Cardiac Autonomic Nervous System Activity and Cardiac Function in Children After Coarctation Repair

Ineke Nederend1, Eco J C de Geus2, Lucia J M Kroft3

  • 1Amsterdam Public Health Research Institute, Department of Biological Psychology, Faculty of Behavioral and Movement Sciences, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands; Department of Pediatric Cardiology, Leiden University Medical Center, Leiden, The Netherlands.

Insights

Children after coarctation of the aorta (CoA) repair show impaired cardiac output and left ventricular function. Autonomic nervous system activity remained unchanged, highlighting the need for ongoing clinical monitoring post-surgery.

Area of Science:

  • Pediatric Cardiology
  • Congenital Heart Disease
  • Autonomic Nervous System

Background:

  • Coarctation of the aorta (CoA) is a common congenital heart defect.
  • Improved surgical outcomes allow most patients to reach adulthood.
  • Late complications like hypertension, recoarctation, and arrhythmias are frequent, suggesting a role for the autonomic nervous system (ANS).

Purpose of the Study:

  • To evaluate cardiac ANS activity and cardiac function in children post-CoA repair.
  • To investigate the relationship between cardiac ANS activity and cardiac function in these patients.

Main Methods:

  • A cohort of 31 children post-CoA repair and 62 healthy controls (ages 8-18) were studied.
  • Ambulatory impedance cardiography monitored cardiac ANS activity and cardiac output over 24 hours.
  • Transthoracic echocardiography and cardiac MRI assessed cardiac function.

Main Results:

  • No significant differences in ambulatory cardiac ANS activity were observed between groups.
  • Patients exhibited significantly decreased ambulatory cardiac output compared to controls.
  • Left ventricular function was also significantly reduced in the post-CoA repair group.

Conclusions:

  • Left ventricular function and cardiac output are impaired in children after CoA repair, irrespective of ANS activity.
  • These findings emphasize the necessity of continued clinical follow-up for pediatric CoA patients, even without detectable residual stenosis.
Abstract

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