A Retrospective Study Evaluating Neonatal Vancomycin Loading Doses to Achieve a Therapeutic Target.

IF 2.8 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Aaqilah Fataar, Veshni Pillay-Fuentes Lorente, Eric H Decloedt, Andrew van Eck, Kessendri Reddy, Angela Dramowski, Adrie Bekker
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引用次数: 0

Abstract

Background: Vancomycin is a glycopeptide antibiotic that has been used to treat hospital-acquired gram-positive infections for more than 5 decades. However, the literature is divided regarding the therapeutic advantages of vancomycin loading doses in neonates.

Objectives: This study aimed to investigate the effect of vancomycin loading doses on therapeutic target attainment in neonates with sepsis.

Methods: A retrospective cohort study was conducted to compare the vancomycin target attainment (area under the curve 0-24 hours/minimum inhibitory concentration ≥400) in neonates before and after the 2019 change in vancomycin prescription guidelines at a neonatal unit in Cape Town, South Africa. As the standard of care, Bayesian modelling software was used to compute the area under the curve from the trough concentrations.

Results: Two hundred ten neonates were included. Multivariate regression analysis showed a 2-fold increase in the odds of target attainment among neonates receiving a loading dose of vancomycin. Early target attainment (within 8-12 hours of treatment initiation) was significantly higher in the loading dose group compared with the no loading dose group [97/105 (92.4%) versus 64/105 (61.0%); P < 0.001]. However, the overall proportion of neonates achieving target attainment at 24 hours was similar between groups [73/105 (69.5%) in the loading dose group versus 62/105 (59.0%) in the no loading dose group; P = 0.110]. The nephrotoxicity rates were low [2/105 (1.9%) in the loading dose group and 2/105 (1.9%) in the no loading dose group].

Conclusions: The addition of a vancomycin loading dose to neonates may facilitate early therapeutic target attainment.

评估新生儿万古霉素加载剂量以达到治疗目标的回顾性研究
背景:万古霉素是一种糖肽类抗生素,用于治疗医院获得性革兰氏阳性感染已有 50 多年的历史。然而,关于新生儿使用万古霉素负荷剂量的治疗优势,文献报道不一:本研究旨在探讨万古霉素负荷剂量对新生儿败血症患者达到治疗目标的影响:方法:在南非开普敦的一家新生儿科室开展了一项回顾性队列研究,比较2019年万古霉素处方指南变更前后新生儿的万古霉素达标率(0-24小时曲线下面积/最低抑制浓度≥400)。作为护理标准,贝叶斯建模软件用于计算谷浓度的曲线下面积:结果:共纳入 210 名新生儿。多变量回归分析显示,接受万古霉素负荷剂量治疗的新生儿达标几率增加了2倍。与无负荷剂量组相比,负荷剂量组的早期达标率(开始治疗后 8-12 小时内)明显更高[97/105 (92.4%) 对 64/105 (61.0%);P < 0.001]。不过,各组 24 小时达标的新生儿总比例相似 [负荷剂量组 73/105 (69.5%) 对无负荷剂量组 62/105 (59.0%);P = 0.110]。肾毒性发生率较低[负荷剂量组为2/105(1.9%),无负荷剂量组为2/105(1.9%)]:结论:新生儿加用万古霉素负荷剂量有助于尽早达到治疗目标。
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
Therapeutic Drug Monitoring
Therapeutic Drug Monitoring 医学-毒理学
CiteScore
5.00
自引率
8.00%
发文量
213
审稿时长
4-8 weeks
期刊介绍: Therapeutic Drug Monitoring is a peer-reviewed, multidisciplinary journal directed to an audience of pharmacologists, clinical chemists, laboratorians, pharmacists, drug researchers and toxicologists. It fosters the exchange of knowledge among the various disciplines–clinical pharmacology, pathology, toxicology, analytical chemistry–that share a common interest in Therapeutic Drug Monitoring. The journal presents studies detailing the various factors that affect the rate and extent drugs are absorbed, metabolized, and excreted. Regular features include review articles on specific classes of drugs, original articles, case reports, technical notes, and continuing education articles.
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