A method and apparatus for evaluating foot inflammation each uses at least one temperature detection modality to form a first thermogram and a second thermogram of the sole of at least one foot. Each thermogram forms a substantially continuous set of two-dimensional temperature values across the sole of the (at least one) foot. The thermograms have features; namely, the first thermogram has first features and the second thermogram has second features. The method and apparatus thus control a device to apply at least one transformation to the first and second thermograms to align the first features with corresponding second features, and determine, at any thermogram location, if at least one of the thermograms presents one of a plurality of patterns indicative of inflammation. Finally, the method and apparatus each produce output information indicating the result of the determination of whether the thermograms present one of the plurality of patterns.

The present subject matter discloses multiside tilt device (100) including a pressure sensing sheet (102) to detect the pressure exerted by the user's body in a pressure build-up area around the pressure sensor and generate a pressure signal indicating a pressure build-up at the pressure build-up area. The multiside tilt device (100) further includes a tilting unit (104) to tilt a portion of the user's body in response to the pressure signal by a predetermined angle. The tilting unit (104) comprises an inflatable base (106) having a first section (108-1) and a second section (108-2) pneumatically separated disposed adjacent to each other to be independently inflated or deflated. Each section (108) comprises one or more cells (112, 304) to be collectively inflated such that each cell (112, 304) is inflated to form an inflated structure having a peak in the center and a trough on either side.

A system and method for facilitating analysis of a wound in a target subject is provided. The method comprises obtaining one or more digital images of at least a portion of the wound; extracting a plurality of feature vectors from the one or more digital images; and identifying, using a first trained deep neural network, a type of wound tissue based on the plurality of extracted feature vectors.

Introduced here are pressure-mitigation systems able to mitigate the pressure applied to a human body by the surface of an object. A system can include a pressure-mitigation device with chambers whose pressure can be varied by a controller that regulates the flow of fluid produced by a pump. The controller may be deployed as part of a closed loop system that autonomously infers information related to the health of a patient based on data related to the pressure of these chambers. For example, the data may be examined to determine whether the values indicate the patient is properly situated. A notification may be presented responsive to determining that the patient is not situated on the pressure-mitigation device, the patient has been improperly situated on the pressure-mitigation device for a certain amount of time, etc. Thus, real-time feedback may be provided to those responsible for monitoring the patient.

Systems, devices, and methods of the present application relate to the diagnostic measurement of condition for pressure ulcers. Preferred embodiments utilize pressure measurements at body locations to determine a diagnostic pressure ulcer value. A pressure sensor device generates patient pressure data that is processed by a data processor which utilizes a diagnostic function to determine the diagnostic value that indicates whether corrective action is needed to prevent pressure ulcer formation. One or more sensor devices can be attached to a patient to measure to transmit data for further processing.

A system or method for pressure related skin injury risk assessment and treatment including measuring extrinsic and intrinsic skin pressure of the patient through assigned ratings responsive to the skin pressure measurement, measuring oxygenation of the patient and assigning a rating responsive to the oxygenation measurement, measuring perfusion of the patient and assigning a rating responsive to the perfusion measurement, summing the skin pressure, oxygenation and perfusion ratings to obtain a POP Box score, determining a risk of pressure related skin injury for the patient in response to the POP Box score, and determining or selecting a recommended treatment from among a plurality of recommended treatments for the patient in response to the determined risk of pressure related skin injury.

A load cell apparatus for use with a bed includes a housing having a top portion and a bottom portion, and a load cell device held by the bottom portion of the housing. The load cell device is structured to generate a signal having a magnitude that is proportional to a first force being applied to the load cell device. The load cell apparatus also includes a button member held by the housing in a manner wherein the button member is structured to engage the load cell device and apply the first force to the load cell device in response to a second force being applied to the top portion of the housing. Also, various systems for monitoring parameters such as weight, sleep quality, fall risk, and/or pressure sore risk that may incorporate such a load cell apparatus.

A system for detecting patient turns includes a person support apparatus including a person support surface and a support frame, a plurality of load cells for generating load cell data, a sensor for sensing at least one of heart rate data and respiration rate data for an individual, and a computing device coupled to the plurality of load cells and the sensor. The computing device receives the load cell data and the at least one of heart rate data and respiration rate data for the individual, detects that a patient turn has occurred on the person support surface based on the load cell data and the at least one of heart rate data and respiration rate data for the individual, and causes an indication that the patient turn occurred to be logged in an electronic medical record corresponding to the individual.

Provided herein are medical devices comprising a plurality of biologically interactive devices configured for interacting with a large area biological surface. The biologically interactive devices each may comprise a sensor for measuring a physiological parameter. A wireless controller is configured to wirelessly operate the plurality of biologically interactive devices. A wireless transmitter is configured for wirelessly communicating an output from said plurality of biologically interactive devices to a remote receiver. The medical devices are particularly suited for measuring one or both of pressure and temperature, with compatibility for incorporating additional sensors of interest.

A handheld, conforming capacitive sensing apparatus configured to measure Sub-Epidermal Moisture (SEM) as a mean to detect and monitor the formation of pressure ulcers. The device incorporates an array of electrodes which are excited to measure and scan SEM in a programmable and multiplexed manner by a battery-less RF-powered chip. The scanning operation is initiated by an interrogator which excites a coil embedded in the apparatus and provides the needed energy burst to support the scanning/reading operation. Each electrode measures the equivalent sub-epidermal capacitance corresponding and representing the moisture content.