使用尼马瑞韦/利托那韦治疗后的 COVID-19 临床反弹。

Daniel Camp, Matthew Caputo, Fabiola Moreno Echevarria, Chad J Achenbach
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摘要

背景介绍尼马瑞韦/利托那韦(NM/r)是一种安全有效的口服抗病毒治疗药物,用于治疗轻度至中度 COVID-19。病例报告描述了一种临床反弹综合征,即患者在成功完成治疗后不久症状复发。关于常规临床治疗中 NM/r 后 COVID-19 反弹的频率、诱因和临床结果的信息尚缺乏。方法:我们查阅了电子病历,以核实 2022 年 1 月至 6 月期间 COVID-19 的诊断、症状和 NM/r 治疗情况。我们将 COVID-19 临床反弹定义为症状明显改善,但在接受 5 天 NM/r 治疗后 30 天内症状复发或恶化。研究结果我们对 268 名成人进行了研究,他们的中位年龄为 57 岁(IQR 47 68),80% 为白种人,85% 为非西班牙裔,55% 为女性,80% 接种过 SARS-CoV-2 疫苗并接受过强化治疗,68% 有任何并发症。在研究的患者中,有 16 人(6.0%)被确定为 COVID-19 临床反弹。从开始使用 NM/r 到病情反弹的中位时间为 11 天(IQR 为 9-13 天)。COVID-19反弹患者中比例较高(无统计学意义)的显著人口统计学和临床因素包括:女性(75%反弹 vs 54.5%未反弹)、黑人(12.5%反弹 vs 4.9%未反弹)、至少患有一种并发症(81.3%反弹 vs 67.5%未反弹)以及既往未感染SARS-CoV-2(100%反弹 vs 92.9%未反弹)。只有一名患者(6.25%)在 COVID-19 反弹后住院治疗。结论使用 NM/r 治疗后,COVID-19 临床反弹程度较轻,治疗效果良好,而且比以前的实际临床治疗研究报告更为常见。
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COVID-19 clinical rebound after treatment with nirmatrelvir/ritonavir.

Background: Nirmatrelvir/ritonavir (NM/r) is a safe and effective oral antiviral therapeutic used for treatment of mild-to-moderate COVID-19. Case reports described a clinical rebound syndrome whereby individuals experience a relapse of symptoms shortly after completing successful treatment. There is a lack of information on frequency of COVID-19 rebound after NM/r in routine clinical care, contributing factors, and clinical outcomes.

Methods: We reviewed electronic medical records to verify COVID-19 diagnosis, symptoms, and treatment with NM/r from January-June 2022. We defined COVID-19 clinical rebound as clear improvement in symptoms followed by recurrence or worsening of symptoms within 30 days of a five-day course of NM/r.

Results: We studied 268 adults with median age 57 (IQR 47, 68), 80% White race, 85% non-Hispanic ethnicity, 55% female, 80% vaccinated and boosted against SARS-CoV-2, and 68% with any co-morbidity. Sixteen (6.0%) of studied patients were determined to have COVID-19 clinical rebound. The median time from starting NM/r to rebound was 11 days (IQR 9, 13). Notable demographic and clinical factors with higher proportion (not statistically significant) among COVID-19 rebound patients were female sex (75% rebound vs 54.5% no rebound), Black race (12.5% rebound vs 4.9% no rebound), presence of at least one co-morbidity (81.3% rebound vs 67.5% no rebound), and lack of prior SARS-CoV-2 infection (100% rebound vs 92.9% no rebound). Only one patient (6.25%) was hospitalized after COVID-19 rebound.

Conclusions: COVID-19 clinical rebound after treatment with NM/r is mild with favorable outcomes and more common than previously reported from real-world clinical care studies.

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