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胸腺球蛋白诱导在活体供肾移植中安全有效:单中心经验

Thymoglobulin induction is safe and effective in live-donor renal transplantation: a single center experience.

作者信息

Hardinger Karen L, Schnitzler Mark A, Koch Matthew J, Labile Emily, Stirnemann Paula M, Miller Brent, Enkvetchakul Decha, Brennan Daniel C

机构信息

Department of Pharmacy Practice, University of Missouri-Kansas City, Kansas City, MO 64108-2792, and Department of Medicine, Barnes-Jewish Hospital at Washington University School of Medicine, St. Louis, MO, USA.

出版信息

Transplantation. 2006 May 15;81(9):1285-9. doi: 10.1097/01.tp.0000209825.91632.ea.

Abstract

BACKGROUND

The relative benefit versus safety of induction therapy in live-donor renal transplant recipients is controversial. This paper presents observational data of live-donor recipients who received Thymoglobulin induction and standard maintenance immunosuppressive therapy.

METHODS

Review and analysis of clinic records and electronic databases of live-donor renal transplants that received Thymoglobulin induction from May 1996 through 2003.

RESULTS

Data analysis included 214 live-donor recipients (146 related, 68 unrelated) with a mean follow-up of 3.0+/-1.9 years. The average age of recipients was 44+/-13 years, with a majority being Caucasian (86%) and male (64%). Nineteen (9%) received previous transplants. No patients experienced delayed graft function and 10 (5%) developed acute rejection. Overall, predicted five-year patient survival was 96% and graft survival was 82%. The rates of CMV infection (5%), malignancy (3%), and lymphoproliferative disorder (0.5%) were low. When compared to live-donor kidney transplant recipients nationwide, the center cohort demonstrated improved five year patient (96% center versus 90% national, P=0.0326) and graft survival (82% center versus 79% national, P=0.0901), and a lower one-year acute rejection rate (2% center versus 21 % national, P<0.001).

CONCLUSIONS

In this analysis, the use of Thymoglobulin in live-donor renal transplantation was associated with an absence of delayed graft function, low acute rejection rates, and high patient and graft survival without increasing the risk of infection or lymphoproliferative disorder.

摘要

背景

活体供肾肾移植受者诱导治疗的相对获益与安全性存在争议。本文呈现了接受胸腺球蛋白诱导治疗及标准维持性免疫抑制治疗的活体供肾受者的观察性数据。

方法

回顾并分析1996年5月至2003年接受胸腺球蛋白诱导治疗的活体供肾移植的临床记录和电子数据库。

结果

数据分析纳入了214例活体供肾受者(146例亲属供肾,68例非亲属供肾),平均随访时间为3.0±1.9年。受者的平均年龄为44±13岁,大多数为白种人(86%)且为男性(64%)。19例(9%)曾接受过移植。无患者发生移植肾功能延迟恢复,10例(5%)发生急性排斥反应。总体而言,预计的5年患者生存率为96%,移植肾生存率为82%。巨细胞病毒感染率(5%)、恶性肿瘤发生率(3%)和淋巴细胞增殖性疾病发生率(0.5%)较低。与全国范围内的活体供肾肾移植受者相比,该中心队列的5年患者生存率(中心为96%,全国为90%,P = 0.0326)和移植肾生存率(中心为82%,全国为79%,P = 0.0901)有所提高,且1年急性排斥反应率较低(中心为2%,全国为21%,P<0.001)。

结论

在本分析中,活体供肾肾移植中使用胸腺球蛋白与无移植肾功能延迟恢复、低急性排斥反应率、高患者及移植肾生存率相关,且未增加感染或淋巴细胞增殖性疾病的风险。

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