References

Akcam FZ, Kaya O, Temel EN An investigation of the effectiveness against bacteriuria of silver-coated catheters in short-term urinary catheter applications: A randomized controlled study. J Infect Chemother. 2019; 25:(10)797-800 https://doi.org/10.1016/j.jiac.2019.04.004

Beattie M, Taylor J. Silver alloy vs. uncoated urinary catheters: a systematic review of the literature. J Clin Nurs. 2011; 20:(15-16)2098-2108 https://doi.org/10.1111/j.1365-2702.2010.03561.x

Bubenik L, Hosgood G. Urinary tract infection in dogs with thoracolumbar intervertebral disc herniation and urinary bladder dysfunction managed by manual expression, indwelling catheterization or intermittent catheterization. Vet Surg. 2008; 37:(8)791-800 https://doi.org/10.1111/j.1532-950X.2008.00452.x

Bubenik LJ, Hosgood GL, Waldron DR, Snow LA. Frequency of urinary tract infection in catheterized dogs and comparison of bacterial culture and susceptibility testing results for catheterized and noncatheterized dogs with urinary tract infections. J Am Vet Med Assoc. 2007; 231:(6)893-899 https://doi.org/10.2460/javma.231.6.893

Chu CM, Lowder JL. Diagnosis and treatment of urinary tract infections across age groups. Am J Obstet Gynecol. 2018; 219:(1)40-51 https://doi.org/10.1016/j.ajog.2017.12.231

Chuang L, Tambyah PA. Catheter-associated urinary tract infection. J Infect Chemother. 2021; 27:(10)1400-1406 https://doi.org/10.1016/j.jiac.2021.07.022

Desai DG, Liao KS, Cevallos ME, Trautner BW. Silver or nitrofurazone impregnation of urinary catheters has a minimal effect on uropathogen adherence. J Urol. 2010; 184:(6)2565-2571 https://doi.org/10.1016/j.juro.2010.07.036

Handler G, Boninger ML. Special issues in randomized controlled trials. In: Hammond F, Malec J, Nick TG, Buschbacher R (eds). New York: Demos Medical Publishing; 2014

Kędziora A, Wieczorek R, Speruda M Comparison of antibacterial mode of action of silver ions and silver nanoformulations with different physico-chemical properties: experimental and computational studies. Front Microbiol. 2021; 12 https://doi.org/10.3389/fmicb.2021.659614

Liedberg H, Lundeberg T. Silver alloy coated catheters reduce catheter-associated bacteriuria. Br J Urol. 1990; 65:(4)379-381 https://doi.org/10.1111/j.1464-410X.1990.tb14760.x

Low DA, Braaten BA, Ling GV, Johnson DL, Ruby AL. Isolation and comparison of Escherichia coli strains from canine and human patients with urinary tract infections. Infect Immun. 1988; 56:(10)2601-2609 https://doi.org/10.1128/iai.56.10.2601-2609.1988

Ogeer-Gyles J, Mathews K, Weese JS Evaluation of catheter-associated urinary tract infections and multi–drug-resistant Escherichia coli isolates from the urine of dogs with indwelling urinary catheters. J Am Vet Med Assoc. 2006; 229:(10)1584-1590 https://doi.org/10.2460/javma.229.10.1584

Ogilvie AT, Brisson BA, Gow WR, Wainberg S, Singh A, Weese JS. Effects of the use of silver-coated urinary catheters on the incidence of catheter-associated bacteriuria and urinary tract infection in dogs. J Am Vet Med Assoc. 2018; 253:(10)1289-1293 https://doi.org/10.2460/javma.253.10.1289

Ogilvie AT, Brisson BA, Singh A, Weese JS. In vitro evaluation of the impact of silver coating on Escherichia coli adherence to urinary catheters. Can Vet J. 2015; 56:(5)490-494

Olin SJ, Bartges JW. Urinary tract infections: treatment/comparative therapeutics. Vet Clin North Am Small Anim Pract. 2015; 45:(4)721-746 https://doi.org/10.1016/j.cvsm.2015.02.005

