Evidence map›Paper›PMID 40083069›Full record

ArticlePrenatal diagnosis2025

Fetal Urinoma Secondary to Posterior Urethral Valve and Its Association to Postnatal Renal Function: A Multicenter Retrospective Study.

Flore-Anne Martin, Matthieu Peycelon, Nicolas Vinit, Thibault Planchamp, Olivier Abbo, Maela Le Lous, Gwenaelle Le Bouar, Yves Ville, Annabelle Paye-Jaouen, Thomas Blanc and 1 more

Abstract readMulticenter Study
In one paragraph

Article in Prenatal diagnosis, 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.

Flore-Anne MartinDepartment of Gynecology, Obstetrics and Reproductive Medicine, CHU Rennes, Université de Rennes, Rennes, France.
Matthieu PeycelonDepartment of Pediatric Urology, National Reference Center for Rare Urinary Tract Malformations (MARVU), University Hospital Robert-Debre, APHP, Université Paris Cité, Paris, France.ORCID 0000-0003-3617-4849
Nicolas VinitDepartment of Pediatric Surgery and Urology, Hôpital Necker-Enfants Malades, APHP, Université Paris Cité, Paris, France.
Thibault PlanchampDepartment of Pediatric Surgery, CHU Purpan, Université de Toulouse, Toulouse, France.
Olivier AbboDepartment of Pediatric Surgery, CHU Purpan, Université de Toulouse, Toulouse, France.
Maela Le Lous
Gwenaelle Le BouarDepartment of Gynecology, Obstetrics and Reproductive Medicine, CHU Rennes, Université de Rennes, Rennes, France.
Yves VilleDepartment of Obstetrics and Fetal Medicine, Surgery and Imaging, Hôpital Necker Enfants Malades, AP-HP Université Paris Cité, Paris, France.
Annabelle Paye-JaouenDepartment of Pediatric Urology, National Reference Center for Rare Urinary Tract Malformations (MARVU), University Hospital Robert-Debre, APHP, Université Paris Cité, Paris, France.
Thomas BlancDepartment of Pediatric Surgery and Urology, Hôpital Necker-Enfants Malades, APHP, Université Paris Cité, Paris, France.
Alexis P ArnaudDepartment of Pediatric Surgery, CHU Rennes, Université de Rennes, Rennes, France.ORCID 0000-0003-4378-3570

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThe role of prenatal urinoma in lower urinary tract obstruction (LUTO) such as posterior urethral valves (PUV) is debated. We aimed to describe the risk factors associated with fetal urinoma and the association between fetal urinoma and postnatal renal function before 2 years of age.

methodsThis retrospective multicenter case-control study from 2000 to 2018 included pregnant patients with suspected LUTO in their male fetus on prenatal ultrasound and postnatal confirmation of PUV. The exposure criterion was prenatal urinoma. The main composit outcome (MCO) was chronic kidney disease stage 3 or higher (CKD3+) before 2 years or death. Descriptive analyses of patient data and crude and multivariate logistic regression analyses were performed in an intent-to-treat fashion, thus including lost-to-follow-up patients. Ethical approval # 20.144.

resultsWe included 299 patients, of whom 39 (13%) had prenatal urinoma. Thirty-eight patients had a termination of pregnancy (12.7%). Sixty-four (24.5%) patients'children were MCO positive. Twenty-one children were lost-to-follow-up, including one prenatal urinoma. Thirty-nine (60.9%) of the remaining children had CKD3+ before the age of two, of whom 6 had a prenatal urinoma (9.4%). Among the 197 children negative to the MCO, 24 had a prenatal urinoma (12.2%, p = 0.42). Four died neonatally. In livebirth patients, prenatal urinoma was associated with obstetrical complications (p = 0.02), prenatal bloodcord sample for fetal beta2-microglobulin (p = 0.01) and uro-amniotic shunt (p = 0.01). Patients with prenatal urinoma more often presented with oligohydramnios (p = 0.01) and dilated posterior urethra (p = 0.01) and were less likely to have urinary tract infections (p = 0.02), although their DMSA scan was more often altered (p = 0.001). Prenatal urinoma was not significantly associated with CKD3+ before 2 years (OR = 0.56, CI98% = 0.20-1.39, p = 0.23).

conclusionRenal function in infants with PUV was not worsened by the presence of a prenatal urinoma. Thus, there should not be any more pejorative message conveyed to concerned couples apart from other already known prenatal poor prognosis risk factors.

Indexed as

Fetal DiseasesRenal Insufficiency, ChronicUrethraUrethral ObstructionUrinomaAdultCase-Control StudiesFemaleHumansInfantInfant, NewbornKidneyMalePregnancyRetrospective StudiesRisk Factors

Identifiers

PMID40083069
PMCPMC12254425

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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.