Paap C M, Sharpe G L
University of Texas College of Pharmacy, Austin.
Dev Pharmacol Ther. 1993;20(3-4):174-9. doi: 10.1159/000457559.
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.
比较了采用荧光偏振免疫分析法(FPIA)和特定高效液相色谱法(HPLC)测定的早产儿血清万古霉素浓度。纳入需要万古霉素治疗并监测血清万古霉素浓度的早产儿(胎龄<38周)。采集血清万古霉素浓度峰值样本,分别采用FPIA和HPLC进行分析。以平均绝对误差和平均百分比误差为因变量,以孕龄、出生后年龄、胎龄、体重和治疗时长为自变量进行多变量和分层数据分析,以描述研究结果。共分析了15对来自平均胎龄为30±4周新生儿的万古霉素浓度。FPIA法与HPLC法测定的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±2.0mg/l。孕龄、体重以及从开始治疗到采集样本的时间是最能表征FPIA法高估万古霉素浓度的自变量。FPIA法测定早产儿万古霉素浓度时高估了实际浓度。孕龄小于30周、体重小于1200g以及在测定浓度前治疗时长大于48小时的早产儿,FPIA法与HPLC法的结果差异最大。当采用FPIA法测定万古霉素浓度时,药代动力学参数估计和剂量调整可能会出现显著误差。