仅使用谷浓度预测万古霉素曲线下面积:儿科人群药代动力学模型的性能评估

Stef Schouwenburg, Tim Preijers, Robert B Flint, Enno D Wildschut, Birgit C P Koch, Brenda C M de Winter, Alan Abdulla
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引用次数: 0

摘要

目的在儿科患者中,万古霉素在抗感染中起着关键作用,需要精确的治疗药物监测以确保疗效和安全性。基于浓度-时间曲线下面积(AUC24h),采用模型信息精确给药(MIPD)已经证明了优化给药策略的潜力。然而,仅使用谷浓度估计AUC24h的群体药代动力学模型的预测性能尚未得到评估。方法回顾性评价23个万古霉素群体药代动力学模型的预测性能;(A) PNA≥50天21例,(B) PNA≥50天124例。使用;(a)峰谷浓度,(b)仅使用峰谷浓度或(c)谷浓度,(d)协变量信息(先验)。所有模型中每个受试者的平均AUC24h被用作“真实”AUC24h。结果在这两个队列中,仅使用谷浓度的AUC24h精度的相对均方根误差(rRMSE)与同时使用峰谷样品的rRMSE相似。对于队列A, Chen、Colin和Mehrotra的模型表现出最佳的低谷型表现,其相对偏差(rBias)最低(-3.3%和-2.6%),rRMSE最低(6.8%和7.3%)。对于队列B, Alsultan和Lv的模型显示了最低的rBias(1.75%和-5.4%)和rRMSE(16.6%和15.1%)。结论本研究表明,基于浓度的AUC24h估计是万古霉素MIPD的可行方法。这些发现支持了儿科晚期MIPD万古霉素治疗的选择模式,尽管建议进一步研究临床结果。
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lPrediction of Vancomycin Area-under-the-curve using Trough Concentrations Only: Performance Evaluation of Pediatric Population Pharmacokinetic Models
Objectives In pediatric patients, vancomycin plays a pivotal role in combating infections, necessitating precise therapeutic drug monitoring to ensure efficacy and safety. The adoption of model-informed precision dosing (MIPD) has demonstrated potential in optimizing dosing strategies based on the area under the concentration-time curve (AUC24h). However, predictive performance of population pharmacokinetic models using only trough concentrations to estimate AUC24h has not been evaluated. Methods Predictive performance of 23 vancomycin population pharmacokinetic models was retrospectively evaluated in two cohorts; (A) 21 subjects with PNA<50 days, (B) 124 subjects with PNA≥50 days. Multiple scenarios were investigated using; (a) peak and trough concentration, (b) using either peak or (c) trough concentration solely, (d) covariate information (a priori). The median AUC24h per subject across all models was used as ‘true’ AUC24h. Results For both cohorts, relative root mean square error (rRMSE) for the AUC24h precision using only trough concentrations was similar to the rRMSE using both a peak and trough sample. For cohort A, the model by Chen, Colin, and Mehrotra showed best trough-based performance with the lowest relative Bias (rBias) (-3.3% and -2.6%) and rRMSE (6.8% and 7.3%). For cohort B, the models from Alsultan and Lv illustrated the lowest rBias (1.75% and -5.4%) and rRMSE (16.6% and 15.1%). Conclusions This study illustrates that trough concentration-based AUC24h estimation is a feasible approach in vancomycin MIPD. These findings endorse the selected models for advanced MIPD vancomycin therapy in pediatrics, though further investigation into clinical outcomes is recommended.
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