ALARMING RATES OF PREVALENCE OF ESBL PRODUCING E. COLI IN URINARY TRACT INFECTION CASES IN A TERTIARY CARE NEUROSPECIALITY HOSPITAL
Abstract
Introduction: Extended spectrum beta-lactamases (ESBL) are enzymes that confer resistance to most beta lactam antibiotics, including Penicillins, Cephalosporins, and the Monobactam, Aztreonam. ESBL strains are on the rise in case of community acquired and healthcare associated infections. Escherichia coli are the most common uropathogen worldwide. Prevalence of ESBL production and their antimicrobial susceptibility patterns in urinary E.coli isolates in a tertiary care Neurospeciality hospital were studied.
Materials and Methods: Urinary E.coli isolates were identified and their susceptibility was tested using Vitek2.Isolates were classified as point of admission UTI (POA-UTI), catheter associated UTI (CAUTI), hospital Acquired UTI (HAUTI). Susceptibility analysis was done.
Results: 198 E.coli urinary isolates were obtained between November, 2015 and March, 2017. Out of 87 POA-UTI cases 73.56% were found to be ESBL producers, among which the sensitivity pattern was Ertapenem (81.6%), Piperacillin (57.47%), Amikacin (80.47%), Fosfomycin (97.70%), Nitrofurantoin ( 82.75%), Ciprofloxacin ( 17.24%). All the E.coli isolates producing CAUTI were ESBL producers, among which the sensitivity pattern was Ertapenem (81.48%), Piperacillin (40.74%), Amikacin (70.37%), Fosfomycin (96.29%), Nitrofurantoin (77.77%), Ciprofloxacin (18.51%). Among other isolates E.coli strains producing HAUTI, the sensitivity pattern was Ertapenem (72.61%), Piperacillin (45.23%), Amikacin (79.76%), Fosfomycin (98.80%), Nitrofurantoin (79.31%), Ciprofloxacin (16.66%).
Conclusion: The strains causing CAUTI are ESBL positive with a limited range of antibiotic susceptibility, possibly due to antibiotic pressure. This shows that irrational use of antibiotics show an increase in ESBL producers. Early institution of antibiotics could be a possible solution to this problem. (BL+BLI) combinations seem to have more usefulness in POA-UTI cases than CAUTI cases. Fosfomycin seems to be a better alternative.
Keywords:
ESBL, Urinary tract infections, Susceptibility testing, Escherichia coliDownloads
References
Crouzet, J., Sotto, A., Picard, E., Lachaud, L. & Bourgeois, N. (2011). A case of Candida haemulonii osteitis: clinical features, biochemical characteristics, and antifungal resistance profile. Cliical Microbiology Infection, 17(7), pp 1068 –1070.
Kathuria, S., Singh, P. K., Sharma, C., Prakash, A., Masih, A., Kumar, A., Meis, J. F. & Chowdhary, A. (2015). Multidrug-resistant Candida auris misidentified as Candida haemulonii: characterization by matrixassisted laser desorption ionization–time of flight mass spectrometry and DNA sequencing and its antifungal susceptibility profile variability by Vitek 2, CLSI broth microdilution, and Etest method. Journal of Clin Microbiology, 53(6), pp 1823–1830.
Khan, Z. U., Al-Sweih, N. A., Ahmad, S., Al-Kazemi, N., Khan, S., Joseph, L. & Chandy, R. (2007). Outbreak of fungemia among neonates caused by Candida haemulonii resistant to amphotericin B, itraconazole, and fluconazole. Journal of Clin Microbiology, 45(6), pp 2025-2027.
Kim, M. N., Shin, J. H., Sung, H., Lee, K., Kim, E. C., Ryoo, N., Lee, J. S., Jung, S. I., Park, K.H., Kee, S. J., Kim, S. H., Shin, M. G., Suh, S. P. & Ryang, D. W. (2009). Candida haemulonii and closely related species at 5 university hospitals in Korea: identification, antifungal susceptibility, and clinical features. Clinical Infectious Diseases, 48(6), pp e57– 61.
Kim, S., Ko, K. S., Moon, S. Y., Lee, M. S., Lee, M. Y. & Son, J. S. (2011). Catheter-related candidemia caused by Candida haemulonii in a patient in long-term hospital care. Journal of Korean Medecal Science, 26(2), pp 297–300.
Kurtzman, C. P., Fell, J. W. & Boekhout, T. (2011). The yeasts: a taxonomic study, 5th edition, Elsevier, Amsterdam, the Netherlands.
Lavarde, V., Daniel, F., Saez, H., Arnold, M. & Faguer, B. (1984). Peritonite mycosique a Torulopsis haemulonii. Bull. Soc. Fr. Mycol. Med, 13, pp 173–176.
Lehmann, P. F., Wu, L. C., Pruitt, W. R., Meyer, S. A. & Ahearn, D. G. (1993). Unrelatedness of groups of yeasts
Oh, B. J, Shin, J. H., Kim, M. N., Sung, H., Lee, K., Joo, M. Y., Shin, M. G., Suh, S. P. & Ryang, D. W. (2011). Biofilm formation and genotyping of Candida haemulonii, Candida pseudohaemulonii, and a proposed new species (Candida auris) isolates from Korea. Medical Mycology, 49(1), pp 98 –102.
Rodero, L., Cuenca-Estrella, M., Córdoba, S., Cahn, P., Davel, G., Kaufman, S., Guelfand, L. & Rodríguez-Tudela, J. L. (2002). Transient fungemia caused by an amphotericin B-resistant isolate of Candida haemulonii. Journal of Clinical Microbiolog, 40(6), pp 2266-2269.
Ruan, S. Y., Kuo, Y. W., Huang, C. T., Hsiue, H. C., Hsueh, P.R. (2010). Infections due to Candida haemulonii: species identification, antifungal susceptibility and outcomes. International Journal of Antimicrobial Agents, 35(1), pp 85– 88.
Sugita, T., Takashima, M., Poonwan, N. & Mekha, N. (2006). Candida pseudohaemulonii sp. nov., an amphotericin B- and azole-resistant yeast species, isolated from the blood of a patient from Thailand. Microbiology and Immunology, 50(6), pp 469–473.
Uden, V. & Kolipinsky, M. C. (1962). Torulopsis haemulonii nov. spec., a yeast from the Atlantic Ocean. Antonie Van Leeuwenhoek, 28, pp 78–80.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2017 Malaysian Journal of Medical Research (MJMR)
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.