Canadian Journal of Infectious Diseases and Medical Microbiology
Volume 2018 (2018), Article ID 3150965, 9 pages
https://doi.org/10.1155/2018/3150965

Research Article

Determinants of Mortality in Patients with Nosocomial Acinetobacter baumannii Bacteremia in Southwest China: A Five-Year Case-Control Study

Shuangshuang Yang, Jide Sun, Xianan Wu, and Liping Zhang

Department of Laboratory Medicine, The First Affiliated Hospital of Chongqing Medical University, No. 1, Youyi Road, Yuzhong District, Chongqing 400016, China

Correspondence should be addressed to Liping Zhang; 1309898173@qq.com

Received 24 February 2018; Revised 2 May 2018; Accepted 10 May 2018; Published 3 June 2018

Academic Editor: Christian Bautista

Copyright © 2018 Shuangshuang Yang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Purpose. This study was aimed to identify the determinants of in-hospital mortality in Acinetobacter baumannii (A. baumannii) bacteremia and to assess impact of carbapenem resistance on mortality. Methods. A five-year case-control study was conducted from January 2011 to December 2015 in a tertiary teaching hospital with 3200 beds, Southwest China. Clinical outcomes and potential determinants of mortality in patients with nosocomial A. baumannii bacteremia and carbapenem-resistant A. baumannii (CRAB) bacteremia were evaluated using Cox and logistic regression analyses. Results. A total of 118 patients with nosocomial A. baumannii bacteremia were included. Seventy-one percent (84/118) of them had carbapenem-resistant A. baumannii (CRAB) bacteremia. The in-hospital mortality of nosocomial A. baumannii bacteremia was 21.2%, and the attributable in-hospital mortality rate due to CRAB was 21.5%. Significant difference of 30-day in-hospital mortality in the Kaplan–Meier curves was found between CRAB and CSAB groups (log-rank test, ). The Cox regression analysis showed that patients with CRAB bacteremia had 2.72 times higher risk for 30-day in-hospital mortality than did those with carbapenem-susceptible A. baumannii (CSAB) bacteremia (95% confidence intervals (CIs) 1.14–6.61, ). The logistic regression analysis reported that mechanical ventilation and respiratory tract as origin of bacteremia were independent predictors of mortality among patients with nosocomial A. baumannii bacteremia and CRAB bacteremia, while high APACHE II score on the day of bacteremia and multiple organ dysfunction syndromes (MODS) during hospitalization were independent predictors of mortality among patients with nosocomial A. baumannii bacteremia but not CRAB bacteremia. Conclusion. It was the severity of illness (high APACHE II score and MODS) not carbapenem resistance that highlighted the mortality of patients with nosocomial A. baumannii bacteremia. The impact of mechanical ventilation on mortality suggested that respiratory dysfunction might prime the poor outcome. Protection of respiratory function during the progression of nosocomial A. baumannii bacteremia should be given more importance. Early identification and intervention of patients with nosocomial A. baumannii bacteremia in critical ill conditions were advocated.

1. Introduction

The past two decades have witnessed a dramatic rise in the incidence of nosocomial infections by Acinetobacter baumannii (A. baumannii) with a worrisome morbidity and mortality [1]. Its global spread is generally attributed to the inherent or acquired ability of environment resilience, transmission, and resistance to broad-spectrum antimicrobials.

As a major nosocomial pathogen, carbapenem-resistant A. baumannii (CRAB) is of particular concern. Recent surveillance has reported its high prevalence and causative agent in ventilation-associated pneumonia (VAP), bloodstream infection, surgical site infection, postsurgical meningitis, and abdominal infection [2]. Bloodstream infection caused by CRAB has been a more tremendous clinical challenge in consideration of the lack of effective antibiotic agents and high mortality [3–6]. Despite colistin and tigecycline as the last resorts, the optimal therapeutic regimen of CRAB bacteremia has not been established, and the unavailability of new antibiotic pipeline in developing countries definitely restricts clinical therapeutic options and facilitates its dissemination. Therefore, surveillance of CRAB bacteremia and selection of patients for CRAB empirical coverage have been considered more essential. Numerous data from different regions have elucidated risk factors for nosocomial colonization or infection of CRAB, whereas impact of nosocomial bacteremia with CRAB has not been well documented, especially in China, and there is ongoing controversy as to whether carbapenem resistance determines a higher mortality of A. baumannii bacteremia.

Accordingly, the aim of this study was to identify the determinants of mortality for nosocomial A. baumannii bacteremia and further to illustrate the potential impact of carbapenem resistance on in-hospital mortality in this setting.

2. Patients and Methods

A five-year study of nosocomial A. baumannii bacteremia was conducted from January 2011 to December 2015 in the First Affiliated Hospital of Chongqing Medical University, which is the surveillance center of antimicrobial resistance in Chongqing, Southwest China. Approval was obtained from the Ethics Committee of the First Affiliated Hospital of Chongqing Medical University.

2.1. Study Design

To meet the objectives, a case-control study design was applied. Nonduplicated hospitalized patients with A. baumannii bacteremia were enrolled. Patients with incomplete medical data, younger than 18 years old, or with multiple microbial infections were excluded. The determinants of mortality of patients with nosocomial A. baumannii bacteremia were studied by comparing demographics, clinical characteristics, and clinical interventions between nonsurvival cases and survival controls. Then nonsurvival cases and survival controls with nosocomial CRAB bacteremia were further compared, and predictors of mortality of patients with nosocomial CRAB bacteremia were determined.

2.2. Microbiological Methods

Blood specimens were obtained by trained nurses and cultured in BD FX200 blood culture systems. Microbiological identification and antibiotic susceptibility testing were performed by the VITEK 2 compact (bioMérieux, France). Carbapenem susceptibility was interpreted by the minimal inhibitory concentration (MIC) breakpoints of Clinical and Laboratory Standards Institute (CLSI) M100-S26.

