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首页> 外文期刊>Molecular genetics and metabolism >Severely impaired health status at diagnosis of Pompe disease: A cross-sectional analysis to explore the potential utility of neonatal screening
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Severely impaired health status at diagnosis of Pompe disease: A cross-sectional analysis to explore the potential utility of neonatal screening

机译:诊断庞贝病时严重损害健康状况:一项横断面分析,探讨新生儿筛查的潜在效用

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摘要

Since the introduction of enzyme replacement therapy for Pompe disease, awareness and early diagnosis have gained importance. Because the therapy is most effective when started early and methods for dried bloodspot screening for Pompe disease are currently being explored, neonatal screening is getting increased attention. The objective of this study was to investigate the gains that might be achieved with earlier diagnosis by neonatal screening. For this purpose we analyzed the health and functional status of non-screened patients with Pompe disease at the time of diagnosis.Previously collected clinical data and results of an international patient-reported questionnaire were used. Cross-sectional data of 53 patients with Pompe disease diagnosed between 1999 and 2009 (aged 0-64. years) were analyzed. According to the World Health Organization's International Classification of Functioning, Disability and Health the following domains are described: body function, activity, participation and contextual factors.In all patients with classic infantile Pompe disease cardiac function, hearing, muscle strength and motor development were considerably impaired at the time of clinical diagnosis. The use of oxygen and/or nasogastric tube-feeding was reported in more than 70% of these cases. Most children, adolescents and adults had advanced muscle weakness and impaired respiratory function at the time of their diagnosis, causing varying degrees of handicap. About 12% of them used a walking device and/or respiratory support at the time of diagnosis.The severely impaired health status reported here provides a strong argument for earlier diagnosis and to further explore the potential of neonatal screening for Pompe disease.
机译:自从对庞贝病引入酶替代疗法以来,认识和早期诊断就变得越来越重要。由于该疗法在早期开始时是最有效的,并且目前正在探索针对庞贝病的干血斑筛查方法,因此新生儿筛查越来越受到关注。这项研究的目的是调查通过新生儿筛查早期诊断可能获得的收益。为此,我们分析了未经筛查的庞贝病患者在诊断时的健康和功能状况,并使用了以前收集的临床数据和国际患者报告的问卷调查结果。分析了1999年至2009年(年龄在0-64岁之间)的53例庞贝病患者的横断面数据。根据世界卫生组织的国际功能,残疾和健康分类,描述了以下领域:身体功能,活动,参与和情境因素。在所有典型婴儿期庞贝病患者中,其心脏功能,听力,肌肉力量和运动发育均相当可观在临床诊断时受损。在这些案例中,有70%以上报告使用氧气和/或鼻胃管喂养。大多数儿童,青少年和成人在诊断时患有晚期肌肉无力和呼吸功能受损,导致不同程度的障碍。他们中约有12%在诊断时使用了步行设备和/或呼吸支持。此处报道的严重健康状况为早期诊断和进一步探索新生儿筛查庞贝病的可能性提供了有力的依据。

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