AI Article Synopsis

  • Right ventricular outflow dysfunction is a common issue in patients with repaired tetralogy of Fallot, leading to increased health risks as they age.
  • The American Heart Association has released an update focusing on how to monitor and treat this condition effectively, including new therapies and techniques for managing complications.
  • The statement highlights the importance of understanding how other health issues and patients' perspectives affect their quality of life and includes discussions on when and how to perform pulmonary valve replacements.

Article Abstract

Right ventricular outflow dysfunction, manifesting as stenosis, regurgitation, or both, is nearly universal in patients with repaired tetralogy of Fallot, precipitating a complex pathophysiological cascade that leads to increasing rates of morbidity and mortality with advancing age. As the number of adolescent and adult patients with repaired tetralogy of Fallot continues to grow as a result of excellent survival during infancy, the need to improve late outcomes has become an urgent priority. This American Heart Association scientific statement provides an update on the current state of knowledge of the pathophysiology, methods of surveillance, risk stratification, and latest available therapies, including transcatheter and surgical pulmonary valve replacement strategies, as well as management of life-threatening arrhythmias. It reviews emerging evidence on the roles of comorbidities and patient-reported outcomes and their impact on quality of life. In addition, this scientific statement explores contemporary evidence for clinical choices such as transcatheter or surgical pulmonary valve replacement, discusses criteria and options for intervention for failing implanted bioprosthetic pulmonary valves, and considers a new approach to determining optimal timing and indications for pulmonary valve replacement.

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Source
http://dx.doi.org/10.1161/CIR.0000000000001291DOI Listing

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