Abstract: The present invention prevents an absorbent body from twisting and splitting while maintaining the capability of fitting onto the buttocks of a wearer even when the absorbent body has a low fabric weight. The absorbent body (4) has a large number of compressed parts (20, 20, . . . ) formed in a region other than a region that extends in a widthwise center section along the longitudinal direction and includes portions corresponding to a body fluid excretion part (H) and the intergluteal cleft of the wearer. A region including a portion corresponding to the intergluteal cleft is an easily deformable region (21) without compressed parts (20). The easily deformable region (21) extends to an intermediate position in the longitudinal direction and does not reach the rear end of the absorbent body (4). The region extending behind the easily deformable region (21) to the rear end of the absorbent body (4) has compressed parts (20) formed thereon.

Abstract: An absorbent core for an absorbent article is provided an absorbent material, the absorbent core comprising one or more first zones comprising a first amount of absorbent material and one or more second zones comprising a second amount of absorbent material, wherein each second zone is at least partly delimited from the other second zones by the one or more first zones characterized in that the first amount of bulk absorbent material is different than the second amount of absorbent material, each amount of absorbent material being determined as weight per unit area.

Abstract: A diaper tab to be secured at a side opening of a diaper, the diaper tab having an elongated body; an adhesive tab extending from a first side of the elongated body; and a hook and loop fastener extending from a second side of the elongated body; the first side is opposite the second side; the adhesive tab is to secure to a first side of the side opening and the hook and loop fastener is to secure to a second side of the side opening; and the elongated body is positioned within the opening.

Abstract: A person support apparatus includes a support adapted to support thereon an occupant of the person support apparatus and a sensor configured to detect an ambient air characteristic. The sensor generates an output signal based on the detected characteristic and communicates the output signal to a controller. The controller is configured to receive the output signal from the sensor and determine a usability status of the person support apparatus. The usability status may include an indication that the person support apparatus is ready for use by an occupant, whether a potential hazard exists for an occupant of the person support apparatus, a cleaning status of the person support apparatus, or a location of the person support apparatus.

Abstract: A bed is provided. The bed may include a lift system which raises and lowers a support deck of the bed. The lift system may include multiple individually actuatable lift systems. The bed may include a powered bed mover system.

Abstract: A bed step stool for assisting a user into and out of bed including opposite sides, a head, and a foot comprising a first support to be disposed closer to the head of the bed; a second support to be disposed closer to the foot of the bed; a step assembly supported between the first support and the second support, the step assembly to enable the user to step thereon for assisting the user into and out of the bed; and a bed attachment that couples the bed step stool to the bed to stabilize the bed step stool.

Abstract: A patient care room, and method of treating a patient includes a patient treatment area that is configured to accept a patient support and an airflow system in said patient care room. The airflow system has an air discharge outlet mounted above the patient support. The outlet has a plenum with at least two laterally outside portions that are aligned with opposite perimeters of the patient support. Each outside portion has at least one large opening that is adapted to direct a curtain of air toward the perimeter of the patient support. The plenum has at least one laterally inside portion within the perimeter of the patient support. A cover over the plenum has small openings distributed over the cover that are smaller than the large opening. The outside portions are adapted to each produce a curtain of air that is passed outside a perimeter of the patient support at a higher flow than air inside the perimeter of the patient support.

Abstract: A hippotherapy device includes a saddle for receiving a person thereon, a programmable movement control, and an automatic movement device for automatically moving the saddle according to a movement pattern program. The program specifies a sequence of target values of positions and orientations of the saddle in the locality of the movement device in order to execute the movement pattern. The hippotherapy device further includes a person securing device having a main support on which a body strap is mounted, at least one sensor for detecting at least one physical variable characterizing the body posture of the person on the saddle, and an auxiliary control device configured to compare expected values of the physical variable with current values of the physical variable detected by the sensor, and to trigger an associated safety function, if a deviation of the current values from the expected values exceeds a predetermined tolerance threshold.

Abstract: The disclosure relates to wearable devices and methods that utilize laryngeal or neck vibro-tactile stimulation (VTS) as a non-invasive form of neuromodulation that induces measurable improvements in the patients with focal dystonia of the head, neck and voice including cervical dystonia and/or spasmodic symptoms.

Abstract: One general aspect of technical solutions described herein includes a biomechanical assistive device that includes one or more sensors, a back-drivable motor system, and a controller. The controller, when the motor system is inactive, records measurements from the one or more sensors for user motion pattern analysis during a user activity being performed by a user. The controller, when the motor system is active, records the measurements from the one or more sensors, and generates an assist torque to assist the user to perform the user activity.

