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July 25, 2011Catheterization and Cardiovascular Interventions150 citations

Predictors of moderate‐to‐severe paravalvular aortic regurgitation immediately after corevalve implantation and the impact of postdilatation

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KTKensuke TakagiALAzeem LatibRARasha Al‐Lamee

Key Points

  • This study aims to identify predictors of moderate-to-severe aortic regurgitation after CoreValve implantation and assess the role of postdilatation in mitigating this condition.
  • Enrolled 79 patients with severe aortic stenosis who underwent CoreValve implantation from July 2008 to July 2010.

Structured PICO

What are the predictors of moderate-to-severe paravalvular aortic regurgitation after CoreValve implantation, and does postdilatation reduce AR severity?

P
Population
79 consecutive patients with severe aortic stenosis who underwent CoreValve implantation
I
Intervention
CoreValve implantation and subsequent postdilatation for moderate-to-severe paravalvular aortic regurgitation
O
Outcome
Moderate-to-severe aortic regurgitation (AR≥2+) immediately after CoreValve implantationsurrogate

Larger annulus diameter, low implantation, and peripheral vascular disease predict moderate-to-severe AR after CoreValve implantation, which can often be effectively reduced by postdilatation.

Abstract

OBJECTIVE: To investigate the predictors of moderate-to-severe aortic regurgitation (AR≥2+) after CoreValve implantation and evaluate the feasibility and safety of postdilatation in reducing the degree of AR. BACKGROUND: Although transcatheter aortic valve implantation is an alternative treatment for high surgical risk patients with severe aortic stenosis, post-implantation paravalvular AR remains a complication. METHODS: From July 2008 to July 2010, we enrolled 79 consecutive patients with severe aortic stenosis who underwent CoreValve implantation. RESULTS: On univariable analysis, the predictors of AR≥2+ immediately after CoreValve implantation were: larger annulus size, low implantation, prosthesis mismatch, chronic renal insufficiency, a history of heart failure, and peripheral vascular disease. On multivariable analysis, the independent predictors of AR≥2+ were: larger annulus diameter (OR 1.78, 95%CI 1.25-2.55; P = 0.002), low implantation (OR 3.67, 95%CI 1.01-13.35, P = 0.05), and peripheral vascular disease (OR 3.54, 95%CI 1.19-10.56, P = 0.02). Post-CoreValve implantation, AR ≥ 2 was seen in 40.5% (32/79). Twenty-one patients underwent postdilatation with improvement in AR grade in the majority (17/21). Of the four patients who did not respond to postdilatation, two underwent valve-in-valve implantation. In one patient, the valve was pulled more proximally by the snare technique. The remaining 10 patients were treated conservatively. CONCLUSION: The appropriate strategy for treating patients with AR≥2+ depends on the causes and severity of AR post-TAVI. This study suggests that we should carefully select the size of CoreValve prosthesis to prevent prosthesis mismatch, especially when implanted in larger annulus sizes. For valves implanted in the appropriate position, postdilatation appears effective in reducing the degree of AR.

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Cite This Study

Takagi et al. (2011) studied this question.

synapsesocial.com/papers/6a053f8f4b242697963807eehttps://doi.org/10.1002/ccd.23003
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