Initial Experience With Intercostal Insertion of an Extravascular ICD Lead Compatible With Existing Pulse Generators

Author:

Burke Martin C.123ORCID,Knops Reinoud E.2ORCID,Reddy Vivek4ORCID,Aasbo Johan5,Husby Michael3ORCID,Marcovecchio Alan3ORCID,O’Connor Mark3,Sanghera Rick3ORCID,Scheck Don3,Pepplinkhuizen Shari2ORCID,Ebner Adrian6

Affiliation:

1. CorVita Science Foundation, Chicago, IL (M.C.B.).

2. Department of Clinical and Experimental Cardiology, Amsterdam UMC, Academic Medical Center, the Netherlands (M.C.B., R.E.K., S.P.).

3. AtaCor Medical, Inc., San Clemente, CA (M.C.B., M.H., A.M., M.O., R.S., D.S.).

4. Mount Sinai Medical School, New York (V.R.).

5. Lexington Cardiology and Baptist Health, KY (J.A.).

6. Cardiovascular Department, Sanatorio Italiano, Asunción, Paraguay (A.E.).

Abstract

BACKGROUND: This study assessed safety and feasibility of a novel extravascular implantable cardioverter defibrillator (ICD) lead when inserted anteriorly through a rib space and connected to various commercially available ICD pulse generators (PGs) placed in either a left mid-axillary or left pectoral pocket. Currently available or investigational, extravascular-ICDs include a subcutaneous or subxiphoid lead connected to customized extravascular-ICD PGs. METHODS: This novel extravascular-ICD (AtaCor Medical Inc, San Clemente, CA) employs a unique intercostal implant technique and is designed to function with commercial DF-4 ICD PGs. In this nonrandomized, single-center, acute study, 36 de novo or replacement ICD (transvenous ICD) patients enrolled to receive a concomitant extravascular-ICD lead inserted through an intercostal space along the left parasternal margin. extravascular-ICD leads were connected to DF-4 compatible ICD PGs positioned in either a left mid-axillary or pectoral pocket for acute sensing and defibrillation testing. Defibrillation testing started at 30 Joules (J) and stepped up or down in 5 to 10 joule increments depending on the success and limitations of the generator used. RESULTS: Successful acute defibrillation using ≤35 J was noted in 100% of left mid-axillary PG subjects (n=27, mean 16.3±8.6 J) and 83% of left pectoral PG subjects (n=6, mean 21.0±8.4 J). Furthermore, 24 of 27 (89%) of patients tested with a left, mid-axillary intermuscular PG had successful VF conversion with defibrillation energies at least 10 J below the maximum delivered output of the device. All evaluable episodes (n=93) were automatically sensed, detected, and shocked. No serious device-related intraoperative adverse events were observed. CONCLUSIONS: This first-in-human study documented the safe and reliable placement of a novel extravascular ICD lead with effective sensing and defibrillation of induced ventricular fibrillation using commercial DF-4 ICD PGs.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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