Comparison between bacteremia caused by carbapenem resistant Acinetobacter baumannii and Acinetobacter nosocomialis.

BACKGROUND: It is unknown whether there are differences between bacteremia caused by carbapenem resistant Acinetobacter baumannii (CRAB) and carbapenem resistant Acinetobacter nosocomialis (CRAN). This study aims to investigate the differences, especially in clinical outcomes, between patients with bacteremia caused by CRAB or CRAN.
METHODS: This is a 9-year retrospective study comparing the clinical manifestations, antimicrobial susceptibilities, and clinical outcomes of 71 patients with CRAB bacteremia and 64 patients with CRAN bacteremia.
RESULTS: Patients with CRAB were more likely to have hematologic malignancies and presented with more shock episodes than those with CRAN. CRAB isolates were more resistant to various classes of antimicrobials except colistin, and therefore the patients with CRAB bacteremia were more likely to receive inappropriate antimicrobial therapies. The 14-day mortality was significantly higher in patients with CRAB (40.8% vs. 14.1%; p = 0.001), and in this study, acquisition of CRAB was identified as an independent risk factor for mortality (odds ratio = 4.003; 95% confidence interval = 1.566-10.231; p = 0.004).
CONCLUSIONS: CRAB and CRAN bacteremia are different in clinical characteristics, antimicrobial susceptibilities, and mortality rates. Genomic species identification should be performed in the study of carbapenem resistant Acinetobacters to better delineate the role of different species.

Background

Acinetobacter species have emerged as important pathogens causing nosocomial infections [1]. Carbapenem resistant Acinetobacter spp. are now increasingly encountered worldwide [2,3], especially in the Asia-Pacific region [4-6]. The three most clinically relevant Acinetobacter species, Acinetobacter baumannii, Acinetobacter nosocomialis (formerly Acinetobacter genomic species 13TU), and Acinetobacter pittii (formerly Acinetobacter genomic species 3), cannot be differentiated by phenotypic tests used in clinical microbiological laboratories and are grouped as the A. baumannii (Ab) group [1]. Though the prevalence of Acinetobacter species in the Ab group vary in different geographic areas and institutions, A. baumannii and A.nosocomialis are commonly isolated clinical Acinetobacter species worldwide [7-12] and accounting for more than 80% of clinical infections caused by the Ab group in Taiwan [10,13,14].

Compared to bacteremia caused by A. nosocomialis, bacteremia caused by A. baumannii is associated with worse clinical outcomes [10,12,13,15]. The higher mortality in patients with A. baumannii might be attributed to a higher pathogenicity of A. baumannii [10,15]. However, it is unknown whether the more severe clinical outcomes of A. baumannii bacteremia compared to A. nosocomialis bacteremia will be the same if both the pathogens are carbapenem resistant, as it has been shown that the virulence of A. baumannii resistant to certain drugs is impaired [16,17]. In this study, we aim to compare the clinical characteristics, antimicrobial susceptibilities of the bacterial isolates, and especially the clinical outcomes of patients with bacteremia caused by carbapenem resistant A. baumannii (CRAB) and A. nosocomialis (CRAN).

Methods

Study population

The study was conducted at the Taipei Veterans General Hospital (T-VGH) during a nine-year period from January 2000 to December 2008. T-VGH is a 2900-bed tertiary-care teaching hospital located in Taipei, Taiwan. Data analyses were performed at the Tri-Service General Hospital (TSGH), National Defense Medical Center in Taipei, Taiwan.

Charts were reviewed from all patients with at least one positive blood culture for A. baumannii or A. nosocomialis who had symptoms and signs of infection. Only the first blood culture from patients with two or more positive blood cultures was included. The source of infection was determined as recommended in Centers of Disease Control guidelines [18,19]. Bacteremia cases without a definite identified source were defined as primary bacteremia. Patients under 18 years of age and those with incomplete medical records were excluded. The protocol was approved by the T-VGH and TSGH Institutional Review Board (approval number: 2011-10-012IC and 2-101-05-074, respectively) with a waiver for informed consent.

