Antimicrobial Pharmacokinetic and Pharmacodynamic Issues in the Critically Ill with Severe Sepsis and Septic Shock

被引:122
作者
Varghese, Julie M. [2 ]
Roberts, Jason A. [1 ,2 ,3 ]
Lipman, Jeffrey [1 ,2 ]
机构
[1] Royal Brisbane & Womens Hosp, Dept Intens Care Med, Brisbane, Qld 4029, Australia
[2] Univ Queensland, Royal Brisbane & Womens Hosp, Burns Trauma & Crit Care Res Ctr, Brisbane, Qld 4029, Australia
[3] Royal Brisbane & Womens Hosp, Dept Pharm, Brisbane, Qld 4029, Australia
基金
英国医学研究理事会;
关键词
Pharmacokinetics; Pharmacodynamics; Volume of distribution; Clearance; Renal failure; Renal replacement therapy; INTENSIVE-CARE-UNIT; VENTILATOR-ASSOCIATED PNEUMONIA; TARGET SITE PENETRATION; CLINICAL PHARMACOKINETICS; CONTINUOUS-INFUSION; CIPROFLOXACIN PHARMACOKINETICS; INTRAPULMONARY CONCENTRATIONS; INTRAVENOUS CIPROFLOXACIN; CREATININE CLEARANCE; PEAK CONCENTRATION;
D O I
10.1016/j.ccc.2010.09.006
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Antimicrobial pharmacokinetics (PK) and pharmacodynamics (PD) are important considerations, particularly in critically ill patients with severe sepsis and septic shock. The pathophysiologic changes that occur in these conditions can have a major effect on pharmacokinetic parameters, which in turn could result in failure to achieve pharmacodynamic targets for antimicrobials thus adversely affecting clinical outcome. This paper discusses the pathophysiologic changes that occur during severe sepsis and septic shock and the consequent effects on antimicrobial PK and PD. The effect of PK/PD on specific antimicrobial classes is discussed and a rational framework for antimicrobial dosing is provided. Knowledge of PK/PD properties of antimicrobials can be used to personalize dosing regimens not only to maximize antimicrobial activity but also to minimize toxicity and reduce the development of antimicrobial resistance.
引用
收藏
页码:19 / +
页数:17
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