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COVID-19 疫苗接种改变了奈玛特韦-利托那韦对急性后死亡率和再住院的影响:一项回顾性队列研究。

COVID-19 vaccination modified the effect of nirmatrelvir-ritonavir on post-acute mortality and rehospitalization: a retrospective cohort study.

机构信息

School of Public Health and Primary Care, The Chinese University of Hong Kong, Hong Kong, China.

Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.

出版信息

Emerg Microbes Infect. 2024 Dec;13(1):2421397. doi: 10.1080/22221751.2024.2421397. Epub 2024 Nov 4.

DOI:10.1080/22221751.2024.2421397
PMID:39497519
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11539398/
Abstract

While previous research examined coronavirus disease 2019 (COVID-19) antiviral-vaccine interactions through exploratory subgroup analysis, none specifically designed for examining this interaction or its impact on post-acute outcomes. This study examined the interaction between nirmatrelvir-ritonavir and complete COVID-19 vaccination on reducing the risk of post-acute outcomes among COVID-19 patients. We followed COVID-19 patients hospitalized between 11 March 2022 and 10 October 2023, until 31 October 2023 in Hong Kong. Exposure groups were based on nirmatrelvir-ritonavir usage and vaccination status (fully or not fully vaccinated). Post-acute death and all-cause rehospitalization were the study outcomes. Propensity score weighting was applied to balance covariates among exposure groups, including age, sex, Charlson Comorbidity Index, and concomitant treatments. Multiplicative and additive interactions between nirmatrelvir-ritonavir and vaccination status were assessed. A total of 50,438 COVID-19 patients were included in this study and arranged into four exposure groups. Significant additive interaction on post-acute rehospitalization was observed (relative excess risk, 0.10; 95% CI, 0.02-0.19; -value, 0.018; attributable proportion, 0.07; 95% CI, 0.01-0.12; -value, 0.017; synergy index, 1.26; 95% CI, 1.02-1.55; -value, 0.032). The interaction on post-acute mortality was marginally significant. In the subgroup analysis, the interaction effect is more pronounced in older adults, female, and CoronaVac recipients. In conclusion, our study demonstrated an additive interaction between nirmatrelvir-ritonavir and complete vaccination on post-acute outcomes, suggesting greater long-term benefits of the antiviral for fully vaccinated individuals compared to not fully vaccinated patients.

摘要

虽然之前的研究通过探索性亚组分析检查了 2019 年冠状病毒病(COVID-19)抗病毒疫苗的相互作用,但没有专门设计用于检查这种相互作用或其对急性后结局的影响。本研究检查了尼马曲韦-利托那韦和完全 COVID-19 疫苗接种在降低 COVID-19 患者急性后结局风险方面的相互作用。我们对 2022 年 3 月 11 日至 2023 年 10 月 10 日期间在香港住院的 COVID-19 患者进行了随访,直至 2023 年 10 月 31 日。暴露组基于尼马曲韦-利托那韦的使用情况和疫苗接种状态(完全或不完全接种)。急性后死亡和全因再入院是本研究的结果。采用倾向评分加权法平衡暴露组中的协变量,包括年龄、性别、Charlson 合并症指数和伴随治疗。评估了尼马曲韦-利托那韦和疫苗接种状态之间的乘法和加法相互作用。本研究共纳入 50438 例 COVID-19 患者,分为四组暴露组。观察到急性后再入院存在显著的加法相互作用(相对超额风险,0.10;95%CI,0.02-0.19;-值,0.018;归因比例,0.07;95%CI,0.01-0.12;-值,0.017;协同指数,1.26;95%CI,1.02-1.55;-值,0.032)。急性后死亡率的相互作用具有边缘统计学意义。在亚组分析中,这种相互作用在老年人、女性和接种科兴疫苗的人群中更为明显。总之,我们的研究表明,尼马曲韦-利托那韦和完全疫苗接种之间存在急性后结局的加法相互作用,这表明与不完全接种的患者相比,抗病毒药物对完全接种的个体具有更大的长期益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/314e/11539398/17549254a486/TEMI_A_2421397_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/314e/11539398/9a37561e87f2/TEMI_A_2421397_F0001_OB.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/314e/11539398/17549254a486/TEMI_A_2421397_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/314e/11539398/9a37561e87f2/TEMI_A_2421397_F0001_OB.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/314e/11539398/17549254a486/TEMI_A_2421397_F0002_OC.jpg

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