Nimodipine monotherapy and carbamazepine augmentation in patients with refractory recurrent affective illness

被引:69
作者
Pazzaglia, PJ
Post, RM
Ketter, TA
Callahan, AM
Marangell, LB
Frye, MA
George, MS
Kimbrell, TA
Leverich, GS
Cora-Locatelli, G
Luckenbaugh, D
机构
[1] NIMH, Biol Psychiat Branch, NIH, Bethesda, MD 20892 USA
[2] NIMH, Clin Sci Lab, NIH, Bethesda, MD 20892 USA
[3] Univ Mississippi, Sch Med, Dept Psychiat & Human Behav, Jackson, MS 39216 USA
[4] Stanford Univ, Sch Med, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA
[5] Brown Univ, Sch Med, Providence, RI USA
[6] Baylor Coll Med, Dallas, TX USA
[7] Med Univ S Carolina, Dept Radiol, Charleston, SC 29425 USA
[8] Vet Adm Med Ctr, N Little Rock, AR USA
关键词
D O I
10.1097/00004714-199810000-00009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Of 30 patients with treatment-refractory affective illness, 10 showed a moderate to marked response to blind nimodipine monotherapy compared with placebo on the Clinical Global Impressions Scale, Fourteens inadequately responsive patients (3 unipolar [UP], 11 bipolar [BP]) were treated with the blind addition of carbamazepine. Carbamazepine augmentation of nimodipine converted four (29%) of the partial responders to more robust responders. Patients who showed an excellent response to the nimodipine-carbamazepine combination included individual patients with patterns of rapid cycling, ultradian cycling, UP recurrent brief depression, and one with BP type II depression. When verapamil was blindly substituted for nimodipine, two BP patients failed to maintain improvement but responded again to nimodipine and remained well with a blind transition to another dihydropyridine L-type calcium channel blocker (CCB), isradipine. Mechanistic implications of the response to the dihydropyridine L-type CCB nimodipine alone and in combination with carbamazepine are discussed.
引用
收藏
页码:404 / 413
页数:10
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