2.3. Definitions

Nosocomial A. baumannii bacteremia was defined as patients with positive blood culture only for A. baumannii and with clinical signs or symptoms of infection at least 48 hours after hospitalization [5].

Carbapenem-susceptible A. baumannii (CSAB) was defined as MIC ≤ 2 μg/mL for imipenem or meropenem, and carbapenem-resistant A. baumannii (CRAB) was defined as MIC ≥ 8 μg/mL for imipenem or meropenem.

Multidurg resistance was defined as resistance to no less than 3 of the following antibiotic agents: antipseudomonal cephalosporins, antipseudomonal carbapenems, ampicillin/sulbactam, fluoroquinolones, and aminoglycosides [7].

Previous use of antibiotic agents was considered if antibiotic therapy had been adopted for more than 3 consecutive days within 30 days prior to the collection of the first blood specimen for culture [8].

Administration of at least one effective antimicrobial agent for 48 h, within 5 days of the onset of bacteremia, is defined as adequate empirical antimicrobial therapy, and if the causative pathogen was susceptible to it in vitro, then it is defined as an effective antimicrobial agent [9].

2.3. Data Collection

Demographics, clinical characteristics, and clinical outcomes were retrieved from electronic database of the hospital information system (HIS), and microbiological characteristics were retrieved from the laboratory information system (LIS). Clinical characteristics were comorbidity, Acute Physiology and Chronic Health Evaluation (APACHE) II score on admission, APACHE II score on the day of bacteremia, multiple organ dysfunction syndromes (MODS), hospital wards, origin of bacteremia, previous antibiotic agent use, the duration of antibiotic agent exposure before the onset of A. baumannii bacteremia, and invasive procedures (abdominal or thoracic drainages, central venous catheterization, mechanical ventilation, nasogastric tube, and urinary catheterization). Clinical outcomes were reported with death or survival by clinicians in the medical records, and only in-hospital mortality was captured.

2.4. Statistical Analysis

Univariate analysis was performed to identify the determinants of mortality of A. baumannii bacteremia and CRAB bacteremia. Chi-square or Fisher’s exact test was used to compare categorical variables. Student’s t-test or the Mann–Whitney U test was used to compare continuous variables. Variables with a value < 0.05 in the univariate test were included in a multivariate logistic remodel. The odds ratio (OR) and its 95% confidence interval (CI) were calculated to evaluate the strength of any association. Kaplan–Merier curves were compared by the log-rank test. Hazard ratio was calculated by the Cox regression analysis. A two-tailed value < 0.05 was considered as statistically significant. SPSS v.21.0 (SPSS Inc., Chicago, IL) was used to perform all of the statistical calculations.

3. Results

3.1. Demographic, Clinical, and Microbiological Characteristics of Nosocomial A. baumannii Bacteremia

During the investigation period, 136 nonduplicate patients were retrieved with nosocomial A. baumannii bacteremia, and due to exclusion criteria, 18 of them were excluded. A total of 118 patients were enrolled from 19 wards in the different parts of this hospital. The mean age of this study population was 58.2 years. Sixty-seven percentage (79/118) of them were male. Sixty-six percentage (78/118) of patients suffered from underlying comorbidities. Hypertension was the most common underlying disease, presenting in 38.1% of the patients. Among the 118 patients, 84 patients had yielded CRAB, and the overall incidence of CRAB was 71.2% (84/118). ICU was the main source of both nosocomial A. baumannii bacteremia (61/118, 51.7%) and CRAB bacteremia (55/61, 90.2%), followed by neurosurgery department and hepatobiliary surgery department. As to subareas of ICU, general ICU contributed a large percentage of CRAB bacteremia cases (33/61, 54.1%), followed by respiratory ICU (15/61, 24.6%).

Of 118 A. baumannii isolates, 77.8% were multidrug resistant and 71.2% were CRAB. Similar but high resistant rates (77.8%) to ampicillin/sulbactam, piperacillin, piperacillin/tazobactam, ceftazidime, ceftriaxone, and ciprofloxacin were observed, whereas those to levofloxacin and sulfamethoxazole were no more than 40%. In comparison, relatively low resistance rates to minocycline and cefoperazone/sulbactam were found with resistance rates of 6.8% and 22.2%, respectively. As to the 84 CRAB strains, all of them were multidrug resistant and resistant to ampicillin/sulbactam, piperacillin, piperacillin/tazobactam, ceftazidime, ceftriaxone, cefepime, and ciprofloxacin. Resistance rates of CRAB strains to minocycline and cefoperazone/sulbactam were 8.6% and 28.6%, respectively.

3.2. Clinical Outcomes of Nosocomial A. baumannii Bacteremia

Totally 25 of 118 patients with nosocomial A. baumannii bacteremia died during the study period, yielding an in-hospital mortality rate of 21.2%. The crude mortality rate of patients with CRAB bacteremia was 27.4% (23/84), while that of patients with CSAB bacteremia was 5.9% (2/34). Significant difference was observed between patients with CRAB and CSAB bacteremia in mortality rate (). The attributable mortality rate due to CRAB was 21.5%, calculated by the subtraction of the crude mortality rate of CSAB patients from that of CRAB patients [10]. Overall, the 30-day in-hospital mortality rate of patients with nosocomial A. baumannii bacteremia was 12.7% (15/118). The 30-day in-hospital mortality rate of CRAB patients was 15.5% (13/84), while that of CSAB patients was 5.9% (2/34). The log-rank test found a significant difference in the Kaplan–Meier curves of 30-day in-hospital mortality between CRAB and CSAB patients (). Furthermore, Cox regression analysis found that patients with CRAB bacteremia suffered 2.72 times higher risk of mortality than did patients with CSAB bacteremia in 30-day hospitalization (hazard ratio (HR) = 2.72; 95% CI 1.14–6.61; ; Figure 1).

