Abstract: A rack for a domestic dishwasher includes a frame and a base. The base can be swung and folded out in order to increase a loading volume of the rack. The base includes a first portion articulated to a first side of the frame via a first articulation, and a second portion articulated to a second side of the frame opposite the first site via a second articulation, and articulated to the first portion via a third articulation. The second portion is configured to change its length between the second and third articulations.

Abstract: A contact detecting apparatus detects contact between a body tissue and a probe for emitting illumination light onto the body tissue and receiving return light of the illumination light scattered from the body tissue. The contact detecting apparatus includes: a laser light source that emits laser light to irradiate a specified region of the body tissue via the probe; a photoelectric conversion unit that converts light received via the probe into an electric signal; and a signal processing unit that determines whether or not there is contact between a distal end of the probe and the body tissue based on whether the electric signal includes a component of a beat signal caused by interference of the return light of the laser light scattered from each of a surface of the body tissue and a surface of the distal end of the probe.

Abstract: A dilation catheter system comprises a guide member, a dilation catheter, and an image sensor. The guide member includes a shaft comprising a distal end and a proximal end. The shaft further defines a longitudinal axis. The dilation catheter is movable relative to the guide catheter member and comprises an expandable dilator. The expandable dilator is sized to fit within one or both of a Eustachian tube or a passageway associated with a paranasal sinus. The image sensor is configured to provide visualization within anatomy of a patient. The image sensor is integral with the guide member.

Abstract: A distal end structure of an endoscope according to the present invention includes a distal end member formed of a metal material, an insulating ring provided in an annular shape around an insertion axis on a proximal end side of the distal end member, a cover formed of a flexible insulative material that covers the distal end member, a projecting section provided integrally with the insulating ring and projecting in a direction crossing the insertion axis, a through-hole provided in the cover and engaging with the projecting section, and a to-be-tom-apart section provided near the through-hole, in which force is applied to the to-be-torn-apart section to tear apart the cover along the insertion axis direction and remove the cover from the distal end member.

Abstract: An endoluminal access system for accessing a body lumen includes a guide track which, when in an operative position, extends through a body lumen to a desired location therewithin and a modular device selectively coupleable to the guide track, the modular device including a drive mechanism for engaging the guide track to move the modular device along the guide track within the body lumen. A method of resecting tissue from a site within a body includes the steps of inserting a guide track to a desired location within the body lumen, coupling a modular device to a proximal end of the guide track and actuating a motor mounted within the modular device to drive the modular device distally along the guide track to the site, drawing tissue at the site into the modular device in combination with the steps of coupling together a portion of tissue adjacent to the site, resecting the tissue from the site and actuating the motor to drive the modular device proximally to withdraw the modular device from the body lumen.

Abstract: The invention relates to an electrical connection piece for a video endoscope having a hermetically closed video unit in a shaft of the endoscope, a video endoscope, and a method for producing an electrical connection in a video endoscope. The electrical connection piece according to the invention includes an at least partially flexible printed circuit board having conductive tracks, wherein the printed circuit board has a base surface with openings for contact pins of a hermetic feedthrough, and a flexible first arm and a flexible second arm that branch off in different, in particular opposite, directions from the base surface, wherein the first arm and the second arm each have a flat end surface at the respective ends facing away from the base surface, wherein the conductive tracks extend between the openings on the base surface and electrical contacting surfaces in the end surfaces.

Abstract: The invention relates to a device for manufacturing an elongated hollow profile element that has at least one pulling wire (13), comprising: two counter-bearings (11, 12), which are arranged on opposite sides of the device and which correspond to the elongated ends of the elongated hollow profile element, wherein one end of the at least one pulling wire (13) is anchored to the distal counter-bearing (11), and a mold (2a, 2b), which forms a sealed elongated cavity (3) that can be filled with a hardening material, wherein the cavity (3) extends between the two counter-bearings (11, 12) and the pulling wire (13) extends in the cavity (3) so as not to touch the cavity wall. The invention further relates to a method for manufacturing an elongated hollow profile element that has at least one pulling wire (13), the elongated hollow profile element, and a bending section for an endoscope.

