Clinical outcomes of linezolid and vancomycin in patients with nosocomial pneumonia caused by methicillin-resistant Staphylococcus aureus stratified by baseline renal function: a retrospective, cohort analysis

被引:13
作者
Liu, Ping [1 ]
Capitano, Blair [2 ]
Stein, Amy [3 ]
El-Solh, Ali A. [4 ,5 ]
机构
[1] Pfizer Inc, Global Established Pharma Business, Clin Pharmacol, Groton, CT 06340 USA
[2] Pfizer Inc, Specialty Care, Med Affairs, Collegeville, PA USA
[3] Customer Solut, Biostat, Quintiles, Durham, NC USA
[4] SUNY Buffalo, Div Pulm Crit Care & Sleep Med, Buffalo, NY 14260 USA
[5] VA Western New York Healthcare Syst, Med Res, Bldg 20 151 VISN02,3495 Bailey Ave, Buffalo, NY 14215 USA
关键词
Outcomes; Linezolid; Vancomycin; Pneumonia; MRSA; Renal function; EFFICACY; PHARMACOKINETICS; NEPHROTOXICITY; INFECTIONS; EXPOSURE; THERAPY;
D O I
10.1186/s12882-017-0581-y
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: The primary objective of this study is to assess whether baseline renal function impacts treatment outcomes of linezolid and vancomycin (with a dose-optimized regimen) for methicillin-resistant Staphylococcus aureus (MRSA) pneumonia. Methods: We conducted a retrospective cohort analysis of data generated from a prospective, randomized, controlled clinical trial (NCT 00084266). The analysis included 405 patients with culture-proven MRSA pneumonia. Baseline renal function was stratified based on creatinine clearance. Clinical and microbiological success rates and presence of nephrotoxicity were assessed at the end of treatment (EOT) and end of study (EOS). Multivariate logistic regression analyses of baseline patient characteristics, including treatment, were performed to identify independent predictors of efficacy. Vancomycin concentrations were analyzed using a nonlinear mixed-effects modeling approach. The relationships between vancomycin exposures, pharmacokinetic-pharmacodynamic index (trough concentration, area under the curve over a 24-h interval [AUC(0-24)], and AUC(0-24)/MIC) and efficacy/nephrotoxicity were assessed in MRSA pneumonia patients using univariate logistic regression or Cox proportional hazards regression analysis approach. Results: After controlling for use of vasoactive agents, choice of antibiotic therapy and bacteremia, baseline renal function was not correlated with clinical and microbiological successes in MRSA pneumonia at either end of treatment or at end of study for both treatment groups. No positive association was identified between vancomycin exposures and efficacy in these patients. Higher vancomycin exposures were correlated with an increased risk of nephrotoxicity (e.g., hazards ratio [95% confidence interval] for a 5 mu g/ml increase in trough concentration: 1.42 [1.10, 1.82]). Conclusions: In non-dialysis patients, baseline renal function did not impact the differences in efficacy or nephrotoxicity with treatment of linezolid versus vancomycin in MRSA pneumonia.
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