Abstract: A fluid control apparatus includes a piezoelectric pump, a pressure vessel, an input unit, a drive control unit, and a driving circuit. The piezoelectric pump has a pump chamber whose volume fluctuates due to displacement of a piezoelectric element, a valve chamber communicated with the pump chamber and has a valve diaphragm, a pump chamber opening that allows the pump chamber to be communicated with an outside of the pump chamber, and a valve chamber opening that allows the valve chamber communicate with an outside of the valve chamber. The pressure vessel is communicated with the valve chamber. The driving circuit drives the piezoelectric element upon application of a driving power-supply voltage from the drive control unit. The drive control unit adjusts the driving power-supply voltage or a driving current corresponding to the driving power-supply voltage in accordance with a vibration state of the valve diaphragm.

Abstract: A device is configured for tracking e.g. the diastolic blood pressure in a patient. The device applies a pressure to a body part, e.g. by use of an inflatable cuff. By performing repeated and alternating pressure changes in the cuff, a specific feature of a signal that relates to the diastolic blood pressure can be tracked and possibly measured. The device may have particular use in conjunction with cardiopulmonary resuscitation devices.

Abstract: An MRI prep scan acquires plural sets of echo signals at a plurality of cardiac time phases which are mutually different from each other for each slice and used to generate a plurality of respectively corresponding prep images. Reference information is acquired and displayed for determining a first cardiac time phase and a second cardiac time phase on the basis of the prep images. The first and second cardiac time phases are set in response to an operator's specification. An imaging scan section for acquiring imaging echo signals by performing an imaging scan is performed upon each of the first and second cardiac time phases to acquire imaging echo signals. A first image is generated based on an echo signal of the first cardiac time phase and a second image is generated based on an echo signal of the second cardiac time phase. A differential image is acquired by calculating a difference between the first image and the second image.

Abstract: A blood pressure monitor includes a cuff to be wound around a living body of a subject, a measuring unit for measuring blood pressure with said cuff wound around the living body of said subject, a detecting unit for detecting an inclination angle of said cuff, a specifying unit for specifying a current inclination level among a plurality of predetermined inclination levels upon measurement by said measuring unit, based on a result of detection by said detecting unit, a memory for storing therein the inclination level specified by said specifying unit, in association with blood pressure data measured by said measuring unit, and a notifying unit for providing notification of at least one past inclination level of the plurality of inclination levels stored in said memory and said current inclination level, in association with each other.

Abstract: A medical blood pressure transducer that provides an identifier to a monitor that conveys characteristics of the transducer. The monitor can use the information to decide whether to function, or in calibration of the system. The transducer may be part of a disposable blood pressure monitoring system, and may include two transducers closely-spaced to provide two separate but identical outputs. In this way, the transducer may be connected to both a patient monitor and a cardiac output monitor at the same time measurements from a single line can be simultaneously supplied to two separate monitoring devices (for example a patient monitor and a cardiac output monitor). The identifier for the transducer may be circuitry, specifically a resistance/capacitance (RC) combination that possesses a characteristic time constant.

Abstract: An electronic sphygmomanometer acquires a patient ID and recommended site information read from an ID card before measurement. The recommended site indicating the site to be attached to a cuff of a left site or a right site is thereby specified for every person to be measured (patient ID). Thereafter, the site to be attached to the cuff is guided by notifying the specified recommended site to the person to be measured.

Abstract: An electronic sphygmomanometer determines whether a position of a measurement site falls within a proper range, and notifies whether the position of the measurement site falls within the proper range. When determination is made that a time in which the position of the measurement site falls within the proper range is not less than a predetermined time (for example, 2 seconds), measurement of a blood pressure is automatically started. When determination is made that a time in which the position of the measurement site is out of the proper range is not less than a predetermined time (for example, 5 seconds), the measurement of the blood pressure is started. Further, whether the position of the measurement site falls within the proper range is notified while correlated with the measurement result.

Abstract: A method for estimating blood pressure includes sensing a sphygmus wave at a body part of a user to which vibration is applied to generate a sensed sphygmus wave, filtering the sensed sphygmus wave to generated a filtered sphygmus wave, and estimating blood pressure of the user based on time differences between peaks of the sensed sphygmus wave and peaks of the filtered sphygmus wave.

