Abstract: An introducer is provided for introducing a sensor into the body of a patient. The introducer connects to a sensor hub. When the sensor hub and introducer are connected, the introducer needle is exposed. When the sensor hub and introducer are disconnected, a needle cover and the needle move with respect to each other so that the needle cover substantially covers the needle, protecting a user from being injured by the needle.

Abstract: A device is configured to monitor a cardiovascular property of a subject. The device obtains measurement data from a primary pressure wave sensor arranged to detect pressure waves in an extracorporeal fluid circuit in fluid communication with the cardiovascular system of the subject. The device has a signal processor configured to generate a time-dependent monitoring signal based on the measurement data, such that the monitoring signal comprises a sequence of heart pulses, wherein each heart pulse represents a pressure wave originating from a heart beat in the subject; determine beat classification data for each heart pulse in the monitoring signal; and calculate, based at least partly on the beat classification data, a parameter value indicative of the cardiovascular property. The beat classification data may distinguish between heart pulses originating from normal heart beats and heart pulses originating from ectopic heart beats.

Abstract: Medical device systems and methods for operating medical device systems conserve energy by efficiently managing computational demands of the systems. A first analysis, having relatively lower computational processing demand than at least a second analysis, processes signals from a subject to determine a first estimate of a propensity for the subject to have a neurological event. If the first estimate meets a set of specified criteria, a second analysis is performed to determine a second estimate of the propensity for the subject to have a neurological event.

Abstract: A system and method is provided for analyzing a glucose state. A method may include identifying a target glucose state and an initial glucose state. The method may include calculating a target return path for a transition from the initial glucose state to the target glucose state. The target return path may comprise at least one intermediate glucose state associated with the transition from the initial glucose state to the target glucose state. The target return path may be calculated based on a hazard associated with the at least one intermediate glucose state of the target return path.

Abstract: Systems and methods are disclosed for determining individual-specific blood flow characteristics. One method includes acquiring, for each of a plurality of individuals, individual-specific anatomic data and blood flow characteristics of at least part of the individual's vascular system; executing a machine learning algorithm on the individual-specific anatomic data and blood flow characteristics for each of the plurality of individuals; relating, based on the executed machine learning algorithm, each individual's individual-specific anatomic data to functional estimates of blood flow characteristics; acquiring, for an individual and individual-specific anatomic data of at least part of the individual's vascular system; and for at least one point in the individual's individual-specific anatomic data, determining a blood flow characteristic of the individual, using relations from the step of relating individual-specific anatomic data to functional estimates of blood flow characteristics.

Abstract: Subject matter disclosed herein relates to monitoring and/or controlling blood glucose levels in patients. In particular, times for obtaining metered blood glucose samples of a patient may be altered based, at least in part, on a blood glucose level of said patient observed from a blood glucose sensor.

Abstract: A wireless circuit includes a housing, such as a hermetic housing, and at least one antenna coil wound about a coil axis within the housing. The coil axis may be substantially parallel to at least one wall of the housing, wherein the wall parallel to the coil axis is substantially thinner than other walls of the housing.

Abstract: A tissue monitoring device includes a light emitter, a light detector, a probe, and a controller. The light emitter emits light through tissue in the subject, such as tissues in the subject's head. The light detector detects light emitted from the light emitter and scattered by the subject's tissue. The probe is inserted into an orifice of the subject and includes one of the light emitter and light detector. The controller communicates with the light detector and the light emitter and detects an oxygenation level of the blood in the subject's tissue based upon measurements of the scattered light. The probe may include one or more bladders for blocking ambient light and/or for ensuring contact exists between the light detector (or emitter) and an interior surface of the subject's orifice.

Abstract: A blood pressure cuff includes a first bladder having a width, and a length transverse to the width. The blood pressure cuff also includes a second bladder connected to the first bladder and a port fluidly connected to at least one of the first and second bladders.

Abstract: Systems and methods are disclosed for estimating patient-specific blood flow characteristics. One method includes acquiring, for each of a plurality of individuals, a geometric model and estimated blood flow characteristics of at least part of the individual's vascular system; executing a machine learning algorithm on the geometric model and estimated blood flow characteristics for each of the plurality of individuals; identifying, using the machine learning algorithm, features predictive of blood flow characteristics corresponding to a plurality of points in the geometric models; acquiring, for a patient, a geometric model of at least part of the patient's vascular system; and using the identified features to produce estimates of the patient's blood flow characteristic for each of a plurality of points in the patient's geometric model.

