患者报告的脊髓性肌萎缩症(SMA)球部功能评估:自我报告量表的验证。

IF 3.4 4区 医学 Q2 CLINICAL NEUROLOGY
Journal of neuromuscular diseases Pub Date : 2025-05-01 Epub Date: 2025-03-20 DOI:10.1177/22143602251325741
Maureen A Lefton-Greif, Lisa Belter, Jill Jarecki, Mary Schroth, Yong Zeng, Thomas O Crawford, Cyd Eaton
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引用次数: 0

摘要

背景:脊髓功能障碍是脊髓性肌萎缩症(SMA)患者所经历的一种公认的负担。缺乏捕捉这些问题影响的度量标准。目的:开发和验证sma -球量表,该量表捕获并量化患者报告的球功能障碍经历。方法:邀请Cure SMA数据库成员完成在线调查和由作者编制的31项球囊量表,该量表参考文献中的球囊功能障碍,并咨询专门的SMA保健提供者、制药公司和受SMA影响的人。结果:166例成人SMA患者报告了一系列的球功能障碍。最常见的问题,超过80%的时间发生,是吃饭时间延长,张嘴困难,吞咽药丸。此外,10%的受访者表示,在他们的一生中,进食功能不断恶化。在各种各样的球功能中,对反应的探索性和验证性因素分析确定了球功能障碍的三个连贯维度:吞咽;用餐时间和交流;呼吸音,语言,声音和分泌物管理。结论:这种由患者报告的严重程度不同的成人的球功能量表捕获并量化了经历过的球功能损伤的各种表现。有了初步的有效性证据,该量表支持标准化准确识别球功能障碍的努力,纳入SMA患者对其日常功能关键领域的观点,为临床试验中有意义的终点提供必要的指标,为实践指南提供信息,并促进评估和开发治疗干预措施所需的监管科学的进步。确定球功能障碍的三个相关维度可以改善进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patient-reported assessment of bulbar function in spinal muscular atrophy (SMA): Validation of a self-report scale.

Background: Bulbar dysfunction is a well-recognized burden experienced by individuals with spinal muscular atrophy (SMA). Metrics that capture the impact of these problems are lacking. Objectives: To develop and validate an SMA-Bulbar Scale that captures and quantifies patient-reported experiences with bulbar dysfunction. Methods: Cure SMA database members were invited to complete online surveys and a 31-item Bulbar Scale developed by the authors with reference to both bulbar dysfunction in the literature and consultations with SMA-dedicated health care providers, pharmaceutical companies, and persons affected by SMA. Results: 166 adults with SMA reported a range of bulbar dysfunctions. The most common problems, occurring more than 80% of the time, were prolonged meal times, difficulty with mouth opening, and swallowing pills. In addition, 10% of the respondents reported a worsening feeding function over the course of their lives. Across the diverse array of bulbar functions, exploratory and confirmatory factor analyses of responses identified three coherent dimensions of bulbar dysfunction: Swallowing; Mealtimes and Communication; and Breath Sounds, Speech, Voice, and Secretion Management. Higher scores of overall bulbar dysfunction, (p < .001) and each factor (p < .001), were reported by respondents with any degree of feeding restrictions. Sex, age, or use of SMA disease-modifying treatment did not correlate with bulbar scores. Conclusions: This patient-reported scale of bulbar function in adults with a wide range of SMA severity captures and quantifies the variable manifestations of experienced bulbar impairment. With preliminary evidence of validity, the scale supports efforts to standardize accurate identification of bulbar dysfunction, incorporate the perspectives of people with SMA on key areas of their daily functioning, provide metrics essential for meaningful endpoints in clinical trials, inform practice guidelines, and promote advancement of the regulatory science needed for the evaluation and development of therapeutic interventions. Identification of three coherent dimensions of bulbar dysfunction may improve further investigations.

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来源期刊
Journal of neuromuscular diseases
Journal of neuromuscular diseases Medicine-Neurology (clinical)
CiteScore
5.10
自引率
6.10%
发文量
102
期刊介绍: The Journal of Neuromuscular Diseases aims to facilitate progress in understanding the molecular genetics/correlates, pathogenesis, pharmacology, diagnosis and treatment of acquired and genetic neuromuscular diseases (including muscular dystrophy, myasthenia gravis, spinal muscular atrophy, neuropathies, myopathies, myotonias and myositis). The journal publishes research reports, reviews, short communications, letters-to-the-editor, and will consider research that has negative findings. The journal is dedicated to providing an open forum for original research in basic science, translational and clinical research that will improve our fundamental understanding and lead to effective treatments of neuromuscular diseases.
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