Abstract: Apparatus is provided for protecting a patient's limb from tourniquet-related injury, comprising: a tourniquet cuff having a length sufficient for encircling a limb protection sleeve applied to a limb at a location having a limb circumference of not less than a predetermined minimum limb circumference and not more than a predetermined maximum limb circumference; limb protection sleeve adapted for applying to the limb at the location, wherein the sleeve has a tubular shape and a tubular circumference predetermined to be less than the predetermined minimum and wherein the sleeve is formed to allow elastic stretching of the tubular shape sufficient to increase the tubular circumference to be substantially equivalent to the limb circumference at the location when the sleeve is applied to the limb, thereby applying a pressure to the limb that is greater than a predetermined minimum pressure and less than a predetermined maximum pressure; and identification means perceptible to a user for providing an indication to

Abstract: The present invention discloses a non-invasive blood pressure measurement apparatus and a safety protection method. In addition to a main pressure measurement circuit and a main microprocessor circuit, the measurement apparatus also includes an independently disposed assist pressure measurement circuit and an independently disposed assist microprocessor circuit. In normal measurement, the assist microprocessor circuit periodically samples a cuff pressure via the assist pressure measurement circuit, and compares the measured cuff pressure with a specified overpressure protection value, and if the cuff pressure exceeds the specified overpressure protection value, the assist microprocessor circuit outputs a control signal to open a deflation valve until the pressure falls to below the safety pressure.

Abstract: A system for remote ischemic preconditioning that includes a cuff, and actuator, and a controller that operates the actuator according to a treatment protocol. The treatment protocol includes a plurality of treatment cycles that each comprise cuff actuation, an ischemic duration, cuff release, and a reperfusion duration.

Abstract: The present invention discloses a non-invasive blood pressure measurement apparatus and a safety protection method. In addition to a main pressure measurement circuit and a main microprocessor circuit, the measurement apparatus also includes an independently disposed assist pressure measurement circuit and an independently disposed assist microprocessor circuit. In normal measurement, the assist microprocessor circuit periodically samples a cuff pressure via the assist pressure measurement circuit, and compares the measured cuff pressure with a specified overpressure protection value, and if the cuff pressure exceeds the specified overpressure protection value, the assist microprocessor circuit outputs a control signal to open a deflation valve until the pressure falls to below the safety pressure.

Abstract: The invention relates to a sphygmomanometer for measuring blood pressure over a long period of time, especially over 24 hours, with a cuff which can be placed against an extremity of the body, a measuring device for determining blood pressure data, a control device for activating automatically the measuring device at specified time intervals, as well as a memory device for storing the blood pressure data determined in different measurements. Pursuant to the invention, the sphygmomanometer is novel owing to the fact that it is constructed as a portable instrument, for which the measuring device, a control device and the memory are part of the body of the device, which is fastened at the cuff.

Abstract: A rising cuff pressure detects the diastolic blood pressure and continues to rise to generate a pulse amplitude profile. The systolic blood pressure is determined by a computation using data from the profile to discriminate against the contribution of a hardened artery, without requiring the cuff pressure to exceed the systolic blood pressure.

Abstract: A non-invasive blood pressure monitoring system is disclosed herein. The non-invasive blood pressure monitoring system includes a pressure cuff comprising a resistive portion and a conductive portion aligned with the resistive portion. The non-invasive blood pressure monitoring system also includes a controller operatively connected to the pressure cuff. The controller is adapted to estimate the circumference of the pressure cuff based on the position of the conductive portion relative to the resistive portion.

Abstract: A manual-driven inflation-powered electronic blood pressure measuring apparatus includes an inflation unit to generate pressurized air by a user through hand squeezing, a power generation unit to receive the pressurized air to generate and output electric power, an electronic blood pressure measurement unit to receive the electric power output from the power generation unit and the pressurized air from the inflation unit to inflate an air pouch, and a sensor to detect a person's blood pressure signals in cooperation with the inflation pouch, and outputs a measurement result through an output unit.

