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不使用放射性进行新生儿甲状腺筛查:促甲状腺素时间分辨荧光免疫测定法的评估

Thyroid screening of neonates without use of radioactivity: evaluation of time-resolved fluoroimmunoassay of thyrotropin.

作者信息

Torresani T E, Scherz R

出版信息

Clin Chem. 1986 Jun;32(6):1013-6.

PMID:3754792
Abstract

We evaluated the usefulness, in routine newborn screening for congenital hypothyroidism, of a time-resolved fluoroimmunoassay kit (DELFIA Neonatal TSH) for the determination of thyrotropin (TSH) in dried blood spots. A total of 11 531 dried blood samples from newborns were tested in parallel in each of two Swiss screening laboratories, by RIA and DELFIA. Six cases of confirmed congenital hypothyroidism were detected during the study period. The rate of false-positive results, after single TSH determination in the DELFIA assay, was 0.16%. Correlation of RIA and DELFIA results for TSH was very good in both laboratories (0.959 and 0.97, respectively). The new method fulfills the criteria for precision and sensitivity of a screening assay. Screening results are usually available the day after the sample arrives in the laboratory, thus favoring early diagnosis and allowing treatment to begin by the seventh or eighth postnatal day.

摘要

我们评估了时间分辨荧光免疫分析试剂盒(DELFIA新生儿促甲状腺激素)在先天性甲状腺功能减退症常规新生儿筛查中用于测定干血斑中促甲状腺激素(TSH)的实用性。在瑞士的两个筛查实验室中,分别采用放射免疫分析法(RIA)和时间分辨荧光免疫分析法(DELFIA)对总共11531份新生儿干血样本进行了平行检测。在研究期间共检测出6例确诊的先天性甲状腺功能减退症病例。在DELFIA检测中单次测定TSH后,假阳性结果率为0.16%。在两个实验室中,RIA和DELFIA检测TSH的结果相关性都非常好(分别为0.959和0.97)。新方法符合筛查检测的精密度和灵敏度标准。筛查结果通常在样本送达实验室后的第二天即可获得,因此有利于早期诊断,并能在出生后第七或第八天开始治疗。

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