Literature DB >> 33679092

Bacteria Causing Urinary Tract Infections and Its Antibiotic Susceptibility Pattern at Tertiary Hospital in Al-Baha Region, Saudi Arabia: A Retrospective Study.

Mohammed Abdullah Alzahrani1,2, Mohamed Salah Ali3, Sirajudheen Anwar4.   

Abstract

CONTEXT: Clinicians face one of the most common bacterial infections in developing countries that is urinary tract infection (UTI). Current knowledge on antimicrobial susceptibility pattern is essential for selecting appropriate therapy. AIMS: In this study, we investigated the various bacteria causing UTI and determined the sensitivity and resistance of antibiotics pattern against most prevalent uropathogens isolated from patients at tertiary hospital, Al-Baha, Saudi Arabia. SETTINGS AND
DESIGN: This was a retrospective study of urine culture conducted in King Fahad Hospital at Al-Baha in Saudi Arabia.
MATERIALS AND METHODS: Laboratory reports and patient medical files of both inpatient and outpatient were collected between June 2017 and May 2018, targeting both male and female of age above 18 years of age, who had been treated for UTI.
RESULTS: A total of 349 patients' urine report was studied to identify the uropathogens. Escherichia coli was the main etiologic agent in community and hospital-acquired infections. The majority of the bacteria was isolated from female (60%), whereas the remaining (40%) was from male. The most common isolates were E. coli, Klebsiella pneumoniae, Enterococcus faecalis, E. coli Extended spectrum beta-lactamases, Pseudomonas, and K. pneumoniae ESBL (these represented 37.82%, 19.20%, 10.89%, 10.32%, 6.59%, and 3.72%, of isolate, respectively). UTI due to E. coli was at a higher rate during summer than during winter. This study showed that ciprofloxacin (20.29%) and cefuroxime (16.14%) are most prescribed medications, followed by ceftriaxone (12.96%) and then tazocin (8.80%). Imipenem, meropenem, amikacin, vancomycin, tigecycline, linezolid, and colistin were highly sensitive for most types of bacteria, but gram-negative bacteria were highly resistant to ampicillin. Gram-positive bacteria showed highly resistance to cefoxitin.
CONCLUSION: The microbial culture and sensitivity of the isolates from urine samples should be carried out as a routine before starting the antimicrobial therapy. Current knowledge of the antibiotic sensitivity/resistance patterns of uropathogens at a particular geographical region is a guiding factor for choosing an appropriate empirical antimicrobial treatment rather than following universal guidelines. Copyright:
© 2020 Journal of Pharmacy and Bioallied Sciences.

Entities:  

Keywords:  Al-Baha; Saudi Arabia; antibiotic susceptibility; predisposing factor; urinary tract infections; uropathogens

Year:  2020        PMID: 33679092      PMCID: PMC7909051          DOI: 10.4103/jpbs.JPBS_294_19

Source DB:  PubMed          Journal:  J Pharm Bioallied Sci        ISSN: 0975-7406


INTRODUCTION

Generally antibiotics are prescribed empirically for urinary tract infection (UTI) before the final urine culture laboratory results are available.[1] Choice of empirical antibiotic prescription depends on the knowledge of bacterial organisms that are prevalent locally and antibiotic sensitivities, rather than on universal guidelines.[234] In recent years, bacterial resistance to various antibiotics has raised dramatically, forcing physicians with few therapeutic choices.[56] Therefore, estimating the epidemiology of UTIs prevalence, risk factors, bacterial isolates, and antibiotic sensitivity is mandatory for the hospital setup and health planners to give appropriate interventions. The aim of this study was to determine the various bacteria causing UTI and the sensitivity and resistance of antibiotic pattern of the urinary pathogens, additionally UTI ratio in gender distribution, antibiotic prescribing pattern, and concomitant disease conditions with UTI at a tertiary hospital at Al-Baha, Saudi Arabia.

SUBJECTS AND METHODS

Sample size

Retrospective study was conducted from past medical files and urine samples’ test report that were obtained from patients treated for UTI at King Fahad Hospital in Al-Baha region, Saudi Arabia, between June, 2017 and May, 2018. Urine specimens’ test report of patients of age 18 years and older, belonging to outpatient clinics and inpatient wards, suspected of having UTI were retrieved from microbiology laboratory. The total number of patients’ medical files assessed was 349.

