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Guideline “Motor neuron diseases” of the German Society of Neurology (Deutsche Gesellschaft für Neurologie)
INTRODUCTION: In 2021, the Deutsche Gesellschaft für Neurology published a new guideline on diagnosis and therapy of motor neuron disorders. Motor neuron disorders affect upper motor neurons in the primary motor cortex and/or lower motor neurons in the brain stem and spinal cord. The most frequent m...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10268388/ https://www.ncbi.nlm.nih.gov/pubmed/37316950 http://dx.doi.org/10.1186/s42466-023-00251-x |
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author | Petri, Susanne Grehl, Torsten Grosskreutz, Julian Hecht, Martin Hermann, Andreas Jesse, Sarah Lingor, Paul Löscher, Wolfgang Maier, André Schoser, Benedikt Weber, Marcus Ludolph, Albert C. |
author_facet | Petri, Susanne Grehl, Torsten Grosskreutz, Julian Hecht, Martin Hermann, Andreas Jesse, Sarah Lingor, Paul Löscher, Wolfgang Maier, André Schoser, Benedikt Weber, Marcus Ludolph, Albert C. |
author_sort | Petri, Susanne |
collection | PubMed |
description | INTRODUCTION: In 2021, the Deutsche Gesellschaft für Neurology published a new guideline on diagnosis and therapy of motor neuron disorders. Motor neuron disorders affect upper motor neurons in the primary motor cortex and/or lower motor neurons in the brain stem and spinal cord. The most frequent motor neuron disease amyotrophic lateral sclerosis (ALS) is a rapidly progressive disease with an average life expectancy of 2–4 years with a yearly incidence of 3.1/100,000 in Central Europe (Rosenbohm et al. in J Neurol 264(4):749–757, 2017. 10.1007/s00415-017-8413-3). It is considered a rare disease mainly due to its low prevalence as a consequence of short disease duration. RECOMMENDATIONS: These guidelines comprise recommendations regarding differential diagnosis, neuroprotective therapies and multidisciplinary palliative care including management of respiration and nutrition as well as provision of assistive devices and end-of-life situations. CONCLUSION: Diagnostic and therapeutic guidelines are necessary due the comparatively high number of cases and the aggressive disease course. Given the low prevalence and the severe impairment of patients, it is often impossible to generate evidence-based data so that ALS guidelines are partially dependent on expert opinion. |
format | Online Article Text |
id | pubmed-10268388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102683882023-06-15 Guideline “Motor neuron diseases” of the German Society of Neurology (Deutsche Gesellschaft für Neurologie) Petri, Susanne Grehl, Torsten Grosskreutz, Julian Hecht, Martin Hermann, Andreas Jesse, Sarah Lingor, Paul Löscher, Wolfgang Maier, André Schoser, Benedikt Weber, Marcus Ludolph, Albert C. Neurol Res Pract Guidelines INTRODUCTION: In 2021, the Deutsche Gesellschaft für Neurology published a new guideline on diagnosis and therapy of motor neuron disorders. Motor neuron disorders affect upper motor neurons in the primary motor cortex and/or lower motor neurons in the brain stem and spinal cord. The most frequent motor neuron disease amyotrophic lateral sclerosis (ALS) is a rapidly progressive disease with an average life expectancy of 2–4 years with a yearly incidence of 3.1/100,000 in Central Europe (Rosenbohm et al. in J Neurol 264(4):749–757, 2017. 10.1007/s00415-017-8413-3). It is considered a rare disease mainly due to its low prevalence as a consequence of short disease duration. RECOMMENDATIONS: These guidelines comprise recommendations regarding differential diagnosis, neuroprotective therapies and multidisciplinary palliative care including management of respiration and nutrition as well as provision of assistive devices and end-of-life situations. CONCLUSION: Diagnostic and therapeutic guidelines are necessary due the comparatively high number of cases and the aggressive disease course. Given the low prevalence and the severe impairment of patients, it is often impossible to generate evidence-based data so that ALS guidelines are partially dependent on expert opinion. BioMed Central 2023-06-15 /pmc/articles/PMC10268388/ /pubmed/37316950 http://dx.doi.org/10.1186/s42466-023-00251-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Guidelines Petri, Susanne Grehl, Torsten Grosskreutz, Julian Hecht, Martin Hermann, Andreas Jesse, Sarah Lingor, Paul Löscher, Wolfgang Maier, André Schoser, Benedikt Weber, Marcus Ludolph, Albert C. Guideline “Motor neuron diseases” of the German Society of Neurology (Deutsche Gesellschaft für Neurologie) |
title | Guideline “Motor neuron diseases” of the German Society of Neurology (Deutsche Gesellschaft für Neurologie) |
title_full | Guideline “Motor neuron diseases” of the German Society of Neurology (Deutsche Gesellschaft für Neurologie) |
title_fullStr | Guideline “Motor neuron diseases” of the German Society of Neurology (Deutsche Gesellschaft für Neurologie) |
title_full_unstemmed | Guideline “Motor neuron diseases” of the German Society of Neurology (Deutsche Gesellschaft für Neurologie) |
title_short | Guideline “Motor neuron diseases” of the German Society of Neurology (Deutsche Gesellschaft für Neurologie) |
title_sort | guideline “motor neuron diseases” of the german society of neurology (deutsche gesellschaft für neurologie) |
topic | Guidelines |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10268388/ https://www.ncbi.nlm.nih.gov/pubmed/37316950 http://dx.doi.org/10.1186/s42466-023-00251-x |
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