A patient interface may include: a plenum chamber pressurisable to a therapeutic pressure; a seal-forming structure connected to the plenum chamber, the plenum chamber being constructed and arranged to seal with a region of the patients face; a positioning and stabilising structure configured to provide a force to hold the seal-forming structure in a therapeutically effective position on the patients head; a vent structure configured to allow a continuous flow of gases exhaled by the patient from an interior of the plenum chamber to ambient; and a material configured to adsorb water vapour from gases exhaled by the patient and desorb water vapour into the flow of air at the therapeutic pressure, the material being positioned within the plenum chamber.

A decision support tool is provided for identifying and assisting clinicians with patient ventilator asynchrony. The information used to make the identification may include data from a patient's ventilator including the volume, flow, and pressure associated with that ventilator. At least some of this information may be used to compute one or more features for a time series of the data received for the patient. These features may be used in connection with heuristic rules and machine learning algorithms to identify instances of patient ventilator asynchrony. Based on the identification, one or more intervening actions may be initiated to reduce the impact of patient ventilator asynchrony.

A shroud for a mask system includes a retaining portion structured to retain a frame, a pair of upper headgear connectors each including an elongated arm and a slot at the free end of the arm adapted to receive a headgear strap, and a pair of lower headgear connectors each adapted to attach to a headgear strap. The retaining portion, the upper headgear connectors, and the lower headgear connectors are integrally formed as a one piece structure.

An air delivery tube for a CPAP system includes a first end configured to connect to a flow generator of the CPAP system and a second end configured to connect to a patient interface of the CPAP system. The air delivery tube also includes a central lumen that is formed by an inner wall of the air delivery tube and is configured to convey pressurized breathable gas from the first end to the second end. In addition, a circumferential chamber surrounds the central lumen and is configured to retain a supply of water. A wick is located within the central lumen and is connected to the inner wall.

A gas delivery system (50) for delivering a flow of breathing gas to a patient (54) includes a blower assembly (100) structured to generate the flow of breathing gas. The blower assembly includes a gas flow path including an inlet manifold, an assembly (130) structured to adjust a pressure and/or flow rate of the flow of breathing gas, and an outlet manifold structured to be coupled to a patient circuit. The gas delivery system additionally includes a light system structured to generate sanitizing light and deliver the sanitizing light to one or more internal surfaces of at least one of the inlet manifold, the assembly and the outlet manifold for sanitizing the one or more internal surfaces.

A feedback device for an acute care provider includes: at least one motion sensor; a haptic output component for providing feedback having a varying haptic pattern to the acute care provider regarding performance of a resuscitation activity; and a controller. The controller can be configured to receive and process a signal representative of performance of the resuscitation activity from the at least one motion sensor, compare the acute care provider's performance of the resuscitation activity to a target performance of the resuscitation activity, and cause the haptic output component to provide haptic feedback to the acute care provider by changing the haptic pattern based, at least in part, on the signal from the at least one motion sensor and the comparison of the acute care provider's performance to the target performance of the resuscitation activity. The device can be adapted to be wrist-worn by the acute care provider.

A filter assembly for filtering a flow of incoming air entering a pressurized breathing gas system includes a filter housing and a filter media. The filter media includes a filtering section and a non-filtering section. The filter housing is structured to be inserted within a pressure generating device used in the pressurized breathing gas system. The filtering section is disposed within the filter housing and is structured to filter contaminant matter from the flow of incoming air. The non-filtering section is disposed outside of the housing and is structured to be separated from the filtering section so as to not make contact with the flow of incoming air. The filtering section and the non-filtering section are structured to be visually compared to one another such that a contaminant matter saturation level of the filter media can be determined.

An information processing method according to an embodiment of the present invention comprises: a step for receiving usage status information representing the usage status of an aerosol generation device for generating aerosol; a step for giving a reward to the user of the aerosol generation device on the basis of the received usage status information; and a step for notifying a terminal device of information relating to the reward, said terminal device being capable of communicatively connecting with the aerosol generation device.

A method of forming a stream having a therapeutic concentration of nitric oxide (NO) is disclosed, along with an apparatus and system suitable to accomplish this method.

The design and structure of a fully automatic oxygen therapy apparatus is exhibited in this disclosure. The apparatus integrates a MEMS mass flow meter, an oximeter, a proportional valve and a smart liquid bottle. The control unit of the apparatus is embedded with a wireless communication device and powered by a battery pack. This apparatus is designed to replace the mechanical oxygen rotameter used in today's hospital or homecare oxygen therapy applications. With a set recipe or parameters locally or remotely, the disclosed apparatus can perform a fully automatic oxygen therapy for recovering the blood oxygen level of patient, without the frequent attention of the therapy administrator, and especially it significantly reduces the possibility of cross infection to the administrator during the attendance of the oxygen therapy process. The therapy process data are relayed to local users as well as a designated cloud or data center. This disclosure will be beneficial for both medical staffs and patient.