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一项为期10周的吸气肌训练计划对多发性硬化症患者下肢活动能力的影响:一项随机对照试验。

Effects of a 10-week inspiratory muscle training program on lower-extremity mobility in people with multiple sclerosis: a randomized controlled trial.

作者信息

Pfalzer Lucinda, Fry Donna

机构信息

Physical Therapy Department, School of Health Professions and Studies, University of Michigan-Flint, Flint, MI, USA.

出版信息

Int J MS Care. 2011 Spring;13(1):32-42. doi: 10.7224/1537-2073-13.1.32.

Abstract

Pulmonary muscle weakness is common in ambulatory people with multiple sclerosis (MS) and may lead to deficits in mobility function. The purpose of this study was to examine the effect of a 10-week home-based exercise program using an inspiratory muscle threshold trainer (IMT) on the results of four lower-extremity physical performance tests in people with MS. The study design was a two-group (experimental-control), pretest-posttest study. Outcome measures consisted of pulmonary function measures including maximal inspiratory pressure (MIP), maximal expiratory pressure (MEP), and maximal voluntary ventilation (MVV), and the following lower-extremity physical performance measures: the 6-Minute Walk (6MW) distance, gait velocity (GV), the Sit-to-Stand Test (SST), the Functional Stair Test (FST), and a balance test (BAL). A total of 46 ambulatory participants (Expanded Disability Status Scale [EDSS] score, 2.0-6.5) with MS were randomly assigned to an intervention group (mean EDSS score, 4.1) that received 10 weeks of home-based inspiratory muscle training or a nontreatment control group (mean EDSS score, 3.2). Of the original 46 participants, 20 intervention group participants and 19 control group participants completed the study. Compared with the control group, the intervention group made significantly greater gains in inspiratory muscle strength (P = .003) and timed balance scores (P = .008). A nonsignificant improvement in 6MW distance (P = .086) was also noted in the IMT-trained group as compared with the control group. This is the first study directly linking improvement in respiratory function to improvement in physical performance function in people with mild-to-moderate disability due to MS.

摘要

肺部肌肉无力在多发性硬化症(MS)的非卧床患者中很常见,可能导致运动功能障碍。本研究的目的是探讨使用吸气肌阈值训练器(IMT)进行为期10周的家庭锻炼计划对MS患者四项下肢身体性能测试结果的影响。研究设计为两组(实验组-对照组)、前后测研究。结果测量包括肺功能测量,包括最大吸气压力(MIP)、最大呼气压力(MEP)和最大自主通气量(MVV),以及以下下肢身体性能测量:6分钟步行(6MW)距离、步态速度(GV)、坐立试验(SST)、功能性楼梯试验(FST)和平衡试验(BAL)。共有46名非卧床MS患者(扩展残疾状态量表[EDSS]评分,2.0 - 6.5)被随机分配到干预组(平均EDSS评分,4.1),接受为期10周的家庭吸气肌训练,或非治疗对照组(平均EDSS评分,3.2)。在最初的46名参与者中,20名干预组参与者和19名对照组参与者完成了研究。与对照组相比,干预组在吸气肌力量(P = .003)和定时平衡评分(P = .008)方面有显著更大的提高。与对照组相比,IMT训练组在6MW距离上也有非显著的改善(P = .086)。这是第一项直接将呼吸功能改善与MS所致轻度至中度残疾患者身体性能功能改善联系起来的研究。

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