Early Failure of the Biotronik Linox Implantable Cardioverter Defibrillator Lead

Author:

PADFIELD GARETH J.1,STEINBERG CHRISTIAN1,KARIM SHAHZAD S.2,TUNG STANLEY1,BENNETT MATTHEW T.3,LE MAITRE JOHN P.2,BASHIR JAMIL1

Affiliation:

1. Divisions of Cardiovascular Surgery and Cardiology; University of British Columbia; St. Paul's Hospital; Vancouver Canada

2. Divisions of Cardiovascular Surgery and Cardiology; University of British Columbia; Royal Columbian Hospital; Vancouver Canada

3. Divisions of Cardiovascular Surgery and Cardiology; University of British Columbia; Vancouver General Hospital; Vancouver Canada

Publisher

Wiley

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference14 articles.

1. Urgent medical device information Sprint Fidelis® lead patient management recommendations;Groves;Medtronic,2007

2. Communication USFadas Premature Insulation Failure in Recalled Riata Implantable Cardioverter Defibrillator (ICD) Leads Manufactured by St. Jude Medical, Inc http://wwwfdagov/MedicalDevices/Safety/AlertsandNotices/ucm314930htm

3. Biotronik Product performance report January 2014 http://wwwbiotronikcom/files/9A51078D1ABE9B35C1257D1800429672/$FILE/2014-01%20PPRpdf

4. The Canadian experience with Durata and Riata ST Optim defibrillator leads: A report from the Canadian Heart Rhythm Society Device Committee;Bennett;Heart Rhythm,2013

5. Failure of a novel silicone-polyurethane copolymer (Optim) to prevent implantable cardioverter-defibrillator lead insulation abrasions;Hauser;Europace,2013

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