Abstract: An infused article includes a substrate infused with an infusion component. The substrate may be an absorbent material and the infusion component may include a soap, dyed soap, or an ink and soap. The infusion component may also include a cleaner, which may include the soap, a wax, or a therapeutic agent. The infused article may be hydrated from a dehydrated state to release the infusion component.

Abstract: An article of manufacture is disclosed. The article of manufacture comprises a package and a disposable sheet. The sheet has a first surface and a second surface. One of the surfaces comprises a texture. The texture is defined by peaks and valleys such that the one textured surface may have an Average Peak to Peak Distance in the range of about 1 mm to about 20 mm, an Average Height Differential in the range of 0.5 mm to 6 mm, and a Surface Topography Index in the range of about 0.01 to about 10. The sheet may be contained within the package.

Abstract: An automatic dishwasher having a tub defining a treating chamber and a housing physically separate from the tub and defining a sump to receive liquid sprayed into the tub, the housing having an inlet fluidly connected to a liquid outlet of the tub and an outlet fluidly coupled to a sprayer located within the tub to define a recirculation path for the sprayed liquid.

Abstract: A dishwasher includes a cabinet defining a washing chamber, a door for closing an opening of the washing chamber and a fan for exhausting moist air from the washing chamber. The fan is arranged between an outer wall and an inner wall of the door, in fluid communication with the washing chamber via at least one vent hole formed in the inner wall, and includes a housing with an inlet and an outlet, an impeller in the housing and an electric motor for driving the impeller. The fan is arranged such that an axial direction of the motor is perpendicular to the inner wall. A flange is formed at an edge of the inlet to restrict water from entering the housing.

Abstract: A dishwasher appliance is provided. The dishwasher appliance includes a tub that defines a wash chamber and a rack assembly disposed within the wash chamber. The rack assembly includes a frame, a first tray and a second tray. The first and second trays are removably mounted to the frame. The first tray is sized and configured for supporting a plurality of flatware therein. The second tray is sized and configured for supporting a plurality of cooking utensils therein.

Abstract: There is provided herein an endoscope assembly comprising at least one front-pointing camera and at least one front illuminator associated therewith, at least one side-pointing camera and at least one of side illuminator associated therewith, a front working channel configured for insertion of a medical tool and a side service channel configured for insertion of a medical tool.

Abstract: An insertion device includes a movement section provided in an inserting section or an attachment unit attached to the inserting section, and moving to cause a propulsive force to act on the inserting section, a holdable grip provided to a proximal direction side with respect to the inserting section, and a driving source driven so as to generate a movement driving force to move the movement section. The insertion device includes a base member to which the grip is abutted, and a coupling member including a driving source-side abutting surface to which an outer peripheral surface of the driving source is abutted, and coupling the driving source to the base member.

Abstract: The present specification provides an apparatus for supporting one or more monitors. The apparatus includes a base stand having one or more wheels for enabling movement of the apparatus; a first rigid frame having a top end and a bottom end attached with the base stand; a second extendable frame having a top end and a bottom end and telescopically movable within the first rigid frame; a monitor arm assembly removably coupled with the top end of the second frame and configured to receive a plurality of monitors. The apparatus is transformable from a first collapsed configuration for transport and storage into a second operational configuration by rotating or removing the monitor arm assembly and by moving the second extendable frame relative to the first rigid frame.

Abstract: The present invention relates to a fully integrated sterilizable one time use disposable tissue visualization device and methods for using such devices. Preferred embodiments of the invention facilitate the visualization of an internal tissue site while causing a minimum of damage to the surrounding tissue. Further preferred embodiments may allow for the delivery of fluids and other treatment to an internal tissue site.

Abstract: The invention encompasses devices and methods used to keep the objective lens of a viewing or illuminating device, specifically an endoscope, free from obstructive fluid and dirt; specifically a device having a hollow body designed to fit over an endoscope, a transparent lens cover film that is retained within the device and that is threaded in front of the objective lens of an endoscope, thereby maintaining a clear and unobstructed transparent window in front of the endoscope lens, and an endcap configured to engage opposing edges of the lens cover film in a sealing manner.

