Abstract: An osseointegrated abutment support socket for a residual limb in which an osseointegrated abutment has been implanted is described. The osseointegrated abutment support socket may include a distal socket base assembly, multiple longitudinal struts and a percutaneous site protector. The distal socket base assembly may include a base plate, a collar extending proximally from the base plate and forming a receptacle for receiving a distal end of the osseointegrated abutment, and a strut support ring disposed around the collar. The struts are connected at their distal ends to the strut support ring and extend proximally upward. The percutaneous site protector contacts a distal surface of the residual limb near a percutaneous site where the distal end of the osseointegrated abutment exits the residual limb.

Abstract: An implant for medical use, and methods of making same, having a body formed of a plurality of single strands of a first material. The body further includes at least one multi-strand of radiopaque material incorporated among the single strands, the multi-strand having at least two side-by-side filaments of radiopaque material that lie substantially contiguous to each other over substantially the entire length of the multi-strand.

Abstract: An implantable prosthesis, including a generally tubular substrate and a continuous shape memory member disposed over the outer surface of the substrate. The shape memory member may include a series of zig-zag struts alternating between a first strut with a first length and a second strut with a second length different from the first length. A graft member may be positioned over the substrate and shape memory member.

Abstract: A vascular device is provided that includes a mesh structure formed of a plurality of spaced members. The structure has (i) a first, collapsed configuration, (ii) a second, expanded configuration, and (iii) a density of the plurality of members. The vascular device further includes an elastic member disposed along a region of the structure, the region having a proximal end and a distal end. The elastic member is configured to increase the density within the region by drawing at least one of the proximal and distal ends of the region toward the other of the proximal and distal ends when the structure is in the second configuration.

Abstract: Methods and devices for increasing flow in the left atrial appendage (LAA) include a conduit directing blood flow from a pulmonary artery into the LAA and/or a conduit drawing blood from the LAA by a Bernoulli effect. In one embodiment, a method comprises implanting a conduit in a pulmonary vein, expanding an inlet portion such that the conduit becomes anchored within the vein and directs blood through an outlet portion of the conduit into or toward the left atrial appendage.

Abstract: A device for moving an elongate member relative to an elongate body through which it extends, the device including a housing, a mover, and a pre-mover. The housing is connectable to the elongate body. The mover is associated with the housing and is connectable to the elongate member for moving the elongate member relative to the housing. The pre-mover is associated with the housing and is connectable to the elongate member for adjusting the elongate member in preparation for moving the elongate member with the mover.

Abstract: The present embodiments provide prosthesis deployment systems. In one embodiment, a sleeve has proximal and distal regions and a lumen extending therebetween, and further comprising a first exit aperture, a first entrance aperture, and a second exit aperture. A trigger wire is disposed at least partially within the lumen of the sleeve. A prosthesis has a delivery state and an expanded state, and further has first and second regions. In the delivery state, the trigger wire extends out of the lumen through the first exit aperture of the sleeve, restrains the first region of the prosthesis, reenters the lumen through the first entrance aperture of the sleeve, extends out of the lumen through the second exit aperture of the sleeve, and restrains the second region of the prosthesis.

Abstract: A wearable apparatus for the treatment or prevention of osteopenia or osteoporosis, stimulating bone growth, preserving or improving bone mineral density, and inhibiting adipogenesis is disclosed where the apparatus may generally comprise one or more vibrating elements configured for imparting repeated mechanical loads to the hip, femur, and/or spine of an individual at a frequency and acceleration sufficient for therapeutic effect. These vibrating elements may be secured to the upper body of an individual via one or more respective securing mechanisms, where the securing mechanisms are configured to position the one or more vibrating elements in a direction lateral to the individual, and the position, tension, and efficacy of these vibrating elements may be monitored and/or regulated by one or more accelerometers.