Microbiological studies

The presumptive identification of the isolates to the level of the Ab group was performed with the API ID 32 GN system (bioMérieux, Marcy l’Etoile, France) or Vitek 2 system (bioMérieux, Marcy l’Etoile, France). A multiplex-PCR method was used to identify A. baumannii to the genomic species level [20]. Isolates identified as non-A. baumannii species of Acinetobacter were identified to the genomic species level by 16S–23S ribosomal DNA intergenic spacer sequence analysis [21]. Antimicrobial susceptibilities were determined by the agar dilution method according to the Clinical Laboratory Standards Institute (CLSI) [22]. Multidrug resistance was defined as resistance to three or more of the following classes of antimicrobial agents: anti-pseudomonal cephalosporins, anti-pseudomonal carbapenems, ampicillin/sulbactam, fluoroquinolones, and aminoglycosides [1].

Molecular typing

The clonal relationships of the clinical isolates were determined by pulsed-field gel electrophoresis (PFGE) [23]. Twenty randomly selected isolates from each Acinetobacter species were performed. PFGE of ApaI-digested genomic DNA was performed using the Bio-Rad CHEF-Mapper apparatus (Bio-Rad Laboratories, Hercules, CA, USA). Cluster analysis was performed using BioNumerics version 5.0 (Applied Maths, Sint-Martens-Latem, Belgium) and the unweighted pair-group method with arithmetic averages (UPGMA). The Dice correlation coefficient was used with a tolerance of 1% in order to analyze any similarities between banding patterns. Isolates showing more than three DNA fragment differences and a similarity of <80% following dendrogram analysis were considered to represent different pulsotypes.

Data collection

Medical records were reviewed to extract clinical information, including demographic characteristics, underlying diseases, duration of stay in an intensive care unit (ICU), hospital stay, time of receipt, dose and route of administration of individual antimicrobials, and the presence of a ventilator, central venous catheters, a nasogastric tube, or a foley catheter at the time of onset of bacteremia. Immunosuppressive therapy was defined as receipt of cytotoxic agents within 6 weeks, corticosteroids at a dosage equivalent to or higher than 10 mg of prednisolone daily for more than 5 days within 4 weeks, or other immunosuppressive agents within 2 weeks prior to the onset of bacteremia. Neutropenia was defined as an absolute neutrophil count <0.5×109 neutrophils/L. Recent surgery was defined as operations performed within 4 weeks prior to the onset of bacteremia. Chronic kidney disease was defined as an estimated glomerular filtration rate <60 mL/min/1.73 m2. Shock was defined as hypotension (systolic blood pressure [SBP] <90 mmHg, mean arterial pressure <70mmHg, or a SBP decrease >40 mmHg) with evidence of end organ dysfunction [24]. Polymicrobial bacteremia was defined as isolation of one or more microorganisms other than A. baumannii or A. nosocomialis from blood during the same bacteremic episode. The severity of illness was evaluated using the Acute Physiology and Chronic Health Evaluation II (APACHE II) score [25] within 24 hours prior to bacteremia onset.

Appropriate antimicrobial therapy was defined as administration of at least one antimicrobial agent, to which the causative pathogen was susceptible, within 48 hours after the onset of bacteremia, with an approved route and dosage for end organ(s) function. Antimicrobial therapy that did not meet this definition was considered inappropriate. Monotherapy with an aminoglycoside was not considered an appropriate therapy. The primary outcome measure was all-cause 14-day mortality following the onset of CRAB or CRAN bacteremia.

Statistical analysis

To assess differences, the chi-square test with Yate’s correction or Fisher’s exact test was used to compare the discrete variables, while the Student’s t-test or Mann–Whitney rank sum test was used to analyze continuous variables. Logistic regression models were used to explore independent risk factors for 14-day mortality. Univariate analyses were performed separately for each of the risk factor variables to ascertain the odds ratio (OR) and 95% confidence interval (CI). All biologically plausible variables with a p value of ≤0.10 in the univariate analysis exhibited by at least 10% of the patients were considered for inclusion in the logistic regression model for the multivariate analysis. A backward selection process was utilized. Time to mortality was analyzed using Kaplan-Meier survival analysis and long-rank test. A p value <0.05 was considered statistically significant. All the analyses were processed with Statistical Package for the Social Sciences (SPSS) software version 18.0 (SPSS, Chicago, IL, USA).

