Abstract: A new born temperature and heart monitor wrap apparatus and method includes a wrap where the wrap is configured such that a new born is substantially covered by the wrap when the wrap is applied to the new born. A heart monitor device is attached to the wrap and a temperature lead retainer is attached to the wrap. A substrate is provided where the wrap is removably connected to the substrate.

Abstract: System comprises a first sensing unit, attached to a proximal portion of a human body with a joint of the human body as a reference, for measuring an acceleration of the proximal portion or an angular velocity of the proximal portion; a second sensing unit, attached to a distal end portion of the human body, for measuring an acceleration of the distal end portion or the angular velocity of the distal end portion; a processing unit for determining an angle of the joint between the proximal portion and the distal end portion on the basis of the measured acceleration or the measured angular velocity and determining a spasticity time point at which resistance to motion of the distal end portion is received; and a display unit for displaying spasticity evaluation information for a spasticity evaluation on the basis of the angle of the joint and the spasticity time point.

Abstract: A syringe-based device includes a housing, a pre-sample reservoir, and an actuator. The housing defines an inner volume between a substantially open proximal end portion and a distal end portion that includes a port couplable to a lumen-defining device. The pre-sample reservoir is fluidically couplable to the port to receive and isolate a first volume of bodily fluid. The actuator is at least partially disposed in the inner volume and has a proximal end portion that includes an engagement portion and a distal end portion that includes a sealing member. The engagement portion is configured to allow a user to selectively move the actuator between a first configuration such that bodily fluid can flow from the port to the pre-sample reservoir, and a second configuration such that bodily fluid can flow from the port to a sample reservoir defined at least in part by the sealing member and the housing.

Abstract: A syringe-based device includes a housing, a pre-sample reservoir, and an actuator. The housing defines an inner volume between a substantially open proximal end portion and a distal end portion that includes a port couplable to a lumen-defining device. The pre-sample reservoir is fluidically couplable to the port to receive and isolate a first volume of bodily fluid. The actuator is at least partially disposed in the inner volume and has a proximal end portion that includes an engagement portion and a distal end portion that includes a sealing member. The engagement portion is configured to allow a user to selectively move the actuator between a first configuration such that bodily fluid can flow from the port to the pre-sample reservoir, and a second configuration such that bodily fluid can flow from the port to a sample reservoir defined at least in part by the sealing member and the housing.

Abstract: An exercise support apparatus is capable of supporting exercise taken by a patient during blood purification treatment and includes an estimation generating device that generates an estimation representing a circulating-blood-volume rate of change regarding a circulating blood volume that is estimated to be observed after the exercise is started, the estimation being generated after the blood purification treatment is started and from a continuous measurement of the circulating-blood-volume rate of change as regarding changes in circulating blood volume that is conducted before the exercise is started; a calculating device that calculates a difference between a measured value of the circulating-blood-volume rate of change that is acquired after the exercise during the blood purification treatment is started and a value of the estimation generated by the estimation generating device; and a first monitoring device that monitors whether the difference or ratio calculated by the first calculating device is over a

Abstract: A blood pressure data processing apparatus including a peak selection unit, a frequency component suppression unit, a respiratory fluctuation calculation unit, an attenuation amount calculation unit, and a respiratory cycle determination unit. The frequency component suppression unit suppresses components of the selected peak frequency within the first spectrum, and generates a second spectrum. The respiratory fluctuation calculation unit calculates a first respiratory fluctuation in second blood pressure data, and calculates a second respiratory fluctuation in third blood pressure data, which is a time domain representation of the second spectrum. The attenuation amount calculation unit calculates an attenuation amount of the second respiratory fluctuation relative to the first respiratory fluctuation. The respiratory cycle determination unit determines a cycle corresponding to the selected peak frequency as a respiratory cycle of a user if the attenuation amount is greater than a threshold.

Abstract: In one embodiment, a system for heel-to-shin testing includes a patient interface configured to be applied to a shin of a patient and extend from a point on the shin adjacent the knee to a point on the shin adjacent the ankle, the patient interface including an elongated medial touch sensor configured to sense contact of a heel of the patient to a centerline of the shin at any axial position between the knee and the ankle, and a control module in electrical communication with the patient interface, the control module being configured to identify a number of times the patient's heel deviates from the centerline of the shin as the patient slides the heel down the shin or drags the heel up the shin.

