Abstract: A system, apparatus, and/or method of determining a health condition of an animal is provided. First data may be received from a first sensor device. The first data may be indicative of an animal event of an animal. Second data may be received from a second sensor device. The second sensor may be separate and/or distinct from the first sensor device. The second data may confirm an occurrence of the animal event. The animal event may be a discharge event and/or a feeding event. The occurrence of the animal event may be identified based on the first data and the second data. The occurrence of the animal event may be displayed via a display device. A health condition of the animal may be determined based on the animal event. The determination of the health condition may be based on a quantity and/or a duration of the animal event.

Abstract: A method of operating an information processing apparatus may include collecting gait information of a walking assistance apparatus; determining a gait feature of a user of the walking assistance apparatus based on the collected gait information; and controlling the walking assistance apparatus by determining a gait group of the user based on the determined gait feature.

Abstract: The embodiments presented herein present a single needle core biopsy instrument and modification required that convert the single needle core biopsy instrument to a dual needle core biopsy instrument. Depending on the design, the dual needle core biopsy instrument permits the simultaneous extraction of tissue or bone specimens taken at between 0.1 mm and 3 mm apart.

Abstract: Methods and devices for performing minimally invasive procedures useful for Fallopian tube diagnostics are disclosed. In at least one embodiment, the proximal os of the Fallopian tube is accessed via an intrauterine approach; an introducer catheter is advanced to cannulate and form a fluid tight seal with the proximal os of the Fallopian tube; a second catheter inside the introducer catheter is provided to track the length of the Fallopian tube and out into the abdominal cavity; a balloon at the end of the second catheter is inflated and the second catheter is retracted until the balloon seals the distal os of the Fallopian tube; irrigation is performed substantially over the length of the Fallopian tube; and the irrigation fluid is recovered for cytology or cell analysis.

Abstract: A biopsy device includes a body, a needle, a hollow cutter, and a tissue sample holder. The needle extends distally from the body and includes a lateral aperture. The cutter is movable relative to the needle to sever a tissue sample and defines a cutter lumen. The tissue sample holder includes a manifold and an outer cover. The manifold includes a plurality of passages and an indexing portion. Each passage of the plurality of passages is configured to selectively index relative to a proximal end of the hollow cutter. The outer cover includes a resilient member. The resilient member is configured to engage with the indexing portion of the manifold to selectively index a passage of the plurality of passages with the distal end of the hollow cutter.

Abstract: An apparatus, method and computer program is described comprising: varying a magnetic field strength of a magnetic field applied to a subject; determining a rate of power loss of the magnetic field, wherein the rate of power loss is a function of the varying magnetic field strength; and providing an output signal based on the determined rate of power loss, wherein the output signal comprises information relating to a conductivity distribution of the subject.

Abstract: Methods, systems and wearable devices for real-time mental stress assessment are provided. The methods and systems employ deep learning using a Gated Recurrent Unit (GRU) gating mechanism in a recurrent neural network with a sliding window approach applied to raw EEG data.

Abstract: A hollow stranded wire (2) has a first layers (4) and second layers (6). The second layer is located outside the first layer. The first layer is formed by twisting eight first element wires (8) which are flat wires. The second layer is formed by twisting eight second element wires (10) which are flat wires. A ratio (Ww/Tw) of a width Ww to a thickness Tw of each flat wire is from 2 to 11. A twisting direction of the second element wires is opposite that of the first element wires. A twisting angle of each first element wire is not greater than 85°. A twisting angle of each second element wire is not greater than 85°. A ratio (D/T) of an average diameter D to a thickness T of the hollow stranded wire is not less than 5 and not greater than 20.

Abstract: Systems and methods for detecting worsening cardiac conditions such as worsening heart failure events are described. A system may include sensor circuits to sense physiological signals and signal processors to generate from the physiological signals first and second signal metrics. The system may include a risk stratifier circuit to produce a cardiac risk indication. The system may use at least the first signal metric to generate a primary detection indication, and use at least the second signal metric and the risk indication to generate a secondary detection indication. The risk indication may be used to modulate the second signal metric. A detector circuit may detect the worsening cardiac event using the primary and secondary detection indications.

Abstract: Methods and devices for performing minimally invasive procedures useful for Fallopian tube diagnostics are disclosed. In at least one embodiment, the proximal os of the Fallopian tube is accessed via an intrauterine approach; an introducer catheter is advanced to cannulate and form a fluid tight seal with the proximal os of the Fallopian tube; a second catheter inside the introducer catheter is provided to track the length of the Fallopian tube and out into the abdominal cavity; a balloon at the end of the second catheter is inflated and the second catheter is retracted until the balloon seals the distal os of the Fallopian tube; irrigation is performed substantially over the length of the Fallopian tube; and the irrigation fluid is recovered for cytology or cell analysis.

