Abstract: In one embodiment, a monitoring system includes a monitoring device configured to removably attach to a tracheotomy tube, the monitoring device including a skin sensor configured to detect contact with skin of a patient's neck.

Abstract: A breathing air supply system (200) is configured to be carried by a person (300) and includes a breathing air supply device (130), a fastening device (1) for the breathing air supply device (130) and a vital parameter sensor (30.1). The vital parameter sensor (30.1) is mounted in or at a back section (22) belonging to a fastening section (20) of the fastening device (1). The vital parameter sensor (30.1) is configured to contactlessly measure a vital parameter of a user (300) of the breathing air supply system (200).

Abstract: The present invention provides a method and apparatus for reducing condensation in a respiratory circuit during a delivery of humidifying agent into the respiratory circuit. A first amount of humidification agent to a first volume of gas is delivered to a patient respiratory circuit during a patient inhalation cycle or immediately after a patient exhalation cycle, and the humidification agent or the first volume of gas is heated. Condensation is removed from the respiratory circuit at least in part by providing, during a patient exhalation cycle or immediately after a patient inhalation cycle, a second amount of the humidification agent to a second volume of gas being delivered from the gas source to the patient respiratory circuit, the second amount of the humidification agent being significantly less than the first amount of the humidification agent.

Abstract: The present disclosure provides a ventilator that includes a first gas path, comprising a first pressurized gas source adaptor and a first flow adjustment device connected in sequence; a second gas path, comprising a second pressurized gas source adaptor and a second flow adjustment device connected in sequence; a third gas path, comprising a third pressurized gas source adaptor; a first inhalation branch for delivering inhalation gas to a patient; a second inhalation branch for delivering inhalation gas to the patient, including a gas compression device; a switching device, including a first mixing mode connecting the first gas path and the second gas path to the first inhalation branch, and a second mixing mode connecting the first gas path and the third gas path to the second inhalation branch; and an exhalation branch for managing exhaled air of the patient.

Abstract: 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.

Abstract: Described herein are various embodiments of an oxygen concentrator system and method of delivering oxygen enriched gas to a user. In some embodiments, oxygen concentrator system includes one or more components that improve the efficiency of oxygen enriched gas delivery during operation of the oxygen concentrator system.

Abstract: The apparatus, method, and system disclosed relates to a headgear assembly for a respiratory system for the delivery of respiratory therapy to a patient. The headgear comprises a yoke at least partially formed from an elastomeric material. The yoke is configured to be stretched under tension to attach the yoke to the headgear assembly.

Abstract: Various control methods can indirectly determine incorrect connections between components in a respiratory therapy system. For example, errors in the connections can occur between a patient interface, a humidifier and/or a gases source. The methods can indirectly detect if a reverse flow condition exists or other error conditions. A reverse flow condition can occur when gases flows in a direction different from an intended direction of flow. The detection of the reverse flow condition can be indicative of likely errors in connections between the humidifier, patient interface and/or gases source.

Abstract: A respiratory apparatus includes components to permit different operations of the apparatus with different power supplies. For example, a respiratory therapy apparatus for controlling a respiratory therapy may include a power input circuit to receive a first power or a second power. The first power may be provided by a connectable low-power power supply and the second power by a connectable high-power power supply. A controller of the respiratory apparatus coupled to the power input circuit may be configured to detect one of the power supplies, and based on the detection, selectively activate one of a first mode of operation and a second mode of operation. The first mode of operation may be a non-therapy mode with the first power such as for a data setup or data transfer with the respiratory therapy apparatus and the second mode of operation may be a therapy mode with the second power.

Abstract: The present invention is a respiratory monitoring device which uses 2+ sensors to map respiratory motion in patients to interpret into a respiratory effort and severity score. The core components of the invention are contact-based sensors that measure relative motion of the chest, abdomen, and/or other key anatomical features, a processing unit which takes in the data from all sensors, an algorithm that analyzes and compares the data from each sensor to understand relative motion and interpret it into clinically-relevant information, and a display screen that shares this information with clinicians. The sensors are connected to each other and the information processing unit which shares data with the screen for display of a respiratory severity score based on analysis of Thoraco-Abdominal Asynchrony (TAA) or similar indicators of respiratory effort as measured by the sensor network and analyzed by the algorithm.

