Next Article in Journal
Assessment of In Vitro Cefiderocol Susceptibility and Comparators against an Epidemiologically Diverse Collection of Acinetobacter baumannii Clinical Isolates
Next Article in Special Issue
Efficacy and Safety of Oral Fosfomycin-Trometamol in Male Urinary Tract Infections with Multidrug-Resistant Enterobacterales
Previous Article in Journal
Antimicrobial Activity of Eucalyptus globulus, Azadirachta indica, Glycyrrhiza glabra, Rheum palmatum Extracts and Rhein against Porphyromonas gingivalis
Previous Article in Special Issue
Antibacterial and Anti-Biofilm Activities of Essential Oil Compounds against New Delhi Metallo-β-Lactamase-1-Producing Uropathogenic Klebsiella pneumoniae Strains
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Influence of Antimicrobial Resistance on the Course of Symptoms in Female Patients Treated for Uncomplicated Cystitis Caused by Escherichia coli

1
Research Unit for General Practice and Section of General Practice, Department of Public Health, University of Copenhagen, 1350 Copenhagen, Denmark
2
University Institute in Primary Care Research Jordi Gol, Via Roma Health Centre, 08007 Barcelona, Spain
3
Department of Public Health, General Practice, University of Southern Denmark, 5000 Odense, Denmark
*
Author to whom correspondence should be addressed.
Antibiotics 2022, 11(2), 188; https://doi.org/10.3390/antibiotics11020188
Submission received: 30 December 2021 / Revised: 26 January 2022 / Accepted: 27 January 2022 / Published: 31 January 2022
(This article belongs to the Special Issue Uropathogens - Antibiotic Resistance and Alternative Therapies)

Abstract

:
Background: Resistance to the prescribed antibiotic causes a longer duration of symptoms in patients with urinary tract infection. Yet, a study found that patients infected with trimethoprim-resistant Escherichia coli (E. coli) had a prolonged duration of symptoms even if treated with an antibiotic to which the strain was susceptible. The purpose of this study was to attempt to reproduce this finding in a different cohort. Methods: We analyzed data from two studies from general practice in the Capital Region of Denmark including patients from 2014 to 2016. The primary outcome was the severity of frequency and dysuria. The secondary outcome was the number of days until symptoms had disappeared. Results: We included 180 women treated for uncomplicated cystitis caused by E. coli. We found that 16.11% (n = 29) of the E. coli strains were resistant to all of the three selected antibiotics (ampicillin, sulfamethizole and trimethoprim). There was no significant difference in severity or time until the symptoms had disappeared between women infected with resistant or susceptible E. coli. Conclusions: Strains of E. coli resistant to ampicillin, sulfamethizole and trimethoprim causing uncomplicated cystitis do not result in more severe symptoms or a longer symptom duration if treated with an antibiotic to which they are susceptible.

1. Introduction

Urinary tract infection (UTI) is one of the most frequent infections encountered in general practice and about one in three women experience a UTI at least once in their life time [1,2].
The increase in antibiotic resistance is a threat to human and animal health worldwide and the excessive use of antibiotics in general practice continues to be an unfortunate driver towards the development of antibiotic resistance, both in society and in the individual patient [3,4,5]. For example, the high use of quinolones for uncomplicated UTIs in the early 2000s resulted in a gradual increase in uropathogens resistant to these antibiotics. As a result, these antimicrobials must now be used more judiciously [6].
E. coli is the most frequent uropathogenic bacteria, and in Denmark, pivmecillinam is the antibiotic most commonly prescribed for UTI [7,8]. In Denmark, the prevalence of E. coli resistant to pivmecillinam is 5% in samples from primary care [9]. In the United Kingdom, trimethoprim is one of the first-line antibiotics recommended for UTI and the resistance rate against trimethoprim for E. coli is 14–17% [10,11,12]. Resistance rates for other antibiotics used in primary health care in Denmark to treat UTIs are ampicillin (36%), sulfamethizole (27%), trimethoprim (21%), nitrofurantoin (0.5%) [9].
Studies from general practice have shown that patients with UTI caused by uropathogen bacterial strains resistant to one or more antibiotics have more severe symptoms and a longer symptom duration than patients with UTI caused by susceptible strains [10,11,13]. Most studies have investigated the influence of uropathogens that are resistant to the prescribed antibiotic. However, a study from the United Kingdom also found a longer symptom duration if the uropathogenic bacteria, Escherichia coli (E. coli), was resistant to trimethoprim in spite of being susceptible to the prescribed antibiotic [11].
The different antibiotic recommendations for UTI in Denmark and the United Kingdom, as well as the different resistance patterns, make it relevant to investigate if the findings from the study from the United Kingdom are applicable to the Danish population.
Hence, the aim of this analysis was to investigate the influence of the antimicrobial resistance (AMR) pattern on the course of symptoms in women with uncomplicated cystitis caused by E. coli treated with an antibiotic to which the bacteria is susceptible. We chose to focus on women with uncomplicated cystitis in order to have a more homogenous group.

