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BACKGROUND : Urinary tract infections (UTIs) are a common disease with a high burden on the healthcare industry. A systematic exploration is necessary of the organisms that cause UTIs, to improve empirical management of patients with acute illness before culture results are obtained. The prevalence of these organisms, both in immunocompetent and immunocompromised patients in Saudi Arabia, needs further clarification.
METHODS: This is a cross-sectional analysis reviewing the charts of patients visiting the emergency department of, and those admitted to, a tertiary hospital in Saudi Arabia during the month of July-August 2021.
RESULT : The total number of participants was 199, with a mean age of 55.8 years (SD=20.02), ranging from 14 to 97 years. 61.8% of patients were immunocompromised, and one-third were from the oncology wards. 40.7% (n=81) were diabetics and 8.54% (n=17) had CKD/ESRD. Females were 25% more likely than males to acquire Candida infections, while Pseudomonas aeruginosa was 26.7% more prevalent in males. Nevertheless, mixed gram-negative bacteria caused the most UTIs, in 40.20% (n=80) of cases, followed by Candida , 16.1% (n=32), and then mixed gram-positive bacteria, in 14.57% (n=29). This was also observed among immunocompromised patients and the subsegment of oncology patients on active chemotherapy, although with variable percentages.
CONCLUSION: This study demonstrates that patients’ immune status is the main determinant of the causative organism of UTIs. The treatment threshold for Candida in diabetic patients and those with CKD/ESRD should be lower, especially when they require admission.
Keywords: Urinary tract infection, Urine culture
Urinary tract infections (UTIs) are a common disease, accounting for 20-25% of all infections and representing 150 million diagnosed cases annually [1-3]. The incidence of such infections differs in relation to age and gender. In adult women, for instance, the lifetime incidence of UTI is greater than 50% [2], while urosepsis is the second-most common cause of sepsis among the elderly popu- lation [4,5]. It has been estimated that UTIs cost approximately $800,000 annually in a local study [6]. As such, the burden of the disease and its relatively high prevalence mandate revisiting this infection and exploring it in greater depth.
There are several predispositions to the develop- ment of UTI beyond the anatomical and physiolog- ical factors, including sexual activity, immunosup- pression, and the use of Foley catheters. Therapeutic use of Foley catheters, for instance, increases the risk for UTI by 10% for every day the catheter is in situ [7,8]. Meanwhile, immunosuppression promotes the development of UTI due to the loss of the body’s defense system [9]. This is seen among people with diabetes, chronic kidney disease, organ transplants, and patients on active chemotherapy. Those with diabetes appear to be affected more than the others. In Saudi Arabia, for example, the prevalence of UTI is around one quarter in those with diabetes mellitus [10], making it the most prevalent infection in this cohort [11,12].
Furthermore, the organisms that cause UTI vary depending on the patients’ comorbidities, previous infections, the use of Foley catheters and instrumen- tation, and prior surgeries. Classically, Escherichia coli is the most common organism, followed by Klebsiella pneumoniae [13,14]. The former remains the most common irrespective of whether the patient is immunocompromised or immunocompetent [9]. In addition, other organisms, including Enterococ- cus species, Candida, Staphylococcus aureus, Pro- teus mirabilis, Pseudomonas aeruginosa, and group B Streptococcus (GBS), were also cultured [13].
The prevalence of these organisms in immuno- competent and immunocompromised patients in Saudi Arabia needs further elucidation. Further- more, an updated exploration of the topic is neces- sary, primarily for physicians working under acute conditions who treat patients empirically before obtaining culture results. We therefore aim, in this study, to explore the organisms causing UTI in emergency patients and inpatients of a tertiary hospital in Saudi Arabia. In addition, we aim to determine whether the type of organism causing the UTI can be predicted on the basis of the patient’s demographic or immune status.
This is a cross-sectional analysis reviewing the charts of patients visiting the emergency department and those admitted during the month of July-August 2021. We tracked patients from the E.D., inpatients in the internal medicine and oncology wards, and those in the intensive care unit. Our sample was selected from a large tertiary hospital in the capital of Saudi Arabia, with a capacity of 1,200 beds.
We estimated a sample size of 200 patients us- ing Raosoft@ online sample size calculator (95% Confidence interval and 6.33% margin of error). Using only information from the medical records, we obtained the demographic details, urine cul- ture method, and whether a clean catch or via a Foley catheter. We also noted any comorbidities, and whether the patient was known to have cancer and was on chemotherapy. Patients were labelled as immunocompromised if they had diabetes, chronic kidney disease/end-stage renal disease, or were on active chemotherapy.
