Dawson D L, Cutler B S, Meissner M H, Strandness D E
Department of Surgery, University of Washington, Seattle, USA.
Circulation. 1998 Aug 18;98(7):678-86. doi: 10.1161/01.cir.98.7.678.
Cilostazol is a new phosphodiesterase inhibitor that suppresses platelet aggregation and also acts as a direct arterial vasodilator. This prospective, randomized, placebo-controlled, parallel-group clinical trial evaluated the efficacy of cilostazol for treatment of stable, moderately severe intermittent claudication.
Study inclusion criteria included age > or =40 years, initial claudication distance (ICD) on treadmill (12.5% incline, 3.2 km/h) between 30 and 200 m, and confirmation of diagnosis of chronic lower-extremity arterial occlusive disease. After stabilization and single-blind placebo lead-in, 81 subjects (62 male, 19 female) from 3 centers were randomized unequally (2:1) to 12 weeks of treatment with cilostazol 100 mg PO BID or placebo. Primary outcome measures included ICD and maximum distance walked (absolute claudication distance, or ACD). Secondary outcome measures included ankle pressures, subjective assessments of benefit by patients and physicians, and safety. Treatment and control groups were similar with respect to age, severity of symptoms, ankle pressures, and smoking status. Statistical analyses used intention-to-treat analyses for each of 77 subjects who had > or =1 treadmill test after initiation of therapy. Comparisons between groups were based on logarithms of ratios of ICD and ACD changes from baseline using ANOVA test at last treatment visit. The estimated treatment effect showed a 35% increase in ICD (P<0.01) and a 41% increase in ACD (P<0.01). There was no significant change in resting or postexercise ankle/brachial indexes. Patients' and physicians' subjective assessments corroborated the measured improvements in walking performance observed in the cilostazol-treated group.
Cilostazol improved walking distances, significantly increasing ICD and ACD. The data suggest cilostazol is safe and well tolerated for the treatment of intermittent claudication.
西洛他唑是一种新型磷酸二酯酶抑制剂,可抑制血小板聚集,并可作为直接的动脉血管扩张剂。这项前瞻性、随机、安慰剂对照、平行组临床试验评估了西洛他唑治疗稳定的、中度严重间歇性跛行的疗效。
研究纳入标准包括年龄≥40岁,跑步机上初始跛行距离(ICD)(坡度12.5%,速度3.2公里/小时)在30至200米之间,以及慢性下肢动脉闭塞性疾病诊断得到确认。在病情稳定并经过单盲安慰剂导入期后,来自3个中心的81名受试者(62名男性,19名女性)被不均衡地(2:1)随机分为两组,分别接受为期12周的口服西洛他唑100毫克每日两次治疗或安慰剂治疗。主要结局指标包括ICD和最大行走距离(绝对跛行距离,或ACD)。次要结局指标包括踝部压力、患者和医生对获益的主观评估以及安全性。治疗组和对照组在年龄、症状严重程度、踝部压力和吸烟状况方面相似。对开始治疗后进行了≥1次跑步机测试的77名受试者中的每一位进行意向性分析。在最后一次治疗访视时,使用方差分析检验,基于ICD和ACD相对于基线变化的比值的对数进行组间比较。估计的治疗效果显示ICD增加35%(P<0.01),ACD增加41%(P<0.01)。静息或运动后踝/臂指数无显著变化。患者和医生的主观评估证实了西洛他唑治疗组观察到的行走能力的改善。
西洛他唑改善了行走距离,显著增加了ICD和ACD。数据表明西洛他唑治疗间歇性跛行安全且耐受性良好。