Atrial and ventricular arrhythmias in patients with cardiac amyloidosis: Incidence, risk factors, and prognostic implications
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Published on: July 25, 2019
Jason Z Li1, Connor P Oates2, Meredith Njus1
1MedStar Heart and Vascular Institute, MedStar Washington Hospital Center, Washington, DC, USA; MedStar Georgetown University Hospital, Washington, DC, USA.
Insights
Arrhythmias are common in cardiac amyloidosis (CA), particularly atrial fibrillation and flutter in ATTR-CA. Sustained ventricular tachycardia in CA increases mortality risk, but implantable cardioverter-defibrillator (ICD) therapy did not improve survival.
Area of Science:
- Cardiology
- Electrophysiology
- Cardiovascular Disease
Background:
- Cardiac amyloidosis (CA) poses significant risks for arrhythmias, with poorly understood prognostic implications.
- The role of implantable cardioverter-defibrillators (ICDs) in managing CA-related arrhythmias remains unclear.
Purpose of the Study:
- To investigate the risk factors, prognostic implications, and outcomes of arrhythmias in patients with cardiac amyloidosis.
- To evaluate the effectiveness of ICD therapy in patients with CA.
Main Methods:
- A retrospective analysis of 186 patients diagnosed with or referred for cardiac amyloidosis between February 2010 and April 2023.
- Assessment of arrhythmia incidence, risk factors for ventricular tachycardia, and survival outcomes in relation to ICD implantation.
Main Results:
- Atrial fibrillation (61.8%) and atrial flutter (24.7%) were common, especially in ATTR-CA. Sustained ventricular tachycardia (VT) occurred in 6.5% of CA patients.
- QRS duration >120 ms and increased left ventricular end-diastolic diameter were associated with VT development.
- Sustained VT independently predicted increased mortality, while ICD implantation did not significantly improve survival.
Conclusions:
- Atrial and ventricular arrhythmias are prevalent in cardiac amyloidosis.
- Adverse electrical and structural remodeling contribute to sustained VT, a significant predictor of mortality in CA.
- Current evidence suggests ICD therapy may not improve survival in this patient population.
Background:
The risk factors for developing arrhythmias, prognostic implications, and value of implantable cardioverter defibrillators (ICD) are poorly understood in patients with cardiac amyloidosis (CA).
Methods:
A single-center retrospective analysis was performed of consecutive patients diagnosed with or referred for cardiac amyloidosis at our center from 2/2010-4/2023.
Results:
A total of 186 patients were diagnosed with CA (AL-CA: 18.3%; ATTR-CA: 81.2%). Atrial fibrillation (AF) occurred in 61.8%, atrial flutter (AFL) in 24.7%, and sustained ventricular tachycardia (VT) in 6.5% of patients with CA. AF and AFL occurred more commonly in patients with ATTR-CA than AL-CA (AF: 66.9% vs 38.2%; p = 0.002; AFL: 28.5% vs 8.8%; p = 0.017). On univariate analysis, QRS duration >120 ms (OR 4.22; 95% CI 1.21-14.64; p = 0.023) and left ventricular end diastolic diameter (OR 3.94; 95% CI 1.45-10.66; p = 0.007) were associated with the development of sustained VT in patients with CA. Incidence of sustained VT in patients with CA was independently associated with increased risk of mortality (HR 2.22; 95% CI 1.10-4.50; p = 0.027), however, ICD implantation was not associated with improved survival (HR 0.59; 95% CI 0.32-1.08; p = 0.090).
Conclusion:
Atrial and ventricular arrhythmias are common in CA. Characteristics of adverse electrical and structural remodeling are associated with the development of sustained VT, which was independently associated with increased mortality in this population. ICD therapy was not associated with improved survival.
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