Prevalence of Klebsiella Bacteriuria and Antimicrobial Susceptibility in a Tertiary Care Hospital, Tiruchirapalli, India

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Available online at www.ijpcr.com International Journal of Pharmaceutical and Clinical Research 216; 8(6): 538-542 Research Article ISSN- 975 1556 Prevalence of Klebsiella Bacteriuria and Antimicrobial Susceptibility in a Tertiary Care Hospital, Tiruchirapalli, India Susethira A R 1 *, Uma A 2 1 Faculty of Medicine and Health Sciences, SRM University, Kattankulathur, India 2 Postgraduate and Research Department of Microbiology, Chennai Medical College Hospital and Research Centre (SRM Group), Tiruchirapalli, India Available Online: 8 th June, 216 ABSTRACT Urinary tract infection is a common health issue encountered in medical practice and leads to frequent antibiotic prescription in outpatient department strains of Klebsiella are challenging for the clinicians when it is become a multidrug resistant Klebsiella either inside the hospital or in outpatient department. Thus this study has its own objective to determine the prevalence of Klebsiella bacteriuria among urine samples received in Clinical Microbiology Laboratory from February 212 to June 215. A battery of 3,958 urine samples was included. All the urine samples which are having the criteria for inclusion were subjected for bacteriological screening. Further confirmation performed by microscopy, biochemical tests and special staining. Among the urine samples processed, 17 samples supported Klebsiella sp isolation. Further, species level determination resulted K. pneumoniae (116) and K. oxytoca (54). All the isolates were subjected to antimicrobial susceptibility test. This study revealed that Klebsiella pneumoniae isolation from UTI in this region is predominant. Keywords: Klebsiella, bacteruria, prevalence, antimicrobial susceptibility test INTRODUCTION Urinary tract infections (UTIs) are very common reason for consultation and antibiotic prescription in current practice 1,2. Excessive and/or inappropriate use of antibiotics in treating UTIs is responsible for the emergence and spread of multi-drug resistant (MDR) urinary bacteria. UTIs caused by MDR Klebsiella pneumonia isolates are a major public health problem, since the therapeutic options significantly reduced and more challenging in clinical scenario. Moreover, MDR pathogens resulting in high morbidity and mortality as they reflect in increased hospital stay and treatment expenditure 3. The development of drug-resistant pathogens in patients with serious infections such as UTIs has generally been ascribed to the widespread use of antimicrobial agents and the limited availability of infection prevention and control programs. As a result, it is increasingly common to encounter individuals infected with bacterial pathogens that are resistant to almost all currently available antibiotics. Of particular concern in the healthcare setting is the emergence of resistant gramnegative pathogens, including drug resistant K. pneumoniae. While antibiotic resistance was previously noted mainly in nosocomial UTIs, it is nowadays also frequently observed in community-acquired UTIs 1,2. Globally, nonsusceptibility of urinary K. pneumoniae to commonly used oral and parenteral antimicrobial agents is rapidly increasing and shows large variation temporally and regionally 4. Empirical antibiotic therapy is based on epidemiological data that are updated and adapted geographically 5. Thus, it is of great importance for institutions to know the local antibiotic resistance patterns of each region in order to implement suitable infection control measures and develop a rational antibiotic policy with local recommendations for antibiotic use. These surveillance data are also used to assess the effectiveness of the measures taken and to identify new points for intervention to control bacterial resistance. Unlike most developed