Amikacin Population Pharmacokinetics in Critically Ill Kuwaiti Patients

被引:8
作者
Matar, Kamal M. [1 ]
Al-lanqawi, Yousef [2 ]
Abdul-Malek, Kefaya [3 ]
Jelliffe, Roger [4 ]
机构
[1] Kuwait Univ, Fac Pharm, Dept Pharmacol & Therapeut, Kuwait 13110, Kuwait
[2] Al Amiri Hosp, Minist Hlth, Dept Pharm, Kuwait 32005, Kuwait
[3] Al Amiri Hosp, Minist Hlth, Intens Care Unit, Kuwait 32005, Kuwait
[4] Univ So Calif, Sch Med, Lab Appl Pharmacokinet, Los Angeles, CA 90033 USA
关键词
AMINOGLYCOSIDE PHARMACOKINETICS; THERAPY;
D O I
10.1155/2013/202818
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Amikacin pharmacokinetic data in Kuwaiti (Arab) intensive care unit (ICU) patients are lacking. Fairly sparse serum amikacin peak and trough concentrations data were obtained from adult Kuwaiti ICU patients. The data were analysed using a nonparametric adaptive grid (NPAG) maximum likelihood algorithm. The estimations of the developed model were assessed using mean error (ME) as a measure of bias and mean squared error (MSE) as a measure of precision. A total of 331 serum amikacin concentrations were obtained from 56 patients. The mean (+/- SD) model parameter values found were V-c = 0.2302 +/- 0.0866 L/kg, k(slope) = 0.00404 +/- 0.00705 min per unit of creatinine clearance, k(12) = 2.2121 +/- 5.506 h(-1), and k(21) = 1.431 +/- 2.796 h(-1). The serum concentration data were estimated with little bias (ME = -0.88) and good precision (MSE = 13.08). The present study suggests that amikacin pharmacokinetics in adult Kuwaiti ICU patients are generally rather similar to those found in other patients. This population model would provide useful guidance in developing initial amikacin dosage regimens for such patients, especially using multiple model (MM) dosage design, followed by appropriate Bayesian adaptive control, to optimize amikacin dosage regimens for each individual patient.
引用
收藏
页数:8
相关论文
共 19 条
[1]   ALTERED AMINOGLYCOSIDE PHARMACOKINETICS IN THE CRITICALLY ILL [J].
BECKHOUSE, MJ ;
WHYTE, IM ;
BYTH, PL ;
NAPIER, JC ;
SMITH, AJ .
ANAESTHESIA AND INTENSIVE CARE, 1988, 16 (04) :418-422
[2]  
Bertsekas Dimitri P., 2018, Abstract Dynamic Programming, V2nd
[3]   Parametric and nonparametric population methods - Their comparative performance in analysing a clinical dataset and two Monte Carlo simulation studies [J].
Bustad, A ;
Terziivanov, D ;
Leary, R ;
Port, R ;
Schumitzky, A ;
Jelliffe, R .
CLINICAL PHARMACOKINETICS, 2006, 45 (04) :365-383
[4]   POPULATION PHARMACOKINETICS OF AMIKACIN IN INTENSIVE-CARE UNIT PATIENTS STUDIED BY NPEM ALGORITHM [J].
DEBORD, J ;
PESSIS, C ;
VOULTOURY, JC ;
MARQUET, P ;
LOTFI, H ;
MERLE, L ;
LACHSATRE, G .
FUNDAMENTAL & CLINICAL PHARMACOLOGY, 1995, 9 (01) :57-61
[5]   POPULATION PHARMACOKINETIC PARAMETERS FOR BAYESIAN MONITORING OF AMIKACIN THERAPY IN INTENSIVE-CARE UNIT PATIENTS [J].
DEBORD, J ;
VOULTOURY, JC ;
LACHATRE, G ;
GAY, C ;
FAVEREAU, JP ;
GAY, R .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1992, 43 (04) :435-436
[6]   Evaluation of population pharmacokinetic models for amikacin dosage individualization in critically ill patients [J].
del Mar Fernandez de Gatta, Maria ;
Romano Moreno, Silvia ;
Victoria Calvo, Maria ;
Ardanuy, Ramon ;
Dominguez-Gil, Alfonso ;
Lanao, Jose M. .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2009, 61 (06) :759-766
[7]  
Domke I, 2000, Clin Lab, V46, P509
[8]   AN UPDATED COMPARISON OF DRUG DOSING METHODS .3. AMINOGLYCOSIDE ANTIBIOTICS [J].
ERDMAN, SM ;
RODVOLD, KA ;
PRYKA, RD .
CLINICAL PHARMACOKINETICS, 1991, 20 (05) :374-388
[9]  
Gauthier T., 1994, International Journal of Bio-Medical Computing, V36, P131, DOI 10.1016/0020-7101(94)90104-X
[10]   Estimation of creatinine clearance in patients with unstable renal function, without a urine specimen [J].
Jelliffe, R .
AMERICAN JOURNAL OF NEPHROLOGY, 2002, 22 (04) :320-324