Figure 1: Risk of 30-day in-hospital mortality comparing patients with CRAB bacteremia and patients with CSAB bacteremia by the log-rank test.

3.3. Predictors for the Mortality of Nosocomial A. baumannii Bacteremia

Although our results have indicated that patients with CRAB bacteremia were vulnerable to death, it is arbitrary to deduce that carbapenem resistance is the predictor for the mortality of A. baumannii bacteremia in nosocomial scenarios. Therefore, we further evaluated the determinants of the mortality of nosocomial A. baumannii bacteremia (Table 1). Twenty-five nonsurvivors and 93 survivors were included. Univariate analysis found that nonsurvivors were more likely to suffer critical conditions than survivors, as indicated by an increased APACHE II score on admission, APACHE II score on the day of bacteremia, and MODS (). As expected, APACHE II score on admission, APACHE II score on the day of bacteremia, carbapenem resistance, central venous catheterization, mechanical ventilation, MODS, ICU stay before the bacteremia day, and respiratory tract as the origin of bacteremia were associated with the mortality of patients with nosocomial A. baumannii bacteremia, while adequate empirical antibiotic therapy was associated with their survival. By logistic regression analysis, high APACHE II score on the day of bacteremia, MODS, mechanical ventilation, and respiratory tract as the origin of bacteremia were identified as independent predictors for the mortality of nosocomial A. baumannii bacteremia (Table 2). Interestingly, carbapenem resistance was not significantly associated with the mortality of nosocomial A. baumannii bacteremia.

Table 1: Univariate analysis of the clinical characteristics of survival and nonsurvival patients suffered from nosocomial bacteremia caused by Acinetobacter baumannii.

Characteristics
Patientsa
value
OR
95% CI

Nonsurvivors ()
Survivors ()

Male
17 (68.0)
62 (66.6)
1.000
1.06
0.41–2.73

Age (median (IQR)) (years)
68 (58, 75)
60 (44.5, 70)
0.104
—
—

Carbapenem resistance
24 (96.0)
60 (64.5)
0.001
13.20
1.71–102.17

Source

Abdominal route
0 (0)
4 (4.3)
0.577
0.39
0.02–7.49

Cerebral spinal route
1 (4)
6 (6.45)
1.000
0.60
0.07–5.27

Central venous route
1 (4)
6 (6.45)
1.000
0.60
0.07–5.27

Primary
11 (44)
60 (64.5)
0.070
0.43
0.18–1.06

Respiratory tract
11 (44)
11 (11.8)
0.001
5.86
2.13–16.08

Skin/soft tissue
1 (4)
4 (4.3)
1.000
0.93
0.09–8.69

Urinary tract
0 (0)
2 (2.2)
1.000
0.72
0.03–15.44

COPD
2 (8)
2 (2.2)
0.197
3.96
0.53–29.62

Coronary heart diseases
5 (20)
12 (12.9)
0.353
1.69
0.53–5.34

Diabetes mellitus
4 (16)
24 (25.8)
0.429
0.55
0.17–1.76

Hepatic diseases
4 (16)
7 (7.5)
0.243
2.34
0.63–8.74

Hypertension
6 (24)
39 (41.9)
0.112
0.44
0.16–1.20

Renal diseases
5 (20)
9 (9.7)
0.172
2.33
0.70–7.73

Malignancy
5 (20)
10 (10.8)
0.307
2.08
0.64–6.75

MODS during hospitalization
5 (20)
2 (2.2)
0.005
11.38
2.06–62.90

APACHE II score on admission (mean ± SD)
21.6 ± 1.4
17.8 ± 0.6
0.010
—
—

APACHE II score on the day of bacteremia (mean ± SD)
22.3 ± 1.3
18.0 ± 0.6
0.001
—
—

ICU stay
22 (88)
62 (66.6)
0.046
3.67
1.02–13.21

Any antibiotic exposure prior to positive blood culture
25 (100)
82 (88.2)
0.117
7.11
0.40–125.0

Duration of previous antimicrobial exposure
11 (8, 24)
13 (6.5, 23)
0.811
—
—

Aminoglycosides
8 (32)
14 (15.1)
0.079
2.66
0.96–7.33

Antifungal azoles
8 (32)
23 (24.7)
0.454
1.43
0.55–3.75

β-Lactam/β-lactamase inhibitors
11 (44)
47 (49.5)
0.654
0.769
0.32–1.87

Cefepime
2 (8)
9 (9.7)
1.000
0.81
0.16–4.02

Carbapenems
19 (76)
52 (55.9)
0.106
2.50
0.91–6.82

Fluoroquinolones
12 (32)
26 (14.0)
0.089
2.38
0.96–5.89

Minocycline
2 (8)
7 (7.5)
1.000
1.068
0.21–5.50

Third-generation cephalosporins
7 (28)
29 (31.2)
0.812
0.86
0.32–2.28

Nitroimidazoles
6 (24)
27 (29.0)
0.803
0.77
0.28–2.14

Abdominal or thoracic drainages
9 (36)
35 (37.6)
1.000
0.93
0.37–2.34

Central venous catheterization
19 (76)
47 (50.5)
0.025
3.10
1.14–8.46

Mechanical ventilation
22 (88)
44 (47.3)
0.000
8.17
2.29–29.18

Nasogastric tube
11 (44)
30 (32.3)
0.345
1.65
0.67–4.07

Urinary catheterization
15 (60)
46 (49.5)
0.376
1.53
0.62–3.76

Adequate empirical antibiotic therapy
7 (28)
53 (57)
0.013
0.29
0.11–0.77

APACHE: Acute Physiology and Chronic Health Evaluation; COPD: chronic obstructive pulmonary disease; CI: confidence interval; ICU: intensive care unit; IQR: interquartile range; OR: odds ratio; SD: standard deviation; MODS: multiple organ dysfunction syndrome. aData were expressed as the number (%) of patients unless stated otherwise.

