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Plasma concentrations of quetiapine, N-desalkylquetiapine, o-desalkylquetiapine, 7-hydroxyquetiapine, and quetiapine sulfoxide in relation to quetiapine dose, formulation, and other factors.与喹硫平剂量、剂型及其他因素有关的喹硫平、N-去烷基喹硫平、奥氮平、7-羟基喹硫平及喹硫平砜的血浆浓度。
Ther Drug Monit. 2012 Aug;34(4):415-21. doi: 10.1097/FTD.0b013e3182603f62.
2
Measurement of quetiapine and four quetiapine metabolites in human plasma by LC-MS/MS.采用液相色谱-串联质谱法测定人血浆中喹硫平和四种喹硫平代谢物。
Biomed Chromatogr. 2012 Sep;26(9):1125-32. doi: 10.1002/bmc.2672. Epub 2012 Jan 12.
3
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Possible drug-drug interaction between quetiapine and lamotrigine--evidence from a Swedish TDM database.可能的喹硫平和拉莫三嗪药物相互作用——来自瑞典 TDM 数据库的证据。
Br J Clin Pharmacol. 2011 Jul;72(1):153-6. doi: 10.1111/j.1365-2125.2011.03941.x.
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Pharmacokinetic variability of quetiapine and the active metabolite N-desalkylquetiapine in psychiatric patients.精神科患者中喹硫平和其活性代谢物 N-去烷基喹硫平的药代动力学变异性。
Ther Drug Monit. 2011 Apr;33(2):222-6. doi: 10.1097/FTD.0b013e31821160c4.
6
Relationship between daily dose, plasma concentrations, dopamine receptor occupancy, and clinical response to quetiapine: a review.喹硫平的日剂量、血浆浓度、多巴胺受体占有率与临床疗效的关系:综述。
J Clin Psychiatry. 2011 Aug;72(8):1108-23. doi: 10.4088/JCP.09r05739yel. Epub 2011 Jan 25.
7
Cytochrome P450 and ABCB1 genetics: association with quetiapine and norquetiapine plasma and cerebrospinal fluid concentrations and with clinical response in patients suffering from schizophrenia. A pilot study.细胞色素 P450 和 ABCB1 基因:与喹硫平和去甲喹硫平的血浆和脑脊液浓度以及精神分裂症患者临床反应的关联。一项初步研究。
J Psychopharmacol. 2011 Jul;25(7):896-907. doi: 10.1177/0269881110389208. Epub 2010 Dec 8.
8
Individual clearance and therapeutic drug monitoring of quetiapine in clinical practice.喹硫平在临床实践中的个体清除率及治疗药物监测
Neuro Endocrinol Lett. 2010;31(2):203-7.
9
Extended-release quetiapine fumarate (quetiapine XR) as adjunctive therapy in major depressive disorder (MDD) in patients with an inadequate response to ongoing antidepressant treatment: a multicentre, randomized, double-blind, placebo-controlled study.富马酸喹硫平缓释片(喹硫平 XR)作为正在进行的抗抑郁治疗应答不足的重性抑郁障碍(MDD)患者的辅助治疗:一项多中心、随机、双盲、安慰剂对照研究。
Int J Neuropsychopharmacol. 2010 Aug;13(7):917-32. doi: 10.1017/S1461145710000015. Epub 2010 Feb 23.
10
Quetiapine: dose-response relationship in schizophrenia.喹硫平:精神分裂症中的剂量-反应关系。
CNS Drugs. 2008;22(1):49-68; discussion 69-72. doi: 10.2165/00023210-200822010-00004.

2000-2011 年治疗药物监测服务中与规定剂量和其他因素有关的血浆喹硫平浓度数据。

Plasma quetiapine in relation to prescribed dose and other factors: data from a therapeutic drug monitoring service, 2000-2011.

机构信息

Toxicology Unit, Department of Clinical Biochemistry, King's College Hospital NHS Foundation Trust, Denmark Hill, London SE5 9RS, UK.

出版信息

Ther Adv Psychopharmacol. 2013 Jun;3(3):129-37. doi: 10.1177/2045125312470677.

DOI:10.1177/2045125312470677
PMID:24167685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3805454/
Abstract

OBJECTIVE

Suggested predose plasma quetiapine target ranges for effective therapy in schizophrenia lie between 50 and 500 µg/l. We aimed to examine data from a quetiapine therapeutic drug monitoring (TDM) service to assess the plasma quetiapine concentrations attained at specified doses in clinical practice.

METHOD

We studied TDM data from patients given immediate-release quetiapine in the period 2000-2011.

RESULTS

There were 946 samples from 487 patients (257 males, age at time of first sample, median [range] 34 [14-87] years, and 230 females, age at time of first sample, median [range] 38 [10-92] years). The plasma quetiapine concentration was <50 and <100 µg/l in 30% and 50% of samples, respectively (no quetiapine detected in 9% of samples). The relationship between dose and plasma quetiapine was poor. The mean (95% confidence interval [CI]) quetiapine dose was higher (t = 3.6, df = 446, p <0.01) in males versus females (641 [600-1240] and 548 [600-943] mg/day, respectively), although there was no difference in median dose (600 mg/day) or in the mean (95% CI) plasma quetiapine concentrations attained. Smoking habit had no discernible effect on plasma quetiapine concentration.

CONCLUSIONS

There was a poor relationship between dose and plasma quetiapine concentration in this study, as found by others. This is probably because of the short plasma half-life of the drug, at least in part. Nevertheless, quetiapine TDM can help assess adherence and measurement of quetiapine metabolites, notably N-desalkylquetiapine, as well as quetiapine itself may enhance the value of quetiapine TDM in future.

摘要

目的

建议精神分裂症有效治疗的喹硫平预剂量血浆靶范围在 50 至 500µg/l 之间。我们旨在通过喹硫平治疗药物监测(TDM)服务的数据来评估在临床实践中特定剂量下达到的血浆喹硫平浓度。

方法

我们研究了 2000-2011 年期间接受即时释放喹硫平的患者的 TDM 数据。

结果

来自 487 名患者的 946 个样本(257 名男性,首次样本时的年龄中位数[范围]为 34[14-87]岁,230 名女性,首次样本时的年龄中位数[范围]为 38[10-92]岁)。分别有 30%和 50%的样本的血浆喹硫平浓度<50 和<100µg/l(9%的样本未检测到喹硫平)。剂量与血浆喹硫平之间的关系不佳。男性与女性的平均(95%置信区间[CI])喹硫平剂量更高(t=3.6,df=446,p<0.01)(分别为 641[600-1240]和 548[600-943]mg/天),尽管中位剂量(600mg/天)或平均(95%CI)达到的血浆喹硫平浓度无差异。吸烟习惯对血浆喹硫平浓度无明显影响。

结论

与其他研究一样,本研究中剂量与血浆喹硫平浓度之间存在不良关系。这可能至少部分是由于该药物的血浆半衰期短。尽管如此,喹硫平 TDM 可以帮助评估依从性和喹硫平代谢物(尤其是 N-去烷基喹硫平)的测量,喹硫平本身可能会提高喹硫平 TDM 的未来价值。