Database: National Oncology Drugs Management System (Ireland): Difference between revisions
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'''Sponsor, manager or home institution:''' [[dataOwner::National Cancer Control Programme (NCCP)]]; [[dataOwner::Health Service Executive]]; [[dataOwner::National Cancer Drug Management Programme]]; [[dataOwner::Primary Care Reimbursement Service (PCRS)]]. | '''Sponsor, manager or home institution:''' [[dataOwner::National Cancer Control Programme (NCCP)]]; [[dataOwner::Health Service Executive]]; [[dataOwner::National Cancer Drug Management Programme]]; [[dataOwner::Primary Care Reimbursement Service (PCRS)]]. | ||
'''Type of information:''' [[databaseStructure::longitudinal]]. Data dictionary is not available. Patient demographics, [[hasVariable::number of drugs]], usage of [[hasVariable:: | '''Type of information:''' [[databaseStructure::longitudinal]]. Data dictionary is not available. Patient demographics, [[hasVariable::number of drugs]], usage of [[hasVariable::medication use|cancer drugs]], and [[hasVariable::healthcare costs|expenditures on cancer medications]]; Other patients' information comprises their name, [[hasVariable::age|date of birth]], [[hasVariable::sex]], [[hasVariable::place of residence|address]], and contact details (if provided), as well as their PPS or medical card number or long-term illness card number (if available). [https://www.hiqa.ie/areas-we-work/health-information/data-collections/national-oncology-drugs-management-system 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. | '''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. | ||
Revision as of 22:20, 23 June 2024
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Type of database: administrative/claims data.
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: longitudinal. Data dictionary is not available. Patient demographics, number of drugs, usage of cancer drugs, and expenditures on cancer medications; Other patients' information comprises their name, date of birth, sex, 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.