Next Article in Journal
Dietary Fiber Intake and Gut Microbiota in Human Health
Previous Article in Journal
Grinding Beads Influence Microbial DNA Extraction from Organic-Rich Sub-Seafloor Sediment
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Stenotrophomonas maltophilia Epidemiology, Resistance Characteristics, and Clinical Outcomes: Understanding of the Recent Three Years’ Trends

1
Clinical Laboratory Sciences Department, College of Applied Medical Sciences, King Saud University, Riyadh 12372, Saudi Arabia
2
Regional Laboratory and Central Blood Bank, Microbiology Department, Albaha 65715, Saudi Arabia
3
Pathology and Clinical Laboratory Medicine, King Fahad Medical City, Riyadh 11525, Saudi Arabia
4
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud bin Abdulaziz University for Health Sciences, Riyadh 11481, Saudi Arabia
5
King Abdullah International Medical Research Center, Riyadh 11481, Saudi Arabia
*
Author to whom correspondence should be addressed.
Microorganisms 2022, 10(12), 2506; https://doi.org/10.3390/microorganisms10122506
Submission received: 21 November 2022 / Revised: 8 December 2022 / Accepted: 15 December 2022 / Published: 18 December 2022
(This article belongs to the Section Public Health Microbiology)

Abstract

:
Background. Stenotrophomonas maltophilia is an emerging pathogen classified as a public health concern, that infects critically ill patients and has expressed resistance against antimicrobial therapy. The aim of this study was to examine the epidemiological pattern, resistance characteristics and clinical outcomes of S. maltophilia infections in hospitalized patients. Methods. The study included 393 S. maltophilia isolates from different clinical specimens as well as the clinical data of 209 Intensive Care Unit (ICU) patients. The patients’ data were obtained from medical and laboratory files. Descriptive statistics and a univariate analysis were used to report and compare the demographics, clinical data, and outcomes. Results. The S. maltophilia was mostly isolated from the respiratory specimens of ICU patients. The adult patients were more likely to develop serious infections and worse outcomes than were pediatric patients. The most common co-infecting pathogens were SARS-CoV2 and Pseudomonas aeruginosa. The death rate was 44.5% and increased to 47.1% in the case of a respiratory infection. Septic shock was the most significant predictor of mortality. Older age and mechanical ventilation were independent and significant risk factors that worsened the outcomes in patients with respiratory infections. Conclusions. The identification of S. maltophilia as a threat highlights the importance of surveillance studies in this region.

1. Introduction

Stenotrophomonas maltophilia (S. maltophilia) is a nonfermenting gram-negative bacillus bacterium [1]. It can be found in different sources of the environment including soil, plants, and animals, as well as it can be detected in an aquatic environment [2]. It is known that S. maltophilia is the only species of the Stenotrophomonas genus that can cause infections in humans, mainly among immunocompromised patients and hospitalized patients, and specifically among Intensive Care Unit (ICU) patients who have undergone prosthetic devices such as catheters, mechanical ventilators, and feeding tubes, as it is capable of producing a biofilm on these surfaces [3]. However, it is uncommon for S. maltophilia to cause community-acquired infections [4]. S. maltophilia is considered to be the most prevalent organism isolated in clinical laboratories after Pseudomonas aeruginosa, Acinetobacter spp., and the Burkholderia cepacia complex [5]. Most of the infections caused by S. maltophilia occur in the lower respiratory tract in the form of tracheobronchitis or pneumonia because of mechanical ventilation, in addition to blood infections such as bacteremia [6]. There are other infections that can be caused by S. maltophilia, such as wound and soft tissue infections, meningitis, peritonitis, urinary tract infections (UTI), and bone/ joint infections [4]. The mortality rate of an S. maltophilia infection is significantly high, as it reaches 75% when associated with pneumonia and 20% when associated with bacteremia [7]. S. maltophilia is identified to be resistant to different types of antimicrobials via different mechanisms, including the production of aminoglycoside acetyltransferase and enzymes, which immobilize erythromycin. In addition, S. maltophilia can possess certain genes that encode efflux pumps [8]. The resistance can be intrinsic or acquired by either mutations or through carrying the resistant genes via a horizontal gene transfer [2]. S. maltophilia has multi-drug resistance (MDR) to certain types of antimicrobials; additionally, pan-resistant strains of S. maltophilia have been found in hospitals as a result of inappropriate antibiotic use, particularly of broad-spectrum antibiotics [8]. The therapeutic options for treating S. maltophilia infections are limited due to its resistance to a wide range of antibiotics such as aminoglycoside and a variety of ß-lactam antibiotics including carbapenem [9]. In addition to the outbreak caused by the virus severe acute respiratory syndrome coronavirus 2 (SARS-CoV2), which was initiated in Wuhan at the end of 2019, there is an elevation in the prevalence of multi-drug resistance (MDR) bacteria including S. maltophilia. This elevation in the resistance occurs as a consequence of the increased utilization of anti-microbial agents among hospitalized COVID-19 patients [10]. However, there are few studies concerned with investigating the resistance pattern of S. maltophilia before and during the outbreak of SARS-CoV-2. The aim of this study was therefore to investigate the epidemiological pattern, resistance characteristics, and clinical outcomes of S. maltophilia in depth over the last three years in Saudi Arabia.

