Abstract: A blood pressure measurement device includes an outer case; a base; a pump provided on the base such that the pump is shifted from a center of the outer case and located on one side as viewed in a circumferential direction of a living body; a drive unit provided on the base and located on one side of the pump as viewed in a direction orthogonal to the circumferential direction; an on-off valve provided on another side of the pump as viewed in the direction orthogonal to the circumferential direction; a pressure sensor provided on said another side of the pump as viewed in the direction orthogonal to the circumferential direction; and packing provided between the on-off valve and the pressure sensor and the base.

Abstract: Disclosed is an analyte measuring patch for invasive measuring a concentration of an analyte, in particular glucose. The analyte measuring patch includes a sensor with a working electrode (101), a counter electrode (103) and a reference electrode 102). The patch further includes an electronics unit with a microcontroller (1200) and a current measurement unit. The microcontroller (1200) includes a control output (DAC), a first analogue input (ADC-1) and a second analogue input (ADC-2). The control output (DAC) is operatively coupled with a control electrode, the control electrode being either of the working electrode or (101) or the counter electrode (103). The first analogue input (ADC-2) is operatively coupled with a measurement electrode via the current measurement unit, the measurement electrode being either of the working electrode (101) or the counter electrode (103). The second analogue input (ADC-1) is operatively coupled with the reference electrode (102).

Abstract: A guidewire comprises a core shaft, a coil body covering a distal end portion of the core shaft, and a coating agent covering an outer periphery of the coil body, wherein the coil body includes a distal coil body disposed on a distal side of the coil body, and a proximal coil body disposed on a proximal side of the distal coil body, a surface roughness of the proximal coil body is higher than a surface roughness of the distal coil body.

Abstract: A blood pressure measurement device includes an outer case; a base; a pump provided on a surface of the base such that the pump is shifted from a center of the outer case and located on one side as viewed in a circumferential direction of a living body; a first pressure sensor and a second pressure sensor that are provided such that the first pressure sensor and the second pressure sensor are arranged side by side in the circumferential direction and located on one side as viewed in a direction orthogonal to the circumferential direction; and a first on-off valve and a second on-off valve that are provided such that the first on-off valve and the second on-off valve are arranged side by side in the circumferential direction with reference to the first pressure sensor and the second pressure sensor.

Abstract: Devices, systems and methods that track various aspects of a person's sleep and environment to optimize one or more aspects of the user's environment and sleep conditions, quality and duration, together or alone, and help make the one or more users maintain and prolong his or her deep sleep status and improve the their sleep duration and quality.

Abstract: Techniques (methods and devices) for neural stimulation through audio with dynamic modulation characteristics are disclosed. The techniques include receiving a mapping of sensor-input values and modulation-characteristic values, wherein each sensor-input value corresponds to a respective modulation-characteristic value; receiving an audio element from an audio source, wherein the audio element comprises at least one audio parameter; identifying an audio-parameter value of the audio parameter; receiving a sensor-input value from a sensor; determining a sensor-input value based on the sensor-input value; selecting from the mapping of sensor-input values and modulation-characteristic values, a modulation-characteristic value that corresponds to the sensor-input value; generating an audio output based on the audio-parameter value and the modulation-characteristic value; and playing the audio output.

Abstract: An allergen delivery system with a tray and delivery set. The delivery set includes a dispensing well. The dispensing well holds a wettable material to receive an allergen and provide it to a delivery barb that has been received into the dispensing well. A conduit is connected to the dispensing well, to receive the allergen and provide it to the dispensing well. A reservoir is connected to the conduit to receive the allergen and provide it to the conduit. A cap is disposed on the reservoir, with a hole, such that when a finger depresses the cap, the finger covers the hole and the depression creates pressure within the reservoir, which motivates an amount of the allergen to flow out from the reservoir through the conduit and into the dispensing well, to be absorbed by the wettable material, where the allergen is available for delivery to the barbed delivery applicator.

Abstract: Parametric model based computer implemented methods for determining the stiffness of a bone, systems for estimating h the stiffness of a bone in vivo, and methods for determining the stiffness of a bone. The computer implemented methods include determining a complex compliance frequency response function Y(f) and an associated complex stiffness frequency response function H(f) and independently fitting a parametric mathematical model to Y(f) and to H(f), and using a first measure of conformity and a second measure of conformity of the collected data to determine accuracy and repeatability of measurements. The systems include a device for measuring the stiffness of the bone in vivo and a data analyzer to determine a complex compliance frequency response function Y(f) and an associated complex stiffness frequency response function H(f).

Abstract: The measurement of electrodermal activity (EDA) can be facilitated by a sensing surface. The sensing surface can have a plurality of electrode pairs. An electrode pair can include a first electrode and a second electrode that are electrically isolated from each other. The plurality of electrode pairs can be electrically isolated from each other. A distance between neighboring electrode pairs can be larger than a distance between the first electrode and a second electrode of each electrode pair. One or more sensors can be configured to detect contact with the sensing surface. In response to the one or more sensors detecting contact with the sensing surface, one or more electrode pairs can be selected to be activated. In response to the one or more electrode pairs being selected to be activated, the selected one or more electrode pairs can be activated.

Abstract: Systems, apparatuses and methods are provided for identifying the position of a catheter relative to internal tissue and controlling injection of a therapeutic substance(s) into the internal tissue. In one embodiment, a catheter includes one or more position sensing electrodes disposed at or near a distal end of the catheter that allow identifying the position of the catheter relative to the internal tissue. The catheter also includes one or more contact sensors that provide an indication of contact and/or contact forces between the catheter and internal tissue before and after a therapy delivery needle is extended from the catheter into the internal tissue. Outputs of the contact sensor(s) allows for confirming insertion of the therapy delivery needle into the internal tissue to a desired depth. Once inserted to the desired depth, a therapeutic substance may be injected into the internal tissue at the desired depth.

