CP-CRE/non-CP-CRE Stratification And CRE Resistance Mechanism Determination Help In Better Managing CRE Bacteremia Using Ceftazidime-Avibactam And Aztreonam-Avibactam.

PURPOSE: This observational study aimed to identify the independent risk factors for both the acquisition and mortality of carbapenemase-producing carbapenem-resistant Enterobacteriaceae (CP-CRE) bacteremia and further assess the in vitro antimicrobial activities of ceftazidime-avibactam (CAZ/AVI) and aztreonam-avibactam (ATM/AVI) against recent CRE bacteremic isolates. PATIENTS AND METHODS: This observational study was conducted to reveal the risk factors and mortality rate for CP-CRE bacteremia between 2012 and 2018 and also evaluate the in vitro antimicrobial activities of CAZ/AVI and ATM/AVI against recent CRE bacteremic isolates from 2016 to 2018.
RESULTS: A total of 81 non-repetitive isolates were collected from 2012 to 2018, with 67.90% (55/81) being CP-CRE. Old age (P = 0.01), transfusion [odds ratio (OR): 17.19; 95% CI: 3.15-93.72; P = 0.001], longer ICU stay (P = 0.02), cancer (OR: 15.91; 95% CI: 3.56-71.37; P < 0.001), and previous carbapenem exposure (OR: 27.86; 95% CI: 5.03-154.19; P = 0.001) were identified as independent risk factors for the acquisition of CP-CRE bacteremia compared with the ESBL bacteremia. The in vitro antimicrobial activities of CAZ/AVI and ATM/AVI against the CRE bacteremic isolates from 2016 to 2018 showed a respective susceptibility rate of 70.68% (41/58) and 100.00% (58/58).
CONCLUSION: The findings indicated that both CP-CRE/non-CP-CRE stratification and CRE resistance mechanism determination were necessary for better guiding the clinical management of CRE bacteremia: ATM/AVI probably works with both non-CP-CRE and CP-CRE bacteremia, even the most notorious double-carbapenemase producer with porin loss/deficiency, whereas CAZ/AVI works with most of the non-CP-CRE and KPC-producers in the region.

Introduction

Carbapenem-resistant Enterobacteriaceae (CRE) has become a serious public health threat worldwide.1,2 Severe CRE infections, especially CRE bacteremia, are associated with an extremely high mortality rate of up to 70%,3 thus, timely, efficient, and targeted antibiotic treatment is of paramount importance.4

CRE arises from one or a combination of the following four mechanisms: carbapenemase production (CP-CRE), production of ESBLs and/or AmpC in combination with porin loss/deficiency (non-CP-CRE), carbapenem efflux, or mutations in penicillin-binding proteins (PBPs),5 among which CP-CRE is the most problematic due to higher-level antimicrobial resistance and plasmid localization of many carbapenemase-encoding genes, potentiating the possibility of horizontal gene transfer.6

Carbapenemases include Ambler class A β-lactamases (e.g., KPC and GES), class B metallo-β-lactamases (MBLs; e.g., NDM, VIM, IMP, and SPM), and class D β-lactamases (e.g., OXA-48 and OXA-181).5 MBLs are particularly worrisome due to their ability to hydrolyze all classes of β-lactams except monobactams (aztreonam) and the inability of the classic serine β-lactamase inhibitors (clavulanic acid, tazobactam, and sulbactam) to inhibit them. On the contrary, the availability of more reliable phenotypic and genotypic carbapenemase assays has led to a better understanding of the implications of resistance heterogeneity in the clinical management of severe CRE infections.6

In the last decade, with polymyxins, tigecycline, fosfomycin, and aminoglycosides being the therapeutic mainstays for CRE infections, double carbapenem, high-dose prolonged carbapenem infusion, and high-dose tigecycline therapies as the combination therapeutic strategies and therapeutic regimens were mainly experience-directed.1,7 With the advent of the newly additional effective therapeutic options for CRE infections, such as the novel β-lactam/β-lactamase inhibitors aztreonam/avibactam (ATM/AVI, active against KPC, MBL, AmpC and OXA producers),8 ceftazidime/avibactam (CAZ/AVI, active against KPC and OXA-48 producers),9 meropenem/vaborbactam (active against KPC producers),10 imipenem/relebactam (active against KPC and AmpC producers),11 and the newly developed antibiotics eravacycline (a novel tetracycline derivative),12 plazomicin (a next-generation aminoglycoside),13 and cefiderocol (a novel siderophore cephalosporin),14 the therapeutic recipe might be targeted and personalized based on the antimicrobial susceptibility profiles, molecular resistance phenotypes, disease severity, and patient characteristics. By prioritizing who should receive novel CP-CRE active antibiotic agents, treatment success can be maximized and drug resistance reduced. More high-quality epidemiology- and resistance mechanism–centered studies are urgently needed to guide effective individualized and targeted therapy for CRE bacteremia. Nevertheless, previous studies exploring the prognosis of CRE bacteremia simply evaluated CRE bloodstream infections as a single cohort, without discriminating between the underlying molecular resistance mechanisms. To date, only one study compared the clinical outcomes of CP-CRE and non-CP-CRE bacteremia by examining 83 CRE bacteremia cases from the Johns Hopkins Hospital between March 2013 and April 2016. It demonstrated that CP-CRE was associated with poorer outcomes, suggesting that CP-CRE might be more virulent compared with non-CP-CRE, highlighting the added significance of deciphering the underlying molecular resistance mechanisms of CRE to direct the personalized antibiotic therapy for CRE bacteremia.15 Thus, for better guidance of the clinical management of CRE bacteremia, additional epidemiology and resistance testing of bacteremia CRE isolates from other countries or regions worldwide are urgently needed.