Abstract: The present invention discloses a method for automatically calibrating an electronic sphygmomanometer, which pumps air at a predetermined air pressure to a testing electronic sphygmomanometer to simultaneously pressurize a set of pressure sensors set for regular use and at least one other set of pressure sensors being interconnected in the electronic sphygmomanometer to detect whether or not the set of pressure sensors used at regular time is normal. The detected change of pressure during the detection is sent to a control module, and the control module will compare the detected value of each pressure sensor. If the comparison is matched, then it means that the set of pressure sensors used at regular time is normal; if the comparison is mismatched, then the pressure sensors are determined as abnormal and the air valve connected to such pressure sensors is shut, such that when a user uses the electronic sphygmomanometer for the next time, another set of pressure sensors will be started.

Abstract: A method and system for operating a non-invasive blood pressure monitor that utilizes an SpO2 plethysmographic signal to reduce the time required to obtain an estimation of a patient's blood pressure. During operation of the NIBP monitor, the NIBP monitor utilizes the SpO2 plethysmographic signal to determine a timing period and a deflation period for each pulse associated with the patient's heartbeat. Upon receiving an oscillation pulse, the NIBP monitor determines the oscillation amplitude during the timing period and deflates the blood pressure cuff during the deflation period immediately following the timing period. Preferably, the deflation period occurs during the same oscillation pulse used to calculate the oscillation pulse amplitude to decrease the amount of time required to obtain a blood pressure estimate from the patient.

Abstract: An apparatus and method for pulse detection based on blood pressure measuring stage is disclosed. Both monitoring of blood pressure and blood vessel pulse are integrated and applied to an apparatus. With the components of the blood pressure monitor, such as an inflatable cuff an air pump and a variable flow valve, with a unique sequential pressure control of reduction and regulation of pressure, not only can blood pressure parameters but also pulse signals under various pressures be measured to provide a complete analysis of blood artery/vessel conditions.

Abstract: A method of operating a non-invasive blood pressure (NIBP) monitor that includes a blood pressure cuff and a pressure transducer. The method initially inflates the blood pressure cuff to a level above systolic pressure and begins to deflate the pressure cuff using a continuous or linear deflation technique. During the linear deflation of the pressure cuff, the oscillation pulses from the pressure transducer are obtained and compared to predicted pulse estimates. If the obtained oscillation pulses vary from the predicted pulse estimates, the linear deflation technique is interrupted and the pressure cuff is then deflated in a sequence of distinct pressure steps. During each pressure step, the oscillation pulses are obtained and the pressure cuff is not deflated to the next pressure step until the oscillation pulses correspond to each other.

Abstract: A method is provided for blood pressure measurement by means of an inflatable cuff (50) applied to a limb of a vertebrate and pneumatically coupled to a first port (112A) and a second port (112B) of a blood pressure measurement apparatus (100). A pump (160) coupled to the second port inflates the cuff pneumatically. During an initial cuff inflation period, a first pressure sensor (180) pneumatically coupled to the first port senses a first pressure and a second pressure sensor (182) pneumatically coupled to the second port senses a second pressure. An analysis module (142) compares the magnitude of the first pressure to the magnitude of the second pressure to determine the relative relationship between the respective magnitudes of the first pressure and the second pressure.

Abstract: An apparatus, system and method for collecting non-invasive blood pressure readings from a patient is provided. A non-invasive blood pressure cuff is arranged to be worn about a wrist of a patient and to be operatively connected to a blood pressure monitor. Communication means are operatively connected to the blood pressure cuff the monitor and arranged to automatically communicate a parameter associated with the cuff to the monitor. The monitor is arranged to automatically adjust blood pressure algorithms based upon the parameter to enhance the accuracy of blood pressure readings.

Abstract: A pressurizing apparatus and method for adjusting an optimal pressurizing rate according to a cuff of various lengths. The pressurizing method measures the pressure values at two reference points and time duration to calculate a pressurizing rate. A control adjustment routine to control an adjustment of the pressurizing rate is decided according the calculated pressurizing rate and at least one control condition. The pump is pressurized according to the adjustment of the pressurizing rate. A diastolic pressure value is measured and the pressurizing of the pump is kept to measure a systolic pressure value. Afterward, the pressurizing is stopped to prevent uncomfortable feeling of user caused by rapidly pressurizing and de-pressurizing process.

