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Association of Molnupiravir and Nirmatrelvir-Ritonavir with reduced mortality and sepsis in hospitalized omicron patients: a territory-wide study

This study evaluates the association between antivirals (Molnupiravir and Nirmatrelvir-Ritonavir) and all-cause and respiratory mortality and organ dysfunction among high-risk COVID-19 patients during an Omicron outbreak. Two cohorts, Nirmatrelvir-Ritonavir versus control and Molnupiravir versus con...

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Autores principales: Wai, Abraham Ka-chung, Lee, Teddy Tai-loy, Chan, Sunny Ching-long, Chan, Crystal Ying, Yip, Edmond Tsz-fung, Luk, Luke Yik-fung, Ho, Joshua Wing-kei, So, Kevin Wang-leong, Tsui, Omar Wai-kiu, Lam, Man-lok, Lee, Shi-yeow, Yamamoto, Tafu, Tong, Chak-kwan, Wong, Man-sing, Wong, Eliza Lai-yi, Rainer, Timothy Hudson
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183691/
https://www.ncbi.nlm.nih.gov/pubmed/37188726
http://dx.doi.org/10.1038/s41598-023-35068-w
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author Wai, Abraham Ka-chung
Lee, Teddy Tai-loy
Chan, Sunny Ching-long
Chan, Crystal Ying
Yip, Edmond Tsz-fung
Luk, Luke Yik-fung
Ho, Joshua Wing-kei
So, Kevin Wang-leong
Tsui, Omar Wai-kiu
Lam, Man-lok
Lee, Shi-yeow
Yamamoto, Tafu
Tong, Chak-kwan
Wong, Man-sing
Wong, Eliza Lai-yi
Rainer, Timothy Hudson
author_facet Wai, Abraham Ka-chung
Lee, Teddy Tai-loy
Chan, Sunny Ching-long
Chan, Crystal Ying
Yip, Edmond Tsz-fung
Luk, Luke Yik-fung
Ho, Joshua Wing-kei
So, Kevin Wang-leong
Tsui, Omar Wai-kiu
Lam, Man-lok
Lee, Shi-yeow
Yamamoto, Tafu
Tong, Chak-kwan
Wong, Man-sing
Wong, Eliza Lai-yi
Rainer, Timothy Hudson
author_sort Wai, Abraham Ka-chung
collection PubMed
description This study evaluates the association between antivirals (Molnupiravir and Nirmatrelvir-Ritonavir) and all-cause and respiratory mortality and organ dysfunction among high-risk COVID-19 patients during an Omicron outbreak. Two cohorts, Nirmatrelvir-Ritonavir versus control and Molnupiravir versus control, were constructed with inverse probability treatment weighting to balance baseline characteristics. Cox proportional hazards models evaluated the association of their use with all-cause mortality, respiratory mortality, and all-cause sepsis (a composite of circulatory shock, respiratory failure, acute liver injury, coagulopathy, and acute liver impairment). Patients recruited were hospitalized and diagnosed with the COVID-19 Omicron variant between February 22, 2022 and April 15, 2022, and followed up until May 15, 2022. The study included 17,704 patients. There were 4.67 and 22.7 total mortalities per 1000 person-days in the Nirmatrelvir-Ritonavir and control groups respectively before adjustment (weighted incidence rate ratio, − 18.1 [95% CI − 23.0 to − 13.2]; hazard ratio, 0.18 [95% CI, 0.11–0.29]). There were 6.64 and 25.9 total mortalities per 1000 person-days in the Molnupiravir and control groups respectively before adjustment (weighted incidence rate ratio per 1000 person-days, − 19.3 [95% CI − 22.6 to − 15.9]; hazard ratio, 0.23 [95% CI 0.18–0.30]). In all-cause sepsis, there were 13.7 and 35.4 organ dysfunction events per 1000 person-days in the Nirmatrelvir-Ritonavir and control groups respectively before adjustment (weighted incidence rate ratio per 1000 person-days, − 21.7 [95% CI − 26.3 to − 17.1]; hazard ratio, 0.44 [95% CI 0.38–0.52]). There were 23.7 and 40.8 organ dysfunction events in the Molnupiravir and control groups respectively before adjustment (weighted incidence ratio per 1000 person-days, − 17.1 [95% CI, − 20.6 to − 13.6]; hazard ratio, 0.63 [95% CI 0.58–0.69]). Among COVID-19 hospitalized patients, use of either Nirmatrelvir-Ritonavir or Molnupiravir compared with no antiviral use was associated with a significantly lower incidence of 28-days all-cause and respiratory mortality and sepsis.
