Surgical treatment for hypertrophic cardiomyopathy: a historical perspective
- PMID: 28944172
- PMCID: PMC5602209
- DOI: 10.21037/acs.2017.04.03
Surgical treatment for hypertrophic cardiomyopathy: a historical perspective
Abstract
Our understanding of hypertrophic cardiomyopathy (HCM) as a disease entity has increased dramatically over the last half century. There has been a concerted effort by several surgical groups to develop operative techniques to relieve left ventricular outflow tract (LVOT) obstruction and alleviate symptoms. This paper traces the development of transaortic septal myectomy, the current gold standard therapy for relief of LVOT obstruction, in symptomatic patients refractory to medical treatment. In addition, we introduce newer methods for myectomy that have expanded the role of surgery in patients with various forms of HCM.
Keywords: Hypertrophic cardiomyopathy (HCM); history; septal myectomy.
Conflict of interest statement
Conflicts of Interest: The authors have no conflicts of interest to declare.
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References
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- American College of Cardiology Foundation/American Heart Association Task Force on Practice .; American Association for Thoracic Surgery.; American Society of Echocardiography.; American Society of Nuclear Cardiology.; Heart Failure Society of America.; Heart Rhythm Society.; Society for Cardiovascular Angiography and Interventions.; Society of Thoracic Surgeons., Gersh BJ, Maron BJ, et al. 2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. J Thorac Cardiovasc Surg 2011;142:e153-203. 10.1016/j.jtcvs.2011.10.020 - DOI - PubMed
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- Authors/Task Force members ., Elliott PM, Anastasakis A, et al. 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC). Eur Heart J 2014;35:2733-79. 10.1093/eurheartj/ehu284 - DOI - PubMed
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