Abstract
Introduction
Non-fermenting Gram-negative bacilli (NFGNB) other than Pseudomonas aeruginosa and Acinetobacter baumannii complex are pathogens of interest due to their ability to cause health-care associated infections and display complex drug resistance phenotypes. However, their clinical and microbiological landscape is still poorly characterized.
Methods
Observational retrospective study including all hospitalized patients presenting with a positive positive blood culture (BC) episode caused by less common NFGNB over a four-year period (January 2020–December 2023). Clinical-microbiological features and factors associated with mortality were investigated.
Results
Sixty-six less common NFGNB isolates other than Pseudomonas and Acinetobacter species causing 63 positive BC episodes were recovered from 60 patients. Positive BC episodes were predominantly sustained by Stenotrophomonas maltophilia (49.2%) followed by Achromobacter species (15.9%) that exhibited the most complex resistance phenotype. Positive BC episodes had bloodstream infection criteria in 95.2% of cases (60 out 63), being intravascular device (30.2%) and respiratory tract (19.1%) the main sources of infection. Fourteen-day, 30-day, and in-hospital mortality rates were 6.4%, 9.5%, and 15.9%, respectively. The longer time from admission to the positive BC episode, older age, diabetes, admission due to sepsis, and higher Charlson Comorbidity Index were identified as the main predictors of in-hospital mortality.
Conclusions
Positive BC episodes sustained by NFGNB other than Pseudomonas and Acinetobacter species were predominantly sustained by Stenotrophomonas maltophilia and Achromobacter species, having bloodstream infection criteria in the vast majority of cases. Factors that have emerged to be associated with mortality highlighted how these species may have more room in prolonged hospitalisation and at the end of life for patients with chronic organ diseases.
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Introduction
Gram-negative bacteria bloodstream infection (BSI) is a serious clinical condition associated with notable mortality and morbidity rates, especially among immunocompromised and elderly patients [1, 2]. The course of infection is heavily influenced by various microbiological and clinical issues as the type of pathogen and burden of drug resistance [3], patients conditions and rapidity and appropriateness of diagnosis and treatment [4, 5]. Among non-fermenting Gram-negative bacilli (NFGNB) [6], Pseudomonas aeruginosa and Acinetobacter baumannii complex are the most frequently isolated pathogens [1, 2]. Given their high burden of antimicrobial resistance [7] they have been placed on the World Health Organisation’s critical priority list for the development of new antibiotics [8]. These two species have therefore been the target of several surveillance [9], clinical [10,11,12] and microbiological studies [13,14,15]. Interest in them even increased during the SARS-CoV-2 pandemic due to their frequent detection especially in patients with prolonged time of invasive ventilation and hospitalisation [16, 17]. Among NFGNB, however, there are other bacteria such as Stenotrophomonas, Achromobacter, Ochrobactrum, Burkholderia, Aeromonas, Roseomonas, Elizabethkingia, Chryseobacterium, Alcaligenes, Ralstonia, Cupriavidus, Sphingomonas, Rhizobium, Empedobacter, Brevundimonas and other species that are less frequently diagnosed but of interest due to their ability to display complex drug resistance phenotypes [18,19,20,21,22,23]. These organisms are widely distributed in the environment, thriving in soil and water supplies [18]. They initially aroused attention due to their ability to colonise and infect cystic fibrosis [24,25,26] and chronic lung disease patients [27]. They have then emerged as healthcare-associated opportunistic pathogens [28, 29], mainly causing pneumonia and/or BSI [6] and nosocomial outbreaks [30,31,32,33], relying on their ability of colonizing medical devices and therapeutic equipment [31, 33].
Risk factors for infection include older age, malignancy, immunodepression, chronic respiratory disease, presence of intravascular device or drain tube, prolonged antibiotic use and hospital length of stay. Stenotrophomonas maltophilia is the most detected aetiology [6]. The mortality rate of infections caused by these species is reported to vary greatly depending on the type of infection, pathogen, and patient involved [6].
