Abstract: A multifunctional mattress having a mattress body and a heating/cooling pressurization apparatus connected to the mattress body; the mattress body comprises independent pressurized circular balloons, alternatingly pressurized square balloons, heating/cooling air supply tubes, and pressurized tubing; the two sides of said heating/cooling air supply tubes are provided with small blow holes; the independent pressurized circular balloons (3) has a surface layer and a bottom layer; the surface layer and bottom layer are joined to form a plurality of independent closed balloons (33); at a position corresponding to the head are independent pressurized circular balloons; the alternatingly pressurized square balloon areas can be inflated or deflated by means of balloons causing the upper layer of sealed balloons to rise or fall.

Abstract: A body lifting device for a bed is provided with a support unit, having a predetermined height, connected to a fixing part of a bed. A movable bed part adjusts an angle between the fixing and movable parts. A driving force transfer member of the device is connected to the movable part at one end, the other end extending toward the fixing part, and has a support point therebetween supported by the support unit. A length between the support point and the other end varies depending on an angle adjustment of the movable part. A lifting unit of the device supports a portion of a user's body, and is connected to the other end of the driving force transfer member. The lifting unit selectively lifts up the user's body depending on movement of the driving force transfer member, which is caused by adjusting an angle of the movable part.

Abstract: A system for use with a bed having a frame and a supporting surface includes a sheet having a bottom surface configured to be placed above the supporting surface and a top surface opposite the bottom surface, the sheet having a sheet engagement member positioned on the bottom surface; and a wedge comprising a wedge body having a base wall, a ramp surface, and a back wall, the ramp surface joined to the base wall to form an apex and having a ramp engagement member. The ramp engagement member is configured to engage the sheet engagement member to form a selective gliding assembly that resists movement of the sheet with respect to the ramp surface in a first direction.

Abstract: An exercise vest including a thoracic belt fitting around a person's midsection. A padded elasticized and reinforced band attached to the thoracic belt at center back designed to come from back around in front of each shoulder and connect to unweighting system. Two elasticized and reinforced straps designed to attach in the front and come around each side of patient attach in an x pattern in the back and attach to the unweighting system. The exercise vest is positioned in such a way that as the patient is unweighted it cinches and hugs the person to distribute forces uniformly throughout a patient's torso, preventing wear on the person and strain on the device. This allows us to lift a patient upright out of a wheel chair in an easy, comfortable and safe manner.

Abstract: The present invention is directed to an adjustable height medical procedure table that can be moved between a first low position and second high position by a scissors lift. The table includes various features to prevent collisions when the table moved to the first low position.

Abstract: A surgical boot mount for mounting a surgical boot to a support rod of a limb holder, the surgical boot mount comprising: a projection having a first section and a second section, wherein the first section is attached to the sole of the surgical boot, wherein the first section comprises a first diameter and the second section comprises a second diameter, and further wherein the second diameter is larger than the first diameter; and a releasable locking mechanism mounted to the support rod of the limb holder, wherein the releasable locking mechanism comprises a first key comprising a first keyway and a second key comprising a second keyway, wherein the second key is slidably connected to the first key, wherein the first key is biased away from the second key, wherein the first keyway and the second keyway overlap to form an opening at least as large as the second diameter when an inwardly-directed force is applied to the first key so as to overcome the bias, and further wherein the opening is reduced to a size

Abstract: An exoskeleton apparatus driven by a pneumatic artificial muscle with functions of upper limb assist and rehabilitation training includes an upper limb frame, a shoulder joint mechanism, and an elbow joint mechanism which are driven by utilizing a processing unit, a first angle sensing unit, a second angle sensing unit, a first proportional pressure valve, a pressure sensing unit and a pneumatic muscle device. The exoskeleton apparatus can be independently used as an upper limb exoskeleton assistive device or can be combined to form an upper limb exoskeleton rehabilitation training system to simulate the upper limb movements in daily life through the upper limb frame to assist with the movements of the wearer's upper limbs, accomplishing the rehabilitation training of each upper and lower arm joint and neurological function.

