A Randomized Study of Defibrillator Lead Implantations in the Right Ventricular Mid‐Septum versus the Apex: The SEPTAL Studyτ

Impact of Recalls on ICD Utilization. Introduction: The study was designed to evaluate the feasibility and performance of right ventricular (RV) mid‐septal versus apical implantable defibrillator (ICD) lead placement. Methods and Results: SEPTAL is a randomized, noninferiority trial, which randomly...

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Published inJournal of cardiovascular electrophysiology Vol. 23; no. 8; pp. 853 - 860
Main Authors MABO, PHILIPPE, DEFAYE, PASCAL, MOUTON, ELISABETH, CEBRON, JEAN‐PIERRE, DAVY, JEAN MARC, TASSIN, AUDE, BABUTY, DOMINIQUE, MONDOLY, PIERRE, PAZIAUD, OLIVIER, ANSELME, FREDERIC, DAUBERT, JEAN‐CLAUDE
Format Journal Article
LanguageEnglish
Published Malden, USA Blackwell Publishing Inc 01.08.2012
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Summary:Impact of Recalls on ICD Utilization. Introduction: The study was designed to evaluate the feasibility and performance of right ventricular (RV) mid‐septal versus apical implantable defibrillator (ICD) lead placement. Methods and Results: SEPTAL is a randomized, noninferiority trial, which randomly assigned patients to implantation of ICD leads in the RV mid‐septum versus apex, with a primary objective of comparing the implant success rate of implant at each site, based on strict electrical predefined criteria. We also compared the (1) pacing lead characteristics, (2) rates of appropriate and inappropriate ICD therapies, and (3) all‐cause mortality between the 2 sites at 1 year. The trial enrolled 215 patients (mean age = 59.7 ± 12.4 years, mean LVEF = 34.0 ± 14.2%, 84.2% men), of whom 148 (68.8%) presented with ischemic heart disease. The ICD indication was primary prevention in 117 patients (54.4%). The lead was successfully implanted in 96/107 patients (89.7%) assigned to the RV mid‐septum, and in 99/108 (91.7%) assigned to the apex (ns). The 1‐year rate of lead‐related adverse events was similar in both groups. A total of 8 first inappropriate ICD therapies (7.9%) were delivered in the RV mid‐septal group, versus 8 (7.8%) in the apical group (ns), while first appropriate therapies were delivered to 22 (21.4%) and 24 patients (23.8%), respectively (ns). All‐cause mortality was 7.9% in the RV mid‐septal versus 2.9% in the RV apical group (ns). Conclusion: This study confirmed the technical feasibility and noninferior performance of ICD leads implanted in the RV mid‐septum versus the apex. (J Cardiovasc Electrophysiol, Vol. 23, pp. 853‐860, August 2012)
Bibliography:This study is sponsored by Boston Scientific/Guidant France S.A.S.
Philippe Mabo, M.D., has received consulting fees and research grants from Biotronik, Boston Scientific, Medtronic, St. Jude Medical, and Sorin Group. Pascal Defaye, M.D., has received consulting fees from Boston Scientific and Sorin Group. Jean‐Pierre Cebron has participated on research grants from Boston Scientific and Sorin Group. Elisabeth Mouton, M.D., is an employee of Boston Scientific. Jean‐Marc Davy, M.D., has received consulting fees and research grants from Boston Scientific, Medtronic, Sorin Group, and St. Jude Medical. Aude Tassin participated on research grants from Boston Scientific and Sorin Group. Dominique Babuty has received consulting fees and/or research grants from Boston Scientific, Medtronic, Sorin Group, and St. Jude Medical. Pierre Mondoly participated on research grants from Boston Scientific, Biotronik, and Sorin Group. Olivier Paziaud, M.D., has received consulting fees and research grants from Boston Scientific, Medtronic, and  Sorin Group. Frederic Anselme, M.D., has received consulting fees and speaker honoraria from Boston Scientific, Sorin Group, St. Jude Medical, and Medtronic. Other authors: No disclosures.
τ
On behalf of the SEPTAL investigators.
ISSN:1045-3873
1540-8167
DOI:10.1111/j.1540-8167.2012.02311.x