Padilla J, Osborne CA, Ward GE. Effects of storage time and temperature on quantitative culture of canine urine. J Am Vet Med Assoc. 1981; 178:(10)1077-1081

Patterson CA, Bishop MA, Pack JD, Cook AK, Lawhon SD. Effects of processing delay, temperature, and transport tube type on results of quantitative bacterial culture of canine urine. J Am Vet Med Assoc. 2016; 248:(2)183-187 https://doi.org/10.2460/javma.248.2.183

Pratt RJ, Pellowe C, Loveday HP The epic project: developing national evidence-based guidelines for preventing healthcare associated infections. Phase I: Guidelines for preventing hospital-acquired infections. Department of Health (England). J Hosp Infect. 2001; S3-S82 https://doi.org/10.1053/jhin.2000.0886

Riley DK, Classen DC, Stevens LE, Burke JP. A large randomized clinical trial of a silver-impregnated urinary catheter: lack of efficacy and staphylococcal superinfection. Am J Med. 1995; 98:(4)349-356 https://doi.org/10.1016/S0002-9343(99)80313-1

Smarick SD, Haskins SC, Aldrich J Incidence of catheter-associated urinary tract infection among dogs in a small animal intensive care unit. J Am Vet Med Assoc. 2004; 224:(12)1936-1940 https://doi.org/10.2460/javma.2004.224.1936

Stiffler KS, Stevenson MAM, Sanchez S Prevalence and characterization of urinary tract infections in dogs with surgically treated type 1 thoracolumbar intervertebral disc extrusion. Vet Surg. 2006; 35:(4)330-336 https://doi.org/10.1111/j.1532-950X.2006.00153.x

Tissot E, Limat S, Cornette C, Capellier G. Risk factors for catheter-associated bacteriuria in a medical intensive care unit. Eur J Clin Microbiol Infect Dis. 2001; 20:(4)0260-0262 https://doi.org/10.1007/s100960100480

Weese JS, Blondeau J, Boothe D International Society for Companion Animal Infectious Diseases (ISCAID) guidelines for the diagnosis and management of bacterial urinary tract infections in dogs and cats. Vet J. 2019; 247:8-25 https://doi.org/10.1016/j.tvjl.2019.02.008

Efficacy of silver-coated urinary catheters for reducing urinary tract infection in dogs

02 July 2023
15 mins read
Volume 14 · Issue 6
Table 1.

Abstract

Indwelling urinary catheters are frequently used in practice, however urinary catheters have been associated with catheter-associated urinary tract infections in dogs. Antimicrobial coating of urinary catheters can reduce catheter-associated urinary tract infections through the initial prevention of bacterial attachment. Historical studies have identified the benefit of silver in reducing bacteriuria in humans. This knowledge summary concluded that no study was able to demonstrate that the use of silver-coated urinary catheters is superior to silicone urinary catheters in reducing the incidence of urinary tract infections in dogs. Further investigation in vivo, with a large sample size, is required to verify the statistical significance of the effect of the silver-coating of urinary catheters in the reduction of urinary tract infections.

Indwelling urinary catheters are frequently used in practice, however urinary catheters have been associated with bacteriuria and catheter-associated urinary tract infections (UTIs) in dogs (Tissot et al, 2001; Ogeer-Gyles et al, 2006). Antimicrobial coating of urinary catheters can reduce catheter-associated UTIs through the initial prevention of bacterial attachment (Beattie and Taylor, 2011). Silver has antibacterial properties, with historical studies identifying its benefit in reducing bacteriuria in humans (Liedberg and Lunderberg, 1990; Riley et al, 1995).

This knowledge summary uses a PICO (Population, Intervention, Comparator, and Outcomes) to investigate the question: in hospitalised dogs, does the use of silver-coated urinary catheters reduce the incidence of UTI when compared to silicone Foley urinary catheters?

A clinical scenario from the perspective of a veterinary nurse was considered and a search of the literature was performed (Table 1) based on this scenario. Exclusion and inclusion criteria are discussed in Tables 2 and 3. Three papers were critically reviewed. Two were prospective, double-blind, randomised controlled clinical trials and one was a controlled, in vitro study.


