A Study of the Effectiveness of Anti-Arrhythmic Medications After Atrial Fibrillation Ablation

Not Applicable

Completed

Conditions: Atrial Fibrillation

Interventions: Drug: propafenone; flecainide; sotalol; dofetilide
Device: Radiofrequency catheter ablation

Registration Number: NCT00408200

Lead Sponsor: University of Pennsylvania

Brief Summary: The purpose of this study is to examine the overall effectiveness of anti-arrhythmic medicines (to control heart rhythm) prescribed after an ablation procedure for atrial fibrillation.

Detailed Description: Atrial fibrillation (AF) is the most common heart rhythm disorder in the US and it is associated with shortness of breath, palpitations, stroke occurrence and increased mortality. Traditional treatment for AF includes anticoagulation, drugs that slow the heart rate and antiarrhythmic agents. More recently, catheter based treatments to address atrial fibrillation have been developed, which involves using radiofrequency energy to isolate the arrhythmogenic foci localized in the pulmonary veins.

During the first weeks following pulmonary vein isolation (PVI), it is not unusual for patients to experience early recurrences of atrial fibrillation or atrial tachycardia due to irritability from the ablation. While these arrhythmias tend to resolve over time, it is nevertheless standard practice to prescribe antiarrhythmic drugs for the first 2-3 months after the intervention to prevent these early recurrences. However, the efficacy of this practice has never been formally evaluated. In addition, we have identified a small group of patients whose atrial tachycardias have terminated after cessation of antiarrhythmic therapy, suggesting that proarrhythmia from these agents may promote reentrant tachycardias in some patients. We therefore designed a study protocol that will evaluate the usefulness of short term antiarrhythmic drug therapy in order to prevent atrial fibrillation and atrial tachycardia episodes during the first 6 weeks following PVI.

The target population of the study includes all patients with paroxysmal atrial fibrillation referred for PVI. After the ablation procedure, patients will be randomized to receive or not receive antiarrhythmic drugs for a period of 6 weeks. Arrhythmia occurrence during this period will be monitored via twice daily transtelephonic monitoring. Clinical visits including a physical exam and 12 lead ECG recording will be scheduled at 6 weeks. The primary endpoint of the study will be a composite endpoint including 1) atrial arrhythmias persisting \> 24 hours or requiring initiation of antiarrhythmic therapy 2) need for cardioversion/hospital admission 3) need for repeat ablation or 4) adverse outcome/intolerance of antiarrhythmic agent requiring drug cessation or change during the 6 week follow up period.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 110

Inclusion Criteria

Adult patients meeting ACC/AHA criteria for paroxysmal atrial fibrillation (episodes typically last no more than 7 days and are self-terminating)
Eligible for pulmonary vein isolation
Able to tolerate antiarrhythmic medication

Exclusion Criteria

Age <18
Persistent or permanent atrial fibrillation (episodes last >7 days and require cardioversion)
Antiarrhythmic treatment for indication other than atrial fibrillation
Contraindication or intolerance to all antiarrhythmic medications
Primary physician unwilling to withhold antiarrhythmic drugs for duration of the study
Failure to obtain informed consent

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
AAD:YES	Radiofrequency catheter ablation	Subjects receive membrane-active anti-arrhythmic medication after ablation. See intervention list below.
AAD:NO	Radiofrequency catheter ablation	Subjects do not receive membrane-active anti-arrhythmic medications after ablation.
AAD:YES	propafenone; flecainide; sotalol; dofetilide	Subjects receive membrane-active anti-arrhythmic medication after ablation. See intervention list below.

Primary Outcome Measures

Name	Time	Method
Composite Endpoint: Atrial Arrhythmias Lasting >24 Hrs or Requiring Antiarrhythmic Drug Therapy; Need for Cardioversion/Repeat Ablation During the Study Period; Adverse Outcome/Intolerance of Antiarrhythmic Agent Requiring Cessation or Change of Drug	6 weeks

Secondary Outcome Measures

Name	Time	Method
Freedom From Atrial Arrhythmia at 6 Months Post Procedure.	6 weeks

Trial Locations

Locations (2): Presbyterian Medical Center
🇺🇸
Philadelphia, Pennsylvania, United States
Hospital of the University of Pennsylvania
🇺🇸
Philadelphia, Pennsylvania, United States