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新生猪肺叶移植:一种治疗先天性膈疝的模型

Pulmonary lobar transplantation in neonatal swine: a model for treatment of congenital diaphragmatic hernia.

作者信息

Crombleholme T M, Adzick N S, Hardy K, Longaker M T, Bradley S M, Duncan B W, Verrier E D, Harrison M R

机构信息

Department of Surgery, University of California, San Francisco 94143.

出版信息

J Pediatr Surg. 1990 Jan;25(1):11-8. doi: 10.1016/s0022-3468(05)80156-3.

DOI:10.1016/s0022-3468(05)80156-3
PMID:2299534
Abstract

Congenital diaphragmatic hernia (CDH) babies born with severe pulmonary hypoplasia are unsalvageable despite maximal therapy including extracorporeal membrane oxygenation (ECMO). Lung transplantation is a potential treatment for these otherwise doomed infants using ECMO as a bridge to transplantation. Cadaveric, or living related donation of a more mature reduced size lung (pulmonary lobe or segment) may help solve the critical donor shortage problem. We evaluated the physiological response of mature left lower lobe (LLL) transplants in neonatal swine with the hemodynamic conditions of CDH simulated by occlusion of the right pulmonary artery (PA), and also studied the pulmonary function of the mature lobar graft compared with the neonatal lung. LLL transplantation was well tolerated and resulted in minimal alteration in hemodynamic parameters. The response to right PA occlusion was similar pre- and posttransplantation with a fall in cardiac output and a significant rise in pulmonary vascular resistance. Compared with the contralateral native lung, the lobar graft was preferentially ventilated with resultant higher pH (7.65 +/- 0.17 v 7.41 +/- 0.08, P less than .01) and lower pCO2 (17 +/- 6 v 36 +/- 5, P less than .001). The more mature lobar graft was preferentially ventilated due to the increased compliance compared with the neonatal right lung (8.16 +/- 1.28 v 5.48 +/- 0.82 mL/cm, P less than .0001). Reduced size lung transplantation is technically feasible and may help solve the donor problem for severe CDH neonates for whom no effective therapy is currently available.

摘要

患有严重肺发育不全的先天性膈疝(CDH)患儿,即便接受包括体外膜肺氧合(ECMO)在内的最大程度治疗,仍无法挽救。肺移植是这些原本注定死亡的婴儿的一种潜在治疗方法,可使用ECMO作为移植桥梁。尸体供肺或活体亲属捐赠的更成熟的缩小尺寸肺(肺叶或肺段)可能有助于解决关键的供体短缺问题。我们通过阻断右肺动脉(PA)模拟CDH的血流动力学状况,评估了新生猪成熟左肺下叶(LLL)移植的生理反应,并研究了成熟肺叶移植物与新生肺相比的肺功能。LLL移植耐受性良好,血流动力学参数变化极小。移植前后对右PA阻断的反应相似,心输出量下降,肺血管阻力显著升高。与对侧的天然肺相比,肺叶移植物优先通气,导致pH值更高(7.65±0.17对7.41±0.08,P<0.01),pCO2更低(17±6对36±5,P<0.001)。与新生右肺相比,由于顺应性增加,更成熟的肺叶移植物优先通气(8.16±1.28对5.48±0.82 mL/cm,P<0.0001)。缩小尺寸肺移植在技术上是可行的,可能有助于解决目前尚无有效治疗方法的严重CDH新生儿的供体问题。

相似文献

1
Pulmonary lobar transplantation in neonatal swine: a model for treatment of congenital diaphragmatic hernia.新生猪肺叶移植:一种治疗先天性膈疝的模型
J Pediatr Surg. 1990 Jan;25(1):11-8. doi: 10.1016/s0022-3468(05)80156-3.
2
Lobar lung transplantation as a treatment for congenital diaphragmatic hernia.肺叶移植治疗先天性膈疝
J Pediatr Surg. 1994 Dec;29(12):1557-60. doi: 10.1016/0022-3468(94)90215-1.
3
Cardiac malposition, redistribution of fetal cardiac output, and left heart hypoplasia reduce survival in neonates with congenital diaphragmatic hernia requiring extracorporeal membrane oxygenation.心脏位置异常、胎儿心输出量重新分布以及左心发育不全降低了患有先天性膈疝且需要体外膜肺氧合的新生儿的存活率。
J Pediatr. 1998 Jul;133(1):57-62. doi: 10.1016/s0022-3476(98)70178-7.
4
Lung volume, pulmonary vasculature, and factors affecting survival in congenital diaphragmatic hernia.先天性膈疝的肺容积、肺血管系统及影响生存的因素
Pediatrics. 1998 Feb;101(2):289-95. doi: 10.1542/peds.101.2.289.
5
Remodeling of pulmonary arteries in human congenital diaphragmatic hernia with or without extracorporeal membrane oxygenation.先天性膈疝患儿肺动脉重塑与体外膜肺氧合的关系
J Pediatr Surg. 2000 Feb;35(2):208-15. doi: 10.1016/s0022-3468(00)90011-3.
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Extracorporeal membrane oxygenation and congenital diaphragmatic hernia: should any infant be excluded?体外膜肺氧合与先天性膈疝:是否应排除任何婴儿?
J Pediatr Surg. 1990 Oct;25(10):1048-52; discussion 1052-3. doi: 10.1016/0022-3468(90)90216-v.
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Reduced-size lung transplantation in neonatal swine: technique and short-term physiological response.新生猪减体积肺移植:技术与短期生理反应
Ann Thorac Surg. 1990 Jan;49(1):55-60. doi: 10.1016/0003-4975(90)90356-b.
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Ventricular Performance is Associated with Need for Extracorporeal Membrane Oxygenation in Newborns with Congenital Diaphragmatic Hernia.先天性膈疝新生儿的心室功能与体外膜肺氧合需求相关。
J Pediatr. 2017 Dec;191:28-34.e1. doi: 10.1016/j.jpeds.2017.08.060. Epub 2017 Oct 13.
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Survival in early- and late-term infants with congenital diaphragmatic hernia treated with extracorporeal membrane oxygenation.接受体外膜肺氧合治疗的先天性膈疝早、晚期婴儿的存活率。
Pediatrics. 2002 Sep;110(3):590-6. doi: 10.1542/peds.110.3.590.
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Surfactant (beractant) therapy for infants with congenital diaphragmatic hernia on ECMO: evidence of persistent surfactant deficiency.体外膜肺氧合(ECMO)支持下的先天性膈疝婴儿的表面活性剂(贝拉克坦)治疗:持续性表面活性剂缺乏的证据
J Pediatr Surg. 1994 Mar;29(3):407-12. doi: 10.1016/0022-3468(94)90580-0.

引用本文的文献

1
Contemporary management of congenital diaphragmatic hernia.
World J Surg. 1993 May-Jun;17(3):350-5. doi: 10.1007/BF01658703.
2
On the horizon: neonatal lung transplantation.展望未来:新生儿肺移植。
Arch Dis Child. 1992 Apr;67(4 Spec No):455-7. doi: 10.1136/adc.67.4_spec_no.455.
3
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.
4
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.