Abstract: The acoustic impedance of the respiratory system can be inferred from oscillations that are generated in an airway of a subject. The impedance describes the frequency-dependent relation between the resulting oscillations in flow and pressure. When the impedance varies from inspiration to expiration, it has to be estimated with a high time resolution. A method is provided that reliably estimates the impedance in time intervals that are short enough for physiological purposes. A simple version of the uncertainty principle has been derived for discrete time and frequency. A discrete time-frequency transform has been developed that gives an optimal time-frequency resolution according to this principle. The transform is orthonormal, which permits an analysis of variance in the discrete time-frequency domain. The impedance follows from bivariate least-squares analysis in the time-frequency domain, under the assumption that noise is present in both flow and pressure.

Abstract: Ultrasonic catheters and methods for determining and/or monitoring reflux volumes during gastroesophageal reflux events.

Abstract: A medical system (100) is disclosed that provides a respiratory-based control of at least one medical procedure. In this regard, the medical system (100) includes one or more appropriate sensors (108) for providing respiratory data on a patient (104). This respiratory data is utilized by respiration assessment logic (116) to determine if the respiratory data has exceeded one or more respiration thresholds and which may be equated with a “sudden” respiratory event. Identification of such a sudden respiratory event by the logic (116) results in the suspension of the noted medical procedure. Patient respiration data may also be displayed, for instance in a color that depends upon its magnitude or level.

Abstract: A blood pressure measurement device includes a cuff, a display, a distance sensor, an acceleration sensor, and a CPU. The display displays a positional relationship between the patient's heart and the device, which includes a flat screen. The distance sensor measures a distance between the device and the patient, and detects a subject to be measured on a line perpendicular to the flat screen of the display and measures the distance. The acceleration sensor measures an angle of inclination of the device when mounted on the patient's wrist. The CPU calculates a positional relationship between the patient's heart and the device based on the distance between the device and the subject to be measured, the angle of inclination of the device mounted on the patient's wrist, the length of the patient's forearm and upper arm, and a vertical distance between the patient's shoulder and heart.

Abstract: A piezoelectric pump is provided with an actuator containing a piezoelectric element and a vibrating sheet; a first diaphragm, positioned opposite the actuator, with a first connecting hole provided therein; a pump chamber formed by the space between the actuator and the first diaphragm; and a second diaphragm positioned opposite the first diaphragm. The part of the second diaphragm opposite the first connecting hole is provided with an opposing wall portion that prevents a fluid that has been introduced into the pump chamber via the first connecting hole from flowing back towards a suction side via the first connecting hole.

Abstract: Various embodiments of the invention disclosed herein comprise a system of wearable devices that collectively allow for the continuous, non-invasive, measurement and monitoring of blood pressure, without the use of an inflatable cuff. The system incorporates: 1) An optical module, which is comprised of a coherent source of light, a semi-transparent hologram, optics for viewing the interference pattern developed between the illuminated hologram and arterial blood, a Charge-Coupled Device (CCD) array, and processing electronics with Bluetooth capability that facilitates digitization and wireless transmission of the fringe pattern to, 2) a personal digital assistant (PDA) that is worn on a waist belt. The PDA and associated software allow for continuous calculation and monitoring of real-time arterial blood pressure from the digitized fringe patterns received. The system further comprises 3) a personal computer (PC) with wireless capacity and connection to the internet.

Abstract: A blood pressure measurement device is characterized in that the said device is designated to arithmetically apply to the computed blood pressure value a correction value that is in accordance with the difference in atmospheric pressure between the position of the blood pressure transmitting part and the position of the heart of the subject wearing the blood pressure transmitting part as obtained from the sensor signal, on the basis of the internal pressure variation of the blood pressure transmitting part.