Abstract: A method and system for determining pulse rate of a patient are disclosed. The method and system include acquiring measured information for at least one pulse at a pressure step, determining and storing quality values for the at least one pulse at the pressure step, analyzing pulse matching criteria for the pressure step, and determining pulse rate based on the measured information, quality values, and pulse matching criteria.

Abstract: A method and system for determining when to make a reversion to smaller cuff pressure steps during an oscillometric blood pressure measurement is disclosed. The method and system comprise comparing conformance of oscillometric envelope blood pressure data with previous blood pressure data, including measuring a shift between the oscillometric envelope blood pressure data and an oscillometric envelope derived from the previous blood pressure data. In addition, the method and system include making a reversion decision based on whether the shift exceeds an allowable threshold. Once a reversion decision is made a subsequent decision may be made as to the need for increasing the cuff pressure level.

Abstract: A vascular sensing system includes blood flow restricting means, a sensor, and means for producing an output representing a return of blood flow after the blood vessel has been temporarily collapsed by the blood flow restricting means. The blood flow restricting means is capable of placement on a human toe having a blood vessel, and is capable of manipulating the blood vessel. The sensor is operably connected to the blood flow restricting means and is physically spaced from the toe. Further, a method of vascular sensing includes taking pressure measurements with an pressure cuff positioned on a toe, and conducting a waveform analysis of the pressure measurements to determine a return of blood flow pressure.

Abstract: A method and system for making pulse rate and blood pressure determinations is disclosed. The method and system comprise collecting oscillometric blood pressure data from pulses, determining individual quality values for feature measurements of the pulses, obtaining an overall quality assessment based on the individual quality values, repeating the collecting step until overall quality level is satisfied, and determining blood pressure and pulse rate using the individual quality values.

Abstract: A method and system for eliminating artifacts in an oscillation envelope are disclosed. The method and system comprise evaluating conformance of the oscillometric envelope blood pressure data with a predetermined expected pattern and excluding one or more data points of the oscillometric envelope blood pressure data based on non-conformance with the expected pattern. The expected pattern is based upon generally known physiological principles relating to oscillometric envelopes, a curve fit representing an oscillometric envelope from a previous determination, or other types of criteria.

Abstract: A method for measuring blood pressure during a limited number of blood pressure cycles at an area overlying an artery of a living subject, includes applying a pressure (P) to the artery for occluding the artery in response to a pressure signal. Subsequently the pressure is released to re-open the artery in response to a pressure release signal. A delay time is computed, by comparing a first time duration with a second time duration. The delay time is from a reference point in time after which a next pressure release signal is to be supplied to a device for applying a pressure. A pressure to be applied to the artery in a next measuring cycle is computed. Subsequently a pressure signal and a pressure release signal corresponding to the computed pressure and delay time are supplied to the device for applying a pressure.

Abstract: A method and apparatus for measuring blood pressure by the oscillometric technique. The method incorporates variable PIP's. The method comprises the steps of obtaining a value for the peak amplitude Amax of an oscillometric envelope; determining a cuff pressure, CP, which corresponds in time with Amax, this pressure representing the MAP of the subject; computing a variable value PIPSBP as a function of MAP; performing the calculation Asbp=Amax*PIPSBP to determine a systolic amplitude value Asbp along the oscillometric envelope; and determining the cuff pressure C which corresponds in time to Asbp, this value representing the systolic blood pressure (SBP) of the subject. PIP can be calculated using a piece-wise linear, polynomial, exponential or other function.

Abstract: Apparatus for measuring a physiological parameter of a patient, such as blood pressure, takes a sequence consisting of a predetermined number of individual measurements. The apparatus computes a best estimate of the physiological parameter from values obtained in two or more of the measurements. The apparatus automatically takes a sequence of measurements and then stops. The apparatus can operate unattended so that it is not necessary for a physician or other health care worker to be present while measurements are being made. The use of the invention to measure blood pressure of a patient reduces the effect of “white coat” hypertension on the best estimate. Preferred embodiments of the apparatus ignore results of a first measurement in the sequence. The patient is already familiar with the apparatus when subsequent measurements are taken. This further reduces the possibility that the patient's reaction to the process of measurement will affect the results of the measurement.

