Clinical and microbiological characteristics of bloodstream infections due to AmpC β-lactamase producing Enterobacteriaceae: an active surveillance cohort in a large centralized Canadian region

Background The objective of this study was to describe the clinical and microbiological characteristics of bloodstream infections (BSIs) due to AmpC producing Enterobacteriaceae (AE) in a large centralized Canadian region over a 9-year period. Methods An active surveillance cohort design in Calgary, Canada. Results A cohort of 458 episodes of BSIs caused by AE was assembled for analysis. The majority of infections were of nosocomial origin with unknown sources. Enterobacter spp. was the most common species while BSIs due to Serratia spp. had a significant higher mortality when compared to other AE. Delays in empiric or definitive antibiotic therapy were not associated with a difference in outcome. However, patients that did not receive any empiric antimicrobial therapy had increased mortality (3/5; 60% vs. 57/453; 13%; p = 0.018) as did those that did not receive definitive therapy (6/17; 35% vs. 54/441; 12%; p = 0.015). Conclusions Delays in therapy were not associated with adverse outcomes although lack of active therapy was associated with increased mortality. A strategy for BSIs due to AE where β-lactam antibiotics (including oxyimino-cephalosporins) are used initially followed by a switch to non-β-lactam antibiotics once susceptibility results are available is effective.

There is controversy about the optimal antibiotic therapy for severe infections caused by AmpC producing Enterobacteriaceae (AE), particularly with regards to those that are chromosomally mediated because of the potential for inducibility and selection of derepressed mutants [4][5][6][7]. Clinical and Laboratory Standards Institute (CLSI) recommends reporting β-lactam susceptibilities of these organisms, with a footnote suggesting that resistance may develop during therapy [8]. Literature has shown the importance of early appropriate antibiotic therapy for severe infections in preventing mortality, [9] but few studies have looked at serious infections caused by AE especially those with chromosomal enzymes. Cephalosporin resistant Enterobacteriaceae have been isolated from patients that have previously received broad-spectrum cephalosporins, [10][11][12] and emergence of cephalosporin resistance has been described during therapy with βlactams [13,14]. These studies have focused on a single species of AE, [10][11][12]14] or have included a limited range of organisms [13]. In addition, these studies have included various types of infections and have not clearly demonstrated that therapy with β-lactams is associated with an increase in mortality.
The objective of this study is to describe the clinical and microbiological characteristics of bloodstream infections (BSIs) due to AE in a large centralized Canadian region over a 9-year period (2000-08). We also investigate the effects of various empiric and definitive antimicrobial treatment regimens on the mortality of patients with BSIs due to AE. Specifically, we look to determine if definitive treatment with β-lactam antibiotics are associated with increased mortality in infections caused by AE.

Study population
The Calgary Zone of Alberta Health Services (previously known as the Calgary Health Region) administers virtually all medical and surgical care to the residents of the cities of Calgary and Airdrie and a large surrounding area (population 1.2 million) in the province of Alberta, Canada. All patients with BSIs caused by AE from January 1, 2000 to December 31 st , 2008 in the Calgary Zone were included in the study. The Conjoint Health Research Ethics Board at the University of Calgary approved this study and granted a waiver of individual patient consent.
We excluded episodes with incomplete data, polymicrobial episodes and those in which the patients died within 24 hours (which may have precluded their receiving appropriate therapy). To investigate the effects of various empiric and definitive antimicrobial treatment regimens on the mortality of patients, patients were divided into two groups. Group I included patients that received definitive therapy with β-lactams that are hydrolyzed by AmpC β-lactamases (i.e. piperacillin-tazobactam), oxyimino-cephalosporins (i.e. cefotaxime, ceftriaxone, ceftazidime) and monobactams (i.e. aztreonam). Group II included patients that received definitive therapy with non-β-lactams and/or β-lactams with sufficient activity in spite of AmpC β-lactamases (i.e. cefepime and carbapenems).

Study protocol
An active surveillance cohort design was utilized. Surveillance for AE were identified using the Electronic Surveillance System at Calgary Laboratory Services [15]. International Statistical Classification of Disease and Health Related Problems (ICD) codes were translated into Charlson Comorbidity Scores using standardized algorithms [16,17]. Antimicrobial therapies were determined using a regional pharmacy database. AE BSIs were defined by the isolation of such bacteria from at least one set of aseptically obtained blood cultures. Repeat isolation from blood from the same patient within 365 days was considered to be the same incident infection.

