加药
医学
治疗药物监测
药品
治疗指标
临床实习
重症监护医学
槽水位
曲线下面积
急性肾损伤
不利影响
药理学
药代动力学
药物开发
万古霉素
抗生素
药物治疗
临床试验
内科学
药物输送
细菌
家庭医学
金黄色葡萄球菌
生物
遗传学
他克莫司
移植
作者
Kazuaki Matsumoto,Kazutaka Oda,Kensuke Shoji,Yuki Hanai,Yoshiko Takahashi,Satoshi Fujii,Yukihiro Hamada,Toshimi Kimura,Toshihiko Mayumi,Takashi Ueda,Kazuhiko Nakajima,Yoshio Takesue
出处
期刊:Pharmaceutics
[MDPI AG]
日期:2022-02-23
卷期号:14 (3): 489-489
被引量:41
标识
DOI:10.3390/pharmaceutics14030489
摘要
To promote model-informed precision dosing (MIPD) for vancomycin (VCM), we developed statements for therapeutic drug monitoring (TDM).Ten clinical questions were selected. The committee conducted a systematic review and meta-analysis as well as clinical studies to establish recommendations for area under the concentration-time curve (AUC)-guided dosing.AUC-guided dosing tended to more strongly decrease the risk of acute kidney injury (AKI) than trough-guided dosing, and a lower risk of treatment failure was demonstrated for higher AUC/minimum inhibitory concentration (MIC) ratios (cut-off of 400). Higher AUCs (cut-off of 600 μg·h/mL) significantly increased the risk of AKI. Although Bayesian estimation with two-point measurement was recommended, the trough concentration alone may be used in patients with mild infections in whom VCM was administered with q12h. To increase the concentration on days 1-2, the routine use of a loading dose is required. TDM on day 2 before steady state is reached should be considered to optimize the dose in patients with serious infections and a high risk of AKI.These VCM TDM guidelines provide recommendations based on MIPD to increase treatment response while preventing adverse effects.
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