INTRODUCTION: A National Diabetes Register was established in the National Board of Health in 2006 following a pilot study showing the feasibility of doing so based on existing registers. CONTENT: The register contains data of birth, date of inclusion, and date of death as well as information on the criteria met for inclusion. VALIDITY AND COVERAGE: The register is more than 90% complete when compared to records of general practitioners, and it covers the entire Danish population. CONCLUSION: The register is a source of demographic information for the diabetes population in itself, but also a source of linkable information for studies of diabetes as outcome and as determinant.
INTRODUCTION: A National Diabetes Register was established in the National Board of Health in 2006 following a pilot study showing the feasibility of doing so based on existing registers. CONTENT: The register contains data of birth, date of inclusion, and date of death as well as information on the criteria met for inclusion. VALIDITY AND COVERAGE: The register is more than 90% complete when compared to records of general practitioners, and it covers the entire Danish population. CONCLUSION: The register is a source of demographic information for the diabetes population in itself, but also a source of linkable information for studies of diabetes as outcome and as determinant.
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