Table 1. Search strategy
Databases searched and dates covered: CAB Abstracts on OVID Platform 2012–2023PubMed accessed via NCBI 2012–2023Science Direct via Elsevier 2012–2023SCOUT on RVC Platform 2012–2023Wiley Online Library on Wiley Science Solutions 2012–2023
Search strategy: CAB Abstracts:
  • (dog or dogs or canine or canines).mp. or exp dogs/
  • (catheter or (silver and coat*)).mp.
  • (urinary tract infection or urinary infection).mp. or exp urinary tract infections/
  • 1 and 2 and 3
PubMed: ((dog OR canine) AND (urinary catheter OR indwelling urinary catheter) AND (silver-coated*) AND (urinary tract infection OR urinary infection))Science Direct:((dog OR canine) AND (urinary catheter OR indwelling urinary catheter) AND (silver-coated) AND (urinary tract infection OR urinary infection))SCOUT:((dog* OR canine) AND (urinary catheter OR indwelling urinary catheter) AND (silver-coated*) AND (urinary tract infection OR urinary infection))Wiley Online Library: ((dog OR canine) AND (urinary catheter OR indwelling urinary catheter) AND (silver-coated) AND (urinary tract infection OR urinary infection))
Dates searches were performed: 13 March 2023

Table 2. Exclusion/inclusion criteria
Exclusion:
  • Papers older than 10 years, for the purpose of evaluating the most recent literature
  • Not relevant to the PICO question
  • Duplicate
  • Systematic reviews
  • Full text not available
  • Book chapters
Inclusion:
  • Any comparative study in which the effect of silver-coated urinary catheters on the development of UTIs was studied
  • Peer-reviewed publication
  • English language

Table 3. Search outcome
Database Number of results Excluded – >10 years old Excluded – systematic review Excluded – full text not available Excluded – does not answer the PICO Excluded – book chapter Total relevant papers
CAB Abstracts 26 4 1 3 16 1 1
PubMed 2 0 0 0 0 0 2
Science Direct 743 496 22 10 17 196 2
SCOUT 2 0 0 0 0 0 2
Wiley Online Library 1184 803 6 246 8 79 2
Total relevant papers after you have removed duplicates 3

Clinical scenario

You are a small animal registered veterinary nurse working in a referral practice. Your practice has seen a high incidence of UTIs in canine patients with indwelling urinary catheters. Recognising that UTIs can hinder patient recovery and increase mortality and morbidity, you are concerned that urinary catheter care in your practice may not be effective. Therefore, you decide to investigate the effectiveness of silver-coated urinary catheters as an implementation that could reduce the risk of UTIs in the catheterised patient.

Strength of evidence

Critical appraisal of the selected papers meeting the inclusion criteria found that they provide moderate evidence in terms of their experimental design and implementation.

The evidence

Two prospective, double-blind, randomised controlled clinical trials compared the efficacy of silver-coated Foley urinary catheters in reducing the incidence of UTIs as compared to a silicone Foley urinary catheter (Ogilvie et al, 2018; Akcam et al, 2019). The study conducted by Akcam et al (2019) (Table 4) evaluated the effectiveness of silver-coated Foley urinary catheters against bacteriuria in human patients admitted to the intensive care unit (ICU), requiring catheterisation for >24 hours. Similarly, the study conducted by Ogilvie et al (2018) (Table 5) evaluated the effectiveness of silver-coated Foley urinary catheters on the incidence of bacteriuria and UTIs in canine patients requiring a urinary catheter for >24 hours. The third study (Table 6) evaluated the impact of silver coating of UCs on the adherence of E. coli in vitro (Ogilvie et al, 2015); however, the clinical application of these findings is limited by the in vitro study design, suggesting that the numerous factors that contribute to the complex environment of urine and the urinary bladder, such as periodic voiding and immune response, were not taken into account (Desai et al, 2010).


