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应用修正后的 Winter-Tozer 方程对神经重症监护病房患者的游离苯妥英钠浓度进行特征描述。

Characterization of unbound phenytoin concentrations in neurointensive care unit patients using a revised Winter-Tozer equation.

机构信息

Department of Pharmacy Practice, Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.

出版信息

Ann Pharmacother. 2013 May;47(5):628-36. doi: 10.1345/aph.1R651. Epub 2013 Apr 19.

Abstract

BACKGROUND

Prior studies examining the accuracy of the Winter-Tozer (WT) equation for correcting total phenytoin concentrations in critically ill patients have yielded conflicting results and are limited by small sample sizes and stringent exclusion criteria, which lessen external validity.

OBJECTIVE

To determine whether the traditional WT equation is appropriate in correcting total phenytoin concentrations in a large sample of patients in a neurointensive care unit (NICU) and whether a new equation may be more predictive.

METHODS

In a retrospective study, NICU patients with reports of a concurrent total and unbound phenytoin concentration and albumin level were analyzed. Two new predictive equations were generated using a revised WT equation and regression model of baseline and laboratory characteristics. Prediction error analysis using a 20% validation cohort was conducted on all 3 equations for comparison.

RESULTS

A total of 140 adults were included for data analysis, with data on 80% used for derivation and 20% as validation of all equations. The mean unbound phenytoin concentration was 1.4 μg/mL, which represented a free fraction of 10%. Most samples were collected within 24 hours of NICU admission. Multivariate regression analysis demonstrated that albumin, total phenytoin concentration, sex, and creatinine clearance were predictive of measured unbound phenytoin concentrations. The traditional WT equation significantly underpredicted true unbound phenytoin concentrations, with 32.1% of patients having a prediction error of more than 50% in the validation cohort.

CONCLUSIONS

The traditional WT equation was significantly biased in underpredicting true unbound phenytoin concentrations in neurointensive care unit patients and should not be used in this setting. Two modified equations were more accurate and precise and should be considered for use when unbound phenytoin concentrations are not readily available in an NICU population.

摘要

背景

先前研究检查 Winter-Tozer(WT)方程修正危重病患者总苯妥英浓度的准确性,得到的结果相互矛盾,且受到小样本量和严格排除标准的限制,降低了外部有效性。

目的

确定传统的 WT 方程是否适用于神经重症监护病房(NICU)中大量患者的总苯妥英浓度校正,以及新方程是否更具预测性。

方法

在回顾性研究中,分析了报告同时存在总苯妥英和未结合苯妥英浓度及白蛋白水平的 NICU 患者。使用修订后的 WT 方程和基础及实验室特征回归模型生成了两个新的预测方程。使用 20%验证队列对所有 3 个方程进行预测误差分析,以进行比较。

结果

共纳入 140 例成人进行数据分析,80%的数据用于推导,20%的数据用于验证所有方程。未结合苯妥英浓度的平均值为 1.4μg/mL,代表游离分数为 10%。大多数样本采集于入住 NICU 后 24 小时内。多变量回归分析表明,白蛋白、总苯妥英浓度、性别和肌酐清除率可预测实测未结合苯妥英浓度。传统的 WT 方程显著低估了真实的未结合苯妥英浓度,在验证队列中,32.1%的患者预测误差超过 50%。

结论

传统的 WT 方程在预测神经重症监护病房患者真实未结合苯妥英浓度时存在显著偏差,不应在此类环境中使用。两个改良方程更准确和精确,当在 NICU 人群中无法获得未结合苯妥英浓度时,应考虑使用。

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