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Diagnosis and management of congenital diaphragmatic hernia: a clinical practice guideline

2018; Canadian Medical Association; Volume: 190; Issue: 4 Linguagem: Inglês

10.1503/cmaj.170206

1488-2329

Pramod S. Puligandla, Erik D. Skarsgard, Martin Offringa, Ian Adatia, Robert Baird, Michelle Bailey, Mary E. Brindle, Priscilla Chiu, Arthur Cogswell, Shyamala Dakshinamurti, Hélène Flageole, Richard Keijzer, Douglas McMillan, Titilayo Oluyomi-Obi, Thomas Pennaforte, Thérèse Perreault, Bruno Piedbœuf, Sean P. Riley, Greg Ryan, Anne Synnes, Michael D. Traynor,

Congenital Anomalies and Fetal Surgery

KEY POINTS Congenital diaphragmatic hernia (CDH), which occurs in about 1 in 3300 live births, is a congenital defect in the diaphragm that allows herniation of abdominal viscera into the thorax.[1][1] The resulting abnormal lung development leads to pulmonary hypoplasia and pulmonary hypertension,