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Primary Adult Liver Transplantation Under Tacrolimus: More Than 90 Months Actual Follow-Up Survival and Adverse Events

机译:他克莫司治疗下的原发性成人肝移植:超过90个月的实际随访生存和不良事件

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摘要

The introduction of tacrolimus has shown decreased rates of acute and steroid-resistant rejection after liver transplantation (LTx). The aim of the present study is to examine the long-term efficacy and safety of tacrolimus in primary liver transplant recipients. The first 121 consecutive adults (aged >16 years) who underwent primary LTx at a single center from August 1989 to February 1990 were followed up until August 1997. The mean follow-up was 93.2 ± 1.2 months (range, 90.5 to 96.5 months). Patient survival, graft survival, rate of rejection, and adverse events were examined. The actual 7-year patient survival rate was 67.8%, and the graft survival rate was 63.6%. Infections, recurrence of disease, de novo malignancies, and cardiovascular events constituted the main causes of graft loss and death in the long term. Graft loss related to acute or chronic rejection was rare. The rate of acute rejection beyond 2 years was approximately 3% per year, and most rejections were steroid responsive. Approximately 70% of the patients received only tacrolimus after 1 year. Four patients developed end-stage renal disease, and 2 patients underwent kidney transplantation. Hyperkalemia and hypertension were observed in one third of the patients. New-onset insulin-dependent diabetes mellitus was observed in 9% and 13% of the patients at the 1-year and 7-year follow-up, respectively. Seven patients developed de novo malignancies, including two skin malignancies. Six patients developed posttransplantation lymphoproliferative disorder during the entire follow-up period. Actual patient and graft survival at 7 years was excellent, and few adverse events developed after the first year. Graft loss from acute or chronic rejection was rare under tacrolimus, and approximately 70% of the patients were steroid free on tacrolimus monatherapy after the first year after LTx.
机译:他克莫司的引入显示出肝移植(LTx)后急性和类固醇耐药性排斥的发生率降低。本研究的目的是检查他克莫司在原发性肝移植受者中的长期疗效和安全性。 1989年8月至1990年2月在单个中心接受初次LTx治疗的连续121位成年人(年龄超过16岁)进行了随访,直至1997年8月。平均随访时间为93.2±1.2个月(范围90.5至96.5个月) 。检查患者存活率,移植物存活率,排斥率和不良事件。实际的7年患者生存率为67.8%,而移植物生存率为63.6%。从长期来看,感染,疾病复发,新发恶性肿瘤和心血管事件是造成移植物丢失和死亡的主要原因。与急性或慢性排斥反应相关的移植物丢失很少见。超过2年的急性排斥反应的发生率约为每年3%,并且大多数排斥反应都是类固醇敏感的。大约70%的患者在1年后仅接受他克莫司治疗。 4名患者发展为终末期肾脏疾病,2名患者接受了肾脏移植。在三分之一的患者中观察到高钾血症和高血压。在1年和7年的随访中,分别有9%和13%的患者观察到新发胰岛素依赖型糖尿病。 7名患者发生了新发恶性肿瘤,其中包括2例皮肤恶性肿瘤。在整个随访期间,六名患者发生了移植后的淋巴增生性疾病。病人和移植物的7年实际生存情况非常好,第一年后几乎没有不良反应发生。他克莫司在急性或慢性排斥反应中很少发生移植物丢失,LTx术后第一年后,他克莫司单抗治疗约70%的患者不含类固醇。

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