Abstract: The present invention provides an eating monitoring method for judging whether chewing is performed or not by a chewing judgment algorithm on the basis of a temporal variation in a measured value of a sensor unit configured to detect a movement of a jaw while a person takes a meal, the person wearing a detection device comprising the sensor unit. The method includes the steps of: adjusting the chewing judgment algorithm on the basis of a variation in a measured value of the sensor unit, the variation corresponding to a chewing action or a mouth opening/closing action of the person wearing the detection device; and judging whether chewing is performed or not by the chewing judgment algorithm which has been adjusted, and measuring the number of chews on the basis of a temporal variation in a measured value of the sensor unit during the meal.

Abstract: The present disclosure describes a system, method and software applications for predicting the KAM of a subject for a plurality of gait cycles of a subject. At least one sensor attachable adjacent to the ankle of at least one leg of the subject provides accelerometer and gyroscopic data for the plurality of gait cycles. A processing means receives subject parameters and accelerometer and gyroscopic data from the at least one sensor for evaluation by a neural network of predicted KAM values for the plurality of gait cycles of the subject. The neural network is configured via determining KAM values for each of the plurality of subjects from measurements during a plurality of gait cycles and other parameters.

Abstract: A method for assessing and reversing exercise impairment in adults having peripheral vascular disease includes quantifying a musculoskeletal deoxygenation level (MDL) of a human subject provided by a wearable near infrared spectroscopy system configured to measure the deoxygenation level during exercise, comparing the quantified MDL to a range of pre-determined healthy MDL values for the subject, and, if the quantified MDL is outside of the pre-determined target MDL values, determining a corrective exercise intensity level or ‘dose’ effective to bring the MDL of the subject within the target MDL values and reverse the exercise impairment.

Abstract: A joint manipulation and evaluation apparatus has a mechanism configured to manipulate a first bone of a joint relative to a second bone of the joint. The apparatus has a joint stabilizer arranged to engage the joint and hold the second bone in place as the first bone is manipulated. A sensor is coupled to the joint stabilizer and is configured and arranged to detect residual movement of a clamped portion of the joint relative to the joint stabilizer as the first bone is manipulated.

Abstract: Automated modular physical health testing systems and associated devices and methods are disclosed herein. A modular system configured in accordance with embodiments of the present technology can include, for example, a housing, a communications hub, and a plurality of physical health testing devices. The housing integrates the communications hub and stores the plurality of physical health testing devices. The physical health testing devices are in wired and/or wireless communication with the communications hub. Each physical health testing device is configured to generate physical health data of a user and to transmit generated physical health data to the communication hub and/or a user's mobile device. The modular physical health testing system provides an automated physical exam that can be performed at user's homes or other convenient locations.

Abstract: A system and method for customized saturation biopsy is provided that facilitates diagnosis, management and treatment of cancer or other disease in a gland or organ. The system includes a pathology mapping unit that identifies a plurality of regions of a biopsy area. A grid assembly is coupled to the pathology mapping unit, the grid assembly including a grid disposed externally to the biopsy area. A display is coupled to the pathology mapping unit that displays information corresponding to the plurality of regions of the biopsy area, the pathology mapping unit controlling a configuration of the grid and the information corresponding to the plurality of regions. An image probe can be provided that acquires at least one image of the biopsy area, and the display displays the at least one image. An interface can be provided that is coupled to the display and supplies information to the pathology mapping unit.

Abstract: A catheter hub assembly includes a body. A pressure sensor is disposed within the body to sense pressure within a catheter and communicating with the body. The body has a chamber formed therein having a predetermined volume. A stopper assembly, slideably moves to engage the body forming a gastight seal within the chamber for pushing a column of gas ahead of the stopper assembly as the stopper assembly moves from a first position to a second position.

Abstract: A sensor assembly for in-vivo monitoring of a body fluid or tissue (F) comprises: a pressure sensor element, comprising a micro-electromechanical system (MEMS) and arranged to detect a pressure of the body fluid or tissue (F) in use; and a shield, which generally surrounds the pressure sensor element such that the pressure sensor element is within an interior volume of the shield, in order to protect and to prevent distortion of the pressure sensor element in use. The pressure sensor element comprises a biocompatible thin film layer, for resisting corrosion and/or fouling of a surface of the pressure sensor element by the body fluid or tissue (F) or biological matter thereof. The pressure sensor element and the shield are in fixed relationship with each other.

Abstract: The goal of the present invention is to calculate with high accuracy a numerical value representing skin barrier function in a wide range of skin conditions. Provided is an operation processing apparatus calculates a first variable based on delay time measured using an alternating-current (AC) signal generated by the AC signal generation circuit and a signal applied by an application electrode and passing through skin and stores the first variable calculated by the processor as a calculation result. The operation processing apparatus calculates a numerical value representing the skin barrier function based on the calculation result.

Abstract: The present disclosure provides systems, methods, devices, and kits for analysis of vaginal biological samples. A device for the analysis of vaginal biological samples can include a sample collector, an extractor, and an assay cartridge. A method for the analysis of vaginal biological samples can include detecting the presence or absence of a pathology, a disease, an immune disorder, a reproductive disorder of a subject. The method may further comprise preserving, storing, or transporting the vaginal biological samples. A kit for the analysis of vaginal biological samples can include probe, reagents and instructions for detecting a nucleic acid in the vaginal biological samples.