Results of a naturalistic study of treatment options: Switching atypical antipsychotic drugs or augmenting with valproate

被引:5
作者
Cramer, JA
Sernyak, M
机构
[1] Yale Univ, Sch Med, Dept Psychiat, West Haven, CT 06516 USA
[2] Vet Affairs Connecticut Healthcare Syst, Mental Hlth Care Line, West Haven, CT USA
关键词
antipsychotic; olanzapine; quetiapine; risperidone; valproate; divalproex;
D O I
10.1016/S0149-2918(04)90134-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Combination therapy with atypical antipsychotic agents has not been well studied. Duration of persistence with a prescribed treatment regimen can be used to estimate overall treatment success. Objective: The aim of this study was to determine whether valproate augmentation improved treatment efficacy (ie, persistence with the prescribed regimen) and efficiency (ie, reduction of antipsychotic dose) with atypical antipsychotic drugs for older and younger patients, using a retrospective database analysis. Methods: Prescription refill data for atypical antipsychotics during calendar-year 2001 from a national pharmacy chain was used for longitudinal analyses. The database was used to identify patients aged 15 to 64 years and greater than or equal to65 years taking risperidone, quetiapine, or olanzapine (but not valproate). Patients who switched to another atypical antipsychotic (group A) or added valproate (group B) were followed after the index prescription to determine the duration of persistence with the treatment regimen and dose changes. Results: We identified 10,262 patients who were prescribed an atypical antipsychotic, of whom 1022 patients switched to an alternative atypical and 1651 added valproate to the index atypical. The addition of valproate provided significantly longer duration of treatment regimen (mean, 155-159 days) than switching from any atypical antipsychotic drug (mean, 127-130 days) for patients aged 15 to 64 years or greater than or equal to65 years (all P < 0.001). Atypical antipsychotic doses did not change significantly from baseline to final prescription in groups A or B. The final mean (SD) dose of valproate added to risperidone (389.1 [130.7] mg/d) was significantly lower than valproate added to quetiapine (424.6 [117.1] mg/d; P = 0.002) or olanzapine (411.6 [122.8] mg/d; P = 0.007). Conclusions: In this naturalistic study, the addition of valproate to an atypical antipsychotic increased the duration of treatment compared with switching among atypical antipsychotics. Valproate augmentation may be a good treatment strategy for patients whose atypical antipsychotic monotherapy is inadequate. Copyright (C) 2004 Excerpta Medica, Inc.
引用
收藏
页码:905 / 914
页数:10
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