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

被引:3
作者
MacArthur, Cassandra [1 ]
Hansen, Michele [2 ]
Baynam, Gareth [3 ,4 ,5 ]
Bower, Carol [2 ]
Kelty, Erin [1 ]
机构
[1] Univ Western Australia, Sch Populat & Global Hlth, Crawley, WA, Australia
[2] Univ Western Australia, Telethon Kids Inst, Crawley, WA, Australia
[3] King Edward Mem Hosp, Western Australian Register Dev Anomalies, Perth, WA, Australia
[4] Univ Western Australia, Inst & Div Paediat, Fac Hlth & Med, Crawley, WA, Australia
[5] Perth Childrens Hosp, Clin Ctr Expertise Rare & Undiagnosed Dis, Rare Care, Perth, WA, Australia
基金
英国医学研究理事会;
关键词
congenital abnormalities; pregnancy; prenatal diagnosis; BIRTH-DEFECTS; MATERNAL AGE; ABNORMALITIES; PREVALENCE; EXPERIENCE; ULTRASOUND; DISEASES; ATLANTA; IMPACT;
D O I
10.1111/ppe.12983
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background Advances in screening and diagnostics have changed the way in which we identify and diagnose congenital anomalies.Objective To examine changes in rates of prenatal diagnosis of congenital anomalies over time and by demographic characteristics.Methods We 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.Results Prenatal 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).Conclusions Increases 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.
引用
收藏
页码:596 / 606
页数:11
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