Impact of the Contamination Mode on the Clinical Evolution During Pseudomonas Aeruginosa Ventilator Acquired Pneumonia (PYO GEN)

Sponsor
University Hospital, Grenoble (Other)
Overall Status
Unknown status
CT.gov ID
NCT01745796
Collaborator
(none)
180
1
36
5

Study Details

Study Description

Brief Summary

Pseudomonas aeruginosa is the main pathogen of nosocomial respiratory infections. Its increasing resistance to antibiotics requires the development of new strategies for prevention and control, demanding a better understanding of the modes of transmission and evolutionary dynamics of this bacteria. In patients under invasive mechanical ventilation, the main mode of contamination by Pseudomonas remains debated, with 3 modes of contamination (endogenous, crossed transmission between patients, or environmental origin) of varying importance, mainly depending on the endemic situation of the place of study.

The emergence of new genotyping technologies (DiversiLab) can now facilitate studies of molecular epidemiology. Thanks to the multidisciplinary collaboration and innovative techniques, the investigators wish to study the impact of the mode of contamination on the outcome of ICU patients, intubated and ventilated for more than 72 hours.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The presence of environmental reservoirs can cause infections and multidrug-resistant P. aeruginosa colonization with P. aeruginosa is itself a prognostic factor, but the impact of the route of infection on the evolution of the history and future of the infectious patient is not established.

    A second factor that may influence the evolution infectious is the degree of genetic heterogeneity of the bacterial population. Multiple exposure pathways could also influence the genetic diversity.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    180 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Impact of the Contamination Mode on the Clinical Evolution During Pseudomonas Aeruginosa Ventilator Acquired Pneumonia
    Study Start Date :
    Jan 1, 2013
    Anticipated Primary Completion Date :
    Jan 1, 2016
    Anticipated Study Completion Date :
    Jan 1, 2016

    Arms and Interventions

    Arm Intervention/Treatment
    Intubated ICU patients

    Outcome Measures

    Primary Outcome Measures

    1. The occurrence of unfavorable patient's outcome, depending on the mode of contamination, such as persistence, relapse or superinfection of the airways at Day 7, and mortality at Day 28 [From day 3 of intubation until the end of mechanical ventilation (an average of 28 days).]

    Secondary Outcome Measures

    1. Number of different clones of P. aeruginosa found in each sample analyzed for the same patient at diagnosis of colonization and VAP. [From day 3 of intubation until the end of mechanical ventilation (an average of 28 days).]

      Samples of infected patients are analyzed once a week, strains are considered from different clones if their genetic homology rate is below 97%

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients> 18 years

    • hospitalized in the intensive care unit

    • with more than 72 hours of mechanical ventilation

    • Presenting a positive bacteriological sample P. aeruginosa.

    Exclusion Criteria:
    • Minors.

    • Pregnant or lactating women.

    • Patients under guardianship, under judiciary placement, or hospitalized without their consent.

    • Patients not affiliated to a social security scheme.

    • Long-term corticosteroid therapy (> 2mg/kg or> 1 month before the onset of established infection suspected)

    • Ongoing chemotherapy, AIDS, transplant patient under immunosuppressive drugs.

    • Bedridden patient or therapeutic decision at ICU arrival

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Medical ICU of Universitary Hospital of Grenoble Grenoble Isère France 38700

    Sponsors and Collaborators

    • University Hospital, Grenoble

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital, Grenoble
    ClinicalTrials.gov Identifier:
    NCT01745796
    Other Study ID Numbers:
    • 12SC02
    First Posted:
    Dec 10, 2012
    Last Update Posted:
    Dec 2, 2015
    Last Verified:
    Dec 1, 2015
    Keywords provided by University Hospital, Grenoble
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 2, 2015