Abstract
Reddy et al (Circulation 2014;129(14):1466-71, PMID 24664277) evaluated the safety and performance of a novel completely self-contained leadless cardiac pacemaker (LCP). The primary safety end point was freedom from complications at 90 days. Secondary end points included implant success rate, implant time, and measures of device performance (pacing/sensing thresholds and rate-responsive performance). The most common indication for cardiac pacing was permanent atrial fibrillation with atrioventricular block (n = 22 [67%]).
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
