Indications for thoracoscopic repair of congenital diaphragmatic hernia in neonates
Indications for thoracoscopic repair of congenital diaphragmatic hernia in neonates
复制标题
胸腔镜新生儿先天性膈疝修补术的适应证
DOI:
10.1007/s00383-010-2724-0
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发表时间:
2010
影响因子:
1.8
通讯作者:
A. Yamataka
中科院分区:
文献类型:
--
作者:
T. Okazaki;Kinya Nishimura;Toshiaki Takahashi;H. Shoji;Toshiaki Shimizu;Toshitaka Tanaka;S. Takeda;E. Inada;Geoffrey J. Lane;A. Yamataka
PurposeWe reviewed 26 consecutive cases of congenital diaphragmatic hernia (CDH) prospectively to establish selection criteria for successful thoracoscopic CDH repair (TR).MethodsFive preoperative deaths were excluded, leaving 21 subjects. TR was only considered once pulmonary hypertension (PH) improved on echocardiography, and if cardiopulmonary status was stable in the decubitus position in the neonatal intensive care unit (NICU) under conventional mechanical or high-frequency oscillatory ventilation (HFOV) with/without nitric oxide (NO) for at least 10 min as a marker for tolerating surgery and manual ventilation was possible for transfer to the operating room. All other patients had open repair (OR).Results8/21 had TR and 13/21 had OR. There were significant differences between TR and OR for prenatal diagnosis (37.5 vs. 84.6%,p< 0.05) and earlier surgery (1.4 ± 0.8 vs. 2.5 ±1.1 days after birth,p< 0.05), respectively. Intraoperative HFOV was required in all OR and 3 TR (p< 0.01). NO was required in 1 TR and 10 OR (p< 0.01). Organ herniation was significantly less in TR (50 vs. 100%,p< 0.01 for stomach; 0 vs. 54%,p< 0.05 for liver). Three TR required conversion to OR because of technical difficulties. One OR died from deteriorating PH.ConclusionsOur selection criteria for TR would appear to be safe and reasonable.