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Updated: Nov 23, 2025

Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
Heart Transplantation for Giant Cell Myocarditis: A Case Series.
Gaurang Nandkishor Vaidya1, Lawrence S C Czer1, Daniel Luthringer2
1Advanced Heart Disease and Heart Transplant Programs, Cedars-Sinai Smidt Heart Institute, Los Angeles, California.
Heart transplant offers excellent survival for giant cell myocarditis (GCM) patients. Immunosuppression with rabbit antithymocyte globulin (rATG) is key, though GCM recurrence is possible and may need intensified treatment.
Area of Science:
- Cardiology
- Transplantation Immunology
- Immunosuppression Therapy
Background:
- Giant cell myocarditis (GCM) presents a significant challenge with a poor prognosis without heart transplantation.
- Limited data exists on long-term survival outcomes following heart transplantation for GCM.
Purpose of the Study:
- To evaluate the post-transplant survival rates of patients who underwent heart transplantation for histologically confirmed GCM.
- To analyze the efficacy of perioperative and maintenance immunosuppressive regimens in GCM patients.
Main Methods:
- Retrospective analysis of seven patients with GCM undergoing heart transplantation.
- Utilized perioperative rabbit antithymocyte globulin (rATG), intravenous immunoglobulin, and early initiation of triple immunosuppressive therapy (tacrolimus, mycophenolate, prednisone).
Main Results:
- Six out of seven patients (86%) survived at a median of 842 days post-transplant.
- One patient experienced asymptomatic GCM recurrence at 3 months, successfully managed with increased immunosuppression.
- No patients experienced high-grade rejection episodes.
Conclusions:
- Heart transplantation provides excellent survival for GCM patients when combined with rATG and triple immunosuppressive therapy.
- Patients with GCM remain at risk for recurrence post-transplant, necessitating vigilant monitoring and potential augmentation of immunosuppression.
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