Prenatal assessment of pulmonary vasculature development in fetuses with congenital diaphragmatic hernia: A literature review

• Published in: Prenatal diagnosis Vol. 43; no. 10; pp. 1296 - 1309
• Main Authors: Weller, Katinka, Edel, Gabriëla G, Steegers, Eric A P, Reiss, Irwin K M, DeKoninck, Philip L J, Rottier, Robbert J, Eggink, Alex J, Peters, Nina C J
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.09.2023
• Subjects: Diaphragm; Fetuses; Hernia; Hernias; Literature reviews; Morbidity; Parameters; Pulmonary arteries; Pulmonary artery; Reversed flow; Vascularization
• ISSN: 0197-3851; 1097-0223
• DOI: 10.1002/pd.6412

Pathophysiological studies have shown that pulmonary vascular development is impaired in fetuses with a congenital diaphragmatic hernia (CDH), leading to a simplified vascular tree and increased vascular resistance. Multiple studies have described prenatal ultrasound parameters for the assessment of the pulmonary vasculature, but none of these parameters are used in daily clinical practice. We provide a comprehensive review of the literature published between January 1990 and February 2022 describing these parameters, and aim to explain the clinical relevance of these parameters from what is known from pathophysiological studies. Prenatal detection of a smaller diameter of the contralateral (i.e. contralateral to the diaphragmatic defect) first branch of the pulmonary artery (PA), higher pulsatility indices (PI), higher peak early diastolic reverse flow values, and a lower vascularization index seem of added value for the prediction of survival and, to a lesser extent, morbidity. Integration within the routine evaluation is complicated by the lack of uniformity of the methods used. To address the main components of the pathophysiological changes, we recommend future prenatal studies in CDH with a focus on PI values, PA diameters and pulmonary vascular branching.