Definitions
Empiric therapy was defined as that therapy initiated prior to the availability of blood culture results and sensitivities. Time to first therapy was defined as the time from blood culture draw to receipt of the first dose of antibiotics. Adequate therapy was defined by the receipt of a standard parenteral dose of an antimicrobial to which the organism was susceptible in vitro or a standard oral dose of an antimicrobial with sufficient bioavailability, to which the organism was susceptible in vitro. If the patient received two drugs from different classes to which the bacterium tested susceptible to one agent but resistant to the other agent, the therapy was considered to be adequate. Adequacy of combination antibiotic therapy required the microorganism to be susceptible to all drugs in the combination. Definitive therapy was defined as the final antibiotic chosen to complete a treatment course after the availability of antimicrobial susceptibilities. If the patient was given adequate antibiotics before or at the time of acquiring the blood culture, the time to first adequate therapy was recorded as zero hours. Mortality was defined as the 30-day mortality of patients as determined by searching provincial databases. Definitions of nosocomial, healthcare associated and community-acquired infections used in this study, have previously been described [18].

Laboratory methods
Clinical isolates were identified and minimum inhibitory concentrations (MICs) were determined by Vitek 2™ (Vitek AMS; bioMérieux Vitek Systems Inc., Hazelwood, MO). Susceptibility testing and reporting was performed according to the CLSI guidelines for broth dilution [8]. Enterobacteriaceae potentially possessing chromosomally mediated AmpC β-lactamases did not undergo confirmatory testing for the AmpC gene and/or inducibility of these genes.
After isolates were first shown to be non-susceptible to cefoxitin, the presence of AmpC β-lactamases in E. coli, K. pneumoniae and Salmonella isolates was confirmed using previously described boronic acid methodology [19].
The policy of the centralized microbiology laboratory is to suppress the susceptibility results of all β-lactam antibiotics for potential AE. Only fluoroquinolones, aminoglycosides and trimethoprim/sulfamethoxazole are routinely reported for infections caused by potential AE. Cefepime and carbapenem susceptibilities are available upon request.

Statistical analysis
Analysis was performed using Stata version 10.0 (Stata Corp, College Station, TX). Non-normally distributed data were described using medians with interquartile ranges (IQR). Categorical data were compared using the two-sided Fisher's exact test. P-values less than 0.05 were considered significant. Logistic regression models were developed to assess the independent effects of various factors on mortality. Treatment adequacy and timing, and all factors found to be significant to the P < 0.1 level in univariate analyses were included in the initial models. Backward stepwise variable elimination was then performed to develop the most parsimonious model. Discrimination was assessed using the area under the receiver operator characteristic (ROC) curve and calibration using the Hosmer-Lemeshow goodness-of-fit test.

Study population
Five hundred and ninety incident episodes of AE BSIs were identified between 2000 and 2008. After excluding patients with incomplete data (n = 64), polymicrobial infection (n = 54, 9) or that died within 24 hours of culture draw (n = 14) a cohort of 458 (78%) episodes remained for further analysis.

for further details)
Empiric therapy was provided in 453 (99%) cases. The most common agents used as empiric therapy included piperacillin-tazobactam (131, 29%) and oxyiminocephalosporins (106, 23%). Empiric therapy was started immediately in 172 (38%) patients, within 8 hours in 277 (60%) patients, within 24 hours in 391 (85%) patients and within 48 hours in 427 (93%) patients. The timing of empiric antibiotic therapy was not associated with a difference in outcome. However, patients that did not receive empiric antimicrobial therapy had a worse outcome (3/5; 60% vs. 57/453; 13%; p = 0.018). The number, combination (at least two antibiotics from different classes), or class of antibiotic was also not associated with any statistically significant improvement in outcome (data not shown). Empiric therapy with piperacillin-tazobactam or an oxyimino-cephalosporin was not associated with a difference in mortality outcome (28/237; 12% vs. 32/221; 14%; p = 0.41). Of 131 that received empiric piperacillintazobactam, the case-fatality rate was 2/19 (11%) for those patients with isolates that tested resistant at baseline as compared to 13/112 (12%) for those isolates that tested sensitive, p = 0.89. Notably, of 106 patients who received oxyimino-cephalosporins as empiric therapy, the case-fatality rate was 5/18 (28%) for those patients with isolates that tested resistant at baseline as compared to 8/88 (9%) for those that were sensitive, p = 0.04.
Adequate therapy was provided in 441 (96%) cases. The most common agents used as adequate therapy included Logistic regression model (see Table 4 for further details) A logistic regression model was developed to assess the effect of timing and adequacy of therapy (n = 458) and had good calibration (Hosmer-Lemeshow goodness of fit p = 0.49 and discrimination (area under ROC = 0.808; ROC curve not shown). Early adequate therapy between 8-24 hours after blood culture draw had worse outcomes (Odds Ratio (OR) 2.01, p = 0.050) while delayed therapy at T > 24 hours to T = 48 hours had increased survival that did not reach statistical significance (OR 0.44, p = 0.70). Never having received definitive therapy demonstrated an increased risk of death (OR 4.78, p = 0.013).

