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Use of Two Intracorporeal Ventricular Assist Devices As a Total Artificial Heart
Published on: May 11, 2018
Ventricular assist device support as a bridge to heart transplantation in patients with giant cell myocarditis
Lindsay K Murray1, Jose González-Costello, Samual N Jonas
1Department of Medicine, Columbia University, New York, NY 10032, USA.
Insights
Ventricular assist devices (VADs) offer a viable bridge to heart transplantation for patients with end-stage giant cell myocarditis (GCM). This approach leads to good survival rates post-transplant, though careful immunosuppression is needed.
Area of Science:
- Cardiology
- Transplantation Immunology
Background:
- Giant cell myocarditis (GCM) is a severe heart condition with a poor prognosis.
- Many GCM patients require advanced therapies like heart transplantation.
Purpose of the Study:
- To evaluate the effectiveness of ventricular assist devices (VADs) as a bridge to orthotopic heart transplantation (OHT) for GCM patients.
- To assess the long-term outcomes of GCM patients undergoing VAD support and subsequent OHT.
Main Methods:
- Retrospective analysis of GCM patients who received VADs.
- Diagnosis confirmed via endomyocardial or explanted heart biopsy.
- Six patients received VADs (biventricular or LVAD) and were bridged to OHT.
Main Results:
- Four of six VAD-supported patients were successfully bridged to OHT and remain alive with a mean follow-up of 5.7 years.
- Two patients died while on VAD support.
- Post-OHT, two patients experienced recurrent GCM (treated with immunosuppression), and three had high-grade rejection. Cardiac function was preserved in all survivors.
Conclusions:
- VADs can successfully bridge patients with end-stage GCM to OHT, resulting in favorable post-transplant survival.
- Further research is needed to optimize immunosuppressive strategies to manage rejection and GCM recurrence post-OHT.
Aims:
Giant cell myocarditis (GCM) carries a poor prognosis and many patients require end-stage therapies. This study sought to determine the outcome of patients bridged with ventricular assist devices (VAD) to orthotopic heart transplantation (OHT).
Methods And Results:
A retrospective data collection of all patients with GCM was performed. Diagnosis was determined by endomyocardial or explanted heart biopsy. Eight patients were found, but two of those patients went directly to OHT and were excluded. The remaining six patients received VADs, and these patients, aged 44 ± 18 years, were included. Five of the six patients were bridged with biventricular support and one patient was supported by left ventricular assist device (LVAD) alone. Two patients died on device support. Four patients were bridged to OHT 77 ± 42 days after device implantation. All four patients bridged with a VAD are alive, with a mean follow-up of 5.7 ± 4.1 years. Two patients were found to have recurrent GCM in the transplanted heart and were treated successfully with immunosuppression. Three patients had high grade (2R) rejection at 66 ± 52 days post-OHT. Cardiac function was preserved in all patients, and only one patient had cardiac allograft vasculopathy.
Conclusion:
Patients with end-stage GCM can be successfully bridged with VADs to OHT with very good post-OHT survival. The proper immunosuppressive regimen for this group needs further investigation given the frequency of rejection and GCM recurrence.
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