Low thromboembolic risk without anticoagulation using advanced-design left ventricular assist devices
Autor: | Howard R. Levin, Alan D. Weinberg, O.H. Frazier, J. Kirk Roberts, Eric A. Rose, James P. Slater, Mehmet C. Oz |
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Rok vydání: | 1996 |
Předmět: |
Pulmonary and Respiratory Medicine
Adult Male medicine.medical_specialty Time Factors Adolescent Waiting Lists medicine.drug_class Ultrasonography Doppler Transcranial medicine.medical_treatment Risk Factors Internal medicine Thromboembolism medicine Humans Prospective Studies Prospective cohort study Aged Heart transplantation Heart Failure business.industry Incidence Anticoagulant Warfarin Anticoagulants Equipment Design Middle Aged medicine.disease Transcranial Doppler Surgery Heart failure Ventricular assist device Cardiology Heart Transplantation Female Heart-Assist Devices Cardiology and Cardiovascular Medicine Complication business medicine.drug |
Zdroj: | The Annals of thoracic surgery. 62(5) |
ISSN: | 0003-4975 |
Popis: | Background. A major limitation of cardiac assist devices has been the high incidence of thromboembolic events and their requirement for systemic anticoagulation. The Thermo Cardiosystems HeartMate 1000 IP left ventricular assist device (LVAD) employs a design that may reduce thromboembolic risk and obviate the need for systemic anticoagulation. Methods. Two hundred twenty-three patients with nonreversible heart failure were supported with the HeartMate LVAD as a bridge to heart transplantation. All patients were monitored prospectively for thromboembolic events. Anticoagulation regimens and occurrence of subclinical thromboembolic events, including those seen by transcranial Doppler examinations in selected patients, were also recorded. Results. Total time of LVAD support use was 531.2 patient-months. Twenty-three patients (10%) received warfarin postoperatively for 42.4 patient-months (8.2% of total support time). Six patients (2.7%) had thromboembolic events, representing 0.011 events per patient-month of device use. Conclusions. The thromboembolic complication rate associated with this LVAD is acceptably low despite the minimal anticoagulation employed in this series, allowing consideration of long-term device use for the treatment of heart failure. |
Databáze: | OpenAIRE |
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