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在接受治疗性亚低温的脑损伤患者持续输注咪达唑仑期间的双相浓度变化。

Biphasic concentration change during continuous midazolam administration in brain-injured patients undergoing therapeutic moderate hypothermia.

作者信息

Fukuoka Noriyasu, Aibiki Mayuki, Tsukamoto Toyohisa, Seki Keisuke, Morita Shushi

机构信息

Hospital Pharmacy Division and Intensive Care Unit, Kagawa Medical University, 1750-1, Ikenobe, Miki, Kita, Kagawa 761-0793, Japan.

出版信息

Resuscitation. 2004 Feb;60(2):225-30. doi: 10.1016/j.resuscitation.2003.09.017.

Abstract

OBJECTIVE

To define the pharmacokinetics of midazolam, a probe for monitoring cytochrome (CYP) 3A 4 activity, during moderate hypothermic therapy.

DESIGN

A prospective randomized study.

SETTING

The intensive care unit of a medical university hospital.

PATIENTS AND INTERVENTIONS

In 15 consecutive brain-injured patients, midazolam concentrations were measured serially using high-performance liquid chromatography (HPLC). Under continuous administration of the agent, eight patients underwent moderate hypothermia of 32-34 degrees C (hypothermia group) and seven received normothermic therapy (normothermia group). A one-compartment model was selected for pharmacokinetic analyses for the continuous administration. Data represent +/-S.D. Statistical analysis was performed using ANOVA followed by Scheffe's F-test or the Mann-Whitney U-test ( P<0.05 ).

MEASUREMENT AND MAIN RESULTS

Serum midazolam concentrations in the hypothermia group increased linearly until the body temperature (BT) reached 35 degrees C without plateauing, even during continuous administration, after which the levels decreased remarkably when BT rose to 36 degrees C. However, the concentrations in the normothermia group remained on a plateau, which lasted until the end of the study. In the hypothermia group, elimination rate constant (k(e)) and clearance (CL) in the phase below 35 degrees C BT were much lesser than those above 35 degrees C BT, whereas distribution volume (V(d)) during the hypothermic phase was greater than that during the period above 35 degrees C BT.

CONCLUSION

This study has demonstrated for the first time that midazolum concentration changes biphasically even during continuous infusion in hypothermic therapy. The mechanisms for the change are unclear. Thus, further studies including confirmation of cytochrome 3A 4 activity are required, while monitoring for the development of undesirable effects from over-dosing is also needed.

摘要

目的

确定咪达唑仑(一种用于监测细胞色素(CYP)3A4活性的探针)在中度低温治疗期间的药代动力学。

设计

一项前瞻性随机研究。

地点

一所医科大学医院的重症监护病房。

患者与干预措施

在15例连续的脑损伤患者中,使用高效液相色谱法(HPLC)连续测定咪达唑仑浓度。在持续给药的情况下,8例患者接受32 - 34摄氏度的中度低温治疗(低温组),7例接受常温治疗(常温组)。选择一室模型对持续给药进行药代动力学分析。数据以±标准差表示。采用方差分析,随后进行谢费尔F检验或曼 - 惠特尼U检验进行统计分析(P<0.05)。

测量与主要结果

低温组血清咪达唑仑浓度在体温(BT)达到35摄氏度之前呈线性增加,即使在持续给药期间也无平台期,之后当BT升至36摄氏度时水平显著下降。然而,常温组的浓度保持在平台期,直至研究结束。在低温组中,体温低于35摄氏度阶段的消除速率常数(k(e))和清除率(CL)远低于体温高于35摄氏度阶段,而低温阶段的分布容积(V(d))大于体温高于35摄氏度阶段。

结论

本研究首次证明,在低温治疗期间即使持续输注,咪达唑仑浓度也会出现双相变化。变化机制尚不清楚。因此,需要进一步研究,包括确认细胞色素3A4活性,同时也需要监测过量用药产生不良影响的情况。

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