Failure of fluoroscopy to detect “inside-out” insulation failure and externalized conductors in a Riata ICD lead

Author:

Cronin Edmond M.,Baranowski Bryan J.,Martin David O.

Publisher

Elsevier BV

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference5 articles.

1. Implantable cardioverter-defibrillator lead disintegration at the level of the tricuspid valve;Duray;Heart Rhythm,2008

2. Food and Drug Administration. St Jude Medical, Riata and Riata ST silicone endocardial defibrillation leads. Silver Spring, MD: FDA. Available from: http://www.fda.gov/MedicalDevices/Safety/ListofRecalls/ucm284360.htm. Accessed September 26, 2012.

3. Food and Drug Administration. FDA recommends X-ray or other imaging on implanted heart defibrillators with St. Jude Medical Riata leads to help guide treatment. Silver Spring, MD: FDA. Available from: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm315684.htm. Accessed September 26, 2012.

4. Fluoroscopic screening of asymptomatic patients implanted with the recalled Riata lead family;Liu;Circ Arrhythm Electrophysiol,2012

5. Prevalence and predictors of cable extrusion and loss of electrical integrity with the Riata defibrillator lead;Shen;J Cardiovasc Electrophysiol,2012

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