Get Permission Reenu S.P, Narayanaswamy, and Kushwaha: Bacterial urinary tract infection in diabetes patients and evaluation for multidrug resistant organisms


Introduction

The most common and ubiquitous disease-causing agent recognized in clinical practice among all age groups is bacterial urinary tract infections (BUTIs). Urinary tract infection is the epidemic routine and repeated infectious disease involved in the urinary tract, kidneys, cystitis. Urinary tract infection affect 150 million people world-wide annually.1 Diabetic mellitus is the universal endocrine disorder. Diabetes is constantly increasing metabolic syndrome based on high blood sugar arising from imperfection or deficiency in insulin secretion, action or both. 2 Diabetic mellitus endures for an extended period. It is distinguished by Type 1 and Type 2. Type 1 diabetes is also known as Juvenile diabetes or Insulin dependent diabetes. Type 2 diabetes is also called as diabetes mellitus and adult-onset diabetes. Type 1 diabetes results from the pancreas inability to generate insulin. Insulin resistance in the body's cells causes type 2 diabetes results when the body’s cells resist the normal effect of insulin. 3 Diabetic Mellitus is the highest barrier causing UTI, because of diabetic mellitus there would be weakness or break in cell-mediated immune response, which results in illness microbial infection. Thus person with diabetes are vulnerable to UTI. Various fungi are too in charge for the cause of UTI in diabetic patients. 4 The up-to-date study predict from the global burden of diseases survey rate 462 million single person appeared to be afflicted with diabetic mellitus. Person with diabetes enlarge unhealthy and risky by UTI being the ultimate infection site.5 Most people visiting health care with diabetes, The physician must enlighten and train the disorder of UTI in diabetic patients could possibly be asymptomatic bacteriuria inflammation of lining the bladder, Kidney infection, Pyelonephritis, Urosepsis, Abdominal pain, recurrent UTI, Perirenal or kidney abscess.6 Patients with diabetes experience more UTIs than people without diabetes. 7 with more serious UTIs that result in consequences like dysuria which leads to total organ failure can result to trauma, because of complicated UTI. 8 The most regular microorganism isolated in UTI diabetes patients were gram-negative microorganisms like E.coli, Klebsiella pneumonia, Proteus species, Enterobacter, E.faecalis. 9 Diabetes patients are exposed and remain competing resistant pathogens in crisis of UTI 10 incorporate with ESBL positive enteric bacteria, fluroquinolones, proof against resistant pathogens, Carbapenem-resistant Enterobacterales. 11 The scope is to invent and illustrate Antimicrobial resistant connected to medical centre related to infections. 12 The appearance and increase of MDRO’s is comprehensive and far-reaching community health threat. 13 MDRO has more prevalent in antimicrobial resistant infection in addition to nosocomial infection/health care-associated infections, However common occurrence may alter by region. 14 Uropathogens show a wide difference in them of varying levels of resistance to their antimicrobial medicines with time and space. 15 According to reports, diabetic persons who take antibiotics experience more severe UTI than those who don't. 16 This is due to the resistance posed by the medications' unchecked usage, which exposes individuals to more severe infection. The purpose of this study is to compare diabetes patients with non-diabetic patients to ascertain the prevalence, risk factors, and antibiotic sensitivity pattern of the organisms causing UTI.

Materials and Methods

This research is a hospital based investigation and analysis experimentation in adult-diabetic patients and non-diabetic people present at Vydehi research hospital, Whitefield Bangalore.

Ethical permission has been issued from Vydehi Institutional Ethical Committee (VIEC). The analysis is done in VIMS and RC.

Study design

The research design is a prospective study consisting for the duration of 6months (April-September 2022). Ethical approval certificate is issued by VIEC. Informed consent were obtained from all participants. After getting permission from the institution patients the process started for urinalysis. Both male and female patients above 18 years with diabetic and non-diabetic who attended Vydehi hospital were compared in this study, disregarding the presence or absence of urinary tract infection symptoms.

