European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERNEURO‐NMD)

Author:

Van Damme Philip1ORCID,Al‐Chalabi Ammar2ORCID,Andersen Peter M.3,Chiò Adriano45ORCID,Couratier Philippe6ORCID,De Carvalho Mamede7ORCID,Hardiman Orla8ORCID,Kuźma‐Kozakiewicz Magdalena9ORCID,Ludolph Albert10,McDermott Christopher J.11ORCID,Mora Jesus S.12,Petri Susanne13ORCID,Probyn Katrin14,Reviers Evy15,Salachas François16,Silani Vincenzo1718ORCID,Tysnes Ole‐Bjørn19,van den Berg Leonard H.20ORCID,Villanueva Gemma14ORCID,Weber Markus21ORCID

Affiliation:

1. Department of Neurology, University Hospitals Leuven, Department of Neuroscience KU Leuven Center for Brain & Disease Research VIB Leuven Belgium

2. Department of Basic and Clinical Neuroscience Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology and Neuroscience, King's College London London UK

3. Department of Clinical Science, Neurosciences Umeå University Umeå Sweden

4. Rita Levi Montalcini Department of Neuroscience University of Turin Turin Italy

5. Azienda Ospedaliero Universitaria Città della Salute e della Scienza di Torino Turin Italy

6. Centre SLA, CHU Limoges Limoges France

7. Faculdade de Medicina Instituto de Medicina Molecular, Universidade de Lisboa, Centro Académico de Medicina de Lisboa Lisbon Portugal

8. Academic Unit of Neurology Trinity Biomedical Sciences Institute, Trinity College Dublin Dublin Ireland

9. Department of Neurology Medical University of Warsaw Warsaw Poland

10. Department of Neurology, Ulm University, German Center for Neurodegenerative Diseases (DZNE) Ulm Germany

11. Sheffield Institute for Translational Neuroscience, University of Sheffield Sheffield UK

12. ALS Unit, Department of Neurology Hospital Universitario San Rafael Madrid Spain

13. Department of Neurology, Hannover Medical School Hannover Germany

14. Cochrane Response London UK

15. EUpALS (European Organization for Professionals and Patients with ALS) and ALS Liga België Leuven Belgium

16. Neurology Department, Paris ALS Center, Groupe Hospitalier Pitié‐Salpêtrière, AP‐HP Paris France

17. Department of Neuroscience and Laboratory of Neuroscience IRCCS Istituto Auxologico Italiano Milan Italy

18. Department of Pathophysiology and Transplantation, Dino Ferrari Center Università degli Studi di Milano Milan Italy

19. Department of Neurology Haukeland University Hospital Bergen Norway

20. Department of Neurology, UMC Utrecht Brain Center University Medical Center Utrecht Utrecht The Netherlands

21. Neuromuscular Diseases Unit/ALS Clinic St. Gallen Switzerland

Abstract

AbstractBackgroundThis update of the guideline on the management of amyotrophic lateral sclerosis (ALS) was commissioned by the European Academy of Neurology (EAN) and prepared in collaboration with the European Reference Network for Neuromuscular Diseases (ERN EURO‐NMD) and the support of the European Network for the Cure ALS (ENCALS) and the European Organization for Professionals and Patients with ALS (EUpALS).MethodsGrading of Recommendations Assessment, Development, and Evaluation (GRADE) methodology was used to assess the effectiveness of interventions for ALS. Two systematic reviewers from Cochrane Response supported the guideline panel. The working group identified a total of 26 research questions, performed systematic reviews, assessed the quality of the available evidence, and made specific recommendations. Expert consensus statements were provided where insufficient evidence was available.ResultsA guideline mapping effort revealed only one other ALS guideline that used GRADE methodology (a National Institute for Health and Care Excellence [NICE] guideline). The available evidence was scarce for many research questions. Of the 26 research questions evaluated, the NICE recommendations could be adapted for 8 questions. Other recommendations required updates of existing systematic reviews or de novo reviews. Recommendations were made on currently available disease‐modifying treatments, multidisciplinary care, nutritional and respiratory support, communication aids, psychological support, treatments for common ALS symptoms (e.g., muscle cramps, spasticity, pseudobulbar affect, thick mucus, sialorrhea, pain), and end‐of‐life management.ConclusionsThis update of the guideline using GRADE methodology provides a framework for the management of ALS. The treatment landscape is changing rapidly, and further updates will be prepared when additional evidence becomes available.

Funder

European Academy of Neurology

Publisher

Wiley

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