Abstract: The present disclosure generally relates to devices, systems, and methods for Fallopian tube diagnostics. In some embodiments, a tube may have a distal end, and a balloon may be coupled to the distal end of the tube. The balloon may be disposed in the tube in a first, inverted position and movable to a second, everted position. The balloon may be extendable a distance distal of the tube distal end such that a surface of the balloon is contactable with an inner surface of the Fallopian tube. A push wire may have a distal end coupled to a second end of the balloon. The balloon may be movable from the first inverted position to the second everted position by actuation of the push wire. The surface of the balloon may include a plurality of surface features for collection of a tissue sample of the inner surface of the Fallopian tube.

Abstract: A biological fluid sampling device for collecting a blood sample from a separate vascular access device and for ejecting a portion of the collected sample to a point-of-care testing device for analysis is provided. The biological fluid sampling device includes a body enclosing a reservoir. The reservoir has an internal volume sufficient to contain enough blood for use in a diagnostic test. The sampling device further includes: an access lumen extending from a distal end of the body for establishing fluid communication between a separate vascular access device and the reservoir; an outflow lumen also in fluid communication with the reservoir; and a removable vented cap attached to the outflow lumen including a gas permeable vent in gaseous communication between the reservoir and ambient air. In addition, several sample and transfer devices are provided for obtaining a sample from a subject and transferring the sample to a point-of-care testing device.

Abstract: Monitoring glucose concentration in aqueous humor can include inserting an implantable device into an eye and determining glucose concentration as a function of glucose sensed at the implantable device. In some implantable device embodiments, the device includes a polymer layer comprising a material that changes volume in response to varying glucose concentrations of the aqueous humor. A pressure sensor in the device can detect the changes in volume. In some implantable device embodiments, the device includes electrodes for determining the glucose concentration.

Abstract: A breast biopsy lateral arm system includes a removable gun mount which attaches to a carriage that traverses along an X-axis defined by a lateral arm in order to position a biopsy needle relative to a patient. The carriage rides along the lateral arm on self-adjusting rollers which are loaded against the lateral arm by spring members. A cam-actuated carriage slide lock can be used to secure the carriage in a desired position relative to the lateral arm. A cam-actuated removable gun mount lock allows the gun mount to be quickly changed and offset orthogonally with respect to the X-axis. An X-axis stop can be used to establish a position to which the carriage can be returned with accuracy.

Abstract: A method for assessing pain caused by administration of a drug solution includes: anesthetizing an experimental animal; inserting a measurement electrode into skeletal muscle of the anesthetized experimental animal; puncturing an injection needle into a predetermined part of the anesthetized experimental animal while measuring a myoelectric potential of the skeletal muscle with the measurement electrode; administering a drug solution to the anesthetized experimental animal; and (i) measuring a duration time of the myoelectric response caused by the administration of the drug solution, and/or (ii) measuring an EMG intensity obtained by integrating absolute values of myoelectric potentials during a period from occurrence of the myoelectric response by the administration of the drug solution to disappearance of the myoelectric response.

Abstract: A mold is used to form a solder joint to join the distal end of the guidewire to a wire coil. The mold has a cavity that can have different configurations so that the solder joint can be any of bullet shaped, micro-J shaped, cone shaped, truncated cone shaped, or have a textured surface.

Abstract: A urine analyzer device, configured to be installed in a toilet bowl, to be used several times, the device comprising a holder member, to attach the device to the rim of the toilet bowl, an electronic unit, enclosed in a housing, a urine reception area, with at least one electro-chemical sensor, configured to measure a quantity of at least one substance contained in urine, such as physiological compound or chemical component, a wireless coupler to send resulting data to a remote computing device, wherein the electro-chemical sensor comprises at least a ion selective Field Effect Transistor (ISFET), configured to sense levels of one or more physiological ions, thereby providing a urine analyzer device, readily available at home, simply installed in a toilet bowl, and that can be used several times subsequently.

