Journal Article

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

Couratier, Philippe, Andersen, Peter M., Van Damme, Philip, Petri, Susanne, Berg, Leonard H., Weber, Markus, Probyn, Katrin, Chiò, Adriano, McDermott, Christopher J., Mora, Jesus S., Ludolph, Albert, Tysnes, Ole‐Bjørn, Villanueva, Gemma, Kuźma‐Kozakiewicz, Magdalena, Reviers, Evy, Al‐Chalabi, Ammar, Silani, Vincenzo, De Carvalho, Mamede, Hardiman, Orla, Salachas, François

2024

Overview

Background This 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). Methods Grading 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. Results A 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. Conclusions This 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.

• Publisher: John Wiley & Sons, Inc
• Subject: Amyotrophic lateral sclerosis / Amyotrophic Lateral Sclerosis - therapy / Collaboration / Cooperation / Cramps / disease-modifying treatment / Europe / Evaluation / Experimental allergic neuritis / gastrostomy / guideline / Humans / Methodology / multidisciplinary care / Neurology / Neurology - methods / Neurology - standards / Neuromuscular diseases / Neuromuscular Diseases - therapy / non-invasive ventilation / Quality / Questions / Saliva / Signs and symptoms / Spasticity