施罗斯运动对特发性脊柱侧凸青少年生活质量和肌肉耐力的影响——一项评估和统计学家盲法随机对照试验:“2015年SOSORT奖得主”。

Scoliosis Pub Date : 2015-09-18 eCollection Date: 2015-01-01 DOI:10.1186/s13013-015-0048-5
Sanja Schreiber, Eric C Parent, Elham Khodayari Moez, Douglas M Hedden, Doug Hill, Marc J Moreau, Edmond Lou, Elise M Watkins, Sarah C Southon
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引用次数: 113

摘要

背景:在北美,青少年小特发性脊柱侧凸(AIS)的护理建议包括观察或支具。在非对照研究中,Schroth脊柱侧凸特异性锻炼在各种结果上显示出有希望的结果。本随机对照试验(RCT)旨在确定与单独标准护理相比,Schroth运动联合标准护理对AIS患者生活质量(QOL)结局和背部肌肉耐力(BME)的影响。材料和方法:50例AIS患者,年龄10-18岁,曲度10-45°,从一个脊柱侧凸诊所招募,随机接受标准治疗或监督Schroth运动加标准治疗6个月。施罗斯练习在前两周分五次进行。每天的家庭计划在每周的监督会议中进行调整。评估员和统计学家被蒙蔽了双眼。结果包括Biering-Sorensen (BME)测试、脊柱侧凸研究协会(SRS-22r)和脊柱外观问卷(SAQ)评分。分析意向治疗(ITT)和每个方案(PP)线性混合效应模型。因为ITT和PP分析得出了相似的结果,所以只有ITT被报道。结果:3个月后,Schroth组BME改善32.3 s,对照组改善4.8 s。两组间27.5 s的差异具有统计学意义(95% CI 1.1至53.8 s, p = 0.04)。3 ~ 6个月,施罗斯组自我形象改善0.13,对照组自我形象恶化0.17 (0.3,95% CI 0.01 ~ 0.59, p = 0.049)。从3个月到6个月,观察到SRS-22r疼痛评分变化的组间差异(85.3,95% CI 8.1至162.5,p = 0.03),其中(SRS-22疼痛评分)(4)在Schroth组增加65.3,在对照组减少20.0。协变量:年龄、自我效能、牙套佩戴、Schroth分类、身高对部分结果有显著主影响。基线上限效应高:SRS-22r(疼痛= 18.4%,功能= 28.6%)和SAQ(突出= 26.5%,腰部= 29.2%,胸部= 46.9%,躯干移位= 12.2%,肩部= 18.4%)。结论:有监督的Schroth练习通过改善SRS-22r疼痛、自我形象评分和BME,为标准护理提供了额外的好处。考虑到SRS-22r和SAQ问卷域的天花板效应的高流行率,我们假设在接受保守治疗的AIS人群中,需要不同的QOL问卷,具有足够的反应性。试验注册:脊柱侧凸Schroth运动试验NCT01610908。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of Schroth exercises added to the standard of care on the quality of life and muscle endurance in adolescents with idiopathic scoliosis-an assessor and statistician blinded randomized controlled trial: "SOSORT 2015 Award Winner".

Background: In North America, care recommendations for adolescents with small idiopathic scoliosis (AIS) curves include observation or bracing. Schroth scoliosis-specific exercises have demonstrated promising results on various outcomes in uncontrolled studies. This randomized controlled trial (RCT) aimed to determine the effect of Schroth exercises combined with the standard of care on quality-of-life (QOL) outcomes and back muscle endurance (BME) compared to standard of care alone in patients with AIS.

Material and methods: Fifty patients with AIS, aged 10-18 years, with curves 10-45 °, recruited from a scoliosis clinic were randomized to receive standard of care or supervised Schroth exercises plus standard of care for 6 months. Schroth exercises were taught over five sessions in the first two weeks. A daily home program was adjusted during weekly supervised sessions. The assessor and the statistician were blinded. Outcomes included the Biering-Sorensen (BME) test, Scoliosis Research Society (SRS-22r) and Spinal Appearance Questionnaires (SAQ) scores. Intention-to-treat (ITT) and per protocol (PP) linear mixed effects models were analyzed. Because ITT and PP analyses produced similar results, only ITT is reported.

Results: After 3 months, BME in the Schroth group improved by 32.3 s, and in the control by 4.8 s. This 27.5 s difference in change between groups was statically significant (95 % CI 1.1 to 53.8 s, p = 0.04). From 3 to 6 months, the self-image improved in the Schroth group by 0.13 and deteriorated in the control by 0.17 (0.3, 95 % CI 0.01 to 0.59, p = 0.049). A difference between groups for the change in the SRS-22r pain score transformed to its power of four was observed from 3 to 6 months (85.3, 95 % CI 8.1 to 162.5, p = 0.03), where (SRS-22 pain score)(4) increased by 65.3 in the Schroth and decreased by 20.0 in the control group. Covariates: age, self-efficacy, brace-wear, Schroth classification, and height had significant main effects on some outcomes. Baseline ceiling effects were high: SRS-22r (pain = 18.4 %, function = 28.6 %), and SAQ (prominence = 26.5 %, waist = 29.2 %, chest = 46.9 %, trunk shift = 12.2 % and shoulders = 18.4 %).

Conclusions: Supervised Schroth exercises provided added benefit to the standard of care by improving SRS-22r pain, self-image scores and BME. Given the high prevalence of ceiling effects on SRS-22r and SAQ questionnaires' domains, we hypothesize that in the AIS population receiving conservative treatments, different QOL questionnaires with adequate responsiveness are needed.

Trial registration: Schroth Exercise Trial for Scoliosis NCT01610908.

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