Abstract: A system and method for cardiovascular monitoring and reporting are disclosed. The system (CV monitoring system) includes a data analysis system and an in-ear biosensor system that preferably includes left and right earbuds. The earbuds include infrasound/vibration sensors that detect biosignals from the individual including signals associated with cardiovascular activity (CV signals). The analysis system calculates cardiovascular function measurements (CV function measurements) based upon the CV signals. The CV monitoring system uses machine learning to predict blood pressure (BP) measurements of the individual based upon the CV signals and the calculated CV function measurements. In an embodiment, the CV monitoring system includes an EKG detection system that detects EKG signals associated with heart function.

Abstract: The present disclosure is a blood collection assembly that has a needle assembly fixedly coupled to a finger-activated actuator and tubing and the needle assembly has a needle. Further, the blood collection assembly has a hub that houses the needle assembly and the hub has a channel in a top surface of the hub. Additionally, the channel slidably engages the finger-activated actuator such that when the finger-activated actuator is moved from a distal end of the hub to a proximal end of the hub the needle retracts within the hub.

Abstract: A urinalysis device includes a target formed from a water-repellent material, an absorbent portion formed from a water-absorbing material and at least partially in contact with the target, a surface structure that forms a pathway for directing urine for application to the target; and a sensor element that is provided in the absorbent portion and outputs signals corresponding to components in the urine.

Abstract: An optical device for the in noninvasive determination of the concentration of glucose or another analyte in blood using a combination of Raman spectrometry and PPG. The device includes an optical detector, preferably a CMOS imager including pinned photodiodes (PPD) to collect a time-variable signal and a logic circuit arranged to determine a glucose concentration based on variations in the optical signal happening in a frequency range compatible with the cardiac rhythm.

Abstract: A steerable biopsy device comprises an outer sheath comprising a sheath body having a proximal sheath section and a distal sheath section. The outer sheath further comprises a distal sheath tip and a sheath lumen terminating at a distal port in the distal sheath tip. The biopsy device further comprises a biopsy needle integrated with the sheath body. The biopsy needle is slidably disposed in the sheath lumen. The biopsy needle comprises a needle shaft and a distal needle tip configured for being displaced between a stored position within the sheath lumen and a deployed position outside of the distal port of the distal sheath tip. The biopsy device further comprises an articulation control actuator configured for articulating the distal sheath section, and a needle actuator configured for distally advancing the distal needle tip from the stored position to the deployed position.

Abstract: A medical syringe useful for administering an injection or withdrawing a bodily fluid, the syringe comprising a barrel, plunger assembly and a needle assembly having a selectively retractable needle, the plunger assembly further comprising a plunger handle with a plunger seal and a front tip extending forwardly of the plunger seal to extend through the barrel and into the an annular fluid seal disposed in a recess between the barrel and a forwardly projecting needle, thereby reducing dead space inside the syringe and helping anchor the annular fluid seal inside the recess.

Abstract: Provided is a blood collection apparatus with which blood can be stably collected from a finger tip of any subject while ensuring safety and ease. This blood collection apparatus is provided with: a puncture site holding mechanism for holding a puncture site; a compression mechanism for performing an operation of compressing and releasing the puncture site when blood is collected from the puncture site; a container holding mechanism for holding a container for collecting blood flowing from a puncture wound at the puncture site; and a driving mechanism for varying the relative distance between the puncture site and the container by vertically moving the puncture site holding mechanism, the container holding mechanism, or the container held by the container holding mechanism when blood flowing from the puncture wound is collected.

Abstract: The present invention provides a spacer device having a flow rate spirometer. The flow rate indicator allows users to use a measured, consistent flow rate leading to improved synchronicity and actuation.

Abstract: A soft conductive composite composition can include a soft matrix containing a conductive member that is associated with a bioactive component. The soft matrix can be formed from a silicone composition. The conductive member can be carbon nanotubes in the silicone composition. The carbon nanotubes can have at least two walls and be conductive. Also, the carbon nanotubes can be a mixture of functionalized carbon nanotubes and non-functionalized carbon nanotubes, which mixture can have a ratio of 1:2 to 1:20 w/w of functionalized to non-functionalized carbon nanotubes per gram of the silicone composition. The bioactive component (e.g., enzyme) can be associated with at least a first portion of the carbon nanotubes. A second portion of the carbon nanotubes can be devoid of the bioactive component.

