ASB: Asymptomatic Bacteriuria & Risk of Urinary Tract Infection in Renal Transplants

Sponsor
Rice, James C., M.D. (Other)
Overall Status
Unknown status
CT.gov ID
NCT01349738
Collaborator
University of Alabama at Birmingham (Other)
200
1
24
8.3

Study Details

Study Description

Brief Summary

The goal of this research program is to understand the natural history of asymptomatic bacteriuria in the renal transplant patients, to determine if screening for asymptomatic bacteriuria and identification of key host characteristics and virulence factors present on uropathogenic bacteria identifies a sub-population of patients with asymptomatic bacteriuria that are at risk to develop symptomatic urinary tract infection. Ultimately, the knowledge obtained from this study will prevent inappropriate antibiotic use and may identify whether certain bacterial isolates predispose to renal allograft injury. We will test the hypothesis that (i) asymptomatic bacteriuria is common in the renal allograft recipient and (ii) that symptomatic urinary tract infection and renal allograft dysfunction do not occur unless key host susceptibility factors and uropathogenic bacterial virulence factors are present.

Detailed Description

Blood samples and urine cultures will be obtained from asymptomatic renal transplant clinic patients. If the urine culture is positive (> or = 105 cfu/ml), we will determine the host and bacterial virulence factors associated with asymptomatic bacteriuria (ASB) and compare these results to transplant patients that develop a symptomatic UTI. The patient's clinical information, laboratory data and the bacterial isolate responsible for the UTI will be collected at the time of their clinic visit and subsequently analyzed.

After the first visit (Day 0 after signing consent) blood and urine will be collected, subjects will be put into either ASB Positive or ASB Negative groups based upon the results of their urine culture. From that point, those who test into the ASB Negative group will have an additional urine culture, either by returning to the clinic or by sending a urine culture mailer kit, and if cultures remain negative, they will be discharged from the study after reviewing medications, adverse events and completing a urinary tract infection risk questionnaire.

For those who test into the ASB Positive group, those subjects will be monitored by the subject returning to the clinic on Day 10-14, at 1 month, 2 month, 3 month and 6 months for blood and urine collection, review of medications and adverse events, and completing a urinary tract infection risk questionnaire. Should the subject have symptoms of a UTI, the subject will be treated with the appropriate antibiotic for which the bacterial isolated from their urine culture is sensitive. Patients will return to the clinic 10-14 days later for a repeat urine culture, complete a urinary tract infection risk questionnaire, and have a repeat urine culture to confirm they are urinary tract infection free. At this point, the subject will be discharged from the study after reviewing medications and adverse events.

It is predicted that 75% of patients will test into the ASB Negative Group and do not require antibiotic therapy. We predict that 25% of patients will test into the ASB Positive Group, but that less than 5% of these patients will ultimately develop a symptomatic UTI and require antibiotic treatment.

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Asymptomatic Bacteriuria & Risk of Urinary Tract Infection in Renal Transplants
Study Start Date :
May 1, 2011
Anticipated Study Completion Date :
May 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Positive Group

Positive for ASB

Drug: Antibiotic
Antibiotic (drug) sensitive to most recent culture for these subjects testing ASB positive and also experience Signs and symptoms of a UTI
Other Names:
  • Trimethoprim sulfamethoxazole (Bactrim)
  • Levofloxacin (Levaquin)
  • Ampicillin
  • SUSCEPTIBILITY
  • Organism >100,000 col/ml Escherichia coli (presumptive)
  • Susceptibility type MIC (BY VITEK 2)
  • Ampicillin >=32 Resistant
  • Ampicillin/Sulbactam 16 Intermediate
  • Cefazolin <=4 Suscep.
  • Ciprofloxacin <=0.25 Suscep.
  • Gentamicin <=1 Suscep.
  • Levofloxacin <=0.12 Suscep.
  • Nitrofurantoin <=16 Suscep.
  • Tobramycin <=1 Suscep.
  • Trimeth-Sulfa >=16/304 Resistant
  • Negative Group

    Negative for ASB

    Outcome Measures

    Primary Outcome Measures

    1. Prevalence of Asymptomatic Bacteriuria and Risk of Developing Symptomatic Urinary Tract Infections or Renal Allograft Injury in Renal Transplant Patients [2 years]

      Determine the prevalence and natural history of asymptomatic bacteriuria (ASB) and the host factors associated with the development of symptomatic UTI in renal allograft recipients. We will enroll renal transplant recipients, perform urine cultures and follow all patients with ASB to determine the prevalence of ASB and the host characteristics associated with ASB and the development of symptomatic UTI.

    Secondary Outcome Measures

    1. Host Characteristics of Renal Transplant Patients with Asymptomatic Bacteriuria at Risk to Develop Symptomatic Urinary Tract Infection [2 years]

      We will measure blood and urine immunoglobulin and cytokine levels in patients with ASB and symptomatic UTI to determine if these host's immune parameters predict the outcome of ASB, including the development of symptomatic UTI.

    2. Determine the characteristics of uropathogenic bacteria that cause acute allograft injury in renal transplant patients. [2 years]

      We will determine the expression of key uropathogenic virulence factors, including P fimbriae, Dr adhesins, and mono-mannose-binding type 1 fimbriae, on E. coli isolated from RTPs with ASB to determine if strains that express such virulence factors are more likely to cause symptomatic UTI and AAI, compared to E. coli that do not express these virulence factors.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • must be 18 years old or older,

    • had a kidney transplant,

    • be at least 30 days post operation.

    Exclusion Criteria:
    • Pregnant women, those planning to become pregnant or nursing mothers;

    • Renal transplant patients less than 30 days post transplant; Use of an indwelling Foley catheter;

    • Patients without a renal transplant;

    • Patients having concurrent surgical/wound infection and presumed hematogenous dissemination for the urinary tract.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Scripps Green Hospital La Jolla California United States 92037

    Sponsors and Collaborators

    • Rice, James C., M.D.
    • University of Alabama at Birmingham

    Investigators

    • Principal Investigator: James C. Rice, MD, Scripps

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT01349738
    Other Study ID Numbers:
    • ASB in Transplants
    First Posted:
    May 9, 2011
    Last Update Posted:
    Sep 1, 2011
    Last Verified:
    Aug 1, 2011

    Study Results

    No Results Posted as of Sep 1, 2011