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Extended septal myectomy for hypertrophic obstructive cardiomyopathy with anomalous mitral papillary muscles or
Kenji Minakata1, Joseph A Dearani, Rick A Nishimura
1Division of Cardiovascular Surgery, Mayo Clinic, Rochester, Minn, USA.
Insights
Surgical relief of mitral valve anomalies and extended septal myectomy effectively treat hypertrophic obstructive cardiomyopathy. This approach avoids mitral valve replacement, significantly reduces obstruction and regurgitation, and yields excellent long-term outcomes.
Area of Science:
- Cardiovascular Surgery
- Cardiology
- Cardiac Surgery
Background:
- Hypertrophic obstructive cardiomyopathy (HOCM) often requires surgical intervention.
- Transaortic septal myectomy is a primary treatment, but mitral subvalvular apparatus anomalies can complicate outcomes.
- Mitral valve replacement is sometimes considered for complex cases.
Purpose of the Study:
- To evaluate the efficacy of preserving the mitral valve in HOCM patients with anomalous mitral subvalvular apparatus.
- To assess surgical techniques aimed at relieving obstruction while maintaining the native mitral valve.
Main Methods:
- A retrospective review of 56 patients (ages 2-77) with HOCM and anomalous mitral subvalvular apparatus (chordae or papillary muscles) undergoing surgery between 1975 and 2002.
- Procedures included resection of anomalous chordae, relief of papillary muscle fusion, and extended septal myectomy.
- 82% of patients were initially in New York Heart Association (NYHA) class III or IV.
Main Results:
- No early mortality or need for mitral valve replacement.
- Significant reduction in mean peak left ventricular outflow tract pressure gradients (70 to 4.9 mm Hg) and mitral regurgitation (grade 2.3 to 1.0; P <.001).
- At a mean follow-up of 2.8 years, 95% freedom from reoperation and 98% of patients in NYHA class I or II.
Conclusions:
- HOCM with mitral subvalvular anomalies can be successfully managed without mitral valve replacement.
- Surgical correction of anomalies combined with extended septal myectomy offers excellent early and late results.
- This strategy significantly alleviates obstruction and mitral regurgitation, improving patient functional status.
Objectives:
Transaortic left ventricular septal myectomy yields excellent results for most severely symptomatic patients with hypertrophic obstructive cardiomyopathy. However, associated anomalies of the mitral subvalvular apparatus may prevent complete relief of obstruction, and mitral valve replacement has been advocated. We reviewed our results of procedures designed to relieve obstruction with preservation of the mitral valve.
Methods:
Among 291 patients undergoing septal myectomy from 1975 to 2002, 56 (ages 2-77 years) had anomalous mitral subvalvular apparatus including anomalous chordae (n = 28) and papillary muscles with direct insertion into mitral leaflets (n = 13) or fusion to septum (n = 31) or free wall (n = 12); 82% of patients were in New York Heart Association class III or IV. Operation included resection of anomalous chordae (28 patients), relief of papillary muscle fusion (36 patients), and extended septal myectomy, wider at the apex than the base.
Results:
There were no early deaths and no patients required mitral valve replacement. Mean peak pressure gradients decreased from 70 +/- 28 to 4.9 +/- 8.4 mm Hg and mean mitral regurgitation grade decreased from 2.3 to 1.0 (P <.001). Mean follow-up was 2.8 +/- 2.6 years. Freedom from reoperation at 4 years was 95%. There were 3 late noncardiac deaths; 98% of patients were in New York Heart Association class I or II.
Conclusions:
Hypertrophic obstructive cardiomyopathy associated with anomalous mitral papillary muscles or chordae can be successfully treated without mitral valve replacement by surgical relief of the anomalies and an extended septal myectomy; early mortality is low, obstruction and mitral regurgitation are significantly reduced, and late results are excellent.
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