A system for influencing the senses of a person in a room for measuring and/or influencing physiological parameters of the person is provided. The person is substantially stationary and lying in the room during the measurement and/or influencing. The system includes a sound insulating apparatus for screening off acoustically active devices with respect to the person. The acoustically active devices serve for measuring and/or influencing the physiological parameters in the room, and an optical display apparatus for offering optical stimuli and/or signals for the person in the field of view of the person.

A system for influencing the senses of a person in a room for measuring and/or influencing physiological parameters of the person is provided. The person is substantially stationary and lying in the room during the measurement and/or influencing. The system includes a sound insulating apparatus for screening off acoustically active devices with respect to the person. The acoustically active devices serve for measuring and/or influencing the physiological parameters in the room, and an optical display apparatus for offering optical stimuli and/or signals for the person in the field of view of the person.

Apparatus for use in providing isolation, the apparatus including an isolation tent having a body including a roof member, at least one wall extending between a supporting surface and the roof member in use to thereby at least partially define an internal volume substantially isolated from a surrounding environment, a plurality of connectors coupled to the body, the plurality of connectors being adapted to physically attach the body to a frame and an electrical component electrically connected to at least one of the plurality of connectors to allow electrical signals to be transferred to or from the electrical component via the connector.

A portable hyperbaric chamber device with forward-facing door includes a frame, an inflatable chamber, a dump valve, at least one primary pressure relief valve, at least one secondary pressure relief valve, a plurality of fill valves. Access to the inflatable chamber is gain through a door panel of the inflatable chamber. The inflatable chamber is positioned within and secured to the frame. The plurality of fill valves is in fluid communication with the inflatable chamber so that the inflatable chamber can be pressured for usage. The dump valve is in fluid communication with the inflatable chamber to deflate the inflatable chamber. The primary pressure relief valve and the secondary pressure relief valve are in fluid communication with the inflatable chamber to maintain a safe internal pressure within the inflatable chamber to protect wellbeing of the users and the structural integrity of the complete apparatus.

A patient isolation tent is disclosed. The tent includes a free-standing frame assembled from individual frame components and corner connectors. A thin, flexible, substantially transparent, disposable membrane having a bottom surface, four side surfaces, and at least partially open top connects to and is supported by the frame to define a patient isolation space. The membrane is formed as a single, continuous piece of material with integral gloves, interior instrument pockets, and a waste catchment. In use, the bottom surface of the membrane in a collapsed folded or unrolled state overlays a patient support. A patient lays on the support and the side surfaces of the membrane are extended to an upright position to create a patient isolation space. When the patient's isolation period or treatment is completed, the membrane and any patient bodily fluids in the waste catchment are properly disposed of The frame may be disassembled, and the frame and patient support may be reused. The entire patient isolation tent may be provided as a compact kit for ready shipment to and use in remote locations.

A negative-pressure dome includes a transparent domed shield, a flexible skirt attached to the perimeter of the domed shield, a hose attachment port formed on the domed shield; and access openings in at least one of the domed shield and the flexible skirt. The transparent domed shield consists of a clear rigid plastic. The access openings may be at least partially occluded by flexible flaps that are deflectable to increase an open cross-section of the access openings. In a first configuration, the access openings are disposed in the domed shield sized to cover a face and are sized to have a cross-section between 3 cm.sup.2 and 200 cm.sup.2. In a second configuration, the access openings are disposed in the flexible skirt and are sized to have a cross-section between 30 cm.sup.2 and 200 cm.sup.2, while the domed shield is sized to cover head and chest of a subject.

A protective equipment includes a rotatable window and an extended member secured to a peripheral edge of the rotatable window. The rotatable window may be configured as a shield to be disposed between a patient and a healthcare worker to minimize exposure of the healthcare worker to at least one of the patient's bodily fluids, bacteria, and viruses. A port provides entrance by one or more instruments through the rotatable window or the extended member, thereby providing access to the patient while protecting the healthcare worker from the patient's bodily fluids, bacteria and/or viruses. The protective equipment may include an air flow system configured to receive and filter air expelled by the patient, to pull the expelled air away from the patient's face and to filter/clean the expelled air.

Personal protective equipment including hygienic barriers and methods of use to provide an improved barrier between a patient and a caregiver.

Methods, apparatus, and systems for reducing transmission of aerosol droplets in a medical or dental procedure are described. One protective shield system includes a base plate, a shield having at least one transparent section, and a pipe or conduit comprising a plurality of holes thereon. The shield is configured to be removably attached to the base plate to allow attachment of the shield to the base plate prior to the medical or dental procedure and removal of the shield from the base plate after the medical or dental procedure. The pipe or conduit is positioned adjacent to an inner surface of the shield and on at least part of a perimeter of the shield. The pipe includes an end that is configured to connect to a suction system to enable removal of the aerosolized particles from below the shield during the medical or dental procedure.

A medial isolette is provided. A flexible enclosure and a collapsible wire-frame structure are provided which supply an economical and easily assembled isolation chamber. A flexible drape is provided to further isolate the patient and effectively control a negative pressure environment within the isolette. Access ports with integrated or removable gloves are provided to access the patient when the isolette is in use. A component access panel is provided for ducted connection of patient gas circuits and leads and source of negative pressure.