Avibactam (AVI) offers a broader β-lactamase inhibition profile compared with any other recently used serine β-lactamase inhibitors.16 When combined with AVI, CAZ/AVI is active in vitro against CP-CRE and non-CP-CRE isolates.17 Notably, recent studies have demonstrated its potent in vitro bactericidal activity against blaKPC- and blaOXA-48-harboring CP-CRE isolates.11

Although aztreonam (ATM) is stable to MBL hydrolysis, it is easily inactivated by ESBLs, KPCs, and AmpC.18 As MBLs-harboring Enterobacteriaceae may frequently harbor additional ATM-inactivating β-lactamases, the bactericidal activity of ATM against these isolates is often mitigated or negated. When combined with AVI, ATM/AVI can kill KPC, AmpC, MBL, and OXA producers.18

CAZ/AVI and ATM/AVI have been used to treat severe cases of CRE infections in the United States, and the resistance had sporadically been reported.19,20 This observational study was conducted to identify the independent risk factors for both the acquisition and mortality of CP-CRE bacteremia and further assess the in vitro antimicrobial activities of CAZ/AVI and ATM/AVI against recent CRE bacteremic isolates.

This study was the first systemic investigation of the possible value of CP-CRE/non-CP-CRE stratification and CRE resistance mechanism determination in better managing CRE bacteremia by both CAZ/AVI and ATM/AVI.

Materials And Methods

Bacterial Strains

A total of 81 non-repetitive nosocomial CRE bacteremic strains were collected between 2012 and 2018 in the First Affiliated Hospital of Chongqing Medical University. All the isolates were identified at the species level by the VITEK MS (bioMérieux, MO, USA) system, and routine antimicrobial susceptibility testing was performed using the VITEK2 compact (bioMérieux, Inc., NC, USA) system. All the bacteremia CRE mono-infection cases with intact medical records and available CRE isolates were included in the study.

Resistance Mechanism Identification

Polymerase chain reaction was used to detect the potential presence of resistance genes, including carbapenemases (blaKPC, blaNDM, blaVIM, blaIMP, blaGES, blaOXA-48-like, blaOXA-181-like, blaOXA-23-like, blaOXA-24-like, and blaOXA-58-like),21 ESBLs, AmpC, Ompk35, Ompk36, OmpF, and OmpC genes, using primers as described previously.22 In addition, the capsular genes of Klebsiella pneumoniae were also amplified. The Carba NP test and eCIM were performed on all isolates to determine whether any bacteria produced carbapenemases by phenotypic methods but were negative by genotypic methods, or vice versa.21

Risk Factors And Clinical Outcomes Of Patients With Bacteremia CP-CRE

This retrospective case–control study was conducted to evaluate the risk factors and clinical outcomes of the patients suffering from CP-CRE bacteremia. All patients with CP-CRE bacteremia were selected as cases. Controls were identified as patients with non-CP-CRE bacteremia or ESBLs-positive Enterobacteriaceae bacteremia.

Antibiotics And In Vitro Susceptibility Testing

CRE bacteremic strains from 2016 to 2018 were recovered for CAZ/AVI and ATM/AVI susceptibility tests. The broth microdilution test method was employed to determine the MICs of CAZ, CAZ/AVI, ATM, and ATM/AVI according to CLSI 2018. MICs of CAZ/AVI >16/4 µg/mL and ATM/AVI >16/4 µg/mL were considered resistant.

Statistical Analysis

All analyses were performed using the SPSS v.25.0 software (SPSS Inc., IL, USA). Univariate analyses were performed separately for each of the variables. All variables with a P value of ≤0.05 in the univariate analyses were considered for inclusion in the multivariate logistic regression model. The odds ratio (OR) and 95% confidence interval (CI) were calculated to evaluate the strength of any association. For all calculations, statistical significance was defined at P <0.05 for two-tailed tests.

