Frequency of Poor Outcome (Death or Poor Quality of Life) After Left Ventricular Assist Device for Destination Therapy
نویسندگان
چکیده
Patients with end-stage heart failure are highly symptomatic and are expected to have a short life expectancy without intervention. For patients who are not candidates for heart transplantation, a left ventricular assist device (LVAD) may be an ideal treatment option as destination therapy, meaning that the patient is expected to live with the device until death (ie, not a bridge to heart transplant). Although an LVAD markedly improves survival and quality of life in the majority of such patients, the risk of mortality remains high even after implantation, despite continued improvements in device technology and surgical experience. Furthermore, many patients who undergo LVAD survive but continue to have poor quality of life because of a myriad of potential reasons, including refractory or recurrent heart failure symptoms, failure to recover from major cardiac surgery, or device-related complications such as bleeding, infections, stroke, and pump malfunction. Finally, the reasons that these patients are ineligible for heart transplantation—advanced age, noncardiac comorbidity, and frailty—may persist after LVAD implantation and can limit the ability of the patients to successfully regain a meaningful quality of life.
منابع مشابه
Frequency of Poor Outcome (Death or Poor Quality of Life) After Left Ventricular Assist Device for Destination Therapy: Results From the INTERMACS Registry.
BACKGROUND A left ventricular assist device (LVAD) improves survival and quality of life for many, but not all, patients with end-stage heart failure who are ineligible for transplantation. We sought to evaluate the frequency of poor outcomes using a novel composite measure that integrates quality of life with mortality. METHODS AND RESULTS Within the INTERMACS (Interagency Registry for Mecha...
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Advances in mechanical circulatory support (MCS) have resulted in improved quality of life (QOL) and survival for the majority of patients implanted for destination therapy (DT). However, some patients will have persistently limiting heart failure (HF) symptoms and poor QOL. Nearly all patients receiving a left ventricular assist device (LVAD) as DT will eventually die with their device in situ...
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The left ventricular assist device was originally designed to be surgically implanted as a bridge to transplantation for patients with chronic end-stage heart failure. On the basis of the REMATCH trial, the US Food and Drug Administration and the US Centers for Medicare & Medicaid Services approved permanent implantation of the left ventricular assist device as a destination therapy in Medicare...
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BACKGROUND INTERMACS (Interagency Registry for Mechanically Assisted Circulatory Support) profiles provide important prognostic information for patients with advanced heart failure (HF) receiving mechanical support. The value of INTERMACS profiling has not been shown for patients followed on medical therapy for advanced HF at centers that also offer mechanical circulatory support. METHODS AND...
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