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体外膜肺氧合对高危先天性膈疝新生儿生存的影响:来自单一机构的45例病例

The effect of extracorporeal membrane oxygenation on the survival of neonates with high-risk congenital diaphragmatic hernia: 45 cases from a single institution.

作者信息

O'Rourke P P, Lillehei C W, Crone R K, Vacanti J P

机构信息

Department of Anesthesia (Pediatrics), Children's Hospital and Medical Center, University of Washington, Seattle 98105.

出版信息

J Pediatr Surg. 1991 Feb;26(2):147-52. doi: 10.1016/0022-3468(91)90896-2.

DOI:10.1016/0022-3468(91)90896-2
PMID:2023071
Abstract

At The Children's Hospital, Boston (TCH), in the 3 years before extracorporeal membrane oxygenation (ECMO) was available, infants with high-risk congenital diaphragmatic hernia (CDH) had a 47% survival rate. In February 1984, ECMO was introduced and offered to all high-risk CDH infants with a 100% predicted mortality. Since February 1984, 45 infants with high-risk CDH presented to TCH. Twenty-six (58%) were supported with ECMO; 19 (42%) never met the criteria for 100% predicted mortality and were supported with conventional mechanical ventilation (CMV). Overall survival was 49%. Nine (35%) of the 26 ECMO patients survived. Thirteen (68%) of the 19 CMV patients survived. Although there was no change in survival, there was a change in the cause of death. Deaths in the ECMO group were either early (n = 8, secondary to a complication of ECMO or lack of pulmonary improvement) or late (n = 9). The late deaths were infants who were successfully weaned from ECMO, never weaned from CMV, and who died secondary to complications of chronic lung disease.

摘要

在波士顿儿童医院(TCH),在体外膜肺氧合(ECMO)可用之前的3年里,患有高危先天性膈疝(CDH)的婴儿存活率为47%。1984年2月,ECMO被引入并提供给所有预测死亡率为100%的高危CDH婴儿。自1984年2月以来,45名高危CDH婴儿被送到TCH。26名(58%)接受了ECMO支持;19名(42%)从未达到预测死亡率为100%的标准,接受了传统机械通气(CMV)支持。总体存活率为49%。26名ECMO患者中有9名(35%)存活。19名CMV患者中有13名(68%)存活。虽然存活率没有变化,但死亡原因发生了变化。ECMO组的死亡要么是早期(n = 8,继发于ECMO并发症或肺部无改善),要么是晚期(n = 9)。晚期死亡的婴儿是那些成功脱离ECMO、从未脱离CMV且死于慢性肺病并发症的婴儿。

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引用本文的文献

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How often is extracorporeal membrane oxygenation needed in cases of congenital diaphragmatic hernia?先天性膈疝病例中需要进行体外膜肺氧合的频率是多少?
Pediatr Surg Int. 1996 Oct;11(8):528-31. doi: 10.1007/BF00626058.
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Congenital diaphragmatic hernia: lung compliance after antenatal tracheal obstruction or surgical correction of the defect.
Pediatr Surg Int. 1996 Oct;11(8):524-7. doi: 10.1007/BF00626057.
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Is there a role for antioxidants in prevention of pulmonary hypoplasia in nitrofen-induced rat model of congenital diaphragmatic hernia?抗氧化剂在硝呋烯腙诱导的先天性膈疝大鼠模型中预防肺发育不全方面是否起作用?
Pediatr Surg Int. 2010 Apr;26(4):401-6. doi: 10.1007/s00383-010-2552-2. Epub 2010 Feb 3.
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Pediatr Surg Int. 2009 Dec;25(12):1059-64. doi: 10.1007/s00383-009-2473-0. Epub 2009 Aug 30.
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Congenital diaphragmatic hernia. Stabilization and repair on ECMO.先天性膈疝。在体外膜肺氧合(ECMO)支持下的稳定与修复。
Ann Surg. 1992 Nov;216(5):569-73. doi: 10.1097/00000658-199211000-00008.
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Delayed surgical repair and ECMO improves survival in congenital diaphragmatic hernia.延迟手术修复和体外膜肺氧合可提高先天性膈疝的生存率。
Ann Surg. 1992 Oct;216(4):454-60; discussion 460-2. doi: 10.1097/00000658-199210000-00009.