2014
DOI: 10.1016/j.athoracsur.2014.05.030
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De Novo Aortic Regurgitation After Continuous-Flow Left Ventricular Assist Device Implantation

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Cited by 48 publications
(38 citation statements)
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“…Clinical studies carried out in the USA, where HM-II has been used as the main device (between 94 and 100% of all studied CF-LVAD patients) with a longer observation period, reported that 52-64% of HM-II patients had developed significant AI. 1,2,6,7 Alternatively, a UK study reported the incidence of mild or greater AI to be 43.1% in HM-II vs. 65.7% in HVAD recipients, 3 the opposite of the present findings. In contrast, Soleimani et al reported that 0/8 patients (0%) developed AI at a mean of 158 days with the HVAD vs. 6/55 (10.9%) with the HM-II at a mean of 314 days.…”
Section: Influence Of Device Type On De Novo Aicontrasting
confidence: 55%
“…Clinical studies carried out in the USA, where HM-II has been used as the main device (between 94 and 100% of all studied CF-LVAD patients) with a longer observation period, reported that 52-64% of HM-II patients had developed significant AI. 1,2,6,7 Alternatively, a UK study reported the incidence of mild or greater AI to be 43.1% in HM-II vs. 65.7% in HVAD recipients, 3 the opposite of the present findings. In contrast, Soleimani et al reported that 0/8 patients (0%) developed AI at a mean of 158 days with the HVAD vs. 6/55 (10.9%) with the HM-II at a mean of 314 days.…”
Section: Influence Of Device Type On De Novo Aicontrasting
confidence: 55%
“…Prior studies have found that 33-52% of LVAD patients develop AI, with two studies noting no difference in survival in the groups with and without significant post-LVAD AI (18)(19)(20). We noted a significant increase in AI at follow-up, which has been noted in several previous studies.…”
Section: Discussionsupporting
confidence: 83%
“…We noted a significant increase in AI at follow-up, which has been noted in several previous studies. Prior studies have found that 33-52% of LVAD patients develop AI, with two studies noting no difference in survival in the groups with and without significant post-LVAD AI (18)(19)(20). In a study by Rajagopal et al, significant development of moderate or worse AI was observed, but those with moderate AI had adequate unloading of the left ventricle (21).…”
Section: Discussionmentioning
confidence: 99%
“…Multiple studies have demonstrated the risk of developing AV pathology, aortic regurgitation and leaflet fusion [20, 21]. This has been shown in patients with the HeartWare HVAD (centrifugal pump), the Thoratec HMI and the HMII (axial flow pump) [22, 23]. The risk of development of AV disease is reduced in patients managed to allow intermittent AV opening [24, 25].…”
Section: Introductionmentioning
confidence: 99%