2. Results

In total, 59 general practices included 851 patients for the two studies. Figure 1 shows a flowchart of the patients included and excluded from the analyses in this paper. We included 180 women with uncomplicated cystitis caused by E. coli and treated with pivmecillinam, sulfamethizole, trimethoprim or nitrofurantoin on the day after consultation for this analysis. Out of the 671 excluded patients, 436 were not infected with E. coli, 79 had a complicated UTI or upper UTI, 127 patients were not prescribed antibiotics as stated in our inclusion criteria and 29 had not returned their symptom diaries.
Table 1 shows the baseline data. The age of the women ranged from 18 to 90 years, with 59 women being 65 years of age or older. The majority of patients (n = 114, 63.33%) were prescribed pivmecillinam. Resistance rates were highest for ampicillin (n = 64, 35.56%), followed by sulfamethizole (n = 48, 26.67%), and trimethoprim (n = 43, 23.89%). Twenty-nine (16.11%) of the urine samples showed growth of E. coli that were resistant to all of the three antibiotics (i.e., ampicillin, sulfamethizole and trimethoprim). The baseline characteristics were similar for women with missing data in their symptom diaries (data not shown).
The mean symptom severity score of frequency and dysuria was not influenced by the AMR pattern (see Figure 2 and Figure 3). The difference in severity score was highest on day one, that is, before the initiation of antibiotic treatment. In patients with E. coli resistant to all three antibiotics (ampicillin, sulfamethizole and trimethoprim), the frequency severity score at day one was 7.0 (95% CI: 6.0–7.9), 7.7 (95% CI: 6.9–8.4) in patients with E. coli resistant to one or two antibiotics and 7.5 (95% CI: 7.0–8.0) in patients with E. coli sensitive to all three antibiotics. The difference was not significant. On day five, the frequency severity scores were below two, irrespective of the AMR pattern. In patients with E. coli resistant to all three antibiotics (ampicillin, sulfamethizole and trimethoprim), the dysuria severity score at day one was 4.0 (95% CI: 3.3–4.7), 4.9 (95% CI: 4.4–5.5) in patients with E. coli resistant to one or two antibiotics and 4.4 (95% CI: 4.1–4.8) in patients with E. coli sensitive to all three antibiotics. At day five, the dysuria severity scores were below one, irrespective of the AMR pattern.
Table 2 shows the influence of the AMR pattern on the mean number of days until symptoms had disappeared. In patients with E. coli resistant to all three antibiotics (ampicillin, sulfamethizole and trimethoprim) the mean number of days until overall cure was non-significantly longer (0.5 days, p > 0.05) than in patients with E. coli susceptible to all three antibiotics.

3. Discussion

3.1. Principal Findings

This analysis shows that the antimicrobial resistance pattern has no influence on the course of symptoms (frequency and dysuria) in women with uncomplicated cystitis caused by E. coli treated with an antibiotic to which the strain is susceptible.

3.2. Strengths and Weaknesses

The most important strength of this analysis is that we used a validated questionnaire to evaluate the symptom scores (Holm–Cordoba UTI Score). It ensures that the most relevant symptoms in patients with uncomplicated cystitis were accurately evaluated. Another strength is the homogeneous study population of women with uncomplicated cystitis caused by E. coli that were prescribed an antibiotic to which the strain was susceptible. With the use of narrow inclusion criteria for the analysis, symptom scores were not compared across a broad spectrum of the disease, which could have biased the thresholds for severity and the number of days until symptoms had disappeared. Furthermore, the population is representative of the source population in that there were no differences in the baseline characteristics between patients returning the symptom diary and those who did not do so.
The relatively small sample of patients could have hidden real differences between the groups. However, the analysis showed only very small differences (less than one day) across groups and the relatively small sample size does not outweigh the importance of the clinical implications of our findings. This means that provided the patient is given an antibiotic to which the E. coli is susceptible, information on the AMR pattern will not change either the decision management or the advice about symptom development given to the patient. This study is based on two previous studies carried out in the primary care setting. The study of virulence genes is not performed in this setting and has therefore not been studied in this paper.

