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奥兰扎平治疗精神分裂症58例临床观察
作者:张新波 谢世平 范俭雄 姚辉 李海林 张宁 张心保 
单位:南京医科大学,附属脑科医院,江苏,南京,210029
关键词:奥兰扎平 精神分裂症 药物治疗 副作用 
分类号:R749.3
出版年·卷·期(页码):2002·21·第四期(324-325)
摘要:

目的:观察奥兰扎平治疗精神分裂症的临床疗效与安全性.方法:选择58例精神分裂症病人,开始给予奥兰扎平5mg*d-1,3d后根据临床疗效、副反应情况酌情增加剂量,最大剂量不超过20mg*d-1,治疗8周.治疗前及治疗后每2周用PANSS、CGI、TESS量表评定1次.结果:治疗后PANSS总分、各因子分较治疗前显著下降(P<0.01),副反应主要有抗胆碱症状、过度镇静、体重增加、一过性丙氨酸氨基转移酶升高.结论:奥兰扎平是一种安全、有效、副作用较轻的抗精神病药.

Objective  To explore the effect and safety of olanzapine.Methods  58 in-patients diagnosed as schizophrenia according to CCMD2R had been given olanzapine at least for 8 weeks.The dosage was 5mg·d    -1 at the beginning.Afterwards,the dosage was adjusted according to clinical effect and side effect,and the maximum dosage was no more than 20mg·d    -1.PANSS,CGI and TESS were evaluated before treatment and every other 2 weeks after treatment.Result  PANSS total score and all factors score were significantly lower (P&lt;0.01) in the end of treatment than in the beginning.The side effects were mainly antimuscarinic activity,somnolence,weight gain,transitory and reversible ALT increasing.Conclusion  Olanzapine is one of the effective and safe antipsychotics.

参考文献:

[1] Ereshefsky L, TRAN-JOHNSON T K, WATANABE M D. Pathophysiologic basis for schizophrenia and the efficacy of antipsychotics, 1990(9)
[2] MELTZER H Y, NASH J F. Effects of antipsychotic drugs on serotonin receptors, 1991(4)
[3] BYMASTER F P, HEMRICK-LUECKE S K, PERRY K W. Neurochemical evidence for antagonism by olanzapine of dopamine,serotonin,α1-adrenergic and muscarinic receptors in vivo in rats. 1996(1-2). doi:10.1007/BF02245608
[4] BEASLEY C M Jr, SANGER T, SATTERLEE W. Olanzapine versus placebo:results of a double-blind,fixed-dose olanzapine trial. 1996(1-2). doi:10.1007/BF02245617
[5] BEASLEY C M Jr, TOLLEFSON G, TRAN P. Olanzapine versus placebo and haloperidol:acute phase results of the North American double-blind olanzapine trial. 1996(2). doi:10.1016/0893-133X(95)00069-P
[6] Street J. Long-term treatment-emergent dyskinetic symptoms in patients treated with olanzapine and haloperidol. 1996(6). doi:10.1016/0924-977X(96)87915-6 

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