Abstract: A method for tracking surgical items with a system including an imaging system, a display, and one or more processors is provided. The method includes capturing a video that depicts a user handling the surgical items, and performing computational analysis of the video to detect a characteristic arm motion of the user which is indicative of the user moving the surgical item to be counted in to a surgical procedure. The method further includes, in response to each instance of the characteristic arm motion being detected, updating a count of surgical items and displaying the updated count on the display.

Abstract: A patient transport apparatus including a base, an intermediate frame, a support deck with a fowler section, and a deck extension assembly with a head deck section, a brace extending between a mount end and a coupling end, and a pivot coupling attached to the coupling end and supporting the head deck section. A mount operatively attached to the fowler section defines a receiver slidably supporting the brace adjacent to the mount end for movement along a brace axis. A retainer interposed between the mount and the brace selectively retains the brace in one of a plurality of extension positions and is operable between: a retained configuration to prevent movement, and a released configuration to permit movement of the brace between the extension positions. Operation changes from the retained configuration to the released configuration in response to force applied to the head deck section along the brace axis.

Abstract: A portable configuration tool for configuring a headwall unit that is adapted to be electrically coupled to an outlet on a headwall communicates with a room device positioned within a common room with the headwall unit. The tool includes a housing, a transceiver for communicating with a portable computer, IR and RF transceivers for communicating with the headwall unit, and a controller adapted to receive a command from the portable computer that instructs the controller to transmit an initial message to the headwall unit using the infrared transceiver, receive an identifier from the headwall unit via the infrared transceiver that uniquely identifies the headwall unit, establish a communication link between the RF transceiver and the headwall unit, receive a configuration setting from the portable computer via the transceiver, and transmit the configuration setting to the headwall unit via at least one of the infrared or RF transceivers.

Abstract: A person support apparatus, such as a bed, cot, stretcher, or the like, includes an exit detection system that has, in some embodiments, multiple user-selectable modes. A first mode issues an alert in response to a static condition being met and the second mode issues an alert in response to a dynamic condition being met. The static condition may be defined by an unchanging boundary that triggers an alert if the occupant's center of gravity crosses the boundary. The dynamic condition may be defined by a changing boundary that triggers an alert if the occupant's center of gravity crosses it. The changing boundary may change based upon the occupant's height, weight, BMI, vital sign, or other characteristic. The changing boundary may also change based upon a position of one or more components of the person support apparatus, such as a siderail or Fowler section.

Abstract: A reconfigurable patient transport system may include a patient support apparatus and a patient transport apparatus. The patient support apparatus may include a hinge member, a left support board, and a right support board each coupled to the hinge member. The left support board may comprise a left proximal segment and a left wing segment each removably coupled to a left distal segment. The right support board may comprise a right proximal segment and a right wing segment each removably coupled to a right distal segment. The patient transport apparatus may comprise a support frame and an intermediate frame coupled to the support frame. The intermediate frame may comprise a support deck configured to support a patient. The patient transport apparatus may further comprise a left siderail bracket and a right siderail bracket each configured for engagement with one of the wing segments of the support boards.

Abstract: A computer-implemented method and system for estimating fluid loss. A graphical representation of a container is displayed. User inputs to display elements may include incrementing or decrementing sliding markers to desired set positions. A first user input may indicate a volume of a second fluid, and a second user input may indicate a total volume of fluid. A first volume of a first fluid may be estimated based on the first and second user inputs. A graphical representation of the first volume of the first fluid may be displayed as a fluid level within the graphical representation of the container. A second volume of the first fluid contained in an absorbent article may be estimated based on a difference between a dry weight and a wet weight measured on a scale. A quantity of the first fluid may be estimated based on the first and second volumes.

Abstract: A patient transport apparatus transports a patient over a floor surface. The patient transport apparatus comprises a support structure and support wheels coupled to the support structure. An auxiliary wheel is coupled to the support structure to influence motion of the patient transport apparatus over the floor surface to assist users. An actuator is operatively coupled to the auxiliary wheel and operable to move the auxiliary wheel relative to the support structure from a retracted position to a deployed position. A user interface sensor is operatively connected to the actuator and configured to generate signals responsive to the user touching the user interface. A controller is operatively coupled to the user interface sensor and the actuator to operate the actuator in response to detection of signals.

Abstract: An orthopedic plate is specifically configured for use in osteotomies, in which part of the plate extends into a portion of a first bone segment and part is external to the cortical surface of an adjacent bone segment to fix the segments to allow them to fuse. The plate has a first end and a second end where the end which is inserted into the bone has a chamfer and a through hole having a hole axis optionally at an oblique angle to the longitudinal axis of the plate, and which can receive a screw, peg or pin. The second end of the plate includes a locking screw hole and optionally including a compression slot extending in a direction toward a screw hole in the opposing end. Optionally, the non-locking hole has a shroud that forms an arc or portion of a cylinder over the hole. A plate driver having a recess that holds the plate is used to insert the plate into the bone.

Abstract: A personal protection system for providing a sterile barrier around medical/surgical personnel. The system includes a helmet over which a hood or a toga suspended. The helmet has a chin bar that extends forward of the face of the individual wearing the system. At least one manually actuated control for regulating one aspect of operation of the system is mounted to the chin bar. Sometimes the control is a button that is depressed to control the operation of a helmet mounted fan that draws air into the hood or toga. A microphone may also be mounted to the chin bar.