Abstract: A wrist brace device has a splint member including an arm portion for support along an inner forearm of a user, and a palm portion for supporting a palm on a palm supporting surface of the palm portion which is oriented generally in the direction of the arm portion to prevent overextension of the hand of the user relative to the forearm. A tool receiving surface is provided on the palm portion opposite from the palm supporting surface for engaging a handle of a tool thereon such that impacts from a tool head of the tool are directed substantially perpendicularly to the upper palm supporting surface and the arm portion of the user.

Abstract: A global osteoarthritis knee brace or orthopedic support includes a flexible, elastic sleeve having a tubular shape with a patella opening at an anterior surface with slits on either side of the opening. The brace includes a first pair of rigid longitudinal stiffeners pivoted therebetween at a hinge that is disposed at the lateral side of the sleeve and likewise at the medial side of the sleeve. The brace further includes an adjustable, flexible patella support having elongated strips at the ends thereof, wherein the patella support is positioned in the interior of the sleeve proximate with the patella opening, where the elongated strips pass from the interior of the sleeve through the slits to the exterior of the sleeve, and extend upward to be adjustably anchored to the sleeve. The wearer pulling on the elongated strips adjusts the patella support.

Abstract: In some embodiments, a system and/or method may include an external spinal brace system. The system may include a plurality of support mechanisms including at least first and second support mechanisms. The first support mechanism may be coupled, during use, to the second support mechanism such that the first and second support mechanisms are inhibited from decoupling. In some embodiments, the system may include a coupling system. The coupling system may couple the plurality of support mechanisms to a subject such that the plurality of support mechanisms are positioned, during use, along at least a portion of the subject's spine. In some embodiments, the external brace system applies a posterior distraction force to the subject.

Abstract: Some embodiments of the present disclosure include a traction device for relieving lower back pain and stiffness and reducing lumbar spine intervertebral disc displacement. The device may include a sliding spine assembly attached to a head rest pad, a torso pad, and a hip pad, an adjustable length vector bar extending outwardly from the spine assembly, wherein the vector bar is rotatably attached to the sliding spine assembly such that the vector bar is configured to move in a plurality of vectors, a cross bar foot brace tube attached to the vector bar; a foot rest positioned on the foot brace tube, a belt positioned proximate to the torso pad, and a strap assembly attached to the foot brace tube or the distal end of the vector bar, the strap assembly configured to attach to the belt and apply traction to a user's back.

Abstract: A patient transfer device is utilized to transport infant patients between locations within a hospital environment. The patient transfer device includes a center, support section and a pair of side sections that can be moved into contact with each other to surround the infant patient. The first and second side sections each include a handle that can be brought into close proximity to each other and can be grasped by a single hand of a clinician. The patient transfer device includes a stiffening device that is positioned within the center section to provide support for the infant patient during transport. A hold down device is included on one or both of the first and second side sections to securely hold tubes and wires connected to the infant patient during transport of the infant patient.

Abstract: An at least partly implantable system for injecting a substance into a patient's body. The system comprises an infusion device for injecting a substance into a part of the body of the patient, the infusion device being adapted for implantation inside the patient's body. The system further comprises at least one reservoir comprising at least one compartment which accommodates and preserves or is adapted to accommodate and preserve the substance to be injected, the reservoir being adapted for implantation inside the patient's body in fluid connection with the infusion device to supply to the infusion device the substance to be injected into the patient's body. The system further comprises an active cooling device adapted for implantation inside the patient's body and adapted to cool the reservoir and thereby keep the substance within said at least one compartment of the reservoir at a temperature below 37° C.

Abstract: An embracing attachment member or sheath and a maxilla attachment subassembly for retaining at least one of a patient's tongue and lip in a desired position. A sheath interlock member extends upward from a dorsal side of a sheath. A tongue receiving cavity is formed within the sheath for insertion and attachment to the patient's tongue. An interlock member is integrated into an accessory for attachment to the sheath interlock member. The accessory can be used to treat sleep apnea, restrain a patient's tongue in a desired position, restrain a patient's upper or lower lip in a desired position, and the like. The interlock design includes a wedge and a retention member that engages with the wedge. The retention member and wedge compress friction surfaces against one another, retaining the sheath interlock and the accessory interlock in a fixed position respective to one another.

