Literature DB >> 26238341

The status of neonatal screening in China, 2013.

Kun Zhong1, Wei Wang1, Falin He1, Zhiguo Wang2.   

Abstract

OBJECTIVES: To investigate the status of neonatal screening in China in 2013.
METHOD: All Chinese neonatal screening laboratories were asked to submit information about the number of newborns screened and for which diseases, the rate of acceptable blood spots, and the time between sample collection and delivery to laboratories and reporting.
RESULTS: Of the 202 laboratories, 194 (96%) submitted data. In 2013, 73.6% (142/193) of laboratories testing for phenylketonuria (PKU), 72.7% (141/194) for congenital hypothyroidism (CH), 58.9% (43/73) for glucose-6-phosphate dehydrogenase (G6PD) deficiency and 53.1% (34/64) for congenital adrenal hyperplasia (CAH) screened more than 30,000 newborns. The incidences of PKU, CH, G6PD deficiency, and CAH were 1:12189, 1:2281, 1:44 and 1:6084, respectively. The estimated coverage of screening for PKU, CH, G6PD deficiency, and CAH were 86.3 ∼ 87.5%, 87.9 ∼ 89.1%, 24.0 ∼ 25.0% and 18.9% ∼ 19.9%, respectively. The rates of acceptable blood spots were ≥98% in 161 (87.0%) of 185 laboratories. More than half the laboratories could not achieve a time from collection to reporting of 5 days.
CONCLUSION: Neonatal screening has developed rapidly in China but the biggest challenge is still to increase coverage and expand the screening disease panel across the entire country. More government support is needed to make neonatal screening more efficient.
© The Author(s) 2015.

Entities:  

Keywords:  G6PD; Neonatal screening; congenital adrenal hyperplasia; congenital hypothyroidism; phenylketonuria

Mesh:

Year:  2015        PMID: 26238341     DOI: 10.1177/0969141315597715

Source DB:  PubMed          Journal:  J Med Screen        ISSN: 0969-1413            Impact factor:   2.136


  18 in total

Review 1.  Newborn screening for Duchenne muscular dystrophy in China: follow-up diagnosis and subsequent treatment.

Authors:  Qing Ke; Zheng-Yan Zhao; Robert Griggs; Veronica Wiley; Anne Connolly; Jennifer Kwon; Ming Qi; Daniel Sheehan; Emma Ciafaloni; R Rodney Howell; Petra Furu; Peter Sazani; Arvind Narayana; Michele Gatheridge
Journal:  World J Pediatr       Date:  2017-05-17       Impact factor: 2.764

2.  Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline.

Authors:  Phyllis W Speiser; Wiebke Arlt; Richard J Auchus; Laurence S Baskin; Gerard S Conway; Deborah P Merke; Heino F L Meyer-Bahlburg; Walter L Miller; M Hassan Murad; Sharon E Oberfield; Perrin C White
Journal:  J Clin Endocrinol Metab       Date:  2018-11-01       Impact factor: 5.958

Review 3.  Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.

Authors:  Hedi L Claahsen-van der Grinten; Phyllis W Speiser; S Faisal Ahmed; Wiebke Arlt; Richard J Auchus; Henrik Falhammar; Christa E Flück; Leonardo Guasti; Angela Huebner; Barbara B M Kortmann; Nils Krone; Deborah P Merke; Walter L Miller; Anna Nordenström; Nicole Reisch; David E Sandberg; Nike M M L Stikkelbroeck; Philippe Touraine; Agustini Utari; Stefan A Wudy; Perrin C White
Journal:  Endocr Rev       Date:  2022-01-12       Impact factor: 19.871

4.  Analysis of the Screening Results for Congenital Adrenal Hyperplasia Involving 7.85 Million Newborns in China: A Systematic Review and Meta-Analysis.

Authors:  Zhuoguang Li; Lianjing Huang; Caiqi Du; Cai Zhang; Mini Zhang; Yan Liang; Xiaoping Luo
Journal:  Front Endocrinol (Lausanne)       Date:  2021-04-23       Impact factor: 5.555

5.  Incidence of Neonatal Hyperphenylalaninemia Based on High-performance Liquid Chromatography Confirmatory Technique in Mazandaran Province, Northern Iran (2007-2015).

Authors:  Ali Abbaskhanian; Daniel Zamanfar; Parvaneh Afshar; Einollah Asadpoor; Hamed Rouhanizadeh; Ali Jafarnia; Mohammad Shokzadeh
Journal:  Int J Prev Med       Date:  2017-11-07

6.  National survey on internal quality control for tumour markers in clinical laboratories in China.

Authors:  Wei Wang; Kun Zhong; Shuai Yuan; Falin He; Yuxuan Du; Zhehui Hu; Zhiguo Wang
Journal:  Biochem Med (Zagreb)       Date:  2018-04-15       Impact factor: 2.313

7.  Expanded newborn screening for inborn errors of metabolism by tandem mass spectrometry in newborns from Xinxiang city in China.

Authors:  Shujun Ma; Qinghe Guo; Zhongxin Zhang; Zhian He; Aizhi Yue; Zhishan Song; Qingwei Zhao; Xia Wang; Ruili Sun
Journal:  J Clin Lab Anal       Date:  2020-01-08       Impact factor: 2.352

8.  Newborn Screening and Molecular Profile of Congenital Hypothyroidism in a Chinese Population.

Authors:  Bin Yu; Wei Long; Yuqi Yang; Ying Wang; Lihua Jiang; Zhengmao Cai; Huaiyan Wang
Journal:  Front Genet       Date:  2018-10-29       Impact factor: 4.599

Review 9.  Genetics of congenital adrenal hyperplasia.

Authors:  Nils Krone; Wiebke Arlt
Journal:  Best Pract Res Clin Endocrinol Metab       Date:  2009-04       Impact factor: 4.690

10.  China's shift from population control to population quality: Implications for neurology.

Authors:  Qing Ke; Li Zhang; Chaying He; Zhengyan Zhao; Ming Qi; Robert C Griggs; Michele A Gatheridge
Journal:  Neurology       Date:  2016-08-23       Impact factor: 9.910

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.