An active implantable stimulating device (10) includes: (a) a tissue coupling unit (40) for being implanted directly onto a vagus nerve (Vn) of a patient, (b) an EEG-unit (70) for measuring an electroencephalogram of the patient, (c) an encapsulation unit (50) configured for being subcutaneously implanted, (d) an energy transfer lead (30) for transferring pulses of electrical and/or optical energy, (e) a signal transfer lead (60) for transferring signals between the EEG unit and the encapsulation unit. EEG electrodes (70a-70d) monitor the electric activity of the brain of a patient. The EEG signal is conveyed to the electronic circuit (53) in the form of EEG conditioned data. The electronic circuit analyses the EEG conditioned data to yield analysis results. The electronic circuit takes a decision to trigger energy pulses to stimulate the vagus nerve (VN).

Treating kenosis may comprise the following steps: measuring the electrodermal activity of a person by means of an EDA sensor; assessing, on the basis of the electrodermal activity measured, whether the person is currently affected by kinetosis; generating electrical pulses at an electrode in contact with the person's skin in order to treat the kinetosis on the basis of the assessment as to whether the person is currently affected by kinetosis. The sensor and the electrode may be integrated in a device that can be worn on the person's body.

The present disclosure relates to establishing bidirectional communication between a brain wave processing device and a vehicle to control at least one vehicle component of the vehicle. For this purpose, a brain-computer communication channel is provided between the brain wave processing device and the respective vehicle component. Subsequently, a control signal is determined as a function of a brain wave of the operator of the brain wave processing device and transmitted via the brain-computer communication channel to adapt at least one operating parameter of the respective vehicle component. This causes a change in the operating state of the respective vehicle component. Depending on this, an output signal is generated and is assigned to the change in the operating state of the vehicle component. This output signal is transmitted back to the brain wave processing device via the brain-computer communication channel and is output to the operator by means of an output unit of the brain wave processing device.

A method for estimating a brain activity response following a stimulus of a person comprises the steps: providing a usage data set of the person from a personal device used by said person, wherein at least one usage attribute is associated to said usage data set, wherein attribute data is associated to each of the at least one usage attribute, providing a computational inference model, generated from a plurality of brain activity data sets and a plurality of usage data sets, wherein each brain activity data set comprises data derived from a brain activity response following a sensory stimulus, submitting the attribute data of each of the at least one usage attributes to said computational inference model, estimating a brain activity response following a sensory stimulus of said person by evaluating said computational inference model for the submitted attribute data. The method is useful to determine, for example the influence of intensive touch pad usage (of a smartphone) on somatosensory evoked potentials.

Some systems, devices and methods detailed herein provide a system for use in determining metrics of a subject. The system can provide, as an output, a function-metric value determined based on a defined relationship between physiological measures and a chronological age.

The present invention relates to a suction instrument, more particularly a bipolar mapping suction instrument, for surgical purposes and to a system for suctioning fluids and tissue and for monitoring nerve tissue. The suction instrument comprises a cannula unit, which comprises an electrically conductive outer cannula tube, an electrically conductive inner cannula tube, and insulation. The electrically conductive inner cannula tube is electrically connected to a first pole of the bipolar electrical connection of the second interface. The electrically conductive inner cannula tube is arranged concentrically in the outer cannula tube which optionally can be insulated from the exterior. The electrically conductive inner cannula tube is mechanically connected to the handpiece and/or the first interface. The electrically conductive outer cannula tube is electrically connected to a second pole of the bipolar electrical connection of the second interface. The insulation is concentrically arranged between the outer cannula tube and the inner cannula tube. The insulation is configured to fully electrically isolate the outer cannula tube and the inner cannula tube in relation to one another.

Described herein are noninvasive electrical stimulation devices, systems and methods for stimulation of the Vagus nerve through its auricular branch to provide beneficial physiological responses in subjects, including alleviation, mitigation or elimination of symptoms of various disorders, including metabolic and inflammatory disorders.

This document discusses a medical system for coupling to one or more implantable electrodes. The medical system includes a sensing circuit, memory, and processing circuitry. The sensing circuit is configured to sense one or more neural signal representative of neural activity of a subject when connected to an implantable electrode of the one or more implantable electrodes, and the memory is to store a reference signal that is representative of a neural response associated with a state of arousal at or near an anatomical location of the implantable electrode. The processing circuitry is configured to compare the one or more sensed neural signals to the reference signal, and to determine a depth of anesthesia of the subject according to the comparison of the one or more sensed neural signals and the reference signal.

To provide objective indications of the progression of peripheral neuropathy of patients, a transmitter apparatus is utilized to produce reproducible pulse signals to specified locations on the human body to determine a minimum level of stimulation necessary to elicit a consciously detectable sensation through the generation of a series of pulse signals of varying intensities, and the recordation of the number of pulse signals felt by the patient. Moreover, the nerve velocity of the patient is additionally determined for a patient via the transmitter apparatus and a receiver apparatus detecting body-signals passing along a nerve within the patient and corresponding to the pulse signals applied to the patient. The results of these tests are recorded over time, thereby enabling generation of patient-specific models indicative of the progression of the patient's peripheral neuropathy over time.

A system provides a burr hole cap assembly configured to secure a position of a lead implanted through a burr hole in a cranium of a patient. One or more electrodes are coupled to one or more components of the burr hole cap assembly. The one or more electrode is disposed within the burr hole cap assembly for sensing signals within a brain of the patient or stimulating a portion of the brain of the patient.