3.3. Relation to the Literature

There is sparse literature in this field. To our knowledge, the study performed by Butler et al. in the United Kingdom is the one most similar to ours [11]. In contrast to our findings, Butler et al. found that the symptoms were longer in duration for patients with UTI caused by E. coli resistant to trimethoprim, who were treated with an antibiotic to which the E. coli was susceptible. Trimethoprim is one of the first-line antibiotics for UTI in the United Kingdom [12]; hence, the decision to prescribe another antibiotic might have been taken based on unregistered reasons. Consequently, Butler et al. argue that due to unidentified causes, these patients might have been different from the remaining study population.
It is worth noting that the study by Butler et al. is different from ours in several ways. Firstly, they had a broader population as they also included men. Secondly, the study design was different, with patients being interviewed to assess symptom duration one month after consultation and this may have caused recall bias. Finally, resistance rates and first-line choices of antibiotics differ between the United Kingdom and the Nordic countries. Pivmecillinam is a first-line antibiotic in Denmark [14], Sweden [15], Norway [16], and Finland [17]. Furthermore, the resistance rates to pivmecillinam are very low (i.e., between 3 and 6%) [9,18,19,20]. Due to this low resistance rate to the first-line antibiotic, we were not able to assess the influence of resistance to the most commonly used antibiotic, as Butler et al. did.
The functional mechanisms of the first-line antibiotics differ as well. Trimethoprim works as a bacteriostatic drug inhibiting the synthesis of one of the important nucleotides in the synthesis of DNA, whereas pivmecillinam (a pro-drug to mecillinam) works as a bactericide targeting the biosynthesis of the bacteria cell wall, and is a very effective drug against Gram-negative bacteria [21].
Another two studies from the United Kingdom investigated the influence of treatment with an antibiotic to which the strain is resistant on the duration of symptoms of uUTI [10,13]. Although the aims are not fully comparable to that of our analysis, the design can be compared, as both studies used symptom diaries. Both Little and McNulty et al. assessed the duration of moderate to severe symptoms. Little et al. also assessed an overall severity score of symptoms at days two to four [13]. In our analysis, we investigated the course of symptoms in different ways: the daily severity of symptoms (frequency and dysuria) and number of days until the symptoms had disappeared, regardless of severity. For future research, it would be relevant to unify scales to compare data across studies.
A recent study from Iran investigated the importance of virulence genes profiling in uropathogenic E.coli and found that one gene, cnf1, was present in all UTIs. Our findings relate to primary care where genetic information is not available at this point. Furthermore, for women with uncomplicated cystitis caused by E. coli we found that the resistance pattern did not affect the course of symptoms. Therefore, for this group genetic profiling does not seem relevant at the moment [22].
Finally, our findings are in line with those from a study investigating the treatment of uncomplicated pyelonephritis. Talan et al. found that all women infected with a strain resistant to trimethoprim–sulfamethizole and treated with ciprofloxacin were cured 11 days after the initiation of treatment [23]. This is in line with our finding regarding the irrelevance of the AMR pattern provided that the patient is given an antibiotic to which the E. coli is susceptible. Nonetheless, it is important to highlight that the use of a broad-spectrum antibiotic (e.g., ciprofloxacin) is not the solution to the problem. This was shown in a recent literature review assessing the efficacy and safety of levofloxacin (a broad-spectrum antibiotic) for complicated UTIs and pyelonephritis [6]. The use of a narrow-spectrum antibiotic (e.g., pivmecillinam) as the first-choice antibiotic is a good option provided there is a low prevalence of resistance.

3.4. Implications

The AMR pattern is not clinically relevant in women with uncomplicated cystitis caused by E. coli and treated with an antibiotic to which the strain is susceptible. Our results apply for women with uncomplicated cystitis caused by E. coli, which is the most frequent cause of uncomplicated cystitis, representing about 80% of all cases [7]. However, we would expect our results to apply for other uropathogens as well, as there is no conclusive evidence that the type of uropathogen influences the course of symptoms for uUTI [10,24,25].
The resistance patterns of E. coli strains causing uncomplicated cystitis vary considerably between regions and countries; therefore, specific treatment recommendations may not be universally suitable for all regions or countries. Hence, up-to-date local surveillance data on E. coli resistance rates at the community level are crucial to optimize the prescription of antibiotics in primary care. A recent Irish study carried out in the Cork area found a high prevalence of resistance towards several of the antibiotics recommended as empirical treatment for UTI in their national guidelines [26]. Updated guidelines are especially important in settings in which empiric prescription is the only option for the management of patients with suspected uncomplicated cystitis due to the lack of access to point-of-care tests (POCTs). Regarding settings such as Denmark, which have a wide availability of POCTs, urine culture is routinely performed in practice [27]. Hence, for women with uncomplicated cystitis caused by E. coli, testing for resistance in this setting is not necessary for GPs to make an appropriate prescription of pivmecillinam, due to the low resistance rates. However, in the Danish setting, the use of sulfamethizole and trimethoprim as first choices for uncomplicated cystitis has been rightfully revised considering the high resistance rates (27% for sulfamethizole and 21% for trimethoprim) [9]. The current first-line treatment for uncomplicated cystitis in Denmark is pivmecillinam, which is also one of the recommendations for first-line treatment according to the newest guidelines from the European Association of Urology [14,28].