Ethical Considerations

The data and samples analyzed in the present study were obtained in accordance with the standards and approved by the Chongqing Medical University Institutional Review Board and the Biomedical Ethics Committee. For this study, samples were collected at the microbiology laboratory of the hospital, with no contact with the patient. This study was retrospective with no patient identification performed during data collection. Therefore, the ethics committee determined that informed consent was not required.

Results

Microbiological Characteristics And Antimicrobial Susceptibility Profiles Of CRE Bacteremic Isolates

As shown in Figure 1, 81 non-repetitive and mono-infected CRE bacteremic isolates were collected during the study period, among which the predominant genus and species were K. pneumoniae (56.79%), followed by Enterobacter cloacae (22.22%) and Escherichia coli (18.52%) (Figure 1A). Resistance mechanism determination revealed that 67.90% of the isolates produced carbapenemases and the proportion of CP-CRE increased every year (Figure 1B). Among all the CP-CRE isolates, K. pneumoniae (65.45%) was the most common species, with E. coli and E. cloacae accounting for 20% and 9.09%, respectively (Figure 1C). It was speculated that the bacteremic CRE isolate might have derived from the tissue origins from which the same-species CRE isolate with the same antibiogram was isolated. As the most common specimen types from which the same-species-same-antibiogram isolate was derived were sputum (50.61%), urine (28.39%), and bile (12.34%) (Figure 1D), it was deduced that the most dominant origins of the CRE bacteremia were respiratory, urinary, and biliary systems.

Figure 1

Distribution of CRE bacteremia cases and bacteremic isolates. (A) Dynamic distribution of species-specific CRE bacteremic isolates. (B) Dynamic distribution of CP-CRE and non-CP-CRE bacteremia cases. (C) Species distribution of CP-CRE and non-CP-CRE bacteremic isolates. (D) Source of CRE bacteremia.

Regarding the antimicrobial susceptibility profiles of the CRE bacteremic isolates (Table 1), CRE showed the highest nonsusceptibility rate to ertapenem (100.00%), with 77.78% and 65.43% nonsusceptibility rates to imipenem and meropenem, respectively. Although these isolates also exhibited high resistance rates to quinolones (>80%) and aminoglycosides (>70%), they showed low resistance rates to tigecycline (2.46%) and colistin (3.70%).

Table 1

Antimicrobial Susceptibility Profiles Of CP-CRE And Non-CP-CRE Bacteremic Isolates

Antimicrobial Agents	Total (N = 81)	Carbapenemase Positive (N = 55)			Carbapenemase Negative (N = 26)			P Value
R (%)	R	I	S	R	I	S
Ertapenem	81 (100.00%)	55 (100.00%)	0 (0.00%)	0 (0.00%)	26 (100.00%)	0 (0.00%)	0 (0.00%)	NA
Imipenem	63 (77.78%)	51 (92.72%)	2 (3.63%)	2 (3.63%)	12 (46.15%)	1 (3.84%)	13 (50.00%)	<0.001
Meropenem	53 (65.43%)	48 (87.27%)	2 (3.63%)	5 (9.09%)	5 (19.23%)	12 (46.15%)	9 (34.62%)	<0.001
Ciprofloxacin	66 (81.48%)	44 (80.00%)	1 (1.81%)	10 (18.18%)	24 (92.30%)	0 (0.00%)	2 (7.69%)	0.16
Levofloxacin	65 (80.24%)	42 (76.36%)	2 (3.63%)	11 (20.00%)	23 (88.46%)	1 (3.84%)	2 (7.69%)	0.20
Gentamycin	65 (80.24%)	46 (83.63%)	0 (0.00%)	9 (16.36%)	19 (73.07%)	0 (0.00%)	7 (26.92%)	0.632
Tobramycin	58 (71.60%)	43 (78.18%)	3 (5.45%)	9 (16.36%)	15 (57.69%)	3 (11.53%)	8 (30.76%)	0.06
Colistin	3 (3.70%)	3 (5.45%)	0 (0.00%)	52 (92.85%)	0 (0.00%)	0 (0.00%)	26 (100.00%)	0.22
Tigecycline	2 (2.46%)	2 (3.63%)	0 (0.00%)	54 (96.42%)	0 (0.00%)	0 (0.00%)	26 (100.00%)	0.32

