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[Foundations for the scientific use of extensive health care data in Germany-results of the Data Sharing working group of the Medical Informatics Initiative]. / Grundlagen für die wissenschaftliche Nutzung umfangreicher Versorgungsdaten in Deutschland ­ Ergebnisse der AG Data Sharing der Medizininformatik-Initiative.
Kirsten, Toralf; Kleinert, Philip; Gebhardt, Marie; Drepper, Johannes; Andreeff, Anne-Katrin; Prasser, Fabian; Kohlbacher, Oliver.
Afiliação
  • Kirsten T; Institut für Medizinische Informatik, Statistik und Epidemiologie, Universität Leipzig, Leipzig, Deutschland.
  • Kleinert P; Medizininformatikzentrum, Dept. Medical Data Science, Universitätsklinikum Leipzig, Leipzig, Deutschland.
  • Gebhardt M; TMF - Technologie- und Methodenplattform für die vernetzte medizinische Forschung e. V., Berlin, Berlin, Deutschland.
  • Drepper J; TMF - Technologie- und Methodenplattform für die vernetzte medizinische Forschung e. V., Berlin, Berlin, Deutschland.
  • Andreeff AK; TMF - Technologie- und Methodenplattform für die vernetzte medizinische Forschung e. V., Berlin, Berlin, Deutschland.
  • Prasser F; Institut für Medizinische Informatik und Biometrie, Medizinische Fakultät Carl Gustav Carus der Technischen Universität Dresden, Dresden, Deutschland.
  • Kohlbacher O; Center of Health Data Science, Medizininformatik, Berliner Institut für Gesundheitsforschung in der Charité - Universitätsmedizin Berlin, Berlin, Deutschland.
Article em De | MEDLINE | ID: mdl-38684526
ABSTRACT
Healthcare data are an important resource in applied medical research. They are available multicentrically. However, it remains a challenge to enable standardized data exchange processes between federal states and their individual laws and regulations. The Medical Informatics Initiative (MII) was founded in 2016 to implement processes that enable cross-clinic access to healthcare data in Germany. Several working groups (WGs) have been set up to coordinate standardized data structures (WG Interoperability), patient information and declarations of consent (WG Consent), and regulations on data exchange (WG Data Sharing). Here we present the most important results of the Data Sharing working group, which include agreed terms of use, legal regulations, and data access processes. They are already being implemented by the established Data Integration Centers (DIZ) and Use and Access Committees (UACs). We describe the services that are necessary to provide researchers with standardized data access. They are implemented with the Research Data Portal for Health, among others. Since the pilot phase, the processes of 385 active researchers have been used on this basis, which, as of April 2024, has resulted in 19 registered projects and 31 submitted research applications.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Disseminação de Informação / Registros Eletrônicos de Saúde Limite: Humans País/Região como assunto: Europa Idioma: De Revista: Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz Assunto da revista: SAUDE PUBLICA Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Disseminação de Informação / Registros Eletrônicos de Saúde Limite: Humans País/Região como assunto: Europa Idioma: De Revista: Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz Assunto da revista: SAUDE PUBLICA Ano de publicação: 2024 Tipo de documento: Article