Inclusion criteria

All adult patients infected with urinary tract infection from June 2017 to May 2018 were included in this study.

Exclusion criteria

All children (younger than 18 years) were excluded from this study.

Data collection

This was a retrospective study, conducted by collecting information from medical files such as date of sample collections, sex and age of patients, bacterial isolate, antibiotics prescribed, and concomitant diseases.

Instruments of data collection

Lab reports

The data were collected from laboratory reports, which had information about uropathogen bacterial isolate, bacterial sensitivity, and resistance to antibiotics.

Medical file

The first-line antibiotics prescribed were recorded that included both empirical antibiotics prescribed before urine laboratory test was conducted and antibiotics after the test result release. Furthermore, concomitant diseases along with UTI and their medications prescribed were recorded from patient medical files.

Urine analysis methodology previously done

Urine analysis was performed according to internal policy and procedure (IPP) conducted at the department of microbiology laboratory, King Fahad Hospital, Al-Baha, Saudi Arabia.

Statistical analysis

Data were entered into a database designed using an MS Excel spreadsheet and analyzed with Statistical Package for Social Sciences (SPSS, Chicago, Illinois) software, version 16.0. Retrospective study statistics shows uropathogen percentage and antibiotics resistance/sensitivity for particular period. The overall 1-year resistance/sensitivity rates of the most common uropathogen to the routinely tested first-line antimicrobials were calculated by dividing the number of urinary isolates resistant/sensitive to each antimicrobial agent by the number of isolates tested against an individual antimicrobial agent. Tables and graphs are presented as frequency (count) and percentages with 95% confidence interval.

RESULTS

Uropathogen percentage for complete study period

The pathogens causing UTIs are well known, Escherichia coli was the main etiologic agent in community as well as hospital-acquired infections. A total of 349 urine bacteria were isolated and identified. The majority of the bacteria was isolated from females (60%), whereas the remaining (40%) was from males. The most common isolates were E. coli, Klebsiella pneumoniae, Enterococcus faecalis, E. coli ESBL, Pseudomonas, K. pneumoniae ESBL, and Proteus (these represented 37.82%, 19.20%, 10.89%, 10.32%, 6.59%, 3.72%, and 2.29% of isolate, respectively). Percentage of uropathogens isolated between June 2017 and May 2018, is shown in Table 1 and Figure 1. Percentage of UTI occurrence during summer was higher than that during winter, which is caused by the most common uropathogen E. coli followed by E. faecalis. Percentage of various uropathogens during summer and winter season is shown in Figure 2.
Table 1

Susceptibility pattern of Escherichia coli

AntibioticsTest done (td)Resistant
95% CI resistantSensitive
95% CI sensitiveTest not done (nd)
N (%)N (%)
Penicillin22 (100)34.2–1000 (0)094
Ampicillin7869 (88.46)79.50–93.819 (11.54)6.19–20.5051
Augmentin3314 (42.42)27.24–59.1919 (57.58)40.81–72.7695
Carbenicillin00000115
Aztreonam223 (13.64)4.75–33.3319 (86.36)66.67–95.2592
Imipenem821 (1.22)0.22–6.5981 (98.78)93.41–99.7848
Meropenem180 (0)018 (100 )82.41–10096
Piperacillin10 (0)01 (100)20.65–100128
Tazocin (Zosyn)384 (10.53)4.17–24.1334 (89.47)75.87–95.8390
Cephalexin4442 (95.45)84.87–98.742 (4.55)1.26–15.1384
Cefoxitin2216 (72.73)51.85–86.856 (27.27)13.15–48.15125
Cefuroxime237 (30.43)15.60–50.8716 (69.57)49.13–84.4056
Ceftriaxone3918 (46.15)31.57–61.4321 (53.85)38.57–68.4357
Ceftazidime130 (0)13 (100.0)77.19–100115
Cefepime268 (30.77)16.50–49.9918 (69.23)50.01–83.50102
Amikacin813 (3.70)1.27–10.3378(96.30)89.67–98.7349
Gentamicin294 (13.79)5.50–30.5625 (86.21)69.44–94.5099
Ciprofloxacin6130 (49.18)37.06–61.4031(50.82)38.60–62.9467
Levofloxacin10 (0)01(100.00)20.65–100.045
Norfloxacin5328 (52.83)39.66–65.6225 (47.17)34.38–60.3466
Erythromycin11 (100.00)20.65–1000 (0)0128
Clindamycin11 (100.00)20.65–1000 (0)0128
Vancomycin10 (0)01 (100.00)20.65–100.00128
Linezolid10 (0)01 (100.00)20.65–100.00128
Tigecycline40 (0)04 (100.00)51.01–100125
Colistin30 (0)03 (100.00)43.85–100126
Nitrofurantoin11211 (9.82)5.57–16.73101 (90.18)83.72-94.4317
TMP-SMX10761 (57.01)47.55–65.9946 (42.99)34.01–52.4522

