Understanding North Star Ambulatory Assessment total scores and their implications for standards of care using observational data

IF 2.3 3区 医学 Q3 CLINICAL NEUROLOGY
Georgia Stimpson , Meredith K. James , Michela Guglieri , Amy Wolfe , Adnan Manzur , Anna Sarkozy , Giovanni Baranello , Francesco Muntoni , Anna Mayhew , UK NorthStar Clinical Network
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引用次数: 0

Abstract

NorthStar Ambulatory Assessment (NSAA) total score (TS) is an ordinal scale to evaluate disease progression and treatment response in ambulatory Duchenne Muscular Dystrophy individuals. Clinical management according to standard of care could be enhanced by understanding how changes in the TS could inform standards of care. Here we describe the associated item performance patterns in the NorthStar Database for ranges of NSAA TS and its timed tests (10 m walk/run and rise from floor). We then compare these patterns depending on whether a participant is on an improving/stable (≤2-point loss in the prior year) or declining (>2-point loss in the prior year) trend. These TS and trends are subsequently linked and referenced to therapy standards of care. We included 761 participants from the UK NorthStar observational clinical database between 5 and 16 years, who were on steroids. Differences and trends in item ability, compensations, and times can suggest specific disease complications and lead towards anticipatory therapy recommendations. Families and therapists can benefit from using the TS and trend to guide therapy management.
利用观察数据了解北辰门诊评估总分及其对护理标准的影响
北星非卧床评估(NSAA)总分(TS)是一种序数量表,用于评估非卧床杜兴氏肌肉萎缩症患者的疾病进展和治疗反应。通过了解TS的变化如何为护理标准提供依据,可以加强根据护理标准进行的临床管理。在此,我们描述了 NorthStar 数据库中 NSAA TS 及其计时测试(10 米步行/跑步和起立)范围的相关项目表现模式。然后,我们将根据参与者是处于改善/稳定(前一年减分≤2 分)趋势还是下降(前一年减分 2 分)趋势来比较这些模式。这些 TS 和趋势随后会与治疗护理标准相联系和参照。我们从英国 NorthStar 观察性临床数据库中纳入了 761 名年龄在 5 到 16 岁之间、服用类固醇的参与者。项目能力、代偿和时间方面的差异和趋势可以提示特定的疾病并发症,从而提出预见性治疗建议。使用TS和趋势来指导治疗管理,可使家庭和治疗师受益匪浅。
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来源期刊
CiteScore
6.30
自引率
3.20%
发文量
115
审稿时长
81 days
期刊介绍: The European Journal of Paediatric Neurology is the Official Journal of the European Paediatric Neurology Society, successor to the long-established European Federation of Child Neurology Societies. Under the guidance of a prestigious International editorial board, this multi-disciplinary journal publishes exciting clinical and experimental research in this rapidly expanding field. High quality papers written by leading experts encompass all the major diseases including epilepsy, movement disorders, neuromuscular disorders, neurodegenerative disorders and intellectual disability. Other exciting highlights include articles on brain imaging and neonatal neurology, and the publication of regularly updated tables relating to the main groups of disorders.
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