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A Cavopulmonary Assist Device for Long-Term Therapy of Fontan Patients
Andreas Escher1, Carsten Strauch2, Emanuel J Hubmann3
1Biofluid Mechanics Laboratory, Institute for Imaging Science and Computational Modelling in Cardiovascular Medicine, Charité-Universitätsmedizin Berlin, Berlin, Germany; Department of Cardiac Surgery, Medical University of Vienna, Vienna, Austria.
Insights
A novel cavopulmonary assist device (CPAD) shows promise for improving Fontan circulation hemodynamics. Preclinical tests demonstrate effective hydraulic performance and low power consumption, suggesting potential for implantable devices in Fontan patients.
Area of Science:
- Biomedical Engineering
- Cardiovascular Surgery
- Medical Devices
Background:
- Fontan pathway surgery is palliative, leading to declining hemodynamics due to lack of subpulmonary pressure.
- A cavopulmonary assist device (CPAD) could restore biventricular equivalency and improve Fontan patient management.
Purpose of the Study:
- To develop a functional CPAD prototype.
- To provide preclinical proof of concept for hydraulic performance, hemocompatibility, and power consumption.
Main Methods:
- Manufactured a CPAD prototype with titanium components, ceramic bearings, and electric motors.
- Assessed hydraulic performance and hemocompatibility using in-silico (CFD) and in-vitro methods.
- Measured power consumption across the device's operational range.
Main Results:
- The CPAD achieved pressure step-ups (0-50 mm Hg) across a wide flow range (0-10 L/min).
- Electric power consumption remained below 1.5 W in the main operating range.
- In-vitro hemolysis tests showed a normalized index of 3.8 ± 1.6 mg/100 L at design point.
- Demonstrated potential for low traumatic and thrombogenic support in a diverse Fontan population.
Conclusions:
- The CPAD prototype exhibits promising hydraulic performance and hemocompatibility for Fontan circulation support.
- Low power consumption supports the feasibility of a small, implantable system with transcutaneous energy transfer.
- Preclinical results warrant further in-vivo trials to confirm hemodynamic benefits.
Abstract:
Treatment of univentricular hearts remains restricted to palliative surgical corrections (Fontan pathway). The established Fontan circulation lacks a subpulmonary pressure source and is commonly accompanied by progressively declining hemodynamics. A novel cavopulmonary assist device (CPAD) may hold the potential for improved therapeutic management of Fontan patients by chronic restoration of biventricular equivalency. This study aimed at translating clinical objectives toward a functional CPAD with preclinical proof regarding hydraulic performance, hemocompatibility and electric power consumption. A prototype composed of hemocompatible titanium components, ceramic bearings, electric motors, and corresponding drive unit was manufactured for preclinical benchtop analysis: hydraulic performance in general and hemocompatibility characteristics in particular were analyzed in-silico (computational fluid dynamics) and validated in-vitro. The CPAD's power consumption was recorded across the entire operational range. The CPAD delivered pressure step-ups across a comprehensive operational range (0-10 L/min, 0-50 mm Hg) with electric power consumption below 1.5 W within the main operating range. In-vitro hemolysis experiments (N = 3) indicated a normalized index of hemolysis of 3.8 ± 1.6 mg/100 L during design point operation (2500 rpm, 4 L/min). Preclinical investigations revealed the CPAD's potential for low traumatic and thrombogenic support of a heterogeneous Fontan population (pediatric and adult) with potentially accompanying secondary disorders (e.g., elevated pulmonary vascular resistance or systemic ventricular insufficiency) at distinct physical activities. The low power consumption implied adequate settings for a small, fully implantable system with transcutaneous energy transfer. The successful preclinical proof provides the rationale for acute and chronic in-vivo trials aiming at the confirmation of laboratory findings and verification of hemodynamic benefit.
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