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Probiotics [LGG-BB12 or RC14-GR1] versus placebo as prophylaxis for urinary tract infection in persons with spinal cord injury [ProSCIUTTU]: a study protocol for a randomised controlled trial
BMC Urologyvolume 16, Article number: 18 (2016)
Urinary tract infections [UTIs] are very common in people with Spinal Cord Injury [SCI]. UTIs are increasingly difficult and expensive to treat as the organisms that cause them become more antibiotic resistant. Among the SCI population, there is a high rate of multi-resistant organism [MRO] colonisation. Non-antibiotic prevention strategies are needed to prevent UTI without increasing resistance. Probiotics have been reported to be beneficial in preventing UTIs in post-menopausal women in several in vivo and in vitro studies. The main aim of this study is to determine whether probiotic therapy with combinations of Lactobacillus reuteri RC-14 + Lactobacillus rhamnosus GR-1 [RC14-GR1] and/or Lactobacillus rhamnosus GG + Bifidobacterium BB-12 [LGG-BB12] are effective in preventing UTI in people with SCI compared to placebo.
This is a multi-site randomised double-blind double-dummy placebo-controlled factorial design study conducted in New South Wales, Australia. All participants have a neurogenic bladder as a result of spinal injury. Recruitment started in April 2011.
Participants are randomised to one of four arms, designed for factorial analysis of LGG-BB12 and/or RC14-GR1 v Placebo. This involves 24 weeks of daily oral treatment with RC14-GR1 + LGG-BB12, RC14-GR1 + placebo, LGG-BB12 + placebo or two placebo capsules. Randomisation is stratified by bladder management type and inpatient status. Participants are assessed at baseline, three months and six months for Short Form Health Survey [SF-36], microbiological swabs of rectum, nose and groin; urine culture and urinary catheters for subjects with indwelling catheters. A bowel questionnaire is administered at baseline and three months to assess effect of probiotics on bowel function.
The primary outcome is time from randomisation to occurrence of symptomatic UTI. The secondary outcomes are change of MRO status and bowel function, quality of life and cost-effectiveness of probiotics in persons with SCI. The primary outcome will be analysed using survival analysis of factorial groups, with Cox regression modelling to test the effect of each treatment while allowing for the other, assuming no interaction effect. Hazard ratios and Kaplan-Meier survival curves will be used to summarise results.
If these probiotics are shown to be effective in preventing UTI and MRO colonisation, they would be a very attractive alternative for UTI prophylaxis and for combating the increasing rate of antibiotic resistance after SCI.
Australian New Zealand Clinical Trials Registry [ACTRN 12610000512022]. Date of registration: 21 June 2010.
Urinary tract infections [UTIs] are very common in people with a neurogenic bladder. People with a spinal cord injury [SCI] and people with the spinal demyelinating form of Multiple Sclerosis [MS] are highly susceptible to the development of neurogenic bladder dysfunction.
UTIs have a high societal cost and current prevention strategies do not work. People with neurogenic bladder are at significant risk from UTI with approximately two  UTI episodes per year on average for persons with SCI . One of the major clinical challenges for SCI patients and clinicians is that when patients get a UTI, simple oral antibiotics frequently are ineffective due to the high numbers of multi-resistant-organism [s] [MROs] within SCI populations [about 40–50 % of SCI people] [1, 2]. This greatly amplifies the health, societal and economic consequences of disease and can even lead to life threatening clinical problems that can spread if not controlled through hospitals and the community. Health care costs associated with cross infection are estimated at US$18–30 billion yearly in the USA and UK combined. Australian costs are expected to be proportionate . Furthermore, based on the existing SCI UTI prevention literature, we have demonstrated that current commonly used methods of non-antibiotic UTI prevention in SCI do not work . The prevention of UTI, particularly the more difficult to treat MRO UTI, is therefore a clinical imperative for those people with SCI and neurogenic bladder. Non-antibiotic prevention is needed to prevent UTI without increasing the antimicrobial resistance burden .
Probiotics are defined as a preparation containing viable, defined micro-organisms in sufficient numbers, which alter the microflora [by implantation or colonization] in a compartment of the host and thus exert beneficial health effects in this host . Reid postulated that probiotics could reduce antibiotic related superinfections, disrupt bacterial biofilms, and enhance generalised mucosal immunity in the gastrointestinal and genitourinary systems . In a systematic review conducted by Falagas et al., it was concluded that several probiotics tested, e.g. Lactobacillus rhamnosus GR-1 and Lactobacillus fermentum RC-14, delivered either intravaginally or orally, were efficacious in restoring vaginal flora and in preventing recurrent UTIs in women . In another trial, Manley et al. demonstrated clearance of vancomycin-related enterococci in stool after treatment with Lactobacillus rhamnosus GG .
