National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia.
Carter Consulting, Incorporated, Atlanta, Georgia.
Birth Defects Res. 2018 Nov 15;110(19):1478-1486. doi: 10.1002/bdr2.1413. Epub 2018 Nov 16.
BACKGROUND/OBJECTIVES: In this data brief, we examine major eye and ear anomalies (anophthalmia/microphthalmia, anotia/microtia, and congenital cataract) for a recent 5-year birth cohort using data from 30 population-based birth defects surveillance programs in the United States.
As a special call for data for the 2018 NBDPN Annual Report, state programs reported expanded data on eye/ear anomalies for birth years 2011-2015. We calculated the combined overall prevalence (per 10,000 live births) and 95% confidence intervals (CI), for the three anomalies as well as by maternal age, maternal race/ethnicity, infant sex, laterality, presence/absence of other major birth defects, and case ascertainment methodology utilized by the program (active vs. passive).
The overall prevalence estimate (per 10,000 live births) was 1.5 (95% CI: 1.4-1.5) for anophthalmia/microphthalmia, 1.5 (95% CI: 1.4-1.6) for congenital cataract, and 1.8 (95% CI: 1.7-1.8) for anotia/microtia. Congenital cataract prevalence varied little by maternal race/ethnicity, infant sex, or case ascertainment methodology; prevalence differences were more apparent across strata for anophthalmia/microphthalmia and anotia/microtia. Prevalence among active vs. passive ascertainment programs was 50% higher for anophthalmia/microphthalmia (1.9 vs. 1.2) and two-fold higher for anotia/microtia (2.6 vs. 1.2). Anophthalmia/microphthalmia was more likely than other conditions to co-occur with other birth defects. All conditions were more frequent among older mothers (40+ years).
This data brief provides recent prevalence estimates for anophthalmia/microphthalmia, congenital cataract, and anotia/microtia that address a data gap by examining pooled data from 30 population-based surveillance systems, covering a five-year birth cohort of about 12.4 million births.
背景/目的:本数据简报使用美国 30 个基于人群的出生缺陷监测项目的数据,研究了最近 5 年出生队列中主要眼部和耳部畸形(无眼/小眼、无耳/小耳和先天性白内障)的情况。
作为 2018 年 NBDPN 年度报告特殊数据征集的一部分,各州项目报告了 2011-2015 年出生年份眼部/耳部畸形的扩展数据。我们计算了这三种畸形的综合总体患病率(每 10000 例活产)和 95%置信区间(CI),并按母亲年龄、母亲种族/族裔、婴儿性别、侧别、是否存在其他主要出生缺陷以及项目使用的病例发现方法(主动与被动)进行了分类。
无眼/小眼的总体患病率估计值(每 10000 例活产)为 1.5(95%CI:1.4-1.5),先天性白内障为 1.5(95%CI:1.4-1.6),无耳/小耳为 1.8(95%CI:1.7-1.8)。先天性白内障的患病率在母亲种族/族裔、婴儿性别或病例发现方法方面差异不大;而在无眼/小眼和无耳/小耳方面,各分层之间的差异更为明显。主动发现与被动发现病例的无眼/小眼患病率相差 50%(1.9 比 1.2),无耳/小耳患病率相差两倍(2.6 比 1.2)。无眼/小眼比其他疾病更有可能与其他出生缺陷同时发生。所有疾病在年龄较大的母亲(40 岁及以上)中更为常见。
本数据简报提供了无眼/小眼、先天性白内障和无耳/小耳的最新患病率估计值,通过检查 30 个基于人群的监测系统的汇总数据,解决了一个数据空白,涵盖了约 1240 万例 5 年出生队列。