Risk Factors And Clinical Outcomes Of Patients With Bacteremia CRE

To investigate the risk factors and prognosis of patients with CP-CRE bacteremia, 55 CP-CRE cases were matched to either 25 non-CP-CRE cases or 60 ESBLs cases in this study where appropriate. The results (Table 2) showed a 50% (40/80) mortality rate among all the patients with CRE bacteremia. However, when stratified into CP-CRE and non-CP-CRE subgroups, the mortality rate was 61.82% and 24%, respectively, showing a significantly higher mortality rate in the CP-CRE subgroup. Moreover, patients with CP-CRE bacteremia showed longer hospital stay. Notably, the CP-CRE, non-CP-CRE, and ESBL groups were well balanced on most of the demographic information, pre-existing medical conditions, and immune-compromising comorbidities, and a likely source of bacteremia (Table 2). Old age (P = 0.04), longer ICU stay (P = 0.03), cancer (OR: 4.35; 95% CI: 1.22–15.46; P = 0.023), and previous carbapenem exposure (OR: 7.67, 95% CI: 1.91–30.77, P = 0.004) were identified as independent risk factors for the acquisition of CP-CRE bacteremia compared with non-CP-CRE bacteremia. Old age (P = 0.01), transfusion (OR: 17.19; 95% CI: 3.15–93.72; P = 0.001), longer ICU stay (P = 0.02), cancer (OR: 15.91; 95% CI: 3.56–71.37; P < 0.001), and previous carbapenem exposure (OR: 27.86; 95% CI: 5.03–154.19; P = 0.001) were identified as independent risk factors for the acquisition of CP-CRE bacteremia compared with the ESBL bacteremia (Table 3). On the other hand, longer ICU stay (P = 0.018) and venous catheterization (OR: 10.29; 95% CI: 3.03–34.87; P = 0.001) were identified as independent risk factors for non-CP-CRE bacteremia compared with the ESBL bacteremia group.

Table 2

Univariate Analysis Of Risk Factors And Outcomes For Patients With CP-CRE, Non-CP-CRE, And ESBL Bacteremia

