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Early Clinical Experience with Molnupiravir for Mild to Moderate Breakthrough COVID-19 among Fully Vaccinated Patients at Risk for Disease Progression
Information on the efficacy and safety of molnupiravir in daily clinical practice is very scarce. We aimed to describe the clinical characteristics and outcomes of fully vaccinated patients with mild to moderate breakthrough COVID-19 treated with molnupiravir between January 2022 and February 2022....
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9318911/ https://www.ncbi.nlm.nih.gov/pubmed/35891305 http://dx.doi.org/10.3390/vaccines10071141 |
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author | Vena, Antonio Traman, Luca Bavastro, Martina Limongelli, Alessandro Dentone, Chiara Magnè, Federica Giacobbe, Daniele Roberto Mikulska, Malgorzata Taramasso, Lucia Di Biagio, Antonio Bassetti, Matteo |
author_facet | Vena, Antonio Traman, Luca Bavastro, Martina Limongelli, Alessandro Dentone, Chiara Magnè, Federica Giacobbe, Daniele Roberto Mikulska, Malgorzata Taramasso, Lucia Di Biagio, Antonio Bassetti, Matteo |
author_sort | Vena, Antonio |
collection | PubMed |
description | Information on the efficacy and safety of molnupiravir in daily clinical practice is very scarce. We aimed to describe the clinical characteristics and outcomes of fully vaccinated patients with mild to moderate breakthrough COVID-19 treated with molnupiravir between January 2022 and February 2022. Overall, 145 patients were enrolled. Their median age was 71.0 years, and 60.7% were males. The most common underlying condition was a severe cardiovascular disease (37.2%), followed by primary or acquired immunodeficiency (22.8%), and oncological/onco-hematological disease in the active phase (22.1%). At 30 days after breakthrough COVID-19 diagnosis, only 4 out of 145 patients (2.7%) required hospital admission. No patients developed severe COVID-19, were admitted to the ICU, or died during the follow-up period. Adverse events, mild in intensity, occurred in 2 patients (1.4%). Our results support the current evidence establishing positive clinical and safety outcomes of molnupiravir in fully vaccinated patients with mild or moderate breakthrough COVID-19. |
format | Online Article Text |
id | pubmed-9318911 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93189112022-07-27 Early Clinical Experience with Molnupiravir for Mild to Moderate Breakthrough COVID-19 among Fully Vaccinated Patients at Risk for Disease Progression Vena, Antonio Traman, Luca Bavastro, Martina Limongelli, Alessandro Dentone, Chiara Magnè, Federica Giacobbe, Daniele Roberto Mikulska, Malgorzata Taramasso, Lucia Di Biagio, Antonio Bassetti, Matteo Vaccines (Basel) Communication Information on the efficacy and safety of molnupiravir in daily clinical practice is very scarce. We aimed to describe the clinical characteristics and outcomes of fully vaccinated patients with mild to moderate breakthrough COVID-19 treated with molnupiravir between January 2022 and February 2022. Overall, 145 patients were enrolled. Their median age was 71.0 years, and 60.7% were males. The most common underlying condition was a severe cardiovascular disease (37.2%), followed by primary or acquired immunodeficiency (22.8%), and oncological/onco-hematological disease in the active phase (22.1%). At 30 days after breakthrough COVID-19 diagnosis, only 4 out of 145 patients (2.7%) required hospital admission. No patients developed severe COVID-19, were admitted to the ICU, or died during the follow-up period. Adverse events, mild in intensity, occurred in 2 patients (1.4%). Our results support the current evidence establishing positive clinical and safety outcomes of molnupiravir in fully vaccinated patients with mild or moderate breakthrough COVID-19. MDPI 2022-07-18 /pmc/articles/PMC9318911/ /pubmed/35891305 http://dx.doi.org/10.3390/vaccines10071141 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Vena, Antonio Traman, Luca Bavastro, Martina Limongelli, Alessandro Dentone, Chiara Magnè, Federica Giacobbe, Daniele Roberto Mikulska, Malgorzata Taramasso, Lucia Di Biagio, Antonio Bassetti, Matteo Early Clinical Experience with Molnupiravir for Mild to Moderate Breakthrough COVID-19 among Fully Vaccinated Patients at Risk for Disease Progression |
title | Early Clinical Experience with Molnupiravir for Mild to Moderate Breakthrough COVID-19 among Fully Vaccinated Patients at Risk for Disease Progression |
title_full | Early Clinical Experience with Molnupiravir for Mild to Moderate Breakthrough COVID-19 among Fully Vaccinated Patients at Risk for Disease Progression |
title_fullStr | Early Clinical Experience with Molnupiravir for Mild to Moderate Breakthrough COVID-19 among Fully Vaccinated Patients at Risk for Disease Progression |
title_full_unstemmed | Early Clinical Experience with Molnupiravir for Mild to Moderate Breakthrough COVID-19 among Fully Vaccinated Patients at Risk for Disease Progression |
title_short | Early Clinical Experience with Molnupiravir for Mild to Moderate Breakthrough COVID-19 among Fully Vaccinated Patients at Risk for Disease Progression |
title_sort | early clinical experience with molnupiravir for mild to moderate breakthrough covid-19 among fully vaccinated patients at risk for disease progression |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9318911/ https://www.ncbi.nlm.nih.gov/pubmed/35891305 http://dx.doi.org/10.3390/vaccines10071141 |
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