Duke Clinical Research Institute, Durham, NC.
Section of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT.
Am Heart J. 2021 Mar;233:59-67. doi: 10.1016/j.ahj.2020.12.004. Epub 2020 Dec 13.
The connection between paclitaxel-coated devices (PCD) use during peripheral vascular interventions (PVI) and mortality is debated. We aimed to analyze patterns of PCD use and the safety and effectiveness of PCD use in the superficial femoral and/or popliteal arteries.
Patients undergoing PVI of femoropopliteal lesions with and without PCD between January 1, 2015 and June 30, 2017 were compared using the American College of Cardiology's National Cardiovascular Data Registry PVI Registry. Outcomes were derived from Centers for Medicare & Medicaid claims data. The primary outcome was all-cause mortality at 6-, 12-, and 24-months following PVI. Inverse probability weighting and frailty models were used to assess the differences between groups. The analysis was IRB-approved.
In the overall cohort consisting of 6,302 femoropopliteal PVIs, PCD-PVI patients were more likely to be treated for claudication (63.5% vs 51.3%, P< .001), less likely to have a chronic total occlusion (24.6% vs 34.7%, P < .001), and more likely to be treated in certain geographic and practice settings. In the analytic cohort consisting of 1,666 femoropopliteal PVIs with linked claims outcomes (888 PCD-PVI, 53.3%), unadjusted rates of all outcomes were lower in PCD-PVI patients. After adjustment, there were no significant differences in mortality following PCD-PVI versus non-PCD PVI at 1 year (adjusted RR 0.78, 95% CI 0.60-1.01, P= .055) or 2 years (aRR 0.98, 95% CI 0.77-1.24, P= .844).
There were significant differences between the patients in whom and settings in which PCD-PVI was versus was not used. PCD-PVI was not associated with an increased risk of 2-year mortality in real-world use.
紫杉醇涂层装置(PCD)在周围血管介入治疗(PVI)中的应用与死亡率之间的关系存在争议。本研究旨在分析 PCD 在股浅动脉和/或腘动脉中的使用模式,以及其安全性和有效性。
本研究回顾性分析了 2015 年 1 月 1 日至 2017 年 6 月 30 日期间接受股浅动脉病变 PVI 治疗的患者,比较了使用和未使用 PCD 的患者。结局数据来源于美国心脏病学会国家心血管数据注册 PVI 注册库和联邦医疗保险和医疗补助服务中心索赔数据。主要结局指标为 PVI 后 6、12 和 24 个月的全因死亡率。采用逆概率加权和脆弱性模型来评估组间差异。本研究经机构审查委员会批准。
在纳入的 6302 例股浅动脉 PVI 患者中,PCD-PVI 患者更可能因跛行(63.5% vs 51.3%,P<.001)接受治疗,而非慢性完全闭塞(24.6% vs 34.7%,P <.001),更可能在某些地理位置和医疗环境中接受治疗。在纳入的 1666 例有相关索赔结局的股浅动脉 PVI 患者中(888 例 PCD-PVI,53.3%),PCD-PVI 患者的全因死亡率在未校正时较低。校正后,PCD-PVI 与非 PCD-PVI 相比,1 年(校正 RR 0.78,95%CI 0.60-1.01,P=.055)和 2 年(aRR 0.98,95%CI 0.77-1.24,P=.844)时死亡率均无显著差异。
PCD-PVI 的使用和实施环境之间存在显著差异。在真实世界中,PCD-PVI 的应用与 2 年死亡率的增加无关。