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Monitoring fluoroquinolone resistance among ESBL-positive and ESBL-negative Escherichia coli strains isolated from urinary tract infections: An alert for empirical treatment

ABSTRACT

Background:

Bacterial resistance to extended-spectrum beta-lactamases (ESBL) is present worldwide. Empirical antibiotic therapy is often needed, and the use of fluoroquinolones, such as ciprofloxacin and norfloxacin, is common. This study aimed to analyze the urine cultures from 2,680 outpatients in January 2019, 2020, 2021, and 2022, with bacterial counts above 100,000 CFU/mL in which Escherichia coli was the etiological agent.

Methods:

We monitored the resistance of ESBL-positive and ESBL-negative strains to ciprofloxacin and norfloxacin and evaluated resistance rates.

Results:

Significantly higher fluoroquinolone resistance rates were observed among ESBL-positive strains in all years studied. Furthermore, a significant increase in the rate of fluoroquinolone resistance was observed between 2021 and 2022 in ESBL-positive and -negative strains, as well as from 2020 to 2021 among the ESBL-positive strains.

Conclusions:

The data obtained in the present study showed a tendency towards an increase in fluoroquinolone resistance among ESBL-positive and -negative E. coli strains isolated from urine cultures in Brazil. Since empirical antibiotic therapy with fluoroquinolones is commonly used to treat diverse types of infections, such as community-acquired urinary tract infections, this work highlights the need for continuous monitoring of fluoroquinolone resistance among E. coli strains circulating in the community, which can mitigate the frequency of therapeutic failures and development of widespread multidrug-resistant strains.

Keywords:
Fluoroquinolones; Urinary tract infection; Escherichia coli; Drug resistance

INTRODUCTION

Urinary tract infections (UTIs) are among the most frequent infections in humans, with an incidence that is high in the community and varies with sex and age. UTIs can be caused by a range of pathogen, mainly Escherichia coli and other Gram-negative bacteria11. Foxman B, Barlow R, D'Arcy H, Gillespie B, Sobel JD. Urinary tract infection: self-reported incidence and associated costs. Ann Epidemiol. 2000;10(8):509-15. Available from: https://doi.org/10.1016/s1047-2797(00)00072-7
https://doi.org/10.1016/s1047-2797(00)00...
. UTI treatment often requires the use of antimicrobials, among which oral beta-lactams and fluoroquinolones are the most prescribed until susceptibility results are acquired. However, owing to the rapid spread of drug resistance among Gram-negative microorganisms, including E. coli, UTIs are becoming increasingly difficult to treat22. Klein RD, Hultgren SJ. Urinary tract infections: microbial pathogenesis, host-pathogen interactions and new treatment strategies. Nat Rev Microbiol. 2020;18(4):211-26. Available from: https://doi.org/10.1038/s41579-020-0324-0
https://doi.org/10.1038/s41579-020-0324-...
.

The production of extended-spectrum beta-lactamases (ESBL) is the most important resistance mechanism that Gram-negative bacteria have against beta-lactam agents33. Teklu DS, Negeri AA, Legese MH, Bedada TL, Woldemariam HK, Tullu KD. Extended-spectrum beta-lactamase production and multi-drug resistance amongEnterobacteriaceaeisolated in Addis Ababa, Ethiopia. Antimicrob Resist Infect Control. 2019;8(39):1-12. Available from: https://doi.org/10.1186/s13756-019-0488-4
https://doi.org/10.1186/s13756-019-0488-...

4. Castanheira M, Simner PJ, Bradford PA. Extended-spectrum β-lactamases: an update on their characteristics, epidemiology and detection. JAC Antimicrob Resist. 2021;3(3):1-22. Available from: https://doi.org/10.1093/jacamr/dlab092
https://doi.org/10.1093/jacamr/dlab092...
-55. Sanders CC, Sanders WEJ. Beta-Lactam resistance in gram-negative bacteria: global trends and clinical impact. Clin Infect Dis. 1992;15(5):824-39. Available from: https://doi.org/10.1093/clind/15.5.824
https://doi.org/10.1093/clind/15.5.824...
. Although there is no direct correlation between the mechanisms involved in resistance to beta-lactams and fluoroquinolones, ESBL-positive strains were found to be more resistant to these agents than ESBL-negative strains. Prior studies have demonstrated that until 58% of ESBL-positive strains harbor resistance genes against quinolones66. Sedighi I, Arabestani MR, Rahimbakhsh A, Karimitabar Z, Alikhani MY. Dissemination of Extended-Spectrum β-Lactamases and Quinolone Resistance Genes Among Clinical Isolates of Uropathogenic Escherichia coli in Children. Jundishapur J Microbiol. 2015 Jul 25;8(7):e19184. Available from: http://doi.org/10.5812/jjm.19184v2
https://doi.org/10.5812/jjm.19184v2...
,77. FarajzadehSheikh A, Veisi H, Shahin M, Getso M, Farahani A. Frequency of quinolone resistance genes among extended-spectrum β-lactamase (ESBL)-producing Escherichia coli strains isolated from urinary tract infections. Trop Med Health. 2019;47(19). Available from: https://doi.org/10.1186/s41182-019-0147-8
https://doi.org/10.1186/s41182-019-0147-...
.

