A pilot study of botulinum toxin A for headache in cervical dystonia

Headache. 2005 Sep;45(8):1073-7. doi: 10.1111/j.1526-4610.2005.05190.x.

Abstract

Objective: To evaluate the prevalence of associated headache (HA) pain with craniocervical dystonia and the therapeutic effect of BoNT-A injections on the HA component when injected for cervical dystonia.

Background: HA associated with craniocervical dystonia is a recent formally codified entity, but has not been systematically studied.

Methods: We identified 44 subjects from three movement disorder clinics who presented with craniocervical dystonia and concurrent HA pain. The subjects were injected with botulinum toxin type A (BoNT-A) and prospectively evaluated with the Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS), headache diaries, Headache Impact Test (HIT-6), and Migraine Disability Assessment Scale (MIDAS), along with HA pain anatomy and adverse events, at baseline, and at 4, 8, and 12 weeks post-injection.

Results: As expected, all aspects of the TWSTRS robustly improved. Headache diaries and the HIT-6 also improved at 4, 8, and 12 weeks post-injection. Sections of the MIDAS improved, and adverse events were minimal.

Conclusion: BoNT-A safely improves headache associated with craniocervical dystonia when administered for the primary condition of craniocervical dystonia.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Botulinum Toxins, Type A / therapeutic use*
  • Female
  • Headache Disorders / drug therapy*
  • Headache Disorders / etiology
  • Humans
  • Male
  • Middle Aged
  • Neuromuscular Agents / therapeutic use
  • Pilot Projects
  • Prospective Studies
  • Torticollis / complications
  • Torticollis / drug therapy*
  • Treatment Outcome

Substances

  • Neuromuscular Agents
  • Botulinum Toxins, Type A