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Born with a Failing Right Heart

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Clinical Cases in Right Heart Failure

Part of the book series: Clinical Cases in Cardiology ((CCC))

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Abstract

Tetralogy of Fallot is one of the most common congenital heart diseases with increasing numbers of patients surviving into adulthood due to advances in surgical and transcatheter techniques. Whereas children undergo surgical repair early, the pathophysiology has a lifetime of consequences, increasing the risk of right heart failure with variable timing and presentation throughout adulthood. Key sequelae of repair include pulmonary regurgitation, pulmonary stenosis, impaired right ventricular function, left ventricular dysfunction, arrhythmias, and conduction abnormalities—all of which contribute to morbidity and mortality later in life. These sequelae are managed using a combination of medical therapy, pacemaker and defibrillator devices, transcatheter and surgical valve replacement, and advanced heart failure therapies, including heart transplantation.

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Correspondence to Michael J. Landzberg .

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Carazo, M.R., Landzberg, M.J., Jokhadar, M. (2020). Born with a Failing Right Heart. In: Tsao, L., Afari, M. (eds) Clinical Cases in Right Heart Failure. Clinical Cases in Cardiology. Springer, Cham. https://doi.org/10.1007/978-3-030-38662-7_4

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  • DOI: https://doi.org/10.1007/978-3-030-38662-7_4

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