School of Medicine, University of Galway, Galway, Ireland.
National Institute for Prevention and Cardiovascular Health, Croí Heart and Stroke Centre, Newcastle, Galway, Ireland.
Cochrane Database Syst Rev. 2024 Feb 14;2(2):CD014717. doi: 10.1002/14651858.CD014717.pub2.
Peripheral arterial disease (PAD) is the obstruction or narrowing of the large arteries of the lower limbs, which can result in impaired oxygen supply to the muscle and other tissues during exercise, or even at rest in more severe cases. PAD is classified into five categories (Fontaine classification). It may be asymptomatic or various levels of claudication pain may be present; at a later stage, there may be ulceration or gangrene of the limb, with amputation occasionally being required. About 20% of people with PAD suffer from intermittent claudication (IC), which is muscular discomfort in the lower extremities induced by exertion and relieved by rest within 10 minutes; IC causes restriction of movement in daily life. Treatment for people with IC involves addressing lifestyle risk factors. Exercise is an important part of treatment, but supervised exercise programmes for individuals with IC have low engagement levels and high attrition rates. The use of mobile technologies has been suggested as a new way to engage people with IC in walking exercise interventions. The novelty of the intervention, low cost for the user, automation, and ease of access are some of the advantages mobile health (mhealth) technologies provide that give them the potential to be effective in boosting physical activity in adults.
To assess the benefits and harms of mobile health (mhealth) technologies to improve walking distance in people with intermittent claudication.
The Cochrane Vascular Information Specialist conducted systematic searches of the Cochrane Vascular Specialised Register, the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, Embase, and CINAHL, and also searched the World Health Organization International Clinical Trials Registry Platform (WHO ICTRP) and ClinicalTrials.gov. The most recent searches were carried out on 19 December 2022.
We included randomised controlled trials (RCTs) in people aged 18 years or over with symptomatic PAD and a clinical diagnosis of IC. We included RCTs comparing mhealth interventions to improve walking distance versus usual care (no intervention or non-exercise advice), exercise advice, or supervised exercise programmes. We excluded people with chronic limb-threatening ischaemia (Fontaine III and IV).
We used standard Cochrane methods. Our primary outcomes were change in absolute walking distance from baseline, change in claudication distance from baseline, amputation-free survival, revascularisation-free survival. Our secondary outcomes were major adverse cardiovascular events, major adverse limb events, above-ankle amputation, quality of life, and adverse events. We used GRADE to assess the certainty of the evidence.
We included four RCTs involving a total of 614 participants with a clinical diagnosis of IC. The duration of intervention of the four included RCTs ranged from 3 to 12 months. Participants were randomised to either mhealth or control (usual care or supervised exercise programme). All four studies had an unclear or high risk of bias in one or several domains. The most prevalent risk of bias was in the area of performance bias, which was rated high risk as it is not possible to blind participants and personnel in this type of trial. Based on GRADE criteria, we downgraded the certainty of the evidence to low, due to concerns about risk of bias, imprecision, and clinical inconsistency. Comparing mhealth with usual care, there was no clear evidence of an effect on absolute walking distance (mean difference 9.99 metres, 95% confidence interval (CI) -27.96 to 47.93; 2 studies, 503 participants; low-certainty evidence). None of the included studies reported on change in claudication walking distance, amputation-free survival, or revascularisation-free survival. Only one study reported on major adverse cardiovascular events (MACE) and found no clear difference between groups (risk ratio 1.37, 95% CI 0.07 to 28.17; 1 study, 305 participants; low-certainty evidence). None of the included studies reported on major adverse limb events (MALE) or above-ankle amputations.
AUTHORS' CONCLUSIONS: Mobile health technologies can be used to provide lifestyle interventions for people with chronic conditions, such as IC. We identified a limited number of studies that met our inclusion criteria. We found no clear difference between mhealth and usual care in improving absolute walking distance in people with IC; however, we judged the evidence to be low certainty. Larger, well-designed RCTs are needed to provide adequate statistical power to reliably evaluate the effects of mhealth technologies on walking distance in people with IC.
