Evidence map›Paper›PMID 40042306›Full record

ArticleMicrobiology spectrum2025

Association between nirmatrelvir/ritonavir treatment and antibiotic prescribing in the outpatient setting among patients with COVID-19.

Aisling R Caffrey, Haley J Appaneal, Vrishali V Lopes, Thomas Lavoie, Laura Puzniak, Evan J Zasowski, Luis Jodar, Iqra Arham, Kerry L LaPlante, John M McLaughlin

Abstract read
In one paragraph

Article in Microbiology spectrum, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. Review
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

10 authors.

Aisling R CaffreyInfectious Diseases Research Program, Providence Veterans Affairs Medical Center, Providence, Rhode Island, USA.ORCID 0000-0002-4180-027X
Haley J AppanealInfectious Diseases Research Program, Providence Veterans Affairs Medical Center, Providence, Rhode Island, USA.ORCID 0000-0002-2407-7032
Vrishali V LopesInfectious Diseases Research Program, Providence Veterans Affairs Medical Center, Providence, Rhode Island, USA.
Thomas LavoieInfectious Diseases Research Program, Providence Veterans Affairs Medical Center, Providence, Rhode Island, USA.
Laura PuzniakPfizer Inc., New York, New York, USA.
Evan J ZasowskiPfizer Inc., New York, New York, USA.
Luis JodarPfizer Inc., New York, New York, USA.
Iqra ArhamPfizer Inc., New York, New York, USA.
Kerry L LaPlanteInfectious Diseases Research Program, Providence Veterans Affairs Medical Center, Providence, Rhode Island, USA.ORCID 0000-0002-9650-4275
John M McLaughlinPfizer Inc., New York, New York, USA.

Funding

Pfizer, Inc
6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) has complicated the management of acute respiratory infections and impacted antibiotic use. We assessed the relationship between nirmatrelvir/ritonavir (NMV/r) receipt and outpatient antibiotic prescribing among patients with COVID-19 in a large national health system. We conducted a retrospective cohort study among outpatients enrolled in the Veterans Affairs Healthcare System who had a positive severe acute respiratory syndrome coronavirus 2 test or COVID-19 diagnosis and were eligible for NMV/r treatment between 1 April 2022 and 31 March 2024. NMV/r-treated patients were compared with those who did not receive NMV/r and were considered unexposed until NMV/r was dispensed. We assessed the relationship between NMV/r receipt and being prescribed an outpatient antibiotic in the 30 days after a COVID-19 diagnosis using adjusted Cox proportional hazards regression. We included 302,600 NMV/r-eligible outpatients with COVID-19, of whom 67,649 received NMV/r and 234,951 did not receive NMV/r. NMV/r-treated patients were less likely to receive outpatient antibiotics compared to those who did not receive NMV/r (7.2% [4,901/67,649] vs 9.2% [21,533/234,951], respectively; adjusted hazard ratio [HR] 0.65, 95% CI: 0.63‒0.68). After excluding patients who received an antibiotic prescription upon COVID-19 diagnosis (i.e., likely empiric therapy), this relationship was attenuated (HR: 0.91, 95% CI: 0.87‒0.95). NMV/r-eligible patients with COVID-19 who received NMV/r were 35% less likely to be prescribed outpatient antibiotics compared to patients who did not receive NMV/r, possibly driven by a diminished perceived need for empiric antibiotic therapy. Treatment with NMV/r may reduce unnecessary outpatient antibiotic use. Antibiotics should be reserved for patients with a high suspicion of bacterial co-infection.IMPORTANCEAntimicrobial resistance, driven by the overuse of antibiotics, is a major global health threat. The coronavirus disease 2019 (COVID-19) pandemic has complicated this issue, with antibiotics often prescribed to patients with COVID-19 despite being ineffective against viruses. These practices, typically aimed at preventing or empirically treating rare bacterial co-infections, have raised concerns about accelerating resistance. The antiviral nirmatrelvir/ritonavir (NMV/r), widely used in high-risk patients with COVID-19 to prevent severe illness, offers an opportunity to reassess antibiotic use in patients with respiratory infections. Our study of over 300,000 patients in a national healthcare system found that those treated with NMV/r for COVID-19 were 35% less likely to receive antibiotics than those who did not receive the antiviral. Lower antibiotic use among patients treated with NMV/r may reflect a reduction in unnecessary outpatient antibiotic use. These findings highlight the potential role of antivirals in supporting antibiotic stewardship and addressing a critical public health challenge.

Indexed as

Anti-Bacterial AgentsAntiviral AgentsCOVID-19COVID-19 Drug TreatmentRitonavirAgedDrug PrescriptionsFemaleHumansMaleMiddle AgedOutpatientsRetrospective StudiesSARS-CoV-2Anti-Bacterial AgentsAntiviral AgentsRitonavirantibioticsco-infectionCOVID-19nirmatrelvir/ritonavirstewardship

Identifiers

PMID40042306
PMCPMC11960072

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.