In recent years, the diagnostic accuracy and frequency of diagnosis of NFGNB other than Pseudomonas and Acinetobacter species have certainly increased, but their pathogenic potential remains a topic yet to be explored. The clinical significance of these species detection from blood cultures (BCs) sometimes can be unclear, especially in case of polymicrobial infections or with a low positive/overall BC samples ratio. However, the treatment of associated infections presents a real challenge, as these organisms, which are difficult to eradicate from healthcare facilities, often exhibit a complex resistance phenotype through the production of β-lactamases and mechanisms favouring drug efflux [18, 34]. This might result in a high rate of empirical therapy misuse and widespread antibiotic consumption.
EUCAST has also recently introduced clinical breakpoints for Stenotrophomonas maltophilia, Aeromonas and Achromobacter species [35], but therapeutic recommendations of the associated infections are only partially present in the most widely consulted guidelines [36].
We conducted this four-year monocentric study with the objective of investigating the factors associated with mortality in a cohort of patients who presented with a positive BC episode caused by NFGNB other than Pseudomonas and Acinetobacter species, contributing to the clinical and microbiological characterization of these infections.
Methods
Study design
In this observational retrospective four-year study (January 2020–December 2023), we included all NFGNB isolates other than Pseudomonas and Acinetobacter species recovered from positive BCs of patients admitted at the “Città della Scienza e della Salute di Torino”, a 1900-bed tertiary referral hospital in Turin, Italy. Duplicate isolates obtained within a 20-day interval from the same patient were considered as part of a single positive BC episode and therefore excluded from the analysis. The electronic medical records of patients who presented with a positive BC episode caused by NFGNB isolates other than Pseudomonas and Acinetobacter species were retrospectively reviewed. Clinical and microbiological characteristics, and factors associated with in-hospital mortality were investigated.
Microbiological diagnostics
The BACT/ALERT FA and FN Plus BC bottles (bioMérieux, Marcy l’Ètoile, France) were incubated in the BACT/ALERT Virtuo (bioMérieux, Marcy l’Ètoile, France). Positive BCs were subjected to Gram staining and subculture on MacConkey and Blood agar media. Bacterial species identification was performed on overnight subcultures by using matrix-assisted laser desorption ionization–time of flight mass spectrometry (MALDI-TOF MS, Bruker DALTONIK GmbH, Bre-men, Germany). Antimicrobial susceptibility testing was performed through a micro-dilution method (Panel NMDR on automated Microscan WalkAway 96 Plus System, Beckman Coulter, Nyon, Switzerland). Cefiderocol susceptibility testing was carried out by disc diffusion method. Antimicrobial susceptibility testing results were interpreted according to the current EUCAST clinical breakpoints (v. 14.0) [35, 37].
Statistical analysis
Descriptive data are shown as relative (%) and absolute (n) frequencies for categorical data and median and interquartile range (IQR) for continuous variables. χ2 test or Fisher’s exact test were employed to assess the association between binary variables and outcomes. For continuous variables, the Mann-Whitney U test was used to com-pare distributions between groups based on outcome status. XGBoost was used as an explanatory model to rank and identify relative feature importance, using SHAP values as a proxy for feature importance measured at the local data point level. SHAP values are reported as log odds. Analyses have been carried out in Python 3.10.
Results
Sixty-six NFGNB isolates other than Pseudomonas and Acinetobacter species causing 63 positive BC episodes (overall prevalence of 1.6% among Gram-negative bacteria) were recovered from 60 patients. Patients had a median age of 65 years [51.5–74.5], were predominantly male (60.3%) and admitted in medical wards (46%), with a median Charlson comorbidity index estimating a 53% probability of surviving in the next ten years (Table 1).
