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Note: Dosing of Aminoglycosides To Rapidly Attain Pharmacodynamic Goals and Hasten Therapeutic Response by Using Individualized Pharmacokinetic Monitoring of Patients with Pneumonia Caused by Gram-Negative Organisms

机译:注意:通过使用个体化的药代动力学监测革兰氏阴性菌引起的肺炎患者氨基糖苷类药物的剂量可快速达到药效目标并加快治疗反应

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摘要

Achieving a peak aminoglycoside concentration (Cmax)/MIC of ≥10 within 48 h of initiation of therapy for pneumonia caused by gram-negative organisms results in a 90% probability of therapeutic response by day 7. Targeting an MIC of 1 μg/ml, empirical aminoglycoside loading doses of 348 (25th- to 75th-percentile range, 275 to 432) mg were calculated to obtain a Cmax/MIC of 10 in our patient population. Individualized pharmacokinetic monitoring coupled with MIC data should determine subsequent dosing regimens to minimize the potential for toxicity and maximize the probability of clinical response.
机译:在革兰氏阴性菌引起的肺炎治疗开始后48小时内,氨基糖苷浓度(Cmax)/ MIC达到≥10的最高结果是,到第7天,治疗反应的可能性为90%,MIC的目标为1μg/ ml,计算得出的348毫克(25%至75%范围,275至432)mg的氨基糖苷类经验加载剂量在我们的患者人群中获得的Cmax / MIC为10。个体化的药代动力学监测以及MIC数据应确定后续的给药方案,以最大程度地降低毒性的可能性并最大程度地提高临床反应的可能性。

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