2020
DOI: 10.3390/diagnostics10121071
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Implantation of a Dual-Chamber Automatic Cardioverter Defibrillator in a Patient with Persistent Left Superior Vena Cava: Case Report and Brief Literature Review

Abstract: Persistence of the left superior vena cava (PLSVC) is a congenital anomaly reported in 0.3–0.5% of patients. Due to the multiple and complex anatomical variations, transvenous lead placement can become challenging. We report the case of a 47-year-old patient diagnosed with non-ischemic dilated cardiomyopathy with reduced left ventricular ejection fraction (LVEF—27%), who was referred to our clinic for implantation of a dual-chamber cardioverter defibrillator for primary prevention of sudden cardiac death. Duri… Show more

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“…However, one of the main challenges that still remains in patients with PLSVC is proper lead placement, lead stability, and preventing lead dislodgement. 12 During left-sided placement, it can be technically challenging to advance and correctly position the defibrillator lead in the right ventricle due to the sharp takeoff between the CS opening into the right atrium and the tricuspid valve. The number of turns that the lead must make to reach this destination increases the risk for dislodgement.…”
Section: Discussionmentioning
confidence: 99%
“…However, one of the main challenges that still remains in patients with PLSVC is proper lead placement, lead stability, and preventing lead dislodgement. 12 During left-sided placement, it can be technically challenging to advance and correctly position the defibrillator lead in the right ventricle due to the sharp takeoff between the CS opening into the right atrium and the tricuspid valve. The number of turns that the lead must make to reach this destination increases the risk for dislodgement.…”
Section: Discussionmentioning
confidence: 99%
“…Among these cases, we identified six patients who had PLSVC, which leads to an incidence of at least 0.15% of this anomaly in the group of patients who required implantable devices in our clinic. It should be mentioned that, in these cases, we met several types of this congenital anomaly (two cases of type II, two cases of type III A, and two cases of type III B according to Schummer’s classification); however, in this article, we will present only four cases, since two of them have already been published [ 5 , 6 ]. None of these patients met the criteria for cardiac resynchronization therapy.…”
Section: Case Reportsmentioning
confidence: 99%