Evidence map›Paper›PMID 40204015›Full record

ArticleAmerican journal of kidney diseases : the official journal of the National Kidney Foundation2025

Safety and Effectiveness of Nirmatrelvir-Ritonavir in Patients With Advanced Kidney Dysfunction and COVID-19.

Marimar Contreras Nieves, Shuchi Anand, I-Chun Thomas, Pascal Geldsetzer, Enrica Fung, Manjula Kurella Tamura, Maria E Montez-Rath

Abstract read
In one paragraph

Article in American journal of kidney diseases : the official journal of the National Kidney Foundation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Marimar Contreras NievesNephrology, Department of Medicine, Stanford University, Stanford, California. Electronic address: mcontre@stanford.edu.
Shuchi AnandNephrology, Department of Medicine, Stanford University, Stanford, California.
I-Chun ThomasNephrology, Department of Medicine, Stanford University, Stanford, California; Geriatric Research and Education Clinical Center, Veterans Affairs Palo Alto, Palo Alto, California.
Pascal GeldsetzerPrimary Care and Population Health, Department of Medicine, Stanford University, Stanford, California.
Enrica FungNephrology, Department of Medicine, Stanford University, Stanford, California.
Manjula Kurella TamuraNephrology, Department of Medicine, Stanford University, Stanford, California; Geriatric Research and Education Clinical Center, Veterans Affairs Palo Alto, Palo Alto, California.
Maria E Montez-RathNephrology, Department of Medicine, Stanford University, Stanford, California.

Funding

Professional Development CoreU2CDK133488 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Marsha J Treadwell · 2023 to 2026
$4.1M
Chronic kidney disease of unknown etiology: applying a multidisciplinary approach to investigate the world's most common tubulointerstitial kidney diseaseR01DK127138 · NIDDK · STANFORD UNIVERSITY · PI MONTEZ RATH, MARIA · 2021 to 2025
$2.7M
A Mentoring Program in Kidney Care for Older AdultsK24AG073615 · NIA · STANFORD UNIVERSITY · PI MANJULA KURELLA TAMURA · 2022 to 2026
$651k
HSRD VA I01 HX002763NIA NIH HHS K24 AG073615NIDDK NIH HHS R01 DK127138NIDDK NIH HHS U2C DK133488
6 · The paper itself

Abstract

RATIONALE &

objectiveNirmatrelvir-ritonavir prevents COVID-19 hospitalization among high-risk adults, but safety concerns limit its use in advanced kidney dysfunction. This study examined safety and effectiveness outcomes from its off-label use in patients with advanced kidney dysfunction. STUDY

designRetrospective matched cohort study. SETTING &

participantsPatients with estimated glomerular filtration rate (eGFR) 15-30mL/min/1.73m EXPOSURE: Treatment with nirmatrelvir-ritonavir, no treatment with nirmatrelvir-ritonavir or molnupiravir, or treatment with molnupiravir. OUTCOME: Incidence of cardiac events, stroke, acute kidney injury, liver injury, hypertension, and infection-related death, respiratory failure, pneumonia, severe infection, and hospitalization within 30-60 days of diagnosis with COVID-19. ANALYTICAL APPROACH: Logistic regression for propensity matching, standardized mean differences for assessment of covariate balance, and conditional logistic regression for estimation of relative risk ratios comparing exposures for each outcome.

resultsAmong 4,020 patients with an eGFR of 15-30mL/min/1.73m LIMITATIONS: Retrospective analysis, predominantly men in the study cohort.

conclusionsNirmatrelvir-ritonavir use in the setting of advanced kidney dysfunction was associated with a reduced risk of acute respiratory failure and pneumonia and no detectable differences in non-respiratory adverse outcomes compared with no treatment with either nirmatrelvir-ritonavir or molnupiravir. PLAIN-LANGUAGE SUMMARY: COVID-19 can cause severe complications in patients with advanced kidney disease, yet nirmatrelvir-ritonavir, one of the first-line antiviral therapies, is not recommended in such patients due to safety concerns. We examined its safety and effectiveness among patients with advanced (stage IV) kidney disease. Using Veterans Health Administration records, we compared patients who received nirmatrelvir-ritonavir with those who were not treated with it nor with molnupiravir (a second-line therapy). We also compared treatment with nirmatrelvir-ritonavir with treatment with molnupiravir. We found that nirmatrelvir-ritonavir was associated with a reduced risk of serious lung problems without any evidence of increased risks of heart, liver, or kidney problems compared with not being treated with nirmatrelvir-ritonavir nor molnupiravir. The effectiveness and safety of nirmatrelvir-ritonavir were similar to that of molnupiravir. This study provides real-world evidence supporting nirmatrelvir-ritonavir use for patients with advanced kidney disease.

Indexed as

Antiviral AgentsCOVID-19COVID-19 Drug TreatmentRitonavirAgedDrug CombinationsFemaleGlomerular Filtration RateHumansMaleMiddle AgedRetrospective StudiesSARS-CoV-2Treatment OutcomeAntiviral AgentsDrug CombinationsRitonavirChronic kidney diseaseCOVID-19Index Wordsmolnupiravirnirmatrelvir-ritonavirpharmacology

Identifiers

PMID40204015
PMCPMC12286726

What OpenQuestion holds

Textmetadata
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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.