Abstract: An apparatus (1) and method for detecting pulse-related parameters, such as pulse arrhythmia is presented. The apparatus (1) detects a series of pulses from a user, e.g. through a cuff-related measurement. Time differences, amplitude and pattern differences between multitudes of N pulses are determined. The apparatus investigates the degree of similarity of multiple pulse periods and/or pulse amplitudes and/or pulse pattern and subsequently generates a statistical set of similarity values based on a plurality of compared results. Basing on this, the apparatus generates a decision value based on the statistical sets of similarity values, and uses the decision value to determine whether or not the user discloses a normal pulse rhythm, atrial fibrillation, premature atrial or ventricular contractions, tachycardia, bradycardia and/or unspecified pulse arrhythmia. Further an artefact index is generated, informing the user whether a measurement was taken under sufficient artefact-free measurement conditions.

Abstract: An apparatus (1) and method for detecting pulse-related parameters, such as pulse arrhythmia is presented. The apparatus (1) detects a series of pulses from a user, e.g. through a cuff-related measurement. Time differences, amplitude and pattern differences between multitudes of N pulses are determined. The apparatus investigates the degree of similarity of multiple pulse periods and/or pulse amplitudes and/or pulse pattern and subsequently generates a statistical set of similarity values based on a plurality of compared results. Basing on this, the apparatus generates a decision value based on the statistical sets of similarity values, and uses the decision value to determine whether or not the user discloses a normal pulse rhythm, atrial fibrillation, premature atrial or ventricular contractions, tachycardia, bradycardia and/or unspecified pulse arrhythmia. Further an artefact index is generated, informing the user whether a measurement was taken under sufficient artefact-free measurement conditions.

Abstract: A blood pressure measuring method, according to which a pulse oscillogram of a patient is defined, the blood pressure is then determined from the pulse oscillogram and displayed. Reliable blood pressure values are obtained without additional cost to the user, by obtaining an evaluation criterion for the presence of haemodynamic stability from the individual pulse oscillogram, the determination of the blood pressure value or the determined blood pressure value being related to the criterion.

Abstract: The device serves to optically determine physiological variables in perfused tissue. The device comprises a first and a second light source which each emit light radiation of a first or a second predetermined wavelength. The light sources are arranged in such a manner that the light radiation exiting them can penetrate into the perfused tissue. At least one photodetector is used, which is arranged so that it detects the light emitted by the light sources and passing through or backscattered by the perfused tissue. The device also comprises a control unit, which furnishes control signals to the light sources so that the light sources continuously emit light alternately, one or more dark phases can be inserted into this sequence, during which at least one light source does not emit any light.

Abstract: The method and the device according to the invention are used for the non-invasive measurement of concentrations of blood components. At least one light source generates light using spectrophotometry and the light is guided to at least one photodetector through a tissue present at the location of application and supplied with pulsating blood. At least the measuring signal of the photodetector is guided to an evaluation unit. The light signals of a first, second, third to (n+1)st wavelength are generated at subsequent pairwise times T1 and T2, T3 and T4 and T5 and T6 to Tn and Tn+1. The evaluation unit takes into consideration the received signals of the photodetector for all wavelengths according to a defined arithmetic pattern and determines a concentration of the blood component. The inventive device comprises at least three light sources that generate light of different wavelength in relation to each other.

Abstract: A method and a device for the identification of at least one substance of content of a body fluid, wherein adjacent to a body tissue containing the body fluid at least one radiation source and a photo receiver are arranged. The radiation source generates radiation of at least two different wavelengths and the radiation is directed onto the body tissue. The photo receiver receives radiation reflected by the body tissue and/or reduced through the body weight. At least at one point radiation from two radiation sources with an essentially same wavelength is directed essentially simultaneously onto the body tissue for penetration and/or reflection.

Abstract: A method and a device for the identification of at least two substances of content of a body fluid, wherein adjacent to a body tissue containing the body fluid, are arranged at least one radiation source and a photo receiver. The radiation source generates radiation of two different wavelengths. The radiation is directed onto the body tissue and the photo receiver receives radiation reflected by the body tissue and/or reduced through the body tissue. At least at times the radiation of a third wavelength is directed onto the body tissue for the identification of a hemoglobin derivate.

Abstract: A blood pressure measuring method, according to which a pulse oscillogram of a patient is defined, the blood pressure is then determined from the pulse oscillogram and displayed. Reliable blood pressure values are obtained without additional cost to the user, by obtaining an evaluation criterion for the presence of haemodynamic stability from the individual pulse oscillogram, the determination of the blood pressure value or the determined blood pressure value being related to the criterion.

