Abstract: Methods and systems for medical imaging including synthesizing virtual projections from acquired real projections and generating reconstruction models and images based on the synthesized virtual projections and acquired real projections. For example, first x-ray imaging data is generated from a detected first x-ray emission at a first angular location and second x-ray imaging data is generated from a detected second x-ray emission at a second angular location. Based on at least the first x-ray imaging data and the second x-ray imaging data, third x-ray imaging data for a third angular location relative to the breast may be synthesized. An image of the breast may be displayed or generated from the third x-ray imaging data.

Abstract: A specimen radiography system may include a controller and a cabinet. The cabinet may include an x-ray source, an x-ray detector, and a specimen drawer disposed between the x-ray source and the x-ray detector. The specimen drawer may be automatically positionable along a vertical axis between the x-ray source and the x-ray detector.

Abstract: A tomosynthesis system has an x-ray source with an addressable array of electron emitting sections on the cathode. The x-ray source moves rotationally about an imaging target, such as a breast. During the rotation, x-rays are emitting from the x-ray source while the x-ray source continues to move. During the emission of x-rays, different subsets of electron-emitting sections of the addressable array are activated to compensate for movement of the x-ray source. By activating the different subsets of electron-emitting sections, an effective focal spot of the x-ray position appears to retain the same shape, size, and position from the perspective of the imaging target, despite movement of the x-ray source itself.

Abstract: Automated systems and methods for evaluating specimens affixed to substrates, such as slides, an exemplary system including a slide imager configured for acquiring a plurality of micro images of a specimen affixed to an substrate, the specimen including a plurality of objects distributed within a three-dimensional volume, and for generating a whole specimen image of the specimen using the micro images, wherein objects contained in the specimen are depicted substantially in focus in the whole specimen image regardless of a z-depth of the respective objects within the specimen. The whole specimen image is stored on a storage medium for subsequent review by a cytotechnologist using a computer-controlled review station including a display and a user interface, wherein the review station user interface is configured such that the cytotechnologist can review and classify the stored whole specimen images.

Abstract: Methods and devices for facilitating post-resection tissue formation to accelerate healing are provided. A hydrogel scaffold with encapsulated cells may be prepared. The encapsulated cells may be cells of the patient undergoing the resection that correspond to a type of the tissue resected. The hydrogel scaffold may be integrated with a frame to form an implantable device for insertion into a cavity created by the resection. The hydrogel scaffold and the frame may be bioabsorbable, and the frame may include non-bioabsorbable, radiopaque markers spaced along the frame. Upon insertion of the implantable device into the cavity, the encapsulated cells may interact with native cells to facilitate new tissue formation within the hydrogel scaffold and other areas of the cavity, the frame may provide temporary structural support for the cavity to reduce deformations as new tissue is being formed, and the markers may enable identification of the resection site.

Abstract: A method for imaging includes acquiring surface image data for a target using a first imaging modality. A visual representation of the target based on the surface image data is generated. Internal image data for the target is acquired using a second imaging modality. During acquisition of the internal image data, the visual representation of the target based on the acquired internal image data is updated.

Abstract: A breast compression paddle for use in an imaging system includes a compression surface and a jacket. The jacket includes at least one inflatable chamber disposed adjacent to the compression surface and a sheet covering at least a portion of the compression surface. The at least one inflatable chamber is configured to selectively inflate and induce the sheet to slide along the compression surface.

Abstract: A system for measuring muscle mass of a patient has a dual-energy radiation emission source. A radiation detector is configured to detect radiation emitted from the dual-energy radiation emission source passed through the patient. A processor has a memory with storing instructions, that when executed by the processor, perform a set of operations. The operations include receiving radiation detection data; generating a scan representation; identifying a primary fat target; determining an amount of fat in the primary fat target; comparing the amount of fat in the primary fat target to a reference; and based on the comparison, correcting an estimated amount of lean tissue to generate a corrected muscle mass value.

Abstract: A biopsy system driver includes a motor having a rotatable output shaft, a support structure, a drive shaft, an elongate lead screw and a biopsy instrument drive member. The drive shaft is rotatably coupled to the support structure and includes or is otherwise operatively connected to the motor output shaft such that activation of the motor rotates the drive shaft. The elongate lead screw is coupled to the drive shaft such that rotation of the drive shaft rotates the lead screw about an axis of the lead screw. The lead screw is axially translatable relative to the drive shaft and to the support structure. The biopsy instrument drive member is threadably coupled to the lead screw such that rotation of the lead screw causes axial translation of one of the lead screw and biopsy instrument drive member relative to the other one and to the support structure.

Abstract: A uterine fibroid tissue removal device includes an inner tube disposed within an outer tube and configured to be translated and rotated relative to the outer tube, and a separately formed unitary distal tip member attached to a distal end of the inner tube, such that the distal tip member translates and rotates relative to the outer tube along with the inner tube, wherein a distal facing open cutting end of the distal tip member in fluid communication with an axial lumen of the distal tip member translates across a tissue resection window in a sidewall of the outer tube so as to sever tissue extending therethrough, the distal tip member axial lumen being in fluid communication with an axial lumen of the inner tube, wherein an outer diameter of the distal tip member is greater than an outer diameter of the inner tube.