Variable	CP-CRE(n = 55)	Non-CP-CRE(n = 25)	ESBLs	CP-CRE vs Non-CP-CRE			CP-CRE vs ESBLs		Non-CP-CRE vs ESBLs
(n = 60)	OR (95% CI)		P Value	OR (95% CI)	P Value	OR (95% CI)	P Value
Demographic characteristics
Gender, male, n (%)	36 (65.45%)	15 (60%)	32 (53.33%)	0.82 (0.30–2.22)		0.70	1.477 (0.58–3.72)	0.41	0.95 (0.32–2.80)	0.93
Age	60.55 ± 14.53	53.04 ± 16.69	54.83 ± 12.26	NA		0.04	NA	0.02	NA	0.45
Pre-existing medical conditions
Surgery in the last 6 months	33 (60.00%)	11 (44.00%)	32 (53.33%)	1.03 (0.33–3.27)		0.95	1.35 (0.64–2.82)	0.42	0.51 (0.16–1.66)	0.26
Cancer	35 (63.63%)	10 (40.00%)	15 (25.00%)	2.84 (1.07–7.53)		0.03	5.22 (2.11–13.00)	0.001	2.24 (0.69–7.30)	0.18
Liver cancer	13 (23.63%)	1 (4.00%)	1 (1.67%)	8.79 (1.07–71.93)		0.04	8.73 (0.23–330.11)	0.22	1.16 (0.02–72.70)	0.94
Pancreatic cancer	8 (14.54%)	1 (4.00%)	1 (1.67%)	4.74 (0.55–41.11)		0.16	11.51 (1.17–112.29)	0.036	7.51 (0.3–89.86)	0.21
Leukemia	4 (7.27%)	4 (16.00%)	5 (8.33%)	0.63 (0.14–2.84)		0.55	0.16 (0.02–1.17)	0.07	0.26 (0.02–2.50)	0.24
Other cancers	10 (18.18%)	4 (16.00%)	7 (11.67%)	0.88 (0.26–2.94)		0.85	1.79 (0.48–6.72)	0.38	0.97 (0.19–4.78)	0.97
Diabetes	13 (23.63%)	5 (20.00%)	12 (20.00%)	0.88 (0.21–3.63)		0.86	1.01 (0.33–3.12)	0.98	1.02 (0.24–4.36)	0.97
Heart failure	12 (21.81%)	2 (8.00%)	4 (6.67%)	1.99 (0.29–13.45)		0.48	3.43 (0.79–14.56)	0.09	1.43 (0.17–12.34)	0.74
Chronic kidney disease	12 (21.81%)	3 (12.00%)	8 (13.33%)	1.18 (0.20–6.83)		0.84	1.46 (0.41–5.16)	0.56	1.94 (0.37–10.11)	0.43
Chronic obstructive pulmonary disease	5 (9.09%)	1 (4.00%)	4 (6.67%)	2.12 (0.21–21.43)		0.52	1.16 (0.24–5.65)	0.85	0.68 (0.05–8.35)	0.76
Liver disease	4 (7.27%)	1 (4.00%)	2 (3.33%)	1.51 (0.14–16.08)		0.74	1.18 (0.14–9.47)	0.87	1.77 (0.15–21.22)	0.65
Immunocompromising comorbidities
Chemotherapy	20 (36.36%)	7 (28.00%)	6 (10.00%)	1.76 (0.44–7.14)		0.42	3.68 (1.16–11.64)	0.026	2.25 (0.48–10.48)	0.30
Solid organ transplantation	5 (9.09%)	1 (4.00%)	1 (1.67%)	1.11 (0.074–16.64)		0.94	0.29 (0.01–11.86)	0.52	2.86 (0.11–74.65)	0.53
Hematopoietic stem cell transplantation	2 (3.63%)	4 (16.00%)	1 (1.67%)	0.21 (0.015–3.02)		0.25	1.55 (0.08–27.24)	0.77	1.95 (0.11–34.63)	0.65
Chronic corticosteroid therapya	9 (16.36%)	3 (12.00%)	1 (1.67%)	1.75 (0.27–11.01)		0.55	2.13 (0.51–8.88)	0.29	1.39 (0.24–8.05)	0.71
Absolute neutrophil count <200 cells/mL	14 (25.45%)	6 (24.00%)	4 (6.67%)	1.14 (0.26–4.98)		0.84	1.42 (0.40–5.01)	0.58	1.96 (0.34–11.38)	0.45
Likely source of bacteremia
Urinary tract	12 (21.81%)	5 (20.00%)	23 (38.33%)	0.57 (0.10–3.18)	0.52		1.06 (0.40–2.63)	0.96	0.85 (0.18–3.94)	0.84
Pneumonia	29 (52.72%)	8 (32.00%)	20 (33.33%)	2.43 (0.51–11.63)	0.26		2.05 (0.82–5.10)	0.12	0.27 (0.05–1.53)	0.14
Intra-abdominal	12 (21.81%)	2 (8.00%)	3 (5.00%)	3.13 (0.32–30.92)	0.32		2.38 (0.53–10.74)	0.26	3.88 (0.61–24.86)	0.15
Biliary tract	11 (20.00%)	4 (16.00%)	6 (10.00%)	0.23 (0.02–2.29)	0.21		1.20 (0.32–4.53)	0.78	1.07 (0.17–6.91)	0.94
Invasive operations
On dialysis	4 (7.27%)	1 (4.00%)	2 (3.33%)	2.37 (0.23–24.11)	0.46		4.42 (0.62–31.99)	0.14	4.60 (0.31–68.38)	0.26
Transfusion	34 (61.82%)	10 (40.00%)	7 (10.17%)	1.74 (0.57–5.36)	0.33		18.44 (4.61–73.79)	0.001	8.23 (1.51–44.79)	0.015
Gastric tube use	29 (52.72%)	9 (36.00%)	7 (11.67%)	0.69 (0.12–3.83)	0.68		2.02 (0.56–7.32)	0.28	2.48 (0.54–11.39)	0.24
Drainage tube use	36 (65.45%)	8 (32.00%)	22 (36.67%)	6.73 (1.05–43.03)	0.04		1.98 (0.77–5.12)	0.17	0.53 (0.15–1.83)	0.31
Urinary catheterization	46 (83.63%)	16 (64.00%)	37 (61.67%)	1.54 (0.29–8.17)	0.61		2.30 (0.75–7.04)	0.15	1.01 (0.27–3.82)	0.98
Tracheal cannula	28 (50.90%)	9 (36.00%)	7 (11.67%)	0.53 (0.07–3.94)	0.54		1.69 (0.40–7.10)	0.47	0.96 (0.18–5.08)	0.96
Venous catheterization	43 (78.18%)	19 (76.00%)	13 (21.67%)	0.80 (0.12–5.48)	0.82		9.29 (2.99–28.822)	0.001	12.69 (3.26–49.31)	0.001
Mechanical ventilation	22 (40.00%)	8 (32.00%)	10 (16.67%)	0.76 (0.17–3.31)	0.72		0.44 (0.12–1.62)	0.28	0.47 (0.10–2.67)	0.34
Antibiotic treatment before the positive bacteria isolation
Penicillin	15 (27.27%)	5 (20.00%)	13 (21.67%)	0.58 (0.10–3.33)		0.54	0.69 (0.17–2.75)	0.60	0.89 (0.23–3.43)	0.87
Cephalosporins	23 (41.82%)	7 (28.00%)	22 (36.60%)	0.63 (0.14–2.83)		0.55	1.36 (0.64–2.89)	0.44	0.44 (0.14–1.44)	0.17
Fluoroquinolone	10 (18.18%)	3 (12.00%)	15 (25.00%)	0.73 (0.10–5.21)		0.76	0.67 (0.27–1.64)	0.38	0.24 (0.05–1.21)	0.08
Aminoglycosides	10 (18.18%)	2 (8.00%)	4 (6.67%)	4.86 (0.55–42.55)		0.15	3.92 (0.89–17.28)	0.07	1.39 (0.21–9.12)	0.73
Carbapenem	29(52.72%)	5 (20.00%)	4 (6.67%)	12.63 (2.30–69.34)		0.004	28.32 (7.71–104.08)	0.001	3.83 (0.68–21.50)	0.12
Prognosis
Mortality	34 (61.82%)	6 (24.00%)	4 (6.67%)	NA		0.002	NA	0.001	NA	0.001
Length of hospitalization	66.64 ± 108.89	33.67 ± 32.76	25.95 ± 14.68	NA		0.04	NA	0.001	NA	0.001
Admission to ICU	34 (61.82%)	8 (32.00%)	13 (21.67%)	4.12 (1.22–13.94)		0.023	4.09 (1.64–10.25)	0.003	0.92 (0.22–3.88)	0.90
Length of ICU stay	20.91 ± 41.43	5.92 ± 20.72	2.67 ± 6.23	NA		0.03	NA	0.001	NA	0.018

