2017
DOI: 10.1111/jocs.13238
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Transfemoral transcatheter aortic valve replacement with a self-expanding valve for severe aortic regurgitation in a patient with left ventricular assist device

Abstract: Aortic insufficiency following left ventricular assist device implantation (LVAD) has been reported in up to 40% of patients and is associated with a worse prognosis. We describe the case of a successful transfemoral transcatheter aortic valve replacement with a self-expanding bioprosthesis for aortic insufficiency following destination LVAD implantation.

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Cited by 9 publications
(6 citation statements)
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“…A similar situation involving the aortic valve has been reported in patients with a left ventricular assist device. This effect is described in both bioprosthetic and native valves …”
Section: Discussionmentioning
confidence: 94%
“…A similar situation involving the aortic valve has been reported in patients with a left ventricular assist device. This effect is described in both bioprosthetic and native valves …”
Section: Discussionmentioning
confidence: 94%
“…However, CF-LVAD has its unique sets of challenges and complications that were not observed with pulsatile LVADs [5]. Incidence of denovo aortic insufficiency (AI) in CF-LVAD patients can be as high as 30–40% and worsens with time [6], [7], [8]. LVAD efficacy diminishes in the presence of moderate to severe AI [7].…”
mentioning
confidence: 99%
“…Moderate to severe AI warrants urgent attention as per International Society of Heart and Lung Transplant (ISHLT) guidelines as a significant portion of blood flow from outflow cannula in the proximal ascending aorta can return back to left ventricle (LV) [7], [10]. Increase in pump output can temporize the situation but at the cost of potentially increasing AI [6]. Unintervened AI not only reduces systemic perfusion, but also leads to LV distension, increased work load on the pump and eventually increased right heart afterload and right ventricular failure.…”
mentioning
confidence: 99%
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“…Although transcatheter approaches have been reported to treat the development of de novo AI, this area remains largely anecdotal and remains to be fully investigated for this off-label use. 3 More than 30% of patients develop de novo, greater-thanmoderate AI by 2 years after LVAD implantation. 4 Existing AI, as in the case presented by Barac and colleagues 5 in this issue of the Journal, must be addressed at the time of implantation.…”
mentioning
confidence: 99%