Cleveland Clinic: First Case Completed in Feasibility Study of Non-Radiation-Based EVAR Navigation Platform

Jan 19, 2021 | News

MOTION study will quantify new technology’s impact on radiation exposure

In December, Cleveland Clinic vascular surgeons successfully completed the first surgical case in the MOTION clinical trial of a new non-radiation-based surgical navigation platform for endovascular aortic interventions.

The trial is a feasibility study of the Intra-Operative Positioning System (IOPS™) from Centerline Biomedical, which received 510(k) marketing clearance from the FDA in 2019. The technology, which serves as an adjunct to X-ray fluoroscopy, is in use at Cleveland Clinic and four other U.S. institutions as part of a limited launch.

“The MOTION trial is being conducted to determine the degree of radiation reduction that’s possible with IOPS and to better characterize its utility in endovascular aortic repair [EVAR],” says Cleveland Clinic vascular surgeon Francis Caputo, MD, who performed the study’s first case and serves as its national principal investigator.

The technology in brief

As detailed in an earlier Consult QD post, the IOPS technology was initially developed at Cleveland Clinic as a platform for enhancing visualization during endovascular aortic interventions with reduced reliance on fluoroscopy.

The portable system employs anatomic mapping algorithms and electromagnetic tracking technology to provide high-definition, three-dimensional (3D) color visualization and guidance in real time during endovascular procedures. “The technology is similar to GPS, in that it uses coordinates derived from prior imaging to guide navigation,” explains Dr. Caputo.

He says an approach like IOPS ultimately has potential to supplant fluoroscopy as the standard of care for visualization during EVAR procedures. “Not only does this system help guide accurate placement of catheters and guidewires as the surgeon navigates the aorta and its branches, but it has the potential to reduce harmful radiation exposure to both surgeons and patients through reduced dependence on fluoroscopy,” Dr. Caputo observes.

Comparative visualization of the left renal artery with the IOPS platform (left) versus fluoroscopy and contrast dye (right).

Study essentials

In fact, radiation dose is one of the main measures being assessed in the MOTION trial, along with use of contrast dye and duration of the EVAR procedure. “IOPS was designed to reduce radiation exposure and use of toxic contrast dye, as well as reduce procedure time through enhanced visualization and coordinate-based navigation assistance,” says Dr. Caputo. “This study aims to formally quantify to what extent it achieves those objectives.”

MOTION is designed to enroll 30 patients between Cleveland Clinic and a second study site, UNC Medical Center in Chapel Hill, North Carolina. Completion of the single-arm study is anticipated by the end of 2021, after which a controlled study may be undertaken to compare IOPS plus fluoroscopy (as needed) versus fluoroscopy alone.

Expected benefits in safety and beyond

If MOTION confirms that IOPS enables substantial reductions in radiation dose, contrast use and procedure time, Dr. Caputo believes the technology is likely to be widely adopted for guiding EVAR procedures in the years ahead — particularly for longer, more complex cases that would otherwise require significant radiation exposure.

“The greatest potential from this system is in more complex cases, ones that involve considerable navigation to target vessels,” he explains. “With fluoroscopy alone, cases like that can require 5 to 10 gray of radiation, and levels above 5 gray raise concern about radiation risk to patients — as well as to providers, despite the lead shields we wear. Beyond safety benefits to patients and staff, reduced-radiation procedures may ultimately become an occupational safety requirement.”

After completing six EVAR repairs using IOPS through the end of 2020, Dr. Caputo says the system also offers advantages to the operator in terms of navigation. “For example,” he notes, “if you are targeting a renal artery, it shows you not only where the artery is but how to use the catheter and wire in conjunction to quickly home in on the artery. Achieving that type of navigation without much or any radiation is a long-sought objective that may be at hand.”

NOTE: Centerline Biomedical is a Cleveland Clinic spinoff company. Cleveland Clinic holds equity in the company and is entitled to royalties from the company.

Published: Jan 18, 2021

Full Article by Consult QD:
https://consultqd.clevelandclinic.org/first-case-completed-in-feasibility-study-of-non-radiation-based-evar-navigation-platform/?utm_medium=social&utm_source=linkedin&utm_campaign=cc+li+posts