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Updated: Jan 22, 2026

ALS - Motor Neuron Disease: Mechanism and Development of New Therapies
Published on: July 29, 2007
Tracheostomy in motor neurone disease
Martin R Turner1, Christina Faull2, Christopher J McDermott3
1Nuffield Department of Clinical Neurosciences, Oxford University, Oxford, UK martin.turner@ndcn.ox.ac.uk.
Tracheostomy ventilation can improve survival and quality of life for patients with amyotrophic lateral sclerosis (motor neurone disease). This article discusses its prevalence, benefits, and practical implementation, including end-of-life care discussions.
Area of Science:
- Neurology
- Respiratory Medicine
- Palliative Care
Background:
- Amyotrophic lateral sclerosis (ALS), also known as motor neurone disease (MND), causes progressive respiratory insufficiency.
- Tracheostomy-associated ventilation is a complex treatment option for advanced ALS.
- Decisions regarding invasive ventilation present significant challenges for patients and clinicians.
Purpose of the Study:
- To review the current prevalence of tracheostomy in MND patients.
- To evaluate the evidence supporting tracheostomy ventilation for survival and quality of life in MND.
- To outline practical considerations and ethical dimensions of implementing tracheostomy ventilation.
Main Methods:
- Literature review on tracheostomy use in amyotrophic lateral sclerosis.
- Analysis of evidence regarding survival benefits.
- Discussion of quality of life implications.
- Exploration of practical and ethical aspects of ventilatory support.
Main Results:
- Tracheostomy ventilation is an option for respiratory insufficiency in MND.
- Evidence suggests potential benefits for both survival and quality of life.
- Implementation involves complex practical, ethical, and economic considerations.
Conclusions:
- Neurologists must openly discuss tracheostomy ventilation with MND patients.
- A framework for decision-making, including therapy withdrawal, is essential.
- Informed patient choice is paramount in managing advanced MND.
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