Disclosed is a barrier tent comprising a canopy, at least a portion of the canopy being composed of flexible sheet material; a frame for supporting the canopy; the canopy and frame being configured such that an internal surface of the canopy defines at least a portion of a patient segregation cavity to enclose a patient's head and at least a portion of the patient's body within the patient segregation cavity; and a gas input extending through the canopy, the gas input being positioned at a location configured such that supply of a gas through the input limits movement of aerosolised particles generated by or adjacent the patient toward the internal surface of the canopy.

Disclosed is a barrier tent comprising a canopy, at least a portion of the canopy being composed of flexible sheet material; a frame for supporting the canopy; the canopy and frame being configured such that an internal surface of the canopy defines at least a portion of a patient segregation cavity to enclose a patient's head and at least a portion of the patient's body within the patient segregation cavity; and a gas input extending through the canopy, the gas input being positioned at a location configured such that supply of a gas through the input limits movement of aerosolised particles generated by or adjacent the patient toward the internal surface of the canopy.

Systems are provided for a patient isolation unit for use with a medical imaging system includes an enclosure comprised of a pathogen impermeable material compatible with one or more imaging systems. The enclosure includes a base, a first end wall coupled to a first end of the base, a second end wall coupled to a second end of the base, and a cover coupled to a first side of the base, second side of the base, the first end wall and the second end wall for substantially enclosing a patient therein. In another exemplary embodiment, a patient isolation unit for use with a medical imaging system includes a head enclosure comprised of a pathogen impermeable material and a body enclosure coupled to the head enclosure and comprised of a pathogen impermeable material.

Systems are provided for a patient isolation unit for use with a medical imaging system includes an enclosure comprised of a pathogen impermeable material compatible with one or more imaging systems. The enclosure includes a base, a first end wall coupled to a first end of the base, a second end wall coupled to a second end of the base, and a cover coupled to a first side of the base, second side of the base, the first end wall and the second end wall for substantially enclosing a patient therein. In another exemplary embodiment, a patient isolation unit for use with a medical imaging system includes a head enclosure comprised of a pathogen impermeable material and a body enclosure coupled to the head enclosure and comprised of a pathogen impermeable material.

The present invention provides a negative-pressure shield device with a simple device structure, which is relatively inexpensive to manufacture, and is extremely effective in preventing infection within an ambulance. The negative-pressure shield device comprises a shield main body that is installed in a patient compartment of an ambulance, includes a ceiling part and a peripheral wall part, and covers at least the head of a patient on a stretcher mounted in the patient compartment, and a connection part which communicates with the interior of the shield main body and connects to a ventilation opening provided in the patient compartment.

The present invention provides a negative-pressure shield device with a simple device structure, which is relatively inexpensive to manufacture, and is extremely effective in preventing infection within an ambulance. The negative-pressure shield device comprises a shield main body that is installed in a patient compartment of an ambulance, includes a ceiling part and a peripheral wall part, and covers at least the head of a patient on a stretcher mounted in the patient compartment, and a connection part which communicates with the interior of the shield main body and connects to a ventilation opening provided in the patient compartment.

An infant care station can include sensors to detect an environmental characteristic of the infant care station, an access point to access a microenvironment of the infant care station, and a processor to obtain a sealed measurement for the infant care station with the access point in a sealed position. The processor can also obtain the environmental characteristic from sensors monitoring the microenvironment. Additionally, the processor can determine a difference between the environmental characteristic and the sealed measurement and generate an alert indicating an access point sealing issue based on the difference exceeding a predetermined threshold.

An infant care station can include sensors to detect an environmental characteristic of the infant care station, an access point to access a microenvironment of the infant care station, and a processor to obtain a sealed measurement for the infant care station with the access point in a sealed position. The processor can also obtain the environmental characteristic from sensors monitoring the microenvironment. Additionally, the processor can determine a difference between the environmental characteristic and the sealed measurement and generate an alert indicating an access point sealing issue based on the difference exceeding a predetermined threshold.

A system and method for maintaining, monitoring and improving air quality and purity in a room or environment, such as a hospital room or operating room.

An interventional operation isolation transfer cabin includes a cabin body, and a lead wire access device and a wire in/out device which two are mounted on the cabin body, the cabin body is provided with a negative pressure generating device at one end and an air inlet at the other end, the negative pressure generating device is provided with an exhaust filter device at its air outlet, and an intake filter device is provided at the air inlet. Several operating openings are provided on side walls of the cabin body, each of the operating openings is in seal connection with an operating glove, and a glove opening of at least one operating glove faces an interior of the cabin body. Equipment wires required by an interventional operation are preset through the lead wire access device, and wires added midway under a sealing condition is guaranteed through the wire in/out device.