Notes: Antibiotic treatment refers to empirical antibiotic treatment before bacterial culture results. aUse of corticosteroids (prednisone equivalent >20 mg/day) for at least 14 days, or other recognized immunosuppressive therapy.

Abbreviation: NA, Not applicable.

Table 3

Multivariate Analyses Of Risk Factors For The Isolation Of CP-CRE Group Versus Non-CP-CRE Group, CP-CRE Group Versus ESBL Group, And Non-CP-CRE Group Versus ESBL Group

Variable	95% CI	OR	P Value
CP-CRE vs non-CP-CRE
Age	NA	NA	0.04
Admission to ICU	0.59–7.55	2.12	0.25
Length of ICU stay	NA	NA	0.03
Cancer	1.22–15.46	4.35	0.023
Liver cancer	0.28–30.16	2.91	0.37
Use of drainage tube	0.62–10.34	2.23	0.19
Previous carbapenem exposure	1.91–30.77	7.67	0.004
CP-CRE vs ESBLs
Age	NA	NA	0.01
Admission to ICU	0.10–2.20	0.46	0.33
Length of ICU stay	NA	NA	0.02
Transfusion	3.15–93.72	17.19	0.001
Cancer	3.56–71.37	15.91	<0.001
Chemotherapy	0.17–5.16	0.94	0.94
Venous catheterization	1.82–35.90	8.10	0.006
Previous carbapenem exposure	5.03–154.19	27.86	0.001
Non-CP-CRE vs ESBLs
Length of ICU stay	NA	NA	0.018
Transfusion	0.32–4.78	1.24	0.75
Venous catheterization	3.03–34.87	10.29	0.001

Abbreviation: NA, Not applicable.

Molecular Analysis Of Carbapenem Resistance Mechanisms

As shown in Table 4, the most common carbapenemase genes were KPC (63.64%, 35/55), NDM (32.73%, 18/55), and IMP (5.45%, 3/55). Notably, a K. pneumoniae isolate that simultaneously expressed KPC-2 and IMP-4 with porin deficiency was identified. All the MBLs-producing (NDM-1, NDM-5, IMP-4, and IMP-8) strains were resistant to all the carbapenem antibiotics tested. For non-CP-CRE bacteremic isolates, ESBL overexpression with OMP loss/deficiency was found to be the most predominant resistance mechanism, accounting for 88.46% (23/26).

Table 4

Distribution And Corresponding Carbapenem MIC Ranges For Strains With Different Resistance Determinants

Carbapenem Resistance Mechanisms	No. Of Isolates	MIC Range (μg/mL)
ETP	IMP	MEM
Carbapenemase positive	55
NDM-1, ESBLs, OMP loss or deficiency	10	8–256	4–64	4–128
NDM-5, ESBLs, OMP loss or deficiency	8	16–256	8–256	4–256
KPC-2, OMP loss or deficiency	34	4–128	1–128	1–128
IMP-4, ESBLs, OMP deficiency	1	64	8	8
IMP-8, ESBLs, OMP loss	1	8	8	8
KPC-2, IMP-4, ESBLs, OMP deficiency	1	256	256	128
Carbapenemase negative	26
AmpC, ESBLs	1	4	2	0.25
AmpC, OMP loss	1	2	2	1
AmpC, ESBLs, OMP loss	1	4	4	0.25
ESBLs, OMP loss or deficiency	23	2–32	0.25–16	0.25–8

Bactericidal Activities Of CAZ/AVI And ATM/AVI Against CRE Bacteremic Isolates

To better define the antimicrobial profiles of CAZ/AVI and ATM/AVI against the CRE bacteremic isolates, a recent (2016–2018) collection of 58 non-repetitive CRE bacteremic isolates, including 44 CP-CRE strains and 14 non-CP-CRE strains, was generated. The in vitro antimicrobial susceptibilities of CAZ, CAZ/AVI, ATM, and ATM/AVI against these isolates were determined using the CLSI broth microdilution method.