Results

During the study period, 801 patients were found to have at least one episode of Ab group bacteremia. Among them, 185 (23.1%) patients with polymicrobial bacteremia were excluded from the study. Following genomic species analysis, 259 (42.0%) and 294 (47.7%) patients were identified as having bacteremia caused by A. baumannii and A. nosocomialis, respectively. The final population that met the entry criteria for this study consisted of 71 patients with CRAB bacteremia and 64 patients with CRAN bacteremia. A total of 43 patients were excluded due to young age (13 patients <18 years) and incomplete medical records (30 patients).

Among the 20 randomly selected CRAB and CRAN isolates, the analysis of PFGE showed that there were 7 and 14 pulsotypes, respectively (data not shown).

The demographic and clinical characteristics of the patients included in the study are summarized in Table 1. The most common source of CRAB and CRAN bacteremia was the respiratory tract (66.2% and 70.3%, respectively). Patients with CRAB had hematologic malignancies more frequently than those with CRAN (12.7% vs. 1.6%, p = 0.019). Though APACHE II scores at the onset of bacteremia were similar in both groups, shock was more frequently present in patients with CRAB.

Table 1

Demographic and clinical characteristics of patients with bacteremia caused by carbapenem resistant and carbapenem resistant *

Demographic or characteristic	A. baumannii (n=71)	A. nosocomialis (n=64)	p value
	n (% or interquartile range)
Age in years	75(61.0–82.0)	76(62.0–81.0)	0.78
Gender, male	54(76.1)	46(71.9)	0.7
Acquired in ICU	60(84.5)	54(84.4)	1
Days of hospitalization prior to culture	22.5(9.5–39.5)	25(8.0–34.0)	0.26
Source
Respiratory tract	47(66.2)	45(70.3)	0.71
Intravenous device	4(5.6)	7(10.9)	0.35
Intra-abdomen	6(8.5)	3(4.7)	0.5
Wound	2(2.8)	1(1.6)	1
Primary bacteremia	12(16.9)	8(12.5)	0.32
Comorbidity
Coronary artery disease	7(9.9)	11(17.2)	0.31
Congestive heart failure	5(7.0)	11(15.6)	0.11
Cerebral vascular disease	13(18.3)	17(26.6)	0.3
Hypertension	22(31.0)	25(39.1)	0.37
COPD	14(19.7)	20(31.2)	0.17
Alcoholism	7(9.9)	1(1.6)	0.07
Liver cirrhosis	3(4.2)	3(4.7)	1
Diabetes mellitus	20(28.2)	22(34.4)	0.46
Collagen vascular disease	4(5.6)	4(6.2)	1
Usage of immunosuppressants	23(32.4)	15(23.4)	0.26
Neutropenia	2(2.8)	1(1.6)	1
Malignancy	27(38.0)	24(37.5)	1
Hematologic malignancy	9(12.7)	1(1.6)	0.019
Solid malignancy	20(28.2)	23(35.9)	0.36
Recent surgery	26(36.6)	29(45.3)	0.38
Trauma	2(2.8)	2(3.1)	1
Procedure†
Abdominal drain	7(9.9)	9(14.1)	0.6
Central venous catheter	49(69.0)	47(73.4)	0.7
Foley catheter	53(74.6)	44(48.8)	0.57
Hemodialysis	9(12.7)	8(12.5)	1
Thoracic drain	1(1.4)	4(6.2)	0.19
Total parental nutrition	9(12.7)	7(10.9)	0.8
Endotracheal tube or tracheostomy	53(74.6)	53(82.8)	0.3
Ventilator	49(69.0)	45(70.3)	1
Arterial line	22(31.0)	12(18.8)	0.12
Nasogastric tube	61(85.9)	51(79.7)	0.37
APACHE II score†	26(19.0–34.0)	26(18.3–31.8)	0.1
Shock	29(40.8)	10(15.6)	0.003
Appropriate antimicrobial therapy	9(12.7)	22(34.4)	0.004
Mortality	43(60.6)	21(32.8)	0.002
14-day mortality	29(40.8)	9(14.1)	0.001
28-day mortality	34(47.9)	13(20.3)	0.001
Time to mortality, day	7(2.0–26.0)	21(9.5–68.5)	0.022

