Pharmacokinetics and pharmacodynamics of beta-lactam antibiotics in critically ill patients

被引:1
|
作者
Sulaiman, Helmi [1 ]
Roberts, Jason A. [2 ,3 ,4 ,5 ]
Abdul-Aziz, Mohd H. [2 ]
机构
[1] Univ Malaya, Fac Med, Dept Med, Kuala Lumpur, Malaysia
[2] Univ Queensland, Fac Med, Univ Queensland Ctr Clin Res UQCCR, Brisbane, Qld 4029, Australia
[3] Royal Brisbane & Womens Hosp, Dept Med Cuidados Intensivos, Brisbane, Qld, Australia
[4] Royal Brisbane & Womens Hosp, Dept Farm, Brisbane, Qld, Australia
[5] Univ Montpellier, Servido Anestesiol Reanimat & Terapia Dolor, Nimes Univ Hosp, Nimes, France
关键词
Antibiotics; Beta-lactamics; Criticaly ill patient; Clinical pharmacocinetics; AUGMENTED RENAL CLEARANCE; EXTRACORPOREAL MEMBRANE-OXYGENATION; CONTINUOUS-INFUSION; POPULATION PHARMACOKINETICS; INTRAVENOUS-INFUSION; REPLACEMENT THERAPY; CLINICAL-OUTCOMES; SEPTIC PATIENTS; BURN PATIENTS; SEPSIS;
D O I
10.7399/fh.13170
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Optimal antibiotic therapy for critically ill patients can be complicated by the altered physiology associated with critical illness. Antibiotic pharmacokinetics and exposures can be altered driven by the underlying critical illness and medical interventions that critically ill patients receive in the intensive care unit. Furthermore, pathogens that are usually isolated in the intensive care unit are commonly less susceptible and "resistant" to common antibiotics. Indeed, antibiotic dosing that does not consider these unique differences will likely fail leading to poor clinical outcomes and the emergence of antibiotic resistance in the intensive care unit. The aims of this narrative review were to describe the pharmacokinetics of beta-lactam antibiotics in critically ill patients, to highlight pharmacokinetic/pharmacodynamic targets for both non- critically ill and critically ill patients, and to discuss important strategies that can be undertaken to optimize beta-lactam antibiotic dosing for critically ill patients in the intensive care unit.
引用
收藏
页码:182 / 190
页数:9
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