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Dose response and atypical antipsychotics in schizophrenia
被引:42
|作者:
Kinon, BJ
[1
]
Ahl, J
[1
]
Stauffer, VL
[1
]
Hill, AL
[1
]
Buckley, PF
[1
]
机构:
[1] Eli Lilly & Co, Lilly Corp Ctr, Res Labs, Indianapolis, IN 46285 USA
来源:
关键词:
D O I:
10.2165/00023210-200418090-00005
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Based on information from clinical trials, both the efficacy and adverse effects of conventional antipsychotics in the treatment of schizophrenia are dose related. The overlapping nature of these dose-response profiles limits the use of these agents. Atypical antipsychotics provide greater relief across the comorbid symptom domains of schizophrenia, but dose-response studies and clinical experience have revealed that some of these drugs also have dose limitations. This article reviews the dose-response relationships of the atypical antipsychotics as presented predominantly in pivotal, randomised studies (double-blind and otherwise). Limited data indicate that clozapine shows dose-related efficacy up to 600 mg/ day in patients with treatment-resistant schizophrenia. However, higher dosages of clozapine may be associated with the risk of seizures. Risperidone demonstrates dose-related adverse events that compromise efficacy. The dose-response relationships for ziprasidone, quetiapine and aripiprazole are less well established. The efficacy of olanzapine appears to be dose related within the recommended dosage range of 10-20 mg/day, but clinical trials that have explored higher dosages suggest improved efficacy. Furthermore, the higher doses are not associated with a significantly increased incidence of adverse events. Further studies are clearly needed to fully characterise the dose-response relationships of atypical antipsychotics.
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页码:597 / 616
页数:20
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