- Research article
- Open Access
- Open Peer Review
Empiric guideline-recommended weight-based vancomycin dosing and mortality in methicillin-resistant Staphylococcus aureus bacteremia: a retrospective cohort study
© Hall et al.; licensee BioMed Central Ltd. 2012
- Received: 2 December 2011
- Accepted: 27 April 2012
- Published: 27 April 2012
No studies have evaluated the effect of guideline-recommended weight-based dosing on in-hospital mortality of patients with methicillin-resistant Staphylococcus aureus bacteremia.
This was a multicenter, retrospective, cohort study of patients with methicillin-resistant Staphylococcus aureus bacteremia receiving at least 48 hours of empiric vancomycin therapy between 01/07/2002 and 30/06/2008. We compared in-hospital mortality for patients treated empirically with weight-based, guideline-recommended vancomycin doses (at least 15 mg/kg/dose) to those treated with less than 15 mg/kg/dose. We used a general linear mixed multivariable model analysis with variables identified a priori through a conceptual framework based on the literature.
A total of 337 patients who were admitted to the three hospitals were included in the cohort. One-third of patients received vancomycin empirically at the guideline-recommended dose. Guideline-recommended dosing was not associated with in-hospital mortality in the univariable (16% vs. 13%, OR 1.26 [95%CI 0.67-2.39]) or multivariable (OR 0.71, 95%CI 0.33-1.55) analysis. Independent predictors of in-hospital mortality were ICU admission, Pitt bacteremia score of 4 or greater, age 53 years or greater, and nephrotoxicity.
Empiric use of weight-based, guideline-recommended empiric vancomycin dosing was not associated with reduced mortality in this multicenter study.
Vancomycin is commonly used for the treatment of methicillin-resistant Staphylococcus aureus (MRSA) bacteremia. The United States of America Food and Drug Administration (FDA) originally approved a dosing regimen of 1 gram administered intravenously (IV) every 12 hours (or 500 mg IV every six hours). The FDA approved dosing regimen has not changed in over 50 years despite several studies demonstrating that vancomycin pharmacokinetics in adults are best predicted by actual body weight [1–4]. Dosing handbooks that are used in clinical practice continue to recommend a fixed dose for all patients regardless of weight [5, 6].
Over the past decade, there has been an increase in the incidence of MRSA strains with vancomycin minimum inhibitory concentration (MIC) values ≥ 1 μg/ml as well as heteroresistant vancomycin-intermediate S. aureus. In response to increasing vancomycin MICs in MRSA isolates, the Infectious Diseases Society of America, the American of Society of Health-Systems Pharmacists, and the Society of Infectious Diseases Pharmacists developed weight-based dosing recommendations for vancomycin based on pharmacokinetic and pharmacodynamic data (15–20 mg/kg/dose IV administered every eight to 12 hours) . The clinical effectiveness of this empiric weight-based, guideline-recommended dosing regimen (at least 15 mg/kg/dose) has yet to be critically evaluated.
Data evaluating guideline-recommended weight-based vancomycin dosing are needed to confirm the efficacy of this approach versus lower traditional dosing. Therefore, we conducted a multicenter retrospective cohort study to evaluate the effectiveness of guideline-recommended weight-based dosing for vancomycin on mortality of patients with MRSA bacteremia.
Study location and patients
We identified a retrospective cohort of patients admitted with MRSA bacteremia (using microbiological records) between 01/07/2002 and 30/06/2008 at three types of hospitals (400 bed urban, 200 bed veteran affairs, and 604 bed university). Patients were included if they were at least 18 years old and had received parenteral vancomycin for at least 48 hours. Patients were excluded if, at the time of the first vancomycin dose, they were receiving dialysis, had a creatinine clearance of 30 ml/min or less based upon the Cockcroft-Gault equation, received prior vancomycin within the hospital stay, had a culture-proven MRSA infection in the previous six months, or were pregnant . The institutional review board of each respective site (North Texas Veterans Health Care System, Texas Tech University Health Sciences Center, and University of Texas Health Science Center, San Antonio) approved the study and waived the need for informed consent.
Study design and data collection
We conducted a retrospective cohort study of patients who received guideline-recommended weight-based dosing with those receiving lower dosing of vancomycin for MRSA bacteremia. Our primary outcome was in-hospital mortality.
