Outcomes of Early Referral to Radiofrequency Ablation in Symptomatic Atrial Fibrillation Patients.

Assiut University

Status: Not yet enrolling

Conditions: Atrial Fibrillation; Radiofrequency Ablation

Treatments: Procedure: Radiofrequency ablation

Study type: Observational

Funder types: Other

Identifiers

NCT05559073

Early Referral to AF Ablation

Details and patient eligibility

About

Atrial fibrillation (AF) is the most common arrhythmia among adults with increasing risk of stroke, heart failure and mortality.

The EAST-AFNET 4 trial showed that rhythm control treatment (Antiarrhythmic drugs AAD or catheter ablation) was associated with a lower risk of adverse cardiovascular outcomes than usual care among patients who had recently (within one year) been diagnosed with atrial fibrillation.

In phase II/III GLORIA AF registry, Early AF ablation within 3 months from initial diagnosis in a contemporary cohort of patients who were predominantly treated with non-vitamin K antagonist oral anticoagulants was associated with a survival advantage compared to medical therapy alone.

Moreover, early AF ablation appeared to provide the greatest benefit compared to other treatments.

The ATTEST trial was a multicenter, randomized, prospective study in patients with paroxysmal atrial fibrillation (AF) designed to assess whether radiofrequency (RF) ablation is more effective in delaying the progression to persistent AF than AADs.

Patients >_65 years were significantly more likely to progress to persistent AF/AT than patients were <65 years, suggesting that early RF ablation may be an effective treatment strategy for delaying AF progression.

So, we hypothesize that early AF ablation within one year after first AF diagnosis may associate with improved procedures outcomes in symptomatic AF patients.

Enrollment: 127 estimated patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Paroxysmal and persistent atrial fibrillation (AF) documented on a 12 lead ECG, trans-telephonic monitoring (TTM) or Holter monitor (episodes of AF must be >30 seconds in duration to qualify as an inclusion criterion)
• Age of 18 years or older on the date of consent.
• Candidate for ablation based on AF that is symptomatic
• Informed Consent

Exclusion criteria

Permenant AF

• Previous left atrial (LA) ablation or LA surgery
• AF due to reversible cause (e.g. hyperthyroidism, cardiothoracic surgery)
• Active intracardiac thrombus
• Pre-existing pulmonary vein stenosis or pulmonary vein stent
• Contraindication to anticoagulation or radiocontrast materials
• Left atrial anteroposterior diameter greater than 5.5 cm by transthoracic echocardiography
• Cardiac valve prosthesis
• Severe mitral valve regurgitation or stenosis
• Myocardial infarction, percutaneous intervention, or coronary artery stenting during the 3-month period preceding the consent date
• Cardiac surgery during the three-month interval preceding the consent date
• Significant unrepaird congenital heart defect (including patent foramen ovale)
• NYHA class IV congestive heart failure
• Significant chronic kidney disease (eGFR <30 mL/min/1.73m2)
• Cerebral ischemic event (stroke or transient ischemic attack) during the six-month interval preceding the consent date
• Pregnancy and Life expectancy less than one year

Trial design

127 participants in 2 patient groups

Early referral to ablation within one year after first documented AF diagnosis

Treatment:

Procedure: Radiofrequency ablation

Delayed referral to ablation after one year after first documented AF diagnosis

Treatment:

Procedure: Radiofrequency ablation