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体外膜肺氧合撤离后先天性膈疝的修复

Repair of congenital diaphragmatic hernia after weaning from extracorporeal membrane oxygenation.

作者信息

Adolph V, Flageole H, Perreault T, Johnston A, Nguyen L, Youssef S, Guttman F, Laberge J M

机构信息

Division of Pediatric Surgery, McGill University, Montreal, Quebec, Canada.

出版信息

J Pediatr Surg. 1995 Feb;30(2):349-52. doi: 10.1016/0022-3468(95)90588-x.

DOI:10.1016/0022-3468(95)90588-x
PMID:7738764
Abstract

Stabilization and delayed operation for patients with congenital diaphragmatic hernia (CDH) is now widely accepted. When preoperative extracorporeal membrane oxygenation (ECMO) is needed, most centers have CDH repaired on ECMO to minimize the risk of postoperative deterioration. The authors adopted a policy of weaning from ECMO before repair in an effort to avoid hemorrhagic risks. They reviewed their experience with CDH patients who required ECMO for stabilization before repair but for whom post-ECMO repair was planned. The records of all high-risk CDH patients with a gestational age of at least 34 weeks were reviewed. Eighteen patients were identified. None of the eight who were stabilized and operated on without ECMO required bypass postoperatively; all survived. Ten were placed on bypass, nine for stabilization before repair. Of the nine, seven (78%) were weaned from ECMO to conventional ventilation. Repair of the diaphragmatic defect was performed an average of 3.8 days later; none of these patients had severe pulmonary hypertension postoperatively, and all survived. Two could not be weaned before repair, one of whom had a complex congenital heart defect. This patient died. The other patient had repair on ECMO because of intrathoracic gastric volvulus. Severe blood loss prompted decannulation, and the patient died. One patient who was placed on bypass was transferred 10 days after having had repair elsewhere (at 4 hours of age). Pulmonary hypertension did not resolve, and the postmortem examination showed alveolar capillary dysplasia, with focal misalignment of the pulmonary vessels.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

先天性膈疝(CDH)患者的稳定治疗及延迟手术目前已被广泛接受。当术前需要体外膜肺氧合(ECMO)时,大多数中心会在ECMO支持下进行CDH修补术,以将术后病情恶化的风险降至最低。作者采取了在修补术前撤离ECMO的策略,以避免出血风险。他们回顾了那些在修补术前需要ECMO稳定病情但计划在ECMO支持下进行修补术的CDH患者的经验。对所有孕周至少34周的高危CDH患者的记录进行了回顾。共确定了18例患者。8例未使用ECMO进行稳定治疗和手术的患者术后均未需要体外循环;全部存活。10例患者接受了体外循环,其中9例是为了在修补术前稳定病情。在这9例患者中,7例(78%)从ECMO撤离至常规通气。平均3.8天后进行了膈肌缺损修补术;这些患者术后均无严重肺动脉高压,全部存活。2例在修补术前无法撤离ECMO,其中1例患有复杂先天性心脏病。该患者死亡。另一例患者因胸腔内胃扭转在ECMO支持下进行了修补术。严重失血导致撤机,患者死亡。1例接受体外循环的患者在其他地方(出生4小时时)进行修补术后10天被转来。肺动脉高压未缓解,尸检显示肺泡毛细血管发育异常,肺血管局部排列紊乱。(摘要截短于250字)

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Repair of congenital diaphragmatic hernia after weaning from extracorporeal membrane oxygenation.体外膜肺氧合撤离后先天性膈疝的修复
J Pediatr Surg. 1995 Feb;30(2):349-52. doi: 10.1016/0022-3468(95)90588-x.
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Late versus early surgical correction for congenital diaphragmatic hernia in newborn infants.新生儿先天性膈疝的晚期与早期手术矫正
Cochrane Database Syst Rev. 2000;2000(3):CD001695. doi: 10.1002/14651858.CD001695.