Table 2: Multivariate logistic analysis of predictors of in-hospital mortality among patients suffered from nosocomial bacteremia caused by Acinetobacter baumannii.

Predictors
aOR
95% CI
value

MODS during hospitalization
10.35
1.20–89.01
0.033

APACHE II score on admission
1.02
0.93–1.12
0.685

APACHE II score on the day of bacteremia
1.82
1.15–2.86
0.010

ICU stay
0.57
0.10–3.36
0.534

Mechanical ventilation
10.13
1.76–58.23
0.009

Central venous catheterization
1.29
0.35–4.80
0.704

Carbapenem resistance
0.93
0.11–7.81
0.94

Respiratory tract origin
10.67
2.61–43.61
0.001

Adequate empirical antibiotic therapy
1.43
0.35–5.92
0.620

aOR: adjusted odds ratio; CI: confidence interval; MODS: multiple organ dysfunction syndrome; ICU: intensive care unit.

3.4. Carbapenem Resistance and the Mortality of Nosocomial A. baumannii Bacteremia

Since carbapenem resistance did not significantly contribute to the mortality of nosocomial A. baumannii bacteremia, the determinants of mortality of nosocomial CRAB bacteremia was further studied. Twenty-three nonsurvivors and 61 survivors with CRAB bacteremia were compared by univariate analysis. Table 3 shows univariate analysis of risk factors for the mortality of nosocomial CRAB bacteremia. No significant difference was found between two groups in terms of male gender, age, and comorbidities. MODS, mechanical ventilation, and respiratory tract as the origin of bacteremia were found significantly associated with the mortality of nosocomial CRAB bacteremia. Logistic regression analysis also found that mechanical ventilation (OR, 7.39; 95% CI, 1.39–39.17; ) and respiratory tract as the origin of bacteremia (OR, 7.41; 95% CI, 2.20–24.89; ) were strong independent risk factors for the mortality of CRAB bacteremia.

Table 3: Univariate analysis of the clinical characteristics of survival and nonsurvival patients suffered from nosocomial bacteremia caused by carbapenem-resistant Acinetobacter baumannii.

Characteristics
Patientsa
value
OR
95% CI

Nonsurvivors
Survivors

()
()

Male
15 (65.2)
43 (70.5)
0.792
0.79
0.28–2.18

Age (median (IQR)) (years)
68 (46, 76)
58 (41, 70)
0.067
—
—

Source

Abdominal route
1 (4.3)
2 (3.3)
1.000
1.34
0.12–15.55

Cerebral spinal route
1 (4.3)
4 (6.6)
1.000
0.65
0.07–6.12

Central venous route
0 (0)
4 (6.6)
0.571
0.27
0.01–5.26

Primary
9 (39.1)
34 (55.7)
0.223
0.51
0.19–1.36

Respiratory tract
11 (47.8)
11 (18.0)
0.011
4.17
1.46–11.87

Skin/soft tissue
1 (4.3)
4 (6.6)
1.000
0.65
0.07–6.12

Urinary tract
0 (0)
2 (3.3)
1.000
0.51
0.02–10.96

Coronary heart diseases
5 (21.7)
9 (14.8)
0.515
1.61
0.48–5.43

Diabetes mellitus
4 (17.4)
12 (19.7)
1.000
0.86
0.25–3.00

Hypertension
6 (26.1)
26 (42.6)
0.211
0.48
0.17–1.37

Hepatic diseases
4 (17.4)
6 (9.8)
0.450
1.93
0.49–7.59

Renal diseases
5 (21.7)
6 (9.8)
0.163
2.55
0.69–9.35

Malignancy
4 (17.4)
4 (6.6)
0.206
3.00
0.68–13.18

MODS during hospitalization
4 (17.4)
2 (3.3)
0.045
6.21
1.05–36.64

APACHE II score on admission (mean ± SD)
21.74 ± 1.42
19.18 ± 0.71
0.116
—
—

APACHE II score on the day of bacteremia (mean ± SD)
22.39 ± 1.38
19.34 ± 0.68
0.056
—
—

ICU stay
22 (95.7)
48 (78.7)
0.098
5.96
0.73–48.47

Any antibiotic exposure prior to positive blood culture
23 (100)
60 (98.4)
1.000
1.17
0.05–29.66

Duration of previous antimicrobial exposure
11 (8, 24)
14 (9, 23)
0.811
—
—

Aminoglycosides
8 (34.8)
10 (16.4)
0.080
2.72
0.91–8.12

Antifungal azoles
7 (30.4)
18 (29.5)
1.000
1.05
0.37–2.97

β-Lactam/β-lactamase inhibitor combinations
11 (47.8)
34 (55.7)
0.517
0.73
0.28–1.91

Carbapenems
18 (78.3)
40 (65.6)
0.302
1.89
0.61–5.81

Cefepime
1 (4.3)
7 (11.5)
0.436
0.35
0.04–3.02

Fluoroquinolones
12 (52.2)
22 (16.4)
0.216
1.93
0.73–5.11

Minocycline
2 (8.7)
6 (9.8)
1.000
0.87
0.16–4.67

Nitroimidazoles
6 (26.1)
23 (37.7)
0.441
0.58
0.20–1.69

Third-generation cephalosporins
6 (26.1)
22 (36.1)
0.446
0.63
0.22–1.82

Abdominal or thoracic drainages
9 (39.1)
24 (39.3)
1.000
0.99
0.37–2.65

Central venous catheterization
18 (78.3)
37 (60.7)
0.198
2.34
0.76–7.13

Mechanical ventilation
21 (91.3)
37 (60.7)
0.007
6.81
1.46–37.74

Nasogastric tube
11 (47.8)
23 (37.7)
0.459
1.51
0.58–3.99

Urinary catheterization
15 (65.2)
34 (55.7)
0.468
1.49
0.55–4.03

Adequate empirical antibiotic therapy
5 (21.8)
21 (34.4)
0.30
0.53
0.17–1.62

APACHE: Acute Physiology and Chronic Health Evaluation; COPD: chronic obstructive pulmonary disease; CI: confidence interval; ICU: intensive care unit; IQR: interquartile range; OR: odds ratio; SD: standard deviation; MODS: multiple organ dysfunction syndrome. aData were expressed as the number (%) of patients unless stated otherwise.

