运动神经元疾病的非运动症状:发病率、评估和影响

Emily Beswick, Deborah Forbes, Kay Johnson, J. Newton, Rachel Dakin, Stella Glasmcher, Sharon Abrahams, Alan Carson, Siddharthan Chandran, S. Pal
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引用次数: 0

摘要

运动神经元疾病患者通常会出现非运动症状,这些症状可能继发于运动退行性变,或与运动退行性变不同,并且可能显著降低生活质量,尽管在临床实践中未得到充分认识和评估。这项以人群为基础的研究探讨的非运动症状包括:疼痛、疲劳、胃肠道问题、睡眠不良、情绪低落、焦虑、唾液问题、冷漠、情绪不稳定、认知不适和性功能障碍。在运动神经元疾病临床、审计、研究和评估平台(苏格兰运动神经元疾病登记处)注册的人被邀请完成一份关于非运动症状的调查问卷和一份自我报告的肌萎缩侧索硬化症功能评定量表。问卷包括一个预先定义的11个潜在的非运动症状列表,并有机会列出其他症状。120人参与了本横断面研究,问卷回复率为39% (n = 311)。99%的参与者(n = 120)经历了至少一种非运动症状,72% (n = 120)报告了五种或更多。最常报告的症状是疼痛和疲劳(分别有76%的参与者报告)。据报道,影响最大的症状是胃肠道问题(54%的参与者报告说他们“严重”),其次是疼痛和唾液问题(分别为51%)。肌萎缩性侧索硬化症功能评定量表得分越低,表明疾病进展越严重,存活时间越长(诊断时间超过8年[1]),报告的症状越多。73%的受访者对临床护理中讨论非运动症状的频率感到满意。80%的参与者表示,他们认为非运动症状的评估很重要,应作为试验结果,独立于他们对这些症状的个人经历。首选的评估方法是在家完成问卷调查。绝大多数患有运动神经元疾病的人报告非运动症状,这些症状经常同时发生。疼痛、疲劳、肠胃问题、睡眠、情绪、焦虑、唾液问题、冷漠、情绪不稳定、认知抱怨和性功能障碍都很普遍。患有运动神经元疾病、身体功能较差的人和那些存活时间较长的人更有可能报告更多的症状。在有报道的地方,这些症状是频繁的,有影响的,并且是临床护理和试验设计中运动神经元疾病患者的优先事项。
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Non-motor symptoms in motor neuron disease: prevalence, assessment and impact
People with motor neuron disease often experience non-motor symptoms that may occur secondary to, or distinct from, motor degeneration, and that may significantly reduce quality of life, despite being under-recognised and evaluated in clinical practice. Non-motor symptoms explored in this population based study include: pain, fatigue, gastrointestinal issues, poor sleep, low mood, anxiety, problematic saliva, apathy, emotional lability, cognitive complaints and sexual dysfunction. People registered on the Clinical, Audit, Research and Evaluation of motor neuron disease platform, the Scottish motor neuron disease register, were invited to complete a questionnaire on non-motor symptoms and a self-reported Amyotrophic Lateral Sclerosis Functional Rating Scale. The questionnaire comprised a pre-defined list of 11 potential non-motor symptoms, with the opportunity to list additional symptoms. 120 individuals participated in this cross-sectional study, a 39% response rate of those sent questionnaires (n = 311). 99% of participants recruited (n = 120) experienced at least one non-motor symptom, with 72% (n = 120) reporting five or more. The symptoms most often reported were pain and fatigue (reported by 76% of participants respectively). The symptoms reported to be most impactful were gastrointestinal issues (reported as ‘severe’ by 54% of participants who experienced them), followed by pain and problematic saliva (51% respectively). Lower Amyotrophic Lateral Sclerosis Functional Rating Scale scores, indicating more advanced disease, and being a long survivor (diagnosed over 8 years ago [1]) were significantly associated with reporting more symptoms. 73% of respondents were satisfied with the frequency that non-motor symptoms were discussed in clinical care. 80% of participants indicated they believe evaluation of non-motor symptom is important to include as outcomes in trials, independent of their personal experience of these symptoms. The preferred method of assessment was completing questionnaires, at home. The overwhelming majority of people with motor neuron disease report non-motor symptoms and these frequently co-occur. Pain, fatigue, gastrointestinal issues, sleep, mood, anxiety, problematic saliva, apathy, emotional lability, cognitive complaints and sexual dysfunction are prevalent. People with motor neuron disease who had worse physical function and those who were long survivors were more likely to report more symptoms. Where reported, these symptoms are frequent, impactful and a priority for people with motor neuron disease in clinical care and trial design.
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