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体重小于20公斤的小儿肝移植受者急性门静脉血栓形成的血管内治疗

Endovascular management of acute portal vein thrombosis in pediatric liver transplant recipients less than 20 kg.

作者信息

Karim Sulaiman, Jefferson Xavior, Moreno Nicolas, Upton Ashley, Chau Alex, Hernandez Alberto

机构信息

Texas Tech University Health Science Center School of Medicine, Lubbock, TX, 79430, USA.

Department of Radiology, Division of Interventional Radiology, Texas Children's Hospital, Houston, TX, USA.

出版信息

Pediatr Radiol. 2025 May;55(5):957-964. doi: 10.1007/s00247-025-06189-3. Epub 2025 Feb 14.

Abstract

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.

摘要

背景

原位肝移植的儿科受者面临移植后并发症的风险,尤其是急性门静脉血栓形成,这会危及患者的生存和移植肝功能。与成人相比,门静脉血栓形成的发生率和影响在儿童中更为严重,5岁以下儿童最易发生血栓事件。

目的

本研究旨在报告我们对11例移植后30天内出现门静脉血栓形成的儿科肝移植受者进行血管内介入治疗的机构经验。

材料和方法

对2019年7月至2022年4月期间在一家三级医疗机构接受原位肝移植并被诊断为急性(<30天)门静脉血栓形成的儿科患者(<18岁)进行了一项经机构审查委员会批准的回顾性研究。记录患者的人口统计学资料、手术特征和结果。

结果

11例患者在移植后中位6天接受了经皮再通治疗门静脉血栓形成。移植时的中位年龄为1.1岁(范围0.64至2.14岁),体重8.7千克(范围6.1至18.9千克),体重指数为18.2(范围14.5至21.9)。在超声引导下,通过经肝(n = 6)或经脾(n = 4)或两者(n = 1)获得门静脉通路。进行了机械血栓切除术(n = 3)、球囊血管成形术(n = 11)和脉冲喷射组织型纤溶酶原激活剂(n = 3)以恢复门静脉系统的血流。所有病例(n = 11)均取得技术成功。门静脉压力梯度的中位降低值为10 mmHg(范围4至15)。一年的原发性通畅率为70%(7/10),原发性辅助通畅率为100%(1/1),继发性通畅率为100%(3/3)。没有立即发生与手术相关的并发症。

结论

移植后急性门静脉血栓形成是儿科肝移植后一种严重的并发症,发病率高。在移植后早期,恢复门静脉血流的血管内介入治疗是安全的,并且可以产生持久的效果。

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