Abstract: A sample collection device that includes a body having a proximal end and a distal end, the body defining a channel extending from the distal end to the proximal end. The sample collection device includes an opening at the proximal end of the body that extends into the channel of the body. The body includes an adhering portion having a depressed surface relative to an adjacent exterior surface of the body, the adhering portion configured to receive a sample in response to the sample contacting the depressed surface of the adhering portion. The body is manually maneuverable in response to the channel receiving a finger of a user through the opening of the body.

Abstract: An apparatus, method and computer program is described comprising: applying an electrical signal to a first electrical circuit formed between a first device electrode and a first eyelid electrode, an eyeball electrical path between the first eyelid electrode and a second eyelid electrode, the second eyelid electrode and a second device electrode, and the second device electrode and the first device electrode; and determining current and/or voltage measurements of the first electrical circuit, wherein a current and/or voltage is generated in the first electrical circuit in response to the applied electrical signal, and wherein the first device electrode is configured to form a first capacitor with the first eyelid electrode and the second device electrode is configured to form a second capacitor with the second eyelid electrode.

Abstract: We describe a capnometer for analysing respiratory system function of a patient, the capnometer comprising: a memory to store patient data which is specific to said patient; and a signal processor to analyse a CO2 waveform representing a variation over time in a CO2 level of air inhaled and/or exhaled by said patient.

Abstract: Systems configured to acquire temperature signals from an Abreu Brain Thermal Tunnel (ABTT), to analyze the temperatures signals, and to determine a condition of a human body from the analysis, and a method for doing the same, are described. In addition, systems for application of thermal signals to the ABTT for treatment of conditions are described.

Abstract: The invention refers to a swab kit for sampling specimens from humans or animals, comprising a swab applicator (1) comprising a swab rod (2) having an extremity (E) and a sampling cloth (4) made of a low-absorbent flexible fabric, wherein the sampling cloth (4) is fixed to and wound, preferably in a spiral, in overlapping turns (T) around the swab rod (2), over a swab rod end region neighboring the extremity (E), in such a manner that at least an edge portion of the sampling cloth (4) overtops the extremity (E) by at least 1 mm when measured in a longitudinal direction of the swab rod (2).

Abstract: In some embodiments, a wound monitoring and/or therapy apparatus includes a wound dressing configured to be positioned in contact with a wound, the wound dressing comprising one or more sensors configured to obtain measurement data of at least one of the wound or periwound. The apparatus can also include a controller configured to maintain a device clock indicative of a non-real time clock, receive measurement data obtained by the one or more sensors, and transmit measurement data to a remote computing device according to a security protocol, the security protocol comprising including the device clock associated with the measurement data in the transmission.

Abstract: A hand held robotic system that remains stiff so long as it is operating within allowed limits, but which become actively controlled once the operator exceeds those limits. The system thus corrects deviations by more than a predetermined amount of the operator's hand motions, so that the tool remains in the allowed region even when the operator's hand deviates from the planned trajectory. The pose and path of the robotic operating head is ascertained by means of a navigation or tracking system, or by means of a proximity device to measure the closeness of the operating head to a damage sensitive feature. As the tool deviates from its predetermined path or pose, or comes too close to the hazardous area, the robot control acts to move the tool back to its predetermined pose or path, or away from the hazardous region, independently of user's hand movement.

Abstract: The present disclosure provides methods for evaluating tissue damage and the use of spatial variation in Sub-Epidermal Moisture (SEM) values to determine damaged tissue for clinical intervention. The present disclosure provides methods of identifying deep and early-stage pressure-induced injuries or ulcers (PI/PU). The present disclosure provides algorithm for computing SEM delta values which inform clinical decision-making for developing intact skin PI/PUs including suspected deep tissue injury (sDTI) and Stage I PI/PUs.

Abstract: A tissue grasping device for use with an endoscope may include a sheath, a control wire slidably disposed within the sheath, and a helical coil disposed over and attached to the control wire. The helical coil may include a proximal region in which adjacent windings are in contact, and a distal region in which adjacent windings are spaced apart. The helical coil may have a sharpened distal tip.

Abstract: A cytology sampling system includes a catheter tube and a cytology tool. The catheter tube has open proximal and distal ends. The cytology tool is insertable through the catheter tube and includes a flexible shaft and a brush. The brush is coupled to the distal end of the flexible shaft. The brush includes a plurality of brush shafts. Each brush shaft has bristles disposed along a portion of a length thereof. The bristles are coupled to and extend radially away from an outer surface of each of the brush shafts. The bristles are configured to collect cell samples from targeted tissue of a patient.

