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Cardiac transplantation for end-stage congenital heart defects: the Mayo Clinic experience. Mayo Cardiothoracic Transplant Team.

AbstractOBJECTIVE:
To review the outcome of cardiac transplantation undertaken in patients with congenital heart defects.
MATERIAL AND METHODS:
Between November 1991 and March 1998 at our institution, cardiac transplantation was performed in 16 patients with congenital heart disease (age range, 3 to 57 years; mean, 26.1). Preoperative diagnoses included univentricular heart (N = 4); complete transposition of the great arteries (N = 3); Ebstein's anomaly (N = 2); tetralogy of Fallot (N = 2); levotransposition (N = 2); dextrocardia, corrected transposition, ventricular and atrial septal defects, and pulmonary stenosis (N = 1); double-outlet right ventricle (N = 1); and hypertrophic obstructive cardiomyopathy (N = 1). All patients had undergone from one to five previous palliative operations.
RESULTS:
Four patients required permanent pacemaker implantation during the first month postoperatively because of bradycardia; more than 2 years later, another patient required a permanent pacemaker because of sick sinus syndrome. In addition, one patient had an automatic implantable cardioverter-defibrillator. Three patients required reconstruction of cardiovascular structures with use of prosthetic material (Teflon patches or donor tissue) at the time of cardiac transplantation. Actuarial 1-, 2-, and 5-year survival was 86.2 +/- 9.1%. During the first year after transplantation, two deaths occurred--one at 41 days of putative vascular rejection and the second at 60 days of severe cellular rejection. All other patients are alive and functionally rehabilitated; the mean follow-up period has been 26.1 months (range, 2 to 89.6).
CONCLUSION:
Cardiac transplantation for patients with congenital heart disease can be accomplished with a low perioperative mortality and an excellent medium-term survival despite the challenges presented by the technical difficulties during invasive diagnostic procedures and at operation and the need for adherence to long-term multiple-drug therapy in this patient population.
AuthorsG Speziali, D J Driscoll, G K Danielson, P R Julsrud, C J Porter, J A Dearani, R C Daly, C G McGregor
JournalMayo Clinic proceedings (Mayo Clin Proc) Vol. 73 Issue 10 Pg. 923-8 (Oct 1998) ISSN: 0025-6196 [Print] England
PMID9787738 (Publication Type: Journal Article)
Chemical References
  • Immunosuppressive Agents
Topics
  • Actuarial Analysis
  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Female
  • Graft Survival
  • Heart Defects, Congenital (surgery)
  • Heart Transplantation
  • Humans
  • Immunosuppressive Agents (therapeutic use)
  • Male
  • Middle Aged
  • Reoperation
  • Survival Analysis
  • Treatment Outcome

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