65 results about "Pulse oximetry" patented technology

A pulse oximetry system includes a wrist portion configured for placement on a wrist of a subject, the wrist portion having a first component and a second component configured to removably secure to one another. The wrist portion can include emitter(s) and detector(s) operably positioned by the wrist portion. In some implementations, the pulse oximetry system further includes a ring member configured to secure around the subject's finger and operably position emitter(s) and detector(s) and a cable connected to the wrist portion in electrical communication with the emitter(s) and the detector(s) of the ring member and configured to transmit the signal(s) from the detector(s) to the wrist portion. The system includes a battery and hardware processor(s) configured to receive and process signal(s) outputted by the detector(s) to determine physiological parameter(s) of the subject.

A wearable system can include an electronic device configured to measure one or more physiological parameters of a patient and a wearable device configured to operably position the electronic device. The electronic device can have at least one light emitter and at least one light detector and be configured to measure at least a pulse oximetry measurement. The wearable device can have a main body with a cavity configured to position the electronic device, a securement portion connected to the main body and configured to secure the main body to the patient, and storage component configured to store patient identification data associated with the patient. When the electronic device and the wearable device are secured to one another, the patient identification data can be transferred from the wearable device to the electronic device.

A medical monitoring system comprises a wearable garment incorporating multiple physiological sensors for real-time patient monitoring. The garment integrates an embedded processing unit that receives sensor data and transmits it wirelessly to a base station or remote server. A multi-modal physiological signal processing unit analyses the data to generate composite physiological indices, including metabolic rate, work of breathing, and fall risk assessments. The garment includes optional monitoring features such as transcutaneous carbon dioxide measurement, electrocardiography, pulse oximetry, blood pressure monitoring, and accelerometer - gyroscope-based motion tracking. The system provides early-warning alerts for clinical deterioration, enabling proactive therapeutic interventions. A wireless communication module ensures real-time data transmission, supporting remote monitoring and integration with hospital networks. The garment's modular design allows for non-invasive physiological assessment while maintaining patient mobility, making it suitable for critical care, ambulatory monitoring, and telemedicine applications.

An Adaptive Neuro-Fuzzy Inference System (ANFIS) for total intravenous anesthesia management is disclosed, enabling control over administration of anesthetic agents and dynamic adjustment according to patient physiological feedback. The system processes patient data, including processed EEG signals, hemodynamic information, capnography, and pulse oximetry, to facilitate real-time anesthetic dosage adjustments.

Existing pulse oximeters have impaired accuracy in measuring blood oxygen levels (SpO2) in patients of color, where the presence of melanin in the skin tends to interfere with measurements of pulse oximetry, resulting in an overestimation of SpO2. Thus, the pulse oximeter often reports a higher oxygen saturation for patients with darker skin tones, often with increasing bias as the actual saturation (SaO2) decreases. This bias is further reinforced by calibration based on individuals with light skin pigmentation, which may lead to inequitable healthcare for patients of color. Our proposed solution is to modify current pulse oximetry calculations—which utilize the relative tissue absorbance of red and infrared light to estimate SpO2—to account for the concentration of melanin by additionally measuring the skin absorbance of UV˜A light. This derived concentration of melanin can then be used to modify the pulse oximetry algorithm output, thus estimating SpO2 more accurately for patients of color.

1. The name of the design product: palm type pulse oximeter. 2. The use of the design product: for measuring the blood oxygen value of human body. 3. The design points of the design product: in the combination of shape, pattern and color. 4. The picture or photo that best shows the design points: front view. 5. The design claimed contains color.

A system for identifying, monitoring the health of an individual and providing for the retrieval of information relating to said individual by a plurality of authorized users. The system comprises an identification device and associated hardware and software components. The identification device a skin wearable, waterproof, non-transferable frangible individual identification device comprising (1) an adhesive and marking arranged on a substrate to provide a physiologically perceptible, humanly understandable information related to said individual, and (2) an electronic device having wireless communication capability with the ability to send, receive, and store information, wherein electronic device comprises at least one sensor for taking vital sign data, wherein once applied to skin, removal of the individual renders the identification device inoperable wherein the marking, substrate, and adhesive are biocompatible. The associated hardware includes a plurality of receivers; a computer interface device receiving information from said individual identification device and from said receivers respecting the individual identified by said individual identification device; a computer system coupled to said computer interface device, said computer system including a memory with an algorithm for processing information collected by said computer system; and a separate set of receivers and a separate service rendering system, each output information from their respective receivers to a common database, the contents of said common database being coupled to a computing device which communicates information to and from a central server. In a preferred embodiment, the identification device is a Bluetooth compatible, battery powered, identification and monitoring device measuring temperature, pulse oximetry and heart rate.