4. Discussion

Limited therapeutic alternatives, a high morbidity, and mortality have rendered surveillance of CRAB a top priority. High prevalence of CRAB (71.2%) was observed in this study, especially in ICU, which is consistent with latest investigations from tertiary teaching hospitals of China, which had observed a steep rise in the incidence of CRAB bacteremia with high carbapenem resistance rates from 62.1% to 91% [11–13]. Furthermore, China’s surveillance of antimicrobial resistance program has detected extensively drug-resistant A. baumannii (XDRAB), the most frequently reported Gram-negative bacteria isolated from bloodstream, and 97.4% of XDRAB were resistant to imipenem [14]. Similar to other studies [15, 16], all the CRAB isolates were multidrug resistant but retained their susceptibility to minocycline and cefoperazone/sulbactam, suggesting the combination of antibiotic therapy of minocycline and/or cefoperazone/sulbactam may benefit the clearance of CRAB in this setting.

Despite high prevalence of CRAB in China, the impact of carbapenem resistance on A. baumannii bacteremia has not been well documented. In this study, the crude and 30-day in-hospital mortality rate of nosocomial A. baumannii bacteremia were 21.2% and 12.7%, respectively, which are similar to the results of a five-year Japanese study [17], but relatively lower than other previous reports with high mortality rates from 29% to 63.5% [12, 18, 19]. This inconsistency is probably ascribed to the heterogeneity of epidemiology, the severity of diseases and the virulence factors of microbes.

Higher mortality rate was detected among the CRAB group during hospitalization, which is consistent with a four-year study of bloodstream infection concerning multidrug-resistant Gram-negative bacteria [20]. Surprisingly, after adjusting for potential confounders, no significant association was found between carbapenem resistance and increased risk of in-hospital mortality.

On the contrary, high APACHE II score on the day of bacteremia, MODS, and respiratory tract as the origin of bacteremia were independent predictors for the mortality of nosocomial A. baumannii bacteremia. Recently, studies focused on ICU patients have shown that it is not antibiotic resistance but the severity of the illness that highlights in-hospital mortality of nosocomial A. baumannii bacteremia [21–23]. These results were compatible with our findings. High APACHE II score on the day of bacteremia and MODS during hospitalization concordantly suggested critical ill conditions, which may lead to rapid death during hospitalization. Furthermore, a recent study in regard of the attributed mortality of nosocomial A. baumannii bacteremia by hospital acquired pneumonia (HAP) in South China found that high APACHE II score was the independent risk factor for HAP patients complicated with bloodstream infection and was associated with high mortality in nosocomial A. baumannii bacteremic pneumonia [24]. Accordingly, it is the severity of illness that predicts the mortality of nosocomial A. baumannii bacteremia in this setting.

Furthermore, this study found that mechanical ventilation increased the risk of mortality of patients with nosocomial A. baumannii and CRAB bacteremia, which is consistent with other studies [11, 19, 25]. Since a majority of patients in this cohort were suffered ICU admission and it has been reported that more than 75% of CRAB bacteremia were due to CRAB ventilation-associated pneumonia in ICU [9, 24], it seems reasonable to expect mechanical ventilation as a pivotal predicator of patients to acquire CRAB bacteremia. However, mechanical ventilation did not predict acquisition but mortality in this cohort. The severity of illness entailed the intervention of mechanical ventilation, but the consequent ventilator-induced lung injury and ventilation associated pneumonia may aggravate the ill conditions and contribute to the mortality [4, 24, 26]. Moreover, this result also suggests that respiratory failure, a critical ill status, is probable to be a hint of poor outcomes of patients with nosocomial A. baumannii bacteremia regardless of CRAB or CSAB. Thus, noninvasive techniques for respiratory support, alternative lung-protective ventilation to prevent ventilator-induced lung injury, and personalization of mechanical ventilation based on individual physiological characteristics and responses to therapy are in urgent need and probably improve outcomes [26].

Interestingly, adequate antibiotic empirical therapy was not associated with mortality of patients with nosocomial A. baumannii and CRAB bacteremia in the current study. Although carbapenem resistance itself increased three- to fivefold risk for receiving inappropriate carbapenem antibiotic therapy [9, 27] and previous studies have found that inappropriate empirical antibiotic therapy increases the mortality of patients with CRAB bacteremia and bacteremic pneumonia [9, 27, 28], our study failed to find that adequate empirical therapy benefitted the survival of patients with nosocomial A. baumannii or CRAB bacteremia. The controversy of the impact of appropriate/inappropriate empirical therapy on mortality of A. baumannii bacteremia is ongoing. Several studies have reported that the appropriateness of antibiotic therapy does not affect early mortality rate, and inappropriate antibiotic therapy is not associated with short-term mortality [19, 29]. Further study illustrated that appropriate antimicrobial therapy did not significantly benefit patients with APACHE II no more than 25 [30]. These results were consistent with our observation, which found an average APACHE II score of 22.2 in nonsurvival patients and that of 18.0 in survival patients with A. baumannii bacteremia. However, it should be noticed that less than 50% of patients received appropriate empirical antibiotic therapy in this present study, due to the unavailability of first-line antibiotic agents: colistin and tigecycline. Two studies concerning about bloodstream infection caused by extensively drug-resistant A. baumannii in critical ill patients found that it was the ineffective management of such infection that increased the risk of death and colistin-vancomycin coadministration was a predictor of a good prognosis [31, 32]. Accordingly, we deduced that the beneficial impact of appropriate empirical antibiotic therapy on clinical outcome might be underestimated in this study.

