What is the best treatment for recurrent UTI?

Introduction

Urinary tract infections [UTIs] are common bacterial infections occurring in both hospital and community settings, affecting individuals of both sexes and in all age ranges.1 Among individuals under 50 years of age, the incidence of UTIs in males is low, with women being up to 30 times more likely to develop a UTI.2 The increased risk among women is attributed to facilitated bacterial entry into the urinary tract on account of anatomical factors including a shorter urethra and urethral proximity increasing contact with vaginal and rectal pathogens, in addition to incomplete voiding of the urinary bladder and exposure to pathogens during intercourse.2,3 Approximately 90% of UTIs are caused by Escherichia coli bacteria, which can be found in the stool and can colonize the urethra, causing urethritis, the urinary bladder [cystitis], and eventually reaching the kidneys [pyelonephritis].1,3,4 Uropathogens other than E. coli, including Klebsiella pneumoniae, Enterobacter spp., P. aeruginosa, Proteus mirabilis, and Enterococcus spp., are most often identified in UTIs among patients under risk factors [RF] for complicated UTIs.2

RFs for UTIs among women include sexual activity, diaphragm and spermicide use, genetic predisposition factors, change in sexual partner, previous UTIs, and post-menopausal state.2,4,5 Uncircumcised men present a higher risk of a UTI compared to circumcised men, and have a higher risk with advancing age due to prostatic hypertrophy.6 Other RFs include urinary catheterization, surgery involving the urinary tract, anatomical alteration or blockage of the urinary tract, inability to fully void the bladder, pregnancy, diabetes, and aged over 65 years.7–9

The European Association of Urology’s ORENUC classification system stratifies UTIs according to clinical presentation, RFs, and severity.9 In this system, adults presenting with uncomplicated UTIs are classified as O [no known/associated RF], R [Recurrent UTI RF, but no risk of severe outcome], and sometimes E [Extra-urogenital RF, with risk of more severe outcome] classes, while complicated UTIs are categorized as N [Nephropathic disease, with risk of more severe outcome], U [Urological RF, with risk of more severe outcome, which can be resolved during therapy] and C [Permanent urinary catheter and non-resolvable urological RF, with risk of more severe outcome].1,9 The typical signs and symptoms of urethral and bladder infection include pollakiuria, alguria and burning on urination, suprapubic discomfort, vesical tenesmus, malaise, cloudy urine or presence of blood, and low fever.1 In cases of pyelonephritis, the symptoms include high fever, headache, chills and low back pain.1,3 The patient may also present a complete clinical picture of UTIs, with cystitis and pyelonephritis.4 Diagnosis is usually based on history and physical examination, and may be complemented with urinalysis and urine culture.9,10

UTI treatment objectives include alleviating symptoms and eliminating the causative agent, thus preventing infection dissemination and the formation of parenchymatous lesions.7,11 The most commonly employed antibiotics include trimethoprim sulfamethoxazole, fluoroquinolones, and cephalosporins.4,7,12

Recurrence of UTIs is common, especially in female patients.5 Recurrent UTIs are associated with both personal [social and psychological impact negatively affecting quality of life] and societal [clinical and economic] disease burden.2,10 Consultations for UTIs account for 1–6% of all medical visits, with an annual cost of approximately US$1.6 billion.11 Preventive measures for UTI recurrence include change of contraceptive method, increased fluid intake, urination after sexual activity, long-term antibiotic therapy, consumption of cranberry juice and fruit products, and urinary antiseptics.7,13

Methenamine is a urinary antiseptic commonly used in the prophylaxis and treatment of chronic and recurrent uncomplicated lower UTIs.13,14 Its bactericidal properties are due to the release of formaldehyde by hydrolysis in acid pH environments, to which most Gram-positive and Gram-negative bacteria are susceptible.13

Methylthioninium hydrochloride, also known as methylene blue, is a thiazine dye related to the monoamine oxidase inhibitor group that exhibits urinary antiseptic action upon oral administration following reduction to leukomethylene blue.15 Repeated and long-term use of both methenamine and methylthioninium hydrochloride as urinary antiseptics is considered attractive since there is no bacterial resistance development.16 In this study, we sought to investigate use of the combination of methenamine and methylene blue, available in commercially available oral formulations in Brazil [Sepurin® and Cystex®], in the symptomatic relief of cystitis prior to initiation of antibacterial treatment.

