Recommendations for optimal interdisciplinary management and healthcare settings for patients with rare neurological diseases

Author:

Graessner HolmORCID,Reinhard Carola,Bäumer Tobias,Baumgärtner Annette,Brockmann Knut,Brüggemann Norbert,Bültmann Eva,Erdmann Jeanette,Heise Kirstin,Höglinger Günter,Hüning Irina,Kaiser Frank J.,Klein Christine,Klopstock Thomas,Krägeloh-Mann Ingeborg,Kraemer Markus,Luedtke Kerstin,Mücke Martin,Musacchio Thomas,Nadke Andreas,Osmanovic Alma,Ritter Gabriele,Röse Katharina,Schippers Christopher,Schöls Ludger,Schüle Rebecca,Schulz Jörg B.,Sproß Joachim,Stasch Eveline,Wunderlich Gilbert,Münchau Alexander

Abstract

Abstract Background In 2017, the German Academy for Rare Neurological Diseases (Deutsche Akademie für Seltene Neurologische Erkrankungen; DASNE) was founded to pave the way for an optimized personalized management of patients with rare neurological diseases (RND) in all age groups. Since then a dynamic national network for rare neurological disorders has been established comprising renowned experts in neurology, pediatric neurology, (neuro-) genetics and neuroradiology. DASNE has successfully implemented case presentations and multidisciplinary discussions both at yearly symposia and monthly virtual case conferences, as well as further educational activities covering a broad spectrum of interdisciplinary expertise associated with RND. Here, we present recommendation statements for optimized personalized management of patients with RND, which have been developed and reviewed in a structured Delphi process by a group of experts. Methods An interdisciplinary group of 37 RND experts comprising DASNE experts, patient representatives, as well as healthcare professionals and managers was involved in the Delphi process. First, an online collection was performed of topics considered relevant for optimal patient care by the expert group. Second, a two-step Delphi process was carried out to rank the importance of the selected topics. Small interdisciplinary working groups then drafted recommendations. In two consensus meetings and one online review round these recommendations were finally consented. Results 38 statements were consented and grouped into 11 topics: health care structure, core neurological expertise and core mission, interdisciplinary team composition, diagnostics, continuous care and therapy development, case conferences, exchange / cooperation between Centers for Rare Diseases and other healthcare partners, patient advocacy group, databases, translation and health policy. Conclusions This German interdisciplinary Delphi expert panel developed consented recommendations for optimal care of patients with RND in a structured Delphi process. These represent a basis for further developments and adjustments in the health care system to improve care for patients with RND and their families.

Funder

Damp Stiftung

Bundesministerium für Bildung und Forschung

Eberhard Karls Universität Tübingen

Publisher

Springer Science and Business Media LLC

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