Efficacy and safety of anticoagulants on venous thromboembolism: a systematic review and network meta-analysis of randomized controlled trials.

IF 4.8 2区 医学 Q1 PHARMACOLOGY & PHARMACY Frontiers in Pharmacology Pub Date : 2025-01-08 eCollection Date: 2024-01-01 DOI:10.3389/fphar.2024.1519869
Weijie Fu, Maolin Zhao, Sheng Ding, Mei Xin, Ke Yang, Li Jiang, Fan Wu, Xiaochen Wu, Jian Wang, Jie Chen, Feng Gao, Siyi He
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Abstract

Background: Anticoagulants are the primary means for the treatment and prevention of venous thromboembolism (VTE), but their clinical standardized application still remains controversial. The present study intends to comprehensively compare the efficacy and safety of various anticoagulants in VTE.

Methods: Medline, Embase, and Cochrane Library from their inception up to August 2023 were searched to compare the efficacy and safety of various anticoagulants in VTE. We extracted data on study settings, baseline characteristics, interventions, and outcomes, applying the intention-to-treat principle. Two researchers assessed study bias using the Cochrane tool, resolving disagreements through discussion or third-party adjudication. Network meta-analyses were performed based on Bayesian generalized linear models, and a frequentist framework with multivariate random effects was used to fit the model.

Results: In terms of treatment, 58 trials with 119,417 patients proved eligible, while 125 trials with 225,414 patients were included in terms of prevention. All anticoagulants were found to reduce the recurrence or incidence of VTE compared with Placebo, of which high-level evidence indicated that direct thrombin inhibitors (TIs) and novel oral anticoagulants (NOACs) were the two most effective drugs. For treatment, low molecular weight heparin (LMWH), unfractionated heparin (UFH), and vitamin K antagonists (VKAs) significantly increased the risk of major bleeding in comparison to Placebo. For prevention, only UFH (OR 2.0, 95% CI 1.2-3.3) and NOACs (OR 1.8, 95% CI 1.2-2.6) showed significant increased risks in major bleeding. Additionally, after an exhaustive analysis of NOACs, analysis showed that apixaban (RR 0.5, 95%CI 0.17-1.46) had a superior performance in major bleeding compared to rivaroxaban (RR 3.87, 95%CI 1.48-10.09).

Conclusion: TIs and NOACs were superior in efficacy with minimal side effects, making them pivotal choices for both prevention and treatment of VTE. Clinical practitioners must carefully weigh drug characteristics, indications, and contraindications to optimize treatment outcomes.

Systematic review registration: https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=466775.

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抗凝剂治疗静脉血栓栓塞的疗效和安全性:随机对照试验的系统回顾和网络荟萃分析。
背景:抗凝剂是治疗和预防静脉血栓栓塞(VTE)的主要手段,但其临床标准化应用仍存在争议。本研究旨在综合比较各种抗凝剂治疗静脉血栓栓塞的疗效和安全性。方法:检索Medline、Embase和Cochrane图书馆自成立以来至2023年8月的资料,比较各种抗凝剂治疗静脉血栓栓塞的疗效和安全性。应用意向治疗原则,我们提取了有关研究设置、基线特征、干预措施和结果的数据。两名研究人员使用Cochrane工具评估研究偏差,通过讨论或第三方裁决解决分歧。网络元分析基于贝叶斯广义线性模型,并使用具有多元随机效应的频率框架来拟合模型。结果:在治疗方面,58项试验纳入119,417例患者,而在预防方面,125项试验纳入225,414例患者。与安慰剂相比,所有抗凝血药物均可降低VTE的复发或发生率,其中高水平证据表明,直接凝血酶抑制剂(TIs)和新型口服抗凝血剂(NOACs)是两种最有效的药物。在治疗方面,与安慰剂相比,低分子肝素(LMWH)、未分离肝素(UFH)和维生素K拮抗剂(VKAs)显著增加了大出血的风险。在预防方面,只有UFH (OR 2.0, 95% CI 1.2-3.3)和NOACs (OR 1.8, 95% CI 1.2-2.6)显示大出血风险显著增加。此外,在对noac进行详尽分析后,分析显示阿哌沙班(RR 0.5, 95%CI 0.17-1.46)在大出血方面优于利伐沙班(RR 3.87, 95%CI 1.48-10.09)。结论:TIs和NOACs疗效优越,副作用小,是预防和治疗静脉血栓栓塞的关键选择。临床医生必须仔细权衡药物特性、适应症和禁忌症,以优化治疗结果。系统评审注册:https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=466775。
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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来源期刊
Frontiers in Pharmacology
Frontiers in Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.80
自引率
8.90%
发文量
5163
审稿时长
14 weeks
期刊介绍: Frontiers in Pharmacology is a leading journal in its field, publishing rigorously peer-reviewed research across disciplines, including basic and clinical pharmacology, medicinal chemistry, pharmacy and toxicology. Field Chief Editor Heike Wulff at UC Davis is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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