A RETROSPECTIVE STUDY ON PREVALENCE OF MULTI DRUG RESISTANT STRAINS OF UROPATHOGENS IN KATHMANDU MODEL HOSPITAL

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Original Article A RETROSPECTIVE STUDY ON PREVALENCE OF MULTI DRUG RESISTANT STRAINS OF UROPATHOGENS IN KATHMANDU MODEL HOSPITAL SB Shrestha*, RB Basnet**, P Shahi* * Abstract Background The emergence of multidrug resistance strains of uropathogens may greatly increase the difficulty of urinary tract infection. Our study was conducted to analyze the antimicrobial susceptibility pattern of uropathogens and to determine the occurrence of multidrug resistant strains among the isolates. Method All mid stream urine samples were cultured by using semi-quantitative method on 5% Blood Agar and Mac Conkey Agar plates. All isolated uropathogens were identified by using Gram stain and biochemical methods. Sensitivity tests were performed on Mueller Hinton agar plate by Kirby Bauer s Disc Diffusion Technique. Result During the study period (December 2006- December 2007), a total of 3648 samples were analyzed. Among 3648 samples, 864(23.6%) showed significant growth. Greater prevalence of urinary tract infection was found in July and August and in 20-29 years age group.e.coli (89.6%) was the most common among the gram negative isolate and Coagulase negative staphylococci was the most common (37.5%) in gram positive isolates. Among the total isolates multidrug resistance was the most commonly associated with Enterococcus faecalis (75.0%) followed by E.coli (68.7%), Pseudomonas aeruginosa (66.6%) and Coagulase negative staphylococci (61.5%).Nitrofurantoin(81.1%) was the most effective first line antibiotic for gram negative isolates and Ciprofloxacin(93.7%) and cefotaxime(93.7%) were for the gram positive isolates.amikacin(80.0%) was the most effective antibiotic tested as extended panel for multidrug resistance strains. Conclusion Multidrug resistance strains of uropathogens are emerging very rapidly which may create serious problem in proper management of urinary tract infection in near future. Keywords 56

Uropathogen, Urinary tract infection, Multidrug resistance * Microbiologist, Kathmandu Model Hospital, Kathmandu ** Consultant Pathologist, Bir Hospital, Kathmandu Introduction Urinary tract infection (UTI) is defined as bacteriuria i.e. multiplication of the organisms in urinary tract and the presence of more than a hundred thousand (10 5 ) organisms per milliliter in the mid stream sample of urine (MSU) 1.Although the widespread availability of antibiotics, UTI remains the most common bacterial infection in the human 2. UTI can occur at anytime in the life of an individual 3.According to the annual report published by Department of Health Services, Kathmandu(1996/1997), the morbidity rate of UTI is 0.42% of total population(21,216,638) and urine samples appear as the second commonest sample(18%) to be submitted to the laboratory after blood(48%) for examination. The incidence of UTI is high in female population about 2% at the age of 15-24 years and increasing 1-2% every decade to a prevalence rate of 10% in 55-64 years 4.Antibiotics today s are the frontline therapeutic means for the medical intervention in an infection, which plays a central role in the control and management of infectious diseases. The current knowledge of antibiotic sensitivity profile of urinary pathogens is mandatory for the proper management of urinary tract infection 5.Since antibiotic resistance pattern may vary in a wide variety of pathogenic organisms even over a short period and depend on site of isolation and on different environments, periodic update in the knowledge about antibacterial activity is needed 6,7. The present study was conducted to determine the antimicrobial susceptibility pattern of uropathogens and to analyze the Multidrug resistant strains of uropathogens from patients suffering with urinary tract infection in Kathmandu Model hospital, Kathmandu. Materials and Methods 3648 urine samples were examined from clinically suspected urinary tract infection in patients attending Kathmandu Model Hospital during this research period of thirteen months (December 2006- December 2007) using culture and sensitivity tests. All the patients were instructed carefully for collection of mid stream urine specimens. They were given a sterile, dry and clean collection bottles for urine collection.all the urine specimens were processed within 30 minutes of collection. Culture of all urine specimens was done on 5% Blood Agar and Mac Conkey Agar plate utilizing semi-quantitative culture method. Shaking with hand to ensure a uniform suspension of bacteria vigorously mixed the urine specimens. Then an inoculating loop of standard dimension was used to take up approximately fixed and known volume (0.001ml) of mixed urine and placed on the center of the plate. The drop was spread in a line and then over the entire surface of the agar plate. After inoculation, the culture plates were incubated in an inverted position 57