Among the characteristics of the patients investigated, presence of a long-term intravascular device (52.4%) and cardiovascular disease (71.4%) followed by having been treated with antibiotic therapy in the previous seven days (47.6%), being colonized by multidrug resistant bacteria (28.6%), and neoplasms (35%) were the most prevalent. Patients were predominantly admitted due to sepsis (27%), surgery (25.4%), and trauma (20.6%). The median time to positive BC episode from admission was 17 days [2–34.5] and 68.3% of patients had at least 50% positive BC bottles out of the total number of BC bottles processed. Almost half (41.3%, n = 26) of the BC samples were polymicrobial mainly with other Gram-negative bacteria (57.7%, n = 15). Positive BC episodes were predominantly sustained by Stenotrophomonas maltophilia (49.2%) followed by Achromobacter (15.9%), Ochrobactrum (9.5%), Aeromonas (9.5%), and Burkholderia species (7.9%, with one imported case of melioidosis). Other species accounted for 14.3% and included Rhizobium radiobacter, Chryseobacterium arthrosphaerae, Roseomonas mucosa, Empedobacter falsenii, Elizabethkingia anophelis, and Brevundimonas diminuita. Positive BC episodes had BSI criteria in 95.2% of cases (60 out 63), being intravascular device (30.2%) and respiratory tract (19.1%) the main sources of infection. Patients suffered from BSI had a median Pitt Bacteremia score of one [0–2], presented with neutropenia in 9.5%, and required ICU admission in 14.3% of the cases. The majority of patients (55.6%) were treated with active antibiotic therapy within 48 h from positive BC episode detection. Targeted antibacterial therapy was carried out in equal proportions between monotherapy and combination (47.6%). The most frequently used antibiotic regimes were those that included meropenem (25.4%), piperacillin/tazobactam (23.8%), fluoroquinolones (22.2%), and trimethoprim/sulfamethoxazole (17.5%). Regarding complications, four patients (6.4%) reoccurred with a positive BC episode caused by the same organism at least 14 days after the first one. Regarding outcomes, 14-day, 30-day, and in-hospital mortality rates were 6.4%, 9.5%, and 15.9%, respectively. The median length of stay was 41 days [19.5–72].
Antimicrobial susceptibility profiles of NFGNB isolates other than Pseudomonas and Acinetobacter species included in the study were reported in Table 2. Stenotrophomonas maltophilia isolates displayed over 90% susceptibility only to cefiderocol and trimethoprim/sulfamethoxazole. Achromobacter species showed high rates of resistance towards all the antibiotics tested and high values of inhibition zone diameter with cefiderocol (range 35–39 mm). Aeromonas species displayed susceptibility to third- and fourth-generation cephalosporins, fluoroquinolones and trimethoprim/sulfamethoxazole. Ochrobactrum anthropi displayed high susceptibility to carbapenems as well as to meropenem in Burkholderia species. High values of the diameter of the zone of inhibition with cefiderocol (range 36–40 mm) were also observed in Burkholderia species.
Patients admitted due to trauma had more episodes of positive BC sustained by at least ≥ 50% of the BC bottles positive (27.9% vs. 5%, p = 0.047, Table 3). Less frequent species included in the ‘other’ group were more detected in patients with less than 50% of positive BC bottles (30% vs. 7%, p = 0.023). No more statistically significant differences in terms of patient characteristics, microbiological findings, source of infection, severity of bacteremia, antibiotic management and outcomes were observed.
Comparison of the clinical characteristics of the patients who died during admission vs. those who survived (Table 4) showed non-survivors suffering more from diabetes (p = 0.025), having a higher Charlson Comorbidity index (p = 0.036), having been treated with antibiotic therapy in the previous seven days (p = 0.038), and having a longer time from admission to positive BC episode (p = 0.003) than survivors. No more statistically significant differences in terms of patient characteristics, microbiological findings, reason for admission, source of infection, severity of bacteremia, antibiotic management and complications were observed.
