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Research Article | Volume 10 Issue 2 (July-December, 2024) | Pages 317 - 321
A prospective study on Microbiological profile and susceptibility pattern of uropathogens at tertiary care hospital
 ,
 ,
1
Associate Professor, Department of Microbiology, Dr Patnam Mahender Reddy Institute of Medical Sciences, Chevella
2
Post graduate Microbiology Dr Patnam Mahender Reddy Institute of Medical Sciences
3
Assistant Professor, Department of Microbiology, Dr Patnam Mahender Reddy Institute of Medical Sciences
Under a Creative Commons license
Open Access
Received
Nov. 2, 2024
Revised
Nov. 18, 2024
Accepted
Nov. 30, 2024
Published
Dec. 30, 2024
Abstract

Introduction Urinary tract infections (UTIs) are a significant public health concern globally, affecting millions of individuals annually. They rank among the most common bacterial infections, especially in women, the elderly, and patients with underlying conditions. UTIs are primarily caused by uropathogenic microorganisms that invade the urinary tract, leading to clinical manifestations ranging from asymptomatic bacteriuria to severe pyelonephritis. The increasing prevalence of antimicrobial resistance (AMR) among uropathogens is a major challenge in clinical management. Resistance to first-line antibiotics, including fluoroquinolones and beta-lactams, has been reported worldwide, necessitating a reevaluation of empirical treatment protocols.  Material and Methods: This cross-sectional study was conducted over six months at a tertiary care hospital. A total of 90 patients with clinical symptoms of UTI were enrolled. Informed consent was obtained from all participants, and ethical approval was secured from the institutional ethics committee. Midstream urine samples were collected under sterile conditions from each participant. Samples were transported to the microbiology laboratory within two hours of collection. Results: Escherichia coli was the predominant pathogen (65%), followed by Klebsiella pneumoniae (15%), Proteus mirabilis (10%), and others (10%). High resistance rates to commonly used antibiotics such as ampicillin and ciprofloxacin were observed, while carbapenems and nitrofurantoin showed better efficacy. Our findings emphasize the importance of routine susceptibility testing to guide empirical treatment and combat antimicrobial resistance. The high prevalence of multidrug-resistant (MDR) and extended-spectrum beta-lactamase (ESBL) producing strains underscores the critical need for judicious antibiotic use. Routine screening for these resistance mechanisms should be integrated into diagnostic protocols. Conclusion:  This study highlights the microbiological profile and antimicrobial susceptibility patterns of uropathogens in a tertiary care setting. Routine surveillance of resistance patterns is critical for optimizing UTI management and curbing the AMR crisis.

Keywords
INTRODUCTION

Urinary tract infections (UTIs) are a significant public health concern globally, affecting millions of individuals annually. They rank among the most common bacterial infections, especially in women, the elderly, and patients with underlying conditions. [1] UTIs are primarily caused by uropathogenic microorganisms that invade the urinary tract, leading to clinical manifestations ranging from asymptomatic bacteriuria to severe pyelonephritis. [2] 

The increasing prevalence of antimicrobial resistance (AMR) among uropathogens is a major challenge in clinical management. [3] Resistance to first-line antibiotics, including fluoroquinolones and beta-lactams, has been reported worldwide, necessitating a reevaluation of empirical treatment protocols. [4]

 

UTIs are predominantly caused by Gram-negative bacteria, with Escherichia coli being the leading pathogen. [5] Other commonly implicated organisms include Klebsiella pneumoniae, Proteus species, Enterococcus species, and Pseudomonas aeruginosa. The epidemiology of UTIs varies with patient demographics, healthcare settings, and local antimicrobial stewardship practices. [6]

 

Accurate identification of uropathogens and their susceptibility patterns is crucial for selecting effective empirical therapy and reducing treatment failure. Inappropriate antibiotic use contributes to the emergence of multidrug-resistant organisms, further complicating UTI management. This study investigates the microbiological profile of uropathogens and their antimicrobial susceptibility patterns, providing insights to inform clinical decision-making.

MATERIALS AND METHODS

This cross-sectional study was conducted over six months at a tertiary care hospital. A total of 90 patients with clinical symptoms of UTI were enrolled. Informed consent was obtained from all participants, and ethical approval was secured from the institutional ethics committee.

 

Sample Collection Midstream urine samples were collected under sterile conditions from each participant. Samples were transported to the microbiology laboratory within two hours of collection.

