A neonatal infant incubator apparatus (10) and a control system module (17), and methods and systems for using the control system module to control the microenvironment of the contained space (16) of the infant incubator apparatus (10). The neonatal infant incubator apparatus (10) including a collapsible frame (12) and a disposable housing (14) to create a closed contained space (16) with a controlled microenvironment. The control system module (17) is comprises a battery (32) and is configured to operate with low voltage; the control system module (17) configured to control the microenvironment, including regulating the temperature and gas composition, of the contained space (16), and includes an air circulation system (72) in air and/or fluid communication with the contained space (16). The systems, apparatus and methods are suitable for containing a full-term or premature infant in need of care in areas where power sources are limited, including e.g., rural or remote regions, third world countries, in a regular clinical setting and/or for transportation of the infant.

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.

A method and a device connects a partially flexible protective cover (2) sealed against the environment and forming a barrier between a contaminated area (12) and an uncontaminated area, to a partially flexible safety cover (20) by transferring the protective cover (2) out of the contaminated area (12) inverting the protective cover (2) over an opening such that its inside is turned out and then severing it from the safety cover (20) and closing the opening; or transferring the protective cover (2) from the contaminated area (12) by sheathing the protective cover (2) with the safety cover (20) as it is pulled through a passage and subsequently severing of both covers (2, 20) from the safety cover (20) and closing the sheathing; or pulling the protective cover (2) back into the contaminated area (12) and then sealing the ends shut to sever the safety cover (20) by forming a further sealed joint between adjacent film parts.

A surgical drape includes a seal connectable with a selected surface of a body disposed with a surgical table. A draping is connected with the seal and a track of the surgical table. The draping is movable relative to the seal to define a sterile region about the body. Surgical instruments, systems and methods are disclosed.

A system configured to create a self-contained negative pressure environment (SCONE) to remove airborne particulates emitted from a patient. The system prevents exposure to pathogenic biological airborne particulates during triage, transportation, and treatment, including aerosol generating procedures (AGPs) and end of life care. This system is directed to a collapsible device having a flexible cover covering two support members, with openings in the flexible cover such that medical professionals can reach in and operate within. The present invention is further adaptable to patients and operating environments of various sizes.

An aerosol containment enclosure is used to isolate an air mass immediately surrounding a patient known or suspected to have a disease which may be transmitted through the air. The enclosure cooperates with a patient support apparatus (PSA). In embodiments, a flexible rod supports a substantially aerosol impermeable covering and is connected to the PSA. The enclosure may be semi-rigid and collapsible to a predetermined collapsed shape. The enclosure may be rapidly erected around a patient in an ambulance or other treatment setting. Embodiments of couplers provide compatibility with a wide diversity of sized and shaped PSAs. One coupler is connectable to the PSA with a coupler end exposed along a frame and upwardly extensible toward a PSA surface. A connector extends from the flexible rod and engages with the coupler end. The coupler may be longitudinally or laterally adjustable along the PSA.

Apparatuses and methods for defining an isolation area around an individual. Such an apparatus includes a frame having two opposing and spaced-apart side walls, an interior region within an interior of the apparatus and defined by and between the side walls, and one or more connecting members spanning the interior region and coupling the opposing side walls. Isolation barriers are coupled to the frame and extend outwardly from the interior region. The isolation barriers are configured to define an isolation zone surrounding the interior region that corresponds with the isolation area around an individual located within the interior region. An opening is providing for access by the individual to and from the interior region within the frame.

Set forth are the structure, function, placement, and applications of vascular valves and servovalves. In the vascular tree, the diversion, shunting, and bypass of flow these provide allow solid organ transplantation which eliminates anoxia and graft organ degradation following harvesting and storage, likely including late term cardiac allograft vasculopathy. Along the lower urinary tract, the diversion of urine from damaged ureters to the native or an artificial bladder or collection bag alleviates problems of intractable urinary incontinence, nocturia, overactive bladder, and frequent urination. Where the lower tract is missing, the synthetics in a valve-based prosthesis preclude infection and degenerative metaplastic transition which can result in malignancy when gut is used to construct a neobladder and/or high maintenance stoma. Accessory channels in side-entry valves and servovalves allow the direct pipe-targeting of medication to sites of disease, anastomoses, or any other trouble spots.

The present disclosure relates to a booth-type mobile infectious disease clinic, and more particularly, to a mobile infectious disease clinic, which is a booth-type mobile infectious disease clinic which makes it possible to assemble and disassemble a large number of mobile infectious disease clinics, that allows a test subject to be tested by a healthcare provider using an infectious disease test kit while exposure of the body parts is minimized and the healthcare provider and the test subject are isolated in the booth-type mobile infectious disease clinic, that performs sterilization of an infectious disease using an ultraviolet C (UV-C) lamp to reduce the time taken for disinfecting the clinic, and that allows the light radiation intensity of the UV-C lamp to be adaptively adjusted according to the body temperature of the test subject.

The present disclosure relates to a tent-type mobile infectious disease clinic, and more particularly, to a mobile infectious disease clinic, which is a tent-type mobile infectious disease clinic that makes it possible to promptly install a large number of mobile infectious disease clinics due to having mobility and being easy to install and remove, that allows a test subject to be tested by a healthcare provider using an infectious disease test kit while the test subject is isolated in the tent-type mobile infectious disease clinic, the healthcare provider is outside the tent-type mobile infectious disease clinic, and exposure of the body parts is minimized, that performs sterilization of an infectious disease using an ultraviolet C (UV-C) lamp to reduce the time taken for disinfecting the clinic, and that allows the light radiation intensity of the UV-C lamp to be adaptively adjusted according to the body temperature of the test subject.