XML Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Nazir A, Kanth F. Bacteriological profile and antimicrobial susceptibility pattern of patients with urinary tract infections in a tertiary care hospital in a tertiary care center. Journal of Research in Applied and Basic Medical Sciences 2024; 10 (2) :110-120
URL: http://ijrabms.umsu.ac.ir/article-1-248-en.html
Microbiology , asifanazir@gmail.com
Full-Text [PDF 601 kb]   (551 Downloads)     |   Abstract (HTML)  (1545 Views)
Full-Text:   (625 Views)
Introduction
Urinary tract infection (UTI) is one of the most common bacterial infections encountered in clinical practice. It is estimated that 150 million cases of UTI occur globally per year resulting in more than 4 billion pounds (6 billion dollars) in direct health care expenditure (1).
Traditionally, UTIs are categorized as uncomplicated or complicated, or by the site of infection. Uncomplicated urinary tract infection (UTI) refers to infection in a structurally and neurologically normal urinary tract. The generally accepted definition of complicated UTI includes infection in the presence of factors that predispose to persistent or relapsing infection, such as foreign bodies (e.g., calculi, indwelling catheters or other drainage devices); obstruction; immunosuppression; renal failure; renal transplantation; and urinary retention from neurologic disease (2). Lower UTIs include urethritis and cystitis, and upper tract infections include pyelonephritis and renal abscesses. Acute infections are usually associated with a single pathogen; chronic infections are usually polymicrobial.
Urinary tract infections can be community acquired or nosocomial. Community-acquired urinary tract infections (CA-UTIs) are defined as the infection of the urinary system that takes place in one’s life in the community setting or in the hospital environment with less than 48 hours of admission. Community-acquired UTI is the second most commonly encountered microbial infection in the community setting (3). Nosocomial urinary tract infections (N-UTIs) are the infections of the urinary tract that occurs after 48 hours of hospital admission, and the patient was not incubating at the time of admission or within 3 days after discharge (4). UTI can be asymptomatic or symptomatic, characterized by a wide spectrum of symptoms ranging from mild burning micturition to bacteremia, sepsis, or even death (5). Although UTI affects both genders, women of the reproductive age group (15-44 years) are the most vulnerable. Young, otherwise healthy, women are commonly affected with an estimated incidence of 0.5–0.7 infections per year (6). Of the women affected, 25%–30% will go on to develop recurrent infections not related to any functional or anatomical urinary tract abnormality. Women are particularly at risk of developing UTIs because of their short urethra, and certain behavioral factors which include delay in micturition, sexual activity and the use of contraceptives which promote colonization of the periurethral area with coliform bacteria (7).
E. coli is the most common organism causing UTI which accounts for up to 65 -90% of cases followed by K. pneumoniae, Staphylococcus, Proteus, Pseudomonas, Enterococcus, and Enterobacter (8). Next to respiratory tract infections UTI is the second most common bacterial disease encountered in the primary care settings (9). Global statistics revealed that 8.3 million outpatient clinic visits are due to UTI and annually emergency department deals with 1 million UTI cases and around 100,000 patients got admitted to the hospitals due to complicated UTI (10).
There are important medical and financial implications associated with UTIs. In the non-obstructed, nonpregnant female adult, acute uncomplicated UTI is believed to be a benign illness with no long-term medical consequences. However, UTI elevates the risk of pyelonephritis, premature delivery, and fetal mortality among pregnant women, and is associated with impaired renal function and end-stage renal disease among pediatric patients. Financially, the estimated annual cost of community-acquired UTI is significant, at approximately $1.6 billion (11).
Management of UTI is largely empirical without the use of a urine culture and susceptibility testing to guide therapy. This practice is a risk for development of antimicrobial resistance among uropathogens. The extensive and inappropriate use of empirical antimicrobial agents has resulted in development of antimicrobial resistance which in recent times has become a major problem worldwide. This emergence and rapid spread of multi-drug resistance among uropathogens has now become a global phenomenon, especially in Japan, China, the US, India, Brazil, Nepal, and Saudi Arabia (12).
It is necessary therefore to have a prior knowledge of the causal organism and its antibiotic susceptibility pattern in order to start a proper empirical antibiotic therapy, and prevent a further rise of antibiotic resistance in uropathogens. Also, the data related to the causal organism and its antibiotic susceptibility pattern changes continuously from one hospital to others and from one region to another; careful monitoring, assembly, and updating of such data is highly recommended.
Thus, the aim of this study was to find out the clinical and microbiological profile of urinary tract infections and to provide knowledge about their etiology, antibiotic susceptibility and appropriate antibiotic treatment.

