TriGUARD 3 Cerebral Embolic Protection Device: First Commercial Case Performed Worldwide

TriGUARD 3 Cerebral Embolic Protection Device  – Today Keystone Heart, LTD. announced the completion of the first worldwide commercial case.

Pieter Stella, MD, Assistant Professor, Medical Department of Cardiology, at UMC Utrecht in the Netherlands, successfully performed the transcatheter aortic valve implantation (TAVI), utilizing the TriGUARD 3™ device, which is designed to minimize the risk of cerebral damage during trans-catheter heart procedures.

“Although we have seen improvement in mortality and morbidity rates during TAVI procedures, the risk of periprocedural stroke has not changed,” commented Professor Stella. “As a physician, I am driven to do anything possible to prevent this rare but terrible complication. I am pleased we can now routinely use the TriGUARD 3™ CEP device in all of our TAVI cases to protect patients from stroke, delirium, and neurocognitive decline.”

The TriGUARD 3™ Cerebral Embolic Protection Device is the only CE Marked product designed to cover and protect all three major cerebral aortic arch vessels. The state-of-the-art Nitinol frame with dome-shaped mesh deflector is delivered transfemorally and designed to “self-position” in the aortic arch.  This design allows the TriGUARD 3™ CEP device to conform to a variety of patient anatomies.

“Our team is thrilled to commercially launch the only CE Marked device designed to cover and protect all three cerebral vessels,” stated Chris Richardson, Keystone Heart President and CEO.  “Our primary objective is to ensure a controlled launch that provides physicians the training and tools necessary to safely and consistently treat all patients undergoing trans-catheter heart procedures with the TriGUARD 3™ CEP device.”

Richardson further commented, “As TAVI procedures continue to expand into treating lower-risk patient groups, the need to protect patients’ brains will also grow. Strokes and minor cognitive events can have devastating outcomes for patients and their families; Keystone Heart is committed to helping physicians minimize those occurrences.”

Keystone Heart began commercialization of the TriGUARD 3™ CEP device in selected TAVI centers of excellence throughout Europe in July 2020.

The TriGUARD 3™ Cerebral Embolic Protection Device

  • Self-positioning, self-stabilizing
  • Polymeric mesh (pore size 115 x 145 µm)
  • 8 Fr OTW delivery
  • Designed to protect all three major arteries that supply blood to the brain
  • Eliminates need for third access site during TAVI
  • Removed upon completion of procedure

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”