Key result
Valve-in-valve implantation using the 23-mm CoreValve Evolut in failing small aortic bioprostheses reduced the mean gradient from 34 mmHg to 14 mmHg with no major adverse events at 30 days.
Why the study?
Is valve-in-valve implantation with a 23-mm CoreValve Evolut feasible and safe in patients with degenerated small aortic bioprostheses?
Observational (n=16)
Yes
Is valve-in-valve implantation with a 23-mm CoreValve Evolut feasible and safe in patients with degenerated small aortic bioprostheses?
Valve-in-valve implantation using the 23-mm CoreValve Evolut is feasible and effectively reduces gradients in patients with degenerated small surgical aortic bioprostheses.
May support use in select high-risk cases; leaves open need for prospective data before broader adoption.
BACKGROUND: Transcatheter valve-in-valve (VIV) implantation has emerged as a novel treatment option in patients with degenerated aortic bioprostheses and high surgical risk. However, VIV implantation in small aortic bioprostheses using first generation TAVI devices has frequently resulted in high postprocedural gradients and small effective orifice areas. Recently, an updated version of the self-expandable Medtronic CoreValve prosthesis, which is particularly suitable for small aortic annuli, has become available. We report on the feasibility and early results of VIV implantation using this novel device in a series of patients with degenerated small aortic bioprostheses. METHODS AND RESULTS: 16 patients from two Hamburg hospitals (age range 72-92 years) underwent implantation of a 23-mm CoreValve Evolut (Medtronic, Minneapolis, MN, USA) transcatheter heart valve into failing aortic bioprostheses with internal diameters below 21 mm. All patients were considered high risk for surgical aortic valve replacement after evaluation by an interdisciplinary heart team mean (logistic EuroSCORE range 9.0-88%). Implantation was successful without relevant remaining aortic regurgitation or signs of stenosis and a marked reduction in postprocedural gradientswas observed in 14 out of 16 patients. The mean gradient was reduced from from 34 mm Hg (SEM 10 mm Hg) to 14 mm Hg (SEM 6 mm Hg). No major device- or procedure-related adverse events occurred during 30-day follow up and clinical improvement was observed. CONCLUSIONS: Failing aortic bioprostheses with small internal diameters continue to be a challenging pathology for TAVI due to the risk of high residual gradients and small aortic orifice areas. This report provides first evidence that the 23-mm CoreValve Evolut, a novel self-expanding prosthesis, provides an improved treatment option in these specific patients due to its low profile which resulted in promising early results.
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Diemert et al. (2014) conducted an observational in degenerated small aortic bioprostheses (n=16). 23-mm CoreValve Evolut transcatheter heart valve was evaluated on mean gradient. Valve-in-valve implantation using the 23-mm CoreValve Evolut in failing small aortic bioprostheses reduced the mean gradient from 34 mmHg to 14 mmHg with no major adverse events at 30 days.
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