Embodiments are directed to a blood pressure measurement device that includes a cuff configured to wrap around a limb of a user when the cuff is worn by the user, a bladder coupled to the cuff and configured to compress the limb when inflated, and a pump operative to inflate the bladder. The blood pressure measurement device can also include a valve positioned between the bladder and the pump and configured to operate in a first state that allows air from the pump to enter the bladder and prevent air from leaving the bladder. The valve can also be configured to operate in a second state that allows air to leave the bladder. The blood pressure measurement device can also include a vent positioned between the bladder and an external environment and configured to continuously release air from the bladder.

Techniques for determining average value of an arterial blood pressure parameter of an examined subject are disclosed. A pressure device is used to apply changing pressure conditions over a body part of a subject and generate pressure measurement data indicative of the pressure applied. A first measuring unit measures blood-pressure-pulse related signals in the pressure-affected body part, and generate blood-pressure-pulse related measurement data indicative thereof, and a second measuring unit measures blood-pressure-pulse related signals in a pressure-free body part of the examined subject, and generate reference blood-pressure-pulse related measurement data indicative thereof. A control unit is used to operate the pressure device to apply the changing pressure conditions over the pressure-affected body part and simultaneously operate the first and second measuring units, determine an initial blood pressure parameter value of the subject based on the measurement data from the pressure device and from the first measuring unit, determine a correction factor based on the measurement data from the second measuring unit and from the first measuring unit, and determine the average blood pressure parameter of the examined subject based on the initial blood pressure parameter value and the correction factor.

Methods and apparatus for optically detecting biologically-sourced acoustic signal(s) are disclosed herein. In some embodiments, K-sounds are detected and/or blood pressure is measured. Alternatively or additionally, an optical stethoscope (e.g. diffused-light interferometer optical stethoscope) is employed.

Protecting a blood pressure cuff and its user is in a sanitary and convenient manner. A shield has upper and lower edges, longitudinal side edges, and interior and exterior surfaces. Stitching couples the side edges. The shield forms a funnel-shaped, generally conical configuration. The upper edge is imperforate, devoid of elastic, and has a first circumference. The shield is fabricated of a flexible material. A continuous elastic band is secured to the shield adjacent the lower edge. The elastic band is adapted to constrict the lower edge to a second circumference when in a relaxed, un-stretched orientation.

The present invention provides an arteriovenous pressure measurement device which allows noninvasive and accurate measurement of arteriovenous pressure, and also provides an arteriovenous pressure measurement method using the measurement device. The noninvasive arteriovenous pressure measurement device comprises a probe (20) for radiating ultrasound toward a blood vessel in the skin, a pressing part (10) for pressing the skin in a state of being placed between the skin and the probe (20), and a pressure sensor (33) for detecting a pressing force applied to the skin at the pressing part (10), the pressing part (10) having water (36) permeable to the ultrasound and a balloon (31) accommodating the water (36), the flexible container (31) being made of a flexible material permeable to the ultrasound, and an outer surface of the balloon (31) presses the skin.

Various systems and methods for collecting patient data are discussed herein. According to some systems and methods, a timer may be started, and a blood pressure data collection system is actuated to obtain a blood pressure measurement of a patient upon the expiration of the timer. The timer may be incorporated into a patient data collection system or method to ensure the patient is relaxed and calm prior to taking a blood pressure measurement. An event may be sensed by an environmental sensor system and the timer may be started in response to sensing the event. A clinician leaving a room where the patient is disposed is one example of an event. An interruption may be sensed by the environmental sensor system and the timer may be terminated in response to sensing the interruption. The clinician entering the room where the patient is disposed in one example of an interruption.

The invention is a type of electronic sphygmomanometer with dynamically calibrated blood pressure reference value, which is determined based on the objective condition of human blood pressure fluctuation influenced by various factors such as age, date and time of measurement, and establishes age/blood pressure reference value, date/blood pressure reference value and time/blood pressure reference. The value database, or through mathematical operations, obtains the real-time standard blood pressure reference value under the specific conditions of the subject's age, test date, and test time, and calibrates it as a benchmark for judging the abnormality state of the real-time blood pressure measurement value. This improves the ability of the sphygmomanometer in producing an accurate judgement of the subject's blood pressure, and reduces the margin of error for false positive tests or false negative tests.

Various systems and methods for collecting patient data are discussed herein. According to some systems and methods, a timer may be started, and a blood pressure data collection system is actuated to obtain a blood pressure measurement of a patient upon the expiration of the timer. The timer may be incorporated into a patient data collection system or method to ensure the patient is relaxed and calm prior to taking a blood pressure measurement. An event may be sensed by an environmental sensor system and the timer may be started in response to sensing the event. A clinician leaving a room where the patient is disposed is one example of an event. An interruption may be sensed by the environmental sensor system and the timer may be terminated in response to sensing the interruption. The clinician entering the room where the patient is disposed in one example of an interruption.

An air circuit structure comprises the air circuit box, an air charging pump, a cuff air nozzle, air discharging valves and an air pressure examination sensor. The air circuit box comprises a shell with a cavity formed inside. The shell is provided with an access port, an air charging port and an air inlet port spaced apart, and the access port, the air charging port and the air inlet port are all connected to the cavity.

[Object] To provide a hemostasis aid and a tourniquet by which a blood vessel at a puncture site can be more reliably distended.

[Solving Means] A hemostasis aid 1 includes a tourniquet 10 including a plurality of pressurizing layers 11a to 11e divided in a width direction and a control device 20 that pressurizes the pressurizing layers 11a to 11e sequentially from the pressurizing layer 11a on one end side A in the width direction W to on the other end side B. Accordingly, a puncture site can be reliably distended by wrapping the tourniquet 10 such that the puncture site is positioned on a patient's distal side with respect to the other end side.