Han Huan-Li, Dai Xiao-Ke, Li Ying-Cun, Zhang Ming-Man
Department of Pediatric Hepatobiliary Surgery, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, China International Science and Technology Cooperation Base of Child Development and Critical Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing 400014, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2022 Sep;53(5):777-781. doi: 10.12182/20220960201.
To evaluate the safety and clinical efficacy of ABO-incompatible living-donor liver transplantation (LDLT) in children.
The clinical data of 62 children who underwent for the first time living donor liver transplantation in our hospital from April 2019 to July 2020 were retrospectively analyzed. According to the blood type matching of donor and recipient, the patients were divided into 3 groups, ABO-identical (ABO-Id, =33), ABO-compatible (ABO-C, =10) and ABO-incompatible (ABO-In, =19), the median age of recipients in the three groups being 5 months. In the ABO-In group, 4 recipients whose condition was combined with liver failure and 2 recipients who had blood group antibody titers≥1∶32 received preoperative plasma exchange. All ABO-incompatible recipients had preoperative blood group antibody titers<1∶32. All recipients in the three groups underwent piggyback liver transplantation and received immunosuppressive and anticoagulation therapy. Postoperative follow-up was 5 to 20 months, the median being 12 months, measured until December 31, 2020 or until the date of death. Baseline clinical data, postoperative survival, and postoperative complications of recipients in the three groups were analyzed.
There were no significant differences in age, gender, underlying disease, operation history, Child Pugh score, donor age, graft to recipient weight ratio (GR/WR), cold ischemia time, warm ischemia time, duration of surgery, intraoperative blood loss and the use of immunosuppressants among the recipients in the three groups (all >0.05). There was one death in the perioperative period and two deaths in the postoperative period in the ABO-Id group. There was one death in the postoperative period in the ABO-C group. There was one death in the perioperative period and one death in the postoperative period in the ABO-In group. There was no significant difference in the overall cumulative survival rate among the three groups ( >0.05). There were no significant differences in the incidence of postoperative infection, acute rejection, biliary anastomotic stenosis and vascular complications among the three groups ( >0.05).
ABO-In LDLT is an effective and safe treatment option that can effectively expand the pool of live donors for liver transplantation and save the life of children with end-stage liver disease.
评估儿童ABO血型不相容活体肝移植(LDLT)的安全性和临床疗效。
回顾性分析2019年4月至2020年7月在我院首次接受活体肝移植的62例儿童的临床资料。根据供受者血型匹配情况,将患者分为3组,即ABO血型相同组(ABO-Id,n=33)、ABO血型相容组(ABO-C,n=10)和ABO血型不相容组(ABO-In,n=19),三组受者的中位年龄均为5个月。在ABO-In组中,4例合并肝衰竭的受者和2例血型抗体效价≥1∶32的受者接受了术前血浆置换。所有ABO血型不相容的受者术前血型抗体效价均<1∶32。三组所有受者均接受背驮式肝移植,并接受免疫抑制和抗凝治疗。术后随访5至20个月,中位随访时间为12个月,至2020年12月31日或直至死亡日期。分析三组受者的基线临床资料、术后生存率及术后并发症。
三组受者在年龄、性别、基础疾病、手术史、Child Pugh评分、供者年龄、移植物与受者体重比(GR/WR)、冷缺血时间、热缺血时间、手术时间、术中出血量及免疫抑制剂使用情况等方面差异均无统计学意义(均P>0.05)。ABO-Id组围手术期死亡1例,术后死亡2例。ABO-C组术后死亡1例。ABO-In组围手术期死亡1例,术后死亡1例。三组总体累积生存率差异无统计学意义(P>0.05)。三组术后感染、急性排斥反应、胆道吻合口狭窄及血管并发症发生率差异均无统计学意义(P>0.05)。
ABO血型不相容活体肝移植是一种有效且安全的治疗选择,可有效扩大肝移植活体供者来源,挽救终末期肝病患儿的生命。