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首页> 外文期刊>European journal of heart failure: journal of the Working Group on Heart Failure of the European Society of Cardiology >High-intensity vs. sham inspiratory muscle training in patients with chronic heart failure: A prospective randomized trial
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High-intensity vs. sham inspiratory muscle training in patients with chronic heart failure: A prospective randomized trial

机译:慢性心力衰竭患者的高强度与假呼吸肌训练:一项前瞻性随机试验

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Aims: The purpose of this study was to evaluate the effectiveness, feasibility, and safety of a 4-week high-intensity inspiratory muscle training (hi-IMT) in patients with chronic heart failure (CHF). Methods and results: A double-blind randomized clinical trial was carried out in 22 patients with CHF. Participants were assigned to the hi-IMT or sham-IMT group. The trainer device was a prototype of the Orygen-Dual Valve?. The training workloads were adjusted weekly at the inspiratory pressure which allowed the performance of 10 consecutive maximal repetitions (10RM). Main outcomes were strength and endurance of the respiratory muscles assessed by maximal respiratory pressures (PImax and PEmax) and a 10RM manoeuvre, respectively. Twenty-one patients presented impairment in respiratory muscle strength and endurance. Patients in the hi-IMT group showed a significant improvement in both strength and endurance: inspiratory muscle strength in the intervention group increased 57.2% compared with 25.9% in the control group (P = 0.001). The percentage change in endurance was 72.7% for the hi-IMT group compared with 18.2% in the sham-IMT group (P 0.001). No adverse effects occurred during the intervention. Conclusion: A 4-week hi-IMT with the use of the Orygen-Dual Valve? is shown to be an effective, feasible, and safe tool to improve weakness and fatigue of the inspiratory muscles. The key point of this study is to discuss immediate practical implications in terms of respiratory muscle dysfunction postulated as a potential prognostic factor and as an additional therapeutic target.
机译:目的:本研究的目的是评估为期4周的高强度吸气肌肉训练(hi-IMT)在慢性心力衰竭(CHF)患者中的有效性,可行性和安全性。方法和结果:对22名CHF患者进行了双盲随机临床试验。参与者被分配到hi-IMT或假IMT组。该训练器设备是Orygen-Dual Valve?的原型。每周在吸气压力下调整训练工作量,以允许进行10次连续最大重复(10RM)。主要结局是分别通过最大呼吸压力(PImax和PEmax)和10RM动作评估的呼吸肌力量和耐力。 21名患者出现呼吸肌力量和耐力受损。 hi-IMT组的患者在强度和耐力上均显示出显着改善:干预组的吸气肌力量增加了57.2%,而对照组为25.9%(P = 0.001)。 hi-IMT组的耐力变化百分比为72.7%,而假IMT组为18.2%(P <0.001)。干预期间未发生不良反应。结论:使用Orygen-Dual瓣膜进行了4周的Hi-IMT?被证明是改善吸气肌无力和疲劳的有效,可行和安全的工具。这项研究的重点是讨论被认为是潜在的预后因素和其他治疗目标的呼吸肌功能障碍的即时实际意义。

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