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间歇性跛行的运动疗法

Exercise for intermittent claudication.

作者信息

Lane Risha, Harwood Amy, Watson Lorna, Leng Gillian C

机构信息

Vascular Unit, Hull Royal Infirmary, Anlaby Road, Hull, UK, HU3 2JZ.

出版信息

Cochrane Database Syst Rev. 2017 Dec 26;12(12):CD000990. doi: 10.1002/14651858.CD000990.pub4.

Abstract

BACKGROUND

Exercise programmes are a relatively inexpensive, low-risk option compared with other, more invasive therapies for treatment of leg pain on walking (intermittent claudication (IC)). This is the fourth update of a review first published in 1998.

OBJECTIVES

Our goal was to determine whether an exercise programme was effective in alleviating symptoms and increasing walking treadmill distances and walking times in people with intermittent claudication. Secondary objectives were to determine whether exercise was effective in preventing deterioration of underlying disease, reducing cardiovascular events, and improving quality of life.

SEARCH METHODS

For this update, the Cochrane Vascular Information Specialist searched the Specialised Register (last searched 15 November 2016) and the Cochrane Central Register of Controlled Trials (CENTRAL; 2016, Issue 10) via the Cochrane Register of Studies Online, along with trials registries.

SELECTION CRITERIA

Randomised controlled trials of an exercise regimen versus control or versus medical therapy for people with IC due to peripheral arterial disease (PAD). We included any exercise programme or regimen used for treatment of IC, such as walking, skipping, and running. Inclusion of trials was not affected by duration, frequency, or intensity of the exercise programme. Outcome measures collected included treadmill walking distance (time to onset of pain or pain-free walking distance and maximum walking time or maximum walking distance), ankle brachial index (ABI), quality of life, morbidity, or amputation; if none of these was reported, we did not include the trial in this review.

DATA COLLECTION AND ANALYSIS

For this update (2017), RAL and AH selected trials and extracted data independently. We assessed study quality by using the Cochrane 'Risk of bias' tool. We analysed continuous data by determining mean differences (MDs) and 95% confidence intervals (CIs), and dichotomous data by determining risk ratios (RRs) and 95% CIs. We pooled data using a fixed-effect model unless we identified significant heterogeneity, in which case we used a random-effects model. We used the GRADE approach to assess the overall quality of evidence supporting the outcomes assessed in this review.

MAIN RESULTS

We included two new studies in this update and identified additional publications for previously included studies, bringing the total number of studies meeting the inclusion criteria to 32, and involving a total of 1835 participants with stable leg pain. The follow-up period ranged from two weeks to two years. Types of exercise varied from strength training to polestriding and upper or lower limb exercises; supervised sessions were generally held at least twice a week. Most trials used a treadmill walking test for one of the primary outcome measures. The methodological quality of included trials was moderate, mainly owing to absence of relevant information. Most trials were small and included 20 to 49 participants. Twenty-seven trials compared exercise versus usual care or placebo, and the five remaining trials compared exercise versus medication (pentoxifylline, iloprost, antiplatelet agents, and vitamin E) or pneumatic calf compression; we generally excluded people with various medical conditions or other pre-existing limitations to their exercise capacity.Meta-analysis from nine studies with 391 participants showed overall improvement in pain-free walking distance in the exercise group compared with the no exercise group (MD 82.11 m, 95% CI 71.73 to 92.48, P < 0.00001, high-quality evidence). Data also showed benefit from exercise in improved maximum walking distance (MD 120.36 m, 95% CI 50.79 to 189.92, P < 0.0007, high-quality evidence), as revealed by pooling data from 10 studies with 500 participants. Improvements were seen for up to two years.Exercise did not improve the ABI (MD 0.04, 95% CI 0.00 to 0.08, 13 trials, 570 participants, moderate-quality evidence). Limited data were available for the outcomes of mortality and amputation; trials provided no evidence of an effect of exercise, when compared with placebo or usual care, on mortality (RR 0.92, 95% CI 0.39 to 2.17, 5 trials, 540 participants, moderate-quality evidence) or amputation (RR 0.20, 95% CI 0.01 to 4.15, 1 trial, 177 participants, low-quality evidence).Researchers measured quality of life using Short Form (SF)-36 at three and six months. At three months, the domains 'physical function', 'vitality', and 'role physical' improved with exercise; however this was a limited finding, as it was reported by only two trials. At six months, meta-analysis showed improvement in 'physical summary score' (MD 2.15, 95% CI 1.26 to 3.04, P = 0.02, 5 trials, 429 participants, moderate-quality evidence) and in 'mental summary score' (MD 3.76, 95% CI 2.70 to 4.82, P < 0.01, 4 trials, 343 participants, moderate-quality evidence) secondary to exercise. Two trials reported the remaining domains of the SF-36. Data showed improvements secondary to exercise in 'physical function' and 'general health'. The other domains - 'role physical', 'bodily pain', 'vitality', 'social', 'role emotional', and 'mental health' - did not show improvement at six months.Evidence was generally limited in trials comparing exercise versus antiplatelet therapy, pentoxifylline, iloprost, vitamin E, and pneumatic foot and calf compression owing to small numbers of trials and participants.Review authors used GRADE to assess the evidence presented in this review and determined that quality was moderate to high. Although results showed significant heterogeneity between trials, populations and outcomes were comparable overall, with findings relevant to the claudicant population. Results were pooled for large sample sizes - over 300 participants for most outcomes - using reproducible methods.

