IV filters are described herein. An IV filter includes a body, a filter media, and a bulb. The body defines a body volume. The filter media is disposed within the body volume. The filter media defines an inlet portion of the body volume and an outlet portion of the body volume. The filter media permits inlet flow from the inlet portion of the body volume to the outlet portion of the body volume and captures particulate from the inlet flow. The bulb defines a bulb volume in fluid communication with the outlet portion of the body volume. The bulb is deformable to compress the bulb volume and direct back flow from the outlet portion of the body volume through the filter media and into the inlet portion of the body volume, displacing particulate captured in the filter media into the inlet portion of the body volume.

An infection containment band (IC Band) that consists of a wrist band with a mouth sized cavity that holds a filter in the filter chamber which is attached to, and/or part of the wrist band-resembling a wrist watch. There are pressure vents on the unit that release the air pressure when coughing or sneezing into the unit. The filter, in preferred embodiments consists of a sub-micron and/or standard filter and/or anti-microbial filter. The foregoing and other objects are intended to be illustrative of the invention and are not meant in a limiting sense. Many possible embodiments of the invention may be made and will be readily evident upon a study of the following specification and accompanying drawings comprising a part thereof. Various features and sub-combinations of invention may be employed without reference to other features and sub-combinations. Other objects and advantages of this invention will become apparent.

A pH-buffer measurement system that has at least one source for modifying the pH of a fluid entering the system, the source selected from an acid source and a base source. The acid source adds an acid equivalent to provide an acid reacted fluid and the base source adds a base equivalent to provide a base reacted fluid. The source is in fluid communication with a flow path and a component for determining a fluid characteristic of the acid reacted fluid or the base reacted fluid. The fluid characteristic that is measured is any one of a gas phase pressure, an electrical conductivity, or thermal conductivity.

A medical airway device includes a housing having at least one breathing circuit port and including an airway filter arranged to filter air flowing through the at least one breathing circuit port. The airway filter includes a layered filter including at least a first separate filter layer and a second separate filter layer being stacked on top of each other so that neighbouring separate filter layers abut each other. The layered filter has a first surface being laminated with a first scrim layer and a second surface being laminated with a second scrim layer. Each separate filter layer is a non-woven fiber layer.

A method for estimating an inhale dose when a drug is delivered to a person using an inhaler is disclosed. A predicted inhale dose (PID) of the drug is estimated based on at least one first-type parameter and at least one second-type parameter. The first-type parameter is related to a breath pattern of the person, and the second-type parameter is related to the inhaler.

A patient interface includes: a plenum chamber; a seal-forming structure; a positioning and stabilising structure; a plenum chamber insert configured to be positioned and retained within the plenum chamber; and a vent structure; wherein the plenum chamber insert has a plenum chamber insert port; wherein the plenum chamber insert has an exterior surface configured to be positioned adjacent to an interior surface of the plenum chamber; wherein when the plenum chamber insert is positioned and retained within the plenum chamber, a radial channel is formed by the interior surface of the plenum chamber and the exterior surface of the plenum chamber insert such that gas is able to pass between a patient-proximal side plenum chamber insert and a patient-distal side of the plenum chamber insert via the radial channel during use.

Disclosed is a method for selectively capturing one or more portions of a patient's breath, comprising: detect one or more parameters regarding the patient's breath during a breathing routine; determine one or more data points from the detected one or more parameters wherein the one or more data points identifies one or more portions of the patient's breath to capture; and capture one or more portions of the patient's breath during the breathing routine.

A filter sterilization system includes an expiratory filter having filter material that collects pathogens present in the exhaled gas stream from a ventilated patient. A filter sterilizer includes an ultraviolet (UV) light source that is activated by the system to emit light towards the expiratory filter. Additionally, the system includes a ventilator coupled to a patient breathing circuit that provides a gas mixture from a gas source to the ventilated patient and transfers exhaled gases of the ventilated patient to the expiratory filter.

A respiratory filter and condensate management apparatus is provided for use in a breathing circuit during patient respiration. The apparatus includes a filter housing having an air inlet port and an air outlet port. A filter member is provided within the filter housing and located in an expiratory air flow path. A collection jar is removably attached to the filter housing and has a liquid reservoir to collect liquid formed by condensation in the flow of expiratory air within the filter housing when the collection jar is attached to the filter housing. A valve assembly moves to an open position when the filter housing is attached to the collection jar to allow drainage of the liquid from the filter housing. The valve assembly moves to a closed position when the filter housing is detached from the collection jar to prevent drainage of the liquid from the filter housing.

A system for conducting inhalation studies includes an inhalation exposure chamber and an aerosol delivery line connected to the inhalation exposure chamber. The aerosol delivery line is configured to produce a bi-directional and symmetrical presentation of aerosol to the inhalation exposure chamber. A laminar flow element is configured to create an ante-chamber where complete and turbulent mixing of the aerosol occurs. A radial exhaust and the laminar flow element enable laminar flow of the aerosol through the inhalation exposure chamber.