Introduction
Transcatheter aortic valve-in-valve implantation (TAVI-ViV) can be associated
with unfavorable hemodynamic outcomes. This study aimed to estimate the
prevalence, identify the risk factors, and evaluate the outcomes and
survival of patients with high residual gradients after TAVI-ViV.
Methods
A total of 85 patients were included in the study. The cohort was divided
into group A, with postprocedural mean pressure gradient (PG) ≥ 20
mmHg, and group B, with mean PG < 20 mmHg.
Results
Postprocedural PG ≥ 20 mmHg was observed in 24.7% of the patients. In
a univariate analysis, preoperative gradient, pre-existing
patient-prosthesis mismatch (PPM), deep valve implantation, small
degenerated valves, and an older generation of transcatheter aortic valves
were found to be risk factors for high residual gradient. Multivariate
analysis showed that preexisting maxPG > 60 mmHg, implantation level of 4
mm below neo-annulus, and degenerated valve size ≤ 23 mm were
independent predictors of high residual gradient. There were no differences
in early morbidity (myocardial infarction, pacemaker implantation, stroke,
acute renal insufficiency) between groups. Kaplan-Meier estimated that the
survival rate was comparable at one and five years regardless of
postoperative gradient. Survivors with high residual mean gradient were
significantly affected by a high New York Heart Association (NYHA)
class.
Conclusion
High residual transvalvular gradient after TAVI-ViV is not rare, but it does
not significantly affect mortality. High residual mean gradient has a
negative impact on NYHA functional class improvement after the procedure.
High preoperative gradient, implantation level, and small failed
bioprosthesis may predispose to increased residual gradient.