Table 4. Summary of evidence: Akcam et al (2019)
Population: Recruitment:
  • Human patients admitted to the intensive care unit (ICU) at Suleyman Demirel University Education and Research Hospital and Isparta State Hospital, Turkey, between 2012 and 2014.
Criteria for eligibility and inclusion:
  • Patients with similar demographic characteristics and primary and underlying diseases admitted to the ICU and anticipated to require long-term catheterisation.
  • Written consent was obtained from patients or patients' relatives.
Criteria for exclusion and rejection:
  • Patients with infectious diseases on admission.
  • Patients with pyuria/bacteriuria in the first urine specimen collected following catheter placement.
Enrolled study population:
  • 54 patients, 27 male and 27 female.
  • Age range between 28-101 years.
  • All patients had a neurological disease.
  • 40 patients had an additional disease.
Sample size: 54 patients
Intervention details: Group allocation: Each patient was assigned to either the silver-coated Foley catheter group or the normal silicone Foley catheter group, on a random basis as catheters were used in sequence.
  • Silver-coated Foley catheter group n=28
  • Normal silicone Foley catheter group n=26
Catheter placement:Catheter placement was performed using aseptic techniques by trained personnel. A closed drainage system was used and care was taken to ensure it was not compromised.Test procedure:
  • Urine specimens were collected at two day intervals.
  • Urine collection was conducted following the guidelines published by the Turkish Society of Hospital Infections and
  • Control's Prevention of Urinary Catheter Infections Guidelines.
  • Urine was collected into a sterile container and immediately transported to the microbiology research lab.
Study design: Prospective, double-blind, randomised controlled clinical trial.
Outcome studied: The presence of bacteriuria [objective]:
  • A sterile calibrated loop was used to streak 1 μl of fresh, unprocessed urine onto one-half of a MacConkey agar plate and a blood agar plate.
  • The plate was incubated at 37°C for two days.
  • Growth of 105 cfu/ml was regarded as representing bacteriuria.
The bacteria present [objective]:
  • Bacteria were identified by an automatic system (BD Phoenix).
Main findings (relevant to PICO question): The presence of bacteriuria:
  • Bacteriuria was determined in 25/54 patients (46.3%).
  • Bacteriuria developed in 12/26 (46.2%) of the patients using silicone Foley urinary catheters.
  • Bacteriuria developed in 13/28 (46.4%) of the patients using silver-coated Foley urinary catheters.
  • No significant difference was found between the use of different catheter types and rates of bacteriuria (P=0.98).
The bacteria present:
  • E. coli was the most commonly detected agent (11/25, 44%), followed by Enterococcus spp (5/25, 20%).
  • E. coli grew in 4/28 (14.3%) of the patients using silver-coated Foley urinary catheters.
  • E. coli grew in 7/26 (26.9%) of the patients using silicone Foley urinary catheters.
  • No significant relation was determined between urinary catheter type and the rate of E. coli growth (P=0.38).
Limitations:
  • Small sample size.
  • Patients enrolled in the study had similar demographic characteristics, primary and underlying diseases, however there was no detailed inclusion criteria.
  • Although kept consistent, the aseptic technique for catheter placement was not outlined.
  • The aseptic technique for catheter maintenance was not described.
  • The process for urine collection was not described, however it was standardised.
  • Blinded operators may have been capable of distinguishing silver-coated Foley urinary catheters from silicone Foley urinary catheters, creating a risk for bias.