Therefore, this study aimed to evaluate the frequency of resistance to ciprofloxacin and norfloxacin among ESBL-positive and ESBL-negative E. coli strains isolated from outpatients with UTIs in January 2019, 2020, 2021, and 2022.

METHODS

In the present retrospective study, data were obtained from the database of one of the largest private laboratories in Latin America. Approximately 120,000 urine cultures originating from all regions of Brazil are processed monthly through an advanced automation system at the Operational Technical Nucleus, a central operation base located in the city of Vespasiano (Minas Gerais). The urine samples were collected at the service units spread throughout the country, preserved in boric acid (Greiner Bio-One®, Brazil), kept under refrigeration, and sent within 24 h to the central operation base. To ensure an adequate conservation time, the samples were transported by air through an integrated logistics system.

We randomly selected the results of 2,680 mid-stream urine cultures carried out in January 2019, 2020, 2021, and 2022 from the database. January was randomly chosen to standardize the time of year. Patients who answered the questionnaire with predefined information or were using antibiotics were excluded. To obtain an overview of the community strains, only information from outpatients was included in the study. Moreover, only data from cultures with bacterial growth above 100,000 CFU/mL, whose identification was conclusive for E. coli were included.

Until 2019, laboratory analyses were manually performed. The specimens were seeded in a laminar flow hood in chromogenic medium plates (chromID® CPS® Elite, bioMérieux®, Brazil) using a 1 μL calibrated loop. After incubation for 24 h at 37 °C in an aerobic atmosphere, biochemical tests were performed using a Modified Rugai medium (Renylab®, Brazil). Antimicrobial Susceptibility Tests (ASTs) were performed using the disk diffusion method in Mueller-Hinton medium (PlastLabor®, Brazil). Additionally, the strains were screened for ESBL production by the disk-approximation method using amoxicillin-clavulanic acid (20/10 µg, Oxoid®, Brazil), ceftriaxone (30 µg, Oxoid®), ceftazidime (30 µg, Oxoid®), aztreonam (30 µg, Oxoid®), and cefotaxime (30 µg, Oxoid®). Although several antibiotics were tested, the compiled results focused on the analysis of ciprofloxacin (5 µg, Oxoid®), norfloxacin (10 µg, Oxoid®), and ESBL production. Standardization followed Clinical and Laboratory Standards Institute (CLSI) guidelines88. Clinical and Laboratory Standard Institute (CLSI). Performance Standards for Antimicrobial Susceptibility Testing. 29th ed. CLSI supplement M100. Wayne, PA: CLSI; 2019. 39 p..

Since 2020, laboratory analyses have been conducted by using automated processes. The samples were processed using AutoPlack® automatic seeders (Beckman Coulter Diagnostics®, USA) and bacterial identification was performed by MALDI-TOF mass spectrometry (VITEK® MS, bioMérieux®, France). The ASTs and screening tests for ESBL were performed using semi-automated cards (VITEK® XL, bioMérieux®). Standardization followed the guidelines established by the BrCAST99. Brazilian Committee on Antimicrobial Susceptibility Testing (BrCAST). Orientações do EUCAST para a detecção de mecanismos de resistência e resistências específicas de importância clínica e/ou epidemiológica. São Paulo: BrCAST. 20 p. 2021. and the Brazilian Ministry of Health. The tests were quality controlled using the standard strains E. coli ATCC 25922 (ESBL-negative), Pseudomonas aeruginosa ATCC 27853 (ESBL-negative), and Klebsiella pneumoniae ATCC 700603 (ESBL-positive).

