Integrated SGRT on the Radixact® System: The Benefits of the VitalHoldTM Package
Surface-guided radiation therapy (SGRT) is rapidly becoming a game-changer in the field of radiotherapy, with data showing it can potentially reduce up to 21% of errors associated with radiation treatments 1. The VitalHold™ Package enables you to efficiently position and monitor patients prior to and during treatment with SGRT on the Radixact® System. In addition, the fully integrated and automated SGRT solution allows you to provide deep inspiration breath hold (DIBH) treatments using TomoDirect™ treatment delivery mode on the Radixact System.
EASY SET-UP
Perform positioning with the clinical flexibility of SGRT and ClearRT® helical kVCT imaging for effective and efficient patient set-up.
CONFIDENT MONITORING
Gate the beam automatically for deep inspiration breath hold (DIBH) treatments using TomoDirect™ delivery.
FAST DELIVERY
Treat precisely in as little as 2 minutes with added patient comfort.
VitalHold Workflow for the Radixact System
The Radixact® Treatment Delivery System integrates Catalyst+ HD surface-guided radiation (SGRT) therapy to expand clinical capabilities, simplify workflows and deliver precise treatments to more patients.
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VitalHold Resources
What’s included in the package
The VitalHold package enables three critical functionalities on the Radixact System: SGRT daily-patient setup, breath-hold gating using TomoDirectTM, in-bore position gating.
Real-world results
Learn how our customers are using VitalHold, take a look at a case study: Deep inspiration breath hold using Vitalhold™ on the Radixact® System.
A deeper look at the technology
Learn more on the latest technologies in treatment planning and delivery to improve radiation therapy treatments for patients with breast cancer.
1Al-Hallaq HA, Batista V, Kügele H, Ford E, Viscariello N, Meyer J The role of surface-guided radiation therapy for improving patient safety. Radiotherapy and Oncology 2021;163:229–236. https://doi.org/10.1016/j.radonc.2021.08.008
* VitalHold is 510(k) cleared and cleared for the EU market. Availability is subject to regulatory clearance or approval in some markets.
