Abstract: The present invention relates generally to implants and tools for the fixation or fusion of joints or bone segments. These tools include tissue dilators and protectors. Other tools include broaches used to shape bores in bone. The tools can also include a system for removing an implant from bone. Implants can include assemblies of one or more implant structures that make possible the achievement of diverse interventions involving the fusion and/or stabilization of lumbar and sacral vertebra in a non-invasive manner, with minimal incision, and without the necessitating the removing the intervertebral disc. Implants for fusing both sacroiliac joints of a patient include a long implant that extends across both sacroiliac joints.

Abstract: An artificial disc to replace a damaged spinal disc in a spinal column includes a resilient core which is fixedly connected to first and second plates. The first and second plates engage upper and lower vertebra in the patient's spine. The inner side of at least one of the first and second plates has an array of recesses into which said resilient core extends. The array of recesses includes a plurality of recesses. Each of the recesses of the plurality of recesses has surfaces which are integrally formed as one piece with the plate.

Abstract: A spinal implant has a proximal region and a distal region, and includes an upper body and a lower body each having inner surfaces disposed in opposed relation relative to each other. A proximal adjustment assembly is disposed between the upper and lower bodies at the proximal region of the spinal implant and is adjustably coupled to the upper and lower bodies, and a distal adjustment assembly is disposed between the upper and lower bodies at the distal region of the spinal implant and is adjustably coupled to the upper and lower bodies. The proximal and distal adjustment assemblies are independently movable with respect to each other to change a vertical height of at least one of the proximal region or the distal region of the spinal implant.

Abstract: A cage or spacer device for harvesting bone graft material for use in bone fusion surgery, e.g., spinal fusion. The device is inserted between facing surfaces of the bones to be fused, and a chamber is formed in the device for containing a slurry of morselized bone and blood to be effused from the bones. In one embodiment, a bone cutter assembly including a cannula having a bend at a distal end is inserted in the chamber for operation. A wire having a cutting tip is passed inside the cannula so that the tip projects a determined distance from the distal end of the cannula. Accordingly, the cutting tip strikes and cuts grooves in the facing surfaces of the bones when the cannula is rotationally driven about its axis. The mentioned slurry effuses from the grooved surfaces and remains in the chamber to promote a solid and healthy fusion.

Abstract: An expandable spinal implant assembly is configured to be inserted between two adjacent vertebral bodies. The expandable spinal implant assembly includes a substantially hollow first body with a first superior endplate with a first top inside face and a first inferior endplate with a first bottom inside face. The first superior endplate and the first inferior endplate are connected together by a lateral wall. At least one strut is arranged within said first body, connecting the first top inside face with the first bottom inside face, said strut including a first threaded through bore. The assembly further includes a substantially hollow second body with a second superior endplate and a second inferior endplate, said second body inserted within said first body. A central screw with a first end including a ball-head and a drive, said central screw further having a threaded shaft is engaged within said first threaded through bore.

Abstract: A lateral plate assembly has an elongated lateral plate for attachment to adjacent vertebrae having a first end portion and a second end portion and a pair of apertures for receiving a first and a second bone screw. The pair of apertures includes a first aperture which is an opening positioned in the first end portion for receiving the first bone screw and a second aperture which is a slotted opening to receive the second bone screw. The second end portion of the lateral plate has an open end with channelled internal sides for receiving and holding a moveable washer on top of the slotted opening. The washer is configured to move along a length of the slotted aperture. The moveable washer has an opening for holding a head of the second bone screw. Movement of the washer relative to the slotted opening increases or decreases the distance between locations of the respective screw heads.

Abstract: A cover for use in protecting a resected surface of a long bone for use in joint arthroplasty includes a body, a plurality of independently moveable members moveably attached to the body, two of the plurality of independently movable members configured to move linearly with respect to the body along a first plane and along a first axis, the body and the plurality of independently moveable members defining a first periphery of the cover along the first plane in one configuration which is smaller than, and encompassed by, a second periphery of the cover along the first plane in a second configuration, and a lip fixedly extending downwardly along an outer radial periphery of one of the body and the plurality of independently moveable members in a direction not co-planar with the first plane.

Abstract: An orthopaedic joint replacement system is shown and described. The system includes a number of prosthetic components configured to be implanted into a patient's knee. The system also includes a number of surgical instruments configured for use in preparing the bones of the patient's knee to receive the implants. A method or technique for using the surgical instruments to prepare the bones is also disclosed.

