在治疗艾勒斯-丹洛斯综合征活动过度症中的 "海马疗法"。

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Hélène Viruega, Célia Loriette, Melissa Quignon, Manuel Gaviria
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引用次数: 0

摘要

活动过度埃勒斯-丹洛斯综合征(EDS)是一种遗传性疾病,主要表现为关节活动过度、不稳定、慢性疼痛和疲劳,严重影响生活质量和自主能力。治疗重点仅在于缓解症状。一位患有活动过度 EDS 的青春期晚期患者在经历了功能能力的迅速衰退后,接受了嬉马疗法康复治疗(30 小时)。她的疲劳、慢性疼痛得到了显著改善,并恢复了行走能力。髋关节疗法在改善她的姿势平衡、运动技能、本体感觉、肌肉功能和耐力方面发挥了至关重要的作用。它还通过刺激感官输入激活神经通路,缓解疼痛和疲劳,对她的认知和情绪调节产生了积极影响。值得注意的是,患者从依赖轮椅过渡到拄着拐杖行走,然后大大提高了步态质量和速度。这些研究结果表明,嬉马疗法对活动过度 EDS 的康复具有重要意义,它减少了对药物干预的需求,并培养了一种积极应对未来挑战的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hippotherapy in the management of hypermobile Ehlers-Danlos syndrome.

Hypermobile Ehlers-Danlos syndrome (EDS) is an inherited condition marked by joint hypermobility, instability, chronic pain and fatigue, significantly impacting quality of life and autonomy. Management focuses solely on symptom alleviation. After experiencing a rapid decline in functional abilities, a patient in late adolescence with hypermobile EDS underwent hippotherapy rehabilitation (30 hours). She saw substantial improvements in fatigue, chronic pain and regained walking abilities. Hippotherapy played a crucial role in refining her postural balance, motor skills, proprioception, muscle function and endurance. It also positively affected her cognitive and emotional regulation by stimulating sensory inputs that activate neural pathways, providing relief from pain and fatigue. Notably, the patient transitioned from wheelchair reliance to walking with crutches, and then greatly enhanced both gait quality and speed. These findings demonstrate the relevance of hippotherapy for the rehabilitation of hypermobile EDS, reducing the need for pharmacological interventions and fostering a proactive approach to future challenges.

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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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