Real-World Effectiveness of Nirmatrelvir in Protecting Long COVID for Outpatient Adult Patients - A Large-Scale Observational Cohort Study from the RECOVER Initiative.

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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Abstract

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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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。
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。
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