Abstract: An apparatus for obtaining information relating to a velocity at which a pulse wave propagates in a living subject, the apparatus including a first inflatable cuff and a second inflatable cuff which are adapted to be worn on two different portions of the subject, respectively, at least one cuff-pulse-wave detecting device which detects the pulse wave occurring to each of the first and second cuffs worn on the two different portions of the subject, and a velocity-relating-information obtaining device which obtains the information relating to the velocity, based on a time difference between a first time when the cuff-pulse-wave detecting device detects the pulse wave occurring to the first cuff, and a second time when the cuff-pulse-wave detecting device detects the pulse wave occurring to the second cuff.

Abstract: A blood pressure monitoring apparatus includes a blood pressure measuring device for measuring blood pressure employing a cuff, a pulse wave propagation time measuring device for measuring the pulse wave propagation time, a hemodynamics measuring device for measuring the hemodynamics, and a control device for controlling the blood pressure measuring device on the basis of a change in pulse wave propagation time measured by the pulse wave propagation time measuring device and a change in hemodynamics measured by the hemodynamics measuring device. The control device controls the blood pressure measuring device to measure the blood pressure on the basis of the amount of change and change trend in the pulse wave propagation time measured by the pulse wave propagation time measuring device, and the amount of change and change trend in the hemodynamics measured by the hemodynamics measuring device.

Abstract: A method and apparatus for measuring blood pressure by the oscillometric technique. The method incorporates variable PIP's. The method comprises the steps of obtaining a value for the peak amplitude Amax of an oscillometric envelope; determining a cuff pressure, CP, which corresponds in time with Amax, this pressure representing the MAP of the subject; computing a variable value PIPSBP as a function of MAP; performing the calculation Asbp=Amax*PIPSBP to determine a systolic amplitude value Asbp along the oscillometric envelope; and determining the cuff pressure C which corresponds in time to Asbp, this value representing the systolic blood pressure (SBP) of the subject. PIP can be calculated using a piece-wise linear, polynomial, exponential or other function.

Abstract: A system (1) for measuring blood pressure during a limited number of blood pressure cycles at an area (2) overlying an artery (3) of a living subject, comprising a mechanism (4) for applying a pressure (P) to the artery for occluding artery in response to a pressure signal (Uprise), and for subsequently releasing said pressure to re-open artery in response to a pressure release signal (Uprelease), and a mechanism (11) for computing, by comparing a first time duration (&Dgr;T1) with a second time duration (&Dgr;T2), a delay time (Tdelay1) from a reference point in time after which a next pressure release signal is to be supplied to a mechanism (4) for applying a pressure, and for computing a pressure (P2) to be applied to artery in a next measuring cycle, and for supplying subsequently a pressure signal (Uprise) and a pressure release signal (Uprelease) corresponding to computed pressure (P2) and delay time (Tdelay1) to a mechanism (4) for applying a pressure.

Abstract: Blood pressure of an human being is read by a process that places a cuff around a portion of the human being's body. The cuff is inflated to a predefined pressure which occludes the flow of blood and then the cuff is deflated in a controlled manner. At a plurality of deflation pressure levels, pressure oscillations that occur in the cuff are measured to produce a series of measurements representing the waveform of the oscillations. The systolic pressure and mean arterial pressure are derived from the measurements in conventional manners. A portion of the waveform for one cardiac cycle is analyzed by locating points which correspond to the occurrence of the systolic and mean arterial pressures. The diastolic pressure, which occurs at the minimum point of the waveform, is derived from those points and the systolic and mean arterial pressures.

Abstract: A blood pressure measurement device and associated operating method utilize a measurement algorithm based on a plurality of measurements, supplying a unique ability to increase diagnostic and analytical success in detection. In an illustrative implementation, three measurement techniques are used in combination to improve overall measurement accuracy. A first of the three techniques is an ascultatory technique. A sound measurement acquired from a microphone located in the measurement cuff detects start and end Korotkoff sounds using a combination of filters. The auscultatory technique is a conventional method that is recommended by the American Heart Association and is similar to manual techniques used by a nurse or technician. The auscultatory technique and associated filtering techniques are well known by those having ordinary skill in the art. A second technique is an oscillometric technique that is commonly found in many low-cost blood pressure measurement devices.

