Key result
Beta-blocker intolerance in cardiac AL amyloidosis is linked to advanced disease and poorer survival.
Why the study?
The utilization and clinical impact of beta-blockers in cardiac amyloidosis were largely unexplored.
Does beta-blocker tolerance affect survival in patients with AL cardiac amyloidosis?
Cohort (n=236)
No
Does beta-blocker tolerance affect survival in patients with AL cardiac amyloidosis?
Beta-blocker use is uncommon in AL cardiac amyloidosis, and intolerance is driven by advanced disease and associated with poorer survival.
Supports cautious beta-blocker assessment in cardiac AL amyloidosis; hypothesis-generating for prognostic impact and prospective trials.
BACKGROUND: The utilization and clinical impact of beta-blockers (BBs) in cardiac amyloidosis (CA) is largely unexplored. METHODS: We conducted a retrospective, single-center analysis of indications, timing of initiation, types and doses of BB used, reasons to discontinue BB and association between BB tolerance and outcomes in a cohort of patients with immunoglobulin light chain amyloidosis (AL). RESULTS: We reviewed 236 patients with AL CA and identified 53 patients taking BB (22.5%). Most patients presented in New York Heart Association Class (NYHA) II or III (74.5%) and 24% presented in Mayo stage IIIB. The most frequent indications for BB initiation were atrial fibrillation (AF) and coronary artery disease (CAD). In most cases (59%) BB was started before the diagnosis of CA. The median duration of BB treatment was 9 months (interquartile range [IQR] 3-24 months). Among patients receiving BB, 28 tolerated BB during follow-up whereas 25 patients discontinued BB. The main causes of BB discontinuation were hypotension and heart failure (HF) exacerbation. Patients intolerant to BB presented with more advanced NYHA class, worse performance status and lower median left ventricular ejection fraction (LVEF) at baseline. At median follow-up duration of 17.7 months, patients who did not tolerate BB had a poor survival. CONCLUSIONS: Although some patients with CA may have indications for treatment with BB, their use is uncommon and those with more advanced disease tolerate BB poorly. Intolerance to BB in patients with cardiac AL is an indicator of poorer outcome.
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Briasoulis et al. (2021) conducted a cohort in Immunoglobulin light chain (AL) cardiac amyloidosis (n=236). Beta-blocker intolerance (discontinuation) vs. Beta-blocker tolerance was evaluated on Survival. Beta-blocker use is uncommon (22.5%) in cardiac AL amyloidosis, and intolerance to beta-blockers is associated with more advanced disease and poorer survival.
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