Blood treatment methods that are combined in a unique manner can provide health benefits to patients by performing the methods and using systems that perform such methods. Methods of treatment include withdrawing the blood from a patient, performing multiple blood treatment methods on the blood, and then inserting the treated blood back into the patient. As a result of the treatments, the blood is cleansed and energized, enabling it to perform at higher levels than it would otherwise perform. The treatment methods can include, for example, performing an oxygen-based treatment, such as ozone generation, in combination with mixing methylene blue with the oxygenated blood. In some embodiments, a red light treatment can also be introduced in conjunction with the use of methylene blue. Systems that enable these treatment methods are also provided.

A positive airway pressure device includes a primary housing and a humidification system. The primary housing includes an outer edge, a first electronic connection portion, and a blower configured to deliver a vapor to a patient. The humidification system includes a water reservoir configured to hold a liquid, a heating plate in thermal communication with the water reservoir, a second electronic connection portion, and a lid configured to selectively shield the second electronic connection portion. The primary housing is configurable between at least two positions relative to the humidification system. The at least two positions include a first position in which the lid at least partially shields the second electronic connection portion and a second position in which the outer edge of the primary housing forces open the lid such that the first electronic connection portion mates with the second electronic connection portion.

A drug delivery system for injecting a medicament includes a housing defining a cavity, a container received within the cavity and configured to receive a medicament, the container comprising a stopper configured to move within the container and a closure, a drive assembly received within the cavity and configured to drive the stopper within the container, a needle actuator assembly received within the cavity and comprising a needle configured to be placed in fluid communication with the container, the needle moveable from a first position and a second position spaced from the first position, and a sterilizer received within the cavity and configured to sterilize at least one of the container, the drive assembly, and the needle actuator assembly upon activation of the drug delivery system.

In an example, a ventilator includes a first container and a second container in fluidic communication with each other via a liquid. The second container includes a second container space surrounded by the second container and a second liquid surface. A hydrostatic pressure in the second container space results from a pressure differential defined by a difference between the first liquid surface elevation in the first container and the second liquid surface elevation. The second container space increases in size with an increase in the breathing gas supplied from a gas supply line to the second container space. An inhalation line is configured to open to permit a flow of the breathing gas from an inhalation inlet in the second container space to an inhalation outlet outside of the liquid and outside of the second container and coupled to a patient, causing the second container space to decrease in size.

An ultraviolet disinfecting cartridge system utilizes an ultraviolet disinfecting cartridge particularly adapted for coupling with a face mask that covers the nose and mouth or to the inhale and exhale tubing of a patient ventilator. The ultraviolet disinfecting cartridge includes multiple UV light emitters that emit UVGI light into the flow channel of the cartridge to neutralize or destroy pathogens. A plurality of baffles may be configured in the flow channel to create a serpentine airflow to increase pathogen exposure time to UV light. A photocatalyst material such as titanium oxide may be configured within the flow channel that is activated by UV light to increase disinfection. An ionizer may be configured proximal to the inlet to produce charged particles that provide disinfection. Any ozone produced may be mitigated by a catalytic converter to a safe level. Inlet and outlet filters may be detachably attachable to the ultraviolet disinfecting cartridge.

A system and method for sleep environment management is provided. The sleep environment comprises a bed within a sleep space, sleep metric sensors, activity metric sensors, and a sleep environment controller. A server comprises a hardware processor, has access to a database, and comprises a non-transitory, computer-readable storage medium for storing program code, comprising program code to receive at least one sleep metric and at least one activity metric from the sleep environment; record the metrics in the database; analyze the metrics over a period of time to generate a user report and one or more product recommendations; and provide the user report and product recommendations to the sleep environment controller as feedback. Such sleep environment management system and method can improve a user's sleep experience, and allows medical and product presentations to be made to the user.

An antimicrobial light dressing device, system and method for a percutaneous treatment that bathes a treatment region around the percutaneous insertion with an antibacterial illumination source for preventing pathogens around the insertion from entering via the dermal puncture created by the insertion. The antimicrobial light dressing device combines a circumferential body centered around the insertion, and an arrangement of LEDs around the body that focus the light around the insertion and onto a therapeutic region of the insertion. An opening in the circumferential body has an articulated protrusion for offsetting a medicinal vessel such as an IV tube off the skin surface to avoid blocking light to an area under the vessel.

A far ultraviolet light application device for killing pathogens on tissue and proximate thereto includes a tube that is to be utilized in a medical procedure. A first fiberoptic cable is engaged to a wall of the tube so that a first end of the first fiberoptic cable is positioned proximate to a first terminus of the tube. The first fiberoptic cable has a second end operationally engaged an ultraviolet C light emitter so that ultraviolet C light is emitted proximate to the first terminus of the tube. The first fiberoptic cable directs the ultraviolet C light from the ultraviolet C light emitter so that the ultraviolet C light impinges upon tissue and pathogens proximate to the first terminus of the tube to inactivate the pathogens.

A far ultraviolet light application device for killing pathogens on tissue and proximate thereto includes a tube that is to be utilized in a medical procedure. A first fiberoptic cable is engaged to a wall of the tube so that a first end of the first fiberoptic cable is positioned proximate to a first terminus of the tube. The first fiberoptic cable has a second end operationally engaged an ultraviolet C light emitter so that ultraviolet C light is emitted proximate to the first terminus of the tube. The first fiberoptic cable directs the ultraviolet C light from the ultraviolet C light emitter so that the ultraviolet C light impinges upon tissue and pathogens proximate to the first terminus of the tube to inactivate the pathogens.

A catheter assembly having the major components: a cap, an introducer tip, four different variations of grip housing, a tube gripper and a catheter. The variations of the housing connected to the catheter assembly allows for safe and effective delivery of the anesthetics to various bodily orifices. The catheter is slowly advanced further while irrigating and dispensing the medication and/or lidocaine gel from the syringe. Once the desired depth is reached the practitioner can mark off the depth in centimeters on the catheter using a variation of the marker.