In April 2022, GE HealthCare earned FDA approval as the first software that helps automate anesthesia delivery in the U.S by conducting a MASTER-Anesthesia Trial (Multi-site Anesthesia randomized controlled STudy of End-tidal control compared to conventional anesthesia Results).
Kyle Herzog, an engineer with GE since 2008, served as the lead engineer on that clinical trial of GE’s End-tidal control* software, which involved 248 patients at four institutions.
In this second video of our three-part series, Herzog delivers a technical overview, examining:
- End-tidal control software and hardware components
- How End-tidal control works
- Which patients benefit from End-tidal control
- Safety mechanisms and checks
- How GE gained FDA-approval
- Results and observations from that US clinical trial
*Et Control is indicated for patients 18 years of age and older in the United States.
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JB29328XX, JB29289XX
Kyle Herzog
Engineering Manager, GE HealthCare – Anesthesia & Respiratory Care
Kyle Herzog has worked as an Engineer at GE HealthCare in Madison, WI since 2008 after graduating with a Biomedical Engineering degree from UW-Madison. He has worked on the Verification and Validation (V&V) team for his entire career with a focus on creating high quality and reliable Anesthesia Machines. He has worked with End-Tidal Control the majority of his career and was a lead engineer on the MASTER trial that eventual lead to FDA Approval of the Et Control feature.
