A wearable cardioverter defibrillator (“WCD”) system includes a support structure that can be worn by a patient, and a defibrillator coupled to the support structure. An ECG input, rendered from an ECG of the patient, may meet a primary shock criterion. One or more sensor modules are further provided, which are worn by the patient at different times. The sensor modules may monitor different physiological parameters of the patient, and transmit signals about them. The WCD system further has a multi-sensor interface to receive the transmitted signals, and a processor to determine from them whether a secondary shock criterion is met. If both the primary and the secondary shock criteria are met, the decision is to shock. The signals increase specificity of the detection, while the patient can wear different modules depending on context.

In some examples, a device includes a catheter insert elongated body defining a body lumen, the catheter insert elongated body being configured to be at least partially inserted to a catheter lumen defined by a catheter without covering a first fluid opening of the catheter and to form a fluidically tight coupling with the catheter, and one or more sensors positioned on the elongated body. At least one of the one or more sensors are configured to sense a substance of interest. The catheter insert elongated body includes a material that is a substantially non-permeable to the substance of interest.

An oral care system includes an oral care implement and a smart device removably retained in a cavity of the oral care implement. The smart device may have a plurality of sensors for sensing conditions of the oral cavity and/or for sensing various parameters associated with the movement of the oral care implement within the oral cavity during use. The smart device may also include a transmitter for transmitting data/information obtained by the sensors to an electronic device, such as a smart phone.

The present application discloses a method of adjusting a parameter, the parameter being used to derive a physiological characteristic of an individual from an image of the user, the method comprising the steps of: obtaining the parameter for the individual; obtaining a corresponding parameter for a plurality of other individuals within a cohort of the individual; comparing the parameter for the individual with a statistically significant parameter for the plurality of other individuals; and adjusting the parameter for the individual in accordance with the difference between the parameter for the individual and the statistically significant parameter for the plurality of other individuals.

To appropriately evaluate skin spots by grasping a quality (characteristic) of the skin spots. A skin spot evaluation apparatus includes an area extracting unit that extracts skin spot areas corresponding to skin spots from a skin image obtained by photographing a skin of a subject; and an evaluation unit that analyzes, based on the skin spot areas extracted by the area extracting unit, at least one of the number of the skin spots, dimension of each of the skin spots and density of each of the skin spots, and generates data obtained by quantifying characteristic of the skin spots of the skin image using the analyzed result.

An integrated sensing system for characterizing blood flow in a subject includes a light source assembly including a light source configured to emit light of a particular wavelength. The integrated sensing system includes an integrated circuit electrically connected to the light source assembly. The integrated circuit includes a light detector assembly including multiple light detectors configured to detect light of the particular wavelength; and a correlator configured to determining a delay between optical signals detected by respective light detectors of the light detector assembly.

Systems and methods for surgical preparation are disclosed. A system may include at least one processor configured to access a repository surgical video footage. The processor may enable a surgeon preparing for a contemplated surgical procedure to input case-specific information corresponding to the contemplated surgical procedure and compare the case-specific information with data associated with the surgical video footage to identify a group of intraoperative events likely to be encountered during the contemplated surgical procedure. The processor may determine that a first set and a second set of video footage from differing patients contain frames associated with intraoperative events sharing a common characteristic and omit the second set from a compilation to be presented to the surgeon and include the first set in the compilation to be presented to the surgeon to enable the surgeon to view a presentation including the compilation.

Disclosed are a device, a system, and a method of providing treatment information for a skin care treatment. The device includes: a patient information providing unit configured to provide patient information; a treatment information generating unit configured to generate treatment information based on the patient information; a progress information input unit configured to receive progress information for the treatment when the treatment is completed based on the treatment information; and a control unit configured to update the treatment information based on the progress information. Therefore, it is possible to provide the skin care treatment in a more objective state by preventing the treatment from being performed under different conditions for each practitioner or according to a condition of the practitioner, and it is further possible to perform a safe and effective treatment by preventing misuse of medical technology due to the misjudgment of the practitioner.

First RGB image signals are inputted. A first B/G ratio and a first G/R ratio are calculated. The first B/G ratio and the first G/R ratio are converted into a second B/G ratio and a second G/R ratio, respectively, through a color information conversion process. Owing to the color information conversion process, a difference between first and second observation areas in a second signal ratio space formed by the second B/G ratio and the second G/R ratio is greater than a difference between the first and second observation areas in a first signal ratio space formed by the first B/G ratio and the first G/R ratio, and a difference between the first and third observation areas in the second signal ratio space is greater than a difference between the first and third observation areas in the first signal ratio space.

An imaging device for monitoring a skin feature includes a camera, at least one processor and memory. The imaging device displays a body area guide, receives a selection of a body area, initiates an image sequence of the body area, the image sequence including capturing, using the camera, a plurality of images, determines whether all body areas have been imaged, analyzes the images, and provides the analyzed images to a clinician. The imaging device can be part of a system including a server in communication with a monitor, where the clinician views the images on the monitor. Additionally, each skin feature can be ranked in order of risk and presented to the clinician in that order.