Key result
Extracellular matrix mitral valve reconstruction yields fully functional valves without regurgitation in a porcine model.
Why the study?
Mitral valve posterior leaflet and subvalvular reconstruction using extracellular matrix sheets has not been characterized in an acute porcine model.
Does mitral valve posterior leaflet reconstruction using extracellular matrix maintain normal valve function in an acute porcine model?
Does mitral valve posterior leaflet reconstruction using extracellular matrix maintain normal valve function in an acute porcine model?
Absolute Event Rate: 11% vs 12%
p-value: p=0.550
Mitral valve posterior leaflet reconstruction using a 2-ply small intestinal submucosal extracellular matrix sheet is feasible and maintains acute valve function in a porcine model.
Acute porcine feasibility does not support clinical mitral reconstruction with submucosal matrix; leaves open translation to durable human repair.
OBJECTIVES: To investigate mitral valve posterior leaflet and subvalvular reconstruction using a 2-ply small intestinal submucosal extracellular matrix sheet. METHODS: Mitral valve posterior leaflet and subvalvular reconstruction was characterized in an acute 80-kg porcine model with 7 pigs acting as their own controls. The characterization was based on pressure catheter measurements of pressure differences to identify mitral regurgitation, stenosis and systolic anterior motion. Furthermore, echocardiography was used for the evaluation of leaflet mobility and geometry, whereas sonomicrometry was used to describe annular and subvalvular geometry. RESULTS: The reconstructed mitral valve was fully functional without any signs of regurgitation (peak left atrial pressure for baseline and reconstruction 12 ± 2 mmHg vs 11 ± 2 mmHg, P = 0.550), mitral valve stenosis (mean pressure difference across the mitral valve 4.8 ± 2.3 mmHg vs 4.1 ± 2.3 mmHg, P = 0.589) or systolic anterior motion. The echocardiographic characterization revealed septal-lateral downsizing, reduced tenting area, increased coaptation length (6.0 ± 0.6 mm vs 8.7 ± 2.3 mm, P = 0.002) and an atrial bend of the reconstructed posterior leaflet. A ballooning effect of the patch material was present at the posterior annular segment. CONCLUSIONS: Mitral valve posterior leaflet and subvalvular reconstruction using a 2-ply small intestinal submucosal extracellular matrix sheet as patch material was possible in an acute porcine model. The reconstructed mitral valve was fully functional without signs of mitral valve stenosis, valve regurgitation, stenosis or systolic anterior motion. The ballooning appearance of the patch material might, however, constitute an altered leaflet stress distribution in this area.
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Tjørnild et al. (2018) studied Mitral valve reconstruction (n=7). Mitral valve posterior leaflet and subvalvular reconstruction using a 2-ply small intestinal submucosal extracellular matrix sheet vs. Baseline was evaluated on Peak left atrial pressure (p=0.550). Mitral valve reconstruction using an extracellular matrix sheet in a porcine model yielded fully functional valves without regurgitation (peak left atrial pressure 11 vs 12 mmHg, P=0.550).
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