The present specification describes a system and method of detecting sleep disordered breathing, that includes acquiring a set of unconditioned sleep test data that includes oximetry data and at least one other physiological sensor data; sampling the set of unconditioned sleep test data; storing the sampled set of unconditioned sleep test data; receiving, through a display, an input indicative of a degree of analyzing to be applied to the sampled set of unconditioned sleep test data; based on said input, applying a corresponding degree of analyzing to the unprocessed sleep test data to generate processed sleep test data; and visually displaying the processed sleep test data.

The utility model relates to a pulse oxyhemoglobin saturation sensor with a current-limiting protection device. The pulse oxyhemoglobin saturation sensor solves the problem that in the prior art, fluctuation of power supply current of a pulse oxyhemoglobin saturation sensor easily affects detection data, and consequently the accuracy of the detection data is reduced. The device comprises a connecting plug, one end of the connecting plug is connected with a monitor for data transmission and power supply transmission, the other end of the connecting plug is connected with a data detection mechanism through a transmission cable, the transmission cable passes through an insulation sleeve structure, and a current limiting protection mechanism used for adjusting current and controlling data transmission is arranged on the circumferential inner side of the insulation sleeve structure. The utility model has the advantages that power supply lines can be quickly switched according to the magnitude of current, the fluctuation adjustment of the current is realized, the accuracy of detection data is ensured, a data transmission line can be replaced when the power supply lines are switched, and the continuity of data transmission is ensured.

A body-worn patch sensor for simultaneously measuring a blood pressure (BP), pulse oximetry (SpO2), and other vital signs and hemodynamic parameters from a patient featuring a sensing portion having a flexible housing that is worn entirely on the patient's chest and encloses a battery, wireless transmitter, and all the sensor's sensing and electronic components. It measures electrocardiogram (ECG), impedance plethysmogram (IPG), photoplethysmogram (PPG), and phonocardiogram (PCG) waveforms, and collectively processes these to determine the vital signs and hemodynamic parameters. The sensor that measures PPG waveforms also includes a heating element to increase perfusion of tissue on the chest.

The invention provides a pulse oxyhemoglobin saturation detection method and system, and the method comprises the steps: receiving an optical signal transmitted to the surface of a light receiving tube through the light receiving tube when the light receiving tube generates red light, converting the optical signal into a first receiving electric signal, and forming a red light sampling channel; when a light receiving tube generates the infrared light, receiving a light signal emitted to the surface of the light receiving tube and converting the light signal into a second receiving electric signal to form an infrared light sampling channel; detecting the first receiving electric signal in real time, identifying the driving output change of the red light emitting tube, and outputting a first signal status bit; the change of the detection rate of the pulse wave is judged based on the signal status bit, and when the detection rate of the pulse wave is increased, the output blood oxygen saturation value is calculated according to the first receiving electric signal and the second receiving electric signal. Comprehensive analysis is carried out in time according to the blood oxygen sampling signal and / or the driving current adjusting state so as to judge and determine whether a suspected non-physiological state mark exists or not.

A system and method to help maintain quality control and reduce cannibalization of accessories and attached probes in a highly sensitive patient monitor, such as a pulse oximetry system. One or more attached components may have information elements designed to designate what quality control mechanisms a patient monitor should look to find on that or another component or designate other components with which the one component may properly work. In a further embodiment, such information elements may also include data indicating the appropriate life of the component.

A wearable system can include an electronic device configured to measure one or more physiological parameters of a patient and a wearable device configured to operably position the electronic device. The electronic device can have at least one light emitter and at least one light detector and be configured to measure at least a pulse oximetry measurement. The wearable device can have a main body with a cavity configured to position the electronic device, a securement portion connected to the main body and configured to secure the main body to the patient, and storage component configured to store patient identification data associated with the patient. When the electronic device and the wearable device are secured to one another, the patient identification data can be transferred from the wearable device to the electronic device.

