Cardiac resynchronisation therapy in paediatric and congenital heart disease: differential effects in various anatomical and functional substrates

Heart. 2009 Jul;95(14):1165-71. doi: 10.1136/hrt.2008.160465. Epub 2009 Mar 22.

Abstract

Background: Cardiac resynchronisation therapy (CRT) is increasingly used in children in a variety of anatomical and pathophysiological conditions, but published data are scarce.

Objective: To record current practice and results of CRT in paediatric and congenital heart disease.

Design: Retrospective multicentre European survey.

Setting: Paediatric cardiology and cardiac surgery centres.

Patients: One hundred and nine patients aged 0.24-73.8 (median 16.9) years with structural congenital heart disease (n = 87), congenital atrioventricular block (n = 12) and dilated cardiomyopathy (n = 10) with systemic left (n = 69), right (n = 36) or single (n = 4) ventricular dysfunction and ventricular dyssynchrony during sinus rhythm (n = 25) or associated with pacing (n = 84).

Interventions: CRT for a median period of 7.5 months (concurrent cardiac surgery in 16/109).

Main outcome measures: Functional improvement and echocardiographic change in systemic ventricular function.

Results: The z score of the systemic ventricular end-diastolic dimension decreased by median 1.1 (p<0.001). Ejection fraction (EF) or fractional area of change increased by a mean (SD) of 11.5 (14.3)% (p<0.001) and New York Heart Association (NYHA) class improved by median 1.0 grade (p<0.001). Non-response to CRT (18.5%) was multivariably predicted by the presence of primary dilated cardiomyopathy (p = 0.002) and poor NYHA class (p = 0.003). Presence of a systemic left ventricle was the strongest multivariable predictor of improvement in EF/fractional area of change (p<0.001). Results were independent of the number of patients treated in each contributing centre.

Conclusion: Heart failure associated with ventricular pacing is the largest indication for CRT in paediatric and congenital heart disease. CRT efficacy varies widely with the underlying anatomical and pathophysiological substrate.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Arrhythmias, Cardiac / etiology
  • Arrhythmias, Cardiac / physiopathology
  • Arrhythmias, Cardiac / therapy*
  • Cardiac Pacing, Artificial*
  • Cardiomyopathy, Dilated / complications*
  • Cardiomyopathy, Dilated / physiopathology
  • Child
  • Child, Preschool
  • Echocardiography
  • Heart Defects, Congenital / complications*
  • Heart Defects, Congenital / physiopathology
  • Heart Transplantation / statistics & numerical data
  • Humans
  • Infant
  • Middle Aged
  • Mitral Valve Insufficiency / etiology
  • Mitral Valve Insufficiency / therapy
  • Pacemaker, Artificial
  • Retrospective Studies
  • Risk Factors
  • Treatment Outcome
  • Ventricular Remodeling
  • Young Adult