Abstract:
The invention relates to a water separator for a gas analyzer, comprising a tube (12) for passing a gas sample into the water separator, wherein water separation is effected in a tubular passage by dividing the flow into two partial flows. The wall or walls (3) of a first tubular passage (17) are made of a porous material, readily permeable to gas, and this main flow, which has penetrated the wall, is passed into a second tubular passage (4) and via a tube (10) on to measuring sensors (5 and 6) but the water, which is not able to penetrate the porous wall of first passage (17), is passed along with a minor amount of gas down a passage (17, 13) into a water receiver (15) and this many times lesser side flow further via a tube (14) into a third tubular passage (16), through its porous wall (3) into a fourth tubular passage (18) and via a tube (11) through a flow throttle (7) on to a pump (8).
Abstract:
The invention relates to a pressure control system and apparatus for the cuff of an automatic blood pressure meter. Pressure reduction is adapted to be effected by using at least two constrictions (3) having a constant constriction, the selection and combination of such constrictions being performed by digitally controlled magnetic valves (4). Such magnetic valves are controlled by a microprocessor (6) depending on a measuring value provided by a sensor (7) for measuring the cuff pressure transition rate so as to obtain a desired, approximately linear rate of pressure reduction. The constrictors (3) comprise thin flexible tubes. The system is capable of compensating automatically for the changes caused in the desired volume air flow by the cuff size and tightness, variations in the circumference of a person's arm, the heartbeat density and pressure range.
Abstract:
The invention relates to a method of recovering nuclear spin or NMR information about a target, such as a human body placed in at least substantially homogenous magnetic field, a desired part of the target being excited by means of a radiofrequency magnetic field which preferably deviates nuclear magnetization through 90.degree., a so-called spin echo is generated by utilizing a second excitation of the target volume which preferably deviates nuclear magnetization through 180.degree., said spin echo is recorded and said excitation sequence is repeated. At least one magnetic field is applied to the target in a manner that the duration and/or amplitude of said magnetic field gradient are varied between various repetitions, so that the difference between the absolute values of time integral of a value following said 180.degree. pulse and a value preceding said 180.degree. pulse of said magnetic field gradient obtains a different value. This way, the use of bipolar current sources is avoided. The invention is well adaptable to recovering information quickly especially about a plurality of image planes from a three-dimensional target.
Abstract:
The invention relates to a method for monitoring a condition of a patient under anesthesia or sedation, whereupon one, two, three or more signals are acquired, and the signal(s) represent(s) cardiovascular and/or combined electrical biopotential on skull activity of the patient. From said signal or signals are derived or calculated at least two parameter values related to a quantity like waveform amplitude, waveform periodicity, waveform morphology, waveform variability, energy, power, signal complexity and frequency content. A predetermined mathematical index for probability of patient comfort is used, in which function said parameters are variables, and successively changing probability index values of said mathematical index is calculated.
Abstract:
The invention relates to a method and apparatus for predicting a sudden heart abnormality for an individual patient. In order to provide a prediction mechanism that is suitable for acute care, three sub-indices are determined based on medical data obtained from the patient. The first sub-index indicates the level of deterministic chaos in the heart rate variability of the patient, the second sub-index indicates the energy level in the myocardium of the patient, and the third sub-index indicates the degree of ventricular arrhythmia of the patient. Based on the first, second, and third sub-indices, at least one overall risk index is then determined, the overall risk index indicating the risk level of a sudden heart abnormality for the patient.
Abstract:
A method for non-invasively determining functional cardiac output (FCO) and/or venous blood CO2 partial pressure (PvCO2). The amount of CO2 (VCO2N) released from the blood and end capillary blood CO2 content (CcCO2N) are determined from measurements from exhaled breathing gases. The CO2 content of the breathing gases inhaled by the subject is increased and values for VCO2R and CcCO2R are obtained. A regression analysis is performed using the obtained VCO2N, VO2R, CcCO2N, and CcCO2R values. The regression line is extrapolated to obtain a value for CcCO2 when (VCO2) is zero so that CvCO2 becomes known. The CvCO2 thus determined can be inserted in a non-differential form in the Fick equation, along with VCO2 and CcCO2 values from normal breathing, to determine FCO. To determine PvCO2, CvCO2 is altered in accordance with the amount of oxygen in the venous blood, to correctly indicate PvCO2. The continuing validity of the FCO measurement can be examined on a breath-by-breath basis by noting changes in an indicator variable, such as VCO2 or end tidal CO2 amounts.
Abstract:
The invention concerns a gas analyzer comprising: a measuring volume (2), a radiation source (1) for providing a beam to pass said measuring volume; a heat sink (16) for said radiation source; at least one thermal detector (3) having a hot junction within a support structure and receiving the radiation and a cold junction for reference within the same support structure and protected from said radiation; at least one optical bandpass filter (9) between said hot junction and said radiation source; and a thermal mass (11), which is formed of a material having high thermal conductance. The thermal mass has a cavity with a bottom step (34) and a rim (32), and a first length therebetween. The support structure has a frontal edge (35) and a base plate lip (33), and a second length therebetween. There is a radial gap between the thermal mass and the support structure. Press means urge said support structure in the cavity, whereupon a more efficient thermal contact is either between said frontal edge and said bottom step, or between said base plate lip and said rim. A first thermal barrier (17) is between the heat sink and the thermal mass, and a second thermal barrier (22) surrounds the thermal mass. A shield (19) formed of a material having high thermal conductance covers said second thermal barrier and is in thermal contact with said heat sink.
Abstract:
A medical X-ray device 5 arrangement for producing three-dimensional information of an object 4 in a medical X-ray imaging comprises an X-ray source 2 for X-radiating the object from at least two different directions; a detector 6 for detecting the X-radiation to form projection data of the object 4; a computational device 15 for modelling the object 4 mathematically utilizing the projection data to solve the imaging geometry and/or the motion of the object, where the solving concerns either some or all parts of the imaging geometry and/or the motion of the object. The computational device 15 utilizes said projection data and said mathematical modelling of the object in Bayesian inversion based on Bayes' formula p ( x , θ ❘ m ) = p pr ( θ ) p pr ( x ) p ( m ❘ x , θ ) p ( m ) to produce three-dimensional information of the object.
Abstract:
A position-independent fluid trap for separating at least a portion of a first fluid of a first density entrained within a flow stream of a second fluid of a second density flowing through a fluid circuit. The trap is connectable within the fluid circuit to a first length of tubing defining an inlet line and to a second length of tubing defining an outlet line, and includes a housing enclosing an interior chamber having a geometric extent of a given volumetric capacity. An inlet port is provided to open in fluid communication with the interior chamber and to be couplable to the inlet line. An outlet tube is provided to extend from a proximal end couplable to the outlet line to a distal end disposed within the housing and opening in fluid communication with the interior chamber. Within the interior chamber, the first and second fluid are separated at an interface into a first and second fluid component according to the relative densities thereof. The outlet line distal end is disposed within the chamber effective to define with respect to the interface a predetermined fill volume of the second fluid maintaining the outlet line distal end within the second fluid component. This fill volume is substantially independent of the orientation of the trap within the fluid circuit.