Since this present study has identified that the severity of illness predicts the fate of patients with nosocomial A. baumannii bacteremia, rapid identification of patients endangered by nosocomial A. baumannii bacteremia deserves top priorities. MALDI-TOF MS in direct blood sample detection may contribute to improve the early management of A. baumannii bacteremia. A recent pre-post, quasi-experimental study witnessed reduced length of time for the clearance of Gram-negative rods in bloodstream infection by the combination of MALDI-TOF MS and real-time antimicrobial stewardship intervention on time [33]. Recently, CarbAcineto NP test (CANP) has been reported with a high sensitivity to detecting OXA-type carbapenemases, which are more frequently identified in carbapenem-resistant Acinetobacter spp. [34]. Its combination with MALDI-TOF MS in direct blood sample detection may contribute to improve the early management of CRAB bacteremia. Based on molecular techniques, the FilmArray System Blood Culture Identification (BCID) panel and novel bioluminescence-based phenotypic method have been found helpful for clinicians to identify patients suspected for A. baumannii and CRAB bacteremia in a timely manner [35, 36]. Moreover, prevention of its acquisition and progression should be emphasized. Recent overview of clinical pathogenesis of A. baumannii infection found that host fate during A. baumannii infection was determined by two stages, which underscored the balancing of host immunological defense and bacteria offense [2]. Our previous study has reported that mucosal immunization with A. baumannii outer membrane protein A (OmpA) is a novel, noninvasive vaccine approach to protect mice against multidrug-resistant A. baumannii infections and suggests the development of OmpA as a promising protein vaccine component against multidrug-resistant A. baumannii in patients, considering that OmpA is immunogenic in humans [37]. A latest study in Italy has further found the potential of immunoglobulin M (IgM) in protecting patients with septic shock from deaths [6]. Further researches will shed light on the pathogenesis of A. baumannii infection in host with comorbidity.

Some limitations of this study are noteworthy. Firstly, as a retrospective study, possible risk or causative factors, such as potential immunocompromised status and confounding complications, were unmeasured. Secondly, molecular mechanism analysis of carbapenem resistance, especially the detection of sequence types and carbapenemase genes, was not conducted. Nevertheless, our previous two-year study of carbapenem-resistant A. baumannii (CRAB) had reported the predominance of sequence type (ST) 75 and ST137, both of which are attributable to clonal complex (CC) 92, and the most common carbapenemase genes were blaOXA-23 and blaOXA-51 [38]. These results are compatible with a national multicenter study in China, which found that the most widely distributed CC of CRAB isolates was blaOXA-23-like-producing and predominantly CC92 [39]. Furthermore, a recent study focusing on bacteremic pneumonia caused by A. baumannii in ICUs of South China also verified the predominance of CC92 [24]. So, it is reasonable to suppose that CC92 may be the predominant genotype and blaOXA-23 may be the most prevalent carbapenemase of CRAB isolates in this setting. Thirdly, single-center findings restricted their applicabilities to other geographical settings.

5. Conclusions

In summary, the results of the present investigation suggest high prevalence of CRAB in nosocomial bloodstream infection, especially in ICU. High in-hospital mortality rate of nosocomial A. baumannii bacteremia, especially among patients with CRAB, was observed, while carbapenem resistance did not predict in-hospital mortality. The severity of the illness (MODS and high APACHE II score), mechanical ventilation, and respiratory tract as the origin of bacteremia were determinants of in-hospital mortality of nosocomial A. baumannii bacteremia, while as to nosocomial CRAB bacteremia, mechanical ventilation and respiratory tract as the origin of bacteremia were risk factors for in-hospital mortality. The role of mechanical ventilation in mortality was highlighted, which suggests respiratory dysfunction may prime the poor outcome. The beneficial impact of adequate empirical antibiotic therapy on survival cannot be concluded but may be underestimated. Early identification, consecutive assessment of the severity of the illness, and protection of respiratory function during the spring of nosocomial A. baumannii bacteremia should be conducted to reduce the risk of mortality of nosocomial A. baumannii bacteremia. Further research should emphasize pathogenetic mechanisms of A. baumannii bacteremia for the evaluation of novel therapy surrogates.

Data Availability

The authors confirm that the data supporting the findings of this study are available within the article.

Conflicts of Interest

The authors declare that there are no conflicts of interest in the research, authorship, and/or publication of this article.

Acknowledgments

The authors are grateful to Minna Ye and Lianlian Liu for providing very useful advice on clinical data collection. This work was supported by both the National Natural Science Foundation of China (Grant no. 81471992) and Chongqing Science and Technology Commission Grant (cstc2016jcyjA0769).

References

R. Amaya-Villar, C. Ferrándiz-Millón, A. Díaz-Martín, J. M. López-Sánchez, and A. Gutiérrez-Pizarraya, “Optimum treatment strategies for carbapenem-resistant Acinetobacter baumannii bacteremia,” Expert Review of Anti-infective Therapy, vol. 13, no. 6, pp. 769–777, 2015.

D. Wong, T. B. Nielsen, R. A. Bonomo, P. Pantapalangkoor, B. Luna, and B. Spellberg, “Clinical and pathophysiological overview of acinetobacter infections: a century of challenges,” Clinical Microbiology Reviews, vol. 30, no. 1, pp. 409–447, 2017.

