Relapse prevention in bipolar I disorder: 18-month comparison of olanzapine plus mood stabiliser <i>v.</i> mood stabiliser alone

Mauricio Tohen(Harvard University), K. N. Roy Chengappa(University of Pittsburgh), Trisha Suppes(The University of Texas Southwestern Medical Center), Robert W. Baker(Eli Lilly (United States)), Carlos A. Zarate(National Institute of Mental Health), Charles L. Bowden(The University of Texas at San Antonio Health Science Center), Gary S. Sachs(Harvard University), David J. Kupfer(University of Pittsburgh), S. Nassir Ghaemi(Harvard University), Peter D. Feldman(Eli Lilly (United States)), Richard C. Risser(Eli Lilly (United States)), Angela R. Evans(Eli Lilly (United States)), Joseph R. Calabrese(Case Western Reserve University)
The British Journal of Psychiatry
March 31, 2004
Cited by 328Open Access
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Abstract

BACKGROUND: Few controlled studies have examined the use of atypical antipsychotic drugs for prevention of relapse in patients with bipolar I disorder. Aims To evaluate whether olanzapine plus either lithium or valproate reduces the rate of relapse, compared with lithium or valproate alone. METHOD: Patients achieving syndromic remission after 6 weeks'treatment with olanzapine plus either lithium (0.6-1.2 mmol/l) or valproate (50-125 microg/ml) received lithium or valproate plus either olanzapine 5-20 mg/day (combination therapy) or placebo (monotherapy), and were followed in a double-masked trial for 18 months. RESULTS: The treatment difference in time to relapse into either mania or depression was not significant for syndromic relapse (median time to relapse: combination therapy 94 days, monotherapy 40.5 days; P=0.742), but was significant for symptomatic relapse (combination therapy 163 days, monotherapy 42 days; P=0.023). CONCLUSIONS: Patients taking olanzapine added to lithium or valproate experienced sustained symptomatic remission, but not syndromic remission, for longer than those receiving lithium or valproate monotherapy.


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