Abstract: A breath analyzer, a system, and a computer program for administering a breath analysis to a donor and recording a breath analysis result. Embodiments of the invention authenticate that the breath analysis was performed correctly, preserves the breath analysis results by communicating with other devices, and presents the breath analysis results by superimposing them on recorded video data. The breath analyzer includes a breath receptor for receiving a breath sample from the donor, an analyzing element for determining a breath analysis result, a communications element for sending information indicative of the breath analysis result to a recording device manager, and a housing for securing the components in a handheld device. The system comprises the breath analyzer, a recording device manager for synchronizing the recordings, and at least one ancillary camera for recording the breath analysis.

Abstract: A bio information measuring device is provided. The bio information measuring device includes a sensor portion and a needle portion including a plurality of needles projecting from a plurality of openings formed in a surface of the sensor portion. The plurality of needles are configured to pierce tissue, wherein the plurality of needles include a biocompatible organic material which includes an enzyme member that reacts with an analysis material and a conductive polymer for transferring an electrical signal generated as a result of a reaction of the enzyme member with the analysis material.

Abstract: A monitoring device for the circulation of a patient includes sensors for recording data, an input unit for inputting patient specific data and a connected a data recording and analysis device configured to determine the right atrial pressure (RAP), the mean arterial pressure (MAP) and the cardiac output (CO) and to determine the mean systemic filling pressure (Pms) and to determine the cardiac efficiency (Eh) therefrom. A device records a pressure value (Pps,char) characterizing the pressure assistance during positive-pressure ventilation. The data recording and analysis device is configured to determine a pressure-corrected mean systemic filling pressure (Pmsp) and a pressure-corrected cardiac efficiency (Ehp) by the difference from the right atrial pressure (RAP) and the pressure value (Pps,char) characteristic of the pressure assistance being used instead of the right atrial pressure (RAP).

Abstract: A medical device includes a housing and an electrode arrangement coupled to the housing and configured to sense an electrical physiologic signal from a patient. The device also includes detection circuitry coupled to the electrode arrangement and configured to obtain a cardiac signal component and a non-cardiac signal component from the physiological signal. A processor is coupled to the detection circuitry. The processor is configured to detect patient activity using at least the non-cardiac signal component and discriminate between voluntary and involuntary activity of the patient based on a comparison of temporally aligned cardiac and non-cardiac signal components.

Abstract: A biological information detection device or the like which can determine a mounted state or an unmounted state with high accuracy, or can appropriately present information on the basis of a determination result is to be provided. A biological information detection device includes a pulse wave detection unit 10 that outputs a pulse wave sensor signal and a processing unit 100 that processes the pulse wave sensor signal, in which the processing unit 100 performs a detachment detection process of the biological information detection device on the basis of a DC component change value of the pulse wave sensor signal in a predetermined period.

Abstract: A method and apparatus for detecting and distinguishing epochs of deep-sleep from epochs of light-sleep of a subject by sensing by a peripheral pulse signal related to the systemic circulation of the subject, preferably a peripheral arterial tone (PAT) sensor for sensing pulsatile arterial volume changes in a digit (e.g., a finger) of the subject reflecting sympathetic tone variations; analyzing the sensed pulse signals for determining therefrom a number of features, particularly seven specific variables in each of two time periods; and utilizing the results of the analysis for determining whether the epoch detected is a light-sleep epoch or a deep-sleep epoch.

Abstract: Disclosed is an electronic device for measuring Electroencephalogram (EEG) signal or electronic stimulation, including at least: electrode modules that measures the EEG signal from a subject's head or apply current to the head; a control module that controls each of the electrode modules or applying current thereto; an EEG signal processing module that processes the EEG signal; an electric stimulation module that provides the electrode modules with a current for electric stimulation. The control module is further configured to: control each electrode module for measuring the EEG signal from the subject's head by controlling a switching module such that the each electrode module is connected with the EEG signal processing module; and control the each electrode module for applying current to the subject's head by controlling the switching module such that the each electrode module is connected with the electric stimulation module.

Abstract: A wireless circuit includes a housing having at least one opening, and sensor connected to the housing at the opening. The sensor includes a first layer having a first dimension and a second layer having a second dimension shorter than the first dimension. The second layer may be positioned entirely within the housing and a surface of said first layer may be exposed to an exterior of the housing.

Abstract: A wearable patch and method for automatically monitoring, screening, and/or reporting events related to one or more health conditions (e.g., sleeping or breathing disorders, physical activity, arrhythmias) of a subject.

Abstract: A second part extending around a first part in a plugged-together state. The second part has snap-in element with an inwardly protruding projection for meshing with a complementary recess on an outer surface of the first part to hold the second part fixed in the axial direction on the first part. Both parts have a central passage opening. One part has an end area expanding towards the outlet opening in a connection area, and the other part is connected to an elastic section, arranged in its interior. The front end of the elastic section is pressed into contact with the expanded end area of the opposite part. The projection of the snap-in element maintains the first and second parts meshed together, so that the elastic section exerts a sealing function due to the pressure on the expanding end area.