All definitions were selected prospectively during the initial trial design. Guideline-recommended weight-based dosing was defined as at least 30 mg/kg/day in the first 24 hours (at least 15 mg/kg/day for patients with a creatinine clearance of 30–50 ml/min). Lower dosing was defined as receiving less than 30 mg/kg/day (less than 15 mg/kg/day for patients with a creatinine clearance of 30–50 ml/min). Pitt bacteremia score was calculated based on the date when the first positive blood culture was obtained [9, 10]. In-hospital mortality was defined as patient death occurring within the index hospital stay. Nephrotoxicity was defined as an increase in creatinine by more than 0.5 mg/dl or greater than a 50% increase from baseline on two consecutive days .
Recursive partitioning was used to ascertain significant cut-points in continuous candidate variables associated with an increased risk of mortality . Univariable associations were explored using either Chi-square or Fisher’s Exact tests. A Pitt bacteremia score cutoff of 4 or higher was used based on previous literature demonstrating significantly higher sensitivity and specificity for predicting severity of illness . A vancomycin trough 15 mcg/ml or greater was based on the guideline recommended trough concentration range of 15–20 mcg/ml . Variables examined in the initial univariable analysis included receipt of guideline recommended weight-based vancomycin dosing, intensive care unit (ICU) admission, age 53 years, Pitt bacteremia score of 4 or higer, vancomycin trough 15 mcg/ml or greater, nephrotoxicity, Charlson comorbidity index score of 5 or higher, weight of 100 kg or greater, and gender.
Variables identified as significant through univariable analysis (p c 0.1) and those conceptually regarded as biologically reasonable causes of mortality were considered for inclusion in the multivariable model. A generalized linear mixed-effect model was utilized to identify independent predictors of mortality. Hospital site was treated as a random effect whereas other covariates were treated as fixed effects. Variables were retained in the multivariable model if their respective p values were < 0.05. Adjusted ORs and 95% confidence intervals were calculated for each variable. Effect measure modification and biologic interaction were also extensively evaluated. All analyses were performed using SAS 9.2 (Cary, North Carolina) and RTREE (Available at: http://c2s2.yale.edu/software.rtree).
Baseline characteristics of the cohort A
Survivors (n = 289)
Non-survivors (n = 47)
Male gender (%)
53 (42, 63)
65 (56, 77)
175.0 (165.1, 180.3)
175.0 (169.5, 183.0)
78.1 (65, 95.6)
80.0 (63.0, 99.0)
Serum Creatinine (mg/dl)
0.90 (0.7, 1.2)
1.10 (0.7, 1.5)
Creatinine Clearence (ml/min)
86.9 (61.0, 122)
64.0 (42.9, 86.3)
Pitt Bacteremia Score
1 (0, 3)
3 (2, 6)
Charlson Comorbidity Index
2 (1, 3)
2 (2, 4)
Guideline-recommended Vancomycin Dose Received (%)
Dose adjusted for renal function (%)
Vancomycin Started in Intensive Care Unit (%)
Initial Vancomycin Dose (mg/kg/day)
24.9 (19.6, 30.4)
21.0 (17.0, 29.0)
Infection source (%)
Central nervous system
The primary sources of bacteremia were skin/soft tissue (32.5%), intravenous catheter (20.2%), and pulmonary (17.8%). Other documented sources included genitourinary (8%), bone (1.2%), gastrointestinal (0.5%), and central nervous system (0.3%). The source of bacteremia was not specified for 19.8% of patients. Non-survivors were less likely to have a skin/muscle source of their bacteremia and more likely to have a bloodstream catheter-related or pulmonary source. Seventy-nine patients (23.4%) received concomitant antimicrobials active against MRSA. Non-survivors were less likely to receive IV contrast dye and more likely to receive vasopressors. Nineteen percent of both groups received aminoglycosides. Nephrotoxicity occurred in 82 patients (23.4%).
The overall median (interquartile range) length of hospital stay was 16 (9, 32) days for survivors and 23 (14, 56) for non-survivors (p = 0.009). The median length of stay after vancomycin initiation was 14 (7.5, 26.5) days for survivors and 19 (9, 42) for non-survivors. Thirty-two percent of patients had a hospital stay longer than 28 days. The median ICU length of stay was 0 (0, 4) days for survivors and 9 (3, 39) for non-survivors.
