Grotti Simone, Liistro Francesco, Angioli Paolo, Ducci Kenneth, Falsini Giovanni, Porto Italo, Ricci Lucia, Ventoruzzo Giorgio, Turini Filippo, Bellandi Guido, Bolognese Leonardo
Cardiovascular Department, San Donato Hospital, Arezzo, Italy.
Cardiovascular Department, San Donato Hospital, Arezzo, Italy
J Endovasc Ther. 2016 Feb;23(1):52-7. doi: 10.1177/1526602815614555. Epub 2015 Oct 28.
To report the 3-year safety and effectiveness outcomes from the prospective all-comers DEBATE-ISR study (ClinicalTrials.gov identifier NCT01558531) of symptomatic diabetic patients with femoropopliteal in-stent restenosis (ISR) undergoing treatment with paclitaxel-eluting balloons compared with historical diabetic controls.
From January 2010 to December 2011, 44 consecutive diabetic patients (mean age 74±11 years; 32 men) were treated with drug-eluting balloons (DEBs) and enrolled in the study. The control group comprised 42 consecutive diabetic patients (age 76±7 years; 23 men) treated with conventional balloon angioplasty (BA) from 2008 to 2009.
No significant differences in terms of clinical, angiographic, or procedural characteristics were observed between the study groups. Critical limb ischemia was present in the majority of patients. Tosaka class III ISR was observed in more than half of the patients. Mean lesion length was 132±86 and 137±82 mm in the DEB and BA groups, respectively (p=0.7). At 3-year follow-up, the rate of target lesion revascularization (TLR) was 40% in the DEB group vs 43% in the BA group (p=0.8); Kaplan-Meier analysis showed no significant differences in terms of freedom from TLR. The presence of a Tosaka class III occlusion was associated with a worse outcome in both study groups (odds ratio 3.96, 95% confidence interval 1.55 to 10.1, p=0.004).
Using DEBs for femoropopliteal ISR yielded similar results to BA in terms of TLR at 3-year follow-up. The treatment of more complex ISR lesions was associated with an increased rate of TLR, irrespective of the technology used.
报告对有症状的股腘动脉支架内再狭窄(ISR)糖尿病患者进行紫杉醇洗脱球囊治疗的前瞻性、面向所有患者的DEBATE-ISR研究(ClinicalTrials.gov标识符NCT01558531)的3年安全性和有效性结果,并与历史糖尿病对照组进行比较。
2010年1月至2011年12月,连续44例糖尿病患者(平均年龄74±11岁;32例男性)接受药物洗脱球囊(DEB)治疗并纳入研究。对照组包括2008年至2009年连续42例接受传统球囊血管成形术(BA)治疗的糖尿病患者(年龄76±7岁;23例男性)。
研究组之间在临床、血管造影或手术特征方面未观察到显著差异。大多数患者存在严重肢体缺血。超过一半的患者观察到托萨卡III级ISR。DEB组和BA组的平均病变长度分别为132±86和137±82mm(p = 0.7)。在3年随访时,DEB组的靶病变血运重建(TLR)率为40%,而BA组为43%(p = 0.8);Kaplan-Meier分析显示在无TLR方面无显著差异。托萨卡III级闭塞的存在与两个研究组中较差的结果相关(比值比3.96,95%置信区间1.55至10.1,p = 0.004)。
在3年随访时,使用DEB治疗股腘动脉ISR在TLR方面产生的结果与BA相似。无论使用何种技术,治疗更复杂的ISR病变均与TLR率增加相关。