Drug Res (Stuttg) 2016; 66(10): 555-560
DOI: 10.1055/s-0042-112027
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Predictions of the Pharmacokinetics in Burn Injury Patients using Regression Models – Case Study with Levofloxacin

N. R. Srinivas
1   Suramus Bio, Bangalore, Karnataka, India
› Author Affiliations
Further Information

Publication History

received 25 March 2016

accepted 06 July 2016

Publication Date:
04 August 2016 (online)

Abstract

Owing to its excellent safety, tolerability, pharmacokinetic and pharmacodynamic profile levofloxacin is widely used. Although pharmacokinetics of levofloxacin was somewhat more variable in burn injury patients, it appeared to be comparable to healthy subjects or other patients. Linear regression model was established for Cmax or Cmin vs. [AUCtau, CL and Vd] of levofloxacin using individual values from burn injury patients. Appropriate regression lines for Cmax or Cmin were subjected to internal and external validation on the ability to predict CL, Vd and AUCtau parameters. The mean absolute error (MAE) and root mean square error (RMSE) of the predictions were used to judge the appropriateness of either Cmax or Cmin models. Cmax models developed for levofloxacin showed moderate to strong correlations with the various parameters such as CL, Vd and AUCtau. The Cmin models showed strong correlation for CL and AUCtau but not for Vd where the correlation was weak. Internal validation using data from individual burn patients showed RMSE of 13.47–25.42% for various predictions. External validation that used mean data from healthy subjects showed RMSE of 13.86–27.13%. Despite the pharmacokinetic variability, linear regression models using either Cmax or Cmin were established for levofloxacin rendering predictions of several key pharmacokinetic parameters. Although there was limitation of Cmin model for predicting Vd, both models may be used as a prospective tool for the prediction of levofloxacin pharmacokinetics in burn care patients.

