A pulse wave detecting device includes: a pressure pulse wave detector which is configured to press a pressing surface in which a pressure detecting element is formed, against a radial artery under a skin of a wrist of a subject, and which is configured to detect a pressure pulse wave from the radial artery; and a housing which accommodates the pressure pulse wave detector in a state where the pressing surface is exposed toward the wrist. The housing is configured so that a compression pressure which is exerted by the housing in an attachment state where the housing is attached to the wrist, and which is applied onto the radial artery is smaller than a compression pressure which is exerted by the pressing surface in the attachment state, and which is applied onto the radial artery.

The invention provides a system and method for measuring vital signs (e.g. SYS, DIA, SpO2, heart rate, and respiratory rate) and motion (e.g. activity level, posture, degree of motion, and arm height) from a patient. The system features: (i) first and second sensors configured to independently generate time-dependent waveforms indicative of one or more contractile properties of the patient's heart; and (ii) at least three motion-detecting sensors positioned on the forearm, upper arm, and a body location other than the forearm or upper arm of the patient. Each motion-detecting sensor generates at least one time-dependent motion waveform indicative of motion of the location on the patient's body to which it is affixed. A processing component, typically worn on the patient's body and featuring a microprocessor, receives the time-dependent waveforms generated by the different sensors and processes them to determine: (i) a pulse transit time calculated using a time difference between features in two separate time-dependent waveforms, (ii) a blood pressure value calculated from the time difference, and (iii) a motion parameter calculated from at least one motion waveform.

The invention provides a system and method for measuring vital signs (e.g. SYS, DIA, SpO2, heart rate, and respiratory rate) and motion (e.g. activity level, posture, degree of motion, and arm height) from a patient. The system features: (i) first and second sensors configured to independently generate time-dependent waveforms indicative of one or more contractile properties of the patient's heart; and (ii) at least three motion-detecting sensors positioned on the forearm, upper arm, and a body location other than the forearm or upper arm of the patient. Each motion-detecting sensor generates at least one time-dependent motion waveform indicative of motion of the location on the patient's body to which it is affixed. A processing component, typically worn on the patient's body and featuring a microprocessor, receives the time-dependent waveforms generated by the different sensors and processes them to determine: (i) a pulse transit time calculated using a time difference between features in two separate time-dependent waveforms, (ii) a blood pressure value calculated from the time difference, and (iii) a motion parameter calculated from at least one motion waveform.

A motion vector coding unit executes processing including a neighboring block specification step of specifying a neighboring block which is located in the neighborhood of a current block; a judgment step of judging whether or not the neighboring block has been coded using a motion vector of another block; a prediction step of deriving a predictive motion vector of the current block using a motion vector calculated from the motion vector of the other block as a motion vector of the neighboring block; and a coding step of coding the motion vector of the current block using the predictive motion vector.

The present invention relates to physiological signal processing, and in particular to methods and systems for processing physiological signals to predict a fluid responsiveness of a patient. A medical monitor for monitoring a patient includes an input receiving a photoplethysmograph (PPG) signal representing light absorption by a patient's tissue. The monitor also includes a perfusion status indicator indicating a perfusion status of the PPG signal, and a fluid responsiveness predictor (FRP) calculator programmed to calculate an FRP value based on a respiratory variation of the PPG signal. The FRP calculator applies a correction factor based on the perfusion status indicator.

Technologies are generally described for systems, devices and methods relating to blood pressure monitors. Blood pressure monitors may include a processor and a structure effective to be in communication with the processor. The structure may be effective to apply pressure to an object. Blood pressure monitors may include at least one photoreceptor effective to be in communication with the processor. Photoreceptors may be located in the device so as to be effective to detect light returned from the object while the pressure is applied. Blood pressure monitors may be effective to determine color values of the returned light, determine changes in the color values of the returned light, and determine a blood pressure based on the changes in the color values.

A method of presenting data from a remote sensor that is monitoring a subject includes obtaining a data stream from the remote sensor, wherein the data stream includes a sensor metric, a metric identifier, dynamically updated integrity information about an accuracy of the sensor metric, and a diagnostic assessment of a health condition of the subject, and then displaying, via a display associated with the client device, the diagnostic assessment of the health condition of the subject, a metric statistic associated with the diagnostic assessment, and a recommendation as to an action to be taken by the subject.

A method of presenting data from a remote sensor that is monitoring a subject includes obtaining a data stream from the remote sensor, wherein the data stream includes a sensor metric, a metric identifier, dynamically updated integrity information about an accuracy of the sensor metric, and a diagnostic assessment of a health condition of the subject, and then displaying, via a display associated with the client device, the diagnostic assessment of the health condition of the subject, a metric statistic associated with the diagnostic assessment, and a recommendation as to an action to be taken by the subject.

A blood pressure measurement method and apparatus, and a wearable device are provided. The blood pressure measurement method includes: detecting a change of a user from a first state to a second state; starting measurement and inflating an airbag (160) to a preset pressure value at a preset rate if determining that the user has changed from the first state to the second state; obtaining first duration of an inflation process; determining a correction value based on the first duration; and after the measurement ends, obtaining a measurement value of a blood pressure, and correcting the measurement value based on the correction value, to obtain a final blood pressure value of the user. The blood pressure measurement method provides an early-morning blood pressure measurement manner in which the early-morning blood pressure can be automatically and accurately measured when the user is insensitive, thereby simplifying user’s operations, and improving user experience.

The blood pressure measuring device (1) is designed as a photoplethysmographic measuring system which functions according to the “vascular unloading technique”. Metrological components and a pressure generating and pressure control system are accommodated in the base part (3). The fitted cuff part (2) has an ergonomic palm support (4), two finger supports (6) divided from one another by a web (5), and also a receiving part (7) which comprises two receiving tubes (9) for fingers. The cuff part (2) projects beyond the base part (3), both towards the front and also towards the rear, and covers the base part (3) almost completely, i.e. by more than 90%. The lateral attachment of the cable (8) facing in the direction of the forearm has the advantage that the cable can be guided along the patient's arm, the wrist does not rub against the cable (8), and in particular the carpal tunnel is also protected.