The Texas Cardiac Arrhythmia Institute (TCAI) at St. David’s Medical Center will host EP Live—a two-day, intensive educational meeting targeting practicing electrophysiologists from across the globe, electrophysiology (EP) fellows in training, general cardiologists, cardiac surgeons with an interest in treating complex arrhythmias and primary care physicians. The meeting consists of four sections: atrial fibrillation ablation, ventricular tachycardia ablation, devices and new technologies. 

More than 2,000 patients in the U.S. have filed suits against Boehringer Ingelheim over its oral anticoagulant dabigatran (Pradaxa). The company confirmed the number to Reuters after a German newspaper initially reported the total.

A subcommittee of the Heart Rhythm Society (HRS) published a list of five treatments and procedures electrophysiologists should avoid in patients with arrhythmias. The five “don’ts” are available on the HRS website.

eCardio Diagnostics, a leader in remote arrhythmia monitoring services, today announced the opening of its second Independent Diagnostic Testing Facility (IDTF) in San Francisco, California.

This February during American Heart Month, Vivek Reddy, MD, of Mount Sinai Heart at The Mount Sinai Hospital implanted the United States' first miniature-sized, leadless cardiac pacemaker directly inside a patient's heart without surgery.

iRhythm Technologies, a healthcare information services company, today announced that Aetna, the third largest health plan in the United States, has issued a positive coverage policy for long-term continuous monitoring of patients with suspected heart arrhythmias, which includes use of the ZIO Service. The new policy now makes iRhythm's solution - comprised of the ZIO Patch, proprietary algorithms and the ZIO report - available as a potential covered service for the insurer's medical members.

Beaumont Health System is the first center outside of Japan to use a new balloon ablation technology to treat atrial fibrillation, the most common heart rhythm disorder that affects about 3 million people in the U.S.

Medtronic, Inc. (NYSE: MDT), today announced that the Medtronic SureScan(r) pacing systems - the first and only pacing systems in the United States that have been approved by the U.S. Food and Drug Administration (FDA) for use with magnetic resonance imaging (MRI) - are now approved for MRI scans positioned on any region of the body. Patients implanted with the Advisa DR MRI(r) or Revo MRI(r) SureScan pacing systems now can have MRI scans without positioning restrictions, including the chest area, which previously had been restricted.