The fluoroquinolone resistance rates among ESBL-positive and -negative groups were calculated and analyzed using the OpenEpi software (version 3.0.1) (Dean AG, Sullivan KM, Soe MM. OpenEpi: Open Source Epidemiologic Statistics for Public Health, http://www.OpenEpi.com). A Chi-square test was performed to compare the resistance rates between the studied groups.

RESULTS

Resistance frequency to ciprofloxacin and norfloxacin was evaluated in 1,340 ESBL-positive (335 per year) and 1,340 ESBL-negative (335 per year) E. coli strains randomly selected during the same period (January) of 2019, 2020, 2021, and 2022. Approximately 43.2% (n=1,158) of the E. coli strains were found to be susceptible to the tested fluoroquinolones, whereas the rest, 56.8% (n=1,522), showed resistance to both antimicrobials.

As shown in Table 1 and Figure 1, the frequency of fluoroquinolone resistance in the ESBL-negative strains was 28.7% (n=96) in 2019, 26.9% (n=90) in 2020, 29% (n=97) in 2021, and 37.6% (n=126) in 2022. The resistance of ESBL-positive strains was verified to be 82.1% (n=275) in 2019, 77% (n=258) in 2020, 83.6% (n=280) in 2021, and 89.6% (n=300) in 2022.

The fluoroquinolone resistance rates among ESBL-positive strains compared to ESBL-negative strains were significantly different (p < 0.0001) in each of the years considered individually. However, there was no statistically significant difference in resistance when the years were compared, specifically, 2019 versus 2020 for ESBL-positive isolates, and for ESBL-negative isolates, in 2019 versus 2020 and 2020 versus 2021. In all other evaluations between years, we found a statistically significant increase in fluoroquinolone resistance as shown in Table 1.

TABLE 1:
Frequency of resistance/susceptibility to ciprofloxacin and norfloxacin among extended-spectrum beta-lactamases (ESBL)-positive and -negative Escherichia coli observed in January 2019, 2020, 2021, and 2022.

FIGURE 1:
Fluoroquinolone resistance among extended-spectrum beta-lactamases (ESBL)-positive and -negative Escherichia coli. Frequency of resistance in each of the groups analyzed individually, demonstrating the trend over the years of study.

DISCUSSION

In routine laboratory tests, several microorganisms can be isolated from urine cultures. Enterobacteria are the main etiological agents of UTIs with E. coli being the most frequent species. The widespread use of empirical antibiotic therapy significantly contributes to the increased prevalence of antimicrobial-resistant strains, as the indiscriminate and incorrect use of therapeutic agents is a risk factor for the emergence and spread of microbial resistance66. Sedighi I, Arabestani MR, Rahimbakhsh A, Karimitabar Z, Alikhani MY. Dissemination of Extended-Spectrum β-Lactamases and Quinolone Resistance Genes Among Clinical Isolates of Uropathogenic Escherichia coli in Children. Jundishapur J Microbiol. 2015 Jul 25;8(7):e19184. Available from: http://doi.org/10.5812/jjm.19184v2
https://doi.org/10.5812/jjm.19184v2...
,1010. Oplustil CP, Zoccoli MC, Tobouti NR, Sinto SI. Procedimentos Básicos em Microbiologia clínica. 3rd ed. Sao Paulo: Savier; 2010, 756 p.,1111. Braoios A, Turatti TF, Meredija LCS, Campos TRS, Denadai FHM. Infecções de trato urinário em pacientes só hospitalizados: etiologia e padrão de Resistência aos antimicrobianos. J Bras Patol Med Lab. 2009;45(6):449-56. Available from: https://doi.org/10.1590/S1676-24442009000600003
https://doi.org/10.1590/S1676-2444200900...
.

Resistance to beta-lactams is often reported for Gram-negative bacteria, occurring mainly due to the production of beta-lactamases or associated with changes in membrane permeability due to the loss of porins. Resistance depends on the amount of enzyme present and the affinity for the substrate, and may not be measured by AST, if the suspension of microorganisms is not adequate and variation in the predominant enzyme can also occur. Therefore, routine susceptibility tests do not always detect ESBL production, but the possibility of their presence cannot be ignored and is relevant1212. Livermore DM. Beta-Lactamases in laboratory and clinical resistance. Clin Microbiol Rev. 1995;8(4):557-84. Available from: https://doi.org/10.1128/CMR.8.4.557
https://doi.org/10.1128/CMR.8.4.557...

