Divalproex sodium in migraine prophylaxis: A dose-controlled study

被引:226
作者
Klapper, J
机构
[1] Colorado Neurol. and Headache Clinic, Denver, CO
[2] Colorado Neurol. and Headache Clinic, Denver, CO 80218
关键词
divalproex sodium; migraine; prophylactic treatment;
D O I
10.1046/j.1468-2982.1997.1702103.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To evaluate the efficacy and safety of divalproex sodium (DVPX) when used as prophylactic monotherapy in patients with migraine. Design: Multicenter, double-blind, placebo-controlled, parallel group. Patients were previously untreated or had failed no more than two adequate trials of prophylactic therapy. During the 4-week (single-blind) baseline, patients received placebo and completed a headache diary. Patients with two or more migraine attacks during the baseline were randomized to receive a DVPX daily dose of 500, 1000, or 1500 mg, or to placebo. The experimental phase (EP) lasted 12 weeks, the first 4 weeks for dose escalation to randomized dose, and the remaining 8 weeks for maintenance at that dose. The primary efficacy variable was 4-week migraine attack frequency during the EP. Results: One-hundred-and-seventy-six patients (44 placebo, 132 DVPX) were randomized; 171 provided efficacy data and 137 completed the study. During the EP, after adjustment for differences in baseline migraine attack frequencies, mean reductions in the DVPX groups were 1.7 (500 mg), 2.0 (1000 mg) and 1.7 (1500 mg) migraine attacks per 4 weeks compared to a mean reduction of 0.5 migraine attacks in the placebo group (p less than or equal to 0.05 vs placebo). Forty-four to 45% of DVPX-treated patients compared to 21% of patients in the placebo group achieved greater than or equal to 50% reduction in their migraine attack frequencies (p less than or equal to 0.05 vs placebo). The recommended initial dose of DVPX in migraine prophylaxis is 500 mg per day, although some patients may benefit from higher doses. Adverse events were similar in the DVPX and placebo treatment groups except for nausea, dizziness and tremor, in which incidence rates were significantly higher in the DVPX 1500 mg group (nausea was also higher in 500 mg group) than in the placebo group. Conclusion: Divalproex sodium is an effective prophylactic treatment in migraine and is generally well tolerated.
引用
收藏
页码:103 / 108
页数:6
相关论文
共 8 条
  • [1] CUTRER FM, 1991, CEPHALALGIA S14, V15, P96
  • [2] NEUROEXCITATORY PLASMA AMINO-ACIDS ARE ELEVATED IN MIGRAINE
    FERRARI, MD
    ODINK, J
    BOS, KD
    MALESSY, MJA
    BRUYN, GW
    [J]. NEUROLOGY, 1990, 40 (10) : 1582 - 1586
  • [3] GELFAND SB, 1991, AC PAIN MAN BALT MAR
  • [4] SODIUM VALPROATE IN THE PROPHYLACTIC TREATMENT OF MIGRAINE - A DOUBLE-BLIND-STUDY VERSUS PLACEBO
    HERING, R
    KURITZKY, A
    [J]. CEPHALALGIA, 1992, 12 (02) : 81 - 84
  • [5] SODIUM VALPROATE HAS A PROPHYLACTIC EFFECT IN MIGRAINE WITHOUT AURA - A TRIPLE-BLIND, PLACEBO-CONTROLLED CROSSOVER STUDY
    JENSEN, R
    BRINCK, T
    OLESEN, J
    [J]. NEUROLOGY, 1994, 44 (04) : 647 - 651
  • [6] MIGRAINE PROPHYLAXIS WITH DIVALPROEX
    MATHEW, NT
    SAPER, JR
    SILBERSTEIN, SD
    RANKIN, L
    MARKLEY, HG
    SOLOMON, S
    RAPOPORT, AM
    SILBER, CJ
    DEATON, RL
    [J]. ARCHIVES OF NEUROLOGY, 1995, 52 (03) : 281 - 286
  • [7] VALPROATE - A NEW DRUG IN MIGRAINE PROPHYLAXIS
    SORENSEN, KV
    [J]. ACTA NEUROLOGICA SCANDINAVICA, 1988, 78 (04): : 346 - 348
  • [8] CEREBROSPINAL-FLUID GAMMA AMINOBUTYRIC-ACID LEVELS IN MIGRAINE
    WELCH, KMA
    CHABI, E
    BARTOSH, K
    ACHAR, VS
    MEYER, JS
    [J]. BRITISH MEDICAL JOURNAL, 1975, 3 (5982) : 516 - 517