Abstract: In various embodiments, methods of treating, improving, or preventing degradation of a user's vision incorporate the display of visual content dichoptically to the left and right eye of the user while the accommodative demand placed on the left eye and/or the right eye is altered.

Abstract: A device for treating dry eye syndrome and strengthening eyesight, of the present invention, comprises: a water goggles main body part into which a saline solution is injected, and which is closely adhered to the facial surface of a user, thereby allowing muscular exercise of the eyeballs to be carried out in the saline solution; a saline solution container coupled to the upper part of the water goggles main body part so as to supply a predetermined amount of saline solution; and a display device fixed to the front of the saline solution container, and in which an ocular muscle strengthening program for guiding the user's line of vision is executed so as to enable eyeball exercise to be performed in the saline solution.

Abstract: In various embodiments, a head-mounted apparatus having first and second display screens for, respectively, displaying visual content dichoptically to left and right eyes of a user is utilized to treat, improve, or prevent degradation of the user's vision.

Abstract: The present disclosure relates generally to devices and methods to relieve tension or stress on tissue and, in particular, tissue that includes a surgical incision site. A shape-setting material is used to conform the device to the tissue without the need for continuous application of negative pressure. The device can support and improve the health of breast tissue after breast augmentation or reconstruction post-mastectomy.

Abstract: A pressure cuff is provided, comprising a plurality of layers and a controller. The layers comprise: an outer covering, an outer surface of which is exposed when the pressure cuff is secured around a body part of a patient; a first conductive layer; a first insulating layer separating the outer covering and the first conductive layer; an inner covering, the inner surface of which contacts the patient or the patient's clothing when the pressure cuff is secured to the patient; a second conductive layer; a second insulating layer separating the inner covering and the second conductive layer; and a first piezoelectric support layer separating the first and second conductive layers. The controller is electrically coupled to the first and second conductive layers and configured to supply a voltage to the first and second conductive layers, whereupon the first piezoelectric support layer constricts around the body part of the patient.

Abstract: A sexual stimulating system with feedback control includes a physiological sensor, a sexual stimulator, and a processing module. The physiological sensor measures a physiological response of a user under sexual stimulation, and generates a sensor signal according to a result of the measurement of the physiological response. The sexual stimulator applies the sexual stimulation. The processing module is electrically connected to the physiological sensor and the sexual stimulator, receives the sensor signal, performs an analytical procedure upon the sensor signal for generating digital data, and generates a driving signal according to the digital data to control a degree of the sexual stimulation.

Abstract: The vibration capsule device disclosed herein comprises a movement generation unit, a movement control unit, a wireless communication unit and a power supply. The movement control unit provides instructions to the movement generation unit, which generates movements in configurable frequencies and duty cycles. The power supply unit provides power to the movement generation unit through movement control unit, which also decides work period and rest period for the capsule device. The vibration capsule device further comprises a capsule movement detection unit, which comprises at least one sensor unit and provides information to the wireless communication unit.

Abstract: A subcutaneous implant, including: (a) a circuitry unit having a first end, a second end, a conducting lateral side, and an opposing lateral side; (b) a first electrode, disposed on an outer surface of the circuitry unit and laterally circumscribing the circuitry unit at the first end; (c) a second electrode, disposed on the outer surface of the circuitry unit and laterally circumscribing the circuitry unit at the second end; (d) circuitry, disposed within the circuitry unit, and configured to be wirelessly powered to drive an electrical current between the electrodes; and (e) an insulating member, disposed on the opposing lateral side such that, on the opposing lateral side, each electrode is sandwiched between the insulating member and the circuitry unit, and the insulating member inhibits electrical conduction from the electrodes into the tissue. Other embodiments are also described.