 
  • References

  • 1 Friedman H, Song X, Crespi S et al. Comparative analysis of length of stay, total costs, and treatment success between intravenous moxifloxacin 400 mg and levofloxacin 750 mg among hospitalized patients with community-acquired pneumonia. Value Health 2009; 12: 1135-1143
  • 2 Frei CR, Jaso TC, Mortensen EM et al. Medical resource utilization among community-acquired pneumonia patients initially treated with levofloxacin 750 mg daily versus ceftriaxone 1000 mg plus azithromycin 500 mg daily: a US based study. Curr Med Res Opin 2009; 25: 859-868
  • 3 Chien SC, Rogge MC, Gisclon LG et al. Pharmacokinetic profile of levofloxacin following once-daily 500-milligram oral or intravenous doses. Antimicrob Agents Chemother 1997; 41: 2256-2260
  • 4 Schein J, Janagap-Benson C, Grant R et al. A comparison of levofloxacin and moxifloxacin use in hospitalized community-acquired pneumonia (CAP) patients in the US: focus on length of stay. Curr Med Res Opin 2008; 24: 895-906
  • 5 Lynch 3rd JP, File Jr TM, Zhanel GG. Levofloxacin for the treatment of community-acquired pneumonia. Expert Rev Anti Infect Ther 2006; 4: 725-742
  • 6 Anderson VR, Perry CM. Levofloxacin: a review of its use as a high-dose, short course treatment for bacterial infection. Drugs 2008; 68: 535-565
  • 7 File Jr TM, Milkovich G, Tennenberg AM et al. Clinical implications of 750 mg, 5-day levofloxacin for the treatment of community acquired pneumonia. Curr Med Res Opin 2004; 20: 1473-1481
  • 8 Bonate PL. Pathophysiology and pharmacokinetics following burn injury. Clin Pharmacokinet 1990; 18: 118-130
  • 9 Weinbren MJ. Pharmacokinetics of antibiotics in burn patients. J Antimicrob Chemother 1999; 44: 319-327
  • 10 Bjerknes R, Vindenes H, Laerum OD. Altered neutrophil functions in patients with large burns. Blood Cells 1990; 16: 127-141
  • 11 Mileski W, Borgstrom D, Lightfoot E et al. Inhibition of leukocyte-endothelial adherence following thermal injury. J Surg Res 1992; 52: 334-339
  • 12 Ün S, Yılmaz Y, Yıldırım M et al. Investigation of prevalance and risk factors for hospital-acquired urinary tract infections in patientswith severe burn injury. Ulus Travma Acil Cerrahi Derg 2015; 21: 57-62
  • 13 Kraft R, Herndon DN, Mlcak RP et al. Bacterial respiratory tract infections are promoted by systemic hyperglycemia after severe burn injury in pediatric patients. Burns 2014; 40: 428-435
  • 14 Brusselaers N, Monstrey S, Snoeij T et al. Morbidity and mortality of bloodstream infections in patients with severe burn injury. Am J Crit Care 2010; 19: e81-e87
  • 15 Kiser TH, Hoody DW, Obritsch MD et al. Levofloxacin pharmacokinetics and pharmacodynamics in patients with severe burn injury. Antimicrob Agents Chemother 2006; 50: 1937-1945
  • 16 Chien SC, Rogge MC, Gisclon LG et al. Pharmacokinetic profile of levofloxacin following once-daily 500-milligram oral or intravenous doses. Antimicrob Agents Chemother 1997; 41: 2256-2260
  • 17 Chien SC, Chow AT, Natarajan J et al. Absence of age and gender effects on the pharmacokinetics of a single 500-milligram oral dose of levofloxacin in healthy subjects. Antimicrob Agents Chemother 1997; 41: 1562-1565
  • 18 Rebuck JA, Fish DN, Abraham E. Pharmacokinetics of intravenous and oral levofloxacin in critically ill adults in a medical intensive care unit. Pharmacotherapy 2002; 22: 1216-1225
  • 19 Chow AT, Fowler C, Williams RR et al. Safety and pharmacokinetics of multiple 750-milligram doses of intravenous levofloxacin in healthy volunteers. Antimicrob Agents Chemother 2001; 45: 2122-2125
  • 20 Kempker RR, Barth AB, Vashakidze S et al. Cavitary penetration of levofloxacin among patients with multidrug-resistant tuberculosis. Antimicrob Agents Chemother 2015; 59: 3149-3155
  • 21 Czyrski A, Kondys K, Szałek E et al. The pharmacokinetic interaction between levofloxacin and sunitinib. Pharmacol Rep 2015; 67: 542-544
  • 22 Garrelts JC, Peterie JD. Altered vancomycin dose vs. serum concentration relationship in burn patients. Clin Pharmacol Ther 1988; 44: 9-13
  • 23 Garrelts JC, Jost G, Kowalsky SF et al. Ciprofloxacin pharmacokinetics in burn patients. Antimicrob. Agents Chemother 1996; 40: 1153-1156
  • 24 Bourget P, Lesne-Hulin A, Le Reveillé R et al. Clinical pharmacokinetics of piperacillin-tazobactam combination in patients with major burns and signs of infection. Antimicrob Agents Chemother 1996; 40: 139-145
  • 25 Farrow SP. Distribution of water and electrolytes in normal and thermally damaged skin. Br J Exp Pathol 1977; 58: 340-351
  • 26 Jaehde U, Sörgel F. Clinical pharmacokinetics in patients with burns. Clin Pharmacokinet 1995; 29: 15-28
  • 27 Srinivas NR, Navickis RJ, Greenhalgh DG et al. Albumin in burn shock resuscitation: A meta-analysis of controlled clinical studies. J Burn Care Res 2014; [Epub]
  • 28 Srinivas NR. Therapeutic drug monitoring of cyclosporine and area under the curve prediction using a single time point strategy: Appraisal using peak concentration data. Biopharmaceutics and Drug Disposition 2015; [Epub]
  • 29 Srinivas NR. Limited sampling strategy for the prediction of extent of absorption (AUC) of statins: Reliability of peak concentration (Cmax) parameter for AUC prediction for pravastatin and simvastatin. Drug Research 2015; [Epub]
  • 30 Srinivas NR. Differences in the prediction of area under the curve for a protease inhibitor using trough versus peak concentration: Feasibility assessment using published pharmacokinetic data for indinavir. American Journal of Therapeutics 2015; [Epub]
  • 31 Srinivas NR. Prediction of area under the curve for a p-glycoprotein, a CYP3A4 and a CYP2C9 substrate using a single time point strategy: Assessment using fexofenadine, itraconazole and losartan and metabolites. Drug Development and Industrial Pharmacy 2015; [Epub]
  • 32 Srinivas NR. Both Ctrough and Cmax can predict the area under the curve for lopinavir boosted therapy with ritonavir with reasonable accuracy in HIV population: Assessment from clinical pharmacokinetic data. American Journal of Health-System Pharmacy 2015; in press)