Luo Jian-jun, Yan Zhi-ping, Wang Jian-hua, Liu Qing-xin, Fang Zhu-ting, Zhang Wen
Department of Interventional Radiology, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Zhonghua Gan Zang Bing Za Zhi. 2013 Nov;21(11):855-9. doi: 10.3760/cma.j.issn.1007-3418.2013.11.013.
To retrospectively analyze the safety and efficacy of mechanical thrombectomy combined with pharmacologic thrombolysis to treat non-acute and symptomatic portal vein thrombosis (PVT) using an intrahepatic portosystemic shunt (IPS) assisted by percutaneous transhepatic approach.
From April 2006 to May 2012, 18 patients with non-acute and symptomatic PVT were treated with balloon dilation, sheath-directed thrombus aspiration and continuous infusion of urokinase using the IPS assisted by percutaneous transhepatic approach. The significance of differences in the portosystemic gradient measured before and after therapy was assessed by paired samples t-test, and survival analysis was made by the Kaplan-Meier method.
IPS was successfully created in all patients. The mean duration of the thrombolytic therapy was 65.3 +/- 29.5 h, and the mean concentration of urokinase used for the thrombolysis was 2324000 +/- 945000 U. Comparison of the mean portosystemic gradients showed a significant improvement in response to the therapy (before: 33.8 +/- 4.9 mm Hg vs. after: 15.4 +/- 2.1 mm Hg; P less than 0.001). The overall rate of clinical improvement was 94.4%. One patient died on day 2 post-therapy and another two patients experienced mild hepatic encephalopathy or right hemothorax, respectively, on day 5 post-therapy, with conservative medical management achieving complete recovery for both. The mean follow-up time was 18.6 +/- 17.5 months, during which only one patient died and five others experienced shunt dysfunction; all remaining patients showed maintenance of shunt patency without symptoms of recurrence.
Mechanical thrombectomy combined with pharmacologic thrombolysis via the IPS assisted by percutaneous transhepatic approach is a safe and effective therapeutic option for patients with non-acute and symptomatic PVT.
回顾性分析经皮经肝途径辅助下,采用肝内门体分流术(IPS)进行机械性血栓切除术联合药物溶栓治疗非急性症状性门静脉血栓形成(PVT)的安全性和有效性。
2006年4月至2012年5月,18例非急性症状性PVT患者采用经皮经肝途径辅助下的IPS,进行球囊扩张、鞘管引导下血栓抽吸及尿激酶持续输注治疗。采用配对样本t检验评估治疗前后门体梯度差异的显著性,并采用Kaplan-Meier法进行生存分析。
所有患者均成功建立IPS。溶栓治疗的平均持续时间为65.3±29.5小时,溶栓所用尿激酶的平均浓度为2324000±945000 U。平均门体梯度比较显示,治疗后有显著改善(治疗前:33.8±4.9 mmHg vs. 治疗后:15.4±2.1 mmHg;P<0.001)。临床改善总率为94.4%。1例患者在治疗后第2天死亡,另外2例患者分别在治疗后第5天出现轻度肝性脑病或右侧血胸,经保守治疗均完全康复。平均随访时间为18.6±17.5个月,在此期间仅1例患者死亡,另外5例出现分流功能障碍;其余所有患者均保持分流通畅,无复发症状。
经皮经肝途径辅助下通过IPS进行机械性血栓切除术联合药物溶栓,是治疗非急性症状性PVT患者的一种安全有效的治疗选择。