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用于慢性肢体缺血的腘下药物洗脱支架

Infrapopliteal drug-eluting stents for chronic limb ischemia.

作者信息

Grant A G, White C J, Collins T J, Jenkins J S, Reilly J P, Ramee S R

机构信息

Department of Cardiovascular Diseases, Section on Invasive and Interventional Cardiology, Ochsner Clinic Foundation, New Orleans, Louisiana 70121, USA.

出版信息

Catheter Cardiovasc Interv. 2008 Jan 1;71(1):108-11. doi: 10.1002/ccd.21367.

Abstract

OBJECTIVE

We report our experience with the elective placement of below-knee, drug-eluting stents in patients with chronic limb ischemia.

BACKGROUND

Infrapopliteal percutaneous transluminal angioplasty has been associated with a lower rate of procedural success and high rate of restenosis because of the small size of the tibial vessels and the prevalence of calcified and diffuse atherosclerotic disease. Prior published data reports 3-year patency rates below 25%. Bare metal stents have been reported in bailout situations. Drug-eluting stents have markedly reduced restenosis compared to bare metal stents in the coronary vasculature, but there is little data supporting the use of these devices below the knee.

METHODS

Elective placement of drug-eluting stents in infrapopliteal lesions was performed on 10 patients with severe (> or =Fontaine Stage IIb) claudication (n = 1) or limb-threatening ischemia (n = 9) (rest pain, nonhealing ulcers and gangrene).

RESULTS

A total of 17 drug-eluting stents were electively placed in 12 below-knee arteries in 10 patients, resulting in an average of 1.7 +/- 0.7 stents per patient. The mean lesion length was 24.8 +/- 10.9 mm, the mean total stent length was 38.3 +/- 19.1 mm, and the mean nominal stent diameter was 2.8 +/- 0.3 mm. One patient required target vessel revascularization (TVR) at 3 weeks because of stent thrombosis. TVR was 10% at 12.4 +/- 6.5 months of follow-up. Clinically driven angiography in three different patients was performed at 4, 15, and 16 months and confirmed drug-eluting stent patency in each case.

CONCLUSIONS

The use of below-knee drug-eluting stents is feasible and appears to be safe in our small series of complex infrapopliteal lesions causing chronic limb ischemia. The occurrence of a single case of stent thrombosis warrants continued observation in this cohort. Prospective clinical trials will be necessary to confirm the benefits and justify the costs of this strategy for treating patients with infrapopliteal culprit lesions and chronic limb ischemia.

摘要

目的

我们报告在慢性肢体缺血患者中选择性置入膝下药物洗脱支架的经验。

背景

由于胫部血管管径小以及钙化和弥漫性动脉粥样硬化疾病的普遍存在,腘下经皮腔内血管成形术的手术成功率较低且再狭窄率较高。先前发表的数据显示3年通畅率低于25%。裸金属支架已被报道用于补救情况。与冠状动脉系统中的裸金属支架相比,药物洗脱支架已显著降低了再狭窄率,但几乎没有数据支持在膝下使用这些装置。

方法

对10例患有严重(≥Fontaine IIb期)间歇性跛行(n = 1)或肢体威胁性缺血(n = 9)(静息痛、不愈合溃疡和坏疽)的患者,在腘下病变处选择性置入药物洗脱支架。

结果

10例患者的12条膝下动脉共选择性置入17枚药物洗脱支架,平均每位患者置入1.7±0.7枚支架。平均病变长度为24.8±10.9毫米,平均支架总长度为38.3±19.1毫米,平均标称支架直径为2.8±0.3毫米。1例患者在3周时因支架血栓形成需要进行靶血管再血管化(TVR)。在12.4±6.5个月的随访中,TVR为10%。在4个月、15个月和16个月时对3例不同患者进行了临床驱动的血管造影,均证实了药物洗脱支架的通畅性。

结论

在我们这一小系列导致慢性肢体缺血的复杂腘下病变中,使用膝下药物洗脱支架是可行的且似乎是安全的。发生1例支架血栓形成事件,需要对该队列继续进行观察。需要进行前瞻性临床试验以证实该策略治疗腘下罪犯病变和慢性肢体缺血患者的益处并证明其成本的合理性。

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