Abstract: A display is connected to at least one sensor for detecting and transmitting physiological measurement values. In addition, one or more displays are used to present the measurement values and/or other associated data visually, acoustically, mechanically, or in some other way perceptible to the senses. A sequence control approach is implemented, according to which the measurement value, before reaching the display, passes through a testing stage, which, on the basis of at least one measured or stored additional value, verifies, checks, or changes the physiological measurement value detected at the sensor or supplements it with additional information. In a process for the noninvasive determination of the oxygen content CaO2 of human and/or animal tissue, the blood oxygen saturation and data on the blood hemoglobin concentration are obtained after the measurements have been acquired by the use of radiation with wavelengths in the range of 400-1,800 nanometers.

Abstract: For detecting and processing a physiological variable, a signal transmitter has devices for processing, using, and/or providing signals, which are generated from measurement values of the physiological variable. In accordance with a sequence control approach, the measurement values are acquired from the detection of electromagnetic waves of different wavelengths. Before the signals are detected, the electromagnetic waves pass through the medium to be examined or are reflected by this medium. For at least a certain percentage of the overall signal quantity, at least two measurement values detected close together in time are used for each generated signal. The signal transmitter is suitable for use in a control circuit, which is designed with an actuator to influence the physiological variable detected instrumentally by the signal transmitter.

Abstract: The method and device serve to measure a proportion of constituents in blood. To this end, electromagnetic radiation of different radiation wavelengths is directed through a tissue (9) containing blood vessels (1). At least a portion of the radiation exiting the vessel is detected using sensors, and a corresponding measured value derived therefrom is fed to an evaluating device. The evaluating device (10) is connected to at least two sensors (2, 3, 4) and has an analyzer (11) for determining a dispersion of radiation by evaluating the intensity of the radiation received by the individual sensors. An individual calibration determination is carried out by evaluating the angle-dependent dispersion and can be drawn upon for conducting a pulse spectroscopic determination of concentrations of substances.

Abstract: By a method to measure the blood pressure of a patient, a series of measurements for the diastolic, the systolic blood pressure and for the pulse rate are made. The results are analysed in order to determine, and to display whether the patient is properly settled to a rest condition, and whether the patients blood pressure variation is found as being normal. Further it is investigated, whether there are high measurement result alterations due to artefacts. Highly altered results are excluded. If the results are sufficiently similar, an average of the result is made. If the results are not sufficiently similar, but still below pre-defined alteration limits, a weighted average is applied to the systolic and the diastolic blood pressure.

Abstract: The method and device serve to measure a proportion of constituents in blood. To this end, electromagnetic radiation of different radiation wavelengths is directed through a tissue (9) containing blood vessels (1). At least a portion of the radiation exiting the vessel is detected using sensors, and a corresponding measured value derived therefrom is fed to an evaluating device. The evaluating device (10) is connected to at least two sensors (2, 3, 4) and has an analyzer (11) for determining a dispersion of radiation by evaluating the intensity of the radiation received by the individual sensors. An individual calibration determination is carried out by evaluating the angle-dependent dispersion and can be drawn upon for conducting a pulse spectroscopic determination of concentrations of substances.

Abstract: By a method to measure the blood pressure of a patient, a series of measurements for the diastolic, the systolic blood pressure and for the pulse rate are made. The results are analysed in order to determine, and to display whether the patient is properly settled to a rest condition, and whether the patients blood pressure variation is found as being normal. Further it is investigated. whether there are high measurement result alterations due to artefacts. Highly altered results are excluded. If the results are sufficiently similar, an average of the result is made. If the results are not sufficiently similar, but still below pre-defined alteration limits, a weighted average is applied to the systolic and the diastolic blood pressure.

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: 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: 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 apparatus (21) which measures the arterial blood pressure at the human wrist (1) is provided with a cuff (22) having a shape adapted to be placed in a predetermined position around the wrist (1). The cuff (22) has one or two inflatable measuring bladders (23a, 23b). The bladders (23a, 23b) are arranged and have a size in such a way that each bladder (23a, 23b) covers only one of either the radial (2) and the ulnar (3) artery.

Abstract: A method is proposed for determining the perfusion by evaluation of the light emitted by at least one light source and influenced by the arterial blood, by use of optical measuring means which measure the intensity variation as a consequence of the variation in arterial blood volume. According to this method, the perfusion is either displayed as variation in thickness from the sum of the parallel tissue enlargements d or as normalized volume. The perfusion is derived by one or more measurements of light intensity. According to the invention, for the first time a method for determining perfusion as a quantitative value is provided.