Abstract: A driving module including a driving source configured to generate power, a gear train including a decelerating gear set configured to receive driving power from the driving source and a ring gear attached to one side thereof, and a rotary joint including at least one planetary gear configured to rotate using power received from an output end of the decelerating gear set and to revolve along the ring gear is disclosed.

Abstract: A method of treating diplopia or convergence insufficiency disorder in a patient; it includes providing a patient having a condition of diplopia or convergence insufficiency disorder with an image pair configured to present a first image to a first weaker eye of the patient and a second image to a second dominant eye of the patient; obtaining performance information of the patient when the patient performs a task requiring the perceiving of at least the information content of the first image; and adjusting, based on the performance information, the at least one image parameter such that the difference in perceptibility of the information content of the first image and the information content of the second image is reduced.

Abstract: The present invention discloses a massager for shoulder and neck which comprises a driving mechanism, a neck massaging mechanism and a shoulder massaging mechanism; wherein the driving mechanism comprises a power assembly and a transmission assembly, the transmission shaft comprises an upper transmission shaft and a lower transmission shaft; the neck massage mechanism comprises a neck kneading massage assembly and a first eccentric block, the first eccentric block is sleeved on the upper transmission shaft, and the neck kneading massage assembly is arranged on the first linked block; the shoulder massaging mechanism comprises a shoulder massage assembly and a second linked block. The massager for shoulder and neck provided by the invention relieves the pain of the muscles of the shoulder and the neck, promotes the blood circulation of the shoulder part and the neck part, and has an obvious effect to keep a healthy body.

Abstract: A massaging apparatus with heating capabilities includes a structural body, an internal chamber, a power source, a control switch, a control panel, and a heating unit. The structural body, which is preferably spherical in shape, is used for massaging purposes. The power source, the control switch, and the control panel, which are positioned within the internal chamber, are used to manage the heating unit that administers heat therapy. To do so, the heating unit is in thermal communication with an outer surface of the structural body. Thus, heat therapy can be provided to a target muscle by positioning the structural body against the skin of a user. Additionally, vibration therapy can also be administered via a vibrating unit.

Abstract: According to an aspect of the present disclosure, a stimulator apparatus is configured for providing stimulation to a human or animal body. In some embodiments, the stimulator apparatus includes a control housing; an electrical power source; contact connection; an object sensor within the control housing adapted to detect at least one control feature of proximity, gesture, movement and colour of an object and/or body part within a motion detection distance range of the control housing; and control circuit means adapted to distinguish the control feature or features of the object or body part in order to vary one or more stimulating parameters of the electrical output of the stimulator apparatus.

Abstract: Aspects of the of the disclosure relate to a non-contact physiological motion sensor and a monitor device that can incorporate use of the Doppler effect. A continuous wave of electromagnetic radiation can be transmitted toward one or more subjects and the Doppler-shifted received signals can be digitized and/or processed subsequently to extract information related to the cardiopulmonary motion in the one or more subjects. The extracted information can be used, for example, to determine apneic events and/or snoring events and/or to provide apnea or snoring therapy to subjects when used in conjunction with an apnea or snoring therapy device. In addition, methods of use are disclosed for sway cancellation, realization of cessation of breath, integration with multi-parameter patient monitoring systems, providing positive providing patient identification, or any combination thereof.

Abstract: A massage device comprising an output shaft, a plurality of permanent magnets arranged on the output shaft, and an electromagnetic driving module arranged radially outside the permanent magnets. The stator yoke of the electromagnetic driving module and the permanent magnets interact to generate a cogging torque. The electromagnetic driving module interacts with the permanent magnets to generate an electromagnetic driving force. The massage device has improvements in efficiency and output, is compact and reduces heat generation. The activation of the electromagnetic driving module actuates the output shaft to strike forward. The cogging torque applies a first pulling force to the output shaft to provide braking and buffering to the output shaft. When the output shaft is urged to move in the direction opposite to the strike forward direction from the idle state, the cogging torque applies a first thrust to the output shaft, to thereby increase the output.

Abstract: A method for performing cardiopulmonary resuscitation (CPR) includes elevating the head, heart and shoulders of an individual from a starting elevation angle to a final elevation angle greater than zero degrees relative to horizontal while performing CPR by repeatedly compressing the chest. The method includes elevating the brain within a time period selected to be slow enough to permit a sufficient amount of blood to flow to the brain throughout the elevation time period. The method also includes regulating the intrathoracic pressure of the individual while performing CPR. The performance of chest compressions is stopped and after stopping the performance of chest compressions, the head, heart, and shoulders are promptly from the final elevation angle within a timeframe selected to prevent significant drainage of blood from the brain until the head, heart and shoulders are lowered.

