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Infant deaths from congenital anomalies: novel use of Child Death Overview Panel data
journal contributionposted on 2018-02-06, 16:55 authored by Catriona Firth, Emily PetherickEmily Petherick, Sam J. Oddie
Objective: We aimed to assess Child Death Overview Panel (CDOP) data validity, and cause of death classification, by comparison with information from a local birth cohort study (Born in Bradford, BiB), and another cause of death coding system (Causes of death and associated conditions – CODAC). We then aimed to use CDOP data to calculate ethnic specific IMRs, and compare characteristics of infants who died of congenital anomalies (CA) to those who died from other causes (non-CA). Design: Retrospective cohort study. Setting: Bradford Metropolitan District. Patients: All infant deaths, 2008 to 2013. Main outcome measures: Infant mortality rates from CA and non-CA causes. Results: 315 infant deaths were included, 56 of whom were BiB recruits. Agreement between CDOP and BiB was moderate to perfect for all characteristics except ethnicity, which showed weak agreement (kappa=0.58). The same deaths (27/56) were classified as CA by CDOP and CODAC. IMRs (per 1000 live births, 2009-2013) were highest in Pakistani infants (all causes 9.8, CA cause 5.5) compared with White British (all causes 4.3, CA cause 1.3), and Other infants (all causes 5.1, CA cause 1.4). In multivariate analysis, infants who died of CA cause were more likely to have been born at term (OR 3.18) and to consanguineous parents (OR 3.28) than infants who died of non-CA cause. Conclusions: Excess Pakistani mortality appears to be partly explained by an excess of deaths from CA, which in this population appears associated with a greater prevalence of consanguinity.
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Published inArchives of Disease in Childhood
CitationFIRTH, C., PETHERICK, E.S. and ODDIE, S.J., 2018. Infant deaths from congenital anomalies: novel use of Child Death Overview Panel data. Archives of Disease in Childhood, 103, pp. 1027-1032.
PublisherBMJ Publishing Group
- AM (Accepted Manuscript)
Publisher statementThis work is made available according to the conditions of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) licence. Full details of this licence are available at: https://creativecommons.org/licenses/by-nc-nd/4.0/
NotesThis paper was published in the journal Archives of Disease in Childhood and the definitive published version is available at http://dx.doi.org/10.1136/archdischild-2017-314256.