at 37 o C for 24 hours 8. After 24 hours, the number of colonies were counted on each plate, which was multiplied by 1000 to calculate the number of organisms per ml in the specimen. Samples showing 10 5 or more organisms per ml of urine were taken as significant. Colony counts less than this was considered as non-significant 9. Gram staining and various biochemical tests were used to identify pure culture of bacterial growth. Different biochemical media used were Triple Sugar Iron Agar,Sulphite Indole motility Agar,Urease agar,simmons s Citrate Agar,MRVP and Oxidation Fermentation medium.catalase, Coagulase and Oxidase Tests were also performed.the primary panel antibiotics used for Gram negative bacteria were Amoxycillin ( 10mcg),Cefotaxime (30 mcg), Ciprofloxacin (5mcg),Cefixime (5 mcg), Cotrimoxazole (1.25/23.75mcg), Norfloxacin (10mcg), Nitrofurantoin (300 mcg) and Ofloxacin (5 mcg) and those used for Gram positive bacteria were Amoxycillin (10mcg), Cefotaxime (30 mcg), Ciprofloxacin (5mcg), Cephalexin (30 mcg), Cotrimoxazole (1.25/23.75mcg) and Cloxacillin (5 mcg). Amikacin(30 mcg), Ceftriaxone 30 mcg), eftazidime(30 cg), hloramphenicol 30 mcg) and Gentamycin 10 mcg) were used as extended panel for Multi Drug Resistance (MDR) Gram negative isolates. All the antibiotics were tested by Kirby Bauer s Disc Diffusion Technique.The colonies picked up and suspended in Nutrient broth and adjusted turbidity to 0.5 Mc Farland Standard. Within 15 minutes a sterilized cotton swab was dipped into the adjusted suspension. Carpet culture was done by streaking the swab over the entire sterile. The antibiotic impregnated discs were placed on the surface of the agar plate and then incubated at 37 o C for 18 hours. The different inhibition zones were measured and interpreted the results on the basis of zone size compared with standard interpretive table given by manufacturer. Result S.No. 1 2 Result Significant Growth No significant Growth Table 1: Source wise and gender wise Distribution of Urine Samples Requested for Culture OPD In Patient Male Female Male Female No % No % No % No % Total No. 230 547 40 47 864 23.6 198 493 30 58 779 21.3 3 No Growth 674 1059 130 142 2005 54.9 % 58

A total of 3648 urine samples, 3201 (87.7%) from Out Patient Department and 447(12.2%) from admitted patients. 864 (23.6%) showed the significant growth and 2005 (54.9%) samples were sterile and 779 (21.3%) samples showed insignificant growth. Urinary Tract Infection was more common in female (68.7%) compared to males (31.2%) Table 2: Month wise Distribution of Urine Samples and uropathogens Year Month Total samples processed Total isolates No. % No % 2006 December 160 4.3 44 5.0 2007 January 201 5.5 42 4.8 2007 February 210 5.7 29 3.3 2007 March 265 7.2 57 6.5 2007 April 302 8.2 70 8.1 2007 May 322 8.8 72 8.3 2007 June 303 8.3 80 9.2 2007 July 385 10.5 120 13.8 2007 August 384 10.5 115 13.3 2007 September 338 9.2 65 7.5 2007 October 251 6.8 60 6.9 2007 November 261 7.1 50 5.7 2007 December 266 7.2 53 6.1 Grand Total 3648 100.0 864 100.0 The no. of samples was significantly higher from July to September and a corresponding higher isolation rates was also observed in this season. Table 3: Profile of Gram negative and Gram positive uropathogens S.No. Uropathogens No. of isolates % Gram negative 1 E.coli 746 89.6 2 Citrobacter freundii 36 4.3 3 Enterobacter aerogens 26 3.1 4 Proteus mirabilis 9 1.0 5 Morganella morganii 8 0.9 6 Proteus mirabilis 3 0.3 7 Pseudomonas aeruginosa 3 0.3 8 Salmonella.typhi 1 0.1 Gram positive 1 Coagulase negative staphylococci 12 37.5 2 Staphylococcus saprophyticus 9 28.1 3 Staphylococcus aureus 7 21.8 4 Enterococcus faecalis 4 12.5 59

