Abstract: A self-learning dynamic electrocardiography analysis method employing artificial intelligence. The method comprises: pre-processing data, performing cardiac activity feature detection, interference signal detection and cardiac activity classification on the basis of a deep learning method, performing signal quality evaluation and lead combination, examining cardiac activity, performing analytic computations on an electrocardiogram event and parameters, and then automatically outputting report data. The method achieves an automatic analysis method for a quick and comprehensive dynamic electrocardiography process, and recording of modification information of an automatic analysis result, while also collecting and feeding back modification data to a deep learning model for continuous training, thereby continuously improving and enhancing the accuracy of the automatic analysis method. Also disclosed is a self-learning dynamic electrocardiography analysis device employing artificial intelligence.

Abstract: A module of implantable cortical and/or intra-cortical comprising a first electrode and a second electrode. Each electrode has a base with interconnect pads adapted to be connected to a processor, a stem having interface pads on a first face, the interface pads adapted to contact soft tissue, routing tracks between the interconnect pads and the interface pads, and abutment surfaces on the second face of each said electrode. The abutment surfaces of the first electrode and of the second electrode are complementary, whereby the first electrode and the second electrode form a translation joint along a length of the stem when the electrodes are joined.

Abstract: An electrocardiogram analysis apparatus includes: an electrocardiogram signal inputting section to which electrocardiogram signals of measurement electrodes attached to a subject are input; a mistaken attachment determining section which, by using the input electrocardiogram signals, determines whether the measurement electrodes are mistakenly attached or not; an outputting section which, if it is determined that the measurement electrodes are mistakenly attached, notifies of mistaken attachment of the measurement electrodes; and an electrocardiogram data storing section which, in a case where there is an input indicative of confirmation of the notification, stores information indicating that the measurement electrodes have been checked, together with the input electrocardiogram signals, and, in a case where there is not an input indicative of confirmation of the notification, stores information indicating that the measurement electrodes have not been checked, together with the input electrocardiogram signals

Abstract: The present technology provides 13C- and 15N-labeled probes for imaging one or more mammalian cells using magnetic resonance. Thus, 13C- and 15N-labeled arginine (compound of formula I), xanthine (compounds of formula II and formula III), urea (compounds of formula IV), and glutamine (compounds of formula V), stereoisomers, tautomers, and pharmaceutically acceptable salts thereof are provided. Further methods of making the labelled probes and methods of using the probes to detect arginase, xanthine oxidase, and glutaminase metabolites and activity are provided.

Abstract: The present invention provides an apparatus and a corresponding method useful for electron paramagnetic resonance imaging, in situ and in vivo, using high-isolation transmit/receive (TX/RX) coils, which, in some embodiments, provide microenvironmental images that are representative of particular internal structures in the human body and spatially resolved images of tissue/cell protein signals responding to conditions (such as hypoxia) that show the temporal sequence of certain biological processes, and, in some embodiments, that distinguish malignant tissue from healthy tissue. In some embodiments, the TX/RX coils are in a surface, volume or surface-volume configuration.

Abstract: An apparatus for capturing the electrical behavior of the human body during respiration and/or ventilation, the apparatus comprising ventilation elements, elements for capturing the impedance of the patient and at least one control unit. The impedance is captured using at least two electrically conductive electrodes, which capture the electrical behavior of the human body. The elements for capturing the impedance are configured to capture the change in the impedance of the human body over time during respiration and/or ventilation.

Abstract: A method and apparatus of determining the condition of a bulk tissue sample, by: positioning a bulk tissue sample between a pair of induction coils (or antennae); passing a spectrum of alternating current (or voltage) through a first of the induction coils (or antennae); measuring spectrum of alternating current (or voltage) produced in the second of the induction coils (or antennae); and comparing the phase shift between the spectrum of alternating currents (or voltages) in the first and second induction coils (or antennae), thereby determining the condition of the bulk tissue sample.

Abstract: Provided herein are devices, systems, and methods for monitoring lesion or treated area in a tissue during focal ablation or cell membrane disruption therapy.

