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 Urology

Study Protocol

Stephen Goodall¹  Scott A. Rice²  Kate Clezy³  Obaydullah Marial⁴  Swee-Ling Toh⁵  James Middleton⁶  Suzanne Ryan⁷  Claire Boswell-Ruys⁷  Laetitia Bossa⁸  Bonsan Bonne Lee⁹  George Kotsiou^1,10  Jasbeer Kaur^1,10  Mark Tudehope^1,10  Gerard Weber^1,11  Judy M. Simpson^1,12 

[1] Centre for Health Economics Research and Evaluation [CHERE], University of Technology Sydney, Sydney, Australia;Centre for Marine Bio-Innovation, University of New South Wales, Sydney, Australia;The Singapore Centre for Life Sciences Engineering and the School of Biological Sciences, Nanyang Technological University, Singapore, Singapore;Department of Infectious Diseases, Prince of Wales Hospital, Sydney, Australia;Department of Spinal and Rehabilitation Medicine, Prince of Wales Hospital, Sydney, Australia;Royal Rehabilitation Centre Sydney, Sydney, Australia;Royal North Shore Hospital, Sydney, Australia;Department of Spinal and Rehabilitation Medicine, Prince of Wales Hospital, Sydney, Australia;School of Public Health, University of Sydney, Sydney, Australia;John Walsh Centre for Rehabilitation Research, Kolling Institute, Northern Sydney Local Health District, 2065, St Leonards, NSW, Australia;Sydney Medical School Northern, University of Sydney, Sydney, Australia;Neuroscience Research Australia [NeuRA] and the University of New South Wales, Sydney, Australia;Neuroscience Research Australia [NeuRA] and the University of New South Wales, Sydney, Australia;Centre for Marine Bio-Innovation, University of New South Wales, Sydney, Australia;Neuroscience Research Australia [NeuRA] and the University of New South Wales, Sydney, Australia;Department of Spinal and Rehabilitation Medicine, Prince of Wales Hospital, Sydney, Australia;Royal North Shore Hospital, Sydney, Australia;Royal Rehabilitation Centre Sydney, Sydney, Australia;School of Public Health, University of Sydney, Sydney, Australia;

关键词: Urinary prophylaxis;    Multi-resistant organisms;    Antibiotic resistance;    Probiotics;    Biofilm;    Microbial community profiles;   

DOI  :  10.1186/s12894-016-0136-8

 received in 2015-11-10, accepted in 2016-03-28,  发布年份 2016

来源: Springer

【 摘 要 】

BackgroundUrinary 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.MethodThis 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.DiscussionIf 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.Trial registrationAustralian New Zealand Clinical Trials Registry [ACTRN 12610000512022]. Date of registration: 21 June 2010.

【 授权许可】

CC BY   
© Lee et al. 2016