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抗精神病药物水平与抗精神病作用:一种难以建立的相关性;游离(或衍生物)与血浆总水平相比的潜在优势。

Neuroleptic drug levels and antipsychotic effects: a difficult correlation; potential advantage of free (or derivative) versus total plasma levels.

作者信息

Garver D L

机构信息

Department of Psychiatry, University of Alabama, Birmingham 35294.

出版信息

J Clin Psychopharmacol. 1989 Aug;9(4):277-81.

PMID:2570087
Abstract

Attempts to demonstrate relationships between neuroleptic plasma levels and antipsychotic response have met with mixed results. Eight studies have attempted to clarify such discrepancies by contrasting drug level-response relationships in which the fit of plasma neuroleptic concentrations with response could be contrasted to the fit with antipsychotic response found with free (unbound) neuroleptic (or close derivations of free drug, such as cerebrospinal fluid or erythrocyte neuroleptic concentrations). In describing such drug level-response relationships, seven of eight studies show superiority of free, cerebrospinal fluid or erythrocyte concentrations of drug, as compared with plasma neuroleptic levels (p less than 0.05). Variance between neuroleptic blood levels and therapeutic response was reduced 12.0% +/- 17.7% (SD) by the use of free, cerebrospinal fluid or erythrocyte neuroleptic concentrations rather than plasma drug concentrations. Neuroleptic assays that monitor metabolites as well as parent neuroleptic may also reduce variance between drug level and response. The state of present information is such that routine monitoring of neuroleptic drug concentrations to guide dosage adjustment is premature.

摘要

试图证明抗精神病药物血浆水平与抗精神病反应之间的关系,结果喜忧参半。八项研究试图通过对比药物水平-反应关系来澄清此类差异,在这些关系中,血浆抗精神病药物浓度与反应的拟合情况可与游离(未结合)抗精神病药物(或游离药物的近似衍生物,如脑脊液或红细胞抗精神病药物浓度)与抗精神病反应的拟合情况进行对比。在描述此类药物水平-反应关系时,八项研究中有七项表明,与血浆抗精神病药物水平相比,游离、脑脊液或红细胞药物浓度具有优势(p小于0.05)。使用游离、脑脊液或红细胞抗精神病药物浓度而非血浆药物浓度,可使抗精神病药物血药水平与治疗反应之间的差异降低12.0%±17.7%(标准差)。监测代谢物以及母体抗精神病药物的抗精神病药物检测方法,也可能减少药物水平与反应之间的差异。目前的信息状况表明,常规监测抗精神病药物浓度以指导剂量调整为时过早。

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