The effect of pathophysiology on pharmacokinetics in the critically ill patient - Concepts appraised by the example of antimicrobial agents

被引:326
|
作者
Blot, Stijn I. [1 ,4 ]
Pea, Federico [2 ,3 ]
Lipman, Jeffrey [4 ,5 ]
机构
[1] Univ Ghent, Fac Med & Hlth Sci, Dept Internal Med, B-9000 Ghent, Belgium
[2] Univ Santa Maria Misericordia, Azienda Osped, Inst Clin Pharmacol, Udine, Italy
[3] Univ Udine, Dept Expt & Clin Med Sci, I-33100 Udine, Italy
[4] Univ Queensland, Burns Trauma & Crit Care Res Ctr, Brisbane, Qld, Australia
[5] Royal Brisbane & Womens Hosp, Dept Intens Care Med, Herston, Qld 4006, Australia
关键词
Antimicrobial agents; Pharmacokinetics; Pharmacodynamics; Intensive care unit; Sepsis; Organ failure; Acute kidney injury; Hepatic failure; INTENSIVE-CARE-UNIT; ACUTE KIDNEY INJURY; AUGMENTED RENAL CLEARANCE; ORGAN BLOOD-FLOW; SEVERE SEPSIS; CONTINUOUS-INFUSION; SEPTIC SHOCK; ATTRIBUTABLE MORTALITY; REPLACEMENT THERAPY; HOSPITAL MORTALITY;
D O I
10.1016/j.addr.2014.07.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Critically ill patients are at high risk for development of life-threatening infection leading to sepsis and multiple organ failure. Adequate antimicrobial therapy is pivotal for optimizing the chances of survival. However, efficient dosing is problematic because pathophysiological changes associated with critical illness impact on pharmacokinetics of mainly hydrophilic antimicrobials. Concentrations of hydrophilic antimicrobials may be increased because of decreased renal clearance due to acute kidney injury. Alternatively, antimicrobial concentrations may be decreased because of increased volume of distribution and augmented renal clearance provoked by systemic inflammatory response syndrome, capillary leak, decreased protein binding and administration of intravenous fluids and inotropes. Often multiple conditions that may influence pharmacokinetics are present at the same time thereby excessively complicating the prediction of adequate concentrations. In general, conditions leading to underdosing are predominant. Yet, since prediction of serum concentrations remains difficult, therapeutic drug monitoring for individual fine-tuning of antimicrobial therapy seems the way forward. (C) 2014 The Authors. Published by Elsevier B.V.
引用
收藏
页码:3 / 11
页数:9
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