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2. Pulsed field ablation - Wikipedia

   en.wikipedia.org/wiki/Pulsed_field_ablation

   Pulsed field ablation (PFA) is a non-thermal (not using extreme heat or cold) method of biological ablation (removal of structure or functionality) utilizing high-amplitude pulsed (microsecond duration) electric fields to create irreversible electroporation in tissues. [1] [2] It is used most widely to treat tumors or cardiac arrhythmias. [3]

3. US FDA approves Medtronic's system for heart condition - AOL

   www.aol.com/news/us-fda-approves-medtronics...

   The system, PulseSelect Pulsed Field Ablation (PFA), is used for the treatment of atrial fibrillation (AF), a condition that is characterized by an irregular rhythm of the heart. PFA is used for ...

4. Fairfield Medical Center becomes first in state to use ... - AOL

   www.aol.com/fairfield-medical-center-becomes...

   LANCASTER – Fairfield Medical Center recently introduced pulsed field ablation (PFA) therapy for the treatment of atrial fibrillation (afib).

5. CHRISTUS Highland first Louisiana hospital to treat atrial ...

   www.aol.com/christus-highland-first-louisiana...

   CHRISTUS Highland Medical Center announced that it is the first hospital in Louisiana to perform a new atrial fibrillation procedure using the Boston Scientific Farapulse Pulsed Field Ablation ...

6. Catheter ablation - Wikipedia

   en.wikipedia.org/wiki/Catheter_ablation

   Catheter ablation is a procedure that uses radio-frequency energy or other sources to terminate or modify a faulty electrical pathway from sections of the heart of those who are prone to developing cardiac arrhythmias such as atrial fibrillation, atrial flutter and Wolff-Parkinson-White syndrome.

7. Pulsed electromagnetic field therapy - Wikipedia

   en.wikipedia.org/wiki/Pulsed_electromagnetic...

   Pulsed electromagnetic field therapy (PEMFT, or PEMF therapy), also known as low field magnetic stimulation (LFMS) is the use of electromagnetic fields in an attempt to heal non-union fractures and depression. [1] By 2007 the FDA had cleared several such stimulation devices. [2]