Abstract: A system for preventing relative motion between bones or sections of bone, for example, an ilium and a sacrum. The system includes an insertion tool and an implant. The implant includes a trunk, a distal anchor, a proximal anchor, and a stem coupled to the trunk. A driver of the insertion tool receives an input for a drive shaft of the insertion tool to draw the stem proximally such that the trunk is drawn towards the insertion tool. The drawing of the trunk and engagement of first and second engagement features is configured to deploy the proximal anchor outwardly. The distal anchor may be an expandable member, and the implant may define a bore extending through the proximal anchor for the distal anchor to receive injectable material. The system may be cannulated such that the insertion tool and the implant may be directed over a guidewire to position the implant.

Abstract: An embolic device for placement in a body lumen, includes: a first segment having a first linear configuration when located inside a catheter, the first segment being configured to form a first three-dimensional structure when outside the catheter, wherein the first three-dimensional structure defines a cavity; and a second segment extending from the first segment, the second segment having a second linear configuration when located inside the catheter, the second segment being configured to form a second three-dimensional structure when outside the catheter; wherein the cavity of the first three-dimensional structure is configured to accommodate at least a majority of the second three-dimensional structure.

Abstract: A device (10) for collecting and processing bone fragments is disclosed. The device comprises a chamber member (12), a press member (14), an intake port (16), and a vacuum port (18). A compression surface (20) and a filter support surface (22) configured to support a filter are defined by said chamber and/or press member. The intake port is on the chamber and/or press member and is configured to receive a composition comprising bone fragments. The vacuum port is on the chamber and/or press member. The chamber member and the press member are rotationally coupled with one another. The composition is acquired through the intake port and collected between the compression surface and the filter support surface. The application of rotational force to the chamber and/or press member in a first direction moves the compression surface and the filter support surface together to compress the composition therebetween to compact, and further remove filtrate from the composition.

Abstract: A protective system for a patient transport apparatus includes the patient transport apparatus with a base arranged for movement along floor surfaces and an intermediate frame coupled to the base and supporting a patient support deck. A mattress is disposed on the patient support deck. The protective system further includes a keeper coupled to the intermediate frame and further includes a cover having a first side configured to absorb fluid and a second side configured to at least partially limit fluid from transferring through the cover towards the first side. The cover is movable by a caregiver between three positions: (i) a stowed position secured within the keeper, (ii) an environmental deployed position with the first side facing towards the mattress, and (iii) a patient deployed position with the first side facing away from the mattress.

Abstract: A method includes displaying visual guidance for guiding a user through an endoscopic camera calibration process. The visual guidance guides the user to direct an endoscopic camera at a plurality of different regions of a field of calibration markers. Images captured by the endoscopic camera while the user directs the endoscopic camera at the calibration markers are received. Suitability of images for use in calibration for the endoscopic camera is determined. In accordance with determining that at least one image is suitable for use in calibration, the visual guidance is updated to indicate to the user that the respective region of the plurality of different regions of the field of calibration markers has been successfully imaged. Calibration factors for calibrating the endoscopic camera are determined based on images determined to be suitable for use in calibration for the endoscopic camera.

Abstract: A patient support system comprises a patient support apparatus for patients. The patient support apparatus comprises a base and a patient support surface supported by the base. The patient support apparatus also comprises powered devices that perform one or more predetermined functions on the patient support apparatus. Multiple input devices are employed to control the powered devices. The input devices are designed to enable caregivers to cause operation of the powered devices, as needed, while freeing the caregivers to perform other tasks.

Abstract: A vaso-occlusive device delivery assembly includes a pusher assembly having proximal and distal ends, a conductive sacrificial link disposed at the distal end of the pusher assembly, and a vaso-occlusive device secured to the pusher assembly by the sacrificial link. The pusher assembly includes first and second conductors extending between the proximal and distal ends thereof. The sacrificial link is electrically coupled between the first and second conductors, such that the first conductor, sacrificial link and second conductor form an electrical circuit, and, when a disintegration current is applied through the sacrificial link through the first and second conductors, the sacrificial link thermally disintegrates, thereby releasing the attachment member and vaso-occlusive device from the pusher assembly.

Abstract: A patient handling device includes a frame for supporting a patient, a controller, and two alert lights which are activated when a controller detects an alert situation, such as, but not limited to, a patient exiting from the patient handling device. The controller is in communication with the alert lights and operable to monitor an integrated bed exit system. The alert lights are positioned adjacent the foot end corners of the frame and are viewable by a user positioned anywhere within a 270 degree section of a circle defined at the center of the patient handling device. The alert lights include one or more Light Emitting Diodes (LEDs).

Abstract: Provided herein are systems and methods for transmitting medical imaging data across a transmission channel that may be bandwidth constrained. In one or more examples, the system and methods can include transmitting the medical imaging data across a channel using a first specification, and then changing the specification in response to a detected reduction in the available bandwidth of the channel. In one or more examples, the second specification can be based on the type of video data being transmitted. In one or more examples, the medical video data can be apportioned into a region of interest and a region of non-interest, and each region can be transmitted across the channel based on the available bandwidth of the channel.