Abstract: A method and a device for detecting physiological indexes. The method includes: obtaining a body temperature fluctuation value associated with a user, where the body temperature fluctuation value is at least obtained by a first difference value between a current shell temperature associated with the user and a basal temperature associated with the user (101); and determining a current physiological index associated with the user based on the body temperature fluctuation value associated with the user (102). The method can be applicable in a detection process for physiological indexes and can perform health-related operations based on the detected physiological indexes including a body temperature measuring result.

Abstract: A system and a method for a medical diagnostic device are described herein. The medical diagnostic device can include an outer sleeve having a hollow interior and open distal and proximal ends, the outer sleeve being defined by a substantially tubular configuration including a proximal section having a substantially conical shape. A core is configured to be inserted axially within the outer sleeve. The core includes an axial inner cavity. The core is further defined by a proximal section having a conical shape substantially conforming to the proximal section of the outer sleeve. The core retains a diagnostic assembly, that can include at least one of a sample collecting assembly and an imaging assembly, that can be integrally or interchangeably attached and wherein the device can be utilized for self-patient or single patient use.

Abstract: Disclosed herein is a biopsy device for efficiently sampling a specimen from a biological tissue, particularly if the biological tissue is a soft tissue. The biopsy device includes: an elongate shaft; a piercing spike for piercing a biological tissue, the piercing spike being disposed on a longitudinally distal end of the elongate shaft; a screw disposed on the elongate shaft, for guiding a specimen sampled from a living body from the longitudinally distal end of the elongate shaft toward a longitudinally proximal end thereof; and a screw cutter disposed on the screw, for peeling the specimen off the living body. The screw cutter peels the specimen off the biological tissue while the piercing spike is piercing the biological tissue.

Abstract: Cognitive function testing. At least some of example embodiments are methods including performing a cognitive function test on a patient without calibrating pupil position of the patient. The performing may include: causing a visual cue on a computer screen in front of the patient to move in a predetermined pattern; reading frames from an eye camera that captures images of an eye of the patient while the visual cue moves on the computer screen and the patient visually tracks the visual cue; determining pupil position within the frames; correcting offsets between the stimulus data and the pupil position data; translating the pupil position data from a coordinate space of the eye camera to a coordinate space of the stimulus data; and generating a test score being the cumulative distance between the stimulus data and pupil position data for each corresponding point in time.

Abstract: In some implementations, a computing device can confirm a sleep determination for a user based on secondary indicia of user activity. For example, the computing device can be a user's primary computing device. The primary device can predict and/or determine when the user is sleeping based on the user's use (e.g., primary indicia), or lack of use, of the primary device. After the primary device determines that the user is sleeping, the primary device can confirm that the user is asleep based on secondary indicia of user activity. In some implementations, the secondary indicia can include user activity reported to the primary computing device by other secondary computing devices (e.g., a second user device, a household appliance, etc.). In some implementations, the secondary indicia can include user activity detected by sensors of the primary computing device (e.g., sound, light, movement, etc.).

Abstract: A method for diagnosing a body malfunction is provided. At least one change in urinary parameter values, being indicative of the body malfunction, is monitored and detected. A volumetric urinary output of kidneys is monitored using a urine flow monitoring apparatus having a low flow metering device. It is determined whether a change exists in at least one of a volume value of the volumetric urinary output, and a trend of the corresponding urinary parameter value during a predetermined period. Signals are received from a plurality of electrodes, representing the urinary parameter values. The body malfunction is detected based on the determination of the change in at least one of the volume value and the trend.

Abstract: Apparatuses and methods for monitoring a patient for seizure activity and for verifying the contact integrity of electrodes included among an EMG sensor may include generating a test signal of known periodicity and applying the signal to at least one electrode in a sensor system. The test signal may be monitored to verify contact integrity of the electrodes.

Abstract: Embodiments include methods, systems and computer program products for monitoring a user of a helmet for cumulative concussions. Aspects include monitoring one or more sensors in the helmet and receiving an output from the one or more sensors corresponding to an impact experienced by the helmet. Aspects also include calculating a cumulative concussion score based on the output of the one or more sensors and displaying an indication of the cumulative concussion score via an indicator on the helmet.

Abstract: The present invention provides a system for monitoring a physiological parameter of players engaged in a sporting activity. The system includes a plurality of reporting units, a controller, and a signaling device. The reporting unit has an arrangement of sensing devices that measure the physiological parameter of an individual player and generate parameter data. The controller receives the parameter data transmitted from each reporting unit and then processes the parameter data to calculate a parameter result. When the parameter result exceeds a predetermined value, the controller communicates with a signaling device that provides an alert to sideline personnel to monitor the player(s) in question. The system also includes a remote storage device for holding historical data collected by the system which permits subsequent analysis.

Abstract: A device for collecting a tissue sample includes an outer needle extending longitudinally from a proximal end to a distal end and including a lumen extending therethrough. The device also includes an inner needle extending longitudinally from a proximal end to a distal end and including an opening extending laterally in and along a length thereof. The inner needle is sized and shaped to be slidably received within the lumen of the outer needle and movable relative thereto between an insertion configuration, in which the opening is covered by the outer needle, to a tissue collecting configuration, in which the opening is exposed. In addition, the device includes a handle assembly for adjusting a throw length of the inner needle relative to the outer needle.

