Cohen R G, Barr M L, Schenkel F A, DeMeester T R, Wells W J, Starnes V A
USC Cardiothoracic Center, Department of Surgery, University of Southern California School of Medicine, Los Angeles 90033-4612.
Ann Thorac Surg. 1994 Jun;57(6):1423-7; discussion 1428. doi: 10.1016/0003-4975(94)90095-7.
Donor lobectomy has been performed in 14 patients enabling 7 recipients with cystic fibrosis to undergo bilateral living-related lobar pulmonary transplantation. Donors included 11 patients, 2 brothers, and 1 uncle. Donor mean age was 43 years (range 24 to 55 years). Their mean height and weight was 170 cm (range, 169 to 180 cm) and 72.4 kg (range, 55 to 90 kg), respectively, compared with 161 cm (range, 140 to 175 cm) and 42.4 kg (range, 27 to 55 kg), respectively, in the recipient group. Donor pulmonary evaluation consisted of a history and physical examination, chest roentgenogram and computed tomographic scan, spirometry with arterial blood gas measurement, echocardiography, and perfusion scanning. From each pair of donors, one was selected for right lower lobectomy and the other for left lower lobectomy. Standard lobectomy techniques were modified to facilitate implantation and optimize preservation of the donor lobes. On the right side, the middle lobe was removed and discarded in the first three donors to provide an adequate cuff of pulmonary artery and bronchus for implantation. With increased experience, this has proved not to be necessary. There have been no deaths and no long-term complications in the donor group. Prolonged postoperative air leaks occurred in the 3 patients who underwent right lower and middle lobectomies. All donors have been able to resume their previous lifestyles. Living-related donor lobectomy provides an alternative to cadaveric organs in select patients in need of pulmonary transplantation.
14例供体接受了肺叶切除术,使7例囊性纤维化患者能够接受双侧亲属活体肺叶移植。供体包括11例患者、2对兄弟和1位叔叔。供体平均年龄为43岁(范围24至55岁)。他们的平均身高和体重分别为170厘米(范围169至180厘米)和72.4千克(范围55至90千克),而受体组的平均身高和体重分别为161厘米(范围140至175厘米)和42.4千克(范围27至55千克)。供体肺部评估包括病史和体格检查、胸部X线片和计算机断层扫描、肺功能测定及动脉血气分析、超声心动图和灌注扫描。从每对供体中,选择1例进行右下肺叶切除术,另1例进行左下肺叶切除术。对标准肺叶切除技术进行了改良,以利于植入并优化供体肺叶的保存。右侧,在前3例供体中切除并丢弃中叶,以便为植入提供足够的肺动脉和支气管袖带。随着经验的增加,已证明这没有必要。供体组无死亡病例,也无长期并发症。接受右下肺和中叶切除术的3例患者术后出现了长时间的气胸漏气。所有供体均已能够恢复其以前的生活方式。亲属活体供体肺叶切除术为某些需要肺移植的患者提供了尸体器官以外的另一种选择。