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A variety of genetically based health care innovations have already reached the marketplace, but information about the clinical use of these treatments and diagnostics is limited. Currently data do not provide information about how a genomic test impacts clinical care and patient health outcomes--other approaches are needed to garner such information.
This volume summarizes a workshop to address central questions related to the development of systems to evaluate clinical use of health care innovations that stem from genome-based research:
What are the practical realities of creating such systems?
What different models could be used?
What are the strengths and weaknesses of each model?
How effectively can such systems address questions about health outcomes?