Abstract: A garment assembly useful for sexual intercourse between a first user and a second user when the penetration of a body-extending member into a body orifice is either not possible or unwanted. The garment assembly includes a front and back panel covering and a crotch piece with the appearance of an ordinary garment normally found in a public environment such as one having the appearance of underwear. A fluid-impenetrable receiver attached to the front panel of the garment assembly will operate as a substitute for a body-orifice. The receiver includes an entryway adjoined to an interior cavity sized to accommodate a body-extending member. A preferred interior cavity includes sexually-interactive textured material for engagement with the body-extending member during use.

Abstract: Systems and methods for improving or preventing a condition, such as the treatment of pain syndromes and migraine headaches are disclosed. A method for treating pain can include one or more of the steps including identifying a region of the patient comprising glabrous tissue; positioning the region of the patient comprising glabrous tissue into an enclosed chamber; adjusting the relative humidity of the enclosed chamber sufficient to create a physiologic effect. The method need not involve altering the temperature within the enclosed chamber.

Abstract: A thermal pack (10) for therapeutic treatment of a mammal that includes a bladder (12, 4) and a separator element insert (22). The bladder (12, 14) is formed of a pair of superposed sheets (12, 14) of flexible, heat conductive liquid impermeable polyurethane material and includes an inlet (18) and an outlet (20). The sheets (12, 14) are welded together at a central spine (17) and along a series of branches (16) so as to provide a turning, tortuous fluid passageway therein. The separator element insert (22) is received within the fluid passageway and provides a fluid conveying track that extends throughout the fluid passageway from the inlet (18) to the outlet (19) to maintain the sheets (12, 14) in spaced apart relationship to mitigate restrictions in fluid flow when the pack (10) is flexed out of the plane of the sheets (12, 14).

Abstract: Disclosed herein are drug delivery devices and methods for the treatment of ocular disorders requiring targeted and controlled administration of a drug to an interior portion of the eye for reduction or prevention of symptoms of the disorder. The devices are capable of controlled release of one or more drugs and may also include structures which allow for treatment of increased intraocular pressure by permitting aqueous humor to flow out of the anterior chamber of the eye through the device.

Abstract: A method for delivering fluids, drugs, or medications to a patient's eye, and a system or apparatus for implementing the method, is disclosed. The system and method comprises the use of a corneal sponge to be deposited onto the cornea of the patient's eye while the patient's eyelids are maintained in open positions, and a scleral contact lens is disposed onto the sponge. The scleral lens has an irrigation fluid supply tube fluidically connected thereto for supplying a fluid, drug, or medication to the sponge which is saturated with the fluid, drug, or medication. Once the sponge and lens are inserted onto the corneal region of the eye, the patient's eyelids are closed thereby trapping and maintaining the sponge and lens upon the corneal region of the eye so as to permit the fluid, drug, or medication to be continuously supplied and applied to the corneal region of the eye.

Abstract: The purpose of the present invention is to provide an injector for an intraocular lens, whereby it is possible to easily set a lens support part to an appropriate position on a lens holder, and to safely carry out insertion work. A lens holder (404) is provided with a base part (441), a release-side guide part (442), and a passing part (443). A concave part (450) for housing the tip of a first lens support part (92) is formed on the release-side guide part (442). The concave part (450) holds the first lens support part (92) above the passing part (443). The release-side guide part (442) guides the first lens support part (92) along the circumference of an optical part (91).

