Switch from abobotulinumtoxinA (Dysport®) to incobotulinumtoxinA (Xeomin®) botulinum toxin formulation: a review of 257 cases.

Authors

  • Donald G. Grosset
  • Elaine G. Tyrrell
  • Katherine A. Grosset

DOI:

https://doi.org/10.2340/16501977-1895

Keywords:

botulinum toxins, type A, incobotulinumtoxinA, abobotulinumtoxinA, blepharospasm, dystonia, torticollis, hemifacial spasm.

Abstract

OBJECTIVE: To explore the dose equivalence ratio and treatment costs for abobotulinumtoxinA and incobotulinumtoxinA for patients with focal dystonias. DESIGN: Patient chart review. SUBJECTS/PATIENTS: Adult patients with blepharospasm (n = 19), cervical dystonia (n = 122), hemifacial spasm (n = 91) or segmental/generalized dystonia (n = 19) at a neurology outpatient clinic. METHODS: Patients were switched from established abobotulinumtoxinA therapy to incobotulinumtoxinA at a ~4:1 unit ratio. Dose requirements, injection intervals, treatment efficacy, and adverse events were evaluated for a period of ≥ 1 year. RESULTS: Patients were switched from abobotulinumtoxinA to incobotulinumtoxinA with a mean dose ratio of 4.07 (standard deviation (SD) 0.50). After switching, incobotulinumtoxinA dose requirements remained stable

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Published

2014-10-01

How to Cite

Grosset, D. G., Tyrrell, E. G., & Grosset, K. A. (2014). Switch from abobotulinumtoxinA (Dysport®) to incobotulinumtoxinA (Xeomin®) botulinum toxin formulation: a review of 257 cases. Journal of Rehabilitation Medicine, 47(2), 183–186. https://doi.org/10.2340/16501977-1895

Issue

Section

Short Communication