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Low-dose subcutaneous injection of botulinum toxin type A for facial synkinesis and hyperlacrimation.

AbstractOBJECTIVE: To investigate the efficacy of low dose of botulinum toxin type A (BTX-A) for facial synkinesis and hyperlacrimation. MATERIAL AND METHODS: Eleven patients suffering from facial synkinesis after Bell's palsy or facial nerve injury were treated with a low dose of BTX-A, 0.5-1.25 U per point into several points. One patient showing hyperlacrimation was also treated with BTX-A. The whole observational period was 43 months. RESULTS: On average, 5.76 U of BTX-A, which was lower than that of previous reports, was injected per treatment. In seven cases, synkinesis disappeared completely after three or fewer sessions of BTX-A injection. The mean interval between treatments was 14.5 weeks. Hyperlacrimation was completely suppressed after a single subcutaneous injection of BTX-A. Only mild subcutaneous hemorrhage was observed as adverse reactions. CONCLUSION: Facial synkinesis can be treated with a lower dose of BTX-A without relevant adverse reactions.
AuthorsH Ito, H Ito, S Nakano, H Kusaka (Affiliation: Department of Neurology, Tokyo-West Tokushukai Hospital, Akishima, Tokyo, Japan. hishashi.ito at tokushukai.jp)
JournalActa neurologica Scandinavica (Acta Neurol Scand) Vol. 115 Issue 4 Pg. 271-4 (Apr 2007) ISSN: 0001-6314 Denmark
PMID17376126 (Publication Type: Clinical Trial, Journal Article)
Chemical References
  • Botulinum Toxin Type A
  • Neuromuscular Agents
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Botulinum Toxin Type A (administration & dosage)
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Injections, Subcutaneous
  • Lacrimal Apparatus Diseases (drug therapy)
  • Male
  • Middle Aged
  • Neuromuscular Agents (administration & dosage)
  • Prospective Studies
  • Synkinesis (drug therapy)
  • Tears (secretion)
  • Treatment Outcome