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Completed

NCT Number: NCT02376387

Evidence Based Evaluation and Acceptance of Donor Hearts for Transplantation

The proposed research will provide evidence-based strategies for the evaluation and acceptance of donor hearts for transplantation. This is relevant to public health because judicious expansion of donor hearts used for transplantation will make this life-saving procedure available to a larger number of patients living with end-stage heart disease.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Donor Network of Arizona, Phoenix, Arizona, United States

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About this study

The demand for donor hearts for transplantation far outstrips the supply; however, only one in three available cardiac grafts are used for transplantation. There are many reasons for graft non-use, but previous studies have failed to demonstrate consistent associations between donor characteristics, donor cardiac function, and adverse recipient outcomes. Thus, there is a critical need to standardize how cardiac allografts are evaluated and accepted for transplantation. The investigators long-term goal is to safely expand the use of available cardiac allografts without adversely affecting transplant recipient outcomes. The investigators propose to carefully characterize the current population of cardiac organ donors, particularly with regards to allograft function; to examine how decisions are made regarding graft acceptance for transplantation; and to systematically evaluate associations between donor characteristics and recipient outcomes. The investigators central hypothesis is that acceptable allografts for heart transplantation are being unnecessarily discarded, and the establishment of an evidence-based process for cardiac donor evaluation and acceptance will increase graft utilization rates while maintaining excellent clinical outcomes. In response to this need, the investigators propose a collaborative study with seven organ procurement organizations representing geographically diverse regions of the United States, to address the following specific aims: (1) To identify clinical correlates of graft function in potential donors being evaluated for heart transplantation. An existing online donor research database will be expanded for standardized collection of data on detailed donor characteristics, especially as pertains to cardiac allograft function. The investigators will perform expert core review of donor echocardiograms, including serial echocardiograms in donors with cardiac allograft dysfunction. Serial electrocardiograms and cardiac biomarkers (Troponin I and B-type natriuretic peptide) will also be studied; (2) To prospectively study reasons for cardiac allograft non-utilization for heart transplantation. Real-time data will be collected on specific reasons for allograft non-acceptance for transplantation in order to study graft acceptance practices and variation in graft utilization nationwide; and (3) To prospectively study associations between donor characteristics and recipient outcomes after heart transplantation. Data will be collected on recipient post-transplant length of hospitalization and survival to identify associations between donor predictors and recipient outcomes. This proposal is innovative because it focuses on an entirely different approach to donor-based research, thereby surmounting the limitations of prior investigations. Completion of the proposed study will have a positive impact by defining how to optimize the evaluation and use of available grafts for heart transplantation, thereby safely expanding the donor pool and increasing the number of heart transplants performed nationwide.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Brain dead (beating heart)
  • 18-65 years of age
  • HIV (-)
  • Donors authorized for research

Exclusion criteria

  • Donors not authorized for research
  • HIV (+)

Treatment and study plan

Primary outcomes

  1. Donor left ventricular ejection fraction, troponin, BNP, EKG changes (arrhythmias, QT prolongation, repolarization abnormalities, LVH, Q waves)

    Time frame: 5 years

    To identify clinical correlates of cardiac function in potential donors being evaluated for heart transplantation.

  2. Identify decline codes for donor hearts not accepted for transplant

    Time frame: 5 years

    To prospectively study reasons for non-acceptance of hearts offered for transplantation.

  3. Create a statistical tools (e.g. risk prediction model) for donor heart acceptance

    Time frame: 5 years

    To develop clinical tools to assist transplant centers with real-time decisions regarding donor heart acceptance.

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Collaborators

  • California Transplant Donor Network
  • Donor Network of Arizona
  • Gift of Hope
  • Gift of Life
  • Kaiser Permanente
  • Life Gift Organ Donation
  • LifeLink
  • National Institutes of Health (NIH)
  • New England Organ Bank
  • Oregon Health and Science University

Registry information

Acronym: DHS

Important dates

Study start
2015
Primary completion
2020
Study completion
2020
First posted
Mar 3, 2015
Registry last updated
Oct 21, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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