Trends in prenatal diagnosis of congenital anomalies in Western Australia between 1980 and 2020: A population‐based study

Author:

MacArthur Cassandra1ORCID,Hansen Michele2ORCID,Baynam Gareth345ORCID,Bower Carol2ORCID,Kelty Erin1ORCID

Affiliation:

1. School of Population and Global Health The University of Western Australia Crawley Western Australia Australia

2. Telethon Kids Institute The University of Western Australia Crawley Western Australia Australia

3. Western Australian Register of Developmental Anomalies King Edward Memorial Hospital Perth Western Australia Australia

4. Faculty of Health and Medicine, Institute and Division of Paediatrics University of Western Australia Crawley Western Australia Australia

5. Rare Care, Clinical Centre of Expertise for Rare and Undiagnosed Diseases Perth Children's Hospital Perth Western Australia Australia

Abstract

AbstractBackgroundAdvances in screening and diagnostics have changed the way in which we identify and diagnose congenital anomalies.ObjectiveTo examine changes in rates of prenatal diagnosis of congenital anomalies over time and by demographic characteristics.MethodsWe undertook a population‐based retrospective cohort study of all children born in Western Australia between 1980 and 2020 and diagnosed with a congenital anomaly. Age at diagnosis (prenatal, neonatal, infancy, early childhood or childhood) prevalence (all‐type and type‐specific), and prevalence ratios (PR) were calculated. We fit joinpoint regression models to describe the average annual percentage change (APC) in prenatal diagnosis over time, and log‐binomial regression models to estimate the association between prenatal diagnosis and demographic characteristics.ResultsPrenatal diagnosis prevalence between the first (1980–1989: 28.3 per 10,000 births) and last (2005–2014: 156.1 per 10,000 births) decades of the study increased 5.5‐fold (95% confidence interval [CI] 5.0, 5.9). Substantial increases were observed for cardiovascular (PR 10.7, 95% CI 8.0, 14.6), urogenital (PR 10.5, 95% CI: 8.7, 12.6) and chromosomal anomalies (PR 7.0, 95% CI 5.9, 8.3). Prenatal diagnosis was positively associated with the birth year (adjusted risk ratio [RR] 1.04, 95% CI 1.03, 1.04), advanced maternal age (RR 1.14, 95% CI 1.11, 1.18), multiple anomalies (RR 2.86, 95% CI 2.77, 2.96) and major anomalies (RR 3.75, 95% CI 3.36, 4.19), and inversely associated with remoteness (RR 0.89, 95% CI: 0.83, 0.95) and Aboriginality (RR 0.90, 95% CI 0.83, 0.97).ConclusionsIncreases in prenatal diagnosis of congenital anomalies were observed in Western Australia from 1980 to 2020, reflecting advances in screening. Prenatal diagnosis was less common in remote regions and in Aboriginal children, strengthening calls for increased provision of antenatal care services for these populations.

Funder

National Health and Medical Research Council

Publisher

Wiley

Subject

Pediatrics, Perinatology and Child Health,Epidemiology

Reference49 articles.

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3