- Research article
- Open Access
- Open Peer Review
Pharmacokinetic-pharmacodynamic profiling of four antimicrobials against Gram-negative bacteria collected from Shenyang, China
BMC Infectious Diseasesvolume 10, Article number: 171 (2010)
To examine common antimicrobial regimens used in eradicating certain nosocomial Gram-negative pathogens and determine which ones are likely to be the most suitable as empirical choices in Shenyang, China.
A 5000-subject Monte Carlo simulation was conducted to determine the cumulative fraction of response (CFR) for meropenem, imipenem, cefepime, piperacillin/tazobactam and levofloxacin against Escherichia coli, Klebsiella pneumoniae, Enterobacter cloacae, Acinetobacter baumannii and Pseudomonas aeruginosa collected in 2006 and 2007 from Shenyang.
Meropenem and imipenem had the highest CFRs against the Enterobacteriaceae (97%-100%), followed by cefepime. No antibiotic simulated regimen achieved optimal CFR against P. aeruginosa and A. baumannii. Piperacillin/tazobactam dosed at 4.5 g q8h achieved the lowest CFR against all bacteria.
This study suggests that the carbapenems provide the greatest likelihood of clinical success for the Enterobacteriaceae, and combination therapy might be needed when choosing empirical therapy, especially when A. baumannii or P. aeruginosa are suspected.
The rapid increase in the prevalence of multidrug resistant microorganisms has threatened the physician's ability to treat serious infections. Since there are a limited number of antimicrobials available that can treat multidrug resistant gram-negative bacteria such as Enterobacteriaceae harboring extended-spectrum β-lactamases (ESBLs), multidrug-resistant P. aeruginosa and A. baumannii, the best approach to combating resistance and providing effective therapy is optimizing the use of currently available antimicrobial agents.
Antibiotic surveillance studies lack consideration of pharmacokinetics and provide little information about optimal dosing. The consideration of minimum inhibitory concentration (MIC) distribution, antibiotic regimen and pharmacokinetic parameter derived from human studies via application of pharmacokinetic/pharmacodynamic (PK/PD) models with Monte Carlo simulation offers a more useful tool for clinicians to predict successful outcomes .
Given that Gram-negative bacteria resistance is increasing rapidly and varies considerably by geographical location in China, location-specific information on pharmacokinetic-pharmacodynamic profiling of common antibiotics (such as meropenem, imipenem, cefepime, piperacillin/tazobactam and levofloxacin) against problem pathogens is of particular concern, thus we conducted this study to assess common antibiotic regimens utilized in Shenyang in order to provide insight into the appropriate antibiotic and dosing options for the empiric therapy of common nosocomial pathogens.
The present study was performed with isolates collected consecutively during 2006 to 2007 from patients hospitalized in The First Hospital of China Medical University, The Second Hospital of China Medical University, and Provincial People Hospital in Shenyang. Included bacterial strains were isolates of non-duplicate E. coli (n = 414), K. pneumoniae (n = 236), E. cloacae (n = 40), P. aeruginosa (n = 281) and A. baumannii (n = 115). Identification of the species level was performed by each laboratory of the participant Hospital with either conventional biochemical methodology or an automated system (Vitek 2, bioMérieux, France).
The MIC data of meropenem, imipenem, cefepime, piperacillin/tazobactam and levofloxacin against these bacteria were determined by the agar dilution method at Department of Laboratory Medicine, The First Hospital of China Medical University according to Clinical and Laboratory Standards Institute guidelines (Table 1). Control strains of E. coli (ATCC 25922) and P. aeruginosa (ATCC 27853) were run with each set of MIC determinations.
The percent of the dosing interval during which free (i.e. unbound) drug was above the MIC (% f T > MIC) was selected as the pharmacodynamic exposure of interest. The following antibiotic regimens were chosen based on the most common regimens used in Shenyang to treat these suspected pathogens modeled as 30-min intravenous (i.v.) infusions: meropenem 0.5 g every 6 hours (q6h), 1 g q8h, and 1 g q12h; imipenem 0.5 g q6h, 1 g q8h and 1 g q12h; cefepime 1 g q8h and 2 g q8h and 2 g q12h; and piperacillin/tazobactam 4.5 g q8h. A one-compartment i.v. -infusion equation was used to calculate % f T > MIC for the β - lactams at steady state as previously described :
where Ln is the natural logarithm, f is the fraction of unbound drug, Vd is the volume of distribution in liters at steady state, CL T is the total body clearance in liters per hour, and DI is the dosing interval for the regimen.
Pharmacokinetic-pharmacodynamic exposures for levofloxacin were measured by calculation of the total drug 24-h area under the concentration-time curve (AUC) to MIC ratio (AUC/MIC). Total drug AUC for levofloxacin regimens (levofloxacin 0.5 every 24 h) were calculated by dividing the daily dose by total plasma clearance
Pharmacokinetic data were obtained from previously published studies with healthy volunteers using previously described selection criteria [2, 3]. Table 2 gives the mean and standard deviation for the total body clearance (total body plasma clearance was calculated as CL = dose/AUC, AUC was determined by the trapezoidal rule and was extrapolated to infinity ) in liters per hour resulting assumptions used to model total plasma clearance (CLT), volume of the central compartment (V d ), fraction unbound and AUC0-24.
