University of Connecticut School of Pharmacy, Storrs, CT, USA.
Evidence-Based Practice Center, Hartford Hospital, Hartford, CT, USA.
Curr Med Res Opin. 2023 Sep;39(9):1183-1194. doi: 10.1080/03007995.2023.2247988. Epub 2023 Aug 24.
Advancing age is a risk factor for developing non-valvular atrial fibrillation (NVAF) or acute venous thromboembolism (VTE). We assessed the comparative effectiveness, safety, costs, and healthcare utilization associated with rivaroxaban versus warfarin in patients of advanced age managed in the United States (US).
We conducted a systematic review of Medline and Embase through April 2023 to identify real-world evidence (RWE) studies of older adults (at least 65+ years of age) with either NVAF or VTE who received either rivaroxaban or warfarin in the US and reported an outcome of stroke or systemic embolism (SSE), ischemic stroke (IS), recurrent VTE, major bleeding, intracranial hemorrhage, costs, or healthcare resource utilization. We classified each outcome of interest per study as "positive" (lower risk), "negative" (higher risk), or "neutral" based upon the summary effect size of rivaroxaban versus warfarin.
Twenty-nine RWE studies met inclusion criteria, mostly (83%) in NVAF populations. For SSE with rivaroxaban versus warfarin, 68.8% of studies showed positive effects and 31.2% showed neutral outcome. For major bleeding, 57.7% showed neutral effects, 38.5% showed negative effects, and 3.8% of studies showed positive effects with rivaroxaban versus warfarin. Of the two studies reporting cost data, both were positive, showing lower costs for SSE for rivaroxaban versus warfarin and neutral cost for major bleeding costs.
This systematic review supports findings from subgroup analyses of randomized controlled trials that, compared with warfarin, rivaroxaban is associated with generally neutral or positive effects on thrombosis and a mixed picture on bleeding outcomes in older adults with either NVAF or VTE treated in the United States.
年龄增长是导致非瓣膜性心房颤动(NVAF)或急性静脉血栓栓塞症(VTE)的一个危险因素。我们评估了利伐沙班与华法林在接受美国治疗的老年患者(至少 65 岁)中与 NVAF 或 VTE 相关的比较有效性、安全性、成本和医疗保健利用情况。
我们通过 2023 年 4 月对 Medline 和 Embase 进行了系统评价,以确定真实世界证据(RWE)研究,这些研究纳入了在美国接受利伐沙班或华法林治疗且报告了中风或全身性栓塞(SSE)、缺血性中风(IS)、复发性 VTE、大出血、颅内出血、成本或医疗保健资源利用情况的老年患者(至少 65 岁)。我们根据利伐沙班与华法林的汇总效应大小,将每个感兴趣的结果在每项研究中分类为“阳性”(风险较低)、“阴性”(风险较高)或“中性”。
29 项 RWE 研究符合纳入标准,其中大部分(83%)研究涉及 NVAF 人群。对于利伐沙班与华法林的 SSE,68.8%的研究显示阳性结果,31.2%显示中性结果。对于大出血,57.7%显示中性结果,38.5%显示阴性结果,3.8%的研究显示利伐沙班与华法林相比阳性结果。在报告成本数据的两项研究中,两者均为阳性,表明利伐沙班在 SSE 方面的成本低于华法林,而大出血的成本则为中性。
本系统评价支持随机对照试验亚组分析的结果,与华法林相比,利伐沙班在接受美国治疗的 NVAF 或 VTE 老年患者中与血栓形成相关的一般为中性或阳性结果,而出血结局则好坏参半。