Northwire Canada EditionSaturday, July 18, 2026
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AII 19.25 +3.9% GGA 5.95 +12.3% VM 0.140 +3.7% GSR 0.365 +1.4% QCX 0.195 +0.0% EAU 0.085 +0.0% MCM 0.310 +0.0% BAT 0.100 +5.3% SFR 0.370 +68.2% FFU 0.125 +4.2% TVI 0.045 −10.0% ZNX 0.080 +0.0% TSK 1.06 +0.9% OMM 0.050 +0.0% EMO 0.320 −7.2% MDM 0.060 +0.0% AII 19.25 +3.9% GGA 5.95 +12.3% VM 0.140 +3.7% GSR 0.365 +1.4% QCX 0.195 +0.0% EAU 0.085 +0.0% MCM 0.310 +0.0% BAT 0.100 +5.3% SFR 0.370 +68.2% FFU 0.125 +4.2% TVI 0.045 −10.0% ZNX 0.080 +0.0% TSK 1.06 +0.9% OMM 0.050 +0.0% EMO 0.320 −7.2% MDM 0.060 +0.0%
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Ventripoint Diagnostics and Providence Health Care Ventures Announce Collaboration to Validate AI-Enabled Cardiac Imaging at St. Paul's Hospital

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Executive Summary

  • Ventripoint Diagnostics entered a collaboration with Providence Health Care Ventures to validate its AI‑enhanced echocardiography platform (VMS+™) at St. Paul’s Hospital, targeting reduction of cardiac MRI demand.
  • The study will compare VMS+™‑derived measurements against MRI, assess workflow integration, potential MRI referral reductions, wait‑time impacts, and system‑level cost efficiencies.
  • Validation work is slated to begin in November 2025 with implementation expected in early 2026, positioning VMS+™ for broader adoption across tertiary, rural and Indigenous health settings.

Key Details

  • Collaboration Partner: Providence Health Care Ventures (PHC Ventures), the commercialization arm of Providence Health Care.
  • Site of Validation: St. Paul’s Hospital, Vancouver, British Columbia – a leading cardiac program in Western Canada.
  • Objective: Demonstrate that AI‑enhanced 2‑D echocardiography can provide MRI‑level cardiac volume and function measurements, thereby reducing reliance on cardiac MRI.
  • Study Components:
  • Direct comparison of VMS+™‑derived measurements with gold‑standard cardiac MRI.
  • Evaluation of workflow integration within the hospital’s imaging pathway.
  • Quantification of potential reductions in MRI referrals and associated wait‑time improvements.
  • Analysis of system‑level cost efficiencies and impact on patient access, especially for rural/Indigenous communities.
  • Technology Highlights:
  • VMS+™ is FDA‑cleared and Health Canada‑licensed; operates on existing 2‑D ultrasound systems without need for new hardware.
  • Prior implementations include Hospital for Sick Children (Toronto), Peter Munk Cardiac Centre (UHN, Toronto), and clinical studies at Mayo Clinic showing close alignment with MRI measurements.
  • Timeline: Collaboration to commence November 2025; implementation phase beginning early 2026.
  • Strategic Impact: Successful validation could expand VMS+™ adoption across Canada’s health system, improve access to advanced cardiac diagnostics in underserved areas, and create a pathway for reduced MRI utilization and associated cost savings.

Notable Quotes

  • “This technology helps identify which patients truly need an MRI and which can be safely assessed using a standard echocardiogram.” – Brian Simmers, President of PHC Ventures.
  • “MRI remains the gold standard for cardiac imaging, but it is not always within reach for every patient… AI‑enhanced echocardiography like VMS+™ could bring MRI‑level precision to a more accessible modality.” – Dr. Robert Moss, Physician Lead, Echocardiography, St. Paul’s Hospital.
  • “Our vision is to make high‑quality cardiac imaging available wherever an echo machine exists.” – Hugh MacNaught, President and CEO, Ventripoint Diagnostics Ltd.
Read the original news release →

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