肝硬化合并门静脉血栓形成的危险因素及抗凝治疗的疗效和安全性:一项meta分析。

IF 2.6 4区 医学 Q2 HEMATOLOGY
Le Zhang, Xia Wang, Pu Ming, Li-Na Ma, Wanlong Ma, Xiang-Chun Ding
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引用次数: 0

摘要

目的:探讨肝硬化并发门静脉血栓形成的危险因素及抗凝治疗的有效性和安全性。方法:通过PubMed、Cochrane library、Embase、Web of Science、万方医学网、CNKI等数据库检索相关文献,纳入符合条件的文献。采用QUADS量表评价纳入文献的质量,采用Stata15.1软件进行meta分析和统计处理。结果:肝硬化合并门静脉血栓形成危险因素分析纳入文献19篇,其中肝硬化合并门静脉血栓形成1563例,肝硬化不合并门静脉血栓形成2579例,均未进行抗凝治疗。meta分析结果显示,与PVT组比较,肌酐(Scr,MD = 0.09,95%CI: -0.03 ~ 0.22,P = 0.132)、总胆红素(TBIL,MD = -0.00, 95%CI: -0.10 ~ 0.09,P = 0.948)差异无统计学意义。白蛋白(ALB,MD = -0.32, 95%CI:-0.43 ~ 0.21,P = 0.000)、PLT(PLT, MD = 0.15, 95%CI: 0.05 ~ 0.26, P = 0.004)差异有统计学意义。两组高血压病史差异无统计学意义(OR = 0.78,95%CI:0.59 ~ 1.03,P = 0.079)。在肝硬化合并门静脉血栓形成的抗凝效果及安全性研究中,共纳入9篇文献。其中,497例肝硬化合并门静脉血栓患者接受了抗凝治疗,633例肝硬化合并门静脉血栓患者未接受抗凝治疗。分析结果显示,肝硬化合并门静脉血栓形成患者抗凝治疗后血栓再通情况优于未抗凝治疗组(OR = 4.052,95%CI: 2.737 ~ 6.000,P = 0.000),且抗凝治疗组与未抗凝治疗组出血事件发生差异无统计学意义(OR = 1.017, 95%CI:0.735 ~ 1.407,P = 0.920)。Stata15.1Egger检验显示所有结果均无显著发表偏倚(P < 0.05)。结论:肝硬化合并低血小板和低白蛋白患者更容易发生PVT,抗凝治疗对肝硬化合并PVT患者溶栓有效且安全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The risk factors of liver cirrhosis complicated with portal vein thrombosis and the efficacy and safety of anticoagulant therapy: a meta analysis.

Objective: To evaluate the risk factors of liver cirrhosis complicated with portal vein thrombosis and the efficacy and safety of anticoagulant therapy.

Methods: Relevant literature was searched through PubMed, Cochrane library, Embase, Web of Science, Wanfang Medical Network and CNKI databases, and eligible literature was included. QUADS scale was used to evaluate the quality of the included literatures, and Stata15.1 software was used for meta-analysis and statistical processing.

Results: For risk factors analysis for cirrhosis with Portal vein thrombosis, 19 literatures were included, including 1563 patients with cirrhosis with portal vein thrombosis and 2579 patients with cirrhosis without portal vein thrombosis, all of which were not treated with anticoagulation. The results of meta-analysis showed that compared with the PVT group, there was no significant difference in creatinine(Scr,MD = 0.09,95%CI: -0.03-0.22,P = 0.132)and total bilirubin(TBIL,MD = -0.00, 95%CI: -0.10 ~ 0.09,P = 0.948).There was significant difference in albumin(ALB,MD = -0.32, 95%CI:-0.43-0.21,P = 0.000)and PLT(PLT, MD = 0.15, 95%CI: 0.05-0.26, P = 0.004).And there was also no difference in hypertension history (OR = 0.78,95%CI:0.59 ~ 1.03,P = 0.079). In the study on the anticoagulant effect and safety of liver cirrhosis complicated with portal vein thrombosis, a total of 9 literatures were included. Among them,497 patients with liver cirrhosis complicated by portal vein thrombosis are treated with Anticoagulation treatment, and 633 patients with cirrhosis complicated by portal vein thrombosis without anticoagulation treatment. The analysis results showed that the thrombus recanalization situation of liver cirrhosis complicated with portal vein thrombosis after anticoagulation treatment was better than that of patients without anticoagulation (OR = 4.052,95%CI: 2.737-6.000,P = 0.000),and there was no significant difference in the occurrence of bleeding events between patients with anticoagulation and those without anticoagulation (OR = 1.017, 95%CI:0.735-1.407,P = 0.920). The Stata15.1Egger test showed no significant publication bias for all the results(P > 0.05).

Conclusions: Patients with liver cirrhosis complicated with low platelet and low albumin are more likely to develop PVT. Anticoagulation is helpful and safe for thrombolysis in patients with liver cirrhosis complicated with PVT.

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来源期刊
Thrombosis Journal
Thrombosis Journal Medicine-Hematology
CiteScore
3.80
自引率
3.20%
发文量
69
审稿时长
16 weeks
期刊介绍: Thrombosis Journal is an open-access journal that publishes original articles on aspects of clinical and basic research, new methodology, case reports and reviews in the areas of thrombosis. Topics of particular interest include the diagnosis of arterial and venous thrombosis, new antithrombotic treatments, new developments in the understanding, diagnosis and treatments of atherosclerotic vessel disease, relations between haemostasis and vascular disease, hypertension, diabetes, immunology and obesity.
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