1. Management and outcome of neonates with a prenatal diagnosis of esophageal atresia type A: A population-based study
- Author
-
Rony Sfeir, Frédéric Gottrand, Elodie Drumez, Véronique Houfflin-Debarge, V. Rousseau, Charles Garabedian, A Bonnard, Cracmo, and Laurent Michaud
- Subjects
medicine.medical_specialty ,Population ,Prenatal diagnosis ,03 medical and health sciences ,0302 clinical medicine ,Prenatal Diagnosis ,030225 pediatrics ,medicine ,Humans ,Registries ,Medical diagnosis ,education ,Esophageal Atresia ,Genetics (clinical) ,education.field_of_study ,030219 obstetrics & reproductive medicine ,Obstetrics ,business.industry ,Infant, Newborn ,Obstetrics and Gynecology ,Gestational age ,medicine.disease ,Population based study ,Atresia ,France ,business - Abstract
OBJECTIVE Evaluate the neonatal management and outcomes of neonates with prenatal diagnosis of esophageal atresia (EA) type A. METHODS This population-based study was conducted using data from the French National Register for infants with EA born from 2008 to 2014, including all cases of EA type A. We compared prenatal and neonatal characteristics and outcomes in children with prenatal diagnosis of EA type A with those with a postnatal diagnosis until the age of 1. RESULTS A total of 1118 live births with EA were recorded among which 88 (7.9%) were EA type A. Prenatal diagnoses were performed in 75 cases (85.2%), and counselling with a prenatal specialist was conducted in 84.8% of the prenatal group. Still within that group, the gestational age at delivery was significantly higher than in the postnatal group (36 [35-38] versus 34 [32-36] weeks; P = .048). Inborn births were more frequent in the prenatal group (86.1% vs 7.7%, P
- Published
- 2018
- Full Text
- View/download PDF