In one instance, a process for predicting and using emotions of a user in a virtual reality environment includes applying a plurality of physiological sensors to a user. The process further includes receiving physiological sensor signals from the physiological sensors and preparing the physiological sensor signals for further processing by removing at least some of the noise and artifacts and doing data augmentation. The process also includes producing an emotion-predictive signal by utilizing an emotion database. The emotion database has been developed based on empirical data from physiological sensors with known emotional states. The method also includes delivering the emotion-predictive signal to a virtual-reality system or other computer-implemented system. Other methods and systems are presented.

In one instance, a process for predicting and using emotions of a user in a virtual reality environment includes applying a plurality of physiological sensors to a user. The process further includes receiving physiological sensor signals from the physiological sensors and preparing the physiological sensor signals for further processing by removing at least some of the noise and artifacts and doing data augmentation. The process also includes producing an emotion-predictive signal by utilizing an emotion database. The emotion database has been developed based on empirical data from physiological sensors with known emotional states. The method also includes delivering the emotion-predictive signal to a virtual-reality system or other computer-implemented system. Other methods and systems are presented.

A disposable patch electrode structure comprises a front flap and a main structure, which is attached to skin for a bio-signal measurement, the patch electrode structure feeding electrical bio-signals to a bio-signal device separate from the patch electrode structure. The front flap is separated from the main structure by a non-enclosing front flap cut, material of the front flap being thus formed as continuous material of the main structure. Materialistic connection of the continuous material between a rear section of the front flap at a non-enclosing side of the front flap cut and the main structure allows tilt of the front flap with respect to the main structure in response to rise of a frontal section of the front flap with respect to the main structure. The front flap is fully surrounded by the main structure. The front flap comprises contact electrodes at the frontal section, the contact electrodes being both connected with measurement electrodes of the main structure through conductors via the materialistic connection and connectable with counter-electrodes of a connector separate from the patch electrode structure.

A disposable patch electrode structure comprises a front flap and a main structure, which is attached to skin for a bio-signal measurement, the patch electrode structure feeding electrical bio-signals to a bio-signal device separate from the patch electrode structure. The front flap is separated from the main structure by a non-enclosing front flap cut, material of the front flap being thus formed as continuous material of the main structure. Materialistic connection of the continuous material between a rear section of the front flap at a non-enclosing side of the front flap cut and the main structure allows tilt of the front flap with respect to the main structure in response to rise of a frontal section of the front flap with respect to the main structure. The front flap is fully surrounded by the main structure. The front flap comprises contact electrodes at the frontal section, the contact electrodes being both connected with measurement electrodes of the main structure through conductors via the materialistic connection and connectable with counter-electrodes of a connector separate from the patch electrode structure.

An electronic vaporizer system includes an anesthetic sump containing anesthetic agent, a vaporizer unit that vaporizes the anesthetic agent from the sump and delivers the vaporized agent to a patient breathing circuit, and a gas sensor configured to measure end tidal concentration of the anesthetic agent and exhalation gasses from the patient. A control system is configured to receive the measured end tidal concentration of anesthetic agent and compare the measured end tidal concentration to a desired end tidal concentration to be maintained for the patient. The vaporizer unit is then automatically controlled to deliver an amount of vaporized agent to the patient based on the comparison.

An implantable electrode device includes a carrier made of a polymer material, at least one measurement electrode formed by an electrically conducting pad located on the carrier, wherein the electrically conducting pad has a contact surface, a barrier layer enclosing the carrier by covering all surfaces of the carrier, wherein the contact surface of the electrically conducting pad is exposed to an outside environment, at least one electrically conducting trace, and at least one electrically conducting terminal. The electrically conducting trace can electrically connect the measurement electrode to the electrically conducting terminal. A surface of the implantable electrode device on a side on which the measurement electrode is located can have a maximum valley depth or a maximum peak height between the contact surface of the measurement electrode and a meanline of a surface of the implantable electrode device, excluding measurement electrodes, being equal to or smaller than 100 micrometres.

An implantable electrode device includes a carrier made of a polymer material, at least one measurement electrode formed by an electrically conducting pad located on the carrier, wherein the electrically conducting pad has a contact surface, a barrier layer enclosing the carrier by covering all surfaces of the carrier, wherein the contact surface of the electrically conducting pad is exposed to an outside environment, at least one electrically conducting trace, and at least one electrically conducting terminal. The electrically conducting trace can electrically connect the measurement electrode to the electrically conducting terminal. A surface of the implantable electrode device on a side on which the measurement electrode is located can have a maximum valley depth or a maximum peak height between the contact surface of the measurement electrode and a meanline of a surface of the implantable electrode device, excluding measurement electrodes, being equal to or smaller than 100 micrometres.

An electrode is provided for recording electroencephalographic signals and/or for stimulating patients. The electrode includes a patient contact part and a transmission part. A layer of electrolyte material is further provided in contact with the patient's skin and interposed between the patient's skin and the contact part. The contact part and/or the transmission part includes of a soft and/or flexible material.

A processing system obtains a deformation signal generated by a deformation sensor. The deformation signal is indicative of a deformation of an outer ear of a user of a hearing instrument. Additionally, the processing system obtains an EMG signal generated by an electrode in a concha of the user, wherein the electrode is configured to detect activity of an intrinsic auricular muscle of the user. Furthermore, the processing system generates information regarding an auditory attention state of the user based on the deformation signal and the EMG signal. The processing system controls, based on the information regarding the auditory attention state of the user, the parameter of the audio system.

A processing system obtains a deformation signal generated by a deformation sensor. The deformation signal is indicative of a deformation of an outer ear of a user of a hearing instrument. Additionally, the processing system obtains an EMG signal generated by an electrode in a concha of the user, wherein the electrode is configured to detect activity of an intrinsic auricular muscle of the user. Furthermore, the processing system generates information regarding an auditory attention state of the user based on the deformation signal and the EMG signal. The processing system controls, based on the information regarding the auditory attention state of the user, the parameter of the audio system.