Department of Surgery, Huntington Memorial Hospital, Pasadena, Calif.
Department of Surgery and Perioperative Care, University of Texas at Austin Dell Medical School, Austin, Tex.
J Vasc Surg. 2018 May;67(5):1472-1479. doi: 10.1016/j.jvs.2017.09.022. Epub 2017 Dec 8.
It has long been known that hydroxymethylglutaryl-coenzyme A reductase inhibitors (statins) broadly reduce cardiovascular events in patients with peripheral vascular disease. It was the goal of this study to determine whether there is an association between statin therapy and primary patency after stenting of superficial femoral and popliteal arteries.
The records of all patients undergoing primary nitinol stenting of the femoral and popliteal arteries at a single institution and by a single surgeon during a 10-year period were reviewed. Demographic characteristics of the patients and risk factors were identified. TransAtlantic Inter-Society Consensus (TASC II) classifications were determined for all stented lesions. Analysis was performed to determine whether the use of statins at the time of stent placement was associated with a change in rates of primary patency. Loss of primary patency was said to have occurred when an intrastent occlusion or a ≥70% stenosis was identified by arterial duplex ultrasound or angiography. Kaplan-Meier survival curves were plotted, and differences between groups were tested by log-rank method.
Between 2004 and 2014, primary femoral or popliteal stenting was performed on 308 limbs in 250 patients. At the time of intervention, 52.4% of these patients were being treated with statin therapy; 137 interventions were done for claudication and 113 for critical limb ischemia. Of the lesions treated, 165 were TASC A or B and 85 were TASC C or D. Primary patency rates for all stented lesions were 75%, 54%, and 35% at 12, 24, and 36 months. The patency rates at 12, 24, and 36 months, respectively, were 80%, 55%, and 40% for those taking statins and 68%, 49%, and 28% for those not taking statins (P = .178). Statin therapy demonstrated a trend toward an association with improved primary patency rates in TASC A/B lesions but had no association in TASC C/D lesions (TASC A/B, P = .056; TASC C/D, P = .537). Statin compliance was found to be 87% at a mean follow-up of 24.1 months.
Although the use of statins has been shown to reduce cardiovascular morbidity and mortality in patients with peripheral vascular disease, overall there is not an association of these drugs with improved primary patency after primary stenting of femoral and popliteal artery lesions. However, when limbs are stratified for severity, less severe (TASC A/B) lesions demonstrated a trend toward a significant association between statin use and improved primary patency. This finding was not seen in more severe (TASC C/D) disease.
人们早就知道羟甲基戊二酰辅酶 A 还原酶抑制剂(他汀类药物)广泛降低外周血管疾病患者的心血管事件。本研究的目的是确定他汀类药物治疗与股浅动脉和腘动脉支架置入后的原发性通畅率之间是否存在关联。
回顾了一家机构和一位外科医生在 10 年内对股浅动脉和腘动脉进行初次镍钛支架置入的所有患者的记录。确定了患者的人口统计学特征和危险因素。对所有支架置入病变进行了跨大西洋腔内血管外科学会共识 (TASC II) 分类。分析了支架置入时使用他汀类药物是否与原发性通畅率的变化相关。当通过动脉双功能超声或血管造影术发现支架内闭塞或≥70%狭窄时,即认为原发性通畅丧失。绘制 Kaplan-Meier 生存曲线,并通过对数秩检验检验组间差异。
2004 年至 2014 年,对 250 名患者的 308 条肢体进行了股浅或腘动脉初次支架置入。在干预时,这些患者中有 52.4%正在接受他汀类药物治疗;137 例用于治疗跛行,113 例用于治疗严重肢体缺血。在治疗的病变中,165 例为 TASC A 或 B,85 例为 TASC C 或 D。所有支架置入病变的 12、24 和 36 个月的通畅率分别为 75%、54%和 35%。服用他汀类药物的患者在 12、24 和 36 个月的通畅率分别为 80%、55%和 40%,而未服用他汀类药物的患者分别为 68%、49%和 28%(P=0.178)。他汀类药物治疗显示出与 TASC A/B 病变原发性通畅率改善相关的趋势,但在 TASC C/D 病变中无相关性(TASC A/B,P=0.056;TASC C/D,P=0.537)。在平均随访 24.1 个月时,发现他汀类药物的依从性为 87%。
尽管他汀类药物的使用已被证明可降低外周血管疾病患者的心血管发病率和死亡率,但总体而言,这些药物与股浅动脉和腘动脉病变初次支架置入后的原发性通畅率改善无关。然而,当根据严重程度对肢体进行分层时,较轻(TASC A/B)病变显示出他汀类药物使用与原发性通畅率改善之间存在显著关联的趋势。在更严重的(TASC C/D)疾病中没有发现这种情况。