Risk Factors for Fluconazole-Resistant Candida glabrata Bloodstream Infections FREE

Candida species are the fourth leading cause of health care–associated bloodstream infections (BSIs) and are associated with significant morbidity and mortality.^1- 3 In the United States, there has been a notable shift in the epidemiology of Candida BSIs. Bloodstream infections caused by Candida albicans have dramatically decreased, and there has been a concomitant increase in certain non–C albicans species, in particular, Candida glabrata.^4- 7

Historically, fluconazole has been the treatment of choice for Candida-related BSIs. However, unlike BSIs caused by C albicans, which are almost always fluconazole-susceptible, C glabrata BSIs are often associated with fluconazole resistance. The emergence of fluconazole-resistant C glabrata BSIs has had important implications because therapy requires higher doses of fluconazole or the use of other antifungal agents such as echinocandins or polyenes.⁸

Fluconazole use has been hypothesized as an important risk factor in the emergence of C glabrata infections. Resistance could be induced either by promoting the development of 1 or more resistance mechanisms including upregulating efflux pumps of the adenosine triphosphate–binding cassette transporter family or by altering patient endogenous flora, enabling colonization and subsequent infection with fluconazole-resistant C glabrata.^9- 10 Although biological plausibility exists, previous studies have reported conflicting results.^11- 15 One limitation of those studies is the absence of susceptibility testing to differentiate fluconazole-resistant from fluconazole-susceptible C glabrata even though resistance is the main concern with C glabrata. We therefore conducted this case-case-control study, which, to our knowledge, is the first to evaluate independent risk factors for BSIs caused by fluconazole-resistant C glabrata.

This study was conducted at 3 hospitals in the University of Pennsylvania Health System: the Hospital of the University of Pennsylvania, a 625-bed academic tertiary- and quaternary-care medical center; Penn Presbyterian Medical Center, a 324-bed urban community hospital; and Pennsylvania Hospital, a 481-bed urban community hospital.

We used a case-case-control study design in which 2 parallel case-control studies were conducted using a shared control group.¹⁶ The first case-control study compared patients with fluconazole-resistant C glabrata BSIs with a random sample of uninfected control subjects. The second case-control study compared patients with fluconazole-susceptible C glabrata BSIs with the same control group.

Case subjects were identified through the Hospital of the University of Pennsylvania Clinical Microbiology Laboratory, which began susceptibility testing of all C glabrata bloodstream isolates from the 3 involved hospitals in January 1, 2003. Candida glabrata was identified by macroscopic and microscopic morphologic features in addition to a positive reaction using the Rapid Assimilation of Trehalose Test (Hardy Diagnostics, Santa Maria, California).¹⁷ Fluconazole susceptibility was performed using Sensititre YeastOne (TREK Diagnostic Systems, Inc, Cleveland, Ohio) in accord with criteria from the Clinical Laboratory Standards Institute.¹⁸ Patients in whom C glabrata bloodstream isolates were detected between January 1, 2003, and May 31, 2007, with minimum inhibitory concentration (MIC) of 16 μg/mL or greater were eligible for inclusion in the fluconazole-resistant C glabrata case group. Patients with isolates with MIC of 8 μg/mL or less were eligible for the fluconazole-susceptible C glabrata case group.¹⁸ Dose-dependent susceptible isolates (MIC of 16-32 μg/mL), which have reduced fluconazole susceptibility and are, therefore, treated with higher fluconazole doses or different antifungal agents than are used to treat C albicans or fluconazole-susceptible C glabrata BSIs, were included in the fluconazole-resistant C glabrata case group.

Inclusion was limited to health care–associated BSIs, defined as C glabrata BSIs that developed after at least 48 hours of hospitalization or within 48 hours in patients who fulfilled at least 1 of the following criteria: (1) receipt within the previous 30 days of intravenous treatment, home health care services, or outpatient hemodialysis or (2) residence for at least 2 of the previous 90 days in a hospital, nursing home, or long-term care facility.¹⁹ Each patient was included only once, and only the initial episode of C glabrata BSI was reviewed. Patients admitted with outpatient blood cultures positive for C glabrata were excluded.

Hospitalized patients without C glabrata BSIs were eligible for inclusion in the control group. Control subjects were selected using a computer-generated random-number table and were frequency matched to case subjects by quartiles on the basis of time at risk. Time at risk was defined as the number of days from admission to a blood culture positive for C glabrata in the case groups and the number of days from admission to discharge in the control group. The number of control subjects selected was approximately 4-fold the total number of case subjects.

Data were abstracted from the Pennsylvania Integrated Clinical and Administrative Research Database, which includes demographic, pharmacy, laboratory, and billing information for more than 800 000 patients with more than 31 000 admissions. This database has been successfully used in studies of antimicrobial resistance.^20- 21

The following data were collected for all subjects: age, sex, race/ethnicity, hospital, time at risk, and comorbid conditions including cancer, cirrhosis, neutropenia (white blood cell count ≤1000/μL or International Classification of Diseases, Ninth Revision code), human immunodeficiency virus infection, solid-organ transplantation, hematopoietic stem cell transplantation, and end-stage renal disease requiring dialysis.