Abstract: An automated infant cry analyzer with high accuracy to detect important acoustic features of cry is provided. The system's accuracy was rigorously tested and was compared to ground truth manual coding. The resulting methods and systems are applied to infant developmental disorders.

Abstract: In some implementations, a computing device can remind a user to perform sleep ritual activities. The computing device can automatically determine the user's sleep ritual. The users sleep ritual can include various activities performed before going to sleep. The computing device can detect when the user performs the various sleep ritual activities. The computing device can remind the user about specific sleep ritual activities when the user forgets to perform the sleep ritual activities before going to sleep. In some implementation, the computing device can perform sleep ritual activities (e.g., turning off devices, locking doors, setting the air conditioning, etc.) on behalf of the user in response to user input. In some implementation, the computing device can perform sleep ritual activities on behalf of the user automatically and without user input.

Abstract: A hearing test system comprising an computerized device (100) having an electro-acoustical output transducer (104) and a graphical user interface (102) and further being adapted to estimate a hearing loss of an individual test person. The invention also relates to a non-transitory computer readable medium carrying instructions which, when executed by a computer, cause a hearing loss of an individual test person to be estimated and a method of estimating a hearing loss.

Abstract: A method and system for detecting a probability of psychogenic non-epileptic seizures using a portable battery powered device placed on the body of a patient and a device for manually logging detected seizures within a time period. The device may, advantageously, have a seizure detection algorithm which automatically records seizures detected within that time period. The two sets of data may then be transferred to a another device where the logged time stamps are matched to the recorded time stamps for determining if the detected seizure is a generalized tonic-clonic seizure (GTCS) or might be a psychogenic nonepileptic seizure (PNES). This provides a cheap and simple method for registering a probability of PNES by using a seizure detection device having an EMG-sensor or an accelerometer.

Abstract: An actuator for a medical device includes a housing, a driving unit mounted in the housing, a first moving unit slidably mounted in the housing and movable by the driving unit. The first moving unit includes a movable first car, an spring with two ends thereof abutting the housing and first car, respectively, and a lock formed between the driving unit and first car. The lock includes a first snap and a first protrusion detachably engagable with the first snap. One of the first snap and first protrusion is formed on the first car, and the other is formed on the driving unit. When the first protrusion disengages from the first snap, the spring moves the first car relative to the housing.

Abstract: Methods and devices for implanting an intra-ocular pressure sensor within an eye of a patient are provided herein. Methods include penetrating a conjunctiva and sclera with a distal tip of a fluid-filled syringe and positioning the pressure sensor within a vitreous body of the eye by injecting the sensor device through the distal tip. The sensor device may be stabilized by one or more anchoring members engaged with the sclera so that the pressure sensor of the sensor device remains within the vitreous body. Methods further include advancing a sensor device having a distal penetrating tip through at least a portion of the sclera to position the sensor within the vitreous body and extracting of the sensor devices described herein by proximally retracting the sensor device using an extraction feature of the sensor device.

Abstract: A pre-sterilized fluid sampling syringe is provided which includes a locking vacuum syringe, 3-way valve, check valve and thermoplastic inlet tubing capable of both aseptic welding and direct connections. The syringe is assembled with components and rendered sterile in its packaging. The packaging permits manipulation of the syringe by the user such that at time of use a vacuum can be generated in the syringe barrel by pulling and locking the plunger into a fully withdrawn position. By using the check valve and vacuum feature of the sampling system the user of the device has a means of aseptically flushing and obtaining fluid samples from a desired system, typically a bioreactor or other process used in biotechnology and/or pharmaceutical laboratories and manufacturing operations.

Abstract: The present disclosure provides an adjustable delivery handle system for interchangeably delivering a needle to a biopsy site. The adjustable delivery handle system includes a delivery handle having an inner hub housing component configured to interchangeably receive a needle subassembly that can be inserted into and withdrawn from the proximal handle member. The needle subassembly includes a biopsy needle having a distinct tissue collection distal end configured to maximize tissue sampling yield and collect a cohesive unit of sampled tissue. The distal end of the needle includes first and second tip portions extending therefrom and radially opposing one another. The first tip portion has a length greater than the second tip portion, thereby resulting in an increased surface area of a curvilinear cutting edge extending from the first tip portion to the second tip portion.

Abstract: Aspects relate to a portable device that may be used to identify a critical intensity and an anaerobic work capacity of an individual. The device may utilize muscle oxygen sensor data, speed data, or power data. The device may utilize data from multiple exercise sessions, or may utilize data from a single exercise session. The device may additionally estimate a critical intensity from a previous race time input from a user.

Abstract: A plug that allows the plug body to be easily and reliably pierced through by a hollow bodily fluid collection needle, makes the bodily fluid collection needle difficult to draw back out of the plug body owing to a resilience of a sheath after the start of bodily fluid collection, and enables easy and reliable collection of the bodily fluid.