Abstract: An indicator device for visually indicating a pressure of blood inside a blood vessel includes: a body, the body comprising a duct extending in the body and having a sealed proximal end; a distal end portion adapted to be positioned inside the blood vessel and including a liquid inlet opening in fluid communication with the duct; and a window including an at least semi-transparent section configured to enable visual observation of blood entering into the duct via the inlet opening when the inlet opening is located inside the blood vessel.

Abstract: Utilization of a contact device placed on the eye in order to detect physical and chemical parameters of the body as well as the non-invasive delivery of compounds according to these physical and chemical parameters, with signals being transmitted continuously as electromagnetic waves, radio waves, infrared and the like. One of the parameters to be detected includes non-invasive blood analysis utilizing chemical changes and chemical products that are found in the conjunctiva and in the tear film. A transensor mounted in the contact device laying on the cornea or the surface of the eye is capable of evaluating and measuring physical and chemical parameters in the eye including non-invasive blood analysis. The system utilizes eye lid motion and/or closure of the eye lid to activate a microminiature radio frequency sensitive transensor mounted in the contact device. The signal can be communicated by wires or radio telemetered to an externally placed receiver.

Abstract: Techniques are provided for use with a pacemaker or other implantable medical device for detecting arterial blood pressure. Briefly, the pacemaker detects aortic electrical resistance using sensing/pacing leads. Aortic electrical resistance pertains to the resistance to an electrical current passing through the aorta. The pacemaker then determines the arterial blood pressure of the patient based on the aortic resistance and a predetermined calibration value that relates aortic resistance to arterial pressure. The calibration value is updated monthly based on blood pressure values detected using an external blood pressure sensor employing a blood pressure cuff. Other techniques described herein pertain to the determination of other physiologic parameters such as stroke volume and cardiac output and to the detection of changes in hematocrit. Any of the various physiological parameters may then be used to trigger or control warning signals and responsive therapy.

Abstract: Devices, systems and methods are disclosed for a neural access device that includes an implant which transcutaneously exits the skin of a patient and provides transport of signals between a sensor implanted in a patient and an external device. The transcutaneous implant has integrated features to provide reduced risk of injury due to mechanical forces as well as electrostatic discharge energy applied to the external portion of the device. Transcutaneous devices which provide wireless communication between a sensor and an external device are also disclosed.

Abstract: The present invention relates to a test instrument (X) including a capillary (5) for moving a sample liquid (B), a liquid pooling portion (4) communicating with the capillary (5) for retaining the sample liquid (B) to be introduced into the capillary (5), and a liquid introduction selector (12) for selecting whether or not the sample liquid (B) retained in the liquid pooling portion (4) is introduced into the capillary (5). The present invention also relates to an attachment provided with the test instrument (X), and a concentration measuring apparatus to which the attachment is mounted for use.

Abstract: The present invention relates generally to systems and methods for measuring an analyte in a host. More particularly, the present invention relates to systems and methods for transcutaneous measurement of glucose in a host.

Abstract: An apparatus for use with a patient having a vessel carrying blood to ascertain characteristics of the blood. The apparatus includes a display module and a probe having a distal extremity adapted to be inserted into the vessel of the patient and having a proximal extremity coupled to the display module. The probe includes a sensor in the distal extremity for providing an electrical signal to the display module when the probe is disposed in the blood. The probe can have an antithrombogenic surface treatment for inhibiting the adhesion of blood components to the probe when disposed in the blood.

Abstract: Methods for determining central systolic pressure are disclosed. A first method determines the time of peak in a measured carotid waveform and then determines the pressure in a measured radial waveform at the corresponding time. A second method utilises only a measured radial waveform. The waveform is analysed to determine a time indicative of lower body waveform and determines the pressure at this time. In each case, the determined pressure is substantially the same as the central systolic pressure.

Abstract: Methods and apparatuses for determining an analyte value are disclosed.

Abstract: A lightweight portable probe or transducer containing a transmissive or reflective electro-optical emitter and receptor in the infrared spectrum is fitted on a subject's finger or toe. Associated electronics energize and monitor the probe, detect cardio-rhythmic fluctuations therefrom, and process digital data over a prescribed window to produce a non-invasive, qualitative or quantitative measure of the subject's circulation. In accordance with one embodiment of the invention, a simple tri-color LED array is used to indicate the subject's circulation as being normal, reduced, or borderline.