S. Chusri, V. Chongsuvivatwong, J. I. Rivera et al., “Molecular epidemiology and spatiotemporal analysis of hospital-acquired Acinetobacter baumannii infection in a tertiary care hospital in southern Thailand,” Journal of Hospital Infection, vol. 95, no. 1, pp. 53–58, 2017.

J. Nowak, E. Zander, D. Stefanik et al., “High incidence of pandrug-resistant Acinetobacter baumannii isolates collected from patients with ventilator-associated pneumonia in Greece, Italy and Spain as part of the MagicBullet clinical trial,” Journal of Antimicrobial Chemotherapy, vol. 72, no. 12, pp. 3277–3282, 2017.

Y. Li, X. L. Cao, H. Ge, Y. H. Jiang, H. Zhou, and W. Zheng, “Targeted surveillance of nosocomial infection in intensive care units of 176 hospitals in Jiangsu Province of China,” Journal of Hospital Infection, vol. 99, no. 1, pp. 36–41, 2018.

S. Busani, G. Serafini, E. Mantovani et al., “Mortality in patients with septic shock by multidrug resistant bacteria,” Journal of Intensive Care Medicine, p. 885066616688165, 2017.

A. Y. Peleg, H. Seifert, and D. L. Paterson, “Acinetobacter baumannii: emergence of a successful pathogen,” Clinical Microbiology Reviews, vol. 21, no. 3, pp. 538–582, 2008.

J. D. Sun, S. F. Huang, S. S. Yang, S. L. Pu, C. M. Zhang, and L. P. Zhang, “Impact of carbapenem heteroresistance among clinical isolates of invasive Escherichia coli in Chongqing, southwestern China,” Clinical Microbiology and Infection, vol. 21, no. 5, pp. 469.e1–469.e10, 2015.

S. Y. Park, E. J. Lee, T. Kim et al., “Early administration of appropriate antimicrobial agents to improve the outcome of carbapenem-resistant Acinetobacter baumannii complex bacteraemic pneumonia,” International Journal of Antimicrobial Agents, vol. 51, no. 3, pp. 407–412, 2018.

A. Hoxha, T. Kärki, C. Giambi et al., “Attributable mortality of carbapenem-resistant Klebsiella pneumoniae infections in a prospective matched cohort study in Italy, 2012-2013,” Journal of Hospital Infection, vol. 92, no. 1, pp. 61–66, 2016.

N. Guo, W. Xue, D. Tang, J. Ding, and B. Zhao, “Risk factors and outcomes of hospitalized patients with blood infections caused by multidrug-resistant Acinetobacter baumannii complex in a hospital of Northern China,” American Journal of Infection Control, vol. 44, no. 4, pp. e37–e39, 2016.

Q. Liu, W. Li, X. Du et al., “Risk and prognostic factors for multidrug-resistant Acinetobacter baumannii complex bacteremia: a retrospective study in a tertiary hospital of west China,” PLoS One, vol. 10, no. 6, Article ID e0130701, 2015.

X. Zhang, B. Gu, Y. Mei, Y. Wen, and W. Xia, “Increasing resistance rate to carbapenem among blood culture isolates of Klebsiella pneumoniae, Acinetobacter baumannii and Pseudomonas aeruginosa in a university-affiliated hospital in China, 2004-2011,” Journal of Antibiotics, vol. 68, no. 2, pp. 115–120, 2015.

A. Xu, B. Zheng, Y. C. Xu, Z. G. Huang, N. S. Zhong, and C. Zhuo, “National epidemiology of carbapenem-resistant and extensively drug-resistant Gram-negative bacteria isolated from blood samples in China in 2013,” Clinical Microbiology and Infection, vol. 22, no. 1, pp. S1–S8, 2016.

G. E. Park, C. I. Kang, M. K. Cha et al., “Bloodstream infections caused by Acinetobacter species with reduced susceptibility to tigecycline: clinical features and risk factors,” International Journal of Infectious Diseases, vol. 62, pp. 26–31, 2017.

M. A. Pfaller, R. K. Flamm, L. R. Duncan, R. E. Mendes, R. N. Jones, and H. S. Sader, “Antimicrobial activity of tigecycline and cefoperazone/sulbactam tested against 18,386 Gram-negative organisms from Europe and the Asia-Pacific region (2013-2014),” Diagnostic Microbiology and Infectious Disease, vol. 88, no. 2, pp. 177–183, 2017.

Y. Fujikura, A. Yuki, T. Hamamoto, A. Kawana, K. Ohkusu, and T. Matsumoto, “Blood stream infections caused by Acinetobacter baumannii group in Japan Epidemiological and clinical investigation,” Journal of Infection and Chemotherapy, vol. 22, no. 6, pp. 366-367, 2016.

Q. Fu, H. Ye, and S. Liu, “Risk factors for extensive drug-resistance and mortality in geriatric inpatients with bacteremia caused by Acinetobacter baumannii,” American Journal of Infection Control, vol. 43, no. 8, pp. 857–860, 2015.

T. Ballouz, J. Aridi, C. Afif et al., “Risk factors, clinical presentation, and outcome of Acinetobacter baumannii bacteremia,” Frontiers in Cellular and Infection Microbiology, vol. 7, p. 156, 2017.

W. Wang, T. Jiang, W. Zhang et al., “Predictors of mortality in bloodstream infections caused by multidrug-resistant gram-negative bacteria: 4 years of collection,” American Journal of Infection Control, vol. 45, no. 1, pp. 59–64, 2017.