Abstract: A blood-circulation monitor including a heartbeat-synchronous-wave sensor, a first judging device for judging whether an arrhythmia has occurred to a living subject, based on a heartbeat-synchronous wave detected by the sensor, a first determining device including a cuff and determining a first blood pressure of the subject based on a first pulse wave produced in the cuff, an information obtaining device for iteratively obtaining a piece of blood-pressure-relating information which changes in relation with blood pressure of the subject, a relationship determining device for determining a relationship between blood pressure and blood-pressure-relating information, a second determining device for iteratively determining, according to the relationship, a second blood pressure of the subject based on each of the pieces of blood-pressure-relating information, a calculating device for calculating a change value of the second blood pressure values, and a second judging device for judging that the condition of blood

Abstract: A blood pressure measuring device is operatable in a first operating mode (M1) and in a second operating mode (M2). In the first operating mode, blood pressure values are based on one single measurement. In a second operating mode (M2), a mean value (SA, DA) of the systolic and the diastolic blood pressure is calculated on the basis of subsequent measurement values. The blood pressure monitor (1) is provided with means (2) for switching between the first operating mode (M1) and the second operating mode (M2).

Abstract: Blood pressure of an human being is read by a process that places a cuff around a portion of the human being's body. The cuff is inflated to a predefined pressure which occludes the flood of blood and then the cuff is deflated in a controlled manner. At a plurality of deflation pressure levels, pressure pulses that occur in the cuff are integrated to produce a plurality of integral values. A diastolic pressure of the human being is derived in response to the deflation pressure level at which occurred the integral value that is greatest in magnitude.

Abstract: An inflatable cuff for being wound and inflated around a body portion pressing a body portion of a living subject to press the body portion in measuring a blood pressure of the subject, the cuff comprising: an inflatable bag which is located in a portion of the cuff in a lengthwise direction thereof and a connector which is attached to a portion of the inflatable bag that is distant, by a predetermined distance, from a distal end of the cuff in a widthwise direction thereof, and which is adapted to connect the inflatable bag to a gas-supply pipe to supply a pressurized gas from the pipe to the inflatable bag.

Abstract: A method for measuring systolic blood pressure includes raising the cuff pressure in such a manner that two conditions are satisfied: (1) The cuff air pressure takes sufficient time to reach the SBP value to avoid blood pressure in the arteries under the PPG sensor being too low, thereby avoiding collapse of the arterioles under the PPG sensor; and (2) The increase of the cuff air pressure between the DBP value and the SBP value is not overly slow in a manner which would cause a relatively high mean blood pressure in the arteries distal to the cuff, and could lead to reduced sensitivity in detecting the restart of blood flow when the cuff air pressure decreases to just below SBP value.

Abstract: An apparatus for automatically measuring a blood pressure of a living subject, including an inflatable cuff which is adapted to be wound around a portion of the subject, an increase-end-pressure determining device for determining, based on a cuff pulse wave occurring to the cuff when a pressure in the cuff is increased at a first rate, an increase-end pressure to which the pressure of the cuff is increased at the first rate, at which the increasing of the pressure of the cuff is ended, and from which the pressure of the cuff is decreased at a second rate lower than the first rate, and a blood-pressure determining device for determining a blood pressure of the subject based on a physical signal obtained from the subject when the pressure of the cuff is decreased at the second rate from the increase-end pressure.

