Abstract
Objective: To propose a list of congenital anomalies having corresponding codes in the International Statistical Classification of Diseases and Related Health Problems, 10th Revision (ICD-10), with the aim of applying it in health surveillance. Methods: In December 2019, the following data sources were searched: ICD-10; ICD-11; anomalies monitored by three surveillance programs; and a database of rare diseases (Orphanet). Anomalies were retrieved from these data sources, processed to check for correspondence with ICD-10 and reviewed manually to compile the list. Results: 898 codes were identified, of which 619 (68.9%) were contained in ICD-10 Chapter XVII. Of the 279 codes contained in other chapters, 19 were exclusive to the ICD-11 search, 72 to the surveillance programs, 79 to Orphanet and 36 to the search for terms in ICD-10. Conclusion: The codes contained in ICD-10 Chapter XVII do not capture the totality of congenital anomalies, indicating the need to adopt an expanded list.
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Bremm, J. M., Cardoso-dos-Santos, A. C., Magalhães, V. S., Medeiros-de-Souza, A. C., Alves, R. F. S., de Araujo, V. E. M., … de França, G. V. A. (2020). Congenital anomalies from the health surveillance perspective: Compilation of a list based on ICD-10. Epidemiologia e Servicos de Saude, 29(5). https://doi.org/10.1590/S1679-49742020000500015
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