2002
DOI: 10.1016/s1053-2498(01)00408-9
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Long-term follow-up of thoratec ventricular assist device bridge-to-recovery patients successfully removed from support after recovery of ventricular function

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Cited by 213 publications
(122 citation statements)
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“…The main complication of mechanical circulatory support in these patients is bleeding. As seen with other systems the DeBakey LVAD comes with a high incidence of bleeding [4,9], our results indicate no significant differences with previously reported figures [11].…”
Section: Discussionsupporting
confidence: 59%
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“…The main complication of mechanical circulatory support in these patients is bleeding. As seen with other systems the DeBakey LVAD comes with a high incidence of bleeding [4,9], our results indicate no significant differences with previously reported figures [11].…”
Section: Discussionsupporting
confidence: 59%
“…Copeland and associates [2] performed the first bridging to HTx by mechanical support in 1985. Mortality of terminal heart failure being very high as disease progresses, HTx candidates die while waiting on long lists [3,4]. According to the recently published REMATCH study [3], the use of left ventricular assist devices (LVAD) resulted in more than twice the survival rate and an improved quality of life, in comparison to optimal medical management.…”
Section: Introductionmentioning
confidence: 99%
“…Furthermore, many cellular processes improve, although they do not completely normalise. [5][6][7][8][9][10][11][12][13][14][15] Sufficient recovery of left ventricular function, allowing LVAD explantation, however, is rare and is mainly feasible in patients suffering from acute myocarditis or PPCM. 10,11,13 In these cases, the LVAD will maintain the patient's life, allowing the myocardium to recover from the underlying disease.…”
Section: Discussionmentioning
confidence: 99%
“…Long-term results after explantation are favourable (one-and five-year survival rate of 86 and 78%, respectively). 14,15 In patients with longstanding idiopathic dilating cardiomyopathy, the concept of reverse remodelling while on the LVAD is intriguing but requires further study to see to what extent this may result in explantation of the device, to investigate the optimal drug regime necessary and the reliable monitoring of this process. 6-9 ■ …”
Section: Discussionmentioning
confidence: 99%
“…It is FDA approved as a bridge to transplant. In the seventh Interagency Registry for Mechanically Assisted Circulatory Support (INTERMACS) report, only 1% of the 1357 patients with continuous flow left ventricular assist devices (CFLVADs) that were implanted with the bridge-to-transplant (BTT) strategy had sufficient myocardial recovery to allow explant of the LVAD at 12 months [1][2][3][4].…”
Section: Introductionmentioning
confidence: 99%