Skip to content
2000
Volume 3, Issue 1
  • ISSN: 2210-299X
  • E-ISSN: 2210-3007

Abstract

Introduction

Urinary Tract Infections (UTIs) represent one of the most common microbial diseases affecting individuals across age groups. This study aimed to investigate the microbiological profile and antibiotic utilization patterns among UTI patients at a tertiary care hospital.

Methods

A prospective observational study was conducted at the Maharishi Markandeshwar Institute of Medical Science and Research (MMIMSR), Mullana, Ambala. The study duration was from January 1, 2021, to April 30, 2021. A total of 323 patients aged 12 years and above with culture-confirmed UTIs receiving antimicrobial treatment were included. Data collected included demographics, urine culture results, and antimicrobial susceptibility patterns.

Results

Out of 323 urine samples analyzed, 165 (51.08%) showed significant microbial growth. The majority of positive cases were from females (54.7%) and patients aged 50–70 years. Escherichia coli (44%) was the most prevalent organism, followed by Enterococcus spp. (11.14%), Klebsiella pneumoniae (8.9%), Pseudomonas aeruginosa (8.04%), and Staphylococcus aureus (6.19%). Gram-negative isolates exhibited high resistance to ampicillin (70%) and nalidixic acid (10.5%), but were more sensitive to nitrofurantoin (10.8%), imipenem (8.6%), and meropenem (7.4%). Gram-positive organisms showed sensitivity to tigecycline (6.5%), linezolid (7.1%), and sulfamethoxazole (7.7%).

Discussion

The study demonstrates a significant prevalence of multidrug-resistant pathogens in UTIs. Escherichia coli remains the most frequent uropathogen. The findings underscore the importance of regular microbiological surveillance and sensitivity profiling to inform empirical treatment decisions. The inclusion of patients aged 12 and above ensures broader representation across age demographics.

Conclusion

UTIs in tertiary care settings are predominantly caused by Escherichia coli, with varying levels of antibiotic resistance. Local sensitivity patterns should guide empirical treatment. The implementation of antimicrobial stewardship programs is essential to combat the rising trend of antimicrobial resistance.

This is an open access article published under CC BY 4.0 https://creativecommons.org/licenses/by/4.0/legalcode
Loading

Article metrics loading...

/content/journals/cis/10.2174/012210299X374625250729115611
2025-08-04
2025-11-08
Loading full text...

Full text loading...

/deliver/fulltext/cis/3/1/CIS-3-E2210299X374625.html?itemId=/content/journals/cis/10.2174/012210299X374625250729115611&mimeType=html&fmt=ahah

