A plurality of devices that provide examination/diagnosis and/or treatment benefits to a patient are presented. The device including a plurality of light sources that provide for the emission of light in a plurality of wavelength ranges, wherein the plurality of light sources are activated by a sensor, configured to determine a proximity of the device to a patient, to control an application of a voltage to selected one of the plurality of light sources for a predetermined time period.

Embodiments of apparatuses and methods for determining an emplacement of sensors in a wound dressing are disclosed. In some embodiments, a wound dressing includes a plurality of sensors configured to measure wound or patient characteristics. One or more processors are configured to receive wound or patient characteristics data as well as emplacement data. The received data can be used to determine an emplacement of the plurality of sensors, the wound dressing, or a wound. The sensors can include a set of nanosensors. The wound dressing can include pH sensitive ink which can be utilized for determining a placement of the wound dressing and determining a pH associated with the wound. The wound dressing can be used in a negative pressure wound therapy system.

A method may include identifying a simulated three-dimensional representation corresponding to an internal anatomy of a subject based on a match between a computed two-dimensional image corresponding to the simulated three-dimensional representation and a two-dimensional image depicting the internal anatomy of the subject. Simulations of the electrical activities measured by a recording device with standard lead placement and nonstandard lead placement may be computed based on the simulated three-dimensional representation. A clinical electrogram and/or a clinical vectorgram for the subject may be corrected based on a difference between the simulations of electrical activities to account for deviations arising from patient-specific lead placement as well as variations in subject anatomy and pathophysiology.

A system (10) is for performing ECG measurements and comprises a probe (12) with an integrated one or more ECG electrodes (22) and an ultrasound sensing means (18), such as a transducer arrangement. The probe thus provides a mobile ECG electrode which can be sequentially moved between a set of different locations on the body for acquiring ECG measurements from different angles relative to the heart (i.e. different ‘leads’). Positioning of the probe in each required location is guided by a position guidance function which uses ultrasound data acquired by the ultrasound sensing means to locate the probe (with reference to an ultrasound body atlas (28) or map), and uses a stored set of reference body locations to guide a user with guidance information as to how to move the probe to arrive at a next target electrode location. In examples, the user may be guided through a sequence of electrode locations, with ECG data acquired at each one, thereby sequentially building up a set of standard ECG lead measurements.

The present document relates to a fetal heart rate monitoring device for monitoring a heart rate of a fetus. The device comprises a carrier that is attachable to a body, a fetal electrocardiographic sensor for providing an output signal, and a reference sensor for filtering the output signal. The device also comprises an actuator arrangement comprising a plurality of actuators distributed in an area around the fetal electrocardiographic sensor. Each actuator is configured for providing a haptic signal to the body. A controller communicatively connects to the fetal electrocardiographic sensor to receive the output signal, and to control the actuators for providing a haptic feedback signal to the body dependent on the output signal. The document also relates to a control method for such a device.

Provided are a system and method for informing of attachment positions of electrocardiogram (ECG) electrodes to improve the quality of ECG data. The system includes a judgment indicator extractor configured to extract a plurality of judgment indicator values from ECG data obtained through ECG electrodes, a reference value setter configured to, in a user-specific reference value setting mode, collect the judgment indicator values for a plurality of pieces of ECG data extracted by the judgment indicator extractor and set user-specific reference values for each judgment indicator, a similarity determiner configured to, in an ECG measurement mode, determine similarity by comparing a plurality of judgment indicator values extracted by the judgment indicator extractor with the user-specific reference values, and an electrode attachment position guide configured to inform a user of attachment positions of the ECG electrodes according to a similarity determination result of each of the judgment indicator values.

A method may include identifying a simulated three-dimensional representation corresponding to an internal anatomy of a subject based on a match between a computed two-dimensional image corresponding to the simulated three-dimensional representation and a two-dimensional image depicting the internal anatomy of the subject. Simulations of the electrical activities measured by a recording device with standard lead placement and nonstandard lead placement may be computed based on the simulated three-dimensional representation. A clinical electrogram and/or a clinical vectorgram for the subject may be corrected based on a difference between the simulations of electrical activities to account for deviations arising from patient-specific lead placement as well as variations in subject anatomy and pathophysiology.

The wearable article 200 comprises an electronics module 100. An electronics module holder 203 holds the electronics module 100. A visual marker 205 is located on an outside surface of the wearable article 200 at a position corresponding to the electronics module holder 203. The module 100 comprises a housing, and a processor 101 and electronics component 111 disposed within the housing. The electronics component 111 detects an object being brought into proximity with the electronics module 100. The visual marker 205 indicates the location of the electronics component 111 in the electronics module holder 203. The electronics component 111 generates a signal in response to the object being brought into the vicinity of the visual marker 205. The processor 101 is arranged to receive the signal generated by the electronics component 111 and is arranged to perform an action in response to receiving the signal.

A chest-worn sensor device, such as a device for daily at-home monitoring of cardiopulmonary health conditions, includes an audio and/or visual interface that provides cues to assist a user in performing a measurement sequence. The sensor device may detect whether there are any body posture issues or device contact issues. In response to detecting an issue, the sensor device provides and audio and/or visual cue to the user indicating the issue. The sensor device may provide additional cues throughout the measurement sequence, such as a cue that a measurement is being taken, a cue for the user to change body posture, and a cue for the user to remove the sensor device.

A vital-data measurement controller is provided for controlling vital-data measurement when a user measures vital data by using a device data measurement. The measurement controller includes a controller that acquires image data including the user’s face and the device by controlling a camera; and an image processor that authenticates the user’s face and the based on the image data. The image processor then determines whether the device is worn by the user based on a positional relationship between the user and the device in the image data, and determines that a period in which the device is determined to be worn by the user after the authentication of the user and the device is a period of a proper state for measurement.