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Pharmacokinetic-pharmacodynamic analysis of ciprofloxacin in elderly Chinese patients with lower respiratory tract infections caused by Gram-negative bacteria 被引量:6

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摘要 Background: Ciprofloxacin is usually used in the treatment of lower respiratory tract infections (LRTIs). Recent studies abroad shown ciprofloxacin is inadequately dosed and might lead to worse outcomes. The aim of this study was to perform pharmacokinetic and pharmacodynamic analyses of ciprofloxacin in elderly Chinese patients with severe LRTIs caused by Gramnegative bacteria. Methods: From September 2012 to June 2014, as many as 33 patients were empirically administered beta-lactam and ciprofloxacin combination therapy. Patients were infused with 200 or 400 mg of ciprofloxacin every 12 h, which was determined empirically by the attending physician based on the severity of the LRTI and the patienfs renal condition. Ciprofloxacin serum concentrations were determined by high-performance liquid chromatography. Bacterial culture was performed from sputum samples and/or endotracheal aspirates, and the minimum inhibitory concentrations (MICs) of ciprofloxacin were determined. The ratios of the area under the serum concentration-time curve to the MIC (AUC/MIC) and of the maximum serum concentration of the drug to the MIC (Cmax/MIC) were calculated. The baseline data and pharmacokinetic parameters were compared between clinical success group and clinical failure group, bacteriologic success group and bacteriologic failure group. Results: Among the 33 patients enrolled in the study, 17 were infected with Pseudomonas aeruginosa, 14 were infected with Acinetobacter baumannii^ and two were infected with Klebsiella pneumoniae. The mean age of the patients was 76.9 土 6.7 years. Thirty-one patients (93.4%) did not reach the target AUC/MIC value of >125, and 29 patients (87.9%) did not reach the target Cmax/MIC value of >8. The AUC/MIC and Cniax/MIC ratios in the clinical success group were significantly higher than those in the clinical failure group (61.1 [31.7-214.9] vs. 10.4 [3.8-66.1], Z =-4.157;9.6 [4.2-17.8] vs, 1.3 [0.4-4.7], Z =-4.018;both P< 0.001). The AUC/MIC and Cmax/MIC ratios in the patients for whom the pathogens were eradicated were significantly higher than those in the patients without the pathogens eradicated (75.3 [31.7-214.9] vs. 10.5 [3.8-66.1], Z =—3.938;11.4 [4.2-17.8] vs. 1.4 [0.4-5.4], Z =—3.793;P < 0.001 for both). Receiver operating characteristic curve analysis showed that the AUC/MIC and Cmax/ MIC values were closely associated with clinical and bacteriologic efficacies (P<0.001 in both). Conclusions: Ciprofloxacin is inadequately dosed against Gram-negative bacteria, especially for those with relatively high MIC values. Consequently, the target values, AUC/MIC > 125 and Cmax/MIC> 8, cannot be reached.
出处 《Chinese Medical Journal》 SCIE CAS CSCD 2019年第6期638-646,共9页 中华医学杂志(英文版)
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  • 1Alan M, Grolimund E, Kutz A, et al. Clinical risk scores and blood biomarkers as predictors of long-term outcome in patients with community-acquired pneumonia: a 6-year prospective follow- up study[J]. J Intern Med, 2014, Dec 19. doi: 10. llll/joim. 12341. [ Et)ub ahead of orintl.
  • 2Cockcroft DW, Gault MH. Prediction of creatinine clearance from serum creatinines[J]. Nephron, 1976, 16(1 ) : 31-41.
  • 3Ferrara AM, Fietta AM. New developments in antibacterial choice for lower respiratory tract infections in elderly patients [ J ]. Drugs Aging, 2004, 21 (3) : 167-186.
  • 4Zhao W, Hill H, Le Guellec C, et al. Population pharmacokinetics of cipmfloxacin in neonates and young infants less than three months of age[ J]. Antimierob Agents Chemother, 2014, 58 ( 11 ) : 6572-6580.
  • 5Adefurin A, Sammons H, Jacqz-Aigrain E, et al. Ciprofloxacin safety in paediatrics : a systematic review [ J ]. Arch Dis Child, 2011,96(9) : 874-880.
  • 6Conil JM, Georges B, de Lussy A, et al. Ciprofloxacin use in critically ill patients: pharmaeokinetie and pharmacodynamie approaches[ J~. Int J Antimicrob Agents, 2008, 32 (6) : 505- 510.
  • 7Khachman D, Conil JM, Georges B, et al. Optimizing ciprofloxacin dosing in intensive care unit patients through the use of population pharmaeokinetic- pharmacodynamic analysis and Monte Carlo simulations[ J]. J Antimierob Chemother, 2011, 66 (8) : 1798-1809.
  • 8van Zanten AR, Polderman KH, van Geijlswijk IM, et al. Ciprofloxacin pharmacokinetics in critically ill patients : a prospective cohort study [ J ]. J Crit Care, 2008, 23 ( 3 ) : 422- 430.
  • 9Cios A, Wyska E, Szymura-Oleksiak J, et al. Population pharmacokinetic analysis of ciprofloxacin in the elderly patients with lower respiratory tract infections [ J ]. Exp Gerontol, 2014, 57(9) : 107-113.
  • 10Campoli-Richards DM, Monk JP, Price A, et al. Ciprofloxacin. A review of its antibacterial activity, pharmacokinetics proprieties and therapeutic useFJ]. Drugs, 1988. 35(4) : 373-44-7.

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