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Efficacy of pregabalin in the treatment of trigeminal neuralgia.

Abstract
This prospective, open-label study aimed to evaluate the efficacy of pregabalin treatment in patients suffering from trigeminal neuralgia with and without concomitant facial pain. Fifty-three patients with trigeminal neuralgia (14 with concomitant chronic facial pain) received pregabalin (PGB) 150-600 mg daily and were prospectively followed for 1 year. The primary outcome was number of patients pain free or with reduction of pain intensity by > 50% and of attack frequency by > 50% after 8 weeks. Secondary outcome was sustained pain relief after 1 year. Thirty-nine patients (74%) improved after 8 weeks with a mean dose of 269.8 mg/day (range 150-600 mg/day) PGB: 13 (25%) experienced complete pain relief and 26 (49%) reported pain reduction > 50%, whereas 14 (26%) did not improve. Patients without concomitant facial pain showed better response rates (32 of 39, 82%) compared with patients with concomitant chronic facial pain (7 of 14, 50%, P = 0.020). Concomitant chronic facial pain appears to be a clinical predictor of poor treatment outcome. PGB appears to be effective in the treatment of trigeminal neuralgia.
AuthorsM Obermann, M S Yoon, K Sensen, M Maschke, H C Diener, Z Katsarava
JournalCephalalgia : an international journal of headache (Cephalalgia) Vol. 28 Issue 2 Pg. 174-81 (Feb 2008) ISSN: 1468-2982 [Electronic] England
PMID18039340 (Publication Type: Journal Article)
Chemical References
  • Analgesics
  • Pregabalin
  • gamma-Aminobutyric Acid
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Analgesics (administration & dosage, therapeutic use)
  • Chronic Disease
  • Dose-Response Relationship, Drug
  • Facial Pain (complications)
  • Female
  • Humans
  • Male
  • Middle Aged
  • Pregabalin
  • Prospective Studies
  • Time Factors
  • Treatment Outcome
  • Trigeminal Neuralgia (complications, drug therapy)
  • gamma-Aminobutyric Acid (administration & dosage, analogs & derivatives, therapeutic use)

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