N = frequency, CI = confidence interval, TMP-SMX = Trimethoprim and sulfamethoxazole, td = respective antibiotic tested against E. coli, nd = respective antibiotic was not tested against E. coli

Figure 1

Percent of uropathogen from June 2017 to May 2018. Total 349 uropathogen isolates were identified between June 2017 and May 2018, among them four major UTI causing bacteria were identified as E. coli = 132, K. pneumoniae = 67, P. aeruginosa = 23, E. faecalis = 38

Figure 2

Percent of uropathogens during summer and winter. Summer season was categorized from March to August month, and September to February was considered as winter season

Susceptibility pattern of Escherichia coli N = frequency, CI = confidence interval, TMP-SMX = Trimethoprim and sulfamethoxazole, td = respective antibiotic tested against E. coli, nd = respective antibiotic was not tested against E. coli Percent of uropathogen from June 2017 to May 2018. Total 349 uropathogen isolates were identified between June 2017 and May 2018, among them four major UTI causing bacteria were identified as E. coli = 132, K. pneumoniae = 67, P. aeruginosa = 23, E. faecalis = 38 Percent of uropathogens during summer and winter. Summer season was categorized from March to August month, and September to February was considered as winter season

Antibacterial susceptibility pattern

Susceptibility pattern of E. coli was observed, it was highly sensitive toward higher and broad range of antibiotics such as meropenem, piperacillin, ceftazidime, levofloxacin, tigecycline, and colistin (100%), followed by imipenem (98.78%), amikacin (96%), nitrofurantoin (90.18%), tazocin (89.47%), aztreonam (86.36%), gentamicin (86.21%), cefuroxime (69.57%), Augmentin (57.58%), ceftriaxone (53.85%), and ciprofloxacin (50.82%). High resistance was observed for ampicillin (88.46%), cephalexin (95.45%), cefoxitin (72.73%), and trimethoprim and sulfamethoxazole (TMP-SMX) (57.01%), and norfloxacin (52.83%). Empirical treatment is based on epidemiological data and guidelines; broad spectrum is generally avoided as first-line treatment.[7] In our study, nitrofurantoin was prescribed as the first choice of antibiotics [Table 1]. Susceptibility patterns against K. pneumoniae had a trend similar to that against E. coli. It was highly sensitive to oxacillin, carbenicillin, colistin (100%), amikacin (94.59%), ceftazidime (90%), imipenem (84.78%), gentamicin (84.62%), tigecycline (83.33%), meropenem and Augmentin (75%), and nitrofurantoin (73.91%). K. pneumoniae was highly resistant against penicillin, ampicillin (100%), cephalexin (93.75%), and cefotaxime (71.43%). Augmentin and nitrofurantoin were prescribed as the first line of therapy for these types of bacteria [Table 2]. E. faecalis was highly sensitive to teicoplanin, colistin, tigecycline, linezolid and vancomycin (100%), and nitrofurantoin (83.33%). It was highly resistant against meropenem (100%), imipenem (87.50%), oxacillin (100%), gentamicin (72.73%), ciprofloxacin (66.67%), erythromycin (88.46%), and most of the beta lactam except ampicillin (53.57%). This bacterium has low susceptibility to doxycycline (50%) and TMP-SMX (52.53%) [Table 3]. P. aeruginosa was highly sensitive to tigecycline and colistin (100%) and tazocin (83.33%), imipenem (73.33%) and meropenem (71.43%), ciprofloxacin (60%), carbenicillin (66.67%), aztreonam (61.54%), ceftazidime, piperacillin, and gentamicin (50%), but highly resistant to most of the beta lactam. This bacterium was resistant against cefepime (66.66%), but it was completely resistant against levofloxacin (100%) [Table 4].
Table 2

