Upper esophageal sphincter myotomy in oculopharyngeal muscular dystrophy: long-term clinical results
- PMID: 9392024
- DOI: 10.1016/s0960-8966(97)00090-4
Upper esophageal sphincter myotomy in oculopharyngeal muscular dystrophy: long-term clinical results
Abstract
From 1980 to 1995, 53 patients with oculopharyngeal muscular dystrophy (OPMD) underwent an upper esophageal sphincter (UES) myotomy for the control of marked dysphagia. From this number, a group of 21 patients had been evaluated for preoperative and postoperative symptoms in 1987. The same clinical assessment was performed in 1995 by an independent evaluator for a total of 37 patients including 12 patients from the first group. As a whole, after a mean follow-up of 6.2 years, surgery succeeded in 18 patients (49%), gave a partial improvement in 12 (32%) and failed in seven (19%). The 12 patients evaluated twice (in 1987 and 1995) have had very good early results, 8-69 months after UES myotomy: dysphagia was totally relieved in eight patients, occurred rarely in three and was moderate in one. Nevertheless, the very long-term follow-up (8 years later) has shown a recurrence of the swallowing and tracheobronchial symptoms in many cases.
Similar articles
-
A pilot study on upper esophageal sphincter dilatation for the treatment of dysphagia in patients with oculopharyngeal muscular dystrophy.Neuromuscul Disord. 1997 Oct;7 Suppl 1:S100-4. doi: 10.1016/s0960-8966(97)00092-8. Neuromuscul Disord. 1997. PMID: 9392026 Clinical Trial.
-
[Oculopharyngeal myopathies: value of myotomy of the superior sphincter of the esophagus. Apropos of a case].Rev Med Interne. 1996;17(12):1017-9. doi: 10.1016/s0248-8663(97)80845-4. Rev Med Interne. 1996. PMID: 9008749 French.
-
Dysphagia in oculopharyngeal muscular dystrophy: a series of 22 French cases.Neuromuscul Disord. 1997 Oct;7 Suppl 1:S96-9. doi: 10.1016/s0960-8966(97)00091-6. Neuromuscul Disord. 1997. PMID: 9392025
-
Management of upper esophageal sphincter disorders: indications and complications of myotomy.Am J Med. 2000 Mar 6;108 Suppl 4a:43S-46S. doi: 10.1016/s0002-9343(99)00334-4. Am J Med. 2000. PMID: 10718451 Review.
-
[Oculopharyngeal muscular dystrophy in a Japanese family].Rinsho Shinkeigaku. 1990 Jan;30(1):29-36. Rinsho Shinkeigaku. 1990. PMID: 2184963 Review. Japanese.
Cited by
-
Transillumination Assisted Cricopharyngeal Myotomy.Indian J Otolaryngol Head Neck Surg. 2022 Oct;74(Suppl 2):2486-2492. doi: 10.1007/s12070-020-02227-8. Epub 2020 Oct 23. Indian J Otolaryngol Head Neck Surg. 2022. PMID: 36452790 Free PMC article.
-
Botulinum toxin for UES dysfunction: therapy or poison?Dysphagia. 2001 Summer;16(3):168-70. doi: 10.1007/s00455-001-0060-1. Dysphagia. 2001. PMID: 11453561 No abstract available.
-
Cricopharyngeal dilatation for the long-term treatment of dysphagia in oculopharyngeal muscular dystrophy.Dysphagia. 2012 Jun;27(2):216-20. doi: 10.1007/s00455-011-9356-y. Epub 2011 Jul 30. Dysphagia. 2012. PMID: 21805106
-
Successful botulinum toxin treatment of dysphagia in a young child with nemaline myopathy.Dysphagia. 2001 Summer;16(3):228-9. doi: 10.1007/s00455-001-0064-x. Dysphagia. 2001. PMID: 11453573 No abstract available.
Publication types
MeSH terms
LinkOut - more resources
Medical
Research Materials