Cystic Fibrosis Cases Missed by Newborn Bloodspot Screening-Towards a Consistent Definition and Data Acquisition.

IF 4 Q1 GENETICS & HEREDITY
Anne Munck, Kevin W Southern, Jared Murphy, Karin M de Winter-de Groot, Silvia Gartner, Bülent Karadag, Nataliya Kashirskaya, Barry Linnane, Marijke Proesmans, Dorota Sands, Olaf Sommerburg, Carlo Castellani, Jürg Barben
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引用次数: 0

Abstract

Repeated European surveys of newborn bloodspot screening (NBS) have shown varied strategies for collecting missed cases, and information on data collection differs among countries/regions, hampering data comparison. The ECFS Neonatal Screening Working Group defined missed cases by NBS as either false negatives, protocol-related, concerning analytical issues, or non-protocol-related, concerning pre- and post-analytical issues. A questionnaire has been designed and sent to all key workers identified in each NBS programme to assess the feasibility of collecting data on missed cases, the stage of the NBS programme when the system failed, and individual patient data on each missed case.

新生儿血斑筛查漏诊的囊性纤维化病例--实现一致的定义和数据采集。
欧洲反复进行的新生儿血斑筛查(NBS)调查显示,收集漏检病例的策略各不相同,而且各国/各地区的数据收集信息也不尽相同,这妨碍了数据比较。ECFS 新生儿筛查工作组将 NBS 的漏检病例定义为假阴性病例、与分析问题有关的协议相关病例或与分析前后问题有关的非协议相关病例。已设计了一份调查问卷,并发送给每个新生儿筛查计划中确定的所有关键工作人员,以评估收集漏报病例数据的可行性、系统出现故障时新生儿筛查计划所处的阶段以及每个漏报病例的单个患者数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Journal of Neonatal Screening
International Journal of Neonatal Screening Medicine-Pediatrics, Perinatology and Child Health
CiteScore
6.70
自引率
20.00%
发文量
56
审稿时长
11 weeks
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