Among the total bacterial isolates (864),gram negative encountered the highest position 832(86.3%)followed by gram positive 32 (13.7%).Out of 832 gram negative uropathogens, the highest numbers of isolates were found to be E.Coli 746 (89.6%) followed by Citrobacter freundii (4.3%) and Enterobacter aerogens (3.1%).Among the total 32 gram positive isolates, Coagulase Negative Staphylococci (37.5%) was the most prevalent followed by Staphylococcus saprophyticus (28.1%), Staphylococcus aureus (21.8%) and Enterococcus faecalis (12.5%). Table 4: Age wise distribution of the uropathogens Bacteria 0-9 10-19 20-29 30-39 40-49 50-59 60-69 70-79 80-89 90-99 E.coli 22 59 243 98 82 85 77 50 26 4 Citrobacter freundii 1 6 11 7 5 2 2 3 - - Enterobacter aerogens 1 1 18 2 - - - 3 1 - Proteus mirabilis - - 4 3 1 1 - - - - Morganella morganii - 1 3-1 1 3 - - - Proteus vulgaris - - 1 1-1 - - - - Pseudomonas aeruginosa - - - 1 - - - 1 1 - Salmonella.typhi - - 1 - - - - - - - Coagulase negative 1 1 3 4 - - 1 2 - - staphylococci Staphylococcus saprophyticus - - 3 2 1 2 1 - - - Staphylococcus aureus - - 1-1 4 1 - - - Enterococcus faecalis - - - - 1 1 2 - - - Maximum infection was found in the age group of 20-29 years followed by age group of 30-39 years. Most of the uropathogens were isolated in these age groups. Table 4: Antibiotic sensitivity profile of gram negative isolates S.No. Antibiotic Isolate Sensitive Intermediate Resistant No. No. % No. % No. % 1 Amoxycillin 832 306 36.7 6 0.7 520 62.5 2 Cefotaxime 832 615 73.9 4 0.4 216 25.9 3 Ciprofloxacin 832 491 59.0 2 0.2 339 40.7 4 Cotrimoxazole 832 472 56.7 2 0.2 358 43.0 5 Cefixime 832 543 65.2 1 0.1 288 34.6 6 Nitrofurantoin 832 675 81.1 - - 157 18.8 7 Norfloxacin 832 502 60.3 4 0.4 326 39.1 60

8 Ofloxacin 832 509 61.1 1 0.1 322 38.7 Among the 832 gram negative isolates, Nitrofurantoin was the most effective antibiotic in 675 (81.1%) isolates followed by Cefotaxime (75.9%), Cefixime (75.9%), (Norfloxacin (63.2%), Ofloxacin (61.1%), Ciprofloxacin (59.0%) and Cotrimoxazole (56.7%).Amoxycillin (36.7%) was the least effective antibiotic. Table 6: Antibiotic sensitivity profile of gram positive isolates S.No. Antibiotic Isolate Sensitive Intermediate Resistant No. No. % No. % No. % 1 Amoxycillin 32 21 65.6 - - 11 34.4 2 Cefotaxime 32 30 93.7 - - 2 6.3 3 Ciprofloxacin 32 30 93.7 - - 2 6.3 4 Cotrimoxazole 32 25 78.1 5 15.6 2 6.3 5 Cephalexin 32 29 90.6 - - 3 9.4 6 Cloxacillin 32 22 68.7 5 15.6 5 15.7 7 Erythromycin 32 20 62.5 - - 12 37.5 8 Norfloxacin 32 25 78.1 - - 7 21.9 Among the 32 gram positive isolates, Cefotaxime and Ciprofloxacin were the most susceptible antibiotics in 30(93.7%) isolates, followed by Cephalexin (90.6%), Cotrimoxazole (78.1%), Norfloxacin (78.1%), Amoxycillin (65.6%) and Erythromycin (62.5%). Table 7: Antibiotic Resistance Pattern of Uropathogens Total Resistance to Organisms Isolate 0 1 2 MDR strains No. drug drug drugs 3 drugs >3 drugs Total % E.coli 746 75 83 75 136 377 513 68.7 Citrobacter freundii 36 12 10 10 2 2 4 11.1 Enterobacter aerogens 26 6 10 2 5 3 8 30.7 Morganella morganii 8 2 2 2 1 1 2 25.0 Pseudomonas aeruginosa 3 - - 1-2 2 66.6 Salmonella.typhi 1 - - 2 - - - - C oagulase negative staphylococci12 3 1-3 5 8 61.5 Staphylococcus aureus 7 2 2 1 2-2 28.5 Enterococcus faecalis 4 - - 1 2 1 3 75.0 Among the total isolates multidrug resistance (MDR= resistance 3drugs) was the most commonly associated with Enterococcus faecalis (75.0%) followed by E.coli (68.7%), Pseudomonas aeruginosa (66.6%), Coagulase negative staphylococci (61.5%), Enterobacter aerogens (30.7%), Staphylococcus aureus (28.5%) and Morganella morganii (25.0%). 61