References

  1. JainS. JainP. MogheV.V. SethV. UpadhyayaP. AbhijitK. GoyalJ. A systematic review of prescription pattern monitoring studies and their effectiveness in promoting rational use of medicines.Perspect. Clin. Res.201562869010.4103/2229‑3485.15400525878953
    [Google Scholar]
  2. FoxmanB. Urinary tract infection syndromes: Occurrence, recurrence, bacteriology, risk factors, and disease burden.Infect. Dis. Clin. North Am.201428111310.1016/j.idc.2013.09.00324484571
    [Google Scholar]
  3. Flores-MirelesA.L. WalkerJ.N. CaparonM. HultgrenS.J. Urinary tract infections: Epidemiology, mechanisms of infection and treatment options.Nat. Rev. Microbiol.201513526928410.1038/nrmicro343225853778
    [Google Scholar]
  4. TullusK. ShaikhN. Urinary tract infections in children.Lancet2020395102371659166810.1016/S0140‑6736(20)30676‑032446408
    [Google Scholar]
  5. FoxmanB. BarlowR. D’ArcyH. GillespieB. SobelJ.D. Urinary tract infection: Self-reported incidence and associated costs.Ann. Epidemiol.200010850951510.1016/S1047‑2797(00)00072‑711118930
    [Google Scholar]
  6. BehzadiP. UrbánE. MatuzM. BenkőR. GajdácsM. The role of gram-negative bacteria in urinary tract infections: current concepts and therapeutic options. Advances in Microbiology.Infectious Diseases and Public Health2021153569
    [Google Scholar]
  7. HootonT.M. Clinical practice. Uncomplicated urinary tract infection.N. Engl. J. Med.2012366111028103710.1056/NEJMcp110442922417256
    [Google Scholar]
  8. KleinR.D. HultgrenS.J. Urinary tract infections: Microbial pathogenesis, host–pathogen interactions and new treatment strategies.Nat. Rev. Microbiol.202018421122610.1038/s41579‑020‑0324‑032071440
    [Google Scholar]
  9. AkramM. ShahidM. KhanA.U. Etiology and antibiotic resistance patterns of community-acquired urinary tract infections in J N M C Hospital Aligarh, India.Ann. Clin. Microbiol. Antimicrob.200761410.1186/1476‑0711‑6‑417378940
    [Google Scholar]
  10. BitewA. MolalignT. ChanieM. Species distribution and antibiotic susceptibility profile of bacterial uropathogens among patients complaining urinary tract infections.BMC Infect. Dis.201717165410.1186/s12879‑017‑2743‑828962545
    [Google Scholar]
  11. GajdácsM. ÁbrókM. LázárA. BuriánK. Comparative epidemiology and resistance trends of common urinary pathogens in a tertiary-care hospital: a 10-year surveillance study.Medicina (Kaunas)201955735610.3390/medicina5507035631324035
    [Google Scholar]
  12. GajdácsM. ÁbrókM. LázárA. BuriánK. Increasing relevance of Gram-positive cocci in urinary tract infections: A 10-year analysis of their prevalence and resistance trends.Sci. Rep.20201011765810.1038/s41598‑020‑74834‑y33077890
    [Google Scholar]
  13. EnanyM.E. AlgammalA.M. ShagarG.I. HanoraA.M. ElfeilW.K. ElshaffyN.M. Molecular typing and evaluation of Sidr honey inhibitory effect on virulence genes of MRSA strains isolated from catfish in Egypt.Pak. J. Pharm. Sci.20183151865187030150182
    [Google Scholar]
  14. AlgammalA.M. El-SayedM.E. YoussefF.M. SaadS.A. ElhaigM.M. BatihaG.E. HozzeinW.N. GhobashyM.O.I. Prevalence, the antibiogram and the frequency of virulence genes of the most predominant bacterial pathogens incriminated in calf pneumonia.AMB Express20201019910.1186/s13568‑020‑01037‑z32472209
    [Google Scholar]
  15. AlgammalA.M. HettaH.F. BatihaG.E. HozzeinW.N. El KazzazW.M. HashemH.R. TawfikA.M. El-TarabiliR.M. Virulence-determinants and antibiotic-resistance genes of MDR-E. coli isolated from secondary infections following FMD-outbreak in cattle.Sci. Rep.20201011977910.1038/s41598‑020‑75914‑933188216
    [Google Scholar]
  16. AlgammalA.M. HettaH.F. ElkelishA. AlkhalifahD.H.H. HozzeinW.N. BatihaG.E.S. El NahhasN. MabrokM.A. Methicillin-resistant Staphylococcus aureus (MRSA): One health perspective approach to the bacterium epidemiology, virulence factors, antibiotic-resistance, and zoonotic impact.Infect. Drug Resist.2020133255326510.2147/IDR.S27273333061472
    [Google Scholar]
  17. AlgammalA.M. HashemH.R. Al-otaibiA.S. AlfifiK.J. El-dawodyE.M. MahrousE. HettaH.F. El-KholyA.W. RamadanH. El-TarabiliR.M. Emerging MDR-Mycobacterium avium subsp. avium in house-reared domestic birds as the first report in Egypt.BMC Microbiol.202121123710.1186/s12866‑021‑02287‑y34445951
    [Google Scholar]
