Geographical variation in infant mortality due to congenital heart disease in the USA: a population-based cohort study

婴儿死亡率 人口学 医学 人口 队列 死亡率 心脏病 队列研究 胎龄 儿科 怀孕 环境卫生 外科 内科学 社会学 生物 遗传学
作者
Michelle Udine,F.J. Evans,Kristin M. Burns,Gail D. Pearson,Jonathan R. Kaltman
出处
期刊:The Lancet Child & Adolescent Health [Elsevier BV]
卷期号:5 (7): 483-490 被引量:34
标识
DOI:10.1016/s2352-4642(21)00105-x
摘要

Summary

Background

Little is known about geographical variation in infant mortality due to congenital heart disease (CHD) and the social determinants of health that might mediate such variation. We aimed to examine US county-level estimates of infant mortality due to CHD to understand geographical patterns and factors that might influence variation in mortality.

Methods

This US population-based cohort study used linked livebirth–infant death cohort files from the US National Center for Health Statistics from Jan 1, 2006, to Dec 31, 2015. All deaths attributable to congenital heart disease in infants in a given year were included. We used hierarchical Bayesian models to estimate rates of infant mortality due to congenital heart disease for all US counties. We mapped model-based estimates to explore geographical patterns. Covariates included infant sex, gestational age, maternal race and ethnicity, percentage of the county population below the poverty level, and proximity of the county to a US News & World Report 2015 top-50 ranked paediatric cardiac centre.

Findings

From 2006 to 2015, 40 847 089 livebirths occurred, of which there were 13 988 infant deaths attributed to congenital heart disease, with an unadjusted infant mortality rate due to CHD of 0·34 per 1000 livebirths (95% CI 0·34–0·35). Kentucky and Mississippi had the greatest proportions of counties with a predicted rate of infant mortality due to CHD above the 95th percentile. All counties in Connecticut, Massachusetts, and Rhode Island had a predicted rate below the fifth percentile. In the model, lower mortality risk correlated with closer proximity to a top-50 ranked paediatric cardiac centre (odds ratio [OR] 0·890, 95% credible interval [CrI] 0·840–0·942), whereas higher mortality risk correlated with higher levels of poverty (OR 1·181, 95% CrI 1·125–1·239).

Interpretation

Substantial geographical variation exists in infant mortality due to CHD in the USA, highlighting the potential importance of bolstering care delivery for infants from economically deprived communities and areas remote from top-performing paediatric cardiac centres.

Funding

None.
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