2006
DOI: 10.2459/01.jcm.0000203847.52149.87
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Bridge to transplantation with the MicroMed DeBakey ventricular assist device axial pump: a single centre report

Abstract: In our experience with the continuous axial flow DeBakey VAD, a high success rate was obtained associated with a low risk of complications. All the patients tolerated continuous blood flow for extended periods that makes this device a valuable alternative to pulsatile VADs as a bridge to transplantation.

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Cited by 11 publications
(4 citation statements)
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“…21,22 However, later studies with improved pumps and more sophisticated protocols did not reproduce such severe symptoms. 23,24 This correlates with findings in long-term clinical studies, [1][2][3][4][25][26][27][28] where no clinical evidence of changes in end-organ microcirculation were observed. To our knowledge, no studies on microcirculation have been performed in patients with cardiac assist devices.…”
Section: Discussionsupporting
confidence: 89%
“…21,22 However, later studies with improved pumps and more sophisticated protocols did not reproduce such severe symptoms. 23,24 This correlates with findings in long-term clinical studies, [1][2][3][4][25][26][27][28] where no clinical evidence of changes in end-organ microcirculation were observed. To our knowledge, no studies on microcirculation have been performed in patients with cardiac assist devices.…”
Section: Discussionsupporting
confidence: 89%
“…4,5 The prevalence of CHF and the shortage of donor hearts have fueled the development of left ventricular assist devices (LVADs), particularly for bridge-totransplant (BTT) purposes. [6][7][8] Nearly 80% of LVADs have been implanted as BTTs 9 and earlier fears of increased panel-reactive antibodies or post-BTT morbidity or mortality are no longer considered significant. 10 The VentrAssist is a novel, third-generation, continuous-flow LVAD designed to overcome earlier LVAD limitations such as size, noise, reliability and mechanical complexity.…”
mentioning
confidence: 99%
“…In contrast to the initial clinical trials with other continuous flow devices, [13][14][15][16] we did not initially test the VA in a conventional BTT cohort. The excellent results achieved in the pre-clinical animal trials 9 gave us the confidence to test the device in a gravely ill DT patient cohort.…”
Section: Discussionmentioning
confidence: 83%