 

Laboratory Procedures

  1. Microscopic Examination: Urine samples were examined for pus cells and bacteria using wet mount and Gram staining.
  2. Culture and Identification: Samples were cultured on MacConkey agar, blood agar, and CLED agar. Plates were incubated at 37°C for 24-48 hours. Colony morphology, Gram staining, and biochemical tests were used for identification.
  3. Antimicrobial Susceptibility Testing (AST): AST was performed using the Kirby-Bauer disk diffusion method on Mueller-Hinton agar. Results were interpreted according to CLSI guidelines.

 

Data Analysis

Data were analyzed using descriptive statistics. The frequency and percentage of isolated pathogens and their susceptibility to various antibiotics were calculated. Chi-square tests were used to assess associations between resistance patterns and clinical variables.

 

RESULTS

Table 1: Distribution of Patient Demographics

Parameter

Frequency (%)

Age range (18-30)

35

Age range (31-50)

40

Age range (51-75)

25

Female

65

Male

35

 

Table 2: Microbiological Profile

Pathogen

Frequency (%)

Escherichia coli

65

Klebsiella pneumoniae

15

Proteus mirabilis

10

Pseudomonas aeruginosa

5

Enterococcus faecalis

5

In table 3, Escherichia coli was the predominant pathogen (65%), followed by Klebsiella pneumoniae (15%), Proteus mirabilis (10%), and others (10%). Escherichia coli emerged as the dominant uropathogen, consistent with global trends, indicating its significant role in UTI pathogenesis. Other pathogens, such as Klebsiella pneumoniae and Proteus mirabilis, accounted for smaller proportions but may represent nosocomial or recurrent infections.

 

Table 3: Antimicrobial Susceptibility of Escherichia coli

Antibiotic

Susceptibility (%)

Ampicillin

20

Ciprofloxacin

35

Nitrofurantoin

85

Carbapenems

95

In table 4, Escherichia coli showed high resistance to commonly prescribed antibiotics like ampicillin and ciprofloxacin, reflecting their overuse. Nitrofurantoin and carbapenems exhibited superior efficacy, underlining their suitability for empirical treatment.

 

Table 4: Antimicrobial Susceptibility of Klebsiella pneumoniae

Antibiotic

Susceptibility (%)

Ampicillin

25

Ciprofloxacin

40

Nitrofurantoin

70

Carbapenems

90

Klebsiella pneumoniae exhibited moderate resistance to ciprofloxacin and ampicillin. The higher susceptibility to carbapenems emphasizes their role in managing resistant infections. Nitrofurantoin remains effective but less so compared to Escherichia coli in table 4.

 

Table 5: Multidrug Resistance

Resistance Type

Frequency (%)

MDR Strains

45

ESBL Producers

30

The high prevalence of multidrug-resistant (MDR) and extended-spectrum beta-lactamase (ESBL) producing strains underscores the critical need for judicious antibiotic use. Routine screening for these resistance mechanisms should be integrated into diagnostic protocols in table 5.

 

Table 6: Clinical Characteristics and Outcomes

Clinical Feature

Frequency (%)

Recurrent UTIs

30

Severe UTI (Hospitalized)

15

Complicated UTIs

25

Uncomplicated UTIs

70

DISCUSSION

The findings of this study provide critical insights into the microbiological and susceptibility profiles of uropathogens in a tertiary care setting, reflecting both global trends and localized resistance patterns.

Escherichia coli, accounting for 65% of isolates, reinforces its role as the most common uropathogen worldwide. This prevalence aligns with its ability to colonize the urinary tract due to virulence factors such as adhesins and toxins. [7] The predominance of E. coli highlights the importance of targeting this pathogen in empirical UTI management. [8,9]

 

The study reveals concerning resistance trends. E. coli showed high resistance to ampicillin (80%) and ciprofloxacin (65%), which are often prescribed for UTIs. These findings are consistent with global reports linking widespread antibiotic misuse to resistance. [10] On the contrary, carbapenems and nitrofurantoin exhibited excellent activity against E. coli, with susceptibility rates of 95% and 85%, respectively. Nitrofurantoin’s efficacy underscores its continued relevance in treating uncomplicated UTIs, particularly given its low systemic absorption and urinary tract-specific action. [11]

 

Klebsiella pneumoniae and Proteus mirabilis, while less prevalent, displayed substantial resistance to first-line agents. The 30% ESBL production rate among isolates further complicates treatment, emphasizing the need for carbapenems in severe cases. [12] Proteus mirabilis’ intrinsic resistance to nitrofurantoin underscores the necessity of species-level identification to optimize therapy. [13,14]

 

