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1999年至2020年德克萨斯州出生缺陷登记处的小脑畸形流行病学

Epidemiology of Colpocephaly in the Texas Birth Defects Registry, 1999 to 2020.

作者信息

Yantz Caitlyn, Shumate Charles, Betancourt Dayana, Allred Rachel, Nguyen Joanne, Agopian A J, Salemi Jason, Ahmad Kaashif

机构信息

Department of State Health Services, Birth Defects Epidemiology and Surveillance Branch, Texas, Austin, Texas.

Department of Epidemiology, University of Texas Health Science Center at Houston, School of Public Health, Houston, Texas.

出版信息

Am J Perinatol. 2025 Sep;42(12):1610-1621. doi: 10.1055/a-2516-1967. Epub 2025 Jan 31.

Abstract

Colpocephaly is a congenital brain defect characterized by enlargement of the occipital horns of the lateral ventricles. Few population-based studies have focused on this central nervous system (CNS) defect. This study aimed to evaluate the birth prevalence and survival of Texas infants with colpocephaly delivered between 1999 and 2020.Cases from the Texas Birth Defects Registry (TBDR) with a diagnosis of colpocephaly were identified. Unadjusted birth prevalence, 1-year survival estimates, and crude hazard ratios with 95% confidence intervals (CIs) were calculated from data collected from the medical record abstraction and linked vital records. Select maternal and infant variables were assessed overall and across four medical classification groups (presence of isolated, chromosomal, syndromic, or multiple major defects).From 1999 to 2020, 1,146 cases with colpocephaly were identified. The overall birth prevalence of colpocephaly was 1.36/10,000 live births (95% CI: 1.28-1.44). Significantly higher prevalence was noted for male infants, infants with low birth weight (<2,500 g), and very preterm (<32 weeks) infants. Overall, 1-year survival was 89.5%, with statistically significant differences observed in each medical classification group (e.g., isolated) across levels of maternal education, Texas/Mexico border maternal residence at delivery, infant birth weight, and gestational age.These findings have important implications for pediatric neurology and future research, such as counseling on the prevalence and prognosis of colpocephaly. Additionally, these findings highlight that the population burden of CNS defects may be higher than previously believed, supporting the expansion of research of rare brain defects. · The overall birth prevalence of colpocephaly for Texas infants delivered between 1999 and 2020 was 1.36/10,000 live births.. · Statistically significant differences in 1-year survival were observed across select maternal and infant variables.. · Longitudinal studies are necessary to fully ascertain the prevalence of colpocephaly beyond the first year of life..

摘要

脑室后角扩大症是一种先天性脑缺陷,其特征为侧脑室枕角增大。很少有基于人群的研究关注这种中枢神经系统(CNS)缺陷。本研究旨在评估1999年至2020年间在得克萨斯州出生的患有脑室后角扩大症的婴儿的出生患病率和生存率。从得克萨斯州出生缺陷登记处(TBDR)中识别出诊断为脑室后角扩大症的病例。根据从病历摘要和关联的生命记录中收集的数据,计算未经调整的出生患病率、1年生存率估计值以及带有95%置信区间(CI)的粗危险比。对选定的母亲和婴儿变量进行了总体评估,并按四个医学分类组(孤立性、染色体性、综合征性或多发性主要缺陷)进行了评估。1999年至2020年期间,共识别出1146例脑室后角扩大症病例。脑室后角扩大症的总体出生患病率为1.36/10000活产(95%CI:1.28 - 1.44)。男婴、低体重(<2500克)婴儿和极早产(<32周)婴儿的患病率明显更高。总体而言,1年生存率为89.5%,在每个医学分类组(如孤立性)中,在母亲教育水平、分娩时母亲居住在得克萨斯州/墨西哥边境、婴儿出生体重和胎龄等方面观察到有统计学显著差异。这些发现对儿科神经学和未来研究具有重要意义,例如关于脑室后角扩大症患病率和预后的咨询。此外,这些发现突出表明中枢神经系统缺陷的人群负担可能高于先前认为的水平,支持扩大对罕见脑缺陷的研究。·1999年至2020年间在得克萨斯州出生的婴儿中,脑室后角扩大症的总体出生患病率为1.36/10000活产。·在选定的母亲和婴儿变量中观察到1年生存率有统计学显著差异。·有必要进行纵向研究以全面确定1岁以后脑室后角扩大症的患病率。

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