Table 5. Summary of evidence: Ogilvie et al (2018)
Population: Recruitment:
  • Female dogs admitted to the Ontario Veterinary College teaching hospital between May 26, 2012 and January 22, 2014, that required urinary catheters for over 24 hours.
  • Male dogs that weighed less than, or 8–10 kg.
  • Recruited patients were enrolled if they met the eligibility and inclusion criteria.
Criteria for eligibility and inclusion:
  • Owned, with the attainment of owner consent.
  • Expected to require urinary catheterisation for more than 24 hours.
Criteria for exclusion and rejection:
  • Male dogs weighing over 10 kg, because of limitations in catheter length.
  • Any dog that had a lower UTI at the time of catheterisation was excluded.
  • Any dog that required catheterisation solely for surgery purposes.
  • Any dog that was expected to be catheterised for less than 24 hours.
Enrolled study population: 36 dogs:
  • 25 females, eight entire and 17 spayed.
  • 11 males.
  • Age range between 6 months and 14 years.
  • Bodyweight ranged from 3–38 kg.
Age, sex and body weight were shown to not significantly differ between groups.
Sample size: 36 dogs
Intervention details: Group allocation: Each dog was randomly assigned via a randomly generated table to receive a silver-coated Foley urinary catheter or the same type of silicone Foley urinary catheter without the silver coating.
  • Silver-coated Foley catheter group n=15
  • Normal silicone Foley catheter group n=21
Catheter placement:
  • All catheters were placed by an experienced veterinary technician or the attending veterinarian.
  • A standardised aseptic catheterisation protocol was used.
  • During this process, any breaks in aseptic technique were recorded.
  • Number of placement attempts were recorded.
Test procedure:
  • Dogs remained enrolled for 7 days unless catheter removal occurred earlier or needed replacing.
  • A urine sample was collected aseptically at the time of catheter placement via a sterile syringe from the catheter end.
  • A urine sample was collected daily for each day the dog was catheterised. The sample was taken from the aseptically prepared sampling port of the collection system.
  • Each sample was placed into two plain evacuated tubes, through the aseptically prepared top via a sterile needle affixed to the syringe.
Study design: Prospective, double-blind, randomised controlled clinical trial
Outcome studied: The presence of cytologically detected bacteriuria [subjective]:
  • Samples for cytology were prepared within 15 minutes after collection, by centrifugation of 200 μL of urine in the collection tube at 400 X g for five minutes.
  • A feathered-edge smear was prepared, air-dried and stained with Wright stain.
  • The smear was evaluated via light microscopy by the same observer, who was unaware of the type of catheter the dog had received.
  • The observer evaluated each sample for pyuria, haematuria and microorganisms.
Positive bacterial culture [objective]:
  • Urine samples for bacterial culture were submitted for testing immediately after collection.
  • 0.01 and 0.001 mL loops were used to transfer each urine sample onto blood agar plates for quantitative analysis. Urine was applied to a MacConkey agar plate using a sterile swab.
  • Plates were incubated in 5% CO2 and MacConkey agar plates incubated in ambient conditions.
  • Plates were checked for growth after 24 and 48 hours of incubation.
  • Matrix-assisted mass spectrometry or biochemical tests were used to identify bacterial colonies.
Main findings (relevant to PICO question):
  • No significant difference was identified in median time to develop cytologically detected bacteriuria between the two groups (P=0.93).
  • Positive bacterial culture results were obtained for 2/13 (15%) dogs with a silver-coated catheter and 2/20 (10%) dogs with a normal silicone catheter (P=1.00).
  • The median time for the development of culture detected bacteriuria did not differ significantly between the two groups (P=0.33).
  • There was no significant difference between the two groups and the development of catheter-associated bacteriuria (P=0.18).
  • Median time to development of catheter-associated bacteriuria differed significantly: 36 hours for dogs with a silver-coated catheter, compared to 96 hours for dogs with normal silicone catheters (P=0.03).
  • There was no significant difference in the incidence of catheter-associated UTI between the two groups (P=1.00).
  • Median time to development of catheter-associated UTI between the two groups did not differ significantly (P=0.83).
Limitations:
  • Small sample size.
  • Antimicrobials were given to a high proportion of dogs in the study, and this could have affected the outcome.
  • Although kept consistent, the aseptic technique for catheter placement was not described.
  • The technique for catheter maintenance was not described.
  • The primary disease, reason for catheterisation and underlying conditions for the dogs enrolled in the study were not considered and may have influenced results.