Abstract: Solutions for non-invasively monitoring blood metabolite levels of a patient are disclosed. In one embodiment, the method includes: repeatedly measuring a plurality of electromagnetic impedance readings with a sensor array from: an epidermis layer of a patient and one of a dermis layer or a subcutaneous layer of the patient, until a difference between the readings exceeds a threshold; calculating an impedance value representing the difference using an equivalent circuit model and individual adjustment factor data representative of a physiological characteristic of the patient; and determining a blood metabolite level of the patient from the impedance value and a blood metabolite level algorithm, the blood metabolite level algorithm including blood metabolite level data versus electromagnetic impedance data value correspondence of the patient.

Abstract: A system for monitoring a patient includes an inflatable cuff configured to at least partially occlude an artery of the patient, and a sensor configured to determine a first parameter associated with the at least partially occluded artery and to generate an output signal indicative of the first parameter. The system also includes a processor configured to receive the output signal and information indicative of an occlusion efficiency of the cuff. The processor is configured to determine a hemodynamic parameter of the patient based on the output signal and the information.

Abstract: Devices and methods useful for sensing or measuring a pressure and remotely indicating or communicating that pressure are provided. The devices and methods have particular utility in sensing pressures in implantable medical devices and more particularly in hydrocephalus shunts. In one exemplary embodiment, an implantable valve can include a housing having a reservoir adapted to receive fluid flow therethrough between an inlet port and an outlet port. The implantable valve can also include a needle-penetrable septum to allow fluid delivery to the reservoir and/or a needle guard disposed within the housing and adapted to protect the radio frequency tag from a needle penetrating into the housing. A radio frequency (RF) tag can be disposed within the reservoir and can be adapted to change one or more of its electromagnetic characteristics in response pressure applied thereto by fluid in or flowing through the reservoir.

Abstract: The present invention is directed to membranes composed liquid crystals having continuous aqueous channels, such as a lyotropic liquid crystal, including a cubic phase lyotropic liquid crystal, and to electrochemical sensors equipped with such membranes. The membranes are useful in limiting the diffusion of an analyte to a working electrode in an electrochemical sensor so that the sensor does not saturate and/or remains linearly responsive over a large range of analyte concentrations. Electrochemical sensors equipped with membranes of the present invention demonstrate considerable sensitivity and stability, and a large signal-to-noise ratio, in a variety of conditions.

Abstract: In a sphygmomanometer for measuring blood pressure according to a volume compensation method, an upper arm V0 equivalent cuff pressure representing a cuff pressure in a state where an inner pressure and an outer pressure of an artery of an upper arm are in equilibrium is specified based on a cuff pressure signal of the upper arm. For example, the upper arm V0 equivalent cuff pressure is detected as an average blood pressure obtained from the cuff pressure signal of the upper arm. After a control target value and an initial cuff pressure in the volume compensation are detected, a difference between the initial cuff pressure and the upper arm V0 equivalent cuff pressure is calculated as a correction value, and the blood pressure value in the volume compensation method is corrected with the calculated correction value.

Abstract: An adjustment device for a hearing aid includes: an audio extraction section for, through an acoustic process of a collected audio signal, utilizing information of a phoneme or syllable contained in the audio signal to output time information, the time information identifying a point of uttering the phoneme or syllable; an electroencephalogram measurement section for measuring an electroencephalogram signal of a user; a determination section for determining a difficulty of hearing of the phoneme or syllable by relying on an event-related potential in the electroencephalogram signal based on the identified point of uttering the phoneme or syllable as a starting point; a phoneme identification section for, when a plurality of phonemes or syllables are determined as difficult to hear, identifying a chronologically preceding phoneme or syllable among them to be difficult to hear; and a gain adjustment section for, with respect to the phoneme or syllable identified by the phoneme identification section, determinin

Abstract: An acoustic means for rendering key respiratory measurements accessible to hand-held mobile digital devices with audio input capabilities (such as mobile phones, personal digital assistants, mobile gaming platforms, and tablets). One or more embodiments comprise: a compact and portable whistle (101) that encodes a user's expiratory airflow rate as audio frequency, and a software process with local or remote access to mobile-device audio that decodes said audio frequency to regain expiratory airflow rate and derive key respiratory measurements, so that these measurements and related information may conveniently be made available to the user (100) and the user's health network of family members (103) and physicians (104). Embodiments enable leveraging the ubiquity and extensive capabilities of hand-held mobile digital devices, while simultaneously simplifying requirements for a dedicated spirometry device.