Abstract: A system and method may display an image stream, where an original image stream may be divided into two or more subset images streams, each subset image stream being displayed simultaneously or substantially simultaneously. The images may be displayed fused. The images may be collected from an ingestible capsule traversing the GI tract.

Abstract: A soft tissue retractor includes a retractor body and a proximal projection extends generally perpendicular to the proximal end of the retractor body. An illumination waveguide engages a slot in the retractor blade to provide illumination to a surgical site while maintaining total internal reflection in the waveguide. An illumination input is formed into the proximal end of the illumination waveguide for conducting light from a source to the illumination waveguide. The proximal projection is configured for application of counter traction without the need for squeezing the retractor body. The proximal projection may be weighted to balance the soft tissue retractor as well as enabling the retractor to provide counter traction by itself. The configuration of the proximal projection further enables self-retraction by including a flat foot to prevent rolling and sliding of the retractor when it is providing self-retraction.

Abstract: The present invention relates to a fully integrated sterilizable one time use disposable tissue visualization device and methods for using such devices. Preferred embodiments of the invention facilitate the visualization of an internal tissue site while causing a minimum of damage to the surrounding tissue. Further preferred embodiments may allow for the delivery of fluids and other treatment to an internal tissue site.

Abstract: A system includes a first element configured to receive a plurality of color components that are spatially separated, wherein each of the plurality of color components comprises light of a respective wavelength, and to focus the plurality of spatially separated color components onto a first surface of a second element. The system also includes a second element having a first surface and a second surface, wherein the second element is configured to receive the plurality of color components via the first surface, to transmit to the second surface uniform light comprising the plurality of color components in a blended state, and to emit the uniform light via the second surface. The system also includes a slit lamp configured to receive the uniform light.

Abstract: An information processing apparatus includes: a light emitting unit configured to emit light; an optical unit configured to induce an optical influence to the light from the light emitting unit, the optical unit having an astigmatic lens configured to generate astigmatism with a plurality of focal lengths; a detecting unit configured to detect the light emitted in the light emitting unit, radiated outside through the optical unit, and reflected by an object; and a measuring unit configured to measure a distance to the object based on astigmatism generated in the reflection light detected in the detecting unit.

Abstract: Non-invasive methods and systems for detection of cancer or arterial vascular disorder involving administering to an individual a composition comprising noble metal nanoparticles that accumulate in a cancerous or injured vascular tissue; optically irradiating an area of a tissue suspected of being a cancerous or injured vascular tissue with a light source outputting an optical signal of at least one wavelength; and measuring diffusion reflection of the area of the irradiated tissue using at least one detector, whereby detection from the measured diffusion reflection of accumulation of the noble metal nanoparticles in this area indicates that the irradiated tissue is a cancerous or injured vascular tissue.

Abstract: A method and system for luminescence molecular imaging or tomography of a region of interest in a scattering medium is disclosed. The system comprises a non-linear luminescent marker material arranged in the scattering medium, one or more light sources positioned by at least one light source position for exciting said luminescent marker by excitation light emitted by said one or more light sources into an excitation volume, a detector at a luminescent light detection position detecting luminescence from said luminescent marker due to said excitation light, wherein said excitation light comprises pulsed excitation light.

Abstract: Systems, catheter and methods for treating Atrial Fibrillation (AF) are provided, which are configure to illuminate a heart tissue having a lesion site; obtain a mitochondrial nicotinamide adenine dinucleotide hydrogen (NADH) fluorescence intensity from the illuminated heart tissue along a first line across the lesion site; create a 2-dimensional (2D) map of the depth of the lesion site along the first line based on the NADH fluorescence intensity; and determine a depth of the lesion site at a selected point along the first line from the 2D map, wherein a lower NADH fluorescence intensity corresponds to a greater depth in the lesion site and a higher NADH fluorescence intensity corresponds to an unablated tissue. The process may be repeated to create a 3 dimensional map of the depth of the lesion.

