Database: National Oncology Drugs Management System (Ireland): Difference between revisions
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'''Date range:''' Data collection started in September [[dataStart::2012]], and reporting procedure began in April 2013 [[dataEnd::onwards]]. | '''Date range:''' Data collection started in September [[dataStart::2012]], and reporting procedure began in April 2013 [[dataEnd::onwards]]. | ||
'''Cancer areas of interest:''' [[ | '''Cancer areas of interest:''' [[hasCancerType::C00-D48: All neoplasms]]. | ||
'''Data access:''' [[dataAvailability::not publicly available]]. Instructions to request data for restricted content [https://www.hse.ie/eng/staff/pcrs/pcrs-publications/ click here to access]. | '''Data access:''' [[dataAvailability::not publicly available]]. Instructions to request data for restricted content [https://www.hse.ie/eng/staff/pcrs/pcrs-publications/ click here to access]. | ||
'''Contact information:''' [https://www.hiqa.ie/areas-we-work/health-information/data-collections/national-oncology-drugs-management-system Click here to access]. | '''Contact information:''' [https://www.hiqa.ie/areas-we-work/health-information/data-collections/national-oncology-drugs-management-system Click here to access]. | ||
Revision as of 19:35, 17 May 2024
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Primary purpose: To organize and oversee the utilization of cancer medications nationally.
Sponsor, manager or home institution: National Cancer Control Programme (NCCP); Health Service Executive; National Cancer Drug Management Programme; Primary Care Reimbursement Service (PCRS).
Type of information: Patient demographics, usage of cancer drugs, and expenditures on cancer medications; Other patients' information comprises their name, date of birth, gender, address, and contact details (if provided), as well as their PPS or medical card number or long-term illness card number (if available). Click here to learn more.
Source of Information: The hospital personnel enters the necessary data into an internet-based system supervised and run by PCRS. PCRS provides NCCP with anonymous and combined reports generated from the system. The data is gathered every month.
Data level: patient level.
Number of records: 21,030 claims submitted – 2021; 17,019 claims submitted – 2020; 15,640 claims submitted - 2019.
Date range: Data collection started in September 2012, and reporting procedure began in April 2013 onwards.
Cancer areas of interest: C00-D48: All neoplasms.
Data access: not publicly available. Instructions to request data for restricted content click here to access.
Contact information: Click here to access.