Materials & Methods
This was a cross-sectional analytical hospital-based study in which analysis of urinary culture results was done. This study was conducted in the Microbiology department of a tertiary health care hospital in Srinagar, from July 2021 to December 2021.
Both out and inpatients presenting or highly suspicious of having UTIs were recruited in the study. The details regarding patient's age, sex, literacy, socioeconomic status, residential area (rural/urban) were recorded along with the sample. Both male and female patients having clinically suspected symptoms of UTI were included in the study.
Culture and Identification: Midstream, clean catch urine samples from all suspected UTI patients were collected in a wide mouth sterile container. The samples were collected aseptically before the starting of antibiotic treatment. These sample were examined and processed within 24-28 hours.
The urine was examined macroscopically for the color and turbidity and wet mount of urine samples were prepared. The wet mounts were observed microscopically to identify the presence of pus cells, red blood cells, epithelial cells, crystals, parasites and yeast. All the findings were recorded. All urine samples were inoculated aseptically on to Hi-Chrome UTI agar using a calibrated wire loop of 28G with an internal diameter of 3.26 mm holding 0.004 ml of urine. The plates were incubated at 37 0 C aerobically and after overnight incubation, they were checked for significant bacteriuria as under by enumeration of colonies [growth of 100 colonies equals to 105 colony forming units (CFU) of bacteria /ml of urine] (13).
A presumptive identification of the isolates was made on the colony color on the Hi-Chrome UTI agar based on the manufacturer’s instructions (Hi-media); Hi-Chrome UTI agar is a chromogenic medium designed to isolate and identify all uropathogens. An important aspect of Hi-Chrome UTI agar is that it allows an easy differentiation of various species from mixed cultures due to specific colony color (14).
Samples showing significant bacterial growth (>105/ml) were subjected to standard biochemical tests for identification and antimicrobial sensitivity testing by Kirby-Bauer disc diffusion method. Interpretation as 'Sensitive' or 'Resistant' was done on the basis of the diameters of zones of inhibition of bacterial growth as per CLSI guidelines (15).
Antimicrobial susceptibility testing: The antibiotics included in our study were co-amoxiclav (20/10 mcg), ampicillin (10 mcg), amikacin (30 mcg), trimethoprim/sulfamethoxazole (co-trimoxazole) (25/23.75 mcg), norfloxacin (5 mcg), ciprofloxacin (5 mcg), levofloxacin (5 mcg), nitrofurantoin (300 mcg), gentamicin (10 mcg), amikacin (30 mcg), cefuroxime (30 mcg), ceftriaxone (30 mcg), ceftazidime (30 mcg), cefotaxime (30 mcg), polymyxin B (2 mcg), piperacillin/tazobactam (100/10 mcg), cefoperazone/sulbactam (75/30 mcg), meropenem (10 mcg), imipenem (10 mcg), and vancomycin (30 mcg).
Descriptive and inferential statistical methods were used. Data were analyzed using SPSS-15th version. A probability of <0.05 was accepted as significant. For continuous variables having normal distribution, data were summarized using mean ± SD, range and median were used for all continuous variables having non-normal distribution (i.e., age).
Results
In our study, out of 2825 samples received in our microbiology laboratory for urine culture from patients suspected with UTI, 804 were reported as bacterial UTIs as per culture and sensitivity reports i.e., the positivity
rate was 28.46% (Figure 1).
 

Fig. 1. The number of positive samples isolated (28%)
 

Gram-negative bacteria accounted for 58.5% (471/804) and Gram-positive 33% (267/804) of the positive results. Among Gram-negative isolates, E. coli (33.8%) and K. pneumoniae (10.8%) were the most prevalent microorganisms in UTI patients, while other gram negatives isolated included Pseudomonas aeruginosa (10.1%), Acinetobacter (1.2%), Proteus sp (1%), Enterobacter sp (1%) and Citrobacter sp (0.2%) as seen in Table 1.
 

