Abstract
The history of the Newborn Screening Program in Mainland China begins in 1981, when a pilot plan was developed that demonstrated the feasibility of its implementation. It has so far focused on the detection of congenital hypothyroidism (CH) and phenylketonuria (PKU) to prevent or reduce mental and physical developmental retardation in children. Throughout this period, a total of 35,795,550 dried blood samples (DBS) of newborns (NB) have been analyzed for PKU, and 35,715,988 for CH. During this period, 3,082 cases with PKU have been diagnosed, resulting in an incidence of 1 case per 11,614 (95% confidence interval 11,218–12,039) live births. In relation to CH, 17,556 cases have been confirmed, arriving at an incidence of 1 case per 2,034(95% confidence interval 2,005–2,065) live births. The biggest challenge for universal newborn screening is still to increase coverage to mid-western area. In Mainland China, MS/MS newborn screening started in 2004. In a pilot study, 371,942 neonates were screened, and 98 cases were detected with one of the metabolic disorders, and the collective estimated prevalence amounted to 1 in 3795 (95% confidence interval 3,168–4,732) live births, with a sensitivity of 98.99%, a specificity of 99.83%, and a positive predictive value of 13.57%. The most important is to get the government’s policy and financial support for expanded screening.
Competing interests: None declared
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We are grateful to the individuals for providing their screening data.
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Communicated by: Verena Peters
Synopsis: Past, Present, and Future of Newborn Screening in Mainland China
Synopsis: Past, Present, and Future of Newborn Screening in Mainland China
In most economically developed countries, blood spot newborn screening (NBS) using biochemical markers to detect certain congenital conditions is a public health activity aimed at the early identification and treatment/management of affected newborns. As an integral part of maternal and child health care in Mainland China, it has so far focused on the detection of congenital hypothyroidism (CH) and phenylketonuria (PKU) to prevent or reduce mental and physical developmental retardation in children. In our country, NBS and other infant screening are just emerging as a priority. This chapter will focus on NBS in the Mainland China, a region of vastly differing newborn screening priorities.
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© 2012 SSIEM and Springer-Verlag Berlin Heidelberg
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Shi, XT. et al. (2012). Newborn Screening for Inborn Errors of Metabolism in Mainland China: 30 Years of Experience. In: JIMD Reports - Case and Research Reports, 2012/3. JIMD Reports, vol 6. Springer, Berlin, Heidelberg. https://doi.org/10.1007/8904_2011_119
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DOI: https://doi.org/10.1007/8904_2011_119
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