Abstract: An apparatus for measuring a systolic blood pressure of a living subject, including an inflatable cuff which is adapted to be wound around a body portion of the subject and includes a first inflatable bag which is inflatable to press an artery of the body portion, a first amplitude determining device for determining a first amplitude of each of a plurality of heartbeat-synchronous pulses of a first pulse wave which is produced in the first inflatable bag when a pressure in the first bag is changed, a pulse-wave detecting device which detects a second pulse wave which propagates from the artery to a downstream-side portion of the cuff as seen in a blood-flow direction in which blood flows in the artery, a second amplitude determining device for determining a second amplitude of each of a plurality of heartbeat-synchronous pulses of the second pulse wave which is detected by the pulse-wave detecting device when the pressure of the first inflatable bag is changed, a ratio calculating device for calculating a rat

Abstract: In a device or in a method for oscillometric measurement of the blood pressure, the pulse time differences are determined associated with the measurement of the blood pressure. Subsequent pulse time differences are stored in a storing unit (15). A distribution of pulse time differences is calculated in a calculating unit (16) and compared in a comparing unit (17) with predetermined reference values. If the distribution or the values of pulse time differences exceed a predetermined amount, an indication means (19) is activated which indicates existence of arrhythmic activities.

Abstract: An electronic sphygmomanometer starts from pressurization and then enters a decompression process. When measurement of blood pressure starts, only a standard pressure release rate voltage is applied to a valve from a standard pressure release rate voltage supply circuit through a decompression control circuit. The valve allows air to be discharged slowly at the standard pressure release rate. If the pressure release rate should be increased for decompression, target pressure release rate acceleration value voltage according to the position of a dial is supplied from an external control signal supply unit. The standard pressure release rate voltage is added to the target voltage and the resultant voltage is supplied to the valve via the decompression control circuit. The valve increases the pressure release rate by the amount corresponding to the external control signal voltage.

Abstract: A blood-pressure monitor, including a blood-pressure measuring device including a cuff, an information obtaining device which iteratively obtains, from a living subject, physical information which changes with change of blood pressure of the subject, a measurement starting device for starting a measurement of the blood-pressure measuring device, when a subsequent piece of information obtained by the obtaining device after the measuring device has measured a last blood pressure of the subject in a last measurement thereof has been deviated by not less than a predetermined amount from an initial piece of information obtained by the obtaining device when the measuring device measured the last blood pressure of the subject, a display device which displays a graph representing the pieces of information obtained by the obtaining device, and a control device which controls the display device to display the graph representing the initial piece of information and each one of subsequent pieces of information iterativel

Abstract: A blood-pressure monitoring apparatus including an inflatable cuff adapted to apply a pressing pressure to a body portion of a living subject, a cuff-pulse-wave detecting device which detects a cuff pulse wave which is produced in the inflatable cuff when the cuff applies the pressing pressure to the body portion of the subject, a pressure control device which increases the pressing pressure of the inflatable cuff to a predetermined value lower than a mean blood-pressure value of the subject, an index-value calculating device for iteratively calculating an index value indicative of a condition of a circulatory system of the living subject, a starting device for judging whether each of the index values calculated by the index-value calculating device is abnormal and, when the each index value is judged as being abnormal, starting the pressure control device to increase the pressing pressure of the cuff to the predetermined value, and an abnormality judging device for judging whether the subject has an abnormal

Abstract: A blood-pressure measurement system accurately monitors a living subject's cardiovascular state, even if the living subject's blood pressure changes during a measurement, the living subject exhibits frequent arrhythmias, or motion artifacts are present during the blood-pressure measurement. The blood-pressure measurement system of this invention provides an arrhythmia-pulse correcting circuit that corrects the amplitudes of oscillometric pulses produced by arrhythmias. An oscillometric-systolic-pressure correcting circuit corrects the measured systolic oscillometric blood pressure when a living subject's blood pressure is changing during the oscillometric blood-pressure measurement.

Abstract: A blood pressure measurement of a blood pressure measuring device is terminated by a blood pressure measurement terminating device, when a difference .vertline.D.sub.M -D.sub.CP .vertline./D.sub.CP between a phase difference D.sub.M obtained according to a phase difference-blood pressure relationship based on a monitor blood pressure value MBP determined by a monitor blood pressure determining device, and an actual phase difference D.sub.CP obtained by a phase difference calculating device, when the blood pressure measurement of the blood pressure measuring device starts, is smaller than a reference value .alpha.. Thus, so long as the pressure pulse wave-blood pressure relationship is effectively applicable, no blood pressure measurement is carried out for updating the current pressure pulse wave-blood pressure relationship, so that the frequency of blood pressure measurements using a cuff is decreased and the discomfort of a living subject is reduced.