Why the study?
Optimizing post-procedural hemostasis is essential as the volume of catheter ablation for arrhythmias increases. This study sought to identify predictors of procedural failure and evaluate long-term safety, specifically the management of rare infectious complications, with an extravascular, bioabsorbable collagen-based venous vascular closure system (VASCADE MVP).
Does an extravascular bioabsorbable collagen-based venous vascular closure system provide effective hemostasis and long-term safety in patients undergoing catheter ablation for arrhythmias?
Observational (n=1,162)
No
Does an extravascular bioabsorbable collagen-based venous vascular closure system provide effective hemostasis and long-term safety in patients undergoing catheter ablation for arrhythmias?
Answers are grounded in this paper and cite their sources.
The bioabsorbable venous vascular closure system achieves a 94% procedural hemostasis rate after arrhythmia ablation—though efficacy is reduced with lower BMI, female sex, and larger sheaths—and has a low 0.6% rate of delayed access-site infection that can be managed conservatively without major surgery.
Background As the volume of catheter ablation for arrhythmias increases, optimizing post-procedural hemostasis is essential for clinical workflow and patient comfort. The VASCADE MVP is an extravascular, bioabsorbable collagen-based venous vascular closure system (VVCS). We conducted a dual-phase study to identify predictors of procedural failure and evaluate long-term safety, specifically focusing on the management of rare infectious complications. Methods This study, conducted at our hospital, utilized a two-phase design. Phase 1 involved a mechanistic analysis of 203 consecutive venous access sites (70 patients) to identify predictors of hemostatic failure. Phase 2 consisted of an expanded safety evaluation of 1,162 consecutive procedures through October 2025. For atrial fibrillation ablation, an uninterrupted DOAC protocol was used with ACT targets of >300s (RF/cryoballoon) or >350s (pulsed-field ablation). Post-deployment, institutional protocol required 3–4 hours of gauze compression before ambulation. Results In Phase 1, the procedural success rate in the initial cohort was 94%. Multivariate analysis identified female sex (P=0.04), lower BMI (22.7 ± 3.5 vs. 25.0 ± 3.6 kg/m², P=0.02), and large-bore sheaths (10.4 ± 1.8 vs. 8.9 ± 1.2 Fr, P=0.01) as significant predictors of failure. In Phase 2, the safety cohort (n=1,162), delayed access-site cellulitis occurred in 0.6% (7/1,162) approximately one-month post-procedure. Management of these infections was limited to oral antibiotics and minor local management (incision, irrigation, and local debridement). Crucially, no patient required major surgical intervention, such as vascular reconstruction or bypass grafting, which are sometimes reported with suture-mediated closure devices. Conclusions This dual-phase evaluation confirms that the bioabsorbable VVCS is highly effective, although its efficacy is influenced by BMI and sheath size. The system’s primary safety advantage is its bioabsorbable nature, which allows rare infectious complications to be managed conservatively, thereby avoiding the invasive surgical interventions associated with permanent suture-based devices.
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Kanda et al. (2026) conducted an observational in Arrhythmias undergoing catheter ablation (n=1,162). VASCADE MVP bioabsorbable venous vascular closure system (VVCS) was evaluated on Procedural hemostatic success (Phase 1) and delayed access-site cellulitis (Phase 2).
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