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中国临床药理学与治疗学 ›› 2024, Vol. 29 ›› Issue (12): 1344-1352.doi: 10.12092/j.issn.1009-2501.2024.12.004

• “特殊人群药物精准治疗服务与研究”专栏 • 上一篇    下一篇

模型引导下的万古霉素血药浓度监测临床研究

袁世轩1,2,吕子彦1,2,杨勇1,2,陈璐1,2,张丽娟1,2   

  1. 1四川省医学科学院·四川省人民医院药学部,成都  610072,四川;2电子科技大学医学院,个体化药物治疗四川省重点实验室,成都  610072,四川

  • 收稿日期:2024-07-01 修回日期:2024-09-04 出版日期:2024-12-26 发布日期:2024-11-18
  • 通讯作者: 张丽娟,女,副主任药师,研究方向:治疗药物监测与个体化用药。 E-mail: Connyzhang@tom.com
  • 作者简介:袁世轩,男,硕士,研究方向:临床药学。 E-mail: 442935675@qq.com
  • 基金资助:
    四川省干部保健科研课题(2023-220)

Clinical study on model-guided vancomycin plasma concentration monitoring

YUAN Shixuan1,2, LV Ziyan1,2, YANG Yong1,2, CHEN Lu1,2, ZHANG Lijuan1,2   

  1. 1 Department of Pharmacy, Personalized Drug Therapy Key Laboratory of Sichuan Province, Sichuan Academy of Medical Sciences & 2 Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610072, Sichuan, China
  • Received:2024-07-01 Revised:2024-09-04 Online:2024-12-26 Published:2024-11-18

摘要:

目的:研究万古霉素在模型引导下精准化给药是否可以达到更佳的临床治疗效果,从而推动其在实践中广泛应用。方法:采用前瞻性队列研究,试验组为使用模型引导下的精准化给药决策万古霉素给药方案的患者,对照组为仅依据现有诊疗流程决策万古霉素给药方案的患者。匹配两组数据,对比两组患者在治疗药物监测(therapeutic drug monitoring,TDM)稳态谷浓度或稳态AUC达标比例上是否存在统计学差异,评估模型软件的应用价值。结果:根据纳入和排除标准,共计280例患者的万古霉素稳态血药浓度数据用于分析。试验最终得到,试验组达标人数10例,达标率为62.50%;对照组达标人数64例,达标率为24.24%(P=0.002)。结论:模型引导下精准化给药方案能更精准地控制患者体内万古霉素血药浓度,显著提高患者稳态谷浓度达标率。因此,建议加大对该方案的研究力度,并推动其在临床实践中广泛应用。

关键词: 模型引导的精准用药, 万古霉素, 治疗药物监测

Abstract:

AIM: The purpose of this paper is to study whether the precise administration of vancomycin under the guidance of the model can achieve better clinical treatment effect by implementing the precise medication model in Sichuan Provincial People's Hospital, so as to promote its wide application in practice. METHODS: A prospective cohort study was conducted. The experimental group was patients who used the Model-informed Precision Dosing to determine the vancomycin dosing regimen, and the control group was patients who only decided the vancomycin dosing regimen based on the existing diagnosis and treatment process. Two sets of data were matched to compare whether there were significant differences between the two groups of patients in the TDM steady-state trough concentration or the steady-state AUC compliance ratio, and to evaluate the application value of the model software. RESULTS: According to the inclusion and exclusion criteria, the steady-state blood concentration data of vancomycin in a total of 280 patients were used for analysis. The final result of the experiment was that the number of people in the experimental group was 10, and the compliance rate was 62.50%. There were 64 cases in the control group, and the compliance rate was 24.24% (P=0.002). CONCLUSION: The study found that the model-guided precise dosing regimen can more accurately control the blood concentration of vancomycin in patients, and significantly improve the patient's steady-state trough concentration compliance rate. Therefore, it is recommended to increase the research on the program and promote its wide application in clinical practice. 

Key words: model-guided precision medication, vancomycin, therapeutic drug monitoring

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