Abstract
The poor prognosis of amyotrophic lateral sclerosis (ALS) makes palliative care a challenge for the neurologist. Most disabilities associated with progressive disease can be ameliorated by symptomatic treatment. Prognosis and treatment options should be openly discussed with the patient and his/her relatives. Nutritional deficiency due to pronounced dysphagia can be efficiently relieved by a percutaneous enterogastrostomy. Respiratory insufficiency can be treated by non-invasive ventilation at home, provided the familial environment is supportive. Adequate assistance and palliative treatment in the terminal phase is of paramount importance. © Springer-Verlag 1997.
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CITATION STYLE
Borasio, G. D., & Voltz, R. (1997). Palliative care in amyotrophic lateral sclerosis. Journal of Neurology, 244(SUPPL. 4). https://doi.org/10.1007/pl00007719
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