Experimental study design

Urine assessment and culture sensitivity test

Clean-voided midstream urine specimen was obtained from outpatients and inpatients in particular aseptic container for the purpose of microscopic examination of routine urine test and antibiotic susceptibility test for 6months. After giving informed consent form to the person who participates in research subject were enlightened on how to collect sample and be germ free and avoid contaminating. The collected samples was inoculated into a culture media (Agar-media).

Sample size

Calculation of sample size was done using the formula.

n=Z2(1-α/2)P(1-P)d2

Where n=required sample size, Z=Z value (from standard normal distribution) that corresponds to the desired confidence level or level of significance is 5% for 95%

confidence level, P=expected proportion of resistance in the target population, which is =0.04, d=absolute precision, which is =2%.

Diabetic – 247, Non- diabetic - 201

Inclusion standards

Studies that looked at the prevalence of UTIs in diabetes and non-diabetic patients as well as descriptive, cross-sectional, and observational studies were all considered. Patients above 18 years with diabetes and UTI was included. Patients with and without diabetes at all gender above 18 years of age, from OPD and also admitted in General medicine department of VIMS & RC, was included.

Exclusion criteria

Patients with pregnancy, known underlying renal pathology, chronic renal disease, and use of antibiotic medication during the previous month was excluded.

Objectives of research work

To screen and identify bacteria from samples of patients with UTI who are diabetes. To evaluate multidrug resistance in the bacterial isolates.

Methodology

Sample size

A total of 247 diabetic & 201 non diabetic urine samples from out patients and in patients was collected for processing in the microbiology laboratory.

Specimen collection & processing

Informed written consent was taken from case. Patient details was collected in data collection form. Patients. and requested a midstream urine sample. Samples taken with a sterile instrument holder that was delivered to bacteriology lab. Plates was inoculated to 24 hours by 37ᵒC and result is considered based on significant or non-significant growth progress. The presence of 105 CFC of bacteria in pure urine culture is notable and considered by standard calibrated units or colony-forming units.

Bacteria resisting treatment more than one or three antimicrobial classes of antibiotics is called Multidrug Resistant Organisms. Identification of bacteria was done as per CLSI guidelines.

Bacterial culture

According to CLSI guidelines, bacterial isolation and antibiotic susceptibility testing was performed. Vitek2 (Bio-Mereuix) was used. Bacterial identification and susceptibility testing. Bacteria was identified Gram's stain is used in fast tests using VITEK 2 system. VITEK 2 C is an automated analyser that identifies the Gram negative and Gram-positive bacteria in 4-6 hrs and sensitivity in 6-8 hours. VITEK 2 C system work as Advanced Colorimetry, diagnose technique that assist and equip high discrimination between strain and average of different and misidentified or mixed-up species.

Multidrug resistant organism

Resistant to all agents tested within at least three antimicrobial classes, including β-lactams, carbapenems, aminoglycosides, & fluroquinolones. New approaches and techniques applied by scientist to sketch microorganisms as Multidrug resistant organisms according to In-Vitro Antibiotic resistant process finding show three or more antimicrobial categories along with Extended Spectrum Beta Lactamase (ESBL), Methicillin Resistant Staphylococcus Aureus (MRSA), and Vancomycin Resistant Enterococcus (VRE), Carbapenems (CRE). 13

Results

Significant bacteria was isolated in 90/247 (36%) & 157(63%) of symptomatic & asymptomatic diabetic patients respectively (Table 2). Prevalence of bacteria isolated among the symptomatic patients: E.coli (55) (61%) is the most common (Table 3). The Prevalence of Multi drug organisms (MDRO) isolated among the symptomatic patients: E.coli (43) (75%) (Table 4). Sensitivity to antibiotics patterns of gram negative & gram-positive bacteria segregates showed that E.coli is resistant to I-group (β-lactams), II–group (Carbapenems), III-group (Aminoglycosides), IV-group (Quinolones), SXT. Pseudomonas aeruginosa is resistant to I-group (β-lactams), III–group (Aminoglycosides), IV- group (Quinolones). Klebsiella pneumoniae is resistant to I-group (β-lactams), III - group (Aminoglycosides), IV- group (Quinolones). Enterococcus faecium is resistant to I - group (β-lactams), II – group (Carbapenems), IV- group (Quinolones). Klebsiella aerogenes I - group (β-lactams), IV- group (Quinolones), SXT, NIT (Table 5).