As was shown in Table 5, CAZ/AVI could inhibit most of the non-CP-CRE isolates (85.71%, 12/14), with low-level resistance (MIC: 16/4 µg/mL) in only two strains. For CP-CRE isolates, most strains carrying the KPC gene could be inhibited by CAZ/AVI (93.55%, 29/31). However, when an isolate expressed class B enzymes (such as NDM and IMP), CAZ/AVI could not inhibit its growth anymore. Compared with CAZ/AVI, ATM/AVI exhibited superior bactericidal activity, inhibiting the growth of all CRE strains.

Table 5

Antibacterial Activities Of CAZ/AVI And ATM/AVI Against 58 CRE Bacteremic Isolates

Resistance Mechanisms	MIC of CAZ/AVI (μg/mL)
0.125/4	0.25/4	0.5/4	1/4	2/4	4/4	8/4	16/4	32/4	64/4	>64/4
Carbapenemase positive
NDM-1, ESBLs, OMP loss or deficiency	0	0	0	0	0	0	0	1	2	0	1
NDM-5, ESBLs, OMP loss or deficiency	0	0	0	0	0	0	0	1	3	0	1
KPC-2, ESBLs, OMP loss or deficiency	0	0	1	2	11	11	4	1	0	0	1
IMP-4, ESBLs, OMP deficiency	0	0	0	0	0	0	0	0	0	1	1
IMP-8, ESBLs, OMP loss	0	0	0	0	0	0	0	1	0	0	0
KPC-2, IMP-4, ESBLs, OMP deficiency	0	0	0	0	0	0	0	0	0	0	1
Carbapenemase negative
AmpC, ESBL	1	0	0	0	0	0	0	0	0	0	0
AmpC, OMP loss	0	0	0	0	0	0	1	0	0	0	0
AmpC, ESBLs, OMP loss	0	0	0	0	0	0	0	1	0	0	0
ESBLs, OMP loss or deficiency	0	0	1	1	4	3	1	1	0	0	0
Resistance mechanisms	MIC of ATM/AVI (μg/mL)
0.125/4	0.25/4	0.5/4	1/4	2/4	4/4	8/4	16/4	32/4	64/4	>64/4
Carbapenemase positive
NDM-1, ESBLs, OMP loss or deficiency	0	2	1	0	0	1	0	0	0	0	0
NDM-5, ESBLs, OMP loss or deficiency	1	0	1	1	0	1	1	0	0	0	0
KPC-2, OMP loss or deficiency	3	9	7	8	2	1	1	0	0	0	0
IMP-4, ESBLs, OMP deficiency	0	1	0	1	0	0	0	0	0	0	0
IMP-8, ESBLs, OMP loss	0	1	0	0	0	0	0	0	0	0	0
KPC-2, IMP-4, ESBLs, OMPs deficiency	0	0	0	0	1	0	0	0	0	0
Carbapenemase negative
AmpC, ESBLs	1	0	0	0	0	0	0	0	0	0	0
AmpC, OMP loss	1	0	0	0	0	0	0	0	0	0	0
AmpC, ESBLs, OMP loss	1	0	0	0	0	0	0	0	0	0	0
ESBLs, OMP loss or deficiency	2	5	2	1	1	0	0	0	0	0	0

Discussion

CRE bacteremia was previously reported to be associated with extremely high mortality, ranging from 20% to 70%.23,24 This cohort study showed a 50% (40/80) mortality rate in general. However, when stratified into CP-CRE and non-CP-CRE groups, the mortality rate of the CP-CRE subgroup (61.82%) was significantly higher than that of the non-CP-CRE group (24%), supporting earlier observations that CP-CRE bacteremia was more harmful than non-CP-CRE bacteremia, with higher levels of antimicrobial resistance and greater mortality.15 Therefore, for the effectiveness of the treatment and prevention of antibiotic resistance, the antibiotics and doses used to treat CP-CRE and non-CP-CRE bacteremia should be different. Of note, CarbaNP and mCIM with or without eCIM were currently recommended by CLSI to be performed on CRE isolates to distinguish CP-CRE and non-CP-CRE for epidemiological or infection control purposes. However, they were not currently recommended for routine clinical use. Thus, the First Affiliated Hospital of Chongqing Medical University Antibiotic Treatment Guidelines did not differentiate treatment recommendations for CP-CRE and non-CP-CRE infections. As clinicians were unaware of carbapenemase gene results when selecting antibiotic therapy for CRE bacteremia, therapeutic regimens were mainly experience-directed. This study was novel in investigating the possible value of CP-CRE/non-CP-CRE stratification and CRE resistance mechanism determination in better managing CRE bacteremia by CAZ/AVI and ATM/AVI.

