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The Failing Right Heart pp 109–126Cite as

The Failing Right Ventricle in Adult Congenital Heart Disease

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Abstract

Given the reproducibility and success of congenital heart surgery in infancy, many patients now survive into adult life with late onset of right heart failure [1]. For these patients right ventricular function may determine symptomatic burden, quality of life and ultimate prognosis. Either naturally or following corrective surgery, the morphological right ventricle usually ejects blood into the pulmonary circulation. In the minority with transposition complexes, it may support the systemic circulation in which case the right ventricle determines longevity [2, 3]. As such this chamber can adapt and pump against systemic afterload for decades. Because of its importance in congenital heart disease, preservation of right ventricular function is increasingly in focus [4, 5].

Keywords

  • Late Gadolinium Enhancement
  • Atrial Septal Defect
  • Tricuspid Valve
  • Ventricular Septal Defect
  • Tricuspid Regurgitation

These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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  1. Department of Cardiac Surgery, Oxford University Hospitals Trust, Oxford, UK

    Stephen Westaby BSc, MS, PhD, FRCS, FETCS, FESC

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  1. Stephen Westaby BSc, MS, PhD, FRCS, FETCS, FESC
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Correspondence to Stephen Westaby BSc, MS, PhD, FRCS, FETCS, FESC .

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  1. Department of Cardiothoracic Surgery, Aristotle University of Thessaloniki AHEPA University Hospital, Thessaloniki, Greece

    Kyriakos Anastasiadis

  2. Department of Cardiac Surgery, Oxford University Hospitals NHS Trust, Oxford, United Kingdom

    Stephen Westaby

  3. Department of Cardiothoracic Surgery, Aristotle University of Thessaloniki AHEPA University Hospital, Thessaloniki, Greece

    Polychronis Antonitsis

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Westaby, S. (2015). The Failing Right Ventricle in Adult Congenital Heart Disease. In: Anastasiadis, K., Westaby, S., Antonitsis, P. (eds) The Failing Right Heart. Springer, Cham. https://doi.org/10.1007/978-3-319-17698-7_8

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