Aydogdu S, Arikan C, Kilic M, Ozgenc F, Akman S, Unal F, Yagci R V, Tokat Y
Department of Pediatrics, Division of Gastroenterology, Ege University School of Medicine, Izmir, Turkey.
Pediatr Transplant. 2005 Dec;9(6):723-8. doi: 10.1111/j.1399-3046.2005.00366.x.
To summarize the evolution of the pediatric liver transplant program in a developing country. Between April 1997, and September 2003, 32 cadaveric (CD) and 35 living donor (LD) liver transplantations were performed on 61 children (median age 3.8 yr, range 0.5-16) at Ege University Organ Transplantation and Research Center. The patient's charts were reviewed retrospectively. The outcome of patient and graft survival was analyzed and the incidence of graft loss, complications and rejections was calculated. Indications for liver transplantation were metabolic liver disease (n = 17), biliary atresia (n = 14), viral hepatitis (n = 4), autoimmune hepatitis (n = 6), cryptogenic cirrhosis (n = 11), fulminant liver failure (n = 5) and others (n = 5). Seven of 61 children with chronic liver disease had hepatocellular carcinoma concomitantly. Median pediatric end-stage liver disease score was 23 (range 1-54). Seven children (11.4%) were UNOS status I, 44 (72%) were UNOS status II and 10 (16.6%) were UNOS status III. The median follow-up of the study population was 3.6 yr (range 0.5-6). Actuarial patient survival rates at 1, 2, 3 and 4 yr were 86, 86, 71.3 and 65% in the CD group vs. 80, 76, 67 and 67% in the LR group, respectively (p = NS). Patients listed as UNOS status 1 had lower survival rates than patients listed as UNOS status 2 and 3 (p < 0.05). The mortality rate was 26.2%. Graft survival rates were 81, 81, 75 and 64% at 1, 2, 3 and 4-yr respectively. Six patients (9%) underwent retransplantation. The main complications were infections (64.7%) and surgical complications (43.2%) (including biliary complication, vascular problems, postoperative bleeding, small for size and large for size). The incidence of acute cellular rejection was 39.3%, whereas chronic rejection was 7.4%. The result of liver transplantation in Turkish children was slightly inferior to those reported for North American and European children. However, an important characteristic of these patients that distinguishes them from Europe and North America is that most were UNOS status IIa and UNOS status I (44%). Despite technical and medical progress, infectious and biliary problems have continued to be an important cause of mortality in these patients.
总结一个发展中国家小儿肝移植项目的发展历程。1997年4月至2003年9月期间,在伊兹密尔埃杰大学器官移植与研究中心,对61名儿童(中位年龄3.8岁,范围0.5 - 16岁)进行了32例尸体供肝(CD)和35例活体供肝(LD)肝移植手术。对患者病历进行回顾性分析。分析患者和移植物的生存结果,并计算移植物丢失、并发症和排斥反应的发生率。肝移植的适应证包括代谢性肝病(n = 17)、胆道闭锁(n = 14)、病毒性肝炎(n = 4)、自身免疫性肝炎(n = 6)、隐源性肝硬化(n = 11)、暴发性肝衰竭(n = 5)及其他(n = 5)。61例慢性肝病患儿中有7例同时患有肝细胞癌。小儿终末期肝病评分中位数为23(范围1 - 54)。7例患儿(11.4%)为美国器官共享联合网络(UNOS)I级,44例(72%)为UNOS II级,10例(16.6%)为UNOS III级。研究人群的中位随访时间为3.6年(范围0.5 - 6年)。CD组1年、2年、3年和4年的精算患者生存率分别为86%、86%、71.3%和65%,而LR组分别为80%、76%、67%和67%(p =无统计学意义)。列为UNOS I级的患者生存率低于列为UNOS II级和III级的患者(p < 0.05)。死亡率为26.2%。移植物1年、2年、3年和4年的生存率分别为81%、81%、75%和64%。6例患者(9%)接受了再次移植。主要并发症为感染(64.7%)和手术并发症(43.2%)(包括胆道并发症、血管问题、术后出血、小肝综合征和大肝综合征)。急性细胞性排斥反应的发生率为39.3%,而慢性排斥反应为7.4%。土耳其儿童肝移植的结果略逊于北美和欧洲儿童报道的结果。然而,这些患者与欧洲和北美患者的一个重要区别特征是,大多数为UNOS IIa级和UNOS I级(44%)。尽管在技术和医学方面取得了进展,但感染和胆道问题仍然是这些患者死亡的重要原因。