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Goadsby, Peter J

0000-0003-3260-5904

Mayo Clinic

NIHR King's Clinical Research Facility and Headache Group, King's College London, London, UK.

Citations 32

Utility of Topiramate for the Treatment of Patients with Chronic Migraine in the Presence or Absence of Acute Medication Overuse
Diener, HC, Dodick, DW, Goadsby, Peter J. , Bigal, ME, Bussone, G. , Silberstein, SD, Mathew, N. T., Ascher, Simon B., Morein, Jacqueline, Hulihan, JF, Biondi, DM, Greenberg, SJ, Ascher, Simon B. , Hulihan, Joseph, Goadsby, Peter J

Cephalalgia | April 23, 2009 | Volume: 29 | Issue: 10 | Pages: 1021-1027

10.1111/j.1468-2982.2009.01859.x Get It

Chronic migraine has been linked to the excessive use of acute headache medications. Medication overuse (MO) is commonly considered the most significant risk factor for the progression of migraine from an episodic to a chronic condition. Managing MO is a challenge. Discontinuation of the acute medication can result in withdrawal headache, nausea, vomiting and sleep disturbances. This review summarizes the results from two similarly designed, randomized, placebo- controlled, multicentre studies of chronic migraine conducted in the USA and European Union. Both studies demonstrate the efficacy and safety of the migraine preventive medication, topiramate, for the treatment of chronic migraine in patient populations both with and without MO. These studies may have important implications for the future of chronic migraine management, suggesting that detoxification prior to initiating prophylactic therapy may not be required in all patients if MO is present.
Identification of Negative Predictors of Pain-Free Response to Triptans: Analysis of the Eletriptan Database
Diener, HC, Dodick, DW, Goadsby, Peter J. , Lipton, RB, Almas, Mary , Parsons, Bruce , Goadsby, Peter J

Cephalalgia | October 18, 2007 | Volume: 28 | Issue: 1 | Pages: 35-40

10.1111/j.1468-2982.2007.01457.x Get It

Thirty to forty percent of migraineurs do not respond to any given triptan treatment. We identified clinical variables that significantly predict therapeutic non-response and evaluated the efficacy of eletriptan (20, 40 and 80 mg) and sumatriptan (100 mg) vs. placebo in a subgroup of patients with all predictor variables. First-attack data were pooled from 10 randomized, double-blind, placebo-controlled migraine trials ( n = 8473). Multivariate regression analyses identified three significant baseline predictors of failure to achieve 2-h pain-free response: severe headache pain, presence of photophobia/phonophobia and presence of nausea. Time of dosing following headache onset did not influence 2-h pain-free response. Among patients with all three risk factors ( n = 2010; 24± of total sample), 2-h pain-free response was significantly higher in patients receiving all three doses of eletriptan or sumatriptan vs. placebo (all P< 0.01). Thus, eletriptan and sumatriptan are efficacious in difficult-to-treat patients at high risk for non-response to triptans.