Royal Philips, a global leader in health technology, on March 12 announced health economic results from the “Define Flair” clinical trial comparing cost-effectiveness between instant wave-free ratio (iFR) and fractional flow reserve (FFR) in the guidance of treatment of ischemic heart disease at the American College of Cardiology (ACC) annual meeting in Orlando, Florida.
The study found that an iFR-guided strategy offers a one-year average cost savings of US$896 per patient compared to an FFR-guided strategy, while delivering consistent patient outcomes. iFR is an innovative pressure-derived index unique to Philips, a global leader in image-guided therapy solutions, allowing a simplified hyperemia-free physiological assessment of coronary blockages.
Coronary artery disease is the most common type of heart disease and is the leading cause of death in the US for men and women (Coronary Artery Disease, NIH, 2015). Coronary physiology has become routine in planning coronary revascularisation, and “Define Flair” compared using iFR and FFR strategies to guide these types of procedures.
With an average saving of nearly US$900per patient per year, the study found that iFR offers a total procedure cost saving of approximately 10 per cent per patient over FFR. Additionally, patients treated with the use of an iFR-guided revascularisation strategy had fewer coronary artery bypass graft procedures and fewer subsequent revascularisations.
Previous data from “Define Flair” released in 2017 found that iFR-guided treatments reduced procedure time by 10 per cent versus FFR-guided treatments, while reducing patient discomfort by 90 per cent (Davies JE, et al., Define-Flair: A Multi- Centre, Prospective, International, Randomised, Blinded Comparison of Clinical Outcomes and Cost Efficiencies of iFR and FFR Decision-Making for Physiological Guided Coronary Revascularisation. New England Journal of Medicine, epub March 18, 2017). The pivotal “Define Flair” study continues to illustrate the advantages of iFR and the superior value it delivers to clinicians and hospital administrators.
“The findings from “Define Flair”continue to demonstrate the benefits of iFR, showing that an iFR-guided treatment offers proven outcomes, reduced costs and procedure time and enhanced patient comfort compared to FFR,” said Dr Manesh Patel, Chief of the Division of Cardiology and Co-Director of the Duke Heart Center at Duke University School of Medicine. “iFR is not only a faster diagnostic solution, but it also offers the advantage of significantly reduced patient discomfort. By implementing an iFR program at a hospital, this solution can deliver the clinical outcome benefits of physiology-driven PCI, while reducing annual health care costs significantly across the organisation.”
In the treatment of coronary artery disease, clinicians have been using FFR in addition to angiographic images to assess the physiology of a suspected blockage in coronary arteries in order to identify the appropriate therapy for each patient. iFR is a next-generation physiologic measurement that uses the same pressure guide wires and equipment as FFR, but avoids the administration of hyperemic agents, which are required with FFR, to the patients.
“The “Define Flair” study has provided further clinical validation of iFR and how it is improving the lives of patients and physicians,” said Christopher Barys, Business Leader of Philips Image Guided Therapy Devices. “An iFR-guided strategy has now been shown to improve patient outcomes and reduce costs for the treatment of coronary artery disease in comparison to an FFR-guided strategy. This is a significant step in our journey to help clinicians decide, guide, treat and confirm the right therapies for their patients, while reducing costs.”
“Define Flair” is a randomised, controlled, single-blinded comparison of clinical outcomes and cost efficiencies of iFR and FFR-guided interventions of 2,492 patients in 49 centres across Europe, Asia, North America and Africa. The study conducted its comparison of iFR versus FFR using pressure guide wires and equipment from Philips. Since the introduction of the hyperemia-free iFR modality in 2013, iFR has been studied in nearly 15,000 patients and is used in more than 4,100 catheterisation labs across the world.