The XGBoost model used to rank features based on their relative importance based on their contribution towards mortality risk patient stratification suggested the most informative features to be the time from admission to the positive BC episode (a high cardinality feature, which inherently increases its importance), older age, diabetes, admission due to sepsis, higher Charlson Comorbidity Index, being treated with combination therapy, and being treated with a meropenem-including regimen. Additionally, the model underscored that male patients and those colonized by multidrug-resistant bacteria were less likely to die compared to female patients and non-carriers under surveillance, respectively (Fig. 1).
Discussion
This study offers a contemporary insight into the clinical–microbiological features of positive BC episodes sustained by NFGNB other than Pseudomonas and Acinetobacter species in a cohort of patients admitted in a reference center of Northern Italy encompassing all major medical and surgical specialties and with multiple challenges in the area of antibiotic resistance [38]. Its findings revealed that positive BC episodes sustained by NFGNB other than Pseudomonas and Acinetobacter species were polymicrobial and microbiologically significant in a remarkable proportion of the samples. Stenotrophomonas maltophilia was the most detected species and, together with Achromobacter species, exhibited the most complex resistance phenotype. Clinically, positive BC episodes were more frequent in patients with a long-term intravascular device and had BSI criteria in the vast majority of cases. In contrast, the degree of severity of bacteremia was quite low, as were the associated mortality rates. Time from admission to the positive BC episode, older age, diabetes, admission due to sepsis, higher Charlson Comorbidity Index, being treated with combination therapy and meropenem-inclusive regimen emerged as factors associated with in-hospital mortality.
Knowledge of the clinical significance of NFGNB other than Pseudomonas and Acinetobacter species is currently very limited [6]. Our study only partially assessed the impact of these species given the high proportion of polymicrobial samples. However, our results reported a high correspondence between positive BC episode, ≥ 50% positive/overall BC samples ratio, BSI criteria and targeted treatment prescription, adding some evidence in favor of the likely pathogenic potential of these species.
Our study also confirmed the epidemiological and clinical relevance of Stenotrophomonas maltophilia within the less common NFGNB [6]. A substantial literature already exists on this species and associated infections [18, 39,40,41,42,43,44,45,46,47] so much so that it is the only one to have been included in the Infectious Diseases Society of America treatment guidelines [36]. Our study also highlighted that resistance to sulfamethoxazole/trimethoprim and cefiderocol remains uncommon as already highlighted in recent studies [13, 48].
Despite the limited sample size, our study showed the complex phenotype of Achromobacter species exhibiting low susceptibility to piperacillin/tazobactam, third-generation cephalosporins, carbapenems, and fluoroquinolones. These findings are not consistent with the results of a Spanish study on patients suffering from Achromobacter xylosoxidans bacteremia that showed high susceptibility to meropenem using EUCAST breakpoints for Pseudomonas aeruginosa [49], highlighting Achromobacter potential for innate resistance to all antibiotics [18]. Of note, high values of inhibition zone diameter with cefiderocol were observed among the isolates included in our study, as also previously described [14]. This might highlight cefiderocol as promising treatment of severe Achromobacter species infections, although clinical evidence on in vivo activity is still limited.
The opportunistic pathogenic nature of the less common NFGNB is highlighted in the literature by the fact that they mainly cause nosocomial infections in an increasingly common population with risk factors such as neoplasia or chronic organ disease, prolonged hospitalizations and the need for systemic therapies, including antibiotics, through long-term intravascular devices [18]. This is consistent with the results of our study which identified the presence of a long-term intravascular device as the most frequent clinical feature among patients and the main source of BSI. On the other hand, although our study showed quite low BSI severity indices and consequently low mortality rates, evidence available so far shows different data according to pathogen and cohort of patients considered [6]. Mortality rates among adult patients suffering from Stenotrophomonas maltophilia BSIs ranged from 32 to 54.8% [50,51,52], while for those sustained by Achromobacter species from 20 to 27% [53, 54]. Similar rates have been reported in Elizabethkingia species BSIs [55,56,57], while lower rates have been reported in Chryseobacterium species [58].
