Gubbins Paul O
University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, USA.
Curr Opin Infect Dis. 2007 Dec;20(6):579-86. doi: 10.1097/QCO.0b013e3282f1be91.
Mould-active azoles are used to treat systemic mycoses in neutropenic patients because of their broad spectrum activity, their availability as intravenous or oral formulations, and their safety. These agents exhibit complex pharmacokinetics and interact with many drugs, however, which can make their use in neutropenic patients challenging. With the addition of two mould-active azoles to the marketplace in the past several years, this paper will provide an overview of the pharmacokinetics and drug-drug interaction profiles of these azoles and will review the issues surrounding the therapeutic drug monitoring of these agents.
New mould-active azoles have sparked interest in correlating their serum concentrations to efficacy and toxicity. Efforts to establish such correlations have, however, generally proved unsuccessful. All mould-active azoles interact significantly with calcineurin inhibitors.
When used in combination with mould-active azoles, calcineurin inhibitor doses should be reduced by at least 50% and their blood or serum concentrations should be closely monitored.
由于具有广谱活性、有静脉或口服制剂且安全性良好,含霉菌活性的唑类药物被用于治疗中性粒细胞减少患者的系统性真菌病。然而,这些药物具有复杂的药代动力学特性,且会与许多药物相互作用,这使得它们在中性粒细胞减少患者中的使用具有挑战性。在过去几年中有两种含霉菌活性的唑类药物进入市场,本文将概述这些唑类药物的药代动力学和药物相互作用情况,并探讨围绕这些药物治疗药物监测的相关问题。
新型含霉菌活性的唑类药物引发了人们将其血清浓度与疗效和毒性相关联的兴趣。然而,建立这种关联的努力通常未获成功。所有含霉菌活性的唑类药物都与钙调神经磷酸酶抑制剂有显著相互作用。
当与含霉菌活性的唑类药物联合使用时,钙调神经磷酸酶抑制剂的剂量应至少减少50%,并应密切监测其血液或血清浓度。