In our analysis, we used the mean and the stan- dard deviation to report the patients’ age, and used proportions to register other demographic details. We used Fisher’s exact test to explore the presence of a nonrandom association between the organisms causing UTI and the patients’ demographics or immune status. We used STATA ® to analyse the results, with a p<0.05 threshold for statistically significant findings. The IRB board approves this study, with IRB registration number 00010471
Demographics: The total number of participants was 199. The mean age of the patients was 55.8 years (SD=20.02), ranging from 14 to 97 years. The patients’ demo- graphic details are illustrated in Table 1. 61.8% of the patients were immunocompromised, and one- third were from the oncology wards. 40.7% (n=81) were diabetic, and 8.54% (n=17) had chronic kidney disease or end-stage renal disease. Most of the urine samples were obtained via clean catch, with 12% via a Foley catheter.
Organisms causing UTI: Most UTIs were caused by mixed gram-negative bacteria, as seen in 40.20% (n=80) of the sample, followed by Candida, in 16.1% (n=32), and then mixed gram-positive bacteria, in 14.57% (n=29). Escherichia coli was cultured in 7.04% (n=14) of the patients. Other organisms are illustrated in Table 2. In oncology patients, the most common organisms causing UTI were mixed gram-negative bacteria, in 45.8% (n=22) of patients, followed by Candida and mixed gram-positive bacteria, both seen in 12.5% (n=6). The proportions of the various organisms in oncology patients are illustrated in Table 3.
Similarly, the most common organisms among immunocompromised patients were mixed gram- negative bacteria, representing 42.3% (n=52) of total infections in this patient cohort. Candida caused 21.1% (n=26) of UTI in this stratum, followed by mixed gram-positive bacteria, at 12.2% (n=15). Table 4 illustrates the prevalence of these organisms according to a subgroup analysis of immunocom- promised and immunocompetent patients.
This study demonstrates that patients’ immune status is the main determinant of the causative organism of UTIs. As such, the treatment threshold for Candida in diabetic patients and those with CKD/ESRD should be lower, especially when they require admission. Emergency physicians should provide antibiotics that cover gram-negative bacteria for patients in general, Candida for immunocom- promised patients, and gram-positive bacteria for immunocompetent patients.
| Demographics | Proportion % (n) |
|---|---|
| Gender | |
| Male | 43.72 (87) |
| Female | 56.28 (112) |
| Oncology patients | 24.12 (48) |
| Diabetics | 40.7 (81) |
| CKD/ESRD | 8.54 (17) |
| Source of urine sample | |
| Clean catch | 80.90 (161) |
| Foley catheter | 12.06 (24) |
| Health status | |
| Immunocompetent | 36.68 (73) |
| Immunocompromised | 61.81 (123) |
| Chronic kidney disease; ESRD: | End-stage renal disease |
| Organism(s) | Proportion % (n) |
|---|---|
| Candida | 16.08 (32) |
| Enterobacter cloacae | 1.01 (2) |
| Enterobacter faecalis | 1.01 (2) |
| Escherichia coli | 7.04 (14) |
| Klebsiella pneumoniae | 4.02 (8) |
| Mixed gram-negative bacteria | 40.20 (80) |
| Mixed gram-negative and positive bacteria | 7.54 (15) |
| Mixed gram-negative bacteria and yeast | 3.02 (6 ) |
| Mixed gram-positive bacteria | 14.57 (29) |
| Proteus mirabilis | 2.51 (5) |
| Pseudomonas aeruginosa | 3.02 (6) |
| Organism(s) | Oncology patient | % (n) Non-oncology patients % (n) |
|---|---|---|
| Candida | 12.5 (6) | 17.6 (26) |
| Enterobacter cloacae | 0 | 1.4 (2) |
| Enterobacter faecalis | 4.2 (2) | 0 |
| Escherichia coli | 8.3 (4) | 6.8 (10) |
| Klebsiella pneumonia | 8.3 (4) | 2.7 (4) |
| Mixed gram-negative bacteria | 45.8 (22) | 37.8 (56) |
| Mixed gram-negative and positive bacteria | 6.3 (3) | 8.1 (12) |
| Mixed gram-negative bacteria and yeast | 0 | 4.1 (6) |
| Mixed gram-positive bacteria | 12.5 (6) | 14.8 (22) |
| Proteus mirabilis | 0 | 3.4 (5) |
| Pseudomonas aeruginosa | 2.1 (1) | 3.4 (5) |
| Total | 100 (48) | 100 (148) |
| Organism(s) Immunocompromised | % (n) Immunocompetent % (n) |
|---|---|
| Candida and other yeast 21.1 (26) | 8.2 (6) |
| Enterobacter cloacae 0 | 2.7 (2) |
| Enterobacter faecalis 1.6 (2) | 0 |
| Escherichia coli 7.3 (9) | 6.8 (5) |
| Klebsiella pneumonia 4.1 (5) | 4.1 (3) |
| Mixed gram-negative bacteria 42.3 (52) | 35.6 (26) |
| Mixed gram-negative and positive bacteria 7.3 (9) | 8.2 (6) |
| Mixed gram-negative bacteria and yeast 1.6 (2) | 5.5 (4) |
| Mixed gram-positive bacteria 12.2 (15) | 17.8 (13) |
| Proteus mirabilis 0.8 (1) | 5.5 (4) |
| Pseudomonas aeruginosa 1.6 (2) | 5.5 (4) |
| Total 100 (123) | 100 (73) |
| Age and urine organisms: | cloacae was only cultured from non-oncology pa- |