13. Bradford PA. Extended-spectrum beta-lactamases in the 21st century: caracterization, epidemiology, and detection of this important resistance threat. Clin Microbiol Rev . 2001;14(4): 933-51. Available from: https://doi.org/10.1128/CMR.14.4.933-951.2001
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-1414. Queenan AM, Foleno B, Gownley C, Wira E, Bush K. Effects of Inoculum and B-lactamase Activity in Ampc- and Extended- Spectrum B-lactamase (ESBL) -Producing Escherichia coli and Klebsiella pneumoniae Clinical isolates Tested by using NCCLS ESBL Methodology. J Clin Microbiol. 2004;42(1):269-75. Available from: https://doi.org/10.1128/JCM.42.1.269-275.2004
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.

The treatment of infections caused by resistant strains offers a substantial challenge, as they can hydrolyze penicillin, cephalosporins of all generations, and monobactam, minimizing therapeutic options, and only some beta-lactam antibiotics maintain their activity against them1515. Lago A, Fuentefria SR, Fuentefria DB. Enterobactérias produtoras de ESBL em Passo Fundo, estado do Rio Grande do Sul, Brasil. Rev. Soc. Bras. Med. Trop. 2010;43(4):430-34. Available from: https://doi.org/10.1590/S0037-86822010000400019
https://doi.org/10.1590/S0037-8682201000...
. To aggravate this issue, two additional facts must be highlighted. First, empirically prescribed antimicrobials that reach a percentage of resistance above 20% in the community run a high risk of therapeutic failure, recommending caution with their usage. Second, a significant increase in the appearance of ESBL-producing strains has been reported worldwide, including in North America and South/Latin America1616. Ibrahim DR, Dodd CER, Stekel DJ, Meshioye RT, Diggle M, Lister M, Hobman JL. Multidrug-Resistant ESBL-Producing E. coli in Clinical Samples from the UK. Antibiotics (Basel). 2023 Jan 13;12(1):169. doi: 10.3390/antibiotics12010169. PMID: 36671370; PMCID: PMC9854697.
https://doi.org/10.3390/antibiotics12010...

17. Gales AC, Sader HS, Jones RN. The SENTRY Participants Group (Latin America). Urinary tract infection trends in Latin American hospitals: report from the SENTRY antimicrobial surveillance program (1997-2000). Diagn Microbiol Infect Dis. 2002;44(3):289-99. Available from: https://doi.org/10.1016/s0732-8893(02)00470-4
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18. Mathai D, Jones RN, Pfaller M. The SENTRY Participant Group North America. Epidemiology and frequency of resistance among pathogens causing urinary tract infections in 1,510 hospitalized patients: a report from the SENTRY Antimicrobial Surveillance Program (North America). Diagn Microbiol Infect Dis . 2001;40(3):129-36. Available from: https://doi.org/10.1016/S0732-8893(01)00254-1
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19. Saurina G, Quale JM, Manikal VM, Oydna E, Landman D. Antimicrobial resistance in Enterobacteriaceae in Brooklyn, NY: epidemiology and relation to antibiotic usage patterns. J Antimicrob Chemother. 2000;45(6):895-8. Available from: https://doi.org/10.1093/jac/45.6.895
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-2020. Winokur PL, Canton R, Casellas JM, Legakis N. Variations in the prevalence of strains expressing an extended-spectrum beta-lactamase phenotype and characterization of isolates from Europe, the Americas, and the Western Pacific region. Clin Infect Dis . 2001;15 (32) Suppl 2:S94-103. Available from: https://doi.org/10.1086/320182
https://doi.org/10.1086/320182...
.

Although fluoroquinolone resistance in E. coli is not new, studies investigating the resistance rates among strains circulating in the community are necessary, especially given the spread of multidrug-resistant (MDR) strains and the recurrent use of empirical therapy with these antimicrobials for the treatment of UTIs. Thus, in the present study, we analyzed the frequency of fluoroquinolone resistance among ESBL-positive and ESBL-negative E. coli strains isolated from outpatients with UTIs in the same month over the past four years.

Our data revealed that the rate of fluoroquinolone resistance in the ESBL-positive strains was approximately 180% higher than that in the ESBL-negative samples in all years evaluated. In addition, our data showed a trend towards increased rates of fluoroquinolone resistance among both ESBL-positive and -negative strains. Once ESBL-negative strains are isolated at high levels in a community, these findings can be considered an alert for the empirical treatment of UTIs.

