| Literature DB >> 29169875 |
Francesca Maria Russo1, Paolo De Coppi2, Karel Allegaert3, Jaan Toelen1, Lennart van der Veeken1, George Attilakos4, Mary Patrice Eastwood5, Anna Louise David4, Jan Deprest6.
Abstract
Congenital diaphragmatic hernia is surgically correctable, yet the poor lung development determines mortality and morbidity. In isolated cases the outcome may be predicted prenatally by medical imaging. Cases with a poor prognosis could be treated before birth. However, prenatal modulation of lung development remains experimental. Fetoscopic endoluminal tracheal occlusion triggers lung growth and is currently being evaluated in a global clinical trial. Prenatal transplacental sildenafil administration may in due course be a therapeutic approach, reducing the occurrence of persistent pulmonary hypertension, either alone or in combination with fetal surgery.Entities:
Keywords: Congenital diaphragmatic hernia; Prenatal therapy; Pulmonary hypertension; Pulmonary hypoplasia; Sildenafil
Mesh:
Year: 2017 PMID: 29169875 DOI: 10.1016/j.siny.2017.11.002
Source DB: PubMed Journal: Semin Fetal Neonatal Med ISSN: 1744-165X Impact factor: 3.926