Effectiveness Of Symbiotic Therapy In Jaundiced Patients

Sponsor
Azienda Ospedaliera Ordine Mauriziano di Torino (Other)
Overall Status
Unknown status
CT.gov ID
NCT01683708
Collaborator
(none)
20

Study Details

Study Description

Brief Summary

The aim of the present study was therefore to evaluate if the perioperative administration of symbiotics reduces postoperative infectious morbidity in jaundiced patients scheduled for hepato-biliary and pancreatic surgery.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Symbiotic therapy

Detailed Description

Despite advances in preoperative patient's selection and anesthetic and surgical techniques, surgery in jaundiced patients is associated with significant morbidity and mortality as a consequence of septic complications. The evidence that nosocomial infections are frequently a consequence of gut-derived organism such as enterobacteriaceae, supports the hypothesis of the "gut derived sepsis". Indeed, several studies have reported that jaundiced patients present an increased intestinal permeability and consequently a higher rate of bacterial migration from gastrointestinal tract across the lamina propria to local mesenteric lymph nodes and from there to extra-intestinal site. This phenomenon increases after surgical decompression of bile duct. The higher prevalence of bacterial translocation in jaundiced patients is related to different mechanisms such as mucosal atrophy secondary to protracted absence of intraluminal bile that open para-cellular route for bacterial translocation and the decreased clearance capacity of Kuppfer secondary to cholestasis.

The mechanisms of action of symbiotics are largely unknown. The probiotic bacteria can improve the mucosal barrier function reducing the bacterial translocation of organism to mesenteric lymph nodes. Indeed symbiotic can affect the intestinal ecosystem by stimulating mucosal immune and non-immune mechanisms through antagonism/competition with potential pathogens.

Study Design

Study Type:
Observational
Anticipated Enrollment :
20 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Effectiveness of Perioperative Symbiotic Therapy to Reduce Infectious Morbidity in Jaundiced Patients: a Randomized Controlled Trial
Study Start Date :
Nov 1, 2008

Arms and Interventions

Arm Intervention/Treatment
Symbiotic group

Jaundiced patients who have symbiotic therapy

Dietary Supplement: Symbiotic therapy
Patients randomized into the Symbiotic group received Prebiotic® in a dose of one sachet twice a day for at least 1 week preoperatively. Postoperatively the medication was reintroduced as tolerated, and continued until discharge from hospital. One 4,5 gr sachet of Prebiotic® contains at least 1010 living Bifidobacterium bifidum, 1010 living Streptococcus Thermophilus, 1010 living Streptococcus Salivarius, 3 109 Lactobacillus Acidophilus, 1010 living Lactobacillus Casei, 1010 living Lactobacillus bulgaricus and galactooligosaccharides (4,5 gr).
Other Names:
  • Prebiotic® (Mediabase s.r.l., Prato, Italy)
  • No Symbiotic therapy

    Jaundiced patients who not have symbiotic therapy

    Outcome Measures

    Primary Outcome Measures

    1. Infectious Morbidity Rate [Participants will followed for the duration of hospital stay, an expected average of 6 weeks]

    Secondary Outcome Measures

    1. IMMUNE PROFILE [The day before and on postoperative day 7]

    2. RATE OF TRANSLOCATION [Intraoperative]

      a lymph node was routinely excised from the ileocaecal mesentery and was immediately transported in sterile saline to the laboratory for culture

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • jaundiced patients scheduled for elective extrahepatic bile duct resections

    • age between 18 and 80 year-old Exclusion Criteria:

    Exclusion Criteria

    • cirrhosis

    • American Society of Anesthesiologists (ASA) score 4

    • intestinal malabsorption

    • emergency surgery

    • intolerance to symbiotic

    • diagnosis of primary or secondary immunodeficiency

    • unresectability

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Azienda Ospedaliera Ordine Mauriziano di Torino

    Investigators

    • Principal Investigator: Lorenzo Capussotti, MD, Mauriziano Hospital, Department of General and Oncological surgery

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    LorenzoCapussotti, Director of Department of General and Oncologica Surgery, Azienda Ospedaliera Ordine Mauriziano di Torino
    ClinicalTrials.gov Identifier:
    NCT01683708
    Other Study ID Numbers:
    • Symbiotic2012
    First Posted:
    Sep 12, 2012
    Last Update Posted:
    Sep 12, 2012
    Last Verified:
    Sep 1, 2012
    Keywords provided by LorenzoCapussotti, Director of Department of General and Oncologica Surgery, Azienda Ospedaliera Ordine Mauriziano di Torino
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 12, 2012