PedsROTEM: Use of ROTEM® in Pediatric Cardiac Surgical Patients

Sponsor
Weill Medical College of Cornell University (Other)
Overall Status
Completed
CT.gov ID
NCT01212289
Collaborator
(none)
23
1
41
0.6

Study Details

Study Description

Brief Summary

Cardiac surgery requiring use of a heart-lung machine, also known as cardiopulmonary bypass (CPB) can induce abnormalities in blood coagulation (clotting) that lead to excessive blood loss during and after operation. While of significant concern in adults, this problem takes on even greater importance in children due to the simple fact that they have a smaller blood volume. It is well known that if a child has previously undergone a heart operation, they are at increased risk of bleeding should more cardiac surgery be required ("reoperation"). The processes regulating blood coagulation are extraordinarily complex, and little is known about the exact mechanisms that contribute to the increased bleeding associated with cardiac reoperation in children. Rotational thromboelastometry (ROTEM®) is a technology that can provide, at the bedside, detailed information about coagulation abnormalities. While not currently approved for general use in the United States, in Europe ROTEM® has been used to guide administration of the blood products in surgery based upon determination of specific coagulation abnormalities. Importantly, there is now evidence that guidelines for transfusion therapy based on ROTEM® reduce transfusion requirements thus decreasing patient exposure to blood products. Whether the use of ROTEM® has potential benefit for pediatric cardiac surgical patients has not been studied. Accordingly, the present study was designed to provide preliminary data comparing coagulation profiles between children undergoing cardiac reoperation to those having primary procedure.

The investigators hypothesize that ROTEM® analysis will detect a pattern of impaired coagulation in children undergoing reoperation. The overall objective of the four assays of ROTEM® analysis therefore, is to provide information that can be used to devise a rational transfusion protocol for pediatric cardiac surgical subjects.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Specific aims of the proposed pilot studies are to:
    1. Use bedside blood analysis with ROTEM® in pediatric cardiac surgical patients to provide preliminary information on the nature of coagulation abnormalities.

    2. Compare ROTEM® coagulation profiles between subjects having primary surgery and those undergoing reoperation.

    In order to test the study hypothesis, pediatric subjects scheduled to undergo cardiac surgery involving CPB will be recruited for two study groups: a) primary surgery; b) reoperation. For each group, a small amount of blood will be obtained for ROTEM® analysis after induction of anesthesia but before skin incision and again following Cardiopulmonary Bypass, 5 minutes after protamine administration.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    23 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    The Use of Rotational Thromboelastometry ROTEM® to Characterize Coagulation Abnormalities in Pediatric Cardiac Surgical Patients: A Prospective Pilot Study
    Study Start Date :
    Sep 1, 2010
    Actual Primary Completion Date :
    Feb 1, 2014
    Actual Study Completion Date :
    Feb 1, 2014

    Arms and Interventions

    Arm Intervention/Treatment
    Primary cardiac surgery

    Pediatric patients receiving primary cardiac surgery

    Reoperation

    Pediatric patients receiving cardiac surgery reoperation

    Outcome Measures

    Primary Outcome Measures

    1. To obtain pre- and post-cardiopulmonary bypass (CPB) coagulation profiles using ROTEM® in pediatric patients undergoing cardiac surgery with CPB [Profiles will be collected after induction of anesthesia and before CPB, and after CPB, 5 minutes after protamine adminsitration]

      A small blood sample from an already existing arterial line will be taken from the patient at these times and analyzed using the ROTEM® machine.

    Secondary Outcome Measures

    1. To compare ROTEM® coagulation profiles between subjects having primary surgery and those having a reoperation [1.3 years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    1 Year to 6 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients with congenital heart disease undergoing cardiac surgery needing cardiopulmonary bypass.

    • Males and females

    • Age 1 year to 6 years

    • Informed consent obtained

    Exclusion Criteria:
    • Known pre-existing haemostatic abnormalities

    • Emergency surgery

    • Pre-operative treatment with prostaglandin infusion or any other medication known to interfere with platelet function or cause coagulation abnormalities .

    • Inclusion in another clinical research study

    • Refusal or inability of patient's parent to sign the Informed Consent Form in English.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 New York Presbyterian Hospital/ Weill Cornell Medical College New York New York United States 10021

    Sponsors and Collaborators

    • Weill Medical College of Cornell University

    Investigators

    • Principal Investigator: Aarti Sharma, M.D., Weill Medical College of Cornell University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Weill Medical College of Cornell University
    ClinicalTrials.gov Identifier:
    NCT01212289
    Other Study ID Numbers:
    • 1005011027
    First Posted:
    Sep 30, 2010
    Last Update Posted:
    Feb 18, 2016
    Last Verified:
    Feb 1, 2016
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 18, 2016