Key result
ProGlide linked to ~20% lower risk of major 30-day complications vs Prostar XL in TAVR.
Why the study?
ProGlide and Prostar XL are widely used for large-bore access during TAVR, but their comparative efficacy and safety remain debated due to conflicting published results.
Does the ProGlide vascular closure device reduce cardiovascular mortality, bleeding, and vascular complications compared to Prostar XL in patients undergoing transfemoral TAVR?
Cohort (n=2,583)
Yes
Does the ProGlide vascular closure device reduce cardiovascular mortality, bleeding, and vascular complications compared to Prostar XL in patients undergoing transfemoral TAVR?
Odds Ratio: 0.8 (95% CI 0.65–0.99)
Absolute Event Rate: 13.8% vs 20.5%
p-value: p=0.043
ProGlide is associated with a lower rate of short-term composite adverse events, primarily driven by fewer bleeding complications, compared to Prostar XL in patients undergoing transfemoral TAVR.
ProGlide was associated with fewer short-term TAVR complications than Prostar XL; leaves open whether randomized trials should change device selection.
Background Transcatheter aortic valve replacement (TAVR) requires large‐bore access, which is associated with bleeding and vascular complications. ProGlide and Prostar XL are vascular closure devices widely used in clinical practice, but their comparative efficacy and safety in TAVR is a subject of debate, owing to conflicting results among published studies. We aimed to compare outcomes with Proglide versus Prostar XL vascular closure devices after TAVR. Methods and Results This large‐scale analysis was conducted using RISPEVA, a multicenter national prospective database of patients undergoing transfemoral TAVR treated with ProGlide versus Prostar XL vascular closure devices. Both multivariate and propensity score adjustments were performed. A total of 2583 patients were selected. Among them, 1361 received ProGlide and 1222 Prostar XL. The predefined primary end point was a composite of cardiovascular mortality, bleeding, and vascular complications assessed at 30 days and 1‐year follow‐up. At 30 days, there was a significantly greater reduction of the primary end point with ProGlide versus Prostar XL (13.8% versus 20.5%, respectively; multivariate adjusted odds ratio, 0.80 [95% CI, 0.65–0.99]; P =0.043), driven by a reduction of bleeding complications (9.1% versus 11.7%, respectively; multivariate adjusted odds ratio, 0.76 [95% CI, 0.58–0.98]; P =0.046). Propensity score analysis confirmed the significant reduction of major adverse cardiovascular events and bleeding risk with ProGlide. No significant differences in the primary end point were found between the 2 vascular closure devices at 1 year of follow‐up (multivariate adjusted hazard ratio, 0.88 [95% CI, 0.72–1.10]; P =0.902). Comparable results were obtained by propensity score analysis. During the procedure, compared with Prostar XL, ProGlide yielded significant higher device success (99.2% versus 97.5%, respectively; P =0.001). Conclusions ProGlide has superior efficacy as compared with Prostar XL in TAVR procedures and is associated with a greater reduction of composite adverse events at short‐term, driven by lower bleeding complications. Registration Information URL: clinicaltrials.gov ; Unique identifier: NCT02713932.
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Berti et al. (2020) conducted a cohort in Transcatheter aortic valve replacement (TAVR) (n=2,583). ProGlide vascular closure device vs. Prostar XL vascular closure device was evaluated on Composite of cardiovascular mortality, bleeding, and vascular complications at 30 days (OR 0.80, 95% CI 0.65-0.99, p=0.043). ProGlide significantly reduced the 30-day composite of cardiovascular mortality, bleeding, and vascular complications compared with Prostar XL in TAVR procedures (13.8% vs 20.5%; OR 0.80; P=0.043).
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