Table 1. The age-wise distribution of study samples (n=804)
Age group  Males (353)
 (n, %)
Females (451)
 (n, %)
15-25 years
26-35 years
36-45 years
46-55 years
56-65 years
>65 years
72 (20.4)
34 (9.6)
45 (12.7)
46 (13.0)
61 (17.3)
95 (26.9)
43 (9.5)
88 (19.5)
126 (27.9)
74 (16.4)
56 (12.4)
64 (14.1)
Total 353 451
 
Enterococcus sp (26.3%) was the most common gram-positive organism isolated followed by Staphylococcus aureus (6.8%), most of which were methicillin resistant (Figure 2).
 


Fig. 2. Showing the frequency of uropathogens isolated


Urinary tract infection was higher in females,451/804 (56.1%) as compared to men, 353/804(43.9%) as shown in Figure 3.

Fig. 3. Gender-wise distribution of study cases
 

As shown in Figure 4, the presence of uropathogens was most common in the age group 36-45 years in females (27.9%) and age group above 65 years in males (26.9%). E. coli was the most organism isolated from both males and females as shown in Figure 4.
 

Fig. 4. Distribution of uropathogens according to gender.

 

Tables 2 and 3 are representative of the overall antibiotic sensitivity pattern of urinary bacterial isolates. E. coli was mostly sensitive to nitrofurantoin (79%%), cefoperazone/sulbactam (40.7%), piperacillin /tazobactam (39.3%). It showed significant resistance to quinolones and carbapenems. Among the isolates of Klebsiella pnuemoniae, nitrofurantoin (71.2%) was the most effective antibiotic while as ceftriaxone was the least effective (28.7%) as shown in Table 2.
 

Table 2: Number and percentage distribution of drug sensitivity of gram-negative uropathogen
Antibiotics E. coli (272)

n%
Klebsiella sp (87)

n%
Pseudomonas aeruginosa (82)
n%
Acinetobacter sp (10)

n%
Nitrofurantoin 215 (79.0) 62 (71.2) 8 (9.7) 4 (40.0)
Co-trimoxazole 106 (38.9) 46 (56.8) 7 (8.5) 2 (20.0)
Norfloxacin 71 (26.1) 31(35.6) 20 (24.3) 1 (10.0)
Ciprofloxacin 81 (29.7) 32(36.7) 30 (36.5) 2 (20.0)
Ceftriaxone 99 (36.3) 25 (28.7) 18 (21.9) 2 (20.0)
Amikacin 101 (37.1) 30(34.4) 19 (23.1) 3 (30.0)
Imipenem 56 (20.5) 29 (33.3) 18 (21.9) 2 (20.0)
Meropenem 102 (37.5) 46 (52.8) 20(24.3)  4 (40.0)
Ampicillin 4 (1.4) - 0 0
Cefoperazone/sulbactam 109 (40.7) 55 (63.2) 21 (25.6) 3 (30.0)
Piperacillin/tazobactam 107(39.3) 54 (62.0) 25(30.4) 4 (40.0)
Aztreonam - - 13 (15.8) -
 
 In gram-positive organisms Enterococcus had maximum sensitivity to linezolid (100%), followed by nitrofurantoin (61.7%) and vancomycin (61.7%). Most of the strains of Staphylococcus were methicillin resistant 51/55 (92.7%) against whom the most effective antibiotics were vancomycin and linezolid. (Table 3).
 

