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1000 Titel
  • Potentials and current shortcomings in the cooperation between German centers for rare diseases and primary care physicians: results from the project TRANSLATE-NAMSE
1000 Autor/in
  1. Druschke, Diana |
  2. Krause, F. |
  3. Müller, G. |
  4. Scharfe, J. |
  5. Hoffmann, G. F. |
  6. Schmitt, J. |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-11-24
1000 Erschienen in
1000 Quellenangabe
  • 16(1):494
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13023-021-02106-7 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611963/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!The TRANSLATE-NAMSE project with the strengthening of the centers for rare diseases with their affiliation to the European Reference Networks was a major step towards the implementation of the German National Plan of Action for People with Rare Diseases establishing better care structures. As primary care physicians, general practitioners and pediatricians play a central role in the diagnosis of patients with rare disease, as it is usually them referring to specialists and rare disease centers. Therefore, the interface management between primary care physicians and the centers for rare diseases is of particular importance.!##!Methods!#!In a mixed-method-approach an anonymous postal survey of 1,500 randomly selected primary care physicians in Germany was conducted with focus on (1) knowledge about a center for rare diseases and how it works, (2) in case of cooperation, satisfaction with the services provided by centers, and (3) expectations and needs they have with regard to the centers. In addition, in-depth telephone interviews were conducted with physicians who had already referred patients to a center.!##!Results!#!In total, 248 physicians responded to the survey, and 15 primary care physicians were interviewed. We observed a wide lack of knowledge about the existence of (45.6% confirmed to know at least one center) about how to access rare disease centers (50.4% of those who know a center confirmed knowledge) and what the center specializes in. In case of cooperation the evaluation was mostly positive.!##!Conclusion!#!To improve medical care, the interplay between primary care physicians and rare disease centers needs to be strengthened. (1) To improve the communication, the objectives and functioning of the rare disease centers should become more visible. (2) Other projects dealing with the analysis and improvement of interface management between centers and primary care physicians, as described in the National Plan of Action for People with Rare Diseases, need to be implemented immediately. (3) If the project is evaluated positively, the structures of TRANSLATE-NAMSE should be introduced nationwide into the German health care system to ensure comprehensive, quality-assured care for people with rare diseases with special consideration of the key role of primary care physicians-also taking into account the financial expenditures of this new care model.
1000 Sacherschließung
lokal Surveys and Questionnaires [MeSH]
lokal Humans [MeSH]
lokal Delivery of Health Care [MeSH]
lokal Interface management
lokal Registries/ Health Planning/ Health Services
lokal Physicians, Primary Care [MeSH]
lokal TRANSLATE-NAMSE
lokal Centers for rare diseases
lokal General practitioners
lokal Research
lokal Germany [MeSH]
lokal Pediatricians
lokal Rare Diseases/diagnosis [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-6365-1404|https://frl.publisso.de/adhoc/uri/S3JhdXNlLCBGLg==|https://frl.publisso.de/adhoc/uri/TcO8bGxlciwgRy4=|https://frl.publisso.de/adhoc/uri/U2NoYXJmZSwgSi4=|https://frl.publisso.de/adhoc/uri/SG9mZm1hbm4sIEcuIEYu|https://frl.publisso.de/adhoc/uri/U2NobWl0dCwgSi4=
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