Abstract: A finger biometric sensor may include a substrate and an array of magnetic field finger biometric sensing pixels carried by the substrate. The finger biometric sensor may also include processing circuitry coupled to the array of magnetic field finger biometric sensing pixels and capable of generating a magnetic field extending into a finger positioned adjacent the array of magnetic field finger biometric sensing pixels to cause eddy currents in the finger. The processing circuitry may also be capable of sensing a counter magnetic field caused by the eddy currents representative of at least one finger biometric characteristic.

Abstract: The invention provides methods for directing a localized biological response of a mammalian body to an implant disposed within the body. In one embodiment, a delivery system is positioned outside the body and adjacent to the implant within the body. The delivery system comprises a first tissue response modifier effective for directing a localized biological response of the body to the implant. The tissue response modifier is nonsurgically delivered from the delivery system into the body in a quantity effective to direct the localized biological response of the body to the implant. The invention also provides an implant system for long-term use comprising an implant and nonsurgical means for delivering a tissue response modifier through the epidermis of the body, the tissue response modifier effective for directing a localized biological response of the body to the implant.

Abstract: A non-invasive, optical-based physiological monitoring system is disclosed. In an embodiment, the non-invasive, optical-based physiological monitoring system comprises an emitter configured to emit light into a tissue site of a living patient; a detector configured to detect the emitted light after attenuation by the tissue site and output a sensor signal responsive to the detected light; and a processor configured determine, based on the sensor signal, a first physiological parameter indicative of a level of pain of the patient.

Abstract: Systems and methods of use for continuous analyte measurement of a host's vascular system are provided. In some embodiments, a continuous glucose measurement system includes an electrochemical sensor incorporating a silver/silver chloride reference electrode, wherein a capacity of the reference electrode is controlled.

Abstract: A biological fluid collection device that is adapted to receive a blood sample having a cellular portion and a plasma portion is disclosed. After collecting the blood sample, the biological fluid collection device is able to transfer the blood sample to a point-of-care testing device or a biological fluid separation and testing device. After transferring the blood sample, the biological fluid separation and testing device is able to separate the plasma portion from the cellular portion and analyze the blood sample and obtain test results.

Abstract: An advancement mechanism of a lancing device operates to sequentially advance lancets in a cartridge. The advancement mechanism includes a rotary drive gear assembly with a first gear and a second gear that co-rotate in a first angular direction by operation of an inter-gear unidirectional drive mechanism such as a ratcheting mechanism. A second-gear unidirectional lock mechanism, such as a ratcheting mechanism, locks the second drive gear from co-rotating with the first drive gear in a second opposite angular direction without impeding rotation in the first direction. The second gear directly or indirectly rotationally drives a pinion gear, which rotationally drives a cartridge gear to advance the lancets in indexed increments for use. The first drive gear is rotated in the first and second directions by a rack gear of a translating operating handle. In addition, a rotary-gear cap-displacement mechanism and a rotary-gear charging/actuation mechanism are provided in other embodiments.

Abstract: A method and system for determining anaerobic threshold intensity (AnT) of a user in a freely performed physical exercise. A physiological response of a user is measured by heart rate and measured heart rate values are recorded as heart rate data. An external workload values are recorded and are each associated with one measured heart rate values to form a plurality of data points. The data points are filtered to form accepted data points, which are classified within a plurality of heart rate segments representing a heart rate within an anaerobic threshold (AnT) of the user. A data point with highest probability is stored for each segment. A first probability factor for each accepted data point is calculated. The calculated first probability factor is compared to a stored probability factor in each segment, and the higher probability factor is retained. AnT is calculated using the stored probabilities in each segment.

Abstract: Provided is an image processing device including a specifying unit configured to specify a part of a living body within a first image on the basis of a characteristic amount of the first image capturing skin of the living body, and a setting unit configured to set a capturing condition under which a second image indicating a state of the skin of the part is captured in response to the specified part.

Abstract: A device for measuring a mechanical property of a tissue includes a probe configured to perturb the tissue with movement relative to a surface of the tissue, an actuator coupled to the probe to move the probe, a detector configured to measure a response of the tissue to the perturbation, and a controller coupled to the actuator and the detector. The controller drives the actuator using a stochastic sequence and determines the mechanical property of the tissue using the measured response received from the detector. The probe can be coupled to the tissue surface. The device can include a reference surface configured to contact the tissue surface. The probe may include a set of interchangeable heads, the set including a head for lateral movement of the probe and a head for perpendicular movement of the probe. The perturbation can include extension of the tissue with the probe or sliding the probe across the tissue surface and may also include indentation of the tissue with the probe.