Table 3: Number and percentage distribution of drug sensitivity of gram-positive uropathogens
Antibiotics Enterococcus sp (212)
n (%)
Staphylococcus aureus (55)
n (%)
Penicillin 14 (4.2) 2(3.9)
Ciprofloxacin 28 (13.2) 30(58.8)
Nitrofurantoin 160 (75.4) 41 (80.3)
Ampicillin 16 (7.5) 1 (1.5)
Tetracycline 117 (55.1) 22 (43.1)
Linezolid 212 (100) 51 (100)
Vancomycin 131 (61.7) 51 (100)
Ceftriaxone - 4 (7.8)
Discussion
UTI is one of the most common diseases diagnosed worldwide and bacterial infection of the urinary tract is one of the common causes for seeking medical attention in the community. Effective management of patients suffering from bacterial UTIs commonly relies on the identification of the type of organisms that caused the disease and the selection of an effective antibiotic agent. The etiology and the antimicrobial susceptibility for urinary tract infection have been changing over the years. Knowledge of local susceptibility patterns is important for the selection of appropriate empirical therapy for UTI.
The present study shows the different types of bacterial pathogens isolated from urine sample of patients suffering from urinary tract infection (UTI) and their antibiotic sensitivity pattern. It focuses on the distribution of UTIs across both genders and various age groups, as well as the resistance patterns exhibited by various uropathogens in response to the antimicrobials.
The prevalence of UTI was found to be 28.46% in this study correlating to the prevalence rate of UTI with study done by Sharma et al. (27.3%) (16).
Some studies from India done by M. Dash et al. (17) and M. Mehta et al. (18) showed prevalence of 34.5% and 36.68%, respectively. Also, higher prevalence was seen in a study by Devanand et al. (53.82%) (19). The higher prevalence of UTIs in this study could have been probably due to the inclusion of a number of risk groups like diabetes, elderly, pregnant women, HIV, infants, and a high number of inpatients who are usually prone to UTIs.
We assessed the relationship between various risk factors and UTI. Sex was one of the considered factors and the result indicated that UTI prevalence was higher in females than males for each isolate. In the present study, 56% of the patients were females and 43.9% of the patients were males, with male: female ratio of 0.78: 1. Similar findings have also been reported by numerous authors in their studies (20,21). The reason behind this high prevalence of UTI in females is due to the proximity of the urethral meatus to the anus, shorter and wider urethra, sexual intercourse, incontinence, less acidic pH of vaginal surface, and poor hygienic conditions (22). On the other hand, some studies show contrary results and in these studies prevalence of UTI was higher in males due to prostate enlargement (23). Thus, it appears that the percentage of UTI in males and females can vary depending on the place of study or physiological characters of the patients.
Prevalence difference was also observed among various age groups. Increased incidence of UTI was seen among female patients in age groups from 36 -45 years (27.9%) followed by 19.5% in 26-35 years age group. The risk factors for recurrent UTI in premenopausal sexually active women include the onset of symptoms briefly after sexual intercourse, the use of spermicides for contraception, the emergence of new sexual partners, the age of the first UTI, maternal history of UTI and the dysfunction in voiding (24). This difference suggests that age is one risk factor associated with UTI. The high incidence of UTI amongst the old age group could be due to genito-urinary atrophy and vaginal prolapse after menopause in females which in turn increases the risk of bacteriuria by increasing vaginal pH and decreasing vaginal Lactobacillus thereby allowing gram-negative bacteria to grow and act as uropathogens (25). Moreover, some studies have indicated that UTI is more common infection in elderly populations (26).
