A prefabricated wall panel includes molds for casting reinforced concrete (RC) elements. The prefabricated wall panel includes foam boards, foam glass panels fixed to the foam boards, fabric mesh fixed to the foam glass panels, wire mesh fixed to the fabric mesh, and an exterior wall finish fixed to the wire mesh. Spaces defined by the foam boards and the foam glass panels form the molds for casting RC columns and beams.

In an embodiment, an interchangeable corner hanger to ornament framing protruding corner structures is provided. The interchangeable corner hanger includes a horizontal portion and a vertical portion. The horizontal portion is designed to rest on an exposed edge of a corner structure, and the vertical portion is designed to hang over the corner of the corner structure and rest against a wall upon which the trim is attached. The vertical portion has a length sufficient to stabilize the corner hanger without the use of other adhesives or attachments. In an embodiment, the vertical portion is configured to allow one or more interlocking elements to be suspended from the vertical portion. For example, the vertical portion may include an interlocking pattern configured to accept a complimentary interlocking pattern on an interlocking element. Further interlocking elements may be attached to the interlocking element.

A flooring system for installation over a surface that provides flooring using artificial wood panels over a plastic base formed from recycled plastics for even durable support over cement or dirt surfaces. The flooring system comprises a plurality of interlocking bases and a plurality of removable clips, wherein each clip has a pair of grippers for engaging at least one board of a plurality of boards, the base and clips supporting the boards apart from the surface and the plurality of boards connected between the grippers are capable of supporting a load of at least 300 pounds.

A unitary safety surface tile is provided. The tile may interlock with at least one other tile. The tiles may be configured for disposing on a base of loose fill and for receiving a covering of loose fill. The tiles may include a plurality of hollow inverted pyramidal shaped pockets. Each of the pockets may connect to at least two other pockets along a top edge of each pocket. Each of the pockets may engage the base of loose fill and/or receive the covering of loose fill. Each of the pockets may include one or more apertures for allowing passage of fluid through each of the pockets. Each tile may further include a plurality of edges. The edges may border the plurality of pockets. Each of at least two of said plurality of edges may be adapted for engaging at least one edge of at least one other tile.

The invention relates to a prefabricated construction element (1) having a permanent form, such as a longitudinal beam or a panel, consisting of two parallel plates that are formed, through molding and spaced apart from each other, from a hydraulic mixture such as concrete and from a built-in metal reinforcement, said plates being separated by an insulating block and connected together by transverse spacers (not shown), characterized in that said construction element (1) comprises consecutive prepositioning and bottom (6, 7) and/or top (8, 9) linking means, said bottom means (6, 7) consisting of a metal male connector (6) secured to the metal reinforcement of a first element (1) and arranged at the end of the bottom portion of said first element, and a metal female connector (7) secured to said metal reinforcement of a consecutive second element and arranged at the end of the bottom portion of said second element, the relative positioning of the male connector (6) and female connector (7) being such that said connectors can be connected together when the two consecutive elements (1) are assembled.

A suspended ceiling system for a building structure includes a plurality of parallel struts for supporting a plurality of parallel vanes suspended from the struts in perpendicular relationship thereto. The vanes can be suspended in downwardly spaced relationship to the struts or in contiguous relationship therewith and occur in different forms including illuminated vanes, adjustable vanes and the like.

This specification describes a tray substrate for tile flooring that can be used in narrow grout line modular floating tile assemblies. The tray is preferably made of plastic and has vertical tray edges around the top of the tray substrate with upward and downward tabs protruding from the sides of the tray substrate wherein some of the tabs are at least partially recessed under the surface of the tray.

