A case of mid-apical obstructive hypertrophic cardiomyopathy treated with a transapical myectomy approach: a case

Thiago Luis Scudeler, Paulo Cury Rezende, Fernando Teiichi Costa Oikawa

  • 1Department of Atherosclerosis, Heart Institute (InCor), University of São Paulo, Avenida Doutor Enéas de Carvalho Aguiar 44, AB, Sala 114, Cerqueira César, 05403-000 São Paulo, SP, Brazil. whady.hueb@incor.usp.br.

Insights

Transapical myectomy offers a new surgical option for mid-apical obstructive hypertrophic cardiomyopathy. This approach effectively resolved symptoms in a patient refractory to medical treatment.

Area of Science:

  • Cardiology
  • Cardiac Surgery
  • Genetics

Background:

  • Hypertrophic cardiomyopathy (HCM) is a genetic heart condition with variable presentation.
  • Myocardial hypertrophy can affect different parts of the left ventricle, including mid-apical segments.
  • Standard treatments include medical therapy, with surgery reserved for specific cases.

Observation:

  • A 63-year-old woman with symptomatic mid-apical obstructive hypertrophic cardiomyopathy despite optimal medical therapy.
  • Transthoracic echocardiography and cardiac MRI confirmed significant left ventricular hypertrophy in the mid-apical region.
  • A transaortic approach was deemed difficult, prompting consideration of an alternative surgical strategy.

Findings:

  • A successful transapical myectomy was performed for mid-apical obstructive hypertrophic cardiomyopathy.
  • The patient experienced complete resolution of symptoms post-procedure.
  • No complications were reported following the transapical approach.

Implications:

  • Transapical myectomy is a viable and effective treatment for mid-apical obstructive hypertrophic cardiomyopathy.
  • This approach should be considered for patients with refractory symptoms.
  • Further research into the transapical approach for HCM is warranted.
Abstract

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