Abstract: A wearable health monitoring includes a monitoring main-body, a wearable component and a biometric monitoring module. The wearable component is connected with the monitoring main-body. The biometric monitoring module is disposed within the monitoring main-body and includes a photoelectric sensor, a pressure sensor and an air-pressure-based blood pressure meter. The air-pressure-based blood pressure meter is embedded and positioned in the embedding slot portion of the embedding seat, and includes a gas-collecting actuator and an elastic air-bag. The gas-collecting actuator transports a gas to the elastic air-bag, and the elastic air-bag is inflated and elastically protrudes to attach to a skin tissue of a wearing user. The pressure sensor measures vasoconstriction pulsation under the skin tissue. A detection signal is generated and converted into health data information, which is outputted to the photoelectric sensor for calibrating a calculation of detection thereof to output precise health data information.

Abstract: A pen format liquid collection device includes an elongate generally tubular housing (12, 112, 212, 312) able to be held by hand and having an opening at one end, and at least one liquid take-up element (30, 130, 230, 330) mounted in the housing so as to be positioned or positionable to project at the opening, the at least one liquid take-up element then further postionable by hand manipulation of the housing to contact a volume of liquid to thereby take-up a sample of the liquid to be analysed. At least one retention element (230a, 330a) is supported in the housing. The at least one liquid take-up element and the at least one retention element are arranged whereby they are relatively movable into contact, and the at least one retention element is adapted on contact to in turn take-up the sample and retain the sample or a component thereof for in situ analysis or later recovery while protected within the housing. The liquid take-up element is preferably a capillary.

Abstract: A device for drawing spinal fluid from a body part or injecting medication into the body part is disclosed. The device may include one or more measurement features (markings) that indicate the subcutaneous depth of the device as well as confirm placement and orientation of the spinal fluid withdrawing or medication injecting end of the device in the body part. The device may include a trocar and a cannula having a patient end, a non-patient end, an outer surface, and a central passage adapted to receive said trocar. One or more windows may be provided in or on the cannula, said windows extending from the outer surface of the cannula to the central passage. The windows may be spaced from the patient end of the cannula and from each other along a specific longitudinal axis of the cannula by a predetermined distance, such as 10 millimeters.

Abstract: An intracranial pressure estimating method includes: an acquisition step (S10) of acquiring time-series data on external ear canal pressure pulse waves of a subject; an analysis step (S12) of analyzing external ear canal pressure pulse wave data obtained by digitalizing the time-series data on the external ear canal pressure pulse waves, to calculate a first formant frequency of the external ear canal pressure pulse wave data; a correction step (S13) of correcting the calculated first formant frequency based on personal information on the subject to calculate a corrected value; and an estimation step (S14) of calculating an estimated value of an intracranial pressure based on the calculated corrected value.

Abstract: The invention discloses a method of operating a system for neurofeedback (NFB) that includes trained animal in a feedback chain. Feedback chain consists of the following steps: A?B?C?D?A wherein said steps are: A. real time recording of the subject's EEG performed by the user module and forwarded to the mobile module; B. analytics of the recorded signal performed by the mobile module and algorithmic decisioning about the stimulation form; C. forwarding the stimulation towards the animal by using of one or more ultrasonic speakers simultaneously wherein the information needed for the animal performance is forwarded in the form of a coded ultrasonic signal; and D. performing of a learned action by the animal triggered by the received ultrasonic signal from the step C which provides a stimulus to the subject exposed to the NBF training.

Abstract: A handheld biopsy punch pen assembly with a first sampling housing selectively removably couplable to a body of the assembly and having a skin puncturing assembly disposed therein that includes a distal tip and with at least one blade member disposed thereon. The assembly includes a spring-loaded pen assembly operably configured to have a loaded position with the distal tip of the skin puncturing assembly recessed, a sampling position with the distal tip projecting outwardly away from the lower end of the first sampling housing for sampling of a user's skin and with the distal end the plunger member directly coupled to the skin puncturing assembly, and a retracted position with the distal tip projecting outwardly away from, and disposed a length away from, the lower end of the first sampling housing and with the distal end the plunger member uncoupled to the skin puncturing assembly.