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Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
Considerations in Patients With Cardiac Implantable Electronic Devices at End of Life
1Melanie T. Gura is Director, Pacemaker & Arrhythmia Services, Northeast Ohio Cardiovascular Specialists, Towbridge Dr, Hudson, OH 44236 (meltg@aol.com).
Abstract:
Since the introduction of implantable cardiac pacemakers in 1958 and implantable cardioverter-defibrillators in 1980, these devices have been proven to save and prolong lives. Pacemakers, implantable cardioverter-defibrillators, and cardiac resynchronization therapy are deemed life-sustaining therapies. Despite these life-saving technologies, all patients ultimately will reach the end of their lives from either their heart disease or development of a terminal illness. Clinicians may be faced with patient and family requests to withdraw these life-sustaining therapies. The purpose of this article is to educate clinicians about the legal and ethical principles that underlie withdrawal of life-sustaining therapies such as device deactivation and to highlight the importance of proactive communication with patients and families in these situations.
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