The present invention is an in vivo non-invasive method and apparatus for the measurement of the arterial blood oxygen saturation status of a patient, the method is a generalized improvement on conventional pulse oximetry to correct for its skin pigmentation bias and significant errors in oxygen saturation assessment in the presence of methemoglobin. The method requires an additional red light sensor with an infrared long pass filter to conventional pulse oximetry, and utilizes red and infrared light and sensors to non-invasively measure the peripheral pulse optical plethysmograph waveforms (PPG) at three light wavelengths, red, long pass red and infrared, positioned over a finger, or ear or other extremity, and from the pulse oximetric ratio of ratios transforms the PPG measurements by a processing device that determines the subject's arterial blood oxygen saturation directly, without the need for an empirical correction as is required in conventional pulse oximetry. The method determines the red transmitted light waveform and thus quantifies the wavelength shift from the incident red light due to the subject's skin pigmentation, and from in vivo hemoglobin extinction coefficients, determines the relative concentrations of oxygenated and deoxygenated hemoglobin and methemoglobin in the subject's arterial blood.

A system and method for monitoring a patient's blood flow waveform require a pulse oximeter to non-invasively measure changes in parametric and blood flow measurements of the waveform. These parametric measurements, namely changes in diastolic pressure, ±Δpd, changes in systolic pressure, ±Δps, and changes in pulse time rate, ±Δtr, collectively affect the patient's blood flow volume. Thus, they can also be used, collectively, to assess the patient's heart muscle function as an indicator of his / her health condition.

The present application relates to the technical field of blood oxygen detection, and more particularly to a pulse blood oxygen saturation detection method based on image processing, which introduces a transfer learning strategy and a domain adaptation network, can be adjusted according to the individual physiological parameters of the user, thereby improving the applicability to different populations. In particular for dark-skinned population, the present application significantly reduces the measurement error, reduces the error rate by more than 30%. The present application designs a set of real-time calculation mechanism of current signal quality index Q, and combines the Bayesian filtering model for dynamic calibration, so as to ensure that reliable blood oxygen saturation estimation value can be obtained even under low signal-to-noise ratio condition. When the signal quality decreases, the historical data is compensated for the current detection value through the LSTM network prediction module, so as to further ensure the accuracy and continuity of the result.

The direct insertion type pulse blood oxygen probe comprises a base, a cover plate is movably installed above the base, a movable rod is movably installed above the base, a rotating rod is movably installed on the surface of one side of the base in an embedded mode, a gear plate is movably installed in the base, and a gear is fixedly installed at the position, close to one end, of the surface of the rotating rod. A rubber plug is movably embedded in one end of the movable rod, a communication line is fixedly embedded in the outer side surface of the cover plate, a lantern ring is fixedly installed on the lower surface of the cover plate, circular rings are fixedly installed on the positions, close to the two sides, of the upper surface of the base, and the movable rod is inserted into the lantern ring and the circular rings in a penetrating mode. And the connecting rod is movably connected with the lantern ring and the circular ring. According to the direct insertion type pulse blood oxygen probe, when a finger is clamped by the probe, the clamping range of the probe can be adjusted according to the thickness of the finger, the comfort degree of the probe is improved, and the spring is convenient to disassemble and replace.

An emergency medical kit may comprise a main body with multiple compartments. A fabric panel may be attached to the main body. The fabric panel may include horizontal and vertical straps forming a grid pattern. The fabric panel may have attachment points for securing medical supplies. A removable medication pack containing pre-selected medications may be included. A removable wound cleaning pack with treatment supplies may also be provided. The kit may further include items like a blood pressure cuff, stethoscope, tourniquet, trauma shears, and pulse oximeter. The fabric panel may have a mesh pocket with a zipper. The main body may open in a T-shaped layout. Elastic bands may secure additional supplies. The grid pattern may comprise a MOLLE system. A medical bag component with a mesh pocket and logo may attach to the main body.

An AI-driven medical intake assistant system includes a computing device having a processor and memory configured to execute an intake module, an abnormality detection module, and an electronic health record (EHR) integration module. The intake module presents a conversational interface that dynamically selects patient intake questions using a rule-based branching decision tree with clinical topic tags and transition rules. One or more connected diagnostic devices automatically capture patient vital sign measurements, including blood pressure, temperature, pulse oximetry, or weight, and transmit the measurements to the computing device. The abnormality detection module compares captured measurements to predefined threshold values or historical baseline data retrieved from the EHR and generates provider-facing alerts when deviation thresholds are exceeded. The EHR integration module maps patient responses and vital sign measurements into predefined structured EHR fields prior to a provider consultation.

