Abstract
Long-term left-ventricular assist device (LVAD) support as destination therapy (DT) is a promising new alternative for the growing population of patients with advanced heart failure. In this article, we summarize the clinical trials that led to the approval of LVAD use as DT in the US national policies regulating candidate selection and DT center accreditation. We review current guidelines for candidate selection, clinical tools to assess candidate operative risk, and outcomes of DT.
MeSH terms
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Angiotensin-Converting Enzyme Inhibitors / therapeutic use
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Antihypertensive Agents / therapeutic use
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Cardiotonic Agents / therapeutic use
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Equipment Design
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Heart Failure / drug therapy
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Heart Failure / mortality
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Heart Failure / surgery*
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Heart-Assist Devices / economics
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Heart-Assist Devices / statistics & numerical data*
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Humans
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Patient Selection*
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Risk Factors
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Treatment Outcome
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United States
Substances
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Angiotensin-Converting Enzyme Inhibitors
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Antihypertensive Agents
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Cardiotonic Agents