*Data are median value (interquartile range) for continuous variables and number of cases (%) for categorical variables. †Within 24 hours prior to bacteremia onset. APACHE II Acute Physiologic and Chronic Health Evaluation II, COPD chronic obstructive pulmonary disease, ICU intensive care units.

The antimicrobial susceptibilities of the clinical isolates of CRAB and CRAN are shown in Table 2. CRAB exhibited significantly higher rates of resistance to all antimicrobials tested, except colistin and piperacillin/tazobactam. Only one A. baumannii isolate was resistant to colistin (1.4%), while in contrast, 45.3% (29/64) of the A. nosocomialis isolates were resistant to colistin (p<0.001). Clinical isolates of CRAB exhibited multidrug resistance more frequently than CRAN (100% vs. 75%, p<0.001). Patients with CRAB more frequently received inappropriate antimicrobial therapies than those with CRAN (Table 1).

Table 2

Comparison of antimicrobial susceptibilities of clinical isolates of carbapenem resistant and carbapenem resistant

	Resistance, n (%)
Antimicrobial agent	A. baumannii (n=71)	A. nosocomialis (n=64)	p value
Amikacin	68(95.8)	30(46.9)	<0.001
Gentamicin	68(95.8)	54(84.4)	0.038
Ceftazidime	69(97.2)	14(21.9)	<0.001
Cefepime or cefpirome	49(69.0)	13(20.3)	<0.001
Ampicillin/sulbactam	43(60.6)	27(42.2)	0.039
Piperacillin/tazobactam	56(78.9)	42(65.6)	0.12
Ciprofloxacin	69(97.2)	4(6.2)	<0.001
Colistin	1(1.4)	29(45.3)	<0.001
Tigecycline	6(8.2)	0(0)	0.03

The antimicrobials used, the APACHE II score, appropriateness of antimicrobial use, and patient outcomes are shown in Table 3. Due to the limited number of cases, differences in illness severity, and appropriateness of therapy in each therapy group, it was difficult to evaluate the effect of different antimicrobial therapies on patients with CRAB and CRAN bacteremia. Overall, the mortality rate of CRAB was higher than CRAN in different antimicrobial therapy groups. For example, in the carbapenem therapy groups, in which the illness of severity was comparable between both groups, the 14-day mortality rates in CRAB and CRAN groups were 41.2% vs. 14.3%, respectively. In the sulbactam therapy group, although the illness severity was lower in the CRAB group, the 14-day mortality rate was still higher (45.5 vs. 0%).

Table 3

Antimicrobials used for the patients with carbapenem resistant and bacteremia*

Main agents used	No. of patients	APACHE II score	No. (%) of patients
		Median (interquartile range)	Appropriate antimicrobial therapy	14–day mortality
Anti-pseudomonal penicillinsa
CRAB	12	31.5(22.8–39.0)	2(16.7)	6(50.0)
CRAN	8	24(19.0–33.0)	7(87.5)	2(25.0)
Anti-pseudomonal cephalosporinsb
CRAB	14	26(22.8–34.0)	2(14.3)	4(28.6)
CRAN	10	26(19.3–30.0)	7(70.0)	1(10.0)
Anti-pseudomonal fluoroquinolonesc
CRAB	5	30(21.0–36.0)	1(20.0)	2(40.0)
CRAN	2	37.5(37.0–38.0)	2(100.0)	0(0)
Anti-pseudomonal carbapenemsd
CRAB	17	32(24.0–38.5)	0(0)	7(41.2)
CRAN	14	30.5(23.0–33.3)	0(0)	2(14.3)
Ampicillin/sulbactam or sulbactam
CRAB	11	17(15.0–33.0)	4(36.4)	5(45.5)
CRAN	8	24(18.0–27.5)	3(37.5)	0(0)
Non-antipseudomonal β-lactamasese
CRAB	6	17.5(15.3–25.3)	0(0)	1(16.7)
CRAN	9	18(15.5–24.0)	3(33.3)	1(11.1)
Miscellaneous
CRAB	6	25(17.8–32.0)	0(0)	2(33.3)
CRAN	13	27(16.0–35.5)	0(0)	3(23.1)