The utility model discloses belong to the blood oxygen saturation sensor technical field, concretely is an improved pulse blood oxygen saturation sensor, including saturation sensor body, the saturation sensor body includes two transmitting light sources and photoelectric detector, the saturation sensor body bottom is set with first annular groove and second annular groove, the first annular groove is installed with rubber ring, the second annular groove is installed with heating ring, through the magic tape, through -hole and rubber ring that set up on the fixing band, can improve the stability of saturation sensor wearing, and improve the comfort degree when wearing, and the user can adjust the tightness of wearing according to own condition through the magic tape that set up on the fixing band, will not cause the saturation sensor wearing too tight or too loose, through the through -hole can with the skin of user's medical adhesive tape is bonded, further improve the stability of saturation sensor wearing, to guarantee the accuracy of data when detecting.

A method for estimating a metabolic rate of a user includes obtaining pulse oximetry data for the user for a period of time. The method includes determining a rate of decline in oxygen saturation of blood of the user that is associated with a breathing rate of the user for the period of time based, at least in part, on the pulse oximetry data. The method includes estimating the metabolic rate of the user for the period of time based, at least in part, on the rate of decline in the oxygen saturation of the blood that is associated with the breathing rate of the user. The method includes providing a notification indicative of the metabolic rate for the period of time.

The utility model discloses an oximeter probe performance testing device in the technical field of oximeters, which comprises a shell, one end of the shell is uniformly and fixedly connected with a plurality of simulation components, the inner wall of the shell is provided with an inner cavity, the inner walls of the two ends of the inner cavity are fixedly connected with liquid storage tanks, and the inner walls of the two liquid storage tanks are provided with liquid storage cavities. The two liquid storage cavities are filled with blood simulation liquid, the inner walls of the two liquid storage cavities are fixedly connected with an oxygenation pump, the end, close to the oxygenation pump, of each liquid storage cavity is fixedly connected with a conveying pump, and the end, close to the conveying pump, of each liquid storage cavity is fixedly connected with an electric heating block. By means of the liquid storage cavity filled with the blood simulation liquid and the skin simulation layer, the real human body environment and the blood oxygen measurement scene can be simulated, and therefore the accuracy and reliability of testing are improved. The oxygen content and the temperature of the blood simulation liquid can be automatically adjusted by utilizing the oxygen increasing pump, the conveying pump, the electric heating block and other components, different physiological states are rapidly simulated, and efficient testing is achieved.

This invention relates to the field of sleep monitoring data fusion processing technology, and discloses a sleep monitoring method based on the fusion of non-invasive brain oxygen saturation (AHI) and multiple physiological parameters. The method includes: S1, simultaneously acquiring multiple physiological parameter signals during the subject's sleep; S2, extracting and analyzing the AHI signal to generate multiple characterization markers; S3, identifying respiratory events related to the subject's apnea information from the respiratory signal and pulse oximetry signal, calculating the apnea-hypopnea index (AHI); and performing correlation analysis on the identified respiratory events and multiple characterization markers to calculate a correlation coefficient; S4, obtaining a comprehensive sleep monitoring assessment report based on the correlation coefficient and the AHI to determine the severity of the subject's current respiratory disturbance and the risk of brain tissue hypoxia. By improving the effectiveness of AHI in non-invasive brain oxygen saturation monitoring, the confirmatory nature of non-invasive brain oxygen saturation information in the respiratory correlation diagnosis during sleep monitoring is ensured.

The utility model provides a kind of monitor capable of displaying pulse breath ratio parameter, including monitor body, still including respiratory data acquisition unit and pulse measurement unit, both are connected with control unit, control unit is connected with display unit in monitor body;Respiratory data acquisition unit is configured to collect the respiratory data of patient, and it is transmitted to control unit after being converted into digital signal, control unit can obtain the respiratory frequency of patient per minute;Pulse measurement unit is configured to be able to collect the pressure signal of patient when measuring pulse, and it is transmitted to control unit after being converted into digital signal, control unit can obtain the pulse number of patient per minute according to pressure signal;Control unit divides the ratio of pulse number per minute by respiratory frequency per minute and transmits to display unit to show, the ratio of pulse number per minute by respiratory frequency per minute is pulse breath ratio parameter. The above-mentioned monitor can display pulse breath ratio parameter on monitor display interface.