Abstract: An endoscope device includes a flexible insertion portion; a flexible tube portion; a first bending portion; a second bending portion; an observation portion; a first drive portion bending the first bending portion; a second drive portion bending the second bending portion; a position detection portion detecting a position of a rigid distal end portion of a medical instrument; first and second bending detection portions detecting radii of curvature of axes of channels formed in the first and second bending portions and directions in which the channels are bent when an input signal generated by the position detection portion is received, respectively; and a control portion configured to control generating a second drive signal driving the second drive portion based on a first drive signal driving the first drive portion, and sending the second drive signal to the second drive portion while sending the first drive signal.

Abstract: An apparatus includes a tubular structure having a proximal end, a distal end, and a body extending between the proximal and distal ends, wherein the body includes a lumen for housing at least a part of an imaging device, and a fluid delivery channel that is fixed in position relative to the body, and an opening that is in fluid communication with the fluid delivery channel, wherein the fluid delivery channel has a first portion, and a second portion that forms an angle with an axis of the first portion.

Abstract: A medical robotic system includes an entry guide with articulatable instruments such as surgical tools and a camera extending out of its distal end. The camera instrument is manipulatable by a camera manipulator, which has a first mechanism for pivoting a focal point of the camera instrument about a pivot of the camera instrument and a second mechanism for positioning the pivot within a three-dimensional space in response to translational commands received from one or a coupled pair of input devices. The system also includes a controller which is configured to receive sensed movement of the input devices, and cause actuation of the first mechanism in response to the sensed movement if the system is in an orientational mode and cause actuation of the second mechanism in response to the sensed movement if the system is in a translational mode.

Abstract: The present invention relates to an illuminated dental prop for holding a patient's mouth open during dental procedures. The illuminated dental prop is completely disposed within the patient's mouth during use and includes a body portion and a lighting assembly that is selectively detachable from the body to allow for intense sterilization of the components after use. Under certain embodiments of the invention, the body portion and/or the lighting assembly will be disposable after a single use.

Abstract: A single imaging platform for making in vivo measurements of an individual's eye, where the measurements are sufficient to construct an optical model of the individual's eye. The platform includes a plenoptic opthalmic camera and an illumination module. In one configuration, the plenoptic opthalmic camera captures a plenoptic image of a corneal anterior surface of the individual's eye. In another configuration, the plenoptic opthalmic camera operates as a wavefront sensor to measure a wavefront produced by the individual's eye.

Abstract: Techniques related to vision correction are disclosed. The techniques involve establishing a visual model associated with a patient. The visual model includes data related to a quality of the patient's vision. A boundary is established as a function of the data associated with the visual model. The boundary is indicative of an area to be corrected within the patient's vision. A retinal map is established as a function of the boundary. An image from a camera associated with the patient is captured and corrections are applied to the image based on the retinal map to generate a corrected image. The corrected image is presented to the eye of the patient.

Abstract: Methods and apparatus are presented for obtaining high-resolution 3-D images of a sample over a range of wavelengths, optionally with polarization-sensitive detection. In preferred embodiments a spectral domain OCT apparatus is used to sample the complex field of light reflected or scattered from a sample, providing full range imaging. In certain embodiments structured illumination is utilized to provide enhanced lateral resolution. In certain embodiments the resolution or depth of field of images is enhanced by digital refocusing or digital correction of aberrations in the sample. Individual sample volumes are imaged using single shot techniques, and larger volumes can be imaged by stitching together images of adjacent volumes.

Abstract: The invention relates to a device for measuring the subjective refraction of a person in near and/or medium vision, which comprises, according to the invention, for each eye of the person, a correction mounting (3) provided with at least one corrective lens, the correction mountings (3) being arranged such that the person looks through the lenses. The position of each correction mounting (3) is variable such as to adjust an angle (a) between the axes of the lenses.

Abstract: A method to determine an ophthalmic tissue structure comprises measuring image data for a range of depths corresponding to a target point in an eye with an axial scanner with a probe; determining an image information by an imaging processor from the image data; identifying a tissue pathology corresponding to the target point by the processor from the image information; and signaling a user by a user indicator based on the identified tissue pathology. A corresponding apparatus comprises an axial scanner with a probe to measure image data for a range of depths corresponding to a target point in an eye; a processor to determine an image information from the image data, and to identify a tissue pathology corresponding to the target point from the image information; and a user indicator to signal a user based on the identified tissue pathology.

