119P Evaluation of physical function before and after medical treatment in patients with Spinal Muscular Atrophy aged 11-25 years

IF 2.7 4区 医学 Q2 CLINICAL NEUROLOGY Neuromuscular Disorders Pub Date : 2024-10-01 DOI:10.1016/j.nmd.2024.07.026
U. Werlauff , L. Busk , P. Drivsholm , B. Heiden , R. Iversen , H. Laustsen , A. Mahoney , L. Olesen , C. Handberg
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Abstract

Medical treatment for 5q spinal muscular atrophy (SMA) is now standard treatment in many countries, and a growing number of studies report on improvement or stabilization in physical function as a result of medical treatment. Different countries have different practices regarding the target group for medical treatment. Age and level of function have been decisive criteria for receiving the treatment. Until July 2023, the Danish medical council had approved initiation of medical treatment for children up to 10 years of age, and during the spring of 2023 it were to be determined whether the patient target group could be expanded. Based on this potential expansion, the aim of the study was to evaluate the current physical functioning in a national cohort of patients > 10 years and – in case treatment was approved – to repeat the evaluation six month after initiation of treatment. Due to the size of the target group (n=136) and the narrow time frame it was decided to narrow the target group to non-ambulant patients and perform the evaluation online. The evaluation included two items from the revised upper limb scale (RULM) (lift hands, pick up and hold coins), the EK2-scale (17 items), Fatigue Severity Scale (7 items), a brief questionnaire on patient expectations before treatment and an online interview about experiences after initiation of treatment. 57 patients accepted the invitation, answered the questionnaire, and were examined online during the spring of 2023. In July 2023, the Danish medical council decided to expand the target group to patients up to 25 years of age. 11/57 patients met the new criteria and accepted treatment. Follow-up examinations of these patients are ongoing. Results will be reported on the poster.
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119P 对 11-25 岁脊髓性肌肉萎缩症患者接受治疗前后的身体功能进行评估
在许多国家,5q脊髓性肌萎缩症(SMA)的药物治疗现已成为标准治疗方法,越来越多的研究报告显示,药物治疗可改善或稳定患者的身体功能。不同国家对药物治疗的目标群体有不同的做法。年龄和功能水平一直是接受治疗的决定性标准。在 2023 年 7 月之前,丹麦医学委员会一直批准对 10 岁以下的儿童进行治疗。根据这一可能的扩大,研究的目的是评估全国 10 岁以下患者目前的身体机能,并在治疗获批的情况下,在开始治疗 6 个月后再次进行评估。由于目标群体人数众多(136 人)且时间紧迫,因此决定将目标群体缩小至非行动不便的患者,并在网上进行评估。评估内容包括修订版上肢量表(RULM)中的两个项目(抬手、拾起和握住硬币)、EK2 量表(17 个项目)、疲劳严重程度量表(7 个项目)、一份关于治疗前患者期望的简短问卷,以及关于开始治疗后体验的在线访谈。57 名患者接受了邀请,回答了问卷,并于 2023 年春季接受了在线检查。2023 年 7 月,丹麦医学委员会决定将目标群体扩大到 25 岁以下的患者。有 11/57 名患者符合新标准并接受了治疗。目前正在对这些患者进行随访检查。结果将在海报上公布。
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来源期刊
Neuromuscular Disorders
Neuromuscular Disorders 医学-临床神经学
CiteScore
4.60
自引率
3.60%
发文量
543
审稿时长
53 days
期刊介绍: This international, multidisciplinary journal covers all aspects of neuromuscular disorders in childhood and adult life (including the muscular dystrophies, spinal muscular atrophies, hereditary neuropathies, congenital myopathies, myasthenias, myotonic syndromes, metabolic myopathies and inflammatory myopathies). The Editors welcome original articles from all areas of the field: • Clinical aspects, such as new clinical entities, case studies of interest, treatment, management and rehabilitation (including biomechanics, orthotic design and surgery). • Basic scientific studies of relevance to the clinical syndromes, including advances in the fields of molecular biology and genetics. • Studies of animal models relevant to the human diseases. The journal is aimed at a wide range of clinicians, pathologists, associated paramedical professionals and clinical and basic scientists with an interest in the study of neuromuscular disorders.
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