Evidence map›Paper›PMID 38380946›Full record

ArticleThe Journal of antimicrobial chemotherapy2024

COVID-19 hospitalization risk after outpatient nirmatrelvir/ritonavir use, January to August 2022, North Carolina.

Heather I Henderson, David A Wohl, William A Fischer, Luther A Bartelt, David van Duin, Deana M Agil, Lindsay E Browne, Kuo-Ping Li, Amanda Moy, Joseph J Eron and 1 more

Abstract read
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

  1. Pooled it
  2. Article
  3. Article
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

11 authors.

Heather I HendersonDepartment of Medicine, University of North Carolina at Chapel Hill, School of Medicine, 130 Mason Farm Road, Chapel Hill, NC 27599, USA.ORCID 0000-0002-2197-3149
David A WohlDepartment of Medicine, University of North Carolina at Chapel Hill, School of Medicine, 130 Mason Farm Road, Chapel Hill, NC 27599, USA.ORCID 0000-0002-7764-0212
William A FischerDepartment of Medicine, University of North Carolina at Chapel Hill, School of Medicine, 130 Mason Farm Road, Chapel Hill, NC 27599, USA.ORCID 0000-0002-4900-098X
Luther A BarteltDepartment of Medicine, University of North Carolina at Chapel Hill, School of Medicine, 130 Mason Farm Road, Chapel Hill, NC 27599, USA.
David van DuinDepartment of Medicine, University of North Carolina at Chapel Hill, School of Medicine, 130 Mason Farm Road, Chapel Hill, NC 27599, USA.ORCID 0000-0003-4784-3227
Deana M AgilDepartment of Medicine, University of North Carolina at Chapel Hill, School of Medicine, 130 Mason Farm Road, Chapel Hill, NC 27599, USA.
Lindsay E BrowneDepartment of Medicine, University of North Carolina at Chapel Hill, School of Medicine, 130 Mason Farm Road, Chapel Hill, NC 27599, USA.
Kuo-Ping LiDepartment of Medicine, University of North Carolina at Chapel Hill, School of Medicine, 130 Mason Farm Road, Chapel Hill, NC 27599, USA.
Amanda MoyDepartment of Medicine, University of North Carolina at Chapel Hill, School of Medicine, 130 Mason Farm Road, Chapel Hill, NC 27599, USA.
Joseph J EronDepartment of Medicine, University of North Carolina at Chapel Hill, School of Medicine, 130 Mason Farm Road, Chapel Hill, NC 27599, USA.
Sonia NapravnikDepartment of Medicine, University of North Carolina at Chapel Hill, School of Medicine, 130 Mason Farm Road, Chapel Hill, NC 27599, USA.ORCID 0000-0002-9032-3713

Funding

Virology, Immunology, and Microbiology CoreP30AI050410 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2001 to 2026
$76.9M
Training in Sexually Transmitted Infections and HIVT32AI007001 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SENA-SOBERANO, ARLENE C. · 1985 to 2025
$10.9M
Project 3: Serological Interactions with the Mucosal Innate Immune System Regulates COVID-19 Associated Tissue Damage.U54CA260543 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WOLFGANG, MATTHEW C · 2020 to 2024
$9.8M
North Carolina Translational and Clinical Science Institute (NC TraCS) TL1TL1TR002491 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ROY-CHAUDHURY, PRABIR · 2018 to 2022
$1.5M
NCATS NIH HHS TL1 TR002491NCI NIH HHS U54 CA260543NIAID NIH HHS P30 AI050410NIAID NIH HHS T32 AI007001NIH HHS TL1TR002491
6 · The paper itself

Abstract

backgroundIn the USA, nirmatrelvir/ritonavir is authorized for the treatment of mild-to-moderate COVID-19 in patients at least 12 years of age, at high risk for progression to severe COVID-19.

objectivesTo estimate the impact of outpatient nirmatrelvir/ritonavir on COVID-19 hospitalization risk in a US healthcare system.

methodsWe conducted a cohort study using electronic health records among outpatients with a positive SARS-CoV-2 PCR test between January and August 2022. We evaluated the association of nirmatrelvir/ritonavir therapy with time to hospitalization by estimating adjusted HRs and assessed the impact of nirmatrelvir/ritonavir on predicted COVID-19 hospitalizations using machine-learning methods.

resultsAmong 44 671 patients, 4948 (11%) received nirmatrelvir/ritonavir, and 201 (0.4%) were hospitalized within 28 days of COVID-19 diagnosis. Nirmatrelvir/ritonavir recipients were more likely to be older, white, vaccinated, have comorbidities and reside in areas with higher average socioeconomic status. The 28 day cumulative incidence of hospitalization was 0.06% (95% CI: 0.02%-0.17%) among nirmatrelvir/ritonavir recipients and 0.52% (95% CI: 0.46%-0.60%) among non-recipients. For nirmatrelvir/ritonavir versus no therapy, the age-adjusted HR was 0.08 (95% CI: 0.03-0.26); the fully adjusted HR was 0.16 (95% CI: 0.05-0.50). In the machine-learning model, the primary features reducing predicted hospitalization risk were nirmatrelvir/ritonavir, younger age, vaccination, female gender and residence in a higher socioeconomic status area.

conclusionsCOVID-19 hospitalization risk was reduced by 84% among nirmatrelvir/ritonavir recipients in a large, diverse healthcare system during the Omicron wave. These results suggest that nirmatrelvir/ritonavir remained highly effective in a setting substantially different than the original clinical trials.

Indexed as

COVID-19LactamsLeucineNitrilesOutpatientsProlineAntiviral AgentsCohort StudiesCOVID-19 Drug TreatmentCOVID-19 TestingFemaleHospitalizationHumansNorth CarolinaRitonavirSARS-CoV-2Antiviral AgentsLactamsLeucinenirmatrelvirNitrilesProlineRitonavir

Identifiers

PMID38380946
PMCPMC10984939

What OpenQuestion holds

Textmetadata
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.