Systems and methods for controlling a pump system for use in negative pressure wound therapy are described herein. In some embodiments, a method for controlling a pump system includes applying a drive signal to a pump assembly of the pump system, the drive signal alternating between a positive amplitude and a negative amplitude and the drive signal having an offset, and sampling a pressure within a fluid flow path configured to connect the pump system to a wound dressing configured to be placed over a wound during one or more time intervals. Each of the one or more time intervals can occur when the drive signal is approximately at an amplitude equal to one or more sampling amplitudes.

Automation for a system and/or method detects and/or controls treatment of inspiratory flow limitation. The system may include a flow rate sensor configured to generate a signal representing a respiratory flow rate of a patient. It may include a recording device configured to record the generated respiratory flow rate signal during a diagnosis session. It may include a computing device (7040) configured to detect a degree of inspiratory flow limitation of the patient on the recorded respiratory flow rate signal. The method may include extracting an inspiratory portion of each breath during a detection and/or monitoring session from a respiratory flow rate signal of the patient, calculating a feature vector from each inspiratory flow portion, labelling each feature vector as flow limited or not flow limited, and/or computing a metric based on the labels, the metric indicating the degree of inspiratory flow limitation of the patient during the session.

Methods and apparatus may implement controlled generation of oxygen enriched air in an oxygen concentrator while implementing control that reduces pneumatic imbalance between the concentrator's canisters, such as dynamic pressure imbalance or other pneumatic characteristic. One or more controllers may regulate operation of a compressor that feeds a pressurised air stream to the concentrator's canisters. This may regulate speed of the compressor to a speed set point for generating the pressurised stream. The regulating may involve generating a compressor control signal having a characteristic parameter such as a power parameter. The controller(s) may operate valve(s) in a cyclic pattern so as to produce oxygen enriched air in an accumulator. A cycle of the cyclic pattern may include a plurality of phases, where each of the plurality of phases has a duration. The controller(s) may then generate a dynamic adjustment to the duration(s) based on an evaluation of the characteristic parameter.

Treatment controllers and methods are provided that can be integrated with treatment systems, such as peritoneal dialysis systems, hemodialysis systems, and nocturnal treatment systems, to manage execution of treatment operations or a course of treatment based on timing information and/or patient sleep state.

An ultrasonic vaporization assembly includes: a piezoelectric drive element provided with a first through hole; a vaporizer plate stacked with the piezoelectric drive element, the vaporizer plate having a microporous zone at a position corresponding to the first through hole; and a loading board arranged on a side surface of the vaporizer plate which faces away from the piezoelectric drive element, the loading board being provided with a second through hole at a position corresponding to the microporous zone. A ratio of a pore size of the second through hole to a diameter of the microporous zone is greater than or equal to 0.75 and less than or equal to 1.5.

An interface pillow for insertion into a nostril of a user for delivering positive air pressure (e.g. during sleep) has a pliable member having a body. The body has an insertion end and a distal sealing end that includes a seal for interfacing with a cannula. An insertion bulge extends from the body limiting an insertion distance into the user's nostrils. An insertion area of the body extends between the insertion end and the insertion bulge, the sides of which angle inwardly towards the insertion end at an angle. The outer shape of the insertion area is flattened on one side for interfacing with a septum of a nose, and an upper interface area of the outer shape of the insertion area is narrower than a lower interface area of the outer shape of the insertion area to conform to a shape of a nostril of the nose.

A respiratory apparatus comprising a base and removable chamber, wherein the chamber is configured to hold a supply of water and include a blower arrangement adapted to provide a supply of pressurized air or gas to the supply of water. In certain embodiments the respiratory apparatus includes a split motor, wherein the stationary components are located within a base and the rotating portions are located within a chamber.

A respiratory assistance component is disclosed that changes shape when an electrical charge is provided. The amount of electrical charge that is applied may be based on values, characteristics, or user controlled parameters of the respiratory assistance system. The component may be all or part of a patient interface, a tube, a flow generator, and/or a sleep mat.

A nasal cannula device includes a cannula body. The cannula body includes an accommodating chamber inside and includes two nasal joint tube extended outwardly and communicating with the accommodating chamber. A junction ring is formed between the cannula body and each nasal joint tube. At least one of the cannula body and each nasal joint tube includes a recessed annular section recessed at one side of each junction ring. The recessed annular section has a thickness smaller than a thickness of the cannula body, a thickness of each nasal joint tube, and a thickness of each junction ring. Accordingly, the nasal cannula device can deliver a therapeutic gas smoothly.

Methods and apparatus for treating a respiratory disorder, in one aspect, include an apparatus that delivers backup breaths at a sustained timed backup rate that is a function of the patient's spontaneous respiratory rate. Other aspects include apparatus that delivers backup breaths at a rate that gradually increases from a spontaneous backup rate to a sustained timed backup rate or, alternatively, apparatus that oscillates a treatment pressure in antiphase with the patient's spontaneous respiratory efforts when a measure indicative of ventilation is greater than a threshold. Other aspects include apparatus configured to treat Cheyne-Stokes respiration by computing the treatment pressure so as to bring a measure indicative of ventilation of the patient towards a target ventilation that is dependent on the measure indicative of ventilation or, alternatively, by periodically elevating the treatment pressure to a high level for a short time, the high level being high enough and the short time being long enough to induce a central apnea in a patient. Depending on functionality, the foregoing apparatus may comprise an adaptive servo-ventilator or CPAP therapy device.