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Data Collection
The patient
NCRI collects information on the diagnosis and primary treatment of the patient’s cancer. Data is collected on primary treatments that take place within approximately 12 months of … -
Data Collection
Quality assurance
Quality assurance measures are implemented at every stage of the data journey, from when the data is imported into the system to the time a tumour is closed on the system. … -
Data Collection
Data sources
NCRI obtains its data from a number of sources. The majority of notifications to NCRI come from histopathology laboratories. The remainder comes from sources such as the Hospital In-Patient Enquiry (HIPE) system, death certificates and … -
Reports & Publications
Cancer projections 2005-2035
This report presents extrapolations of National Cancer Registry incidence data for 1994-2006 to the years 2010-2035. Between 2005 and 2035, the overall number of invasive cancers is projected to increase by 17,063 (165%, 6% annually) for females and by …Publication date -
Data Collection
The data journey
The data journey refers to the various stages through which an organisation’s data moves from collection to use. Here is a detailed look at the data journey of the National Cancer Registry. … -
Data Collection
Record linkage
Once the data has been imported and put into the correct format, new registrations are created or existing registrations updated. … -
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Reports & Publications
Cancer trends - Cancers of the brain and central nervous system
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Reports & Publications
Cancer in Ireland 1994-2012: Annual Report of the National Cancer Registry
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Reports & Publications
Cancer in Ireland 1994-2018 with Estimates for 2018-2020: Annual Report of the National Cancer Registry
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Reports & Publications
Cancer in Ireland 1994-2020: Annual Statistical Report of the National Cancer Registry
Over 50% increase in numbers of cancer survivors compared with a decade ago …Publication date