2. Materials and Methods

2.1. Study Design and Setting

A retrospective study was conducted over three years from January 2019 to December 2021 at King Fahad Medical City (KFMC), with a capacity of 1200 beds, in Riyadh, Saudi Arabia. A total of 393 S. maltophilia isolates from various clinical samples were analyzed. The clinical histories of 209 ICU patients were also included in this study.

2.2. Data Collection

A total of 393 samples of S. maltophilia were collected from various sources, which included blood (central and peripheral lines), respiratory (sputum and endotracheal), urine (mid-stream urine, indwelling catheter, and in and out catheter), and miscellaneous (abscess, wound, tissue, body fluid, and device) sources. The inclusion criteria were: (A) Age was divided into pediatric and adult categories. The pediatric category included three sub-categories: infant (age 1 Y); children (age from 1 to 10 Y); and adolescent (age from 11 to 18 Y). The adults were divided into four groups: group one (from 19 to 44 Y), group two (from 45 to 64 Y), group three (from 65 to 84 Y), and group four (age 85 and above). (B) Ward or clinic that the patient was admitted to, including emergency, ICU, ward, and outpatient clinic. (C) Sample source and location/site. (D) Bacterial resistant category. Any growth other than S. maltophilia was excluded from the data. The clinical histories were collected from the KFMC databases for patients admitted to the ICU, including pediatric and adult patients. The clinical histories collected for the ICU patients included different criteria, which were: (1) co-infection, if present or not; (2) exposure to carbapenem or other antibiotic in the past 14 to 30 days; (3) renal dialysis at isolation or not; (4) on mechanical ventilation or not; (5) chronic disease such as DM, hypertension, renal disease, or malignancy; (6) the presence of clinical symptoms such as fever, GIT symptoms, or respiratory symptoms; (7) the presence of a wound or urinary tract infection; (8) the presence of bacteremia or septicemia; (9) clinical outcomes for the patient and additional notes if present.

2.3. S. maltophilia Identification and Antimicrobial Susceptibility Testing

All of the isolates were presumptively identified as Stenotrophomonas species by the aid of a Phoenix BD instrument for full identification and sensitivity testing. Only patients whose isolates were definitively identified as S. maltophilia were included. Antimicrobial sensitivity testing (AST) was done for the following antibiotics: ceftazidime (CTZ), levofloxacin (LVX), and trimethoprim-sulfamethoxazole (TMP-SMX). The results were interpreted and reported according to the 32nd Edition of the CLSI-M100 document and classified as susceptible (S), intermediate (I), and resistant (R). The confirmation of resistant isolates was performed by an E-test. The S. maltophilia isolates were categorized based on their resistance to antibiotics, according to International Consensus [11].

2.4. Statistical Analysis

All data were analyzed using a GraphPad prism statistical project version 9.3.1. The demographic characteristics of the entire study population with an S. maltophilia infection were summarized. A univariate analysis to compare clinical characteristics between adults and pediatric ICU-admitted patients was obtained using Fisher’s exact test, with a p-value of less than 0.05 being statistically significant. Similarly, a multivariate analysis was used to compare the outcomes and risk factors linked to death among ICU patients. Relative risk (RR) was calculated to indicate how much the risk factors increased the risk of death among those patients with a respiratory infection, and the results were reported as RR and 95% confidence interval (CI). Additionally, the AMT was presented in percentages.

