2001
DOI: 10.1016/s0003-4975(00)02614-x
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Research and development of an implantable, axial-flow left ventricular assist device: the Jarvik 2000 Heart

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Cited by 117 publications
(71 citation statements)
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References 22 publications
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“…Survival of children after heart transplantation with pre-transplantation IPC (ECMO and Left Ventricular Bypass) and without mechanical support of blood circulation xas США) [57] и HeartWareHvad (HeartWare, Framingham, MA. США), осевые насосы HeartMate II (Thoratec Corporation США), Jarvik 2000 FlowMaker (Jarvik Heart, Inc., New York, CША) [58][59][60].…”
Section: результатыunclassified
“…Survival of children after heart transplantation with pre-transplantation IPC (ECMO and Left Ventricular Bypass) and without mechanical support of blood circulation xas США) [57] и HeartWareHvad (HeartWare, Framingham, MA. США), осевые насосы HeartMate II (Thoratec Corporation США), Jarvik 2000 FlowMaker (Jarvik Heart, Inc., New York, CША) [58][59][60].…”
Section: результатыunclassified
“…Two case series studies evaluating the Jarvik 2000 LVAD were judged to be methodologically weak, [94][95][96][97][98][99][100] with poor reporting of the selection criteria for participants and the methods of data collection (Appendix 16). Outcome assessment was not blinded, providing the opportunity for ascertainment bias.…”
Section: Jarvikmentioning
confidence: 99%
“…80 Similarly, the study of the Novacor LVAD included male patients (100%) with a mean age of 47-51 years with ischaemic aetiology (40-80%), whereas the study of the Toyobo LVAD was of males (100%) with a mean age of 40 years and idiopathic dilated cardiomyopathy. One study of the Jarvik 2000 LVAD focused on males (66%) with a mean age of 47 years and suffering from ischaemic aetiology, 94 whereas in the other case study patient ages ranged from 30 to 70 years, 73% were male and 50% suffered from dilated cardiomyopathy and 50% from ischaemic cardiomyopathy. [94][95][96][97][98][99][100] The patients in the MicroMed DeBakey studies range in age from 33 to 65 years and were predominantly male.…”
Section: Generalisabilitymentioning
confidence: 99%
“…[28][29][30] The HeartMate II was FDA approved in January 2010 for use as destination therapy in adults with heart failure. Over 4000 HeartMate II devices have been implanted world-wide, 85 making it one of the most frequently used and successful VAD's in the current era.…”
Section: First-generation Vadsmentioning
confidence: 99%