Susceptibility pattern of Klebsiella pneumoniae

AntibioticsTest Done (td)Resistant, N (%)95% CI resistantSensitive, N (%)95% CI sensitiveTest not done (nd)
Penicillin22 (100)34.24–1000(0)049
Ampicillin3939 (100)91.03–1000 (0)028
Augmentin164 (25)10.18–49.5012 (75)50.50–89.9251
Oxacillin10 (0)01 (100)20.65–10063
Carbenicillin10 (0)01 (100)20.65–10061
Aztreonam124 (33.33)13.81–60.948 (66.67)25.38–74.6246
Imipenem467 (15.22)7.57–28.2239 (84.78)71.78–92.4320
Meropenem164 (25)10.18–49.5012 (75)50.50–89.8248
Tazocin (Zosyn)2110 (47.61)28.34–67.6311 (52.38)32.37–71.6646
Cephalexin1615 (93.75)71.67–98.891 (6.25)1.11–28.3351
Cefoxitin127 (58.33)31.95–80.675 (41.67)19.33–68.0555
Cefuroxime139 (69.23)42.37–87.324 (30.77)12.68–57.6337
Ceftriaxone2213 (59.09)38.73–76.749 (40.91)23.26–61.2731
Ceftazidime101 (10)1.79–40.429 (90)59.58–98.2157
Cefotaxime75 (71.43)35.89–91.782 (28.57)8.22–64.1158
Cefepime124 (33.33)13.81–60.948 (66.67)39.06–86.1951
Amikacin372 (5.41)1.50–17.7035 (94.59)82.30–98.5030
Gentamicin132 (15.38)4.33–42.2311 (84.62)57.77–95.6750
Ciprofloxacin4320 (46.51)32.51–61.0823 (53.49)38.92–67.4937
Levofloxacin32 (66.67)20.77–93.851 (33.33)6.15–79.2318
Norfloxacin2810 (35.71)20.71–54.1718 (64.29)33.45–64.1137
Clindamycin11 (100)20.65–1000 (0)066
Tigecycline61 (16.67)3.01–56.355 (83.33)3.55–17.7961
Colistin50 (0)05 (100)56.55–10062
Nitrofurantoin4612 (26.09)15.60–40.2634 (73.91)59.74–84.4021
TMP-SMX5729 (50.88)38.26–63.3828 (49.12)36.62–61.7414

N = frequency, CI = confidence interval, TMP-SMX = trimethoprim and sulfamethoxazole, td = respective antibiotic tested against K. pneumoniae nd = respective antibiotic was not tested against K. pneumoniae

Table 3

Susceptibility pattern of Enterococcus faecalis

AntibioticsTest done (td)Resistant, N (%)95% CI resistantSensitive, N (%)95% CI, sensitiveTest not done (nd)
Penicillin44 (100.00)51.01–1000 (0)023
Ampicillin2813 (46.43)29.53–64.1915 (53.57)35.81–70.477
Augmentin43 (75.00)30.06–95.441 (25.00)4.56–69.9434
Oxacillin33 (100.00)43.85–1000 (0)031
Imipenem87 (87.50)52.91–97.761 (12.50)2.24–47.0925
Meropenem11 (100.00)20.65–1000 (0)038
Cephalexin44 (100.00)51.01–1000.00030
Cefoxitin1514 (93.33)70.18–98.811 (6.67)1.19–29.8223
Gentamicin2216 (72.73)51.85–86.856 (27.27)13.15–48.1516
Ciprofloxacin128 (66.67)39.06–86.194 (33.33)13.81–60.9426
Norfloxacin11 (100.00)20.65–1000 (0)037
Erythromycin2623 (88.46)71.02–96.003 (11.54)4.0–28.9812
Tetracycline43 (75.00)30.06–95.441 (25.00)4.56–69.9427
Doxycycline21 (50.00)9.45–90.551 (50.00)9.45–90.5528
Clindamycin1514 (93.33)70.18–98.811 (6.67)1.19–29.8223
Vancomycin290 (0)029 (100.00)88.30–1009
Linezolid220 (0)022 (100.00)85.13–10016
Tigecycline40 (0)04 (100.00)51.01–10040
Colistin10 (0)01 (100.00)20.65–10033
Nitrofurantoin244 (16.67)6.68–35.8520 (83.33)64.15–93.3214
TMP-SMX199 (47.37)27.33–68.2910 (52.63)31.71–72.6719
Teicoplanin130 (0)013 (100.00)77.19–10018

