Evidence map›Paper›PMID 38175151›Full record

Observational studyJournal of medical virology2024

Association of nirmatrelvir for acute SARS-CoV-2 infection with subsequent Long COVID symptoms in an observational cohort study.

Matthew S Durstenfeld, Michael J Peluso, Feng Lin, Noah D Peyser, Carmen Isasi, Thomas W Carton, Timothy J Henrich, Steven G Deeks, Jeffrey E Olgin, Mark J Pletcher and 3 more

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Journal of medical virology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
18.8field-weighted citation impact, top 1% of its field
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

31 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  4. Combination antiviral and anti-inflammatory therapy mitigates persistent neurological deficits in mice post SARS-CoV-2 infection.Proceedings of the National Academy of Sciences of the United States of America · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 1 country.

Matthew S DurstenfeldDivision of Cardiology at ZSFG, Department of Medicine, University of California, San Francisco (UCSF), San Francisco, California, USA.ORCID 0000-0002-7612-3352
Michael J PelusoDivision of HIV, Infectious Disease, & Global Medicine, UCSF, San Francisco, California, USA.
Feng LinDepartment of Epidemiology and Biostatistics, UCSF, San Francisco, California, USA.
Noah D PeyserDepartment of Epidemiology and Biostatistics, UCSF, San Francisco, California, USA.
Carmen IsasiDepartment of Epidemiology & Population Health, Albert Einstein College of Medicine, New York City, New York, USA.
Thomas W CartonLouisiana Public Health Institute, New Orleans, Louisiana, USA.
Timothy J HenrichDepartment of Experimental Medicine, UCSF, San Francisco, California, USA.
Steven G DeeksDivision of HIV, Infectious Disease, & Global Medicine, UCSF, San Francisco, California, USA.
Jeffrey E OlginDivision of Cardiology, Department of Medicine, UCSF, San Francisco, California, USA.
Mark J PletcherDepartment of Epidemiology and Biostatistics, UCSF, San Francisco, California, USA.
Alexis L BeattyDivision of Cardiology, Department of Epidemiology and Biostatistics, Department of Medicine, UCSF, San Francisco, California, USA.
Gregory M MarcusDivision of Cardiology, Department of Medicine, UCSF, San Francisco, California, USA.
Priscilla Y HsueDivision of Cardiology at ZSFG, Department of Medicine, University of California, San Francisco (UCSF), San Francisco, California, USA.
University of California, San Francisco · USGlobal Solutions for Infectious Diseases · USAlbert Einstein College of Medicine · USLouisiana Public Health Institute · US

Funding

MHC Variation in Host Response to SARS-CoV2 and COVID-19 OutcomesR01AI159260 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HOLLENBACH, JILL ALLISON · 2021 to 2025
$4.0M
Role of Hematopoietic System and Proteomics in HIV-Associated CardiovascularDiseaseK24AI112393 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HSUE, PRISCILLA Y. · 2014 to 2024
$1.9M
UCSF Career Development Program in Cardiopulmonary, Hematologic, and Immunologic Comorbidities of HIV (CHIC)K12HL143961 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HSUE, PRISCILLA Y., HUANG, LAURENCE · 2018 to 2022
$1.8M
Characterizing the virologic and immunologic signatures of HIV exceptional controlK23AI157875 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PELUSO, MICHAEL JOSEPH · 2021 to 2025
$927k
Mentoring Scientists for Careers in HIV Translational Clinical ResearchK24AI174971 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Timothy Jensen Henrich · 2023 to 2026
$766k
Evaluation of the Impact of HIV Status on the Immune Response to mRNA COVID-19 VaccinesR21AI167648 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GANDHI, MONICA, SPINELLI, MATTHEW A. · 2022 to 2023
$444k
NHLBI NIH HHS K12 HL143961NIAID NIH HHS K23 AI157875NIAID NIH HHS K24 AI112393NIAID NIH HHS K24 AI174971NIAID NIH HHS L30 AI147159NIAID NIH HHS R01 AI159260NIAID NIH HHS R21 AI167648Patient-Centered Outcomes Research Institute
6 · The paper itself

Abstract

Oral nirmatrelvir/ritonavir is approved as treatment for acute COVID-19, but the effect of treatment during acute infection on risk of Long COVID is unknown. We hypothesized that nirmatrelvir treatment during acute SARS-CoV-2 infection reduces risk of developing Long COVID and rebound after treatment is associated with Long COVID. We conducted an observational cohort study within the Covid Citizen Science (CCS) study, an online cohort study with over 100 000 participants. We included vaccinated, nonhospitalized, nonpregnant individuals who reported their first SARS-CoV-2 positive test March-August 2022. Oral nirmatrelvir/ritonavir treatment was ascertained during acute SARS-CoV-2 infection. Patient-reported Long COVID symptoms, symptom rebound and test-positivity rebound were asked on subsequent surveys at least 3 months after SARS-CoV-2 infection. A total of 4684 individuals met the eligibility criteria, of whom 988 (21.1%) were treated and 3696 (78.9%) were untreated; 353/988 (35.7%) treated and 1258/3696 (34.0%) untreated responded to the Long COVID survey (n = 1611). Among 1611 participants, median age was 55 years and 66% were female. At 5.4 ± 1.3 months after infection, nirmatrelvir treatment was not associated with subsequent Long COVID symptoms (odds ratio [OR]: 1.15; 95% confidence interval [CI]: 0.80-1.64; p = 0.45). Among 666 treated who answered rebound questions, rebound symptoms or test positivity were not associated with Long COVID symptoms (OR: 1.34; 95% CI: 0.74-2.41; p = 0.33). Within this cohort of vaccinated, nonhospitalized individuals, oral nirmatrelvir treatment during acute SARS-CoV-2 infection and rebound after nirmatrelvir treatment were not associated with Long COVID symptoms more than 90 days after infection.

Indexed as

COVID-19Post-Acute COVID-19 SyndromeCohort StudiesFemaleHumansMaleMiddle AgedRitonavirSARS-CoV-2RitonavirLong COVIDnirmatrelvirPaxlovidpost-acute sequelae of COVID-19rebound

Identifiers

PMID38175151
PMCPMC10786003
OpenAlexW4390589544

What OpenQuestion holds

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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.