Morrissey P E, Gordon F, Shaffer D, Madras P N, Silva P, Sahyoun A I, Monaco A P, Hill T, Lewis W D, Jenkins R L
Division of Organ Transplantation, Beth Israel-Deaconess Medical Center, Boston, MA, USA.
Liver Transpl Surg. 1998 Sep;4(5):363-9. doi: 10.1002/lt.500040512.
Patients with renal failure after liver transplantation have a particularly poor prognosis. Therefore, in the setting of end-stage renal disease requiring dialysis or severe renal insufficiency that will not improve after liver replacement, combined liver-kidney transplantation (LKT) is the preferred approach. We have adopted a policy of LKT in patients with end-stage liver disease and renal insufficiency undergoing dialysis or with a creatinine clearance less than 35 mL/min and evidence of chronic renal dysfunction. Since 1991, we have performed 208 orthotopic liver transplantations. Fourteen patients (8%) have undergone combined LKT, including 6 patients undergoing hemodialysis. Cytotoxic cross-matches (modified Amos technique and antihuman globulin method) were performed on 13 of 14 patients and were positive in 3 patients. Two patients died less than 4 months after LKT and 12 patients are alive and well. Graft survival censored for patient death was 100% for liver allografts and 93% for renal allografts, with a mean follow-up of 39 +/- 24 months. The most recent serum creatinine level in the patients with the 11 functioning grafts was 1.1 +/- 0.6 mg/dL. Biopsy-proven acute rejection occurred in 50% of simultaneous liver allografts. By contrast, only a single episode (6%) of renal allograft dysfunction was attributable to acute rejection. All rejection episodes occurred in the first 90 days after transplantation and were steroid sensitive. Three of 14 combined procedures were performed in the setting of a positive cytotoxic cross-match. In 2 recent patients, the results were confirmed by positive cross-matches to the donor's T and B cells by flow cytometry. Flow cytometric cross-matches reverted to negative 1 hour after liver transplantation and several hours before the administration of antithymocyte globulin. The cross-matches remained negative on postoperative days 1 and 7. Presently, all 3 patients with a positive cross-match enjoy normal hepatic and renal function at 631, 706, and 2275 days follow-up. Renal scans were performed in 4 LKT recipients not previously undergoing hemodialysis and indicated varying and unpredictable degrees of function in the native and transplanted kidneys. In conclusion, combined LKT can be performed safely and is associated with a low rate of acute rejection, even in the setting of a positive cross-match. Predicting which patients with renal insufficiency will benefit from LKT remains challenging; however, these results suggest that LKT should be encouraged in patients with evidence of irreversible renal insufficiency who require liver transplantation.
肝移植后出现肾衰竭的患者预后特别差。因此,对于需要透析的终末期肾病或肝移植后肾功能严重不全且无法改善的患者,肝肾联合移植(LKT)是首选方法。我们对终末期肝病合并肾功能不全且正在接受透析或肌酐清除率低于35 mL/分钟并有慢性肾功能不全证据的患者采取了LKT策略。自1991年以来,我们共进行了208例原位肝移植。14例患者(8%)接受了肝肾联合移植,其中6例患者正在接受血液透析。14例患者中的13例进行了细胞毒性交叉配型(改良阿莫斯技术和抗人球蛋白法),3例结果为阳性。2例患者在LKT后不到4个月死亡,12例患者存活且情况良好。以患者死亡为截尾因素的肝移植移植物存活率为100%,肾移植移植物存活率为93%,平均随访时间为39±24个月。11例有功能移植物的患者最近一次血清肌酐水平为1.1±0.6 mg/dL。经活检证实,50%的同期肝移植发生了急性排斥反应。相比之下,只有单次(6%)肾移植功能障碍归因于急性排斥反应。所有排斥反应均发生在移植后的前90天内,且对类固醇敏感。14例联合手术中有3例是在细胞毒性交叉配型阳性的情况下进行的。在最近的2例患者中,流式细胞术检测证实与供体T细胞和B细胞的交叉配型均为阳性。肝移植后一小时以及给予抗胸腺细胞球蛋白前数小时,流式细胞术交叉配型结果转为阴性。术后第1天和第7天交叉配型结果仍为阴性。目前,3例交叉配型阳性的患者在随访631、706和2275天时肝肾功能均正常。对4例此前未接受血液透析的LKT受者进行了肾脏扫描,结果显示天然肾和移植肾的功能程度各异且难以预测。总之,即使在交叉配型阳性的情况下,肝肾联合移植也可安全进行,且急性排斥反应发生率较低。预测哪些肾功能不全患者将从LKT中获益仍然具有挑战性;然而,这些结果表明,对于有不可逆肾功能不全证据且需要肝移植的患者,应鼓励进行LKT。