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Preserve Transfemoral TAVI

Enable simple and safe TF TAVI in patients with calcified iliacs
  • Calcified iliacs increase risk of serious complications during TAVI
  • Transfemoral TAVI has lower morbidity & mortality vs. alternative access
  • IVL safely fractures calcium, preserving TF access as primary option
Featured Case
Pre-TAVR/TAVI IVL in Calcified Iliacs; Courtesy of Brian Kolski, MD, St Joseph Hospital, Orange, CA, USA

Enable First-Choice Transfemoral TAVI

Hear from Prof. Carlo Di Mario about how IVL has lowered his use of alternative TAVI access

"Clearly a Better Way"

Learn from Dr. Dean Kereiakes on how IVL facilitates transfemoral access safely and intuitively

Publications

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IVL-Facilitated Pre-TAVR Registry Published. Di Mario et al, A Prospective Registry of Intravascular Lithotripsy-Enabled Vascular Access for Transfemoral Transcatheter Aortic Valve Replacement, JACC Interventions, March 2019.
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Gorla et al, Transfemoral aortic valve implantation following lithoplasty of iliac artery in a patient with poor vascular access, Catheter Cardiovasc Interv Oct 2018
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Di Mario et al, Lithoplasty-assisted transfemoral aortic valve implantation, Eur Heart J, Feb 2018
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MINIMIZE TRAUMA

Minimize trauma to soft tissue by safely selecting and fracturing intimal and medial calcium

 

OPTIMIZE OUTCOMES

Optimize outcomes while reducing complications and cost escalation

 

SIMPLIFY PROCEDURES

Simple and intuitive system that makes complex calcified procedures more predictable

 

 

SHOCKWAVE M5 IN-DEPTH

Ready to Make Waves with Shockwave IVL?

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We're excited about IVL's potential in aortic stenosis, too!

But, right now we're in the early phases of the R&D program. In the meantime, don't miss the IVL application that heart teams are embracing already — maintaining transfemoral TAVR access through heavily calcified iliacs by using IVL.

MORE ON TAVR ENABLING TRANSFEMORAL ACCESS
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Wow - you're ready to start cracking, aren't you?

Too bad our coronary technology is not yet approved in the United States. Good news is that we have initiated our U.S. FDA IDE study. Learn more about the Disrupt CAD III study on our clinical research portion of the website.

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