Abstract: A medical device for the measurement of brain temperature data through the Abreu brain thermal tunnel (ABTT) is described. Brain temperature measurement is the key and universal indicator of both disease and health equally, and is the only vital sign that cannot be artificially changed by emotional states. Currently, brain temperature is difficult to measure. However, the present disclosure describes a device that readily locates the Abreu brain thermal tunnel, and is configured to provide a non-contact temperature reading of the brain. Embodiments of the disclosed device enable an individual to measure their own temperature and enable medical professionals to measure the temperature of others.

Abstract: Improved apparatus and methods for non-invasively assessing one or more hemodynamic parameters associated with the circulatory system of a living organism. In one aspect, the invention comprises apparatus adapted to accurately place and maintain a sensor (e.g., tonometric pressure sensor) with respect to the anatomy of the subject, including an alignment apparatus which is separable from an adjustable fixture. The alignment apparatus moveably captures the sensor to, inter alia, facilitate coupling thereof to an actuator used to position the sensor during measurements. The alignment apparatus also advantageously allows the sensor position to be maintained when the fixture is removed from the subject, such as during patient transport. Methods for positioning the alignment apparatus and sensor, correcting for hydrostatic pressure effects, and providing treatment to the subject are also disclosed.

Abstract: A contactless cardiopulmonary signal estimation method and apparatus are provided. A cardiopulmonary signal estimation apparatus may estimate a cardiopulmonary signal of a user from a heartbeat signal and a respiratory signal of the user in response to movement of a chest based on a cardiopulmonary exercise of the user.

Abstract: A CPU detects pulse waves in a pressure signal of a cuff detected during a period of reducing pressure applied by the cuff to a measurement site and acquires blood flow sound signals corresponding to blood flow sounds occurring in the pressure reduction period. Then, data for a pulse wave envelope that associates the amplitude values of the detected pulse waves with the pressurizing pressures at the pulse wave generation times, and data for a blood flow sound envelope that associates the amplitude values of the blood flow sound signals with the pressurizing pressures at the blood flow sound generation times are generated, and the data for the pulse wave envelope and the data for the blood flow sound envelope are used to determine whether or not there is periodic variation in the blood pressure during the pressure reduction period.

Abstract: The present disclosure relates to a method of assessing heart function and a system for assessing heart function. In detail, the present disclosure relates to a measuring a change in oxygenation or blood flow in the heart of the subject in response to a breathing maneuver and comparing the change in oxygenation or blood flow to a control. The change in oxygenation may be measured by segmenting an image of a heart, determining the signal intensity of a region of interest in a segment of the image and comparing the signal intensity to a control. An abnormal change in oxygenation blood flow or signal intensity in the heart compared to the control is indicative of reduced heart function. The disclosure further relates to a system for diagnosing heart disease which comprises an imaging device and processor configured to assess heart function.

Abstract: Vessel perfusion and myocardial blush are determined by analyzing fluorescence signals obtained in a static region-of-interest (ROI) in a collection of fluorescence images of myocardial tissue. The blush value is determined from the total intensity of the intensity values of image elements located within the smallest contiguous range of image intensity values containing a predefined fraction of a total measured image intensity of all image elements within the ROI. Vessel (arterial) peak intensity is determined from image elements located within the ROI that have the smallest contiguous range of highest measured image intensity values and contain a predefined fraction of a total measured image intensity of all image elements within the ROI. Cardiac function can be established by comparing the time differential between the time of peak intensity in a blood vessel and that in a region of neighboring myocardial tissue both pre and post procedure.

Abstract: Various technologies described herein pertain to sensing cardiovascular risk factors of a user. A chair includes one or more sensors configured to output signals indicative of conditions at site(s) on a body of a user. A seat of the chair, a back of the chair, and/or arms of the chair can include the sensor(s). Moreover, the chair includes a collection circuit configured to receive the signals from the sensor(s). A risk factor evaluation component is configured to detect a pulse wave velocity of the user based on the signals from the sensor(s). The risk factor evaluation component is further configured to perform a pulse wave analysis of the user based on a morphology of a pulse pressure waveform of the user, and the pulse pressure waveform is detected based on the signals from the sensor(s).