Table 8: Extended Panel of Antibiotics for MDR Gram Negative Uropathogens S.No. Antibiotic Isolate Sensitive Intermediate Resistant No. No. % No. % No. % 1 Amikacin 350 280 80.0 13 3.7 57 16.2 2 Ceftriaxone 350 225 64.2 - - 125 35.7 3 Gentamycin 350 206 58.8 - - 144 41.1 4 Chloramphenicol 350 156 44.5 12 3.4 194 55.4 5 Ceftazidime 350 123 35.1 14 4.0 227 64.8 Among 350 Multi Drug Resistance gram negative uropathogens, Amikacin (78.9%) was the most effective drug followed by Ceftriaxone (62.4%) and Gentamycin (56.7%). Discussions Urinary tract infection is a common cause of morbidity and can lead to a significant mortality. Careful diagnosis and treatment result in successful resolution of infection in most instances. Bacteriological examination of the urine is major aid in the diagnosis of infection. During the study period (December 2006- December2007), 3648 urine samples were analyzed. Out of 3648 samples 864 (23.6%) showed significant growth. The rate of growth positivity was found to be 68.7% in female whereas it was found to be 31.2% in males. Such high rate of growth possibility in 10, 11, women is reported by other investigators 12. The higher no. of requests and higher growth positivity in females is attributed to their anatomical structure (short urethra and proximity to anal orifice).in this study, the highest percentage of the infected patients (30%) belonged to age group 20-29 year. This age group of the patient is sexually active and is of childbearing age in case of female. This finding corresponds to other results 10, 12. Reports from world wide suggest a significant peak of UTI for a few months in post summer season each year. They attribute this to hot and humid conditions during these months. We have observed that the samples were maximum in July and August with corresponding high recovery of isolates during this period 13,14. E.coli (86.3%) was the commonest isolate resembles to various other reports 10, 12. E.coli is the most important pathogen for uncomplicated as the complicated UTI and has shown a slow and steady increase in resistance to several antibiotics over the past decade 15,16. Nitrofurantoin was found to be the most effective for gram negative isolates (81.1%).Similar data is presented in other reports 10,12,17. In our study, Enterococcus faecalis (75.0%) was found to be the most common Multi Drug Resistance (MDR) uropathogens followed by E.Coli (68.7%) and Pseudomonas aeruginosa (66.6%).MDR was defined as resistance to 2 or >2 classes of the antimicrobials ( 3drugs) of first line tested in this study.enterococcus faecalis and Pseudomonas aeruginosa were commonly 62

associated with the patients admitted in the hospital, in whom there is increase intake of antibiotics and increased urological manipulation. According to Hasan et al, multidrug resistance was the commonest with Enterococcus faecalis (78.8%) followed by Pseudomonas aeruginosa (65.1%) 14. Infectious Diseases Society of America (IDSA) recently recommended that each hospital should establish mechanisms to determine the local resistance rates among uropathogens and that the standard antimicrobial regimens for empirical treatment of UTIs should be reassessed periodically in light of changing susceptibility pattern. Clinicians should be aware of current antimicrobial susceptibility patterns for E.coli and other uropathogens in their local communities as antimicrobial susceptibility changes over time 18.The overall high resistance to Amoxycillin and Cotrimoxazole found in this study resembles to other studies 18,19,20.Similar to our study the resistance rate of Ciprofloxacin in other studies 18,19.In E.coli uropathogen, a correlation between Ampicillin, Cotrimoxazole and Ciprofloxacin resistances has previously reported 21.A decline in the activity of Ciprofloxacin would be especially problematic in view of the ability of gram negative bacilli to acquire resistance to all other classes of antimicrobials 22. Among the total isolates multidrug resistance (MDR= resistance 3drugs) was the most commonly associated with Enterococcus faecalis (75.0%) followed by E.coli (68.7%), and Pseudomonas aeruginosa (66.6%). This study is closely related to the study done by Hasan et.al 14.The most useful first line antibiotic for the treatment of urinary tract infection is Nitrofurantoin which is also reported to other studies 10, 12.In extended panel of antibiotics for the treatment of MDR uropathogens, Amikacin was the most effective antimicrobial agent and this was also shown in this study 14. Conclusion In conclusion, the alarming finding of this study was the high prevalence of MDR uropathogens which are resistant to almost all antimicrobial agents. Higher resistance rates to all antibiotics tested in our study may be due to high and uncontrolled consumption of these antibiotics. All the antibiotics are easily available in the market and can be purchased without requiring the doctor s prescription in our country. Further study is needed to find out the clear reason of such high prevalence of MDR uropathogens.this is an urgency to recognize all the factors involved in the prevalence of MDR, control and regular monitoring of the usage of antimicrobial agents and select the best strategies for the prevention and control the development of resistance. Acknowledgement We are very thankful to Mr Ashok Manandhar for his assistance in data analysis, Mr Sanjit Shrestha for manuscript preparation and all the laboratory staffs for their valuable contributions during the study period. References 63

