Megacystis in the first trimester of pregnancy: Prognostic factors and perinatal outcomes.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 18 12 2020
accepted: 26 07 2021
entrez: 7 9 2021
pubmed: 8 9 2021
medline: 15 12 2021
Statut: epublish

Résumé

To determine whether bladder size is associated with an unfavorable neonatal outcome, in the case of first-trimester megacystis. This was a retrospective observational study between 2009 and 2019 in two prenatal diagnosis centers. The inclusion criterion was an enlarged bladder (> 7 mm) diagnosed at the first ultrasound exam between 11 and 13+6 weeks of gestation. The main study endpoint was neonatal outcome based on bladder size. An adverse outcome was defined by the completion of a medical termination of pregnancy, the occurrence of in utero fetal death, or a neonatal death. Neonatal survival was considered as a favorable outcome and was defined by a live birth, with or without normal renal function, and with a normal karyotype. Among 75 cases of first-trimester megacystis referred to prenatal diagnosis centers and included, there were 63 (84%) adverse outcomes and 12 (16%) live births. Fetuses with a bladder diameter of less than 12.5 mm may have a favorable outcome, with or without urological problems, with a high sensitivity (83.3%) and specificity (87.3%), area under the ROC curve = 0.93, 95% CI (0.86-0.99), p< 0.001. Fetal autopsy was performed in 52 (82.5%) cases of adverse outcome. In the 12 cases of favorable outcome, pediatric follow-up was normal and non-pathological in 8 (66.7%). Bladder diameter appears to be a predictive marker for neonatal outcome. Fetuses with smaller megacystis (7-10 mm) have a significantly higher chance of progressing to a favorable outcome. Urethral stenosis and atresia are the main diagnoses made when first-trimester megacystis is observed. Karyotyping is important regardless of bladder diameter.

Identifiants

pubmed: 34492029
doi: 10.1371/journal.pone.0255890
pii: PONE-D-20-39804
pmc: PMC8423287
doi:

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0255890

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Emmanuelle Lesieur (E)

Maternité Port-Royal, AP-HP, Hôpital Cochin, FHU PREMA, Paris, France.

Mathilde Barrois (M)

Maternité Port-Royal, AP-HP, Hôpital Cochin, FHU PREMA, Paris, France.

Mathilde Bourdon (M)

Faculté de Médecine Paris Centre, Faculté de Santé, Université de Paris, Paris, France.
Service de Gynécologie-Obstétrique II et de Médecine de la Reproduction, AP-HP, Centre Hospitalier Universitaire (CHU) Cochin, Paris, France.
Department "Infection, Immunity and Inflammation", Université de Paris, Institut Cochin, Paris, France.

Julie Blanc (J)

Service de Gynécologie Obstétrique, Hôpital Nord, AP-HM, Chemin des Bourrely, Marseille, France.
EA3279, CEReSS, Health Service Research and Quality of Life Center, Université Aix-Marseille, Marseille, France.

Laurence Loeuillet (L)

Service d'Histologie-Embryologie-Cytogénétique, Hôpital Necker-Enfants Malades, AP-HP, Paris, France.

Clémence Delteil (C)

Institut Médicolégal de Marseille, Hôpital Timone Adultes, Marseille, France.
CNRS, EFS, ADES UMR 7268, Aix-Marseille université, Marseille, France.

Julia Torrents (J)

Service d'Anatomo-Cytopathologie et Fœtopathologie, Hôpital de la Timone, Marseille, France.

Florence Bretelle (F)

Service de Gynécologie Obstétrique, Hôpital Nord, AP-HM, Chemin des Bourrely, Marseille, France.
Aix Marseille Univ, IRD, AP-HM, MEФI, Marseille, France.

Gilles Grangé (G)

Maternité Port-Royal, AP-HP, Hôpital Cochin, FHU PREMA, Paris, France.

Vassilis Tsatsaris (V)

Maternité Port-Royal, AP-HP, Hôpital Cochin, FHU PREMA, Paris, France.
Université de Paris, Inserm UMR-S 1139, Physiopathologie et Pharmacotoxicologie Placentaire Humaine, Paris, France.

Olivia Anselem (O)

Maternité Port-Royal, AP-HP, Hôpital Cochin, FHU PREMA, Paris, France.

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Classifications MeSH