viernes, 28 de junio de 2019

The German National Action League for people with rare diseases: translating the three tiers center system into active co-operation, a one center experience | Orphanet Journal of Rare Diseases | Full Text

The German National Action League for people with rare diseases: translating the three tiers center system into active co-operation, a one center experience | Orphanet Journal of Rare Diseases | Full Text



Orphanet Journal of Rare Diseases

The German National Action League for people with rare diseases: translating the three tiers center system into active co-operation, a one center experience

Orphanet Journal of Rare Diseases201914:158
  • Received: 12 April 2019
  • Accepted: 12 June 2019
  • Published: 

Abstract

Introduction

In 2009 the European Commission called for National action plans (NAP) to improve the care for persons with rare diseases. Germany set up a NAP in 2013 suggesting a three-tiered structure of co-operating centers (CC), centers of excellence (CE) and reference centers (CR). Since then CEs and CRs were organized in the framework of university hospitals. However, realization of CCs taking into account the requirements of the NAP has been slow. We therefore set-up a 12-months program to initiate co-operation and to support the development of structured CCs.

Methods

Our center invited 3000 physicians from Berlin and/or Brandenburg to participate. They were chosen either due to already referring patients with rare metabolic diseases to the center, residing in a neighborhood with diverse ethnic background, known to have a high prevalence for specific metabolic diseases, or working as a medical sub-specialist (gastroenterology, hematology, rheumatology) with a high probability to diagnose a rare metabolic disease. The center offered co-operation contracts, administrative and structured medical support, privileged access to the center for physicians and their patients, as well as a program of continuous medical education (CME) over a period of 12 months.

Results

Between 0.1 to 0.5% (mean 0.2%) of the invited physicians participated in CME meetings. None of them was interested in setting up a co-operating center. The physicians were interested in broadening their knowledge about rare diseases, but less so in direct care for these patients and not at all in fulfilling the requirements of the NAP.

Conclusions

The requirements of the NAP for CC are thought of as unrealistic due to their demands on structural re-organization, quality measurements and additional work-load for outpatient-care. Especially so, with respect for the low number of patients profiting from these efforts and the lack of re-imbursement. We suggest a reconsideration of the German NAP.

Keywords

  • Rare diseases
  • National action plan
  • Co-operation

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