A 20-month, double-blind, maintenance trial of lithium versus divalproex in rapid-cycling bipolar disorder

被引:144
作者
Calabrese, JR [1 ]
Shelton, MD [1 ]
Rapport, DJ [1 ]
Youngstrom, EA [1 ]
Jackson, K [1 ]
Bilali, S [1 ]
Ganocy, SJ [1 ]
Findling, RL [1 ]
机构
[1] Case Western Reserve Univ, Univ Hosp Cleveland, Cleveland, OH 44106 USA
关键词
D O I
10.1176/appi.ajp.162.11.2152
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: The authors tested the hypothesis that divalproex would be more effective than lithium in the long-term management of patients with recently stabilized rapid-cycling bipolar disorder. Method: A 20-month, double-blind, parallel-group comparison was carried out in recently hypomanic/manic patients who had experienced a persistent bimodal response to combined treatment with lithium and divalproex. Sixty patients were randomly assigned to lithium or divalproex monotherapy in a balanced design after stratification for illness type ( bipolar I versus bipolar II disorder). Results: Of the 254 patients enrolled in the open-label acute stabilization phase, 76% discontinued the study prematurely ( poor adherence: 28%; nonresponse: 26% [of whom 74% remained depressed and 26% remained in a hypomanic/manic/mixed episode], intolerable side effects: 19%). Of the 60 patients (24%) randomly assigned to double-blind maintenance monotherapy, 53% relapsed (59% into depression and 41% into a hypomanic/manic/mixed episode), 22% completed the study, 10% had intolerable side effects, and 10% were poorly adherent. The rates of relapse into any mood episode for those given lithium versus divalproex were 56% and 50%, respectively; the rates were 34% and 29% for a depressive relapse and 19% and 22% for a hypomania/mania relapse. There were no significant differences in time to relapse. The proportion discontinuing prematurely because of side effects was 16% for lithium and 4% for divalproex. Conclusions: The hypothesis that divalproex is more effective than lithium in the long-term management of rapid-cycling bipolar disorder is not supported by these data. Preliminary data suggest highly recurrent refractory depression may be the hallmark of rapid-cycling bipolar disorder.
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页码:2152 / 2161
页数:10
相关论文
共 20 条
[1]  
ALLEN MH, 2004, 2004 ANN M NEW RES P
[2]  
*AM PSYCH ASS, 2002, AM J PSYCHIAT S, V159
[3]   A randomized, placebo-controlled 12-month trial of divalproex and lithium in treatment of outpatients with bipolar I disorder [J].
Bowden, CL ;
Calabrese, JR ;
McElroy, SL ;
Gyulai, L ;
Wassef, A ;
Petty, F ;
Pope, HG ;
Chou, JCY ;
Keck, PE ;
Rhodes, LJ ;
Swann, AC ;
Hirschfeld, RMA ;
Wozniak, PJ .
ARCHIVES OF GENERAL PSYCHIATRY, 2000, 57 (05) :481-489
[4]   A placebo-controlled 18-month trial of lamotrigine and lithium maintenance treatment in recently manic or hypomanic patients with bipolar I disorder [J].
Bowden, CL ;
Calabrese, JR ;
Sachs, G ;
Yatham, LN ;
Asghar, SA ;
Hompland, M ;
Montgomery, P ;
Earl, N ;
Smoot, TM ;
DeVeaugh-Geiss, J .
ARCHIVES OF GENERAL PSYCHIATRY, 2003, 60 (04) :392-400
[5]  
BOWDEN CL, 2004, ARCH GEN PSYCHIAT, V61, P680
[6]   A placebo-controlled 18-month trial of lamotrigine and lithium maintenance treatment in recently depressed patients with bipolar I disorder [J].
Calabrese, JR ;
Bowden, CL ;
Sachs, G ;
Yatham, LN ;
Behnke, K ;
Mehtonen, OP ;
Montgomery, P ;
Ascher, J ;
Paska, W ;
Earl, N ;
DeVeaugh-Geiss, J .
JOURNAL OF CLINICAL PSYCHIATRY, 2003, 64 (09) :1013-1024
[7]   A double-blind placebo-controlled study of lamotrigine monotherapy in outpatients with bipolar I depression [J].
Calabrese, JR ;
Bowden, CL ;
Sachs, GS ;
Ascher, JA ;
Monaghan, E ;
Rudd, GD .
JOURNAL OF CLINICAL PSYCHIATRY, 1999, 60 (02) :79-+
[8]  
CALABRESE JR, 1990, AM J PSYCHIAT, V147, P431
[9]   A double-blind, placebo-controlled, prophylaxis study of lamotrigine in rapid-cycling bipolar disorder [J].
Calabrese, JR ;
Suppes, T ;
Bowden, CL ;
Sachs, GS ;
Swann, AC ;
McElroy, SL ;
Kusumakar, V ;
Ascher, JA ;
Earl, NL ;
Greene, PL ;
Monaghan, ET .
JOURNAL OF CLINICAL PSYCHIATRY, 2000, 61 (11) :841-850
[10]  
DUNNER DL, 1974, ARCH GEN PSYCHIAT, V30, P229