Table 6. Summary of evidence: Ogilvie et al (2015)
Population:
  • In vitro
  • Six isolates of E. coli from dogs with UTIs that had been demonstrated to produce biofilm in vitro.
Exclusion criteria:
  • Apparent contaminants in the sample
Sample size: Six isolates of E. coli
Intervention details: Preparation:
  • Silicone catheters were coated with a non-eluting, amino-acid based polymer coating containing silver salt.
  • Uncoated silicone catheters were used as controls.
  • Six isolates of E. coli from dogs with UTIs were studied.
  • Isolates were grown overnight on 5% Columbia Sheep Blood Agar at 35°C.
  • After growth, 10 mL of tryptic soy broth (TSB) was inoculated with E. coli.
  • A sterile 2.5 cm segment of a silver-coated 10 French, or uncoated catheter was aseptically cut and incubated in the broth at 37°C in a water bath under continuous agitation.
Test procedure:
  • Two segments of catheter were inoculated for each combination of catheter type and time point.
  • Two negative controls for each time point were monitored visually and cultured for contamination.
Study design: Controlled in vitro study
Outcome studied: Inhibition of bacterial growth in broth with the silver-coated catheter [objective]:
  • 1 mL of the TSB was collected at zero, 24, 48 and 72 hours.
  • Serial 10-fold dilutions were performed in TSB and 100 μL of each was spread onto Columbia blood agar.
  • After incubation for 24 hours at 37°C, colonies were counted and the bacterial concentration in the broth was calculated.
Impact of silver coating on bacterial attachment [objective]:
  • One catheter segment was aseptically removed from the inoculum at each time point.
  • It was rinsed three times using 9 mL of sterile phosphate-buffered saline.
  • It was then placed in 10 mL of TSB and sonicated for two minutes to remove adherent bacteria.
  • The catheter and sonicate were vortexed and serial 10-fold dilutions were made in TSB.
  • Quantitative culture was performed as described above.
Main findings (relevant to PICO question):
  • Bacterial growth was evident in broth containing both coated and non-coated catheters.
  • Bacterial numbers were significantly lower in broth from silver-coated catheters compared with those from non-coated catheters at 24 hours (P=0.0023), but not after 48 hours and 72 hours.
  • Adherent bacteria were identified on all catheters.
  • There were significantly fewer adherent bacteria on silver-coated catheters compared to non-coated catheters after 24 hours (P=0.0488), 48 hours (P=0.0137) and 72 hours (P=0.0023).
Limitations:
  • Conducted in vitro, which does not represent the complex environment of urine and the bladder. The adherence of bacteria in the canine urinary tract could be different to the laboratory setting.
  • E. coli was the only isolate tested.
  • Small sample size.

Summary of evidence

UTI detection

Urine culture is gold standard for UTI detection in humans and canines (Chu and Lowder, 2018). Akcam et al (2019) and Ogilvie et al (2018) confirm bacteriuria in their human and canine population, respectively, with a culture exam. The culture exams differ between studies, with Akcam et al (2019) not outlining the urine collection procedure. The handling of urine samples can affect culture results, suggesting that Akcam et al's (2019) results must be considered with caution due to ambiguity surrounding possible sample contamination (Padilla et al, 1981). Chu and Lowder (2018) argue that the process for sample collection is irrelevant if it is sterile and standardised, reducing the likelihood of contamination.

Urine samples were analysed immediately after collection, confirmed by Patterson et al (2016) as providing optimum results; however, the term ‘immediate’ is non-specific (Ogilvie et al, 2018; Akcam et al, 2019). The distance between the laboratory and practice could cause the time surpassed between sample collection and culture exam to differ between studies. The storing of urine samples collected out of hours by Ogilvie et al (2018) increased the processing time by 12–36 hours, with Patterson et al (2016) identifying the unreliability of urine samples stored incorrectly for 24 hours. It would have been beneficial for the authors to specify the processing time of the sample.

Antimicrobial treatment

Antimicrobial use can increase the UTI risk in dogs (Bubenik et al, 2007). When studied in vitro, silver-coating reduced the risk of UTIs, a finding that was not mirrored by Akcam et al (2019) and Ogilvie et al (2018). This discrepancy could be owed to Akcam et al (2019) and Ogilvie et al (2018) including patients receiving antimicrobials in their population. Ogilvie et al (2018) concluded that antimicrobial use did not increase UTI risk, contradicting Bubenik et al (2007). This could be due to the majority of patients receiving antimicrobials, leaving too few dogs untreated to determine a significant association. Contrarily, as the majority of dogs received antimicrobials, their influence on the development of a UTI could be uniform for both catheter groups. Although identified as a confounding factor, it is common for patients undergoing surgery to be administered prophylactic antimicrobials, highlighting the applicability to the hospitalised canine (Bubenik et al, 2007).