Abstract: A medical device configured to enable concurrent collection of two tissue samples associated with an area of interest. The medical device can include a first needle hub having a fixed position and a second needle hub having an adjustable position. A position of the second needle hub can be adjusted using an adjustment mechanism of the medical device. The medical device can include an aspiration mechanism (e.g., a bulb) with tubing connecting the individual needles to create a suction mechanism to collect samples via aspiration.

Abstract: A medical testing apparatus and method of use for penetrating a patient's tissue with an agent, the apparatus comprises an arcuate rail having spaced first and second sides supported by upper and lower arcuate surfaces and an arcuate handle having first and second ends extending from the upper surface of the arcuate rail. A plurality of tips extend substantially from and normally outward as the lower arcuate surface. The plurality of tips comprises alternating blunt tips and reed tips.

Abstract: An apparatus for delivery of a biopsy marker to a biopsy site includes a grip, a cannula, at least one biopsy marker, and a sterile guide. The cannula extends distally from the grip and includes a lumen extending at least partially therethrough. A maker exit opening is defined by the cannula and is in communication with the lumen. The at least one biopsy marker is disposed in the lumen for deployment through the marker exit opening. The sterile guide is slidable along the cannula and is configured to selectively fasten to the grip.

Abstract: A non-invasive blood pressure monitoring device includes an inflatable blood pressure cuff, a pump device for pressurizing the cuff, a pressure sensor to monitor blood pressure as physiological parameter, and an electrically actuated, normally-open solenoid valve configured to maintain a cuff pressure. A control unit configured to regulate a valve hold value for holding the normally-open solenoid valve at a desired closed position, wherein the valve hold value is at least one of a voltage value and a current value for controlling actuation of the normally-open solenoid valve. At least one inertial sensor configured to detect and transmit motion signals representative of external motions applied to the portable medical device, wherein the control unit is configured to regulate the valve hold value as a function of the motion signals of the at least one inertial sensor to maintain the normally-open solenoid valve in the closed position.

Abstract: A computer-implemented method and system includes a head-mounted wearable device with two current electrodes that provide input alternating currents over a range of frequencies to a subject during at least one intervention. The head-mounted wearable device includes at least two sense electrodes that collect voltage difference measurements in response to the input alternating currents. A measurement validation module applies a Hilbert transform or a Kramer-Kronig test to the voltage difference measurements to generate validated time-series impedance spectra. A cranial fluid dynamics module fits the validated time-series impedance spectra to an electrical circuit model to determine a glymphatic flow response to the at least one intervention.

Abstract: A thermographic sensing device for measuring temperatures at one or more regions of the human body, particularly the breast, utilizes a thermographic composition deposited into linear arrays of recesses formed in the lobes of a conformable medium which is disposable against the skin. The thermographic composition includes a binary solvent system and at least one colorant, wherein the compositions in each array are formulated to melt at precise temperatures, within a diagnostically temperature relevant range, to change from a first visible color to a second visible color.

Abstract: Disclosed herein is a machine learning platform and system for data analysis including for purposes of providing digital evaluations and therapeutics.

Abstract: Elderly people suffer from health issues, and timely detection can save lives. State of the art techniques either make certain assumptions or require clinical data in order to perform the frailty detection, which affects the quality as well as cause inconvenience to the users. The disclosure herein generally relates to patient monitoring and, more particularly, to frailty detection using pedometer sensor data, PIR sensor data, and door sensor data. The system determines activity levels of the user being monitored, based on data from the pedometer sensors, PIR sensors, and door sensors, and based on the determined activity levels, further determines whether the user has frailty or not.

Abstract: A core collector is shaped as a crescent in cross-section and has lateral sides formed into axially extending rows of axially spaced teeth. The arc angle of the crescent shape is sufficient to keep the core collector radially centered in a cannula by having the crescent's lateral sides bear against the inside of the cannula. The set of a core collector and cannula can be used in a known biopsy system to replace the known cannula and core collector of can be used in a new core biopsy instrument.

Abstract: A temperature probe for monitoring temperatures of a surface of a tissue or organ within the body of a subject includes a section with a substantially two-dimensional arrangement and a plurality of temperature sensors positioned across an area defined by the substantially two-dimensional arrangement. Such an apparatus may be used in conjunction with procedures in which thermal techniques are used to diagnose a disease state or treat diseased tissue. Specifically, a temperature probe may be used to monitor temperatures across an area of a surface of a tissue or organ located close to the treated tissue to prevent subjection of the monitored tissue or organ to potentially damaging temperatures.