外周动脉疾病(PAD)是下肢大血管的阻塞或狭窄,可导致运动时肌肉和其他组织供氧不足,甚至在更严重的情况下在休息时也会出现这种情况。PAD 分为五类(Fontaine 分类)。它可能无症状,也可能存在不同程度的跛行疼痛;在后期,可能会出现肢体溃疡或坏疽,偶尔需要截肢。约 20%的 PAD 患者患有间歇性跛行(IC),即下肢肌肉不适,在 10 分钟内通过休息得到缓解;IC 限制了日常生活中的活动。针对 IC 患者的治疗包括解决生活方式风险因素。运动是治疗的重要组成部分,但针对 IC 患者的监督运动计划参与度低,退出率高。有人提出使用移动技术是让 IC 患者参与步行运动干预的一种新方法。移动健康(mhealth)技术的新颖性、对用户的低成本、自动化和易于访问是它们具有提高成年人身体活动潜力的一些优势。
评估移动健康(mhealth)技术在改善间歇性跛行患者步行距离方面的益处和危害。
Cochrane 血管信息专家对 Cochrane 血管专科注册库、Cochrane 中心对照试验注册库(CENTRAL)、MEDLINE、Embase 和 CINAHL 进行了系统检索,还对世界卫生组织国际临床试验注册平台(WHO ICTRP)和 ClinicalTrials.gov 进行了检索。最近一次检索是在 2022 年 12 月 19 日进行的。
我们纳入了年龄在 18 岁及以上、有症状 PAD 和临床诊断为 IC 的随机对照试验(RCT)。我们纳入了 RCT,比较 mhealth 干预措施与改善步行距离与常规护理(无干预或非运动建议)、运动建议或监督运动计划的效果。我们排除了慢性肢体威胁性缺血(Fontaine III 和 IV)的患者。
我们使用了标准的 Cochrane 方法。我们的主要结局是从基线到绝对步行距离的变化,从基线到跛行距离的变化,无截肢生存率,无血运重建生存率。我们的次要结局是主要不良心血管事件、主要不良肢体事件、踝上截肢、生活质量和不良事件。我们使用 GRADE 来评估证据的确定性。
我们纳入了四项 RCT,共涉及 614 名有 IC 临床诊断的患者。四项纳入 RCT 的干预持续时间从 3 个月到 12 个月不等。参与者被随机分配到 mhealth 或对照组(常规护理或监督运动计划)。四项研究都存在一个或多个领域的高偏倚风险。最常见的偏倚风险是在实施偏倚领域,由于在这种类型的试验中无法对参与者和人员进行盲法,因此被评为高风险。根据 GRADE 标准,由于对偏倚、不精确性和临床不一致性的担忧,我们将证据的确定性降低到低水平。基于 GRADE 标准,我们将证据的确定性降低至低水平,因为存在偏倚、不精确性和临床异质性的担忧。将 mhealth 与常规护理相比,绝对步行距离没有明显的改善效果(平均差异 9.99 米,95%置信区间(CI)-27.96 至 47.93;2 项研究,503 名参与者;低质量证据)。没有纳入的研究报告跛行距离、无截肢生存率或无血运重建生存率的变化。只有一项研究报告了主要不良心血管事件(MACE),发现两组之间没有明显差异(风险比 1.37,95%CI 0.07 至 28.17;1 项研究,305 名参与者;低质量证据)。纳入的研究均未报告主要不良肢体事件(MALE)或踝上截肢。
移动健康技术可用于为慢性疾病患者,如 IC,提供生活方式干预。我们发现符合纳入标准的研究数量有限。我们发现 mhealth 与常规护理在改善 IC 患者的绝对步行距离方面没有明显差异;然而,我们认为证据的确定性较低。需要更大、设计良好的 RCT 来提供足够的统计效力,以可靠地评估 mhealth 技术对 IC 患者步行距离的影响。