2.5. Ethical Approval

The project was approved by the local ethical research committee of King Fahad Medical City. Consent was obtained from KFMC according to ICH GCP guidelines with the ethical code of IRB log number: 21-426E.

3. Results

3.1. Demographic Characteristics of Patients with S. maltophilia Infection

A total of 393 isolates of S. maltophilia were isolated from different clinical specimens including the sputum, endotracheal secretions, the urine, the blood, and other miscellaneous body fluids. The majority of the isolates were obtained from respiratory specimens (65.4%), followed by blood cultures (17.3%). Approximately half of the S. maltophilia isolates (53.2%) mainly originated from the ICU (209/393). The demographic characteristics of patients are summarized in Table 1.

3.2. Comparison of Clinical Characteristics among Adult and Pediatric ICU Patients

A univariant analysis was conducted to compare the clinical characteristics between adult and pediatric ICU patients (n = 209). The adult patients infected with S. maltophilia were significantly more likely to develop a co-infection, a urinary tract infection, septic shock, and death than were pediatric patients. Almost half of the ICU patients were co-infected with another organism (n = 106; 50.7%). The co-infection was mostly caused by gram-negative bacteria (64%; Pseudomonas aeruginosa, Klebsiella pneumoniae, Klebsiella oxytoca, Acinetobacter baumannii, Enterobacter cloacae, Escherichia coli, Serratia species, and Proteus mirabilis), followed by a SARS-CoV-2 infection (48%). The most frequent co-isolated species were P. aeruginosa (28%), K. pneumoniae (12%), and A. baumannii (9%). Co-infections with the influenza A virus, fungi, and gram-positive bacteria (Staphylococcus aureus, Staphylococcus epidermidis, and Enterococcus faecium) were also detected. In addition, there was a significant association between adults aged more than 18 and some clinical characteristics including fever, respiratory symptoms, mechanical ventilation, recent antibiotic pre-exposure, and chronic diseases (Table 2). Diabetes mellitus and hypertension were the most significant chronic illnesses associated with S. maltophilia infections among adult ICU patients.

3.3. Clinical Outcomes and Factors Associated with Mortality of ICU Patients with S. maltophilia Infection

The overall mortality rate of an S. maltophilia infection among ICU patients was 44.5% and a respiratory infection increased the mortality rate to 47.1%. To evaluate the risk factors associated with mortality between the resolved and the deceased patients, univariant analysis was conducted (Table 3). Several factors were tested for their potential associations with mortality among the infected ICU patients with S. maltophilia: age above 18 years, a positive respiratory culture, septicemia, septic shock, malignancy, prior exposure to antimicrobials, and the use of mechanical ventilation. Upon univariate analysis, there were three factors significantly associated with mortality among the infected ICU patients with S. maltophilia: age above 18 years, septicemia, and septic shock at p = 0.0049, p = 0.0321, and p < 0.0001, respectively. However, septic shock was the leading cause of death in S. maltophilia infected ICU patients (p < 0.0001).
There was a considerable percentage (82%) of ICU patients who had an S. maltophilia respiratory infection. Therefore, a multivariate analysis was conducted to identify the significant predictors for mortality among those patients (Table 4). The results of the multivariate analysis indicated that only the age above 18 years (RR = 1.264; 95% CI: 1.036–1.557; p = 0.031) and the use of mechanical ventilation (RR = 1.138; 95% CI: 1.020–1.290; p = 0.034) were independent and significant risk factors for mortality among the infected ICU patients with respiratory S. maltophilia infections as shown in Table 4. In other words, the risk of mortality was increased by 26% in patients aged above 18 years. Furthermore, the risk of death was increased by 14% among mechanically ventilated patients relative to non-ventilated ICU patients.

3.4. Antibiotic Susceptibility of S. maltophilia Isolates

The antimicrobial susceptibility testing (AST) of S. maltophilia isolates from the 393 patients is illustrated in Figure 1. S. maltophilia susceptibility to TMP/SMX was the highest (95.9%), followed by levofloxacin (68.9%) and ceftazidime (33.1%). Therefore, the isolates showed higher resistance to ceftazidime (62.1%) than to levofloxacin (14.8%) and TMP/SMX (4.1%).