Gram-negative bacteria accounted for 58.5% (471/804) and Gram-positive 33% (267/804) of the positive results which were in agreement with other studies also (27). E. coli was the most common organism isolated (33.8%) among the gram negatives followed by Klebsiella sp (10.8%) while other gram negatives isolated included Pseudomonas aeruginosa (10.1%), Acinetobacter (1.2%), Proteus sp (1%), Enterobacter sp (1%) and Citrobacter sp (.2%). These finding correlates with the findings of Bharti et al., where the prevalence of E. coli and Klebsiella was found to be 36.84% and 7.66%, respectively (28). This result is also consistent with reports from other studies by Devanand et al., (19), Arghya Das et al., (29) Ahmed Naeem et al. (30) where 42.58%, 53.69%, 34.1% cultures grew E. coli, respectively; and it was the most frequent pathogen causing UTI in all these studies. Higher incidence of gram-negative bacteria, related to Enterobacteriaceae, in causing UTI has many factors which are responsible for their attachment to the uroepithelium such as they are able to colonize in the urogenital mucosa with adhesins, pili, fimbriae, and P-1 blood group phenotype receptor (31).
In the present study E. coli was sensitive to nitrofurantoin, imipenem and amikacin which was contrary to the findings of Pattanayak C et al., (32) who found that the organism was mainly sensitive to polymyxin B, gatifloxacin and ceftriaxone. In this study, E. coli was mostly resistant to cephalosporins, which are consistent with the findings of other studies. (33).
In our study Klebsiella sp were sensitive to nitrofurantoin (71.2%), meropenem (52.8%) and ceftriaxone (56.8%). Study by Ahmed Naeem et al. (30) has reported highest sensitivity to
gentamicin (92.3%) followed by imipenem (90.2%) and less sensitivity was shown to cefotaxime. Arghya Das et al. (29) in his study observed highest resistance to ampicillin, fluoroquinolones and ceftriaxone whereas gentamicin and nitrofurantoin were the antibiotics to which organisms were most sensitive. Our findings are consistent with another study showing alarmingly high resistance for fluoroquinolones and third-generation cephalosporins. (34).
Enterococcus sp (26.3%) was the most common gram-positive organism isolated followed by Staphylococcus aureus (6.8%), most of which were methicillin resistant. These findings were similar to study of Chooramani et al. (35) who showed the incidence Enterococcus spp (20.7%) and Klebsiella spp (10.3%). The sensitivity pattern of Enterococcus revealed that the most effective drugs against it were linezolid (100%), Vancomycin (61.7%) and nitrofurantoin (75.4%). A study by Goel et al. in New Delhi (36) also revealed a high degree of resistance of Enterococcus to tetracycline and ciprofloxacin. Variations in sensitivity may be due to the inappropriate exposure of different localities as to antibiotics which can drive the development of resistance.
The increasing rates resistance to antibiotics such as ampicillin, cephalosporins, trimethoprim-sulfamethoxazole, and quinolones, especially in E. coli and Klebsiella strains, which are the most common pathological agents of UTI in our region, have limited the use of these treatments. Nitrofurantoin, one of the oldest oral antibiotics, emerged as the drug which showed high sensitivity in our study. It was effective against most of the uropathogens especially among the OPD patients. This may be because of localized action of this drug only on the urinary tract. So, nitrofurantoin can be considered as the first line, cost saving and effective oral therapy in UTI patients at OPD level.
Conclusion
Urinary tract infections pose a major health problem for human society worldwide. The results of the present study reveal that UTI occurs in all age groups and both genders but prevalence was higher in females. The need of the hour is periodic assessment of the susceptibility pattern of urinary pathogens as it serves as a guide for antibiotic therapy as these organisms exhibit resistance to many first-line drugs used for UTI infection. In order to prevent resistance to antibiotics, appropriate therapy as per antibiotic sensitivity pattern needs to be initiated. The small size of the sample is the main limitation of this study, so it is recommended to do more studies in this case with more study populatiuon.