Abstract: A method of treating red blood cells of a human patient has the steps of activating an acoustic shock wave generator or source to emit acoustic shock waves and subjecting a vascular system containing red blood cells and surrounding muscle tissue peripherally through an extremity of a patient to the acoustic shock waves by stimulating the extremity wherein the extremity is positioned within a path of the emitted shock waves and away from a geometric focal volume or point of the emitted shock waves. The methods also treat muscle tissue of aging patients, from muscle regeneration or athletes for legal performance enhancement without drugs.

Abstract: The vibration capsule device disclosed herein comprises a movement generation unit, a movement control unit, a wireless communication unit and a power supply. The movement control unit provides instructions to the movement generation unit, which generates movements in configurable frequencies and duty cycles. The power supply unit provides power to the movement generation unit through movement control unit, which also decides work period and rest period for the capsule device. The vibration capsule device further comprises a capsule movement detection unit, which comprises at least one sensor unit and provides information to the wireless communication unit.

Abstract: A method for providing a therapeutic benefit to a patient includes positioning a first tactile stimulator in therapeutic contact with a body of a patient and positioning a second tactile stimulator in therapeutic contact with the body of the patient in a bilateral position to the first tactile stimulator. A controller (mobile device) activates the first tactile stimulator to provide a first stimulation for a first time period and activating the second tactile stimulator to apply a second stimulation for a second time period beginning at least commensurate with a cessation of the first time period.

Abstract: For allowing an access to an eye during a rinsing process it is suggested to configure an eye opening device in such a way that the eye opening device comprises two wing-like spreading elements for pulling the upper eyelid and the lower eyelid of the eye apart so as to support the opening of the eye during a rinsing process, wherein two access gaps are formed laterally between the two wing-like spreading elements of the eye opening device.

Abstract: In certain embodiments, a vial adaptor comprises a housing configured to couple the adaptor with a vial, an access channel, a regulator channel, and a regulator assembly. The access channel is configured to facilitate withdrawal of fluid from the vial when the adaptor is coupled to the vial. The regulator channel is configured to facilitate a flow of a regulating fluid from the regulator assembly to compensate for changes in volume of a medical fluid in the vial. The regulator assembly can include a valve configured to transition between a closed configuration and an opened configuration.

Abstract: A method and a medication organizer tray apparatus for organizing medications and collecting medication adherence information are provided. The medication organizer tray apparatus includes a support frame, multiple medication bins accommodating multiple medications, a bin cover layer with multiple customized bin labels, and a conductive circuit layer. The support frame includes multiple apertures positioned at predefined intervals from each other for placement of the medication bins. The customized bin labels having medical information printed thereon seal openings of the medication bins. The conductive circuit layer includes conductive lines running along one or more of a lower surface of the bin cover layer, around each medication bin, and a lower surface of each medication bin. The conductive circuit layer electrically communicates with a receptacle base to enable detection of removal of each medication bin from the support frame and detection of tampering of the medication bins.

Abstract: A fluid connector for selectively establishing fluid communication between a first medical container and a second medical container is provided. The fluid connector includes an adapter configured to removably attach to the first container. The adapter includes an access port and a cap. The connector further includes an outer sleeve connected to the adapter and a tubular body retained at least partially within the outer sleeve. The body has a proximal end connected to the adapter and a distal end connected to the second container. The fluid connector is transitionable from a first position in which the first container and the second container are in fluid isolation to a second position in which the first container and the second container are in fluid communication. At least a portion of the cap of the adapter is retained within the outer sleeve.

Abstract: A syringe assembly (2) comprises a syringe barrel (4) comprising an inner chamber (14) filled or adapted to be filled with medicament, and a channel (18) in fluid communication with the chamber and through which medicament is dispensed. The assembly further comprises an outer sheath (6) configured to be removably attached to the syringe barrel, and comprising a projection (40) which is received by the channel when the outer sheath is attached to the barrel, thereby creating a seal, which prevents medicament from flowing therethrough.