3.5. S. maltophilia Infection before and during COVID-19 Pandemic

The trends of S. maltophilia infections before and during the COVID-19 pandemic were investigated among ICU and non-ICU patients. As detailed in Table 5, before and during the COVID-19 pandemic, the frequency of positive respiratory cultures isolated from ICU patients was consistently higher than non-ICU patients (p < 0.0001) over a three year period (2019, 2020, and 2021). On the contrary, the number of S. maltophilia isolates from non-respiratory specimens was higher among non-ICU patients compared to ICU patients before and during the COVID-19 pandemic. Furthermore, the frequency of bloodstream infections increased consistently, especially among non-ICU patients, at 17.7%, 27.9%, and 31.2% in 2019, 2020, and 2021, respectively.

4. Discussion

S. maltophilia is commonly circulated in natural environments such as water and soil. This bacterium can also be present in hospital environments, which may result in nosocomial infections. Unfortunately, the detection of S. maltophilia in ICUs has increased over the past few years, which has raised concerns that urge an in-depth study of the risk factors associated with this pathogen in ICUs. To our knowledge, there were no studies performed in Saudi Arabia concerning S. maltophilia clinical isolates before and during the COVID-19 era, and no studies have considered both adult and pediatric patients.
Our study included 393 isolates of S. maltophilia collected from January 2019 to December 2021 at KFMC. The isolates were collected from different sites, but most were from respiratory, followed by blood, and more than half of the specimens were obtained from ICU patients. These findings are not surprising, as a study that was performed in KKUH in Riyadh (2012) also reported that S. maltophilia mainly causes respiratory infections and is predominantly isolated from ICU patients [12].
Our study revealed that the numbers of S. maltophilia isolates before and during the COVID-19 pandemic have not changed significantly in both the ICU and non-ICU patients (Table 5). One reason for this is that during the pandemic, most of the non-urgent surgeries were canceled, therefore the number of patients admitted was reduced to allow beds to be available for COVID-19 cases. Moreover, the infection control measures that were taken in hospitals during the COVID-19 era may affect the rate of nosocomial infections caused by S. maltophilia. Our study showed that the severity of S. maltophilia and the risk of developing co-infections is more in adult patients compared with pediatric patients. To our knowledge, there were no previous studies that compared adults to children in terms of severity; most studies of S. maltophilia in Saudi Arabia focused on pediatrics [13,14].
The results presented herein indicate that respiratory infections of S. maltophilia are the highest among other types of infections (Table 5), which is consistent with what was reported in the previous study [15]. This might be due to the ability of S. maltophilia to form biofilms and colonize on the respiratory tracts of hospitalized patients [16]. The observed higher number of respiratory infections among ICU patients might be reflected using mechanical ventilation, which was reported previously as a risk factor for the development of an S. maltophilia respiratory infection [15].
The most common co-infections with S. maltophilia were found in this study to be gram-negative bacterial infections. Similarly, various studies have reported that the polymicrobial infection associated with S. maltophilia was caused by gram-negative bacteria [14,17]. Additionally, a recent study has reported the presence of S. maltophilia as a secondary bacterial infection in ICU-COVID-19 patients [18]. We found some clinical characteristics that were more significantly associated with adult ICU patients than pediatric ICU patients, such as fever, septic shock, and underlying conditions such as hypertension and diabetes mellitus. Our study reported the mortality rate among S. maltophilia ICU patients to be 44.4%, which is consistent with a study performed in KKUH in Riyadh [12]. Septic shock was the most significant predictor of mortality, which is in line with other studies that investigated S. maltophilia mortality risk factors [6], followed by septicemia, and then being above 18 years.
The relative risk of mortality among ICU patients with respiratory infections was investigated. Being on a mechanical ventilator and being over 18 years increased the risk of mortality by 14% and 26%, respectively. A recent metanalytic study has also identified a strong correlation between mechanical ventilators and S. maltophilia pneumonia in ICU patients [19]. Therefore, physicians are required to firmly follow the indications for invasive procedures and minimize unnecessary invasive procedures. Understanding the risk factors associated with S. maltophilia infections in the ICU and early targeted empirical treatment is crucial to reducing the mortality from S. maltophilia. The treatment of S. maltophilia is difficult, as this pathogen demonstrates high levels of intrinsic or acquired resistance to different antimicrobial agents, limiting the available options for treatment [6]. Our study showed that S. maltophilia isolates were mostly resistant to ceftazidime (62.1%), followed by levofloxacin (14.8%), and then TMP/SMX (4.1%). According to the study performed in KKUH in 2012, S. maltophilia isolates resistant to ceftazidime were (57.21%) and those resistant to TMP/SMX were (9.45%). These data indicate that ceftazidime resistance has increased, which is probably due to the extensive use of the antibiotic over the past few years, especially during the pandemic. Fortunately, TMP/SMX remained effective as empirical therapy for S. maltophilia infections, but resistance to this drug must be continuously monitored.
The study’s sample size included a range of diverse sample sources from various sites that identified the types of infections, which helped to clarify the sources of the S. maltophilia infections. Additionally, the large sample size from the ICU patients allowed us to draw very exact conclusions from the statistical analysis. However, the study’s main drawback is that it only used data from a single tertiary institution. A large-scale multicenter effective surveillance system in Riyadh and other cities in Saudi Arabia with a larger sample size is needed for a better understanding of the S. maltophilia threat.