Patients and Methods

Study Design

This was a double-blind, randomized, double-dummy, comparative study in parallel groups of patients with recurrent cystitis [defined as ≥2 episodes within the last 6 months] performed at UNIFESO in the State of Rio de Janeiro, Brazil. The primary objective of this study was to evaluate the use of the combination of methenamine and methylene blue in the treatment of recurrent cystitis. The secondary objectives were to evaluate safety and efficacy of the combination of methenamine and methylene blue in the treatment of cystitis symptoms, and to compare the efficacy and safety of the combination of methenamine and methylene blue versus the combination of acriflavine + methenamine + methylene blue + Atropa belladonna L. in the treatment of cystitis symptoms.

Written informed consent was obtained from each patient. The protocol was conducted in accordance with the Declaration of Helsinki and Good Clinical Practice guidelines. The study protocol and related documents received approval from the institution’s ethical committee [Comitê de Ética em Pesquisa do UNIFESO approval no. 2.434.612] and the study was registered at ClinicalTrials.gov under the number NCT03379389.

Patient Population

Inclusion criteria specified age ≥18 years, recurrent cystitis, and required that female patients be neither pregnant nor breastfeeding and used birth control during the treatment period. Subjects presenting history of nephritis or renal calculi, diabetes, open-angle glaucoma or anatomical changes contributing to recurrent cystitis [as evidenced by imaging exams] were not included in the study. Subjects with urine culture identifying Proteus spp. and Pseudomonas spp. were withdrawn at Visit 2.

Study Procedures

After obtaining informed consent and screening for inclusion and non-inclusion criteria, subjects were randomized into one of two treatment groups in order of arrival to study center.

The randomization list was generated using a random-allocation software. Randomization was generated sequentially, at a ratio of 1:1 for two treatment groups, in blocks of 10. Table 1 summarizes the schedule of study procedures. At Visit 1, randomized subjects underwent pretreatment assessments [medical history, physical exam, vital signs, cystitis history], and urine was collected for culture and antibiotic sensitivity tests. Visit 2 occurred at the end of 3 days of treatment with the urinary antiseptics; patients returned to the study center for evaluations, and antibiotic therapy was initiated based on the urine culture/bacterial sensitivity result. Visit 3/Final Study Visit occurred after 3 additional days of treatment with antibiotic and study medication.

Efficacy was evaluated using the Urinary Tract Infection Symptoms Assessment Questionnaire [UTISA].17 Using this questionnaire, the patient assessed the degree of severity and bothersomeness on a scale of 0–3 [0= absence of symptom; 3= most severe/bothersome] of the following 7 UTI symptoms: urgency of urination, frequency of urination, pain or burning when passing urine, urinary retention, pressure in the lower abdomen or pelvic area, lower back pain, and blood in the urine. The UTI symptoms scored with the UTISA are divided into four domains: urination regularity, problems with urination, pain associated with UTIs and hematuria. The questionnaire also includes an overall rating of UTI severity on a scale of 0 [no symptoms] to 3 [severe symptoms]. Follow-up UTISA includes two questions regarding improvement from previous evaluation, [0= about the same; 1= better; 2= worse], and how much improvement from previous evaluation, on a scale of 1–6 [1= a little better; 6= a very great deal better].

The investigating physician also evaluated patient global condition on a 10-point scale with 1 point representing the worst possible evaluation and 10 the best possible global condition. Overall efficacy and tolerability were evaluated by the investigating physician during the final study visit, who classified both as “Very Good,” “Good,” “Fair” or “Poor.”

Safety evaluations throughout the treatment period included adverse event monitoring, in terms of: occurrence, severity [mild/moderate/severe], duration and causality [relation to study medication] as well as monitoring of laboratory tests performed at each study visit, including: CBC, fasting blood glucose, AST, ALT, urea, uric acid, and creatinine.

