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无反应的慢性精神分裂症患者的抗精神病药物血药浓度

Blood levels of neuroleptic drugs in nonresponding chronic schizophrenic patients.

作者信息

Smith R C, Crayton J, Dekirmenjian H, Klass D, Davis J M

出版信息

Arch Gen Psychiatry. 1979 May;36(5):579-84. doi: 10.1001/archpsyc.1979.01780050089011.

Abstract

Blood levels of butaperazine were measured in schizophrenic patients who were chronic nonresponders to their psychotropic medication. The blood levels were compared with those in patients who had shown a better clinical response to this neuroleptic. Nonresponders had two to seven times lower levels of butaperazine in plasma and RBCs after a single dose or chronic dosing. Some of the patients later treated with thioridazine or haloperidol had lower plasma levels of these neuroleptics also. No significant differences were found between nonresponders and relative responders in either the alpha- or beta-phase half-life of butaperazine in plasma and RBCs after administration of a single dose of the drug. Butaperazine and thioridazine levels were not related to previously administered amounts of neuroleptic drugs. These findings do not support the hypothesis that low blood levels are the result of faster systemic metabolism of the drug after it reaches the central circulation. Our results suggest that low blood levels of neuroleptics may be one important factor in the poor clinical response of some chronic schizophrenic patients.

摘要

对那些对精神药物长期无反应的精神分裂症患者测定了丁酰拉嗪的血药浓度。将这些血药浓度与对这种抗精神病药物临床反应较好的患者的血药浓度进行了比较。单次给药或长期给药后,无反应者血浆和红细胞中的丁酰拉嗪水平比有反应者低两到七倍。后来接受硫利达嗪或氟哌啶醇治疗的一些患者,这些抗精神病药物的血浆水平也较低。在单次给药后,无反应者与相对有反应者在丁酰拉嗪在血浆和红细胞中的α相或β相半衰期方面均未发现显著差异。丁酰拉嗪和硫利达嗪的水平与先前服用的抗精神病药物剂量无关。这些发现不支持血药浓度低是药物到达体循环后全身代谢加快所致的假说。我们的结果表明,抗精神病药物血药浓度低可能是一些慢性精神分裂症患者临床反应不佳的一个重要因素。

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