An neonatal care unit comprising: a hood defining an interior space and having a bottom opening, wherein the hood is dimensioned to accommodate a neonate; a sealing skirt extending along at least a portion of a peripheral edge of the bottom opening and configured to engage at least part of a front torso region of a human in a sealing engagement; at least one access opening located about a sidewall of the hood and dimensioned to allow passage of the neonate therethrough; at least two arm ports located about the sidewall and dimensioned to allow passage of a hand therethrough; and at least one port configured to allow passage of a medical conduit therethrough.

A positive exhalation pressure device increases the pressure gradient in the airways, thereby increasing oxygen saturation levels and decreasing the severity of hypoxia. Various embodiments of the device may be inserted into the nasal and/or oral cavities, or configured as mask devices covering the nasal and/or oral cavities. In some embodiments, the resistance of the device may be varied.

An isolation hood for respiratory treatment is disclosed. The isolation hood may include a head enclosure defining an interior volume configured to receive the head of a patient, and a neck seal configured to couple the head enclosure to a neck of the patient. The isolation hood may include an inlet port configured to be coupled to a distal end of a treatment source tube and to a first end of a treatment delivery tube, and an outlet port configured to be coupled to an inline particle filter configured to permit air to flow through the head enclosure. The neck seal and the inline particle filter are each configured to prevent viral/bacterial aerosolization outside the hood. The inlet and outlet ports may be attached to respiratory tubing and non-invasive ventilatory equipment to permit aerosol-generating procedures within the hood while preventing viral/bacterial aerosolization outside the hood.

An air circuit for use in an air therapy device that is lightweight and comfortable for a user that is configured to also limit air leakage. The air circuit may include a tubular structure formed from various textile structures including circular weaving, circular knitting, braiding and other structures.

A headgear for use with a patient interface for providing a flow of pressurized breathing gas to the airway of a patient includes a pair of wrapping panels positioned at a rear thereof. The wrapping panels prevent the tension in the neck of a patient that commonly results when non-wrapping headgear is tightened.

A respiratory protection hood having a sealed flexible shell including a pressurized oxygen vessel provided with a calibrated output opening leading into the inside space of the flexible shell and a device for trapping at least one portion of the carbon dioxide exhaled by the user that includes a cartridge for adsorbing carbon dioxide having a perforated tube arranged around a volume of carbon dioxide absorbing material. At least one portion of the perforated tube being arranged around the volume of absorbent material in direct communication with the inside space of the hood.

A patient airway dome including an adjustable frame having a hinge such that the hinge allows the frame to adjust between an erected position to create an airway dome and a collapsed position that allows the frame to lay flat, a dome covering located over the retractable frame, a suction port which is connected to a conventional device in order to provide negative pressure to patient airway dome, and an arm access assembly operatively connected to the dome covering, wherein the arm access assembly includes an opening in the dome covering and a closure assembly located adjacent to the opening.

A stand-alone chamber or multi-chamber inhalation system has at least two alternative vaporized test liquid supply systems for passive or self-administered delivery of vaporized test fluid and air to one or more test chambers, which can be passive or restraint chambers, based on operator selection of delivery on and off times in a passive mode or actuation of an actuator in the chamber by a test animal in a self-administered mode. In one case, a multiple inhalation chamber system has two or more separate test fluid delivery systems and provides options for selective passive uniform drug delivery to multiple chambers or selective delivery of two or more different drugs to different groups of chambers from different delivery systems so that two different drugs or different concentrations of delivered drugs can be tested simultaneously.

An apparatus for providing a pressurized atmosphere to a patient including one or more flat sheets of plastic arranged in an envelope and sealed around the periphery to form an airtight container. The helmet has an airtight collar that is configured to accommodate a patient's neck and form an airtight seal. An intake port is integrated into the helmet and receives pressurized air. An exhaust port is integrated into the helmet near the patient's mouth when the helmet is in use. Additional ports can be added to the helmet to provide more functionality such as feeding or supplemental oxygen.

A pathogen protection device includes an enclosure made of air-tight material configured to seal a user's head from the outside and allow the user to see through; and a filter is disposed on a wall of the enclosure to allow filtered air to enter and exit the enclosure.