2016
DOI: 10.1016/j.jacep.2015.10.008
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Subcutaneous Implantable Cardioverter-Defibrillator and Left Ventricular Assist Device

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Cited by 11 publications
(5 citation statements)
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“…Also, there is a likely assertation bias because normal functioning devices are unlikely to be reported. In this regard, we only found three such reports of S‐ICD with confirmed lack of EMI in the literature 36‐38 . It is noteworthy that the largest published patient series of LVADs and S‐ICDs demonstrated that 10% of the patients (2/20) experienced EMI from LVADs 14 .…”
Section: Limitationsmentioning
confidence: 88%
“…Also, there is a likely assertation bias because normal functioning devices are unlikely to be reported. In this regard, we only found three such reports of S‐ICD with confirmed lack of EMI in the literature 36‐38 . It is noteworthy that the largest published patient series of LVADs and S‐ICDs demonstrated that 10% of the patients (2/20) experienced EMI from LVADs 14 .…”
Section: Limitationsmentioning
confidence: 88%
“…Electromagnetic interference were not observed in patients with HeartMate II™ and Jarvik 2000 ® 7 , 8 , 10 as opposed to patients with HeartWare ® 6 , 11 and HeartMate 3™ 9 , 12 . S-ICD algorithms for EMI discrimination have not been modified in the three generations of this device, suggesting that the occurrence of disturbances in S-ICD sensing depends on the type of LVAD implanted.…”
Section: Discussionmentioning
confidence: 91%
“…All reported patients with EMI detection had thoracic LVAD pump location, 6 , 9 , 11 , 12 while two out of three cases with a correct cardiac signal detection had a Heart Mate II™, which pump is contained in a subdiaphragmatic pocket ( Figure 4 ). 7 , 8 A patient with a Jarvik 2000 ® , 10 with the pump located in the thorax, did sense correctly. Noteworthy, this latter device runs at a very high rate, which makes sensing of EMI less likely.…”
Section: Discussionmentioning
confidence: 96%
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“…However, there are emerging and encouraging data demonstrating that S-ICD, if all sensing vectors before and after LVAD activation are correctly tested or its speed increases, is a safe and effective alternative to conventional ICD in terminating ventricular arrhythmias without evidence of mechanical interferences also with different types of LVAD. 12,14 A potential limitation of this novel technique could be a potential greater complexity for battery replacement. However, we believe that both the long battery duration of the current new-generation S-ICD system and reduction of acute and late complications may overcome this potential limitation.…”
mentioning
confidence: 99%