Association between vancomycin trough concentration monitoring and gestational age in neonates: a single-center, retrospective observational study.

IF 2.3 3区 医学 Q2 PEDIATRICS
Hui Chen, Xing Liu, Kanglu Ju, Xiao Song, Kai Zhao, Zeyang Wei, Bo Guo
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Abstract

Background: The vancomycin dosing regimen for neonates is primarily determined by gestational age (GA) and postnatal age(PNA). Nonetheless, initial trough concentrations frequently fall below therapeutic levels in neonates administered vancomycin. This study seeks to examine the relationship between vancomycin trough concentrations and gestational age in neonates, thereby offering a reference for individualized vancomycin dosing tailored to neonates of varying gestational ages.

Methods: A retrospective observational study was undertaken to collect clinical data on neonates treated with vancomycin and subjected to trough concentration monitoring in the Neonatal Intensive Care Unit (NICU) at Northwest Women's and Children's Hospital over the preceding six years.

Results: Utilizing a two-piecewise linear regression model, the P-value for the log-likelihood ratio was 0.007, indicating statistical significance, and an inflection point was identified at 34.6 weeks(approximately 242 days). For gestational ages less than 34.6 weeks, a positive correlation was observed between GA and the initial vancomycin trough concentration (TCV) (β = 0.08, 95% CI: 0.01, 0.14, p = 0.021). Conversely, for gestational ages exceeding 34.6 weeks, a negative trend of borderline significance (β = -0.10, 95% CI: -0.20 to 0.00, P = 0.059).

Conclusion: Vancomycin trough concentrations in neonates exhibit a significant correlation with GA. This retrospective study, conducted at a single center, revealed a non-linear relationship between gestational age and initial vancomycin trough concentrations in neonates, identifying an inflection point at approximately 34.6 weeks. The results indicate that existing gestational age-based dosing protocols may inadequately account for pharmacokinetic transitions, underscoring the necessity for prospective studies to validate therapeutic drug monitoring protocols stratified by gestational age.

万古霉素谷浓度监测与新生儿胎龄的关系:一项单中心、回顾性观察性研究。
背景:新生儿万古霉素给药方案主要由胎龄(GA)和出生后年龄(PNA)决定。尽管如此,初始谷浓度经常低于治疗水平的新生儿给予万古霉素。本研究旨在探讨万古霉素谷浓度与新生儿胎龄的关系,为不同胎龄新生儿万古霉素个体化用药提供参考。方法:采用回顾性观察性研究,收集西北妇幼医院新生儿重症监护病房(NICU)接受万古霉素治疗并进行谷浓度监测的新生儿6年来的临床资料。结果:利用两分段线性回归模型,对数似然比的p值为0.007,具有统计学意义,并在34.6周(约242天)时发现拐点。胎龄小于34.6周时,GA与初始万古霉素谷浓度(TCV)呈正相关(β = 0.08, 95% CI: 0.01, 0.14, p = 0.021)。相反,对于胎龄超过34.6周的孕妇,呈负性趋势(β = -0.10, 95% CI: -0.20 ~ 0.00, P = 0.059)。结论:新生儿万古霉素谷浓度与GA有显著相关性。这项在单中心进行的回顾性研究揭示了胎龄与新生儿初始万古霉素谷浓度之间的非线性关系,并在大约34.6周时确定了拐点。结果表明,现有的基于胎龄的给药方案可能不足以解释药代动力学转变,强调了前瞻性研究的必要性,以验证按胎龄分层的治疗药物监测方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Pediatrics
BMC Pediatrics PEDIATRICS-
CiteScore
3.70
自引率
4.20%
发文量
683
审稿时长
3-8 weeks
期刊介绍: BMC Pediatrics is an open access journal publishing peer-reviewed research articles in all aspects of health care in neonates, children and adolescents, as well as related molecular genetics, pathophysiology, and epidemiology.
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