Division of Pediatric Cardiology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas.
Arkansas Reproductive Health Monitoring System, Arkansas Children's Research Institute & University of Arkansas for Medical Sciences, Little Rock, Arkansas.
Birth Defects Res. 2018 Mar 1;110(4):352-363. doi: 10.1002/bdr2.1157. Epub 2017 Dec 1.
Previous studies demonstrate that infant and childhood mortality differ among children with birth defects by maternal race/ethnicity, but limited mortality information is published for Hispanic ethnic subgroups.
We performed a retrospective cohort study using data for children with birth defects born to Hispanic mothers during 1999-2007 from 12 population-based state birth defects surveillance programs. Deaths were ascertained through multiple sources. Survival probabilities were estimated by the Kaplan-Meier method. Cox proportional hazards regression was used to examine the effect of clinical and demographic factors on mortality risk.
Among 28,497 Hispanic infants and children with major birth defects, 1-year survival was highest for infants born to Cuban mothers at 94.6% (95% confidence intervals [CI] 92.7-96.0) and the lowest for Mexicans at 90.2% (95% CI 89.7-90.6; p < .0001). For children aged up to 8 years, survival remained highest for Cuban Americans at 94.1% (95% CI 91.8-95.7) and lowest for Mexican Americans at 89.2% (95% CI 88.7-89.7; p = .0002). In the multivariable analysis using non-Hispanic White as the reference group, only infants and children born to Mexican mothers were noted to have a higher risk of mortality for cardiovascular defects.
This analysis provides a better understanding of survival and mortality for Hispanic infants and children with selected birth defects. The differences found in survival, particularly the highest survival rates for Cuban American children and lowest for Mexican American children with birth defects, underscores the importance of assessing Hispanic ethnic subgroups, as differences among subgroups appear to exist.
先前的研究表明,出生缺陷儿童的母婴种族/民族不同,其婴儿和儿童死亡率也不同,但关于西班牙裔亚群的死亡率信息有限。
我们对 1999 年至 2007 年期间来自 12 个基于人群的州出生缺陷监测项目的西班牙裔母亲所生患有重大出生缺陷的儿童进行了回顾性队列研究。通过多种来源确定死亡情况。通过 Kaplan-Meier 方法估计生存率。Cox 比例风险回归用于检查临床和人口统计学因素对死亡率风险的影响。
在 28497 名患有重大出生缺陷的西班牙裔婴儿和儿童中,古巴裔母亲所生婴儿的 1 年生存率最高,为 94.6%(95%置信区间 [CI] 92.7-96.0),而墨西哥裔母亲所生婴儿的生存率最低,为 90.2%(95% CI 89.7-90.6;p<.0001)。对于 8 岁以下的儿童,古巴裔美国人的生存率仍然最高,为 94.1%(95% CI 91.8-95.7),而墨西哥裔美国人的生存率最低,为 89.2%(95% CI 88.7-89.7;p=0.0002)。在使用非西班牙裔白人为参考组的多变量分析中,只有母亲为墨西哥裔的婴儿和儿童被认为患有心血管缺陷的死亡率更高。
本分析更好地了解了患有特定出生缺陷的西班牙裔婴儿和儿童的生存率和死亡率。在生存率方面发现的差异,特别是古巴裔美国儿童的生存率最高,而墨西哥裔美国儿童的生存率最低,这突出了评估西班牙裔亚群的重要性,因为亚群之间似乎存在差异。