Abstract: A method for ventilating a patient during CPR including repeatedly compressing the patient's chest and delivering a positive pressure ventilation to the patient primarily during a decompression phase of the repeated compressions of the patient's chest.

Abstract: An adjustable respirator shell, suitable for being worn on a human body trunk, includes a body, a belt and a buffer. The body includes a protrusive portion and a contact portion. The protrusive portion has an opening connecting a fluid pressure controller, and the contact portion is to contact the human body trunk. The belt, connecting the body, is to surround the human body trunk so as to fasten the adjustable respirator shell on the human body trunk. The buffer covers a circumference of the contact portion, and the contact portion contacts the human body trunk via the buffer. In addition, the buffer includes at least one cushion.

Abstract: A method is provided for a novel application of trigger point dry needling. A target tissue is identified based on the observation of a series of movement patterns performed by the patient. Once identified, a needle movement protocol is used to insert a needle into the target tissue to a myofascial trigger point during one or more movement patterns. The needle protocol is adjusted until a local twitch response is induced.

Abstract: Embodiments for managing photographic capture by one or more processors are described. An image is received. The image includes at least one individual and is associated with a location. A signal indicative of a recommendation with respect to a posture of the at least one individual in the image is generated based on information associated with the at least one individual, the location, or a combination thereof.

Abstract: The present disclosure describes a kit for peritoneal dialysis that includes at least two bags. The kit also includes an overwrap for accommodating the at least two bags. At least one bag of the at least two bags forms at least a portion of the overwrap. According to the present disclosure, it is advantageously possible to reduce the material consumption of the overwrap, lower the cost of the kit, and reduce the amount of the disposable waste.

Abstract: There is provided means with which, during frozen storage of a biological sample or a drug, the biological sample or drug stored inside a frozen storage container is not susceptible to contamination. A frozen storage container 10 includes a container body 11 with an internal space 13, and a partition wall 12 which divides the internal space 13 of the container body 11 at least into a first space 14 and a second space 15. In the container body 11, the first space 14 is liquid-tightly sealed, the second space 15 has an opening 22 which is in communication with the outside, and the second space 15 is liquid-tightly sealable by welding the container body 11.

Abstract: An apparatus, method, and article of manufacture for transferring fluid contained in a syringe. The apparatus includes an airlock component having a cylindrical body with a first end, a second end, and a hollow tube disposed between the first end and the second end. An annular opening is located at the first end of the cylindrical body. The hollow tube includes a gas inlet aperture and a gas outlet aperture. The hollow tube also includes an inwardly-facing airtight material coupled to the interior surface of the hollow tube, and a septum coupled to the second end of the cylindrical body. The method includes transferring fluid from one container to a second container using the apparatus. The article of manufacture includes the apparatus, a syringe, and a needle.

Abstract: The invention is directed to a method and a device for the dosing of active substances for the preparation of medicaments. In the context of the dosing method, one or more active substances dissolved in a liquid are stored in a storage container, and, in order to permit dosing, a number of drops corresponding to the desired amount of active substance are forced actively through a nozzle onto a substrate or into a collecting vessel; the device used for this purpose comprises at least one storage container for storage of a liquid, and one or more active substances dissolved therein, and also a nozzle through which a number of drops corresponding to the desired amount of active substance are forced out onto a substrate or into a collecting vessel.

Abstract: A device for the metered filling of a container with a filling material includes a receiving unit for receiving a container and at least one material store as a storage container for the filling material. A defined quantity of the filling material is able to be removed from the at least one material store and transferred into the container by a filling unit. The filling unit includes at least one metering chamber which is displaceably mounted so that the metering chamber is present alternately in a first position and in a second position. In its first position the metering chamber is in contact with the material store so that filling material is able to be filled into the metering chamber from the material store. In its second position the metering chamber is arranged above the container so that the filling material located in the metering chamber is able to be emptied into the container. The container may, in particular, be a drinking straw.

Abstract: Devices for inducing satiety in enterally fed patients are provided. In one aspect, an enteral feeding device is provided that includes a catheter tube and an expandable bladder secured to a distal end of the catheter tube. The expandable bladder is positionable within a body lumen of a patient for receiving and dispensing nutrients to the patient. In another aspect, a satiety-inducing device for continuously dispensing nutrients to a patient is provided that includes an enteral feeding tube and an expandable bladder secured to the feeding tube near a distal end of the feeding tube such that the expandable bladder is positionable within a body lumen of the patient. The expandable bladder expands upon receipt of nutrients to occupy a volume of the body lumen and contracts as nutrients are continuously dispensed to the patient.

