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肺叶移植。适应证、技术及结果。

Lobar transplantation. Indications, technique, and outcome.

作者信息

Starnes V A, Barr M L, Cohen R G

机构信息

Department of Surgery, University of Southern California School of Medicine, Los Angeles 90033.

出版信息

J Thorac Cardiovasc Surg. 1994 Sep;108(3):403-10; discussion 410-1.

PMID:8078333
Abstract

Lobar transplantation represents a therapeutic option for children and some adults with severe end-stage pulmonary disease. Six patients including two neonates, three children, and one adult underwent lobar transplantation. Ages ranged from 17 days to 21 years. Transplant procedures were unilateral in the neonates and two of the children and bilateral in the child and adult who had cystic fibrosis. The donor lobes were from cadavers in the two neonates and living related donors in the children and the adult. Unilateral grafts involved use of the right upper lobe in the 12-year-old patient with bronchopulmonary dysplasia; right middle lobe with a ventricular septal defect repair in the 4-year-old patient with Eisenmenger's syndrome, left upper lobe in the 28-day-old patient with primary pulmonary hypertension, and the right upper and middle lobes in the 17-day-old patient with diaphragmatic hernia. Bilateral lobar transplantations were performed with the right lower and left lower lobes in the two patients with cystic fibrosis (aged 13 and 21 years). The two neonates underwent emergency transplantation with the use of extracorporeal membrane oxygenation as a bridge. Perioperative survival was 83%, with only the 4-year-old patient with ventricular septal defect/Eisenmenger's syndrome dying early. No airway complications were observed. The unilateral grafts received most of the blood flow as shown by perfusion scanning (range 74% to 99%). Living related donor complications included prolonged air leaks (> 6 days) in two patients. In urgent situations, such as an infant requiring extracorporeal membrane oxygenation, and in the existing milieu of donor shortage, lobar transplantation (living related or cadaveric) is a surgically feasible procedure and can provide a donor source in the limited time frame of these clinical situations. Bilateral lobe transplantation may be a viable option for patients with cystic fibrosis and life-threatening respiratory decompensation.

摘要

肺叶移植是治疗患有严重终末期肺病的儿童和部分成人的一种治疗选择。6例患者接受了肺叶移植,其中包括2例新生儿、3例儿童和1例成人。年龄范围从17天至21岁。新生儿和2例儿童接受的是单侧移植手术,患有囊性纤维化的儿童和成人接受的是双侧移植手术。2例新生儿的供体肺叶来自尸体,儿童和成人的供体肺叶来自活体亲属供体。单侧移植中,12岁患有支气管肺发育不良的患者接受的是右上叶移植;4岁患有艾森曼格综合征且行室间隔缺损修补术的患者接受的是右中叶移植;28天患有原发性肺动脉高压的患者接受的是左上叶移植;17天患有膈疝的患者接受的是右上叶和中叶移植。2例患有囊性纤维化(年龄分别为13岁和21岁)的患者接受的是右下叶和左下叶的双侧肺叶移植。2例新生儿在体外膜肺氧合作为过渡的情况下接受了急诊移植。围手术期生存率为83%,只有4岁患有室间隔缺损/艾森曼格综合征的患者早期死亡。未观察到气道并发症。灌注扫描显示单侧移植肺叶接受了大部分血流(范围为74%至99%)。活体亲属供体的并发症包括2例患者出现持续漏气(>6天)。在紧急情况下,如婴儿需要体外膜肺氧合,以及在供体短缺的现有环境下,肺叶移植(活体亲属供体或尸体供体)是一种手术可行的方法,并且可以在这些临床情况的有限时间框架内提供供体来源。双侧肺叶移植对于患有囊性纤维化且有危及生命的呼吸功能不全的患者可能是一种可行的选择。

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