5. Conclusions

S. maltophilia is an emerging pathogen causing a relatively high mortality rate in ICU patients. In the cases of respiratory infections, the fatality rate climbed to 47.1%. Septic shock was the most important predictor of death. In patients with respiratory infections, older age and mechanical ventilation were independent and substantial risk factors. Knowing the risk factors, whether they are related to the host and/or medical factors associated with S. maltophilia mortality, is the key to the monitoring, prevention, and control of the infections. This study will help physicians in assessing the risks of S. maltophilia infections in ICU patients and will enhance the management of high-risk groups.

Author Contributions

T.A.H. theorized and designed the study, reviewed the literature, acquired the data, and critically commented and wrote the original draft of the manuscript. S.S.A. contributed to the data analysis and interpreted the results. A.A. contributed to the study design, managed data collection, and analyzed the results. M.G.A. contributed to the study design, interpreted the results, performed critical revisions, and edited the final version of the manuscript. E.A. contributed to the design and discussion of the study. A.S.A. and M.A.M. contributed to the study design, managed data collection, and interpreted the results. All authors have read and agreed to the published version of the manuscript.

Funding

The Deputyship for Research & Innovation, Ministry of Education in Saudi Arabia for funding this research work through the project no. (IFKSURG-2-363).

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Institutional Review Board of King Fahad, Saudi Arabia.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Data available in the KFMC institute data system and could be available for public upon special request.

Acknowledgments

The authors would like to thank the Deputyship for Research & Innovation, Ministry of Education in Saudi Arabia for funding this research work through the project No. (IFKSURG-2-363) and the Deanship of Scientific Research, King Saud University for support. The authors also express their appreciation to the Microbiology Department at King Fahad Medical City in Riyadh for facilitating the data collection process and to Abeer AlMazyed, who contributed to data collection.

Conflicts of Interest

All authors declare that they have no competing interest.

