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小儿肝肾联合移植术后即刻强化监护治疗:结局和预后因素。

Immediate postoperative intensive care treatment of pediatric combined liver-kidney transplantation: outcome and prognostic factors.

机构信息

Department of Pediatrics, Pediatric Intensive Care Unit, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Transplantation. 2011 May 27;91(10):1127-31. doi: 10.1097/TP.0b013e318216c1bb.

DOI:10.1097/TP.0b013e318216c1bb
PMID:21544033
Abstract

BACKGROUND

Studies reporting the immediate pediatric intensive care unit (PICU) treatment after combined liver-kidney transplantation (CLKT) are scarce, although this period is pivotal for survival and long-term outcome.

METHODS

We retrospectively analyzed all pediatric CLKT performed in our center between 1998 and 2010.

RESULTS

Sixteen patients underwent 17 CLKT at a median age of 5.3 years (range, 1.3-15.9 years). Median body weight at CLKT was 17.7 kg (range, 9.2-55 kg). Underlying diagnosis was primary hyperoxaluria type 1 in nine patients and autosomal recessive polycystic kidney disease in seven patients. Median time on PICU was 8.5 days (range, 3-68 days); however, patients with primary hyperoxaluria type 1 had a significantly longer stay (P=0.031). Median duration of ventilation was 1 day; however, five patients required ventilation for 25 to 52 days. Continuous veno-venous hemofiltration was applied in nine patients due to delayed kidney graft function, volume overload, or high plasma oxalate. Overall, the survival rate after CLKT was 100% and long-term outcome was very good at a mean follow-up of 3.6 years (range, 0.5-12.2 years). Waiting time, donor age, and donor-to-recipient weight ratio were found to be significant risk factors for an extended PICU stay (P=0.02, 0.0031, and 0.014, respectively).

CONCLUSIONS

Immediate postoperative course after CLKT may be challenging and complex. However, excellent results can be achieved, even in small children.

摘要

背景

虽然此时期对患儿的存活和长期预后至关重要,但联合肝-肾移植(CLKT)后即刻转入儿科重症监护病房(PICU)接受治疗的相关研究却十分有限。

方法

我们对 1998 年至 2010 年期间在本中心接受的所有小儿 CLKT 进行了回顾性分析。

结果

16 例患儿共接受了 17 次 CLKT,中位年龄为 5.3 岁(范围,1.3-15.9 岁)。CLKT 时的中位体重为 17.7kg(范围,9.2-55kg)。9 例患儿的基础诊断为 1 型原发性高草酸尿症,7 例患儿的基础诊断为常染色体隐性多囊肾病。PICU 中位停留时间为 8.5 天(范围,3-68 天);但 1 型原发性高草酸尿症患儿的停留时间明显更长(P=0.031)。中位通气时间为 1 天;但有 5 例患儿需要通气 25-52 天。9 例患儿因移植肾功能延迟、容量超负荷或血浆草酸盐水平过高而应用连续静脉-静脉血液滤过。总的来说,CLKT 后的生存率为 100%,在中位随访 3.6 年(范围,0.5-12.2 年)后,长期预后非常好。研究发现,等待时间、供体年龄和供体与受体体重比是 PICU 停留时间延长的显著危险因素(P=0.02、0.0031 和 0.014)。

结论

CLKT 后即刻的术后过程可能具有挑战性且复杂,但即使是在小患儿中,也可以获得良好的效果。

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