Requirements for fetal surgery: the diaphragmatic hernia model.

Abstract

Fetal surgery for congenital diaphragmatic hernia and other fetal conditions can only be considered if (1) the morbidity of antenatal intervention is acceptable, (2) the diagnosis of the condition can be made accurately, (3) the condition can be differentiated from other, non-surgical anomalies. In addition, (4) the natural evolution of the disease, if left untreated, should be predictable, and the condition should be lethal or severely debilitating, (5) there should not exist adequate postnatal treatment, and (6) the proposed in utero operation should be technically feasible. Open fetal surgery has proven too invasive to be justified for the treatment of diaphragmatic hernia, and progress in postnatal therapy (including ECMO) has dramatically improved the neonatal outcome in all but a severe subgroup of patients. Recently, advances in endoscopic fetal surgery (which appears to be less stressful for the fetus and the gravid uterus) and a new approach to accelerate fetal lung growth and maturation have renewed the feasibility of in utero intervention for diaphragmatic hernia.

• Authors: F I Luks
• Journal: European journal of obstetrics, gynecology, and reproductive biology (Eur J Obstet Gynecol Reprod Biol) Vol. 92 Issue 1 Pg. 115-8 (Sep 2000) ISSN: 0301-2115 [Print] Ireland
• PMID: 10986444 (Publication Type: Journal Article, Review)

Topics

• Female
• Fetal Diseases (diagnosis, etiology, surgery)
• Hernia, Diaphragmatic (complications, diagnosis, surgery)
• Humans
• Hypertension, Pulmonary (etiology)
• Pregnancy
• Prenatal Diagnosis
• Risk Assessment