Evidence map›Paper›PMID 40495087›Full record

ArticleEuropean journal of pediatrics2025

Morbidity in children with major kidney anomalies: a European population-based study.

Ester Garne, Mads Damkjær, Anke Rissmann, Clara Cavero-Carbonell, Mika Gissler, Amanda Neville, Michele Santoro, Joachim Tan, David Tucker, Maria Loane and 1 more

Abstract read
In one paragraph

Article in European journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Ester GarneDepartment of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Sygehusvej 24, 6000, Kolding, Denmark. Ester.garne@rsyd.dk.
Mads DamkjærDepartment of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Sygehusvej 24, 6000, Kolding, Denmark.
Anke RissmannMedical Faculty, Malformation Monitoring Centre Saxony-Anhalt, Otto-Von-Guericke-University Magdeburg, Magdeburg, Germany.ORCID http://orcid.org/0000-0002-9437-2790
Clara Cavero-CarbonellRare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
Mika GisslerDepartment of Data and Analytics, THL Finnish Institute for Health and Welfare, Helsinki, Finland.
Amanda NevilleCentre for Clinical and Epidemiological Research, University of Ferrara and Azienda Ospedaliero Universitario Di Ferrara, Ferrara, Italy.
Michele SantoroUnit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.ORCID http://orcid.org/0000-0003-0676-3036
Joachim TanNIHR Great Ormond Street Hospital Biomedical Research Centre, UCL GOS Institute of Child Health, London, UK.
David TuckerData & Digital Directorate, Public Health Wales, Swansea, UK.
Maria LoaneInstitute of Nursing and Health Research, Ulster University, Belfast, UK.
Joan MorrisSchool of Health and Medical Sciences, City St George's, University of London, London, UK.

Funding

European Union's Horizon 2020 733001
6 · The paper itself

Abstract

Knowledge about the prognosis for children born with congenital anomalies is important for counselling parents after a prenatal diagnosis. Nine population-based European Congenital Anomaly registries provided data on all children born 1995-2014 diagnosed with congenital hydronephrosis, multicystic kidney disease (MCKD), or posterior urethral valves (PUV) and on reference children from the same populations. Data up to 2015 on prescriptions, hospital diagnosis, and surgical procedures up to the 10th birthday were obtained by linkage to prescription and hospital databases. The study included 5624 children diagnosed with congenital hydronephrosis, 1314 with MCKD, and 414 with PUV. Children with hydronephrosis or MCKD were 13 times more likely to have prescriptions for antihypertensives compared to reference children before 10 years of age. Around 3% of children with congenital hydronephrosis or MCKD had a diagnosis of kidney failure at the age of 5 years; however, only 1% had a kidney transplantation by the age of 5 years. For children with PUV, 18.3% had a diagnosis of kidney failure and 5% had a kidney transplantation by the age of 5 years.

conclusionChildren born with congenital hydronephrosis and MCKD generally have a low absolute risk of developing kidney failure. Children with PUV have much higher morbidity, with 1 in 5 (18.3%) being diagnosed with kidney failure before the age of 5 years. It is important to monitor these children closely in early childhood in order to prevent or delay kidney failure. WHAT IS KNOWN: • Congenital kidney anomalies are a leading cause of pediatric end-stage kidney disease. Children with hydronephrosis, MCKD, and PUV have increased morbidity, but long-term data on medication use and kidney outcomes are limited. WHAT IS NEW: • This population-based study shows a low absolute risk of kidney failure in children born with hydronephrosis or MCKD but a high relative risk. PUV has high morbidity, with 1 in 4 developing kidney failure by age 10. Antibiotic use is high in early childhood, and antihypertensive use increases with age.

Indexed as

HydronephrosisKidneyMulticystic Dysplastic KidneyRenal InsufficiencyAdolescentChildChild, PreschoolEuropeFemaleHumansInfantInfant, NewbornKidney TransplantationMaleMorbidityRegistriesCongenital hydronephrosisKidney failureKidney transplantationMulticystic kidney dysplasiaPosterior urethral valves

Identifiers

PMID40495087
PMCPMC12152065

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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.