Abstract: An orthopedic joint replacement system is shown and described. The system includes a number of prosthetic components configured to be implanted into a patient's knee. The system also includes a number of surgical instruments configured for use in preparing the bones of the patient's knee to receive the implants. A method or technique for using the surgical instruments to prepare the bones is also disclosed.

Abstract: A hip joint navigation system is provided that includes a base having at least one channel disposed therethrough for receiving a pin for mounting the base to the pelvis. A mount feature is disposed on a top surface. A registration jig is configured to couple with the base and to engage anatomical landmarks. In some aspects, a patient specific jig system for hip replacement is provided including an engagement surface formed to closely mate to acetabular bone contours of a specific patient and a registration feature configured to be in a pre-determined orientation relative to an acetabulum of the patient when the jig is coupled with acetabular bone contours of the specific patient. In other aspects, methods of using the systems are provided.

Abstract: A prosthetic device having a rotatable pyramid and lateral travel limit is provided. A first member has a first end connectable to a prosthetic component and a second end with a bar having sides and a distal face. The distal face has ribs thereon. A central hole is provided through the first member. A second member has a first end with a pyramid and a second end with a ring that defines a recess with a solid face. A third member has a dome on a first end and a channel on the second end. The pyramid extends through a central hole through the dome. A screw passes through the central hole of the first member wherein it can engage the second member within the recess. The lateral movement of the bar within the channel is bound by the screw contacting the second member.

Abstract: An intraluminal vascular prosthesis assembly, having a hollow cylindrical body with a first end and a second end is provided. The assembly includes, at its first end, a first vascular prosthesis portion, and at its second end, a second vascular prosthesis portion which has only a prosthesis material. The vascular prosthesis assembly has a stent portion which is provided between the first vascular prosthesis portion and the second vascular prosthesis portion, the stent portion being free of prosthesis material to allow fluid flow therethrough and received within the aortic arch and spanning the brachiocephalic artery, left common carotid artery, and left subclavian artery when placed within the aortic arch of a patient.

Abstract: An expandable helical stent is provided, wherein the stent may be formed of an amorphous metal alloy or other non-amorphous metal with a securement. The stent is formed from flat or tubular metal in a helical coiled structure which has an undulating pattern. The main stent component may be formed of a single helically coiled component. Alternatively, a plurality of helically coiled ribbons may be used to form a stent heterogeneous in design, material, or other characteristic particular to that stent. The helical tubular structure may be secured with a securement, such as a weld, interlock or a polymer, to maintain the helical coils in a tubular configuration. The helical coils of the main stent component may be spaced apart or nestled to each other-maintain the tubular shape of the helically coiled stent and prevent the polymer layer from sagging at any point between cycles of the coils.

Abstract: Provided is a superfine polyester fiber containing at least 98 wt % of a polyethylene terephthalate component, and characterized by fulfilling the following conditions: (1) the reduced viscosity (?sp/c) is at least 0.80 dl/g; (2) the total fineness is 7-120 dtex, and the single filament fineness is no more than 0.5 dtex; and (3) the toughness parameter (X) indicated by formula (1) is at least 2.0, the tensile strength is at least 3.5 cN/dtex and the tensile elongation is at least 12%. X=(tensile strength×?tensile elongation)/(total fineness×single filament fineness)??formula (1).

Abstract: The present embodiments provide a stent for use in a medical procedure that comprises a series of proximal apices disposed at a proximal end of the stent and a series of distal apices disposed at a distal end of the stent. A trigger wire is adapted to be coupled to at least one of the proximal apices to restrain a proximal end of the stent during delivery. In a first embodiment, a first proximal apex comprises a bore for receiving the trigger wire, and a second proximal apex, disposed adjacent to the first proximal apex, comprises at least one barb. The trigger wire therefore is only coupled to selected ones of the proximal apices. In an alternative embodiment, a first proximal apex comprises a first bore and a second, adjacent proximal apex comprises a second bore, such that a single trigger wire may be disposed through the first and second bores to restrain the first and second proximal apices during delivery.

Abstract: A stent graft comprises a hollow cylindrical body and a sleeve catheter, wherein the body comprises at least a self-expanding stent and prosthetic material, wherein the body has a circumference in a compressed state which is smaller than a circumference of the body in an expanded state. The sleeve catheter is embodied as a flap-shaped compression element comprising two longitudinal edges, wherein a first longitudinal edge is attached to the body, wherein an extent of the flap-shaped compression element perpendicular to the first longitudinal edge is smaller than the circumference of the body in the expanded state, wherein, for compressing the body, the flap-shaped compression element can be placed around the body and a free second longitudinal edge is detachably fixable to fixation points arranged on the body and/or on the flap-shaped compression element.

