Evidence map›Paper›PMID 39500807›Full record

ArticlePrenatal diagnosis2024

Hypospadias Associated With Fetal Growth Restriction: A Multicentric Descriptive and Prognostic Cohort Study.

Manon Marquet, Olivia Anselem, Claire Bouvattier, Alexandre J Vivanti, Alexandra Benachi, Jean-Marie Jouannic, Olivier Picone, Jonathan Rosenblatt, Laurent J Salomon, Vassilis Tsatsaris and 1 more

Abstract readMulticenter Study
In one paragraph

Article in Prenatal diagnosis, 2024. 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. Review
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.

Manon MarquetDepartment of Obstetrics and Gynecology, AP-HP, Port-Royal Maternity, Université Paris Cité, Paris, France.
Olivia AnselemDepartment of Obstetrics and Gynecology, AP-HP, Port-Royal Maternity, Université Paris Cité, Paris, France.ORCID 0000-0002-1516-3203
Claire BouvattierDepartment of Pediatric Endocrinology, AP-HP, Bicêtre Hospital, Université Paris-Saclay, Le Kremlin-Bicêtre, France.
Alexandre J VivantiDepartment of Obstetrics and Gynecology, DMU Santé des Femmes et des Nouveau-nés, AP-HP, Antoine Béclère Hospital, Université Paris Saclay, Clamart, France.
Alexandra BenachiDepartment of Obstetrics and Gynecology, DMU Santé des Femmes et des Nouveau-nés, AP-HP, Antoine Béclère Hospital, Université Paris Saclay, Clamart, France.ORCID 0000-0001-6045-0765
Jean-Marie JouannicFetal Medicine Department, Armand Trousseau Hospital, AP-HP, Sorbonne University, Paris, France.ORCID 0000-0002-7890-3790
Olivier PiconeDepartment of Obstetrics and Gynecology, APHP, Louis Mourier Hospital, Université Paris Cité, Paris, France.ORCID 0000-0001-8421-9971
Jonathan RosenblattDepartment of Obstetrics and Gynecology, AP-HP, Robert Debré Hospital, Université Paris Cité, Paris, France.ORCID 0000-0001-8877-0381
Laurent J SalomonMaternity and Foetal Medicine Department, AP-HP, Necker Enfant Malades Hospital, Université Paris Cité, Paris, France.
Vassilis TsatsarisDepartment of Obstetrics and Gynecology, AP-HP, Port-Royal Maternity, Université Paris Cité, Paris, France.
Yoann AthielDepartment of Obstetrics and Gynecology, AP-HP, Port-Royal Maternity, Université Paris Cité, Paris, France.ORCID 0000-0003-2665-8292

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo determine the prevalence of genetic and endocrine abnormalities and to assess fetal, neonatal and surgical outcomes in cases of hypospadias associated with fetal growth restriction.

methodA multicentric retrospective study was conducted across five prenatal diagnosis centers in Paris. The cohort encompassed all fetuses diagnosed with the combination of fetal growth restriction < 10th percentile (FGR) and hypospadias from 2013 to 2021. Maternal data, fetal outcome and results of prenatal investigations were collected, along with postnatal data, encompassing endocrinological and genetic assessments, functional aspects and surgical outcomes.

resultsAmong the 82 patients included in the cohort, there were 14 (17%) terminations of pregnancy and four (5%) in utero deaths, leaving 64 (78%) live neonates, including five (6%) with early neonatal death. Among the 52 (63%) cases where hypospadias and FGR were considered as ultrasound-isolated anomalies, six (12%, [3.2%-20.8%]) exhibited chromosomic, genetic, or endocrinological abnormalities diagnosed half prenatally and half postnatally. Fifty percent of the overall hypospadias were proximal. Most children underwent surgical intervention before reaching 2 years of age, with 50% encountering complications and often required reintervention.

conclusionThe association of FGR and hypospadias should not be underestimated as genetic or endocrinological abnormalities were identified even when hypospadias and FGR initially appear isolated. Additionally, the overall prognosis may be worsened using complex and iterative surgical procedures.

Indexed as

Fetal Growth RetardationHypospadiasAdultCohort StudiesFemaleHumansInfantInfant, NewbornMalePregnancyPrognosisRetrospective StudiesUltrasonography, Prenatal

Identifiers

PMID39500807
PMCPMC11628206

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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.