Abstract: An improved teething device is provided. The device comprises a body portion (3) and a head portion (5) extending from the body portion. A plurality of nodules (11) project from a surface (9) of the head portion (5).

Abstract: The invention relates to nail composition sets including mirror pigment, as well as to methods and kits related to such composition sets.

Abstract: The present invention relates to toiletry products and more particularly to shower products that are manufactured in shaped forms and/or comprise shaped gels. Certain embodiments relate to formulations for shower products comprising gelatin, water and surfactant wherein the shower product is in shaped gel form and/or comprises a shaped gel form. Other embodiments relate to shower products per se for example in shaped gel form and/or comprising shaped gel form. Further embodiments relate to a process for the manufacture of such formulations and shower products.

Abstract: An antiperspirant aerosol product having good environmental sustainability and comprising an anhydrous antiperspirant aerosol composition comprising an AP active comprising a basic aluminium chloride compound 5 of formula Al2OH4.4Cl1.6 to Al2OH4.9Cl1.1, water soluble calcium salt and amino acid, and an aerosol dispenser comprising a container body, an aerosol valve, and a valve actuator; characterised in that the product has a Combined Sustainability Index (CSI) of less than 3.0, where: CSI=AlF+VOCF+MCB/N10 AlF being the weight (in centigrams) of aluminium expelled per spray; VOCF being the weight of VOC (in grams) expelled per spray; MCB being the weight of metal (in grams) in the container body; and N is the number of spray applications possible from the fully charged product, each figure being based on a spray duration of 2 seconds.

Abstract: The present invention discloses an ultraviolet (UV) block cosmetic composition in the form of a water-in-oil (W/O) emulsion in which a discontinuous water phase is uniformly distributed in a continuous oil phase, or in the form of an oil-in-water (O/W) emulsion in which a discontinuous oil phase is uniformly distributed in a continuous water phase, the UV block cosmetic composition comprising a water phase, an oil phase, and an emulsifier, wherein the water phase includes a water phase medium and cerium oxide particles, and the oil phase includes any one or more selected from a group consisting of an oil phase medium, a hydrophobic UV blocking agent, and an oil UV blocking agent. A UV block cosmetic composition according to the present invention has a superior UVA and UVB blocking effect and a good feeling of use.

Abstract: The present invention provides a bicontinuous microemulsion composition, including: (A) polyglycerin group-containing organo(poly)siloxane shown by the general formula (1): wherein R1 represents an alkyl group or a phenyl group, R2 represents a group having a polyglycerin structure shown by the formula (2) or the formula (3), R3 represents R1 or R2, “a” is 0 to 6, “b” is 0 to 4, a+b is 0 to 10, and at least one of R3 is R2 when “b” is 0: wherein R4 represents an alkylene group or an aralkylene group, “c” is 0 to 10, and “d” is 2 to 6; (B) silicone oil having a viscosity of 20 mm2/s or less at 25° C., volatile hydrocarbon oil, or ester oil; and (C) water. This provide a transparent bicontinuous microemulsion composition in which anionic or cationic surfactant, and water-soluble monovalent or polyvalent alcohol are unnecessary; and a cosmetic with excellent pleasantness of use.

Abstract: A reloadable microcapsule contains a microcapsule core and a microcapsule wall encapsulating the microcapsule core. The microcapsule core contains a hydrophobic core solvent and a hydrophilic core solvent, and the microcapsule wall, formed of an encapsulating polymer, is permeable to the hydrophilic core solvent. Also disclosed are methods of preparing the reloadable microcapsule and consumer products having the microcapsules.

Abstract: A cosmetic composition for brightening skin and a method for brightening skin using the cosmetic composition are provided. The cosmetic composition is ammonia-free and persulfate-free, and includes hydrogen peroxide, at least one alkaline booster and at least one fatty compound present from about at least 30% by weight, based upon the total weight of the composition. The method for brightening skin includes applying to the skin a composition provided as a multi-part system, the parts separately containing two or more sub-compositions each of which comprises one of the hydrogen peroxide and the alkaline booster, one or both comprising a fatty compound component, the sub-combinations combinable at the time of use.

Abstract: Oral care compositions and methods for the same are provided herein. The oral care composition may include an orally acceptable vehicle, a peroxide whitening agent, and one or more gelling agents. The gelling agents may include a fatty acid. The gelling agents may be free or substantially free of fatty alcohols. The gelling agents may include at least one of palmitic acid, stearic acid, or mixtures thereof.

