Assessing Changes in Myocardial Tissue and Blood in Patients With Advanced Heart Disease

Purpose

Hypothesis: Tissue and serum samples collected from end-stage heart failure patients receiving left ventricular assist device implantation (LVAD) or heart transplantation will provide information regarding the basic science of heart disease. Tissue and serum samples collected from a limited numbers of "healthy controls" (donor grafts that were not utilized for heart transplantation) will serve as a comparator in research database projects. Design: This is a registry project; there are no investigational treatments, drug or procedures associated with participation in registry activities. This project is an organized functional data and tissue data gathering and storing (database) endeavor with specific focus on the functional, structural, and molecular aspects of heart failure. Data collection will not immediately influence the course of treatment for any patient.

Condition

  • Congestive Heart Failure

Eligibility

Eligible Ages
Over 13 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • >18 years of age diagnosed with heart failure undergoing either LVAD implantation or heart transplantation - 13 to 18 years of age, specifically, older children with heart failure whose body mass index is large enough to accommodate and LVAD

Exclusion Criteria

  • Neither patient nor patient representative understands spoken English - Neither patient nor patient's personal representative is willing to give written consent for participation.

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Advanced Heart Failure Therapy Group Patients diagnosed with end stage heart failure undergoing either VAD implantation or heart transplantation.
Normal Hearts Group Control samples will be obtained from individuals undergoing other types of cardiac surgery during which it is routine to discard some tissue intraoperatively.

Recruiting Locations

Intermountain Medical Center
Murray, Utah 84157
Contact:
Abdallah Kfoury, M.D.
801-507-7000
a.kfoury@imail.org

University of Utah Health Sciences Center
Salt Lake City, Utah 84132
Contact:
Stavros Drakos, M.D, Ph.D
801-585-2340
stavros.drakos@hsc.utah.edu

VA Salt Lake City Health Care System
Salt Lake City, Utah 84148
Contact:
Stavros Drakos, M.D, Ph.D
801-585-2340
stavros.drakos@hsc.utah.edu

More Details

Status
Recruiting
Sponsor
University of Utah

Study Contact

John Kirk
801-585-2944
john.kirk@hsc.utah.edu

Detailed Description

Brief description of procedures: After informed consent is obtained from the patient, the blood samples will be obtained either during a procedure from access lines inserted for the procedure or they will be drawn when other ordered lab work is done at specific time points during the study. Tissue samples will be obtained at the time of LVAD implantation by keeping the part of the left ventricular apex that the surgeon is removing in order to place the inflow cannula of the LVAD. No extra tissue sample, other than the tissue that has to be removed as a part of a standard LVAD, will be collected.