A corner block has spaced-apart front and rear sections interconnected by two spaced-apart side sections that jointly define an internal cavity. Upper protrusions are provided on the top face of the block, and inner protrusions are provided inside the cavity at the bottom of the block. The upper and inner protrusions are configured and arranged relative to one another so that when two corner blocks are stacked one atop another with one block rotated 90° relative to the other, the upper protrusions of the lower block interlock with the inner protrusions of the upper block to interlock the two blocks. The corner blocks are constructed in two variants, a corner block A and a corner block B, which are mirror images of each other. The corner blocks A and B are alternately stacked upon one another to construct a 90° corner of a segmental wall structure.

Trusses comprising natural round timbers as top and bottom cords are provided. Also provided are truss and column assemblies comprising natural branched round timber columns connected to a truss.

The present subject matter is directed to a lattice tower covering and/or assembly for a wind turbine. The lattice tower assembly includes a plurality of structural members connected together to define an open lattice tower. The structural members include a plurality of supports, a plurality of inner cross-support members, and a plurality of outer cross-support members. The inner and outer cross-support members are connected between the supports so as to define one or more openings. The lattice tower covering includes one or more panel elements. Each of the panel elements are retained in position between the supports and cover at least a portion of one or more of the openings. Further, the lattice tower covering has a surface area defined by the plurality of supports and the one or more panel elements.

An extrudable keder rail and a clamping anchor for the keder rail are cooperative to secure keder fabric to a building support beam. The clamping anchor allows the keder rail to be securely attached to a standard beam without drilling holes or strapping about the beam. A temporary clamp and movable tensioning device allow the keder rails and keder fabric to be applied to the building support beams after the support beams have been assembled and installed.

A dovetail anchoring system for cavity walls is disclosed and includes a sheetmetal dovetail anchor and one-piece sheetmetal dovetail veneer tie. The anchoring system is used in conjunction with building structures that have a masonry outer wythe anchored to a poured masonry inner wythe. A thermally-isolating coating is optionally applied to the high-strength veneer tie, which is interconnected with the wall anchor. The thermally-isolating coating is selected from a distinct grouping of materials, that are applied using a specific variety of methods, in one or more layers and cured and cross-linked to provide high-strength adhesion. The thermally-coated veneer ties provide an in-cavity thermal break that severs the thermal threads running throughout the cavity wall structure, reducing the U- and K-values of the anchoring system by thermally-isolating the metal components.

Thermally-isolating wall anchors and reinforcement devices and anchoring systems employing the same are disclosed for use in masonry cavity walls. A thermally-isolating coating is applied to the wall anchor, which is interconnected with a wire formative veneer tie. The thermally-isolating coating is selected from a distinct grouping of materials, that are applied using a specific variety of methods, in one or more layers and cured and cross-linked to provide high-strength adhesion. The thermally-coated wall anchors provide an in-cavity thermal break that severs the thermal threads running throughout the cavity wall structure, reducing the U- and K-values of the anchoring system by thermally-isolating the metal components.

The invention concerns a half shell element (10) for the production of a hollow body with an identical further half shell element (10), with at least one guide (20 . . . 20'″) for the further element (10), which is constructed in the region of a first half periphery (11) of its encircling edge (12), so that the further element (10) can be pushed onto the half shell element (10) from the second half periphery (11') of the edge (12) lying opposite this first half periphery (11) and guided on the edge (12) and held in a final position. The hollow bodies which are thus produced can be both inserted into steel cages and also connected with each other via bars and built into concrete layers.

A pole splint, generally for use with a broken wooden utility pole, which can provide for a strong repair at a pole breakpoint and which uses relatively little manpower and equipment to install, even under difficult conditions. The splint generally comprises two panels which are designed to be interconnected with elongated connectors. The connectors will generally interact with one of the panels through the use of a nut and washer, and may connect with the other panel through a nut and washer or via a chain formed of chain links.