countries, we unfortunately do not yet have nationwide surveillance programs for monitoring antimicrobial resistance. However, surveillance studies of bacterial resistance are among the most important measures in terms of controlling the spread of resistant bacteria. Therefore, the objectives of this regional study were to analyze the prevalence of Klebsiella sp prospectively and to determine the antibiotic resistant pattern that add valuable data to assist the medical community in the development of a plan for a rational use Table 1: Results of culture Results of culture Number of Percentage samples 163 4.1 Significant bacteriuria (Klebsiella) Insignificant bacteriuria 7.2 (Klebsiella) Other isolates 356 9. Commensals 565 14.3 Sterile 2867 72.4 Total 3958 1 *Author for Correspondence

No. of samples supported Klebsiella No. of samples supported Susethira et al. / Prevalence of Klebsiella Table 2: Distribution of Klebsiella positive samples with respect to the patients age Age group Distribution of Klebsiella positive samples in years (in 212 213 214 215* Total years) 1-1 - 1 2 2 5 11-2 1-5 4 1 21-3 1 7 4 5 17 31 4 6 5 12 8 31 41-5 5 7 12 9 33 51-6 7 7 7 5 26 61-7 8 5 6 7 26 71-8 8 4 2 6 2 81-9 - - 1 1 2 Total 36 36 51 47 17 *Upto June only of therapeutics including antimicrobial agents in the treatment of UTIs due to K. pneumoniae. MATERIALS AND METHODS This was a prospective study which was conducted in the Department of Microbiology in Chennai Medical College Hospital and Research Centre, Tiruchirapalli, India over a period of 3 years and 5 months, starting from February 212 to June 215. Study area and patients A battery of 3,958 urine samples received in the Clinical Microbiology Laboratory was included. All the urine samples which were having the criteria for inclusion were subjected for bacteriological screening. 4 Specimen collection After getting clearance from the Institutional ethical committee, this study was conducted. Urine samples were collected by standard mid-stream clean catch/ catheterized/ suprapubic method in sterile, wide mouthed containers that were covered with tight-fitting lids. Culture The samples were processed by using standard microbiological procedures. The specimens were inoculated on dried plates of Nutrient agar, MacConkey agar and Blood agar (in 5-1% CO 2 atmosphere) by standard loop method and the plates were incubated at 37 C overnight. The isolates were confirmed by using standard bacteriological identification techniques. Culture results were interpreted as significant and insignificant according to the standard criteria. Biochemical confirmation After colony determination and microscopy, the isolates were confirmed by biochemical methods and special staining technique (capsular staining) to confirm capsulated Klebsiella species). Antimicrobial Susceptibility test Antimicrobial Susceptibility test was performed using Kirby-Bauer disc diffusion method and interpretation was done according to Clinical and Laboratory Standards Institute (formerly NCCLS) guidelines 6,7,8. The antibiotics included tested were ampicillin (1mcg), amoxyclav (2/1mcg), amikacin (3mcg), gentamycin, cefipime (3mcg), ceftriaxone (3mcg), cefuroxime (3mcg), cefotaxime, ceftazidime, cefoxitin, cefeperazonesulbactam, piperacillin-tazobactam, ciprofloxacin (5mcg), co-trimaxazole (25mcg), norfloxacin (1mcg), 3 2 1 212 213 214 215 Year Male Female 4 3 2 1 Figure 1: Gender wise distribution of positive Klebsiella cultures 34 33 25 24 23 18 11 Klebsiella pneumoniae 2 Klebsiella oxytoca 212 213 214 215* Years Figure 2: Distribution of Klebsiella species IJPCR, June 216, Volume 8, Issue 6 Page 539