N = frequency, CI = confidence interval, TMP-SMX = Trimethoprim and sulfamethoxazole, td = respective antibiotic tested against E. faecalis, nd = respective antibiotic was not tested against E. faecalis

Table 4

Susceptibility pattern of Pseudomonas aeruginosa

AntibioticsTest done (td)Resistant, N (%)95% CI resistantSensitive, N (%)95% CI sensitiveTest not done (nd)
Ampicillin44 (100)51.01–1000 (0)019
Augmentin11 (100)20.65–1000 (0)022
Carbenicillin31 (33.33)6.15–79.232 (66.67)20.77–93.8519
Aztreonam135 (38.46)17.71–64.488 (61.54)35.52–82.299
Imipenem154 (26.67)10.90–51.9511 (73.33)48.05–89.108
Meropenem72 (28.57)8.22–64.115 (71.43)35.89–91.7815
Piperacillin21 (50.00)9.45–90.551 (50.00)9.45–90.5521
Tazocin (Zosyn)122 (16.67)4.70–44.8010 (83.33)55.20–95.3011
Cephalexin33 (100)43.85–1000 (0)019
Cefuroxime22 (100)34.24–1000 (0)018
Ceftriaxone33 (100)43.85–1000 (0)018
Ceftazidime84 (50)21.52–78.484 (50)21.52–78.4816
Cefepime64 (66.67)30.00–90.322 (33.33)9.68–70.0017
Amikacin103 (30)10.78–60.327 (70)39.68–89.2213
Gentamicin42 (50)15.00–85.002 (50)15.00–85.0019
Ciprofloxacin156 (40)19.83–64.259 (60)35.75–80.188
Levofloxacin11 (100)20.65–1000 (0)011
Norfloxacin61 (16.67)3.01–56.355 (83.33)43.65–96.9917
Tigecycline10 (0)01 (100)20.65–10022
Colistin40 (0)04 (100)51.01–10016
Nitrofurantoin63 (50)18.76–81.243 (50)18.76–81.2417
TMP-SMX54 (80)37.55–96.381 (20)37.55–96.3818

N = frequency, CI = confidence interval, td = respective antibiotic tested against P. aeruginosa, nd = respective antibiotic was not tested against P. aeruginosa, TMP-SMX = trimethoprim and sulfamethoxazole

Susceptibility pattern of Klebsiella pneumoniae N = frequency, CI = confidence interval, TMP-SMX = trimethoprim and sulfamethoxazole, td = respective antibiotic tested against K. pneumoniae nd = respective antibiotic was not tested against K. pneumoniae Susceptibility pattern of Enterococcus faecalis N = frequency, CI = confidence interval, TMP-SMX = Trimethoprim and sulfamethoxazole, td = respective antibiotic tested against E. faecalis, nd = respective antibiotic was not tested against E. faecalis Susceptibility pattern of Pseudomonas aeruginosa N = frequency, CI = confidence interval, td = respective antibiotic tested against P. aeruginosa, nd = respective antibiotic was not tested against P. aeruginosa, TMP-SMX = trimethoprim and sulfamethoxazole

Antibiotics prescribed for urinary tract infection

This study shows us that ciprofloxacin is the most prescribed medication in inpatient and outpatient departments (20.29%), followed by cefuroxime—second-generation cephalosporin (16.14%), ceftriaxone—third generation-cephalosporin (12.96%), piperacillin/tazobactam–tazocin (8.80%), nitrofurantoin (5.13%), meropenem (4.16%), imipenem and colistin (3.67%), metronidazole, and linezolid (2.69%), whereas ampicillin has shown us that it is less commonly used because of high rate of resistance [Table 5].
Table 5

