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休斯顿德克萨斯大学肾移植结果的决定因素。

Factors determining renal transplant outcome at the University of Texas at Houston.

作者信息

Smith A Y, Van Buren C T, Lewis R M, Kerman R H, Kahan B D

机构信息

Department of Surgery, University of Texas Medical School, Houston 77030.

出版信息

Clin Transpl. 1987:155-66.

PMID:3154393
Abstract

CsA-Pred therapy yields equivalently good patient survival for LRD and 2 degrees CAD versus 1 degree CAD transplants. There is a long-term graft survival advantage for LRD versus 1 degree CAD transplants (5 years; 83% vs 58%). 2 degrees CAD transplants have inferior graft survival when compared with 1 degree CAD grafts (one year; 78% vs 67%). Multiple donor factors adversely affecting graft outcome include increased warm and cold ischemia times, pulsatile perfusion, use of pressors or diuretics in the donor, donor age less than 10 years, donor blood transfusions, and kidneys shipped from other centers. Recipient factors adversely affecting graft outcome include retransplantation and CMV infection as well as noncompliance with therapy. HLA-matching and pretransplant blood transfusions have not contributed in a statistically significant way to graft outcome although they may affect the quality of graft function at this center. Immunosuppressive therapy with CsA-Pred must be tailored to the individual patient. Continuous IV CsA infusion in the preoperative period and slow steroid taper impact favorably on graft outcome. The complications of CsA therapy include neuroectodermal toxicity, hepatotoxicity, and most importantly, nephrotoxicity. Other problems unique to CsA-Pred therapy include hypertension, delayed graft thrombosis, and de novo hemolytic uremic syndrome. Hepatotoxicity may eventuate in biliary and pancreatic complications necessitating surgical therapy. The overall incidence of infection and neoplasm remains low with CsA-Pred therapy. The use of therapeutic trough CsA level monitoring, as well as pharmacokinetic and pharmacodynamic analyses may assist in clinical decision making regarding administered doses, dosing interval, and discrimination between rejection and nephrotoxicity.

摘要

与1级CAD移植相比,环孢素-泼尼松疗法在LRD和2级CAD患者中产生了同样良好的生存率。LRD移植相对于1级CAD移植具有长期移植物存活优势(5年;83%对58%)。与1级CAD移植物相比,2级CAD移植的移植物存活率较低(1年;78%对67%)。对移植物结果产生不利影响的多个供体因素包括热缺血和冷缺血时间延长、搏动灌注、供体使用升压药或利尿剂、供体年龄小于10岁、供体输血以及从其他中心运送的肾脏。对移植物结果产生不利影响的受体因素包括再次移植和巨细胞病毒感染以及不遵守治疗。尽管HLA匹配和移植前输血可能会影响该中心的移植物功能质量,但对移植物结果没有统计学上的显著贡献。环孢素-泼尼松免疫抑制治疗必须根据个体患者进行调整。术前持续静脉输注环孢素和缓慢减量类固醇对移植物结果有有利影响。环孢素治疗的并发症包括神经外胚层毒性、肝毒性,最重要的是肾毒性。环孢素-泼尼松治疗特有的其他问题包括高血压、移植物延迟血栓形成和新发溶血尿毒综合征。肝毒性可能导致胆道和胰腺并发症,需要手术治疗。环孢素-泼尼松治疗的感染和肿瘤总体发生率仍然较低。使用治疗性环孢素谷浓度监测以及药代动力学和药效学分析可能有助于临床决策,包括给药剂量、给药间隔以及区分排斥反应和肾毒性。

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