Right ventricular dysplasia: the Mayo Clinic experience

Mayo Clin Proc. 1995 Jun;70(6):541-8. doi: 10.4065/70.6.541.

Abstract

Objective: To determine the initial clinical manifestations and echocardiographic features of right ventricular dysplasia as encountered in a major cardiovascular referral center in the United States.

Design: We conducted a retrospective study of cases of right ventricular dysplasia diagnosed at the Mayo Clinic between January 1978 and January 1993.

Material and methods: In an institutional data-base search, we identified 20 patients with right ventricular dysplasia. Echocardiographic, electrophysiologic, Holter monitoring, cardiac catheterization, and endomyocardial biopsy results were analyzed. The mean duration of follow-up was 7 years.

Results: In the 12 female and 8 male patients (mean age, 30 years; range, 3 to 60), the initial manifestations of right ventricular dysplasia included ventricular arrhythmia (45%), congestive heart failure (25%), heart murmur (10%), asymptomatic (10%), complete heart block (5%), and sudden death (5%). First-order relatives were affected in 30% of the patients. Ventricular tachycardia with morphologic features of left bundle branch block was inducible in seven of nine patients. On Holter monitoring, all but 2 of 15 patients studied had frequent ventricular ectopic activity (Lown grade 2 or more). Characteristic fatty infiltration of the myocardium was present in 7 of 13 right ventricular biopsy specimens. Inordinate right ventricular enlargement was present in 60% of the patients at first echocardiographic assessment and in two other patients on follow-up assessment. Variable left ventricular involvement was noted in 50% of the cases. During the follow-up period, four patients died: two died suddenly, one died of congestive heart failure, and one died of respiratory failure after a coronary artery bypass operation. Of the 16 living patients, 8 are doing well, 3 have an implanted cardiac defibrillator, 3 are receiving antiarrhythmic agents, and 2 have undergone cardiac transplantation because of progressive biventricular failure.

Conclusion: Patients with right ventricular dysplasia have varied initial manifestations and a high frequency of serious cardiovascular symptoms and complications.

MeSH terms

  • Adolescent
  • Adult
  • Cardiac Catheterization
  • Child
  • Child, Preschool
  • Death, Sudden, Cardiac / etiology
  • Echocardiography
  • Electrocardiography, Ambulatory
  • Female
  • Follow-Up Studies
  • Heart Block / diagnosis
  • Heart Block / etiology
  • Heart Block / physiopathology
  • Heart Failure / diagnosis
  • Heart Failure / etiology
  • Heart Failure / physiopathology
  • Heart Murmurs / diagnosis
  • Heart Murmurs / etiology
  • Heart Murmurs / physiopathology
  • Heart Ventricles / pathology*
  • Humans
  • Hypertrophy, Right Ventricular / complications
  • Hypertrophy, Right Ventricular / diagnosis*
  • Hypertrophy, Right Ventricular / physiopathology
  • Male
  • Middle Aged
  • Retrospective Studies
  • Tachycardia, Ventricular / diagnosis
  • Tachycardia, Ventricular / etiology
  • Tachycardia, Ventricular / physiopathology
  • Ventricular Dysfunction, Right / complications
  • Ventricular Dysfunction, Right / diagnosis*
  • Ventricular Dysfunction, Right / physiopathology
  • Ventricular Function, Right