Study Drugs

Urinary Antiseptics

Subjects were randomized into one of two treatment groups: Group A or Group B. Group A received a combination of 120mg methenamine and 20mg methylthioninium at the dose of 2 coated tablets, 3 times a day. Group B received a combination of 15mg acriflavine + 250mg methenamine + 20mg methylthioninium + 15mg Atropa belladonna L., at the dose of 3 coated tablets, twice daily. Treatment duration with urinary antiseptics lasted a total of six consecutive days. The urinary antiseptics were administered in double-dummy fashion in order to maintain double-blind evaluation between the two treatments.

Antibiotic Therapy

At Visit 2, patients were prescribed open-label antibiotic therapy based on the results of the urine bacterial sensitivity testing performed at Visit 1. Treatment duration was determined on an individual basis, depending on the antibiotic prescribed according to the urine bacterial sensitivity test result.

Statistical Analysis

The primary study endpoint was the percentage of patients presenting improvement in cystitis manifestations on the UTISA domain “Urination Regularity” at Visit 2. Secondary endpoints included Visit 2 evolution of the total UTISA score, evolution of the remaining UTISA domain scores, percentage of subjects with improvement in UTISA question 9 [changes in UTI severity], and the incidence of adverse events related to the study medication in each treatment group.

Sample size determination was based on the primary endpoint, estimating a difference between proportions with a two-tailed test, with an alpha of 0.05 and power of 90.2%. The study n was determined with 109 patients per treatment group, considering a maximum acceptable difference between the treatment groups of 0.20. Based on these parameters it would be possible to report the difference between proportions with an accuracy of approximately 0.12 points [95% confidence interval]. Taking into account an estimated 30% loss rate [dropouts, loss of follow-up and withdrawal of patients with positive cultures for Proteus spp. and Pseudomonas spp.], the total number of subjects required for this study was 284 evaluable patients.

Study data were analyzed using GraphPad Prism software, version 8.4.3 for Windows [GraphPad Software, San Diego, California USA, www.graphpad.com]. Baseline and demographic data were compared between groups using unpaired t-test or Fisher’s exact test for continuous and categorical variables, respectively. Primary and efficacy endpoint analysis was performed using the Fisher’s exact test for the intent-to-treat [ITT] population. For analysis of continuous variables, data were analyzed for the ITT population using mixed effects analysis followed by Tukey’s multiple comparisons test. For comparisons of categorical variables, we used the χ2 or Fisher’s test, or mixed effects analysis for repeated measures.

Results

Subject Disposition

A total of 503 subjects were screened between March and November 2018 and 288 subjects were randomized to treatment, with 144 subjects in each treatment group [Figure 1]. Sixteen subjects were removed at the end of Visit 2 for the following reasons: Adverse event [Group A: n= 1; Group B n= 3]; Urine culture positive for Proteus spp., [Group A: n= 1; Group B: n= 1]; Need for parenteral antibiotics [Group A: n= 3; Group B n= 3]; Withdrawn consent [Group A: n= 3; Group B: n= 1]. A total of 272 subjects completed the study, 136 per treatment group.

Baseline Characteristics

The demographic and pretreatment data are summarized in Table 2. With the exception of mean participant age, where there was a statistically significant difference between the two treatment groups, pretreatment and demographic characteristics were comparable between groups. A majority of patients in both treatment groups reported previous cystitis treatment with antibiotics and half of all patients in both treatment groups reported previous treatment with urinary antiseptics.

Table 3 displays the UTISA total and domain scores at each study visit. Mean pretreatment UTISA total domain scores were comparable between treatment groups [19.0 and 17.8 in Group A and Group B, respectively; p= 0.11]. Pretreatment patient overall UTI severity assessment was comparable between groups [Group A: 15 patients with score of 1, 80 patients with score of 2 and 49 patients with score of 3; Group B: 26 patients with score of 1, 67 patients with score of 2 and 51 patients with score of 3; χ2= 4.141, df= 3; p= 0.247] Physician global evaluation scores at pretreatment were also comparable between treatment groups [p= 0.097].

Results at Visit 2 [3 Days of Treatment]

Study Drug Efficacy

Analysis of the primary endpoint [UTISA domain “Urination Regularity” after 3 days of treatment] reveals homogeneity between treatment groups [χ2= 0.278; df= 2; p= 0.87], with 69.4% and 72.2% of patients in Group A and Group B, respectively, showing significant score improvement after 3 days of treatment [mean reduction of −6.778 in Group A and −8.813 in Group B; p