  18. AlgammalA.M. HashemH.R. AlfifiK.J. HettaH.F. SherabaN.S. RamadanH. El-TarabiliR.M. atpD gene sequencing, multidrug resistance traits, virulence-determinants, and antimicrobial resistance genes of emerging XDR and MDR-Proteus mirabilis.Sci. Rep.2021111947610.1038/s41598‑021‑88861‑w33947875
    [Google Scholar]
  19. ChuC.M. LowderJ.L. Diagnosis and treatment of urinary tract infections across age groups.Am. J. Obstet. Gynecol.20182191405110.1016/j.ajog.2017.12.23129305250
    [Google Scholar]
  20. GajdácsM. ÁbrókM. LázárA. BuriánK. Urinary tract infections in elderly patients: A 10-year study on their epidemiology and antibiotic resistance based on the WHO Access, Watch, Reserve (AWaRe) classification.Antibiotics2021109109810.3390/antibiotics1009109834572680
    [Google Scholar]
  21. Available from: https://www.linkedin.com/pulse/what-microbial-profiling-kashef qaadri#:~:text=Microbial%20profiling%20is%20usually%20based,microbes%20present%20in%20a%20sample
  22. AbrahamianF.M. KrishnadasanA. MowerW.R. MoranG.J. TalanD.A. Association of pyuria and clinical characteristics with the presence of urinary tract infection among patients with acute nephrolithiasis.Ann. Emerg. Med.201362552653310.1016/j.annemergmed.2013.06.00623850311
    [Google Scholar]
  23. TavichakorntrakoolR. PrasongwattanaV. SungkeereeS. SaisudP. SribenjaluxP. PimratanaC. BovornpadungkittiS. SriboonlueP. ThongboonkerdV. Extensive characterizations of bacteria isolated from catheterized urine and stone matrices in patients with nephrolithiasis.Nephrol. Dial. Transplant.201227114125413010.1093/ndt/gfs05722461670
    [Google Scholar]
  24. RaheemO.A. KhandwalaY.S. SurR.L. GhaniK.R. DenstedtJ.D. Burden of urolithiasis: Trends in prevalence, treatments, and costs.Eur. Urol. Focus201731182610.1016/j.euf.2017.04.00128720363
    [Google Scholar]
  25. GutierrezJ. SmithA. GeavleteP. ShahH. KuralA.R. de SioM. Amón SesmeroJ.H. HoznekA. de la RosetteJ. CROES PCNL Study Group Urinary tract infections and post-operative fever in percutaneous nephrolithotomy.World J. Urol.20133151135114010.1007/s00345‑012‑0836‑y22367718
    [Google Scholar]
  26. MaierA. ManA. ChibeleanC. CighirT. Nemes-NagyE. MaierI. TodeaC. VidaO. MarthaO. Bacteriological evaluation of the non-struvite nephrolithiasis and its association with urinary tract infections.Rev. Rom. Med. Lab.201523445746810.1515/rrlm‑2015‑0045
    [Google Scholar]
  27. ChenD. ZhangY. HuangJ. LiangX. ZengT. LanC. DuanX. ZhaoZ. ZengG. TiseliusH.G. LuX. WuW. The analysis of microbial spectrum and antibiotic resistance of uropathogens isolated from patients with urinary stones.Int. J. Clin. Pract.2018726e1320510.1111/ijcp.1320529790623
    [Google Scholar]
  28. BiancaT. AdrianM. EmilM. AdrianT. Microbiological study of urinary calculi in patients with urinary infections.Acta Medica Transilvanica201322245249
    [Google Scholar]
  29. BellB.G. SchellevisF. StobberinghE. GoossensH. PringleM. A systematic review and meta-analysis of the effects of antibiotic consumption on antibiotic resistance.BMC Infect. Dis.20141411310.1186/1471‑2334‑14‑1324405683
    [Google Scholar]
  30. SongraM. DamorM. NamdevR. PatbamniyaN. NawalakheP. JainR. A study on positive stone culture and its association with rate of sepsis after urological procedures.Int. Surg. J.20152223924610.5455/2349‑2902.isj20150522
    [Google Scholar]
  31. YongzhiL. ShiY. JiaL. YiliL. XingwangZ. XueG. Risk factors for urinary tract infection in patients with urolithiasis—primary report of a single center cohort.BMC Urol.20181814510.1186/s12894‑018‑0359‑y29783970
    [Google Scholar]
  32. HedelinH. Uropathogens and urinary tract concretion formation and catheter encrustations.Int. J. Antimicrob. Agents200219648448710.1016/S0924‑8579(02)00095‑X12135838
    [Google Scholar]
  33. BoraD.I. LyngdohD.W. KhyriemD.B. Bacteriological profile of rena.Int. J. Curr. Res.2015761689816901
    [Google Scholar]
  34. TabassumD.S.K. AhmedS.I. BaigD.M.A. Bacteriological profile of clinical isolates from urinary samples and prevalence of CAUTI at a tertiary care hospital.Scholars J. Appl. Medical. Sciences20221091492149910.36347/sjams.2022.v10i09.012
    [Google Scholar]
/content/journals/cis/10.2174/012210299X374625250729115611
Loading
/content/journals/cis/10.2174/012210299X374625250729115611
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test