Abstract: The present invention relates to hair band EEGs. More particularly, the present invention relates to hair bands.

Abstract: An implantable sensor module and medical device includes a housing having an inner shell having a thickness extending between an inner wall and an outer wall and an outer layer, wherein the inner shell and the outer layer form a substantially flat portion. A shoulder extends adjacent to a diaphragm to extend the outer layer laterally away from a central medial line extending between edges of the diaphragm. A recess portion is formed between the diaphragm and an inner side of the outer layer, and an over-fill channel is formed by the outer layer extending through the outer layer from an opening formed at the outer wall to an opening formed along the inner side of the outer layer extending along the substantially flat portion.

Abstract: A magnetic resonance imaging apparatus performs myocardial perfusion imaging of an object. An imaging unit acquires image data by imaging a heart of the object in synchronism with a biological signal from the object. An image generating unit generates an image concerning the heart of the object based on the image data. The imaging unit applies a probe pulse for detecting body motion of the object before imaging of the heart, and applies a spatial non-selective saturation pulse before application of the probe pulse, and a local selective pulse for flipping back a flip angle of the spatial non-selective saturation pulse with regard to a region to which the probe pulse is applied.

Abstract: A system that monitors various conditions of a plurality of hospital beds located in different rooms of a healthcare facility is provided. Alternatively or additionally, other types of equipment may be monitored by the system. Various configurations of network interface units that are coupleable to or integrated into a hospital bed are also disclosed. The system receives data from the hospital beds and/or other equipment and initiates a communication to a wireless communication device of at least one designated caregiver in response to the received data being indicative of an alarm condition.

Abstract: A graphical audio station of a nurse call system is operable to permit a user to perform one or more of the following functions: establish a two-way voice communication link with another computer device in another patient and/or with a another computer device located in another staff work area and/or with a wireless communication device carried by caregiver and/or with a telephone of the healthcare facility; broadcast a voice page to a group of other selected computer devices; compose and send a text message to a portable device that is carried by a caregiver and that has wireless communication capability; browse web pages and/or view multimedia content, such as videos, hosted on servers of the healthcare facility and/or that are accessible via the Internet; view and/or acknowledge and/or answer and/or cancel alerts or nurse calls originating in a plurality of patient rooms.

Abstract: An imaging system includes a radiation source, a positioner configured to rotate the radiation source along an arc path at a rate less than 0.5 degree/sec, an imager in operative position relative to the radiation source, wherein the radiation source and the imager are configured to obtain a plurality of images while the radiation source is at different positions along the arc path, and a processor configured to determine a digital tomosynthesis image using a subset of the plurality of images. An imaging method includes generating a control signal to control a positioner to rotate a radiation source through an arc path at a rate less than 0.5 degree/sec, obtaining a plurality of images that are generated using radiation from the radiation source while the radiation source is at different positions along the arc path, and determining a digital tomosynthesis image using a subset of the plurality of images.

Abstract: A SPECT diagnostic method of performing myocardial perfusion imaging on a patient, consisting of (A) administering a rest radiotracer to the patient while the patient is at rest; then (B) when the rest radiotracer is fixed in a heart of the patient, scanning the heart to obtain rest heart pumping ability information; (C) scanning the heart of the patient to obtain a rest perfusion image; (D) administering a stressing agent to the patient to place the patient's heart under stress; (E) scanning the heart of the patient to obtain stress heart pumping ability information; then (F) administering a stress radiotracer while the heart of the patient is under stress; then (G) when the stress radiotracer is fixed in the heart, scanning the heart to obtain a stress perfusion image.

Abstract: This application discusses, among other things, curved plates for immobilizing a breast of a subject for medical imaging. In an example, an immobilization assembly Can include a curved compression plate assembly, a curved support plate assembly, an assembly coupling configured to position a first concave major surface of the curved compression plate assembly opposite a second concave major surface of the curved support plate assembly, wherein a cross section view through the curved compression assembly and the curved support plate assembly includes two portions of a single ellipse separated by a distance, and wherein the curved compression plate assembly and the curved support plate assembly are configured to immobilize the biological specimen between the first concave major surface and the second concave major surface.