Abstract: Oral care compositions and methods for whitening and preventing stains on teeth are provided. The oral care composition may include an orally acceptable vehicle, a peroxide whitening agent, and an abrasive system. The orally acceptable vehicle may include a block copolymer of ethylene oxide and propylene oxide, and the abrasive system may include at least one insoluble phosphate salt.

Abstract: Anhydrous oral care compositions and methods for making and using the same are described herein. The anhydrous oral care compositions may include an orally acceptable vehicle, a peroxide whitening agent, and an abrasive system. The abrasive system may include at least one abrasive having a pellicle cleaning ratio (PCR) greater than or equal to 100.

Abstract: Compounds and methods for preparing and using the compounds are disclosed herein. The method for preparing the compounds may include contacting a metal ion or salt thereof with an alkali metal polyphosphate salt in an aqueous medium. The method may also include adding a base to increase a pH of the aqueous medium.

Abstract: The invention relates to compositions for removing nail polish including at least about 20% by weight of a C2-C3 monoalcohol, at least about 10% by weight of glycerin, and a diester of a dicarboxylic acid. The compositions optionally include water. The water, if present, is present in a concentration by weight that is less than the concentration by weight of glycerin. If the concentration of glycerin is from 30% to 60% by weight, then the concentration of C2-C3 monoalcohol is at least about 30% by weight.

Abstract: Provided among other things is a lubricant formulation comprising by weight: water about 20 to about 45%; propylene glycol about 40 to about 50%; siloxane/emulsifier about 15 to about 30%; and C6 to C12 glycol about 0.5 to about 2%, wherein the formulation is clear to slightly hazy, and wherein additional components are about 5% by weight of the formulation or less.

Abstract: The present invention provides a salicylic acid aqueous solution comprising salicylic acid, tromethamine as a dissolution-enhancing agent to enhance dissolution of salicylic acid, and water for dissolving salicylic acid.

Abstract: Methods and compositions for stimulating the growth of hair are disclosed wherein said compositions include a cyclopentane heptanoic acid, 2-cycloalkyl or arylalkyl compound represented by the formula I wherein the dashed bonds represent a single or double bond which can be in the cis or trans configuration, A, B, Z, X, R1 and R2 are as defined in the specification. Such compositions are used in treating the skin or scalp of a human or non-human animal. Bimatoprost is preferred for this treatment.

Abstract: A cosmetic composition and a method of preparing a cosmetic composition that includes mangiferin characterized as demonstrating soluble and chemically stable mangiferin, wherein stability includes resistance to crystallization of mangiferin that is independent of temperature and pH.

Abstract: The invention relates to compositions for removing nail polish comprising a C2-C3 monoalcohol, glycerin, and propylene carbonate, wherein the glycerin and propylene carbonate are present in a glycerin to propylene carbonate ratio by weight of at least 1:3 and the concentration by weight of ethanol is at least about 16%. Methods of removing nail polish and moisturizing the hands are also provided.

Abstract: This invention relates to a skin care formulation containing, among others, Vitamins A, C, and E, and derivatives thereof and to a skin care product where the formulation is impregnated in a delivery system, which can be made of pure heavy-metals-free silk membrane or mask, to retard the effects of aging of the skin and generally improve the quality of the skin, particularly human facial skin.

Abstract: A cosmetic article that includes a hydrophobically-modified biopolymer and a cosmetic application. The cosmetic application is selected from the group consisting of mascara, moisturizing creams, moisturizing lotions, facial cleansers, wrinkle-reducing gels/creams/lotions, shampoos, conditioners, soaps, deodorants, acne treatment, thy-skin treatment, blemish concealers, coloring make-up, and controlled molecular release matrices for fragrances.

Abstract: A mascara composition including a film-forming polymer portion and a particulate portion is provided. The film-forming polymer portion comprises a high molecular weight vinylpyrrolidone homopolymer and the particulate portion comprises an inorganic particulate. The mascara composition comprises at least about ten percent by weight of the vinylpyrrolidone homopolymer and is substantially free of wax. Methods of applying makeup to the eyelashes are also provided.

Abstract: A mascara composition includes a film-forming polymer portion. The film-forming polymer portion is stabilized in a vehicle that includes water. The film-forming polymer portion includes a high molecular weight vinylpyrrolidone homopolymer and one or more secondary film-forming polymers each having one or more repeat units. The one or more repeat units of the one or more secondary film-forming polymers include imide and/or acid-anhydride functionality. The mascara composition includes at least about 10 percent by weight of the vinylpyrrolidone homopolymer and is substantially free of wax.