Abstract: Certain aspects of the present disclosure provide a platform for monitoring patient adherence to a medical regimen. Certain aspects of the present disclosure also proved various components that may help enable such a platform, such as a smart collar capable of detecting removal and/or insertion of objects from a container (such as a pill container). In some cases, a smart collar may include a first portion having sides adapted to guide objects toward an opening in the first portion sized to allow the objects to pass, at least one detector proximate the opening and responsive to removal of objects from the container as they pass through the opening in the first portion, and a processor configured to process a first signal generated by the detector to update a monitored count of objects in the container.

Abstract: Certain aspects of the present disclosure provide a platform for monitoring patient adherence to a medication regimen. Certain aspects of the present disclosure also proved various components that may help enable such a platform, such as a smart collar capable of detecting removal and/or insertion of objects from a container (such as a pill container). Aspects of the present disclosure also provide for tailored communications with a patient. For example, a mode of communicating with the patient to encourage adherence with a medication regimen may be adjusted based on feedback regarding why the patient is not adhering to the regimen.

Abstract: A teat including at least a shaft and a nipple, wherein structured surface areas are provided at least in a partial region thereof, and the structured surface areas are formed by at least one rough surface zone having a surface roughness of 100 ?m at the most, or 50 ?m at the most.

Abstract: This disclosure includes intraluminal tubes comprising: an elongated tube (e.g., having a proximal portion, a distal portion configured to be disposed inside of an internal cavity of a patient, and a sidewall defining a lumen extending from the proximal portion to the distal portion, the distal portion defining one or more openings in fluid communication with the lumen) and a plurality of deployable tines, each coupled to the tube and disposed outside the sidewall of the distal portion, where each tine is movable from a collapsed state to a deployed state in which a portion of the tine extends laterally away from the distal portion of the tube. In some of the present intraluminal tubes, the sidewall of the distal portion defines a plurality of longitudinal grooves, and each tine is disposed in a different one of the grooves when the tines are in the collapsed state.

Abstract: An apparatus 100 for use in tube feeding comprises a cylindrical body 110 provided with a first opening 120 and a second opening 130 connected by a flow channel 140. The body 110 comprises reagent 111, for determining a characteristic of fluid disposed in the body and a transparent window 112 through which the reagent 111 is visible. In use, a first end of an enternal feeding tube releasably engages with the first opening 120. The second, distal end of said feeding tube is disposed inside a patient to be fed. A second feeding tube engages with the second opening 130. The second feeding tube connects the apparatus 100 to a bi-directional pump operable: to pump enternal fluid from a reservoir, through the apparatus and into the enternal feeding tube; and to pump fluid from the patient into the body 110 of the apparatus 100. This allows a user to pump fluid from the patient into the body 110 of the apparatus 100 to react with the reagent 111.

Abstract: A composition comprising microcapsules functionalized with polymerizable functional groups on the surface of said microcapsules wherein the functional groups form covalent bonds with monomers in the continuous phase to enhance the mechanical properties of the composition.

Abstract: The present disclosure relates to an aqueous dental glass ionomer composition comprising a reactive particulate glass, a water-soluble, polymerizable polymer which is reactive with the particulate glass in a cement reaction, a hydrolysis-stable, water-soluble monomer having a single polymerizable double bond and optionally a carboxylic acid group or hydroxyl group; and a polymerization initiator system, wherein the polymerizable polymer is obtainable by a process comprising a step of polymerizing a mixture comprising a first polymerizable monomer comprising at least one optionally protected carboxylic acid group and a first polymerizable organic moiety, and optionally a second copolymerizable monomer comprising one or more optionally protected primary and/or secondary hydroxyl and/or amino group(s) and a second polymerizable organic moiety, for obtaining an water-soluble polymer; a step of coupling to the water-soluble polymer a compound having a olymerizable moiety and a functional group reactive with an opt

Abstract: An aqueous dental glass ionomer composition comprising (A) a reactive particulate glass, (B) a water-soluble polymer comprising acidic groups, which is reactive with the particulate glass in a cement reaction, (C) a water-soluble, hydrolysis-stable monomer having a single polymerizable double bond and optionally a carboxylic acid group or hydroxyl group; (D) a water-soluble, hydrolysis-stable polymerizable crosslinker having at least two polymerizable carbon-carbon double bonds; and (E) a polymerization initiator system.

