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Updated: Feb 22, 2026

Implantation of the Syncardia Total Artificial Heart
Published on: July 18, 2014
Experience with the SynCardia total artificial heart in a Canadian centre
Anthony Nguyen1, Michel Pellerin1, Louis P Perrault1
1From the Department of Cardiac Surgery, Montreal Heart Institute and Université de Montréal, Montreal, Que. (Nguyen, Pellerin, Perrault, Carrier); and the Department of Medicine, Montreal Heart Institute and Université de Montréal, Montreal, Que. (White, Ducharme, Racine).
Insights
The SynCardia total artificial heart (TAH) offers a vital option for patients awaiting heart transplants, demonstrating a low rate of neurological complications. This TAH therapy supports critically ill individuals with complex conditions.
Area of Science:
- Cardiology
- Medical Devices
- Surgical Innovation
Background:
- The SynCardia total artificial heart (TAH) is a device for complete circulatory support, replacing native ventricles.
- Indications include bridge to transplantation and destination therapy.
- This review examines TAH implantation experiences alongside the availability of axial flow pumps.
Purpose of the Study:
- To review the clinical experience with SynCardia total artificial heart (TAH) implantation.
- To evaluate patient outcomes and survival during a specific period of TAH use.
Main Methods:
- Retrospective analysis of patient demographics and clinical characteristics.
- Evaluation of survival data for all patients who received a TAH.
Main Results:
- 13 patients received TAH for refractory cardiogenic shock; mean ejection fraction was 14%.
- Survival on support was 77% at 30 days; 77% survived to transplantation after a mean of 52 days.
- Complications included stroke (8%), ARDS (38%), and renal failure (38%).
Conclusions:
- TAH is a viable option for extremely fragile patients awaiting heart transplantation, with a low incidence of neurologic events.
- Complex and unusual patient anatomy influenced the utilization of TAH.
Background:
The SynCardia total artificial heart (TAH) provides complete circulatory support by replacing both native ventricles. Accepted indications include bridge to transplantation and destination therapy. We review our experience with TAH implantation during a period when axial flow pump became available.
Methods:
We retrospectively analyzed the demographics, clinical characteristics and survival of all patients receiving the TAH.
Results:
From September 2004 to November 2016, 13 patients (12 men, mean age 45 ± 13 yr) received the TAH for refractory cardiogenic shock secondary to idiopathic (56%) or ischemic (17%) cardiomyopathy and to other various causes (33%). Before implantation, mean ejection fraction was 14% ± 4%, 7 (54%) patients had previous cardiac surgery, 4 (31%) were on mechanical ventilation, and 3 (23%) patients were on dialysis. The mean duration of TAH support was 46 ± 40 days. Three (23%) patients died while on support after a mean of 15 days. Actuarial survival on support was 77% ± 12% at 30 days after implantation. Complications on support included stroke (n = 1, 8%), acute respiratory distress syndrome requiring prolonged intubation (n = 5, 38%) and acute renal failure requiring temporary dialysis (n = 5, 38%). Ten (77%) patients survived to be transplanted after a mean of 52 ± 42 days of support. Actuarial survival rates after transplant were 67% ± 16% at 1 month and 56% ± 17% at 1 year after transplantation.
Conclusion:
The TAH provides an alternative with low incidence of neurologic events in extremely fragile and complex patients waiting for heart transplantation. Complex and unusual anatomic conditions explained the current use of TAH.
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