https://doi.org/10.55788/9fe58be8
The new ALS guidelines were presented by Prof. Philip van Damme (University Hospital Gasthuisberg, Belgium) [1]. This version replaces the previous guidelines dating back to 2012 [2]. Prof. Van Damme explained that 26 research questions were identified using the PICO framework. Of these, 8 were recommendations adapted from the British NICE guidelines (NICE guideline NG42: Motor neurone disease) [3]; the other 16 were de novo recommendations.
A cornerstone of ALS management is multidisciplinary care; the evidence is based mostly on observational studies. A team ideally consists of an ALS neurologist, a respiratory specialist, a nursing professional, a mental health professional, a social worker, a speech/language pathologist, a dietician, and a physical therapist.
The main recommendations concerning disease-modifying therapies are the following:
- Riluzole should be offered as a lifelong treatment option to all ALS patients at diagnosis. “A single daily dose of 50 mg can already be effective,” added Prof. Van Damme.
- Cell-based therapies are not recommended outside the context of clinical trials until positive phase 3 trial data is available.
- Edaravone and AMX0035 both receive temporary recommendations; the guideline committee wants to await the phase 3 trial results before issuing a final recommendation.
- Tofersen should be offered as first-line treatment in patients with progressive ALS caused by mutations in the superoxide dismutase 1 (SOD1) gene. The possibility of serious adverse events should be discussed with the patient.
There are ongoing RCTs for nutritional interventions. Despite there currently being no RCTs for gastrostomy, it should be discussed at an early stage with the patient. Furthermore, healthcare professionals should also explain the benefits of early placement and the possible risks of a late gastrostomy.
In conclusion, Prof. Van Damme expressed his hope that an update of these guidelines will be necessary shortly, as 3 additional drugs are likely to be evaluated by the EMA in the coming year.
- Van Damme P, et al. EAN guideline on the management of amyotrophic lateral sclerosis in collaboration with ERN Euro-NMD. EAN 2023 Annual Meeting, 1-4 July, Budapest, Hungary.
- Andersen PM, et al. Eur J Neurol. 2012;19(3):360–75.
- https://www.nice.org.uk/guidance/ng42
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Table of Contents: EAN 2023
Featured articles
Letter from the Editor
Alzheimer’s disease and dementia: the road towards proactive and preventive care
Overarching Theme: Big Data
Contribution of genomics and genetics to personalised medicine
How big data can boost care for neurodegenerative disorders
COVID-19
Amantadine in early COVID-19 enhances recovery
SARS-CoV-2 vaccination in CIDP and MMN: more benefit than harm
Cerebrovascular Disease and Stroke
Intensive BP reduction associated with smaller haematoma
Cognition and Dementia
Towards cell biology of Alzheimer’s disease
Epilepsy
Minimising co-medication optimises cenobamate efficacy in drug-resistant epilepsy
Headache and Pain
GLP-1 agonists induce weight loss and alleviate headache in idiopathic intracranial hypertension
Cannabis-based medicine does not beat placebo in central neuropathic pain
80% of patients reverse from chronic to episodic migraine on anti-CGRP antibodies
Multiple Sclerosis
Which patients can initially be treated with platform DMT?
Retinal layer thickness predicts disability accumulation in early RMS
Withdrawing DMF in early pregnancy does not increase relapse risk in pregnant patients with MS
Immunosenescence and MS: relevance to immunopathogenesis and treatment
Sleep Disorders
Nightmares during childhood linked to cognitive decline later in life
Sleep changes contribute to the pathogenesis of neurodegenerative diseases
Miscellaneous
EAN guidelines on the management of ALS
What neurologists should know about bladder and sexual problems
Laughing gas abuse often leads to polyneuropathy, myelopathy, and encephalopathy
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