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

Authors :
Holm Graessner
Carola Reinhard
Tobias Bäumer
Annette Baumgärtner
Knut Brockmann
Norbert Brüggemann
Eva Bültmann
Jeanette Erdmann
Kirstin Heise
Günter Höglinger
Irina Hüning
Frank J. Kaiser
Christine Klein
Thomas Klopstock
Ingeborg Krägeloh-Mann
Markus Kraemer
Kerstin Luedtke
Martin Mücke
Thomas Musacchio
Andreas Nadke
Alma Osmanovic
Gabriele Ritter
Katharina Röse
Christopher Schippers
Ludger Schöls
Rebecca Schüle
Jörg B. Schulz
Joachim Sproß
Eveline Stasch
Gilbert Wunderlich
Alexander Münchau
Source :
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-9 (2024)
Publication Year :
2024
Publisher :
BMC, 2024.

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.

Details

Language :
English
ISSN :
17501172
Volume :
19
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Orphanet Journal of Rare Diseases
Publication Type :
Academic Journal
Accession number :
edsdoj.4649b5a064957935d72b149d0ec67
Document Type :
article
Full Text :
https://doi.org/10.1186/s13023-024-03023-1