*Data are median value (interquartile range) for continuous variables and number of cases (%) for categorical variables. aIncluding piperacillin, piperacillin/tazobactam, and ticarcillin/clavulanate. bIncluding cefoperazone, ceftazidime, cefepime, and cefpirome. cIncluding ciprofloxacin and levofloxacin. dIncluding imipenem and meropenem. eIncluding penicillin, amoxicillin/clavulanate, cefazolin, cefuroxime, cefotaxime, cefmetazole, and flomoxef. APACHE II Acute Physiologic and Chronic Health Evaluation II, CRAB carbapenem resistant A. baumannii, CRAN carbapenem resistant A. nosocomialis.

The mortality rates by 14 and 28 days after bacteremia onset were significantly higher in patients with bacteremia caused by CRAB than CRAN (p = 0.001). The 14-day mortality for CRAB was 40.8% (29/71) compared with 14.1% (9/64) for CRAN. The average time from admission to death was significantly shorter in CRAB than CRAN(16.7 days vs. 39.4 days, p = 0.022). Kaplan-Meier survival curves reflected the early occurrence of death within a few days following bacteremia for patients infected with CRAB. This was followed by higher rates of death in the CRAB group than the CRAN group (p = 0.001, by log-rank test) (Figure 1).

Figure 1

Kaplan-Meier survival curves for patients with carbapenem resistant bacteremia and carbapenem resistant bacteremia.

Factors associated with 14-day mortality are summarized in Table 4. Bacteremia with CRAB, higher APACHE II score, use of immunosuppressants and shock were univariable risk factors for mortality. Following logistic regression analysis, A. baumannii itself was found to be an independent risk factor for mortality among all patients (odds ratio = 4.003; 95% confidence interval = 1.566-10.231; p = 0.004). The usage of immunosuppressants was also an independent risk factor for mortality.

Table 4

Factors associated with 14-day mortality in patients with carbapenem resistant and bacteremia

Demographic and characteristics	Univariate analysis		Multivariate analysis
	Odds ratio	p value	Odds ratio	p value
	(95% CI)		(95% CI)
A. baumannii	4.220(1.806–9.861)	0.001	4.003(1.566–10.231)	0.004
APACHE II score*	1.165(1.098–1.237)	<0.001
Score ≤25	1.127(0.965–1.317)	0.131
Score >25	1.062(0.986–1.144)	0.113
Score ≤35	1.086(1.012–1.166)	0.022
Score >35	1.056(0.895–1.247)	0.113
Cerebral vascular disease	0.222(0.063–0.783)	0.019	0.194(0.048–0.789)	0.022
Usage of immunosuppressants	4.105(1.827–9.227)	0.001	3.921(1.516–10.143)	0.005
Appropriate antimicrobial therapy	0.381(0.144–1.004)	0.051
Recent surgery	0.190(0.073–0.494)	0.001	0.222(0.079–0.628)	0.005
Shock	2.760(1.244–6.122)	0.013

*Every one increase in APACHE II score is accompanied by an increase of 1.165 in the odds ratio. APACHE II Acute Physiologic and Chronic Health Evaluation II, CI Confidence interval.

