首页> 外文期刊>Journal of Infection and Chemotherapy >Recommended initial loading dose of teicoplanin, established by therapeutic drug monitoring, and outcome in terms of optimal trough level
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Recommended initial loading dose of teicoplanin, established by therapeutic drug monitoring, and outcome in terms of optimal trough level

机译:通过治疗药物监测确定的替考拉宁的建议初始负荷剂量,以及根据最佳谷水平得出的结果

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摘要

Teicoplanin has a long serum half-life, and therefore it takes time to reach a steady-state concentration. An initial loading procedure has been recommended for teicoplanin to enable prompt reaching of the optimal serum trough level (10–15 µg/ml). However, the dose of teicoplanin that should be administered to patients with varying renal function levels remains inconclusive. In this study, we monitored the serum concentrations of teicoplanin in patients with methicillin-resistant Staphylococcus aureus (MRSA) pneumonia and compared different teicoplanin serum concentrations and their clinical efficacy, investigating the significance of the mean dose administered during the initial 3 days. The study included 48 patients with MRSA pneumonia. The peak and trough concentrations of teicoplanin were determined utilizing a fluorescence polarization immunoassay and a two-compartment Bayesian population model. Teicoplanin was given at a loading dose of 400 or 800 mg on the first day, followed by maintenance doses of 200 or 400 mg. The mean initial dose (MID) over the first 3 days was calculated as: (loading dose + dose on 2nd day + dose on 3rd day)/3. Patients with an MID of 266.7 mg or less (400 mg for loading, 200 mg over the 2nd and 3rd days) did not have a trough level that exceeded 10 µg/ml at the point before the injection on the 4th day. Even in patients with hemodialysis (HD), an MID of 266.7 mg was not enough to provide a trough level of 10 µg/ml. Patients with an MID than 533.3 mg had significantly elevated trough levels, showing better outcomes. A multiple regression formula for predicting trough level before the fourth day of administration is given as: 0.034 + 0.030 × (MID; mg) − 0.057 × creatinine clearance (Ccr; ml/min). These findings suggest that 800 mg as an initial dose, followed by 400 mg maintenance doses over the following 2 days, makes it possible to safely attain an optimal trough level, even in the patients with HD.
机译:Teicoplanin具有较长的血清半衰期,因此达到稳态浓度需要时间。对于替考拉宁,建议采用初始上样程序,以迅速达到最佳血清谷水平(10–15 µg / ml)。但是,替考拉宁应给予肾功能水平不同的患者的剂量尚无定论。在这项研究中,我们监测了耐甲氧西林金黄色葡萄球菌(MRSA)肺炎患者的替考拉宁的血清浓度,并比较了不同的替考拉宁血清浓度和它们的临床疗效,调查了最初3天平均剂量的意义。该研究纳入了48例MRSA肺炎患者。使用荧光偏振免疫测定法和两室贝叶斯种群模型确定替考拉宁的峰谷浓度。在第一天以400或800 mg的负载剂量给予替考拉宁,然后维持200或400 mg的维持剂量。前3天的平均初始剂量(MID)计算为:(加药量+第2天的剂量+第3天的剂量)/ 3。 MID为266.7 mg或更低(400 mg负荷,在第2天和第3天为200 mg)的患者在注射前第4天的谷值未超过10 µg / ml。即使在血液透析(HD)患者中,266.7 mg的MID仍不足以提供10 µg / ml的谷值。 MID高于533.3 mg的患者的谷值明显升高,显示出更好的结果。用于预测给药第四天之前谷值水平的多元回归公式为:0.034 + 0.030×(MID; mg)− 0.057×肌酐清除率(Ccr; ml / min)。这些发现表明,即使在患有HD的患者中,初始剂量为800 mg,随后在接下来的2天中维持剂量为400 mg,也可以安全地达到最佳谷值。

著录项

  • 来源
    《Journal of Infection and Chemotherapy》 |2006年第4期|185-189|共5页
  • 作者单位

    Second Division Department of Internal Medicine Hamamatsu University School of Medicine Hamamatsu Japan;

    Second Division Department of Internal Medicine Hamamatsu University School of Medicine Hamamatsu Japan;

    Second Division Department of Internal Medicine Hamamatsu University School of Medicine Hamamatsu Japan;

    Department of Pharmacy Hamamatsu University School of Medicine Hamamatsu Japan;

    Department of Pharmacy Hamamatsu University School of Medicine Hamamatsu Japan;

    Department of Pharmacy Hamamatsu University School of Medicine Hamamatsu Japan;

    Second Division Department of Internal Medicine Hamamatsu University School of Medicine Hamamatsu Japan;

    Second Division Department of Internal Medicine Hamamatsu University School of Medicine Hamamatsu Japan;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Therapeutic drug monitoring; Teicoplanin; Loading dose; MRSA;

    机译:治疗药物监测;替考拉宁;负荷剂量;MRSA;

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