Abstract: A system and method for localizing medical instruments during cardiovascular medical procedures is described. One embodiment comprises an electromagnetic field generator; an antenna reference instrument adapted to be introduced into the heart of a subject and including at least one electromagnetic sensor and at least one electrode; at least one roving instrument adapted to be introduced into the thorax cavity of the subject and including at least one electrode; and a control unit configured to determine position coordinates of the antenna reference instrument based on an electromagnetic signal from the electromagnetic field generator sensed by the electromagnetic sensor, measure an electrical-potential difference between the electrode of the antenna reference instrument and the electrode of the roving instrument, and calibrate the measured electrical-potential difference using the determined position coordinates of the antenna reference instrument to determine position coordinates of the roving instrument.

Abstract: A system for determining a location of a tool within a patient includes a tool and a sensor. The tool is configured to be introduced into a patient. The tool includes a flexible tubular member, a laser coupled to the flexible tubular member, and a cap coupled to the laser. A plurality of waves are generated when a beam of light from the laser shines upon the cap. The sensor is configured to be coupled to an exterior of the patient. The sensor is configured to receive the waves, and a location of the tool within the patient is configured to be determined based at least partially upon the waves received by the first sensor.

Abstract: The system of the present invention includes a conductive element, an electronic component, and a partial power source in the form of dissimilar materials. Upon contact with a conducting fluid, a voltage potential is created and the power source is completed, which activates the system. The electronic component controls the conductance between the dissimilar materials to produce a unique current signature. The system can also measure the conditions of the environment surrounding the system.

Abstract: Disclosed is an implant and method of making an implant. The implant having a housing that defines a cavity. The housing includes a sensor comprising a base attached to a diaphragm wherein said base may be positioned within said cavity. The sensor may be a capacitive pressure sensor. The diaphragm may be connected to the housing to hermetically seal said housing. The sensor may include electrical contacts positioned on the diaphragm. The base may define a capacitive gap and a vent wherein the electrodes may be positioned within said capacitive gap such that at least a portion of the electrical contacts extend through the vent. The implant may include a coil in electric communication with the sensor, said coil may be positioned within said housing. A printed circuit board having at least one component may be attached to the floating base.

Abstract: An Internet-based disease monitoring system may include a network-based disease sensor device, which is coupled to a sensor, such as a spirometer. A remote server may be coupled to the network-based disease sensor device to provide analysis of input signals from the sensor. The remote server may be able to provide various services for grouping or handling functions relating to such input signals. A service may provide the ability to aggregate input signals from multiple sensors coupled to sensor devices and provide predictive modeling or statistical analysis, which may then be used to adjust future input signals. A service may also contain instructions how to handle billing based on usage of the network-based disease sensor device.

Abstract: An apparatus for providing a classification of an angular position of a limb relative to a torso of a vertebral mammal is provided. The apparatus includes a first sensor, a second sensor, a memory device and a processor. The first sensor is for measuring position of the torso relative to a first frame of reference and for providing first data indicative of the torso position. The second sensor is for measuring position of the limb relative to a second frame of reference and for providing second data indicative of the limb position. The memory device is adapted for storing the first and second data at least temporarily. The processor is adapted for processing the first and second data to derive the angular position of the limb relative to the torso in at least one anatomical plane of the mammal's body, and to provide the classification based at least on the derived torso and limb positions.

Abstract: A sensing device including a sensor, a triggering mechanism is provided. The sensing device is attachable to a covering positioned in contact with a body such that the triggering mechanism extends between first and second segments of the body. Movement of at least one of the first and second segments activates the triggering mechanism to provide an input to the sensor, actuating the sensor to generate an output defining at least one measurement of the movement. The measurement may be one or more of rotation, translation, velocity, acceleration, and joint angle. An intermediate mechanism may be interposed between the triggering mechanism and the sensor. The sensing device may include a means to process or record measurements corresponding to movement. A system and method of measuring the movement is also provided.

Abstract: In a system and method for monitoring movement, a movement monitoring device is configured to engage with a rotating belt of a treadmill. The movement monitoring device includes a rotational tracking device to measure rotational motion of the belt and send the rotational motion measurement to a computing device, and a vertical tracking device to measure vertical motion of the belt and to send a vertical motion measurement to the computing device. The system further includes a computing device for receiving the rotational motion measurement and the vertical motion measurement and to generate a Symmetry Index for the user on the rotating belt of the treadmill, the Symmetry Index being a comparison of more than one measure of symmetry for a first leg and a second leg of the user derived from the rotational motion measurement and the vertical motion measurement.