4. Materials and Methods

This analysis was based on data from two studies on the diagnosis and management of UTI in general practice performed in the Capital Region of Denmark between 2014 and 2016 [27,29]. The inclusion and exclusion criteria of these studies can be found in the previously published protocols [30,31].
For this analysis, we included women ≥ 18 years with symptoms of uncomplicated cystitis (dysuria, frequency or urgency) and a positive urine culture with significant growth of E. coli (≥103 CFU/mL) [32]. In Denmark, four different antibiotic regimes were recommended for uncomplicated cystitis at the time the data were collected: 400 mg of pivmecillinam three times a day for three days, 1 g of sulfamethizole twice a day for three days, 200 mg of trimethoprim twice a day for three days and 50 mg of nitrofurantoin four times a day for three days [8]. We analyzed patients who initiated antibiotic treatment with one of the recommended antibiotics one day after the initial consultation to obtain a homogenous sample of patients in terms of recovery time and since this was the most common day for initiating antibiotics in our two study samples.

4.1. Antimicrobial Resistance

At the initial consultation, the patient was instructed to deliver a mid-stream urine sample, which was sent to the microbiological laboratory for culture and susceptibility testing.
The urine was sent in tubes containing boric acid to stabilize the bacterial count. The culture was performed on blood agar and CHROMagar or “blue” agar plates. Samples were incubated aerobically over night at 35 °C.
All samples were quantified. E. coli was specified based on colonial morphology. Significant growth was defined as ≥103 colony forming units per milliliter (cfu/mL) for E. coli. [27,29]. Antimicrobial susceptibility testing was performed with discs containing antibiotics on Mueller–Hinton agar plates according to EUCAST standards (version 3.1, year 2013) [33]. Testing was performed for mecillinam, trimethoprim, nitrofurantoin, sulfamethizole, ampicillin and ciprofloxacin.

4.2. Outcome and Covariates

The primary outcome was the symptom severity score measured daily during one week after the index consultation. In this analysis, we focused on the most common symptoms of uncomplicated cystitis: frequency and dysuria [34]. We used the Holm–Cordoba UTI Score which is a validated UTI-specific patient-reported outcome measure (PROM) [35]. According to the Holm-Cordoba UTI Score, frequency is an aggregated symptom complex, based on four specific symptoms (increased daytime frequency, increased urge, increased hurry to visit the toilet, increased incontinence), measured on a scale from 0 to 12. Correspondingly, dysuria is an aggregated symptom complex, based on three specific symptoms (pain by urination, difficulty emptying the bladder, suprapubic tension), measured on a scale from 0 to 9.
The secondary outcomes were (a) the number of days until all frequency symptoms had disappeared, (b) the number of days until all dysuria symptoms had disappeared, and (c) the number of days until all UTI symptoms had disappeared (the latter was assessed through a global item, which was the overall assessment of the symptom burden by the patient), hereafter referred to as the ‘overall cure’.
The exposure was the antimicrobial resistance pattern. In this analysis, we only investigated the influence of antibiotics with a known resistance rate of more than 10%, i.e., ampicillin, trimethoprim and sulfamethizole. We carried out two analyses. First, we examined the influence of an overall AMR pattern with the following three groups: (1) resistant to all three antibiotics (i.e., ampicillin, trimethoprim and sulfamethizole); (2) resistant to one or two of these antibiotics; and (3) sensitive to all three antibiotics. Secondly, we investigated the influence of resistance toward the specific antibiotic: (1) resistance to ampicillin compared to sensitivity to all the three antibiotics; (2) resistance to sulfamethizole compared to sensitivity to the three antibiotics; and (3) resistance to trimethoprim compared to sensitivity to all three antibiotics.
We did not control for confounders, since we had a very limited number of relevant co-variates available in both datasets.