Abstract: This assisting tool is a multi-functional tool that is used in X-ray measurements of a subject. The multi-functionality is achieved by using the outer form and the inner structure of the tool in combination. More specifically, this assisting tool has two inclined surfaces that constitute the outer form. By inserting this assisting tool under the two legs, the two legs can be kept in a posture in which the knees are bent. The side end structure that constitutes the outer form keeps the two feet in a twisted state. A measurement chamber that constitutes the inner structure is for measuring the forearm.

Abstract: Embodiments include a system for providing blood flow information for a patient. The system may include at least one computer system including a touchscreen. The at least one computer system may be configured to display, on the touchscreen, a three-dimensional model representing at least a portion of an anatomical structure of the patient based on patient-specific data. The at least one computer system may also be configured to receive a first input relating to a first location on the touchscreen indicated by at least one pointing object controlled by a user, and the first location on the touchscreen may indicate a first location on the displayed three-dimensional model. The at least one computer system may be further configured to display first information on the touchscreen, and the first information may indicate a blood flow characteristic at the first location.

Abstract: An x-ray system comprising: at least one x-ray tube assembly; a collimator; an image detector; a monitor; means for determining the location of a Region of Interest (ROI) of a patient on said displayed image; a first controller; an image processing unit configured to modify the detected image for display on said monitor according to the image parts in said ROI; each x-ray tube assembly comprising a plurality of cathodes; and at least one anode; a second controller configured to control operating parameters of each one of said at least one x-ray tube assembly, said parameters comprising at least one collision location of electrons emitted from said plurality of cathodes on said at least one anode in reference to said collimator aperture; and means for controlling the directions of emitted x-ray beams.

Abstract: An imaging system includes a computed tomography (CT) acquisition unit and a processing unit. The CT acquisition unit includes an X-ray source and a CT detector configured to collect CT imaging data of an object to be imaged. The processing unit includes at least one processor operably coupled to the CT acquisition unit. The processing unit is configured to control the CT acquisition unit to collect at least one sample projection during rotation of the CT acquisition unit about the object to be imaged, compare an intensity of the at least one sample projection to an intensity of a reference projection, select a time to perform an imaging scan based on the comparison of the intensity of the at least one sample projection to the intensity of the reference projection, and control the CT acquisition unit to perform the imaging scan.

Abstract: A multi-source radiation generator in which plural radiation sources are arranged in series includes a control unit that controls a dose of radiation emitted from each of the radiation sources depending on positions of the radiation sources, and reduces variation in a radiation dose resulting from differences in positions of the radiation sources by changing an irradiation time, an anodic current value of each of the radiation sources depending on a distance from each of the radiation sources to a subject.

Abstract: A system and method to perform image acquisition of a subject is provided. The system includes a mobile device to move an imaging system across a floor, and a brake system that restrains movement of the mobile device. A controller includes a memory having program instructions to instruct a processor to perform the steps of: instructing movement of the mobile device in support of the imaging system to a first position for image acquisition of the subject; receiving feedback that the mobile device is located at the first position; and applying a brake force to restrain movement of the mobile device. The step of applying the brake force includes generating a vacuum in restraint of movement of the mobile device with respect to the floor.

Abstract: Provided are a radiographic imaging apparatus and a method of controlling the same. The radiographic imaging apparatus includes a radiographic source configured to emit radiographic rays in a discontinuous eigen energy spectrum, a radiographic detector configured to receive the radiographic rays, convert the received radiographic rays into electrical signals, and count the number of photons having energy that exceeds a threshold energy, and a controller configured to adjust the threshold energy by comparing an energy spectrum of the detected radiographic rays with the eigen energy spectrum of the emitted radiographic rays from the radiographic source.

Abstract: An ultrasound imaging system includes a transducer array, with an array of transducer elements that transmits an ultrasound signal and receives a set of echoes generated in response to the ultrasound signal traversing a flowing structure. The ultrasound imaging system further includes a beamformer that beamforms the set of echoes, generating a beamformed signal. The ultrasound imaging system further includes a pre-processor that performs basebanding, averaging and decimation of the beamformed signal and determines an autocorrelation of the basebanded, averaged and decimated beamformed signal. The ultrasound imaging system further includes a velocity processor that generates an axial velocity component signal and a lateral velocity component signal based on the autocorrelation. The axial and lateral velocity components indicate a direction and a speed of the flowing structure in the field of view.