Abstract: The invention relates to a method and apparatus for processing a cyclic physiological signal (30, 40, 52, 53, 54). The method comprises the steps of repeatedly collecting (2) the physiological signal (30, 40, 52, 53, 54) over a time period (31, 32, 33) covering two or more cycles of the cyclic physiological signal (30, 40, 52, 53, 54), wherein a next time period (31, 32, 33) is adjacent to or overlaps with a previous time period (31, 32, 33), extracting values (3, 13) of a set of predefined parameters from the physiological signal (30, 40, 52, 53, 54) within each time period (31, 32, 33) which parameter values characterize the physiological signal (30, 40, 52, 53, 54) within the time period (31, 32, 33), and classifying (4, 14) the physiological signal (30, 40, 52, 53, 54) within each time period (31, 32, 33) based upon the extracted set of predefined parameter values.

Abstract: Tools and techniques for providing joint position error test system are provided. A system includes a head sensing unit coupled to a joint position error processor. The head sensing unit may include a positional sensor and further be configured to be coupled to the head of a test subject. The joint position error processor may include a processor, and non-transitory computer readable media comprising instructions executable by the processor to record reference sensor data from the positional sensor when the test subject's head is in a reference position, record return sensor data when the test subject's head is in a return position. The instructions may further be executable to determine a position error based on the reference sensor data and the return sensor data, and to further determine the presence of a condition of the test subject based on the position error.

Abstract: A wearable motion monitoring device including: a housing sized and shaped to be positioned between a body region of a subject and a garment worn by the patient; a marker included in said housing, said marker including at least one light emitter, wherein said light emitter is positioned to emit light from an upper surface of said marker, such that said at least one light emitter is indicative of displacements of said body region; at least one garment holder incorporated in said housing, said holder serves as an anchoring point between said marker and said garment, said garment overlies said marker when anchored by said at least one garment holder.

Abstract: Techniques for user identification by a biometric monitoring device are disclosed. In one aspect, a method of operating a biometric monitoring device may involve measuring a weight of a user in response to detecting that the user is standing on a platform, determining, based on sensor data generated by a sensor, a user parameter indicative of the user's identification, identifying one of a plurality of user profiles as corresponding to the user based on a comparison of the user parameter to parameter values and a comparison of the measured weight of the user to weight values, and updating the identified user profile based on at least one of the measured weight and the user parameter.

Abstract: The present invention provides a device for measuring biological information including a sensor array, wherein the sensor array includes a plurality of sensors that are either sensors for amplifying photoreactivity or sensors forming an island network connected by a plurality of multi-channels and, in the device, the average value of biological information about the skin tissues is measured based on values output from the sensor array, and a method of measuring biological information using the device.

Abstract: Disclose is a dry adhesive patch comprising: a plurality of embossed pillars formed on a substrate; a hemi-spherical adsorbing cup defining a top portion of each pillar, wherein a hemi-spherical hole is defined in a top portion of the adsorbing cup and is exposed to an outside; and an annular extension extending radially from an outer perimeter of a distal end of each adsorbing cup.

Abstract: Compact medical device inserters, systems incorporating the same, and related methods of use are described. The inserters can include a housing, a sharp support, a sharp body, and a shroud, and can apply a sensor control device to a recipient with a sensor implanted in the recipient's body. The shroud can extend from the sensor control device in a position that covers or protects the sensor and a sharp, and can be retracted by pressure placed upon the inserter against the recipient's body to cause the sharp and sensor to penetrate the body, after which the sharp can be automatically withdrawn with the aid of a biasing element.

Abstract: A method of estimating a concentration of an analyte may include obtaining a plurality of in vivo estimation spectra, generating a plurality of noise detection models by varying a number of principal components based on the plurality of in vivo estimation spectra, comparing the generated plurality of noise detection models with a plurality of concentration estimation models for each number of principal components, extracting a noise spectrum and a concentration estimation model for use in estimating the concentration of the analyte based on the comparison, updating the extracted concentration estimation model based on the extracted noise spectrum, and estimating the concentration of the analyte by using the updated concentration estimation model and an in vivo estimation spectrum from among the plurality of in vivo estimation spectra.

