调整儿科万古霉素剂量:达到治疗水平和最小化肿瘤患者的毒性。

Nadeen Hossam, Dalia Makhlouf, Ahmed Elzeiny, Akram Elzeiny, Sherif Kamal, Omneya Hassanien, Lobna Shalaby, Mohamed Nagy
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引用次数: 0

摘要

背景:万古霉素是儿科肿瘤中广泛使用的肾毒性药物。我们的目的是评估万古霉素的初始剂量方案,以达到万古霉素的目标治疗浓度在10至20微克/毫升之间。方法:我们分析了在CCHE 57357(2017-2023)治疗的1678例儿科肿瘤患者的4134例万古霉素谷水平。结果:较高的万古霉素初始剂量(80和100 mg/kg/天)比60 mg/kg/天(38.1%)产生更好的目标水平(45.5%,51.4%)。结论:儿童肿瘤可能需要更高的初始万古霉素剂量(80- 100mg /kg/天)才能达到治疗水平。Kg剂量超过上限达到目标而不增加毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tailoring pediatric vancomycin doses: achieving therapeutic levels and minimizing toxicity in oncology patients.

Background: Vancomycin is a widely used nephrotoxic drug in pediatric oncology. Our aim was to assess the initial vancomycin dosing protocols required for achieving the target therapeutic concentrations of vancomycin between 10 and 20 mcg/ml.

Methods: We analyzed 4134 vancomycin trough levels from 1678 pediatric oncology patients treated at CCHE 57357 (2017-2023).

Results: Higher initial Vancomycin doses (80 and 100 mg/kg/day) yielded better target levels (45.5%, 51.4%) compared to 60 mg/kg/day (38.1%). Younger patients (<10 years) showed higher sub-therapeutic levels than older ones (53.4% vs. 24.8%, p < 0.0001). Co-administration of nephrotoxic medications increased vancomycin toxicity risk (13.3% vs. 8.9%, p < 0.0001). Weight-based dosing of vancomycin resulted in higher therapeutic levels compared to capping doses at 500 mg.

Conclusion: Higher initial vancomycin doses (80-100 mg/kg/day) may be necessary to achieve therapeutic levels in pediatric oncology. Kg dosing beats capping for reaching targets without raising toxicity.

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