Some Conclusions Of This Study Were Noteworthy

First, the study explored the independent risk factors leading to the acquisition of CP-CRE bacteremia. Notably, besides old age, transfusion, longer ICU stay, and cancer, previous carbapenem exposure was identified as an independent risk factor for bacteremia CP-CRE acquisition, which was in agreement with a previous report.24

Second, CAZ/AVI was reported to be active in vitro against non-CP-CRE as well as blaKPC- and blaOXA-48-harboring CP-CRE isolates.25 Emerging clinical data demonstrated that CAZ/AVI treatment in CRE infections achieved clinical response rates that were superior to those attained with regimens including colistin or an aminoglycoside.26,27 At our center, in vitro CAZ/AVI resistance emerged in 29.31% of the CRE bacteremic isolates, which was congruent with a previous report by Shields who declared a 75% success rate for CAZ/AVI in treating CRE bacteremia.28 Moreover, consistent with previous reports, in vitro susceptibility testing showed that most CP-CRE bacteremia strains carrying the blaKPC-2 gene were sensitive to CAZ/AVI. However, 2 out of 31 blaKPC-2-harboring strains (with ESBL overexpression and OMP loss) were revealed to be CAZ/AVI-resistant, mirroring the strains described in prior reports by Shields, who demonstrated a stepwise increase in CAZ/AVI MICs in KPC-2-producing K. pneumoniae isolates co-harboring ESBLs and ompK36 porin gene mutations.29 Humphries thought that the extensive prior treatment with meropenem and cefepime might have provided the selective pressure required for a mutation to OmpK36.30 Giddins identified CAZ/AVI resistance in the newly emerging K. pneumoniae ST307 clonal background after only 12 days of CAZ/AVI exposure, with the induction of a 532G-T mutation in the blaKPC-2 gene leading to a D179Y protein substitution as the putative initial mechanism of CAZ/AVI resistance.31 The characterization of some CAZ/AVI-resistant Pseudomonas aeruginosa isolates demonstrated that the entry of CAZ/AVI into the periplasmic space depended on outer membrane permeability.32 Also, the patients infected with KPC2-producing CRE had no previous exposure to CAZ/AVI, but instead had frequent previous exposures to meropenem and cefepime. Hence, it was postulated that their resistance to CAZ/AVI might be also due to the lack of membrane porin proteins.

Third, ATM/AVI combination is currently in clinical development for treating serious infections caused by MBL-producing Enterobacteriaceae,19 with sporadically reported resistance. Fortunately, this study demonstrated that all the studied CRE bacteremic isolates, including both the CP-CRE and non-CP-CRE ones, were highly sensitive to ATM/AVI in vitro. Nevertheless, Alm already found a special NDM-producing E. coli isolate with decreased susceptibility to ATM/AVI caused by a four-amino-acid insertion in PBP3, leading to decreased binding.33 Hence, it is necessary to investigate whether ATM/AVI resistance or a stepwise increase in ATM/AVI MICs would be rapidly induced during ATM/AVI treatment, especially in the most notorious double-carbapenemase producers with porin loss/deficiency.

In general, with the advancement of individualized medicine, the selection and use of antibiotics should gradually be personalized and standardized. CP-CRE/non-CP-CRE bacteremia stratification and CRE resistance mechanism determination can better guide the clinical management of CRE bacteremia. For example, ATM/AVI can be prescribed to treat CP-CRE bacteremia for patients with high risks of contracting CP-CRE bacteremia, such as those with advanced age, transfusion, longer ICU stay, cancer, and previous exposure of carbapenems, while patients without risk factors can be treated with CAZ/AVI.

A limitation of the present study was that only the in vitro susceptibility tests of CAZ/AVI and ATM/AVI were performed. Animal experiments and prospective clinical trials are still needed to validate the risk factors and therapeutic recommendations based on CRE resistance mechanism stratification for CRE bacteremia. Furthermore, multi-center retrospective and prospective studies are still awaited to move from a proof of concept to practical applications of risk factors and management of CRE bacteremia guided by molecular resistance mechanism stratification. In addition, CP-CRE/non-CP-CRE stratification and CRE resistance mechanism determination might also better guide the clinical management of CRE bacteremia using other novel antibiotics, such as meropenem/vaborbactam, imipenem/relebactam, and cefiderocol, which needs further investigation. Last but not the least, possible synergy of CAZ/AVI with meropenem, amikacin, aztreonam, colistin, or fosfomycin against the aforementioned CAZ/AVI-resistant isolates deserves further explorations. Although much remains to be elucidated concerning the therapeutic recommendations for CRE bacteremia guided by the resistance mechanism stratification, this study laid an invaluable groundwork for future studies.