Factors affecting the health-related quality of life of patients with cervical dystonia and impact of treatment with abobotulinumtoxinA (Dysport): results from a randomised, double-blind, placebo-controlled study

BMJ Open. 2014 Oct 16;4(10):e005150. doi: 10.1136/bmjopen-2014-005150.

Abstract

Objective: To describe the health-related quality of life (HRQOL) burden of cervical dystonia (CD) and report on the HRQOL and patient perception of treatment benefits of abobotulinumtoxinA (Dysport).

Design: The safety and efficacy of a single injection of abobotulinumtoxinA for CD treatment were evaluated in a previously reported international, multicenter, double-blind, randomised trial. HRQOL measures were assessed in the trial and have not been previously reported.

Setting: Movement disorder clinics in the USA and Russia.

Participants: Patients had to have a diagnosis of CD with symptoms for at least 18 months, as well as a total Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS) score of at least 30; a Severity domain score of at least 15; and a Disability domain score of at least 3. Key exclusion criteria included treatment with botulinum toxin type A (BoNT-A) or botulinum toxin type B (BoNT-B) within 16 weeks of enrolment.

Interventions: Patients were randomised to receive either 500 U abobotulinumtoxinA (n=55) or placebo (n=61).

Primary and secondary outcome measures: Efficacy assessments included TWSTRS total (primary end point) and subscale scores at weeks 0, 4, 8, 12; a pain visual analogue scale at weeks 0 and 4; and HRQOL assessed by the SF-36 Health Survey (SF-36; secondary end point) at weeks 0 and 8.

Results: Patients with CD reported significantly greater impairment for all SF-36 domains relative to US norms. Patients treated with abobotulinumtoxinA reported significantly greater improvements in Physical Functioning, Role Physical, Bodily Pain, General Health and Role Emotional domains than placebo patients (p≤0.03 for all). The TWSTRS was significantly correlated with Physical Functioning, Role Physical and Bodily Pain scores, for those on active treatment.

Conclusions: CD has a marked impact on HRQOL. Treatment with a single abobotulinumtoxinA injection results in significant improvement in patients' HRQOL.

Trial registration number: The trial is registered at ClinicalTrials.gov, numbers NCT00257660 and NCT00288509.

Keywords: QUALITATIVE RESEARCH.

Publication types

  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine Release Inhibitors / therapeutic use*
  • Adult
  • Aged
  • Botulinum Toxins, Type A / therapeutic use*
  • Double-Blind Method
  • Dystonia / complications
  • Dystonia / drug therapy*
  • Female
  • Health Status
  • Humans
  • Injections, Intramuscular
  • Male
  • Middle Aged
  • Neck Muscles*
  • Neck Pain / drug therapy*
  • Neck Pain / etiology
  • Pain Measurement
  • Patient Satisfaction*
  • Quality of Life*
  • Treatment Outcome
  • Young Adult

Substances

  • Acetylcholine Release Inhibitors
  • Botulinum Toxins, Type A
  • abobotulinumtoxinA

Associated data

  • ClinicalTrials.gov/NCT00257660
  • ClinicalTrials.gov/NCT00288509