In 2020, the microbiology laboratory standards were changed. A committee formed by members of the Societies of Clinical Analysis, Infectious Diseases, Microbiology, Clinical Pathology, and Laboratory Medicine began to determine and periodically review procedures for the interpretation of susceptibility tests to antimicrobials for clinical use and epidemiological purposes, proposing to the National Agency of Sanitary Surveillance the implementation of these procedures in Brazilian clinical laboratories. The CLSI standards fell into disuse, and this change was implemented in our study at its inception. Thus, it is necessary to consider the change in breakpoints for fluoroquinolones. For example, resistance to ciprofloxacin was previously determined by a minimum inhibitory concentration of ≥1 µg/mL but is now determined when >0.5 µg/mL. Initially, we believed that this would increase the number of resistant strains. However, as the change was only one dilution point, this was not occurred. In fact, as shown in Table 1, the number of resistant strains in 2020 was not statistically different from that in 2019, with p values of 0.051 and 0.302 (resistance in ESBL-positive and ESBL-negative, respectively). For the ESBL-negative group there was a decrease in the absolute number (from 96 to 90 strains).

In Brazil, a similar study found a fluoroquinolone resistance rate of approximately 76%2121. Araújo MRB, Batista AL, Sousa MAB. Perfil de Resistência aos Antimicrobianos em Escherichia coli, Proteus mirabilis e Klebsiella pneumoniae produtoras de Beta-Lactamase de Espectro Ampliado (ESBL), isoladas de pacientes com infecção do trato urinário. LAES/HAES. 2018;39:66-80. Available from: http://www.mcwill.com.br/revistavirtual/233/mobile/index.html#p=66
http://www.mcwill.com.br/revistavirtual/...
among ESBL-positive strains. In Latin America, resistance rates of 58% and 90% have been reported in Peru2222. Yabar M, Curi B, Torres C, Calderon R, Riveros M, Ochoa T. Multirresistencia y factores asociados a la presencia de betalactamasas de espectro extendido en cepas de Escherichia coli provenientes de urocultivos. Rev Peru Med Exp Salud Publica. 2017;34(4):660-5. Available from: https://doi.org/10.17843/rpmesp.2017.344.2922.
https://doi.org/10.17843/rpmesp.2017.344...
and Venezuela2323. Guevara N, Guzmán M, Merentes A, Rizzi A, Papaptzikos J, Rivero N, et al. Patrones de susceptibilidad antimicrobiana de bacterias gramnegativas aisladas de infecciones del tracto urinario en Venezuela: Resultados del estudio SMART 2009-2012. Rev. Chil. Infectol. 2015;32(6):639-48. Available from: http://dx.doi.org/10.4067/S0716-10182015000700005
https://doi.org/10.4067/S0716-1018201500...
, respectively. Moreover, a rate of 80% has been reported in Mexico, 60% in Ecuador2424. Chavez JAD, Castillo ARP, Alcocer DAQ, Flores WIG, Puga MEJ, Buitrón DEO. Resistencia y sensibilidad bacteriana en urocultivos en una población de mujeres de ecuador. Ver Fac Med [online]. 2018;26(2):.22-8. Available from: http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0121-52562018000200022&lng=en&nrm=iso.
http://www.scielo.org.co/scielo.php?scri...
and 12% in Chile2525. Merino MM, Morales IO, Badilla JB, Vallejos CM. Resistencia antimicrobiana en infección del tracto urinario con bacteriuria en el servicio de urgencia de un hospital comunitario de la región de Ñuble, Chile. Rev Virtual Soc Parag Med Int. 2021;8(1):117-25. Available from: https://doi.org/10.18004/rvspmi/2312-3893/2021.08.01.117
https://doi.org/10.18004/rvspmi/2312-389...
. In Brazil, rates of 43%2626. Leite MS, Gusmão AC, Gontijo BAV, Garcia PG. Perfil de resistência aos antimicrobianos de Escherichia coli isoladas de amostras de urina de pacientes de uma Unidade de Terapia Intensiva. Rev Bras Anal Clin. 2020;52(3):243-7. Available from: https://doi.org/10.21877/2448-3877.202100877
https://doi.org/10.21877/2448-3877.20210...
and 56%2727. Diniz AMM, Santos RMC. Escherichia coli resistente a ciprofloxacina em pacientes internados em hospital universitário de Manaus, 2015. Rev Epidemiol Control Infec. 2017;7(1):20-4. Available from: https://doi.org/10.17058/reci.v7i1.7758
https://doi.org/10.17058/reci.v7i1.7758...
have been reported. In earlier studies, rates of 12%2828. Kiffer CR, Mendes C, Oplustil CP, Sampaio JL. Antibiotic Resistance and Trend of Urinary Pathogens in General Outpatients from a Major Urban City. Int Braz J Urol. 2007;33:42-9. Available from: https://doi.org/10.1590/s1677-55382007000100007
https://doi.org/10.1590/s1677-5538200700...
,2929. Moreira ED Jr, De Siqueira IC, Alcantara AP, Guereiro De Moura CG, De Carvalho WA, Riley L. Antimicrobial resistance of Escherichia coli Strains causing community-acquired urinary tract infections among insured and uninsured populations in a large urban center. Journal of Chemotherapy. 2006;18:255-60. Available from: http://dx.doi.org/ 10.1179/joc.2006.18.3.255
https://doi.org/10.1179/joc.2006.18.3.25...
and 22%3030. Dias Neto JA, Martins ACP, Tiraboschi RB, Domingos ALA, Cologna AJ, Paschoalin EL, et al. Prevalence and bacterial susceptibility of hospital acquired urinary tract infection. Acta Cir Bras. 2003;18(5):36-38. Available from: http://dx.doi.org/10.1590/S0102-86502003001200013
https://doi.org/10.1590/S0102-8650200300...
were found. In a Russian study, a resistance rate of 25% was obtained in 2017, which was 23% higher than the rate found in 19993131. Rafalskiy V, Pushkar D, Yakovlev S, Epstein O, Putilovskiy M, Tarasov S, et al. Distribution and antibiotic resistance profile of key Gram-negative bacteria that cause community-onset urinary tract infections in the Russian Federation: RESOURCE multicentre surveillance 2017 study. J Glob Antimicrob Resist. 2020;21:188-94. Available from: https://doi.org/10.1016/j.jgar.2019.09.008
https://doi.org/10.1016/j.jgar.2019.09.0...
.