Abstract: Needle deployment and imaging system includes a sheath, an imaging core, and interventional core. The imaging core and interventional core are received in first and second axial passages in the sheath and at least one of said cores will be removable and replaceable within the sheath. The imaging core may be extended from the sheath or be sealed within the first axial passage of the sheath. The interventional core will typically be advanced laterally or axially from a location near the distal end of the sheath.

Abstract: An ultrasound endoscope, having a cable for connecting the ultrasound endoscope to a driving apparatus, includes an insertion section insertable into a subject, a plurality of transducers provided at a distal end portion, an electrode formed in each of the transducers, a wiring section connected to the electrode to electrically connect the electrode and the cable, and matching circuits, at least one of which is provided at an end of or partway in each of the wiring section. The electrode, the wiring section, and the matching circuits are provided in each of the plurality of transducers. The cable includes a core wire and an insulating layer enwrapping the core wire and functions as a matching section that matches electric impedance of each of the transducers between the plurality of transducers and the driving apparatus by varying a thickness or quality of material of the insulating layer.

Abstract: An ultrasonic probe connected to an ultrasonic diagnostic apparatus having a display unit configured to display an ultrasonic image is provided. The ultrasonic probe includes a transducer array aligned in a predetermined direction for and configured to transmit an ultrasonic beam to a target object and receive a reflected ultrasonic beam, a probe display unit fixed to said ultrasonic probe and having a length at least as long as a length of said transducer array, and a display control unit configured to, based on a specific information specified in the ultrasonic image displayed on the image display unit, display a corresponding position of the specific information on said probe display unit.

Abstract: An apparatus for dispensing gel for use with a medical device comprising a storage container for storing a quantity of gel of at least one gallon, a pump for delivering gel to a user, a first delivery conduit connected to the outlet of the storage container and the inlet of the pump, and a second delivery conduit connected to the outlet of the pump on one end and having a second end terminating at a location near the patient. The apparatus includes a heat source positioned proximal to the storage container for warming the gel so that is at a comfortable temperature when it is applied to a patient.

Abstract: An ultrasound endoscope according to the invention includes: an ultrasound transducer that transmits/receives ultrasound; a housing in which the ultrasound transducer is fixed via an adhesive, and which houses the ultrasound transducer; an inner peripheral face forming a rectangular first opening portion for exposing the ultrasound transducer, the first opening portion being formed in the housing; an acoustic lens forming a part from an upper face to at least a side face of the ultrasound transducer; and a chamfered portion provided at a side face of the acoustic lens, an adhesive outlet port for the adhesive to flow to an outside from the first opening portion being formed between the chamfered portion and the inner peripheral face.

Abstract: A compact, high power, dual mode, emitting and receiving ultrasound transducer and method for applying ultrasonic energy within a living subject and for monitoring the effects it induces in tissue comprises a set of piezoelectric polymeric transducer elements and a set of piezoelectric ceramic elements, bonded together. The polymeric transducer elements have electrodes enabling their use for low power diagnostic imaging interrogation of the tissue and the ceramic transducer elements have electrodes enabling their use for high power therapy applications.

Abstract: An ultrasound observation apparatus includes: an analysis unit that analyzes a frequency of a signal using a parameter that differs depending on presence or absence of a contrast agent in a specimen to calculate a frequency spectrum, the signal being generated based on an echo signal reflected from the specimen; a calculation unit configured to calculate a feature of the frequency spectrum; a generating unit that generates feature image data for displaying visual information related to the feature in a display pattern that differs depending on the presence or absence of the contrast agent in the specimen; a determination unit that determines the presence or absence of the contrast agent using the frequency spectrum and information on a known frequency spectrum in the presence of the contrast agent in the specimen; and a control unit that changes a setting of the parameter in accordance with a result of the determination.