Acknowledgments
Not declared.
Conflict of interest:
The authors declare that they have no conflicts of interest.

Funding/support:
No financial support was received for the work within this manuscript.

Data Availability
The raw data supporting the conclusions of this article are available from the authors upon reasonable request.

Ethical statement:
The study was a retrospective analysis of existing data and did not involve any direct patient contact or intervention. All patient data were anonymized and de-identified to protect patient confidentiality.
 
Type of Study: orginal article | Subject: General

References
1. Harding GKM, Ronald AR. The management of urinary infections: what we have learned in the past decade. Inter J Antimicrob Agents 1994;4:83-8. [DOI:10.1016/0924-8579(94)90038-8] [PMID]
2. Levison ME, Kaye, D. Treatment of complicated urinary tract infections with an emphasis on drug-resistant gram-negative uropathogens. Curr Infect Dis Rep 2013;15:109-15. [DOI:10.1007/s11908-013-0315-7] [PMID]
3. Sabrina J. Antimicrobial resistance among producers and non-producers of extended spectrum beta-lactamases in urinary isolates at a tertiary Hospital in Tanzania. BMC Res Notes 2010;3:348. [DOI:10.1186/1756-0500-3-348] [PMID] []
4. Iacovelli V, Gaziev G, Topazio L, Bove P, Vespasiani G, Finazzi Agrò E. Nosocomial urinary tract infections: A review. Urologia 2014;81(4):222-7. [DOI:10.5301/uro.5000092] [PMID]
5. Stamm WE, Hooton TM. Management of urinary tract infections in adults. N Eng J Med 1993;329:1328-34. [DOI:10.1056/NEJM199310283291808] [PMID]
6. Hooton TM, Scholes D, Hughes JP, et al. A prospective study of risk factors for symptomatic urinary tract infection in young women. N Engl J Med 1996;335:468-74. [DOI:10.1056/NEJM199608153350703] [PMID]
7. Litza JA, Brill JR. Urinary tract infections. Primary Health Care 2010;37(3):491-507. [DOI:10.1016/j.pop.2010.04.001] [PMID]
8. Manges AR, Natarajan P, Solberg OD, Dietrich PS, Riley LW. The changing prevalence of drug-resistant Escherichia coli clonal groups in a community: evidence for community outbreaks of urinary tract infections. Epidemiol Infect 2006;134(2):425-31. [DOI:10.1017/S0950268805005005] [PMID] []
9. Hotchandani R, Aggarwal KK. Urinary Tract Infections in Women. Indian J Clin Practice. 2012;23(4):187-94. [PMID]
10. Naber KG, Schito G, Botto, H, Palou J. and Mazzei T. Surveillance study in Europe and Brazil on clinical aspects and Antimicrobial Resistance Epidemiology in Females with Cystitis (ARESC): implications for empiric therapy. Eur Urol 2008;54(5):1164-75. [DOI:10.1016/j.eururo.2008.05.010] [PMID]
11. Foxman B. Epidemiology of urinary tract infections: incidence, morbidity, and economic costs.Am J Med 2002;113:5-13. [DOI:10.1016/S0002-9343(02)01054-9] [PMID]
12. Dehbanipour R, Rastaghi S, Sedighi M, Maleki N, Faghri J. High prevalence of multidrug-resistance uropathogenic Escherichia coli strains, Isfahan, Iran. J Nat Sci Biol Med 2016;7:22-6. [DOI:10.4103/0976-9668.175020] [PMID] []
13. Collee JG, Marr W. Specimen collection, culture containers and media. In: Collee JG, Fraser AG, Marmion BP, Simmons A. eds. Mackie & McCartney Practical Medical Microbiology, 14th edition New York, Churchill Livingstone. 1996:85-111. [URL]
14. Samra Z, Heifetz M, Talmor J, Bain E, Bahar J. Evaluation of use of a new chromogenic agar in detection of urinary tract pathogens. Journal Clin Microbiol 1998;36:990-4. [DOI:10.1128/JCM.36.4.990-994.1998] [PMID] []
15. Clinical and Laboratory Standards Institute. Performance Standards for Antimicrobial Susceptibility Testing: Thirty-First Edition M100-S31. Wayne: CLSI.2021. [URL]
16. Sharma AR, Bhatta DR, Shrestha J, Banjara MR: Antimicrobial Susceptibility Pattern of Escherichia coli Isolated from Urinary Tract Infected Patients Attending Bir Hospital. Nepal J Sci Techn 2013;14(1):177-84. [DOI:10.3126/njst.v14i1.8938]
17. Dash M, Padhi S, Mohanty I, Panda P, Parida B. Antimicrobial resistance in pathogens causing urinary tract infections in a rural community of Odisha, India. J Family Community Med 2013;20(1):20-6. [DOI:10.4103/2230-8229.108180] [PMID] []
18. Mehta M, Bhardwaj S, Sharma J. Screening of urinary isolates for the prevalence and antimicrobial susceptibility of Enterobacteria other than Escherichia coli. Int J Life Sci Pharma Res 2013;3(1):100-4. [Google Scholar]