Abstract: A gastric tube for use in a bariatric procedure includes an elongate tube and a cannulated plug coupled to the elongate tube. The elongate tube has a proximal end portion and a distal end portion. The elongate tube defines a lumen along a length thereof. The proximal end portion defines an opening in communication with the lumen. The elongate tube includes a blunt tip and an outer surface. The blunt tip is formed on the distal end portion. The outer surface defines a side opening in communication with the lumen. The cannulated plug includes a proximal end and a distal end. The proximal end is configured for connection to a vacuum source. The distal end is configured for removable receipt in the opening of the proximal end portion of the elongate tube to control a flow of one of aspiration and irrigation through the lumen.

Abstract: Systems and methods for providing torque to an assistive device are disclosed. In an embodiment, an apparatus comprises a material arranged to define a volume of space. The material may comprise a flexible portion and having a first surface and a second surface. The material may have a first position, in which the material is bent along the flexible portion and the first surface contacts the second surface. When the material is in the first position, an increase in pressure to the space creates a force between the first surface and the second surface. The material transitions from the first position to a second position in response to the force between the first surface and the second surface. The apparatus may be attached to an assistive device or other machine, such as an orthosis or prosthesis, in order to provide a torque.

Abstract: A guard for protecting a finger without interfering with athletic performance, having a rigid core that protects the finger from hyperextension and impact injuries. The guard has a proximal segment and a distal segment, each having a top surface, and a hinge assembly attached and extending above the top surfaces of the distal segment and proximal segment. The hinge assembly allows the distal segment to vary in position between a minimum position and a maximum position while remaining out of the way of adjacent fingers. The guard securely engages the finger by a distal strap that secures to a distal part of the finger, and a proximal strap that secures to a proximal part of the finger. The proximal part has sides that extend alongside the finger, and the distal segment only extends along the superior surface of the finger toward but not reaching the fingertip.

Abstract: An improved pain management and post-operative hip orthosis includes a waist strap having first and second ends and a lateral portion therebetween, a lower strap having first and second ends and a lateral portion therebetween, and a pocket extending between the waist strap and lower strap. The pocket has inner and outer panel fastened to each other to define an upper opening and a lower opening. The orthosis further includes an abduction harness including two upper straps and a lower strap coupled to each other at a central union, wherein the upper straps are secured to the top of the pocket and the lower strap is secured to the bottom of the pocket. The orthosis still further includes a rotation strap extending from the bottom of the pocket to a location on the waist strap proximate to the top of the pocket.

Abstract: An intra-oral device comprising an upper splint (7100), a lower splint (7200) and a pair of lateral connecting rods (7300). Each connecting rod has a first rod end (7310) that connects to the lower splint and a second rod end (7320) that connects to the upper splint. The connecting rods (7300) are configured to maintain the mandible in an advanced position relative to the maxilla. The upper splint (7100) includes at least one upper gutter portion (7110) that retains the upper splint on the maxilla. The lower splint (7200) includes at least one lower gutter portion (7210) that retains the lower splint on the mandible. The thickness of the at least one upper gutter portion and/or the at least one lower gutter portion may vary across the profile of the teeth.

Abstract: A sleep apnea oral appliance in which a pair of appliance trays are worn over respective orthodontic trays. The appliance trays are adjustable in order to allow them to be used with a series of orthodontic trays.

Abstract: Relatively non-invasive devices and methods for heating or cooling a patient's body are disclosed. Devices and methods for treating ischemic conditions by inducing therapeutic hypothermia are disclosed. Devices and methods for inducing therapeutic hypothermia through esophageal cooling are disclosed. Devices and methods for operative temperature management are disclosed.

Abstract: The devices and methods described herein relate to injector devices for delivering payloads to a tissue.

Abstract: A force-sensing tool includes a tool shaft that has a proximal end and a distal end, a flexure section attached at a first end to the distal end of the tool shaft, a tool tip operatively connected to the flexure section such that axial forces applied to the tool tip are coupled primarily to a first portion of the flexure section and transverse forces applied to the tool tip are coupled primarily to a second portion of the flexure section, an axial force sensor coupled to the first portion of the flexure section, and a transverse force sensor coupled to the second portion of the flexure section. The axial force sensor responds to axial forces applied to the tool tip substantially independently of the transverse forces applied to the tool tip under a designed operating range of forces, and the transverse force sensor responds to transverse forces applied to the tool tip substantially independently of the axial forces applied to the tool tip under the designed operating range of forces.

