Pharmacodynamic profiling of continuously infused piperacillin/tazobactam against Pseudomonas aeruginosa using Monte Carlo analysis

被引:35
作者
Kuti, JL
Nightingale, CH
Quintiliani, R
Nicolau, DP [1 ]
机构
[1] Hartford Hosp, Dept Pharm Res, Hartford, CT 06115 USA
[2] Hartford Hosp, Off Res Adm, Hartford, CT 06115 USA
[3] Hartford Hosp, Div Infect Dis, Dept Med, Hartford, CT 06115 USA
[4] Univ Connecticut, Sch Med, Farmington, CT USA
关键词
D O I
10.1016/S0732-8893(02)00416-9
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Standard doses of piperacillin/tazobactam (9-13.5 g over 24 h) administered by continuous infusion (CI) routinely provide serum concentrations in excess of the susceptibility breakpoint (less than or equal to16/4 mug/ml) for most Enterobacteriaceae. Since the breakpoint of this agent for Pseudomonas aeruginosa is considerably higher (less than or equal to64/4 mug/ml), the likelihood of obtaining adequate drug exposures with these doses against this bacterium is currently unknown. Monte Carlo simulation was utilized to determine the probability of obtaining adequate piperacillin concentrations above its MICs for P. aeruginosa in patients receiving Cl. MICs of 557 P. aeruginosa isolates were determined by E-test and a distribution was constructed for the 496 susceptible isolates. Using a previously validated population pharmacokinetic equation, steady-state serum concentrations were estimated for 210 patients who received piperacillin/tazobactam via Cl. A Monte Carlo simulation was performed to predict the probability of obtaining concentrations at the MIC, 2xMIC, 4xMIC, 5xMIC, and 6xMIC for patients infected with susceptible P. aeruginosa isolates. MICs ranged from 0.09 to 64 mug/ml with modal and median values of 3 and 4 mug/ml, respectively. Steady-state concentrations of 51.14 +/- 17.52 mug/ml were estimated in our patient population. The simulation resulted in a median level of exposure 12.62 times the MIC. The level of certainty of obtaining concentrations at the MIC, 2xMIC, 4xMIC, 5xMIC, and 6xMIC for piperacillin administered by CI was 97, 93, 85, 81, and 77%, respectively. Despite concern for the place of CI piperacillin/tazobactam in the management of P. aeruginosa infections due to the higher established breakpoint, these data suggest a high probability of achieving adequate drug exposure against susceptible isolates with this dosing regimen. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:51 / 57
页数:7
相关论文
共 28 条
[1]   Continuous vs. intermittent infusion of cefuroxime for the treatment of community-acquired pneumonia [J].
Ambrose, PG ;
Quintiliani, R ;
Nightingale, CH ;
Nicolau, DP .
INFECTIOUS DISEASES IN CLINICAL PRACTICE, 1998, 7 (09) :463-470
[2]   The use of Monte Carlo simulation to examine pharmacodynamic variance of drugs:: fluoroquinolone pharmacodynamics against Streptococcus pneumoniae [J].
Ambrose, PG ;
Grasela, DM .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2000, 38 (03) :151-157
[3]   Treatment of ventilator-associated pneumonia with piperacillin-tazobactam/amikacin versus ceftazidime/amikacin:: A multicenter, randomized controlled trial [J].
Brun-Buisson, C ;
Sollet, JP ;
Schweich, H ;
Brière, S ;
Petit, C .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (02) :346-354
[4]   PHARMACODYNAMICS OF CEFTAZIDIME ADMINISTERED AS CONTINUOUS-INFUSION OR INTERMITTENT BOLUS ALONE AND IN COMBINATION WITH SINGLE DAILY-DOSE AMIKACIN AGAINST PSEUDOMONAS-AERUGINOSA IN AN IN-VITRO INFECTION MODEL [J].
CAPPELLETTY, DM ;
KANG, SL ;
PALMER, SM ;
RYBAK, MJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (08) :1797-1801
[5]   PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE [J].
COCKCROFT, DW ;
GAULT, MH .
NEPHRON, 1976, 16 (01) :31-41
[6]   PIPERACILLIN-TAZOBACTAM PLUS AMIKACIN VERSUS CEFTAZIDIME PLUS AMIKACIN AS EMPIRIC THERAPY FOR FEVER IN GRANULOCYTOPENIC PATIENTS WITH CANCER [J].
COMETTA, A ;
ZINNER, S ;
DEBOCK, R ;
CALANDRA, T ;
GAYA, H ;
KLASTERSKY, J ;
LANGENAEKEN, J ;
PAESMANS, M ;
VISCOLI, C ;
GLAUSER, MP ;
GIBSON, B ;
SANZ, M ;
HANN, IM ;
FOLLATH, F ;
FATIO, R ;
FERSTER, A ;
VANHOOF, A ;
VANLANDUYT, H ;
ARENDT, V ;
HEMMER, R ;
PEETERMANS, M ;
PADMOS, A ;
SEITANIDES, B ;
HATZIYANNI, M ;
LOPEZ, A ;
PORCELLINI, A ;
GREK, V ;
CABALLERO, D ;
TOGNI, P ;
GALLAGHER, JG ;
GARAVENTA, A ;
MASSIMO, L ;
SUGAR, A ;
LEGRAND, JC ;
OPPENHEIM, B ;
PETRIKKOS, G ;
BEYTOUT, J ;
NIKOSKELAINEN, J ;
SHAPIRO, M ;
ESTAVOYER, JM ;
KERN, W .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (02) :445-452
[7]   CONTINUOUS INFUSION OF BETA-LACTAM ANTIBIOTICS [J].
CRAIG, WA ;
EBERT, SC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (12) :2577-2583
[8]  
Daniel KP, 1996, PHARMACOTHERAPY, V16, P149
[9]  
Diekema DJ, 1999, CLIN INFECT DIS, V29, P595, DOI 10.1086/598640
[10]  
FACCA BF, 2002, IN PRESS J INFEECT D