| Non-parametric analysis was conducted to explore | tients, while none of this cohort had Enterobacter |
| the association between age and the organism cul- | faecalis. However, the difference was not statisti- |
| tured from the urine. We were unable to uncover a | cally significant, p=0.23. |
| significant association; p=0.07. | |
| Foley catheters and urine organisms: | |
| Gender and urine organisms: | Urine samples obtained using Foley catheters did |
| We used Fisher’s exact test to determine the asso- | not differ significantly from clean catch samples |
| ciation between patients’ gender and the cultured | with regard to the organism implicated; X2=9.93, |
| organism, p=0.049. We noted that females were | p=0.54. |
| more likely to acquire Candida infection than males, | |
| with a difference of 25%. Pseudomonas aeruginosa | IV. DISCUSSION |
| was 26.7% more in males. Furthermore, females | It is crucial to explore the prevalence of the |
| were more likely to acquire Escherichia coli and | causative organisms for UTIs within the different |
| Klebsiella, with a difference of 25.7% and 25% | geographic regions. In our analysis, mixed gram- |
| respectively. Enterobacter faecalis was only seen in | negative bacteria were far more common than Es- |
| females. Mixed gram-negative bacteria were more | cherichia coli. Indeed, this emerges as the most |
| in males, with a 25% difference. | common cause among patients admitted with UTI, |
| in general and for those with diabetes, CKD/ESRD, | |
| Immune status and urine organisms: | and oncology patients on active treatment. These |
| The patients’ immune status also revealed an as- | findings are distinct and incongruent with other |
| sociation with the cultured organisms using Fisher’s | studies in which E. coli was the most prevalent |
| exact test. Immunocompromised patients were more | uropathogen, followed by Klebsiella and Staphylo- |
| likely than their immunocompetent counterparts to | coccus [15-18]. |
| have Candida, with a difference of 51.25%. Mixed | Candida was observed among diabetic and |
| gram-negative bacteria were also common among | CKD/ESRD patients, and less among oncology |
| the former segment, seen in 50.7%. Enterobacter | patients. Our sample revealed a total of 32 pa- |
| faecalis was only cultured from immunocompro- | tients with Candida in their urine culture, repre- |
| mised patients, whereas Enterobacter cloacae was | senting 16.08% of all UTIs in this sample. Only |
| only seen in the immunocompetent; p=0.031. | six patients were oncology patients, representing |
| Fisher’s exact test was also used to analyse the | 12.5%, whereas the prevalence of Candida increased |
| difference between organisms causing UTI in on- | to 21.1% (n=26) when we included diabetic and |
| cology patients versus those seen in non-oncology | CKD/ESRD patients It is also important to note |
| Candida’s prevalence among immunocompetent pa- | [4] Martín S, Pérez A, Aldecoa C. Sepsis and |
| tients in our sample was 8.2% (n=6), indicating that | Immunosenescence in the Elderly Patient: A Re- |
| there is still a high infection burden among the | view. Front Med (Lausanne). 2017 Feb 28;4:20. doi: |
| immunocompetent. Nevertheless, immunocom- | 10.3389/fmed.2017.00020. PMID: 28293557; |
| promised patients are prone to invasive candidiasis | PMCID: PMC5329014. |
| [19], which should be considered when managing | [5] Mayr FB, Yende S, Angus DC. Epidemiology |
| critically ill patients. | of severe sepsis. Virulence. 2014 Jan 1;5(1):4-11. |
| Mixed gram-positive bacteria were seen more | doi: 10.4161/viru.27372. Epub 2013 Dec 11. PMID: |
| among immunocompetent and non-oncology pa- | 24335434; PMCID: PMC3916382. |
| tients. Whether this bacterium needs to be covered | [6] Alanazi MQ. An evaluation of community- |
| empirically with antibiotics in the E.D. requires | acquired urinary tract infection and appropriateness |
| further analysis. | of treatment in an emergency department in Saudi |
| It is prudent to assert that our study examined | Arabia. Ther Clin Risk Manag. 2018;14:2363–2373. |
| patients in the E.D., those admitted to various wards, | doi:10.2147/tcrm.S178855 |
| and in the ICU. Therefore, patients discharged be- | [7] Lo E, Nicolle LE, Coffin SE, Gould C, |
| yond the E.D. might not be represented appropri- | Maragakis LL, Meddings J, Pegues DA, Pet- |
| ately. This might suggest a sampling bias, as more | tis AM, Saint S, Yokoe DS. Strategies to pre- |
| severe UTI is represented in our sample than in | vent catheter-associated urinary tract infections in |
| those treated and discharged. Further analysis of | acute care hospitals: 2014 update. Infect Con- |
| discharged patients is needed. | trol Hosp Epidemiol. 2014 May;35(5):464-79. doi: |
| 10.1086/675718. PMID: 24709715. |