Evidence map›Paper›PMID 39762640›Full record

ArticleCommunications medicine2025

Impact of extended-course oral nirmatrelvir/ritonavir in established Long COVID: a case series.

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 and 5 more

Abstract read
In one paragraph

Article in Communications medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. A pain from the nose to the head: neurological commitment during long COVID.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Alison K CohenDepartment 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. alison.cohen@ucsf.edu.ORCID http://orcid.org/0000-0001-9848-934X
Toni Wall JaudonPatient-Led Research Collaborative & University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Eric M SchurmanIndependent scholar, Seattle, WA, USA.ORCID http://orcid.org/0009-0006-5085-871X
Lisa KavaPatient-Led Research Collaborative, Brisbane, QLD, Australia.
Julia Moore VogelScripps Research Translational Institute and Patient-Led Research Collaborative, La Jolla, CA, USA.ORCID http://orcid.org/0000-0002-4902-3540
Julia Haas-GodsilIndependent scholar, Stamford, CT, USA.
Daniel LewisPatient-Led Research Collaborative, Campbell, CA, USA.
Samantha CrausmanIndependent scholar, Rehoboth, MA, USA.
Kate LeslieIndependent scholar, Boulder, CO, USA.
Siobhan Christine BlighIndependent scholar, London, UK.
Gillian LizarsIndependent scholar, Oakland, CA, USA.
J D DavidsStrategies for High Impact/Long COVID Justice, Patient-Led Research Collaborative, New York City, NY, USA.
Saniya SranIndependent scholar, Los Angeles, CA, USA.
Michael PelusoDivision of HIV, Infectious Diseases, and Global Medicine, University of California San Francisco, San Francisco, CA, USA.
Lisa McCorkellPatient-Led Research Collaborative, Oakland, CA, USA.ORCID http://orcid.org/0000-0002-3261-6737

Funding

Characterizing the virologic and immunologic signatures of HIV exceptional controlK23AI157875 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PELUSO, MICHAEL JOSEPH · 2021 to 2025
$927k
NIAID NIH HHS K23 AI157875
6 · The paper itself

Abstract

backgroundPrior 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.

methodsWe 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.

resultsAmong 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.

conclusionsExtended 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.

Identifiers

PMID39762640
PMCPMC11704346

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.