{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,22]],"date-time":"2026-01-22T21:58:02Z","timestamp":1769119082223,"version":"3.49.0"},"reference-count":19,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2020,10,14]],"date-time":"2020-10-14T00:00:00Z","timestamp":1602633600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Cardiovasc electrophysiol"],"published-print":{"date-parts":[[2020,12]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Introduction<\/jats:title><jats:p>In patients with a left ventricular assist device (LVAD), the subcutaneous implantable cardioverter\u2010defibrillator (S\u2010ICD) can be an alternative to transvenous ICD systems due to reduced risk of systemic infection, which could lead to extraction of the ICD as well as the LVAD. S\u2010ICD eligibility is lower in patients with LVAD than in patients with end\u2010stage heart failure without LVAD. Several reports have shown inappropriate S\u2010ICD therapy in the coexistence of LVAD and S\u2010ICD. The aim of the present study was to evaluate S\u2010ICD eligibility in patients with LVAD using the established electrocardiogram (ECG)\u2010based screening test as well as a novel device\u2010based screening test to identify potentially inappropriate S\u2010ICD sensing in this specific patient cohort.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods and Results<\/jats:title><jats:p>The present study included 115 patients implanted with an LVAD. The standard ECG\u2010based screening test and a novel device\u2010based screening test were performed in all patients. Eighty patients (70%) were eligible for S\u2010ICD therapy with the standard ECG\u2010based screening test. Performance of the novel device\u2010based screening test identified device\u2010device interference in 14 of these 80 patients (12%).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Using a novel extended device\u2010based S\u2010ICD screening method, a small number of patients with LVAD deemed eligible for S\u2010ICD with the standard ECG\u2010based screening test exhibit device\u2010device interference. Careful S\u2010ICD screening should be performed in patients with LVAD, who are candidates for S\u2010ICD therapy, to prevent inappropriate sensing or ICD therapy.<\/jats:p><\/jats:sec>","DOI":"10.1111\/jce.14769","type":"journal-article","created":{"date-parts":[[2020,10,5]],"date-time":"2020-10-05T15:01:50Z","timestamp":1601910110000},"page":"3286-3292","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":8,"title":["A novel screening tool to unmask potential interference between S\u2010ICD and left ventricular assist device"],"prefix":"10.1111","volume":"31","author":[{"given":"Christos","family":"Zormpas","sequence":"first","affiliation":[{"name":"Hannover Heart Rhythm Center, Department of Cardiology and Angiology Hannover Medical School Hannover Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J\u00f6rg","family":"Eiringhaus","sequence":"additional","affiliation":[{"name":"Hannover Heart Rhythm Center, Department of Cardiology and Angiology Hannover Medical School Hannover Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Henrike A. 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