Epidemiology and Control, School of Public Health, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.
  • Krug RM; WHO Collaborating Center for Infectious Disease Epidemiology and Control, School of Public Health, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.
  • Cowling BJ; Laboratory of Data Discovery for Health Limited, Hong Kong, China.
  • Meyers LA; Center for Infectious Disease Modeling and Analysis, Yale School of Public Health, New Haven, United States.
Elife ; 132024 Apr 16.
Article en En | MEDLINE | ID: mdl-38622989
ABSTRACT
Paxlovid, a SARS-CoV-2 antiviral, not only prevents severe illness but also curtails viral shedding, lowering transmission risks from treated patients. By fitting a mathematical model of within-host Omicron viral dynamics to electronic health records data from 208 hospitalized patients in Hong Kong, we estimate that Paxlovid can inhibit over 90% of viral replication. However, its effectiveness critically depends on the timing of treatment. If treatment is initiated three days after symptoms first appear, we estimate a 17% chance of a post-treatment viral rebound and a 12% (95% CI 0-16%) reduction in overall infectiousness for non-rebound cases. Earlier treatment significantly elevates the risk of rebound without further reducing infectiousness, whereas starting beyond five days reduces its efficacy in curbing peak viral shedding. Among the 104 patients who received Paxlovid, 62% began treatment within an optimal three-to-five-day day window after symptoms appeared. Our findings indicate that broader global access to Paxlovid, coupled with appropriately timed treatment, can mitigate the severity and transmission of SARS-Cov-2.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Antivirales / SARS-CoV-2 / COVID-19 / Tratamiento Farmacológico de COVID-19 Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Elife Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Antivirales / SARS-CoV-2 / COVID-19 / Tratamiento Farmacológico de COVID-19 Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Elife Año: 2024 Tipo del documento: Article País de afiliación: China