There are currently no known trials of oral probiotics and its efficacy in prevention of UTIs in people with neurogenic bladders. Darouiche and others have conducted more invasive trials involving inoculating neurogenic bladders with benign strains of Escherichia coli and showed this approach was effective at lowering the rate of UTIs per year [10–12].
To test the effectiveness of combination oral probiotic therapy Lactobacillus reuteri RC-14 + Lactobacillus rhamnosus GR-1 [RC14-GR1 capsules] and/or Lactobacillus rhamnosus GG + Bifidobacterium BB-12 [LGG-BB12 capsules] in preventing UTI in people with SCI compared to placebo.
To examine whether probiotics may change or prevent colonisation or infection with MROs in persons with SCI.
To examine the effects of probiotics on bowel function in persons with SCI
Examination of indwelling and suprapubic catheters to determine:
How probiotic intervention affects microbial community composition in the urine and urinary catheter.
Differences between microbial communities in individuals who are symptomatic versus asymptomatic for UTI.
To estimate the cost-effectiveness of probiotics in persons with SCI
A randomised controlled trial [RCT] was selected as the design most likely to provide a definitive conclusion to the primary aim.
This is a prospective multi-site randomised, double-blind, double-dummy, placebo-controlled factorial design trial conducted in the state of New South Wales [NSW] Australia, in order to test the effectiveness of two probiotic therapies in preventing UTI in people with SCI. Participants will be recruited from the NSW SCI community and all the specialist SCI units in NSW hospitals, including their regional and rural affiliations. These units are located at the Prince of Wales Hospital [POWH], Royal Rehabilitation Centre Sydney [RRCS] and Royal North Shore Hospital [RNSH].
A multi-site ethics approval was obtained from the Human Research Ethics Committee [HREC] at each of the three SCI units in NSW, Australia. HREC Protocol no: 1008-282-CTN-GG [POWH SSA 1008-282 CTN, RR SSA 11/SSA03, RNSH SSA10/HAWKE/171].
The protocol for catheter sampling and culture independent technique of bacterial community identification was categorised as a low-risk study with separate ethics approval obtained from the HREC at each site [POWH HREC ref no. 11/036, RNSH HREC/10/HARBR/102 and SSA/10/HAWKE/171].
The trial was registered with the Australian New Zealand Clinical Trials Registry [ACTRN 12610000512022] on 21 June 2010. Informed consent will be provided prior to recruitment and participation. Participant recruitment commenced in April 2011.
The trial uses a factorial design which allows the two probiotics to be compared with placebo simultaneously without inflating the sample size, on the assumption that they do not interact with each other. [Refer Table 1].
UTI prevention: In our previous RCT with the same study population , 45 % of participants had a symptomatic UTI within six months. To have 80 % power to detect [at 5 % two-sided significance level] a 30 % reduction in the treatment group requires a total sample size of 350. Allowing for a 5 % loss to follow-up a final sample size of 372 is required, 93 participants being randomly allocated to each of the four study groups.
MRO treatment: It is expected that approximately 40 % participants will be MRO-positive at enrolment. Assuming 5-10 % become MRO-negative in the control group, a 15–20 % reduction in MRO-positive colonisation rate with probiotics would be detectable as significant at the 5 % level, with 80 % power, with a sample size of 372.
Randomisation and blinding of assessors
A simple stratified [computer generated] randomisation protocol is used. JS is responsible for generating the allocation sequence. Randomisation is stratified by bladder management types [indwelling/suprapubic vs intermittent catheters vs condom drainage/reflex voiding] as well as inpatient/outpatient status. Randomisation occurs following participant’s compliance check at Day 4. One central pharmacy is responsible for the assignment and distribution of the intervention for the entire study. All four treatment regimens will be indistinguishable by appearance and taste, and all participants receive the same quantity of tablets. All clinical staff, researchers and participants remain blind to treatment allocation throughout this process. An audit of randomisation, product allocation and dispensing stock will be performed at the completion of the study by MT, who is not affiliated with the final analysis and the clinical management of the study or study participants.
All participants are to be over 18 years of age and are required to provide written consent. All participants with known neurogenic bladder as a result of SCI who meet inclusion criteria and gave written consent are enrolled. BL, ST, SR, JK, LB, GW and CBR are responsible for enrolling participants.