4.3. Statistical Analysis

The association of the AMR patterns with the course of the symptom severity one week after the index consultation was assessed in linear mixed models including a subject random effect to account for repeated measurement. The association of the AMR patterns with the number of days until symptoms had disappeared was also assessed in linear models.
In all the statistical analyses, missing information on resistance for the three antibiotics was imputed and the results from multiple (25) imputations were aggregated using Rubin’s rule. Imputation was carried out with chained equations in augmented data on the 356 patients with UTI caused by E. coli. Variables used for the imputation with chained equations were as follows: resistance to ampicillin, sulfamethizole, trimethoprim, mecillinam and ciprofloxacin, and sex, (un)complicated UTI and pyelonephritis, clinic area and age. Analyses were carried out with SAS version 9.4.

Author Contributions

Conceptualization, M.S.W., G.C., L.B., A.H. and C.L.; methodology, M.S.W., G.C., L.B., A.H. and V.S.; formal analysis, V.S., C.B. and M.S.W.; writing—original draft preparation, M.S.W.; writing—review and editing, M.S.W., G.C., L.B., A.H., C.L., V.S. and C.B.; supervision, G.C., L.B. and A.H.; funding acquisition, M.S.W. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by ‘Den lægevidenskabelige del af Det Sundhedsvidenskabelige Fakultets fond for videnskabeligt ansatte kandidater og studerende ved Københavns Universitet’, grant number 2018-0087. The studies from which the data were obtained were funded by the 2016 fund (grant from the University of Copenhagen to promote interdisciplinary research), Læge Sofus Carl Emil Friis og Hustru Olga Doris Friis’ legat, KAP-H (agency for quality in primary care in the Capital Region), and SSI Diagnostika (materials).

Institutional Review Board Statement

The Ethical Committee of the Capital Region of Denmark approved the studies from which the data were obtained.

Informed Consent Statement

Informed written consent was obtained from all patients participating in the two studies. The data for this analysis were received in an anonymized form.

Data Availability Statement

Patient-level data in an anonymized format are available on reasonable request to the primary author.