Abstract: A catheter is disclosed for providing pressure measurements at a vascular lesion. The catheter includes an outer component having a side opening the providing transverse access to a lumen thereof and an inner component slidably disposed within the lumen. The inner component has a guidewire lumen with a proximal side port. When the inner component is longitudinally translated relative to the outer component, the side port of the inner component is accessible through the side opening of the outer component for providing transverse access to a guidewire. A first pressure sensor is disposed proximate of a distal end of the outer component and a second pressure sensor is disposed proximate of a distal end of the inner component, such that relative longitudinal translation between the inner and outer components permits a distance between the first and second pressure sensors to be varied.

Abstract: Tools and devices are provided for determining whether a patient is well suited to receiving an implantable cardiac stimulation device by analyzing cardiac signals captured using external or cutaneous electrodes. Some of the illustrative tools include shapes for visual comparison to printed ECG strips. Kits for use of illustrative tools are also shown. Automatic devices are also disclosed which perform at least some analytical functions electronically for a user. In an example, a printed ECG strip is visually compared to a shape in order to ensure a patient is well suited to receiving a cardiac stimulation device having a particular implant location and/or cardiac signal analysis method implementation.

Abstract: In a system and method for reconstructing cardiac activation information, an analysis cardiac signal and a reference cardiac signal are processed to determine a first point of change in a derivative of the analysis cardiac signal with respect to a derivative of the reference cardiac signal. The analysis cardiac signal and the reference cardiac signal are processed to determine a second point of change in a different derivative of the analysis cardiac signal with respect to a different derivative of the reference cardiac signal. An activation onset time is assigned in the analysis cardiac signal at a point based on a mathematical association of the first point of change and the second point of change to define cardiac activation indicating a beat in the analysis cardiac signal.

Abstract: A heart monitor includes a single chest accelerometer (210), an analog signal conditioning and sampling section (215) responsive to said accelerometer to produce a digital signal substantially representing acceleration, and a digital processor (220) operable to filter the acceleration signal into a signal affected by body motion and to cancel the body motion signal from the acceleration signal, thereby to produce an acceleration-based cardiac-related signal. Other processes and electronic systems are also disclosed.

Abstract: Medical devices and methods for making and using medical devices are disclosed. An example medical device may include a catheter shaft with a plurality of electrodes coupled thereto and a processor coupled to the catheter shaft. The processor may be capable of collecting a set of signals from the plurality of electrodes, characterizing the set of signals, generating a visual representation of the set of signals and refining the visual representation.

Abstract: Medical devices and methods for making and using medical devices are disclosed. An example medical device may include a catheter shaft with a plurality of electrodes coupled thereto and a processor coupled to the catheter shaft. The processor may be capable of collecting a set of signals from the plurality of electrodes and generating a data set from at least one of the set of signals. The data set may include at least one known data point and one or more unknown data points. The processor may also be capable of interpolating at least one of the unknown data points by conditioning the data set and assigning a value to at least one of the unknown data points.

Abstract: Medical devices and methods for making and using medical devices are disclosed. An example medical device may include a catheter shaft with a plurality of electrodes coupled thereto and a processor coupled to the catheter shaft. The processor may be capable of collecting a set of signals from the plurality of electrodes, generating a set of data from at least one of the set of signals, wherein the data set includes at least one known data point and one or more unknown data points, determining a non-linear distance between the at least one known data point and the one or more unknown data points, and assigning a value to at least one of the unknown data points.

Abstract: A non-contact cardiac mapping method is disclosed that includes: (i) inserting a catheter into a heart cavity having an endocardium surface, the catheter including multiple, spatially distributed electrodes; (ii) measuring signals at the catheter electrodes in response to electrical activity in the heart cavity with the catheter spaced from the endocardium surface; and (iii) determining physiological information at multiple locations of the endocardium surface based on the measured signals and positions of the electrodes with respect to the endocardium surface. Related systems and computer programs are also disclosed.

Abstract: Implantable medical devices (IMD) configured for implantation within a recess formed in a cranium of a patient, as well as associated methods, are described. In some embodiments, the IMD includes a top external surface and another adjacent external surface, e.g., a side surface, which are oriented with respect to each other to define an acute angle. A connection module for an electrical lead or catheter may be included on the top external surface. Embodiments of the invention may facilitate implantation of an IMD within a recess formed in the cranium of a patient at a location remote to an incision made in the scalp of the patient.

