Correction of posaconazole concentrations for hypoalbuminemia.

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Pharmacotherapy Pub Date : 2025-04-18 DOI:10.1002/phar.70021
David E Nix, Fekade Sime, Jason A Roberts
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引用次数: 0

Abstract

Background: Posaconazole is an example of a highly protein-bound drug (>98%) in which therapeutic drug monitoring (TDM) is commonplace. Total drug concentration is typically measured, and in the setting of hypoalbuminemia, total concentrations are lower despite no anticipated change in unbound concentration. Data support that unbound posaconazole concentration is responsible for antifungal activity and, in theory, is responsible for adverse effects that are dose-related. However, the therapeutic range of posaconazole is expressed as total concentration. The objective of this study was to investigate the use of an equation to correct posaconazole concentrations for albumin concentration as a surrogate for measurement of unbound concentration.

Methods: Data on unbound and total posaconazole concentration were acquired retrospectively from a study of posaconazole pharmacokinetics in critically ill patients. The relationship between total and unbound concentration was explored with and without albumin as a covariate using linear regression. Correction equations were used to normalize total concentration to an albumin concentration of 4.4 g/dL.

Results: A total of 78 pairs of total and unbound concentrations were available. Total and unbound posaconazole concentrations were determined using ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). The median fraction unbound was 0.00645 (interquartile range of 0.00331-0.00794). Albumin concentration plays a highly significant role in the interpretation of TDM results. In a patient with hypoalbuminemia, a corrected concentration (Ccorr) = Ct/(0.01 + 0.99·Alb/4.4), where Ct is the total concentration and Alb is the albumin concentration in units of g/dL, is suggested. This equation can be further simplified to Csim = Ct·4.4/Alb, where Csim is a close approximation of Ccorr.

Conclusions: Hypoalbuminemia is associated with lower total concentrations of posaconazole; however, the "active" unbound concentration is not expected to systematically change. As a result, total posaconazole concentrations in the therapeutic range for patients with hypoalbuminemia are more likely to be associated with toxicity, especially when doses are increased to achieve "therapeutic" concentrations.

泊沙康唑治疗低白蛋白血症的浓度校正。
背景:泊沙康唑是一种高度蛋白结合的药物(>98%),其中治疗药物监测(TDM)是常见的。通常测量药物总浓度,在低白蛋白血症的情况下,尽管未结合浓度没有预期的变化,但总浓度较低。数据支持未结合的泊沙康唑浓度对抗真菌活性负责,并且在理论上对剂量相关的不良反应负责。泊沙康唑的治疗范围以总浓度表示。本研究的目的是研究使用一个方程来校正泊沙康唑浓度的白蛋白浓度,以代替未结合浓度的测量。方法:回顾性分析危重病人泊沙康唑药动学资料,获取泊沙康唑非结合浓度和总浓度。用线性回归方法探讨了总浓度和未结合浓度之间的关系,并将白蛋白作为协变量。用校正方程将总浓度归一化为4.4 g/dL的白蛋白浓度。结果:共获得78对总浓度和未结合浓度。采用超高效液相色谱-串联质谱法(UHPLC-MS/MS)测定泊沙康唑总浓度和未结合浓度。未绑定的中位分数为0.00645(四分位数范围为0.00331-0.00794)。白蛋白浓度在TDM结果的解释中起着非常重要的作用。对于低白蛋白血症患者,建议校正浓度(Ccorr) = Ct/(0.01 + 0.99·Alb/4.4),其中Ct为总浓度,Alb为白蛋白浓度,单位为g/dL。该式可以进一步简化为Csim = Ct·4.4/Alb,其中Csim是Ccorr的近似值。结论:低白蛋白血症与泊沙康唑总浓度降低有关;然而,“活性”非结合浓度预计不会系统性地改变。因此,泊沙康唑在低白蛋白血症患者治疗范围内的总浓度更可能与毒性有关,特别是当剂量增加以达到“治疗”浓度时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmacotherapy
Pharmacotherapy 医学-药学
CiteScore
7.80
自引率
2.40%
发文量
93
审稿时长
4-8 weeks
期刊介绍: Pharmacotherapy is devoted to publication of original research articles on all aspects of human pharmacology and review articles on drugs and drug therapy. The Editors and Editorial Board invite original research reports on pharmacokinetic, bioavailability, and drug interaction studies, clinical trials, investigations of specific pharmacological properties of drugs, and related topics.
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