Abstract: A method is disclosed for generating sinograms by sampling transducers acoustically coupled with a surface of a volume after a pulse of light, each transducer being associated with a channel in an optoacoustic imaging system, and processing at least two multi-channel sinograms, each corresponding to a different one of the at least two different predominant wavelengths, to create at least two processed sinograms. The processing step includes a step of sub-band acoustic compensation. Image reconstruction is performed based upon the processed sinograms to generate at least two optoacoustic images. Image post processing is performed on the optoacoustic images to generate post-processed images. A parametric map is generated based upon information contained in the post-processed images, and an ultrasound image is generated using the transducers. The parametric map and the ultrasound image are co-registered and a co-registered image is displayed.

Abstract: A shaft of a laparoscopic instrument, having a ceramic tube which extends over the main length of the shaft and has a sheath which encloses the ceramic tube in at least some regions, is situated to cover those regions of the ceramic tube that are at risk of breakage and is designed to prevent the splinters of ceramic from penetrating through the sheath. The ceramic tube forms a predetermined breaking point in the region of the sheath.

Abstract: A method of repairing a pelvic floor disorder and a system for carrying out the method are provided. The method is effected by positioning an imaging device in an abdominal, rectal, perianal or vaginal cavity, advancing a surgical instrument through a vaginal wall under guidance of the imaging device to thereby reach a target tissue and using the surgical instrument to attach the tissue repair device to the target tissue.

Abstract: A surgical instrument comprises a steering mechanism. The steering mechanism comprises a handle at a proximal end of the surgical instrument. The handle includes a plurality of controls for controlling a movement of the surgical instrument. The steering mechanism also comprises a hub that rotatably mates with the handle and a housing positioned about the hub. The handle, the housing, and the hub communicate with each other to provide at least a first degree of freedom and a second degree of freedom. An articulation region is at a distal end of the surgical instrument. A movement of the steering mechanism handle in one and only one of the first or second degrees of freedom relative to at least one of the housing or the hub translates to a movement of the articulation region in a single plane of motion.

Abstract: A wound closure device including a first tissue anchor with a first suture filament fixedly coupled thereto at a proximal end and extending along a length to a free distal end, and a second tissue anchor with a second suture filament fixedly coupled thereto at a proximal end and extending along a length to a free distal end. The first suture filament is configured to form a slip knot at its proximal end substantially adjacent the first tissue anchor, and the second suture is configured to form a slip knot at its proximal end substantially adjacent the second tissue anchor. The length of the first suture filament passes through the slip knot of the second suture and the length of the second suture filament passes through the slip knot of the first suture filament.

Abstract: A method and a device for anchoring a suture to an object includes a shuttle and a pin made of a material which can be liquefied by means of ultrasonic vibrations. A suture is attached to a rear end of the pin. The shuttle has a shuttle body, a shuttle arm and a suture reception, wherein the shuttle arm is suitable for releasably holding the pin in a predetermined position relative to the shuttle body such that the pin can be reliably introduced into a hole in an object.

Abstract: A method and device for securing a tissue graft within a bone passage includes providing a graft fixation device that houses a closed loop having both braided and non-braided portions. A tissue graft is looped through the closed loop at the non-braided portion to attach the tissue graft to the graft fixation device. The graft fixation device is passed through the bone passage and seated against the surface of the bone to secure the tissue graft within the bone passage.

Abstract: A cutting blade for a surgical cutting and stapling instrument is disclosed therein. The cutting blade can include one or more features to direct or displace substances released from within the tissue thickness compensators used with the surgical instrument. The cutting blade may include a textured surface that can cause substances from the tissue thickness compensator to spread across the blade surface.

Abstract: Disclosed is a surgical clip for end-to-end or end-to-side vascular anastomosis and for suturing blood conduits, which comprises a V-shaped base from which at least two branches project in a direction opposed to an apex of the V-shaped base. The branches each have a hook pointing toward the base, the branches are parallel to one another before plastic deformation and each branch forms with the corresponding hook a re-entrant corner with an apex angle of between 30° and 80°. The clip has three zones of preferential deformation, at an the apex of the V-shaped base and at connecting zones between the base and the branches. After plastic deformation, the two branches remain substantially parallel. The deformation of the clip has been concentrated on the apex of the base, the angle of which has narrowed under the stress of the gripper, and on the apices, which have opened.