References

  1. Adegoke, A.A.; Stenström, T.A.; Okoh, A.I. Stenotrophomonas maltophilia as an Emerging Ubiquitous Pathogen: Looking Beyond Contemporary Antibiotic Therapy. Front. Microbiol. 2017, 8, 2276. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Sánchez, M.B. Antibiotic resistance in the opportunistic pathogen Stenotrophomonas maltophilia. Front. Microbiol. 2015, 6, 658. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Geller, M.; Nunes, C.P.; Oliveira, L.; Nigri, R.S. maltophilia pneumonia: A case report. Respir. Med. Case Rep. 2018, 24, 44–45. [Google Scholar] [CrossRef] [PubMed]
  4. Rajkumari, N.; Mathur, P.; Gupta, A.K.; Sharma, K.; Misra, M.C. Epidemiology and outcomes of Stenotrophomonas maltophilia and Burkholderia cepacia infections among trauma patients of India: A five year experience. J. Infect. Prev. 2015, 16, 103–110. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Gajdács, M.; Urbán, E. Prevalence and Antibiotic Resistance of Stenotrophomonas maltophilia in Respiratory Tract Samples: A 10-Year Epidemiological Snapshot. Health Serv. Res. Manag. Epidemiol. 2019, 6, 2333392819870774. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Brooke, J.S. Stenotrophomonas maltophilia: An Emerging Global Opportunistic Pathogen. Clin. Microbiol. Rev. 2012, 25, 2–41. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Singhal, L.; Kaur, P.; Gautam, V. Stenotrophomonas maltophilia: From trivial to grievous. Indian J. Med. Microbiol. 2017, 35, 469–479. [Google Scholar] [CrossRef] [PubMed]
  8. Çıkman, A.; Parlak, M.; Bayram, Y.; Güdücüoğlu, H.; Berktaş, M. Antibiotics resistance of Stenotrophomonas maltophilia strains isolated from various clinical specimens. Afr. Health Sci. 2016, 16, 149–152. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  9. Brooke, J.S. New strategies against Stenotrophomonas maltophilia: A serious worldwide intrinsically drug-resistant opportunistic pathogen. Expert Rev. Anti-Infect. Ther. 2014, 12, 1–4. [Google Scholar] [CrossRef] [PubMed]
  10. Lai, C.C.; Chen, S.Y.; Ko, W.C.; Hsueh, P.R. Increased antimicrobial resistance during the COVID-19 pandemic. Int. J. Antimicrob. Agents 2021, 57, 106324. [Google Scholar] [CrossRef] [PubMed]
  11. Magiorakos, A.P.; Srinivasan, A.; Carey, R.B.; Carmeli, Y.; Falagas, M.E.; Giske, C.G.; Harbarth, S.; Hindler, J.F.; Kahlmeter, G.; Olsson-Liljequist, B.; et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: An international expert proposal for interim standard definitions for acquired resistance. Clin. Microbiol. Infect. 2012, 18, 268–281. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Naeem, T.; Absar, M.; Somily, A.M. Antibiotic resistance among clinical isolates of Stenotrophomonas maltophilia at a teaching hospital in Riyadh, Saudi Arabia. J. Ayub Med. Coll. Abbottabad 2012, 24, 30–33. [Google Scholar] [PubMed]
  13. Alqahtani, J.M. Emergence of Stenotrophomonas maltophilia nosocomial isolates in a Saudi children’s hospital: Risk factors and clinical characteristics. Saudi Med. J. 2017, 38, 521–527. [Google Scholar] [CrossRef] [PubMed]
  14. Alsuhaibani, M.; Aljarbou, A.; Althawadi, S.; Alsweed, A.; Al-Hajjar, S. Stenotrophomonas maltophilia bacteremia in children: Risk factors and mortality rate. Antimicrob. Resist. Infect. Control 2021, 10, 19. [Google Scholar] [CrossRef] [PubMed]
  15. Falagas, M.E.; Valkimadi, P.E.; Huang, Y.T.; Matthaiou, D.K.; Hsueh, P.R. Therapeutic options for Stenotrophomonas maltophilia infections beyond co-trimoxazole: A systematic review. J. Antimicrob. Chemother. 2008, 62, 889–894. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  16. Chawla, K.; Vishwanath, S.; Gupta, A. Stenotrophomonas maltophilia in lower respiratory tract infections. J. Clin. Diagn. Res. 2014, 8, DC20–DC22. [Google Scholar] [CrossRef] [PubMed]