An ambulatory surgical center can include a hybrid operating room. The hybrid operating room can include at least four lead-shielded walls, a floor, and a ceiling. The ambulatory surgical center can also include an imaging device disposed in a central area of the hybrid operating room. The ambulatory surgical center can further include an operating table disposed in the central area of the hybrid operating room. The ambulatory surgical center can additionally include a power room adjacent to the operating room. The power room can include a power supply for the imaging device. The ambulatory surgical center can also include a conduit from the power room to the imaging device configured to deliver power to the imaging device. The ambulatory surgical center can further include an emergency power source for the imaging device configured to permit continuity of surgery in the hybrid operating room during a power outage.

A method of modulating oxygen saturation levels can include measuring oxygen saturation levels in a patient, administering inhaled nitric oxide, adjusting the dose of oxygen in real time to a second dose based on the inhaled nitric oxide.

The present invention relates to the administration of warm humidified oxygen to patients suffering with breathing problems. The present invention more specifically relates to the high flow of warm humidified oxygen to patients suffering with breathing problems or suffering with asthma.

A breathable gas inlet control device permits flow regulation at the inlet of a flow generator for a respiratory treatment apparatus such as a ventilator or continuous positive airway pressure device. The device may implement a variable inlet aperture size based on flow conditions. In one embodiment, an inlet flow seal opens or closes the inlet to a blower in accordance with changes in pressure within a seal activation chamber near the seal. The seal may be formed by a flexible membrane. A controller selectively changes the pressure of the seal activation chamber by controlling a set of one or more flow control valves to selectively stop forward flow, prevent back flow or lock open the seal to permit either back flow or forward flow. The controller may set the flow control valves as a function of detected respiratory conditions based on data from pressure and/or flow sensors.

A system and method are presented that electrically stimulates the phrenic nerve whereby said stimulation results in muscle activation of the diaphragm as observed by a measurement of work or power of breathing associated with the inspiratory portion of a stimulated breath.

A method comprises receiving an input coupling adjacent to a drive input, the drive input being driven by an actuating element, the input coupling being coupled to a joint output, the joint output being connected to a movable object. The method further comprises rotating the actuating element until a resistance torque is experienced by the actuating element and determining, based upon the resistance torque, whether the drive input has engaged the input coupling.

The present disclosure provides devices for preventing or absorbing fluid (e.g., sweat) and/or odors from the intergluteal cleft of a subject. In some embodiments, the present disclosure provides devices for treating or preventing hemorrhoids and methods of using same.

A method of forming oral orthotic systems includes providing an upper dental member adapted to be placed in connection with upper dentition of the patient, providing a lower dental member adapted to be placed in connection with lower dentition of the patient and providing a plurality of posterior mounting structures. Each of the posterior mounting structure is configured to be attached to one of the upper dental member or the lower dental member at a posterior, buccal position thereon. Force may be applied to the mandible of the patient via at least one of a plurality of different types mechanisms via attachment of a component of a selected type mechanism to at least one of the posterior mounting structures.

Embodiments according to the invention include coated condoms in which a fluidic coating material substantially covers an entire length of the condom, and methods for manufacturing such condoms. In some embodiments, a condom includes a tubular shaft having a tip on a closed end of the tubular shaft and an open end opposite the closed end on the tubular shaft, and a lubricant disposed along a length of the tubular shaft that extends from the open end of the tubular shaft to the tip on the closed end of the tubular shaft.

A system and method for creating a medicated atmosphere in an organ, or body cavity is disclosed. The system includes a flexible nebulization catheter that can be manipulated during use, a device for the introduction of the nebulization catheter, a medication delivery apparatus configured to control delivery of a medication to the catheter, a gas delivery apparatus in communication with the catheter, a gas pressure relief apparatus configured to relieve pressure in the organ or body cavity, and a central controller. The system may include a liquid source having a mixture of hyaluronic acid and heparin that, in conjunction with the nebulizing catheter, are designed to generate an aerosol with a particle size of 10-25 microns in a body cavity. The method includes providing an aerosol of anti-adhesive medication to an organ or body cavity while controlling overall pressure in the organ or cavity.