Abstract: A method is disclosed for motivating a user of a spirometry system 20 having a display screen 12, an air-tube 22, a flow measurement sensor 24 operatively associated with the air-tube 22, a display screen 26, and an associated processor 30. A motivational animation is displayed on the display screen 12 having a first aspect that reflects a relative evaluation of a determined peak flow rate to a goal value therefor and having a second aspect that reflects a relative evaluation of a determined total flow volume to a goal value therefor. The processor 30 repeatedly updates the motivational animation during the period of use of the spirometer to reflect the degree of achievement of both of the goal values by the user.

Abstract: A probe for application to a selected area of a subject's skin covering a body part, which selected area serves as a measurement site for measuring changes in the pulsatile arterial blood volume thereat, includes: a base for application to the selected area of the subject's skin at the measurement site; a pressure applicator for applying a static pressure to the subject's skin at the measurement site; and a sensor for sensing changes in the pulsatile arterial blood volume at the measurement site. The pressure applicator is designed to apply to the measurement site a static pressure of a magnitude to partially unload the wall tension of, but not to occlude, the arteries. The pressure applicator is configured to substantially prevent venous distention and blood pooling at the measurement site by permitting free venous drainage through tissues surrounding the measurement site.

Abstract: Methods and apparatuses including determining a calibration parameter associated with a detected analyte value, calibrating the analyte value based on the calibration parameter, and dynamically updating the calibration parameter are disclosed. Also provided are systems, kits, and computer program products.

Abstract: Methods and apparatus for providing a power supply to a device, including an inductive rechargeable power supply for a data monitoring and management system in which a high frequency magnetic field is generated to provide power supply to a rechargeable rower source such as a battery of a transmitter unit in the data monitoring and management system are provided.

Abstract: A venous-arterial detector is disclosed. The detector includes a first chamber in fluid communication with a needle, and an indicator chamber in selective fluid communication with the first chamber through a valve. The indicator chamber is pre-pressurized to a defined pressure that preferably exceeds typical venous pressure, and the valve retains that pressure within the indicator chamber. When the needle is inserted into a vessel, if the pressure in the vessel is greater than the defined pressure in the indicator chamber, blood will flow into the indicator chamber, indicating that the vessel is most likely to be an artery.

Abstract: A breath biofeedback method and system for encouraging a subject to modify respiration. The system includes a thoracic volume input module measuring thoracic volume data of the subject and a pattern module providing target breathing patterns in communication with a display generator. The display generator producing display information representing a displayable image including a first object having a first position determined as a function of the thoracic volume data and a second object having a second position determined as a function of the target breathing pattern and the thoracic volume data. The displayable image is designed such that when displayed on the display device the displayable image encourages the subject viewing the displayable image to modify respiration.

Abstract: The invention provides a devices, methods and systems to measure and record uterine tissue environment components such as pH during the course of uterine artery occlusion. The uterus becomes ischemic due to the occlusion thereof, and its pH drops sharply within minutes of uterine artery occlusion and remains relatively low for a period of time. The return of normal pH is an indicator of return of blood to the ischemic tissue. In use, a catheter with a pH measuring tip is advanced through the patient's vaginal canal and into the patient's uterine cavity until the pH measuring active electrode on the distal end of the catheter contacts or penetrates the uterine fundus. The active electrode detects the pH and a signal representing pH is transmitted to a pH recording and monitoring device which preferably displays the pH. The signal may be transmitted through a conductor or by a radio transmitter. Components other than pH may be monitored such a pCO2, and pO2.

Abstract: A method of evaluating human stress using photoplethysmography (PPG) includes defining at least one PPG parameter, radiating light having at least one wavelength, which reacts to a blood component to be measured, at a measuring target and measuring a PPG signal from the measuring target during a predetermined period of time, and evaluating a level of human stress using a plurality of stress indexes obtained from the PPG parameter.

Abstract: The present invention relates to a predictive-kinetic method for use with data processing of a sensor-generated signal, as well as, microprocessors and monitoring systems employing such a predictive-kinetic method. Data from a transient region of a signal is used with suitable models and curve-fitting methods to predict the signal that would be measured for the system at the completion of the reaction. The values resulting from data processing of sensor response using the methods of the present invention are less sensitive to measurement variables.

Abstract: The present invention discloses a detection device for detecting irregular intravascular pressure, the device including an analyzer for automatically analyzing intravascular pressure upstream of the suspected location of irregular blood flow, and a comparing device that correlates the recorded intravascular pressure to a standard whereby variation in the intravascular pressure during multiple tests is indicative of irregular blood flow. Also disclosed is a system for providing a warning of potential health problems due to irregular blood flow, the system including a detecting device as set forth above and a communicating device operatively connected to the detecting device for communicating a warning when the device indicates an irregularity of intravascular pressure during at least two uses of the device.