Dödsorsaksregistret

Dödsorsaksregistret, which translates to the Cause of Death Register, is a national registry maintained in Sweden. Its primary purpose is to collect and process information on the causes of death for all individuals who die in Sweden. This data is crucial for public health monitoring, epidemiological research, and the compilation of national statistics.

The register is managed by the National Board of Health and Welfare (Socialstyrelsen). Medical professionals, primarily physicians, are responsible for certifying the cause of death on a death certificate. This information is then reported to the Dödsorsaksregistret. The data collected includes not only the immediate cause of death but also underlying and contributing factors, as well as demographic information about the deceased.

The information within the Dödsorsaksregistret is used for various analytical purposes. It helps track mortality trends, identify public health challenges, and evaluate the effectiveness of health interventions. Researchers utilize the anonymized data to study diseases, risk factors, and patterns of mortality across different populations and time periods. The register plays a vital role in informing health policy decisions and resource allocation in Sweden. Access to the detailed data is restricted to authorized personnel and researchers for specific studies, ensuring the privacy of individuals while maximizing the utility of the information for public good.