Provided is a respiratory rate measurement device (4), the respiratory rate measurement device (4) including a detection unit (6) that detects an in-tube pressure and/or an in-tube gas flow rate in a tube (2) supplying concentrated oxygen gas to a patient from a pressure swing adsorption oxygen concentration device (1) connected to the patient and concentrating oxygen in the air by periodically repeating pressurization and depressurization, and outputs pressure data and/or gas flow rate data, an arithmetic operation unit (722) that extracts patient respiratory information data, based on the pressure data and/or the gas flow rate data, and an estimation unit (723) that estimates a respiratory rate per predetermined time, based on the patient respiratory information data, wherein the estimation unit (723) estimates the respiratory rate using, as a respiratory interval, a time Δt in which the autocorrelation coefficient takes a peak.

An active breathing assistance apparatus is disclosed. A simple apparatus includes first, second and third sets of balloons in a base compartment; a compression component on or over the balloons, configured to expel air from the balloons; a tubing network connected to the balloons; a wearable breathing compartment at an outlet of the tubing network; first and second check valves in the tubing network, between the breathing compartment and (i) the third set of balloons and (ii) the first and/or second balloons, respectively; third and fourth check valves between atmospheric air and the first and second balloons, respectively; a cover securing the compression component to the base compartment; and a motion restricting component controlling movement of the compression component. The first and second sets of balloons are between the compression component and the base compartment, and the third set of balloons is between the compression component and the cover.

The systems and methods include providing, displaying, and/or utilizing leak estimation during ventilation of a patient with a ventilator. The systems and methods include providing, displaying, and/or utilizing internal leak estimation, total leak estimation, and/or external leak estimation during ventilation of a patient with a ventilator.

A modular compressor assembly comprises a common motor assembly, an impeller, a blower housing and an engagement mechanism. The common motor assembly includes a stator housing containing a stator assembly and having a rotor magnet rotatably disposed therewithin. The impeller is mounted to and rotatable with the rotor magnet. The blower housing is selectable from among a plurality of blower housings each having a different cross-sectional geometry. The engagement mechanism is formed on the stator housing and/or the blower housing and allows interchangeable mounting of different blower housing configurations to the common motor assembly in order to achieve varying flow characteristics of the compressor assembly.

A method for measuring the anesthetic agent consumption in a ventilation system has a breathing circuit which contains a gas mixer (1) and an anesthetic agent metering device (2). The anesthetic agent quantity, which is consumed over a pregiven time interval in the ventilation system, is determined from the sum of the determined anesthetic gas volume flows in the ventilation system which are integrated over the pregiven time interval.

This disclosure describes embodiments of alarm systems and methods for use in devices such as medical ventilators. Embodiments described provide for an apparatus of an interactive multilevel alarm system. Embodiments of the alarms also provide, at a glance, current alarm and device status information and historical alarm information to the operator. Embodiments also direct interaction with the alarming functions of the device by the operator. In some embodiments, additional visual indicators may be provided to identify non-normal or noteworthy operating conditions, such as the use of a therapeutic gas by a mechanical ventilator, so that the operator can assess the impact of that non-normal condition on any current and historical alarm information simultaneously provided.

An oxygen concentrator is provided with a controller for recovering an oxygen concentration to a level suitable for treatment in a short period of time by selecting an optimum purge time corresponding to the deterioration state of an adsorbent. The judgment of moisture-absorption deterioration is performed when the detected value of the oxygen concentration sensor is equal to or less than a control value of the oxygen concentration in the oxygen-enriched gas and the detected value of the pressure sensor is equal to or more than an adsorption pressure at which the oxygen concentration increases significantly before and after the control to reduce the purge time, and control of reducing a time for the purge step shorter than a preset time is performed.

Systems and methods for humidifying ventilator delivered breathing gases are disclosed. These systems and methods utilize a hollow cone atomizer (e.g., a pressure swirl atomizer) and/or a heating element associated with a heating circuit and/or a heating tube. In some aspect, the systems and methods utilize received flow, temperature, and/or humidity information to determine an amount of water to add to breathing gases to reach a desired humidity of the breathing gases delivered to the patient. In further aspects, the humidification system can serve as a nebulization system for delivering nebulized medicine.

An example aerosol delivery device includes a mouthpiece having an airflow outlet, and an airflow passage extending between an airflow inlet and the airflow outlet. The example aerosol delivery device further includes a housing configured to receive a cartridge that includes an aerosolizable substance and a vapor element configured to heat the aerosolizable substance, and an internal power source configured to provide electrical power. The example aerosol delivery device further includes a controller coupled to the internal power source to receive a portion of the electrical power and configured to, when the cartridge is installed at the housing, cause the vapor element of the cartridge to heat the aerosolizable substance to release an aerosol into the airflow passage during an inhalation through the airflow outlet, and a connector configured to receive power from an external source to recharge the internal power source.

A method of providing a breath to a human patient. The patient has a patient connection connected, by a patient circuit, to a ventilator having a first ventilator connection and a different second ventilator connection. Each of the first and second ventilator connections are in fluid communication with the patient circuit. The method includes identifying, with the ventilator, initiation of an inspiratory phase of the breath, delivering a bolus of oxygen to the first ventilator connection before or during the inspiratory phase, and delivering breathing gases comprising air to the second ventilator connection during the inspiratory phase. The ventilator isolates the bolus of oxygen delivered to the first ventilator connection from the breathing gases delivered to the second ventilator connection.