Antibiotic use in critical illness

医学 重症监护医学 抗菌剂 药效学 经验性治疗 抗生素 药品 药代动力学 抗生素耐药性 人口 治疗药物监测 危重病 抗药性 病危 药理学 病理 微生物学 生物 替代医学 环境卫生
作者
Samuel D. Stewart,Sarah Allen
出处
期刊:Journal of Veterinary Emergency and Critical Care [Wiley]
卷期号:29 (3): 227-238 被引量:16
标识
DOI:10.1111/vec.12842
摘要

Abstract Objective To provide a review on the current use of antimicrobials with a discussion on the pharmacokinetic and pharmacodynamic profiles of antimicrobials in critically ill patients, the challenges of drug resistance, the use of diagnostic testing to direct therapy, and the selection of the most likely efficacious antimicrobial protocol. Etiology Patients in the intensive care unit often possess profound pathophysiologic changes that can complicate antimicrobial therapy. Although many antimicrobials have known pharmacodynamic profiles, critical illness can cause wide variations in their pharmacokinetics. The two principal factors affecting pharmacokinetics are volume of distribution and drug clearance. Understanding the interplay between critical illness, drug pharmacokinetics, and antimicrobial characteristics (ie, time‐dependent vs concentration‐dependent) may improve antimicrobial efficacy and patient outcome. Diagnosis Utilizing bacterial culture and susceptibility can aid in identifying drug resistant infections, selecting the most appropriate antimicrobials, and hindering the future development of drug resistance. Therapy Having a basic knowledge of antimicrobial function and how to use diagnostics to direct therapeutic treatment is paramount in managing this patient population. Diagnostic testing is not always available at the time of initiation of antimicrobial therapy, so empiric selections are often necessary. These empiric choices should be made based on the location of the infection and the most likely infecting bacteria. Prognosis Studies have demonstrated the importance of moving away from a “one dose fits all” approach to antimicrobial therapy. Instead there has been a move toward an individualized approach that takes into consideration the pharmacokinetic and pharmacodynamic variabilities that can occur in critically ill patients.
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