Abstract: An apparatus for treating a respiratory disorder in a patient includes a power supply, a first power supply circuit coupled to the power supply, a pressure generator to generate a flow of air, a transducer to generate a flow signal representing a property of the flow of air, and motor power supply circuitry. The motor power supply circuitry includes: a motor controller to control operation of a motor in the pressure generator based on the flow signal; one or more storage elements to store energy generated by motor deceleration; an energy dissipation circuit to dissipate a portion the energy generated by the deceleration of the motor; and an energy transfer circuit to couple the one or more storage elements to the first power supply circuit and transfer the energy generated by motor deceleration and/or the energy stored by the one or more storage elements to the first power supply circuit.

Abstract: A photo-resist (21) is applied in a pattern or vertical columns having the dimensions of holes or pores of the aperture plate to be produced. This mask pattern provides the apertures which define the aerosol particle size, having up to 2500 holes per square mm. There is electro-deposition of metal (22) into the spaces around the columns (21). There is further application of a second photo-resist mask (25) of much larger (wider and taller) columns, encompassing the area of a number of first columns (21). The hole diameter in the second plating layer is chosen according to a desired flow rate.

Abstract: A vent adaptor for a for a respiratory pressure therapy (RPT) system, the vent adaptor comprising: a vent assembly comprising: a vent housing defining a central orifice for the flow of pressurized gas to pass through the vent assembly from the delivery conduit to the patient interface, the vent housing having an annular surface around the central orifice, and the annular surface having a plurality of holes to discharge pressurized gas to atmosphere; and a membrane positioned adjacent to the annular surface; a heat and moisture exchanger (HME); and a diffusing member.

Abstract: Disclosed is a respirator which comprises an electronic control device and a pneumatic main line in which the following are connected pneumatically: a respiratory gas source, a valve, a mixing chamber, a gas-dosing unit, and a supply line. The gas-dosing unit is configured to convey external air and/or oxygen and/or anesthetic gas into the mixing chamber, the respiratory gas source is configured to deliver respiratory gas to the supply line, the mixing chamber is configured to make available respiratory gas, the supply line is configured to supply the patient with respiratory gas, and the valve is configured to at least temporarily reduce a stream of respiratory gas to a patient.

Abstract: A computer-implemented method is described. The method includes receiving an indication and determining a subject's oxygen consumption based on the indication. The indication refers to an oxygen fraction in a sample of inhalation gas delivered by a ventilator for inhalation by a subject. The indication further refers to an oxygen fraction in a sample of exhalation gas exhaled by the subject. The indication further refers a measurement of a flow rate of the exhalation gas.

Abstract: The present disclosure relates to an oxygen mask comprising: a mask body defining a cavity configured to be positioned over the mouth and nose of a patient, an oxygen port formed on the upper half of the mask body, an annular aperture formed on the mask body, and at least one vent port formed on the mask body, wherein each vent port is formed on the bottom half of the mask body in a manner that patient's exhaled gases are directed towards the vent port.

Abstract: The present invention provides a new inhaler device for the storage and/or administration of inhalable liquids to a patient offering one or more advantages or improvements over known inhalers, particularly inhalers for the delivery of halogenated volatile liquids such as methoxyflurane for use as an analgesic.

Abstract: Start-up protocols for a device and method for administering NO is described.

Abstract: An elbow assembly for a patient interface includes a swivel component adapted to connect to a patient interface and an elbow component adapted to connect to an air circuit. The swivel component is coupled to the elbow component by a ball and socket joint and a hinge joint which allows the elbow component to pivot relative to the swivel component about a single axis.

Abstract: A positive airway pressure device is disclosed herein. The positive airway pressure device includes a blower, a buffer chamber, a gas manifold, a first sensor, a second sensor, and a controller. The buffer chamber is downstream of the blower. The buffer chamber configured to receive gas generated by the blower and output the gas to a patient. The gas manifold is fluidly coupling the blower to the buffer chamber. The first sensor is at least partially disposed in the gas manifold. The first sensor is configured to measure a first pressure in the gas manifold. The second sensor is at least partially disposed in the buffer chamber. The second sensor is configured to measure a second sensor in the buffer chamber.