Evaluation of Coagulation Testing in Patients Undergoing Cardiac Surgery

Sponsor
Boston Children's Hospital (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT02410473
Collaborator
(none)
200
1
92
2.2

Study Details

Study Description

Brief Summary

Neonates, children with single ventricle congenital heart disease, and those undergoing multiple complex cardiac surgeries are at high risk of increased perioperative blood loss, and blood product transfusions. In addition, some of these patients will present an increased risk of postoperative thromboembolic complications. For a long time, bleeding management has been based on the empiric administration of different blood products (e.g. platelet concentrates, cryoprecipitates, and/or activated factor VII), topical hemostatic agents, and surgical manipulation. Recently, the use of viscoelastic tests (e.g. thromboelastography (TEG) or thromboelastometry (ROTEM)) increased, and allowed a better assessment of perioperative coagulopathy, and a more 'rational' treatment of bleeding. While TEG and ROTEM record the viscoelastic properties of whole blood by measuring mechanical impedance and related changes during clot formation, T2MR, a miniaturized, magnetic resonance-based diagnostic platform, measures how water molecules react in the presence of magnetic fields to evaluate a broad range of hemostasis measurements. In this study, we will prospectively collect demographic data, surgical characteristics, the amount of perioperative bleeding and blood product transfusion, results of laboratory assays, and postoperative outcomes (30-day follow-up or until discharge), with the aim to assess our current practice, and develop an algorithm-based approach for the administration of targeted blood product and pro-coagulant therapies. Our goals are: the reduction of blood product utilization, the reduction of the incidence of massive bleeding and postoperative thrombosis.

Condition or Disease Intervention/Treatment Phase
  • Other: Discarded blood samples
  • Other: Discarded Urine Sample

Study Design

Study Type:
Observational
Actual Enrollment :
200 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Evaluation of Coagulation Testing in Patients Undergoing Cardiac Surgery
Actual Study Start Date :
Apr 1, 2015
Actual Primary Completion Date :
Jul 1, 2017
Anticipated Study Completion Date :
Dec 1, 2022

Outcome Measures

Primary Outcome Measures

  1. Evaluate newer technologies for coagulation diagnostics with the aim to standardize bleeding management in high risk cardiac patients [1 year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Neonates and infant patients (0 -12 months of age) undergoing complex cardiac surgical procedures

  • cardiac surgery patient > 12 months of age who has previously undergone 2 or more sternotomies

Exclusion Criteria:
  • child in a moribund condition (American Society of Anesthesiology (ASA 5)

  • children with a hematological and/or oncological disease

  • Jehovah witnesses

  • If the child is only undergoing a patent ductus arteriosus (PDA) ligation or other procedures not considered at risk for thrombosis and/or bleeding or they do not provide consent for enrollment (e.g. Ventricular Septal Defect repair)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Boston Children's Hospital Boston Massachusetts United States 02115

Sponsors and Collaborators

  • Boston Children's Hospital

Investigators

  • Principal Investigator: Juan Ibla, MD, Boston Children's Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Juan Ibla, Cardiac Anesthesiologist, Boston Children's Hospital
ClinicalTrials.gov Identifier:
NCT02410473
Other Study ID Numbers:
  • P00016625
First Posted:
Apr 7, 2015
Last Update Posted:
May 12, 2022
Last Verified:
May 1, 2022
Keywords provided by Juan Ibla, Cardiac Anesthesiologist, Boston Children's Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 12, 2022