小于20kg儿童肝移植受者急性门静脉血栓的血管内处理。

IF 2.1 3区 医学 Q2 PEDIATRICS
Sulaiman Karim, Xavior Jefferson, Nicolas Moreno, Ashley Upton, Alex Chau, Alberto Hernandez
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引用次数: 0

摘要

背景:儿童原位肝移植受者存在移植后并发症的风险,尤其是急性门静脉血栓形成,危及患者生存和移植物功能。门静脉血栓的发生率和影响在儿童中比成人更严重,5岁以下的儿童最容易发生血栓事件。目的:本研究旨在报告我们的机构经验,血管内介入治疗11例移植后30天内出现门静脉血栓的儿童肝移植受者。材料和方法:对经irb批准的儿科患者进行回顾性研究(结果:11例患者因门静脉血栓形成在移植后6天中位数接受经皮再通治疗。移植时的中位年龄为1.1岁(范围0.64至2.14),体重为8.7 kg(范围6.1至18.9 kg),体重指数为18.2(范围14.5至21.9)。在超声引导下经肝(n = 6)或经脾(n = 4)或经肝经脾(n = 1)获得门静脉通路。通过机械取栓(n = 3)、球囊成形术(n = 11)和脉冲喷雾tPA (n = 3)来恢复门静脉系统的血流。所有病例均取得技术成功(n = 11)。门静脉压力梯度中值降低10 mmHg(范围4 ~ 15)。一年一期通畅率为70%(7/10),一期辅助通畅率为100%(1/1),二期通畅率为100%(3/3)。没有立即出现手术相关的并发症。结论:急性门静脉血栓形成是小儿肝移植术后的重要并发症,发病率高。在移植后早期,血管内介入恢复门静脉血流是安全的,并且可以产生持久的效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endovascular management of acute portal vein thrombosis in pediatric liver transplant recipients less than 20 kg.

Background: Pediatric recipients of orthotopic liver transplants are at risk for post-transplant complications, particularly acute portal vein thrombosis, which jeopardizes patient survival and graft function. The incidence and impact of portal vein thrombosis are more severe in children compared to adults, with those under 5 most vulnerable to thrombotic events.

Objective: This study aims to report our institutional experience with endovascular interventions for treating portal vein thrombosis in 11 pediatric liver transplant recipients who presented within 30-days post-transplant.

Materials and methods: An IRB-approved retrospective review was conducted on pediatric patients (< 18 years of age) from a single tertiary care institution who received an orthotopic liver transplant and were diagnosed with acute (< 30 days) portal vein thrombosis, from July 2019 to April 2022. Patient demographics, procedural characteristics, and outcomes were recorded.

Results: Eleven patients were treated with percutaneous recanalization at a median of 6-days post-transplant for portal vein thrombosis. Median age at the time of transplant was 1.1 years (range 0.64 to 2.14), weight of 8.7 kg (range 6.1 to 18.9 kg), and body mass index of 18.2 (range 14.5 to 21.9). Portal venous access was obtained via trans-hepatic (n = 6) or trans-splenic (n = 4), or both (n = 1) under ultrasound guidance. Mechanical thrombectomy (n = 3), balloon angioplasty (n = 11), and pulse-spray tPA (n = 3) were performed to restore flow to the portal system. Technical success was achieved in all cases (n = 11). The median reduction in portal venous pressure gradient was 10 mmHg (range 4 to 15). One-year primary patency was 70% (7/10), primary-assisted was 100% (1/1), and secondary patency was 100% (3/3). There were no immediate procedure-related complications.

Conclusion: Acute post-transplant portal vein thrombosis is a significant complication following pediatric liver transplantation with high morbidity. In the early post-transplant period, endovascular interventions to restore portal flow are safe and can produce durable results.

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来源期刊
Pediatric Radiology
Pediatric Radiology 医学-核医学
CiteScore
4.40
自引率
17.40%
发文量
300
审稿时长
3-6 weeks
期刊介绍: Official Journal of the European Society of Pediatric Radiology, the Society for Pediatric Radiology and the Asian and Oceanic Society for Pediatric Radiology Pediatric Radiology informs its readers of new findings and progress in all areas of pediatric imaging and in related fields. This is achieved by a blend of original papers, complemented by reviews that set out the present state of knowledge in a particular area of the specialty or summarize specific topics in which discussion has led to clear conclusions. Advances in technology, methodology, apparatus and auxiliary equipment are presented, and modifications of standard techniques are described. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been reviewed by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in an appropriate version of the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted.
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