VIST® Case-It
Patient-specific simulation, powered by clinically proven segmentation solutions to allow creation of patient specific training cases.
Patient-specific simulation, powered by clinically proven segmentation solutions to allow creation of patient specific training cases.
Case-It is a paradigm shift in simulation solutions for image-guided interventional therapies, powered by clinically proven segmentation solutions to allow the creation of patient-specific training cases.
Case-It is a unique solution that creates a Mentice simulation case from existing patient anatomies with only a few clicks.
The resulting case can be used for sharing and teaching after the actual procedure has been done, allowing peers and students to re-enact the experience and practice various treatment approaches. It is possible to build an expansive library of varying cases. Ultimately, it can be used as a warm-up or rehearsal before an actual procedure.
Case-It technology eliminates the learning curve by interfacing with the user’s existing segmentation workstation.
Mentice builds easy-to-use and reliable simulation solutions without compromising quality and realism. Case-It combines state-of-the-art segmentation with the only fully validated simulator for image-guided interventional therapies.
Import your patient anatomy data and prepare yourself and your team for challenging cases.
Build your own unlimited case library
Share complex cases with colleagues
Add pathologies to your case to create the best possible training
Our Vision
Simulation plays an increasingly important role in medical education settings, certification, and recertification. However, as with clinical practice, curriculums change over time, and the needs differ between settings and regions. This creates a growing demand for content that matches specific needs. Case-It technology allows users to select and utilize the cases that best suit their individual training needs.
Case-It is the first step in a comprehensive environment that allows the creation of individualized training cases and content.
History
Mentice is a pioneer in patient-specific training and was the first company to show a ‘Mission Rehearsal’ case for Carotids live at EuroPCR 2004. Since then, we have also created patient-specific cases for both coronary and neuro interventions.
How it works
Case-It technology harnesses the power of professional segmentation tools. This ensures the highest possible quality of the 3D reconstruction using market-leading and clinically proven workstations.
From CT or MRI data, the operator will reconstruct the relevant anatomy using the available, preferred segmentation solution. The benefit is that the user is well versed with the respective workstation and will be able to reconstruct from a variety of data qualities.
The reconstructed anatomy is imported using Case-It technology and stitched onto a template anatomy to create a complete vascular anatomy for procedural training (even if the CT data are limited to only a part of the patient’s anatomy).
Thanks to this, Mentice clients can now robustly and simply create their own patient-specific simulated cases with a minimum of extra work, using segmentation software they are already familiar with and without a significant learning curve.
Certification Program
To ensure that Case-It always works seamlessly with anatomy data from the user’s preferred segmentation workstation, Mentice has launched the Case-It Certified program. Within this program, Mentice validates the output of professional and FDA-approved segmentation solutions to make sure Case-It is fully compatible.
Flow Diverter Case planning in Ankyras®
Import Case directly into VIST® simulator
Practice deployment in patient-specific anatomy
Contact us to learn more or see a web demo of this product
Disclaimer & Regulatory Information
VIST® Ankyras® Flow Diverter Rehearsal is a training solution not intended for clinical use or decision making. Ankyras® is a medical device manufactured by Mentice Spain S.L. Mentice Spain S.L. is ISO 13485 certified. Ankyras® complies with the EU Medical Device Regulation (EU CE Mark, MDR 784032). ANKYRAS® is a medical software intended to assist healthcare professionals in the selection of a proper braided device for treatment of intracranial aneurysms. ANKYRAS® is intended for exclusive use by professional users.
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