Vancomycin Associated Red Man Syndrome (RMS)

Sponsor
Children's Mercy Hospital Kansas City (Other)
Overall Status
Completed
CT.gov ID
NCT00824122
Collaborator
Katherine Berry Richardson Foundation (Other)
544
1
45
12.1

Study Details

Study Description

Brief Summary

This study proposes to identify patients who developed RMS with vancomycin infusion, and determine presence or absence of variant alleles involved in histamine biotransformation. The implications of this study are important, as identification of variant alleles in these patients, may alter the current standard of care for vancomycin infusions.

The hypothesis of this study is that the development of red man syndrome (RMS) during receipt of intravenous vancomycin is associated with the presence of variant alleles for genes involved in the histamine pathway. The primary outcome that will be measured will be the history of RMS and the presence or absence of variant alleles for the genes responsible for histamine metabolism (i.e. histamine n-methyltransferase and diamine oxidase). As a secondary endpoint, the study will also attempt to determine the incidence of RMS in pediatric patients.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Vancomycin has been utilized as an antimicrobial therapeutic agent for serious gram positive infections for more than half a century.The pharmacokinetics of vancomycin has been well studied, and in general there are few side effects from this medication. The most common side effect that occurs with receipt of vancomycin is red man syndrome (RMS), which is also known as red neck, or red person syndrome.1 RMS encompasses a spectrum that ranges from a mild reaction such as flushing, urticarial rash, pruritis, to a severe reaction that includes generalized erythema,intense pruritis, and even hypotension. RMS has been estimated to occur in 5- 50% of hospitalized patients who receive this drug.

    RMS is considered an anaphylactoid type of reaction that is due to mast cell degranulation with a concomitant rise in blood histamine levels. The resultant symptomatology varies from mild itching and erythematous rash to a more generalized reaction with hypotension. This reaction has been shown to be modified by pre-treatment with various types of antihistamines including diphenhydramine and cimetidine.

    There is now evidence to suggest that altered histamine metabolism contributes to the pathogenesis of various disorders. Histamine is almost exclusively metabolized by the enzymes histamine N-methyltranserase (HNMT)and diamine oxidase (DAO) both of which are polymorphically expressed in people with varying frequencies.HNMT catalyzes the N- methylation of histamine. This is the predominant pathway for histamine metabolism,accounting for 50-80% of its biotransformation. Diamine oxidase (DAO) likely contributes in a significant manner of the remaining metabolism of histamine as only 2-3% of this autocoid is excreted unchanged in the urine. It is plausible that allelic variants of HNMT and/or DAO may contribute to histmaminergic reactions in a given patient with resultant propagation of its pharmacologic effects, and that polymorphically expressed enzymes primarily responsible for terminating the pharmacologic activity of histamine (via biotransformation)may play a crucial role in determining disease phenotype for disorders (e.g., RMS) where histamine is a key mediator.

    This is a prospective study that will be conducted over a one year period of time. Eligible patients will be identified by a search of patients who are receiving vancomycin therapy throughout the study period. Chart review/patient interview will then be performed to identify patients who developed symptomatology consistent with RMS while receiving vancomycin infusion. For the purposes of this study, red man syndrome (RMS) will be defined as: erythematous rash, flushing of the face, neck, or torso, itching, or a lowering of systolic or diastolic blood pressure by >10mm/hg. A subset of patients who remained asymptomatic throughout their vancomycin therapy will also be evaluated as a control group.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    544 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Genetic Polymorphisms Associated With Histamine Disposition in Children With Vancomycin Associated Red Man Syndrome (RMS)
    Study Start Date :
    Jan 1, 2008
    Actual Primary Completion Date :
    Dec 1, 2008
    Actual Study Completion Date :
    Oct 1, 2011

    Arms and Interventions

    Arm Intervention/Treatment
    1

    Children greater than 6 months receiving at least one dose of Vancomycin and Red Man Syndrome

    2

    Children greater than 6 months receiving at least one dose of Vancomycin and has not had Red Man Syndrome

    Outcome Measures

    Primary Outcome Measures

    1. Presence or abscence of genetic polymorphisms in the histamine pathway in patients with vancomycin related RMS. [During Hospital Admission]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    6 Months to 21 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients must have received vancomycin
    Exclusion Criteria:
    • Patients who have received antihistamines at the time of vancomycin administration or

    • Patients who have been on steroids or tricyclic antidepressants within 30 days prior to the vancomycin administration

    • People receiving ECMO or have multiorgan failure

    • Currently receiving dialysis

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Children's Mercy Hospital & Clinics Kansas City Missouri United States 64108

    Sponsors and Collaborators

    • Children's Mercy Hospital Kansas City
    • Katherine Berry Richardson Foundation

    Investigators

    • Principal Investigator: Angela Myers, MD, MPH, Children's Mercy Hosptials and Clinics

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Angela Myers, Assistant Professor of Pediatrics, Children's Mercy Hospital Kansas City
    ClinicalTrials.gov Identifier:
    NCT00824122
    Other Study ID Numbers:
    • 10914
    First Posted:
    Jan 16, 2009
    Last Update Posted:
    Oct 12, 2011
    Last Verified:
    Oct 1, 2011
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 12, 2011