Low-dose botulinum toxin type A for the treatment of refractory piriformis syndrome

Pharmacotherapy. 2007 May;27(5):657-65. doi: 10.1592/phco.27.5.657.

Abstract

Study objectives: To evaluate the efficacy of a single, low-dose injection of botulinum toxin type A in relieving pain in Korean patients with piriformis syndrome resistant to conventional therapy, and to assess the drug's influence on these patients' quality of life.

Design: Prospective, single-site, open-label trial.

Setting: Rehabilitation medicine clinic in Seoul, Korea.

Patients: Twenty-nine patients with a confirmed diagnosis of chronic piriformis syndrome and 82 age- and sex-matched healthy subjects were enrolled from April 1, 2003-February 28, 2004. Intervention. In 20 of the patients, botulinum toxin type A 150 U was injected using computed tomographic guidance into the affected unilateral piriformis muscle. The other nine patients served as active controls and received an injection of dexamethasone 5 mg and 1% lidocaine. The healthy subjects did not receive any injection.

Measurements and main results: The patients' pain at baseline and at 4, 8, and 12 weeks after treatment was rated by using a numeric rating scale. Health-related quality of life was assessed by using the validated Korean version of the Medical Outcomes Study 36-Item Short Form Health Survey (SF-36) at baseline and at 4 weeks of treatment. Healthy subjects also completed the SF-36 at baseline. Pain intensity scores were significantly lower at 4, 8, and 12 weeks after treatment than at baseline (p<0.0001). Baseline scores from the SF-36 subscales, including those for physical functioning (p<0.0001), role physical (p<0.0001), bodily pain (p<0.0001), general health (p<0.0001), vitality (p<0.0001), and social functioning (p<0.002), were significantly lower in the patients than in the healthy subjects. Four weeks after treatment, physical functioning (p=0.003), role physical (p=0.021), bodily pain (p=0.016), general health (p=0.013), vitality (p=0.031) and social functioning (p=0.035) improved significantly from baseline in the patients. However, at 4 weeks, patients in the active control group were withdrawn from the study because their pain did not improve, and continuation without further medical care was considered unethical.

Conclusion: A low dose of botulinum toxin type A relieved pain and improved quality of life in patients with refractory piriformis syndrome.

Publication types

  • Clinical Trial
  • Comparative Study

MeSH terms

  • Adult
  • Anesthetics, Local / therapeutic use
  • Asian People
  • Botulinum Toxins, Type A / adverse effects
  • Botulinum Toxins, Type A / therapeutic use*
  • Dexamethasone / therapeutic use
  • Female
  • Glucocorticoids / therapeutic use
  • Humans
  • Korea
  • Lidocaine / therapeutic use
  • Male
  • Middle Aged
  • Muscle Contraction / drug effects
  • Muscle Stretching Exercises
  • Muscle, Skeletal / drug effects*
  • Neuromuscular Agents / adverse effects
  • Neuromuscular Agents / therapeutic use*
  • Pain / drug therapy*
  • Pain Measurement
  • Prospective Studies
  • Quality of Life
  • Rehabilitation Centers
  • Sciatic Nerve / physiopathology
  • Syndrome
  • Tomography, X-Ray Computed

Substances

  • Anesthetics, Local
  • Glucocorticoids
  • Neuromuscular Agents
  • Dexamethasone
  • Lidocaine
  • Botulinum Toxins, Type A