Treatment of severe congenital diaphragmatic hernia by fetal tracheal occlusion: Clinical experience with fifteen cases

被引:170
作者
Flake, AW
Crombleholme, TM
Johnson, MP
Howell, LJ
Adzick, NS
机构
[1] Childrens Hosp Philadelphia, Dept Surg, Ctr Fetal Diag & Treatment, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Surg, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Dept Obstet, Philadelphia, PA 19104 USA
关键词
fetal surgery; congenital diaphragmatic hernia; tracheal occlusion; fetal lung growth;
D O I
10.1067/mob.2000.108871
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: Our purpose was to determine whether prenatal tracheal occlusion improves survival in a selected population of fetuses affected by severe congenital diaphragmatic hernia. STUDY DESIGN: Fetuses with isolated congenital diaphragmatic hernia were selected as candidates for fetal intervention by specific criteria designed to predict a 90% mortality rate with conventional postnatal treatment. RESULTS: Fifteen fetuses underwent tracheal occlusion with 5 survivors (33%). Two fetuses were lost to early preterm labor. In 13 mothers, postoperative gestation ranged from 19 to 68 days, with a mean duration of pregnancy after tracheal occlusion of 38 days. The 5 survivors were hospitalized for an average of 76 days. Despite dramatic lung growth in some fetuses after tracheal occlusion, intensive management was required, and most deaths were caused by respiratory insufficiency. CONCLUSION: Prenatal tracheal occlusion can result in impressive lung growth in a subset of fetuses with severe congenital diaphragmatic hernia. However, survival remains compromised by pulmonary functional abnormality and the consequences of prematurity.
引用
收藏
页码:1059 / 1066
页数:8
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