Urinary Tract Infection Clinical Trial
Official title:
Probiotics Improvement of Gastrointestinal and Genitourinary Health in Girls With Spina Bifida (H-23245)
Girls with spina bifida also have bladder problems. This is because they need temporary
placement of a tube into the bladder to remove urine. This thin flexible tube is called a
catheter. It can increase the risk of having bacteria in the urine. This in turn can lead to
urinary tract infection (UTI).
Some girls with spina bifida are given antibiotics. These are medicines used to treat
infections caused by bacteria. The medicine is used to prevent UTI. However, long-term
treatment with these medicines can have side effects. For example, the bacteria may become
resistant to the antibiotics. Also, bacteria in the urine can persist. UTI can still occur
in patients on antibiotics.
UTI in girls occurs because bacteria migrate from the rectum to the vagina area. This gives
the bacteria access to the bladder. Also, in girls with spina bifida, the access to the
bladder is easier because of the catheter.
Probiotics are friendly bacteria. They are available as dietary supplements and as food.
They contain helpful bacteria. Yogurt is an example of a food that contains probiotics.
The purpose of this study is to find out, if probiotics taken for 6 months can prevent UTI
in girls with spina bifida. We will also try to find out whether changes in urine bacteria
are associated with the taking of the probiotics. A vaginal and rectal swab will also be
done to find out if taking probiotics has any benefits on preventing bacteria.
In children with spina bifida and neurogenic bladder dysfunction, the need for intermittent
bladder catheterization increases the risk of bacteriuria. In many patients, this leads to a
clinically significant urinary tract infection (UTI). Many of these children are placed on
long term, low dose antibiotic suppression to prevent recurrent urinary infection.
Unfortunately, bacteriuria often persists despite daily antibiotic therapy, and breakthrough
UTIs are common. Furthermore, this approach carries the potential for deleterious side
effects, and may promote the development of antibiotic-resistant bacteria.
UTI in girls occur when virulent bacteria migrate from the rectum and colonize the vagina
and peri-urethral mucosa, thus gaining access to the bladder. In girls with spina bifida,
access to the bladder is greatly facilitated by catheter passage. Antibiotic prophylaxis
relies on maintaining a low dose of antibiotic in the urinary stream, which decreases
peri-urethral colonization, and prevents proliferation of bacteria after they gain access to
the bladder. An alternative approach to daily antibiotic prophylaxis is to decrease the risk
of urinary colonization with virulent bacteria by supplementing the normal bacteria flora
with non-infection causing strains of bacteria.
Probiotics are dietary supplements containing potentially beneficial bacterial strains such
as Lactobacillus. The safety of oral administration of probiotics has been demonstrated in
several studies over the last 30 years. Studies using Lactobacillus rhamnosus GG, a
probiotic introduced in the late 1980s to alleviate diarrhea, have shown promising results
when used for UTI prevention. In one study, researchers found that the subjects consuming GG
drinks had fewer episodes of UTI compared to those women not receiving probiotics. A
placebo-controlled study in premature infants also used GG in an attempt to prevent UTI. The
number of urinary infections was reduced but statistically the difference was not
significant. Finally, a recent randomized clinical trial demonstrated that the rate of UTI
in children taking prophylactic antibiotics was similar to that of patients taking
Lactobacillus acidophilus alone. The efficacy of probiotic usage in the spina bifida
population has not been reported.
Clinical trials have suggested that oral ingestion of the probiotic strains Lactobacillus
reuteri RC-14 and Lactobacillus rhamnosus GR-1 results in vaginal colonization and
prevention of adult UTI, potentially by inhibiting uropathogen ascension from the vagina to
the urinary tract.
A total of 60 patients will be enrolled for this pilot study, half of whom will be
randomized to receive probiotics and the reminder of which will receive placebo [1:1 ratio;
50% chance of being in each group (A and B)]. Treatment assignment will be double blinded
and will last 6 months.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
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