Nirmatrelvir/ritonavir prescription and the risk of hospitalization and death in COVID-19 outpatients

IF 0.9 Q4 PRIMARY HEALTH CARE
H.R. Vargas-Sánchez , J.C. Tomás-López , E. Guzmán-Medina , A. Alarcón-López , E. Krug-Llamas , E. Arizmendi-Uribe , H. Domínguez-Zárate , J.E. Fernández-Gárate , I.J. Ascencio-Montiel
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引用次数: 0

Abstract

Objective

The nirmatrelvir/ritonavir is an oral combination of antiviral drugs used to treat the COVID-19. In this study we evaluated the risk of hospitalization and death, comparing COVID-19 patients who received and did not receive ambulatory nirmatrelvir/ritonavir prescription.

Material and methods

A two-group comparative study was carried out using data from the Mexican Institute of Social Security medical information systems. We analyzed of 83,348 ambulatory patients aged 18 years old and over and with laboratory confirmed SARS-CoV-2 infection during the period from September 12th, 2022, to September 30th, 2023. Of them, 27,437 received nirmatrelvir/ritonavir prescription (32.9%) and 55,911 did not (67.1%). We compared the 60-day COVID-19 related hospitalization and all-cause death risk among groups using a multivariate Poisson regression model.

Results

The 60-day COVID-19 related hospitalization and all-cause death combined incidence was 0.13% in the patients who received nirmatrelvir/ritonavir and 0.26% among the cases who did not receive the prescription. In the multivariate model, after adjusting for age, sex, and previous medical conditions such as chronic kidney disease, chronic obstructive pulmonary disease and cardiovascular disease, the nirmatrelvir/ritonavir prescription was associated with a decrease in 60-day hospitalization and death, with an adjusted risk ratio of 0.52 (95% confidence interval from 0.36 to 0.75).

Conclusions

Our data supports that nirmatrelvir/ritonavir prescription is associated with a risk reduction of 60-day COVID-19 related hospitalization and death, in outpatients with COVID-19.
尼马特瑞韦/利托那韦处方与COVID-19门诊患者住院和死亡风险
目的尼马特利韦/利托那韦是一种用于治疗COVID-19的口服抗病毒药物组合。在这项研究中,我们评估了住院和死亡的风险,比较了接受和未接受尼马特里韦/利托那韦门诊处方的COVID-19患者。材料与方法采用墨西哥社会保障医疗信息系统研究所的数据进行两组比较研究。我们分析了2022年9月12日至2023年9月30日期间18岁及以上实验室确诊的SARS-CoV-2感染的83348例门诊患者。其中,接受尼马特瑞韦/利托那韦处方的有27437人(32.9%),未接受处方的有55911人(67.1%)。我们使用多变量泊松回归模型比较各组60天COVID-19相关住院和全因死亡风险。结果接受尼马替韦/利托那韦治疗的患者与COVID-19相关的60天住院和全因死亡的综合发生率为0.13%,未接受处方治疗的患者为0.26%。在多变量模型中,在调整了年龄、性别和既往医疗状况(如慢性肾病、慢性阻塞性肺病和心血管疾病)后,尼马特利韦/利托那韦处方与60天住院和死亡减少相关,调整后的风险比为0.52(95%置信区间为0.36 ~ 0.75)。结论我们的数据支持,在COVID-19门诊患者中,尼马特利韦/利托那韦处方与60天COVID-19相关住院和死亡风险降低相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medicina de Familia-SEMERGEN
Medicina de Familia-SEMERGEN PRIMARY HEALTH CARE-
CiteScore
1.40
自引率
18.20%
发文量
83
审稿时长
39 days
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