Percentage of antibiotics prescribed between June 2017 and May 2018

AntibioticsTotal* prescribedPrescribed percentage95% CI
Ampicillin10.240.04–1.37
Amoxicillin61.470.67–3.16
Augmentin102.441.33–4.44
Imipenem153.672.23–5.96
Meropenem174.162.61–6.56
Colistin153.672.23–5.96
Tazocin368.806.43–11.95
Cefepime10.240.04–1.37
Ceftriaxone5312.9610.05–16.56
Cefuroxime6616.1412.89–20.01
Cefazolin71.710.83–3.49
Cephalexin10.240.04–1.37
Ceftazidime81.960.99–3.81
Levofloxacin71.710.83–3.49
Metronidazole112.691.51–4.75
Nitrofurantoin215.133.38–7.72
Linezolid112.691.51–4.75
Azithromycin102.441.33–4.44
Doxycycline30.730.25–2.13
Ciprofloxacin8320.2916.68–24.46
Co-trimoxazole30.730.25–2.13
Amikacin51.220.52–2.83
Gentamicin10.240.04–1.37
Tigecycline81.960.99–3.81
Vancomycin30.730.25–2.13
Clindamycin20.490.13–1.77
Total409

*Total antibiotics prescribed during June 2017 to May 2018, for all UTI cases

Percentage of antibiotics prescribed between June 2017 and May 2018 *Total antibiotics prescribed during June 2017 to May 2018, for all UTI cases

Concomitant disease with urinary tract infection

The patients with UTI during study period had following concomitant diseases: diabetes mellitus was the greatest risk of UTIs (21.11%), then hypertension (20.49%), urinary tract disorders (9.55%), chronic kidney disease (6.47%), and pregnancy (3.85%) [Figure 3].
Figure 3

Concomitant diseases with urinary tract infection.

Concomitant diseases with urinary tract infection.