Discussion

This study clearly demonstrates significant differences in the risk factors, antimicrobial resistances, and especially clinical outcomes between bacteremia caused by CRAB and CRAN. Patients infected with CRAB were more likely to have hematologic malignancies and a greater frequency of shock. Even though both pathogens were carbapenem resistant, CRAB exhibited resistance to more antimicrobial agents. CRAB bacteremia was also associated with more frequent instances of inappropriate antimicrobial use, as well as more rapid and higher mortality rates. Among the patients with CRAB and CRAN bacteremia, acquisition of CRAB was found to be an independent factor for 14-day mortality.

Compared with CRAN, CRAB had higher resistance rates toward most commonly used antimicrobial agents, and all CRAB isolates were multidrug resistant. This resistance is responsible for the increased chance of receiving an inappropriate antimicrobial therapy in patients infected with these microorganisms. On the contrary, there were still some therapeutic options available for the treatment of CRAN bloodstream infections. A higher rate of colistin resistance in A. nosocomialis than A. baumannii was also observed in previous reports [14,26,27], where the resistance of colistin in A. nosocomialis was about 20%. In this study, it was even higher in CRAN isolates (45.3%).

The higher mortality of patients infected with CRAB compared to CRAN may be attributed to unfavorable underlying diseases, an increased likelihood of inappropriate antimicrobial therapy in the former group, and possibly higher pathogenicity of A. baumannii[10,13]. According to our findings, there were more shock episodes in patients with CRAB than with CRAN of similar disease severity. Furthermore, CRAB was identified as an independent risk factor for mortality after adjustment for other risk factors for mortality, including underlying diseases, severity of illness, and appropriateness of antimicrobial therapy. This result indicates a possible higher pathogenicity of CRAB compared to CRAN. Because of the diversity of the clonality of CRAB and CRAN isolates, we believe that the result is due to species but not strain effect. Genomic species identification is therefore important to better delineate the role of different species of carbapenem resistant Acinetobacters[21,28].

The prevalence of Acinetobacter species in the Ab group can vary in different geographic areas and institutions. For example, A. pittii was found to be the predominant species accounting for clinical infections in Germany during 2005-2009 [11]. Although A. baumannii and A. nosocomialis account for more than 80% of clinical infections caused by the Ab group, their ratio differs among centers in Taiwan [10,13-15]. Three centers demonstrated a >2:1 relative ratio of A. baumannii to A. nosocomialis[10,13,15], however, the ratio has consistently been around 1:1 in our center in recent years [26,29].

This study is subject to several limitations regularly found in retrospective studies. Several confounding factors, especially the antimicrobials used during the whole treatment course, could not be well controlled in both groups. However, it is not likely that certain antimicrobial regimens that might affect clinical outcomes were used more often in either group as the primary physicians were unaware of the genomic species.

Conclusions

CRAB and CRAN bacteremia are different in clinical characteristics, antimicrobial susceptibilities, and mortality rates. Genomic species identification should be performed in the study of carbapenem resistant Acinetobacters to better delineate the role of different species.

Abbreviations

A. baumannii: Acinetobacter baumannii; Ab group: A. baumannii group; A. nosocomialis: Acinetobacter nosocomialis; APACHE II: Acute Physiology and Chronic Health Evaluation II; CLSI: Clinical Laboratory Standards Institute; COPD: Chronic obstructive pulmonary disease; CRAB: Carbapenem resistant A. baumannii; CRAN: Carbapenem resistant A. nosocomialis; DNA: Deoxyribonucleic acid; ICU: Intensive care unit; PCR: Polymerase chain reaction; PFGE: Pulsed-field gel electrophoresis; SBP: Systolic blood pressure; SPSS: Statistical Package for the Social Sciences; TSGH: Tri-Service General Hospital; T-VGH: Taipei Veterans General Hospital.

Competing interests

Te-Li Chen is a medical advisor for TTY Biopharm. Other authors declare that they have no competing interests.

Authors’ contributions

YSY, YTL, and TLC participated in the study design, analysis of data, and writing of the manuscript. JRS and SCK participated in the data collection, while WCT and CHY participated in the data analysis. JCL, CPF, and FYC revised the manuscript with important intellectual contributions. All authors read and approved the final manuscript.

Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1471-2334/13/311/prepub