T. Chopra, D. Marchaim, R. A. Awali et al., “Epidemiology of bloodstream infections caused by Acinetobacter baumannii and impact of drug resistance to both carbapenems and ampicillin sulbactam on clinical outcomes,” Antimicrobial Agents and Chemotherapy, vol. 57, no. 12, pp. 6270–6275, 2013.

E. Brotfain, A. Borer, L. Koyfman et al., “Multidrug resistance acinetobacter bacteremia secondary to ventilator-associated pneumonia: risk factors and outcome,” Journal of Intensive Care Medicine, vol. 32, no. 9, pp. 528–534, 2017.

A. Nutman, R. Glick, E. Temkin et al., “A case-control study to identify predictors of 14-day mortality following carbapenem-resistant Acinetobacter baumannii bacteraemia,” Clinical Microbiology and Infection, vol. 20, no. 12, pp. O1028–O1034, 2014.

Y. Tan, K. Zhou, X. Tang et al., “Bacteremic and non-bacteremic pneumonia caused by Acinetobacter baumannii in ICUs of South China: a clinical and microbiological study,” Scientific Reports, vol. 7, no. 1, p. 15279, 2017.

C. P. Liu, S. C. Shih, N. Y. Wang et al., “Risk factors of mortality in patients with carbapenem-resistant Acinetobacter baumannii bacteremia,” Journal of Microbiology, Immunology and Infection, vol. 49, no. 6, pp. 934–940, 2016.

E. C. Goligher, N. D. Ferguson, and L. J. Brochard, “Clinical challenges in mechanical ventilation,” The Lancet, vol. 387, no. 10030, pp. 1856–1866, 2016.

M. D. Zilberberg, B. H. Nathanson, K. Sulham, W. Fan, and A. F. Shorr, “Multidrug resistance, inappropriate empiric therapy, and hospital mortality in Acinetobacter baumannii pneumonia and sepsis,” Critical Care, vol. 20, no. 1, p. 221, 2016.

H. Y. Lee, C. L. Chen, S. R. Wu, C. W. Huang, and C. H. Chiu, “Risk factors and outcome analysis of acinetobacter baumannii complex bacteremia in critical patients,” Critical Care Medicine, vol. 42, no. 5, pp. 1081–1088, 2014.

K. O. Gradel, U. S. Jensen, H. C. Schønheyder et al., “Danish collaborative bacteraemia network (DACOBAN). Impact of appropriate empirical antibiotic treatment on recurrence and mortality in patients with bacteraemia: a population-based cohort study,” BMC Infectious Diseases, vol. 17, no. 1, p. 122, 2017.

Y. T. Lee, S. C. Kuo, S. P. Yang et al., “Impact of appropriate antimicrobial therapy on mortality associated with Acinetobacter baumannii bacteremia: relation to severity of infection,” Clinical Infectious Diseases, vol. 55, no. 2, pp. 209–215, 2012.

M. P. Freire, D. de Oliveira Garcia, C. P. Garcia et al., “Bloodstream infection caused by extensively drug-resistant Acinetobacter baumannii in cancer patients: high mortality associated with delayed treatment rather than with the degree of neutropenia,” Clinical Microbiology and Infection, vol. 22, no. 4, pp. 352–358, 2016.

M. Papadimitriou-Olivgeris, F. Fligou, A. Spiliopoulou et al., “Risk factors and predictors of carbapenem-resistant Pseudomonas aeruginosa and Acinetobacter baumannii mortality in critically ill bacteraemic patients over a 6-year period (2010-15): antibiotics do matter,” Journal of Medical Microbiology, vol. 66, no. 8, pp. 1092–1101, 2017.

M. Beganovic, M. Costello, and S. M. Wieczorkiewicz, “Effect of matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) alone versus MALDI-TOF MS combined with real-time antimicrobial stewardship interventions on time to optimal antimicrobial therapy in patients with positive blood cultures,” Journal of Clinical Microbiology, vol. 55, no. 5, pp. 1437–1445, 2017.

E. Literacka, M. Herda, A. Baraniak et al., “Evaluation of the Carba NP test for carbapenemase detection in Enterobacteriaceae, Pseudomonas spp. and Acinetobacter spp., and its practical use in the routine work of a national reference laboratory for susceptibility testing,” European Journal of Clinical Microbiology and Infectious Diseases, vol. 36, no. 11, pp. 2281–2287, 2017.

H. Salimnia, M. R. Fairfax, P. R. Lephart et al., “Evaluation of the film array blood culture identification panel: results of a multicenter controlled trial,” Journal of Clinical Microbiology, vol. 54, no. 3, pp. 687–698, 2016.

V. van Almsick, B. Ghebremedhin, N. Pfennigwerth, and P. Ahmad-Nejad, “Rapid detection of carbapenemase-producing Acinetobacter baumannii and carbapenem-resistant Enterobacteriaceae using a bioluminescence-based phenotypic method,” Journal of Microbiological Methods, vol. 147, pp. 20–25, 2018.

X. Zhang, T. Yang, J. Cao, J. Sun, W. Dai, and L. Zhang, “Mucosal immunization with purified OmpA elicited protective immunity against infections caused by multidrug-resistant Acinetobacter baumannii,” Microbial Pathogenesis, vol. 96, pp. 20–25, 2016.

W. Dai, S. Huang, S. Sun, J. Cao, and L. Zhang, “Nosocomial spread of carbapenem- resistant Acinetobacter baumannii (types ST75 and ST137) carrying blaOXA-23-like gene with an upstream ISAba1 in a Chinese hospital,” Infection, Genetics and Evolution, vol. 14, pp. 98–101, 2013.

Z. Ruan, Y. Chen, Y. Jiang et al., “Wide distribution of CC92 carbapenem-resistant and OXA-23-producing Acinetobacter baumannii in multiple provinces of China,” International Journal of Antimicrobial Agents, vol. 42, no. 4, pp. 322–328, 2013.