A Single-Group Study on the Effect of OnabotulinumtoxinA in Patients with Chronic Migraine Associated with Medication Overuse Headache: Pain Catastrophizing Plays a Role

Toxins (Basel). 2023 Jan 17;15(2):86. doi: 10.3390/toxins15020086.

Abstract

Pain catastrophizing and cutaneous allodynia are commonly altered in patients with chronic migraine associated with medication overuse headache (CM-MOH) and tend to improve in parallel with clinical improvement. The relation between pain catastrophizing and cutaneous allodynia is poorly understood in patients with CM-MOH receiving OnabotulinumtoxinA therapy. In this single-arm open-label longitudinal observational study, patients with CM-MOH were assigned to structured withdrawal and then administered OnabotulinumtoxinA (5 sessions on a three-month basis, 195 UI per 31 sites). Headache frequency, medication intake, disability, impact, cutaneous allodynia and pain catastrophizing were evaluated with specific questionnaires. In total, 96 patients were enrolled and 79 completed the 12-month follow-up. With the exclusion of cutaneous allodynia and the magnification subscale of the pain catastrophizing questionnaire, all variables showed significant improvement by the sixth month, which was maintained at 12 months. Reduction of pain catastrophizing, and particularly of its helplessness subscale, was a significant predictor of reduction in headache frequency and medication intake. Pain catastrophizing is often implicated in the clinical improvement in patients with CM-MOH receiving behavioral treatments, but, in this study, also showed a role in patients receiving OnabotulinumtoxinA; combining OnabotulinumtoxinA and behavioral treatments specifically addressing pain catastrophizing might further enhance patients' clinical outcome.

Keywords: OnabotulinumtoxinA; PREEMPT; chronic migraine; cutaneous allodynia; medication overuse headache; pain catastrophizing.

Publication types

  • Observational Study

MeSH terms

  • Botulinum Toxins, Type A* / therapeutic use
  • Catastrophization
  • Chronic Disease
  • Headache / drug therapy
  • Headache Disorders, Secondary* / chemically induced
  • Headache Disorders, Secondary* / complications
  • Headache Disorders, Secondary* / drug therapy
  • Humans
  • Hyperalgesia / drug therapy
  • Migraine Disorders* / drug therapy
  • Pain / drug therapy

Substances

  • Botulinum Toxins, Type A

Grants and funding

This research received no external funding.