Neurodevelopmental Outcome in Children With Single Ventricle After Total Cavopulmonary Connection

Nicole Vahsen1, Arndt Bröder2, Viktor Hraska3

  • 1German Paediatric Heart Centre Sankt Augustin, Paediatric Cardiology, Sankt Augustin, Germany.

Klinische Padiatrie
|December 20, 2017
PubMed

Insights

Children with single ventricle hearts after total cavopulmonary connection show increased neurodevelopmental delays and behavioral issues. However, their quality of life is comparable to the general population, highlighting the need for early intervention.

Area of Science:

  • Pediatric Cardiology
  • Neurodevelopmental Pediatrics
  • Congenital Heart Disease

Background:

  • Single ventricle heart physiology presents unique challenges.
  • Total cavopulmonary connection (TCPC) is a palliative surgical procedure.
  • Neurodevelopmental outcomes after TCPC require thorough assessment.

Purpose of the Study:

  • To evaluate neuropsychological outcomes in children with single ventricle hearts post-TCPC.
  • To identify risk factors associated with impaired neurodevelopment in this population.

Main Methods:

  • 104 patients aged 2-20 years underwent standardized neuropsychological testing.
  • Assessments included intelligence, motor function, visuospatial abilities, and behavior.
  • Health-related quality of life was measured via self-report.

Main Results:

  • Patients scored significantly lower in fluid and crystallized intelligence compared to the general population.
  • Reduced motor function (34%), impaired visuospatial abilities (51%), and behavioral problems were prevalent.
  • Deep hypothermic circulatory arrest and pre-TCPC brain perfusion complications were risk factors for reduced fluid intelligence.

Conclusions:

  • Children with single ventricle hearts undergoing TCPC face higher risks of neurodevelopmental delays and behavioral disorders.
  • Despite these challenges, quality of life is generally well-maintained.
  • Prompt diagnosis and intervention are crucial for suspected developmental delays.
Abstract