Terumo Health Outcomes and Medis Medical Imaging Announce Strategic Partnership to Enhance Cardiovascular Care

In This Article:

– Collaboration combines Terumo's ePRISM™ precision medicine software platform with Medis' QFR® technology –

SOMERSET, N.J., Dec. 10, 2024 /PRNewswire/ -- Terumo Health Outcomes (THO), a division of Terumo Interventional Systems (TIS), and Medis Medical Imaging, a leading cardiac imaging software company, announced today that they have entered into a strategic partnership, in the United States, to enhance cardiovascular care through the utilization of both ePRISM – Terumo's proprietary clinical decision support platform – and Medis' Quantitative Flow Ratio (QFR) technology, a non-invasive software solution designed to assess angiography-derived coronary physiology. The use of ePRISM and Medis QFR will be piloted at selected clinical sites, leveraging real-time data from electronic health records to provide prospective insights to help enhance patient care.

(PRNewsfoto/Terumo Corporation)
(PRNewsfoto/Terumo Corporation)

THO's partnership with Netherlands-based Medis Medical Imaging represents a significant step in enhancing clinical decision support capabilities, streamlining workflows and, most importantly, improving patient outcomes by providing interventional cardiologists with precise anatomical and physiological assessments of coronary artery disease (CAD).

More than 60 million people currently suffer from coronary artery disease (CAD) worldwide1. Percutaneous Coronary Intervention (PCI)  is a common method for treatment and management of patients with CAD. As Medis QFR is an angiographic image-based approach, it eliminates the need for a more invasive wire-based approach in assessing coronary physiology. It is also capable of evaluating multiple areas from the same images versus the wire-based approach which is vessel- and often lesion-specific. This can potentially increase efficiency and safety while reducing procedure time.

The FAVOR trials, performed in the EU, have proven the efficacy of the Medis QFR solution in practical use during and after an interventional procedure. The FAVOR III China trial demonstrated a 34% reduction in major adverse cardiac events (MACE) in a one-year follow-up of patients treated with Medis QFR-guided versus standard angiography-guided procedures, and similar results were obtained after two years2. The FAVOR Trials, which used the first-generation QFR technology, demonstrated high accuracy compared to the pressure wire. This led to Medis QFR being approved and reimbursed in Japan, and included in the 2024 ESC guidelines for chronic coronary syndromes with a Class I recommendation. The PIONEER IV trial, a 2,540-patient study, aims to evaluate the superiority of the next-generation QFR technology – for both pre- and post-procedure stenting recommendations – which will be integrated with THO's ePRISM platform.