Significant bacteria was isolated in 29/201 (14%) & 114(56%) of symptomatic & asymptomatic non-diabetic patients respectively (Table 6). Prevalence of bacteria isolated among the symptomatic patients: E.coli (20) (64%) (Table 7). The Prevalence of Multi drug organisms (MDRO) isolated among the symptomatic patients: E.coli(2) (66%) klebsiella pneumoniae (1) (Table 8). The prevalence of Antibiotic sensitivity profile of MDRO bacterial isolates in non-diabetic patients: E.coli is resistant to I - group (β-lactams)

II – group (Carbapenems), Trimethoprim/sulfamethoxazole. Klebsiella pneumoniae is resistant to I - group (β-lactams), II – group (Carbapenems), III - group (Aminoglycosides), IV- group (Quinolones) (Table 9).

Table 1

Organisms identified from urine cultures of diabetic and non-diabetic patients

Isolates

Diabetic

Non-diabetic

Total

No(%)

No(%)

Escherichia coli

55(61%)

23(79%)

78

P. aeruginosa

6(6.67%)

-

6

K. pneumoniae

13(14%)

1(12.9%)

14

K. aerogenes

1(1.1%)

-

1

E. faecium

2(2.2%)

-

2

E. faecalis

1(1.1%)

-

1

A. baumanii

1(1.1%)

-

1

Serratia Maresus

1(1.1%)

-

1

S. aureus

-

1(3.2%)

1

Enterobacter cloacae

-

2(3.2%)

2

Table 2

Diabetic patients with UTI (n=247)

Total No. of patients

Total No. of organisms isolated (%)

No growth (%)

247

90(36%)

157(63%)

Table 3

Bacterial isolates from Diabetic patients with UTI (n=90)

Name of the bacteria

Total No. of isolate (%)

Escherichia coli

55 (61%)

Pseudomonas aeruginosa

6 (6.67%)

Klebsiella pneumoniae

13(14%)

Klebsiella aerogenes

1(1.1%)

Enterococcus faecium

2(2.2%)

Enterococci faecalis

1(1.1%)

Acinetobacter baumanii

1(1.1%)

Serratia Maresus

1(1.1%)

Total   

90

Table 4

MDRO bacterial isolates in diabetic patients with UTI

Name of the bacteria

No. of MDRO isolates

Escherichia coli

43(75%)

Pseudomonas aeruginosa

1 (6.2%)

Klebsiella pneumoniae

1 (6.2%)

Klebsiella aerogenes

1(6.2%)

Enterococcus faecium

1(6.2%)

Total

48(53%)

Figure 1

Percentage of bacterial isolates in diabetic and non-diabetic patients

https://s3-us-west-2.amazonaws.com/typeset-prod-media-server/dadbc3b6-9063-4cb9-b99b-9c24829b00afimage1.png
Table 5

Antibiotic sensitivity profile of MDRO bacterial isolates in diabetic patients with UTI

Name of the organism

MDRO antibiotic resistance

Sensitive antibiotics

1. E.coli

I - group (β-lactams)

Fosfomycin

III - group (Aminoglycosides)

IV- group (Quinolones), SXT

2. E.coli

I - group (β-lactams)

III - group (Aminoglycosides) Fosfomycin, Ertapenem, Nitrofurantoin

IV- group (Quinolones),

Trimethoprim/sulfamethoxazole

3. E.coli

I - group (β-lactams)

Fosfomycin, Gentamicin, Nitrofurantoin

IV- group (Quinolones),

Trimethoprim/sulfamethoxazole

4. E.coli

I - group (β-lactams)

Fosfomycin, Ertapenem, Nitrofurantoin, Piperacillin-tazobactam

IV- group (Quinolones),

Trimethoprim/sulfamethoxazole

5. E.coli

I - group (β-lactams)

III - group (Aminoglycosides) Fosfomycin, Ertapenem,

II – group (Carbapenems)

