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[MSB-73] Hypertrophic Obstructive Cardiomyopathy Management in the Pediatric Population: The Dilemma of Mitral Valve
Nazlı Melis Coşkun Yücel1, Ahmet Aydın1, Timuçin Sabuncu1
1Department of Cardiovascular Surgery, Hacettepe University Faculty of Medicine, Ankara, Türkiye.
Insights
Mitral valve replacement combined with myectomy is more effective for pediatric hypertrophic cardiomyopathy (HOCM) patients, improving left ventricular cavity and reducing obstruction. This combined approach safely manages HOCM in children.
Area of Science:
- Cardiovascular Surgery
- Pediatric Cardiology
- Congenital Heart Disease
Background:
- Hypertrophic cardiomyopathy (HOCM) in pediatric patients presents unique surgical challenges.
- Left ventricular outflow tract (LVOT) obstruction and systolic anterior motion (SAM) are common complications.
- Surgical intervention is necessary for symptomatic HOCM in children.
Purpose of the Study:
- To evaluate the surgical experience with pediatric HOCM patients.
- To compare outcomes of isolated myectomy versus combined myectomy and mitral valve replacement (MVR).
- To assess the safety and efficacy of MVR in conjunction with myectomy for pediatric HOCM.
Main Methods:
- Retrospective review of 10 pediatric HOCM patients undergoing surgery.
- Procedures included isolated myectomy or myectomy with MVR.
- Surgical approach involved aortotomy, left atriotomy, and apical ventriculotomy.
Main Results:
- Eight patients underwent myectomy with MVR; two had isolated myectomy.
- Isolated myectomy resulted in persistent SAM and higher LVOT gradients.
- MVR in pediatric patients with narrow annuli was well-tolerated using low-profile valves.
Conclusions:
- Combined MVR and myectomy is more effective in pediatric HOCM for LVOT gradient reduction and cavity enlargement.
- This approach prevents SAM and offers greater cavity volume gain.
- MVR combined with myectomy is a safe and effective surgical option for pediatric HOCM.
Objective:
This study aimed to share our surgical experience with 10 pediatric patients with hypertrophic cardiomyopathy (HOCM).
Methods:
This study included 10 HOCM patients, aged between 8 months and 18 years, who underwent surgery due to conditions such as aortic insufficiency, mitral insufficiency, significant narrowing of the left ventricular cavity, and left ventricular outflow tract (LVOT) obstruction.
Results:
Two patients underwent isolated myectomy, while the remaining eight underwent myectomy combined with mitral valve replacement (MVR). Myectomy was performed via aortotomy, left atriotomy, and apical ventriculotomy. All patients had preoperative signs of systolic anterior motion (SAM) and a gradient in the LVOT. In the two patients who underwent isolated myectomy, SAM signs persisted postoperatively. Additionally, the gradient in the LVOT was measured to be higher in isolated myectomy cases compared to cases in which MVR was performed. Despite being in the pediatric age group with narrow annuli, all patients tolerated the MVR procedure with low-profile valves.
Conclusion:
According to our experience, simultaneous MVR in pediatric HOCM cases requiring surgery is more effective in enlarging the left ventricular cavity and reducing the gradient in the LVOT, as it allows both the removal of the mitral valvular apparatus and the prevention of SAM. It provides a greater cavity volume gain compared to the alternative manipulation of the mitral valve apparatus. In our clinic, MVR surgery combined with myectomy is safely performed in pediatric HOCM cases.
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