Cohen Alison K, Jaudon Toni Wall, Schurman Eric M, Kava Lisa, Vogel Julia Moore, Haas-Godsil Julia, Lewis Daniel, Crausman Samantha, Leslie Kate, Bligh Siobhan Christine, Lizars Gillian, Davids J D, Sran Saniya, Peluso Michael, McCorkell Lisa
Department of Epidemiology & Biostatistics and Philip R. Lee Institute for Health Policy Studies, School of Medicine, University of California San Francisco and Patient-Led Research Collaborative, San Francisco, CA, USA.
Patient-Led Research Collaborative & University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Commun Med (Lond). 2025 Jan 6;4(1):261. doi: 10.1038/s43856-024-00668-8.
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.
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.
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.
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.
先前的病例系列研究表明,为期5天的口服帕罗韦德(奈玛特韦/利托那韦)疗程对一些患有长期新冠的患者有益,无论是否处于急性再感染的情况下。据我们所知,此前尚无针对尝试更长疗程奈玛特韦/利托那韦的长期新冠患者的病例系列研究。
我们记录了一个病例系列,其中13名长期新冠患者在急性SARS-CoV-2感染之外(n = 11)和之内(n = 2)开始了口服奈玛特韦/利托那韦的延长疗程(>5天;范围:7.5 - 30天)。参与者报告了在使用奈玛特韦/利托那韦之前、期间和之后的症状及健康状况。
在急性感染之外接受奈玛特韦/利托那韦延长疗程的患者中,一些人的症状有显著减轻,尽管并非所有益处都能持续。其他人则症状未受影响。一名参与者因剧烈胃痛提前停药。对于在急性再感染情况下接受奈玛特韦/利托那韦延长疗程的两名参与者,两人均报告最终恢复到再感染前的基线水平。
奈玛特韦/利托那韦的延长疗程可能对一些长期新冠患者有显著益处,但对另一些患者则不然。我们鼓励研究人员研究奈玛特韦/利托那韦如何以及为何对部分患者有益,以及何种疗程长度最为有效,以期为使用奈玛特韦/利托那韦和/或其他抗病毒药物作为长期新冠潜在治疗方法的临床建议提供依据。