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To be called Version 9
yes correct AJCC Version 9- old habits...and thank you
Galaxy S7 edge
Just to emphasize - it seems we struggle to accurately follow a patient through a network of care using current NCDB tools.
Some Cancer Registry vendors do allow reporting mutually exclusive patients one time with information from all sites within an INCP or large organization. It would help if NCDB would require demographics for merging pts so full information and end-results can be obtained.
It is equally if not more important for patients that travel between networks.
Are clinical pathways important in the future for tracking patients through the staging an treatment process and generating data?
If a single National Patient Identifier can be achieved, then NCDB should consider and two way data exchange to assist with closing the treatment loop for patient who seek treatment at other facilities which would reduce cancer registry burden