Embodiments provide an aeromedical bio-containment module for use in a cargo plane. The aeromedical bio-containment module includes a fully integrated pallet system allowing for the module to roll onto the cargo plane. An integrated set of lugs allows the module to be locked into the cargo plane floor without the use of chains or other pallets. The aeromedical bio-containment module features a ward area for safe treatment of patients, an anteroom, and an office area for personnel. The aeromedical bio-containment module operates under a negative pressure system, and includes a full air filtration system to remove pathogens, particulates, and other airborne contaminants.

The present disclosure relates to a field-type negative pressure isolation room system including main facilities necessary for constructing a negative pressure isolation room defined by the legal regulations, wherein the main facilities are manufactured in a plant in a modular way, so these modular facilities are usually stored in a warehouse, etc., and are installed in an outdoor site such as a parking lot, playground, vacant lot, and the like in case of emergency to utilize as a negative pressure isolation room, and these modular facilities are disinfected and dismantled during demolition and stored in the warehouse again, whereby these modular facilities can be used repeatedly regardless of the number of times of use, and can be quickly constructed and dismantled.

The present disclosure relates to a field-type negative pressure isolation room system including main facilities necessary for constructing a negative pressure isolation room defined by the legal regulations, wherein the main facilities are manufactured in a plant in a modular way, so these modular facilities are usually stored in a warehouse, etc., and are installed in an outdoor site such as a parking lot, playground, vacant lot, and the like in case of emergency to utilize as a negative pressure isolation room, and these modular facilities are disinfected and dismantled during demolition and stored in the warehouse again, whereby these modular facilities can be used repeatedly regardless of the number of times of use, and can be quickly constructed and dismantled.

The disclosed infection control systems and devices can be easily and quickly deployed by clinicians and staff in emergent and routine medical environments to provide adequate protection from bio-aerosolized and droplet material while allowing appropriate access to and visibility of the patient during such procedures. The infection control devices may include a base member and a frame disposed on the base member. The frame may be configured to move between a collapsed state and an expanded state with respect to the base member. The frame may include a first support member and a second support member configured to extend vertically from the base member when in the expanded state. The devices may include an enclosure member that is disposed on the frame and the base member and configured to define an enclosure above the base member. The devices may also include access member(s) configured to provide access to the enclosure.

A differential air pressure system has a pressure bag with windows and preferred folding configuration such that when the bag is folded no window is folded. The pressure bag is supported by a lift support that is proximal to a user control panel and adjacent to or nearly adjacent to the user who is coupled to the pressure bag. A treadmill base for use with differential air pressure equipment is provided. There are various improvements provided to adapt the operations of the DAP system via the use of separate pressure volume and non-pressure volume portions of the treadmill base. Various improvements to serviceability and repairs are provided by placement of components outside of the pressure volume portion or by providing one or more pressure volume access points.

A differential air pressure system has a pressure bag with windows and preferred folding configuration such that when the bag is folded no window is folded. The pressure bag is supported by a lift support that is proximal to a user control panel and adjacent to or nearly adjacent to the user who is coupled to the pressure bag. A treadmill base for use with differential air pressure equipment is provided. There are various improvements provided to adapt the operations of the DAP system via the use of separate pressure volume and non-pressure volume portions of the treadmill base. Various improvements to serviceability and repairs are provided by placement of components outside of the pressure volume portion or by providing one or more pressure volume access points.

The subject matter of the invention is a therapeutic device in the form of a cylindrical chamber which comprises a hyperbaric chamber, LED matrices (5) and inductive coil rings (10, 11, 12, 13), constructed in one inseparable set in the form of a chamber of 200-280 cm in length and diameter of the round cylinder (70-130 cm).

The present invention relates to a resuscitation chamber apparatus for administering hyperbaric oxygen to a patient. More particularly, the present invention relates to a hyperbaric oxygen compatible critical care chamber apparatus preferably for use in emergency departments and/or prehospital ambulance management of patients. In a preferred embodiment of the present invention, the apparatus is a resuscitation monoplace hyperbaric chamber preferably used in critical care management of acutely ill or injured patients in prehospital emergency medical services (EMS) settings or in hospital emergency departments. The apparatus preferably allows a critical care shock or arrested patient to be pressurized preferably without compromise for application of best medical equipment, medications and human resuscitating intervention.

The present disclosure relates to methods for lengthening telomeres. administering a hyperbaric oxygen therapy protocol; prescribing an exercise regimen that is performed inside of a hyperbaric chamber during the administration of the hyperbaric oxygen protocol; and prescribing a specialized nutrition plan comprising a daily intake of high fiber.

A personal respiratory isolation system (PRIS) provides a personal, negative pressure environment for a patient or user that reduces contamination and spread of pathogens exhaled by the patient into the environment. The PRIS includes an enclosure to receive the patient's head (such as a hood and a drape) and a negative pressure source which draws ambient air into the interior of the enclosure and draws air within the enclosure's interior (including the exhalations of the patient, including any contaminants and/or pathogens) out of the enclosure via a fluid port into a container for biohazard processing or disposal. The PRIS may allow positive air pressure therapeutic treatments to be delivered to the patient within the negative pressure environment, and the PRIS may maintain a constant pressure within the interior of the enclosure. The PRIS may include a transparent, hinged face shield for ease of patient observation and/or access.