Impact of Pre-Existing Urinary Antimicrobial Agents on Culture Yield, Diagnostic Accuracy, and the Detection of Significant Bacteriuria in Community-Acquired Urinary Tract Infections
- PMID: 40510091
- PMCID: PMC12161482
- DOI: 10.7759/cureus.84038
Impact of Pre-Existing Urinary Antimicrobial Agents on Culture Yield, Diagnostic Accuracy, and the Detection of Significant Bacteriuria in Community-Acquired Urinary Tract Infections
Abstract
Introduction: Pre-existing antibacterial substances (ABS) in urine can significantly impact the diagnostic and therapeutic management of urinary tract infections (UTIs) by altering microbial culture outcomes and influencing the detection and resistance profiles of uropathogens. The presence of pre-existing ABS may lead to false-negative or insignificant culture results, affecting clinical decision-making. This study aims to assess the impact of pre-existing ABS on culture positivity, microbial distribution, and antibiotic susceptibility patterns in outpatients, particularly those with prior antimicrobial exposure.
Methods: A prospective observational study was conducted at a tertiary care hospital on 621 outpatients with clinical symptoms suggestive of UTI. Urine samples were analyzed for pre-existing ABS and classified into pre-existing ABS-positive (n = 158) and pre-existing ABS-negative (n = 463) groups. Data on demographics, clinical characteristics, comorbidities, and microbiological profiles were collected. Associations between pre-existing ABS presence and variables such as prior antibiotic exposure, requisition form completeness, and diabetes mellitus were evaluated using chi-square tests. A p-value of <0.05 was considered statistically significant.
Results: The study population comprised 356 females (57.32%), with a mean age of 30.68 years. The most common presenting symptom was an increased urinary frequency (76.16%), followed by abdominal pain (62.47%). Pre-existing ABS were detected in 158 (25.44%) cases. Significant associations were observed between pre-existing ABS presence and prior antibiotic use (χ² = 31.61 p < 1.88 × 10 ⁻⁸,), adequate requisition form documentation (χ² (df) = 40.58, p < 1.88 × 10 ⁻¹⁰), and diabetes mellitus (χ² (df) = 9.02, p = 0.0027). Culture positivity was significantly reduced in pre-existing ABS-positive samples, with lower isolation rates of Escherichia coli (27.21% vs. 39.52%, p = 0.007) and an increased prevalence of Proteus mirabilis (10.75% vs. 4.96%, p = 0.018). Pre-existing ABS-positive samples also showed significantly higher rates of no growth (17.49% vs. 9.49%, p = 0.023) and insignificant growth (19.62% vs. 12.00%, p = 0.026). Antibiotic susceptibility analysis revealed that pre-existing ABS-positive isolates of E. coli and Klebsiella pneumoniae exhibited reduced susceptibility to amoxicillin-clavulanic acid, cefazolin, and imipenem compared to pre-existing ABS-negative isolates, suggesting a potential impact of prior antimicrobial exposure on resistance patterns.
Conclusion: The presence of pre-existing ABS in urine significantly alters microbial culture outcomes, leading to reduced detection of common uropathogens and an increased likelihood of false-negative or insignificant culture results. Additionally, pre-existing ABS-positive isolates demonstrate higher resistance to key antibiotics, highlighting the need for careful interpretation of urine culture results in patients with prior antimicrobial exposure. Comprehensive documentation of antibiotic history and requisition form completeness is essential to improve diagnostic accuracy. Further research is warranted to explore the role of pre-existing ABS in promoting antimicrobial resistance in community-acquired UTIs and to refine diagnostic criteria for significant bacteriuria in the presence of pre-existing ABS.
Keywords: antimicrobial agents; antimicrobial sensitivity tests; diagnosis drug resistance; significant bacteriuria; urinary tract infections.
Copyright © 2025, Jadhav et al.
Conflict of interest statement
Human subjects: Consent for treatment and open access publication was obtained or waived by all participants in this study. LNCTMC issued approval LNCTMC & SH-IEC VU/LNCTMC/IEC/2024/14. Ethics Approval: The study was conducted using anonymised clinical samples obtained during routine diagnostic procedures, without direct patient interaction or the use of identifiable personal data. Ethical approval for the study was obtained from the Institutional Ethics Committee of LNCT Medical College, Indore (Approval No. VU/LNCTMC/IEC/2024/14, dated 28/08/2024). All procedures were carried out in accordance with relevant guidelines and regulations. Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.
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