Development of Strategies to Decrease False Positive Results in Newborn Screening

被引:35
作者
Malvagia, Sabrina [1 ]
Forni, Giulia [1 ]
Ombrone, Daniela [1 ]
la Marca, Giancarlo [1 ,2 ]
机构
[1] Meyer Childrens Univ Hosp, Newborn Screening Clin Chem & Pharmacol Lab, I-50139 Florence, Italy
[2] Univ Florence, Dept Expt & Clin Biomed Sci, I-50139 Florence, Italy
关键词
newborn screening; second-tier test; false positives; tandem mass spectrometry; inborn error of metabolism; DRIED BLOOD SPOTS; CONGENITAL ADRENAL-HYPERPLASIA; TANDEM MASS-SPECTROMETRY; TYROSINEMIA TYPE-I; SEVERE COMBINED IMMUNODEFICIENCY; 2ND TIER TEST; 2ND-TIER TEST; DERMATAN SULFATE; HEPARAN-SULFATE; INBORN-ERRORS;
D O I
10.3390/ijns6040084
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The expansion of national newborn screening (NBS) programmes has provided significant benefits in the diagnosis and early treatment of several rare, heritable conditions, preventing adverse health outcomes for most affected infants. New technological developments have enabled the implementation of testing panel covering over 50 disorders. Consequently, the increment of false positive rate has led to a high number of healthy infants recalled for expensive and often invasive additional testing, opening a debate about the harm-benefit ratio of the expanded newborn screening. The false-positive rate represents a challenge for healthcare providers working in NBS systems. Here, we give an overview on the most commonly used strategies for decreasing the adverse effects due to inconclusive screening results. The focus is on NBS performance improvement through the implementation of analytical methods, the application of new and more informative biomarkers, and by using post-analytical interpretive tools. These strategies, used as part of the NBS process, can to enhance the positive predictive value of the test and reduce the parental anxiety and healthcare costs related to the unnecessary tests and procedures.
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页数:16
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