Faculty of Health and Wellbeing, Sheffield Hallam University, Sheffield, UK.
Disabil Rehabil. 2013 Jul;35(15):1284-92. doi: 10.3109/09638288.2012.726691. Epub 2013 Feb 4.
Multiple sclerosis (MS) is the most common disabling neurological condition affecting young adults. One third of people on an American registry of people with MS (PWMS) reported having activities affected by spasticity. The psychosocial effects of spasticity in people with MS have been shown to be distressing and detrimental to emotional and social relationships when investigated from a psychology perspective. This paper investigates the impact of spasticity on the lives of people living with MS from a physiotherapeutic perspective.
This study involved 12 semi-structured interviews with individuals experiencing MS-related spasticity. Ten sets of data were analyzed following framework analysis principles.
Results suggest spasticity effects life experience of these PWMS in diverse and complex ways. Physical, psychological and social consequences of spasticity are closely linked and can be far reaching.
Therapists need to be aware of links between specific physical symptoms and their psychosocial consequences if they want to improve peoples' quality of life. This paper provides in depth qualitative research evidence for the complexity of the spasticity experience for each individual, strengthening the argument for a patient-centred approach to treatment. These results also support the case for targeted interventions with effectiveness recorded in a patient-centred way.
• Spasticity is suggested here to affect the lives of individuals with multiple sclerosis in diverse and far reaching ways. Therapists need to investigate this fully in subjective assessment to impact on people's quality of life. • Direct links were identified between treatable physical symptoms and far reaching consequences of spasticity. • Knowledge about the complexity of the spasticity experience for each individual will allow therapists to target interventions appropriately and accurately record effectiveness in a patient-centred way.
多发性硬化症(MS)是影响年轻人的最常见的使人丧失能力的神经疾病。在美国 MS 患者登记处(PWMS)的三分之一的人报告说他们的活动受到痉挛的影响。从心理学角度研究 MS 患者痉挛的心理社会影响表明,当涉及到情绪和社会关系时,这种影响是令人痛苦和有害的。本文从物理治疗的角度调查痉挛对 MS 患者生活的影响。
本研究涉及对 12 名患有 MS 相关痉挛的个体进行了半结构式访谈。根据框架分析原则,分析了十组数据。
结果表明,痉挛以不同和复杂的方式影响这些 PWMS 的生活体验。痉挛的身体、心理和社会后果密切相关,可能影响深远。
如果治疗师希望提高人们的生活质量,他们需要意识到特定的身体症状与他们的心理社会后果之间的联系。本文提供了深入的定性研究证据,证明了每个个体痉挛体验的复杂性,为以患者为中心的治疗方法提供了强有力的论据。这些结果也支持以患者为中心的方式记录有效性的针对性干预措施。
这里建议痉挛以不同和深远的方式影响多发性硬化症患者的生活。治疗师需要在主观评估中充分调查这一点,以影响人们的生活质量。
直接联系被确定为可治疗的身体症状和痉挛的深远后果之间的联系。
了解每个个体痉挛体验的复杂性将使治疗师能够适当地针对干预措施,并以患者为中心的方式准确记录有效性。