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VentriPoint Diagnostics Ltd V.VPT

Alternate Symbol(s):  VPTDF

Ventripoint Diagnostics Ltd. is a Canada-based medical device company. It is engaged in the development and commercialization of diagnostic tools to monitor patients with heart disease. It develops a suite of applications for all heart diseases and imaging modalities, including congenital heart disease, pregnancy, pulmonary hypertension, COVID-19, technically difficult imaging and cardiotoxicity in oncology patients. It provides application of artificial intelligence to echocardiography. Its flagship product, Ventripoint Medical System (VMS+), enhances echocardiography to deliver cMRI levels of accuracy for volumetric measurements and ejection fractions for all four chambers of the heart. It has developed a solution that transforms cardiac care through its 3D ECHO and MRI software. VMS products are powered by its proprietary Knowledge Based Reconstruction technology, which is the result of a decade of development and provides accurate volumetric cardiac measurements equivalent to MRI.


TSXV:VPT - Post by User

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Comment by eyeNteeon Nov 18, 2015 8:52pm
98 Views
Post# 24303475

RE:Another new article

RE:Another new articleStill an overall positive article reguarding Ventipoints technology fiveniner. Thnx.
                                                                                                                                                                        The commercial application of this technology is the Ventripoint imaging system, which was evaluated in a multicenter clinical trial in PAH patients in comparison to CMR. Though full results of the study have not been published to date, the Ventripoint system reportedly generated similar volumes to Figure 2: Definition of anatomic points from standard 2D-TTE views using the Ventripoint system (Panels A–D) to generate 3D reconstruction of the RV (Panel E) in both diastole and systole (Panel F). Advances in Pulmonary Hypertension Volume 14, Number 1; 2015 31 CMR performed within 24 hours of the Ventripoint echocardiogram, and based on the results of this trial data, the Ventripoint system has been approved by the United States Food and Drug Administration for RV quantification. To date there has been relatively little clinical experience with this technology in PAH patients outside of the clinical trial arena, but this system certainly has the potential to significantly enhance routine echocardiographic assessment of RV volume and EF. Using the Ventripoint technology might be a less costly secondary endpoint in future PAH clinical trials. 

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