Increased amikacin dosage requirements in burn patients receiving a once-daily regimen

被引:39
作者
Conil, J. M. [1 ]
Georges, B.
Breden, A.
Segonds, C.
Lavit, M.
Seguin, T.
Coley, N.
Samii, K.
Chabanon, G.
Houin, G.
Saivin, S.
机构
[1] Hop Rangueil, Serv Anesthesie Reanimat, Toulouse, France
[2] Fac Pharmaceut Sci, Lab Cinet Xenobiot, UMR Physiopathol & Toxicol Expt 181, UPTE INRA,ENVT, Toulouse, France
[3] Hop Rangueil, Lab Bacteriol Hyg, Toulouse, France
[4] Hop Rangueil, Lab Pharmacocinet & Toxicol Clin, F-31403 Toulouse, France
关键词
burn patients; amikacin; once-daily dosing; creatinine clearance; doses >= 20mg/kg;
D O I
10.1016/j.ijantimicag.2006.04.015
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Altered pharmacokinetics in burn patients may affect antibiotic plasma concentrations. Typical once-daily dosing (ODD) of 15 mg/kg amikacin (AMK) in burn patients does not always produce peak concentrations (C(max)) reaching the therapeutic objective of six to eight times the minimal inhibitory concentration (MIC). We recorded plasma concentrations following administration of 20 mg/kg AMK in burn patients and studied factors affecting pharmacokinetics. Mean C(max) was 48.3 +/- 10.8 mg/L and the C(max)/MIC ratio was 6 +/- 1.35. Statistical analysis demonstrated a relationship between C(max) and the area of the burn and Unit Burn Standard, and between AMK clearance and creatinine clearance (Cl(CR)). We conclude that ODD regimens of AMK in patients with burns > 15% body surface area and/or with Cl(CR) > 120 mL/min could require doses > 20 mg/kg to reach adequate C(max). In all cases, patient therapeutic drug monitoring is essential to ensure the safe usage of these dosing recommendations. (c) 2006 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:226 / 230
页数:5
相关论文
共 23 条
[1]  
Barza M, 1996, BRIT MED J, V312, P338
[2]   CLINICAL AND BACTERIOLOGICAL EFFICACY, AND PRACTICAL ASPECTS OF AMIKACIN GIVEN ONCE DAILY FOR SEVERE INFECTIONS [J].
BEAUCAIRE, G ;
LEROY, O ;
BEUSCART, C ;
KARP, P ;
CHIDIAC, C ;
CAILLAUX, M .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1991, 27 :91-103
[3]   PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE [J].
COCKCROFT, DW ;
GAULT, MH .
NEPHRON, 1976, 16 (01) :31-41
[4]   Single daily amikacin intake in burned patients: A pharmacokinetic and clinical study [J].
Conil, JM ;
Laguerre, J ;
Marty, N ;
Chabanon, G ;
Favarel, H ;
Brouchet, A ;
Houin, G ;
Virenque, C ;
Costagliola, M .
MEDECINE ET MALADIES INFECTIEUSES, 1997, 27 (10) :848-855
[5]  
FLANDROIS JP, 1979, NOUV PRESSE MED, V8, P3501
[6]  
GALIZIA JP, 1986, CAH ANESTHESIOL, V6, P495
[7]  
GARRAFO R, 2000, INFECT ANTIBOTHERAPI, P395
[8]  
Hoey Lori L., 1997, Journal of Burn Care and Rehabilitation, V18, P116, DOI 10.1097/00004630-199703000-00005
[9]   Optimisation of antimicrobial therapy using pharmacokinetic and pharmacodynamic parameters [J].
Jacobs, MR .
CLINICAL MICROBIOLOGY AND INFECTION, 2001, 7 (11) :589-596
[10]   Achieving an optimal outcome in the treatment of infections - The role of clinical pharmacokinetics and pharmacodynamics of antimicrobials [J].
Li, RC ;
Zhu, M ;
Schentag, JJ .
CLINICAL PHARMACOKINETICS, 1999, 37 (01) :1-16