Nirmatrelvir在保护门诊成人患者长期COVID方面的实际效果--来自RECOVER倡议的一项大规模观察性队列研究。

Fei Wang, Chengxi Zang, Haoyang Li, Dhru Khullar, Yongkang Zhang, Stephenson Strobel, Yong Chen, Marc Sala, Payal Patel, Alejandro Comellas, Andrew Wylam, Mark Weiner, Christopher Forrest, Thomas Carton, Rainu Kaushal
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引用次数: 0

摘要

Paxlovid 已被批准用于严重急性 COVID-19 疾病的高危患者。有关 Paxlovid 是否能预防 SARS-CoV-2 感染急性后遗症(PASC)或长 COVID 的证据在高风险患者中不尽相同,而在低风险患者中则缺乏。我们采用目标试验仿真框架,利用以患者为中心的临床研究网络(PCORnet)RECOVER 存储库中的电子病历,评估了在感染 SARS-CoV-2 后 5 天内进行 Paxlovid 治疗与感染后急性期(感染后 30-180 天)发生的 Long COVID 以及因任何原因住院或死亡的相关性。研究对象包括2022年3月1日至2023年2月1日期间的497,499名SARS-CoV-2阳性患者,其中165,256人在感染后5天内接受了Paxlovid治疗,307,922人未接受Paxlovid或其他COVID-19治疗。与未接受治疗组相比,Paxlovid治疗与长COVID风险降低相关,危险比(HR)为0.88(95% CI,0.87至0.89),绝对风险降低为每百人2.99例(95% CI,2.65至3.32)。帕克洛维治疗可降低急性期后的全因死亡风险(HR,0.53,95% CI 0.46至0.60;风险降低率为每百人0.23例,95% CI 0.19至0.28)和住院风险(HR,0.70,95% CI 0.68至0.73;风险降低率为每百人2.37例,95% CI 2.19至2.56)。对于没有记录风险因素的患者,相关性(HR,1.03,95% CI 0.95 至 1.11;每 100 人风险增加 0.80 例,95% CI -0.84 至 2.45)尚无定论。总体而言,在感染 SARS-CoV-2 后 5 天内接受 Paxlovid 治疗的 COVID-19 高危、非住院成年患者在急性期后发生 Long COVID 和全因住院或死亡的风险较低。然而,在低风险患者中未观察到 Paxlovid 可降低长 COVID 风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-World Effectiveness of Nirmatrelvir in Protecting Long COVID for Outpatient Adult Patients - A Large-Scale Observational Cohort Study from the RECOVER Initiative.

Paxlovid has been approved for use in patients who are at high risk for severe acute COVID-19 illness. Evidence regarding whether Paxlovid protects against Post-Acute Sequelae of SARS-CoV-2 infection (PASC), or Long COVID, is mixed in high-risk patients and lacking in low-risk patients. With a target trial emulation framework, we evaluated the association of Paxlovid treatment within 5 days of SARS-CoV-2 infection with incident Long COVID and hospitalization or death from any cause in the post-acute period (30-180 days after infection) using electronic health records from the Patient-Centered Clinical Research Networks (PCORnet) RECOVER repository. The study population included 497,499 SARS-CoV-2 positive patients between March 1, 2022, to February 1, 2023, and among which 165,256 were treated with Paxlovid within 5 days since infection and 307,922 were not treated with Paxlovid or other COVID-19 treatments. Compared with the non-treated group, Paxlovid treatment was associated with reduced risk of Long COVID with a Hazard Ratio (HR) of 0.88 (95% CI, 0.87 to 0.89) and absolute risk reduction of 2.99 events per 100 persons (95% CI, 2.65 to 3.32). Paxlovid treatment was associated with reduced risk of all-cause death (HR, 0.53, 95% CI 0.46 to 0.60; risk reduction 0.23 events per 100 persons, 95% CI 0.19 to 0.28) and hospitalization (HR, 0.70, 95% CI 0.68 to 0.73; risk reduction 2.37 events per 100 persons, 95% CI 2.19 to 2.56) in the post-acute phase. For those without documented risk factors, the associations (HR, 1.03, 95% CI 0.95 to 1.11; risk increase 0.80 events per 100 persons, 95% CI -0.84 to 2.45) were inconclusive. Overall, high-risk, nonhospitalized adult patients with COVID-19 who were treated with Paxlovid within 5 days of SARS-CoV-2 infection had a lower risk of Long COVID and all-cause hospitalization or death in the post-acute period. However, Long COVID risk reduction with Paxlovid was not observed in low-risk patients.

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