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小体积供肝右半肝活体肝移植患者的结局。

Outcome of patients undergoing right lobe living donor liver transplantation with small-for-size grafts.

机构信息

Pei-Xian Chen, Lu-Nan Yan, Wen-Tao Wang, Department of Liver and Vascular Surgery, West China Hospital of Sichuan University, Chengdu 610041, Sichuan Province, China.

出版信息

World J Gastroenterol. 2014 Jan 7;20(1):282-9. doi: 10.3748/wjg.v20.i1.282.

DOI:10.3748/wjg.v20.i1.282
PMID:24415883
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3886020/
Abstract

AIM

To investigate the outcome of living donor liver transplantation (LDLT) recipients transplanted with small-for-size grafts (SFSGs).

METHODS

Between November 2001 and December 2010, 196 patients underwent LDLT with right lobe liver grafts at our center. Recipients were divided into 2 treatment groups: group A with an actuarial graft-to-recipient weight ratio (aGRWR) < 0.8% (n = 45) and group B with an aGRWR ≥ 0.8% (n = 151). We evaluated serum liver function markers within 4 wk after transplantation. We also retrospectively evaluated the outcomes of these patients for potential effects related to the recipients, the donors and the transplantation procedures based upon a review of their medical records.

RESULTS

Small-for-size syndrome (SFSS) developed in 7 of 45 patients (15.56%) in group A and 9 of 151 patients (5.96%) in group B (P = 0.080). The levels of alanine aminotransferase and aspartate aminotransferase in group A were higher than those in group B during early period after transplantation, albeit not significantly. The cumulative 1-, 3- and 5-year liver graft survival rates were 82.22%, 71.11% and 71.11% for group A and 81.46%, 76.82%, and 75.50% for group B patients, respectively (P = 0.623). However, univariate analysis of risk factors associated with graft survival in group A demonstrated that the occurrence of SFSS after LDLT was the only significant risk factor affecting graft survival (P < 0.001). Furthermore, multivariate analysis of our data did not identify any additional significant risk factors accounting for poor graft survival.

CONCLUSION

Our study suggests that LDLT recipients with an aGRWR < 0.8% may have liver graft outcomes comparable to those who received larger size grafts. Further studies are required to ascertain the safety of using SFSGs.

摘要

目的

研究小体积供肝肝移植(LDLT)受者的预后。

方法

2001 年 11 月至 2010 年 12 月,我们中心对 196 例患者进行了右半肝 LDLT。将受者分为 2 个治疗组:A 组为计算的移植物与受体重量比(aGRWR)<0.8%(n=45),B 组为 aGRWR≥0.8%(n=151)。我们在移植后 4 周内评估血清肝功能标志物。我们还回顾性评估了这些患者的结果,根据他们的病历,评估与受者、供者和移植程序相关的潜在影响。

结果

A 组中 7 例(15.56%)和 B 组中 9 例(5.96%)患者发生小肝综合征(SFSS)(P=0.080)。尽管差异无统计学意义,但 A 组患者在移植后早期的丙氨酸氨基转移酶和天冬氨酸氨基转移酶水平高于 B 组。A 组患者的累积 1、3 和 5 年肝移植物存活率分别为 82.22%、71.11%和 71.11%,B 组分别为 81.46%、76.82%和 75.50%(P=0.623)。然而,A 组移植物存活率相关风险因素的单因素分析显示,LDLT 后发生 SFSS 是影响移植物存活率的唯一显著危险因素(P<0.001)。此外,我们数据的多因素分析没有发现任何其他导致移植物存活率较差的显著危险因素。

结论

我们的研究表明,aGRWR<0.8%的 LDLT 受者的肝移植物预后可能与接受较大体积移植物的受者相当。需要进一步的研究来确定使用小体积供肝的安全性。

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本文引用的文献

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Risk factors for in-hospital mortality of patients with high model for end-stage liver disease scores following living donor liver transplantation.高终末期肝病模型评分患者行活体肝移植术后院内死亡的风险因素。
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Safety of small-for-size grafts in adult-to-adult living donor liver transplantation using the right lobe.成人对成人活体肝移植中使用右叶的小体积供肝的安全性。
Liver Transpl. 2010 Jul;16(7):864-9. doi: 10.1002/lt.22094.
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Increasing donor body weight to prevent small-for-size syndrome in living donor liver transplantation.增加供体体重以预防活体肝移植中的小肝综合征。
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Increasing donor body weight to prevent small-for-size syndrome in living donor liver transplantation.增加供体体重以预防活体肝移植中的小肝综合征。
World J Surg. 2010 Oct;34(10):2409-10. doi: 10.1007/s00268-010-0671-5.
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Alleviating the burden of small-for-size graft in right liver living donor liver transplantation through accumulation of experience.通过积累经验缓解右半肝活体肝移植中小体积供肝的负担。
Am J Transplant. 2010 Apr;10(4):859-867. doi: 10.1111/j.1600-6143.2010.03017.x. Epub 2010 Feb 10.
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Liver Transpl. 2009 Dec;15(12):1776-82. doi: 10.1002/lt.21955.
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Delayed splenic artery occlusion for treatment of established small-for-size syndrome after partial liver transplantation.延迟性脾动脉闭塞术治疗部分肝移植术后已形成的小肝综合征
Liver Transpl. 2009 Oct;15(10):1381-2. doi: 10.1002/lt.21844.