Abstract: A surgical device and procedure for accessing tissue to perform microsurgery, including a capsulotomy of a lens capsule of an eye. The device includes a handpiece with a tip for insertion into an incision. A sliding element is disposed within the handpiece and a suction cup is mounted to the sliding element. The sliding element can be translated to move the suction cup into and out of the handpiece. A compression mechanism associated with the suction cup and the handpiece compresses the suction cup for deployment through the tip of the handpiece. The suction cup can expand inside the anterior chamber into a cutting position. A cutting element mounted to the suction cup is used to cut a portion and to remove the portion. The cutting element may be mounted to a cutting element support structure in a way that prevents heating of the device.

Abstract: Laser assisted cataract surgery methods and devices utilizing one or more treatment laser beams to create a shaped opening in the anterior lens capsule of the eye when performing a capsulorrhexis procedure. A light absorbing agent may optionally be added onto or into the lens capsule tissue, and the treatment laser wavelength selected to be strongly absorbed by the light absorbing agent. Alternatively, the treatment laser wavelength may be selected to be absorbed or strongly absorbed by the tissue itself, in which case no additional light absorbing agent need be used. Visualization patterns produced with one or more target laser beams may be projected onto the lens capsule tissue to aid in the procedure. The devices may be attached to or integrated with microscopes.

Abstract: An ophthalmic system may comprise an imaging device having a field of view oriented toward the eye of the patient; a patient interface housing defining a passage therethrough, having a distal end coupled to one or more seals configured to be directly engaged with one or more surfaces of the eye of the patient, and wherein the proximal end is configured to be coupled to the patient workstation such that at least a portion of the field of view of the imaging device passes through the passage; and two or more registration fiducials coupled to the patient interface housing in a predetermined geometric configuration relative to the patient interface housing within the field of view of the imaging device such that they may be imaged by the imaging device in reference to predetermined geometric markers on the eye of the patient which may also be imaged by the imaging device.

Abstract: The present invention is to provide a swimming goggle swimming goggle cushion pad in contact with a wearer's face around the eye socket, comprising: a connection frame defined with an inner peripheral face and an outer peripheral face, a circumferential fitting groove mounted between the inner peripheral face and the outer peripheral face to receive a circumference of the swimming goggle frame; a face contact portion extending along the inner peripheral face of the connection frame and defined with an outer ring surface and an inner ring surface; a buffer unit disposed between the inner peripheral face of the connection frame and the outer ring surface of the face contact portion; wherein the buffer unit provides the face contact portion with support and restoring forces against a deformation stress produced between the cushion pad and the wearer's face when worn, to ensure a comfortable engagement with the wearer's face skin.

Abstract: A percutaneous implant for reducing the risk of post-implant infection by reducing the likelihood of epidermal down-growth between the dermis of the skin and the implant. In one example, the implant comprises a barrier member between the epidermis and the dermis about the implant. In another example, a barrier is provided by removing a portion of the epidermis from the dermis about the implant.

Abstract: An apparatus comprises a shaft, an expandable dilator, and at least one ventilation pathway. The shaft defines a longitudinal axis and comprises a distal and proximal ends with at least one shaft lumen. The expandable dilator comprises body with its own proximal and distal ends. The body is configured to transition between a contracted state and an expanded state. The body is configured to dilate a Eustachian tube of a patient in the expanded state. The at least one ventilation pathway is configured to provide ventilation from the distal end of the body to the proximal end of the body when the body is in the expanded state. In some examples, the ventilation pathway comprises a set of transversely oriented vent openings formed through the shaft. In some other examples, the ventilation pathway comprises a space defined between one or more radially outwardly protruding features of the expandable dilator.

Abstract: The present device includes a rotor that is rotated around a cam drum and includes a plurality of units, each unit including: a mover that is guided by the cam drum and reciprocates in an axial direction of the cam drum by virtue of the rotation of the rotor; a first belt linked to the mover; a first pulley and a second pulley that rotate with the first belt wound therebetween; a pad that reciprocates in the axial direction in accordance with the reciprocation of the mover, while holding a sheet piece; a second belt linked to the pad; a third pulley and a fourth pulley that rotate with the second belt wound therebetween; and a transmission mechanism that transmits the rotation of the second pulley to the third pulley and changes a rotation speed of the third pulley with respect to a rotation speed of the second pulley.

