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Recommended data elements for health registries: a survey from a German funding initiative.
Harkener, Sonja; Jenetzky, Ekkehart; Rupp, Rüdiger; Dell, Jennifer; Engel, Christoph; von Bargen, Maximilian Ferry; Finger, Robert; Glienke, Maximilian; Heinz, Carsten; Jersch, Patrick; Martin, David; Schmutzler, Rita; Schönthaler, Martin; Suwelack, Barbara; Wegner, Jeannine; Stausberg, Jürgen.
Afiliación
  • Harkener S; Faculty of Medicine, University Duisburg-Essen, IMIBE, Essen, Germany.
  • Jenetzky E; Faculty of Health/School of Medicine, Witten/Herdecke University, Witten, Germany.
  • Rupp R; University Medical Center of the Johannes-Gutenberg-University, Mainz, Germany.
  • Dell J; Spinal Cord Injury Center, Heidelberg University Hospital, Heidelberg, Germany.
  • Engel C; Department of Ophthalmology, University Hospital Bonn, Bonn, Germany.
  • von Bargen MF; Leipzig University, IMISE, Leipzig, Germany.
  • Finger R; Department of Urology, Faculty of Medicine, Medical Centre - University of Freiburg, University of Freiburg, Freiburg, Germany.
  • Glienke M; Department of Ophthalmology, University Hospital Mannheim, Mannheim, Germany.
  • Heinz C; Department of Urology, Faculty of Medicine, Medical Centre - University of Freiburg, University of Freiburg, Freiburg, Germany.
  • Jersch P; Department of Ophthalmology, St. Franziskus-Hospital Münster, Münster, Germany.
  • Martin D; Department of Ophthalmology at University Essen, Essen, Germany.
  • Schmutzler R; Spinal Cord Injury Center, Heidelberg University Hospital, Heidelberg, Germany.
  • Schönthaler M; Faculty of Health/School of Medicine, Witten/Herdecke University, Witten, Germany.
  • Suwelack B; Department of Pediatrics, Eberhard-Karls University Tübingen, Tübingen, Germany.
  • Wegner J; Center for Familial Breast and Ovarian Cancer, University of Cologne, Cologne, Germany.
  • Stausberg J; Department of Urology, Faculty of Medicine, Medical Centre - University of Freiburg, University of Freiburg, Freiburg, Germany.
BMC Med Inform Decis Mak ; 24(1): 136, 2024 May 27.
Article en En | MEDLINE | ID: mdl-38802886
ABSTRACT

BACKGROUND:

The selection of data elements is a decisive task within the development of a health registry. Having the right metadata is crucial for answering the particular research questions. Furthermore, the set of data elements determines the registries' readiness of interoperability and data reusability to a major extent. Six health registries shared and published their metadata within a German funding initiative. As one step in the direction of a common set of data elements, a selection of those metadata was evaluated with regard to their appropriateness for a broader usage.

METHODS:

Each registry was asked to contribute a 10%-selection of their data elements to an evaluation sample. The survey was set up with the online survey tool "LimeSurvey Cloud". The registries and an accompanying project participated in the survey with one vote for each project. The data elements were offered in content groups along with the question of whether the data element is appropriate for health registries on a broader scale. The question could be answered using a Likert scale with five options. Furthermore, "no answer" was allowed. The level of agreement was assessed using weighted Cohen's kappa and Kendall's coefficient of concordance.

RESULTS:

The evaluation sample consisted of 269 data elements. With a grade of "perhaps recommendable" or higher in the mean, 169 data elements were selected. These data elements belong preferably to groups' demography, education/occupation, medication, and nutrition. Half of the registries lost significance compared with their percentage of data elements in the evaluation sample, one remained stable. The level of concordance was adequate.

CONCLUSIONS:

The survey revealed a set of 169 data elements recommended for health registries. When developing a registry, this set could be valuable help in selecting the metadata appropriate to answer the registry's research questions. However, due to the high specificity of research questions, data elements beyond this set will be needed to cover the whole range of interests of a register. A broader discussion and subsequent surveys are needed to establish a common set of data elements on an international scale.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sistema de Registros Límite: Humans País/Región como asunto: Europa Idioma: En Revista: BMC Med Inform Decis Mak Asunto de la revista: INFORMATICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Sistema de Registros Límite: Humans País/Región como asunto: Europa Idioma: En Revista: BMC Med Inform Decis Mak Asunto de la revista: INFORMATICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Alemania