3D printing of severe hypertrophic cardiomyopathy in a child with Rasopathy

N F Johnston1, T Prendiville1, C J McMahon2

  • 1Department of Paediatric Cardiology, Our Lady's Children's Hospital, Crumlin, Dublin, 12, Ireland.

Insights

Three-dimensional (3D) printing aids in assessing hypertrophic cardiomyopathy, especially in complex cases like Rasopathy. This innovative technique complements traditional imaging methods for better cardiac evaluation.

Area of Science:

  • Cardiology
  • Biomedical Engineering
  • Medical Imaging

Background:

  • Hypertrophic cardiomyopathy (HCM) is a significant cardiac condition often requiring advanced imaging for diagnosis and management.
  • Rasopathies are genetic disorders that can present with complex cardiac anomalies, including HCM.
  • Echocardiography and cardiac MRI are standard tools for evaluating HCM, but may have limitations in visualizing complex 3D structures.

Observation:

  • A case study involving a boy with Rasopathy and hypertrophic cardiomyopathy is presented.
  • Three-dimensional (3D) printing was utilized in conjunction with echocardiography to assess the cardiac condition.
  • The 3D printed model provided an additional perspective on the patient's specific cardiac anatomy.

Findings:

  • Three-dimensional printing offers a supplementary method for evaluating hypertrophic cardiomyopathy.
  • The integration of 3D printing with echocardiography enhanced the assessment of complex cardiac morphology in this patient.
  • This approach may improve the understanding of structural abnormalities in HCM.

Implications:

  • 3D printing holds potential as an adjunct to conventional imaging modalities like echocardiography and MRI for HCM.
  • This technology could improve surgical planning and patient education in cases of complex congenital heart disease.
  • Further research into the application of 3D printing in cardiology is warranted to explore its full clinical utility.