使用荧光偏振免疫分析法(Tdx)对早产儿血清万古霉素浓度的高估。

C M Paap, G L Sharpe
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引用次数: 9

摘要

比较了荧光偏振免疫分析法(FPIA)和高效液相色谱法(HPLC)测定早产儿血清万古霉素浓度的差异。纳入需要万古霉素治疗和血清万古霉素浓度监测的早产儿(< 38周胎龄)。采集血清万古霉素峰值浓度样品,分别用fia和HPLC进行独立分析。多变量和分层数据分析以平均绝对误差和平均百分比误差作为因变量,以怀孕后年龄、出生后年龄、胎龄、体重和治疗持续时间为自变量来描述结果。对平均胎龄为30 +/- 4周的新生儿共15对万古霉素浓度进行了分析。FPIA与HPLC测定万古霉素浓度的平均百分比误差为18.1 +/- 11.1%,平均绝对误差为3.7 +/- 2.0 mg/l。孕后年龄、体重和从开始治疗到样本收集的时间是最能表征FPIA万古霉素浓度高估的独立变量。FPIA万古霉素测定法高估了早产儿万古霉素的实际浓度。孕龄小于30周、体重小于1200g、治疗时间大于48 h的早产儿在浓度测定前的fia和HPLC结果差异最大。当使用FPIA测定万古霉素浓度时,可能会出现药代动力学参数估计和剂量调整的显著误差。
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Overestimation of serum vancomycin concentrations using a fluorescence polarization immunoassay (Tdx) in preterm neonates.

Serum vancomycin concentrations determined by fluorescence polarization immunoassay (FPIA) with a specific high-performance liquid chromatography (HPLC) method in preterm neonates were compared. Preterm neonates (< 38 weeks gestational age) requiring vancomycin therapy and serum vancomycin concentration monitoring were enrolled. Peak serum vancomycin concentration samples were collected and independently analyzed by FPIA and HPLC. Multivariate and stratified data analysis was done with mean absolute error and mean percent error as dependent variables and independent variables as postconceptional age, postnatal age, gestational age, weight, and duration of therapy to characterize the findings. A total of 15 paired vancomycin concentrations were analyzed from neonates with a mean gestational age of 30 +/- 4 weeks. The mean percentage error of FPIA versus HPLC vancomycin concentrations was 18.1 +/- 11.1% and the mean absolute error was 3.7 +/- 2.0 mg/l. Postconceptional age, weight, and time from initiation of therapy to sample collection were independent variables which best characterized the overestimation of FPIA vancomycin concentrations. The FPIA vancomycin assay method overestimated actual vancomycin concentrations in preterm neonates. Preterm neonates less than 30 weeks postconceptional age, less than 1,200 g body weight, and duration of therapy greater than 48 h prior to concentration determination had the greatest difference in FPIA and HPLC results. Significant error in pharmacokinetic parameter estimations and dosage adjustments is possible when vancomycin concentrations are determined by FPIA.

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