A method for the objective determination of capillary refill behavior on a human body surface in which a spatially and spectrally resolved optical detection is carried out by at least one detector device (1) at a skin surface area (2) having a predefined areal size and outer contour. Subsequently a predefined pressure p constant over the skin surface area (2) is exerted over a predefined time t1; and the pressure effect is ended after expiry of this time t1. The spatially and spectrally resolved optical detection is carried out by the detector device (1) and the respective capillary refill behavior is spatially and temporally determined at a time t2 up to which at least one first threshold value of the measurement values detected simultaneously with spatial resolution has reached the measurement value that had been optically detected before the start of the pressure effect.

This invention relates to apparatus and method for detection of human skin lesion malignancy. The method relies on two independent wavelengths regions: (a) visible and Near IR circa (0.4-1.3 um); (b) Far Infrared (6-12 um). The visible and NIR wavelengths will analyze sub-skin scattering and absorbance to detect structural and diffusion abnormalities, and the FIR wavelengths will monitor the thermal blood perfusion, as reflected by monitoring temperature variation of suspected region. An apparatus according to the present invention would comprise a cooling/heating component which encloses the suspected area, MIR camera or thermal sensors, visible and NIR camera. Evaluation of the rate of the skin temperature changes and propagation in the suspected area will enable to detect increased blood perfusion and metabolic heat, identifying alarming signals related to skin diseases. Parallelly, the sub-skin density and coagulation will be analyzed by peripheral illumination. Evaluation procedure will include image analysis and artificial intelligence to enhance the detection capabilities. Using two independent technologies minimizes the false-negative detection and increases sensitivity and specificity. This invention relates to different body parts without limitations.

Self-directed health screening systems and methods utilizing user navigation and device integration, health analyzing algorithms, and/or self-learning techniques for the detection, quantifying, prevention, and management of health risks and discoverable health conditions. Implementations herein may include components or involve aspects associated with information collection, information processing, display/provision/rendering of professional advice, and/or processing of various associated data and information via network(s). Implementations herein provide for innovatively configured, easily upgradable, efficient, portable, scalable, easy-to-use, usage-encouraging, and/or effective implementations for screening, predicting points of inflection of pending health issues, preventing and/or managing users' health, provided via various and multiple embodiments having numerous advantages over other known techniques. Screenings, health information, and user-selectable choices may be optimized for each unit by offering different combinations over a period of time and iterating to produce the greatest usage and user traffic thereby best serving the specific health needs of the user base and sponsoring advertisers.

A finger insert for use with a nailfold imaging device includes a housing to receive the user's finger and an immersion substance (e.g., immersion oil), and a deformable pad that holds the user's finger in place during imaging, as well as prevent bubble formation in the substance. The housing includes a transparent wall to facilitate imaging of the finger. The transparent wall includes multiple angled portions that prevent or reduce contact between the nailfold and the wall, to ensure sufficient blood flow through the nailfold region for imaging.

Provided are an electronic device and method for providing information related to a skin type of an object. The electronic device includes: a camera configured to capture at least one image including a skin portion and a non-skin portion of an object; and a processor configured to determine at least one color ratio between the skin portion and the non-skin portion from the at least one image, and determine a skin type of the object based on the determined at least one color ratio.

A treatment system can include a channel generation system configured to expose an infected region of a target tissue with a laser beam traveling along an optical axis and focused at a focal volume located in or adjacent to the target tissue. The laser beam can have a wavelength ranging from about 100 nm to about 400 nm. The laser beam can be configured to generate at least a first channel in the infected region. The treatment system can also include a detection system configured to detect a first radiation generated by one or more of (i) the target tissue, (ii) a fungi coupled to the infected region in the target tissue, and (iii) an adjacent tissue located proximal to the target tissue as a result of interaction with the laser beam. The treatment system can also include a delivery system configured to deposit an active treatment agent in the at least first channel.

An analysis method and a diagnostic device, enabling one to determine whether a longitudinal melanonychia is caused by a malignant melanoma or a benign nevus by correcting color variation in a dermoscopic image through standardization of color balance without depending on an imaging device or an operator; and a computer program for allowing a computer to function as the diagnostic device. Proposed is a structure including: an image reading step of reading a color image of a longitudinal melanonychia or an affected skin site of a subject as a digital color image; an image processing step involving an image size conversion step of converting the whole size of the digital color image into a preset size through pixel size conversion, and a region of interest (ROI)-extraction step of extracting an ROI required for the diagnosis from the digital color image; a chromatic adaptation transformation step of controlling the color balance of the digital color image data through chromatic adaptation transformation; and a discrimination index (DI) calculation step of determining a DI value using the image after the chromatic adaptation transformation.

A sensor includes a bridge circuit including one or more strain gauges mounted on a nail plate, the bridge circuit outputting a voltage signal, an amplifier circuit amplifying the voltage signal output by the bridge circuit to generate an amplified signal, an analog-to-digital (A/D) converter converting the amplified signal into a digital signal, a controller receiving the digital signal and facilitating communication with a receiver, and an antenna configured to transmit the digital signal.

Systems, computer-implemented methods and/or computer program products that facilitate wearable multiplatform sensing are provided. In one embodiment, a computer-implemented method comprises: measuring, by a system operatively coupled to a processor, wirelessly on a nail plate, physiological data of an entity; integrating and synchronizing, by the system, the physiological data with other physiological data from one or more devices to form integrated physiological data; and analyzing, by the system, the integrated physiological data to detect one or more disorders.

A method for determining a body area condition is provided. The method may includes determining at least one body condition parameter and determining the body area condition using the at least one body condition parameter. The determining of the body condition parameter includes recording, during a sequential exposing of a body area of a user to light of different colors by a display of a portable data processing device, a plurality of images of at least a part of the light which has interacted with the body area, determining a spectral characteristic of the body area by the plurality of images, comparing the spectral characteristic with calibration spectral characteristics obtained for a plurality of calibration body areas, and determining the body condition parameter including a result of the comparison.