cerca CERCA
Lunedì 02 Dicembre 2024
Aggiornato: 21:44
10 ultim'ora BREAKING NEWS

comunicato stampa

Transpara Announces New FDA Clearance Designed to Improve Breast Cancer Detection at RSNA

02 dicembre 2024 | 18.51
LETTURA: 3 minuti

ScreenPoint Medical to Showcase Innovative FDA Cleared Capabilities including Breast Density Assessment and Temporal Comparison to Elevate Radiologist Performance

CHICAGO, Dec. 2, 2024 /PRNewswire/ -- ScreenPoint Medical is showcasing a new FDA clearance for innovative new capabilities of its industry leading Breast AI Transpara here at the 110th Annual Radiological Society of North America (RSNA) meeting, December 1-4, 2024 (South Hall #5316). The most clinically validated Breast AI on the market, Transpara provides radiologists with a 'second pair' of eyes to help detect cancers earlier and reduce recall rates.

ScreenPoint will highlight its latest advancements, which include Transpara 2.1: an updated algorithm based on additional training and insights gathered from luminary users around the world. Transpara 2.1 is compatible with options for breast density (BIRADS and volumetric) and temporal comparison. Allowing suspicious areas on a current study to be analyzed against up to 3 priors over 6 years, the robust temporal comparison capability will be the first of its kind in the market. The Transpara 2.1 algorithm is both CE marked and FDA cleared.

With the  algorithm improvements, the system standalone performance is demonstrated to be in the top 10% of radiologists in a presentation by Alejandro Rodriguez Ruiz, PhD at ECR 2024.

"Taking tissue changes into account for characterization of findings is a long awaited feature of AI," said Professor Nico Karssemeijer, PhD, co-founder and Chief Scientific Officer of ScreenPoint Medical. "We are very excited about the significant improvement of Transpara performance when priors are used, especially when more priors with a longer time interval are included, which is in line with radiologists' experience. Our solution is designed for screening and diagnostic use to truly improve clinical workflow. Use of priors hardly increases computation time, and we provide the user with information about the effect of priors on the final result to increase confidence and transparency."

In addition to the introduction of Transpara 2.1, the clinical and workflow benefits of Transpara on improving the mammography screening process are the subject of several studies being presented this week at RSNA in scientific sessions:

With 35+ peer-reviewed publications, Transpara is the only breast AI algorithm evaluated in large-scale real-world screening populations multiple times (including UCLA, Capital Region of Denmark, Lund University in Sweden, Norwegian Cancer Registry, Reina Sofia Hospital Cordoba). Research shows that up to 45% of interval cancers can be found earlier using Transpara, while helping to reduce workload and optimize workflow.

About ScreenPoint Medical 

ScreenPoint Medical translates cutting edge machine learning research into technology accessible by radiologists to improve screening workflow, decision confidence and breast cancer risk assessment. Transpara is trusted by radiologists globally because it has been developed by experts in machine learning and image analysis and updated with user feedback from world-renowned breast imagers. See all the proof at: https://screenpoint-medical.com/published-evidence/peer-reviewed-publications 

Logo -  https://mma.prnewswire.com/media/1582198/ScreenPoint_Medical_Logo.jpg

 

View original content:https://www.prnewswire.co.uk/news-releases/transpara-announces-new-fda-clearance-designed-to-improve-breast-cancer-detection-at-rsna-302319868.html

Riproduzione riservata
© Copyright Adnkronos
Tag
Vedi anche


SEGUICI SUI SOCIAL



threads whatsapp linkedin twitter youtube facebook instagram
ora in
Prima pagina
articoli
in Evidenza