Lung size and liver herniation predict need for extracorporeal membrane oxygenation but not pulmonary hypertension in isolated congenital diaphragmatic hernia: systematic review and meta-analysis

Author:

Russo F. M.12,Eastwood M. P.1,Keijzer R.3,Al-Maary J.3,Toelen J.14,Van Mieghem T.12,Deprest J. A.125

Affiliation:

1. Academic Department of Development and Regeneration, Organ Systems Cluster; KU Leuven; Leuven Belgium

2. Clinical Department of Obstetrics and Gynaecology; University Hospitals Leuven; Leuven Belgium

3. Departments of Surgery, Pediatrics & Child Health and Physiology; University of Manitoba, and Children's Hospital Research Institute of Manitoba, Biology of Breathing; Winnipeg Manitoba Canada

4. Clinical Department of Pediatrics; University Hospitals Leuven; Leuven Belgium

5. Institute of Women's Health; University College London Hospitals; London UK

Funder

Erasmus + Programme of the European Union

University Hospitals Leuven (KOOR)

Publisher

Wiley

Subject

Obstetrics and Gynecology,Radiology, Nuclear Medicine and imaging,Reproductive Medicine,General Medicine,Radiological and Ultrasound Technology

Reference74 articles.

1. Congenital diaphragmatic hernia. A cause of persistent pulmonary hypertension of the newborn which lacks an effective therapy;Thébaud;Biol Neonate,1998

2. Congenital diaphragmatic hernia;Bohn;Am J Respir Crit Care Med,2002

3. Cardiopulmonary consequences of congenital diaphragmatic hernia;O'Toole;J Perinatol,1996

4. Prevention of heart failure in the management of congenital diaphragmatic hernia by maintaining ductal patency. A case report;Buss;J Pediatr Surg,2006

5. Neonatal pulmonary hypertension;Steinhorn;Pediatr Crit Care Med,2010

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