The Percept™ family with BrainSense™ technology† is the only sensing-enabled DBS system offering insights into a patient’s condition inside and outside of the clinic throughout the patient journey.
Now with cutting-edge advancements exclusive to the Medtronic Percept™ family of devices for Parkinson’s disease
BrainSense™ Electrode Identifier
The BrainSense™ Electrode Identifier feature guides you to the sensing “sweet spot” on the lead, providing a starting point for DBS programming and identification of initial contacts for stimulation delivery.
BrainSense™ Adaptive DBS (aDBS)
aDBS uses BrainSense™ technology to automatically adjust therapeutic stimulation to effectively control motor symptoms throughout the day and night.
of patients with Parkinson’s disease preferred BrainSense™ aDBS over traditional DBS after using for 30 days.¶
Safety
There are risks and benefits of DBS: Risks include surgical complications, infection, failure to deliver therapy as needed and/or worsening of some symptoms.
The safety profile observed for aDBS is consistent with the safety profile for traditional DBS (cDBS). Stimulation-related side effects are expected during initial aDBS setup, such as worsening of Parkinson’s disease symptoms and dyskinesias, and are expected to resolve with reprogramming. It’s important to ensure patients have regular follow up visits to monitor response to therapy, optimize programming, and manage any stimulation-related side effects promptly, especially within aDBS adjustment and set up periods (at least within the first few months of aDBS programming). aDBS is an optional programming feature and may not work for everyone.
† The sensing feature of the Percept™ PC system and Percept™ RC system is intended for use in patients receiving DBS where chronically-recorded bioelectric data may provide useful, objective information regarding patient clinical status.
‡ Improved motor symptom control results were based on post hoc analysis averaging overall patient aDBS on time results compared to cDBS. Results presented for dual threshold aDBS. N=40. Based on results from an open-label comparison.
§ Study data with 40 patients evaluated on Dual Threshold mode.
◊ 16 hours.
¶ Clinical Summary, Data from 45 patients who were previously stable on traditional DBS (cDBS).
# Medtronic DBS systems are MR Conditional. Refer to product labeling for full list of conditions. https:manuals.medtronic.com/manuals/mri/region