Nirmatrelvir/ritonavir and remdesivir against symptomatic treatment in high-risk COVID-19 outpatients to prevent hospitalization or death during the Omicron era: a propensity score-matched study.

IF 3.8 Q2 INFECTIOUS DISEASES
Therapeutic Advances in Infectious Disease Pub Date : 2024-03-26 eCollection Date: 2024-01-01 DOI:10.1177/20499361241236582
Sandra Rajme-López, Bernardo A Martinez-Guerra, Carla M Román-Montes, Karla M Tamez-Torres, Andrea C Tello-Mercado, Karen M Tepo-Ponce, Zurisadai Segura-Ortíz, Abigail López-Aguirre, Orianlid Del Rocío Gutiérrez-Mazariegos, Oswaldo Lazcano-Delgadillo, Rafael Nares-López, María F González-Lara, David Kershenobich-Stalnikowitz, José Sifuentes-Osornio, Alfredo Ponce-de-León, Guillermo M Ruíz-Palacios
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引用次数: 0

Abstract

Background: Even though worldwide death rates from coronavirus disease 2019 (COVID-19) have decreased, the threat of disease progression and death for high-risk groups continues. Few direct comparisons between the available severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antivirals have been made.

Objective: We aimed to compare two SARS-CoV-2 antivirals (nirmatrelvir/ritonavir and remdesivir) against all-cause hospitalization or death.

Design: This is a propensity score-matched cohort study.

Methods: We included all high-risk outpatients with COVID-19 in a tertiary referral center in Mexico City from 1 January 2022 to 31 July 2023. The primary outcome was all-cause hospitalization or death 28 days after symptom onset. The secondary outcome was COVID-19-associated hospitalization or death 28 days after symptom onset. Logistic regression analysis for characteristics associated with the primary outcome and a multi-group comparison with Kaplan-Meier survival estimates were performed.

Results: Of 1566 patients analyzed, 783 did not receive antiviral treatment, 451 received remdesivir, and 332 received nirmatrelvir/ritonavir. The median age was 60 years (interquartile range: 46-72), 62.5% were female and 97.8% had at least one comorbidity. The use of nirmatrelvir/ritonavir was associated with an absolute risk reduction of 8.8% and a relative risk reduction of 90% for all-cause hospitalization or death. The use of remdesivir was associated with an absolute risk reduction of 6.4% and a relative risk reduction of 66% for all-cause hospitalization or death. In multivariable analysis, both antivirals reduced the odds of 28-day all-cause hospitalization or death [nirmatrelvir/ritonavir odds ratio (OR) 0.08 - 95% confidence interval (CI): 0.03-0.19, remdesivir OR 0.29 - 95% CI: 0.18-0.45].

Conclusion: In high-risk COVID-19 outpatients, early antiviral treatment with nirmatrelvir/ritonavir or remdesivir was associated with lower 28-day all-cause hospitalization or death.

尼马瑞韦/利托那韦和雷米地韦对高危 COVID-19 门诊患者进行对症治疗,以预防 Omicron 时代的住院或死亡:倾向得分匹配研究。
背景:尽管2019年冠状病毒病(COVID-19)的全球死亡率已经下降,但疾病进展和高危人群死亡的威胁仍在继续。很少有人对现有的严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)抗病毒药物进行直接比较:我们旨在比较两种 SARS-CoV-2 抗病毒药物(尼尔马特韦/利托那韦和雷米地韦)对全因住院或死亡的影响:这是一项倾向得分匹配队列研究:我们纳入了2022年1月1日至2023年7月31日期间墨西哥城一家三级转诊中心的所有COVID-19高危门诊患者。主要结果是症状出现 28 天后全因住院或死亡。次要结果是症状出现 28 天后与 COVID-19 相关的住院或死亡。研究人员对与主要结果相关的特征进行了逻辑回归分析,并对卡普兰-梅耶生存率进行了多组比较:在分析的 1566 名患者中,783 人未接受抗病毒治疗,451 人接受了雷米替韦治疗,332 人接受了尼马替韦/利托那韦治疗。中位年龄为 60 岁(四分位间范围:46-72 岁),62.5% 为女性,97.8% 至少患有一种合并症。使用尼马瑞韦/利托那韦可使全因住院或死亡的绝对风险降低 8.8%,相对风险降低 90%。使用雷米替韦可使全因住院或死亡的绝对风险降低 6.4%,相对风险降低 66%。在多变量分析中,两种抗病毒药物都降低了28天全因住院或死亡的几率[尼马瑞韦/利托那韦的几率比(OR)为0.08 - 95%置信区间(CI):0.03-0.19,雷米地韦的几率比为0.29 - 95%置信区间(CI):0.18-0.45]:结论:在COVID-19高危门诊患者中,早期使用尼马瑞韦/利托那韦或雷米替韦进行抗病毒治疗与降低28天全因住院或死亡相关。
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
CiteScore
5.30
自引率
8.80%
发文量
64
审稿时长
9 weeks
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