Feasibility, Efficacy, and Safety of the Mitral Annulo-TRIpsy in eXtreme Risk Patients.
Document Type
Article
Publication Date
6-24-2025
Publication Title
Structural heart : the journal of the Heart Team
Abstract
BACKGROUND: Severe calcific mitral stenosis is common and therapeutically challenging. Intravascular lithotripsy (IVL) can facilitate percutaneous balloon mitral valvuloplasty in patients not amenable to conventional therapies. We describe a modified technique using larger IVL balloons to ensure maximal annular contact and delivery of ultrasonic shockwaves to restore mitral leaflet pliability and reduce transvalvular gradients without the need for noncompliant valvuloplasty balloons.
METHODS: Seven patients underwent the Mitral Annulo-TRIpsy in eXtreme risk patients (MATRIX) procedure at 3 tertiary structural heart disease centers in the United States. Transcatheter mitral valve replacement was contraindicated due to prohibitive risk of left ventricular outflow tract obstruction or insufficient annular calcification for anchoring of a balloon-expandable valve. IVL balloons were delivered using a large-bore transseptal sheath over three 0.014 wires. Runs of delivery of IVL therapy were repeated until satisfactory results in terms of mean mitral gradient (mMG) reduction were achieved.
RESULTS: Median age was 78 years, and 14.3% were female. All patients presented with progressive New York Heart Association class III-IV symptoms and functional limitations. Pre-MATRIX mMG was 9.0 mmHg. The final mMG was 3.0 mmHg (absolute difference 6.3 mmHg; 95% CI 2.6-10.1 mmHg;
CONCLUSIONS: This small multicenter series demonstrates that IVL of calcified mitral stenosis using the MATRIX technique is feasible and safe and associated with effective reductions in mMG.
Volume
9
Issue
8
First Page
100683
Recommended Citation
Giustino G, Asselin CY, Naguib M, Jabri A, Lok Lai LK, Kipperman R et al [Abbas A] Feasibility, efficacy, and safety of the mitral annulo-tripsy in extreme risk patients. Struct Heart. 2025 Jun 24;9(8):100683. doi: 10.1016/j.shj.2025.100683. PMID: 40894366
DOI
10.1016/j.shj.2025.100683
ISSN
2474-8714
PubMed ID
40894366