Studies have also indicated that microorganisms with the ESBL phenotype may show in vitro susceptibility to some drugs, but the use of these drugs leads to a lower clinical response due to the inoculum effect, resulting in an increase in the minimum inhibitory concentration when faced with a large bacterial inoculum or when the drug fails to reach its pharmacodynamic targets3232. Endimiani A, Luzzaro F, Perilli M, Lombardi G, Colì A, Tamborini A, et al. Bacteremia due to Klebsiella pneumoniae isolates producing the TEM-52 extended-spectrum β-lactamase: treatment outcome of patients receiving imipenem or ciprofloxacin. Clin Infect Dis . 2004;38(2):243-51. Available from: http://doi.org/10.1086/380645
https://doi.org/10.1086/380645...
,3333. Paterson DL, Ko WC, Von Gottberg A, Mohapatra S, Casellas JM, Goossens H, et al. Antibiotic therapy for Klebsiella pneumoniae bacteremia: implications of production of extended-spectrum β-lactamases. Clin Infect Dis . 2004;39(1):31-7. Available from: http://doi.org/10.1086/420816
https://doi.org/10.1086/420816...
. Thus, the decrease in antimicrobial susceptibility of ESBL-positive strains may also represent a significant possibility for therapeutic failure in situations where AST is not performed.

In cases of UTIs, particularly community-acquired UTIs, it is common to not perform urine cultures and apply empirical treatment. However, with the high rates of resistance in ESBL-positive strains, empiric therapy can result not only in therapeutic failure, but also increase bacterial resistance rates, which is an unfavorable outcome. Infection control is extremely important, and studies such as this one have value in guiding health professionals in this difficult mission. Bacterial multidrug resistance must be considered, and therapeutic options, which are often limited, become even scarcer when ESBL-producing bacteria cause infection.

The clinical significance of ESBL strains is high because limitation in antibiotic choice for treatment, thus making it evident that monitoring the resistance profile of bacteria is beneficial and recommended, as it reduces the chance of failure and spread of MDR strains. Finally, increased fluoroquinolone resistance among ESBL-negative strains, which is more common in the community (non-hospital environments), should also be monitored to prevent rising resistance rates in infections.

ETHICAL APPROVAL

Since the study was a retrospective analysis of laboratory data collected, and no additional investigations were performed with submitted specimens, no ethical approval was applied.

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  • Financial Support: Funding information is not applicable. No funding was received.

Publication Dates

  • Publication in this collection
    14 Apr 2023
  • Date of issue
    2023

History

  • Received
    11 Nov 2022
  • Accepted
    10 Mar 2023
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