Disclosed herein are vials and devices containing a ketorolac solution for intranasal administration and a head space comprising no more than about 10% v/v oxygen and which vials and devices are stored in an oxygen-impermeable pouch. Also disclosed are processes for preparing the vials and devices.

The present disclosure relates to a dose indicator comprising, a chassis comprising a 42 chassis frame and a displacement portion, an indexable first display unit, mountable on the chassis, the first display unit being indexable about a first display axis, the indexable first display unit comprising a plurality of indexing teeth, a first display non-return arm, and a drive pawl connected at its proximal part to the displacement portion, the drive pawl comprising a socket at its distal part, the socket being adapted to engage an indexing tooth of the first display unit during indexing. The disclosure further relates to an actuator for an inhaler, wherein the actuator comprises a dose indicator as described above. The present disclosure is also directed to an inhaler comprising such actuator.

A nasal mask has a flexible bottom edge portion and side portions. A delivery device includes a holding chamber coupled to the nasal mask. A method of delivering an inhalable substance includes positioning a nose of a user in a cavity of the nasal mask, inhaling through the nose, and orally soothing the user with a soothing device.

A positive exhalation pressure device (1) is described. The device (1) comprises a housing (2) having an annular chamber (5), a chamber inlet (6) configured to permit air into the chamber, a chamber outlet (7) configured to permit air out of the chamber, and a mouthpiece (8) in fluid communication with the chamber inlet. A movable body such as a ball (3) is disposed in the housing within the annular chamber and configured to revolve around the annular chamber in response to flow of air through the chamber from the chamber inlet to the chamber outlet. The movable body is configured to at least partially block the chamber outlet as it revolves around the annular chamber causing cyclical fluctuations in airflow resistance.

In certain example embodiments, a system and/or method of guiding transitions between therapy modes in connection with the treatment and/or diagnosis of a patient for a respiratory disorder is/are provided. Respiratory disorder treatment according to a first therapy mode is provided. Input indicating a second therapy mode to be transitioned to following provision of the first therapy mode is received, with the second therapy mode being different from the first therapy mode. At least one default treatment parameter suitable for the second therapy mode is assigned or calculated. Each default treatment parameter of the second therapy mode is presented, with each default treatment parameter being adjustable by an operator during the presenting. Transitioning from the first therapy mode to the second therapy mode is performed by providing respiratory disorder treatment in accordance with the second therapy mode and each default treatment parameter and any adjustments made thereto prior to the transitioning. Advantageously, the chances of a patient being disturbed by transitioning from mode-to-mode are reduced.

An inner cannula (20) for a tracheostomy tube assembly includes a thin, inner sheath (22) supported externally by a structural frame (23) having a longitudinal portion (25) and a plurality of ribs (26) extending circumferentially and spaced along the cannula. The inner cannula (20) is inserted within and is removable from an outer tracheostomy tube (1). The inner cannula (20) is made by coating a plastic layer on a core to form the sheath and then placing the sheath on a curved core. The structural frame (23) is then moulded about the sheath (22) in a mould 80.

The present disclosure provides a device that can be used to secure an endotracheal tube. In one embodiment, the device is a one-time use device that has a flexible construction with an adhesive side. The device is configured to be adhered to the endotracheal tube and subsequently secure unto the patient's face. The device is quick and easy to deploy, it reliably secure the endotracheal tube, is comfortable for the patient, and that minimized the chances of infection.

A gas ventilation mask includes an anesthesia nasal mask and a mouth mask defining respectively a nasal chamber and an oral chamber, detachably connected to one another so that the nasal mask and the mouth mask may be used either separately as a nasal mask or as a mouth mask, or as a combination nasal-mouth mask. Also provided is a mask anchor for holding a face mask on a patient, includes a head support for engaging a back of a patient's head, a posterior head strap that originates from behind the patient's head, in contact with the patient's head and attaches either directly or indirectly to the mask when the mask is on the patient's face, wherein the strap can be tightened to create a seal to allow for positive pressure ventilation or left loose and for providing supplement oxygen. Also provided is an anesthesia mask strap system having a first expandable strap portion having the ability to extend; second and third non-expandable strap sections fixed to ends of the first expandable strap section; and an adhesion section for fixing a length of the strap system when the second and third non-expandable strap sections are pulled to tension the expandable strap section.