1. Chakrabarti P. Textbook of Microbiology.1 st edition, New Central Book Agency, Calcutta 2001. 2. Sharm a S. C urrent understanding of pathogenic m echanism s in urinary tract infections. A nn N at l A ca M ed Sci 1997; 33:31-8 3. Simon N, McRae, Linda M, Dairiki Shortliffe.Bacterial infections of genitourinary tract.smith s General Urology 15 th edition, Large Medical Book /McGrew Hill Health Professional Division,2000:p237-264 4. Kass E H.Asyptomatic infections of urinary tract.trans Am phys 1978;69:56 5. Gruneber4g G N.Antibiotic sensitivities of urinary pathogens: 1971-1982.J Antimicrob Chemthr 1984;14:17-23 6. Jones R N, Thronsberry C.Cefotaxime:a review of in vitro antimicrobial properties and spectrum of activity 7. Fu K P,Neu H C.Betalactamase stability of HR 750 a novel cephalosporin compared to that of cefuroxime and cefotaxime. Antimicrob Agents Chemother 1978;14:322-6 8. Barons B J, Finegold S M.Bailey and Scott s Diagnostic Microbiology.8 th edition.st Louis Missouri Baltimore: CV Mosby-yearbook, 1990. 9. Cheesebrough M.District Laboratory Practices in Tropical Countries Part 2.Cambridge University Press 2001. 10. Jha VC, Y adav JN.B acterial Species isolated from urine of U TI Patients and their sensitivity to com m onaly available antibiotics.j N epal M ed A ssoc 1992; 30:222-225 11. Rajbhandari R, Shrestha J.Bacteriological study of urinary tract infection and its antibiotic sensitivity test( Hospital Based Study).J Nepal Assoc.for Med Lab Sci 2002; 4:26-32 12. Shrestha B,Basnet RB,Shrestha P,Shahi P.Prevalence of urinary tract infection in female patients attending Kathmandu Model Hospital.J Nepal Assoc for Med Lab Sci 2005;7:10-14 13. Anderson JE.Seasonality of symptomatic bacterial urinary infections in women. J Epidemiol Community Health.1983; 37(4):286-90 14. Hasan AS, Nair D, Kaur J, Baweja G, Deb M, Aggrawal P.Resistance Patterns of urinary Isolates in a Tertiary Indian Hospital.J Ayb Med Coll Abbottabad 2007;19(1):39-41 15. Kahlmeter G.Prevalence and antimicrobial susceptibility of pathogens in uncomplicated cystitis in Europe.The ECO.SENS study.int J Antimicrob agents 2003; 22:49-52. 16. Gales AC,sader HS and Jones RN.Urinary Tract infections trends in latin American Hospitals:report from the SENTRY antimicrobial surveillance program91997-2000).diagn Microbiol Infect Dis.2002;44:289-299 17. Chhetri PK, Rai SK, Pathak UN.Retrospective Study On urinary tract infection at Nepal Medical College 64

Teaching Hospital, Kathmandu. Nepal Medical college J 2001;3(2):83-85 18. Sahm DF, Thornsberry C, Mayfield DC, Jones ME, Karlowsky JA.Multidrug Resistance Urinary Tract Isolates of Escherichia coli : Prevalence and patient demographics in the United States in 2000.Antimicrob Agents Chemother 2001;45:1402-1406 19. Moniri R, khorsidi A, Akbari H.Emergence of Multidrug resistance strains of Escherichia coli isolated from urinary tract infection. Iranian J Publ Health 2003;32(4):42-46 20. 21. Gupta N, Kundra S, Sharma S,Gautam V, Arora DR.Antimicrobial susceptibility of uropathogens in India.J Infect Dis Antimicrob Agents 2007;24(1):13-18 22. Zhanel GG, Karlowsky JA, harding GK et.al.a Canadian National Surveillance Study of urinary Tract Isolates Outpatients:Comparision of the activities of Trimethoprim-Sulfamethoxazole, Ampicillin,Mecillinam, Nitrofurantoin and Ciprofloxacin.The Canadian Urinary Isolate Study Group.Antimicrob Agents Chemother 2000;44:1089-92 23. Sahm DF, Critchley IA,Kelly LJ et.al.evaluation of Current activities of fluroquinolones against gram negative bacilli centralized in vitro testing and electronic surveillance.antimicrob agents chemotherapy 2001;45(1):267-274 65