Abstract: Embodiments of the disclosure provide an oximeter, including a blood oxygen collecting unit that has a first light emitting unit, a second light emitting unit, and a light receiving sensor, the first light emitting unit emitting a red light, the second light emitting unit emitting an infrared light, and the light receiving sensor receiving the red light emitted by the first light emitting unit and the infrared light emitted by the second light emitting unit and not absorbed by the human body, and converting them into an electrical signal, a storage unit that stores a first threshold value, a microprocessor that calculates a blood oxygen saturation of the human body based on the electrical signal detected by the light receiving sensor, and includes a judging unit that judges whether the blood oxygen saturation is lower than the first threshold value, and a display unit.

Abstract: A device, system and method of non-invasive monitoring of physiological measurements of a subject are disclosed. The method may include: emitting light beams towards skin of the subject, with at least one light source having at least one predetermined polarization, wherein the light beams are emitted at an angle 0°??<90° relative to the normal to the skin surface of the subject; sensing In light beams with at least one light sensor positioned at a predetermined distance from the at least one light emitting source; filtering out signals corresponding to detected light beams based on the at least one predetermined polarization of the at least one light source; and determining at least one physiological signal, based on the sensed light beams after filtering. The sensed light beams may pass through at least one of epidermis, dermis, subcutaneous tissue and blood vessel of the subject.

Abstract: A method for manufacturing a sensor for detecting an analyte in a body fluid is disclosed. In the inventive method a membrane layer is provided, and at least one first electrically conductive material is directly or indirectly deposited onto the membrane layer. At least one electrically insulating material is directly or indirectly deposited onto the at least one membrane layer and the at least one first electrically conductive material, and at least one second electrically conductive material is deposited directly or indirectly onto the electrically insulating material. An associated sensor is also disclosed.

Abstract: Various components of an interventional therapy assembly are disclosed. One such component is a pointer which may be configured to indicate the disposition of another portion or component of the assembly. A rotary indexing device which may be configured to control or facilitate rotation of other components is also disclosed. Further, various components of an elongate instrument having flexible segments and operative segments are also disclosed. In some embodiments, the elongate instrument may comprise a biopsy assembly and may be used in connection with other components of the disclosed assembly.

Abstract: An electronic device attached to a user's skin is provided to determine a user emotion based on measured bio-signals. An image corresponding to the determined emotion is displayed. The electronic device includes a skin-attachment apparatus having a bonding unit for bonding to a user's skin and a bio-signal sensor that measures the bio-signals of the user. A display unit and a controller are connected with the skin-attachment apparatus. The controller determines the user emotion based on the bio-signals acquired from the bio-signal sensor and operates the display unit to display at least one of a color and a pattern corresponding to the determined emotion.

Abstract: A system for detecting unsafe equipment operation conditions using physiological sensors includes a plurality of wearable physiological sensors, each physiological sensor of the plurality of wearable physiological sensors configured to detect at least a physiological parameter of an operator of an item of equipment, and a processor in communication with the at least a physiological sensor and designed and configured to determine an equipment operation parametric model, wherein the equipment operation parametric rule relates physiological parameter sets to equipment operation requirements, detect using the equipment operation parametric model and the plurality of physiological parameters, a violation of an equipment operation requirement, and generate a violation response action in response to detecting the violation.

Abstract: A method is provided for monitoring and managing muscle activity and soft tissue loading. The method includes providing to a subject a plurality of sensors for measuring muscle activity and soft tissue loading levels; directing the subject to undertake a program of exercise; measuring muscle activity and soft tissue loading during the program of exercise; comparing the measured muscle activity and soft tissue loading levels against calibrated muscle activity and soft tissue loading levels for the subject; and alerting the subject if the comparison of measured muscle activity and soft tissue loading levels against calibrated muscle activity and soft tissue loading levels indicates that a desirable level of muscle activity and/or soft tissue loading is being exceeded.

Abstract: A method, device and a computer program product for determining a training load distribution of a user is provided. Heart rate is continuously measured by a heart rate sensor. An aerobic training effect and load are calculated using intensity values and divided into categories of Aerobic Low and Aerobic High. An anaerobic training effect and load are calculated using determined characteristics related to high intensity periods of an exercise.

Abstract: A method and system for monitoring therapeutic interventions for treating a patient with PTSD comprises using a scanner to obtain pre-treatment neural spectroscopic data of at least one neuromarker chemical in the brain of the patient before treatment, treating the patient with at least one treatment protocol, after treatment, obtaining post-treatment neural spectroscopic data of the at least one neuromarker chemical in the brain of the patient, and comparing the results of the pre-treatment and post-treatment data to enable a determination of the effectiveness of the treatment.

