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内镜胎儿手术中的插管及拔管技术能够将早产儿胎膜早破的发生率降到最低
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作者 Chang J. Tracy Jr.T.F. +2 位作者 Carr S.R. F.I. Luks 李丹 《世界核心医学期刊文摘(儿科学分册)》 2006年第A10期43-44,共2页
Background: Premature rupture of membranes (PROM) remains a significant complication of fetal surgery. Rates of 40% to 100% have been reported after both open and endoscopic fetal surgery. We describe a technique of e... Background: Premature rupture of membranes (PROM) remains a significant complication of fetal surgery. Rates of 40% to 100% have been reported after both open and endoscopic fetal surgery. We describe a technique of endoscopic port insertion and removal that minimizes trauma to the membranes. Methods: Twenty- seven consecutive patients undergoing endoscopic laser ablation for twin- to- twin transfusion syndrome were reviewed. In each case, a mini laparotomy was performed, and the amniotic cavity was entered under direct vision of the uterus using a Seldinger technique. The entry site was carefully dilated to accommodate a 4.0- mm- diameter cannula. A gelatin sponge plug was placed at port removal. Postoperative management and outcome were evaluated. Results: Median gestational age at operation was 21.3 weeks. Median operating time was 60 minutes. One patient delivered intraoperatively because of fetal distress. Seventeen (65.4% ) patients required postoperative tocolysis (median duration, 12 hours). Median postoperative gestation was 6.5 weeks (range, 1- 20 weeks). Only 1 (4.2% ) of 24 patients with successful gelatin sponge placement developed PROM. Conclusions: Meticulous technique and atraumatic insertion and removal of ports help minimize the risk of postoperative amniotic leak after endoscopic fetal surgery. Our PROM rate of 4.2% contrasts sharply with previously reported rates after similar operations. 展开更多
关键词 胎膜早破 胎儿期 拔管 手术时间 平均胎龄 明胶海绵 保胎治疗 激光消融 剖腹术 小切口
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微创外科时代的先天性多囊肺的围生期管理
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作者 Truitt A.K. Carr S.R. +2 位作者 Cassese J. F.I. Luks 刘凯 《世界核心医学期刊文摘(儿科学分册)》 2006年第A10期36-37,共2页
Background: Most congenital cystic lung lesions (CCLLs) do not require in utero or perinatal intervention. The management of asymptomatic lesions is controversial: the theoretical risk of infection and malignancy is o... Background: Most congenital cystic lung lesions (CCLLs) do not require in utero or perinatal intervention. The management of asymptomatic lesions is controversial: the theoretical risk of infection and malignancy is offset by whether thoracotomy in asymptomatic children is justified. We examined our recent experience and the role of minimally invasive surgery. Methods: We analyzed the pre- , peri- , and postnatal findings of all consecutive CCLLs diagnosed between 1997 and 2005. We reviewed records for pre- , and postnatal imaging, management, and outcome. Results: Thirty- five CCLL were diagnosed prenatally. Since 2000, all asymptomatic lesions were removed endoscopically at 6 to 18 months (thoracoscopy for 6 extralobar sequestrations, 3 intralobar sequestrations/- congenital cystic adenomatoid malformations, 5 bronchogenic cysts, and retroperitoneal laparoscopy for 2 intraabdominal sequestrations). Congenital cystic adenomatoid malformation elements were present in more than 70% . Two abdominal lesions have regressed, and 2 patients are awaiting intervention. One symptomatic infant underwent thoracotomy for congenital lobar emphysema. Conclusions: It has been argued that the risks associated with congenital lung lesions (infection and malignancy) justify intervention in the asymptomatic patient. In our experience, all these lesions could be safely removed using endosurgical techniques. Counseling of (future) parents should be updated to include minimally invasive surgery in the management algorithm. 展开更多
关键词 围生期 微创外科 腔镜治疗 叶性肺气肿 囊性腺瘤样畸形 支气管囊肿 开胸术 无症状型 出生后 肺病变
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