Depolarization and repolarization parameters on ECG predict recurrence after atrial fibrillation ablation in patients

Song-Nan Wen1, Hao-Jie Zhu1, Peng-Yu Sun1

  • 1Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.

Insights

QTc prolongation and fragmented QRS (fQRS) predict atrial fibrillation (AF) ablation failure in hypertrophic cardiomyopathy (HCM) patients. Combining these markers improves risk prediction for AF recurrence after ablation.

Area of Science:

  • Cardiology
  • Electrophysiology
  • Medical Diagnostics

Background:

  • Atrial fibrillation (AF) ablation outcomes are suboptimal, particularly in patients with structural heart disease like hypertrophic cardiomyopathy (HCM).
  • Identifying patients likely to benefit from AF ablation or experience treatment failure is crucial for personalized management.

Purpose of the Study:

  • To investigate preprocedural QTc interval and fragmented QRS (fQRS) as predictors of AF recurrence after ablation in HCM patients.
  • To evaluate the combined predictive value of QTc prolongation and fQRS for AF recurrence in this population.

Main Methods:

  • 120 HCM patients undergoing primary AF ablation were enrolled.
  • Preprocedural QTc interval and fQRS presence were assessed.
  • Arrhythmia recurrence was monitored over a median follow-up period.

Main Results:

  • Arrhythmia recurrence was observed in 69 patients (57.5%) after 13.4 months.
  • fQRS was present in 59.17% of patients, predominantly in inferior leads.
  • QTc > 448 ms (HR: 1.982) and fQRS+ (HR: 1.922) were independent risk factors for recurrence.
  • The combination of fQRS+ and QTc > 448 ms showed superior predictive value for recurrence.

Conclusions:

  • QTc prolongation (>448 ms) and fQRS are independent risk factors for AF recurrence post-ablation in HCM patients.
  • The combination of fQRS and prolonged QTc offers enhanced predictive value for procedural failure.
  • These findings can aid in identifying high-risk HCM patients for AF ablation.
Abstract

Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
418
ECG Interpretation of Arrhythmias II: Atrial, Junctional and Ventricular Arrhythmias01:25

ECG Interpretation of Arrhythmias II: Atrial, Junctional and Ventricular Arrhythmias

Arrhythmia is a condition characterized by an irregular heart rhythm, with ECG changes that differ based on its origin and nature. The types of arrhythmias discussed below include atrial, junctional, and ventricular arrhythmias.Atrial ArrhythmiasPremature Atrial Complexes (PACs): PACs are early atrial beats caused by stress, caffeine, alcohol, electrolyte imbalances, hypoxia, hyperthyroidism, or certain medications (e.g., bronchodilators and decongestants). The ECG shows early P waves with an...
483
Amyloid Fibrils03:03

Amyloid Fibrils

Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining,...
11.7K
Amyloid Fibrils03:03

Amyloid Fibrils

6.3K
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
489
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
481