Progress of newborn screening in China.

Hongli Jiang, Rulai Yang, Ao Dong, Benqing Wu, Zhengyan Zhao
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Abstract

Newborn screening (NBS) plays a significant role in reducing the risk of birth defects. NBS in China began in the early 1980s. Under the protection of laws and regulations and the leadership of the national health administration, approved screening centers in public hospitals took the responsibility for publicity, screening, diagnosis, treatment, follow-up and management of birth defects. As of 2022, 31 provinces (autonomous regions and municipalities directly under the central government) have carried out NBS for phenylketonuria, congenital hypothyroidism, and hearing loss, 23 provinces have carried out screening for glucose-6-phosphate dehydrogenase (with a screening rate of 89.24%), and 24 provinces have carried out screening for congenital adrenal cortical hyperplasia (91.45% screening rate). Over the past four decades, screening techniques have evolved from bacterial inhibition, fluorescence analysis, and tandem mass spectrometry for the detection of biochemical markers to genetic testing, which has greatly contributed to the expansion of the types of diseases screened for. The combined use of metabolomics and genomics is currently being explored. Effective management and rigorous quality control of NBS are prerequisites for improving the quality and ensuring the accuracy of screening. The Quality Management System for Newborn Screening System Network (QMS-NBS), established by the National Center for Clinical Laboratories, covers all screening centers and related blood collection agencies. The operation of the QMS-NBS allows the quality and performance of screening to be transparent and measurable, ensuring the quality and efficiency of screening. This article provides an overview of the history of NBS, especially the evolution of policies for the NBS in China, the construction of screening institutions, the number of newborns screened, the incidence rates of screened diseases, the changes in screening technology, the expansion of new diseases screened for, and the quality control of NBS. Overall, the progress in NBS in China has not only benefited from the development and standardization at the technological level, but also benefited from the construction of policies, regulations and ethics.

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中国新生儿疾病筛查的进展。
新生儿疾病筛查(NBS)在降低出生缺陷风险方面具有重要意义。中国的新生儿疾病筛查始于 20 世纪 80 年代初。截至 2022 年,全国 31 个省(区、市)已全部开展新生儿苯丙酮尿症(PKU)、先天性甲状腺功能减低症(CH)和听力损失筛查。22个省(区、市)开展了葡萄糖-6-磷酸脱氢酶缺乏症(G6PD)筛查,筛查率为89.24%。24个省(区、市)开展先天性肾上腺皮质增生症筛查,筛查率为91.45%。脂肪酸代谢障碍、有机酸代谢障碍、氨基酸代谢障碍筛查率分别为 49.78%、50.86%、50.01%。有效的新生儿疾病筛查管理和严格的质量控制是提高筛查质量、确保筛查准确性的前提。推广和实施新生儿筛查系统质量管理体系(QMS-NBS)网络,可实现质量绩效的可视化和可测量。
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CiteScore
3.80
自引率
0.00%
发文量
67
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