Abstract: A touch panel apparatus for sensing a biosignal and a method of acquiring information about respiration of a user by the touch panel apparatus are provided. The touch panel apparatus includes a touch panel configured to sense a biosignal of a user based on a touch input through the touch panel; a detector configured to detect a respiratory signal from the biosignal; and a processor configured to acquire information about respiration of the user based on characteristics of the detected respiratory signal.

Abstract: An apparatus comprises a data processing unit and a stimulator. The data processing unit receives first electroencephalographic data based on a measurement of a brain of a person exposed to one or more estimated or measured non-zero amounts of anesthetic drug substance. The data processing unit performs a first comparison between the first electroencephalographic data and corresponding data of a reference brain function, and outputs information about the first comparison. The stimulator provides the brain of the person exposed to the anesthetic drug substance with brain stimulation on the basis of a direct or indirect reception of the information about the first comparison.

Abstract: The present system is directed in various embodiments to methods, devices and systems for sensing, measuring and evaluating compliance in a bodily conduit. In other embodiments, the methods, devices and systems sense, measure, determine, display and/or interpret compliance in a bodily conduit and/or a lesion within the bodily conduit. In all embodiments, the sensing, measuring, determining, displaying and/or interpreting may occur before, during and/or after a procedure performed within the bodily conduit. An exemplary conduit comprises a blood vessel and an exemplary procedure comprises a vascular procedure such as atherectomy, angioplasty, stent placement and/or biovascular scaffolding.

Abstract: The invention is directed to a system and method for providing an ARDS indication of a patient comprising a sampling device for obtaining a gas sample of the exhaled breath of a patient, a measuring unit for measuring a content of n-octane in the exhaled breath of a patient, a controller which is able to distinguish if the patient has or may develop ARDS based on the content of n-octane in the exhaled breath of a patient resulting in a ARDS indication of the patient and provided with a protocol for providing output regarding the ARDS indication of the patient, and a user interface for indicating the ARDS indication to a user.

Abstract: A bodily information measurement apparatus includes a band-shaped belt to be wrapped around a measurement site; a main body that is connected to a base end portion in the lengthwise direction of the belt and on which a pressure detection unit and a fluid supply unit are mounted; and a fastening unit for fastening the base end portion and the leading end portion of the belt. The belt is formed by stacking an outer circumferential layer and a fluid bladder for compressing the measurement site. The bodily information measurement apparatus is attached to the measurement site due to the base end portion and the leading end portion being fastened by the fastening portion in a state in which the fluid bladder and the leading end portion of the belt overlap.

Abstract: The present invention relates to a non-invasive health indicator monitoring system including a sensing module, an electric power storage module, and a circuit module to collect health indicator information by contacting with a subject. In addition, the present invention also relates to a method for monitoring health indicator continuously by using the health indicator monitoring system.

Abstract: Method for determining the stroke volume of a heart comprising: attaching electrodes to the front legs or arms or head, and the hind legs of the body; connecting an alternating current source to the left pair of front legs/arms or head, and hind legs; connecting an alternating current source to the right pair of front legs/arms or head, and hind legs; attaching a number of electrode pairs to the thoracic skin, such that the electrodes are in contact with the skin of the thorax at predetermined positions, wherein the electrode pairs are each connected to an independent input of a data acquisition/calculation device; determining the beginning the cardiac cycle and measuring with the number of electrode pairs on the thorax the voltage at the beginning of the cardiac cycle at the predetermined positions; measuring during the cardiac cycle with the number of electrode pairs on the thorax the voltages at the predetermined positions and determining the voltage changes Vmeas(?) compared to the voltage at the beginnin

Abstract: Disclosed herein is a framework for facilitating adaptive control of monitoring devices. In accordance with one aspect, a position detector detects a chest elevation level and provides chest elevation level data. A processor uses the chest elevation level data to determine a heart elevation level with respect to a reference level. A comparator compares the determined heart elevation level with an elevation level of a monitoring device with respect to the reference level. In response to the comparison, a movement system adjusts the elevation level of the monitoring device.

Abstract: Certain exemplary embodiments can provide a system, machine, device, manufacture, circuit, composition of matter, and/or user interface adapted for and/or resulting from, and/or a method and/or machine-readable medium comprising machine-implementable instructions for, activities that can comprise and/or relate to, facilitating determination of the oxygen consumption, carbon dioxide production, respiratory exchange ratio, and/or energy expenditure of a mammal.

Abstract: Embodiments provide physiological measurement systems, devices and methods for continuous health and fitness monitoring. A wearable strap may detect reflected light from a user's skin, where data corresponding to the reflected light is used to automatically and continually determine a heart rate of the user. The wearable strap may include a motion sensor that is used to determine a motion status of the user. Based upon the motion status of the user, the system may activate light emitters on the wearable strap to determine the heart rate of the user.

