1 Division of Cardiology, VA Eastern Colorado Health Care System and University of Colorado, Denver, CO, USA.
2 Division of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center and VA North Texas Health Care System, Dallas, TX, USA.
Vasc Med. 2018 Aug;23(4):358-364. doi: 10.1177/1358863X18775593. Epub 2018 Jun 20.
With growing use of drug-coated balloons (DCB) for femoropopliteal (FP) artery interventions, there is limited information on rates of real-world adjunctive stent use and its association with short and long-term outcomes. We report on 225 DCB treated FP lesions in 224 patients from the Excellence in Peripheral Artery Disease (XLPAD) registry (NCT01904851) between 2014 and 2016. Cochran-Mantel-Haenszel and Wilcoxon rank sum statistics were used to compare stented (planned or 'bail-out') versus non-stented DCB treated lesions. Stents were implanted in 31% of FP DCB interventions. Among the 70 stents implanted, 46% were for 'bail-out' indications and 54% were planned. Lesions treated with stents were longer (mean 150 mm vs 100 mm; p < 0.001) and less likely to be in-stent restenosis lesions (10% vs 28%; p=0.003). Stenting was significantly more frequent in complex FP lesions, including chronic total occlusions (66% vs 34%; p < 0.001). For bail-out stenting, interwoven nitinol stents were the most common type (50%) followed by drug-eluting stents (34%) and bare-metal stents (22%). There were no differences in peri-procedural complication rates or 12-month target limb revascularization rates (18.6% vs 11.6%; p=0.162) or 12-month amputation rates (11.4% vs 11%; p=0.92) between lesions where adjunctive stenting was used versus lesions without adjunctive stenting, respectively. In conclusion, in a contemporary 'real-world' adjudicated multicenter US registry, adjunctive stenting was necessary in nearly a third of the lesions, primarily for the treatment of more complex FP lesions, with similar short and intermediate-term clinical outcomes compared with non-stented lesions. ClinicalTrials.gov Identifier: NCT01904851.
随着药物涂层球囊(DCB)在股腘动脉(FP)介入治疗中的应用越来越广泛,关于真实世界中辅助支架使用的情况及其与短期和长期结果的关系的信息有限。我们报告了 2014 年至 2016 年期间,来自卓越外周动脉疾病(XLPAD)登记处(NCT01904851)的 224 名患者的 225 例 FP 病变的 DCB 治疗情况。采用 Cochran-Mantel-Haenszel 和 Wilcoxon 秩和检验比较了支架(计划或“紧急”)与非支架 DCB 治疗病变。在 FP DCB 介入治疗中,有 31%的患者植入了支架。在植入的 70 个支架中,46%是用于“紧急”适应证,54%是计划植入的。支架治疗的病变更长(平均 150mm 与 100mm;p<0.001),支架内再狭窄病变的可能性较小(10%与 28%;p=0.003)。支架治疗在复杂的 FP 病变中更为常见,包括慢性完全闭塞(66%与 34%;p<0.001)。对于紧急支架治疗,编织型镍钛合金支架最为常见(50%),其次是药物洗脱支架(34%)和裸金属支架(22%)。在围手术期并发症发生率或 12 个月靶肢体血运重建率(18.6%与 11.6%;p=0.162)或 12 个月截肢率(11.4%与 11%;p=0.92)方面,支架辅助治疗与无支架辅助治疗的病变之间没有差异。总之,在当代“真实世界”的经裁决的多中心美国登记处,近三分之一的病变需要辅助支架治疗,主要是为了治疗更复杂的 FP 病变,与非支架治疗的病变相比,短期和中期临床结果相似。临床试验.gov 标识符:NCT01904851。