The antimicrobial used was not disclosed by Ogilvie et al (2018), and it is unclear whether urine samples were subject to antimicrobial sensitivity testing. Differing antimicrobials could justify the discrepancy between studies, as the effect on UTI development differs based on the antimicrobial used (Olin and Bartges, 2015). To reduce the impact of confounding factors and improve reliability of future studies, all dogs receiving antimicrobials should be excluded. However, the applicability to practice due to the varied requirements for antimicrobials in the hospitalised patient would be reduced. This highlights the relevance of Akcam et al (2019) and Ogilvie et al's (2018) findings to clinical practice, despite the variation in antimicrobials.

Duration of catheterisation

The duration of catheterisation can impact the UTI risk in both humans and dogs (Bubenik and Hosgood, 2008). Akcam et al (2019) and Ogilvie et al (2018) identified a significant association between the duration of catheterisation and increased bacteriuria, regardless of the urinary catheter used. Canine studies have demonstrated an increased UTI risk associated with catheterisation for over 3 days, with a 27% increase in risk for each additional day (Smarick et al, 2004; Bubenik and Hosgood, 2008). Ogeer-Gyles et al (2006) identified a similar trend specific to catheter-associated UTIs, where infection rose from 19% following catheterisation for 12 hours to 79% after 72 hours. Ogilvie et al (2018) found the association between catheterisation length and catheter-associated UTI to not be significant; however, their median catheterisation length was 48 hours, compared to 72 hours in Ogeer-Gyles et al's (2006) study. Smarick et al (2004) define catheter-associated UTI as a UTI in canine patients catheterised for greater than 24 hours, highlighting the relevance of Ogilvie et al's (2018) findings to practice.

Ogilvie et al (2015) identified reduced bacterial adherence on silver-coated urinary catheters, with fewer bacteria identified after 72 hours. The in vitro study design differs to the complex environment of the urinary bladder, with bacterial adherence inevitably differing in the laboratory setting, highlighting the requirement for in vivo evaluation of silver-coated urinary catheters on canine UTIs.

Uropathogen

E. coli is the prevailing bacteria present in canine and human UTIs; however, it is not the sole causative urophathogen (Stiffler et al, 2006; Chuang and Tambyah, 2021). Akcam et al (2019) identified higher rates of uropathogens other than E. coli in patients with silver-coated urinary catheters. Kędziora et al (2021) identify E. coli as having greater sensitivity to silver ions, explaining why Ogilvie et al (2015), having only tested the efficacy of silver-coated urinary catheters on E. coli isolates, found there to be a significant impact on bacterial adherence. The conduction of a further in vitro study comparing the sensitivity of different uropathogens to silver could assess their effectiveness in the canine patient, where E. coli is often not the sole causative uropathogen (Chuang and Tambyah, 2021).

Ogilvie et al (2018) omit to identify the uropathogens isolated, however the previous identification of E. coli as the primary isolate in urinary catheters suggests that it was likely the causative uropathogen in their study (Chuang and Tambayah, 2021). The identification of uropathogens by Ogilvie et al (2018) could have compared the effectiveness of silvercoating against E. coli and other uropathogens.

Sample size

Sample size is imperative in determining whether a significant difference between treatments can be detected (Handler and Boninger, 2014). During the planning stage, a sample size power calculation should be performed, as a too small sample size can result in reduced validity, while a too large sample size is unnecessary and unethical (Handler and Boninger, 2014). Akcam et al (2019) and Ogilvie et al (2015) performed a sample size power calculation, however Ogilvie et al (2015) does not report the results and thus cannot be externally verified. The robustness should be considered alongside sample size when determining the validity of a study; however, when being applied to a large population such as canine patients with urinary catheters, studies with a small sample size should be handled with caution.

