Key result
Extended septal myectomy for HOCM shows ~78% long-term survival and complete freedom from cardiac reoperations.
Why the study?
Secondary mitral regurgitation due to systolic anterior motion affects 30-60% of HOCM patients, prompting evaluation of extended septal myectomy and its impact on concomitant mitral valve procedures.
Does extended septal myectomy reduce the need for concomitant mitral valve procedures in patients with hypertrophic obstructive cardiomyopathy?
Cohort (n=84)
Does extended septal myectomy reduce the need for concomitant mitral valve procedures in patients with hypertrophic obstructive cardiomyopathy?
Extended septal myectomy for hypertrophic obstructive cardiomyopathy provides good long-term outcomes and largely eliminates the need for concomitant mitral valve surgery unless intrinsic mitral valve disease is present.
May support avoiding routine mitral surgery with extended myectomy in HOCM; leaves open randomized confirmation of survival benefit.
AIMS: Septal myectomy is the treatment of choice for hypertrophic obstructive cardiomyopathy (HOCM). Around 30-60% of patients with HOCM have a secondary mitral valve regurgitation due to systolic anterior motion (SAM). We report our experience with extended septal myectomy and its impact on the incidence of concomitant mitral valve procedures. METHODS: This is a retrospective study on 84 patients who underwent SM from January 2008 to February 2022. Surgical procedure was performed according to the concept of 'extended myectomy' described by Messmer in 1994. Follow-up outcomes in terms of survival, hospital admissions for heart failure or MV disease, cardiac reoperations, and pacemaker (PMK) implantation were recorded. RESULTS: Mean age was 61 ± 15 years. Mitral valve surgery was performed in seven cases (8%); particularly only one patient without degenerative mitral valve disease underwent mitral valve surgery, with a plicature of the posterior leaflet. In-hospital mortality was 5%. Mitral valve regurgitation greater than mild was present in four patients (5%) at discharge. Twelve-year survival was 78 ± 22%. Cumulative incidence of rehospitalization for heart failure and rehospitalization for mitral valve disease was 10 ± 4 and 2.5 ± 2.5%, respectively. PMK implantation was 5% at discharge, with a cumulative incidence of 15 ± 7%. Freedom from cardiac reoperations was 100%. CONCLUSION: Septal myectomy for HOCM is associated with good outcomes. Although concomitant surgery on the mitral valve to address SAM and associated regurgitation has been advocated, these procedures were needed in our practice only in patients with intrinsic mitral valve disease. Adequate myectomy addresses the underlying pathophysiology in most patients.
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Lio et al. (2024) conducted a cohort in Hypertrophic obstructive cardiomyopathy (HOCM) (n=84). Extended septal myectomy was evaluated on Survival, hospital admissions for heart failure or MV disease, cardiac reoperations, and pacemaker implantation. Extended septal myectomy for hypertrophic obstructive cardiomyopathy resulted in a 12-year survival of 78% and 100% freedom from cardiac reoperations, with low need for concomitant mitral surgery.
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