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spelling pubmed-101836912023-05-16 Association of Molnupiravir and Nirmatrelvir-Ritonavir with reduced mortality and sepsis in hospitalized omicron patients: a territory-wide study Wai, Abraham Ka-chung Lee, Teddy Tai-loy Chan, Sunny Ching-long Chan, Crystal Ying Yip, Edmond Tsz-fung Luk, Luke Yik-fung Ho, Joshua Wing-kei So, Kevin Wang-leong Tsui, Omar Wai-kiu Lam, Man-lok Lee, Shi-yeow Yamamoto, Tafu Tong, Chak-kwan Wong, Man-sing Wong, Eliza Lai-yi Rainer, Timothy Hudson Sci Rep Article This study evaluates the association between antivirals (Molnupiravir and Nirmatrelvir-Ritonavir) and all-cause and respiratory mortality and organ dysfunction among high-risk COVID-19 patients during an Omicron outbreak. Two cohorts, Nirmatrelvir-Ritonavir versus control and Molnupiravir versus control, were constructed with inverse probability treatment weighting to balance baseline characteristics. Cox proportional hazards models evaluated the association of their use with all-cause mortality, respiratory mortality, and all-cause sepsis (a composite of circulatory shock, respiratory failure, acute liver injury, coagulopathy, and acute liver impairment). Patients recruited were hospitalized and diagnosed with the COVID-19 Omicron variant between February 22, 2022 and April 15, 2022, and followed up until May 15, 2022. The study included 17,704 patients. There were 4.67 and 22.7 total mortalities per 1000 person-days in the Nirmatrelvir-Ritonavir and control groups respectively before adjustment (weighted incidence rate ratio, − 18.1 [95% CI − 23.0 to − 13.2]; hazard ratio, 0.18 [95% CI, 0.11–0.29]). There were 6.64 and 25.9 total mortalities per 1000 person-days in the Molnupiravir and control groups respectively before adjustment (weighted incidence rate ratio per 1000 person-days, − 19.3 [95% CI − 22.6 to − 15.9]; hazard ratio, 0.23 [95% CI 0.18–0.30]). In all-cause sepsis, there were 13.7 and 35.4 organ dysfunction events per 1000 person-days in the Nirmatrelvir-Ritonavir and control groups respectively before adjustment (weighted incidence rate ratio per 1000 person-days, − 21.7 [95% CI − 26.3 to − 17.1]; hazard ratio, 0.44 [95% CI 0.38–0.52]). There were 23.7 and 40.8 organ dysfunction events in the Molnupiravir and control groups respectively before adjustment (weighted incidence ratio per 1000 person-days, − 17.1 [95% CI, − 20.6 to − 13.6]; hazard ratio, 0.63 [95% CI 0.58–0.69]). Among COVID-19 hospitalized patients, use of either Nirmatrelvir-Ritonavir or Molnupiravir compared with no antiviral use was associated with a significantly lower incidence of 28-days all-cause and respiratory mortality and sepsis. Nature Publishing Group UK 2023-05-15 /pmc/articles/PMC10183691/ /pubmed/37188726 http://dx.doi.org/10.1038/s41598-023-35068-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wai, Abraham Ka-chung
Lee, Teddy Tai-loy
Chan, Sunny Ching-long
Chan, Crystal Ying
Yip, Edmond Tsz-fung
Luk, Luke Yik-fung
Ho, Joshua Wing-kei
So, Kevin Wang-leong
Tsui, Omar Wai-kiu
Lam, Man-lok
Lee, Shi-yeow
Yamamoto, Tafu
Tong, Chak-kwan
Wong, Man-sing
Wong, Eliza Lai-yi
Rainer, Timothy Hudson
Association of Molnupiravir and Nirmatrelvir-Ritonavir with reduced mortality and sepsis in hospitalized omicron patients: a territory-wide study
title Association of Molnupiravir and Nirmatrelvir-Ritonavir with reduced mortality and sepsis in hospitalized omicron patients: a territory-wide study
title_full Association of Molnupiravir and Nirmatrelvir-Ritonavir with reduced mortality and sepsis in hospitalized omicron patients: a territory-wide study
title_fullStr Association of Molnupiravir and Nirmatrelvir-Ritonavir with reduced mortality and sepsis in hospitalized omicron patients: a territory-wide study
title_full_unstemmed Association of Molnupiravir and Nirmatrelvir-Ritonavir with reduced mortality and sepsis in hospitalized omicron patients: a territory-wide study
title_short Association of Molnupiravir and Nirmatrelvir-Ritonavir with reduced mortality and sepsis in hospitalized omicron patients: a territory-wide study
title_sort association of molnupiravir and nirmatrelvir-ritonavir with reduced mortality and sepsis in hospitalized omicron patients: a territory-wide study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183691/
https://www.ncbi.nlm.nih.gov/pubmed/37188726
http://dx.doi.org/10.1038/s41598-023-35068-w
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