Reports: Swedish Palliative Registry (Sweden): Difference between revisions
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'''Sponsor, manager or home institution:''' Svenska Palliativ Registret. | '''Sponsor, manager or home institution:''' [[dataOwner::Svenska Palliativ Registret]]. | ||
'''Primary purpose:''' To improve end-of-life care for patients and their relatives by collecting data on care quality, identifying areas for improvement, and providing knowledge support for healthcare professionals, with research based on the registry's results. | '''Primary purpose:''' To improve end-of-life care for patients and their relatives by collecting data on care quality, identifying areas for improvement, and providing knowledge support for healthcare professionals, with research based on the registry's results. | ||
'''Type of information:''' General and specialized [[availableVariable::palliative care]]; Quality assurance; National care plan; Indicators; Coverage; Survival and death interview; Care in numbers. | '''Type of information:''' General and specialized [[availableVariable::palliative care]]; Quality assurance; National care plan; Indicators; Coverage; Survival and death interview; Care in numbers. [https://www.palliativregistret.se/arkiv/arsrapporter/ Click here to learn more]. | ||
'''Data level:''' [[dataLevel::national level]]. | '''Data level:''' [[dataLevel::national level]]. | ||
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'''Cancer areas of interest:''' [[hasCancerType::C00-D48: All neoplasms]]. [https://www.palliativregistret.se/ Click here to learn more]. | '''Cancer areas of interest:''' [[hasCancerType::C00-D48: All neoplasms]]. [https://www.palliativregistret.se/ Click here to learn more]. | ||
'''Access to information:''' [https://www.palliativregistret.se/arkiv/arsrapporter/ Click here to | '''Access to information:''' [https://www.palliativregistret.se/arkiv/arsrapporter/ Click here to access]. | ||
Revision as of 17:50, 11 July 2024
Go back to Sweden page
Sponsor, manager or home institution: Svenska Palliativ Registret.
Primary purpose: To improve end-of-life care for patients and their relatives by collecting data on care quality, identifying areas for improvement, and providing knowledge support for healthcare professionals, with research based on the registry's results.
Type of information: General and specialized palliative care; Quality assurance; National care plan; Indicators; Coverage; Survival and death interview; Care in numbers. Click here to learn more.
Data level: national level.
Cancer areas of interest: C00-D48: All neoplasms. Click here to learn more.
Access to information: Click here to access.
