Retrospective analysis of the efficacy and safety of rivaroxaban in the treatment of hepatic sinus obstruction syndrome caused by Gynura segetum

Hao Bing, Dan Li, B. Chang, Yiling Li, Xiang-dong He, J. Tong, Ying Wang, R. Ao, Ningning Wang
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Abstract

Background PA-HSOS is a rare disease and there is no specific treatment for PA-HSOS. Anticoagulant, antithrombotic and microcirculation therapy can alleviate the progression of PA-HSOS. The application of rivaroxaban in patients with PA-HSOS has not yet been reported. The aim of this study was to analyze the efficacy and safety of rivaroxaban in the treatment of pyrrolizidine alkaloid-induced hepatic sinusoidal obstruction syndromecaused by Gynura segetum (PA-HSOS) . Methods A retrospective analysis was conducted with the clinical data of patients with PA-HSOS in the acute/subacute phase caused by taking Gynura segetum. The patients were divided into warfarin and rivaroxaban groups according to the anticoagulant therapy they received. Related biochemical indicators were monitored during hospitalization. Liver ultrasound, liver elastography and related biochemical indicators were reviewed every two weeks or one month after discharge. The patients were followed until 1 year after complete remission or death. The efficacy and safety of rivaroxaban was compared with that of warfarin according to the patients’ hepatic venous recanalization rates and the occurrence of bleeding events. Results The study included 20 patients, with 10 patients in the warfarin group and 10 patients in the rivaroxaban group. The results showed that the average anticoagulant course in the rivaroxaban group was significantly shorter than that in the warfarin group (P=0.007). With treatment, the remission rates of the rivaroxaban group and the warfarin group reached 90%. There was no significant difference in the incidence of adverse reactions or bleeding events between the two groups (P>0.05). Conclusions Compared with warfarin, rivaroxaban, a new oral anticoagulant, is convenient and safe for clinical use. It has an obvious effect on PA-HSOS and a low risk of bleeding. It provides a new anticoagulant treatment for PA-HSOS.
回顾性分析利伐沙班治疗黄花菊所致肝窦阻塞综合征的疗效和安全性
背景:PA-HSOS是一种罕见的疾病,目前尚无针对PA-HSOS的特异性治疗方法。抗凝、抗栓和微循环治疗可缓解PA-HSOS的进展。利伐沙班在PA-HSOS患者中的应用尚未见报道。本研究的目的是分析利伐沙班治疗吡咯利西定生物碱所致的黄花草引起的肝窦阻塞综合征(PA-HSOS)的有效性和安全性。方法回顾性分析服用黄花草引起的急性/亚急性期PA-HSOS患者的临床资料。根据患者接受的抗凝治疗情况分为华法林组和利伐沙班组。住院期间监测相关生化指标。出院后每2周或1个月复查肝脏超声、肝脏弹性图及相关生化指标。患者随访至完全缓解或死亡后1年。根据患者肝静脉再通率及出血事件发生情况,比较利伐沙班与华法林的疗效和安全性。结果共纳入20例患者,其中华法林组10例,利伐沙班组10例。结果显示,利伐沙班组平均抗凝疗程明显短于华法林组(P=0.007)。经治疗,利伐沙班组和华法林组的缓解率均达90%。两组患者不良反应及出血事件发生率比较,差异均无统计学意义(P>0.05)。结论与华法林相比,利伐沙班是一种新型口服抗凝剂,临床使用方便、安全。对PA-HSOS有明显疗效,出血风险低。为PA-HSOS提供了一种新的抗凝治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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