All three studies identify sample size as a limitation (Ogilvie et al, 2015; Ogilvie et al, 2018; Akcam et al, 2019). The sample size was smaller than that calculated to be required to detect a significant difference, thus contributing to differences being statistically insignificant. This highlights the requirement for a larger study to determine whether silver-coated urinary catheters reduce the UTI risk in dogs.

Application

The frequency of UTIs in dogs with urinary catheters high-lights the importance of reducing this risk to improve patient care. Although not avoidable, a significant proportion of UTIs are preventable (Pratt et al, 2001). Silver-coated urinary catheters have proved to reduce UTIs in humans, however veterinary studies are limited. Where results are extrapolated from human studies, their applicability to the veterinary setting must be evaluated. Akcam et al's (2019) study design in humans is comparable to that of Ogilvie et al (2018) on a canine population. The complex environment of the urinary tract and the development of UTIs occurs analogously in both species. Having identified E. coli as the predominant causative bacteria for UTIs in humans and dogs, with a historic study by Low et al (1988) confirming the E. coli strains isolated from human and canine UTIs as identical, the effect of silver-coated urinary catheters is expected to be comparable in both species. This highlights the applicability of Akcam et al's (2019) study to the veterinary setting.

Urinary catheter placement and maintenance may differ between human and veterinary practice, with an increased risk of patient interference and contamination in dogs (Bubenik et al, 2007). Weese et al (2019) identify urinary catheter maintenance as a risk factor for UTIs. Akcam et al (2019) and Ogilvie et al (2018) omit to outline urinary catheter maintenance, however as conducted in a teaching hospital, it can be presumed that evidence-based veterinary medicine was practiced by Ogilvie et al (2018), where protocols are commonly extrapolated from human medicine. This suggests that urinary catheter maintenance was comparable between the studies, highlighting the applicability of Akcam et al's (2019) study to the canine population.

Ogilvie et al (2015) studied E. coli isolates from canine urine in vitro, investigating the adherence of E. coli to silver-coated urinary catheters. Bacterial adherence in the canine urinary tract is influenced by numerous factors, such as periodic voiding, immune response and attachment to the bladder wall (Desai et al, 2010). This creates a complex evironment that is impossible to replicate in vitro, limiting the applicability of the findings to the canine patient. It provides evidence supportive of the use of silver-coated urinary catheters, however the conduction of an in vivo study is necessary to justify their use in practice.

Conclusions

Overall, Ogilvie et al (2015) demonstrate moderate evidence that silver-coating reduces the adherence of E. coli to urinary catheters, however the in vitro nature limits its applicability to the canine patient. The complexity of the urinary system is made apparent by Akcam et al (2019) and Ogilvie et al (2018) who identify the ineffectiveness of silver-coating in reducing UTIs in humans and dogs. All studies concluded with caution because of study design or lack of statistical significance. No study was able to demonstrate that the use of silver-coated urinary catheters is superior to silicone urinary catheters in reducing the incidence of UTIs in dogs.

The available evidence does not support the hypothesis that silver-coated urinary catheters reduce the incidence of UTIs compared to silicone Foley urinary catheters (Ogilvie et al, 2015; Ogilvie et al, 2018; Akcam et al, 2019). Due to the limited evidence supporting the effectiveness of the antibacterial properties of silver-coated urinary catheters and the increased cost associated with them, their use in practice is currently not justifiable.

Given that all three studies were weakened by limitations, a further study conducted in hospitalised dogs not undergoing antimicrobial treatment, using a larger population size and standardised maintenance of silver-coated catheters, would be valuable.

KEY POINTS

  • Indwelling urinary catheters are frequently used in practice, however urinary catheters have been associated with bacteriuria and catheter-associated UTIs in dogs.
  • The frequency of UTIs in dogs with urinary catheters highlights the importance of reducing this risk to improve patient care.
  • The available evidence does not support the hypothesis that silver-coated urinary catheters reduce the incidence of UTIs compared to silicone Foley urinary catheters.