  17. Sattler, C.A.; Mason, E.O.; Kaplan, S.L. Nonrespiratory Stenotrophomonas maltophilia infection at a children’s hospital. Clin. Infect. Dis. 2000, 31, 1321–1330. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  18. Chong, W.H.; Saha, B.K.; Ramani, A.; Chopra, A. State-of-the-art review of secondary pulmonary infections in patients with COVID-19 pneumonia. Infection 2021, 49, 591–605. [Google Scholar] [CrossRef] [PubMed]
  19. Wang, N.; Tang, C.; Wang, L. Risk Factors for Acquired Stenotrophomonas maltophilia Pneumonia in Intensive Care Unit: A Systematic Review and Meta-Analysis. Front. Med. 2022, 8, 808391. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Antibiotic susceptibility of S. maltophilia isolates (n = 393).
Figure 1. Antibiotic susceptibility of S. maltophilia isolates (n = 393).
Microorganisms 10 02506 g001
Table 1. Demographic characteristics of patients with S. maltophilia infections.
Table 1. Demographic characteristics of patients with S. maltophilia infections.
CharacteristicPatients, n = 393
Gender, n (%)
Male231 (58.8)
Female162 (41.2)
Age group, n (%)
Infants < 1 y59 (15)
Children 1–10 y40 (10.2)
Adolescents 11–18 y15 (3.8)
Adults 19–44 y65 (16.5)
Adults 45–64 y95 (24.2)
Adults 65–84 y101 (25.7)
Adults > 85 y18 (4.6)
Specimen source, n (%)
Respiratory257 (65.4)
Blood68 (17.3)
Urine35 (8.9)
Miscellaneous 133 (8.4)
Type of ward/clinic (%)
ICU 2209 (53.2)
ER 334 (8.7)
OPC 423 (5.8)
Wards127 (32.3)
Note: Data are presented as number of patients (n) with the corresponding percentage in parentheses (%). 1 Miscellaneous samples were abscess, wound, tissue, body fluid, and device; 2 ICU, Intensive Care Unit; 3 ER, Emergency; 4 OPC, Outpatient Clinic.
Table 2. Comparison of clinical characteristics of adult and pediatric ICU patients with S. maltophilia infections.
Table 2. Comparison of clinical characteristics of adult and pediatric ICU patients with S. maltophilia infections.
CharacteristicAdult Patients,
>18 Y (n = 140)
Pediatric Patients,
≤18 Y (n = 69)
p Value
Mortality, n (%)72 (51.4)21 (30.3)0.0049 **
Clinical presentation, n (%)
Fever60 (42.9)18 (26.1)0.0224 *
Septicemia38 (27.1)10 (14.5)0.0780
Septic shock52 (37. 1)10 (14.5)0.0007 ***
Bacteremia40 (28.0)18 (27.3)>0.9999
GIT 1 symptoms56 (40.0)21 (30.4)0.2226
WI 228 (20. 0)10 (14.5)0.4458
UTI 341 (29.3)7 (10.1)0.0016 **
Respiratory symptoms99 (70. 7)37 (53.6)0.0203 *
Co-infection81 (57.9)25 (36.2)0.0050 **
Underlying disease, n (%)
Diabetes mellitus66 (47.1)12 (17.4)<0.0001 ****
Hypertension60 (42.9)13 (18.9)0.0006 ***
Malignancy23 (16.4)5 (7.3)0.0841
Kidney illnesses41 (29.3)11 (16.0)0.0414 *
Risk factors, n (%)
Mechanical ventilation132 (94.3)49 (71.0)<0.0001 ****
Recent antibiotic exposure25 (17.7)4 (5.8)0.0189 *
Dialysis20 (14.3)5 (7.3)0.1763
Note: Univariant analysis (Fisher’s exact test; p ≤ 0.05). The statistical significance differences between adult and pediatric patients are indicated by a (*) symbol and the number of * represent the strength of the significance difference. Data are presented as number of patients (n) with the corresponding percentage in parentheses (%). 1 GIT, Gastrointestinal Tract; 2 WI, Wound Infection; 3 UTI, Urinary Tract Infection.
Table 3. Univariate analysis for factors associated with mortality of ICU patients with Stenotrophomonas maltophilia infections.
Table 3. Univariate analysis for factors associated with mortality of ICU patients with Stenotrophomonas maltophilia infections.
FactorOutcome
Dead, n = 93Resolved, n = 116p Value
Age above 18 y, n (%)
Yes72 (77.4)68 (58.6)0.0049 **
No21 (22.6)48 (41.4)