Abstract: A disposable diaper having features that improve its ability to lay open in a flat configuration is disclosed. The diaper may include fastening members having a minimum basis weight, and a minimum width and a minimum surface area relative the chassis dimensions, along with other features that tend to cause the diaper to lay open in a flat configuration, for the convenience of the caregiver during application of the diaper to a baby.

Abstract: A transversely extensible elastic laminar web material comprising a first and a second web material each of which defines a first and a second distal region adjacent to corresponding longitudinal side edges and a central region between the aforesaid distal regions, at least one web of elastomeric material applied to these central regions of the first and second web materials and a plurality of connection formations applied to at least one distal region of said first and second web materials and projecting from a respective longitudinal edge. In the transversely extensible elastic laminar web material, the elastomeric web material and the connection formations are interposed between said first and second web materials and are joined thereto by mechanical welds.

Abstract: A disposable absorbent article may include a topsheet, a backsheet, an absorbent core disposed between the topsheet and the backsheet, and a leg gasketing system. The leg gasketing system may include an inner cuff and an outer cuff; the inner cuff may include an inner cuff folded edge and an inner cuff material edge and the outer cuff may include an outer cuff folded edge and an outer cuff material edge such that the web of material is folded laterally inward to form the outer cuff folded edge and folded laterally outward to form the inner cuff folded edge.

Abstract: A liquid permeable substrate for an absorbent article is disclosed. The substrate includes a first layer including a hydrophobic material and a second layer including a hydrophilic material. The first layer is joined to the second layer. The substrate includes a plurality of recesses, a plurality of projections, and a plurality of land areas. The land areas surround at least a majority of the plurality of projections and a plurality of the recesses. The plurality of recesses, the plurality of projections, and the plurality of land areas together form a first three-dimensional surface on a first side of the substrate and a second three-dimensional surface on a second side of the substrate. The substrate has an overall z-directional height in the range of about 1000 ?m to about 6000 ?m according to the Overall Substrate Height Test.

Abstract: A hygiene article including a nonwoven web having nanofibers. The hygiene articles include diapers, training pants, adult incontinence pads, catamenials products, tampons, personal cleansing articles, and personal care articles. The nanofiber webs can be used as a barrier, wipe, or absorbent material. Particularly, the nanofiber web is used in a diaper as a barrier-on-core, outercover, and/or leg cuff. It may also be used as a wipe.

Abstract: A method is disclosed for modifying the physical characteristics of a web which involves passing the web between at least one pair of interengaged rolls to incrementally stretch the web, and then withdrawing the incrementally stretched web from between the rolls under tension. A web modified according to the disclosed method has desirable breathability and liquid impermeability, as well as extensibility and a soft, cloth-like textured surface.

Abstract: The invention relates to the use of a fleece composed of plastic filaments, in particular made of a thermoplastic, as a sustained-released system or as a storage system for at least one active substance, in particular for at least one active liquid. The filaments are spun using a spinneret, and the plastic material of the filaments is foamed so that pores are formed at least on the surface or in surface regions of the filaments and at least some of the pores are pores that are open outward, and at least some of the open pores are filled with the active substance, in particular with the active liquid.

Abstract: An apparatus is configured for use with a chair having a supporting surface, and includes a cushioning member adapted to be placed above the supporting surface, a bottom sheet connected to the cushioning member and having an engagement surface opposite the cushioning member, a top sheet having a bottom surface positioned in confronting relation to the engagement surface and a top surface opposite the bottom surface, and a selective gliding assembly positioned between the top and bottom sheets. The top sheet has at least one end connected to the bottom sheet, and the top sheet further has a slip resistant material positioned on the top surface. The selective gliding assembly includes engagement members positioned on the engagement surface and on the bottom surface of the top sheet, and the engagement members engage each other to resist forward sliding of the top sheet and to permit rearward sliding of the top sheet.

