A protective air supply system for controlling air supply flows in a clean room comprises a first air supply diffuser and a second air supply diffuser, arranged within a ceiling of the clean room on opposite sides of the clean area and spaced from side walls of the clean room, wherein each supply air diffuser is provided with nozzles configured to diffuse a first air flow having a first air flow volume directed along a ceiling of the clean room and towards the clean area and a second air flow having a second air flow volume directed along the ceiling of the clean room and towards a perimeter of the clean room, and a controller coupled to the air supply diffusers and configured to adjust the first and second air flow volumes and their ratio.

A simplified examination room includes a first booth and a second booth provided adjacent to each other, interposing a partition wall therebetween, and the partition wall is formed with a through hole allowing an arm to pass through and is provided, at least at an intermediate portion of the partition wall in an up-down direction, with a transparent region allowing a person having entered the first booth and a person having entered the second booth to face each other. A simplified examination room assembly set for producing the simplified examination room includes a frame constituting a framework of the first booth and the second booth, and a panel constituting at least one side of a ceiling part, a floor part, a side face wall, or a back face wall, and a partition wall partitioning the first booth and the second booth.

The present invention relates to an adaptive hyperbaric oxygen chamber designed to function as a medical apparatus in order to treat a subject suffering from any FDA approved medical condition. The hyperbaric oxygen chamber is designed and constructed in such a way that only one subject can be allowed to sit in an upright seated position, unless the pediatric seat is occupied by a pediatric patient and the adult is seated in the standard seat to accompany the pediatric patient. The upright patient seat when treating a pediatric patient is in the extended position while the occupant enters and exits the mono medical hyperbaric oxygen chamber and the seat is returned to the fixed position inside the hyperbaric oxygen chamber while the overhead door is closed, the seat being operated by an extension device. The hyperbaric oxygen chamber is made, using additive manufacturing technology. The hyperbaric oxygen chamber provides two hundred to five hundred liters of one hundred percent oxygen per minute to the pressure vessel. A nitrogen scrubber is connected to a discharge air duct of this hyperbaric oxygen chamber that converts the oxygen being expelled through the air duct to one hundred percent nitrogen.

The present invention relates to an ambulance having an infectious disease blocking function and an interior pressure control method therefor, the ambulance having a driver seat, a vehicle body and an emergency care compartment which is mounted on the vehicle body and which has a space in which a patient can be placed, and comprising an air pressure regulation part for setting the inside of the emergency care compartment to have a positive pressure or a negative pressure, and a control part for selectively controlling a positive pressure or a negative pressure of the air pressure regulation part.

Various systems and devices are provided for determining a weaning readiness for weaning a patient from a thermoregulated microenvironment. In one example, a method includes receiving current patient parameters of the patient and applying a weaning model to the current patient parameters to calculate a weaning index representing a likelihood that the patient can be successfully weaned from the microenvironment. The method also includes outputting the weaning index for display on a display device or for storage in a medical record of the patient and upon outputting the weaning index, receiving one or more subsequent patient outcomes, the one or more subsequent patient outcomes comprising whether the patient developed any complications within the duration since being weaned from the microenvironment. The method also includes updating the weaning model based on the one or more received subsequent patient outcomes.

Various systems and devices are provided for determining a weaning readiness for weaning a patient from a thermoregulated microenvironment. In one example, a method includes receiving current patient parameters of the patient and applying a weaning model to the current patient parameters to calculate a weaning index representing a likelihood that the patient can be successfully weaned from the microenvironment. The method also includes outputting the weaning index for display on a display device or for storage in a medical record of the patient and upon outputting the weaning index, receiving one or more subsequent patient outcomes, the one or more subsequent patient outcomes comprising whether the patient developed any complications within the duration since being weaned from the microenvironment. The method also includes updating the weaning model based on the one or more received subsequent patient outcomes.

An isolette comprising an array of support structures is provided, covered by sheeting, and a drape. The arrays provide vertical or peripheral wire frame supports which are easily assembled and attached to the flexible sheeting. Access ports allow patient access. A component access panel is provided. The drape includes an optional sealing ring held in position by a strap or medical tape. The access ports can include iris diaphragms, covering flaps, integrated gloves, and removable gloves.

An oxygen distributor (1) positionable, in use, in a wound for supplying oxygen to the wound has an oxygen delivery area (17) for, in use, receiving a supply of oxygen. At least one tube (19A) extends from the oxygen delivery area, having a tube wall with an oxygen-permeable, liquid-impermeable section. Oxygen delivered to the oxygen delivery area can flow away from the oxygen delivery area along the, or each, tube.

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 negative pressure protection system has a cover enclosing an inner space, a ventilation duct fluidly communicating with an air outlet port of the cover, a filter having an inlet end communicating with the ventilation duct, and an air exhausting device connected to an outlet end of the filter. The air exhausting device draws air out from the inner space of the cover via the ventilation duct. The air is filtered and purified by the filter and then is exhausted away by the exhausting device.