Abstract: An optical tomographic imaging apparatus includes a first lens having a first focal length, a second lens having a second focal length longer that the first focal length, a scanning unit disposed at a focal position of the second lens, and an optical path branching unit disposed between the first and second lenses. An observation optical path located on a transmission optical path of the optical path branching unit, and an optical path of measurement light located on a reflection optical path of the optical path branching unit. The second lens is disposed on the optical path of the measurement light between the first lens and the scanning unit, such that an angle at which the measurement light scanned by the scanning unit is incident on the optical path branching unit is maintained substantially unchanged during scanning.

Abstract: A method of correcting wavefront aberrations of an eye includes determining a high precision conventional intrastromal corneal ablation profile based on a direct removal of the intrastromal corneal tissue. An expanded ablation volume profile is constructed based on the direct tissue removal profile and the expanded tissue volume is to be ablated instead to correct to the wavefront aberrations. The thickness of the ablated profile of a conventional ablation profile is expanded by an expansion factor (Nc?1)/(Nm?Nc), Nc is the index of refraction of the cornea and Nm the index of fill material. An expanded ablation volume filled with the fill material produces the effect of correcting wavefront aberrations as if a much smaller tissue volume were ablated without the fill material.

Abstract: A method in support of health management services acts upon active and passive data, in which the active data is communicated by a patient or healthcare professional and in which the passive data is detected by at least one sensor detectably coupled to the patient. These data are correlated with each other and if a predefined correlation is not met, further data can be solicited, patient-specific queries can be generated, alerts can be communicated, or a combination of these can be done in embodiments of the invention. Any Irregularity or trend in the data can be identified and processed in embodiments of the invention. Also in some embodiments, these data can be used in connection with intelligent, machine-based decisions to send communications concerning the provision of further healthcare resources to patients, such as in view of their relative acuity rank. Systems can be constructed to implement the methods described herein.

Abstract: An identifying and monitoring system to be worn at all times that includes a bracelet that can locate lost or missing children, adults, and pets. The bracelet provides emergency personnel with pertinent identifying information including medical history and family contacts. The system includes GPS capabilities and the use of the internet and a web page to upload and download information per each individual bracelet. The bracelet also incorporates a unique locking system that when disengaged from a wearer's wrist an emergency signal and location information is immediately sent to emergency responders.

Abstract: The present invention provides a transmitted light detection type measurement apparatus for skin fluorescence, which is configured to perform light irradiation and light detection on a reference sample and a measurement target. The apparatus includes a first light source, a second light source, a first optical detector and a second optical detector, a light source switching controller, and an operator.

Abstract: Described are embodiments of methods of obtaining three-dimensional (3D) surface data of an object scene such as an intra-oral cavity. For example, measured surfaces may include the enamel surface of teeth, the dentin substructure of teeth, gum tissue and various dental structures. The methods can also be applied in medical applications and other applications in which 3D measurement data are acquired with maneuverable 3D measurement devices. In certain embodiments, the measurement device is positioned and translated to enable 3D data to be acquired for a backbone 3D data set. Subsequent controlled motion of the measurement device enables additional 3D data to be acquired and accurately joined to the backbone 3D data set.

Abstract: Provided are a photoacoustic probe and photoacoustic diagnostic apparatus. The photoacoustic probe includes a light irradiation unit for irradiating first light that is used for photoacoustic imaging on an object and an indicator for providing information about whether the first light is irradiated by using the first light.

Abstract: This invention provides a phantom whose light propagation characteristics and acoustic propagation characteristics are similar to those of human tissues and which allows detection of an absorber also with an ultrasonic wave diagnostic apparatus and allows adjustment of the oxygen saturation. A phantom has light absorbers 12a to 12d in a phantom base material 11, in which the light absorbers 12a to 12d approximate the light absorption coefficient ratio at two or more wavelengths to that of biological tissues, and the acoustic propagation characteristics of the phantom base material 11 and the light absorbers 12a to 12d are different from each other.

Abstract: Improved apparatus and methods for monitoring, diagnosing and treating at least one medical respiratory condition of a patient are provided, including a medical data input interface adapted to provide at least one medical parameter relating at least to the respiration of the patient, and a medical parameter interpretation functionality (104, 110) adapted to receive the at least one medical parameter relating at least to the respiration (102) of the patient and to provide at least one output indication (112) relating to a degree of severity of at least one medical condition indicated by the at least one medical parameter.

Abstract: The invention consists of a device and method for the prediction of left ventricular ejection fraction (EF) and other cardiac hemodynamic parameters using systolic time intervals in patients with narrow QRS, right bundle branch block, left bundle branch block, right ventricular and/or left ventricular cardiac pacing and in the presence of arrhythmia, such as atrial fibrillation. The device has three inputs: the ECG, a peripheral pulse and a phonocardiogram. Timing parameters are obtained from these signals to calculate a systolic function index, used for the prediction of ejection fraction. Given the invention's features it would be now possible to assess cardiac performance and specifically left ventricular ejection fraction in ambulatory patients as well as during invasive procedures such as the implant of cardiac rhythm management devices.

Abstract: A wearable, wireless, non-invasive device applicable to the hand or foot, a wireless system, and a method for reducing the risk of different critical situations of hypoxia and/or bradycardia possibly occurring in victims of sudden infant death syndrome (SIDS), Pierre Robin Sequence patients, preterm babies, and adults, and for the prevention of the sleep apnea, is based on use of a sensor and a computing algorithm sufficient to reduce false alarms and save lives. The device is worn on the hand or foot of a user. Part of the device may be placed on the proximal phalange of a finger or a foot, or even in the palm. The electronics of the device may be placed inside gloves or booties of different sizes to accommodate the hands or feet of different wearers. The device measures blood oxygen saturation and heart rate through a sensor that is preferably a pulse oximeter.

Abstract: Intravascular devices, systems, and methods are disclosed. In some instances, the intravascular device is a guide wire with electrical conductors embedded within a core wire. In some instances, the electrical conductors are coupled to conductive bands adjacent a proximal portion of the guide wire and a sensing element adjacent a distal portion of the guide wire. Methods of making, manufacturing, and/or assembling such intravascular devices and associated systems are also provided.

Abstract: A system to generate a representation of a rhythm disorder includes a plurality of sensors disposed at multiple locations spatially in relation to the heart, wherein cardiac information signals are sensed. A processor receives and analyzes the activation onsets of the cardiac information signals to determine an arrangement of activation onsets. A representation that indicates the clinical source of the rhythm disorder is generated based on the arrangement of the activation onsets.

Abstract: A physiological parameter measurement device comprising a processor and a video processing module coupled to the processor to divide each of a plurality of frames of a video into a plurality of blocks, where the video is of a body part of a subject whose physiological parameter is to be determined. The video processing module further is to select a block having highest peak signal to noise ratio (PSNR) from amongst the plurality of blocks. Further, the video processing module is to extract a photoplethysmogram (PPG) signal from the video based on a block identifier associated with the block. The physiological parameter measurement device further comprises a signal enhancement module coupled to the processor, to process the PPG signal to obtain an enhanced PPG signal for determining a value of the physiological parameter for the subject.

Abstract: An electrode system include a flowable and cohesive surface contact element comprising a hydrophilic polymer swollen with an electrolyte fluid, the contact element having a Q? ratio of at least 5 as defined by the equation Q ? = W W W G wherein WG is the dry weight of the hydrophilic polymer and WW is weight of water in the sample after absorption of the electrolyte fluid comprising water and an electrolyte salt. The surface contact element can consist essentially of the hydrophilic polymer swollen by the electrolyte fluid. Another electrode system includes a contact element including a crosslinked hydrophilic polymer matrix. The contact element has a Q? ratio of at least 5 as defined by the equation Q ? = W W W G . The contact elements can also have a Q? ratio of at least 6, at least 7, at least 10 or even at least 11.

Abstract: A stimulation electrode assembly configured to be positioned relative to a patient for an operative procedure is disclosed. The stimulation electrode may be a connection or self-contained component to contact a portion of a nerve. The stimulation electrode may provide or receive a signal to and/or from the nerve to assist in testing integrity of the nerve.

Abstract: Methods and systems for evaluating the electrical activity of the heart to identify novel ECG patterns closely linked to the subsequent development of serious heart rhythm disturbances and fatal cardiac events. Two approaches are describe, for example a model-based analysis and space-time analysis, which are used to study the dynamical and geometrical properties of the ECG data. In the first a model is derived using a modified Matching Pursuit (MMP) algorithm. Various metrics and subspaces are extracted to characterize the risk for serious heart rhythm disturbances, sudden cardiac death, other modes of death, and all-cause mortality linked to different electrical abnormalities of the heart. In the second method, space-time domain is divided into a number of regions (e.g., 12 regions), the density of the ECG signal is computed in each region and input to a learning algorithm to associate them with these events.

Abstract: A method of monitoring the cardiac function of a patient includes receiving a position input from a position sensor attached to the patient and classifying the position input into a position class. Cardiac waveform data is received for the patient and then the cardiac waveform data is compared to model waveform parameters for the position class.

Abstract: A system and method for secure physiological data processing and delivery are provided. A log of identifiers of physiological monitoring patches and of passwords is maintained in a secure database. Physiological monitoring data obtained using one of the patches is received by at least one server together with the identifier and the password associated with that patch. The received identifier and password are compared with the identifiers and passwords stored in the log. The received physiological monitoring data is stored in electronic medical records associated with the matching identifier. The password and the identifier associated with the physiological monitoring data are received from a user device over the data communications network. The received password and identifier are compared to the password and the identifier associated with the electrical medical records. The electronic medical records are provided by to the user device over the data communication network based on the comparison.

Abstract: Neural signal recording apparatus and method is described, in which a micro electrode array is utilized for performing a weighted matrix as a moving window providing superpositioning of electrode signals. A voltage distribution across the electrode array is determined as a Laplacian. The apparatus and method can be utilized in a variety of electrode sensing applications involving registering neural activity, and for electrode stimulation applications, or combinations thereof.

Abstract: The present disclosure relates to a wearable monitor device and methods and systems for using such a device. In certain embodiments, the wearable monitor records cardiac data from a mammal and extracts particular features of interest. These features are then transmitted and used to provide health-related information about the mammal.

Abstract: Physiological monitoring can be provided through a lightweight wearable monitor that includes two components, a flexible extended wear electrode patch and a reusable monitor recorder that removably snaps into a receptacle on the electrode patch. The wearable monitor sits centrally (in the midline) on the patient's chest along the sternum oriented top-to-bottom. The placement of the wearable monitor in a location at the sternal midline, with its unique narrow “hourglass”-like shape, significantly improves the ability of the wearable monitor to cutaneously sense cardiac electrical potential signals, particularly the P-wave and, to a lesser extent, the QRS interval signals indicating ventricular activity in the ECG waveforms. Additionally, the monitor recorder includes an ECG sensing circuit that measures raw cutaneous electrical signals and performs signal processing prior to outputting the processed signals for sampling and storage.

Abstract: Cardiac catheterization is facilitated by generating first and second electroanatomic maps of a heart of a subject and designating common spatial locations that correspond to first electrical events on the first electroanatomic map and second electrical events on the second electroanatomic map. The common spatial locations of the first electroanatomic map and the second electroanatomic map are aligned to establish an aligned map, and using the location data on the aligned map to guide a probe to a point of interest.

Abstract: A system automatically detects and measures ST deviation of a heart wave ECG signal in the presence of noise and accommodates baseline variation of the signal and other artifacts. A system identifies a particular point in an electrophysiological signal representing heart electrical activity using an interface for receiving an electrical signal waveform comprising an R-wave and including an ST segment portion associated with heart electrical activity of a patient over a heart beat cycle. A signal processor processes data representing the electrical signal waveform by identifying an S point and T point in the electrical signal waveform and determining a first candidate J point in the electrical signal waveform having substantially a maximum distance from a line between the identified S and T points, the distance being measured perpendicularly to the line.

Abstract: Systems and methods are provided to detect subwaveforms of an ECG waveform. Electrical impulses are detected between at least one pair of electrodes of two or more electrodes placed proximate to a beating heart and are converted to an ECG waveform for each heartbeat of the beating heart using the detector. One or more subwaveforms within P, Q, R, S, T, U, and J waveforms of the ECG waveform for each heartbeat or in an interval between the P, Q, R, S, T, U, and J waveforms that represent the depolarization or repolarization of an anatomically distinct portion of muscle tissue of the beating heart are detected using a signal processor. A processed ECG waveform that includes the one or more subwaveforms for each heartbeat is produced using the signal processor. The processed ECG waveform is received from the signal processor is displayed using a display device.

Abstract: A method of targeting fibrosis or autonomic nerve tissue for ablation in a subject is provided. The method includes performing at least one EGM analysis of a plurality of recorded atrial EGMs for a tissue in a region suspected of having fibrosis or autonomic nerve tissue. With regard to targeting fibrosis for ablation, the method includes determining one or more correlations of at least one AF EGM characteristic to a region having fibrosis from the plurality of recorded atrial EGMs for the tissue and determining whether the tissue contains dense fibrosis that would preclude effective ablation of the analysis region of the tissue. With regard to targeting autonomic nerve for ablation, the method includes determining whether one or more significant changes in EGM characteristics with autonomic blockade exist that would indicate the need to perform ablation of the analysis region of the tissue.

