Effect of Intercurrent Operation and Cerebral Oxygenation on Developmental Trajectory in Congenital Heart Disease

George M Hoffman1, Cheryl L Brosig1, Laurel M Bear2

  • 1Herma Heart Center, Children's Hospital of Wisconsin, Milwaukee, Wisconsin; Departments of Pediatric Anesthesiology, Pediatrics, and Pediatric Critical Care Medicine, Cardiology, and Cardiothoracic Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin.

Insights

Children with congenital heart disease (CHD) face neurodevelopmental risks. Improved physiological status, not just surgical procedures, is linked to better cognitive and motor outcomes in these children.

Area of Science:

  • Pediatric Cardiology
  • Neurodevelopmental Pediatrics
  • Medical Engineering

Background:

  • Children with congenital heart disease (CHD) exhibit elevated risks for abnormal neurodevelopment (ND).
  • Both demographic and perioperative physiological factors influence developmental outcomes in these children.
  • The precise impact of surgical procedures on ND, balancing risks against benefits of improved physiology, remains unclear.

Purpose of the Study:

  • To identify procedural and physiological factors associated with neurodevelopmental outcomes in children with CHD.
  • To assess the relationship between outpatient assessments and long-term developmental trajectories.
  • To investigate the risk-benefit balance of surgical interventions on neurodevelopment.

Main Methods:

  • Utilized Bayley Scales of Infant Development-III for at least three assessments in the first three years of life for 178 high-risk CHD children.
  • Recorded cardiac procedures, hospitalization duration, feeding status, anthropometrics, and arterial, cerebral, and somatic oxygen saturations via near-infrared spectroscopy (NIRS) at each visit.
  • Employed general linear models to predict language, motor, and cognitive composite scores and their changes over time.

Main Results:

  • Motor performance improved with age across all diagnostic groups; cognitive and language skills improved in single-ventricle (1V) patients but not in two-ventricle (2V) or genetic syndrome groups.
  • 1V patients showed lower initial motor scores but higher improvement rates, achieving normal scores by 24 months, unlike genetic syndrome patients who remained below normal.
  • Higher arterial saturation and narrower NIRS saturation differences correlated with better motor performance; increased cardiopulmonary bypass time, hospital stay, and tube feeding were risk factors.

Conclusions:

  • Physiological status, particularly as assessed by NIRS-derived cerebral and somatic oxygenation, is significantly associated with neurodevelopmental performance in children with CHD.
  • The number of surgical procedures itself is not a risk factor for neurodevelopment when adjusted for cardiopulmonary bypass time and physiological status.
  • Interventions aimed at optimizing physiological status hold promise for improving neurodevelopmental outcomes in this vulnerable population.
Abstract

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