Trimethoprim/sulfamethoxazole

Nitrofurantoin

6. E.coli

I - group (β-lactams)

SXT, Fosfomycin

II – group (Carbapenems)

IV- group (Quinolones)

7. E.coli

I - group (β-lactams)

I - group (β-lactams) III - group (Aminoglycosides)

IV- group (Quinolones),

Trimethoprim/sulfamethoxazole

Nitrofurantoin

8. E.coli

I - group (β-lactams)

Fosfomycin, Nitrofurantoin, Trimethoprim/sulfamethoxazole

III - group (Aminoglycosides)

IV- group (Quinolones)

9. E.coli

I - group (β-lactams)

Fosfomycin

II – group (Carbapenems)

III - group (Aminoglycosides)

IV- group (Quinolones)

10. E.coli

I - group (β-lactams)

Amikacin, Fosfomycin, Ertapenem

Nitrofurantoin,

Trimethoprim/sulfamethoxazole

11. E.coli

I - group (β-lactams) III - group (Aminoglycosides)

III - group (Aminoglycosides) Piperacillin-tazobactam

IV- group (Quinolones)

12. E.coli

I - group (β-lactams)

Nitrofurantoin,

Trimethoprim/sulfamethoxazole

13. Pseudomonas Aeruginosa

I - group (β-lactams)

Cefoxitin, Polymyxin B

III - group (Aminoglycosides)

IV- group (Quinolones)

14. Klebsiella pneumoniae

I - group (β-lactams)

Fosfomycin, Nitrofurantoin

III - group (Aminoglycosides)

IV- group (Quinolones)

15. Enterococcus faecium

I - group (β-lactams)

Trimethoprim/sulfamethoxazole Nitrofurantoin Piperacillin-tazobactam

II – group (Carbapenems)

IV- group (Quinolones)

16. Klebsiella aerogenes

I - group (β-lactams)

Amikacin, Fosfomycin

IV- group (Quinolones), SXT, NIT

Table 6

Non-diabetic UTI patients (n=201)

Number of patients overall

Number of Isolates Overall

No growth (%)

201

29(14%)

114(56%)

Table 7

Bacterial isolates from non-diabetic patients with UTI (n=29)

Name of organisms

Total No. of isolated (%)

E.coli

23(79%)

Enterococcus faecium

2 (6%)

Klebsiella pneumoniae

1 (12.9%)

Staphylococcus aureus

1(3.2%)

Enterobacter cloacae

2(3.2%)

Total

29(17%)

Table 8

MDRO bacterial isolates in Non-diabetic patients with UTI

Name of the MDRO organisms

No. of organisms

E.coli

2 (66%)

Klebsiella pneumoniae

1 (33%)

Total

3

Table 9

Antibiotic sensitivity profile of MDRO bacterial isolates in diabetic patients with UTI

Name of the organism

MDRO antibiotic resistance

Sensitive antibiotics

E.coli

I - group (β-lactams)

Amikacin, Fosfomycin

II – group (Carbapenems)

Trimethoprim/sulfamethoxazole

E.coli

I - group (β-lactams)

Ertapenem, Fosfomycin, amikacin, Nitrofurantoin

IV- group (Quinolones)

Trimethoprim/sulfamethoxazole

Klebsiella pneumoniae

I - group (β-lactams)

Trimethoprim/sulfamethoxazole

II – group (Carbapenems)

III - group (Aminoglycosides)

IV- group (Quinolones)

Discussion

The research outcome and findings depicted that many patients encountered Urinary Tract Infection(UTI) long-suffering and short period diabetic cases was considered int his study. Significant bacteria was isolated in 90/247 (36%) & 157(63%) of symptomatic & asymptomatic diabetic patients respectively. The most common cause of UTI is asymptomatic bacteriuria because, in favourable circumstances, colonised bacteria in the urinary system may climb towards the bladder and cause cystitis, which is typically accompanied by the classic UTI symptoms. If an untreated UTI spreads via the ureters to the kidneys, it may result in pyelonephritis, which can cause fatal renal failure and irreparable kidney damage.17

The distinctive outcome were described in advance research prevailed no significant variation with recurrence showing up of bacteria in urine considering male and females. In comparison, Geerling’s et al9 suggested with the purpose that UTI is increased in women.

