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Holter monitoring in AL amyloidosis: prognostic implications

G Palladini1, G Malamani, F Cò

  • 1Department of Internal Medicine and Medical Oncology, University of Pavia, Italy.

Insights

Primary (AL) amyloidosis frequently affects the heart, leading to death. Holter monitoring reveals arrhythmias like couplets, which predict survival and sudden cardiac death in these patients.

Area of Science:

  • Cardiology
  • Electrophysiology
  • Amyloidosis Research

Background:

  • Cardiac involvement is prevalent in primary (AL) amyloidosis, often causing mortality.
  • Rhythm and conduction disturbances are common terminal events in AL amyloidosis.
  • Understanding cardiac abnormalities is crucial for prognosis.

Purpose of the Study:

  • To identify Holter monitoring abnormalities in AL amyloidosis patients.
  • To evaluate the prognostic value of these Holter findings, especially for sudden death.
  • To correlate Holter data with echocardiographic findings and clinical outcomes.

Main Methods:

  • Fifty-one AL amyloidosis patients underwent comprehensive clinical evaluation, echocardiography, and 24-hour Holter monitoring.
  • Echocardiographic signs of cardiac involvement and heart failure were assessed.
  • Ventricular arrhythmias, including couplets and nonsustained ventricular tachycardia, were analyzed from Holter recordings.

Main Results:

  • Cardiac involvement was present in 55% of patients; 23% had heart failure.
  • Complex ventricular arrhythmias were detected in 57%, with couplets in 29% and nonsustained ventricular tachycardia in 18%.
  • Congestive heart failure, echocardiographic abnormalities, and Holter abnormalities negatively impacted survival (median 23.4 months).

Conclusions:

  • Interventricular septum thickness and the presence of couplets on Holter monitoring are independent predictors of survival in AL amyloidosis.
  • Couplets on Holter monitoring correlate significantly with sudden cardiac death.
  • Holter monitoring is a valuable tool for assessing prognosis in patients with AL amyloidosis.

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