Abstract: A steering attachment for a wheelchair includes an arm assembly configured to engage a wheelchair fork comprising two outer bars connected to a shorter center member, thereby defining a gap on one end of the arm assembly to engage the fork. Attachment apertures extend through the outer bars and center member configured to receive attachment members to adjustably assemble the arm assembly to accommodate a particular fork blade. A link pivotally is connected to an opposite end of the bar assembly, and is hinged to move between an extended position and a folded position. A foot support is pivotally connected to an upper wall of the link and configured to pivot about an axis perpendicular to the pivot axis of the link. The steering attachment is connectable to a wheelchair with a single pull pin.

Abstract: The present disclosure relates to a swing arm linkage (1) for a mid-wheel drive wheelchair, comprising: a first swing arm (3) having a first swing arm pivot point (3a) and a linkage member first mounting point (3b), a second swing arm (5) having a second swing arm pivot point (5a) and a linkage member second mounting point (5b), a linkage member (7) configured to be connected to the linkage member first mounting point (3b) and to the linkage member second mounting point (5b), to enable force transfer between the second swing arm (5) and the first swing arm (3), wherein the linkage member (7) has an elongated shape defining a linkage axis (A) extending between the linkage member first mounting point (3b) and the linkage member second mounting point (5b), a first straight line being formed between the first swing arm pivot point (3a) and the linkage member first mounting point (3b), and a second straight line being formed between the second swing arm pivot point (5a) and the linkage member second mounting point

Abstract: An assist chair includes a base portion, a pair of armrests, a backrest, an uplifting apparatus, a seat cushion and a waist rest cushion, wherein the uplifting apparatus further includes a pair of assist handles. When the uplifting apparatus is activated, the assist handles is capable of being driven out of inner sides of the pair of armrests, leaving the inner sides of the armrests or being retracted back to the inner sides of the pair of armrests after being pushed out of the armrests, such that the configuration can support the elderly when standing up or sitting down.

Abstract: Systems and methods for detecting a pinch event or obstruction to a movable component of a patient support. In some embodiments, the patient support apparatus may include a control system capable of controlling one or more actuator systems coupled to one or more movable components of the patient support apparatus. The control system may operate according to one or more modes of operation in controlling the actuator system to move a component from a first position to a second position. In one embodiment, the control system may receive sensor feedback indicative of one or more operating characteristics of an actuator system, and analyze the sensor feedback differently in one mode than in another. In one embodiment, the controller may receive sensor feedback indicative of both a speed of a component coupled to the movable component and a current of power supplied to an electric motor of the actuator system.

Abstract: A bed for maintaining the patient in horizontal position includes a patient support, undercarriage provided with casters and a system for propelling the bed which includes a controller and a control panel both connected to a processor unit. The controller includes a touch sensor connected to the processing unit. An activation member is also connected to processor unit. The activation member is a part of the control panel and it serves to activate the system and to initialize the calibration process of the touch sensor. An essential condition for propelling the bed is activated touch sensor and concurrently any of the function buttons being pressed. The touch sensor is being recalibrated before every system initialization hence the control of the system for propelling the bed is safe for the patient and the propelling of the bed is comfortable and simple for the personnel.

Abstract: A person support apparatus with an extendable mattress, a night light message display system, a screen key pendant, egress handle siderails, and various other features. The extendable mattress includes hinged extensions along the sides of the extendable mattress that are moved from a nested position to the extension position. The screen key pendant includes a plurality of screen keys that can be pressed to cycle through various control modes for the person support apparatus. The night light message display system can be configured to display a message or image on the floor communicating information to the person and/or alerting the person as to when they are able to exit the bed.