Abstract: Disclosed herein is a dental impression material that includes a two part addition curing silicone composition. The disclosed impression material contains a surfactant system composed of a fluorosurfactant and a fatty alcohol ethoxylate. The impression material disclosed herein exhibits improved storage stability than known systems using fluorosurfactants and silicone ether compounds.

Abstract: The invention relates to a cosmetic spray which consists of a) an oil-in-water emulsion (O/W emulsion) that contains i) polyglyceryl-3 methylglucose distearate and ii) acrylate/C10-30 alkyl acrylate crosspolymer, and b) a spray applicator system.

Abstract: The invention relates to a cosmetic spray consisting of a) an oil-in-water emulsion (O/W emulsion) containing poly glyceryl-10 stearate and b) a spray applicator system.

Abstract: A reduction treatment agent made of a powder with a particle size within a range of 1500 to 3000 mesh, the powder containing: 20 to 40 parts of a mixed-oxide powder containing magnesium oxide and zinc oxide; and 60 to 80 parts of an organic acid powder containing calcium, ascorbic acid, citric acid and salt. The reduction treatment agent may further contain one to six kinds of metal powder selected from the group of copper, molybdenum, nickel, cobalt, iron and aluminum, each in an amount of one part. Due to this configuration, the reduction treatment agent can be easily mixed with various substances when added to those substances. Even if the target substance is not water, the agent can entirely and uniformly change that substance into a reduced state. Additionally, the reduction treatment agent can act as a surfactant, and therefore, can be used as cosmetics or food.

Abstract: Described herein are oral care compositions comprising a thickening system comprising a first thickening agent and a second thickening agent, wherein the first thickening agent comprises greater than 15 wt % of the mixture of the first and second thickening agents in the thickening system.

Abstract: A solid stick antiperspirant composition is provided. The antiperspirant composition includes aluminum zirconium tetrachlorohydrex glycine having a concentration from about 10% to about 35% by weight of the composition, an anhydrous liquid carrier, one or more structurants having a concentration from about 15% to about 25% by weight of the composition, wherein the one or more structurants comprises one or more waxes and a non-ionic exthoxylated linear alcohol having a carbon chain length from about 20 to about 40. The solid stick antiperspirant composition is a single phase.

Abstract: Methods of making personal care compositions including microcapsules and methods of enhancing the efficacy of the microcapsules in said personal care compositions.

Abstract: This document provides methods and materials for delivering agents to hair, skin, and/or nails using one or more adhesive molecules alone or in combination with one or more interlocking metals, one or more dyes, and/or one or more polypeptides. For example, methods and materials for delivering interlocking metals, dyes, or polypeptides to hair, skin, or nails of a mammal (e.g., a human) are provided.

Abstract: A method for colouring hair. The method comprises the formation of a first plurality of coated hair fibre portions by applying a first composition to a first plurality of hair fibre portions and subsequently styling the hair. The first plurality of coated hair fibre portions is contacted with a second plurality of coated hair fibre portions but does not comprise the application of a solid barrier means in order to separate the first plurality of coated hair fibre portions from the second plurality of coated hair fibre portions. The composition comprises from about 0.2% to about 20% of viscosity-increasing agent and the viscosity-increasing agent is selected from the group consisting of: clays; polysaccharides; silicas; block copolymers of polypropylene oxide (PPO) and polyethylene oxide (PEO); and mixtures thereof. Also provided are a hair colouring composition being in ready to use form, the use of the composition, a developing formulation, and a process for creating a hair colouring composition.