Abstract: A biological tissue cutting and fluid aspiration system provides a plurality of surgical instruments operable independent of an external control console. In some embodiments, each surgical instrument may include all sensors and controls directly applicable to the surgical instrument, and may be used independently. In some embodiments, instruments communicate status information to each other, and adjust operating parameters based on the communications.

Abstract: A method and system for use in an ocular surgical procedure is provided. The design includes a handpiece having an ultrasonically vibrating tip operational within a plurality of operating modes including a first operating mode and a sensing device, such as a vacuum pressure sensor. A controller is connected to the handpiece and sensing device and is configured to receive data from the sensing device and adjust at least one operational parameter (time/duty cycle of operation, power during operation) associated with the first operating mode and adjust at least one parameter associated with another operating mode based on the data received from the sensing device. Operational modes may include multiple longitudinal or non-longitudinal modes (torsional, transversal, etc.) or combinations of longitudinal and/or non-longitudinal modes.

Abstract: A surgical device is disclosed for cutting tissue, including for performing a capsulotomy of a lens capsule of an eye. This device includes a reversibly collapsible cutting element for cutting a portion of a capsule membrane of the eye. The cutting element includes an outer layer, an inner layer, and a bottom layer that has a higher electrical resistance than the electrical resistance of the outer layer and the inner layer. The bottom layer is configured to conduct an electrical current between the outer layer and the inner layer, which causes a temperature increase in the bottom layer for cutting tissue.

Abstract: An ocular implant adapted to reside at least partially in a portion of Schlemm's canal of an eye. The implant includes a spine extending along a longitudinal axis of the implant, a plurality of curved supports extending from the spine, each support comprising a first end extending from a first location on a first side of the spine and a second end extending from a second location on a second side of the spine, the second location being proximal to the first location, so that each support forms a portion of a helix, the spine and supports defining a volume having a maximum width perpendicular to the longitudinal axis between 0.005 inches and 0.04 inches, the ocular implant being configured to bend preferentially in a preferential bending plane.

Abstract: A system and method are presented for use in delivering electromagnetic radiation to a limbal area of an eye, for example for treatment of glaucoma. The system includes an illumination unit, a beam shaping device and a control unit. The illumination unit includes a first source of electromagnetic radiation configured and operable for producing a beam of electromagnetic radiation having first optical properties to be delivered to the limbal area of a patient's eye to interact therewith and produce a desired effect, and a second source of electromagnetic radiation configured and operable for producing a beam of electromagnetic radiation having second optical properties. The beam shaping device when accommodated in an optical path of said first and second beams defines one or more regions along a path substantially aligned with a limbus of the patient's eye.

Abstract: An apparatus for corneal crosslinking, the use of the apparatus for corneal crosslinking, and a method for corneal crosslinking are provided. The apparatus comprises a source of laser radiation; a scanner device for scanning the laser radiation; and a control computer for controlling the scanner device.

Abstract: A process for performing retinal phototherapy or photostimulation includes generating a laser light that creates a therapeutic effect to retinal and/or foveal tissues exposed to the laser light without destroying or permanently damaging the retinal or foveal tissue. The laser light is applied to a first treatment area of the retina. After a predetermined interval of time, within a single treatment session, the laser light is reapplied to the first treatment area of the retina. During the interval of time between the laser light applications to the first treatment area, the laser light is applied to one or more additional areas of the retina that is spaced apart from the first treatment area and one another. The laser light is repeatedly applied to each of the areas to be treated until a predetermined number of laser light applications to each area to be treated has been achieved.

Abstract: An ophthalmic laser treatment apparatus includes: an aiming optical system configured to irradiate an aiming beam to a patient's eye; a laser irradiation optical system configured to irradiate a laser beam for treatment to the patient's eye; a shift unit configured to make a shift of a focus shift position corresponding to a focus position of the laser beam to a posterior or anterior position with respect to a focus position of the aiming beam; a selection receiving unit configured to receive an instruction to select any one of a plurality of treatment modes; and a control unit configured to control operations of the ophthalmic laser treatment apparatus. The control unit sets a value of a parameter related to irradiation of the laser beam, the parameter including a parameter related to the shift of the focus shift position, according to the treatment mode selected with the selection receiving unit.