Abstract: A system for use with a hospital bed having circuitry and a standard AC power outlet spaced from the hospital bed is provided. The system includes a cable assembly couplable to the circuitry of the hospital bed. The cable assembly has power conductors and at least one data conductor. The cable assembly also has a plug including a first power coupler coupled to the power conductors and a first data coupler coupled to the at least one data conductor. The system also includes a second data coupler mountable adjacent the standard AC power outlet. The second data coupler is configured to couple to the first data coupler when the first power coupler is coupled to the standard AC power outlet.

Abstract: An incubator of the disclosure is configured such that a top hood is detachable from a peripheral frame by unlatching first latch mechanisms that latch the top hood. The incubator is also configured such that any of wall portion among four wall portions configuring the peripheral frame are detachable from an incubator base by unlatching any of corresponding second to fifth latch mechanisms.

Abstract: The present invention provides an incubator in which there is no concern of a user feeling pain or injuring their arm, even if their arm makes comparatively hard contact with an upper end of baby guards when the user has placed their arm inside an infant accommodation space. The baby guards are formed with a protrusion and have sufficient strength as a guard configuration body at an outer periphery of the infant accommodation space, and the width of a region inside the baby guards where observation by the user is slightly inconvenienced does not become particularly large. In the incubator, at least one of the baby guards includes the substantially rod shaped protrusion configuring an upper end of the at least one baby guard when in a substantially upright state that is substantially upward.

Abstract: A bed is stably mounted on a body when located at a first position. The bed is mounted on the body via buffering members so that the buffering members absorb and prevent vibration and shock from being transmitted from the body to the bed, when located at the second position.

Abstract: An actuation system having a table, a lifting column for raising and lowering the table, first and second actuators pivotally mounted to a top section of the lifting column. The first and second actuators are coupled to a first end of the table. A guide plate having a top portion and at least one track is provided. The at least one track is slidingly engaged with at least one guide, the at least one guide is vertically mounted to a third side of the lifting column. The top portion of the guide plate is vertically driven by the third actuator and is universally coupled to a second end of the table. A controller for controls the movement of the lifting column in the vertical plane, and of the table in the longitudinal and lateral planes by varying the position of the three actuators relative to each other.

Abstract: A patient support apparatus, comprising a patient support having one or more pads for supporting a patient's torso and hip in a generally horizontal orientation. At least one, elongated leg support extends from the patient support. The leg support is movable through a generally horizontal plane. A portion of the leg support is declinable and inclinable from the horizontal plane. A traction device is connected to the leg support. The traction device is attachable to a patient's leg and operable to exert a traction force on the patient's leg along an axis generally parallel to the leg support. The traction device is connected to the leg support by a slide assembly and the traction device can be secured stationary relative to the leg support or the traction device can slide relative to the leg support.

Abstract: Described herein are exemplary embodiments of patient positioning systems for supporting and positioning a patient in an inclined position during medical treatment, such as in the Reverse Trendelenburg position. Some embodiments comprise a flexible, air-impermeable shell having a torso portion configured to support the patient's torso and secure the positioner to the support surface, an intermediate portion integrally coupled to an inferior end of the torso portion, and a suprapubic portion integrally coupled to an inferior end of the intermediate portion opposite the torso portion and configured to extend along the patient's perineal-pubic region when the shell is evacuated of air. When evacuated of air, the positioner is configured to hold the patient in an inclined position on an inclined support surface with the patient's head above the patient's hips such that the intermediate and/or suprapubic portions physically block the patient from sliding feet-first down the inclined support surface.

Abstract: A lower extremity orthosis, including at least one actuator configured to control a motion of at least one joint of a person wearing the orthosis, is provided with a handle including a force sensor configured to produce a signal representing a force applied to the handle. A controller, which is in communication with the force sensor and the at least one actuator, is configured to modify the motion based on the signal from the force sensor. The system can be particularly employed to enable a physical therapist to have input in controlling and modifying the positions and/or forces prescribed by the lower extremity orthosis during rehabilitation of the person.