Abstract: There is provided herein systems and methods for managing a subject suffering from cognitive impairment, the method comprising: providing to a subject a cognitive training session; determining at least one aspect of the subject's cognitive performance based on and/or in response to said training session; monitoring one or more life style, physiological and/or medical parameters of the subject before, during and/or after said training session; identifying peaks in the subject's cognitive performance; wherein the identifying comprises comparing the determined cognitive performance to stored cognitive performance data; identifying changes in one or more life style, physiological and/or medical parameters positively or negatively associated with the peak in the cognitive performance; and providing the subject with a life style, physiological and/or medical recommendation based on the on identified association.

Abstract: A cognitive function evaluation device includes: an instruction unit that instructs quick pronunciation of pseudoword in which a predetermined syllable is repeated; an obtainment unit that obtains voice data indicating a voice of an evaluatee who has received an instruction; a calculation unit that calculates a feature from the voice data obtained by the obtainment unit; an evaluation unit that evaluates a cognitive function of the evaluatee from the feature calculated by the calculation unit; and an output unit that outputs a result of the evaluation by the evaluation unit.

Abstract: A method for indexing cognitive function includes giving, to a subject, a work for inducing biological activity related to cognitive function, acquiring measurement data, and acquiring an index indicating the cognitive function of the subject from the measurement data of the subject using a model constructed in advance.

Abstract: An imaging device for monitoring a skin feature includes a camera, at least one processor and memory. The imaging device displays a body area guide, receives a selection of a body area, initiates an image sequence of the body area, the image sequence including capturing, using the camera, a plurality of images, determines whether all body areas have been imaged, analyzes the images, and provides the analyzed images to a clinician. The imaging device can be part of a system including a server in communication with a monitor, where the clinician views the images on the monitor. Additionally, each skin feature can be ranked in order of risk and presented to the clinician in that order.

Abstract: Various implementations include approaches for monitoring the workload of a pilot, such as an aircraft pilot. Certain approaches include: receiving flight condition data and aircraft configuration data about an aircraft; comparing the flight condition data and aircraft configuration data with corresponding thresholds to determine flight condition and aircraft configuration workload components; applying respective weights to the flight condition and aircraft configuration workload components; and providing a report indicating a workload for the pilot based upon the weighted flight condition and aircraft configuration workload components.

Abstract: Methods, apparatus, and processor-readable storage media for facilitating a secure platform for point-to-point brain sensing are provided herein. An exemplary method includes presenting a user of a brain-computer interface with learning content; monitoring brain signals of the user using a brain-computer interface while the learning content is being presented; determining, based at least in part on said monitoring, that a confusion state of the user exceeds a personalized confusion threshold in regard to at least a part of the learning content; in response to said determining, outputting information to assist the user in understanding the part of the learning content until the confusion state of the user is below the personalized confusion threshold.

Abstract: Systems and methods for providing a preferred fitness state of a use are disclosed. The system includes at least a sensor that detects at least a biological parameter of a user and a fitness state soring module that generates a current user fitness state using machine-learning and the at least a biological parameter. Methods of providing a preferred fitness state of a user include detecting at least a biological parameter of a user, determining by a fitness state sorting module a current user fitness state and determining a user specific recommendation by the fitness state sorting module.

Abstract: Systems and methods for assessing compliance with position therapy. In an embodiment, position therapy is provided to a user while the user is wearing a position therapy device. The position therapy comprises, by the device, collecting positional data, determining positions of the user over a time period based on the positional data, and, when it is determined that the user is in a target position, providing feedback to the user to influence the user to change to a non-target position. In addition, the device stores a duration of use in its memory. The duration of use indicates a duration that the user has used the wearable position therapy device in each of one or more positions. An assessment of the user's compliance with the position therapy is then provided based, at least in part, on the duration of use.

Abstract: One embodiment includes a method for monitoring nerve tissue which includes inserting a dilator into muscle, the dilator including first and second electrodes at the distal tip. While the dilator is in muscle, a system may communicate (a) a first series of unequal current amplitude applications (e.g., a series including 0.5, 7, 3, 5 mA applications) to the first electrode to produce at least a first evoked potential (e.g., a MAP or NAP), and (b) a second series of unequal current amplitude applications to the second electrode to produce at least a second evoked potential. The method further includes sensing the first and second evoked potentials and determining a relative location of a nerve based on the sensing of at least one of the first and second evoked potentials.

