Hospital Universitario Getafe, Angiology and Vascular Surgery Department, Madrid, Spain.
J Vasc Surg. 2010 Apr;51(4):857-62. doi: 10.1016/j.jvs.2009.10.116.
The study tested the feasibility of using a new portable mechanical compression device for the treatment of claudication. The device applies intermittent non-pneumatic mechanical compression (IMC) to the calf. It was hypothesized that it can offer a low-cost convenient option for patients and achieve good compliance and improved clinical outcomes.
Thirty patients were enrolled in a randomized controlled single blind study. Fourteen patients were assigned to active IMC. Sixteen control patients continued with medical treatment alone. Outcomes were recorded at baseline, after one month, three months, and six months. The study examined changes in exercise tolerance using Initial Claudiacation Distance (ICD) and Absolute Claudiaction Distance (ACD) as well as ankle-brachial index at rest (ABI-r) and post-exercise (ABI-pe). All patients had stable claudication due to peripheral arterial disease (PAD) and were already under best medical treatment (BMT). To be eligible for inclusion, patients had to be between the ages of 50 and 75 years, had to have stable claudication with an absolute claudication distance >40 meters but <300 meters on a standardized treadmill stress test (3.8 km/h at a 10% grade), have a resting ABI in the affected limb <0.8 with a drop of at least 0.15 following exercise, in whom surgical intervention was not expected for at least three months. Fourteen patients were assigned to active IMC consisting of compressions 65 mm Hg in amplitude, applied for three 3-second compressions/minute, two hours/day for three months. Sixteen control patients continued with BMT alone.
One month after treatment, ICD increased by 66% (P = .001), ACD increased by 51.75% (P = .005), and ABI-pe increased by 42% (P = .01). Treatment effects were maintained or further improved after three months. ABI-r did not increase at any time. Compliance exceeded 80%. Three months following cessation of therapy, claudication distances and ABI-pe did not decrease significantly.
We concluded that the use of IMC of the calf for three months increased claudication distances and led to objective improvements in ABI-pe. Intermittent mechanical compression may be a useful approach to patients with continued claudication despite standard medical treatment.
本研究旨在测试一种新型便携式机械压缩装置治疗跛行的可行性。该设备对小腿施加间歇性非气动机械压缩(IMC)。研究假设它可为患者提供一种低成本、方便的选择,并实现良好的依从性和改善临床结局。
本研究共纳入 30 例患者,采用随机对照单盲研究设计。14 例患者被分配至主动 IMC 组,16 例对照组患者继续接受单纯药物治疗。在基线、1 个月、3 个月和 6 个月时记录结局。本研究通过初始跛行距离(ICD)和绝对跛行距离(ACD)评估运动耐量的变化,同时检测静息踝肱指数(ABI-r)和运动后踝肱指数(ABI-pe)。所有患者均因外周动脉疾病(PAD)而出现稳定型跛行,且已接受最佳药物治疗(BMT)。为符合纳入标准,患者年龄需在 50 至 75 岁之间,静息状态下的下肢 ABI<0.8,且下肢运动后 ABI 下降至少 0.15,在接受标准跑步机压力测试时(3.8km/h,坡度 10%),跛行距离>40 米但<300 米,预计在至少 3 个月内无需进行手术干预。14 例患者被分配至主动 IMC 组,采用振幅为 65mmHg 的压缩装置,以每分钟 3 次、每次 3 秒的频率进行压缩,每天 2 小时,持续 3 个月。16 例对照组患者继续接受单纯 BMT。
治疗 1 个月后,ICD 增加了 66%(P=0.001),ACD 增加了 51.75%(P=0.005),ABI-pe 增加了 42%(P=0.01)。治疗 3 个月后,治疗效果得以维持或进一步改善。ABI-r 在任何时间点均未增加。依从性超过 80%。停止治疗 3 个月后,跛行距离和 ABI-pe 无明显下降。
本研究结果表明,小腿 IMC 治疗 3 个月可增加跛行距离,并使 ABI-pe 得到客观改善。间歇性机械压缩可能是一种对持续跛行但已接受标准药物治疗的患者有益的治疗方法。