A 5000-patient Monte Carlo simulation (Crystal Ball 2000; Decisioneering Inc., Denver, CO) was conducted to calculate estimates of % f T > MIC or AUC/MIC ratio for each antibiotic dosage regimen and bacterial population combination. Five thousand estimates of pharmacodynamic exposure were generated for each antibiotic regimen against each bacterial population using values for CL T , Vd, f, and MIC based on probability distributions, as previously described . During simulations, pharmacokinetic parameters were assumed to follow log-Gaussian distributions and the fraction unbound f followed a uniform distribution. Discrete MIC distributions were built for each population of bacteria based on the MIC frequencies, whereby the percentage of bacteria for which each MIC applies is treated as a frequency and values in between the MIC do not exist. The cumulative fraction of response (CFR) was calculated over the MIC distributions using weighted summation . For comparative purpose, bactericidal pharmacodynamic breakpoints were defined as 40% f T > MIC for meropenem and imipenem, 50% f T > MIC for cefepime, and piperacillin-tazobactam, and a total drug AUC/MIC ≥ 125 for levofloxacin. A regimen that achieved > 90% CFR against a population of organisms was considered optimal .
The CFRs for each antibiotic dosage regimen against each population of bacteria are given in Table 3. Overall, CFRs were highest against the Enterobacteriaceae, followed by P. aeruginosa and then A. baumannii.
Against the Enterobacteriaceae, meropenem and imipenem at all simulated dosage regimens achieved the highest CFRs. Because lower doses of meropenem and imipenem (0.5 g q8h or q6h) by the standard 30-minute infusion obtained 97%-100% CFR against Enterobacteriaceae, increasing the dose of meropenem to 1 g q8h had no clinical significance for these three species (98%-100% CFR) (Table 3).
Against E. coli, cefepime also fared well, with higher CFRs (95%) than the optimal CFR (90%) at the simulated regimen of 2 g q8h and slightly lower CFRs (90%) at the lower dose of 1 g q8h and 2 g q12h. Piperacillin/tazobactam dosed at 4.5 g q8h achieved the lowest CFR against all bacteria. Particularly, levofloxacin regimens achieved significantly less exposure against E. coli (30%) than E. cloacae (68%) and K. pneumoniae (44%).
No antibiotic simulated regimen achieved high enough CFRs against the nonfermenters to warrant its use empirically as monotherapy. Against P. aeruginosa and A. baumannii, all antibiotic regimens achieved very low CFRs (≤ 60%) with the exception of cefepime dosed at 2000 mg every 8 hours against P. aeruginosa (68%).
Our simulations demonstrated that meropenem and imipenem achieved a high likelihood of bactericidal activity against the Enterobacteriaceae, with CFRs close to 100%. These findings support other studies [2, 7, 8] indicating that for mild to moderate infections caused by pathogens with inherently low MICs, such as the Enterobacteriaceae, meropenem and imipenem 0.5 g q8h as a 30-minute infusion may be as effective as standard therapy (1 g, q8h), resulting in decreased costs; whereas for treatment of more severe infections and higher risk of P. aeruginosa or other antibiotic-resistant, gram-negative pathogens, meropenem at higher dose (2 g, q8h) would optimize the pharmacodynamic parameter of %T > MIC.
Additionally, larger or more frequent doses of antibiotic against the nonfermenters resulted in increases in the CFRs, but not enough to justify the use of any of these agents empirically as monotherapy. This may have clinical relevance, since dosage increase is a common response to try to curb resistance. The data shown here clearly demonstrate that for the regimens evaluated, dosage increase would not be a good option for empiric treatment. Instead, because no single regimen had high CFR against A. baumannii and P. aeruginosa, the use of empiric combination therapy to treat these pathogens may be worthwhile. A recent study demonstrated that the use of combination antimicrobial therapy for the P. aeruginosa bacteremia resulted in an improvement in 30-day survival; at least until the antibiotic susceptibility results were available to help guide therapy .
In addition, being different from other study , the results of these simulations are strongly supported by the dramatically increasing resistance emerging in carbapenem-resistant A. baumannii in Shenyang (China), with only 38%- 36% susceptible to meropenem and imipenem respectively (data not shown). Other study suggests that the carbapenemase blaOXA-23 and the AdeABC efflux pump were the importance mechanism of imipenem-resistance in this region (this was done in a separate project). It alludes to the fact that it is critical to know local trends in resistance and MIC distributions, since information from elsewhere (even within the same country) could lead one to utilize less optimal dosing regimens. Ideally, the use of hospital- or unit-specific (i.e. ICU) MIC distributions in those Monte Carlo simulations would provide the most reliable data for designing empirical dosing regimens .
