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American Heart Association

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Final ID: MP1021

The Association Between Cardiac Resynchronization Therapy and Survival in Patients with Cardiac Amyloidosis: A Multicenter Retrospective Study.

Abstract Body (Do not enter title and authors here): Background: Cardiac amyloidosis (CA) patients with reduced left ventricular ejection fraction (EF) are at increased risk for mortality. The benefit of cardiac resynchronization therapy (CRT) in terms of mortality reduction has not been established in this population.
Aim: To evaluate the survival benefit of CRT, either CRT-D or CRT-P, in a large cohort of patients with cardiac amyloidosis and reduced EF.
Methods: We retrospectively analyzed patients with confirmed CA and reduced EF (<40%) between 2009 and 2023 across Mayo Clinic sites. Patients were stratified into three groups: no device, CRT with pacemaker function (CRT-P), and CRT with defibrillator function (CRT-D). CRT devices were indicated for low ejection fraction less than 40% and patients who had chronic heart failure with a wide QRS. Kaplan-Meier survival estimates were generated, and log-rank tests were used for comparison. A secondary analysis was conducted combining CRT-P and CRT-D versus no device (EF <40%), and a tertiary analysis compared CRT-P versus CRT-D.
Results: Among 184 patients [36 AL (20%), 148 ATTR (80%)], 38 (19%) had no cardiac device and EF <40%, 20 (11%) received CRT-P, and 116 (63%) received CRT-D. The median follow-up was 3.4 years (1.7, 5.0). The probability of survival was significantly higher in the CRT group compared to the no device-EF<40 group (Log Rank p=0.013; figure B). Among patients receiving CRT, there was no significant difference in all-cause mortality between those receiving CRT-P and those receiving CRT-D (Log Rank p=0.5; figure C).
Conclusion: In patients with cardiac amyloidosis and reduced EF, CRT is associated with significantly improved survival compared to no device. No mortality difference was observed between CRT-P and CRT-D. Prospective studies are warranted.
  • Raslan, M. Alaa  ( Mayo Clinic , Lansing , Michigan , United States )
  • Jamal, Fares  ( Mayo Clinic Arizona , Scottsdale , Arizona , United States )
  • Youssef, Amal  ( Mayo Clinic Arizona , Scottsdale , Arizona , United States )
  • Abdul Nabi, Hussein  ( Mayo Clinic Arizona , Phoenix , Arizona , United States )
  • Abbas, Mohammed Tiseer  ( Mayo Clinic Arizona , Phoenix , Arizona , United States )
  • Abdalla, Hesham  ( Mayo Clinic Arizona , Scottsdale , Arizona , United States )
  • Baqal, Omar  ( Mayo Clinic , Phoenix , Arizona , United States )
  • El Masry, Hicham  ( Mayo CLinic AZ , Phoenix , Arizona , United States )
  • Author Disclosures:
    M. Alaa Raslan: DO NOT have relevant financial relationships | Fares Jamal: DO NOT have relevant financial relationships | Amal Youssef: DO NOT have relevant financial relationships | Hussein Abdul Nabi: DO NOT have relevant financial relationships | Mohammed Tiseer Abbas: DO NOT have relevant financial relationships | Hesham Abdalla: No Answer | Omar Baqal: DO NOT have relevant financial relationships | Hicham El Masry: No Answer
Meeting Info:

Scientific Sessions 2025

2025

New Orleans, Louisiana

Session Info:

Arrhythmic Risks in Infiltrative Cardiomyopathy: Pathophysiology and Management

Saturday, 11/08/2025 , 03:15PM - 04:30PM

Moderated Digital Poster Session

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