Susethira et al. / Prevalence of Klebsiella Table 3: Antibiotic resistance pattern of the Klebsiella isolates Antibiotics Percentage distribution of antibiotic resistance among Klebsiella isolates 212 (n=36) 213 (n=36) 214 (n=51) 215 (n=47) Penicillin Group Ampicillin 36 (1) 36 (1) 51 (1) 47 (1) Cotrimoxazole 19 (52.8) 19 (52.7) 2 (39.2) 24 (51) Fluroquinolones Norfloxacin 29 (8.5) 22 (61.1) 28 (45.1) 25 (53.2) Ciprofloxacin 17 (47.2) 21 (58.3) 34 (33.3) 27 (57.4) Levofloxacin 13 (36.1) 12 (33.1) 4 (21.6) 26 (55.3) Aminoglycosides Gentamicin 18 (5) 16 (44.4) 32 (37.3) 22 (46.8) Amikacin 13 (36.1) 8 (22.2) 11 (21.6) 13 (27.7) II generation cephalosporin Cefuroxime 29 (8.5) 24 (66.6) 32 (62.7) 32 (66) III generation cephalosporin Cefatoxime 28 (77.8) 24 (66.6) 19 (62.7) 33 (7.2) Ceftriaxone 28 (77.8) 24 (66.6) 31 (6.8) 33 (7.2) Ceftazidime 28 (77.8) 24 (66.6) 3 (58.8) 28 (59.6) IV generation cephalosporin Cefipime 28 (77.8) 24 (66.6) 28 (54.9) 26 (55.3) β lactum and β lactamase inhibitors Amoxycillin clavulanic acid 34 (94.4) 35 (97.2) 42 (82.4) 45 (95.7) Cefaperazone - sulbactum 12 (33.3) 15 (41.7) 12 (23.5) 18 (38.3) Piperacillin - tazobactam 9 (25) 11 (3.6) 14 (27.4) 14 (29.8) Carbapenem Imepenem 2 (5.5) 1 (2.7) 5 (1.7) Meropenem 2 (5.5) 1 (2.7) 5 (1.7) Ertapenem 2 (5.5) 1 (2.7) 5 (1.7) [Figure in parenthesis denoted percentages] levofloxacin (5mcg), ertapenam, imipenem (1mcg) and meropenem (1mcg) (Himedia, India). RESULTS AND DISCUSSION Among 3,958 urine samples screened, significant Klebsiella bacteriuria was found in only 17 (4.3%) samples and depicted in table 1. Among positive cultures which were obtained, all supported to monobacteriuria. Highest incidence (33%) was reported in the age group of 41-5 years (Table 2). The sexwise distribution of the positive Klebsiella isolates was depicted in figure 1. Overall, 17 Klebsiella isolates were determined in this study. Among them, K. pneumoniae isolates were possible to 116 samples and 54 samples supported K. oxytoca (Figure 2). The distribution of K. pneumoniae was observed as 25, 34, 33 and 24 in 212, 213, 214 and 215 respectively. Klebsiella pneumonaie, the most common isolate, was found to be sensitive to carbapenems (Imipenem, meropenem and ertapenam) followed by amikacin and levofloxacin. K. oxytoca, the second most frequent organism which was grown on culture while sensitivity to the abovesaid antibiotics. In this study, we are not concentrating the species variations among the Klebsiella isolates for sensitivity pattern. High resistance pattern was observed among ampicillin, amoxycillinclavulanic acid, norfloxacin, cefuroxime and other third generation cephalosporins (Table 3). The distribution of multi drug resistance (MDR) was also determined and analyzed the sensitivity to carbapenem group of antibiotics. The overall determination of MDR among Klebsiella isolates was depicted in figure 3. It was observed that there is an increase MDR yearly and also increasing resistance of carbapenem (Figure 4). This study was carried out to determine the prevalence of Klebsiella isolates among the urine samples processed in the Department of Microbiology, Chennai Medical College Hospital and Research Centre, Tiruchirapalli, India. The percentage of susceptibility of K. pneumoniae and K. oxytoca isolates to the antibiotics which are commonly used to treat Klebsiella infections as shown in table 3. The most predictable and primary etiological bacteria involved in urinary tract infections (UTI) are Escherichia coli followed by K. pneumoniae in both outpatient and inpatient 9,1. Lot of research papers are published related to E. coli infections among urinary tract infectious patients. Thus in this present study we concentrating on Klebsiella species as the observable bacterial isolates from urine samples and this finding is not observed in other studies that compared. In general, the prevalence of UTI occurred more in females than in males due to shorter urethra, closer proximity to the perirectal area in females. But in this study, the prevalence was found to be more or less equal. Most of the studies suggested that UTIs are more frequent in females than males during childhood 11,12,13. Out of 17 Klebsiella isolates, 116 of K. pneumoniae and 54 of K. oxytoca were recorded. IJPCR, June 216, Volume 8, Issue 6 Page 54

