Philips announces FDA approval for enhanced LumiGuide guidewire and marks the 1000th patient treated with its breakthrough 3D device guidance technology
September 17 2024 - 7:56AM
- Enhanced longer version of Philips LumiGuide Navigation Wire
enables US clinicians to visualize a broader range of
catheters
- Internationally recognized vascular surgeon Carlos Timaran, MD,
was the first to use the new LumiGuide wire to perform a complex
aortic repair,
- Procedure marks the world’s 1000th procedure assisted by
Philips’ unique Fiber Optic RealShape (FORS) guidance
technology
Amsterdam, the Netherlands – Royal Philips (NYSE: PHG,
AEX: PHIA), a global leader in health technology, today announced
the introduction of the 160cm FDA approved version of its unique
LumiGuide endovascular navigation wire. This enhanced LumiGuide
guidewire, which utilizes the company’s breakthrough Fiber Optic
RealShape (FORS) technology, was used for the first time on a
patient by Professor and vascular surgeon Carlos Timaran, MD, an
internationally recognized expert in advanced endovascular
techniques. He used the technology during a complex aortic aneurism
repair operation, marking the 1000th patient treated milestone
using FORS technology since first clinical use of the technology in
2020. The introduction of a longer FORS-enabled LumiGuide
Navigation Wire enables US clinicians to visualize a broader range
of catheters and expands usage of this technology to patients in
America treated in centers equipped with LumiGuide.
"The new enhanced Philips LumiGuide navigation guidewire
represents a significant leap forward in endovascular surgery,
offering unprecedented 3D visualization and precision during
complex procedures,” said Carlos Timaran, MD. “As the first to use
this guidewire for a complex aortic repair, I experienced firsthand
its potential to revolutionize how we approach minimally invasive
vascular interventions. The patient who underwent this
groundbreaking procedure is doing well, further validating the
efficacy of this innovative technology.” Usually during
minimally-invasive surgeries, doctors have to rely on live X-ray
imaging (fluoroscopy) to help them manipulate interventional
devices such as catheters inside the patient’s body. But real-time
X-ray fluoroscopy comes with radiation risks for both patients and
physicians and only provides grayscale, 2D images of these devices.
LumiGuide – powered by Philips’ unique FORS technology – changes
the game by allowing doctors to see their guidewires and catheters
in 3D and color as they manipulate them inside the patient's body,
from any angle, in real-time, and with minimal radiation. Philips’
FORS technology simplifies navigation in tortuous vessels (blood
vessels that are twisted or winding). Using this advanced
technology, complex cases such as aortic repair procedures can be
done 37% faster and use 70% less X-ray imaging during the process
[1][2]. Providing greater reach and enhanced catheter loading
possibilities than the company’s existing 120cm (47 inch)
guidewire, Philips’ new 160cm (63 inch) LumiGuide wire enables US
physicians to experience 3D device guidance with more catheters
than before, enabling use of the technology for more patients and
procedures.
“LumiGuide unlocks the color visualization of wires, catheters,
and patient anatomies in 3D from any angle, including simultaneous
angles to generate ‘virtual biplane’ images. Combined with device
navigation viewed from angles physically unachievable using
conventional C-arm systems, it has already been shown to improve
workflows, reduce procedure times, and decrease patient and staff
radiation dose," said Dr. Atul Gupta, Chief Medical Officer for
Diagnosis and Treatment at Philips and a practicing interventional
radiologist. Philips LumiGuide integrates
seamlessly into the company’s Image Guided Therapy System – Azurion
– allowing its use alongside pre-operative cross-sectional imaging.
The solution recently won the ‘Best of the Best’ 2024 Red Dot
Design Award with the jury stating the innovation ‘not only
revolutionizes instrument guidance in minimally-invasive
procedures, but also aims to protect patients and medical staff’.
[1] Eric J. Finnesgard, Jessica P. Simons, Douglas W. Jones,
Caitlin M. Sorensen, Tammy T. Nguyen, Andres Schanzer. Initial
single-center experience using Fiber Optic RealShape guidance in
complex endovascular aortic repair, Journal of Vascular Surgery,
November 12, 2022. DOI:https://doi.org/10.1016/j.jvs.2022.11.041.
[2] Interim analysis report of FORS Learn Registry Bart Wessels;
Philips, May 2023For further information, please
contact:
Joost Maltha Philips External Relations Tel:
+31 6 10 55
8116 Email: joost.maltha@philips.com
About Royal Philips
Royal Philips (NYSE: PHG, AEX: PHIA) is a leading health
technology company focused on improving people's health and
well-being through meaningful innovation. Philips’ patient- and
people-centric innovation leverages advanced technology and deep
clinical and consumer insights to deliver personal health solutions
for consumers and professional health solutions for healthcare
providers and their patients in the hospital and the home.
Headquartered in the Netherlands, the company is a leader in
diagnostic imaging, ultrasound, image-guided therapy, monitoring
and enterprise informatics, as well as in personal health. Philips
generated 2023 sales of EUR 18.2 billion and employs approximately
68,700 employees with sales and services in more than 100
countries. News about Philips can be found at
www.philips.com/newscenter.
- Philips LumiGuide Procedure JPG
- Philips LumiGuide JPG
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