The high prevalence of MDR strains (45%) and ESBL producers (30%) is alarming. These pathogens complicate clinical management and increase the risk of treatment failure. [15] The findings underscore the need for routine ESBL screening and judicious antibiotic stewardship programs to curb the spread of resistant strains. [16]

 

Empirical therapy for UTIs should consider local resistance patterns. For uncomplicated cases, nitrofurantoin remains a first-line option, while carbapenems should be reserved for resistant infections to minimize resistance development. [17] The high rate of recurrent and complicated UTIs (30% and 25%, respectively) further highlights the importance of tailored treatment strategies. [18] These results reflect global AMR trends while also highlighting the specific resistance dynamics within the study’s geographical region. Continued surveillance and collaboration with global AMR networks are crucial for formulating effective interventions. [19]

 

Future research should focus on multicentric studies to validate these findings and explore innovative therapeutic options, such as bacteriophage therapy or combination regimens, to combat resistant uropathogens. Additionally, public health initiatives to promote responsible antibiotic use and improve hygiene practices are essential.

CONCLUSION

This study highlights the microbiological profile and antimicrobial susceptibility patterns of uropathogens in a tertiary care setting. Routine surveillance of resistance patterns is critical for optimizing UTI management and curbing the AMR crisis.

REFERENCES
  1. Gupta, K., et al. (2017). International clinical practice guidelines for the treatment of acute uncomplicated cystitis and pyelonephritis. Clinical Infectious Diseases, 64(6), e25-e42.
  2. Flores-Mireles, A. L., et al. (2015). Urinary tract infections: epidemiology, mechanisms of infection, and treatment options. Nature Reviews Microbiology, 13(5), 269-284.
  3. Clinical and Laboratory Standards Institute (CLSI). (2021). Performance Standards for Antimicrobial Susceptibility Testing. CLSI Document M100.
  4. Tansarli, G. S., et al. (2013). Clinical outcomes of patients with UTIs caused by ESBL-producing Enterobacteriaceae. International Journal of Antimicrobial Agents, 42(5), 409-419.
  5. Hooton, T. M. (2012). Uncomplicated urinary tract infection. New England Journal of Medicine, 366(11), 1028-1037.
  6. Raz, R. (2011). Urinary tract infection in postmenopausal women. Karger Medical and Scientific Publishers, 18(1), 21-25.
  7. Foxman, B. (2014). Epidemiology of urinary tract infections: incidence, morbidity, and economic costs. American Journal of Medicine, 113(1A), 5S-13S.
  8. Martinez, J. L. (2008). Antibiotics and antibiotic resistance genes in natural environments. Science, 321(5887), 365-367.
  9. Nicolle, L. E. (2008). Uncomplicated urinary tract infection in adults including uncomplicated pyelonephritis. Urological Clinics of North America, 35(1), 1-12.
  10. Warren, J. W., et al. (1999). Guidelines for antimicrobial treatment of uncomplicated acute bacterial cystitis and acute pyelonephritis in women. Infectious Diseases Society of America, 29(4), 745-758.
  11. Wagenlehner, F. M., et al. (2011). Emerging resistance and treatment strategies for urinary tract infections. Clinical Microbiology and Infection, 17(4), 795-799.
  12. Stamm, W. E., & Norrby, S. R. (2001). Urinary tract infections: disease panorama and challenges. Journal of Infectious Diseases, 183(S1), S1-S4.
  13. Goossens, H., et al. (2005). Outpatient antibiotic use in Europe and association with resistance: a cross-national database study. Lancet, 365(9459), 579-587.
  14. Kahlmeter, G. (2003). An international survey of the antimicrobial susceptibility of pathogens from uncomplicated UTIs: the ECO.SENS project. Journal of Antimicrobial Chemotherapy, 51(1), 69-76.
  15. Al-Badr, A., & Al-Shaikh, G. (2013). Recurrent urinary tract infections management in women: a review. Sultan Qaboos University Medical Journal, 13(3), 359.
  16. Tenney, J., et al. (2018). Risk factors for aquiring multidrug-resistant organisms in urinary tract infections: a systematic literature review. Journal of Hospital Medicine, 13(5), 343-350.
  17. Costelloe, C., et al. (2010). Effect of antibiotic prescribing in primary care on antimicrobial resistance in individual patients: systematic review and meta-analysis. BMJ, 340, c2096.
  18. Colgan, R., et al. (2001). Diagnosis and treatment of acute pyelonephritis in women. American Family Physician, 63(5), 927-932.
  19. Wilson, M. L., & Gaido, L. (2004). Laboratory diagnosis of urinary tract infections in adult patients. Clinical Infectious Diseases, 38(8), 1150-1158.

 

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