No. of isolates showing IS and IR Number of isolates supported MDR Susethira et al. / Prevalence of Klebsiella 2 13 12 13 17 1 212 213 214 215 Year 14 12 1 8 6 4 2 Figure 3: Carbapenem resistance among MDR Klebsiella strains 9 3 11 1 212 213 Year 214 215 Figure 4: Carbapenem resistance among MDR Klebsiella strains [IR Imepenem Resistant; IS Imipenem Sensitive] 13 12 5 MDR-IS MDR-IR Most of the studies suggested that the older men of 61 7 years were observed positive to K. pneumoniae urinary culture, mainly due to prostate obstruction or subsequent instrumentation like catheter 14. Other study suggested that the incidence of UTI in females was more at an earlier age compared to that in males 13. Antibiotic resistance is a major clinical problem in treating Klebsiella infections and the issue was increasing over the years where the resistance rates vary from country to country 15. K. pneumoniae is becoming resistant to co-trimoxazole and norfloxacin due to use for a long period and must have been abused and a result the organisms must have developed a different mode of action 13. Overall resistance to various generations of cephalosporins and penicillins alone was high on account of the production of extended spectrum β lactamases (ESBLs) by the bacteria involved. Based on the observations of this study, we recommend the use of levofloxacin, ciprofloxacin or 3 rd generation cephalosporins along with β lactamase inhibitors (clavulanate or sulbactam) against infection caused by Klebsiella species after proper laboratory investigation. The posological determination and incidence of toxicity subsequently reduced with the usage of piperacillin or cephalosporins 3. Furthermore, carbapenem groups including imepenem, carbapenem etc showed very effective but relatively expensive. The restriction in procurement and indiscriminate use are making the organisms susceptible to it. Hence, there is a need to emphasize the rational use of antimicrobials and strictly adhere to the concept of reserve drugs to minimize the misuse of available antimicrobials. Carbapenem (imipenem or meropenem) and amikacin or gentamicin should be considered as a reserved drug for the treatment of severe nosocomial infections caused by K. pneumoniae. In fact, the irrational and inappropriate use of antibiotics is responsible for the development of resistance of the Enterobacteriaceae family including K. pneumonia 12. In addition, regular antimicrobial susceptibility surveillance is essential for endemic monitoring of the resistance patterns. An effective national and state level antibiotic policy and draft guidelines should be introduced to preserve the effectiveness of antibiotics and for better patient management 5,15. Though carbapenem resistance was observed among the MDR Klebseilla, there is no observation of pan drug resistance in this study. Further, the carbapenem resistance strains were found to be sensitive to colistin and tigecycline. In vitro sensitivity is an important factor yet other factors given below should also be seriously considered in selecting the antimicrobial agents for an infection. For example cost of drugs for complete treatment, route of administration (oral, parenteral etc.), age (if the patient is neonate chloramphenicol is contraindicated) and pregnancy (tetracyclines are contraindicated). Other factors like allergic reactions to drugs like β lactam antibiotic, kinetics of drugs and its concentration at the target site and mode and frequency of administration, bactericidal or bacteriostatic, efficacy/safety ratio, immunological status of the patient, MDR should also be considered 9,11. IJPCR, June 216, Volume 8, Issue 6 Page 541

