Related Experiment Video
Updated: May 7, 2026

Utilizing Percutaneous Ventricular Assist Devices in Acute Myocardial Infarction Complicated by Cardiogenic Shock
Published on: June 12, 2021
Pediatric Mechanical Support with an External Cardiac Compression Device
Minoo N Kavarana1, Howard M Loree, Robert B Stewart
1Department of Surgery, Medical University of South Carolina, Charleston, SC, 29425, USA.
Insights
The PediBooster, a novel pediatric cardiac support device, shows promise in stabilizing acute right ventricular dysfunction. Further research is needed to optimize its design for improved ventricular filling during support.
Area of Science:
- Biomedical Engineering
- Pediatric Cardiology
- Medical Devices
Background:
- Acute Postcardiotomy Shock (PCS) presents a critical challenge in pediatric cardiac surgery.
- Existing treatments for PCS have limitations, necessitating novel therapeutic approaches.
- Biventricular Assist Devices (BiVAD) offer potential for hemodynamic support in pediatric patients.
Purpose of the Study:
- To evaluate the feasibility and efficacy of the PediBooster, a novel pediatric external cardiac compression device.
- To assess the PediBooster's performance in a porcine model of acute right ventricular dysfunction.
- To determine the stability and functional outcomes of the PediBooster in supporting pediatric hearts.
Main Methods:
- Development and testing of the PediBooster extracardiac wrap with a novel hydrogel coating.
- Utilized a porcine model (5.1 ± 0.3 kg) with induced acute right ventricular dysfunction via ASD and PA banding.
- Collected hemodynamic data, transesophageal echocardiography (TEE), video recordings, and cardiac histology over 2-16 hour support durations.
Main Results:
- The PediBooster demonstrated stable support for up to 16 hours in the pediatric model.
- TEE and video data confirmed good attachment and function of the wrap.
- Wrap-induced end-diastolic restriction was observed in 3 out of 4 animals, indicating a need for design optimization.
Conclusions:
- The PediBooster shows potential as a palliative therapy for pediatric Postcardiotomy Shock.
- The developed congenital heart disease model is suitable for further chronic studies.
- Adjusting wrap dimensions may improve ventricular filling and mitigate restriction during PediBooster support.
Abstract:
The PediBooster external cardiac compression device is a minimally invasive, non-blood contacting Biventricular Assist Device (BiVAD) intended for pediatric use. It is being developed as a palliative therapy for acute Postcardiotomy Shock (PCS). The PediBooster extracardiac wrap is pneumatically actuated to circumferentially compress the heart, providing co-pulsation support. Attachment is via a novel hydrogel coating. Early versions of the wrap were tested in vivo using a single ventricle congenital heart disease model with postcardiotomy shock, which proved unstable and demonstrated high peri-operative mortality. The final wrap design was tested in 4 acute studies with piglets (5.1 ± 0.3 kg), where the combination of ASD and PA banding induced acute right ventricular dysfunction. Data collected included routine hemodynamic values, TEE, video of the exposed heart, and cardiac histology. The model proved stable for support durations ranging from 2 to 16 hours. The wrap restricted the heart in 3 of the 4 animals, as evidenced by increased diastolic LVP during support compared to the baseline failure condition. TEE and video data showed good attachment and function of the wrap, particularly during the final 16 hr study. This model of congenital heart disease shows promise for chronic (24-72 hr) studies. Ventricular filling during support may be improved by adjusting wrap dimensions to eliminate end diastolic restriction.
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