Donas K P, Schwindt A, Schönefeld T, Tessarek J, Torsello G
Department of Vascular Surgery, St. Franziskus Hospital, Münster, Germany.
Eur J Vasc Endovasc Surg. 2009 Jun;37(6):688-93. doi: 10.1016/j.ejvs.2009.01.023. Epub 2009 Mar 27.
To evaluate the effectiveness of nitinol stent placement in long infrapopliteal lesions in patients with critical limb ischaemia.
Between January 2005 and January 2008, 34 high-risk patients (18 female; mean age: 73.8+/-6.1 years) with critical limb ischaemia underwent infragenicular stenting. They had serious cardiovascular co-morbidities (>3, such as chronic obstructive pulmonary disease (COPD), congestive heart failure and coronary artery occlusive disease), American Society of Anaesthesiologists score of 3 or more, previous myocardial infarction, coronary stent or bypass. The mean stenosis length was 6.5+/-0.9 cm (range: 2.2-8 cm), and the mean occlusion length was 7.5+/-2.9 cm (range: 3-9.6 cm). Primary stent implantation was performed for long stenosis or occlusion based on the TransAtlantic InterSociety Consensus (TASC) C and D classification, secondary stenting for flow-limiting dissections or elastic recoil after balloon dilatation. All patients who returned to the outpatient clinic were assessed for claudication by clinical examination, ankle-brachial index (ABI) measurements, colour flow and duplex Doppler ultrasound (US). Digital subtraction angiography was performed if restenosis or re-occlusion was identified by Doppler US or transcutaneous measurement of partial oxygen pressure (TcpO(2)) measurements, when appropriate.
The technical success rate was 97.1% (33 of 34 cases). The crude rate of primary patency rate was 91.1% during a follow-up period of 10.4+/-7.3 months. The mean ankle-brachial index increased significantly following intervention (0.45+/-0.25-0.92+/-0.13, p<0.001). Two patients underwent successful redo angioplasty after tibioperoneal interventions due to in-stent restenosis (>70%) with relevant limitation of pain-free walking distance. In another patient, bypass surgery to the anterior tibial artery 6 months after primary intervention was necessary due to rest pain. Two patients required surgical revision of the femoral artery after antegrade access. No procedure-related death was recorded in the entire follow-up period.
The mid-term outcome underscores infrapopliteal stent placement as a reliable treatment option in patients with critical limb ischaemia. In patients at high risk for crural bypass, with no flow-limiting supragenicular lesions, below-knee stent-supported angioplasty should be considered as a first choice of treatment.
评估镍钛合金支架置入术治疗严重下肢缺血患者腘动脉以下长病变的有效性。
2005年1月至2008年1月期间,34例严重下肢缺血的高危患者(18例女性;平均年龄:73.8±6.1岁)接受了膝下支架置入术。他们患有严重的心血管合并症(>3种,如慢性阻塞性肺疾病(COPD)、充血性心力衰竭和冠状动脉闭塞性疾病),美国麻醉医师协会评分3分或更高,既往有心肌梗死、冠状动脉支架置入或搭桥手术史。平均狭窄长度为6.5±0.9 cm(范围:2.2 - 8 cm),平均闭塞长度为7.5±2.9 cm(范围:3 - 9.6 cm)。根据跨大西洋两岸心血管介入治疗协作组(TASC)C和D级分类,对长段狭窄或闭塞进行一期支架植入,对球囊扩张后出现的限流性夹层或弹性回缩进行二期支架植入。所有返回门诊的患者均通过临床检查、踝肱指数(ABI)测量、彩色血流和双功多普勒超声(US)评估跛行情况。如果通过多普勒超声或经皮测量局部氧分压(TcpO₂)测量发现再狭窄或再闭塞,酌情进行数字减影血管造影。
技术成功率为97.1%(34例中的33例)。在10.4±7.3个月的随访期内,一期通畅率的粗率为91.1%。干预后平均踝肱指数显著增加(从0.45±0.25增至0.92±0.13,p<0.001)。2例患者因支架内再狭窄(>70%)导致无痛步行距离受限,在胫腓动脉干预后成功进行了再次血管成形术。另1例患者在初次干预6个月后因静息痛需要进行胫前动脉搭桥手术。2例患者在顺行入路后需要对股动脉进行手术修复。在整个随访期内未记录到与手术相关的死亡病例。
中期结果强调了腘动脉以下支架置入术是严重下肢缺血患者可靠的治疗选择。对于有小腿旁路手术高风险且无膝上限流性病变的患者,膝下支架辅助血管成形术应被视为首选治疗方法。