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Development of a cardiac loading device to monitor cardiac function during ex vivo graft perfusion
Emilie Farine1, Manuel U Egle1, Alice C Boone1
1Department of Cardiovascular Surgery, Inselspital, Bern University Hospital, Bern, Switzerland.
Insights
A new cardiac loading device allows for reliable measurement of myocardial function in ex vivo perfused hearts. This innovation enables better assessment of donor heart viability before transplantation.
Area of Science:
- Cardiovascular Research
- Biomedical Engineering
- Transplantation Science
Background:
- Ex vivo heart perfusion limits donor heart ischemic time.
- Current systems perfuse hearts in an unloaded state, preventing functional assessment.
- Reliable evaluation of cardiac contractile function is crucial for transplantation.
Purpose of the Study:
- Develop a ventricular loading device for ex vivo heart perfusion systems.
- Enable monitoring of myocardial function during perfusion.
- Create a prototype for rat experimentation.
Main Methods:
- Designed a device with ventricular and reservoir balloons and an electronic check valve.
- Characterized balloon properties and pressure-volume relationships.
- Evaluated the device using a mock ventricle and ex vivo perfused rat hearts.
Main Results:
- Consistent balloon production with maintained properties.
- Device demonstrated appropriate function in vitro and ex vivo.
- Measured hemodynamic function compared favorably to isolated working heart preparations.
Conclusions:
- The cardiac loading device reliably measures left ventricular hemodynamic parameters.
- The device allows for controlled ventricular loading.
- This technology enhances functional assessment of ex vivo perfused hearts.
Background:
Ex vivo heart perfusion systems, allowing continuous perfusion of the coronary vasculature, have recently been introduced to limit ischemic time of donor hearts prior to transplantation. Hearts are, however, perfused in an unloaded manner (via the aorta) and therefore, cardiac contractile function cannot be reliably evaluated.
Objectives:
We aim to develop a ventricular loading device that enables monitoring of myocardial function in an ex vivo perfusion system. In this initial study, was to develop a prototype for rat experimentation.
Methods:
We designed a device consisting of a ventricular balloon and a reservoir balloon, connected through an electronic check valve, which opens and closes in coordination with changes in ventricular pressure. All balloons were produced in our laboratory and their properties, particularly pressure-volume relationships, were characterized. We developed a mock ventricle in vitro test system to evaluate the device, which was ultimately tested in ex vivo perfused rat hearts.
Results:
Balloon production was consistent and balloon properties were maintained over time and with use on the device. Results from in vitro and ex vivo experiments show that the device functions appropriately; hemodynamic function can be measured and compares well to measurements made in an isolated, working (loaded) rat heart preparation.
Conclusions:
Our cardiac loading device appears to reliably allow measurement of several left ventricular hemodynamic parameters and provides the opportunity to control ventricular load.
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