Had a known neurogenic bladder;
Had a stable SCI or stable multiple sclerosis with a known spinal demyelinating lesion;
Had a stable bladder management technique [i.e. not receiving bladder management education for at least 4 weeks] and using a bladder management technique such as indwelling catheter, suprapubic catheter, clean intermittent self-catheterisation or reflex/condom drainage;
Agreed to fortnightly telephone consultation for themselves and their care team during the six month study period;
Agreed not to take any other probiotic in addition to the allocated intervention during the course of the study. This includes all oral or topical preparations of yoghurt and urinary antiseptics [e.g. methenamine hippurate (hiprex) or cranberry preparations].
Receiving bladder management education within the last 4 weeks;
Being treated for, or symptomatic from a current infection or long-standing pressure sore;
Known to have a complex bladder disturbance requiring surgical intervention e.g. known cystoplasty, renal or bladder calculus, significant hydronephrosis, or current pyelonephritis;
Known to have chronic open wound/s or known long-standing osteomyelitis [greater than 6 weeks];
On long-term antibiotic therapy for any indication;
Known to have a history of adverse drug reaction to yoghurt products or a demonstrated intolerance to the probiotics used. Lactose intolerance was NOT an exclusion criterion;
Known to have severe renal or hepatic failure;
Requiring full [invasive] mechanical ventilation;
Receiving immunosuppressant medications or have an underlying immunosuppressive disease [for example HIV or end-stage/ progressive diabetes mellitus, multiple sclerosis or cerebrovascular disease];
Planning to have oral surgery during the intervention period;
Concurrently enrolled in another intervention study [observational studies or inclusion following completion of another study was allowed].
Each participant is enrolled for a six month study period, which includes 24 weeks of treatment [see Fig. 1]. Each participant randomised is required to take two tablets orally each day consisting of either RC14-GR1 + LGG-BB12 or RC14-GR1 + placebo or LGG-BB12 + placebo or 2 placebo tablets.
GR1-RC14. Concentration per capsule is 5.4 × 109 colony forming units.
LGG-BB12. Concentration per capsule is 7 × 109 colony forming units.
Participants will be assessed at Day 0, 3 months and 6 months, supported by fortnightly phone calls to determine health status and confirm intercurrent symptomatic UTI status. [Fig. 1] Following witnessed informed consent, evaluations conducted will be:
Intervention issues and compliance.
Quality of life assessment with the Short Form Health Survey [SF-36] – baseline and 6 months plus study endpoint if reached.
Microbiological swabs of rectum, nose and groin, urine culture and collection of urinary catheters for participants with indwelling or suprapubic catheters – baseline, 3 months and 6 months. Urine cultures also performed if at study endpoint. Specific instructions for sampling were given by study co-ordinator to research assistants and community nurses performing the swabs to ensure consistency.
The indwelling urethral and suprapubic catheter biofilm is examined as a proxy for the urinary tract microbial community. Culture-independent techniques in profiling human microbes will be used to determine the composition of adherent microbes through the examination of the bacterial 16S rDNA gene by Terminal Restriction Fragment Length Polymorphism [TRFLP]  and via next-generation sequencing [16–19]
Samples are selected irrespective of interventional grouping.
Samples are also selected from groups with recurrent symptomatic UTI compared to no-UTI symptoms over the study follow-up period. All TRFLP and sequencing analysis will be conducted blinded by the use of a participant identification key that de-identifies the data.
TRFLP is done in collaboration with the Ramaciotti Centre for Genomics, University of New South Wales and sequencing through the Singapore Centre for Environmental Life Sciences Engineering at Nanyang Technological University, Singapore.
The primary outcome measure is the time from randomisation to occurrence of “symptomatic UTI” [Fig. 2]. The date of the endpoint is the date participants develop symptoms consistent with a “symptomatic UTI” as per the algorithm, not the date participants start developing any symptoms. Table 2 outlines the definition of “symptomatic UTI” as primary endpoint for ProSCIUTTU. For participants who do not experience a “symptomatic UTI”, the primary outcome is at six months. Participants who cease intervention early are followed up until the end of the study period.
The secondary endpoint is time to change of MRO colonisation status as determined by two successive cultures [See guidelines for MRO change or clearance in Additional file 1].
All analyses of outcomes will be by intention to treat, apart from safety outcomes which will be according to actual treatment received. Primary and MRO outcomes will be analysed using survival analysis. Cox regression modelling will be performed to test the effect of each treatment while allowing for the other, assuming no interaction effect. Hazard ratios and Kaplan-Meier survival curves will be used to summarise results. The extremely high prevalence of MRO in SCI will also allow us to explore whether probiotics can treat [or prevent] MRO colonisation in this group.
A survey was sent out to selected co-authors for determining the strength of association of several variables in regards to UTI in the SCI population [pre hoc review]. Only variables which have strong or moderate association will be included in the analysis.
