Zoekresultaten - 6 results
Methodological choices in brucellosis burden of disease assessments: A systematic review
Most studies retrieved brucellosis epidemiological data from administrative registries. Incidence data were often estimated on the basis of laboratory-confirmed tests. Not all studies included mortality ...
Burden of non-communicable disease studies in Europe: a systematic review of data sources and methodological choices
Morbidity data were frequently (40%) drawn from routine administrative and survey datasets, including disease registries and hospital discharge databases. The majority (60%) of national BoD studies reported ...
The non-fatal burden of cancer in Belgium, 2004–2019: a nationwide registry-based study
registry data and international disease models. We developed a microsimulation model to translate incidence- into prevalence-based estimates, and used expert elicitation to integrate the long-term impact of ...
Conducting national burden of disease studies in small countries in Europe– a feasible challenge?
expertise, and engage with countries and institutions that have long-standing experience with BoD assessment. Conclusion Apart from mortality registries, adequate health data sources, notably for cancer, are ...
Melanoma burden by melanoma stage: Assessment through a disease transition model
The model was applied to a large cohort of 8016 melanoma patients recorded by the Belgian Cancer Registry for incidence years 2009-2011. DALY s were calculated for each American Joint Committee on ...
The burden of cystic fibrosis in Belgium: a registry-based study
elaborate the disease burden of cystic fibrosis in Belgium. Methodology: The Belgian Cystic Fibrosis Registry provides data concerning cystic fibrosis patients in Belgium. These data are used as the primary ...