Susethira et al. / Prevalence of Klebsiella Most of the isolates had a high level of resistance further laboratory evidence of infection and antibiotic susceptibility testing should be carried out to help in the choice of systemic drugs. Continuous monitoring of antimicrobial susceptibility pattern in individual settings together with their judicious use is emphasized to minimize emergence of drug resistant bacteria. Thus, it is highly recommended that practicing physicians should become aware of the magnitude of the existing problem of antimicrobial resistance and help in fighting this deadly threat by rational prescribing. REFERENCES 1. Yeshitele B, Gebre SS, Feleke Y. Asymptomatic bacteriuria and symptomatic urinary tract infections (UTI) in patients with diabetes mellitus in Tikur Anbesa specialized University hospital, Addis Ababa, Ehtiopia. Ethiop Med J 212; 5: 239-249. 2. Alemu A, Moges F, Shiferaw Y, Tafess K, Kassu A, Anaqaw B, Aqeqn A. Bacterial profile and drug susceptibility pattern of urinary tract infection in pregnant women at University of Gondar Teaching Hospital, Northwest Ethiopia. BMC Res Notes 212; 25: 197-22. 3. Wondimeneh Y, Muluye D, Alemu A, Atinafu A, Yitayew G, Gebrecherkos T, Damtie D, Ferede G. urinary tract infection among obstetric fistula patients at Gondar University Hospital, Northwest Ethiopia. BMC Womens Health 214; 17: 14-22. 4. Melaku S, Kibret M, Abera B, Gebre SS. Antibiogram of nosocomial urinary tract infections in Felege Hiwot referral hospital, Ethiopia. Afr Health Sci 212; 12: 134-139. 5. Akinbami AA, Ajibola S, Bode SI, Oshinaike O, Adediran A, Ojelabi O, Osikomaiya B, Ismail K, Uche E, Moronke R. Prevalence of significant bacteriuria among symptomatic and asymptomatic homozygous sickle cell disease in a tertiary hospital in Lagos, Nigeria. Niger J Clin Pract 214; 17: 163-167. 6. Clinical and Laboratory Standards Institute 212. Reference method for broth dilution antifungal susceptibility testing of yeasts; 4 th informational supplement. CLSI document M27-S4. Clinical and Laboratory Standards Institute, Wayne, PA. 7. Clinical and Laboratory Standards Institute. 213. Performance standards for antimicrobial susceptibility testing; 23 rd informational supplement. CLSI M1-S23. Clinical and Laboratory Standards Institute, Wayne, PA. 8. Clinical and Laboratory Standards Institute. 214. Performance standards for antimicrobial susceptibility testing; 24 th informational supplement. CLSI M1-S24. Clinical and Laboratory Standards Institute, Wayne, PA. 9. Gupta K, Hooton TM, Wobbe CL, Stamm WE. The prevalence of antimicrobial resistance among uropathogens causing uncomplicated cystitisin young women. Int J Antimicrob Agents 1999; 11: 35-38. 1. Gales CA, Jones R, Gordon KA, Sader SH, Wilke WW, Beach ML, Pfaller MA, Doern GV. Activity and spectrum of 22 antimicrobial agents tested against urinary tract infectious pathogens in hospitalized patients in Latin America: Report from the second year of the SENTRY antimicrobial surveillance programme. J Antimicrob Chemother 2; 45: 295-33. 11. Akinyemi KO, Alabi SA, Taiwo NA, omonighehin EA. Antimicrobial susceptibility pattern and plasmid profile of pathogenic bacteria isolated from subjects with urinary tract infections in Lagos, Nigeria. Nig Qt J Hosp Med 1997; 1: 7-11. 12. Ibeawuchi R, Mbata TI. Rational and irrational use of antibiotics. Afr Hlth 22; 24: 16-18. 13. Asati RK, Sadawarte K. Prevalence and antimicrobial susceptibility pattern of Klebseilla pneumoniae causing urinary tract infection and issues related to the rational selection of antimicrobials. Sch J Appl Med Sci 213; 1: 395-399. 14. Jung SY, Kun HS. Effects of electro acupuncture on benign prostate hyperplasia patients with lower urinary tract symptoms: a single blinded randomized controlled trail. Evid Bas Complem Altern Med 211; 13: 198-25. 15. Kahan NR, Chinitz DP, Waltman DA, Dushnitzky D, Kahan E, Shapiro M. Empiric treatment of uncomplicated urinary tract infection with fluoroquinolones in older women in Israel: another lost treatment option. Ann Pharmacother 26; 4: 2223-2227. IJPCR, June 216, Volume 8, Issue 6 Page 542