Botulinum toxin A and B: a comparative dosing study for spasmodic dysphonia

Otolaryngol Head Neck Surg. 2005 Dec;133(6):836-8. doi: 10.1016/j.otohns.2005.09.008.

Abstract

Objective: The purpose of this study was to find the conversion factor, safety, and efficacy of type A to type B toxin for laryngeal muscles.

Methods: Thirty-two patients with adductor spasmodic dysphonia with stable doses of A toxin to manage their symptom were given type B toxin starting at a conversion of 1 U of BTX-A to 50 U of BTX-B. The patients were followed for 1 year, and doses adjusted according to response.

Results: The conversion factor was found to be 52.3 U:1 U. The onset of action of type B was more rapid (2.09 days vs 3.2 days [P = 0.028]), with a shorter duration of benefit (10.8 weeks vs 17 weeks [P = 0.002). The safety profile for A and B toxin appeared the same, with 3 patients receiving Myobloc reporting dry mouth.

Conclusion: This study shows that a conversion factor of 52.3:1 Myobloc (BTX-B) to Botox (BTX-A) and that Myobloc is an effective alternative to Botox (BTX-A) for patients with spasmodic dysphonia.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Botulinum Toxins / administration & dosage*
  • Botulinum Toxins / therapeutic use
  • Botulinum Toxins, Type A / administration & dosage*
  • Botulinum Toxins, Type A / therapeutic use
  • Dose-Response Relationship, Drug
  • Female
  • Follow-Up Studies
  • Humans
  • Laryngeal Muscles / drug effects
  • Laryngeal Muscles / physiopathology
  • Male
  • Metalloendopeptidases / administration & dosage*
  • Metalloendopeptidases / therapeutic use
  • Muscle Contraction / drug effects
  • Neuromuscular Agents / administration & dosage*
  • Neuromuscular Agents / therapeutic use
  • Treatment Outcome
  • Voice Disorders / drug therapy*
  • Voice Disorders / physiopathology

Substances

  • Neuromuscular Agents
  • rimabotulinumtoxinB
  • Metalloendopeptidases
  • Botulinum Toxins
  • Botulinum Toxins, Type A