Abstract: A system can include a near-field instrument to be placed inside a chamber of a heart, a far-field instrument to be placed in a stable position in relation to the heart, and a control unit. The control unit is configured to identify a unique pattern in electrogram information received from the far-field instrument when the near-field instrument is in one or more positions within the heart. When the unique pattern is detected, the control unit is configured to receive electrogram information from the near-field instrument. While recording electrogram information from the near-field instrument, the control unit is also configured to record voltage and complex fractionated atrial electrogram (CFAE) characteristics of the tissue inside a heart chamber. This information combined with rotor information can be used to identify substrate versus non-substrate rotor characteristics.

Abstract: Methods and systems are presented for determining physiological information in a physiological monitor. A physiological signal (e.g., an EEG signal) received from a subject is wavelet transformed and first and second related features that vary in scale over time are identified in the transformed signal. First and second coupled ridges of the respective first and second related features may also be identified in the transformed signal. A non-stationary relationship parameter is determined and is indicative of the relationship between the first and second features and/or between the first and second ridges. Physiological information, which may be indicative of a level of awareness of a subject, is determined based on the non-stationary relationship parameter.

Abstract: A apparatus for detecting electrooculograph (EOG) signals, comprising: a pair of temple pieces connected to a bridging structure; at least one electrode on each temple piece configured to contact the skin at the temple, and to receive an EOG signal from a proximate orbital socket; a reference electrode displaced from each temple; and a processor configured to process signals from the sensors to detect saccade movements of the eyes. A wavelet-based algorithm permits analysis and coding of the saccade movements.

Abstract: The system and method may measure and monitor physiological changes in a body. In some embodiments, the system and method may measure the impedance at a site in the body. In some embodiments, the system and method identify, quantify, and localize leaks from a site following surgery, measure cardiac contractility, or lung compliance. In an embodiment, the system includes a measuring device with one or more sensors embedded in a porous matrix. Changes in the electrical properties of one or more sensors may be used to determine the presence of leaks from a site following surgery, measure cardiac contractility, or lung compliance, depending on the position of the device.

Abstract: A magnetic resonance imaging sequence is defined by an imaging protocol and parameter values for a set of parameters of the imaging protocol. A contrast signal score is computed for the magnetic resonance imaging sequence respective to a contrast type to be scored using a scoring equation. A contrast type is determined for the magnetic resonance imaging sequence based on the computed contrast signal score. In one approach, the computing is repeated for a plurality of different contrast types to be scored, and the determining is based on the computed contrast signal scores.

Abstract: A method for diagnosing cancer, comprises detecting volatile organic compounds (VOCs) contained specifically in exhaled breath of cancer patients, and more particularly, to a method for providing information for cancer diagnosis, which comprises a step of measuring whether ionized fragments of cancer-specific VOCs, which have molecular weights of (i) 69, (ii) 131 and (iii) 181, are present in exhaled breath gas collected from patients suspected of having cancer. Cancer can be early diagnosed with high sensitivity in a non-invasive manner by use of exhaled breath sampled from cancer patients. Thus, the cancer diagnosis method can diagnose cancer in a more cost-effective and rapid manner compared to conventional cancer diagnosis methods.

Abstract: A respiratory waveform analyzer, operable to analyze a respiratory waveform, which is generated based on a temporal change of a concentration of a component in respiratory gas of a subject, includes: a respiratory gas concentration generator which generates a concentration signal based on an output signal from a sensor that is placed to measure the concentration of the component; a flatness calculator which calculates a flatness indicative of flat degree of the respiratory waveform based on a temporal change of the concentration signal; and a reliability calculator which calculates a reliability of the respiratory waveform based on the flatness and the concentration signal.

Abstract: A device for monitoring human feet can include: a transmissive sheet configured to bear at least 90 kg supported at a height of no more than 23 cm, and a foot image capture system below the sheet. An optical image sensor can capture a field of view including at least 250 cm2 of the surface of the sheet. The device can have a central reflective element positioned below the sheet directly above the sensor and two outer mirrors such that two fields of view at least 250 cm2 each can be focused onto the sensor by a lens. Foot sole images can be automatically captured when a patient stands on the device. Images can be transmitted to a database and associated with the patient by analyzing the images for a unique predetermined metric.