Pulsed Field Ablation

Pulsed Field Ablation
(PFA)

Pulsed field ablation is the newest and most technologically advanced form of catheter ablation. It uses precisely controlled electrical pulses to eliminate arrhythmia-causing tissue — with greater precision and a better safety profile than traditional thermal ablation methods.

⚠ This page provides general educational information only. Please consult your electrophysiologist about whether PFA is appropriate for your situation.
FDA approved
PFA approved in the U.S. in 2023
Tissue selective
Spares surrounding structures
Faster
Shorter procedure times vs traditional ablation

Video coming soon — Dr. Luni explains pulsed field ablation in plain language

How is PFA different from traditional ablation?

Traditional catheter ablation uses heat (radiofrequency) or cold (cryoablation) to destroy tissue. These thermal approaches work well, but because heat and cold spread beyond the intended target, they carry risks of damage to nearby structures — including the esophagus, phrenic nerve, and pulmonary veins.

Pulsed field ablation uses a different mechanism entirely. Instead of heat or cold, PFA delivers precisely timed electrical pulses that cause irreversible electroporation — a process that destroys cardiac cells selectively while largely sparing other tissue types. This tissue selectivity is the key advantage.

What are the benefits of PFA?

Who is PFA used for?

PFA is currently used primarily for atrial fibrillation ablation, where it has shown excellent results in isolating the pulmonary veins — the most common source of AFib triggers. Research is ongoing for its use in other arrhythmias.

What should I expect?

The PFA procedure is similar to traditional catheter ablation from the patient's perspective. You will be sedated, catheters will be inserted through the groin, and the procedure typically takes 2-3 hours. Most patients go home the next day and return to normal activities within 1-2 weeks.

Dr. Luni performs pulsed field ablation using the FARAPULSE system (Boston Scientific) — the first FDA-approved PFA platform in the United States — as part of his AFib ablation program at Timpanogos Regional Hospital.

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