Evidence map›Paper›PMID 42584658›Full record

ArticlePediatric nephrology (Berlin, Germany)2026

Acute kidney diseases and disorders in children with bloodstream infection: frequency, predictors, and outcomes.

Misaki Akiyama, Kentaro Nishi, Toshihiro Matsui, Kaoru Tsuboi, Satoshi Okada, Tomoya Kaneda, Masao Ogura, Chiba Hirotaka, Norihiko Tsuboi, Kentaro Ide and 2 more

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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. Not yet cited 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

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Misaki AkiyamaDivision of Nephrology and Rheumatology, National Center for Child Health and Development, Tokyo, Japan.
Kentaro NishiDivision of Nephrology and Rheumatology, National Center for Child Health and Development, Tokyo, Japan. nishi-k@ncchd.go.jp.ORCID http://orcid.org/0000-0002-3436-0392
Toshihiro MatsuiDivision of Infectious Diseases, National Center for Child Health and Development, Tokyo, Japan.
Kaoru TsuboiDivision of Critical Care Medicine, National Center for Child Health and Development, Tokyo, Japan.
Satoshi OkadaDivision of Nephrology and Rheumatology, National Center for Child Health and Development, Tokyo, Japan.
Tomoya KanedaDivision of Nephrology and Rheumatology, National Center for Child Health and Development, Tokyo, Japan.
Masao OguraDivision of Nephrology and Rheumatology, National Center for Child Health and Development, Tokyo, Japan.
Chiba HirotakaDivision of Information Management Department Information Analysis Office, National Center for Child Health and Development, Tokyo, Japan.
Norihiko TsuboiDivision of Critical Care Medicine, National Center for Child Health and Development, Tokyo, Japan.
Kentaro IdeDivision of Critical Care Medicine, National Center for Child Health and Development, Tokyo, Japan.
Shotaro MatsumotoDivision of Critical Care Medicine, National Center for Child Health and Development, Tokyo, Japan.
Koichi KameiDivision of Nephrology and Rheumatology, National Center for Child Health and Development, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPediatric acute kidney diseases and disorders (AKDs) are a new concept defined as kidney damage lasting 7-90 days from onset. Data on AKD after bloodstream infection (BSI) are limited.

methodsThis single-center, retrospective observational study included patients aged < 20 years with BSI who were subsequently diagnosed with acute kidney injury (AKI) and/or AKD between 1 May 2013 and 31 May 2023. The index day was the date of the first positive blood culture. AKI (days 0-7) and AKD (days 7-90) were defined according to the Kidney Disease: Improving Global Outcomes/Acute Disease Quality Initiative criteria. Patients were categorized as those with AKI without AKD, AKD with AKI, and AKD without AKI. Primary comparisons included AKD (with/without AKI) versus AKI without AKD. Logistic regression analyses were conducted to identify predictors of AKD.

resultsAmong 1427 patients with positive blood cultures, 197 developed kidney dysfunction. The final cohort comprised 96 patients, including 41 patients (43%) who developed AKD. In the final cohort, 55 patients had AKI without AKD, 33 patients had AKD with AKI, and 8 patients had AKD without AKI. By multivariable logistic regression analysis, younger age (odds ratio, 0.91; 95% confidence interval, 0.84-0.99; P = 0.046) was independently associated with AKD after adjusting for intensive care unit onset, glycopeptide exposure, and white blood cell count. Compared to AKI without AKD (0/55), those with AKD (with/without AKI) had higher rates of death (6/41, 15%) and major adverse kidney events at days 30 (7/41, 17%) and 90 (8/41, 20%). All adverse outcomes occurred in the AKD with AKI subgroup.

conclusionsIn children with bloodstream infection-associated kidney dysfunction, AKD occurred in a substantial proportion, including those not meeting the AKI criteria. Younger age was associated with AKD development.

Indexed as

Acute kidney diseaseAcute kidney injuryBacteremiaPediatricSepsis

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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 Socratic graph.