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June 19, 2026Journal of the American College of Cardiology140 citations

Influence of Transcatheter Aortic Valve Replacement Strategy and Valve Design on Stroke After Transcatheter Aortic Valve Replacement

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GAGanesh AthappanRGRama Dilip GajulapalliPSPrasanna Sengodan

Key Result

The risk of 30-day stroke after TAVR was similar between transfemoral and transapical approaches (2.8% vs 2.8% in multicenter studies) and between CoreValve and Edwards Valve designs.

Key Points

  • The aim is to compare the risk of stroke associated with different TAVR approaches and valve designs.
  • Conducted systematic review of studies on stroke risk post-TAVR.
  • Pooled data from 25 multicenter registries and 33 single-center studies.
  • Followed established meta-analytical guidelines for analysis.
  • No significant difference in 30-day stroke rates between transfemoral and transapical approaches.
  • Stroke rates were similar for CoreValve and Edwards Valve types after TAVR.
  • Overall decline in stroke risk noted with improved technology and experience.

Study Design

Type

Meta-Analysis

Multicenter

Yes

Structured PICO

Does the TAVR approach (transfemoral vs. transapical) or valve design (CoreValve vs. Edwards Valve) affect the risk of 30-day stroke in patients undergoing TAVR?

P
Population
Patients undergoing transcatheter aortic valve replacement across 25 multicenter registries and 33 single-center studies.
I
Intervention
Transfemoral (TF) approach or CoreValve design for TAVR
C
Comparator
Transapical (TA) approach or Edwards Valve design for TAVR
O
Outcome
30-day stroke post-TAVRhard clinical

The risk of 30-day stroke after TAVR is similar regardless of the approach (transfemoral vs. transapical) or valve type (CoreValve vs. Edwards Valve).

Main Result

Absolute Event Rate: 2.8% vs 2.8%

Abstract

OBJECTIVES: The study undertook a systematic review to establish and compare the risk of stroke between the 2 widely used approaches (transfemoral TF vs. transapical TA) and valve designs (CoreValve, Medtronic, Minneapolis, Minnesota vs. Edwards Valve, Edwards Lifesciences, Irvine, California) for transcatheter aortic valve replacement (TAVR). BACKGROUND: There has been a rapid adoption and expansion in the use of TAVR. The technique is however far from perfect and requires further refinement to alleviate safety concerns that include stroke. METHODS: All studies reporting on the risk of stroke after TAVR were identified using an electronic search and pooled using established meta-analytical guidelines. RESULTS: 25 multicenter registries and 33 single-center studies were included in the analysis. There was no difference in pooled 30-day stroke post-TAVR between the TF and TA approach in multicenter (2.8% 95% confidence interval (CI): 2.4 to 3.4 vs. 2.8% 95% CI: 2.0 to 3.9) and single-center studies (3.8% 95% CI: 3.1 to 4.6 vs. 3.4% 95% CI: 2.5 to 4.5). Similarly, there was no difference in pooled 30-day stroke post TAVR between the CoreValve and Edwards Valve in multicenter (2.4% 95% CI: 1.9 to 3.2 vs. 3.0% 95% CI: 2.4 to 3.7) and single-center studies (3.8% 95% CI: 2.8 to 4.9 vs. 3.2% 95% CI: 2.4 to 4.3). There was a decline in stroke risk with experience and technological advancement. There was no difference in the outcome of 30-day stroke between TAVR and surgical aortic valve replacement. CONCLUSIONS: Our findings suggest that the risk of 30-day stroke after TAVR is similar between the approaches and valve types. There has been a decline in stroke risk after TAVR with improvements in valve technology, patient selection, and operator experience.

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Cite This Study

Athappan et al. (2014) conducted a meta-analysis in Aortic valve disease requiring TAVR. Transfemoral approach and CoreValve vs. Transapical approach and Edwards Valve was evaluated on 30-day stroke post-TAVR. The risk of 30-day stroke after TAVR was similar between transfemoral and transapical approaches (2.8% vs 2.8% in multicenter studies) and between CoreValve and Edwards Valve designs.

synapsesocial.com/papers/6a35b2457f329793c62de3c6https://doi.org/10.1016/j.jacc.2014.02.540
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