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Real-Time Therapeutic Drug Monitoring-Based Pharmacokinetic/Pharmacodynamic Optimization of Complex Antimicrobial Therapy in a Critically Ill Morbidly Obese Patient. Grand Round/A Case Study

机译:基于治疗药物监测的基于治疗药物监测的药代动力学/药效学优化复合抗菌治疗患者危重病害患者。 大轮/案例研究

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The authors present the case of a critically ill morbidly obese patient (body mass index, 51.2 kg/m(2)) who suffered from methicillin-resistant Staphylococcus epidermidis, and Candida albicans bloodstream infections. Initial treatment with caspofungin and daptomycin was deemed inappropriate, because blood cultures remained positive for both isolates after 14 days. The clinical pharmacological consultant suggested adding fluconazole and ceftobiprole to the ongoing antimicrobial therapy, and starting a real-time therapeutic drug monitoring program of daptomycin, ceftobiprole, and fluconazole, aimed at optimizing plasma exposures. Punctual minimum inhibitory concentration knowledge on the clinical isolates allowed attainment of the desired pharmacodynamic efficacy targets. Within few days, the patient greatly improved, as blood cultures became negative, and the inflammatory markers decreased to near normal values. This is a proof-of-concept of the importance of a therapeutic drug monitoring-based multidisciplinary approach in the proper management of complex antimicrobial therapy in special populations.
机译:作者呈现出一种严重生病的病态肥胖患者(体重指数,51.2千克/米(2))的患者,他患有甲氧西林葡萄球菌的葡萄球菌,以及念珠菌血栓性感染。用Caspofungin和Daptomycin的初始治疗被认为是不适当的,因为在14天后两种分离株血液培养仍然是阳性的。临床药理学顾问建议将氟康唑和头孢虫渗至正在进行的抗微生物治疗,并开始达摩霉素,头虫和氟康唑的实时治疗药物监测程序,旨在优化血浆曝光。对临床分离株的准时的最小抑制浓度知识允许获得所需的药效学疗效靶标。在几天之内,患者随着血液培养变为阴性而大大提高,炎症标记减少到正常值附近。这是基于治疗药物监测的多学科方法在特殊人群中复杂抗菌治疗的适当管理中的重要性概念。

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