A device 10 withdraws a breathing gas stream (A) from a ventilation system (B) and transports the breathing gas stream (A) to a gas analysis system (G). The device 10 has a tubular configuration with an inner side (41) and with an outer side (42) and includes two tube sections (11, 11′) and a drying stage (12, 14, 22) with an inner side (43, 43′) and with an outer side (44, 44′), and at least one liquid storage device (13, 21). The drying stage (12, 14, 22) includes a gas-tight and moisture-permeable material that transports moisture from the inner side (43, 43′) of the drying stage (12, 14, 22) through the gas-tight and moisture-permeable material to the outer side (42) of the tubular device (10). The drying stage (12, 14, 22) and/or the liquid storage device (13, 21) is arranged at least partially between the two tube sections (11, 11′).

The present disclosure relates to determining a corrected exhaled gas measurement during high flow respiratory therapy. Measuring exhaled gas concentration during high flow respiratory therapy is difficult and inaccurate due to a phenomenon known as flushing. The high flows delivered to the patient flush the dead space in the conducting airways, which causes a dilution effect that results in underestimated or overestimated exhaled gas measurement depending on the gas composition delivered by the high flow system. This can lead to incorrect clinical measurements and diagnoses. Various algorithms are disclosed herein to account for the dilution effect caused by flushing, allowing for the method of measuring gas concentrations to still be used accurately for clinical measurements.

The present disclosure relates to a filter apparatus for filtering liquid from a gas, the apparatus having a first housing having a gas inlet and a gas outlet; a first filter media disposed in the first housing; a second filter media disposed in the housing; and a second housing forming a first collection basin disposed in the flow path between the first filter media and the second filter media, so that a path is defined for the gas flowing from the inlet, through the first filter media, past the collection basin, through the second filter media, and to the outlet. The present disclosure also relates to a method of passing a gas through a coalescing filter media and through a hydrophobic filter media.

A method for determining a chance to enable a zeroing of gas analysis is disclosed herein. The method includes emitting radiation, and receiving emitted radiation, the received radiation comprising a first wavelength range absorbed by the at least one desired gas component and one or more disturbing factor, and a second wavelength range absorbed by the disturbing factor, the first wavelength range differing from the second wavelength range. The method also includes providing to a processing unit a first signal data indicative of a concentration of the at least one desired gas component and absorption of the disturbing factor, and a second signal data indicative of absorption of the disturbing factor. The method also includes determining a stability of the first and second signal data as a function of time, and if they are substantially stable enabling the zeroing to improve a measurement accuracy.

A medical breathing gas filter housing includes a first housing body including a first port, and a second housing body including a second port. The gas filter housing is configurable between a closed state and an open state. In the closed state, the first housing body is snap fit to the second housing body such that first and second interior sides of the first and second housing bodies, respectively, define a cavity, the cavity sized to receive a replaceable gas filter media. In the open state, the first housing body is separated from the second housing body to provide access to the cavity.

A mask assembly includes a mask frame including a lower portion and a neck extending from the lower portion, a cushion provided to the mask frame and adapted to contact a patient's face, a forehead support assembly provided to the neck of the mask frame, the forehead support assembly including a forehead support and a forehead pad provided to the forehead support, and an elbow assembly provided to the mask frame. The neck includes a pair of side walls spaced apart from one another along an entire length of the neck, the side walls providing an open space therebetween along the entire length of the neck that opens towards a front side of the mask assembly. The pair of side walls comprise an upper converging section wherein the pair of side walls converge towards one another in a downward direction.

The invention relates to a monitoring and/or respiratory assistance apparatus that can be used during a cardiopulmonary resuscitation (CPR) with successive chest compressions of duration (dt) performed on the patient and with relaxations, said apparatus comprising a CO.sub.2 content measurement sensor (10) a graphical user interface (14), and signal-processing system (11) configured to process the CO.sub.2 content measurement signals in such a way as to determine at least one maximum CO.sub.2 content value (Vmax) and at least one minimum CO.sub.2 content value (Vmin), during at least one duration (dt) of at least one chest contraction, and then to calculate at least one airway opening index AOI or mean index AOI.sub.mean on the basis of the CO.sub.2 content values. Said one or more indices are displayed on the GUI in the form of numerical values or graphical representations, especially curves or pictograms.

Present invention is a oral airway with a flexible air connector and tubing built into the trachea tube distal end. Additional access channels are also provided.

A nasal cannula including a manifold having a delivery channel and a collection channel fluidly connected to a delivery nasal prong for delivering a gas to be inhaled from a patient's nose and to a collection prong for collecting gas exhaled from the patient's nose. The prongs are composed of a resilient material having sufficient memory that allows the prongs to be resiliently spread apart to be inserted into the respective nares of the patient's nose and when released, gently grasp the columella of the patient's nose to secure the cannula in position. The prongs are oriented leftwardly or rightwardly of the channels so that the right or left portions of the patient's face remain unobscured during surgery.

The present disclosure describes systems and apparatuses related to a bronchial isolation tube, a laryngeal mask or similar device, and/or adapters and connectors for use with the same, as well as methods for using the same. In an exemplary airway device, the device may comprise a mask portion being defined at a distal end of the airway device, and may be configured and dimensioned to be positioned in a hypopharyngeal area of a patient to cover and seal around a glottis of the patient; and a channel portion extending from a proximal end of the airway device to the mask portion. The channel portion may include first and second channels, wherein the second channel may obliquely merge with the first channel proximate to an opening of the first channel. In an exemplary embodiment, a third channel may form a combined pharyngeal-gastric access channel.