Evidence map›Paper›PMID 41217467›Full record

ArticlePediatric nephrology (Berlin, Germany)2026

A multi-center collaborative highlights the differences in nephrotoxic medication exposure and associated AKI in pediatric bone marrow transplant, oncology, and pulmonary service lines.

Julia M Steinke, Katja M Gist, David Askenazi, Richard K Ogden, Stella Shin, Scott Sutherland, Karyn Yonekawa, Allison Redpath Mahon, Jeffrey Fadrowski, Jason Misurac and 2 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2026. 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. Preventing pediatric acute kidney injury: is it even possible?Pediatric nephrology (Berlin, Germany) · 2026
    Review
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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

12 authors.

Julia M SteinkeHelen DeVos Children's Hospital, Grand Rapids, MI, USA. jxsteink@texaschildrens.org.ORCID http://orcid.org/0000-0002-8601-9479
Katja M GistUniversity of Colorado Anschutz Medical Campus, Children's Hospital Colorado, Aurora, CO, USA.
David AskenaziChildren's Hospital of Alabama, Birmingham, AL, USA.
Richard K OgdenChildren's Mercy Hospital and Clinics, Kansas City, MO, USA.
Stella ShinChildren's Healthcare of Atlanta, Atlanta, GA, USA.
Scott SutherlandLucille Packard Stanford Children's Hospital, Palo Alto, CA, USA.
Karyn YonekawaSeattle Children's Hospital, Seattle, WA, USA.
Allison Redpath MahonAmerican Family Children's Hospital, Madison, WI, USA.
Jeffrey FadrowskiJohns Hopkins School of Medicine, Baltimore, MD, USA.
Jason MisuracStead Family Children's Hospital, Iowa City, IA, USA.
Michael SemanikAmerican Family Children's Hospital, Madison, WI, USA.
Stuart L GoldsteinCincinnati Children's Hospital Medical Centerand , University of Cincinnati College of Medicine, Cincinnati, OH, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNephrotoxic medication (NTMx) exposure is a common cause of hospital-acquired acute kidney injury (AKI) in non-critically ill, hospitalized children. NINJA (Nephrotoxic Injury Negated by Just-In-Time Action), an AKI screening and quality improvement tool, has successfully decreased exposure to NTMx and associated AKI at various US children's hospitals. We explored NTMx exposure and AKI rates by admitting service to understand patient risk profiles further.

methodsAKI screening was performed by daily serum creatinine when high NTMx exposure criteria were met (≥ 3 NTMx or ≥ 3 days of intravenous aminoglycosides or vancomycin). Centers separately reported data from children admitted to hematology-oncology (heme), bone marrow transplant (BMT), and pulmonary services over 5 years (n = 11, 2016-2021). Rates for NTMx exposure and AKI were expressed as events per 1000 patient days. AKI intensity (#AKI days/100 exposure days) was assessed. Adherence to recommended serum creatinine monitoring was a surrogate for AKI event reliability (observed/expected × 100).

resultsMean exposure rates were highest in BMT (26.92), then pulmonary (22.73), and heme (13.01). AKI rates were highest in BMT (6.27), then pulmonary (4.24), and heme (1.82). Heme and BMT had the highest AKI intensity (12.93 and 12.25 AKI days per 100 high-NTMx exposure days, respectively) compared to pulmonary (7.50 AKI days/100 high-NTMx exposure days). Serum creatinine monitoring compliance varied between institutions (62.5-100%).

conclusionsNephrotoxic exposure and AKI rates vary by patient population, with BMT patients having the highest NTMx exposure, AKI rates, and AKI intensity. These findings suggest that sub-populations have different levels of exposure and may require different strategies to reduce the burden of nephrotoxic medications.

Indexed as

Acute Kidney InjuryAnti-Bacterial AgentsBone Marrow TransplantationAdolescentAminoglycosidesChildChild, PreschoolCreatinineFemaleHospitals, PediatricHumansInfantMaleRetrospective StudiesUnited StatesVancomycinAminoglycosidesAnti-Bacterial AgentsCreatinineVancomycinAcute kidney injuryNephrotoxicPediatricsQuality improvementSurveillance

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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.