Database: Socialstyrelsen Cancer Registry (Sweden): Difference between revisions
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'''Data level:''' [[dataLevel::patient level]]. | '''Data level:''' [[dataLevel::patient level]]. | ||
'''Available data level:''' [[availableDataLevel::regional level]]. | '''Available data level:''' [[availableDataLevel::regional level]] and [[availableDataLevel::national level]]. | ||
'''Number of records:''' 60,000 cases registered every year. [https://www.healthinformationportal.eu/health-information-sources/swedish-national-cancer-register Click here to learn more]. | '''Number of records:''' 60,000 cases registered every year. [https://www.healthinformationportal.eu/health-information-sources/swedish-national-cancer-register Click here to learn more]. | ||
Revision as of 16:51, 19 May 2024
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Primary purpose: To map the occurrence and change of cancer diseases over time.
Sponsor, manager or home institution: Socialstyrelsen.
Type of information: Data Dictionary: Socialstyrelsen Cancer Registry. Click here to learn more.
Available type of information: number of diagnostics; Cases per 100,000; cancer incidence; age; sex; diagnosis, and year.
Source of Information: The data is sent from hospitals to six regional cancer centers for coding and registration. Once the material has been verified, it is then transmitted to the National Board of Health and Welfare to become part of the cancer registry. The registry is updated annually.
Data level: patient level.
Available data level: regional level and national level.
Number of records: 60,000 cases registered every year. Click here to learn more.
Date range: 1970 onwards.
Cancer areas of interest: C00-D48: All neoplasms. Click here to learn more.
Data access: partially publicly available: click here to access. Instructions to request data for restricted content: click here to learn more.
Contact information: Click here to learn more.
