A portable suction pump for aspirating secretions from a patient's artificial airway includes a peristaltic pump head, a suction tube extending from a patient through the peristaltic pump head, the suction tube having a tee-fitting conduit, and a collection container having a plurality of ports for collecting patient media. A clinician has an ability to increase or decrease vacuum levels without increasing or decreasing flowrate and/or an ability to increase or decrease the flow rate without increasing or decreasing the vacuum levels. The tee-fitting conduit extends to a vacuum sensor port connecting to a vacuum sensor in communication with a processor, the processor controlling a proportional valve employed to regulate the vacuum levels.

This disclosure describes systems and methods for providing a high pressure controlled proportional assist ventilation breath type during ventilation of a patient. The disclosure describes a novel breath type that reduces ventilator support (or a percent support setting) based on the occurrence of a predetermined number of high pressure alarms.

A nebulizer for producing an inhalable mist of droplets, comprising at least an aerosol generator, a housing having a liquid reservoir and control electronics, the aerosol generator consisting at least of a membrane, a piezo element and a substrate plate, and the control electronics comprising at least an RF generator, a controller, memory and switching elements, and an inductor. The aerosol generator forms a resonant circuit together with the inductor and the control electronics are configured to at least partly excite the aerosol generator to vibrate. The aerosol generator is configured such that aerosol droplets are producible by vibrations and the RF generator is configured to vary the amount of aerosol produced.

A high flow therapy system for delivering heated and humidified respiratory gas to an airway of a patient includes a respiratory gas flow pathway for delivering the respiratory gas to the airway of the patient by way of a non-sealing respiratory interface; wherein flow rate of the respiratory gas is controlled by a microprocessor, a mixing area for mixing a first gas and a second gas in the respiratory gas flow pathway, a humidification area downstream of the mixing area and configured for humidifying respiratory gas in the respiratory gas flow pathway, and a heated delivery conduit for minimizing condensation of humidified respiratory gas.

A valve assembly for adjustably regulating communication with medical tubing applied to a patient including a housing having a hollow interior and a primary connector interconnecting the medical tubing to the hollow interior. First and second ports are attached to and movable with a closure segment, concurrently and alternately, between an open orientation and a closed orientation. The concurrent and alternate disposition of the first and second ports comprising each disposed in the open orientation concurrent to the other disposed in the closed orientation. The open orientation of each of said first and second ports comprising disposition thereof in communicating relation with the medical tubing, via said hollow interior and said primary connector.

A humidification system can include a heater base, a chamber, and a breathing circuit. The heater base includes a heater plate positioned in a recessed region, and a heat conductive portion of the chamber is configured to contact the heater plate. The heater base includes a guard configured to control movement of the chamber into and out of the recessed region. The guard includes an anti-racking mechanism. The chamber includes an inlet port, an outlet port. A downward extension extends into the chamber from the inlet port, and a baffle is disposed at a lower end of the downward extension. A component of the breathing circuit can include a conduit hanging end cap for shipping and storage. The end cap can include a hanging component to allow the breathing circuit component to be hung from a medical stand. The system can detect when breathing circuits are connected in reverse.

An automatic control system for a manual mechanical ventilation device comprising a servomotor, an actuator and a stepper cylinder adapted to compress the mechanical ventilation device in response to signals sent by a controller. The controller is further connected to at least one flow sensor and one pressure sensor and has a human-machine interface for the insertion of pressure and oxygen flow output values to be received by a patient.

An oxygen mask may include a convex shell having an upper portion and a lower portion and defining a chamber, a rim at least partially around the chamber, a nasal access port in the upper portion, and an oral access port in the lower portion. The nasal access port that is penetratable and/or puncturable to provide access to the chamber, and the oral access port may include a bite block defining a lumen and a valve in the lumen. The oxygen mask may include an inlet into the chamber, an outlet from the chamber, and a sampling port in communication with the chamber. The oxygen mask may include at least one fold or crease configured to allow the bite block to tilt relative to the horizontal axis and/or to translate along the vertical axis.

A patient interface for treating sleep disorder breathing includes a textile tube that also provides support for the seal forming structure. The textile tube includes an inner and outer layer that are joined along seams to form an air chamber or passageway. The textile tube can be pre-shaped so that the textile tube resiliently returns to a pre-determined shape prior to the introduction of pressurized air.

A connection unit establishes a fluid connection between a patient and a ventilator. The connection unit includes a patient-side connection piece, a device-side connection piece, a port piece and a central piece, which provides a tube with a curved tube segment and is connected with a fluid-tight connection to the two connection pieces. The port piece includes a straight tube segment and a bent surface with a bent surface and with a passage opening. The port piece is inserted into a receiving opening of the central piece. The bent surface of the port piece forms a part of a wall of the curved tube segment. The straight tube segment of the port piece and the central piece provide a straight tube, which is interrupted by the passage opening. An additional device is insertable through the straight tube segment and through the passage opening into the provided tube.