Biofilms will be analysed using a combination of RNA based meta-community sequencing, TRFLP fingerprinting and culture based methods.
Trial data management
The data will be collected on trial specific case record forms. OM is responsible for designing and maintaining the trial database. Following each study visit, a study team member will ensure data is complete. Databases will be commissioned within the SCI units and will contain non-identifiable data. Re-identifiable data will be available for use only by the study team. Primary outcome measure endpoint determination will be verified by BL and ST. The two assessors will be blinded by each other’s assessment. Discrepancies will be decided by a third investigator [KC].
Feasability, safety, efficacy
Hospital admissions and intensive care unit admissions related to infection.
A diagnosis of laboratory infection defined by a positive blood culture.
Clinical adverse events [grade 3–4] regardless of causality.
All causes of mortality.
Use of antibiotics.
Change in of MRO colonisation/infection status as defined by two consecutive MRO swabs three months apart.
Modifications of bladder management.
A cost-effectiveness analysis will be undertaken using SF-6D utility weights derived from the SF-36. In addition to antibiotic use, the following resource data will also be collected during the study:
Use of isolation precautions: Single room; Personal Protective Equipment [PPE];
Infection control auditing
An independent Safety Monitoring Committee [SMC] is established. Clinicians or investigators responsible for the clinical care of study participants were not permitted to be members of the SMC. The SMC will monitor the trial and review safety data by treatment allocation. Safety monitoring will be carried out at various intervals through the trial depending on frequency of adverse events. The Committee will review laboratory data, Grade 3, Grade 4 and Grade 5 adverse events and serious adverse events [SAEs] and adverse events leading to cessation of study therapy [refer Table 3]. A summary of safety data will be undertaken when all recruited participants have completed 20 weeks on study.
The SMC Chairman had no formal affiliation with the trial and coordinated this process.
Project governance and administration support
The chief investigator Dr. Bon San Bonne Lee will be responsible for overall project management, but is assisted and advised by a project steering committee comprised of the collaborating researchers and administrative support from the administering institution [NeuRA]. The project steering committee will meet regularly and all agendas and minutes circulated to all stakeholders.
Trial commencement date: April 2011
Trial follow-up completion date: March 2014
Number of participants recruited: 207
lactobacillus rhamnosus GR-1
lactobacillus rhamnosus GG
National Health and Medical Research Council of Australia
personal protective equipment
lactobacillus reuteri RC-14
serious adverse event
short form health survey
spinal cord injury
safety monitoring committee
terminal restriction fragment length polymorphism
urinary tract infection
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The authors would like to acknowledge Dr. Marcella Kwan and Ms. Elizabeth Rose, for their contributions as research assistants for the trial. The authors would like to thank Professor Ian Cameron for his role as the SMC Chairman. The authors would also like to thank Ms. Hanan Youssef and Ms. Alysia Wong for administrative support.
NHMRC is the organisation responsible for funding the supply of probiotics and matching placebo selected by the researchers for this study and budgeted within the NHMRC grant.
CHR Hansen has been paid commercial rates for providing the intervention product and placebo. The company had no input into the design of the trial.
BL, JS, SG and JM have received competitive research funding support from the National Health and Medical Research Council of Australia [NHMRC]. They declare that they have no other financial or non-financial competing interests. The rest of the authors have no competing financial or non-financial interests.
The trial protocol has been developed by all authors over a series of teleconferences and workshops in Sydney, Australia in late 2009 and early 2010 from an original study design developed by BL and JS. LB and SAR were responsible for the protocol design and analysis of culture independent techniques of microbioflora identification. SR is the overall study project co-ordinator. SR is responsible for the study regulatory processes including designing the data collection forms, ethics and regulatory submissions as well as co-ordinating packaging of the investigational products. OM is responsible for designing and maintaining the trial database. JS is responsible for designing the biostatistical aspects of the trial and reviewing the statistical analysis. SG is responsible for designing the health economics aspects of the protocol and analysing the health economics data. GK is responsible in co-ordinating the microbiological sample analysis. MT is responsible for auditing the pharmacy compliance with protocol. BL, JK and GW are site investigators at the respective three spinal units. Recruitment is undertaken by BL, ST, SR, JK, GW, LB, CBR. Data collection is conducted by BL, SR, ST, OM, LB and CBR. ST, BL and KC are responsible for study endpoint determination. BL, SR and ST are responsible for initial manuscript preparation. All authors reviewed and were involved in writing up the final version of the manuscript prior to submission.
Guidelines for MRO change and clearance. (DOC 27 kb)