Abstract: The invention discloses a method, a system, a computer program and a device for determining the surface charge and/or dipole densities on heart walls. Using the foregoing, a table of dipole densities ?(P?, t) and/or a table of surface charge densities ?(P?, t) of a given heart chamber can be generated.

Abstract: Electrical impedance myography (EIM) can be used for the assessment and diagnosis of muscular disorders. EIM includes applying an electrical signal to a region of tissue and measuring a resulting signal. A characteristic of the region of tissue is determined based on the measurement. Performing EIM at different frequencies and/or different angular orientations with respect to a muscle can aid in the assessment and diagnosis. Devices are described that facilitate assessment and diagnosis using EIM.

Abstract: A cryogenic cooling apparatus comprises a supply gas line and a return gas line adapted to be coupled to a compressor. A coupling element is positioned in gaseous communication with the supply and return gas lines, the coupling element being adapted in use to supply gas to a mechanical refrigerator so that the pressure of said supplied gas is modulated by the coupling element in a cyclical manner. A sensing system is used to monitor the operational state of the mechanical refrigerator and a control system modulates the frequency of the cyclical gas pressure supplied by the coupling element in accordance with the monitored operational state. The mechanical refrigerator has a first cooled stage and a second cooled stage, the second cooled stage being adapted to be coupled thermally with target apparatus to be cooled.

Abstract: A system (10) and method generate one or more MR data sets of an imaging volume (16) using an MR scanner (14). The imaging volume (16) includes one or more of a region of interest (ROI), the ROI including a metal element, and a local receive coil (18) of the MR scanner (14). At least one of an attenuation, confidence or density map accounting for the metal element is generated and the location of the local receive coil (18) within the imaging volume (16) is determined. The generating includes identification of the metal element within the ROI based on a phase map of the ROI generated from the MR data sets. The determining includes registering a known sensitivity profile of the local receive coil (18) to a sensitivity map of the local receive coil (18) generated from the MR data sets.

Abstract: Systems and methods for magnetic resonance imaging (“MRI”), in which accurate and conspicuous visualization of vascular calcifications and other bony structures can be achieved. An MRI system is operated to perform a pulse sequence that generates substantially similar signal intensity from soft tissues (e.g. muscle, fat, blood) within the body. For instance, blood can be rendered to have a signal intensity that is substantially similar to the vessel wall, while fat and muscle are rendered to appear substantially similar to the vessel wall. With this “neutral” contrast, arterial calcifications, which appear dark due to their low proton density, can be more readily and efficiently visualized by an interpreting physician.

Abstract: The present invention relates to an implantable sensor configured to be implanted within the body of the subject and being configured to measure impedance within a body tissue of the subject resulting from an electrical current flowing through the body tissue, wherein the body tissue is sub-dermal or subcutaneous tissue of the subject. One pair of injection electrodes is configured for injection of electrical current into the body tissue and one pair of sensing electrodes is configured to detect the resulting voltage. A detector is operatively connected to the sensing electrodes and is configured to receive the voltage detected by the sensing electrodes, wherein the detector is configured to measure the impedance of the body tissue based on the voltage detected by the pair of sensing electrodes.

Abstract: The present invention relates to a health monitoring system comprising an implantable sensor configured to measure impedance within a body tissue of the subject resulting from an electrical current flowing through said body tissue, wherein the body tissue is sub-dermal or subcutaneous tissue of said subject, the sensor including a powering and communication circuit having a coil configured to be powered by an electromagnetic field and to communicate with external devices.

Abstract: Apparatus and method for imaging a patient in an MRI system. This includes a frame, and at least one assembly that includes a patient-interface positioner connected to a reference position on the frame, a first lockable joint on the positioner; and a patient interface connected to a patient-proximal end of the positioner by a second joint, wherein the first patient-interface is moveably positioned to a selected pitch angle, a selected yaw angle, and a selected one of a plurality of distances relative to the reference position on the frame. The first lockable joint is configured to be tightened to yieldably hold the first patient-interface at the selected pitch and yaw angles, and at the selected one of the plurality of distances, relative to the reference position. Optionally a second substantially similar patient-interface and assembly are provided. The earpiece(s) optionally include audio transducer(s) and/or RF coil(s).

