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己酮可可碱、丁咯地尔和硝苯地平治疗下肢间歇性跛行的比较评价

Comparative evaluation of pentoxifylline, buflomedil, and nifedipine in the treatment of intermittent claudication of the lower limbs.

作者信息

Chacón-Quevedo A, Eguaras M G, Calleja F, Garcia M A, Roman M, Casares J, Muñoz I, Concha M

机构信息

Cardiovascular Unit, Reina Sofia Hospital, Cordoba, Spain.

出版信息

Angiology. 1994 Jul;45(7):647-53. doi: 10.1177/000331979404500708.

Abstract

In the light of the current controversy surrounding the use of hemorheologic and vasodilator drugs in the treatment of peripheral arteriosclerosis, a comparative study was designed in order to evaluate the efficacy of pentoxifylline, buflomedil, and nifedipine in 45 patients with peripheral arterial disease (Fontaine stage II). The patients in this prospective randomized study were divided into three groups: 15 patients received pentoxifylline treatment (1,200 mg/day), 15 were treated with buflomedil (600 mg/day), and 15 with nifedipine (60 mg/day). Response to treatment was assessed at the start of the study and after forty-five and ninety days, by clinical examination, Doppler test, strain test, and digital occlusion plethysmography using a strain gauge ring. Pentoxifylline was significantly more effective (P < 0.05) than buflomedil and nifedipine at ninety days in improving walking performance, resting toe pressure, resting and postexercise ankle/brachial pressure ratio, and basal/postischemic toe-pulse ratio. Significant differences within groups were also noted for initial claudication, toe peak-flow time, pulse reappearance time (PRT/2), and maximum postischemic flow time, together with significant intergroup variables. In conclusion, pentoxifylline proved more effective than the other drugs tested in: 1. improving distal pressure and resting microcirculatory blood flow; 2. increasing postexercise distal flow, ratios, and pressures and enabling faster recuperation of basal pulse rates; 3. increasing initial claudication distance in the strain test within the test group and achieving a greater absolute subjective claudication distance than that obtained using the other treatments.

摘要

鉴于目前围绕血液流变学药物和血管扩张剂在治疗外周动脉硬化中的应用存在争议,设计了一项比较研究,以评估己酮可可碱、丁咯地尔和硝苯地平对45例外周动脉疾病(Fontaine II期)患者的疗效。在这项前瞻性随机研究中,患者被分为三组:15例患者接受己酮可可碱治疗(1200毫克/天),15例接受丁咯地尔治疗(600毫克/天),15例接受硝苯地平治疗(60毫克/天)。在研究开始时以及45天和90天后,通过临床检查、多普勒测试、应变测试以及使用应变仪环进行数字式闭塞体积描记法来评估治疗反应。在90天时,己酮可可碱在改善步行能力、静息趾压、静息及运动后踝/臂压力比值以及基础/缺血后趾脉搏比值方面比丁咯地尔和硝苯地平显著更有效(P<0.05)。在初始跛行、趾峰值血流时间、脉搏重现时间(PRT/2)和最大缺血后血流时间方面,组内也存在显著差异,同时组间变量也有显著差异。总之,己酮可可碱在以下方面比其他受试药物更有效:1. 改善远端压力和静息微循环血流量;2. 增加运动后远端血流量、比值和压力,并使基础脉搏率更快恢复;3. 在测试组的应变测试中增加初始跛行距离,并比使用其他治疗方法获得更大的绝对主观跛行距离。

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