Acknowledgments

We would like to acknowledge the GPs and patients who took part in the two studies and hereby made this analysis possible.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Moth, G.; Vedsted, P.; Olesen, F. Kontakt- og Sygdomsmønsteret i almen praksis: KOS 2008. 1. udg. Århus: Forskningsenheden for Almen Praksis [Report on Contact and Disease Pattern 2008]; Aarhus Universitet: Aarhus, Denmark, 2010. [Google Scholar]
  2. Butler, C.C.; Hawking, M.K.; Quigley, A.; McNulty, C.A. Incidence, severity, help seeking, and management of uncomplicated urinary tract infection: A population-based survey. Br. J. Gen. Pract. 2015, 65, 702–707. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Costelloe, C.; Metcalfe, C.; Lovering, A.; Mant, D.; Hay, A.D. Effect of antibiotic prescribing in primary care on antimicrobial resistance in individual patients: Systematic review and meta-analysis. BMJ 2010, 340, c2096. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Goossens, H.; Ferech, M.; Vander, R.; Md, S.; Goossens, H.; Ferech, M.; Stichele, R.V.; Elseviers, M. Outpatient antibiotic use in Europe and association with resistance: A cross-national database study. Lancet 2005, 365, 579–587. [Google Scholar] [CrossRef]
  5. World Health Organization. Global Action Plan on Antimicrobial Resistance; World Health Organization: Geneva, Switzerland, 2015; pp. 1–28.
  6. Bientinesi, R.; Murri, R.; Sacco, E. Efficacy and safety of levofloxacin as a treatment for complicated urinary tract infections and pyelonephritis. Expert Opin. Pharmacother. 2020, 21, 637–644. [Google Scholar] [CrossRef] [PubMed]
  7. Schito, G.C.; Naber, K.G.; Botto, H.; Palou, J.; Mazzei, T.; Gualco, L.; Marchese, A. The ARESC study: An international survey on the antimicrobial resistance of pathogens involved in uncomplicated urinary tract infections. Int. J. Antimicrob. Agents 2009, 34, 407–413. [Google Scholar] [CrossRef] [Green Version]
  8. Holm, A.; Cordoba, G.; Aabenhus, R. Prescription of antibiotics for urinary tract infection in general practice in Denmark. Scand. J. Prim. Health Care 2019, 37, 83–89. [Google Scholar] [CrossRef] [Green Version]
  9. Statens Serum Insitut; National Veterinary Institue; National Food Institue. Danmap 2020. 2021. Available online: https://www.danmap.org/reports/2020 (accessed on 21 December 2021).
  10. McNulty, C.A.; Richards, J.; Livermore, D.M.; Little, P.; Charlett, A.; Freeman, E.; Harvey, I.; Thomas, M. Clinical relevance of laboratory-reported antibiotic resistance in acute uncomplicated urinary tract infection in primary care. J. Antimicrob. Chemother. 2006, 58, 1000–1008. [Google Scholar] [CrossRef]
  11. Butler, C.C.; Hillier, S.; Roberts, Z.; Dunstan, F.; Howard, A.; Palmer, S. Antibiotic-resistant infections in primary care are symptomatic for longer and increase workload: Outcomes for patients with E. coli UTIs. Br. J. Gen. Pract. 2006, 56, 686–692. [Google Scholar] [CrossRef]
  12. National Institue for Health and Care Exelence; Public Health England. Urinary Tract Infection (Lower): Antimicrobial Prescribing. 2018. Available online: https://www.nice.org.uk/guidance (accessed on 18 March 2019).
  13. Little, P.; Merriman, R.; Turner, S.; Rumsby, K.; Warner, G.; Lowes, J.A.; Smith, H.; Hawke, C.; Leydon, G.; Mullee, M.; et al. Presentation, pattern, and natural course of severe symptoms, and role of antibiotics and antibiotic resistance among patients presenting with suspected uncomplicated urinary tract infection in primary care: Observational study. BMJ 2010, 340, b5633. [Google Scholar] [CrossRef] [Green Version]
  14. Johansen, I.S.; Gerstof, J.; Engberg, J.H.; Frimodt-Møller, N.; Böcher, S.; Møller, J.K.; Hansen, M.P. Akut Ukompliceret Cystitis Acute Uncomplicated Cystitis. Available online: https://pro.medicin.dk/Specielleemner/Emner/318565 (accessed on 29 December 2021).
  15. Läkemedelsverket Läkemedelsbehandling av Urinvägsinfektioner i Öppenvård—Behandlingsrekommendation Guideline for Treatment of Urinary Tract Infections in Outpatient Care. 2017, pp. 21–36. Available online: https://lakemedelsverket.se/uvi (accessed on 20 March 2019).
  16. Bærheim, A.; Grude, N.; Antibiotikabruk i Primærhelsetjenesten. Cystitt. Use of Antibiotics in Primary Care. Urinary Tract Infection. 2018. Available online: http://www.antibiotikaiallmennpraksis.no/index.php?action=showtopic&topic=vXmA4Spa (accessed on 20 March 2019).
