Hepatic and splenic venous access tract closure using the VASCADE vascular closure system following percutaneous

Lindsay F Eilers1, Manish Bansal1, Asra Khan1

  • 1Charles E. Mullins Cardiac Catheterization Laboratories, Texas Children's Hospital, and Lillie Frank Abercrombie Section of Cardiology, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.

Cardiology in the Young
|September 13, 2024
PubMed

Insights

The VASCADE Vascular Closure System safely closed hepatic and splenic venous access sites in pediatric cardiac catheterization procedures. This novel approach shows promise in reducing bleeding complications in young patients.

Area of Science:

  • Interventional Cardiology
  • Vascular Access Management
  • Pediatric Cardiac Procedures

Background:

  • Hepatic and splenic venous access are specialized techniques for cardiac catheterization.
  • Bleeding is a common complication of these venous access methods.
  • The VASCADE Vascular Closure System is approved for femoral access closure in adults.

Purpose of the Study:

  • To evaluate the safety and efficacy of the VASCADE Vascular Closure System for hepatic or splenic venous access sites.
  • To assess the potential of VASCADE in reducing post-procedural bleeding complications in pediatric patients undergoing cardiac catheterization.

Main Methods:

  • Single-center retrospective review of patients undergoing percutaneous hepatic or splenic venous access.
  • Tract closure was performed using the VASCADE Vascular Closure System.
  • Data collected from March 2022 to October 2023.

Main Results:

  • Ten pediatric patients (16 procedures) underwent closure with VASCADE.
  • Successful closure was achieved in all patients (15 hepatic, 2 splenic access sites).
  • No major adverse events related to VASCADE closure were reported.

Conclusions:

  • VASCADE is a safe option for closing transhepatic and trans-splenic venous access sites in pediatric cardiac catheterization.
  • The device may reduce the risk of bleeding complications.
  • Further studies in larger pediatric cohorts are warranted to confirm safety and efficacy.
Abstract