## Abstract There is accumulating evidence that ALS is a multisystem degenerative disease, raising the question of whether some symptoms are of extrapyramidal origin. The objective was to better characterize the type of stiffness in a series of ALS patients and to study correlations with balance an
Palliative surgery in patients with bulbar amyotrophic lateral sclerosis
β Scribed by Steven O. Short; Dr. Allen D. Hillel
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 629 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1043-3074
No coin nor oath required. For personal study only.
β¦ Synopsis
Patients with amyotrophic lateral sclerosis (ALS), a progressive neurodegenerative disorder, commonly develop bulbar symptoms including dysphagia, dysarthria, and defective airway protection. Otolaryngologists/head and neck surgeons are frequently asked to assist in the management of these problems. We reviewed our experience of 13 surgical procedures in 7 patients with advanced bulbar ALS. In spite of technically good surgery, 3 patients died within 1 week of hospitalization. Four patients appeared to benefit from the surgery. Patients with bulbar ALS are a high risk group because of chronic malnutrition and dehydration, covert aspiration and pneumonitis, and diminished ventilation. A team approach to these problems is stressed. Perioperative morbidity can be reduced with careful preoperative preparation and patient selection. HEAD & NECK 11 :364-369,1989 Amyotrophic lateral sclerosis (ALS) is a progressive neurologic disorder characterized by asymmetric muscular weakness, atrophy, and hyperactive reflexes with cramping and spasticity. Sensory pathways and autonomic functions
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