Abstract: A skin care composition having from about 0.01% to about 5%, by weight, of an superabsorbent polymer which is a sodium polyacrylate, sodium polacrylate starch, sodium acrylates crosspolymer-2 or mixtures of these and a portion of the polymer comprises a grafted starch material. The superabsorbent polymer is particulate where the particles have an average particle size in the range of from about 5?-30?, and the individual particles in their dry or un-swollen condition are substantially non-spherical, flat, platelet, or elongated in shape. The particles have an absorption capacity of at least about 1000 times their initial dry or un-swollen volume. Additionally, the skin care composition contains from about 0.01-10% of a dry powder that is either starch or silicone based and wherein the dry powder is coated with a silicone based material. Further there is provided a UV active.

Abstract: A cosmetic, dermatological and/or pharmaceutical composition, in particular for topical use, in the form of a dispersion of a discontinuous internal phase in a continuous external phase. One of the phases is an aqueous phase and the other is an oily phase. The composition contains a polyacrylic polymer and a consistency factor. The composition is free of surfactant and of preservative. A method for preparing the composition includes mixing the aqueous phase and the oily phase so as to form a homogeneous dispersion. The dispersion thus formed is sterilized by ultra-high temperature infusion sterilization.

Abstract: Compositions are provided that provide release of fragrance over an extended period of time. The compositions comprise a hydrophilically-modified cross-linked silicone elastomer and an acrylic rheology modifier.

Abstract: Described herein is a granulated dry composition comprising at least one non-elastomeric polyorganosiloxane, agglomerated onto solid carrier particles. The granulated dry compositions can be used as a dry cleanser for keratinous substrates with high speed of absorption of body fluids together with improved sensory feel and release of care agents.

Abstract: The application is directed, generally, to an array of products and methods for treating periorbital dyschromia. More specifically, the application discloses an array of products and methods for treating different types of periorbital dyschromia. The products and methods utilize extracts of Vicia faba.

Abstract: The present application is directed, generally, to an array of products and methods for treating periorbital dyschromia. More specifically, the present application discloses an array of products and methods for treating different types of periorbital dyschromia. The products and methods utilize extracts of Cucurbita pepo.

Abstract: A cosmetic composition for improving the appearance of Type II and/or Type III periorbital dyschromia. The composition includes an effective amount of an extract of Vicia faba and a dermatologically acceptable carrier. The composition may be disposed in a package that includes verbal and/or non-verbal indicia to communicate to a user that the composition is intended to treat a particular type of periorbital dyschromia.

Abstract: A method of improving the appearance of periorbital dyschromia by identifying a target portion of skin in the periorbital region of a person that exhibits periorbital dyschromia and applying a personal care composition to the target portion of skin. The personal care composition includes an effective amount of an extract of Vicia faba and a dermatologically acceptable carrier. The personal care composition is applied for a sufficient amount of time for the extract of Vicia faba to improve the appearance of the periorbital dyschromia.

Abstract: A method of improving the appearance of periorbital dyschromia by identifying a target portion of skin in the periorbital region of a person that exhibits periorbital dyschromia and applying a personal care composition to the target portion of skin. The personal care composition includes an effective amount of an extract of Cucurbita pepo and a dermatologically acceptable carrier. The personal care composition is applied for a sufficient amount of time for the extract of Cucurbita pepo to improve the appearance of the periorbital dyschromia.

Abstract: A method of improving the appearance of periorbital dyschromia by identifying a target portion of skin in the periorbital region of a person that exhibits periorbital dyschromia and applying a personal care composition to the target portion of skin during a treatment period. The personal care composition includes an effective amount of Type I active, an effective amount of a Type II active, and a dermatologically acceptable carrier. The treatment period is of sufficient length for at least one of the actives to improve the appearance of the periorbital dyschromia.