Abstract: This disclosure is directed to systems and techniques for detecting change in patient health based upon peak and non-peak patient activity data. In some examples, the peak and non-peak patient activity data correspond to one or more peak (time) periods and the one or more non-peak periods, respectively, where at least one peak period and at least one non-peak period corresponds a highest activity level and a lowest activity level, respectively, for a single day. If a change in patient health is detected, the techniques described herein may direct a medical device to generate for display output indicating the detection of the change in patient health.

Abstract: A bodily-fluid transfer 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 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: Disclosed are devices and systems for monitoring and measuring arterial carbon dioxide, including those with an occlusive earpiece, a housing and a carbon dioxide sensor. A pressure sensor may also be provided. The devices and methods can monitor for altered carbon dioxide production and ventilator impairment and provide alerts.

Abstract: A strain gauge (10, 40, 50), a pressure sensor (20, 60), and an interventional medical catheter. The strain gauge (10, 40, 50) comprises a substrate (11) and at least two sensitive gages (1, 2) provided on the substrate (11), the at least two sensitive gages (1, 2) being arranged along two mutually perpendicular directions and sharing one ground port (3). The pressure sensor (20, 60) comprises an elastic body (21, 61) and the strain gauge (10, 40, 50) provided on the elastic body (21, 61). The interventional medical catheter comprises a catheter distal end and the pressure sensor (20, 60) provided at the catheter distal end.

Abstract: There is provided a wheeze detection apparatus including: a sound measurer configured to measure a pulmonary sound of a measurement subject; a respiratory sound volume deriver configured to derive a respiratory sound volume of the measurement subject based on the sound measured by the sound measurer; and a wheeze detector configured to extract a maximum point from an intensity distribution for each frequency of the sound and to detect wheeze based on information on the maximum point. The wheeze detector sets, in a case where the respiratory sound volume is outside a predetermined range, detection sensitivity of the wheeze to a higher value than the detection sensitivity in a case where the respiratory sound volume is within the range.

Abstract: An arterial blood module (16) that is removably connectable to an arterial blood collection element (14) is disclosed. The arterial blood module includes a housing (30), a needle (32), a cap (34) removably securable over the needle, a mixing chamber (36), and a safety shield (38) engaged with a portion of the housing and transitionable from a first shield position in which a portion of the needle is exposed to a second shield position in which the needle is shielded by a portion of the safety shield. In one embodiment, the present disclosure includes an arterial blood collection system (10) that includes an arterial blood collection element (14) defining a collection chamber (20) and an arterial blood module (16) removably connectable to a portion of the arterial blood collection element.

Abstract: The apparatus for evaluating force control ability according to an embodiment includes: a display unit configured to display a target force direction; a measuring unit configured to measure a direction and magnitude of a force applied by a user; and a processing unit configured to evaluate force control ability of the user by comparing the measured force direction with the target force direction and comparing the measured force magnitude with a predetermined reference force magnitude.

Abstract: Electrophysiologic biomarkers for prognostication of neurological outcome are described herein. An inverse correlation was found between timing of a cortical spreading depolarization (SD) wave and neurological outcome as tested at 24 hours post-CPR. Additionally, a minor image of this SD was identified as a “repolarization (RP) wave.” Quantifying features of SD and RP during cardiac arrest and cardiopulmonary resuscitation (CPR) provide important metrics for diagnosis and prognosis of neurological injury from hypoxia-ischemia and can serve as an early prognostication tool for predicting outcome at subsequent days after successful CPR. This discovery may also allow for novel therapeutic interventions to improve neurological recovery after hypoxia-ischemia insults.

Abstract: An IV catheter device can include or being configured to employ a probe assembly having an integrated fluid flushing mechanism. The probe assembly can be configured in a variety of ways to cause flushing fluid to be injected through a fluid permeable structure of the probe as the probe is advanced distally from a catheter. In this way, the fluid permeable structure can be kept clear of any occlusion that may otherwise form. With the probe extending distally from the catheter, a blood sample may be collected.

Abstract: A sensorized garment is provided. The sensorized garment includes an wearable element on a skin having a hand-tightening or a closure device to securely constrain sensors, for example electrodes to detect electrophysiological signals, during a physical activity. The wearable element has a three-dimensional shape to uniquely define a right side and a left part of a circumferential zone when the wearable element is worn. The sensorized garment further includes a band carried by the circumferential zone, and at least one conductor connected between the sensor and a zone of the sensorized garment.

Abstract: Disclosed is a guidewire configured to provide high torsional stiffness without detrimentally increasing bending stiffness. Such a device provides a high ratio of torsional stiffness to bending stiffness. The guidewire device includes a core with a proximal section and a distal section. The distal section of the core is coupled to a microfabricated outer tube such that the distal section of the core passes into and is encompassed by the outer tube.