Amyloid cardiomyopathy (ACM) is an infiltrative disease, with the majority of cases attributable to aggregation of immunoglobulin light chains (AL) or misfolded transthyretin (ATTR). Due to enhanced, noninvasive diagnostic approaches and recently available therapeutic agents, clinicians are increasingly seeking, and making, the diagnosis of ACM.
Despite these advancements, however, some patients with ACM will progress to advanced heart failure or be diagnosed late in their disease course. Heart transplantation is an available option for highly selected patients with advanced ACM, but some patients may be too ill to wait for a donor; others may simply not be good candidates for heart transplantation. For such patients, mechanical circulatory support devices (MCSDs) are a consideration, but prior studies of their use in these patients have been limited to smaller populations with limited generalizability.