Investigation of Teicoplanin Trough Concentrations and Safety Following High-Dose Loading in a Pediatric Population.

IF 2.8 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Therapeutic Drug Monitoring Pub Date : 2025-01-07 DOI:10.1097/FTD.0000000000001302
Sayaka Okuzono, Takaaki Yamada, Yoshitomo Motomura, Hikaru Kanemasa, Masataka Ishimura, Yuhki Koga, Hiroyuki Torisu, Shunsuke Kanno, Ichiro Ieiri, Shouichi Ohga
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Abstract

Background: Therapeutic drug monitoring-informed teicoplanin dosage adjustments are recommended for safe and effective use. The authors' group previously reported that only half of children reached the recommended blood concentration range at the standard teicoplanin loading dose. It has been suggested that higher loading doses are necessary; however, the usefulness and safety of high-dose loading in pediatric patients in clinical practice are unknown.

Methods: This retrospective cohort study was conducted between January 2018 and June 2021 using electronic medical records. The analysis included 2- to 16-year-old patients treated with teicoplanin who met the eligibility criteria. We assessed the trough concentration of teicoplanin and its safety after high-dose loading in pediatric patients.

Results: Overall, 86 patients received a high-dose loading regimen (15 mg/kg every 12 hours for 3 doses, followed by 10 mg/kg once daily). Notably, 55 of the 86 patients (64%) achieved the target trough concentration (>15 mg/L) at significantly higher rates without increasing the incidence of organ damage compared with the standard loading regimen. Multivariate analysis revealed significant differences in age and renal function as factors that inhibited the attainment of the target trough concentration. Simulation analysis using a nomogram stratified by age and renal function revealed that the predicted teicoplanin trough levels were within the target trough values in 73% of patients.

Conclusions: High-dose teicoplanin loading safely increases trough blood concentrations in the pediatric population. For further optimization, the dose selection should be stratified according to age and renal function.

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替柯planin在儿童人群中高剂量负荷后谷浓度和安全性的研究。
背景:为了安全有效地使用,建议根据治疗药物监测情况调整替柯planin的剂量。作者小组先前报道,在标准teicoplanin负荷剂量下,只有一半的儿童达到推荐的血药浓度范围。有人建议需要更高的负荷剂量;然而,在临床实践中,高剂量负荷在儿科患者中的有效性和安全性尚不清楚。方法:本回顾性队列研究于2018年1月至2021年6月期间使用电子病历进行。该分析包括符合资格标准的2- 16岁接受替可普兰治疗的患者。我们评估了替柯planin的谷浓度及其在儿科患者高剂量负荷后的安全性。结果:总体而言,86例患者接受了高剂量负荷方案(每12小时15 mg/kg,共3次剂量,随后每天1次10 mg/kg)。值得注意的是,与标准负荷方案相比,86例患者中有55例(64%)以更高的速率达到了目标谷浓度(> 15mg /L),而没有增加器官损伤的发生率。多因素分析显示,年龄和肾功能是抑制达到目标谷浓度的因素。使用年龄和肾功能分层的nomogram模拟分析显示,73%的患者的teicoplanin谷值预测值在目标谷值之内。结论:在儿科人群中,大剂量替柯planin可安全地增加经血药浓度。为了进一步优化,剂量选择应根据年龄和肾功能分层。
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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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