Abstract: A capsule configured for collecting samples in the intestine, comprising a body delimiting at least one compartment for receiving samples and comprising at least one opening for samples intake, and a mobile mechanism for opening and/or closing the opening controlled by the dissolution of a material which is dissolvable in the intestine.

Abstract: A blood pressure measurement device includes a bag-like pressing cuff wound around a measurement target site of a living body; a back plate arranged on the living body side of the pressing cuff; a bag-like sensing cuff arranged on the living body side of the back plate; a supply device configured to supply a fluid into the cuffs; first guides arranged on the living body side of the pressing cuff and configured to form wrinkles in a direction intersecting the winding direction; and second guides arranged on the living body side of the sensing cuff and configured to form wrinkles in the direction intersecting the winding direction.

Abstract: An example of a system for monitoring and treating respiratory distress in a patient may include one or more non-invasive monitoring devices to acquire patient condition signals and a respiratory distress monitoring circuit to monitor a state of the respiratory distress using the patient condition signals. The respiratory distress monitoring circuit may include a signal processing circuit to generate patient condition parameters using the patient condition signals and a respiratory distress analyzer, which may include a parameter analysis circuit and a notification circuit. The parameter analysis circuit may be configured to produce a patient condition metric being a function of the patient condition parameters and to perform prediction and/or detection of an exacerbation of the respiratory distress based on the patient condition metric. The notification circuit may be configured to produce an alert notifying a result of the performance of the prediction and/or detection.

Abstract: High blood pressure measurement accuracy can be achieved with a blood pressure monitor employing a double cuff structure. A blood pressure monitor of the present invention includes a pressing member that includes a pressure cuff having a bag shape capable of containing fluid and generates a pressing force toward a measurement site of a subject when the pressing member is wound around the measurement site and the pressure cuff is inflated, and a controller that controls an operation of the adjuster such that the fluid is contained in the sensing cuff in an amount corresponding to biometric information about the subject and the pressure cuff is inflated or inflated and deflated in this state when performing a blood pressure measurement, and calculates a blood pressure value of the subject based on an output from the pressure sensor.

Abstract: Medical devices configured for in vivo assays of one or more analytes can sometimes be problematic if left inserted in a tissue, such as skin, for an extended time. Certain medical device surface profiles may aid in alleviating this issue. Accordingly, medical devices may comprise a base surface having a tissue-facing surface profile defined thereon, and a sensor extending through the base surface and at least a portion of the tissue-facing surface profile. The tissue-facing surface profile deviates from the base surface, and the tissue-facing surface profile is also configured to undergo a change in shape, hardness, or a combination thereof after contacting a tissue for a length of time. A dynamic material may be present in at least a portion of the tissue-facing surface profile.

Abstract: An automated allergy office system and method provides a medical professional with a new allergy treatment plan to administer to a patient. The automated allergy office system comprises a viewing device to select a test site on the patient's skin that is clear. A multiple test applicator is in cooperative engagement with a fluid tray and delivers a small amount of a first allergen to a first test site on the patient's skin as a small amount of a second allergen is delivered to a second test site on the patient's skin. The allergy condition of the patient is detected as a wheal forms at the first test site after fifteen minutes. The elements of the treatment plan are retrieved from a database for treating the patient's allergy condition. The patient's electronic medical record is checked to confirm that the allergy treatment is new for this patient.

Abstract: Provided is an apparatus for non-invasively monitoring a health condition. The apparatus for monitoring health according to an example embodiment of the disclosure includes: a pulse wave sensor configured to obtain a first pulse wave signal in a first contact state of an object and a second pulse wave signal in a second contact state of the object; and a processor configured to estimate a degree of vasodilation based on an alternating current (AC) component of each of the first pulse wave signal and the second pulse wave signal, configured to monitor a vascular health condition based on the estimated degree of vasodilation, and configured to output a result of monitoring the vascular health condition.

Abstract: An apparatus for estimating bio-information includes a sensor part configured to measure a pulse wave signal and a contact force of an object, while the object is in contact with the sensor part. The apparatus further includes a processor configured to extract a first feature from the measured pulse wave signal and the measured contact force, select one estimation model from a plurality of estimation models, based on a second feature of a user corresponding to the object, and estimate the bio-information, by inputting the extracted first features in the selected estimation model.

Abstract: Systems, devices, apparatus, methods, and computer-readable storage media for developmental assessment using eye tracking are provided. In one aspect, a system for development assessment via eye tracking includes: a patient-side computing device having a screen for presenting visual stimuli to a patient, an eye-tracking device integrated with the patient-side computing device and configured to collect eye-tracking data of the patient while the visual stimuli are presented to the patient on the screen of the patient-side computing device, and an operator-side computing device configured to present a user interface for an operator to communicate with the patient-side computing device.

Abstract: Systems, computer-implemented methods and/or computer program products that facilitate wearable multiplatform sensing are provided. In one embodiment, a computer-implemented method comprises: measuring, by a system operatively coupled to a processor, wirelessly on a nail plate, physiological data of an entity; integrating and synchronizing, by the system, the physiological data with other physiological data from one or more devices to form integrated physiological data; and analyzing, by the system, the integrated physiological data to detect one or more disorders.