Evidence map›Paper›PMID 42474745›Full record

ArticlePediatric nephrology (Berlin, Germany)2026

Major adverse kidney events at pediatric intensive care unit discharge in a nationwide Japanese pediatric continuous kidney replacement therapy registry.

Taiki Haga, Takahiro Matsudo, Ryuta Itakura, Yuji Yamagami, Kenji Sonota, Takuya Miyazawa, Shunsuke Noda, Sho Wada, Hiroshi Sakihama, Takuya Hayashi and 15 more

Abstract read
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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. 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

25 authors.

Taiki HagaDepartment of Critical Care Medicine, Osaka City General Hospital, 2-13-22, Miyakojima-Hondori, Miyakojima, Osaka, Osaka, 534-0021, Japan. taiki-haga@umin.ac.jp.ORCID http://orcid.org/0000-0001-5401-6479
Takahiro MatsudoDivision of Pediatric Critical Care Medicine, Matsudo City General Hospital, Matsudo, Chiba, Japan.
Ryuta ItakuraDepartment of Pediatric Emergency and Critical Care Medicine, Tokyo Metropolitan Children's Medical Center, Fuchu, Tokyo, Japan.
Yuji YamagamiDepartment of Pediatric Emergency and Critical Care Medicine, Hyogo Prefectural Amagasaki General Medical Center, Amagasaki, Hyogo, Japan.
Kenji SonotaDepartment of Intensive Care Medicine, Miyagi Children's Hospital, Sendai, Miyagi, Japan.
Takuya MiyazawaPediatric Critical Care Medicine, Shizuoka Children's Hospital, Shizuoka, Shizuoka, Japan.
Shunsuke NodaPediatric Critical Care Medicine, Nagano Children's Hospital, Azumino, Nagano, Japan.
Sho WadaDivision of Pediatric Critical Care Medicine, Aichi Children's Health and Medical Center, Obu, Aichi, Japan.
Hiroshi SakihamaCenter for Pediatric Critical Care Medicine, Hyogo Prefectural Kobe Children's Hospital, Kobe, Hyogo, Japan.
Takuya HayashiEmergency & Intensive Care Department, Kanagawa Children's Medical Center, Yokohama, Kanagawa, Japan.
Naoki FujiwaraPediatric Critical Care Medicine, Okinawa Prefectural Nanbu Medical Center & Children's Medical Center, Haebaru, Okinawa, Japan.
Yuki IchisakaDepartment of Pediatric Critical Care Medicine, Hokkaido Medical Center for Child Health and Rehabilitation, Sapporo, Hokkaido, Japan.
Hiroshi OkadaDivision of Pediatric Critical Care Medicine, Matsudo City General Hospital, Matsudo, Chiba, Japan.
Kohei TsukaharaDepartment of Emergency, Critical Care, and Disaster Medicine, Faculty of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University, Okayama, Okayama, Japan.
Mai MiyajiPediatric Intensive Care Unit, Department of Pediatrics, School of Medicine, St. Marianna University, Kawasaki, Kanagawa, Japan.
Kazufumi YaginumaDepartment of Pediatric Anesthesiology and Intensive Care Medicine, Jichi Children's Medical Center Tochigi, Shimotsuke, Tochigi, Japan.
Akito HorikawaDepartment of Pediatric Emergency and Critical Care Medicine, Tokyo Metropolitan Children's Medical Center, Fuchu, Tokyo, Japan.
Taku KoizumiDepartment of Intensive Care Medicine, Miyagi Children's Hospital, Sendai, Miyagi, Japan.
Shinya TakaradaPediatric Critical Care Medicine, Shizuoka Children's Hospital, Shizuoka, Shizuoka, Japan.
Norio OmoriPediatric Critical Care Medicine, Nagano Children's Hospital, Azumino, Nagano, Japan.
Keiichiro TomaPediatric Critical Care Medicine, Okinawa Prefectural Nanbu Medical Center & Children's Medical Center, Haebaru, Okinawa, Japan.
Wataru SakaiDepartment of Pediatric Critical Care Medicine, Hokkaido Medical Center for Child Health and Rehabilitation, Sapporo, Hokkaido, Japan.
Takafumi ObaraDepartment of Emergency, Critical Care, and Disaster Medicine, Faculty of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University, Okayama, Okayama, Japan.
Noriaki KuritaDepartment of Clinical Epidemiology, Graduate School of Medicine, Fukushima Medical University, Fukushima, Fukushima, Japan.
jpCRRT Registry Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMajor adverse kidney events (MAKE)-a composite of death, new dialysis dependence, and persistent kidney dysfunction-are key outcomes in pediatric patients receiving continuous kidney replacement therapy (CKRT). Due to limited Asian pediatric population data, we determined MAKE incidence at pediatric intensive care unit (PICU) discharge and explored associated factors using the first nationwide Japanese pediatric continuous renal replacement therapy (jpCRRT) registry.

methodsThis cohort study included children (aged < 16 years) who underwent CKRT for acute conditions between 2023 and 2025 in 17 Japanese PICUs. The primary outcome, MAKE at PICU discharge, was defined as death, new dialysis dependence, or persistent kidney dysfunction (≥ 25% increase in serum creatinine from baseline or ≥ 25% decrease in estimated glomerular filtration rate). Multivariable logistic regression, with variable selection using the least absolute shrinkage and selection operator and adjustment for clinically relevant covariates, was used to identify independent predictors of MAKE.

resultsOf 139 patients, 76 (54.7%) developed MAKE, comprising death, new dialysis dependence, and persistent kidney dysfunction in 25 (18.0%), 18 (13.0%), and 33 (23.7%), respectively. Independent MAKE factors were primary admission diagnoses of kidney disease (adjusted odds ratio (AOR), 60.7; 95% confidence interval (CI), 5.8-639), infection/sepsis (AOR, 37.0; 95% CI, 3.7-373), higher vasoactive-inotropic score (per 1-point increase; AOR, 1.04; 95% CI, 1.004-1.08), and hyperkalemia (per 1 mmol/L increase; AOR, 2.0; 95% CI, 1.1-3.6). High vasoactive support and hyperkalemia were associated with mortality, whereas kidney and infectious admission diagnoses were associated with new dialysis dependence or persistent kidney dysfunction.

conclusionAmong children receiving CKRT, more than half experienced MAKE at PICU discharge. Notably, a primary admission diagnosis of kidney disease was associated with adverse short-term outcomes, along with infectious/septic admission diagnoses, higher vasoactive-inotropic scores, and hyperkalemia. Longer-term follow-up is needed to clarify subsequent kidney recovery and post-discharge outcomes.

Indexed as

ChildrenContinuous kidney replacement therapyMajor adverse kidney eventsMortalityNew dialysis dependence

Identifiers

PMID42474745

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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.