Evidence map›Paper›PMID 41488217›Full record

ArticleAmerican journal of medicine open2026

Inpatient NSAID Exposure and Development of Acute Kidney Injury in Medical Inpatients: A Retrospective Cohort Study.

Katie M Rieck, Darrell R Schroeder, Michael A Mao

Abstract read
In one paragraph

Article in American journal of medicine open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Katie M RieckDivision of Hospital Internal Medicine, Mayo Clinic, Rochester, Minn.
Darrell R SchroederDivision of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, Minn.
Michael A MaoDivision of Nephrology and Hypertension, Mayo Clinic, Jacksonville, Fla.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To assess the risk of hospital-acquired acute kidney injury after nonsteroidal anti-inflammatory drug (NSAID) administration in the general medical population. Methods: This was a retrospective cohort study conducted at an academic medical center (Mayo Clinic, Rochester, MN) that included all general care medical patients for 2 years. Patients were analyzed in a propensity-adjusted approach using inverse probability of treatment weighting (IPTW) according to NSAID exposure on hospital day 0 or 1 categorized as follows: (1) no NSAID exposure; (2) only low-dose aspirin; (3) topical exposures, or (4) systemic NSAIDs. Results: A total of 17,885 patients met the initial inclusion criteria, and 11,840 were included in the study. The systemic NSAID cohort were the healthiest and youngest patients at baseline with fewer comorbidities. After adjustment, there was no significant difference seen in the rate of AKI (using the inverse probability of treatment weighting) between cohorts. The odds ratio of hospital-acquired AKI was 1.16 (0.80-1.70) in the Low-dose Aspirin group, 0.65 (0.21-2.03) in the Topical group, and 0.82 (0.27-1.85) in the Systemic NSAID group, with the No NSAID serving as the reference. Adjusted AKI incidence was 3.4% with No NSAIDs, 3.9% with Low-dose Aspirin, 2.2% with Topicals, and 2.8% with Systemic NSAIDs. These differences were not statistically significant. Conclusion: This study provides evidence that carefully selected hospitalized patients may be able to receive NSAIDs without increasing their AKI risk. This increases options for the treatment of pain, which may improve patient satisfaction and decrease opioid-related complications. Further prospective research is required to verify the findings of our study.

Indexed as

Acute kidney injuryAcute renal failureHospitalistInpatient analgesiaNSAIDOpioid epidemic

Identifiers

PMID41488217
PMCPMC12757445

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