The following variables were collected if they occurred within 30 days preceding a blood culture positive for C glabrata in the case groups or the date of discharge in the control group: receipt of chemotherapy, immunosuppression, antibiotic therapy, or total parenteral nutrition, and stay in the intensive care unit. The following antimicrobial agents were assessed individually²²: amikacin, amoxicillin, amoxicillin-clavulanate, amphotericin, ampicillin, ampicillin-sulbactam, azithromycin, aztreonam, caspofungin, cephalexin, cefazolin, cefepime, ceftazidime, ceftriaxone, chloramphenicol, ciprofloxacin, clarithromycin, clindamycin, doxycycline, erythromycin, fluconazole, gentamicin, imipenem, kanamycin, levofloxacin, linezolid, meropenem, metronidazole, nafcillin, ofloxacin, penicillin, piperacillin, piperacillin-tazobactam, quinupristin-dalfopristin, tobramycin, trimethoprim-sulfamethoxazole, vancomycin, and voriconazole.

Bivariate analyses were conducted for each case-control study to identify potential risk factors for fluconazole-resistant and fluconazole-susceptible C glabrata BSIs. The χ² or Fisher exact test was used for categorical variables, and the t test or Wilcoxon rank sum test was used for continuous variables. The primary association of interest (ie, previous fluconazole use and fluconazole-resistant C glabrata BSIs) was stratified by hospital, year of hospitalization, oncologic status, and receipt of chemotherapy.

Adjusted odds ratios (ORs) were calculated using multiple logistic regression. The first multivariate model identified independent risk factors for fluconazole-resistant C glabrata BSIs, and the second model evaluated independent risk factors for fluconazole-susceptible C glabrata BSIs. Both models included fluconazole as the primary risk factor of interest. Variables with P values ≤.20 at bivariate analyses were included separately in multivariate modeling and maintained if their inclusion changed the OR for the primary risk factor of interest by 15% or greater.²³ We qualitatively compared the adjusted OR of the 2 models to identify risk factors unique to fluconazole-resistant vs fluconazole-susceptible C glabrata BSIs. Subgroup analysis of the first multivariate model, in which the fluconazole-resistant C glabrata case group was limited to isolates with an MIC of 64 μg/mL or higher, was also performed. All statistical calculations were performed using commercially available software (STATA version 10.0; Stata Corp LP, College Station, Texas).

We identified 76 patients with fluconazole-resistant C glabrata BSIs and 68 patients with fluconazole-susceptible C glabrata BSIs. The control group included 512 patients without C glabrata BSIs. Of patients with C glabrata BSIs, half were from the Hospital of the University of Pennsylvania, where 45% of the isolates were fluconazole-resistant and one-fourth each were from Pennsylvania Presbyterian Medical Center and Pennsylvania Hospital, where 60% to 62% of isolates were fluconazole-resistant.

Results at bivariate analyses are given in Table 1 and Table 2. Patients with fluconazole-resistant C glabrata BSIs were more likely to have previously used fluconazole (unadjusted OR [95% CI], 4.6 [2.6-8.0]; P < .001), less likely to have been hospitalized at the Hospital of the University of Pennsylvania (0.6 [0.3-0.9]; P = .02), and had significantly longer median time at risk (23 vs 17 days; P = .003). Previous fluconazole use was also significantly associated with fluconazole-susceptible C glabrata BSIs (unadjusted OR [95% CI], 2.0 [1.0-3.9]; P = .02). There was no effect modification by year, hospital, oncologic status, or chemotherapy status found in either of the case-control studies.

At multivariate analyses, previous fluconazole use (adjusted OR, 2.3 [1.3-4.2]; P = .007) and linezolid use (4.6 [2.2-9.3]; P < .001) were independent risk factors for fluconazole-resistant C glabrata BSIs (Table 3). In the subgroup analysis, in which fluconazole-resistant C glabrata was limited to those isolates with MIC greater than or equal to 64 μg/mL (n = 19), previous fluconazole use (5.2 [1.8-15.6]; P = .003), linezolid use (6 [1.4-14.5]; P = .01), and time at risk (1.02 [1.01-1.04]; P = .009) were independent risk factors. Previous cefepime use (adjusted OR [95% CI], 2.2 [1.2-3.9]; P = .007) and metronidazole use (2.0 [1.1-3.5]; P = .02) were independent risk factors for fluconazole-susceptible C glabrata BSIs (Table 3).

To our knowledge, the present study is the first to evaluate independent risk factors for fluconazole-resistant C glabrata BSIs. We found that previous fluconazole use and linezolid use were independent risk factors for fluconazole-resistant C glabrata BSIs. Previous cefepime use and metronidazole use were independent risk factors for fluconazole-susceptible C glabrata BSIs.