Abstract: An analyte test device is constructed as an integrated, single-use, disposable cartridge which can be releasably installed into a compatible analyte test monitor. In use, the device can be used in conjunction with the monitor to lance the skin of a patient to create a blood sample, express the blood sample from the wound site using vacuum forces and calculate the concentration of a particular analyte in the expressed blood sample. In one embodiment, the device includes a base which includes a top surface and a bottom surface. The base is also shaped to define an aperture which extends transversely through its top and bottom surfaces. An electrochemical test sensor is affixed to the base in such a manner so that a vacuum path is at least partially defined between the base and the test sensor, the vacuum path being in fluid communication with the aperture.

Abstract: A sleep apnea diagnostic system includes a housing that is configured to be attached to near the nose of a patient's face to sense physiological information of a patient. The housing includes sensors to sense the physiological information. The physiological information may be, for example, air flow through the nose or the mouth or both. The physiological information further may be, for example, blood volume. The sleep apnea diagnostic system includes at least one processor in the housing or external to the housing or both to analyze the physiological information to determine whether the patient has experienced irregular or abnormal respiratory activity and to detect respiratory effort. The analysis may be real time or delayed.

Abstract: A respiration pattern of a number of respiration cycles is detected and breath intervals (BI) and tidal volume (TVOL) measurements of each of the respiration cycles are respectively determined. An unevenly sampled instantaneous minute ventilation (iMV) signal is produced using the BI and TVOL measurements, and an evenly sampled iMV signal (resampled iMV signal) is produced using the unevenly sampled iMV signal. Disordered breathing is detected based on a comparison between a baseline threshold and the resampled iMV signal.

Abstract: A method and device for generating a signal that mirrors changes in the level of effort exerted by respiratory muscles of patients on mechanical ventilatory support comprising: monitoring and storing airway pressure (Paw), rate of gas flow (F), and volume of gas flow (V), and generating a composite pressure signal using resistive pressure units (KF) determined from elapsed data and selected to minimize step changes in the calculated signal and elastic pressure units (Kv) determined from elapsed data by steps comprising: —scanning stored F or Paw during exhalation and identifying where their trajectory transiently reverses direction to detect transients; —selecting points within the exhalation that are at preselected distances away from the transients; —calculating the value of Kv required to force the values of the calculated signal at said selected points in elapsed breaths to be substantially equal when the selected value of KF is used as the flow coefficient.

Abstract: The present invention relates to a quantitative electroencephalogram (QEEG) monitor and system capable of monitoring and displaying simultaneously neuropathological characteristic and activity of both sides of a subject's brain. The methods include various indices and examination of differences in these indices by which neurophysiological conditions or problems can be identified and treated. These methods, and the systems and devices using these methods preferably can be used for identifying these neurophysiological conditions or brain dysfunction with monitors and methods for seizure detection, for sedation monitoring, for anesthesia monitoring, and the like. These bilateral brain monitoring methods and systems, and the devices using these methods can be used by individuals or clinicians with little or no training in signal analysis or processing. These bilateral monitoring methods can also be used in a range of applications.

Abstract: Disclosed herein are methods, systems, and apparatus for detecting an epilepsy event in a patient using a medical device. The medical device is capable of determining an occurring epilepsy event, for example a seizure or an increased risk of a seizure. The determination is performed by determining at least one NNXX value from the beat sequence of the patient's heart. The medical device may then take a responsive action, such as warning, logging the time of the seizure, computing and storing one or more seizure severity indices, and treating the epilepsy event.