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.
Meta-Analysis
Yes
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?
The risk of 30-day stroke after TAVR is similar regardless of the approach (transfemoral vs. transapical) or valve type (CoreValve vs. Edwards Valve).
Absolute Event Rate: 2.8% vs 2.8%
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.
Athappan et al. (Sun,) 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.