CDIP-58 can measure the impact of botulinum toxin treatment in cervical dystonia

Neurology. 2006 Dec 26;67(12):2230-2. doi: 10.1212/01.wnl.0000249310.25427.f2.

Abstract

We compared the responsiveness of the Cervical Dystonia Impact Profile (CDIP-58), Medical Outcome Study Short Form-Health Survey (SF-36), Functional Disability Questionnaire (FDQ), and Pain and Activities of Daily Living subscales of the Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS) in participants with cervical dystonia treated with botulinum toxin A. Subscales of CDIP-58 were more sensitive in detecting statistical and clinical change than comparable subscales of the SF-36, FDQ, and TWSTRS.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Botulinum Toxins, Type A / therapeutic use*
  • England / epidemiology
  • Female
  • Humans
  • Male
  • Middle Aged
  • Neck Pain / diagnosis
  • Neck Pain / epidemiology*
  • Neck Pain / prevention & control*
  • Outcome Assessment, Health Care / methods*
  • Prevalence
  • Prognosis
  • Psychometrics / methods
  • Quality of Life
  • Reproducibility of Results
  • Risk Assessment / methods
  • Risk Factors
  • Sensitivity and Specificity
  • Sickness Impact Profile*
  • Torticollis / diagnosis
  • Torticollis / drug therapy*
  • Torticollis / epidemiology*
  • Treatment Outcome

Substances

  • Botulinum Toxins, Type A