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首页> 外文期刊>Journal of child neurology >Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): case definition in surveillance for childhood-onset Duchenne/Becker muscular dystrophy.
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Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): case definition in surveillance for childhood-onset Duchenne/Becker muscular dystrophy.

机译:肌营养不良监测跟踪和研究网络(MD Starnet):儿童诊断监测的案例定义Duchenne / Becker肌肉营养不良。

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摘要

The Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet) is a multisite collaboration to determine the prevalence of childhood-onset Duchenne/Becker muscular dystrophy and to characterize health care and health outcomes in this population. MD STARnet uses medical record abstraction to identify patients with Duchenne/Becker muscular dystrophy born January 1, 1982 or later who resided in 1 of the participating sites. Critical diagnostic elements of each abstracted record are reviewed independently by >4 clinicians and assigned to 1 of 6 case definition categories (definite, probable, possible, asymptomatic, female, not Duchenne/Becker muscular dystrophy) by consensus. As of November 2009, 815 potential cases were reviewed. Of the cases included in analysis, 674 (82%) were either ''definite'' or ''probable'' Duchenne/Becker muscular dystrophy. These data reflect a change in diagnostic testing, as case assignment based on genetic testing increased from 67% in the oldest cohort (born 1982-1987) to 94% in the cohort born 2004 to 2009.
机译:肌营养不良监测跟踪和研究网络(MD Starnet)是多路关的合作,以确定儿童发病患者患者患有肌肉营养不良营养不良的患病率,并在这群人群中表征医疗保健和健康结果。 MD Starnet使用医疗记录抽象来识别1982年1月1日出生的Duchenne / Becker肌营养不良患者,或者在参加场所的1位。每个抽象记录的关键诊断要素由> 4个临床医生独立审查,并分配给6个案例定义类别中的1个(明确,可能的,可能,无症状,女性,而不是Duchenne / Becker肌营养不良营养不良)。截至2009年11月,审查了815个潜在案件。在分析中包含的病例,674名(82%)是“明确”的“或”可能“的”杜氏/ Becker肌肉营养不良症。这些数据反映了诊断测试的变化,因为基于遗传检测的案例分配在最旧的队列(1982-1987)中的67%增加到2004年至2009年的队列中的94%。

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