Abstract: Featured are impact detection sensors that include a nonconductive layer disposed between two conductive layers. Each conductive layer includes an electrical circuit configured to generate a signal in response to an impact. Also featured are devices (e.g., a wearable device or device configured for use with a piece of equipment, such as a vehicle) including a plurality of impact detection sensors. The device having sensors can receive and process data from the sensors and provide situational awareness for users in adverse conditions, such as during combat or wartime. The wearable device may further include one or more inflatable bladders configured to apply pressure to a wound site for treatment.

Abstract: Athlete technology including athlete garments, athlete sensors, athlete data processors, athlete data networks, and other features, functions, and components.

Abstract: An oesophageal electrode probe for bioimpedance measurement and/or for neurostimulation is provided; a device for transoesophageal cardiological treatment and/or cardiological diagnosis is also provided; a method for the open-loop or closed-loop control of a cardiological catheter ablation device and/or a cardiological, circulatory and/or respiratory support device is also provided. The oesophageal electrode probe comprises a bioimpedance measuring device for measuring the bioimpedance of at least one part of tissue surrounding the oesophageal electrode probe. The bioimpedance device comprises at least one first and one second electrode. The at least one first electrode is arranged on a side of the oesophageal electrode probe facing towards the heart. The at least one second electrode is arranged on a side of the oesophageal electrode probe facing away from the heart. The device comprises the oesophageal electrode probe and a control and/or evaluation device.

Abstract: A flexible probe includes a probe body having a distal end and a proximal end, and comprises at least one flexible nanoelectronic thread having a distal end and a proximal end and a length therebetween, the nanoelectronic thread comprising at least one electrode positioned on a top surface of the nanoelectronic thread, and at least one nanoscale wire is partially encapsulated, having a first portion electrically connected to at least one of the electrodes and a second portion surrounded by a dielectric insulator, the probe further including at least one external trace electrically connected to the at least one nanoscale wire at the proximal end of the at least one nanoelectronic thread, the at least one external trace having a width larger than the width of the at least one nanoscale wire, and an interface connector near the proximal end of the probe body, electrically connected to the at least one electrode via the at least one nanoscale wire and the at least one external trace, wherein the at least one nano

Abstract: A measurement method includes a first measurement in which a characteristic amount of a specific analyte in a biological fluid is measured with a biosensor. The method also includes a second measurement in which motion information of living activity is measured. Additionally, the method may include recording the motion information and the characteristic amount measured in the first measurement with the motion information and characteristic amount associated with each other.

Abstract: A monitoring device configured for insertion into a conduit of a subject includes a housing, at least one physiological sensor coupled to the housing, a transmitter coupled to the housing, an expandable element, inflatable element, stretched membrane or balloon coupled to the housing and configured to occlude at least a portion of the conduit, a power source attached to the housing, and a processor coupled to the housing and operatively coupled to memory containing computer instruction causing the monitoring device to obtain physiological information via the at least one physiological sensor where the physiological information includes one or more of pulse rate information, body temperature information, breathing rate information, blood pressure information, cardiac output information, or blood gas level information, and processing and analyzing the physiological information to provide a result.

Abstract: An embodiment in accordance with the present invention provides a non-invasive solution to risk stratify the risk of in arrhythmia in patients with TOF. Currently, no reliable method for non-invasive risk stratification exists. In the realm of congenital heart disease, cardiac MRI is now used routinely for patients with Tetralogy of Fallot (TOF), the most common form of cyanotic congenital heart disease. An innovative platform for using clinical MRI data to create 3D electromechanical models of the heart enables predictions of whether or not patients with ischemic heart disease have the substrate for arrhythmia and what their relative risk for such an event is. An embodiment of the current invention provides a non-invasive solution to risk stratify the risk of arrhythmia in patients with TOF. Currently, no reliable method for non-invasive risk stratification exists.

Abstract: A patient monitoring system and method are disclosed which provide a caregiver with more easily identifiable indications of the state of multiple physiological parameters in order to give the caregiver an indication of the patient's overall wellness in an efficient manner. Multiple physiological parameter sets are plotted on a graph, along with an indication of each parameter set's normal range. An overlapping area for all set's normal ranges provides an indication of an ideal patient state. In an embodiment, alerts are generated based on parameters distance from normal readings.