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Published on: May 10, 2022
Mechanical circulatory support for cardiac amyloidosis
Michelle M Kittleson1, Robert M Cole1, Jignesh Patel1
1Cedars-Sinai Medical Center, Smidt Heart Institute, Los Angeles, California.
Mechanical circulatory support (MCS) can be a viable bridge to heart transplantation (HTx) for patients with cardiac amyloidosis. This study found durable biventricular MCS feasible with acceptable outcomes in carefully selected amyloid cardiomyopathy patients.
Area of Science:
- Cardiology
- Cardiovascular Surgery
- Transplantation Medicine
Background:
- Cardiac amyloidosis, caused by abnormal AL or ATTR amyloid protein deposition, frequently leads to heart failure.
- Heart failure in cardiac amyloidosis often necessitates heart transplantation (HTx).
- The efficacy of mechanical circulatory support (MCS) in managing cardiac amyloidosis remains unclear.
Purpose of the Study:
- To evaluate the use and outcomes of MCS in patients with cardiac amyloidosis.
- To present institutional experience with MCS as a bridge to HTx for cardiac amyloidosis.
Main Methods:
- A retrospective review of consecutive cardiac amyloidosis patients who received MCS between 2010 and 2018.
- Comparison of clinical characteristics and outcomes between the MCS-Amyloid group and a matched control group (MCS-No Amyloid) at a 2:1 ratio.
- Analysis of patient demographics, INTERMACS Profile, and survival rates.
Main Results:
- 11 patients with cardiac amyloidosis received durable MCS, primarily total artificial hearts (9) or paracorporeal biventricular assist devices (2).
- Within one year, 82% of the MCS-Amyloid group were transplanted, with 18% mortality.
- In the control group, 36% were transplanted, 46% died, and 18% remained on MCS at one year.
Conclusions:
- Durable biventricular MCS is a feasible treatment option for carefully selected patients with amyloid cardiomyopathy.
- MCS can provide acceptable outcomes as a bridge to heart transplantation in this patient population.
- This approach demonstrates potential for improving survival in advanced cardiac amyloidosis.
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