Abstract: An apparatus includes a body, a shaft in communication with the body, and an end effector in communication with the shaft. The end effector is operable to drive staples through tissue. The end effector comprises an anvil and a cartridge. The anvil is operable to move pivotally relative to the cartridge. The cartridge is positioned to drive staples upwardly toward the anvil. The cartridge comprises a plurality of protrusions operable to prevent lateral rocking of the anvil. The plurality of protrusions is pointed toward the anvil. In some versions, an alignment member and/or a lateral stabilization member may be used between the anvil and the cartridge.

Abstract: In accordance with the present disclosure a cartridge for use with a surgical stapler is disclosed. The cartridge has a plurality of individual directionally biased surgical staples therein and associated pushers for ejecting the staples from the cartridge, each of the staples being supported within the cartridge in spaced relation from adjacent staples and each of the staples comprising a backspan, and a pair of deformable legs depending from the backspan. The legs are configured to come into contact with anvil pockets for formation of the staple. Each of the staples has a substantially uniform cross-section along substantially the entire length of each leg, the cross-section includes a shape that is selected from the group consisting of a trapezoid, a triangle and a semicircle.

Abstract: The present disclosure is directed to an implantable repository including a housing comprising at least one bioactive agent and at least one attachment member coupled to the housing, the at least one attachment member configured to couple the implantable repository to at least one of a medical device and a tissue surface.

Abstract: A surgical instrument is disclosed. The surgical instrument comprises a handle, a shaft comprising a proximal portion extending from the handle and a distal portion, and a firing member. The surgical instrument further comprises a motor, wherein the motor is configured to be operated in a first direction to advance the firing member toward the distal portion during a firing stroke, wherein the firing stroke comprises a firing stroke end, and wherein the motor is configured to be operated in a second direction to retract the firing member away from the distal portion. The surgical instrument further comprises a switch configured to detect when the firing member has reached the firing stroke end, wherein the motor is configured to be automatically operated in the second direction when the switch detects the firing stroke end.

Abstract: Stents and methods of using stents are provided. Stents of the invention provide external support structure for a blood vessel segment disposed within, wherein the stents are capable of resilient radial expansion in a manner mimicking the compliance properties of an artery. The stent may be formed of a knitted or braided mesh formed so as to provide the needed compliance properties. A venous graft with the stent and a vein segment disposed within is provided, wherein graft is capable of mimicking the compliance properties of an artery. Methods of selecting stents for downsizing and methods of using the stents of the invention in downsizing and smoothening are provided. Methods of replacing a section of an artery with a venous graft including a stent of the invention are provided. Methods of reducing intimal hyperplasia in implanted vein segment in a venous graft using stents of the invention are provided.

Abstract: An anvil assembly suitable for trans-oral delivery includes an anvil head configured to receive a guide suture that is severed during a stapling procedure. An anvil delivery assembly includes the anvil assembly and a suture guide assembly secured to the anvil assembly.

Abstract: A tissue ligating device for ligating a tissue includes a suture having an elastic restoring force, and a hook-shaped member including a groove portion, connected to a first end of the suture, and disposed in a direction along a derivation direction of the suture and in a direction opposite to the derivation direction of the suture with respect to the first end of the suture.

Abstract: Apparatus for advancing a vascular implant into a blood vessel. The apparatus comprises a first elongate member, the first elongate member having sufficient column strength to function as a pusher member; and a second elongate member, the second elongate member being thinner than the first elongate member and extending to a distal end located at a first point which is at or near a distal end of the first elongate member. The elongate members form an implant retaining portion while the distal end of the second elongate member is located at the first point. The implant retaining portion is located proximal of the first point. The implant retaining portion comprises a space located between the elongate members and configured for receiving an implant portion, with the first elongate member on one side of the space and the second elongate member on another side. The implant retaining portion further comprises a proximal side and a distal side which further circumscribe the space.

Abstract: A method for confined and controlled treatment of a target area of an internal body lumen using negative pressure applied to the target area, the method permitting treatment to proceed without interrupting the flow of bodily fluid through the body lumen, the method including deploying a resilient stent having a liner to define the target area and passages within the liner connected to a catheter tube so that the negative pressure may be applied through a lumen of the catheter tube from a source connected to the catheter tube without impacting the inflated stent and without impacting the ability of body lumen fluid to flow through the stent, thereby permitting therapy to proceed without disrupting the natural flow of bodily fluids or the delivery of nutrients within the body lumen during therapy.