延长疗程口服尼马特韦/利托那韦对长期确诊COVID的影响:一个病例系列。

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Communications medicine Pub Date : 2025-01-06 DOI:10.1038/s43856-024-00668-8
Alison K Cohen, Toni Wall Jaudon, Eric M Schurman, Lisa Kava, Julia Moore Vogel, Julia Haas-Godsil, Daniel Lewis, Samantha Crausman, Kate Leslie, Siobhan Christine Bligh, Gillian Lizars, J D Davids, Saniya Sran, Michael Peluso, Lisa McCorkell
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引用次数: 0

摘要

背景:先前的病例系列表明,5天的口服Paxlovid (nirmatrelvir/ritonavir)疗程对一些长COVID患者有益,无论是在急性再感染的情况下还是在急性再感染的情况下。据我们所知,此前还没有出现过Long COVID患者尝试过更长疗程的尼马特韦/利托那韦病例系列。方法:我们记录了13例长COVID患者的病例系列,他们开始延长疗程(bbb50天;范围:7.5-30天),在急性SARS-CoV-2感染的背景下(n = 11)和(n = 2)之外(n = 11)口服尼马特韦/利托那韦。参与者报告了在使用尼马特韦/利托那韦之前、期间和之后的症状和健康经历。结果:在非急性感染的情况下延长服用nirmatrelvir/ritonavir疗程的患者中,一些患者的症状明显减轻,尽管并非所有的益处都能持续。另一些则对症状没有影响。一名参与者由于剧烈的胃痛而提前停药。对于两名在急性再感染的情况下服用了延长疗程的尼马特韦/利托那韦的参与者,他们都报告最终回到了再感染前的基线。结论:延长nirmatrelvir/ritonavir疗程可能对一些长COVID患者有意义,但对其他患者没有意义。我们鼓励研究人员研究尼马特利韦/利托那韦如何以及为什么对一些人有益,以及什么疗程最有效,目的是为临床推荐使用尼马特利韦/利托那韦和/或其他抗病毒药物作为长期COVID的潜在治疗提供信息。
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Impact of extended-course oral nirmatrelvir/ritonavir in established Long COVID: a case series.

Background: Prior case series suggest that a 5-day course of oral Paxlovid (nirmatrelvir/ritonavir) benefits some people with Long COVID, within and/or outside of the context of an acute reinfection. To the best of our knowledge, there have been no prior case series of people with Long COVID who have attempted longer courses of nirmatrelvir/ritonavir.

Methods: We documented a case series of 13 individuals with Long COVID who initiated extended courses (>5 days; range: 7.5-30 days) of oral nirmatrelvir/ritonavir outside (n = 11) of and within (n = 2) the context of an acute SARS-CoV-2 infection. Participants reported on symptoms and health experiences before, during, and after their use of nirmatrelvir/ritonavir.

Results: Among those who take an extended course of nirmatrelvir/ritonavir outside of the context of an acute infection, some experience a meaningful reduction in symptoms, although not all benefits persist. Others experience no effect on symptoms. One participant stopped early due to intense stomach pain. For the two participants who took an extended course of nirmatrelvir/ritonavir within the context of an acute reinfection, both report eventually returning to their pre-re-infection baseline.

Conclusions: Extended courses of nirmatrelvir/ritonavir may have meaningful benefits for some people with Long COVID but not others. We encourage researchers to study how and why nirmatrelvir/ritonavir benefits some and what course length is most effective, with the goal of informing clinical recommendations for using nirmatrelvir/ritonavir and/or other antivirals as a potential treatment for Long COVID.

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