Fishbein Thomas M, Kaufman Stuart S, Florman Sander S, Gondolesi Gabriel E, Schiano Thomas, Kim-Schluger Leona, Magid Margaret, Harpaz Noam, Tschernia Alan, Leibowitz Andrew, LeLeiko Neal S
Georgetown University Hospital, Washington, DC 20007, USA.
Transplantation. 2003 Aug 27;76(4):636-40. doi: 10.1097/01.TP.0000083042.03188.6C.
Isolated intestinal transplantation has been limited by poor patient and graft survival. If high survival could be achieved and if parenteral nutrition-associated liver disease were reversible, this procedure could be more widely applied, with early liver dysfunction indicating the need for transplant evaluation.
Twenty-six patients who had failed parenteral nutrition received 28 isolated intestinal transplants. We analyzed patient and graft survival, the effect of sirolimus on the severity and frequency of rejection, and the reversibility of liver dysfunction after transplant.
Three-year actuarial patient and primary graft survival were 88% and 71%, respectively. Two patients underwent successful retransplants. Twenty-two patients are alive at a mean of 21+/-15 (median 18; range 3-51) months. Actuarial survival with freedom from parenteral support is 81% at 3 years (21 of 26 patients). Actuarial freedom from parenteral support among survivors is 95.5% at 3 years (21 of 22 patients). Early rejection was less frequent with sirolimus (34% vs. 70% without sirolimus) (P=0.007). Moderate and severe rejection was less frequent with sirolimus (1/11 episodes vs. 9/17 episodes without sirolimus) (P=0.05). No grafts were lost after introduction of sirolimus. In all four patients with advanced liver dysfunction, fibrosis and cholestasis regressed within 1 year.
High patient survival and parenteral nutrition-free survival can be achieved after isolated intestinal transplantation. Sirolimus treatment has eliminated graft loss. Parenteral nutrition-associated liver disease is reversible with intestinal transplantation. Refractory liver dysfunction in patients receiving parenteral nutrition should prompt consideration for isolated intestinal transplantation.
孤立性肠移植受限于患者和移植物的低生存率。若能实现高生存率且肠外营养相关肝病可逆,该手术可能会得到更广泛应用,早期肝功能障碍提示需要进行移植评估。
26例肠外营养失败的患者接受了28例孤立性肠移植。我们分析了患者和移植物的生存率、西罗莫司对排斥反应严重程度和频率的影响以及移植后肝功能障碍的可逆性。
三年精算患者生存率和原发性移植物生存率分别为88%和71%。2例患者成功接受再次移植。22例患者存活,平均存活时间为21±15(中位数18;范围3 - 51)个月。三年无需肠外支持的精算生存率为81%(26例患者中的21例)。幸存者中三年无需肠外支持的精算生存率为95.5%(22例患者中的21例)。使用西罗莫司时早期排斥反应较少见(34%对未使用西罗莫司时的70%)(P = 0.007)。使用西罗莫司时中度和重度排斥反应较少见(1/11次发作对未使用西罗莫司时的9/17次发作)(P = 0.05)。引入西罗莫司后无移植物丢失。在所有4例晚期肝功能障碍患者中,纤维化和胆汁淤积在1年内消退。
孤立性肠移植后可实现高患者生存率和无需肠外营养的生存。西罗莫司治疗消除了移植物丢失。肠外营养相关肝病通过肠移植是可逆的。接受肠外营养患者出现难治性肝功能障碍应促使考虑进行孤立性肠移植。