van Maarseveen Erik M, Sprij Arwen, Touw Daniel J
*Department of Clinical Pharmacy, University Medical Center Utrecht; †Department of Pediatrics, Haga Teaching Hospital, The Hague; and ‡Department of Hospital and Clinical Pharmacy and Pharmacology, University Medical Center Groningen, University of Groningen, the Netherlands.
Ther Drug Monit. 2016 Jun;38(3):402-6. doi: 10.1097/FTD.0000000000000283.
Current gentamicin dosing algorithms in adult populations target a high peak concentration (Cmax) assuring efficacy and a drug-free period (concentration <0.5 mg/L) preventing toxicity. In contrast, gentamicin-based regimens in neonatal sepsis often aim for lower peak levels and trough concentrations of 0.5-2.0 mg·L. The latter concentrations are associated with an increased risk of aminoglycoside-related toxicity. Therefore, the primary aim of this study was to assess the target attainment of a simple and practical dosing regimen designed to attain drug-free periods in newborns.
The study was of prospective observational design. Neonates admitted to a level II neonatal nursery diagnosed with (suspected) early-onset sepsis and commencing intravenous gentamicin therapy of 5 mg·kg every 36 hours were eligible for inclusion. Gentamicin dosing was guided by drug concentration monitoring targeting Cmax values >8 mg·L and estimated trough concentrations <0.5 mg·L. Relationships between body weight (BW), gestational age (GA), postnatal age, and pharmacokinetic parameters were analyzed using the Pearson correlation test, and univariate and multivariate logistic regression analyses were performed to identify covariates predictive of target attainment failure.
A total of 184 patients were included. 90.4% of patients (n = 166) achieved a Cmax value >8 mg·L with a Cmin value <0.5 mg·L. Subsequently, significant correlations were found between GA and Cmax (r = 0.58, P < 0.001) between GA and Cmin (r = 0.44, P < 0.001), between BW and Cmax (r = 0.50, P < 0.001), and between BW and Cmin (r = 0.42, P < 0.001). Correlations between area under the curve (AUC) and GA (r = 0.064, P = 0.4), and between AUC and BW (r = 0.028, P = 0.7) were not significant. During multivariate analysis, only GA (P < 0.001) was retained as an independent predictor of underexposure.
Extended interval dosing of gentamicin resulted in high target attainment rates in neonates admitted to a level II unit. In line with previous reports, low GA and BW were predictive of subtherapeutic peak and toxic trough levels. The AUC, however, was unaffected by the interpatient variation in GA and BW. Since AUC-guided dosing is gaining interest worldwide, the latter finding deserves further exploration in other neonatal cohorts.
目前成人人群中庆大霉素给药算法的目标是获得较高的峰浓度(Cmax)以确保疗效,并设定无药期(浓度<0.5mg/L)以预防毒性。相比之下,新生儿败血症中基于庆大霉素的治疗方案通常旨在达到较低的峰浓度,谷浓度为0.5 - 2.0mg·L。后一种浓度与氨基糖苷类相关毒性风险增加有关。因此,本研究的主要目的是评估一种旨在使新生儿达到无药期的简单实用给药方案的目标达成情况。
本研究为前瞻性观察性设计。入住二级新生儿重症监护室、诊断为(疑似)早发型败血症且开始每36小时静脉注射5mg·kg庆大霉素治疗的新生儿符合纳入标准。庆大霉素给药以药物浓度监测为指导,目标是Cmax值>8mg·L,估计谷浓度<0.5mg·L。使用Pearson相关检验分析体重(BW)、胎龄(GA)、出生后年龄与药代动力学参数之间的关系,并进行单因素和多因素逻辑回归分析以确定预测目标达成失败的协变量。
共纳入184例患者。90.4%的患者(n = 166)达到了Cmax值>8mg·L且Cmin值<0.5mg·L。随后,发现GA与Cmax之间(r = 0.58,P < 0.001)、GA与Cmin之间(r = 0.44,P < 0.001)、BW与Cmax之间(r = 0.50,P < 0.001)以及BW与Cmin之间(r = 0.42,P < 0.001)存在显著相关性。曲线下面积(AUC)与GA之间(r = 0.064,P = 0.4)以及AUC与BW之间(r = 0.028,P = 0.7)的相关性不显著。在多因素分析中,只有GA(P < 0.001)被保留为暴露不足的独立预测因素。
庆大霉素延长间隔给药在入住二级病房的新生儿中目标达成率较高。与先前的报告一致,低GA和BW可预测治疗不足的峰浓度和毒性谷浓度。然而,AUC不受患者间GA和BW差异的影响。由于AUC指导给药在全球范围内越来越受到关注,后一发现值得在其他新生儿队列中进一步探索。