| Literature DB >> 9402548 |
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.Entities:
Mesh:
Year: 1997 PMID: 9402548 DOI: 10.1007/pl00007719
Source DB: PubMed Journal: J Neurol ISSN: 0340-5354 Impact factor: 4.849