Abstract: Embodiments of this disclosure disclose an imaging system, including an eye interface device, a scanning assembly, a beam source, a free-floating mechanism, and a detection assembly. The beam source generates an electromagnetic radiation beam. The detection assembly generates a signal indicative of an intensity of a portion of the electromagnetic radiation beam reflected from the focal point location. A subsequent focal point of the electromagnetic radiation beam may be adjusted per the measured intensity signal. In some embodiments, an intensity signal below a lower threshold value may suggest a depth increase for a subsequent focal point. An intensity signal above an upper threshold value may suggest a depth decrease for a subsequent focal point. And, an intensity signal between the lower and upper thresholds may suggest a depth be maintained for a subsequent focal point. The focal point may be adjusted after each pulse or after a plurality of pulses.

Abstract: A compact system for performing laser ophthalmic surgery is disclosed. The systems and methods may be used to measure corneal thickness or other anatomy to prepare a treatment plan for any of numerous treatments, such as LASIK, PRK, intra stromal lenticular lens incisions, cornea replacement, or any other treatment. By using a reduced power femtosecond laser backscatter may be measured to calculate distances such as distances between an interior boundary and an exterior boundary of a cornea or other tissue.

Abstract: A reclosable carton being capable and being adapted for accommodating a multiplicity of disposable absorbent articles is provided. The reclosable carton has a substantially parallelepiped-shape. A blank having a substantially folded flat-shape able to be converted in the reclosable carton is also provided.

Abstract: A refastenable disposable garment defines a longitudinal direction and a transverse direction, and comprises a first waist region contiguous with a first waist edge. The first waist region defines first and second side edges transversely spaced apart and defines first and second surfaces. The first waist region is elastomeric proximal both the first and second side edges. The garment can include a second waist region and a crotch region that interconnects the first and second waist regions. The garment comprises non-extensible, relatively rigid first and second fastening components attached to the first surface of the first waist region adjacent the first and second side edges, respectively. The first waist region defines first and second flange portions transversely outward of the first and second fastening components, respectively. Each flange portion is transversely curled toward the second surface. A process for making such an article is also disclosed.

Abstract: A rescue device includes at least two parallel columns defining a core section. The columns are located in a substantially flat plane with each column lying adjacent at least one other column. Each column includes rods, a connection device, and at least one sleeve. Each rod is located within a sleeve and the rods are connectable in series by the connection devices to form a column. The rescue device further includes at least one linking element. Each sleeve is connected to at least one linking element.

Abstract: The disclosure concerns a motor vehicle with a mobile vehicle seat. The seat includes a frame that forms a seating surface and a backrest. An energy source is arranged in the frame. A drive motor is arranged in the frame and connected to the energy source. At least one wheel is arranged on the frame and in drive connection with the drive motor. A control device controls the drive motor, and a first coupling is arranged on the frame to releasably fix the frame to the motor vehicle. A second coupling corresponding to the first coupling of the vehicle seat is arranged on an inside of a vehicle door, which is mounted pivotably on a vehicle superstructure. The second coupling can be brought into releasable engagement with the first coupling of the vehicle seat.

Abstract: A wheelchair is provided includes driving wheels, a pair of side frames, and an accommodation pocket. The frames rotatably support the driving wheels coupled to the exterior sides of the side frames. Each of side frames includes an elbow rest frame portion, a vertical frame portion, and a lower frame portion. The elbow rest frame portion has an elbow rest. The vertical frame portion is coupled to the rear end part of the elbow rest frame portion. The lower frame portion is arranged under the elbow rest frame portion. The vertical frame portion is coupled to the rear end part of the lower frame portion. The accommodation pocket is arranged above the front part of the driving wheel as viewed in side view, and is at least partially positioned on the exterior side relative to the elbow rest frame portion as viewed in front view.

Abstract: A support assembly includes a fixable portion and a rotatable portion. The fixable portion is adapted to be fixedly mounted to a wheelchair and includes a shaft having a keyway formed therein that is supported by one or more mounts. The rotatable portion is received on the shaft and is in selective locked engagement therewith. The rotatable portion includes a bracket body with an opening into which the shaft of the fixable portion is received and a key member providing a key. The key member is supported by the bracket body and is movable in linear translation between an engaged position in which the key is engaged with the keyway to lock a rotational orientation of the bracket body relative to the shaft and a disengaged position in which the key is disengaged from the keyway permitting the rotatable portion to rotate relative to the fixable portion.

