Suppr超能文献

梅尔辛省囊性纤维化的新生儿筛查:国家项目年度评估

Newborn Screening for Cystic Fibrosis in Mersin Province: Yearly Assessment of the National Program.

作者信息

Özdemir Ali, Doğruel Dilek

机构信息

Pediatric Pulmonary Section, Department of Pediatrics, Mersin City Training and Research Hospital, Mersin, Turkey.

Pediatric Allergy Section, Department of Pediatrics, Çukurova University School of Medicine, Adana, Turkey.

出版信息

Turk Thorac J. 2020 Mar 1;21(2):100-104. doi: 10.5152/TurkThoracJ.2019.18187. Print 2020 Mar.

Abstract

OBJECTIVES

A national newborn screening program for cystic fibrosis (CF) was started using immunoreactive trypsinogen (IRT) test on January 1, 2015, in Turkey. We aimed to analyze the characteristics of newborn screen-positive (NBSP) infants in Mersin province.

MATERIALS AND METHODS

The data on NBSP infants were retrospectively analyzed between 2015 and 2017 from records of Mersin Women & Children's Hospital and Mersin City Training and Research Hospital.

RESULTS

A total of 82,273 newborns were screened for CF by IRT test between January 2015 and December 2017 in Mersin. Among those, 512 infants were defined as NBSP after two repeated IRT tests (IRT/IRT) (138 infants in 2015, 217 in 2016, and 157 in 2017). Sweat test was normal in the majority of infants (115 infants [83.3%] in 2015, 189 [87.1%] in 2016, and 129 [82.2%] in 2017). Overall, between 2015 and 2017, after two repeated sweat tests, 4 infants had sweat test results in the intermediate range and 9 infants had positive sweat tests. The incidence of CF for a 3-year period was approximately 1/9300 in our region. The positive predictive value of IRT test for defining CF was 1.8%, with a sensitivity of 90.0% and specificity of 99.4%.

CONCLUSION

IRT/IRT test as a newborn screening strategy provides the opportunity for earlier diagnosis and treatment of CF patients. More data are needed to understand the frequency of CF on a national level.

摘要

目的

2015年1月1日起,土耳其启动了一项使用免疫反应性胰蛋白酶原(IRT)检测的全国新生儿囊性纤维化(CF)筛查项目。我们旨在分析梅尔辛省新生儿筛查呈阳性(NBSP)婴儿的特征。

材料与方法

回顾性分析2015年至2017年梅尔辛妇女儿童医院和梅尔辛市培训与研究医院记录中的NBSP婴儿数据。

结果

2015年1月至2017年12月期间,梅尔辛共有82273名新生儿接受了IRT检测以筛查CF。其中,经过两次重复IRT检测(IRT/IRT)后,512名婴儿被定义为NBSP(2015年138名婴儿,2016年217名,2017年157名)。大多数婴儿的汗液检测结果正常(2015年115名婴儿[83.3%],2016年189名[87.1%],2017年129名[82.2%])。总体而言,2015年至2017年期间,经过两次重复汗液检测后,4名婴儿的汗液检测结果处于中间范围,9名婴儿汗液检测呈阳性。我们地区3年期间CF的发病率约为1/9300。IRT检测用于定义CF的阳性预测值为1.8%,敏感性为90.0%,特异性为99.4%。

结论

IRT/IRT检测作为一种新生儿筛查策略,为CF患者的早期诊断和治疗提供了机会。需要更多数据来了解全国范围内CF的发病频率。

相似文献

6
A survey of newborn screening for cystic fibrosis in Europe.欧洲囊性纤维化新生儿筛查调查。
J Cyst Fibros. 2007 Jan;6(1):57-65. doi: 10.1016/j.jcf.2006.05.008. Epub 2006 Jul 25.

本文引用的文献

3
Cystic fibrosis screen positive, inconclusive diagnosis.囊性纤维化筛查呈阳性,诊断结果不确定。
Curr Opin Pulm Med. 2016 Nov;22(6):617-22. doi: 10.1097/MCP.0000000000000314.
8
Cystic fibrosis carrier screening in a North American population.北美人群中的囊性纤维化携带者筛查。
Genet Med. 2014 Jul;16(7):539-46. doi: 10.1038/gim.2013.188. Epub 2013 Dec 19.
10
Thirty-years of screening for cystic fibrosis in East Anglia.东英吉利地区 30 年的囊性纤维化筛查。
Arch Dis Child. 2012 Dec;97(12):1043-7. doi: 10.1136/archdischild-2012-301968. Epub 2012 Oct 16.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验