Existing pulse oximeters have impaired accuracy in measuring blood oxygen levels (SpO2) in patients of color, where the presence of melanin in the skin tends to interfere with measurements of pulse oximetry, resulting in an overestimation of SpO2. Thus, the pulse oximeter often reports a higher oxygen saturation for patients with darker skin tones, often with increasing bias as the actual saturation (SaO2) decreases. This bias is further reinforced by calibration based on individuals with light skin pigmentation, which may lead to inequitable healthcare for patients of color. Our proposed solution is to modify current pulse oximetry calculations - which utilize the relative tissue absorbance of red and infrared light to estimate SpO2 - to account for the concentration of melanin by additionally measuring the skin absorbance of UV~A light. This derived concentration of melanin can then be used to modify the pulse oximetry algorithm output, thus estimating SpO2 more accurately for patients of color.

An Adaptive Neuro-Fuzzy Inference System (ANFIS) for total intravenous anesthesia management is disclosed, enabling control over administration of anesthetic agents and dynamic adjustment according to patient physiological feedback. The system processes patient data, including processed EEG signals, hemodynamic information, capnography, and pulse oximetry, to facilitate real-time anesthetic dosage adjustments.

Disclosed herein are devices, systems, and methods for reducing skin pigmentation bias in pulse oximetry measurements. The systems and methods can include devices, systems, and methods for narrowing the full-width-half-maximum bandwidth of light used to calculate SpO2.

Disclosed herein are apparatuses for monitoring user health via an inhaler as well as systems and methods thereof. The apparatus can include the inhaler as well as a power source, sensors, and a computing system. The sensors can include a first sensor configured to capture expiratory flow data from within the inhaler and a second sensor configured to capture pulse oximetry or heart rate data from a user of the inhaler. The computing system can be configured to process the data captured by the sensors and record the data as corresponding peak expiratory flow information and pulse oximetry or heart rate information. The apparatus can also include an electronics board, configured to communicatively couple the power source, the sensors, and the computing system.

The invention is applied to the technical field of medical treatment, and discloses a thoracic surgery postoperative complication intelligent prediction system, which comprises a data acquisition and transmission module, a feature extraction and model training module, a real-time monitoring and prediction module and a decision support module. According to the intelligent prediction system for the postoperative complications of the thoracic surgery department, the flexible silica gel intelligent pectoral girdle integrating the pulse oximeter, the respiratory rate sensor and the micro-pressure sensor is adopted, and continuous and real-time collection of physiological data such as the heart rate, the blood oxygen saturation degree, the respiratory rate and the thoracic tiny pressure change is achieved; the problem of prediction lag caused by traditional intermittent manual monitoring is solved, the endurance of equipment reaches 72 hours or above, the integrity and comfort of data acquisition are ensured by combining a low-power reminding function, the monitoring effect is prevented from being influenced by equipment defects, key information such as operation types, duration and bleeding amount is automatically obtained through a hospital information system (HIS), and the operation efficiency is improved. The postoperative physiological status and the operative wound influence of the patient are comprehensively reflected.

The present application relates to the technical field of medical equipment, and proposes a pulse blood oxygen detection device and method thereof, which comprises a lower clamp cover and an upper clamp cover hinged to the lower clamp cover, the opposite sides of the lower clamp cover and the upper clamp cover are both provided with clamping grooves for clamping fingers, a detection module is arranged in the clamping groove of the lower clamp cover, a motor one for driving the opening and closing of the lower clamp cover is fixed to one side of the tail of the lower clamp cover, and two pressing rods are fixed in the clamping groove of the upper clamp cover; in the present application, the upper clamp cover is closed on the lower clamp cover to clamp the fingers, so that the pulse blood oxygen can be detected by the detection module; in this state, the two clamping mechanisms are in a relaxed state under the extrusion of the two pressing rods on the bottom surface of the upper clamp cover, the ventilation mechanism can work to ventilate the fingers, thereby increasing the circulation of air to prevent the appearance of sweat stains around the fingers to affect the detection results; compared with the prior art, the ventilation method is adopted in the detection process to improve the detection efficiency.