Discussion
Our study described the clinical and microbiological characteristics of BSIs due to AE over a 9-year period. The majority of infections were of nosocomial origin with unknown sources. Patients often had underlying malignancy and the highest rates of mortality were associated with underlying pneumonia. Enterobacter spp. was by far the most common bacteria responsible for BSIs due to AE and was associated with underlying BTIs. Interestingly, we found that BSIs due to Serratia spp. had a significant higher mortality when compared to other AE.
Early and adequate antimicrobial therapy is a cornerstone of treatment of severe infections including BSIs. Several studies have found a clear relationship between time to first adequate therapy and mortality [9,[30][31][32]. Most of these studies utilize in vitro susceptibility to establish adequacy of therapy and this may not be appropriate   in the specific case of AE organisms. Our study revealed that delays in active antibiotic therapy were not associated with a poor outcome. However, patients that did not receive any empiric or definitive antimicrobial therapy had increased mortality. While the importance of appropriate early antimicrobial therapy is generally accepted, there are several studies that do not support this premise [33][34][35][36][37]. Our patient population was not limited to the critically ill and this may explain why we were not able to demonstrate an association between early adequate antimicrobial therapy and increased survival. Previous studies have investigated the issue of resistance development during treatment with oxyiminocephalosporins of infections due to AE. A previous study had shown a low risk of emergence of resistance during therapy and a low risk of associated mortality [13]. However that study included only a select number of AE and included a broad range of infections types. Another study showed that after treatment, 477 patients with susceptible Enterobacter spp. infections, 49 (10.3%) subsequently developed cephalosporin resistant isolates [11]. This study did not specifically address mortality. The policy of the centralized laboratory to suppress susceptibilities for all β-lactam antibiotics for infections caused by AE resulted in clinicians changing the definitive antimicrobial therapy to non-β-lactam antibiotics once susceptibility results were available. After excluding all patients that died early and that did not receive definitive therapy only 22 of 441 patients completed definitive therapy with oxyimino-cephalosporins. The low numbers of patients treated with oxyimino-cephalosporins thus precluded us from determining the efficacy of this regimen. Our study did however reveal that patients empirically treated with oxyimino-cephalosporins, when the isolate was resistant at baseline, had a statistically worse outcome. This supports the notion that initial empiric therapy with oxyimino-cephalosporins may be effective for AE that test in vitro sensitive to these agents. We recommend that patients who previously received oxyimino-cephalosporins should be treated empirically with an alternate class of agent because of the risk of being colonized with oxyimino-cephalosporin resistant AE.
In the multivariate model it was noted that adequate therapy at between 8-24 hours after blood culture draw had worse outcomes while delayed adequate therapy at T > 24 hours to T = 48 hours had increased survival; findings that did not reach statistical significance. Our group has previously reported similar results [34]. This interesting finding was most likely the result of sicker patients receiving broader and more prompt empiric antimicrobials as a result of their clinical condition. Again, our study is limited in that we did not collect data regarding severity of illness. Furthermore, since these findings did not reach statistical significance they may have occurred by chance alone. It should be mentioned that the numbers of patients that did not receive empiric or definitive therapy were small, 5 and 17 respectfully. As such, any specific conclusions could not be generated.
There are several limitations of our study mostly arising from our pharmacy database. This database did not capture all outpatient data. It is conceivable that the 22   (or a proportion thereof ) patients that are classified as having completed definitive β-lactam therapy may have received outpatient definitive non-β-lactam therapy after initial improvement. In addition, the pharmacy database may have not captured all ward stock antibiotics dispensed and the pharmacy database captured the time the antibiotic was dispensed which may not have correlated with the time the antibiotic was administered. Finally, the cohort assembled for this study included potential AmpC producers, and it is possible that some of the isolates may not have had the AmpC β-lactamase gene. In the clinical context it is impractical due to time and financial constraints to test each isolate for the presence of the AmpC gene and/or inducibility of these genes. As such our study attempted to answer this question from a feasibility perspective.

Conclusion
In conclusion, Enterobacter spp. is the most common AE that causes BSIs in the Calgary region. A strategy where β-lactam therapy (including oxyimino-cephalosporins) is used as initial therapy for severe infections caused by AE followed by a switch to non-β-lactam therapy once susceptibility results are available is effective. The efficacy of using oxyimino-cephalosporins as definitive therapy for severe AE infections remains unknown.