Abstract: An electrode attachment state determination system includes: an electroencephalogram measurement section for measuring an electroencephalogram signal of a user by using at least one set of electrodes including a ground electrode, a reference electrode, and a measurement electrode; a frequency analysis section for performing a frequency analysis of the electroencephalogram signal; an insufficient electrode determination section for extracting at least one parameter of a total frequency power and a noise amount from a result of the frequency analysis, and through a comparison of a value of the parameter against a predetermined threshold value, determining whether the ground electrode, the reference electrode, or the measurement electrode has an insufficient state of attachment; and an output section for, when an insufficient state of attachment is determined, presenting information indicating the insufficient state of electrode attachment to the user.

Abstract: What is disclosed is a system and method for identifying a patient's breathing pattern for respiratory function assessment without contact and with a depth-capable imaging system. In one embodiment, a time-varying sequence of depth maps are received of a target region of a subject of interest over a period of inspiration and expiration. Once received, the depth maps are processed to obtain a breathing signal for the subject. The subject's breathing signal comprises a temporal sequence of instantaneous volumes. One or more segments of the subject's breathing signal are then compared against one or more reference breathing signals each associated with a known pattern of breathing. As a result of the comparison, a breathing pattern for the subject is identified. The identified breathing pattern is then used to assess the subject's respiratory function. The teachings hereof find their uses in an array of diverse medical applications. Various embodiments are disclosed.

Abstract: Continuous monitoring of a plurality of physiological data may be used for health and fitness improvements for a user. To this end, a physiological monitoring and measurement device may include a wearable strap that receives heart rate data for a user including a time series of heart rate data, a maximum heart rate, and a resting heart rate. A processor may transform the heart rate data into a time series of heart rate reserve data that is weighted, e.g., to account for cardiovascular efficiencies at different intensity levels, to provide a weighted time series of heart rate reserve values. An intensity score that provides an indicator of cardiovascular intensity for an exercise routine may be generated from the weighted time series of heart rate reserve values and displayed to the user on the wearable strap.

Abstract: A system and method for assessing treatment effects on obstructive sleep apnea are provided. The apparatus includes a bio-signal measurement unit, a combined index calculation unit, and a treatment response assessment unit. The bio-signal measurement unit measures each of the electrocardiogram and respiratory rhythm of a patient. The combined index calculation unit calculates a combined cardiac and respiratory index by combining the heart rate variability and respiratory rhythm signals measured by the bio-signal measurement unit. The treatment response assessment unit assesses a response of the patient to the treatment of obstructive sleep apnea.

Abstract: A plethysmographic respiration processor is responsive to respiratory effects appearing on a blood volume waveform and the corresponding detected intensity waveform measured with an optical sensor at a blood perfused peripheral tissue site so as to provide a measurement of respiration rate. A preprocessor identifies a windowed pleth corresponding to a physiologically acceptable series of plethysmograph waveform pulses. Multiple processors derive different parameters responsive to particular respiratory effects on the windowed pleth. Decision logic determines a respiration rate based upon at least a portion of these parameters.

Abstract: A method of calibrating an analyte measurement system is provided.

Abstract: The Portable Unit for Metabolic Analysis measures human metabolic function. The compact invention attaches to the face of a subject and it is able to record highly time-resolved measurements of air temperature and pressure, flow rates during inhalation and exhalation, and oxygen and carbon dioxide partial pressure. The device is capable of ‘breath-by-breath’ analysis and ‘within-breath’ analysis at high temporal resolution.

Abstract: There is provided herein methods, apparatus and systems for evaluating carbon dioxide (CO2) concentration in a subject's breath, for example in subjects ventilated with High Frequency Ventilation (HFV), the method includes inserting to a trachea of a subject an endotrachial tube (ETT), sampling breath from an area in the trachea located in proximity to a distal end of the endotrachial tube (ETT) and evaluating one or more CO2 related parameters of the sampled breath.

Abstract: A monitoring system for cardiac operations with cardiopulmonary bypass comprising: a processor operatively connected to a heart-lung machine; a pump flow detecting device connected to a pump of the heart-lung machine to continuously measure the pump flow value and send it to the processor; a hematocrit reading device to continuously measure the blood hematocrit value and to send it to the processor; a data input device to allow the operator to manually input data regarding the arterial oxygen saturation and the arterial oxygen tension; computing means integrated in the processor to compute the oxygen delivery value on the basis of the measured pump flow, the measured hematocrit value, the preset value of arterial oxygen saturation, and the preset value of arterial oxygen tension; and a display connected to the processor to display in real-time the computed oxygen delivery value.

Abstract: A blood pressure measurement cuff wrapped a direction along circumferential direction around a measurement site, the blood pressure measurement cuff containing fluid bladder between belt-shaped body composed of inner cloth to be in contact with the measurement site and outer cloth opposing the inner cloth. Ring attachment member attached to a region on inner circumferential end-side of the outer cloth and hook-and-loop fastener provided in a region on outer circumferential end-side of the inner cloth are included. The ring has a temporary fastening structure that allows a region continuous with outer circumferential end of the belt-shaped body to be pulled through ring with arm strength in a direction away from measurement site during attachment and suppresses a case in which the region continuous with the outer circumferential end of the belt-shaped body pulled by the arm strength is pulled back through the ring by elastic force of the measurement site.