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胆道闭锁患儿肝移植的时机——71例患儿由多学科团队管理的结果

Timing of liver transplantation in biliary atresia-results in 71 children managed by a multidisciplinary team.

作者信息

Cowles Robert A, Lobritto Steven J, Ventura Kara A, Harren Patricia A, Gelbard Rondi, Emond Jean C, Altman R Peter, Jan Dominique M

机构信息

Division of Pediatric Surgery, Morgan Stanley Children's Hospital of New York-Presbyterian and Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.

出版信息

J Pediatr Surg. 2008 Sep;43(9):1605-9. doi: 10.1016/j.jpedsurg.2008.04.012.

Abstract

BACKGROUND

Kasai portoenterostomy (KP) remains the initial surgical therapy for biliary atresia (BA). Liver transplantation (LTx) is offered after a failed KP or if KP is not feasible. The timing of LTx in these children is not well established. We attempted to define factors that may help choose the optimal timing for LTx in children with BA managed by a multidisciplinary team including a pediatric surgeon, hepatologist, and liver transplant surgeon.

METHODS

Records of children who underwent LTx for BA at our institution between January 1998 and December 2006 were reviewed. Clinical data such as pre-LTx pediatric end-stage liver disease (PELD) score, location of KP, and outcome were evaluated.

RESULTS

Seventy one children underwent 77 liver transplants for BA at an average age of 25 months (range, 3-216 months). Sixty-one had a previous KP, 30 at our institution. Ten had LTx without KP. The overall patient survival was 94.4% and overall graft survival was 87% at median follow-up of 58 months (range, 6-111 months). Four patients died, 1 because of vascular thrombosis despite repeat LTx, 1 because of fungal infection after LTx, and 2 because of causes unrelated to LTx. Six children required retransplantation. Living donor liver transplantation was performed in 32 of these children with 91% patient and graft survival. Fifty-three children had a PELD score of 10 or higher with patient and graft survivals of 92% and 86%, respectively. Eighteen children had a PELD score of less than 10 with patient and graft survivals of 100%. For the 30 children who underwent KP at our institution, the median age at LTx was 9 months (range, 3-168 months), and patient and graft survival were both 93%.

CONCLUSIONS

Outcome of LTx for BA is excellent. Children with higher PELD scores (>/=10) at LTx may have worse outcome. Children with a PELD score of less than 10 survived with their original grafts. In children with BA, the PELD score should be monitored and may help stratify patients for eventual LTx. When a child with BA is deemed a candidate for LTx, the PELD score should be determined. A PELD score that approaches 10 should trigger discussion of LTx and living donor liver transplantation with the family.

摘要

背景

肝门空肠吻合术(KP)仍是胆道闭锁(BA)的初始手术治疗方法。若KP手术失败或不可行,则考虑肝移植(LTx)。这些患儿接受肝移植的时机尚未明确。我们试图确定一些因素,以帮助为由小儿外科医生、肝病学家和肝移植外科医生组成的多学科团队管理的BA患儿选择最佳肝移植时机。

方法

回顾了1998年1月至2006年12月期间在我院接受BA肝移植的患儿记录。评估了肝移植前小儿终末期肝病(PELD)评分、KP位置及预后等临床数据。

结果

71例患儿接受了77次BA肝移植,平均年龄25个月(范围3 - 216个月)。61例曾接受过KP手术,其中30例在我院进行。10例未行KP直接接受肝移植。中位随访58个月(范围6 - 111个月)时,总体患者生存率为94.4%,总体移植物生存率为87%。4例患者死亡,1例尽管再次肝移植仍因血管血栓形成死亡,1例肝移植后因真菌感染死亡,2例因与肝移植无关的原因死亡。6例患儿需要再次移植。其中32例患儿接受了活体供肝肝移植,患者和移植物生存率分别为91%。53例患儿PELD评分为10分或更高,患者和移植物生存率分别为92%和86%。18例患儿PELD评分低于10分,患者和移植物生存率均为100%。对于在我院接受KP手术的30例患儿,肝移植时的中位年龄为9个月(范围3 - 168个月),患者和移植物生存率均为93%。

结论

BA肝移植的预后良好。肝移植时PELD评分较高(≥10分)的患儿预后可能较差。PELD评分低于10分的患儿其原移植物存活。对于BA患儿,应监测PELD评分,这可能有助于对最终进行肝移植的患者进行分层。当BA患儿被认为是肝移植候选者时,应确定PELD评分。接近10分的PELD评分应促使与家属讨论肝移植和活体供肝肝移植。

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