Interventional Cardiology Unit, EMO-GVM Centro Cuore Columbus, Milan, Italy.
J Interv Cardiol. 2013 Jun;26(3):259-63. doi: 10.1111/j.1540-8183.2013.12010.x. Epub 2013 Feb 4.
To assess the safety and efficacy of combining drug-eluting balloon (DEB) and drug-eluting stents (DES) in the same coronary lesion.
Use of DEB may not always produce optimal results or even result in dissection, compelling the operators to consider bailout stenting with bare metal stents (BMS). However, BMS may not be ideal in patients who have significant risk-profile for restenosis. We have opted for DES over BMS in such situations and present our follow-up data.
Between 2009 and 2011, 46 patients (57 lesions) requiring bailout stenting following DEB use were treated with second-generation DES. All patients had at-least one or more risk-factors that made them vulnerable for restenosis (diabetes, chronic kidney disease, previous in-stent restenosis [ISR], and/or long diffuse lesions ≥ 30 mm).
Of the 57 lesions, 34 (60%) were previous ISR. The mean length of the DEB was: 36.2 ± 5.6 mm. All patients had TIMI-3 flow post PCI with no in-lab complications. At median follow-up of 12.3 months (interquartile range [IQR]: 7.5-18.1), the rates target lesion revascularization (TLR) and target vessel revascularization (TVR) were 3 (5.3%) and 4 (7%), respectively. One patient had died 3 months following treatment. There were no episodes of myocardial infarction, definite or probable stent thrombosis. The major adverse cardiovascular events (MACE) rate defined as cardiac-death, MI, and TVR occurred in 11% of patients.
The results from this novel strategy of combining "Paclitaxel" eluting balloon and "Limus" eluting stent in a same lesion are encouraging. Dual drug-elution acting on two different pathways may provide potential synergy that may explain the favorable outcome.
评估药物洗脱球囊(DEB)与药物洗脱支架(DES)联合应用于同一冠状动脉病变的安全性和疗效。
尽管使用 DEB 不一定能产生最佳效果,甚至可能导致夹层,迫使操作者考虑使用裸金属支架(BMS)进行紧急支架置入。然而,对于那些存在明显再狭窄风险的患者,BMS 可能并不是理想的选择。在这种情况下,我们选择使用 DES 而不是 BMS,并呈现我们的随访数据。
在 2009 年至 2011 年期间,46 例(57 处病变)在使用 DEB 后需要紧急支架置入的患者接受了第二代 DES 治疗。所有患者均至少存在一个或多个使他们易发生再狭窄的危险因素(糖尿病、慢性肾脏病、既往支架内再狭窄[ISR]和/或≥30mm 的长弥漫性病变)。
57 处病变中,34 处(60%)为既往 ISR。DEB 的平均长度为:36.2±5.6mm。所有患者经 PCI 后均获得 TIMI 3 级血流,无实验室并发症。在中位数为 12.3 个月(四分位距[IQR]:7.5-18.1)的随访中,靶病变血运重建(TLR)和靶血管血运重建(TVR)的发生率分别为 3 例(5.3%)和 4 例(7%)。1 例患者在治疗后 3 个月死亡。无心肌梗死、确定或可能的支架血栓形成事件。定义为心脏死亡、心肌梗死和 TVR 的主要不良心血管事件(MACE)发生率为 11%。
这种将“紫杉醇”洗脱球囊和“雷帕霉素”洗脱支架联合应用于同一病变的新策略的结果令人鼓舞。双重药物洗脱作用于两种不同途径可能提供潜在的协同作用,这可以解释其良好的结果。