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Pharmacoepidemiol Drug Saf · Apr 2015
Historical ArticleAccuracy of ICD-9-CM coding to identify small for gestational age newborns.
- Kelesitse Phiri, Sonia Hernandez-Diaz, Lawrence C Tsen, Karen M Puopolo, John D Seeger, and Brian T Bateman.
- Department of Epidemiology, Harvard School of Public Health, Boston, MA, USA.
- Pharmacoepidemiol Drug Saf. 2015 Apr 1; 24 (4): 381-8.
PurposeThis study aimed to evaluate the accuracy of the International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) diagnosis code for small for gestational age (SGA) recorded in administrative healthcare records using birthweight and gestational age information recorded in electronic medical records.MethodsWe used billing and medical records from women aged 13-55 years who delivered at a tertiary care center in the USA between 2004 and 2011. Information on birthweight, gestational age at birth, and ICD-9-CM code for SGA, 656.5x, was abstracted from the database. Each infant's birthweight percentile for gestational age was calculated on the basis of published US references; infants below the 10th percentile were classified as SGA. The performance characteristics of SGA ICD-9-CM diagnosis code against SGA classification based on birthweight and gestational age were calculated, for all deliveries and by strata of demographic and delivery characteristics.ResultsWe identified 51 292 singleton live birth deliveries. The prevalence of SGA infants calculated from birthweight and gestational age at birth was higher (13%) than the prevalence based on ICD-9-CM code (2%). Sensitivity of the SGA ICD-9-CM code was 14.2%, specificity was 99.7%, positive predictive value was 86.8%, and negative predictive value was 88.4%. Stratification by demographic and delivery characteristics yielded similar results.ConclusionsIdentification of SGA infants using ICD-9-CM code, 656.5x, from administrative healthcare records has low sensitivity but high specificity; the accuracy did not differ across demographic and delivery characteristics. Thus, although this source of information would underestimate the prevalence of SGA, it could produce valid relative risk estimates.Copyright © 2015 John Wiley & Sons, Ltd.
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