Comparative research agreement of UTI in people with and without diabetes women unregulated and connected with increasing severity of infectious pathogen. The most commonly isolated pathogen is E.coli.18 The most prevalent strains of Gram-negative isolate were Klebsiella pnueumoniae, Pseudomonas aeruginosa.

Escherichia coli was the most frequently isolated bacterium, according to several investigations. In this study, individuals with poor glycaemic control accounted for the majority of the 16 UTI cases (84.21%). In patients with adequate glycaemic control, only 3 (15.79%) incidences of UTI were discovered. 9, 19 Among gram positive, Enterococcus represented 6.2% of isolated pathogens further more Staphylococcus aureus 3.2% was found in few cases at most 1% specimens exist to Candida species. Gram-negative infections reveal disturbing resistant to first and second-line agents Ampicillin, Fluroquinolones, Trimethoprim/sulfamethoxazole, Amoxicillin, in this investigation.

In comparison analysis by Bhargava et al20 exposed remarkably amikacin, gentamycin, cefepime, cefalotin The best treatments for GNB were and imipenem. Vancomycin, chloramphenicol, and nitrofurantoin, on the other hand, were the highest effectual medicine in opposition to Gram negative and Gram-positive bacteria. Various studies published resistant to the β-lactam group of antibiotic drug comparable with investigation of sensitivity pattern is observed.21 The purpose of the study Daniel, Betty et al estimate the frequency of urethral infections with hose with and without diabetes22 Whereas our study is to isolate and identify bacteria from samples of people with UTI who are diabetes. To evaluate multidrug resistance in the isolates of bacteria.

Conclusion

Infection of the urinary tract are frequent along with diabetic symptoms. UTI is an enhancing factor which give rise to infection in diabetic patients. The habitual utilize of common antibiotics created particular bacteria resistant’s reaching consequences of antibiotics.

The prolonged case assuming that UTI endures in diabetic patients, later can have dangerous complications. Diabetic people remain on increased risk of infections, with UTI amongst the most chronic situation. Urinary tract infection in diabetic mellitus act as a common intention of mortality and will result in mortality. E.coli is the major recurrent and regular infectious agent in charge between diabetics and non-diabetics of UTI, accompanied by Klebsiella. Examination of bacteriuria (UTI) is high in both diabetes and non-diabetic people. Significant remedy in medical care.

Source of Funding

None.

Conflicts of Interest

There is no conflict of interest.

References

1 

OH Barahim AM AL-Kadassy H Pyar LSB Dahman Prevalence of bacterial urinary tract infections amongst diabetes mellitus patients attending Ibn-Sina General Hospital in Mukalla, YemenJ Med Sci2022221071210.3923/jms.2022.107.112

2 

S Jagadeesan B K Tripathi P Patel S Muthathal Urinary tract infection and Diabetes Mellitus-Etio-clinical profile and antibiogram: A North Indian perspectiveJ Family Med Prim Care20221151902610.4103/jfmpc.jfmpc_2017_21

3 

O Nitzan M Elias B Chazan W Saliba Urinary tract infections in patients with type 2 diabetes mellitus: review of prevalence, diagnosis, and managementDiabetes Metab Syndr Obes201581293610.2147/DMSO.S51792

4 

M Sahu Z Bhagat Pervasiveness of urinary tract infection in diabetic patients and their causative organisms with antibiotic sensitivity patternApollo Med2020171263010.4103/am.am_2_20

5 

MAB Khan MJ Hashim JK King RD Govender H Mustafa JA Kaabi Epidemiology of Type 2 Diabetes - Global Burden of Disease and Forecasted TrendsJ Epidemiol Glob Health20201011071110.2991/jegh.k.191028.001

6 

JS Brown H Wessells MB Chancellor SS Howards WE Stamm AE Stapleton Urologic complications of diabetesDiabetes Care20052811778510.2337/diacare.28.1.177

7 

V De Lastours B Foxman Urinary tract infection in diabetes: epidemiologic considerationsCurr Infect Dis Rep201416138910.1007/s11908-013-0389-2.