AUTHORS' CONCLUSIONS: High-quality evidence shows that exercise programmes provided important benefit compared with placebo or usual care in improving both pain-free and maximum walking distance in people with leg pain from IC who were considered to be fit for exercise intervention. Exercise did not improve ABI, and we found no evidence of an effect of exercise on amputation or mortality. Exercise may improve quality of life when compared with placebo or usual care. As time has progressed, the trials undertaken have begun to include exercise versus exercise or other modalities; therefore we can include fewer of the new trials in this update.

摘要

背景

与其他更具侵入性的治疗行走时腿部疼痛(间歇性跛行(IC))的疗法相比,运动方案是一种相对廉价、低风险的选择。这是首次发表于1998年的一篇综述的第四次更新。

目的

我们的目标是确定运动方案是否能有效缓解间歇性跛行患者的症状,并增加其在跑步机上的行走距离和行走时间。次要目标是确定运动是否能有效预防基础疾病的恶化、减少心血管事件并改善生活质量。

检索方法

对于本次更新,Cochrane血管信息专家通过Cochrane在线研究注册库检索了专业注册库(最后检索时间为2016年11月15日)和Cochrane对照试验中心注册库(CENTRAL;2016年第10期),以及试验注册库。

选择标准

针对因外周动脉疾病(PAD)导致间歇性跛行的患者,比较运动方案与对照或与药物治疗的随机对照试验。我们纳入了任何用于治疗间歇性跛行的运动方案或疗法,如步行、跳绳和跑步。试验的纳入不受运动方案的持续时间、频率或强度的影响。收集的结局指标包括跑步机行走距离(疼痛发作时间或无痛行走距离以及最大行走时间或最大行走距离)、踝臂指数(ABI)、生活质量、发病率或截肢情况;如果未报告这些指标中的任何一项,我们就不将该试验纳入本综述。

数据收集与分析

对于本次更新(2017年),RAL和AH独立选择试验并提取数据。我们使用Cochrane“偏倚风险”工具评估研究质量。我们通过确定平均差(MDs)和95%置信区间(CIs)来分析连续数据,通过确定风险比(RRs)和95% CIs来分析二分数据。除非我们识别出显著的异质性,否则我们使用固定效应模型汇总数据,在这种情况下我们使用随机效应模型。我们使用GRADE方法评估支持本综述中评估结局的证据的总体质量。

主要结果

在本次更新中我们纳入了两项新研究,并为先前纳入的研究确定了更多的出版物,使符合纳入标准的研究总数达到32项,共涉及1835名有稳定腿部疼痛的参与者。随访期从两周到两年不等。运动类型从力量训练到竞走以及上肢或下肢运动各不相同;监督课程通常每周至少进行两次。大多数试验使用跑步机行走试验作为主要结局指标之一。纳入试验的方法学质量中等,主要是因为缺乏相关信息。大多数试验规模较小,纳入20至49名参与者。27项试验比较了运动与常规护理或安慰剂,其余5项试验比较了运动与药物(己酮可可碱、伊洛前列素、抗血小板药物和维生素E)或小腿充气加压;我们通常排除了有各种医疗状况或其他预先存在的运动能力限制的人。对9项研究(391名参与者)的荟萃分析表明,与无运动组相比,运动组的无痛行走距离总体有所改善(MD 82.11 m,95% CI 71.73至92.48,P < 0.00001,高质量证据)。数据还显示运动对改善最大行走距离有益(MD 120.36 m,95% CI 50.79至189.92,P < 0.0007,高质量证据),这是通过汇总10项研究(500名参与者)的数据得出的。改善可持续长达两年。运动并未改善ABI(MD 0.04,95% CI 0.00至0.08,13项试验,570名参与者,中等质量证据)。关于死亡率和截肢结局的数据有限;与安慰剂或常规护理相比,试验未提供运动对死亡率(RR 0.92,95% CI 0.39至2.17,5项试验,540名参与者,中等质量证据)或截肢(RR 0.20,95% CI 0.01至4.15,1项试验,177名参与者,低质量证据)有影响的证据。研究人员在三个月和六个月时使用简短健康调查问卷(SF - 36)测量生活质量。在三个月时,“身体功能”、“活力”和“角色身体”领域因运动而有所改善;然而,这是一个有限的发现,因为只有两项试验报告了这一点。在六个月时,荟萃分析显示运动后“身体总结评分”有所改善(MD 2.15,95% CI 1.26至3.04,P = 0.02,5项试验,429名参与者,中等质量证据)以及“精神总结评分”有所改善(MD 3.76,95% CI 2.70至4.82,P < 0.01,4项试验,343名参与者,中等质量证据)。两项试验报告了SF - 36的其余领域。数据显示运动后“身体功能”和“总体健康”有所改善。其他领域——“角色身体”、“身体疼痛”、“活力”、“社会功能”、“角色情感”和“心理健康”——在六个月时未显示出改善。在比较运动与抗血小板治疗、己酮可可碱、伊洛前列素、维生素E以及足部和小腿充气加压的试验中,由于试验和参与者数量较少,证据通常有限。综述作者使用GRADE评估本综述中呈现的证据,并确定质量为中等至高。尽管结果显示试验之间存在显著异质性,但总体而言人群和结局具有可比性,研究结果与跛行患者群体相关。对于大多数结局,样本量超过300名参与者时,使用可重复方法汇总数据。

作者结论

高质量证据表明,与安慰剂或常规护理相比,运动方案在改善适合运动干预的间歇性跛行腿部疼痛患者的无痛和最大行走距离方面提供了重要益处。运动并未改善ABI,并且我们未发现运动对截肢或死亡率有影响的证据。与安慰剂或常规护理相比,运动可能会改善生活质量。随着时间的推移,所进行的试验开始纳入运动与运动或其他方式的比较;因此在本次更新中我们能够纳入的新试验较少。

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