Abstract: A patient table system includes a patient table that includes a bed board fixed component, a bed board moving component, a linear barcode and a barcode sensor. The bed board moving component is movably disposed on the bed board fixed component. One of the linear barcode and the barcode sensor is disposed on the bed board fixed component, while the other one is disposed on the bed board moving component. The barcode sensor faces the linear barcode and is separated therefrom. The linear barcode marks the position of the bed board moving component in the direction of movement of the bed board moving component relative to the bed board fixed component.

Abstract: An endoscope system includes: a position and posture calculating portion that estimates a position of a distal end and a longitudinal direction of a distal end portion; a condition determining portion that, based on the shape information at the position of the distal end that is estimated, determines whether or not an angle that a core line direction of the luminal organ and the longitudinal direction estimated by the position and posture calculating portion form is equal to or less than a predetermined threshold value; and a position and posture information recording portion that, when the angle that the core line direction and the longitudinal direction form is equal to or less than the predetermined threshold value, records information regarding the position and the longitudinal direction of the distal end.

Abstract: Systems and methods described herein use near field communications to locate a radiating transponder, such as a pill swallowed by a patient. The system can be triggered to turn on and transmit a waveform to a set of antennas attached to, coupled with, or near the patient. The magnetic field emitted by the transponder can be measured by the receiving antennas, for example, using principles of mutual inductance. The differential phase and/or time shifts between the antennas can contain sufficient information to find the location of the transponder and optionally its orientation relative to body coordinates. The system can display the location and/or orientation of the transponder. Further, the pill can include a reservoir to deliver a payload at a particular site of the patient's body based at least in part on the determined location.

Abstract: A balloon catheter is used for dilating tubular members of the body such as dilating stenotic aortic valve leaflets found in the aortic root, and measuring the shape and dimensions of the annulus. The balloon has two larger diameter bulbous regions; one is positioned in the left ventricular outflow tract (LVOT) and the other in the aortic sinus; a smaller diameter waist region is positioned across the aortic annulus. During inflation of the balloon, the balloon waist expands in diameter until it comes into contact with the aortic annulus. The balloon pressure and inflation volume is monitored during inflation so that an inflection point in the dP/dV curve is seen at the point of contact of the waist with the annulus. Radiopaque rings and/or marker bands in the device allow the size and orientation of the elliptical annulus to be calculated.

Abstract: A method for acquiring gait parameters of an individual is disclosed. The method includes capturing calibration images from foot marker placed on feet or shoes of an individual while an individual is standing still, the calibration images are obtained from a camera worn by the individual, capturing subsequent time-varying images from the foot markers while the individual is walking, and comparing the calibration images to the subsequent time-varying images by a processing unit that is coupled to the camera to determine changes between the initial relative image size of the foot markers and the time-varying images of the foot markers as a function of time to analyze gait of the individual.

Abstract: A system for testing motor and/or performance of a human subject with a mobile device is provided. The system features a mobile device including a processor subsystem and configured to receive taps from a hand or part of a hand of a human subject on a screen of the mobile device. A tap application for the mobile device is executed by the processor subsystem and is responsive to taps by the hand or part of the hand on the screen and is configured to measure the frequency and duration of each tap by the hand or part of the hand on the screen to determine the motor and/or cognitive performance of the human subject.

Abstract: A system includes a light source and a light detector. The system further includes a first optical system configured to direct a transmitted portion of light onto the detector. The first optical system is further configured to block a scattered portion of the light. The system also includes a second optical system configured to direct the transmitted and scattered portions of the light onto the detector.

Abstract: A first temperature sensor is formed in a first measurement area so that a measurement surface thereof is exposed to an inner surface of a liquid tank (a storage body). The first temperature sensor can detect a temperature of liquid injected into the liquid tank. Further, a first input part is formed in the first measurement area so that an output surface thereof is exposed to the inner surface of the liquid tank.