Prevalence and timing of bend relief disconnection in patients supported by the late version HeartMate II left ventricular assist device

Author:

Yuzefpolskaya Melana,Uriel Nir,Chow Daniel S.,Restaino Susan W.,Mancini Donna M.,Flannery Margaret,Te-Frey Rosie,Chichetti JoAnne,Ota Takeyoshi,Kim Hyonah,Dano Drew D.,Pearson Gregory D.,Takayama Hiroo,Naka Yoshifumi,Jorde Ulrich P.

Publisher

Elsevier BV

Subject

Transplantation,Cardiology and Cardiovascular Medicine,Pulmonary and Respiratory Medicine,Surgery

Reference5 articles.

1. Extended mechanical circulatory support with a continuous-flow rotary left ventricular assist device;Pagani;J Am Coll Cardiol,2009

2. Long-term use of a left ventricular assist device for end- stage heart failure;Rose;N Engl J Med,2001

3. U.S. Food and Drug Administration. Thoratec Corporation, HeartMate II Left Ventricular Assist System (LVAS): Class 1 Recall—outflow graft may kink or deform. http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm298710.htm. Accessed: September 13, 2012.

4. Development of a novel echocardiography ramp test for speed optimization and diagnosis of device thrombosis in continuous flow left ventricular assist devices: The Columbia Ramp Study;Uriel;J Am Coll Cardiol,2012

5. Clinical impact, diagnosis, and management of a disconnected outflow graft bend relief in a patient supported by the HeartMate II Left Ventricular Assist System;Agarwal;J Heart Lung Transplant,2012

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