Abstract:
A method and apparatus for improving the calculation of oxygen saturation by non-invasive pulse oximeters during transient conditions. Transient conditions introduce artifactual errors into the detected optical signal because of changes in transmittance of the light with localized blood volume changes and as the average background oxygen saturation level of the patient's blood changes. The invention relates to correcting the detected optical pulses by selective frequency filtering and compensating the detected optical signal using the filtered signal to provide accurate estimates of oxygen saturation during transient conditions.
Abstract:
@ A pulse oximeter is disclosed of the type wherein light of two different wavelengths is passed through human or animal body tissue, such as a finger, an ear, the nasal septum or the scalp, so as to be modulated by the pulsatile component of arterial blood therein, and thereby allowing indication of oxygen saturation. The level of incident light is continually adjusted for optimal detection of the pulsatile component, while permitting accommodation to variable attenuations due to skin color, flesh thickness and other invariants. At significant slope reversal of the pulsatile component to negative (indicating a wave maximum), wave form analysis of blood flow occurs. A quotient of the pulsatile component of light transmission over the constant component of light transmission is measured for each of two wave lengths by direct digital tracking. The respective quotients are thereafter converted to a ratio, which ratio may be thereafter fitted to a curve of independently derived of oxygen saturation. Calibration is disclosed by solving four unknowns at at least four differing saturations. An output of pulse rate, pulse flow and oxygen saturation is given. An incident light source duty cycle is chosen to be at least 1 in 4 so that noise, inevitably present in the signal, may be substantially eliminated and filtered. Provision is made for a local battery-driven low power consumption instrument capable of being substantially independent of ambient light noise.
Abstract:
The present invention provides a method and apparatus for adapting to noise sources affecting a pulse oximeter. Various available frequencies are evaluated to determine their respective noise levels and one is selected to act as the operating demultiplexer frequency. During normal operation of the pulse oximeter, the various available demultiplexer frequencies are periodically scanned to determine which has the lowest associated noise. The noise level associated with the operating frequency is used to determine the signal-to-noise ratio of the pulse oximeter signals and thereby qualify certain signals from the pulse oximeter. Those pulses associated with a signal-to-noise ratio below a predetermined threshold are rejected and excluded from use in calculating blood oxygen saturation.
Abstract:
An object of the invention is to display target data in modes different from one another. Such an arrangement is adopted that a multi-color display section (1) capable of displaying in at least two colors is provided, and a color and a state (on/off) of a light are selected in accordance with examination and treatment data to be displayed. According to the present invention, by use of the combinations of a color and a state of the light, various data can be displayed in modes different from one another, so that displayed meanings and details can be identified at a glance.
Abstract:
A sensor placement and retention mechanism for use with fetal sensor sites beyond the user's reach are disclosed. The preferred embodiment of this invention is a fetal pulse oximetry sensor (2,200) having an active face (4) through which a light source (6) and a light detector (8) operate. The sensor includes a handle (15) that facilitates placement of the active face at a sensor site in a preferred region beyond the transcervical region and beyond the reach of the user. A pair of electrodes (210,212)--one disposed against the fetus' skin (211) and one exposed to the amniotic fluid--are used to confirm that the sensor is firmly in place on the fetus. In an optional sensor retention feature, a self-inflating bladder (40) presses the active face of the sensor against the fetus' skin to optically couple the sensor with the tissue at the sensor site.
Abstract:
A CO₂ monitor which has a reusable portion and a disposable portion is disclosed. The disposable portion includes an airway sensor (4) for connecting between a ventilator output and an endotracheal tube. The airway sensor has ports (16,18) on opposite sides. In one port (16) a disposable infrared light source (20) is inserted with wire contacts extending to the exterior of the airway sensor body. The reusable portion is a detector module (6) which includes a detector (24) and an amplifier. The detector module attaches to the airway sensor so that the detector is disposed in the second port (18) and so that contacts in the detector module communicate with the wire contacts of the light source. The detector module may be removed from the airway sensor without removing the light source from the airway sensor.
Abstract:
A sensor placement and retention mechanism for use with fetal sensor sites beyond the user's reach are disclosed. The preferred embodiment of this invention is a fetal pulse oximetry sensor (2,200) having an active face (4) through which a light source (6) and a light detector (8) operate. The sensor includes a handle (15) that facilitates placement of the active face at a sensor site in a preferred region beyond the transcervical region and beyond the reach of the user. A pair of electrodes (210,212)--one disposed against the fetus' skin (211) and one exposed to the amniotic fluid--are used to confirm that the sensor is firmly in place on the fetus. In an optional sensor retention feature, a self-inflating bladder (40) presses the active face of the sensor against the fetus' skin to optically couple the sensor with the tissue at the sensor site.
Abstract:
A gas analyzer airway adapter (12) that permits insertion of a suction tube (22) into the patient without removal of the airway adapter (12) from the patient. The adapter body has three ports. A patient port (30) is formed in the main section of the adapter body and has a fitting that attaches to the endotracheal tube (10). A sample port (34) is formed in a smaller diameter passage extending from the main body and attaches to the sample intake of a gas analyzer (14). The central axis of the smaller diameter passage is preferably parallel to the central axis of the main body of the adapter (12). Finally, a ventilator port (32) is formed in a passage whose central axis extends at approximately a 31 degree angle from the central axis of the main body. A hub/filter (36) assembly is disposed in the smaller diameter passage of the airway adapter (12), and a longitudinal filter (36) extends into the main body of the adapter (12). A tube guide (42) is disposed below the filter (36) within the main body of the adapter (12). The purpose of the guide (42) is to protect the longitudinal filter (36) and to direct the movement of the suction tube (22) as discussed below.
Abstract:
Un appareil de mesure des caractéristiques de la circulation sanguine de foetus comprend une sonde oxymétrique non invasive (100; 700; 800; 900) de détection du pouls qui est insérée dans l'utérus, entre le foetus et la paroi utérine. La sonde est déformable et positivement fixée à la surface du tissu foetal au moyen d'une pompe à vide qui déforme la sonde, modifiant sa courbure initiale de façon à l'adapter à la courbure de la surface du tissu foetal et à former une liaison étanche (122; 712; 826; 922) avec la surface du tissu foetal. On insère manuellement la sonde dans l'utérus au moyen d'un outil d'insertion courbe (400). La forme de la sonde est telle que la sonde passe à travers un col légèrement dilaté. Dans un mode préférentiel de réalisation, la sonde comprend des capteurs électrocardiographiques (702, 720; 806, 802) de la mère et du foetus et des dispositifs additionnels de détection (704, 706, 818, 820). La sonde est également pourvue d'appareils (902, 904) qui améliorent l'efficacité des éléments optiques de détection oxymétrique du pouls.
Abstract:
A pulse oximeter wherein light of two different wavelengths is passed through body tissue, such as a finger, an ear or the scalp, so as to be modulated by the pulsatile component of arterial blood therein and thereby indicate oxygen saturation. A tonal signal is emitted having a pitch proportional to the ratio of oxygen saturation and a sequential repetition proportional to pulse. A visual cue consisting of an array of strobed light emitting diodes is flashed having a total light output proportional to the magnitude of the pulse and a sequential flashing rate proportional to pulse rate. A systematic rejection of extraneous or irregular detected data prevents undue sounding of alarms.