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Pulsed field ablation beats antiarrhythmic drugs as first-line persistent AF therapyPulsed field ablation shows higher success than drugs for heart rhythm

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Key Takeaway
Consider pulsed field ablation as first-line therapy for persistent atrial fibrillation based on superior 12-month success versus antiarrhythmic drugs.

This randomized trial compared pulsed field ablation (PFA) using a pentaspline catheter versus antiarrhythmic-drug therapy as first-line treatment in 207 patients with previously untreated persistent atrial fibrillation. An additional PFA-only group was included for safety analysis. The primary outcome was treatment success (short-term and long-term) through 12 months.

At 12 months, treatment success was 56% in the PFA group (128 of 207 patients) versus 30% in the antiarrhythmic-drug group (40 of 103 patients). The hazard ratio for composite treatment failure was 0.46 (95% CI 0.33 to 0.65; P<0.001), favoring PFA.

Serious adverse events occurred in 13 of 257 patients (5.1%) in the combined PFA group. At 12 months, adverse events were reported in 45 patients (25%) in the PFA group versus 20 patients (21%) in the antiarrhythmic-drug group. Specific adverse events and discontinuations were not reported.

The study was funded by Boston Scientific. Limitations were not reported. The risk of recurrence of atrial arrhythmia was significantly lower with PFA as first-line treatment compared to antiarrhythmic-drug therapy. Clinicians should consider PFA as an initial strategy for persistent AF, though longer-term data and broader safety profiles are needed.

How this fits prior evidence

This trial extends prior evidence on ablation strategies for persistent AF. Prior coverage showed that rotational activity ablation plus PVI achieved 91.5% sinus rhythm in an observational cohort, and that rhythm control improved LVEF in CRT recipients with persistent AF. The current randomized data provide higher-certainty evidence that PFA, a newer ablation modality, is superior to antiarrhythmic drugs as first-line therapy, with a 46% reduction in treatment failure risk. It also contrasts with the evidence gap noted for amiodarone in chronic Chagas cardiomyopathy, as amiodarone was not specifically studied here.

Living with an irregular heartbeat, known as persistent atrial fibrillation, can be frustrating and difficult to manage. For many people, the first line of defense is taking antiarrhythmic drugs. However, a recent trial looked at whether a procedure called pulsed field ablation (PFA) could offer a more effective way to keep the heart's rhythm steady.

The study followed 207 patients who had never been treated for this condition before. The results showed that 56% of those who received the PFA procedure were successful after 12 months. In contrast, only 30% of those who took antiarrhythmic drugs saw success over the same period. This suggests that PFA may be a more reliable way to manage heart rhythm in the short and long term.

While the results favor the PFA procedure, it is important to look at the safety data. The study noted some serious adverse events related to the device or procedure, occurring in about 5% of the total group. Because this trial was funded by a medical device company, patients should discuss these specific results and their own health risks with a doctor to decide on the best treatment path.

What this means for you:
Pulsed field ablation showed a significantly higher success rate than antiarrhythmic drugs for persistent atrial fibrillation.

Common questions

How effective is pulsed field ablation for heart rhythm?

The study found that 56% of patients who received pulsed field ablation (PFA) had successful outcomes at the 12-month mark. This was significantly higher than the 30% success rate seen in the group treated with antiarrhythmic drugs.

Is pulsed field ablation safe for atrial fibrillation?

The study reported that serious adverse events related to the device or procedure occurred in about 5.1% of the combined PFA group. You should talk to your doctor to discuss these risks and how they apply to your specific health situation.

How does this treatment compare to standard drugs?

The trial showed that patients receiving pulsed field ablation as their first treatment had a much lower risk of heart rhythm issues returning compared to those who were treated with antiarrhythmic drugs for 12 months.

Study Details

Study typeRct
Sample sizen = 207
EvidenceLevel 2
Follow-up12.0 mo
PublishedJun 2026
View Original Abstract ↓
BACKGROUND: Guidelines recommend a trial of antiarrhythmic drugs before catheter ablation for persistent atrial fibrillation. Whether pulsed field ablation (PFA) may be a preferred initial treatment is unclear. METHODS: We conducted an international, randomized trial involving patients with previously untreated persistent atrial fibrillation. The patients were randomly assigned in a 2:1 ratio to receive PFA performed with a pentaspline catheter or to receive antiarrhythmic-drug therapy. An additional group of patients (PFA-assigned) underwent PFA for the analysis of the primary safety end point alone. All the patients received an insertable cardiac monitor. The primary effectiveness end point was the short-term and long-term success of treatment through 12 months. Short-term success was defined as procedural success in the PFA group and the absence of ablation during the blanking period (90 days after treatment initiation) in the antiarrhythmic-drug group. Long-term success was defined as freedom from recurrence of atrial arrhythmias, repeat ablation, or need for antiarrhythmic drugs from 90 days through 12 months (in the PFA group) and freedom from amiodarone use at any time. The primary safety end point was device- and procedure-related serious adverse events. RESULTS: At 12 months, treatment success was observed in 128 of 207 patients (Kaplan-Meier estimate, 56%; 95% confidence interval [CI], 48 to 63) in the PFA group and in 40 of 103 patients (Kaplan-Meier estimate, 30%; 95% CI, 21 to 40) in the antiarrhythmic-drug group (hazard ratio for composite treatment failure [a lack of short- and long-term success], 0.46; 95% CI, 0.33 to 0.65; P<0.001). A primary safety end-point event occurred in 13 of 257 patients (5.1%) in the combined PFA group (both randomized and PFA-assigned groups). At 12 months, serious adverse events had occurred in 45 patients (25%) in the PFA group and in 20 patients (21%) in the antiarrhythmic-drug group. CONCLUSIONS: Among patients with persistent atrial fibrillation, the risk of recurrence of atrial arrhythmia was significantly lower among those who received PFA as first-line treatment than among those who received antiarrhythmic-drug therapy. (Funded by Boston Scientific; AVANT GUARD ClinicalTrials.gov number, NCT06096337.).
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