  17. Wuorela, M.; Kouri, T.; Laato, M.; Lipponen, P.; Sammalkorpi, K.; Uhari, M.; Uusitalo, L.; Vuento, R. Käypä hoito—Suosituksen päivitystiivistelmä. Virtsatieinfektiot [Update on current care guidelines: Urinary tract infections]. Duodecim 2011, 127, 2334–2335. [Google Scholar]
  18. Public Health Agency of Sweden; National Veterinary Institue. Consumption of Antibiotics and Occurence of Antibiotics Resistance in Sweden. Swedres-Svarm 2017. Available online: https://www.sva.se/en/our-topics/antibiotics/svarm-resistance-monitoring/swedres-svarm-reports/ (accessed on 10 April 2019).
  19. FiRE and National Institute for Health and Welfare. Antimicrobial Resistance in Finland, Finres 2012. Available online: https://thl.fi/en/web/infectious-diseases/surveillance/antimicrobial-resistance/fire-finnish-study-group-for-antimicrobial-resistance (accessed on 10 April 2019).
  20. Norsk Overvåkningssystem for Antibiotikaresistens for Mikrober (NORM). Usage of Antimicrobial Agents and Occurence of Antimicrobial Resistance in Norway. NORM/NORM-VET 2017; Norwgian Veterinary Institute. Folkehelseinstituttet. 2018. Available online: https://www.vetinst.no/en/surveillance-programmes/norm-norm-vet-report (accessed on 10 April 2019).
  21. Issakhanian, L.; Behzadi, P. Antimicrobial Agents and Urinary Tract Infections. Curr. Pharm. Des. 2019, 25, 1409–1423. [Google Scholar] [CrossRef] [PubMed]
  22. Hozzari, A.; Behzadi, P.; Kerishchi Khiabani, P.; Sholeh, M.; Sabokroo, N. Clinical cases, drug resistance, and virulence genes profiling in Uropathogenic Escherichia coli. J. Appl. Genet. 2020, 61, 265–273. [Google Scholar] [CrossRef] [PubMed]
  23. Talan, D.A.; Stamm, W.E.; Hooton, T.M.; Moran, G.J.; Burke, T.; Iravani, A.; Reuning-scherer, J. Acute Uncomplicated Pyelonephritis in Women. JAMA 2000, 283, 1583–1590. [Google Scholar] [CrossRef] [PubMed]
  24. Ferry, S.A.; Holm, S.E.; Stenlund, H.; Lundholm, R.; Monsen, T.J. The natural course of uncomplicated lower urinary tract infection in women illustrated by a randomized placebo controlled study. Scand. J. Infect. Dis. 2004, 36, 296–301. [Google Scholar] [CrossRef]
  25. Monsen, T.J.; Holm, S.E.; Ferry, B.M.; Ferry, S.A. Mecillinam resistance and outcome of pivmecillinam treatment in uncomplicated lower urinary tract infection in women. Apmis 2014, 122, 317–323. [Google Scholar] [CrossRef] [PubMed]
  26. O’Grady, M.C.; Barry, L.; Corcoran, G.D.; Hooton, C.; Sleator, R.D.; Lucey, B. Empirical treatment of urinary tract infections: How rational are our guidelines? J. Antimicrob. Chemother. 2019, 74, 214–217. [Google Scholar] [CrossRef]
  27. Córdoba, G.; Holm, A.; Sørensen, T.M.; Siersma, V.; Sandholdt, H.; Makela, M.; Frimodt-Møller, N.; Bjerrum, L. Use of diagnostic tests and the appropriateness of the treatment decision in patients with suspected urinary tract infection in primary care in Denmark—Observational study. BMC Fam. Pract. 2018, 19, 65. [Google Scholar] [CrossRef] [Green Version]
  28. Grabe, M.; Bartoletti, R.; Bjerklund-Johansen, T.E.; Cai, T.; Çek, M.; Koves, B.; Naber, K.G.; Pickard, R.S.; Tenke, P.; Wagenlehner, F.; et al. EAU 2020 Guidelines on Urological Infections; European Association of Urology: Arnhem, The Netherlands, 2020; pp. 33–40. Available online: https://uroweb.org/guideline/urological-infections/#3 (accessed on 23 December 2021).
  29. Holm, A.; Cordoba, G.; Sørensen, T.M.; Jessen, L.R.; Frimodt-Møller, N.; Siersma, V.; Bjerrum, L. Effect of point-of-care susceptibility testing in general practice on appropriate prescription of antibiotics for patients with uncomplicated urinary tract infection: A diagnostic randomised controlled trial. BMJ Open 2017, 7, e018028. [Google Scholar] [CrossRef] [Green Version]
  30. Cordoba, G.; Sørensen, T.M.; Holm, A.; Bjørnvad, C.R.; Bjerrum, L.; Jessen, L.R. Exploring the feasibility and synergistic value of the One Health approach in clinical research: Protocol for a prospective observational study of diagnostic pathways in human and canine patients with suspected urinary tract infection. Pilot Feasibility Stud. 2015, 1, 38. [Google Scholar] [CrossRef] [Green Version]
  31. Holm, A.; Cordoba, G.; Sørensen, T.M.; Jessen, L.R.; Siersma, V.; Bjerrum, L. Point of care susceptibility testing in primary care—does it lead to a more appropriate prescription of antibiotics in patients with uncomplicated urinary tract infections? Protocol for a randomized controlled trial. BMC Fam. Pract. 2015, 16, 106. [Google Scholar] [CrossRef] [Green Version]
  32. European confederation of laboratory medicine. European Urinalysis Guidelines. Scand J. Clin. Lab. Investig. 2000, 60, 1–96. [Google Scholar]
