2001
DOI: 10.1067/mtc.2001.118274
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Multicenter clinical evaluation of the HeartMate vented electric left ventricular assist system in patients awaiting heart transplantation

Abstract: The HeartMate VE LVAS provides adequate hemodynamic support, has an acceptably low incidence of adverse effects, and improves survival in heart transplant candidates both inside and outside the hospital. The studies of the HeartMate LVAS (both pneumatic and electric) for Food and Drug Administration approval are the only studies with a valid control group to show a survival benefit for cardiac transplantation.

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Cited by 498 publications
(164 citation statements)
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“…A prospective trial was designed to investigate this necessary comparison [22]. Twenty-four centers throughout the United States enrolled 280 transplant candidates who had been unresponsive to inotropic support with or without intra-aortic balloon counterpulsation.…”
Section: Ventricular Assist Devices In Clinical Usementioning
confidence: 99%
“…A prospective trial was designed to investigate this necessary comparison [22]. Twenty-four centers throughout the United States enrolled 280 transplant candidates who had been unresponsive to inotropic support with or without intra-aortic balloon counterpulsation.…”
Section: Ventricular Assist Devices In Clinical Usementioning
confidence: 99%
“…Second, pulsatile LVADs employed the use of a volume displacement chamber, resulting in a relatively large device. In turn, this required both a patient with a large body habitus and extensive dissection to accommodate implantation [10,11]. Third, owing to the mechanism of the volume displacement chamber, these pumps were often noisy.…”
Section: Introductionmentioning
confidence: 99%
“…Potentially, the use of a VAD could be associated with acute organ failure [6]. Interaction mechanisms between VAD and internal organs have been hypothesized [7,8,9,10].…”
Section: Introductionmentioning
confidence: 99%