EUROlinkCAT: A linked European cohort of children with congenital anomalies

Maria Loane, Joan Morris, Ester Garne, None EUROlinkCAT Working Group
{"title":"EUROlinkCAT: A linked European cohort of children with congenital anomalies","authors":"Maria Loane, Joan Morris, Ester Garne, None EUROlinkCAT Working Group","doi":"10.23889/ijpds.v8i2.2346","DOIUrl":null,"url":null,"abstract":"ObjectiveTo establish a linked European cohort of children with congenital anomalies (CAs) to evaluate mortality and morbidity outcomes of these children up to the age of 10 years.&#x0D; MethodEUROlinkCAT supported 22 EUROCAT population-based congenital anomaly registries in 14 countries to link their data on children with CAs to mortality, vital statistics, hospital discharge and prescription databases. All live births with a CA born 1995-2014 recorded in the registries were followed up to age 10 years or to 31st December 2015. Each registry transformed their local mortality and morbidity data to a Common Data Model (CDM) and ran centrally created syntax scripts and produced tables/outputs in a standard form for meta-analysis. Analyses were performed on 100 different congenital anomaly subgroups for children <1 year,1-4 years, and 5-9 years.&#x0D; ResultsSixteen registries linked their data on children with CAs to mortality databases, eleven to regional/national hospital databases, and six to prescription databases. Data on children without a CA born during the same time-period and from the same population area (reference population) were available for seven registries linking to hospital databases and for all six registries linking to prescription databases. For the mortality studies, linked information on survival was available for 96% of children recorded in the anomaly registries (180,00 live births). For the morbidity studies, 89% of children with a CA (n=99,000) and 95% of reference children (n=2 million) were linked. For the prescription studies, 95% of children with a CA (n=60,000) and 95% of reference children (n= 1,700,000) were linked.&#x0D; ConclusionThe EUROlinkCAT project was successful in creating a linked cohort of children with and without CAs in Western Europe. More efforts are needed to support data linkage in Eastern European countries. We have developed a set of recommendations for data linkage studies based on our experiences in establishing this cohort.","PeriodicalId":132937,"journal":{"name":"International Journal for Population Data Science","volume":"29 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal for Population Data Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.23889/ijpds.v8i2.2346","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

ObjectiveTo establish a linked European cohort of children with congenital anomalies (CAs) to evaluate mortality and morbidity outcomes of these children up to the age of 10 years. MethodEUROlinkCAT supported 22 EUROCAT population-based congenital anomaly registries in 14 countries to link their data on children with CAs to mortality, vital statistics, hospital discharge and prescription databases. All live births with a CA born 1995-2014 recorded in the registries were followed up to age 10 years or to 31st December 2015. Each registry transformed their local mortality and morbidity data to a Common Data Model (CDM) and ran centrally created syntax scripts and produced tables/outputs in a standard form for meta-analysis. Analyses were performed on 100 different congenital anomaly subgroups for children <1 year,1-4 years, and 5-9 years. ResultsSixteen registries linked their data on children with CAs to mortality databases, eleven to regional/national hospital databases, and six to prescription databases. Data on children without a CA born during the same time-period and from the same population area (reference population) were available for seven registries linking to hospital databases and for all six registries linking to prescription databases. For the mortality studies, linked information on survival was available for 96% of children recorded in the anomaly registries (180,00 live births). For the morbidity studies, 89% of children with a CA (n=99,000) and 95% of reference children (n=2 million) were linked. For the prescription studies, 95% of children with a CA (n=60,000) and 95% of reference children (n= 1,700,000) were linked. ConclusionThe EUROlinkCAT project was successful in creating a linked cohort of children with and without CAs in Western Europe. More efforts are needed to support data linkage in Eastern European countries. We have developed a set of recommendations for data linkage studies based on our experiences in establishing this cohort.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
EUROlinkCAT:先天性畸形儿童的欧洲队列
目的建立一个欧洲先天性异常儿童(CAs)的关联队列,以评估这些儿童10岁以下的死亡率和发病率。方法eurolinkcat支持14个国家的22个EUROCAT基于人口的先天性异常登记处,将其患有ca的儿童数据与死亡率、生命统计、出院和处方数据库联系起来。所有在登记处记录的1995-2014年出生的CA活产婴儿均被随访至10岁或至2015年12月31日。每个注册中心将其本地死亡率和发病率数据转换为公共数据模型(CDM),并运行集中创建的语法脚本,以标准形式生成用于元分析的表/输出。对1岁、1-4岁和5-9岁儿童进行了100个不同的先天性异常亚组分析。结果16个注册中心将ca患儿数据与死亡率数据库相关联,11个注册中心与地区/国家医院数据库相关联,6个注册中心与处方数据库相关联。与医院数据库相连的7个登记处和与处方数据库相连的所有6个登记处均可获得在同一时期和同一人口地区(参考人口)出生的无CA儿童的数据。对于死亡率研究,在异常登记(18万活产)中记录的96%的儿童的生存相关信息是可用的。在发病率研究中,89%的CA患儿(n=99,000)和95%的对照患儿(n= 200万)被联系起来。在处方研究中,95%的CA患儿(n=6万)和95%的参考患儿(n= 170万)被关联。 结论EUROlinkCAT项目成功地建立了西欧患有和没有ca的儿童的关联队列。需要作出更多努力来支持东欧国家的数据联系。根据我们建立这一队列的经验,我们为数据链接研究制定了一套建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Using novel data linkage of biobank data with administrative health data to inform genomic analysis for future precision medicine treatment of congenital heart disease Common governance model: a way to avoid data segregation between existing trusted research environment Federated learning for generating synthetic data: a scoping review Health Data Governance for Research Use in Alberta Establishment of a birth-to-education cohort of 1 million Palestinian refugees using electronic medical records and electronic education records
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1