Abstract: A tissue removal device includes a housing, an outer tube having a distal portion configured for transcervical insertion into a uterus, an inner tube slidably disposed within the outer tube lumen, a vacuum generation chamber disposed within the housing, a movable piston slidably disposed in the vacuum generation chamber, a collection chamber, a manual actuator moveably coupled to the housing and operatively coupled to the piston, and proximal and distal one-way valves. The outer tube has an outer tube lumen, a tissue in-take opening proximate a distal end thereof, and a proximal end coupled to the housing. The inner tube has an inner tube lumen extending from an open inner tube distal end to an open inner tube proximal end, the open inner tube distal end comprising a cutting edge configured to sever intrauterine tissue extending through the tissue in-take opening in the outer tube.

Abstract: A method includes moving a radiation source and a radiation detector along a scan path substantially transverse to a longitudinal axis of a patient. A beam of radiation is emitted from the radiation source. The beam of radiation is detected at the radiation detector. The detected beam is processed so as to form a first image of a first area of the patient along the scan path.

Abstract: A breast support platform for an x-ray imaging system includes a housing having a compression plate and a front wall, and a heating system disposed at least partially within the housing. The heating system is configured to heat at least a portion of the compression plate, at least a portion of the front wall, or at least a portion of the compression plate and the front wall. In an example, the heating system includes a transparent conducting film coupled to an inner surface of the housing. In another example, the heating system includes a blower disposed at least partially within the housing, and the blower is configured to channel hot air across an inner surface of the housing.

Abstract: An x-ray tube having at least one focusing cup and an anode. The x-ray tube may have a first filament positioned in a first location between the focusing cup and the anode, the first filament having a first size, and a second filament positioned in a second location between the focusing cup and anode, the second filament having a second size that is substantially the same as the first size. The x-ray tube may also include a switching mechanism configured to engage the second filament upon failure of the first filament.

Abstract: A pump cartridge for mounting on a drive rotor includes a roller assembly having first and second hubs maintained in a spaced apart relationship and defining an axis, and a plurality of planetary rollers arranged in a circumferentially spaced orientation about the axis, the rollers mounted to the hubs displacement radially outward. One or more compressible tubing lines are interposed between the rollers and an interior wall of the pump cartridge housing. The housing and the first and second hubs collectively define a passageway through which a spreader on the drive rotor extends and may be rotated relative to the roller assembly to displace the rollers radially outward to thereby compress the tubing lines against the interior wall. A coupling feature on the first hub engages a roller driving feature of the rotor, so that rotation of the rotor causes rotation of the roller assembly about the axis.

Abstract: A breast securement device for an imaging system is provided. The securement device includes a retainer configured to attach to at least a portion of a patient's breast and a tensioning system coupled to the retainer. The tensioning system is configured to pull the retainer away from a chest wall of the patient so as to apply a pulling force to the patient's breast. The retainer may include a substantially tubular-shaped mesh material having a first end configured to receive at least a portion of the patient's breast and an opposite second end coupled to the tensioning system. In another example, the retainer may include a vacuum bag having a first end configured to receive at least a portion of the patient's breast. In still another example, the retainer may include an adhesive member configured to adhere to the patient's breast.

Abstract: Methods and devices for testing effects of external stimuli on breast appearance in an x-ray image are provided. A model for testing may include a breast phantom with an encapsulated hydrogel. In some examples, a three-dimensional cell culture and/or microfluidic channels may be encapsulated in the hydrogel. A first set of x-ray images of the model may be captured, thermal energy may be applied to the model, and a second set of x-ray images of the model may be captured while the thermal energy is being applied for comparison with the first set to determine effects of the thermal energy on appearance of the model. By incrementally increasing an amount of thermal energy applied and capturing subsequent x-ray images for comparison, an appropriate temperature range may be determined for heating compression surfaces of a breast imaging system to reduce compression-related pain and discomfort for patients without compromising x-ray image quality.

Abstract: A bracket body releasably secures a compression element to the compression arm of a breast imaging system. A pair of parallel lateral arms extends from a rigid frame which extends from the bracket. A span connects the ends of the lateral arms opposite the bracket and a flexible membrane extends from the span towards the bracket body.

Abstract: An automated system for processing a sample contained in a liquid sample container includes an automated tool head configured to rotate about a first axis, and to translate along a second axis different than the first axis, an analytic element positioner having an analytic element holder configured to releasably grip an analytic element, and a specimen transfer device carried by the tool head, wherein the tool head is configured to automatically position a working end of the specimen transfer device to obtain a specimen from a sample container held in the sample container holder, and to transfer the obtained specimen to an analytic element held by the analytic element holder, respectively, through one or both of rotation of the tool head about the first axis and translation of the tool head along the second axis.