Lallier M, St-Vil D, Dubois J, Paradis K, Laberge J M, Bensoussan A L, Guttman F M, Blanchard H
Division of Pediatric General Surgery, Hôpital Sainte-Justine, Montreal, Quebec.
J Pediatr Surg. 1995 Aug;30(8):1122-6. doi: 10.1016/0022-3468(95)90002-0.
From February 1986 to July 1994, 81 hepatic transplantations were performed in 73 children, with an overall patient survival rate of 83%. Forty-two patients received whole-liver grafts (WLG) and 39 had reduced-size grafts (RSG). The mean patient weight was 19.7 kg, with 29 patients weighing less than 10 kg. Seventeen vascular complications (21%) occurred in 13 children: 8 (10%) had hepatic artery thrombosis (HAT), 5 (6%) had portal vein thrombosis (PVT), 1 had both HAT and PVT (1%), and 3 (4%) had aortic conduit perforation (ACP). There was no significant difference in the incidence of HAT between RSG (5%) and WLG (14%) or between children weighing less than 10 kg (10%) and those weighing more than 10 kg (10%). The site of arterial reconstruction, end-to-end to the recipient common hepatic artery or end-to-side to the infrarenal aorta, had no significant effect on the occurrence of HAT (7% v 8%), but HAT occurred in 2 of 6 cases (33%) in which an aortic conduit was used. PVT documented in 5 cases (6%) was associated with technical complications (2), preduodenal portal vein (2), and a circulating cardiolipid antibody (1), and required thrombectomy, with no graft loss. Combined HAT and PVT was found in one patient 2 years postretransplantation for HAT. Although graft function is normal, portal hypertension persists. The aortic conduit, used in six patients, led to arterial perforation (3), HAT (2), and death (2). Of the 8 cases of HAT, 1 was diagnosed during autopsy and 7 occurred within 30 days and required retransplantation (6) or thrombectomy with rearterialization (1).(ABSTRACT TRUNCATED AT 250 WORDS)
1986年2月至1994年7月,对73名儿童进行了81例肝移植手术,患者总体生存率为83%。42例患者接受了全肝移植(WLG),39例接受了减体积肝移植(RSG)。患者平均体重为19.7千克,其中29例患者体重不足10千克。13名儿童发生了17例血管并发症(21%):8例(10%)发生肝动脉血栓形成(HAT),5例(6%)发生门静脉血栓形成(PVT),1例同时发生HAT和PVT(1%),3例(4%)发生主动脉管道穿孔(ACP)。RSG组(5%)和WLG组(14%)之间,以及体重不足10千克的儿童(10%)和体重超过10千克的儿童(10%)之间,HAT的发生率无显著差异。动脉重建的部位,即与受体肝总动脉端端吻合或与肾下主动脉端侧吻合,对HAT的发生无显著影响(7%对8%),但在使用主动脉管道的6例病例中有2例(33%)发生了HAT。记录在案的5例PVT(6%)与技术并发症(2例)、十二指肠前门静脉(2例)和循环心磷脂抗体(1例)有关,需要进行血栓切除术,且无移植肝丢失。1例患者在因HAT再次移植术后2年发现合并HAT和PVT。尽管移植肝功能正常,但门静脉高压仍然存在。6例患者使用的主动脉管道导致动脉穿孔(3例)、HAT(2例)和死亡(2例)。在8例HAT病例中,1例在尸检时确诊,7例发生在30天内,需要再次移植(6例)或进行血栓切除并再次动脉化(1例)。(摘要截选至250词)