DISCUSSION

UTI is reported as one of the most common microorganism infections despite widely accessible diagnostic aids, antibiotics, and increased knowledge about its pathogenesis. The first line of defense in the lower urinary tract will, in most cases, succeed in preventing bacterial attachment and establishment. However, sometimes, and more often in certain risk groups, namely the elderly and the pregnant women, patients with diabetes, with preexisting urinary tract structural abnormalities/obstruction, and transplanted kidney, bacteria will establish themselves in the urinary tract to cause infection.[7] Less commonly, bacteria spread to the upper urinary tract causing pyelonephritis. The patients with recurrent UTI are often had been prescribed antibiotics repeatedly or as prophylaxis for longer period. The problem of bacterial resistance to antibiotics used in UTI is increasing at a high speed, and new treatment strategies are therefore needed. To be able to therapeutically intervene in the host–pathogen interaction in the urinary tract, better understanding of the antibiotic sensitivity and resistance is needed.[8] In our study, high prevalence of UTI in females than that in males was observed, which correlates with the findings of Akhtar et al.,[9] which revealed that the frequency of UTI is greater in females as compared to males. In another short period study from March to June in Qassim province by Alzohairy and Khadri,[5] it was found that females had more UTI than males, principally due to anatomical and physical factors. The most common uropathogens associated with uncomplicated UTI are E. coli, Staphylococcus saprophyticus, Enterococcus species, K. pneumoniae, Proteus mirabilis; complicated UTI is caused by E. coli, P. aeruginosa, Acinetobacter baumannii, Enterococcus species, and Staphylococcus spp. Catheter-associated urinary tract infection is caused by P. mirabilis, Morganella morganii, Providencia stuartii, Corynebacterium urealyticum, Candida species; and recurrent UTI is caused by P. mirabilis, K. pneumoniae, Enterobacter species, antibiotic-resistant E. coli, Enterococcus species, and Staphylococcus species.[10] The predominant isolates in our study were E. coli, followed by Klebsiella species. These findings are in conformity with the reports by other researchers.[911] According to Alzohairy and Khadri[9] and Patil and Jain,[1]Pseudomonas species was the third most common uropathogen, but this is contrary to our study, which showed that E. faecalis is the third one. The resistance to antibiotic drugs has been observed since its use and is an increasing worldwide problem. In this study, high rate of E. coli and K. pneumoniae isolates were resistant to ampicillin, this result is same as that of another study in Ethiopia[4] and central Riyadh hospital in Saudi Arabia.[3] In agreement with El-Kersh et al.,[12] our susceptibility data indicated that all tested gram-negative bacteria showed high resistance to ampicillin. Moreover, E. coli, K. pneumoniae, and other gram-negative bacteria showed susceptibility against meropenem, amikacin, and gentamicin. Also as similar to a study by El-Kersh et al.,[12] we observed that most tested bacteria were far more susceptible to amikacin than that toward gentamicin. In another Saudi study conducted in a major tertiary hospital, the King Saud University Medical City (formerly known as King Khalid University Hospital) Riyadh,[13]E. coli showed highest resistance to ampicillin, followed by TMP-SMX and ciprofloxacin, whereas K. pneumoniae showed highest resistance to ampicillin, TMP-SMX, followed by cefuroxime. Compared to our results, E. coli showed high resistance to ampicillin followed by cephalexin, then TMP-SMX and norfloxacin, whereas K. pneumoniae showed high resistance against penicillin ˃ ampicillin ˃ cephalexin ˃ cefotaxime. Similar results were that ESBL producing E. coli were resistant to third-generation cephalosporin and fluoroquinolone, but highly susceptible to carbapenems, amikacin, and piperacillin/tazobactam. Hence, nitrofurantoin and TMP-SMX can be used as first line of treatment. Previous study in Riyadh had shown that the drugs commonly used to treat P. aeruginosa infection was limited, which includes ciprofloxacin, amikacin, gentamicin, ceftazidime, piperacillin, tazocin, and imipenem.[14] This report was parallel with our data for these antibiotics; additionally, last but not the least, colistin and tigecycline can be used. It is recommended to use nitrofurantoin as first line because it has good susceptibility to most microorganisms. This is consistent with the findings by Biswas et al.[15] and Shaifali et al.[2] We suggest that nitrofurantoin may be considered as a viable alternative to fluoroquinolones. When comparing our result of uropathogen sensitivity and resistance treated with co-trimoxazole (TMP-SMX) versus the result of a study by Biswas et al.[15] conducted in Bangladesh, an increasing pattern of resistance of E. coli and P. aeruginosa was observed in our study. However, this drug shows good susceptibility similar to that observed in the study by Biswas et al.[15] study for E. coli ESBL and Klebsiella, but low sensitivity, particularly, to E. coli in Al-Baha region, Saudi Arabia. Additionally, Al-Mijalli, in Central Riyadh Hospital, has revealed high resistance when compared to our study. Their result stated that trimethoprim was more resistant to E. coli and K. pneumoniae.[15] Also Balkhi et al.[13] stated that the gram-positive organism Enterococcus faecium showed a high resistance to ampicillin and ciprofloxacin. This was similar to our study in resistance against ciprofloxacin except ampicillin. Staphylococcus Coa negative (gram positive) showed high susceptible to gentamicin and ciprofloxacin, on the contrary, erythromycin and Augmentin were fully resistant. Okopi et al.,[16] following sensitivity pattern, observed ciprofloxacin ˃ gentamicin ˃ erythromycin but no resistance was found for these antibiotics. Generally, the drug of choice as short-term therapy with nitrofurantoin was successful in most of the cases. Co-trimoxazole, fluoroquinolone, or cephalosporin is not considered as the first choice of treatment. We found that UTIs are common among patients with type 2 diabetes mellitus due to an impaired immune status and increased glucose content of the urine. This is in consistence with the finding of a study that was carried out as systematic review on observational studies by evaluating 37 articles.[17] All kidney and urinary tract related diseases also had UTI, which was prominent in our study. Broad-spectrum antibiotics should be avoided as empirical treatment. E. coli > K. pneumoniae > E. faecalis seems to be common causative uropathogen. Strong evidence of resistance have been noted for penicillin, ampicillin, cephalexin and cefoxitin against E.coli induced UTI. Fluoroquinolones, Augmentin, cephalosporin, and nitrofurantoin are good choice of drugs as empirical treatment. Fluoroquinolone-resistant cases can be treated with nitrofurantoin. Broad-spectrum antibiotics, namely carbapenam, piperacillin, vancomycin, linezolid, tigecycline, and colistin should be reserved for special cases of complicated UTI.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.
  6 in total