  33. The European Committee on Antimicrobial Susceptibility Testing. Breakpoint Tables for Interpretation of MICs and Zone Diameters. Version 3.1. 2013. Available online: http://www.eucast.org. (accessed on 3 May 2019).
  34. Johansen, T.E.B.; Botto, H.; Cek, M.; Grabe, M.; Tenke, P.; Wagenlehner, F.M.E.; Naber, K.G. Critical review of current definitions of urinary tract infections and proposal of an EAU/ESIU classification system. Int. J. Antimicrob. Agents 2011, 38, 64–70. [Google Scholar] [CrossRef] [PubMed]
  35. Holm, A.; Cordoba, G.; Siersma, V.; Brodersen, J. Development and validation of a condition-specific diary to measure severity, bothersomeness and impact on daily activities for patients with acute urinary tract infection in primary care. Health Qual. Life Outcomes 2017, 15, 57. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Figure 1. Included patients.
Figure 1. Included patients.
Antibiotics 11 00188 g001
Figure 2. Influence of the overall AMR pattern on daily mean symptom severity scores for frequency and dysuria, with 95% confidence intervals for each day.
Figure 2. Influence of the overall AMR pattern on daily mean symptom severity scores for frequency and dysuria, with 95% confidence intervals for each day.
Antibiotics 11 00188 g002
Figure 3. Influence of the AMR pattern on daily mean symptom severity scores for frequency and dysuria. Data are presented per antibiotic with 95% confidence intervals for each day.
Figure 3. Influence of the AMR pattern on daily mean symptom severity scores for frequency and dysuria. Data are presented per antibiotic with 95% confidence intervals for each day.
Antibiotics 11 00188 g003
Table 1. Baseline characteristics.
Table 1. Baseline characteristics.
n (%)
Age
<65 years121 (67.22)
≥65 years59 (32.78)
Antibiotic prescribed
Pivmecillinam114 (63.33)
Sulfamethizole32 (17.78)
Trimethoprim11 (6.11)
Nitrofurantoin23 (12.78)
AMR pattern (missing data n = 42, imputated)
Sensitive to all three103 (57.22)
Resistant to one or two48 (26.67)
Resistant to all three29 (16.11)
Table 2. Influence of the antimicrobial resistance pattern on the number of days until symptoms had disappeared.
Table 2. Influence of the antimicrobial resistance pattern on the number of days until symptoms had disappeared.
Number of Days Until Symptoms Had Disappeared
Overall Cure *FrequencyDysuria
Mean (95% CI)DaysMean (95% CI)DaysMean (95% CI)Days
AMR pattern overall
  Sensitive to all three4.2 (3.9–4.5)Ref3.8 (3.4–4.1)Ref3.6 (3.2–3.9)Ref
  Resistant to one or two4.5 (4.0–5.0)+0.33.6 (3.1–4.1)−0.24.1 (3.5–4.7)+0.5
  Resistant to all three4.7 (4.1–5.3)+0.54.1 (3.5–4.8)+0.33.9 (3.2–4.7)+0.4
AMR pattern focusing on specific antibiotics
  Resistant to ampicillin4.5 (4.1–5.0)+0.33.8 (3.3–4.2)03.9 (3.4–4.4)+0.3
  Resistant to sulfamethizole4.6 (4.1–5.1)+0.43.8 (3.3–4.3)04.0 (3.4–4.6)+0.4
  Resistant to trimethoprim4.7 (4.2–5.2)+0.54.1 (3.6–4.7)+0.44.0 (3.4–4.6)+0.5
Antimicrobial resistance to ampicillin, sulfamethizole and trimethoprim. Resistant groups are compared to ‘sensitive to all three’ in linear models. All analyses have p-values > 0.05. * Overall cure: Patients felt all UTI symptoms had disappeared.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Waldorff, M.S.; Bjerrum, L.; Holm, A.; Siersma, V.; Bang, C.; Llor, C.; Cordoba, G. Influence of Antimicrobial Resistance on the Course of Symptoms in Female Patients Treated for Uncomplicated Cystitis Caused by Escherichia coli. Antibiotics 2022, 11, 188. https://doi.org/10.3390/antibiotics11020188

AMA Style

Waldorff MS, Bjerrum L, Holm A, Siersma V, Bang C, Llor C, Cordoba G. Influence of Antimicrobial Resistance on the Course of Symptoms in Female Patients Treated for Uncomplicated Cystitis Caused by Escherichia coli. Antibiotics. 2022; 11(2):188. https://doi.org/10.3390/antibiotics11020188

Chicago/Turabian Style

Waldorff, Marie Soees, Lars Bjerrum, Anne Holm, Volkert Siersma, Christine Bang, Carl Llor, and Gloria Cordoba. 2022. "Influence of Antimicrobial Resistance on the Course of Symptoms in Female Patients Treated for Uncomplicated Cystitis Caused by Escherichia coli" Antibiotics 11, no. 2: 188. https://doi.org/10.3390/antibiotics11020188

APA Style

Waldorff, M. S., Bjerrum, L., Holm, A., Siersma, V., Bang, C., Llor, C., & Cordoba, G. (2022). Influence of Antimicrobial Resistance on the Course of Symptoms in Female Patients Treated for Uncomplicated Cystitis Caused by Escherichia coli. Antibiotics, 11(2), 188. https://doi.org/10.3390/antibiotics11020188

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop