Abstract: A cleaning system may include a first mobile robot, a communication unit configured to communicate with a second mobile robot that emits a second signal, and a controller configured to recognize the location of the second mobile robot using the second signal, and control a moving speed of the first mobile robot such that the second mobile robot follows a trajectory corresponding to the movement of the first mobile robot based on the recognized location. The controller may transmit a first signal to the second mobile robot in response to the first mobile robot approaching the second mobile robot to within a distance less than a threshold distance from the second mobile robot, and control avoidance moving of the first mobile robot and the second mobile robot based on the second signal of the second mobile robot responding to the first signal.

Abstract: An extractor is provided. The extractor comprises: a base movable along a surface; a handle configured to be gripped by a user to move the base; a nozzle in fluid communication with a suction motor configured to generate a suction airflow through the nozzle; an encoder operable to generate an encoder signal as a first signal based on user-initiated movement of the base along the surface in a forward direction and as a second signal based on movement in a rearward direction; and a controller operatively connected to the encoder and the suction motor, the controller being configured to change a power to the suction motor to a forward power level based on the first signal during operation of the extractor and to a rearward power level based on the second signal during operation of the extractor, wherein the forward power level is less than the rearward power level.

Abstract: A method of operating an autonomous cleaning robot includes receiving, at a handheld computing device, a first input representing a first set of cleaning schedule parameters for a first cleaning schedule for the autonomous cleaning robot, the first cleaning schedule corresponding to a first area. The method includes presenting, on a display of the handheld computing device, the first cleaning schedule. The method includes receiving, at the handheld computing device, a second input representing a second set of cleaning schedule parameters for a second cleaning schedule for the autonomous cleaning robot, the second cleaning schedule corresponding to a second area different from the first area. The method includes presenting, on the display, the first and second cleaning schedules, and initiating a transmission to the autonomous cleaning robot, based on the first or second cleaning schedules, the transmission including data for causing the robot to initiate a cleaning mission.

Abstract: The present invention provides a mop cleaning cloth and a method for manufacturing the same. The mop cleaning cloth comprises, sequentially from bottom to top, a base cloth layer, a water-absorption layer and a dirt removal layer. The dirt removal layer is formed by high terry fabrics and low terry fabrics. The ratio of the terry height of the high terry fabrics to the terry height of the low terry fabrics is 1.1-5:1. The high terry fabrics have a terry height of 2-20 mm and low terry fabrics have a terry height of 1-10 mm. The water-absorption layer is formed by a water-absorption fabric made from water-absorption fibers. The base cloth layer is formed by a terry fabric. The manufacturing method is simple, and the mop cleaning cloth is easy to manufacture and has the advantages of being small in resistance, high in water absorptivity and dirt collection and removal capacity, and the like.

Abstract: A dishwasher can include a tub defining a treating chamber receiving dishes for treatment, a spray system providing treating liquid to the treating chamber, a first dish rack located in the tub and having a bottom wall with inclined portions configured to cradle a glass therebetween and prevent the glass from rolling.

Abstract: A dishwasher, in particular a household dishwasher, includes a mechanism for modifying odor. The mechanism for modifying odor includes an ozone generator for odor neutralization in a dishwasher cavity and a system for fragrance introduction into the dishwasher cavity. A control device has stored therein a process, which firstly provides for the odor neutralization by the ozone generator and then introduction of a new fragrance by the system for fragrance introduction.

Abstract: A dishwashing appliance includes a tub defining a wash chamber. The tub includes an inlet and an outlet. The dishwashing appliance also includes a drying system in fluid communication with the wash chamber. The drying system includes a heat pipe heat exchanger having a condenser section and an evaporator section. The evaporator section is downstream of the outlet. The condenser section is downstream of the evaporator section and upstream of the inlet. A thermoelectric assembly is in thermal communication with the heat pipe heat exchanger.

Abstract: A method and appliance utilize one or more sprayers that are coupled to both a liquid supply and an air supply through a common hydraulic circuit such that both liquid and pressurized air can be supplied to the one or more sprayers. A common motor may operate both an air pump and/or a water pump of the appliance. The air pump and/or water pump may supply fluid to one or more sprayers and/or other apparatuses within the appliance.

Abstract: A three-dimensional endoscope comprises a video signal input portion to which a first video signal is obtained by a first imaging system and a second video signal is obtained by a second imaging system are inputted. A video signal identification portion that identifies a two-dimensional video signal and a three-dimensional video signal are obtained from the video signal input portion. An image condition detection portion that when the video signal identification portion has detected the two-dimensional video signal, analyzes a display area of a two-dimensional image to detect a foggy region. An image combining portion that, when the image condition detection portion has detected a foggy region in a video of at least one of the first imaging system and the second imaging system, combines both of the first video signal and the second video signal to generate a composite image in which fogginess of the foggy region being eliminated.

Abstract: A system may control an illuminator to illuminate a surgical site with non-white light and control a camera to capture light reflected from the surgical site. The camera may separate the captured light into a plurality of color components. The plurality of color components may be captured by the camera as a plurality of sets of pixels of a frame in a video stream, and each set of the plurality of sets of pixels may be in a different color channel of the camera. The system may further control, based on color component characteristics of the light captured by the camera, the illuminator to configure the non-white light such that each color channel of the camera has an about equal response to the light captured by the camera for a subsequently captured frame in the video stream.

Abstract: An endoscopic system comprises an image capturing device. The image capturing device captures an image of an examinee and generates a captured image signal with respect to the examinee. A control device is connected to the endoscope. A first controller is disposed in the endoscope and having a first sender/receiver communicating with the control device during a predetermined period when the endoscope is connected to the control device so as to send a plurality of parameters for driving the image capturing device to the control device. A second controller is disposed in the control device and having a second sender/receiver receiving the parameters sent from the first controller during the predetermined period when the endoscope is connected to the control device. An output value controller is disposed in the control device and setting predetermined output values relative to the control device required to drive the image capturing device.

Abstract: A surgical equipment holder is disclosed. The surgical equipment holder includes a first arm pivotable relative to a base, a second arm pivotably coupled to the first arm and an end effector pivotable relative to the second arm. The surgical equipment holder also includes a lever configured to actuate between a locked and unlocked position by use of a single hand by an operator. The end effector of the surgical equipment holder is configured to support and finely adjust the position of any number of surgical accessories during surgical procedures.

Abstract: A disposable air/water valve for an endoscope, including a shaft having a passage from an opening to a vent. The shaft has grooves and ridges and a protrusion formed at the vent. Seals are set within some of the grooves. An inner ring, having a diaphragm, extends from an outer circumference of the inner ring to an internal circumference of an outer cap. Hinges extend vertically downward from the diaphragm and ribs are formed along the internal circumference of the outer cap. A button cap has an internal ring that securely attaches to the shaft. A resilient member is securely disposed between the button cap and the diaphragm. The outer cap, inner ring, and internal ring of the button cap define a central bore to accommodate the shaft therein.

Abstract: An endoscope, including: a handle, a sheath tube, an endoscopic cannula, and a tensioning mechanism. The sheath tube includes a first axial guide hole and a first joint pin disposed in the first axial guide hole. The handle includes a second axial guide hole and a second joint pin disposed in the second axial guide hole. The first joint pin matches and is directly connected to the second joint pin. The sheath tube matches and connects to the handle. The handle includes a cavity and the tensioning mechanism is disposed in the cavity. The endoscopic cannula includes a flexible part extending out of the sheath tube and a rigid part fixed in the sheath tube. The flexible part includes a steering wire. The first joint pin is connected to the steering wire. The tensioning mechanism is connected to the second joint pin.

Abstract: An apparatus for dental irrigation may be provided to project fluid onto the surfaces of, and the interproximal spaces between, a user's teeth and gum-line. The apparatus may comprise two hollow U-shaped manifolds having orifices located on their interior faces used as fluid jets. The manifolds may be connected, at a central point of reflection, by a rotating inlet joint which supplies the fluid flow. When placed in the user's mouth, the apparatus may be designed to receive the top and bottom sets of teeth in each corresponding U-shaped manifold, with orifices configured to provide fluid jets aligned towards the lingual and buccal side of the teeth. The orifices may be staggered to provide staggered fluid flow. A user's teeth may be cleaned with a controlled fluid flow by moving the apparatus in a sweeping motion between each set of rear molars.

Abstract: In some embodiments, endoscopy systems and/or methods of using endoscopy systems are described. In some embodiments, an endoscopy system comprises a shaft having an image sensor within a distal tip of the shaft. The shaft can have an expandable cuff disposed on an outer surface of the shaft. The expandable cuff can be moved from a contracted configuration to a deployed configuration. In the deployed configuration, an outer surface of the expandable cuff can inhibit, reduce, or prevent fluid (e.g., blood) flow in the vessel. Inhibiting or preventing the fluid flow can permit direct visualization of the interior of the vessel by the image sensor without interference from the fluid.

Abstract: A machine for treating a medical apparatus, such as an endoscope washer-disinfector, can be integrated into a wall at an opening of the wall. The wall can separate a first enclosure with a controlled/non-controlled atmosphere from a second enclosure with a non-controlled/controlled atmosphere. The machine may include first and second openings configured to allow the medical apparatus to be loaded into/unloaded from the machine. The machine may also include first and second doors sealingly closing the openings. The machine may include a partitioning interface attached to the wall that closes the opening in the wall and a movable part that can be removed from the partitioning interface. The movable part can at least partially carry a pump and solenoid valve of the treatment system. The movable part can be positioned immediately adjacent to the partitioning interface when the treatment machine is in an operating position.

Abstract: An image capturing device comprises an elongated body, an imaging window coupled to a distal end of the elongated body, and a heat source within the elongated body. The heat source is configured to apply heat to the imaging window to remove condensation from or prevent condensation from forming on the imaging window.

Abstract: A method and apparatus for improving a heat dissipation capacity. An apparatus comprises an elongate member, a housing, and a heat pump device. The elongate member has a distal end and a proximal end. The housing is coupled to the proximal end of the elongate member. The heat pump device is coupled between the elongate member and the housing. The heat pump device is configured to transfer thermal energy between the elongate member and the housing.

Abstract: A handheld endoscope has a disposable, single-use portion that includes a fluid hub, cannula, distal tip and is steerable by the operator though actuation of one or two levers. The endoscope also includes re-usable portion that has a handle and display module. The distal tip includes LED illumination and an imaging module that feeds live video to the display module that is rotatable to allow viewing by the operator and others. The single-use and re-usable portions mate and un-mate with each other via physically separated mechanical and electrical connectors. The single use portion can include grasper device that can be actuated by an operator using an actuation tab.

Abstract: An excitation force (internal or external) and phase-sensitive optical coherence elastography (OCE) system, used in conjunction with a data analyzing algorithm, is capable of measuring and quantifying biomechanical parameters of tissues in situ and in vivo. The method was approbated and demonstrated on an example of the system that combines a pulsed ultrasound system capable of producing an acoustic radiation force on the crystalline lens surface and a phase-sensitive optical coherence tomography (OCT) system for measuring the lens displacement caused by the acoustic radiation force. The method allows noninvasive and nondestructive quantification of tissue mechanical properties. The noninvasive measurement method also utilizes phase-stabilized swept source optical coherence elastography (PhS-SSOCE) to distinguish between tissue stiffness, such as that attributable to disease, and effects on measured stiffness that result from external factors, such as pressure applied to the tissue.

Abstract: An ophthalmic apparatus includes: a light source; a measurement optical system that irradiates an eye with light from the source and guides reflected light from the eye; a reference optical system that guides the light from the source to use the light from the source as reference light; an abnormality detection optical system that has an optical path length of a predetermined length and to guide the light from the source to use the light from the source as abnormality detection light; a light receiving element that receives measurement interference light being combination of the reflected light from the eye and the reference light and abnormality detection interference light being combination of the abnormality detection light and the reference light, and the ophthalmic apparatus determines whether the measurement interference light is abnormal based on waveform of an abnormality detection interference signal outputted from the light receiving element.

Abstract: Systems and methods are provided for evaluating an eye using retinal fluid volumes to provide a clinical parameter. An optical coherence tomography (OCT) image of an eye of a patient is obtained. The OCT image is segmented to produce a total retinal volume and one or both of a subretinal fluid volume and an intraretinal fluid volume for a region of interest within the eye. A metric is generated as a function of the total retinal volume and one or both of the subretinal fluid volume and the intraretinal fluid volume. A clinical parameter for the patient is determined from the metric. The determined clinical parameter is provided to a user at a display.

Abstract: Provided is a technique with which it is possible to measure a subject's reaction by moving a visual target object in an arbitrarily defined direction as well as a horizontal direction. A dynamic visual acuity measuring device includes a projector projecting an index image pattern, a reflecting mirror reflecting light from the projector, a screen receiving light from the reflecting mirror and displaying the index image pattern, a movable casing holding and maintaining relative positions of the projector, the reflecting mirror, and the screen, a fixed casing supporting the movable casing, and a rotating shaft linking the movable casing rotatably to the fixed casing. In this device, the index image pattern displayed on the screen is moved in one direction by the reflecting mirror being displaced and a direction of movement of the index image pattern is changed in a coordinate system fixed to the fixed casing by the rotating shaft being rotated.

Abstract: A wavefront device produces adjustable amplitudes in optical path differences and adjustable axis orientation angles. Two substantially identical wave plates have a wavefront profile of at least the third order Zernike polynomial function which are not circularly symmetric, as denoted by Z(i,j) where i?3 and j?0. The wave plates are mounted in rotatable mounts with their optical centers substantially aligned with each other. An subjective wavefront refraction instrument and method are provided to correct low and high order aberrations of the eye, using the adjustable wave plates that have astigmatism and higher order Zernike function optical path difference wavefront profiles.

Abstract: Disclosed embodiments may include a device, system and method for providing a low cost device that can measure refractive errors very accurately via attachment to a smart phone. A disclosed device may use ambient light or a light source in simulating the cross cylinder procedure that optometrists use by utilizing the inverse Shack-Hartman technique. Using an optical device, in conjunction with a smart phone, the user first changes the angle of the axis until he/she sees a cross pattern (the vertical and horizontal lines are equally spaced). The user adjusts the display, using motorized controls on the on the optical device, to make the lines come together and overlap, which corresponds to bringing the view into sharp focus, thus determining the appropriate optical prescription for the user.

Abstract: The disclosure herein provides methods, systems, and devices for improving optical coherence tomography machine outputs through multiple enface optical coherence tomography angiography averaging techniques. The embodiments disclosed herein can be utilized in ophthalmology for employing optical coherence tomography (OCT) for in vivo visualization of blood vessels and the flow of blood in an eye of a patient, which is also known generally as optical coherence tomography angiography (OCTA).

Abstract: An ophthalmological device according to the embodiments comprises an objective lens, a subjective inspection optical system, and an interference optical system. The subjective inspection optical system includes an optical element capable of correcting aberration of a subject's eye and projects a visual target onto the subject's eye via the objective lens and the optical element. The interference optical system splits light from a light source into reference light and measurement light, projects the measurement light onto the subject's eye via the objective lens and the optical element, generates interference light between returning light of the measurement light and the reference light, and detects the generated interference light.

Abstract: The object of the present invention is to develop an ophthalmologic microscope of a new method that increases the degree of freedom in the optical design in the Galilean ophthalmologic microscope provided with an OCT optical system. The present invention provides an ophthalmologic microscope 1, wherein an observation optical system 400, an objective lens 2, and an OCT optical system 500 are placed in such a way that the optical axis of the OCT optical system O-500 does not penetrate through objective lens 2, and the optical axis of the observation optical system O-400 and the optical axis of the OCT optical system O-500 are non-coaxial, and wherein the ophthalmologic microscope further comprises a SLO optical system 1500 that scans a light ray which is a visible ray, a near infrared ray, or an infrared ray and guides the light to the subject's eye so as to become substantially coaxial with the optical axis of the OCT optical system O-500.

Abstract: An ophthalmological device according to one aspect of the present disclosure includes a support structure, an illumination light source, an observation optical system, and a controller. The support structure is configured to support a subject's face. The illumination light source is configured to illuminate a subject's eye. The observation optical system includes an imaging element configured to receive light reflecting off the subject's eye. The controller is configured to acquire, from the imaging element, a first image captured when the illumination light source is on and a second image captured when the illumination light source is off and determine whether the subject's face is placed on the support structure based on a difference between the first image and the second image.

Abstract: An analyte monitoring system may include an analyte sensor, two or more devices including a display device and a second device, and a transceiver. The transceiver may be configured to (i) receive measurement information from the analyte sensor, (ii) establish a connection with the display device while being connected with no other device of the two or more devices, (iii) convey first information to the display device while connected with the display device, (iv) establish a connection with the second device while being connected with no other device of the two or more devices, and (v) convey or receive second information to or from the second device while connected with the second device. The display device may be configured to (i) receive the first information from the transceiver and (ii) display an analyte level based on at least the first information.

Abstract: A monitoring system a user activity sensor to determine patterns of activity based upon the user activity occurring over time.

Abstract: An automatic clipping technique capable of satisfactorily extracting blood vessels to be extracted is provided. A specific tissue extraction mask image which is created by extracting a specific tissue (for example, a brain) from a three-dimensional image acquired by magnetic resonance angiography and a blood vessel extraction mask image which is created by extracting a blood vessel from an area (a blood vessel search area) which is determined using a preset landmark position and the specific tissue extraction mask image are integrated to create an integrated mask. By applying the integrated mask to the three-dimensional image, a blood vessel is clipped from the three-dimensional image.

Abstract: Method for diagnosing conditions consistent with the presence of cranial blood vessel blockage and large vessel occlusions (LVO's) using the framework of a small head-harness that is transportable, field-expedient, and durable. A single pulse set using ultrasonic or near-infrared energy is broadcast into a patient's brain allowing the apparatus to perform an area scan of the brain and detect and decipher cranial blood vessel blockage and LVO signal patterns. The interpretation of the pattern lies within the internal programming which produces a binary signal as to whether an LVO is suspected or not.

Abstract: An image processing apparatus is described herein including an image input unit that receives an input of a tomographic image of a heart imaged from outside a body; a low motion site estimation unit that estimates a low motion site of the heart on the basis of the tomographic image; an infarct site estimation unit that estimates an infarct site of the heart; and a target site identification unit that identifies a site other than the infarct site among the low motion sites, as a target site.

Abstract: Methods and apparatuses for 3D imaging to measure the shape of orthodontic aligners, teeth, and other oral structures simultaneously, in-vivo or in-vitro. These methods and apparatuses may be used to determine contact locations of aligners with teeth and/or teeth with other teeth with very high precision, including determining the size of gaps where they are not in contact. These measurements may be used design, modify or replace an aligner and/or to verify aligner fit. 3D models of the whole aligner and teeth may be generated.

Abstract: A device according to an embodiment includes an optical system employing the OCT, and tomographically visualizes the viscoelasticity of tissue of an object. The device includes an optical mechanism that guides light from a light source to the tissue of the object to scan the tissue, a loading device that applies deformation energy to the tissue, a control computation unit that computes tomographic distribution of the viscoelasticity of the tissue by controlling driving of the loading device and the optical mechanism and processing an optical interference signal from the optical system on the basis of the driving, and a display device that displays the viscoelasticity of the tissue in a form of tomographic visualization. The loading device is a non-contact loading device that loads acoustic radiation pressure in the tissue by outputting ultrasonic waves toward a focus point set in the object.

Abstract: A measurement system is provided with a light source that is configured to increase signal-to-noise ratio by increasing a light intensity from at least one of a plurality of semiconductor sources. An apparatus to receive a portion of the output optical beam, and deliver an analysis output beam to a sample. A receiver to: receive and process at least a portion of the analysis output beam reflected or transmitted from the sample, generate an output signal, and synchronize to the light source. A smart phone or tablet to: receive and process at least a portion of the output signal, store and display the processed output signal, and transmit at least a portion of the processed output signal. A cloud to: receive an output status comprising the at least a portion of the processed output signal, process the received output status to generate processed data, and store the processed data.

Abstract: A physiological signal processing system for a physiological waveform that includes a cardiovascular signal component provides a variable high pass filter that is responsive to the physiological waveform, and that is configured to high pass filter the physiological waveform in response to a corner frequency that is applied. A heart rate metric extractor is responsive to the variable high pass filter and is configured to extract a heart rate metric from the physiological waveform that is high pass filtered. A corner frequency adjuster is responsive to the heart rate metric extractor and is configured to determine the corner frequency that is applied to the variable high pass filter, based on the heart rate metric that was extracted. Analogous methods may also be provided.

Abstract: An exemplary system, method and computer-accessible medium for generating a magnetic resonance imaging (MRI) temperature profiles of a portion(s) of a patient(s) can be provided, which can include, for example receiving first imaging information related to an MRI scan of the portion(s) of the patient(s), generating second imaging information by segmenting the first imaging information into a plurality of layers, and generating the MRI temperature profile(s) by applying a bioheat equation(s) to the second imaging information. The first imaging information can be based on a point-by-point MRI scan of the patient(s). The first imaging information can be a Digital Imaging and Communications in Medicine data set produced by an MRI apparatus.

Abstract: An apparatus for measuring a bio-signal includes a pulse wave sensor that may measure a pulse wave signal, of an object of interest, that is non-equidistantly sampled based on a sampling rate of the pulse wave sensor, and a processor that may identify, using a sampling profile, a first interval based on a health index to be measured. The processor may identify, using the sampling profile, a second interval based on the health index to be measured. The processor may set the sampling rate of the pulse wave sensor to a first sampling rate in the first interval. The processor may set the sampling rate of the pulse wave sensor to a second sampling rate, that is less than the first sampling rate, in the second interval.

Abstract: A system for monitoring neural activity of a living subject is provided. The system may comprise a correspondence module configured to be in communication with (1) a neural module and (2) one or more additional modules comprising a sensing module, another neural module, and/or a data storage module. The neural module(s) are configured to collect neural data indicative of perceptions experienced by the living subject. The sensing module may be configured to collect (1) sensor data indicative of real-world information about an environment around the living subject, and/or (2) sensor data indicative of a physical state or physiological state of the living subject. The data storage module may be configured to store prior neural data and/or prior sensor data.

Abstract: A camera coupled to a processor is disclosed. The camera is configured to capture images of the subject. The processor is configured to amplify microscopic temporal variations between the images of the subject and generate a profile of at least one microscopic temporally detected physiological variation of the subject. The processor is further configured to compare the profile of the subject to a pre-existing first aggregate profile of a plurality of third-party subjects, said aggregate profile corresponding to the at least one microscopic temporally detected physiological variation of the third-party subjects, the aggregate third-party profile corresponding to a known state of the third-party subjects.

Abstract: A bio-information estimating apparatus includes a sensor part configured to measure a pulse wave signal from an object, a contact force that is applied by the object to the sensor part, and a contact area of the object that is applied to the sensor part, and a processor configured to obtain a first feature value, based on a first change in the contact area with respect to a second change in the contact force, obtain a second feature value, based on the pulse wave signal, and estimate bio-information, based on the first feature value and the second feature value.

Abstract: A system for measuring a pressure in a vein includes a needle sized and shaped to be inserted through a working channel of an endoscope. The needle is extending longitudinally and including a channel extending longitudinally therethrough. The system also includes a pressure sensing device including a longitudinally extending body sized and shaped to be slidably inserted through the channel of the needle and a sensor mounted on a distal portion of the body and connected to a proximal portion of the pressure sensing device via a connection cable. The sensor is configured to detect information corresponding to a pressure of a flow of blood through a vein.

Abstract: Embodiments of the present systems and methods may provide improved, automated monitoring of brain function. In embodiments, a multimodal, multi-sensor monitoring device may provide to monitoring of the full spectrum of brain function. In an embodiment, a system for monitoring brain function of a subject may include an apparatus for mounting a plurality of stimulus and response sensors on a head of the subject, including a cognizance stimuli-sensor suite, a physiologic sensor suite, and advance monitoring devices such as a transcranial Doppler puck, an electroencephalograph monitor, and an optic nerve sheath parameter sensor.

Abstract: An intraluminal microneurography probe has a probe body configured to be introduced into an artery near an organ of a body without preventing the flow of blood through the artery. An expandable sense electrode and an expandable stimulation electrode are fixed to the probe body at one end of each electrode such that movement of the other end toward the fixed end causes the sense electrode to expand from the probe body toward a wall of the artery. A ground electrode is configured to couple to the body, and a plurality of electrical connections are operable to electrically couple the electrodes to electrical circuitry. The sense electrode is operable to measure sympathetic nerve activity in response to excitation of the stimulation electrode. A radio frequency ablation element is located between the expandable sense electrode and expandable stimulation electrode, and is operable to ablate nerves proximate to the artery.

Abstract: A method of displaying a virtual electrogram for a virtual bipole includes receiving a plurality of electrophysiological signals from a respective plurality of electrodes carried by a multi-dimensional catheter; using the received electrophysiological signals to compute a plurality of virtual electrograms associated with a respective plurality of virtual bipoles, each having a corresponding virtual bipole orientation; selecting a virtual bipole orientation; and displaying the virtual electrogram associated with the virtual bipole having the selected virtual bipole orientation. Aspects of the disclosure can be executed through a graphical user interface of an electroanatomical mapping system that also incorporates a visualization processor.

Abstract: A magnetometer system for medical use comprises one or more induction coils for detecting a time varying magnetic field. Each coil has a maximum outer diameter of 10 cm or less, and a configuration such that the ratio of the coil's length to its outer diameter is 0.9 or more, and the ratio of the coil's inner diameter to its outer diameter is 0.6 or more. Each induction coil comprises a magnetic core. The magnetometer system further comprises a detection circuit coupled to each coil and configured to convert a current or voltage generated in the coil by a time varying magnetic field to an output signal for use to analyse the time varying magnetic field.

Abstract: Methods and systems are provided for detecting arrhythmias in cardiac activity is provided. The method and systems are under control of one or more processors configured with specific executable instructions. The method and systems obtain a far field cardiac activity (CA) signal that includes a series of beats, the CA signal including paced events. The method and systems identify the paced events in the CA signals. The method and systems determine a score based on an amount of paced events and adjust at least one parameter of an atrial fibrillation (AF) detection process based on the score.