预防静脉血栓栓塞复发的初级/二级治疗持续时间:系统回顾和荟萃分析

IF 7.4 1区 医学 Q1 HEMATOLOGY
Anqi Li, Rasha Khatib, Luciane Cruz Lopes, Fazila Aloweni, Liming Lu, Qingyong He, Jiaming Wu, Peiming Zhang, Yuyuan Tang, Sureka Pavalagantharajah, Nigar Sekercioglu, Carlos A Cuello Garcia, Serge Koujanian, Arnav Agarwal, Sean Alexander Kennedy, Ignacio Neumann, Sam Schulman, Wojtek Wiercioch, Gabriel Rada, Andrew M Peseski, Thomas L Ortel, Yu-Qing Zhang
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引用次数: 0

摘要

摘要:抗血栓治疗可以预防复发性深静脉血栓形成(DVT)和肺栓塞(PE)。然而,它与大出血的风险增加有关。本荟萃分析系统地回顾了有关抗血栓治疗持续时间的证据,以评估其益处和危害。我们系统地检索了比较较短疗程(3-6个月)和较长疗程(6 -6个月)抗凝治疗用于静脉血栓栓塞(VTE)初级治疗的随机对照试验(RCTs),或比较停药与无限期抗凝治疗用于VTE二级预防的随机对照试验(RCTs)。成对的审稿人筛选符合条件的试验并收集数据。本研究纳入22项随机对照试验(11617名受试者)。汇总估计显示,对于非诱发性静脉血栓栓塞、慢性危险因素或短暂性危险因素诱发的静脉血栓栓塞的初级治疗,较短疗程(3-6个月)的抗凝治疗较长疗程(6 -6个月)的患者可能减少复发性PE(风险比[RR], 0.66;95%可信区间[CI], 0.42-1.02)和DVT (RR, 0.85;95% CI, 0.63-1.14),但与死亡率增加相关(RR, 1.43;95% CI, 0.85-2.41)(中等确定性),大出血风险较高(RR, 2.02;95% ci, 1.02-3.98;高确定性)。对于非诱发性静脉血栓栓塞和慢性危险因素诱发的静脉血栓栓塞的二级预防,与停止治疗相比,无限期抗凝治疗与死亡率降低相关(RR, 0.54;95% CI, 0.36-0.81),复发性PE减少(RR, 0.25;95% CI, 0.16-0.41)和DVT (RR, 0.15;95% CI, 0.10-0.21),出血风险增加(RR, 1.98;95% CI, 1.18-3.30),均有高确定性支持。无限期抗血小板治疗可能与死亡率降低相关(RR, 0.95;95% ci: 0.53-1.68;低确定性),可能会减少复发性PE (RR, 0.65;95% CI, 0.41-1.03)和DVT (RR, 0.44;95% CI, 0.17-1.13)(中等确定性),并可能增加出血的风险(RR, 1.28;95% ci, 0.48-3.41;低确定性)。综上所述,对于所有类型VTE的初级治疗,较短的抗凝时间(3-6个月)更有益。对于非诱发性静脉血栓栓塞或由慢性危险因素引起的静脉血栓栓塞的二级预防,无限期抗栓治疗更有益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Duration of primary/secondary treatment to prevent recurrent venous thromboembolism: a systematic review and meta-analysis.

Abstract: Antithrombotic therapy can prevent recurrent deep vein thrombosis (DVT) and pulmonary embolism (PE). It is, however, associated with an increased risk for major bleeding. This meta-analysis systematically reviewed the evidence regarding the duration of antithrombotic therapy to assess benefits and harms. We systematically searched for randomized controlled trials (RCTs) that compared shorter (3-6 months) with longer (>6 months) courses of anticoagulation for the primary treatment of venous thromboembolism (VTE) or that compared discontinued with indefinite antithrombotic therapy for the secondary prevention of VTE. Pairs of reviewers screened the eligible trials and collected data. This study included 22 RCTs (11 617 participants). Pooled estimates showed that, for the primary treatment of unprovoked VTE, VTE provoked by chronic risk factors or transient risk factors, treating patients with a longer course (>6 months) of anticoagulation, as opposed to a shorter course (3-6 months), probably reduced recurrent PE (risk ratio [RR], 0.66; 95% confidence interval [CI], 0.42-1.02) and DVT (RR, 0.85; 95% CI, 0.63-1.14), but it was associated with increased mortality (RR, 1.43; 95% CI, 0.85-2.41) (moderate certainty) and a higher risk for major bleeding (RR, 2.02; 95% CI, 1.02-3.98; high certainty). For the secondary prevention of unprovoked VTE and VTE provoked by chronic risk factors, when compared with discontinuing treatment, indefinite anticoagulation therapy was associated with decreased mortality (RR, 0.54; 95% CI, 0.36-0.81), a reduction in recurrent PE (RR, 0.25; 95% CI, 0.16-0.41) and DVT (RR, 0.15; 95% CI, 0.10-0.21), and an increase in the risk for bleeding (RR, 1.98; 95% CI, 1.18-3.30), all supported by high certainty. Indefinite antiplatelet therapy may be associated with decreased mortality (RR, 0.95; 95% CI: 0.53-1.68; low certainty), probably a reduction in recurrent PE (RR, 0.65; 95% CI, 0.41-1.03) and DVT (RR, 0.44; 95% CI, 0.17-1.13) (moderate certainty), and may increase the risk for bleeding (RR, 1.28; 95% CI, 0.48-3.41; low certainty). In summary, for the primary treatment of all types of VTE, shorter (3-6 months) duration of anticoagulation is more beneficial. For the secondary prevention of unprovoked VTE or VTE provoked by chronic risk factors, indefinite antithrombotic treatment is more beneficial.

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来源期刊
Blood advances
Blood advances Medicine-Hematology
CiteScore
12.70
自引率
2.70%
发文量
840
期刊介绍: Blood Advances, a semimonthly medical journal published by the American Society of Hematology, marks the first addition to the Blood family in 70 years. This peer-reviewed, online-only, open-access journal was launched under the leadership of founding editor-in-chief Robert Negrin, MD, from Stanford University Medical Center in Stanford, CA, with its inaugural issue released on November 29, 2016. Blood Advances serves as an international platform for original articles detailing basic laboratory, translational, and clinical investigations in hematology. The journal comprehensively covers all aspects of hematology, including disorders of leukocytes (both benign and malignant), erythrocytes, platelets, hemostatic mechanisms, vascular biology, immunology, and hematologic oncology. Each article undergoes a rigorous peer-review process, with selection based on the originality of the findings, the high quality of the work presented, and the clarity of the presentation.
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