Storm H H, Michelsen E V, Clemmensen I H, Pihl J
Department of Cancer Registration, Danish Cancer Society, København.
Dan Med Bull. 1997 Nov;44(5):535-9.
The Danish Cancer Registry is a population-based registry containing data on the incidence of cancer throughout Denmark since 1943. Reporting of cancer was made mandatory by administrative order in 1987. Details of individual cases of cancer are available according to the 7th revision of the International Classification of Diseases (ICD) for all years, and according to the ICD-O since 1978. A core data set is kept on each individual which includes date of birth, sex, date of cancer diagnosis, method of verification, date of death and cause of death. This paper describes the history of the registry, its data sources and its procedures, including quality control and access to data. Integration of both research activities and registration since the inception of the Registry has maintained the completeness and validity of the data for 1943-1996.
丹麦癌症登记处是一个基于人群的登记机构，自1943年起记录丹麦全国的癌症发病率。1987年，行政命令规定癌症报告为强制性。所有年份的癌症个案详情均按照《国际疾病分类》第7版记录，自1978年起按照国际疾病分类肿瘤学专辑记录。每个个体都有一个核心数据集，包括出生日期、性别、癌症诊断日期、核实方法、死亡日期和死亡原因。本文介绍了该登记处的历史、数据来源及其程序，包括质量控制和数据访问。自登记处成立以来，研究活动与登记工作的整合保持了1943 - 1996年数据的完整性和有效性。