Positive respiratory culture, n (%)
Yes81 (87.1)91 (78.5)0.1440
No12 (12. 9)25 (21.6)
Septicemia, n (%)
Yes28 (30.1)20 (17.2)0.0321 *
No65 (69.9)96 (82.8)
Septic shock, n (%)
Yes42 (45.2)20 (17.2)<0.0001 ****
No51 (54.8)96 (82.8)
Malignancy, n (%)
Yes17 (18.3)11 (9.5)0.0694
No76 (81.7)105 (90.5)
Prior use of carbapenem or other antimicrobials in the past 30 days, n (%)
Yes17 (18.3)12 (10.3)0.1106
No76 (81.7)104 (89.7)
Mechanical ventilation, n (%)
Yes85 (91.4)96 (82.8)0.1009
No8 (8.6)20 (17.2)
Note: Univariant analysis (Fisher’s exact test; p ≤ 0.05). The statistical significance differences between dead and resolved patients are indicated by a (*) symbol and the number of * represent the strength of significance difference. Data are presented as number of patients (n) with the corresponding percentage in parentheses (%).
Table 4. Risk factors and relative risk of mortality among ICU patients with S. maltophilia respiratory infections.
Table 4. Risk factors and relative risk of mortality among ICU patients with S. maltophilia respiratory infections.
VariableRRCI 95%p Value
Antibiotic pre-exposure1.7480.817 to 3.7650.1818
Mechanical ventilation1.1381.020 to 1.2900.0340 *
Co-infection1.2640.934 to 1.7180.1690
Bacteremia1.1230.677 to 1.8620.7272
Age above 18 y1.2641.036 to 1.5570.0310 *
Total S. maltophilia respiratory positive culture (n = 172). The statistical significance, p ≤ 0.05 indicated by a (*).
Table 5. Comparison between ICU and Non-ICU patients with S. maltophilia infections.
Table 5. Comparison between ICU and Non-ICU patients with S. maltophilia infections.
CharacteristicICU Patients,
n = 209
Non-ICU Patients,
n =184
p Value
Year of 2019n = 68n = 62
Source of sample
Respiratory56 (82.4)24 (38.7)<0.0001 ****
Blood5 (7.4)11 (17.7)0.1075
Urine4 (5. 9)15 (24.2)0.0052 **
Miscellaneous3 (4.4)12 19.4)0.0116 *
Year of 2020n = 68n = 61
Source of sample
Respiratory58 (85.3)31 (34.8)<0.0001 ****
Blood6 (8.8)17 (27.9)0.0057 **
Urine0 (0)9 (14.8)0.0008 ***
Miscellaneous4 (5.9)4 (6.56)>0.9999
Year of 2021n = 73n = 61
Source of sample
Respiratory59 (80.8)29 (47.5)<0.0001 ****
Blood10 (13.7)19 (31.2)0.0200 *
Urine2 (2.7)5 (8.2)0.2448
Miscellaneous2 (2.7)8 (13.1)0.0429 *
Note: Univariant analysis (Fisher’s exact test; p ≤ 0.05). The statistical significance differences between ICU and Non-ICU patients during the study period are indicated by a (*) symbol and the number of * represent the strength of significance difference. Data are presented as number of patients (n) with the corresponding percentage in parentheses (%).
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Hafiz, T.A.; Aldawood, E.; Albloshi, A.; Alghamdi, S.S.; Mubaraki, M.A.; Alyami, A.S.; Aldriwesh, M.G. Stenotrophomonas maltophilia Epidemiology, Resistance Characteristics, and Clinical Outcomes: Understanding of the Recent Three Years’ Trends. Microorganisms 2022, 10, 2506. https://doi.org/10.3390/microorganisms10122506

AMA Style

Hafiz TA, Aldawood E, Albloshi A, Alghamdi SS, Mubaraki MA, Alyami AS, Aldriwesh MG. Stenotrophomonas maltophilia Epidemiology, Resistance Characteristics, and Clinical Outcomes: Understanding of the Recent Three Years’ Trends. Microorganisms. 2022; 10(12):2506. https://doi.org/10.3390/microorganisms10122506

Chicago/Turabian Style

Hafiz, Taghreed A., Esraa Aldawood, Alaa Albloshi, Shahad S. Alghamdi, Murad A. Mubaraki, Ahmed S. Alyami, and Marwh G. Aldriwesh. 2022. "Stenotrophomonas maltophilia Epidemiology, Resistance Characteristics, and Clinical Outcomes: Understanding of the Recent Three Years’ Trends" Microorganisms 10, no. 12: 2506. https://doi.org/10.3390/microorganisms10122506

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop