Reyes J, Bueno J, Kocoshis S, Green M, Abu-Elmagd K, Furukawa H, Barksdale E M, Strom S, Fung J J, Todo S, Irish W, Starzl T E
Thomas E. Starzl Transplantation Institute, University of Pittsburgh Medical Center, Children's Hospital of Pittsburgh, PA 15213, USA.
J Pediatr Surg. 1998 Feb;33(2):243-54. doi: 10.1016/s0022-3468(98)90440-7.
A clinical trial of intestinal transplantation (Itx) under tacrolimus and prednisone immunosuppression was initiated in June 1990 in children with irreversible intestinal failure and who were dependent on total parenteral nutrition (TPN).
Fifty-five patients (28 girls, 27 boys) with a median age of 3.2 years (range, 0.5 to 18 years) received 58 intestinal transplants that included isolated small bowel (SB) (n = 17), liver SB (LSB) (n=33), and multivisceral (MV) (n=8) allografts. Nine patients also received bone marrow infusion, and there were 20 colonic allografts. Azathioprine, cyclophosphamide, or mycophenolate mofetil were used in different phases of the series. Indications for Itx included: gastroschisis (n=14), volvulus (n=13), necrotizing enterocolitis (n=6), intestinal atresia (n=8), chronic intestinal pseudoobstruction (n=5), Hirschsprung's disease (n=4), microvillus inclusion disease (n=3), multiple polyposis (n=1), and trauma [n=1).
Currently, 30 patients are alive (patient survival, 55%; graft survival, 52%). Twenty-nine children with functioning grafts are living at home and off TPN, with a mean follow-up of 962 (range, 75 to 2,424) days. Immunologic complications have included liver allograft rejection (n=18), intestinal allograft rejection (n=52), posttransplant lymphoproliferative disease (n=16), cytomegalovirus (n=16) and graft-versus-host disease (n=4). A combination of associated complications included intestinal perforation (n=4), biliary leak (n=3), bile duct stenosis (n=1), intestinal leak (n=6), dehiscence with evisceration (n=4), hepatic artery thrombosis (n=3), bleeding (n=9), portal vein stenosis (n=1), intraabdominal abscess (n=11), and chylous ascites (n=4). Graft loss occurred as a result of rejection (n=8), infection (n=12), technical complications (n=8), and complications of TPN after graft removal (n=3). There were four retransplants (SB, n=1; LSB n=3).
Intestinal transplantation is a valid therapeutic option for patients with intestinal failure suffering complications of TPN. The complex clinical and immunologic course of these patients is reflected in a higher complication rate as well as patient and graft loss than seen after heart, liver, and kidney transplantation, although better than after lung transplantation.
1990年6月,针对不可逆性肠衰竭且依赖全胃肠外营养(TPN)的儿童,开展了一项在他克莫司和泼尼松免疫抑制下进行肠移植(Itx)的临床试验。
55例患者(28例女孩,27例男孩),中位年龄3.2岁(范围0.5至18岁),接受了58例肠移植,包括孤立小肠(SB)移植(n = 17)、肝小肠(LSB)移植(n = 33)和多脏器(MV)移植(n = 8)。9例患者还接受了骨髓输注,有20例结肠移植。在该系列的不同阶段使用了硫唑嘌呤、环磷酰胺或霉酚酸酯。肠移植的适应证包括:腹裂(n = 14)、肠扭转(n = 13)、坏死性小肠结肠炎(n = 6)、肠闭锁(n = 8)、慢性肠假性梗阻(n = 5)、先天性巨结肠(n = 4)微绒毛包涵体病(n = 3)、多发性息肉病(n = 1)和创伤(n = 1)。
目前,30例患者存活(患者生存率55%;移植物生存率52%)。29例移植物功能良好的儿童在家中生活且停用了TPN,平均随访962天(范围75至2424天)。免疫并发症包括肝移植排斥反应(n = 18)、肠移植排斥反应(n = 52)、移植后淋巴细胞增殖性疾病(n = 16)、巨细胞病毒感染(n = 16)和移植物抗宿主病(n = 4)。相关并发症的组合包括肠穿孔(n = 4)、胆漏(n = 3)、胆管狭窄(n = 1)、肠漏(n = 6)、裂开伴脏器脱出(n = 4)、肝动脉血栓形成(n = 3)、出血(n = 9)、门静脉狭窄(n = 1)、腹腔内脓肿(n = 11)和乳糜性腹水(n = 4)。移植物丢失的原因包括排斥反应(n = 8)、感染(n = 12)、技术并发症(n = 8)和移植物切除后TPN的并发症(n = 3)。有4例再次移植(SB移植,n = 1;LSB移植,n = 3)。
肠移植对于患有TPN并发症的肠衰竭患者是一种有效的治疗选择。这些患者复杂的临床和免疫过程表现为并发症发生率较高,以及患者和移植物丢失率高于心脏、肝脏和肾脏移植,但优于肺移植。