Universidade Federal do Rio Grande Sul, Departamento de Genética, Porto Alegre, RS, Brasil.
Ministério da Saúde, Secretaria de Vigilância em Saúde, Brasília, DF, Brasil.
Epidemiol Serv Saude. 2020 Dec 4;29(5):e2020164. doi: 10.1590/S1679-49742020000500015. eCollection 2020.
To propose a list of congenital anomalies having corresponding codes in the International Statistical Classification of Diseases and Related Health Problems, 10thRevision (ICD-10), with the aim of applying it in health surveillance.
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.
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.
The codes contained in ICD-10 Chapter XVII do not capture the totality of congenital anomalies, indicating the need to adopt an expanded list.
提出一份包含国际疾病分类第十版（ICD-10）中相应编码的先天性畸形清单，旨在应用于健康监测。
2019 年 12 月，检索了以下数据源：ICD-10；ICD-11；三个监测计划监测的畸形；以及罕见疾病数据库（Orphanet）。从这些数据源中检索到畸形，进行处理以检查与 ICD-10 的对应关系，并进行手动审查以编制清单。
确定了 898 个代码，其中 619 个（68.9%）包含在 ICD-10 第十七章中。在其他章节中包含的 279 个代码中，有 19 个是 ICD-11 搜索独有的，72 个是监测计划独有的，79 个是 Orphanet 独有的，36 个是 ICD-10 中术语搜索独有的。
ICD-10 第十七章中包含的代码没有涵盖所有先天性畸形，表明需要采用扩展的清单。
