Kickuth Ralph, Keo Hong Hak, Triller Jürgen, Ludwig Karin, Do Dai-Do
Department of Diagnostic, Inselspital, University of Berne, Freiburgstrasse 20, CH-3010 Berne, Switzerland.
J Vasc Interv Radiol. 2007 Jun;18(6):703-8. doi: 10.1016/j.jvir.2007.03.012.
To evaluate the primary success and short-term patency associated with a new 4-F sheath-compatible self-expanding nitinol stent after failed conventional angioplasty of distal popliteal and infrapopliteal lesions in severe lifestyle-limiting claudication (LLC) and chronic critical limb ischemia (CLI).
Between May 2003 and July 2005, 35 patients with Rutherford category 3-5 disease (16 patients with CLI, 19 patients with LLC) underwent percutaneous transluminal angioplasty (PTA) and stent implantation. Indications for stent placement were residual stenosis, flow-limiting dissections, or elastic recoil after PTA. Before and after the intervention and during the 6-month follow-up, clinical investigation, color-flow and duplex Doppler ultrasonography, and digital subtraction angiography were performed. Technical success, primary patency at 6 months, clinical improvement as defined by Rutherford with clinical and hemodynamic measures, and complications were evaluated.
A total of 22 patients underwent distal popliteal artery stent placement and 13 underwent tibioperoneal artery stent placement. Stent implantation was successfully performed in all patients. After stent placement, the primary cumulative patency rate for the study group at 6 months was 82%. The mean resting ankle-brachial index at baseline was 0.50 +/- 0.16 and significantly increased to 0.90 +/- 0.17 at 12-24 hours after intervention and 0.82 +/- 0.24 at latest follow-up (P < .001 for both). The sustained clinical improvement rate was 80% at the 6-month follow-up. The 6-month limb salvage rate regarding major amputation was 100%. The rate of major complications was 17%.
Infrapopliteal application of the new nitinol stent is a safe, feasible, and effective method with good short-term patency rate in the treatment of severe LLC and chronic CLI.
评估在严重影响生活方式的间歇性跛行(LLC)和慢性严重肢体缺血(CLI)患者中,腘动脉远端和腘以下病变常规血管成形术失败后,一种新型与4F鞘兼容的自膨式镍钛合金支架的初次成功率和短期通畅率。
2003年5月至2005年7月期间,35例卢瑟福分级为3 - 5级疾病的患者(16例CLI患者,19例LLC患者)接受了经皮腔内血管成形术(PTA)和支架植入。支架置入的指征为PTA后残余狭窄、限流性夹层或弹性回缩。在干预前后以及6个月的随访期间,进行了临床检查、彩色血流和双功多普勒超声检查以及数字减影血管造影。评估了技术成功率、6个月时的初次通畅率、卢瑟福定义的临床和血流动力学指标的临床改善情况以及并发症。
共22例患者接受了腘动脉远端支架置入,13例接受了胫腓动脉支架置入。所有患者均成功进行了支架植入。支架置入后,研究组6个月时的初次累积通畅率为82%。基线时平均静息踝肱指数为0.50±0.16,干预后12 - 24小时显著增加至0.90±0.17,最新随访时为0.82±0.24(两者P均<0.001)。6个月随访时持续临床改善率为80%。关于大截肢的6个月肢体挽救率为100%。主要并发症发生率为17%。
新型镍钛合金支架在腘以下的应用是一种安全、可行且有效的方法,在治疗严重LLC和慢性CLI方面具有良好的短期通畅率。