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The risk of gastrointestinal hemorrhage with non-vitamin K antagonist oral anticoagulants

机译:具有非维生素K拮抗剂口腔抗凝血剂胃肠出血的风险

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BACKGROUND:Non-vitamin K antagonist oral anticoagulants (NOACs) have been widely used for stroke prevention in atrial fibrillation (AF) and the treatment and prevention of venous thromboembolism. There is an issue with safety, especially in clinically relevant bleeding. We performed a network meta-analysis to evaluate the risk of major gastrointestinal (GI) bleeding associated with NOACs.METHODS:Interventions were warfarin, enoxaparin, apixaban, dabigatran, edoxaban, and rivaroxaban. The primary outcome was the incidence of major GI bleeding. A subgroup analysis was performed according to the following indications: AF, deep venous thrombosis/pulmonary embolism, and postsurgical prophylaxis.RESULTS:A total of 29 randomized controlled trials (RCTs) and 4 large observation population studies were included. Compared with warfarin, apixaban showed a decreased the risk of major GI bleeding (relative risk [RR] 0.54, 95% confidence interval [CI] 0.25-0.76), and rivaroxaban tended to increase this risk (RR 1.40, 95% CI 1.06-1.85). Dabigatran (RR 1.25, 95% CI 0.98-1.60), edoxaban (RR 1.07, 95% CI 0.69-1.65), and enoxaparin (RR 1.24, 95% CI 0.63-2.43) did not significantly increase the risk of GI bleeding than did warfarin. In the subgroup analysis, according to indications, apixaban showed a decreased risk of major GI bleeding (RR 0.50, 95% CI 0.34-0.74) than did warfarin in AF studies. Dabigatran (RR 2.36, 95% CI 1.55-3.60, and rivaroxaban (RR 1.75, 95% CI 1.10-6.41) increased the risk of major GI bleeding than did apixaban. An analysis of studies on venous thromboembolism or pulmonary embolism showed that no individual NOAC or enoxaparin was associated with an increased risk of major GI bleeding compared to warfarin.CONCLUSION:Individual NOACs had varying profiles of GI bleeding risk. Results of analyses including only RCTs and those including both RCTs and population studies showed similar trends, but also showed several differences.Copyright ? 2021 the Author(s). Published by Wolters Kluwer Health, Inc.
机译:背景:非维生素K拮抗剂口腔抗凝血剂(NOACS)已广泛用于心房颤动(AF)中的中风预防和治疗和预防静脉血栓栓塞。安全有一个问题,特别是在临床相关的出血中。我们进行了网络荟萃分析,以评估与Noacs相关的主要胃肠道(GI)出血的风险。方法:干预措施是华法林,烯脱蒿素,Apixaban,Dabigatran,Edoxaban和Rivaroxaban。主要结果是主要GI出血的发病率。根据以下适应症进行亚组分析:AF,深静脉血栓形成/肺栓塞和后期预防。结果:包括29项随机对照试验(RCT)和4种大观察人口研究。与华法林相比,Apixaban表现出重大Gi出血的风险(相对风险[RR] 0.54,95%置信区间[CI] 0.25-0.76),rivaroxaban倾向于增加这种风险(RR 1.40,95%CI 1.06- 1.85)。 Dabigatran(RR 1.25,95%CI 0.98-1.60),Edoxaban(RR 1.07,95%CI 0.69-1.65)和烯脱蒿素(RR 1.24,95%CI 0.63-2.43)没有显着增加Gi出血的风险华法林。在亚组分析中,根据适应症,Apixaban表现出主要的Gi出血的风险降低(RR 0.50,95%CI 0.34-0.74),而不是AF研究的Warfarin。 Dabigatran(RR 2.36,95%CI 1.55-3.60和Rivaroxaban(RR 1.75,95%CI 1.10-6.41)增加了主要GI出血的风险而不是Apixaban。对静脉血栓栓塞或肺栓塞研究的分析表明没有个体与Warfarin相比,Noac或烯库蛋白与主要GI出血的风险增加有关几个差异。2021年作者。由Wolters Kluwer Health,Inc。发布

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