There are a few issues that require discussion. With regard to the pharmacokinetic data, the parameters chosen were selected from healthy adults rather than patients. This is due to the lack of comparable pharmacokinetic trials of all these agents in the same patient population; we utilized healthy volunteer data to make a conservative estimate, similar to other studies [2, 9]. Additionally, some studies showed that the pharmacodynamic target attainment calculated with healthy subject pharmacokinetic data was predictive of patient target attainment for the β-lactams .
Additional limitations of the study are that it does not look at the new carbapenem, doripenem, and neither does it evaluate prolonged nor continuous infusion regimens.
This pharmacokinetic-pharmacodynamic simulation provides a useful tool that complements susceptibility data to help in the selection of appropriate empirical antibiotic therapy on the regional level. It suggests that the carbapenems, and specifically meropenem, remain the most potent agents for the Enterobacteriaceae, and owing to high antibiotic MICs among many Gram-negative rods in Shenyang, combination therapy might be needed when choosing empirical therapy, especially when A. baumannii or P. aeruginosa are suspected.
Conflict of interests
The authors declare that they have no competing interests.
Bradley JS, Dudley MN, Drusano GL: Predicting efficacy of anti-infectives with pharmacodynamics and Monte Carlo simulation. Pediatr Infect Dis J. 2003, 22 (11): 982-992. 10.1097/01.inf.0000094940.81959.14.
Kuti JL, Nightingale CH, Nicolau DP: Optimizing Pharmacodynamic Target Attainment Using the MYSTIC Antibiogram: Data Collected in North America in 2002. Antimicrob Agents Chemother. 2004, 48 (2): 2464-2470. 10.1128/AAC.48.7.2464-2470.2004.
Frei CR, Wiederhold NP, Burgess DS: Antimicrobial breakpionts for Gram-negative aerobic bacteria based on pharmacokinetic-pharmadynamic models with Monte Carlo simulation. J Antimicrob Chemother. 2008, 61 (3): 621-628. 10.1093/jac/dkm536.
Leroy A, Fillastre JP, Borsa-Lebas F, Etienne I, Humbert G: Pharmacokinetics of meropenem (ICI 194,660) and its metabolite (ICI 213,689) in healthy subjects and in patients with renal impairment. Antimicrob Agents Chemother. 1992, 36 (12): 2794-2798.
Drusano GL, Preston SL, Hardalo C, Hare R, Banfield C, Andes D, Vesga O, Craig WA: Use of preclinical data for selection of a phase II/III dose for evernimicin and identification of a preclinical MIC breakpoint. Antimicrob Agents Chemother. 2001, 45 (1): 13-22. 10.1128/AAC.45.1.13-22.2001.
Mouton JW, Dudley MN, Cars O, Derendorf H, Drusano GL: Standardization of pharmacokinetic/pharmacodynamic (PK/PD) terminology for anti-infective drugs: an update. J Antimicrob Chemother. 2005, 55 (5): 601-607. 10.1093/jac/dki079.
Mattoes HM, Kuti JL, Drusano GL, Nicolau DP: Optimizing Antimicrobial Pharmacodynamics: Dosage Strategies for Meropenem. Clin Ther. 2004, 26 (8): 1187-1198. 10.1016/S0149-2918(04)80001-8.
Chamot E, Boffi El Amari E, Rohner P, Van Delden C: Effectiveness of combination antimicrobial therapy for Pseudomonas aeruginosa bacteremia. Antimicrob Agents Chemother. 2003, 47 (9): 2756-2764. 10.1128/AAC.47.9.2756-2764.2003.
Wang H, Zhang B, Ni Y, Kuli JL, Chen B, Chen M, Nicolau DP: Pharmacodynamic target attainment of seven antimicrobials against Gram-negative bacteria collected from China in 2003 and 2004. Int J Antimicrob Agents. 2007, 30 (5): 452-457. 10.1016/j.ijantimicag.2007.06.005.
Kuti JL, Nicolau DP: Making the most of surveillance studies: summary of the OPTAMA Program. Diagn Microbiol Infect Dis. 2005, 53 (4): 281-287. 10.1016/j.diagmicrobio.2005.10.004.
Kuti JL, Horowitz S, Nightingale CH, Nicolau DP: Comparison of pharmacodynamic target attainment between healthy subjects and patients for ceftazidime and meropenem. Pharmacotherapy. 2005, 25 (7): 935-941. 10.1592/phco.2005.25.7.935.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/10/171/prepub
We thank The First Hospital of China Medical University, The Second Hospital of China Medical University, and Provincial People Hospital for kindly providing clinical isolates.
No funding of any kind has been received.
Presented in part for poster presentation: 7th International Symposium on Antimicrobial Agents and Resistance, Bangkok, March 18, 2009 (poster submission number: GN113).
YZC and SFT have made substantial contributions to conception and design, or acquisition of data, or analysis and interpretation of data. HN and GQS have been involved in drafting the manuscript. HS conceived of the study, and participated in its design and coordination. BYC carried out the revision for important intellectual content. All authors read and approved the final manuscript.
Bai Yi Chen, Hong Shang contributed equally to this work.