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Meta-analysis of efficacy and safety of rivaroxaban compared with warfarin or dabigatran in patients undergoing catheter ablation for atrial fibrillation

机译:与华法林或达比加群相比,利伐沙班与华法林或达比加群相比在房室导管消融术中的疗效和安全性的荟萃分析

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Several studies have been conducted to study the efficacy and safety of rivaroxaban in the atrial fibrillation periprocedural ablation period with similar rates of thromboembolism and major bleeding risks compared with warfarin or dabigatran. We sought to systematically review this evidence using pooled data from multiple studies. Studies comparing rivaroxaban with warfarin or dabigatran in patients undergoing catheter ablation for atrial fibrillation were identified through electronic literature searches of MEDLINE, EMBASE, clinicaltrials.gov, and the Cochrane library up to March 2014. Study-specific risk ratios (RRs) were calculated and combined using a random-effects model meta-analysis. In an analysis involving 3,575 patients, thromboembolism (composite of stroke, transient ischemic attack, and systemic and pulmonary emboli) occurred in 3 of 789 patients (0.4%) in the rivaroxaban group and 10 of 2,786 patients (0.4%) in the warfarin group (RR 0.71, 95% CI 0.26 to 1.96, I2 = 0%, p = 0.51). Major hemorrhage occurred in 9 of 749 patients (1.2%) in the rivaroxaban group and 22 of 975 patients (2.3%) in the warfarin group (RR 0.49, 95% CI 0.24 to 1.02, I2 = 0%, p = 0.06). Furthermore, direct efficacy and safety comparisons between rivaroxaban and dabigatran showed nonsignificant differences in rates of thromboembolism (0.5% vs 0.4%, respectively, RR 1.12, 95% CI 0.25 to 4.99, I2 = 0%, p = 0.88) and major bleeding (1.0% vs 1.6%, respectively, RR = 0.71, 95% CI 0.16 to 3.15, I2 = 22%, p = 0.66). In conclusion, our study suggests that patients treated with rivaroxaban during periprocedural catheter ablation have similar rates of thromboembolic events and major hemorrhage. Similar results were seen in direct comparisons between dabigatran and rivaroxaban.
机译:与华法林或达比加群相比,利伐沙班在房颤围手术期消融期中利伐沙班的疗效和安全性研究相似,具有相似的血栓栓塞发生率和主要出血风险。我们试图使用来自多个研究的汇总数据系统地审查该证据。截止到2014年3月,通过MEDLINE,EMBASE,clinicaltrials.gov和Cochrane库的电子文献检索,鉴定出了将利伐沙班与华法林或达比加群用于接受导管消融治疗房颤的患者的比较研究。计算了特定于研究的风险比(RRs),结合使用随机效应模型的荟萃分析。在一项涉及3,575例患者的分析中,利伐沙班组789例患者中有3例(0.4%)发生了血栓栓塞(中风,短暂性脑缺血发作以及全身性和肺栓塞的复合物),华法林组则有2 786例患者中有10例(0.4%)发生了血栓栓塞(RR 0.71,95%CI 0.26至1.96,I2 = 0%,p = 0.51)。利伐沙班组749例患者中有9例(1.2%)发生大出血,华法林组975例患者中有22例(2.3%)发生大出血(RR 0.49,95%CI 0.24至1.02,I2 = 0%,p = 0.06)。此外,利伐沙班和达比加群之间的直接疗效和安全性比较显示血栓栓塞发生率(分别为0.5%和0.4%,RR 1.12、95%CI 0.25至4.99,I2 = 0%,p = 0.88)无显着差异。分别为1.0%和1.6%,RR = 0.71,95%CI为0.16至3.15,I2 = 22%,p = 0.66)。总之,我们的研究表明,在术中导管消融期间使用利伐沙班治疗的患者发生血栓栓塞事件和严重出血的发生率相似。在达比加群和利伐沙班之间的直接比较中看到了相似的结果。

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