Transapical Ventricular Remodeling for Hypertrophic Cardiomyopathy With Systolic Cavity Obliteration
Daokun Sun1, Hartzell V Schaff1, Rick A Nishimura2
1Department of Cardiovascular Surgery, Mayo Clinic, Rochester, Minnesota.
Insights
Transapical septal myectomy safely improves heart function in hypertrophic cardiomyopathy (HCM) patients with systolic obliteration. This procedure offers a viable alternative to heart transplantation for advanced heart failure.
Area of Science:
- Cardiology
- Cardiac Surgery
- Heart Failure Management
Background:
- Hypertrophic cardiomyopathy (HCM) can cause reduced left ventricular (LV) stroke volume and systolic cavity obliteration due to symmetric LV hypertrophy.
- This specific subgroup of HCM patients presents unique challenges in managing heart failure.
- Current treatment options may be limited for these patients.
Purpose of the Study:
- To detail the experience with transapical septal myectomy in patients with HCM and systolic cavity obliteration.
- To evaluate the safety and efficacy of this surgical approach in enlarging LV volume and relieving cavity obliteration.
- To assess early survival and functional outcomes in this patient cohort.
Main Methods:
- Analysis of 38 patients with HCM and symmetric LV hypertrophy who underwent transapical septal myectomy between February 2001 and May 2021.
- Evaluation of preoperative clinical status, including New York Heart Association (NYHA) class and exercise capacity.
- Assessment of postoperative outcomes, including survival rates and functional improvement.
Main Results:
- Most patients (84.2%) presented in NYHA class III/IV, with significantly reduced peak oxygen consumption and enlarged left atrial size.
- Transapical septal myectomy was performed on all patients to increase LV cavity size.
- No in-hospital mortality occurred; 1, 3, and 5-year survival rates were 100%, 92%, and 87%, respectively, with significant functional improvement reported in most patients.
Conclusions:
- Transapical myectomy is a safe procedure for enlarging LV cavity volume in selected HCM patients.
- The procedure demonstrates good early survival and functional outcomes.
- It represents a valuable alternative to cardiac transplantation for HCM patients experiencing systolic cavity obliteration and progressive heart failure.
Background:
Some patients with hypertrophic cardiomyopathy (HCM) present with reduced left ventricular (LV) stroke volume and elongated systolic cavity obliteration due to symmetric LV hypertrophy. In this report, we detail our experience with transapical septal myectomy to enlarge the LV volume and to relieve cavity obliteration in this unique subgroup of patients with HCM.
Methods:
We analyzed 38 patients with HCM who had extended symmetric LV hypertrophy and underwent transapical septal myectomy to enlarge the LV cavity from February 2001 to May 2021.
Results:
At the time of evaluation for operation, 84.2% (n = 32) of the patients were in New York Heart Association class III/IV. The peak oxygen consumption was 51.5% (44.0%-58.0%) of the normal predicted values on the preoperative exercise stress test (n = 16). Preoperative left atrial sizes in this cohort were enlarged (left atrial volume index, 39.0 [33.5-51.5] mL/m2), despite only 4 patients with moderate or greater mitral valve regurgitation. All patients underwent transapical septal myectomy to enlarge the LV cavity size. There was no postoperative (within 30 days) death. During a median (interquartile range) follow-up of 3.4 (0.7-6.9) years, the estimated survival rates were 100%, 92%, and 87% at 1, 3, and 5 years, respectively. Follow-up surveys suggested that 16 of the 17 contacted patients experienced improvement in their heart function after the procedure.
Conclusions:
Transapical myectomy to enlarge LV cavity volume can be performed safely with good early survival and functional results. This procedure is an important alternative to cardiac transplantation for HCM patients with systolic cavity obliteration and progressive heart failure.
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