A new treatment option for laryngeal sensory neuropathy
β Scribed by Stacey L. Halum; David L. Sycamore; Bryan R. McRae
- Book ID
- 102449039
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 87 KB
- Volume
- 119
- Category
- Article
- ISSN
- 0023-852X
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β¦ Synopsis
Abstract
Objectives/Hypothesis:
Laryngeal sensory neuropathy (LSN) may produce a variety of symptoms, including chronic cough, globus sensation, odynophonia, and/or odynophagia. Etiologies are often iatrogenic, viral, or idiopathic, although the diagnosis is generally one of exclusion. The aim of this study is to introduce pregabalin (Lyrica, Pfizer Inc., New York, NY) as a potential new therapy for LSN.
Study Design:
Retrospective clinical investigation.
Methods:
Charts were reviewed from 12 consecutive patients who were prescribed pregabalin for symptoms of LSN. Outcomes were reviewed by analyzing pre and postβtreatment questionnaires asking patients to rate symptoms on a scale from 0 to 5. Adverse effects and evidence of drug tolerance were also recorded.
Results:
Two patients did not tolerate pregabalin due to somnolence. Of those that tolerated the medication, mean pretreatment chief complaint symptom severity rating was 3.9, whereas mean postβtreatment symptom rating was 1.2 after 1 month of pregabalin therapy. None of the patients developed drug tolerance effects over time.
Conclusions:
Pregabalin therapy appears to be an effective treatment option for laryngeal sensory neuropathy. Future prospective studies are needed to compare outcomes between pregabalin and other medications as treatments for LSN. Laryngoscope, 2009
π SIMILAR VOLUMES
Two brothers with a new type of hereditary sensory neuropathy are described. The main clinical feature is late onset sensory ataxia without ulcerating acropathy or other autonomic abnormality. The older patient also has oculomotor dysfunction and extensor plantar responses.
A pedigree with a new form of hereditary sensory neuropathy is described. Ataxia and scoliosis rather than loss of pain and ulcerating acropathy are the principal clinical features. Analysis of the pedigree suggests a dominant mode of transmission with variable age of onset and perhaps reduced penet