老年房颤患者口服非维生素K拮抗剂的安全性和有效性:22项研究和440281例患者的系统评价和荟萃分析

Angelo Silverio, Marco Di Maio, Costantina Prota, Elena De Angelis, Ilaria Radano, Rodolfo Citro, Albino Carrizzo, Michele Ciccarelli, Carmine Vecchione, Davide Capodanno, Gennaro Galasso
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引用次数: 27

摘要

目的:本荟萃分析的目的是评估非维生素K口服拮抗剂(NOACs)与维生素K拮抗剂(VKAs)在老年房颤(AF)患者中的疗效和安全性,并间接比较NOACs在该人群中的作用。方法和结果:检索MEDLINE、Cochrane、ISI Web of Sciences和SCOPUS,比较NOACs和vka在≥75岁AF患者卒中预防中的随机或调整观察性研究。该荟萃分析的主要疗效和安全性结果分别是卒中和系统性栓塞(SSE)和大出血的综合结果。其他次要结局也进行了分析。该分析包括22项研究,纳入440281例≥75岁的房颤患者。与VKAs相比,noac的SSE风险显著降低[风险比(HR) 0.79;95%可信区间(CI) 0.70-0.89],而在大出血方面没有发现差异(HR 0.94;95% ci 0.85-1.05)。NOACs降低颅内出血风险(HR 0.46;95% CI 0.38-0.58),出血性卒中(HR 0.61;95% CI 0.48-0.79)和致死性出血(HR 0.46;95% CI 0.30-0.72),但胃肠道出血增加(HR 1.46;95% CI 1.30-1.65),与vka相比。经调整后的间接比较显示,NOAC制剂在SSE方面无显著差异。相反,利伐沙班与阿哌沙班发生大出血的风险更高(HR 1.69;95% CI 1.39-2.08)和依多沙班(HR 1.37;95% CI 1.14-1.67),达比加群与阿哌沙班比较(HR 1.47;95% ci 1.18-1.85)。结论:在老年房颤患者中,与vka相比,NOACs与SSE、颅内出血、出血性卒中和致死性出血的风险较低,但增加了胃肠道出血。在本分析中,单个NOAC制剂的安全性存在显著差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety and efficacy of non-vitamin K antagonist oral anticoagulants in elderly patients with atrial fibrillation: systematic review and meta-analysis of 22 studies and 440 281 patients.

Aims: The aim of the present meta-analysis was to evaluate the efficacy and safety of non-vitamin K oral antagonists (NOACs) vs. vitamin K antagonists (VKAs) in elderly patients with atrial fibrillation (AF) and indirectly compare NOACs in this population.

Methods and results: MEDLINE, Cochrane, ISI Web of Sciences, and SCOPUS were searched for randomized or adjusted observational studies comparing NOACs vs. VKAs for stroke prevention in AF patients ≥75 years. The primary efficacy and safety outcomes of this meta-analysis were the composite of stroke and systemic embolism (SSE) and major bleedings, respectively. Other secondary outcomes were also analysed. The analysis included 22 studies enrolling 440 281 AF patients ≥ 75 years. The risk of SSE was significantly lower with NOACs vs. VKAs [hazard ratio (HR) 0.79; 95% confidence interval (CI) 0.70-0.89], whereas no differences were found for major bleedings (HR 0.94; 95% CI 0.85-1.05). NOACs reduced the risk of intracranial bleeding (HR 0.46; 95% CI 0.38-0.58), haemorrhagic stroke (HR 0.61; 95% CI 0.48-0.79) and fatal bleeding (HR 0.46; 95% CI 0.30-0.72) but increased gastrointestinal (GI) bleedings (HR 1.46; 95% CI 1.30-1.65), compared to VKAs. The adjusted indirect comparison showed no significant differences in term of SSE between NOAC agents. Conversely, the risk of major bleeding was higher for rivaroxaban vs. apixaban (HR 1.69; 95% CI 1.39-2.08) and edoxaban (HR 1.37; 95% CI 1.14-1.67), and for dabigatran vs. apixaban (HR 1.47; 95% CI 1.18-1.85).

Conclusion: In elderly patients with AF, NOACs are associated to a lower risk of SSE, intracranial bleeding, haemorrhagic stroke and fatal bleeding than VKAs, but increase GI bleedings. In this analysis, the safety profile of individual NOAC agents was significantly different.

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