Ex Situ Left Ventricular Pressure-Volume Loop Analyses for Donor Hearts: Proof of Concept in an Ovine Experimental

I A Ertugrul1, R A D A Puspitarani2, B Wijntjes3

  • 1Department of Cardiothoracic Surgery, University Medical Centre Groningen, University of Groningen, Groningen, Netherlands.

Insights

A new pressure-volume loop system accurately assesses left ventricular function during ex situ heart perfusion (ESHP). This method offers improved graft selection for donation after brain death (DBD) and donation after circulatory death (DCD) donor hearts.

Area of Science:

  • Cardiology
  • Transplantation Medicine
  • Physiology

Background:

  • Ex situ heart perfusion (ESHP) is crucial for preserving donor hearts from both brain death (DBD) and circulatory death (DCD) donors.
  • Current viability assessment relies on biochemical markers, lacking a reliable method for evaluating graft function in a working state.
  • Functional assessment during ESHP is critical for predicting post-transplantation outcomes.

Purpose of the Study:

  • To evaluate a novel pressure-volume loop analysis system for assessing left ventricular function during normothermic ESHP.
  • To introduce a method for real-time functional graft assessment in a physiologic working mode.

Main Methods:

  • Ovine hearts underwent functional evaluation using a novel pressure-volume loop system during normothermic ESHP.
  • The system provided adjustable preload and afterload to the left ventricle.
  • Left ventricular function was assessed by measuring end-systolic elastance at varying preloads.

Main Results:

  • The novel pressure-volume loop system successfully assessed ovine left ventricular function during ESHP.
  • End-systolic elastance values were recorded at 60 minutes (2.8 ± 1.8 mmHg/mL) and 120 minutes (2.7 ± 0.7 mmHg/mL).

Conclusions:

  • A novel method using ex situ pressure-volume loop analysis for functional graft assessment during ESHP has been demonstrated.
  • This validated pressure-volume assessment technique could enhance graft selection for both DBD and DCD donor hearts.

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