Perhaps not surprising, in our study patients who did not survive admission were older, suffered from more baseline comorbidities, were admitted due to sepsis, and experienced both longer time from admission to the positive BC episode and more broad-spectrum antibiotic therapy. Therefore, patient’s general condition prevailed over etiology in patients suffering from less common NFGNB BSIs. The relevance of comorbidities in predicting mortality was well highlighted in an Australian population study over the period 2000–2019 [53]. In a recent meta-analysis on patients with Stenotrophomonas maltophilia bloodstream infection, poor outcomes were associated with infection severity (ICU admission, septic shock, need for mechanical ventilation), comorbidities (indwelling central venous catheter, neutropenia, hematological neoplasms, chronic kidney disease) and antibiotic prescription (inappropriate antimicrobial therapy and prior antibiotic use) [59]. However, our finding differs significantly from a recent multicenter study conducted in Northern Italy on patients suffering from NFGNB BSI (including Pseudomonas aeruginosa and Acinetobacter baumannii complex) that identified older age, septic shock and Acinetobacter baumannii complex etiology as predictors of 30-day mortality [11]. The strength of this study is the collection of data from a surveillance study on a group of bacteria sporadically reported in the literature and investigating their pathogenic potential. Some limitations should be also acknowledged, including its retrospective nature with possible confounders and potential bias not considered and the fact that it was conducted in a single center. The narrow nature of our findings, due to the limited sample size, does not allow generalized conclusions to be drawn.
In conclusion, this study investigated the clinical and microbiological findings of positive BC episodes caused by NFGNB other than Pseudomonas and Acinetobacter species. Positive BC episodes were predominantly sustained by Stenotrophomonas maltophilia and Achromobacter species, having BSI criteria in the vast majority of cases. Achromobacter species isolates showed the most complex resistance phenotype and from the in vitro results, cefiderocol appeared to be a possible option for treating infections caused by these multidrug resistance strains. Long-term intravascular device and respiratory tract were the main sources of infection. No differences in patient comorbidities, infection severity and outcomes were observed on the basis of the percentage of positive BC samples, providing an argument in favor of those who consider these species to have substantial pathogenic potential. The longer time from admission to positive BC episode, older age, diabetes, admission due to sepsis, higher Charlson Comorbidity Index, being treated with combination therapy and meropenem-including regimen emerged as the strongest predictors of in-hospital mortality. This might highlight how these species may have more room in prolonged hospitalisation and at the end of life for patients with chronic organ diseases. Further studies are needed to validate our results, notwithstanding the need for continuous surveillance of these species and their antimicrobial susceptibility profiles.
Data availability
Data is provided within the manuscript or supplementary information files.
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Open access funding provided by Università degli Studi di Torino within the CRUI-CARE Agreement. This research was supported by EU funding within the MUR PNRR Extended Partnership initiative on Emerging Infectious Diseases (Project no. PE00000007, INF-ACT).
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G.B. and M.B. designed the study; R.C, S.C. (Sara Comini), S.C. (Silvia Corcione) acquired data; M.B. and P.B. analyzed and interpreted data; R.C. and M.B. wrote the paper; F.G.D.R. and C.C. supervised the study; all authors revised the article critically. All authors have read and agreed to the published version of the manuscript.
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This study was conducted in accordance with the Declaration of Helsinki and approved by the Ethics Committee of A.O.U. Città della Salute e della Scienza di Torino-A.O. Ordine Mauriziano-A.S.L. Città di Torino (protocol code 0048443 on 29 April 2022).
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Informed consent was waived due to the retrospective nature of the study.
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Casale, R., Boattini, M., Comini, S. et al. Clinical and microbiological features of positive blood culture episodes caused by non-fermenting gram-negative bacilli other than Pseudomonas and Acinetobacter species (2020–2023). Infection (2024). https://doi.org/10.1007/s15010-024-02342-6
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DOI: https://doi.org/10.1007/s15010-024-02342-6