19. Prakash D, Saxena RS. Distribution and antimicrobial susceptibility pattern of bacterial pathogens causing urinary tract infection in urban community of meerut city, India. ISRN Microbiol 2013;2013:749629. [DOI:10.1155/2013/749629] [PMID] []
20. Kumari SS, Ramaya T, Reddy K, Gundela S, Venkata S, Reddy BS, et al. Etiology and antibiotic resistance pattern of uropathogens in a tertiary care hospital from South India. Tropical J Pathol Microbiol 2019;5(6):1-10. [PMID]
21. Ahmed SS, Shariq A, Alsalloom AA, Babikir IH, Alhomoud BN. Uropathogens and their antimicrobial resistance patterns: Relationship with urinary tract infections. Int J Health Sci (Qassim) 2019;13(2):48-55. [PMID]
22. Ghadage DP, Muley VA, Sharma J, Bhore AV. Bacteriological profile and antibiogram of urinary tract infections at a tertiary care hospital. Natl J Lab Med 2016;5:20-24. [Google Scholar]
23. Karishetti MS, Shaikh HS. Clinicomicrobial assessment of urinary tract infection in a tertiary care hospital. Ind J Health Sci Biomed Res 2019;12(1):69-74. [DOI:10.4103/kleuhsj.kleuhsj_296_17]
24. Al-Badr A, Al-Shaikh G. Recurrent urinary tract infections management in women: a review. Sultan Qaboos Univ Med J 2013;13(3):359-67. [DOI:10.12816/0003256] [PMID] []
25. Scholes D, Hooton TM, Roberts PL, Stapleton AE, Gupta K, Stamm WE. Risk factors for recurrent urinary tract infection in young women. J Infect Dis 2000;182(4):1177-82. [DOI:10.1086/315827] [PMID]
26. Shortliffe LM, McCue JD. Urinary tract infection at the age extremes: pediatrics and geriatrics. Am J Med 2002;113(Suppl 1A):55s-66s. [DOI:10.1016/S0002-9343(02)01060-4] [PMID]
27. Mirzarazi M, Rezatofighi SE, Pourmahdi M, Mohajeri MR. Antibiotic resistance of isolated gram-negative bacteria from urinary tract infections (UTIs) in Isfahan. Jundishapur J Microbiol 2013; 6(8):6883. [DOI:10.5812/jjm.6883]
28. Bharti AK, Farooq U, Singh S, Kaur N, Ahmed R, Singh K. Incidence of Enterococcal Urinary Tract Infection and its Sensitivity Pattern among Patients Attending Teerthanker Mahaveer Medical College and Research Centre, Moradabad, India. Int J Sci Stud 2016;3(12):115-9.
29. Das A, Banerjee T. Prevalence of Urinary Tract Infections and Susceptibily Pattern of Uropathogens in Women of Reproductive age Group from North India. J Adv Med 2015;4(1-2). [DOI:10.5958/2319-4324.2015.00002.4]
30. Ahmad Naeem Sajed, Uzma Batool. Prevalence of urinary tract infections and their antibiotic sensitivity in tertiary care hospital Lahore. IOSR J Dent Med Sci 2014;13(12):57-61. [DOI:10.9790/0853-131225761]
31. Johnson JR: Virulence factors in Escherichia coli urinary tract infection. Clin Microbiol Rev 1991;4:80-128. [DOI:10.1128/CMR.4.1.80] [PMID] []
32. Pattanayak C, Patanaik SK, Datta PP, Panda P. A study on antibiotic sensitivity pattern of bacterial isolates in the intensive care unit of a tertiary care hospital in Eastern India. Int J Basic Clin Pharmacol 2013;2:153-9. [DOI:10.5455/2319-2003.ijbcp20130307]
33. Barai L, Fatema K, Ashraful Haq J, Omar Faruq M, Areef Ahsan ASM, Golam Morshed MAH, et al. Bacterial profile and their antimicrobial resistance pattern in an intensive care unit of a tertiary care hospital in Dhaka. Ibrahim Med Coll J 2010;4:66. [DOI:10.3329/imcj.v4i2.6499]
34. Baral P, Neupane S, Marasini BP, Ghimire KR, Lekhak B, Shrestha B. High prevalence of multidrug resistance in bacterial uropathogens from Kathmandu, Nepal. BMC Res Notes 2012;5(1):38. [DOI:10.1186/1756-0500-5-38] [PMID] []
35. Chooramani G, Jain B, Chauhan PS. Prevalence and antimicrobial sensitivity pattern of bacteria causing urinary tract infection; study of a tertiary care hospital in North India. Clin Epidemiol Glob Health 2020;8(3):890-3. [DOI:10.1016/j.cegh.2020.02.018]
36. Goel V, Kumar D, Kumar R, Mathur P, Singh S: Community-acquired enterococcal urinary tract infections and antibiotic resistance profile in North India. J Lab Physicians 2016;8:50-4. [DOI:10.4103/0974-2727.176237] [PMID] []

Add your comments about this article : Your username or Email:
CAPTCHA

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2025 CC BY-NC 4.0 | Journal of Research in Applied and Basic Medical Sciences

Designed & Developed by : Yektaweb