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Nirmatrelvir‐ritonavir therapy and COVID‐19 vaccination improve clinical outcomes of SARS‐CoV‐2 Omicron variant infection

To evaluate the effect of Nirmatrelvir‐ritonavir therapy and coronavirus disease 2019 (COVID‐19) vaccination on clinical outcomes of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) Omicron infection, we retrospectively analyzed the clinical data of 762 adult patients with confirmed Omic...

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Autores principales: Qi, Tangkai, Jin, Yinpeng, Wang, He, Liao, Yixin, Liu, Tiefu, Mao, Enqiang, Li, Feng, Li, Yinchuan, Fan, Xiaohong, Ling, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107277/
https://www.ncbi.nlm.nih.gov/pubmed/36651302
http://dx.doi.org/10.1002/jmv.28497
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author Qi, Tangkai
Jin, Yinpeng
Wang, He
Liao, Yixin
Liu, Tiefu
Mao, Enqiang
Li, Feng
Li, Yinchuan
Fan, Xiaohong
Ling, Yun
author_facet Qi, Tangkai
Jin, Yinpeng
Wang, He
Liao, Yixin
Liu, Tiefu
Mao, Enqiang
Li, Feng
Li, Yinchuan
Fan, Xiaohong
Ling, Yun
author_sort Qi, Tangkai
collection PubMed
description To evaluate the effect of Nirmatrelvir‐ritonavir therapy and coronavirus disease 2019 (COVID‐19) vaccination on clinical outcomes of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) Omicron infection, we retrospectively analyzed the clinical data of 762 adult patients with confirmed Omicron BA2.2 variant infection, of them 488 patients received standard therapy and 274 patients received Nirmatrelvir‐ritonavir therapy. Subjects were matched by propensity score matching using R language, the baseline factors were balanced by the nearest‐neighbor matching method and were compared, together with the factors including progression to severe/critical disease, viral clearance time, length of hospital stay, and virological rebound of SARS‐CoV‐2 infection. Nirmatrelvir‐ritonavir therapy significantly accelerated viral clearance at Days 14 and  28 during hospitalization, but it had no impact on disease progression, length of hospital stay, or infection rebound. In contrast, COVID‐19 vaccination before admission was positively correlated with the viral clearance rate and negatively correlated with disease progression in a dose‐dependent way. COVID‐19 vaccination reduced the probability of infection rebound. Other factors such as the number of comorbidities, pneumonia on‐admission, and high D2 levels were positively correlated with disease progression. Our study strongly recommended booster COVID‐19 vaccination for the elderly population, particularly patients with comorbidities to prevent critical disease.
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spelling pubmed-101072772023-04-18 Nirmatrelvir‐ritonavir therapy and COVID‐19 vaccination improve clinical outcomes of SARS‐CoV‐2 Omicron variant infection Qi, Tangkai Jin, Yinpeng Wang, He Liao, Yixin Liu, Tiefu Mao, Enqiang Li, Feng Li, Yinchuan Fan, Xiaohong Ling, Yun J Med Virol Research Articles To evaluate the effect of Nirmatrelvir‐ritonavir therapy and coronavirus disease 2019 (COVID‐19) vaccination on clinical outcomes of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) Omicron infection, we retrospectively analyzed the clinical data of 762 adult patients with confirmed Omicron BA2.2 variant infection, of them 488 patients received standard therapy and 274 patients received Nirmatrelvir‐ritonavir therapy. Subjects were matched by propensity score matching using R language, the baseline factors were balanced by the nearest‐neighbor matching method and were compared, together with the factors including progression to severe/critical disease, viral clearance time, length of hospital stay, and virological rebound of SARS‐CoV‐2 infection. Nirmatrelvir‐ritonavir therapy significantly accelerated viral clearance at Days 14 and  28 during hospitalization, but it had no impact on disease progression, length of hospital stay, or infection rebound. In contrast, COVID‐19 vaccination before admission was positively correlated with the viral clearance rate and negatively correlated with disease progression in a dose‐dependent way. COVID‐19 vaccination reduced the probability of infection rebound. Other factors such as the number of comorbidities, pneumonia on‐admission, and high D2 levels were positively correlated with disease progression. Our study strongly recommended booster COVID‐19 vaccination for the elderly population, particularly patients with comorbidities to prevent critical disease. John Wiley and Sons Inc. 2023-01-26 2023-02 /pmc/articles/PMC10107277/ /pubmed/36651302 http://dx.doi.org/10.1002/jmv.28497 Text en © 2023 The Authors. Journal of Medical Virology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Qi, Tangkai
Jin, Yinpeng
Wang, He
Liao, Yixin
Liu, Tiefu
Mao, Enqiang
Li, Feng
Li, Yinchuan
Fan, Xiaohong
Ling, Yun
Nirmatrelvir‐ritonavir therapy and COVID‐19 vaccination improve clinical outcomes of SARS‐CoV‐2 Omicron variant infection
title Nirmatrelvir‐ritonavir therapy and COVID‐19 vaccination improve clinical outcomes of SARS‐CoV‐2 Omicron variant infection
title_full Nirmatrelvir‐ritonavir therapy and COVID‐19 vaccination improve clinical outcomes of SARS‐CoV‐2 Omicron variant infection
title_fullStr Nirmatrelvir‐ritonavir therapy and COVID‐19 vaccination improve clinical outcomes of SARS‐CoV‐2 Omicron variant infection
title_full_unstemmed Nirmatrelvir‐ritonavir therapy and COVID‐19 vaccination improve clinical outcomes of SARS‐CoV‐2 Omicron variant infection
title_short Nirmatrelvir‐ritonavir therapy and COVID‐19 vaccination improve clinical outcomes of SARS‐CoV‐2 Omicron variant infection
title_sort nirmatrelvir‐ritonavir therapy and covid‐19 vaccination improve clinical outcomes of sars‐cov‐2 omicron variant infection
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10107277/
https://www.ncbi.nlm.nih.gov/pubmed/36651302
http://dx.doi.org/10.1002/jmv.28497
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