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奈玛特韦-利托那韦和莫努匹拉韦在非住院COVID-19成年患者中的真实世界疗效:一项基于人群的回顾性队列研究。

Real-world effectiveness of nirmatrelvir-ritonavir and molnupiravir in non-hospitalized adults with COVID-19: a population-based, retrospective cohort study.

作者信息

Jorda Anselm, Ensle Dominik, Eser Hubert, Glötzl Florentin, Riedl Benjamin, Szell Marton, Valipour Arschang, Zoufaly Alexander, Wenisch Christoph, Haider Doris, Burgmann Heinz, Thalhammer Florian, Götzinger Florian, Jilma Bernd, Ristl Robin, Karnthaler Ursula, Zeitlinger Markus

机构信息

Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.

Municipal Department for Public Health Services of the City of Vienna, Vienna, Austria.

出版信息

Clin Microbiol Infect. 2025 Mar;31(3):451-458. doi: 10.1016/j.cmi.2024.10.026. Epub 2024 Nov 4.

Abstract

OBJECTIVES

The real-world effectiveness of the oral antivirals nirmatrelvir-ritonavir and molnupiravir against the SARS-CoV-2 Omicron variant remains uncertain. We aimed to estimate their effectiveness in non-hospitalized adults with COVID-19.

METHODS

This retrospective cohort study used data from the Municipal Department for Public Health Services of Vienna, Austria, to identify non-hospitalized adults with confirmed SARS-CoV-2 infection between January 2022 and May 2023. Nirmatrelvir-ritonavir users were compared with untreated controls and molnupiravir users with untreated controls by calculating adjusted risk differences (aRDs) using a covariate-adjusted logistic regression model with inverse probability weighting. Outcomes were hospitalization and all-cause death within 28 days.

RESULTS

We identified 113 399 eligible cases (90 481 untreated controls, 12 166 nirmatrelvir-ritonavir users, and 10 752 molnupiravir users). Over 96% of the patients were immunized by previous infection or vaccination. In the nirmatrelvir-ritonavir analysis, the estimated risk of hospitalization was 0.57% (95% CI, 0.35-0.78) in nirmatrelvir-ritonavir users and 1.09% (95% CI, 0.86-1.32) in untreated controls (aRD, -0.53%; 95% CI, -0.77 to -0.28). The estimated risk of death was 0.0% (95% CI, 0.0-0.0) in nirmatrelvir-ritonavir users and 0.13% (95% CI, 0.08-0.18) in untreated controls (aRD, -0.13%, 95% CI, -0.18 to -0.08). The number needed to treat to prevent hospitalization and death was 190 (95% CI, 130-356) and 792 (95% CI, 571-1289), respectively. These statistically significant aRDs were restricted to the subgroup of patients ≥60 years. In the molnupiravir analysis, the estimated risk of hospitalization was 1.36% (95% CI, 0.95-1.77) in molnupiravir users and 1.16% (95% CI, 0.93-1.39) in untreated controls (aRD, 0.2%; 95% CI, -0.08 to 0.49). The estimated risk of death was 0.12% (95% CI, 0.01-0.23) in molnupiravir users and 0.14% (95% CI, 0.06-0.21) in untreated controls (aRD, -0.01%; 95% CI, -0.08 to -0.06).

DISCUSSION

Among outpatients aged ≥60 years with COVID-19 in an Omicron-dominated era, treatment with nirmatrelvir-ritonavir was associated with a lower risk of hospitalization and all-cause death within 28 days, albeit with wide CIs and high numbers needed to treat. This finding was not observed in molnupiravir users and younger nirmatrelvir-ritonavir users.

摘要

目的

口服抗病毒药物奈玛特韦-利托那韦和莫努匹韦针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)奥密克戎变异株的实际疗效仍不确定。我们旨在评估它们在非住院成人新冠病毒感染者中的疗效。

方法

这项回顾性队列研究使用了奥地利维也纳市公共卫生服务部的数据,以确定2022年1月至2023年5月期间确诊感染SARS-CoV-2的非住院成人。通过使用具有逆概率加权的协变量调整逻辑回归模型计算调整风险差异(aRDs),将使用奈玛特韦-利托那韦的患者与未治疗的对照组进行比较,以及将使用莫努匹韦的患者与未治疗的对照组进行比较。观察的结局为28天内的住院治疗和全因死亡。

结果

我们确定了113399例符合条件的病例(90481例未治疗的对照组、12166例使用奈玛特韦-利托那韦的患者和10752例使用莫努匹韦的患者)。超过96%的患者曾因既往感染或接种疫苗而获得免疫。在奈玛特韦-利托那韦的分析中,使用奈玛特韦-利托那韦的患者住院风险估计为0.57%(95%CI,0.35-0.78),未治疗对照组为1.09%(95%CI,0.86-1.32)(aRD,-0.53%;95%CI,-0.77至-0.28)。使用奈玛特韦-利托那韦的患者死亡风险估计为0.0%(95%CI,0.0-0.0),未治疗对照组为0.13%(95%CI,0.08-0.18)(aRD,-0.13%,95%CI,-0.18至-0.08)。预防住院和死亡所需治疗的人数分别为190(95%CI,130-356)和792(95%CI,571-1289)。这些具有统计学意义的aRDs仅限于年龄≥60岁的患者亚组。在莫努匹韦的分析中,使用莫努匹韦的患者住院风险估计为1.36%(95%CI,0.95-1.77),未治疗对照组为1.16%(95%CI,0.93-1.39)(aRD,0.2%;95%CI,-0.08至0.49)。使用莫努匹韦的患者死亡风险估计为0.12%(95%CI,0.01-0.23),未治疗对照组为0.14%(95%CI,0.06-0.21)(aRD,-0.01%;95%CI,-0.08至-0.06)。

讨论

在奥密克戎为主的时代,年龄≥60岁的门诊新冠病毒感染者中,使用奈玛特韦-利托那韦治疗与28天内较低的住院风险和全因死亡风险相关,尽管置信区间较宽且所需治疗人数较多。这一发现未在使用莫努匹韦的患者以及年龄较轻的使用奈玛特韦-利托那韦的患者中观察到。

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