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预防医学  2023, Vol. 35 Issue (11): 1001-1004    DOI: 10.19485/j.cnki.issn2096-5087.2023.11.019
  妇幼保健 本期目录 | 过刊浏览 | 高级检索 |
2012—2021年朝阳区新生儿遗传代谢病筛查工作质量评价
王川, 赵秋玲, 马艳艳, 高倩, 赵月, 罗佳
北京市朝阳区妇幼保健院儿童保健科,北京 100021
Quality assessment of screening for neonatal inherited metabolic disease in Chaoyang District from 2012 to 2021
WANG Chuan, ZHAO Qiuling, MA Yanyan, GAO Qian, ZHAO Yue, LUO Jia
Department of Child Healthcare, Maternal and Child Health Hospital of Chaoyang District, Beijing 100021, China
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摘要 目的 评价2012—2021年北京市朝阳区新生儿遗传代谢病筛查工作质量,为提高新生儿遗传代谢病筛查管理质量和效率提供参考。方法 通过北京市新生儿疾病筛查中心收集2012—2021年朝阳区新生儿遗传代谢病筛查资料,分析筛查率、血片采集合格率、可疑病例复查率,以及先天性甲状腺功能低下症(CH)、苯丙酮尿症(PKU)和先天性肾上腺皮质增生症(CAH)等疾病确诊情况,以评价朝阳区新生儿遗传代谢病筛查工作质量。结果 2012—2021年朝阳区活产新生儿484 002人,累计筛查新生儿481 395人,筛查率为99.46%,血片采集合格率为99.71%。筛查检出可疑阳性病例4 305例,召回复查4 148例,可疑病例复查率为96.35%;其中CH、PKU和CAH复查率分别为96.37%、96.79%和95.65%。累计确诊遗传代谢病482例,总发病率为1/999;其中CH 307例,发病率为1/1 568;高促甲状腺激素血症103例,发病率为1/4 674;PKU 66例,发病率为1/7 294;CAH 6例,发病率为1/20 233。结论 2012—2021年朝阳区新生儿遗传代谢病筛查率和复查率均保持在95%以上,需继续完善新生儿筛查管理模式,进一步提高可疑病例召回复查率。
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王川
赵秋玲
马艳艳
高倩
赵月
罗佳
关键词 新生儿筛查遗传代谢病苯丙酮尿症先天性甲状腺功能减低症先天性肾上腺皮质增生症    
AbstractObjective To evaluate the quality of neonatal inherited metabolic diseases screening in Chaoyang District, Beijing Municipality from 2012 to 2021, so as to provide insights into improvements in the screening quality and efficiency of neonatal inherited metabolic diseases. Methods Data pertaining to screening of neonatal inherited metabolic disease in Chaoyang District from 2012 to 2021 were captured from Beijing Center for Neonatal Disease Screening. The percentage of screening, eligible rate of blood smears collection, re-examination rate of suspected cases, and definitive diagnosis of congenital hypothyroidism (CH), phenylketonuria (PKU) and congenital adrenal hyperplasia (CAH) were analyzed to evaluate the quality of neonatal inherited metabolic diseases screening in Chaoyang District. Results There were 484 002 live neonates in Chaoyang District from 2012 to 2021, and 481 395 neonates were screened for inherited metabolic diseases, with a screening rate of 99.46% and 99.71% eligible rate of blood smears collection. A total of 4 305 suspected positive cases were screened, including 4 148 cases recalled for re-examinations, with a 96.35% re-examination rate of suspected cases, and the re-examination rates of CH, PKU and CAH were 96.37%, 96.79% and 95.65%, respectively. Totally 482 neonates were definitively diagnosed with inherited metabolic diseases, with an overall incidence rate of 1/999, and the incidence rates of CH (307 cases), hyperthyrotropinemia (103 cases), PKU (66 cases) and CAH (6 cases) were 1/1 568, 1/4 674, 1/7 294 and 1/20 233, respectively. Conclusions The screening rate and re-examination rate of neonatal inherited metabolic diseases was both more than 95% in Chaoyang District from 2012 to 2021. Improving the management of neonatal inherited metabolic diseases screening and the recall of suspected cases is required.
Key wordsneonatal screening    inherited metabolic disease    phenylketonuria    congenital hypothyroidism    congenital adrenal hyperplasia
收稿日期: 2023-08-24      修回日期: 2023-10-17      出版日期: 2023-11-10
中图分类号:  R725.8  
通信作者: 罗佳,E-mail:carejiajia@126.com   
作者简介: 王川,硕士,主管医师,主要从事儿童保健工作
引用本文:   
王川, 赵秋玲, 马艳艳, 高倩, 赵月, 罗佳. 2012—2021年朝阳区新生儿遗传代谢病筛查工作质量评价[J]. 预防医学, 2023, 35(11): 1001-1004.
WANG Chuan, ZHAO Qiuling, MA Yanyan, GAO Qian, ZHAO Yue, LUO Jia. Quality assessment of screening for neonatal inherited metabolic disease in Chaoyang District from 2012 to 2021. Preventive Medicine, 2023, 35(11): 1001-1004.
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http://www.zjyfyxzz.com/CN/10.19485/j.cnki.issn2096-5087.2023.11.019      或      http://www.zjyfyxzz.com/CN/Y2023/V35/I11/1001
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