We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

MedImaging

Download Mobile App
Recent News Radiography MRI Ultrasound Nuclear Medicine General/Advanced Imaging Imaging IT Industry News

Software Designed for the Assessment of Orthopedic Implant Fixation and Bone Segment Motion

By MedImaging International staff writers
Posted on 26 Mar 2014
Print article
Model-based roentgen stereophotogrammetric analysis (MBRSA) software has been developed for evaluation of orthopedic implant fixation and bone segment motion. The software is the first to measure the in vivo three-dimensional (3D) position and/or relative motion of metal implants, markers beads, and/or bone segments in 3D from calibrated stereo X-ray images.

When interpreted by trained physicians these measurements may be useful to derive conclusions for critical patient treatment decisions. Halifax Biomedical, Inc. (HBI; Mabou, NS, Canada), a company specializing in precision assessment of spine and joint-replacement microinstability, reported that their image processing software has received US Food and Drug Administration (FDA) clearance.

The MBRSA software has been developed and maintained by HBI partner RSAcore of the department of orthopedics at Leiden University Medical Center (LUMC; The Netherlands). “Our strong and longstanding partnership with Leiden University Medical Center has enabled us to complete the final regulatory step in our transition from clinical research use of our technology to everyday clinical use,” said Chad Munro, chief executive officer for HBI.

“This FDA clearance will enable HBI to provide image processing services for two key clinical issues: deciding whether to intervene to stabilize a total knee replacement due to implant fixation concerns and deciding whether sufficient spine instability is present to justify spine fusion surgery,” said Chad Munro, chief executive officer for HBI.

“The FDA clearance of this analytical software is not only a major milestone for HBI but also for the orthopedic community as we shift toward broad clinical use in the United States. The HALIFAX program now includes FDA clearance for Halifax intraoperative bone markers, Halifax SR imaging systems, and now, SR image processing services,” said Crystal Jones, VP operations for HBI.

“This approval represents an important step forward in independent and quantitative assessment of orthopedic patients,” said Bart Kaptein, MSc, PhD, and Prof. Rob Nelissen, MD, PhD, of the department of orthopedics at LUMC. “MBRSA is a leading edge analysis platform, we are proud of the many years of intense research and development at LUMC to create this orthopedic research tool.”

Related Links:
Halifax Biomedical
Leiden University Medical Center 


New
Cylindrical Water Scanning System
SunSCAN 3D
Portable Color Doppler Ultrasound Scanner
DCU10
Portable X-ray Unit
AJEX140H
Diagnostic Ultrasound System
MS1700C

Print article

Channels

MRI

view channel
Image: The AI tool can help interpret and assess how well treatments are working for MS patients (Photo courtesy of Shutterstock)

AI Tool Tracks Effectiveness of Multiple Sclerosis Treatments Using Brain MRI Scans

Multiple sclerosis (MS) is a condition in which the immune system attacks the brain and spinal cord, leading to impairments in movement, sensation, and cognition. Magnetic Resonance Imaging (MRI) markers... Read more