Abstract: A patient support apparatus includes a patient support surface to support a patient. The patient support surface has at least one air bladder that is inflated and/or deflated to achieve a turn assist function and/or a therapy function of the patient support surface. A graphical user interface (GUI) is configured to receive user inputs from a caregiver to initiate the turn assist or therapy functions. The patient support apparatus has control circuitry coupled to the GUI. The GUI is controlled by the control circuitry to display information indicating that the patient is improperly positioned on the patient support surface for either the turn assist function or the therapy function. Alternatively or additionally, the control circuitry indicates that the patient is improperly positioned for raising a head section of a bed frame.

Abstract: A patient control unit for controlling functions of a hospital bed includes a housing having a first side that includes a plurality of user inputs to control the functions of the hospital bed. The housing has a second side that includes a dock to secure a handheld phone in place on the housing. A hospital bed has a head-of-bed angle (HOBA) lockout selector that is used to signal a controller to prevent a head section of the bed from being moved below a threshold.

Abstract: Catheter monitor integration with patient support systems, such as patient beds, and with other healthcare communication systems including hand hygiene systems is provided. A patient bed that transmits bed data and catheter monitor data is disclosed. When catheter tubing is connected to a catheter monitor integrated into a patient bed, the bed automatically implements a falls prevention protocol. A countdown timer pertaining to removal of catheter tubing from a patient is displayed on one or more display devices. Monitoring for caregiver handwashing compliance in connection with use of a catheter monitor or a catheter kit is also provided.

Abstract: A patient support apparatus includes an upper frame that is movable to raise and lower relative to a base frame frame. A mattress support deck is coupled to the upper frame and includes a foot deck section. The foot deck section is movable with respect to the rest of the mattress support deck to raise and lower. A drainage bag support is coupled to the foot deck section and is configured to support a drainage bag. Control circuitry controls movement of the upper frame and the foot deck section. The control circuitry has a lockout mode to limit the movement of the upper frame and foot deck section to prevent the drainage bag from touching a floor.

Abstract: The present invention relates to a system and method for support and off-loading. The system includes an inner bladder filled with a flowable composition. An outer bladder filled with a flowable composition is positioned adjacent to the inner bladder. The composition of the inner bladder has greater flow characteristics than the composition of the outer bladder. The inner bladder micro-contours to the received body part and the outer bladder macro-contours to the inner bladder after the inner bladder is micro-contoured to the received body part. Alternatively, the system provides a pair of ultra low pressure plenums and a positioner. The patient body size and size and corresponding surface area of the positioner control the amount of gas which is displaced evenly against the walls of the ultra low pressure plenums.

Abstract: A modular, deformable, repositionable, cushioned gentle cushioned, resistive infant positioning system and method for use with infants is provided that includes first and second tubular pillows each having two longitudinally-elongated chambers adjoined at a first and second pillow lateral flexure-enabling element, respectively, and a third compact pillow. The second tubular pillow is preferably wider than the first tubular pillow and includes two straps. Methods of using the three pillows of the cushioned, resistive infant positioning system are presented that provide positioning, calming, and/or the prevention and/or the correction of head shape deformations.

Abstract: An apparatus for moving a patient from a reclining position to an upright sitting position, and methods of using same, are described. The apparatus includes an articulating patient support platform with first, second and third panels. The first panel includes opposite first and second ends and the second panel is movably attached to the first panel first end and is upwardly pivotable from a substantially co-planar relationship with the first panel to a substantially orthogonal relationship with the first panel. The third panel is secured to the second panel in spaced-apart, substantially co-planar relationship therewith. A patient is positioned on the patient support platform with the patient's upper body supported by the first and second panels and the patient's legs supported by the third panel. The second panel is caused to pivot upwardly, thereby moving the patient to a generally upright sitting position.

Abstract: A patient maneuvering apparatus including a substantially planar body having a top surface, a bottom surface opposing the top surface, a left end, and a right end. The patient maneuvering apparatus also includes a first handle disposed at the left end of the body and a second handle disposed at the right end of the body, a mesh layer with a mesh layer thickness at least partially defining the bottom surface, a fabric layer of an absorbent material at least partially defining the top surface and with a fabric layer thickness, and a border spanning the perimeter of the body, surrounding the mesh and fabric layers, and with a border thickness greater than the mesh layer thickness and the fabric layer thickness.

Abstract: According to the present disclosure, a surgical patient support provides support to a patient. The surgical patient support may include configuration to accommodate various patient body positions to provide a variety of access to the patient's body.