Surgical management of hypertrophic cardiomyopathy

Chandrasekaran Ananthanarayanan1, SriKrishna Reddy Modugula1, Vincent Chauvette1

  • 1Department of Thoracic and Cardiovascular Surgery, Heart Vascular and Thoracic Institute, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH 44195 USA.

Insights

Surgical myectomy offers a curative solution for symptomatic hypertrophic cardiomyopathy (HCM) patients unresponsive to medication. This procedure safely reduces left ventricular outflow tract obstruction, improving long-term survival and quality of life.

Area of Science:

  • Cardiology
  • Cardiac Surgery
  • Medical Research

Background:

  • Hypertrophic cardiomyopathy (HCM) presents a wide clinical spectrum, from incidental findings to sudden cardiac death.
  • Medical management is the initial approach for symptomatic patients, with new drugs under investigation.
  • Invasive therapy, specifically surgical myectomy, is indicated for patients with persistent symptoms despite maximal medical therapy and offers better long-term survival.

Purpose of the Study:

  • To analyze the outcomes of surgical myectomy for hypertrophic cardiomyopathy (HCM) performed between 2005 and 2015.
  • To evaluate the effectiveness of septal myectomy in reducing left ventricular outflow tract (LVOT) obstruction.
  • To assess the safety and complication rates associated with surgical myectomy in a large patient cohort.

Main Methods:

  • Retrospective analysis of 1549 patients who underwent surgical myectomy for HCM.
  • Evaluation of pre- and post-operative left ventricular outflow tract (LVOT) gradients.
  • Assessment of operative parameters including aortic cross-clamp time and muscle resection mass.
  • Review of complication rates, operative mortality, hospital stay, and post-operative functional status (NYHA class).

Main Results:

  • Surgical myectomy significantly reduced the mean LVOT gradient from 63 mmHg pre-operatively to 15 mmHg post-operatively.
  • The mean aortic cross-clamp time was 28 minutes, with an average of 8.1 g of muscle resected.
  • Low complication rates were observed, including 4.2% pacemaker insertion, two iatrogenic ventricular septal defects, and an operative mortality of 0.38%.
  • Mean hospital stay was 6 days, with most patients achieving New York Heart Association (NYHA) class I post-operatively.

Conclusions:

  • Septal myectomy is a curative treatment for symptomatic HCM patients refractory to medical management.
  • A thorough understanding of individual septal anatomy and LVOT obstruction mechanisms is crucial for successful surgical outcomes.
  • Surgical myectomy can be performed safely, yielding excellent long-term results and significantly improving patient functional status.
Abstract

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