A patient interface assembly having an improved support for use in securing a patient interface device to the head of a patient overcomes the shortcomings of conventional headgear. The improved support provides a self-adjusting anchor point situated anterior to the ear of the patient that provides enhanced stability in mounting the patient interface device to the patient.

A system provides warm, humidified gas to a patient via a patient interface. Horizontal connections can be used between the humidification chamber and conduit. To reduce the likelihood of condensate flowing back to the humidification chamber, or dead space or gases recirculation regions occurring within the gases flow path, a raised portion is positioned inside of the flow path to improve flow characteristics and to provide a barrier for condensate back flow. The raised portion also reduces the amount of condensate that is formed in the system and provides better flow characteristics for sensing purposes.

An electronic device is provided. The electronic device includes a capsule container configured to contain at least one capsule, a discharge structure configured to discharge a material included in the capsule, a transceiver configured to transmit data to an external device or to receive data from the external device, and at least one processor. The at least one processor is configured to receive, user state information and biometric information from the external device via the transceiver, select at least one capsule in the capsule container on the basis of the received user state information and biometric information, determine a spray amount of a material contained in the selected at least one capsule, and spray the material via the discharge structure.

An umbilical system for sourcing and delivering within a flexible protective covering, a plurality of different breathing gasses, safety tether, a plurality of ancillary lines for remotely distributable, documentable, multidirectional, multi-format data/communications acquisition and delivery, personal/situational awareness and ancillary power sources for tool, accessory or device enervation, to a plurality of Users in an adverse environment.

A method for manufacturing an impregnated filter material includes preparing at least one impregnating solution comprising sulphate and phosphate; providing a filter material; and impregnating the filter material with at least one impregnating solution, at least once. In this manner, it is possible to manufacture an impregnated filter material for the removal of noxious substances and/or toxins, which includes sulphate and phosphate. The noxious substances and/or toxins can thereby be present in the form of gases and/or vapours.

An oral-nasal cannula receives exhaled gases from the nose and mouth of a patient. The exhaled gases are transported to variable flow valves that can variably restrict the flow of the gases through the valves upon software generated signals. The exhaled gases pass through the variable flow valves and mix so that they can be measured by a single sensor such as a sensor of a capnometer. Based upon information gathered by the capnometer, the variable valves can be adjusted in real-time according to a software method in order to identify a variable valve flow configuration that maximizes the amount of CO2 received and measured by the capnometer. In this manner, the software can adapt a single capnometer to measure exhaled gases regardless of whether a patient breathes primarily through their nose or mouth or some proportion of the two.

An example method for detecting respiratory disturbances experienced by a subject can include receiving an airflow signal and at least one of an acoustic or vibration signal, where the airflow, acoustic, and/or vibration signals are associated with the subjects breathing. At least one feature can be extracted from the airflow signal and at least one feature can be extracted from at least one of the acoustic or vibration signal. Based on the extracted features, at least one respiratory disturbance can be detected. The respiratory disturbance can be flow limited breath or inspiratory flow limitation (“IFL”).

Certain embodiments are directed to a specimen retrieval device having a high friction inner lining for reducing specimen deformation during removal. Certain embodiments are directed to a device that facilitates isolation and removal of specimens during minimally invasive surgery. In certain aspects the device is configured to disperse pulling tension over a larger area reducing the likelihood of specimen tearing during removal. The device enables quicker removal through a smaller hole or opening in the body wall.

