April 21, 2022
- First use of Philips’ breakthrough CavaClear solution to help patients with embedded IVC filters, including an athlete suffering from a 16-year old penetrating filter
- Only FDA-cleared solution for advanced IVC filter removal safely ablates tissue and removes embedded IVC filters in first patients
- In the USA, estimates show more than one million patients with IVC filters would benefit from filter removal to reduce the risk of long-term complications [1,2]
Amsterdam, the Netherlands – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced that the first patients have been successfully treated for Inferior Vena Cava (IVC) filter removal using its IVC Filter Removal Laser Sheath – CavaClear. CavaClear provides an effective, minimally invasive solution for embedded IVC filters, to help physicians reduce risk of significant filter-related complications in patients and improve workflow performance. The first two patients were successfully treated at Northwestern Medicine (Chicago, IL) by Kush R. Desai, MD, FSIR, Associate Professor of Radiology, Surgery, and Medicine, and Director of Deep Venous Interventions, Division of Interventional Radiology at Northwestern University Feinberg School of Medicine, and at Stanford Hospital (Palo Alto, CA) by William T. Kuo, MD, FSIR, FCCP, FSVM, FACR, FCIRSE, Professor of Interventional Radiology and Director of the Stanford IVC Filter Clinic at Stanford University School of Medicine.
IVC filters are used to treat patients with venous thromboembolism, in which blood clots form in the deep veins of the leg and groin and can travel through the circulatory system. They are placed in the inferior vena cava to capture blood clots from moving to the lungs. However, research has shown that IVC filters may have long-term complications . The filters can fracture and travel through the bloodstream to other parts of the body. Other identified long-term risks associated with IVC filters include penetration into adjacent organs and IVC occlusion. The FDA recommends that implanting physicians consider removing retrievable IVC filters as soon as they are no longer indicated .
CavaClear uses circumferential tissue ablation to aid in capturing the filter within seconds of laser activation, which can help increase procedural efficiency during removal and may help lower costs by reducing the number of retrieval attempts needed to remove an embedded filter. In addition, the simple and safe design is easy for physicians to integrate into their workflow and reduce the need for high-force retrievals that could increase the chance of a complication.
“Millions of patients have IVC filters that are no longer indicated, and CavaClear helps physicians experienced in IVC filter retrieval work towards the goal of safely removing such devices, in line with regulatory guidance,” said Dr. Desai.
Dr. Desai treated the first patient with CavaClear at Northwestern Medicine by removing an IVC filter that was placed over 6 months prior for deep vein thromboembolism. An attempt to retrieve the filter was made approximately 4 months post implant at another institution, however, the procedure was unsuccessful and then referred to Dr. Desai. CavaClear was later successfully applied to quickly and safely free the embedded filter from the caval wall, enabling the patient to now be filter-free.
At Stanford Hospital, Dr. Kuo performed the first CavaClear retrieval on a chronically embedded IVC filter that was placed more than 16 years ago. The filter was rediscovered after the patient developed lifestyle-limiting pain and blood vessel occlusions related to the filter. Due to case complexity, none of the patient’s original physicians outside of the USA were able to provide a safe treatment plan and so referred the patient to the Stanford IVC Filter Clinic.
The patient commented on his experience, “I am so thankful to Dr. Kuo and the team for accepting me as a patient when none of my doctors back home would even attempt removal of my 16-year-old IVC filter, which was causing painful penetration and blood vessel blockage requiring blood thinners. The worst thing is that I was previously a cyclist and sportsman who used to ride more than 7000 miles per year, but after these blockages, I became so weak that I could not even climb the stairs of my home. I now look forward to exercising again. I want to thank all members of the team involved. I will never get tired of saying thank you!”
“We chose to use CavaClear on a chronic filter implant that was embedded for over 16 years and completely encased in scar tissue. Prior to our discovery of the laser technique, pioneered at Stanford , percutaneous removal would have been impossible, but the use of CavaClear allowed us to achieve successful removal within minutes – highlighting the first ever use of CavaClear to remove a chronic filter implant. Although the device is now cleared in the USA, embedded IVC filters remain a worldwide problem,” said Dr. Kuo.
“We are deeply moved to see Philips IVC Filter Removal Laser Sheath – CavaClear – have a positive impact on the lives of patients, and the ability to provide physicians with access to a safe, effective and efficient option for advanced IVC filter removal,” said Atul Gupta, MD, Interventional Radiologist and Chief Medical Officer for Image Guided Therapy at Philips. “These are just the first of many successful cases to come, and a testament of the Philips commitment to innovating procedures and solutions with physician collaboration to improve patient outcomes.”
Regulatory recognition and research in support of laser-assisted removal
In December 2021, Philips CavaClear IVC Filter Removal Laser Sheath received FDA De Novo clearance, becoming the first and only FDA-cleared solution for advanced IVC filter removal. Failure rates for IVC filter removal can be high and prior to CavaClear, limited options for removal existed if the filter became difficult to remove. Advanced retrieval tools and techniques are required if the IVC filter becomes embedded in the vasculature. Physicians previously had very few tools to remove the filter when complications occurred and until now there were no FDA-approved devices for this type of advanced removal.
Philips IVC Filter Removal Laser Sheath – CavaClear is available in the USA. For more information please go to www.philips.com/CavaClear.
 Philips internal market research data calculation.
 Health, C. for D. and R. Safety Communications – Removing Retrievable Inferior Vena Cava Filters: FDA Safety Communication. (2014).
 Van Ha, T. G. Complications of inferior vena caval filters. Semin. Interv. Radiol. 23, 150–155 (2006).
 Kuo, W. et al. Laser‐Assisted Removal of Embedded Vena Cava Filters: A First‐In‐Human Escalation Trial in 500 Patients Refractory to High‐Force Retrieval. Journal of the American Heart Association 9:24, 1-9 (2020).
For further information, please contact:
Philips Global Press Office
Tel: +31 6 10 55 8116
Fabienne van der Feer
Philips Image Guided Therapy
Tel: + 31 622 698 001
About Royal Philips
Royal Philips (NYSE: PHG, AEX: PHIA) is a leading health technology company focused on improving people’s health and well-being, and enabling better outcomes across the health continuum – from healthy living and prevention, to diagnosis, treatment and home care. Philips leverages advanced technology and deep clinical and consumer insights to deliver integrated solutions. Headquartered in the Netherlands, the company is a leader in diagnostic imaging, image-guided therapy, patient monitoring and health informatics, as well as in consumer health and home care. Philips generated 2020 sales of EUR 17.3 billion and employs approximately 78,000 employees with sales and services in more than 100 countries. News about Philips can be found at www.philips.com/newscenter.
- Philips IVC Filter Removal Laser Sheath – CavaClear – 1
- Philips IVC Filter Removal Laser Sheath – CavaClear – 2
- Philips IVC Filter Removal Laser Sheath – CavaClear – 3
The content is by GlobeNewswire. DKODING Media is not responsible for the content provided or any links related to this content. DKODING Media is not responsible for the correctness, topicality or the quality of the content.