1.  A survey on urinary tract infections associated with the three most common uropathogenic bacteria.

Authors:  Payam Behzadi; Elham Behzadi; Hodjjat Yazdanbod; Roghiyyeh Aghapour; Mahboubeh Akbari Cheshmeh; Djaafar Salehian Omran
Journal:  Maedica (Buchar)       Date:  2010-04

2.  Antimicrobial susceptibility of microorganisms causing Urinary Tract Infections in Saudi Arabia.

Authors:  Bander Balkhi; Wael Mansy; Sultan AlGhadeer; Abdulrahman Alnuaim; Abdullah Alshehri; Ali Somily
Journal:  J Infect Dev Ctries       Date:  2018-04-30       Impact factor: 0.968

3.  Bacterial uropathogens in urinary tract infection and antibiotic susceptibility pattern in jimma university specialized hospital, southwest ethiopia.

Authors:  Getenet Beyene; Wondewosen Tsegaye
Journal:  Ethiop J Health Sci       Date:  2011-07

4.  Antibiotic susceptibility patterns of urinary pathogens in female outpatients.

Authors:  Iram Shaifali; Uma Gupta; Syed Esam Mahmood; Jawed Ahmed
Journal:  N Am J Med Sci       Date:  2012-04

5.  Five-Year Antimicrobial Resistance Patterns of Urinary Escherichia coli at an Australian Tertiary Hospital: Time Series Analyses of Prevalence Data.

Authors:  Oyebola Fasugba; Brett G Mitchell; George Mnatzaganian; Anindita Das; Peter Collignon; Anne Gardner
Journal:  PLoS One       Date:  2016-10-06       Impact factor: 3.240

6.  Clinical Practice Guidelines for the Antibiotic Treatment of Community-Acquired Urinary Tract Infections.

Authors:  Cheol In Kang; Jieun Kim; Dae Won Park; Baek Nam Kim; U Syn Ha; Seung Ju Lee; Jeong Kyun Yeo; Seung Ki Min; Heeyoung Lee; Seong Heon Wie
Journal:  Infect Chemother       Date:  2018-03
  6 in total
  5 in total

1.  Antimicrobial Surveillance for Bacterial Uropathogens in Ha'il, Saudi Arabia: A Five-Year Multicenter Retrospective Study.

Authors:  Abdulrahman S Bazaid; Amir Saeed; Abdulaziz Alrashidi; Abdulkarim Alrashidi; Khalid Alshaghdali; Sahar A Hammam; Talal Alreshidi; Munif Alshammary; Abdullah Alarfaj; Rawan Thallab; Abdu Aldarhami
Journal:  Infect Drug Resist       Date:  2021-04-16       Impact factor: 4.003

2.  Urinary tract infection, antimicrobial susceptibility pattern of isolates, and associated factors among women with a post-fistula at public health facilities, Harar, eastern Ethiopia: A cross-sectional study.

Authors:  Dadi Marami; Degu Abate; Shiferaw Letta
Journal:  SAGE Open Med       Date:  2022-02-21

3.  A Retrospective Study on Bile Culture and Antibiotic Susceptibility Patterns of Patients with Biliary Tract Infections.

Authors:  Chenwei Zhao; Shanshan Liu; Xue Bai; Jitao Song; Qiaowei Fan; Jing Chen
Journal:  Evid Based Complement Alternat Med       Date:  2022-04-13       Impact factor: 2.650

4.  Catheter-Associated Urinary Tract Infection in Intensive Care Unit Patients at a Tertiary Care Hospital, Hail, Kingdom of Saudi Arabia.

Authors:  Mohd Saleem; Azharuddin Sajid Syed Khaja; Ashfaque Hossain; Fahaad Alenazi; Kamaleldin B Said; Soha Abdallah Moursi; Homoud Abdulmohsin Almalaq; Hamza Mohamed; Ehab Rakha; Sunit Kumar Mishra
Journal:  Diagnostics (Basel)       Date:  2022-07-12

5.  Urinary Tract Infection as the Diagnosis for Admission Through the Emergency Department: Its Prevalence, Seasonality, Diagnostic Methods, and Diagnostic Decisions.

Authors:  Sarah Alrashid; Ramah Ashoor; Sahar Alruhaimi; Amirah Hamed; Shahad Alzahrani; Abdulla Al Sayyari
Journal:  Cureus       Date:  2022-08-09
  5 in total

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