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The Use of the MyoDK for Mechanical Pressure in the Treatment of Chronic Lateral Epicondylalgia: A Pilot Study

机译:MyoDK在机械压力治疗慢性外侧上con痛中的应用:一项初步研究。

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Introduction: Chronic Lateral Epicondylalgia (CLE) is potentially associated with a significant reduction of the patient?s quality of life; its treatment by manual Deep Transverse Friction (DTF), although widely accepted, lacks standardization. The purpose of our study was to evaluate the efficacy of the MyoDK device, which allows deep transverse pressure (DTP) monitoring, for treatment of CLE. Materials and Methods: This is a single centre observational study for treatment of CLE by the MyoDK device. In a given year, all patients who appeared at our institution with a diagnostic of CLE were screened for possible inclusion. Exclusion criteria were: confounding factors on pain and function of the upper limb, cognitive impairment, inability or unwilling to give informed consent or to comply with treatment protocol. Our primary outcome measure was the pain reduction measured by the VAS pain scale (VAS) at 6 weeks. Our intervention consisted in applying a pressure from 0.5 to 10kg/100mm2 for 20 minutes, once a week for 6 weeks, using the MyoDK device. Results: Thirty patients were screened. Two were excluded for incomplete protocol, remaining 28 for analysis. Mean age was 47.3, 23 were male (82.1%), 24 were affected on their dominant side (85.7%). We had a significant reduction in VAS pain score at 12 weeks (80.8 vs 13.0; p<0.01). There were no side effects reported. Conclusion: Our study showed the safety of the use of a standard protocol using the MyoDK device for treatment of CLE. We believe that further controlled studies will establish the MyoDK as a reliable option for treatment of CLE.
机译:简介:慢性外侧上con痛(CLE)可能与患者生活质量的显着降低有关。它的手动深部横向摩擦(DTF)处理虽然被广泛接受,但缺乏标准化。我们研究的目的是评估MyoDK装置的功效,该装置允许深度横向压力(DTP)监测,用于治疗CLE。材料和方法:这是一项用MyoDK装置治疗CLE的单中心观察性研究。在给定的一年中,对所有出现在我们机构并诊断为CLE的患者进行了筛查,以寻找可能的纳入对象。排除标准为:上肢疼痛和功能,认知障碍,不能或不愿给予知情同意或不遵守治疗方案的混杂因素。我们的主要结局指标是6周时通过VAS疼痛量表(VAS)衡量的疼痛减轻情况。我们的干预措施包括使用MyoDK设备对0.5到10kg / 100mm2的压力施加20分钟,每周一次,持续6周。结果:筛选了30例患者。不完整的方案排除了两个,其余28个用于分析。平均年龄为47.3岁,其中23例为男性(82.1%),24例患侧为显性一侧(85.7%)。在12周时,VAS疼痛评分显着降低(80.8比13.0; p <0.01)。没有副作用的报道。结论:我们的研究表明,使用MyoDK装置治疗CLE的标准方案的安全性。我们相信,进一步的对照研究将使MyoDK成为治疗CLE的可靠选择。

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