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©The Author(s) 2015.
World J Crit Care Med. May 4, 2015; 4(2): 139-151
Published online May 4, 2015. doi: 10.5492/wjccm.v4.i2.139
Published online May 4, 2015. doi: 10.5492/wjccm.v4.i2.139
Table 5 Pharmacokinetic considerations in the critically ill patient
Data from pharmacokinetic studies are no substitute for clinical monitoring of the individual patient’s response to therapy |
Pharmacokinetic parameters derived from studies involving normal volunteers or less severely ill patients are not directly applicable to the critically ill patient |
Average parameters for volume of distribution and clearance are larger and have much greater variability in critically ill patients compared with less severely ill patients |
The duration of action of single or isolated IV doses of more lipophilic drugs used in the ICU is a function more of distribution than of clearance |
The values for volume of distribution and clearance frequently change from baseline with prolonged drug administration because of factors such as accumulation or altered elimination |
For drugs with active metabolites, the pharmacokinetics of the metabolites as well as the parent compound must be considered |
Drug absorption is important not only with oral or enteral administration but also with intramuscular and subcutaneous injections |
- Citation: Erstad BL. Designing drug regimens for special intensive care unit populations. World J Crit Care Med 2015; 4(2): 139-151
- URL: https://www.wjgnet.com/2220-3141/full/v4/i2/139.htm
- DOI: https://dx.doi.org/10.5492/wjccm.v4.i2.139