Previous fluconazole use could promote either de novo resistance by 1 or more mechanisms including upregulating efflux pumps or resistance by changing a patient's endogenous flora, enabling colonization and infection with fluconazole-resistant C glabrata.^9- 10 Our results are similar to those of 2 previous studies in patients with cancer that identified previous fluconazole use as a risk factor for invasive C glabrata infections (OR, 5-11).^11- 12 However, subsequent studies that broadened the study population to include the general inpatient population did not find this association. Several ecologic studies did not enable identification of significant increases in C glabrata BSIs despite significant increases in fluconazole use.^13- 14 A case-case-control study by Lin et al¹⁵ found that previous fluconazole use was not a risk factor for C glabrata and Candida krusei BSIs at bivariate or multivariate analyses. Malani et al²⁴ reported no difference in fluconazole-resistance rates between patients with and without previous fluconazole exposure. Limitations of the study by Malani et al, however, include that multivariate analysis was not performed and that the study may not have been powered to detect this difference.

The difference between the present study and previous studies in general inpatient populations may be related to case group selection. Although previous studies focused on C glabrata because of its association with fluconazole resistance, susceptibility testing was typically absent. Both patients with fluconazole-resistant and fluconazole-susceptible isolates were included in the case group. This may have decreased the ability to detect risk factors for fluconazole-resistant C glabrata, particularly given the results of this study, which found that previous fluconazole use was significantly associated with fluconazole-resistant C glabrata BSIs but not with fluconazole-susceptible C glabrata BSIs. High rates of fluconazole use in patients with cancer, however, may have resulted in higher rates of resistance in this population, enabling the investigators to find a strong association.

Linezolid use was also identified as an independent risk factor for fluconazole-resistant C glabrata BSIs. Linezolid has broad gram-positive coverage that could alter skin and possibly gastrointestinal flora such as Enterococcus species, enabling colonization and subsequent infection with fluconazole-resistant C glabrata. Lin et al¹⁵ found vancomycin, another antibiotic with broad gram-positive coverage, to be an independent risk factor for C glabrata and C krusei BSIs.

Cefepime use and metronidazole use were found to be independent risk factors for fluconazole-susceptible C glabrata BSIs. Lin et al¹⁵ identified piperacillin-tazobactam, an antimicrobial agent with both gram-negative and anaerobic coverage, as a significant risk factor for C glabrata and C krusei BSIs. Animal models have suggested that C glabrata may have fewer virulence factors.^25- 26 If C glabrata is less pathogenic than C albicans, C glabrata may require selection pressure from antecedent antibiotic use for colonization and infection. Previous studies have also suggested that Candida infections can occur via horizontal transfer, and this mode of transmission may be particularly important in C glabrata infections, the incidence of which increases with age.^27- 28

There are several potential limitations of the present study. Misclassification of risk factors is possible because data were not collected prospectively (ie, the database may be missing comorbid conditions not identified via International Classification of Diseases, Ninth Revision, coding and medications prescribed outside of the University of Pennsylvania Health System). However, the percentage of missing data is unlikely to be dissimilar between groups, and this nondifferential misclassification would bias results toward null. In addition, the study was conducted in 3 hospitals in the same city. Geographic and hospital-associated differences in the susceptibility patterns of C glabrata have been previously demonstrated.^2,29

To our knowledge, the present study is the first to evaluate independent risk factors for fluconazole-resistant C glabrata BSIs and to identify previous fluconazole use as a significant risk factor for resistance in the general inpatient population. Future studies will be needed to identify the effect of decreasing fluconazole use on the rates of fluconazole-resistant C glabrata BSIs.

Correspondence: Ingi Lee, MD, MSCE, Division of Infectious Diseases, Department of Medicine, Hospital of the University of Pennsylvania, 3400 Spruce St, Third Floor, Silverstein Bldg, Ste E, Philadelphia, PA 19104 (ingi.lee@uphs.upenn.edu).

Accepted for Publication: September 14, 2008.

Author Contributions: Dr Lee had full access to all of the study data and takes responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: Lee, Fishman, Zaoutis, and Lautenbach. Acquisition of data: Lee, Weiner, Synnestvedt, and Nachamkin. Analysis and interpretation of data: Lee, Morales, and Lautenbach. Drafting of the manuscript: Lee and Lautenbach. Critical revision of the manuscript for important intellectual content: Lee, Fishman, Zaoutis, Morales, Weiner, Synnestvedt, Nachamkin, and Lautenbach. Statistical analysis: Lee, Morales, and Lautenbach. Obtained funding: Lee. Administrative, technical, and material support: Lee, Weiner, Synnestvedt, and Nachamkin. Study supervision: Fishman, Zaoutis, and Lautenbach.

Financial Disclosure: Dr Lautenbach received research grant support from Merck Pharmaceuticals and Ortho-McNeil Pharmaceuticals. Dr Zaoutis received research grant support from Merck Pharmaceuticals.

Funding/Support: This study was supported by Institutional National Research Service Award T32 AI055435 (Dr Lee) and by grants U18HS016946 and U18HS10399 from the Agency for Healthcare Research and Quality (AHRQ).

Role of the Sponsor: The AHRQ had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; or preparation, review, or approval of the manuscript. The content is solely the responsibility of the authors and does not necessarily represent the official views of the AHRQ.

Additional Contributions: John Stern, MD, facilitated the conduct of this study at Pennsylvania Hospital.