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Long-term post-transplantation outcomes in patients with hypertrophic cardiomyopathy: Single-center 35-year
Matylda Mazur1, Geetha Bhat1, Eric Popjes1
1Heart and Vascular Institute, Pennsylvania State Health Milton S. Hershey Medical Center, Hershey, Pennsylvania, USA.
Insights
Heart transplantation (HT) outcomes for hypertrophic cardiomyopathy (HCM) patients are favorable long-term. Despite a more challenging initial recovery, HCM individuals experience similar survival and freedom from rejection as other cardiomyopathy groups.
Area of Science:
- Cardiology
- Transplantation Medicine
- Cardiovascular Surgery
Background:
- Heart transplantation (HT) is a critical treatment for end-stage heart failure and hypertrophic cardiomyopathy (HCM) unresponsive to medical therapy.
- Long-term outcomes following HT in patients with HCM are not well-documented.
Purpose of the Study:
- To evaluate and compare the long-term outcomes of heart transplantation in adult patients with hypertrophic cardiomyopathy (HCM) versus those with ischemic or dilated cardiomyopathy.
- To assess survival rates, allograft rejection, cardiac allograft vasculopathy (CAV), and need for post-transplant support.
Main Methods:
- A retrospective analysis of 319 adult patients who underwent HT between 1984 and 2019.
- Comparison of outcomes among 24 HCM patients, 160 ischemic cardiomyopathy patients, and 135 dilated cardiomyopathy patients.
- Follow-up included monitoring for rejection, CAV, death, re-transplantation, and immediate post-HT support requirements.
Main Results:
- The 10-year survival rate was comparable across groups (67% HCM, 62% ischemic, 69% dilated; p=0.04).
- HCM patients required more prolonged inotropic support (37%), mechanical circulatory support (45%), and renal replacement therapy (55%) immediately post-HT.
- No significant differences were observed in 10-year freedom from acute rejection (38%) or CAV (88%) among the groups.
Conclusions:
- Adult patients with HCM have a favorable long-term prognosis after heart transplantation.
- The immediate post-transplant period for HCM patients is more complex, requiring intensive support.
- Long-term graft survival and rejection rates are similar to other common cardiomyopathy indications for HT.
Background:
Heart transplantation (HT) is the only option for most patients with end-stage heart failure and hypertrophic cardiomyopathy (HCM) who fail medical therapy. Data on the long-term outcomes post-transplant in HCM individuals remain scarce.
Methods:
We analyzed data of 319 adult patients who underwent HT between 1984 and 2019. Patients were followed for cardiac allograft rejection, cardiac allograft vasculopathy (CAV), death, or re-transplantation.
Results:
Outcomes of 24 patients with HCM, 160 with ischemic, and 135 with dilated cardiomyopathy were compared. During a mean follow-up of 11.6 ± 7.2 (max 27.8), 16.7 ± 8.2 (max 32.7), and 16.1 ± 9.7 (max 34.6) years after HT in hypertrophic, ischemic, and dilated cardiomyopathy groups, respectively: 10-year survival rate was 67%, 62%, 69%, respectively (p = .04). Post-transplantation, HCM individuals more often than the other two studied groups required prolonged inotropic support (37%, 12%, 17%, respectively, p = .02), temporary mechanical circulatory support (45%, 13%, 14%, respectively, p < .01), and renal replacement therapy immediately post-HT (55%, 19%, 24%, respectively, p < .01). No significant inter-group differences were noted in the 10-year freedom from acute allograft rejection (38%, 46%, 43%, respectively, p = .38) or 10-year freedom from CAV (88%, 78%, 81%, respectively, p = .57).
Conclusions:
The long-term post-transplant prognosis of adult patients with hypertrophic cardiomyopathy is favorable despite more challenging immediate post-HT course.
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