Virk Ghazala S, Javed Sana, Chaudhry Raheel, Moazam Mustafa M, Mahmood Arhum, Mahmood Faraz, Zaheer Mohammed, Khan Shahroz M, Rajasekaran Vedika
Internal Medicine, Avalon University School of Medicine, Ohio, USA.
Medicine, University of Birmingham, Royal College of General Practitioners, Birmingham, GBR.
Cureus. 2024 Feb 15;16(2):e54252. doi: 10.7759/cureus.54252. eCollection 2024 Feb.
An effective anticoagulation therapy is required for patients with atrial fibrillation because it presents a significant risk of stroke. The current study evaluates the relative safety as well as efficacy of rivaroxaban in patients who are diagnosed with atrial fibrillation. A thorough literature review of relevant databases was conducted, focusing on academic and clinical studies that were published from 2017 onward. Inclusion criteria comprised randomized controlled trials and other observational studies comparing the incidence of stroke and the safety index of rivaroxaban in atrial fibrillation. We followed the Preferred Reporting Items for Systematic Review and Meta-Analyses (PRISMA) for data overview reporting and overview. A total of 21 studies were selected based on the inclusion criteria. A total of 19/21 studies advocated the adoption of rivaroxaban for minimizing stroke incidence. Rivaroxaban also showed superiority in achieving the therapeutic objectives, i.e., reduction in the incidence of stroke. The results for rivaroxaban against warfarin showed an improved safety index and effectiveness of rivaroxaban. The total effect size for the analysis was calculated to be Z=2.62 (p-value=0.009). The individual effect of all studies favored the "rivaroxaban" group. The heterogeneity in the study was as follows: tau=0.10; chi=110.10, df=6; I=95%. The second analysis for risk reduction and incidence of stroke after rivaroxaban therapy also showed a bias towards rivaroxaban therapy. The combined effect for the analysis was found to be as follows: HR=0.73 ((95% CI: 0.50, 1.07). The total effect was calculated to be Z=1.61 (p-value= 0.10). The heterogeneity was found to be as follows: tau= 0.20, chi=89.97, df=6, I=93%. Standard dosing of rivaroxaban emerges as a preferred strategy for stroke prevention, balancing efficacy and safety. Clinical decision-making should consider individual patient characteristics and future research should delve into specific subpopulations and long-term outcomes to further refine treatment guidelines.
心房颤动患者需要有效的抗凝治疗,因为其存在显著的中风风险。本研究评估了利伐沙班在被诊断为心房颤动患者中的相对安全性和疗效。对相关数据库进行了全面的文献综述,重点关注2017年以后发表的学术和临床研究。纳入标准包括比较利伐沙班在心房颤动中的中风发生率和安全指数的随机对照试验及其他观察性研究。我们遵循系统评价和Meta分析的首选报告项目(PRISMA)进行数据概述报告和综述。根据纳入标准共选择了21项研究。21项研究中有19项主张采用利伐沙班以尽量降低中风发生率。利伐沙班在实现治疗目标方面也显示出优势,即降低中风发生率。利伐沙班与华法林对比的结果显示利伐沙班的安全指数和有效性有所提高。分析的总效应量计算为Z = 2.62(p值 = 0.009)。所有研究的个体效应均有利于“利伐沙班”组。研究中的异质性如下:tau = 0.10;chi = 110.10,自由度 = 6;I = 95%。利伐沙班治疗后中风风险降低和发生率的第二项分析也显示出倾向于利伐沙班治疗的偏差。分析的合并效应如下:HR = 0.73(95% CI:0.50,1.07)。总效应计算为Z = 1.61(p值 = 0.10)。发现异质性如下:tau = 0.20,chi = 89.97,自由度 = 6,I = 93%。利伐沙班的标准剂量成为预防中风的首选策略,平衡了疗效和安全性。临床决策应考虑个体患者特征,未来研究应深入探讨特定亚群和长期结果,以进一步完善治疗指南。