8 

M Saleem B Daniel Prevalence of urinary tract infection among patients with diabetes in Bangalore CityInt J Emerg Sci201112133

9 

R Meiland SE Geerlings S Langermann EC Brouwer FEJ Coenjaerts AIM Hoepelman Fimch antiserum inhibits the adherence of Escherichia coli to cells collected by voided urine specimens of diabetic womenJ Urol2004171415899310.1097/01.ju.0000118402.01034.fb

10 

T Inns S Millership L Teare W Rice M Reacher Service evaluation of selected risk factors for extended-spectrum beta-lactamase Escherichia coli urinary tract infections: a case-control studyJ Hosp Infect20148821169

11 

R Colodner W Rock B Chazan N Keller N Guy W Sakran Risk factors for the development of extended-spectrum beta-lactamase-producing bacteria in nonhospitalized patientsEur J Clin Microbiol20042331637

12 

J W Tapsall F Ndowa D A Lewis M Unemo Meeting the public health challenge of multidrug- and extensively drug-resistant Neisseria gonorrhoeaeExpert Rev Anti Infect Ther20097782134

13 

A-P Magiorakos A Srinivasan RB Carey Y Carmeli ME Falagas CG Giske Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistanceClin Microbiol Infect201218326881

14 

N Dayan H Dabbah I Weissman I Aga L Even D Glikman Urinary tract infections caused by community-acquired extended-spectrum β-lactamase-producing and nonproducing bacteria: A comparative studyJ Pediatr 20131635141721

15 

S Kotgire S Siddiqui Prevalence and Antibiogram of Uropathogens from Patients Attending Tertiary Care HospitalInt J Med Microbiol Trop Dis20173120310.18231/2455-6807.2017.0005

16 

UM Chukwuocha CO Emerole TN Njokuobi IC Nwawume Urinary Tract Infections (UTIs) Associated with Diabetic Patients in the Federal Medical Center owerri, NigeriaGlobal Adv Res J Microbiol201215626

17 

YB Ngwai H Iliyasu E Young G Owuna Bacteriuria and Antimicrobial Susceptibility of Escherichia coli Isolated From urine of Asymptomatic University Students in Keffi, NigeriaJundishapur J Microbiol2012513237

18 

V Garg A Bose J Jindal A Goyal Comparison of Clinical Presentation and Risk Factors in Diabetic and Non-Diabetic Females with Urinary Tract Infection Assessed as Per the European Association of Urology ClassificationJ Clin Diagn Res.20159612410.7860/JCDR/2015/14177.6029

19 

AH Aamir UY Raja A Asghar Asymptomatic urinary tract infections and associated risk factors in Pakistani Muslim type 2 diabetic patientsBMC Infect Dis202121138810.1186/s12879-021-06106-7

20 

K Bhargava G Nath A Bhargava R Kumari GK Aseri N Jain Bacterial profile and antibiotic susceptibility pattern of uropathogens causing urinary tract infection in the eastern part of Northern IndiaFront Microbiol20221396505310.3389/fmicb.2022.965053

21 

S Sood R Gupta Antibiotic Resistance Pattern of Community Acquired Uropathogens at a Tertiary Care Hospital in Jaipur, RajasthanIndian J Community Med2012371394410.4103/0970-0218.94023

22 

M Saleem B Daniel Prevalence of Urinary Tract Infection among Patients with Diabetes in Bangalore CityInt J Emerg Sci20111213342



jats-html.xsl


This is an Open Access (OA) journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.

  • Article highlights
  • Article tables
  • Article images

Article History

Received : 17-08-2022

Accepted : 30-10-2022


View Article

PDF File   Full Text Article


Copyright permission

Get article permission for commercial use

Downlaod

PDF File   XML File   ePub File


Digital Object Identifier (DOI)

Article DOI

https://doi.org/10.18231/j.ijmmtd.2022.062


Article Metrics






Article Access statistics

Viewed: 846

PDF Downloaded: 186