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Case fatality among infants with congenital malformations by lethality

✍ Scribed by Kirk A. Bol; Russel S. Rickard; Russell S. Kirby


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
90 KB
Volume
70
Category
Article
ISSN
1542-0752

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✦ Synopsis


Abstract

OBJECTIVE

Infant mortality rates continue to show that congenital anomalies are the leading cause of infant death in the United States. However, studies of factors contributing to increased mortality across different types of congenital anomalies have been limited. The objective of this study was to assess whether the likelihood of infant mortality varied by maternal race and ethnic group while considering the severity of the birth defect.

METHODS

A retrospective cohort analysis was conducted using data from Colorado's statewide, population‐based birth defects surveillance system (CRCSN). The cohort included infants, born between 1995 and 2000 to Colorado resident mothers, who were diagnosed with major congenital malformations stratified by degree of lethality. Multiple logistic regression was performed for each level of lethality, and included the following potential explanatory variables: maternal race/ethnicity, clinical gestation, birth weight, maternal education level, maternal age, and sex of child.

RESULTS

Within the low/very low lethality cohort, maternal race/ethnicity of Black/non‐Hispanic was associated with increased risk of infant mortality, OR 2.81 (1.41–5.19), as were low and very low birth weight, OR 2.21 (1.12–4.04) and 19.31 (11.84–31.01), respectively. Maternal race/ethnicity was not a significant risk factor in either high or very high lethality groups; however, the interaction between birth weight and gestational age significantly increased the risk of mortality.

CONCLUSIONS

Through the use of statewide, population‐based birth defects surveillance data, a disparity in infant mortality has been identified in a specific subset of the population that could be investigated further and targeted for prevention activities. Birth Defects Research (Part A) 70:580–585, 2004. © 2004 Wiley‐Liss, Inc.


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