Database: Andmebaas Cancer Registry (Estonia): Difference between revisions
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
'''Sponsor, manager or home institution:''' The Health Statistics and Health Research Database; The National Institute for Health Development. | '''Sponsor, manager or home institution:''' The Health Statistics and Health Research Database; The National Institute for Health Development. | ||
Revision as of 19:24, 13 November 2023
Sponsor, manager or home institution: The Health Statistics and Health Research Database; The National Institute for Health Development.
Primary purpose: The main task of the cancer registry is to ensure the most complete and reliable registration of cancer cases.
Type of information: Data Dictionary: Andmebaas Cancer Registry[1].
Available type of information: Andmebaas Cancer Registry [2].
Source of Information: Data is updated from the Estonian population register (personal data, including time of leaving the country) from the register of causes of death (death data, including the cause of death). Reporting cancer cases is mandatory for all doctors working in Estonia who diagnose or treat cancer. Forensic experts also submit data to the register.
Data level: Patient level.
Number of Records: Unknown.
Date Range: 1968 onwards.
Cancer Areas of Interest: All malignant tumors (C00-C97); Tumors in situ (D00–D09); Benign and unclear and unspecified tumors of the brain and central nervous system, as well as endocrine glands located in the brain region (D32.0–D33.9, D35.2–D35.4, D42.0–D43.9, D44.3–D44.5); Other neoplasms of lymphoid and hematopoietic tissue and similar tissues (D45-D47).
Data access: Partially publicly available [3], to access go to Population > Morbidity > Malignant neoplasms. Instructions to request data for restricted content [4].
Contact information: Information [5].