Systems and methods for effecting posture of a subject who is to be positioned on a support surface having an inclinable portion such that the subject's thorax is inclinable relative to the subject's legs, are provided. An example system includes a detachedly coupleable thoracic harness having at least an inner surface and an outer surface. The inner surface being contoured to fit over shoulders of the subject. The outer surface having a fastening surface that releasable attaches to a corresponding fastening surface disposed on the inclinable portion of the support surface.

The invention pertains to positioning a patient in prone position, comprising: positioning a patient in a supine position,attaching a chest body contact sheet to the chest of the patient with an attached inflatable chest cushion in the deflated state,attaching a pelvic body contact sheet to the pelvic region of the patient with an attached inflatable pelvis cushion in the deflated state,transferring the patient from the supine position to a prone position,with the chest body contact sheet attached to the chest of the patient and the pelvic body contact sheet attached to the pelvic region of the patient and the patient in the prone position, inflating the chest cushion and the pelvis cushion, thereby making that the chest cushion and the pelvis cushion together bear the weight of the torso of the patient with the abdominal region of the patient being decompressed. The invention is based on a combination of anatomy and physiology that is used for a reliable positioning the patient, which is safe for the patient and safe, hygienic and user friendly for the medical team.

A nozzle received by a patient. The nozzle has at least two portions. A first portion that has an upper end and a lower end in which a central aperture extends between the upper and lower ends of the nozzle. The central aperture terminates at the opening of the lower end of the nozzle. A second portion that has two ends, the second end is rounded. There is at least one support arm joining the first and second body portions but holding the second body portion a set distance from the first body portion.

Provided are systems, methods, and electronic vapor devices configured to provide spirometer functionality and respiratory medication dispensing which can couple and function symbiotically with a portable electronic communication device.

An assembly for a counter mechanism for a drug delivery device is described comprising a drive member, wherein the drive member is adapted and arranged to be rotated in a first rotational direction and to be prevented from rotation in a second rotational direction which direction is opposite to the first rotational direction, an advancing member adapted and arranged to be axially moved and rotated with respect to the drive member, wherein the advancing member is adapted and arranged to mechanically cooperate with the drive member such that the drive member is rotated in the first rotational direction, and a display member which is configured to count a number of doses and to display the counted number of doses, wherein the assembly is adapted and arranged such that rotation of the drive member in the first rotational direction is converted into a counting movement of the display member. Furthermore, a drug delivery device comprising the assembly is described.

This disclosure describes systems and methods for controlling pressure and/or flow during exhalation. The disclosure describes novel exhalation modes for ventilating a patient.

A method and a control program for operating an anesthesia apparatus, as well as an anesthesia apparatus (12), which operates according to the method are provided. The anesthesia apparatus includes a breathing gas feed unit (22) intended for displacing a breathing gas volume in a breathing circuit (10). A piston (23) brings about the displacement of the breathing gas. Switching over between a first mode of operation and a second mode of operation during the return of the piston (23) allows for a presetting of a corresponding piston return velocity. The piston return velocity depends on a volume flow in an exhalation branch (34) of the breathing circuit (10) in the first mode of operation. The piston return velocity depends on a minimally necessary piston return velocity in the second mode of operation.

A smart oronasal mask for a positive-airway-pressure device includes a mask body and a temperature sensor. The mask body has an air inlet and an air outlet. The temperature sensor is deposited in the mask body and located between the air inlet and the air outlet for sensing a temperature of a mixture formed by gas entering the mask body through the air inlet of the mask body and gas entering the mask body through the air outlet of the mask body. Then the positive airway pressure device adjusts air feed according to the temperature sensed by the temperature sensor in a real-time manner, so as to help keep a patient's respiratory tract clear.

A system for determining an optimal hardness of a patient interface device includes a fit score determination unit structured to receive a 3-D model of the patient interface device and a 3-D model of a patient's face and to determine a fit score between the patient interface device and the patient's face based on the 3-D model of the patient interface device and the 3-D model of the patient's face, and a hardness determination unit structured to determine a hardness value of the patient interface device based on the determined fit score.