A ventilator system includes a gas flow chamber configured to receive ventilation gas circulating in a ventilation gas pathway of the ventilator and at least one UVC lamp. The UVC lamp is configured to radiate UVC spectrum light into the gas flow chamber to inactivate pathogens in the ventilation gas. A flow sensor is configured to measure a gas flow rate of the ventilation gas and a controller is configured to receive the gas flow rate, determine an intensity based on the gas flow rate, and control power to the UVC lamp based on the intensity.

A positive airway pressure device includes a blower and a base. A blower outlet passage is connected to the blower and has a central tubular portion and a flexible sealing portion surrounding an outer circumferential surface of the central tubular portion. The base receives a tub with a heat conducting base plate, an internal air passage configured to receive the pressurized flow of respiratory gas from the blower outlet passage, and a pair of tub flanges extending laterally from respective side walls of the tub. Each tub flange has a horizontal portion and a tapered portion. The base further includes a floor with a heater plate a pair of base flanges. Each base flange extends laterally inward from a respective one of the side walls and engages a respective tub flange as the tub is inserted into the base with the tapered portions of the tub flanges being received first.

An exercise with oxygen therapy (EWOT) apparatus for rejuvenating oxygen-depleted cell tissue and simulating high altitude oxygen conditions. The EWOT apparatus includes a first cylindrical bladder for providing oxygen-enriched air and a second bladder for providing lower-purity hypoxic air. The first bladder is retained within an open, lightweight rectangular-shaped frame having vertical frame members. An air supply source provides the oxygen-enriched and hypoxic air to the first and second bladders, respectively. A control switch, which can be manually and/or programmed to automatically operate, selectively delivers the oxygen-enriched and/or hypoxic air to a breathing mask worn by a user while exercising on exercise equipment. The first bladder includes a plurality of weights which provide a positive pressure to the air therein. The cylindrical first bladder is attached to the vertical frame members with slidable rings and expands and collapses in a vertical direction when being filled or during use, respectively.

An integrated respiratory pressure therapy device and humidifier for pressurising and humidifying breathable air to treat a respiratory disorder in a patient, includes a blower configured to pressurise the breathable air; a water reservoir configured to hold a volume of water to be used for humidification of the breathable air, the water reservoir comprising a water reservoir base, a water reservoir lid connected to the water reservoir base, and a compliant portion. The compliant portion is constructed from an elastomeric material and configured to seal between the water reservoir base and the water reservoir lid. A water reservoir dock forms a cavity configured to partially receive the water reservoir. The water reservoir lid includes a protrusion and the water reservoir dock includes a recess configured to releasably engage one another to secure the water reservoir to the water reservoir dock.

A method includes receiving a pressure signal from a pressure sensor and/or a flow signal from a flow sensor and receiving signals from one or more sensors that measure different physiological parameters from the pressure sensor and the flow sensor. The method includes detecting the onset of the spontaneous breath by the patient based on the pressure signal and/or the flow signal and synchronizing providing breathing support to the patient with the onset of the spontaneous breath detected utilizing the pressure signal and/or the flow signal. The method includes calibrating parameters and thresholds to be utilized in detecting the onset of the spontaneous breath based on the signals. The method includes after calibration, switching to: detecting the onset of the spontaneous breath by the patient based on the signals and synchronizing providing breathing support to the patient with the onset of the spontaneous breath detected utilizing the signals.

A CPAP device is configured to deliver a pressurized flow of respiratory gas to a patient's airways and includes a flow generator with a blower configured to pressurize the flow of respiratory gas. A flexible face seal is positioned at an outlet end of a blower discharge path. The flexible face seal includes an aperture and a lip curling inwardly from a perimeter of the flexible face seal. A tub configured to hold a body of water and humidify the pressurized flow of respiratory gas includes a heat conducting base plate and a side wall. The side wall has a substantially flat portion that surrounds an air inlet opening. A base supports both the flow generator and the tub and includes a floor with a heater plate. A laterally positioned guide prevents the tub from being removed from the base in a vertical direction and includes a pair of C-shaped channel portions with open sides that face each other.

A device and method for adjusting a tidal breath delivered to a patient. The device includes a moving frame which is configured to move over a stationary frame that is nested within the moving frame itself. Disposed between the moving frame and the stationary frame is a compressible bellows which delivers a tidal breath to the patient each time the moving frame is passed over the stationary frame. The specific volume of the tidal breath that is delivered may adjusted according to the estimated weight of the patient, thereby preventing over inflation of the patient's lungs while undergoing treatment. To adjust the tidal breath volume, the user quickly changes the relative position of a slide adjuster which dictates the range of possible movement between the moving frame and the stationary frame, thereby limiting the volume of air/oxygen which may be drawn into the bellows.

A water reservoir for an apparatus for humidifying a flow of air for delivery to an entrance of the airways of a patient for respiratory therapy includes a reservoir base configured to hold a volume of water, a reservoir lid comprising an inlet and an outlet, a hinge joint to pivotally couple the reservoir lid to the reservoir base for pivotal movement between an open position and a closed position, wherein the reservoir lid and the reservoir base cooperate to form a sealed internal volume at the closed position, and a rotation stop, wherein the rotation stop is arranged between the reservoir lid and the reservoir base at the open position, and wherein the rotation stop is configured and arranged to disconnect the reservoir lid from the reservoir base at the hinge joint when the reservoir lid is over-pivoted beyond the open position.

Disclosed are systems and processes related to cardiopulmonary resuscitation (CPR). One embodiment of the system comprises an inspiration chamber and an expiration chamber, which work cooperatively to provide gas (e.g., Oxygen (O.sub.2)) to a subject (e.g., human patient) during inspiration and extract and expel expired gas (e.g., Carbon Dioxide (CO.sub.2)) from the subject during expiration as a medical professional applies CPR to the subject. In other words, this disclosure provides systems and processes that allow for substantially synchronous chest compressions with positive pressure active inspirations and, also, substantially synchronous chest decompressions with negative pressure active expirations.

A device and method for adjusting a tidal breath delivered to a patient. The device includes a moving frame which is configured to move over a stationary frame that is nested within the moving frame itself. Disposed between the moving frame and the stationary frame is a compressible bellows which delivers a tidal breath to the patient each time the moving frame is passed over the stationary frame. The specific volume of the tidal breath that is delivered may adjusted according to the estimated weight of the patient, thereby preventing over inflation of the patient's lungs while undergoing treatment. To adjust the tidal breath volume, the user quickly changes the relative position of a slide selector which dictates the range of possible movement for the bellows to be compressed, thereby limiting the volume of air/oxygen which may be delivered by the bellows.