Database: Socialstyrelsen National Patient Register (Sweden): Difference between revisions
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'''Sponsor, manager or home institution:''' [[dataOwner::Socialstyrelsen]]. | '''Sponsor, manager or home institution:''' [[dataOwner::Socialstyrelsen]]. | ||
Revision as of 17:25, 5 December 2023
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Sponsor, manager or home institution: Socialstyrelsen.
Primary purpose: The patient register serves multiple purposes. One of its main functions is to track the health development of the population over an extended period. In doing so, it helps to improve the possibilities of preventing and treating diseases. Additionally, the patient register contributes to the overall development of healthcare by providing valuable data and insights. It also enables healthcare providers to monitor the quality of their operations and identify areas where improvements may be needed.
Type of information: Data Dictionary: Socialstyrelsen National Patient Register. Full list of variables [1].
Source of Information: Healthcare providers must submit patient information to the patient register monthly, including hospital code and medical area. Data is submitted via a reporting portal or register service.
Data level: patient level.
Number of Records: unknown.
Date Range: 1964 onwards.
Cancer Areas of Interest: unknown.
Data access: not publicly available. Instructions to request data for restricted content [2].
Contact information: Information [3].