Univariable and multivariable analysis
Univariable analysis of risk factors for mortality
95% Confidence Interval
Guideline-Recommended Vancomycin Dosing
Intensive Care Unit Admission
Age of 53 years or greater
Pitt Bacteremia Score of four or greater
Vancomycin trough of 15 mcg/ml or greater
Charlson Comorbidity Index of five or greater
Weight of 100 kg or greater
Multivariable analysis of independent risk factors for mortality
95% Confidence interval
Guideline-Recommended Vancomycin Dosing
Intensive Care Unit Admission
Age of 53 years or greater
Pitt Bacteremia Score of four or greater
Vancomycin trough of 15 mcg/ml or greater
To our knowledge, this is the first published multicenter study to evaluate the effect of empiric guideline-recommended weight-based dosing on mortality in MRSA bacteremia. We did not observe any significant relationship between empiric guideline-recommended weight-based vancomycin dosing and in-hospital mortality. Independent predictors of in-hospital mortality were ICU admission, Pitt bacteremia score of 4 or greater, age 53 years or greater, and nephrotoxicity.
Most studies evaluating the effectiveness of vancomycin dosing for MRSA infections have compared high vs. low vancomycin trough concentrations. Our results parallel the findings of these studies. A recently published prospective cohort study assessing patients with MRSA pneumonia and bacteremia failed to demonstrate that achieving vancomycin trough concentrations to 4 to 5 times the MIC were associated with any difference in clinical response rates . Another study of 102 patients evaluated the association between vancomycin trough concentrations and mortality in MRSA pneumonia; 11% of patients had concomitant bacteremia . This study did not find a difference in vancomycin trough concentrations between survivors and non-survivors (13.6 vs. 13.9 mcg/ml). Using vancomycin trough concentrations to evaluate mortality is potentially confounded by the fact that vancomycin is eliminated by the kidneys. Acute renal failure is an independent risk factor for mortality, which also results in increased vancomycin trough concentrations (regardless of the cause of acute renal failure).
Our findings suggest that other patient factors play are more important factors in determining in-hospital mortality for patients with MRSA bacteremia than vancomycin dosing. The empiric use of guideline-recommended weight-based dosing in the absence of compelling efficacy or effectiveness data has the potential to place patients at an increased risk of concentration-related adverse events with an uncertain benefit to the patient. Clinicians should critically evaluate vancomycin trough concentrations and kidney function to help minimize this risk in patients receiving guideline-recommended weight-based vancomycin regimens.
The implications of this study on clinical practice are limited by its retrospective design, use of in-hospital mortality, lack of MIC data, and lack of data regarding time to a therapeutic vancomycin trough concentration. Utilizing in-hospital mortality as our primary endpoint resulted in fewer events than utilizing 30 day mortality or vancomycin failure [15–17]. This difference created greater variability in the multivariable model and limited the number of candidate variables evaluated in the multivariable model. In spite of this limitations, the factors associated with mortality in this study are similar to others . The study’s retrospective design allowed a more realistic estimate of clinical effectiveness than could be observed in a randomized, controlled trial. Increased vancomycin MIC values may have also played a role in the lack of benefit associated with guideline-recommended dosing. However, clinicians rarely have vancomycin MIC data available when selecting an empiric vancomycin dose. We did not collect data regarding the time to the first therapeutic vancomycin trough, as quicker times to therapeutic trough concentrations may improve vancomycin efficacy. However, this information may have been biased in this retrospective evaluation by clinician judgment regarding when trough concentrations were ordered. Our results may have also been subject to a selection bias that patients weighing greater than 70 kilograms were less likely to receive guideline-recommended, weight-based vancomycin dosing since most patients (85%) received 1 gram every 12 hours. Furthermore, the implications of loading doses on mortality need further evaluation since none of the study institutions utilized this dosing strategy.
In our study, we did not observe any significant association between guideline-recommended dosing and mortality. These results, in concert with the findings of others, call for a prospective, randomized comparison of empiric use of guideline-recommended weight-based vs. traditional dosing of vancomycin to ensure that patients treated with vancomycin receive doses that maximize efficacy and safety.
Dr. Hall and Alvarez’s effort was supported by Grant Number KL2RR024983, titled, “North and Central Texas Clinical and Translational Science Initiative” (Milton Packer, M.D., PI) from the National Center for Research Resources (NCRR), a component of the National Institutes of Health (NIH), and NIH Roadmap for Medical Research, and its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NCRR or NIH. Information on NCRR is available at http://www.ncrr.nih.gov/. Information on Re-engineering the Clinical Research Enterprise can be obtained from http://nihroadmap.nih.gov/clinicalresearch/overview-translational.asp. Dr. Frei’s time was supported by NIH grant KL2RR025766. The NIH had no role in the study design, data collection, analysis/interpretation, manuscript drafting, or submission.
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