Abstract: A breathing apparatus includes a compressed air source with a compressed air source valve, a breathing regulator with a pressure reducer and a demand valve, a breathing mask connected to the demand valve at a first inlet connector, a second air source, a switching mechanism having an actuating member for switching between the compressed air source and the second air source and an exhalation valve, on the breathing mask, movable between a higher internal pressure in a second operating state than in a first operating state. The actuating member is provided on the breathing regulator. The switching mechanism, upon being switching to compressed air breathing, activates the lung-governed demand valve and adjusts the exhalation valve to the second operating state. Upon switching to breathing via the second air source, the lung-governed demand valve is deactivated and the exhalation valve (30) is adjusted to the first operating state.

Abstract: A device (102) provides respiratory treatment for SDB (including mild OSA) and other respiratory conditions. A flow generator warms and humidifies gas at controlled flow levels. For example, the device (102) delivers breathable gas to the upper airway at flow rates of about 10-35 Liters/minute. Levels of flow rate, temperature and/or humidification of the device may be automatically adjusted in response to the detection of SDB events. The device may also automatically deliver adjustments of any of the levels in accordance with detected phases of respiratory cycles. In some embodiments, the device automatically delivers distinct levels to either of the nares based on independent control of flow to each nare. A warm-up procedure controls temperature and humidity at a desired target during a ramp-up of flow to the set therapy level. A cool-down procedure controls temperature above the dewpoint to avoid condensation internal to the device and patient interface.

Abstract: A metered droplet medicament delivery device for delivering metered doses of medicament includes a proximal part and a distal part having opposite distal and proximal ends; a medicament container with a movable stopper; and a dose delivery mechanism that includes a plunger rod, operably arranged to act on the stopper. The proximal and distal parts are releasably connectable to each other. The proximal part includes a medicament container holder accommodating the medicament container, and the distal part includes the dose delivery mechanism. A plunger rod positioning member is engageable with a proximal end of the plunger rod and with a proximal area of the distal part for positioning the plunger rod in a longitudinal direction in relation to the proximal area.

Abstract: A headgear for securing a patient airway interface device to a patient's head comprising a concave partial helmet having an outer surface and an inner surface and having a left lateral element, a right lateral element, a top portion and a back portion, wherein the left lateral element and the right lateral element are separated at a front half of the concave partial helmet by a void between the front half top portion of the concave partial helmet and the left lateral element and the right lateral element; when on the patient's head the top portion of the concave partial helmet terminates at the forehead of the patient's head with a front face of the top portion of the concave partial helmet that is proximal to the forehead having a stabilizer for supporting a hub and wherein the left lateral element and the right lateral element is structured to terminate on either side of a patient's face near a cheek portion without directly touching the check portion and wherein a section of the right lateral element and t

Abstract: This invention relates to a treatment device (10) and method of use, and in particular to a treatment device adapted to assist the clearance of bronchial secretions in persons whose cough function is impaired. The invention provides a treatment device having a pump (12) with a negative pressure inlet side (22) and a positive pressure outlet side (24). The device has a breathing tube (14) for connection to a patient, and a pressure sensor (18) adapted to determine the pressure within the breathing tube. A valve (16) selectively connects the breathing tube to the inlet side or the outlet side of the pump whereby to provide cycles of positive and negative pressure within the breathing tube. A controller (26) is provided to control the valve. An indicator (20) alerts the patient to an operational status of the device so that the patient can breathe in time with the device and in particular can seek to cough at the same time as the pressure within the breathing tube is rapidly reduced.

Abstract: A respiratory treatment device having an inlet configured to receive exhaled air into the device and an outlet configured to permit exhaled air to exit the device. A blocking member is moveable between a closed position where the flow of air through the device is restricted, and an open position where the flow of air through the device is less restricted. A biasing member is configured to bias the blocking member toward the closed position, wherein a level of bias decreases as the blocking member moves from the closed position to the open position.

Abstract: An interfacing structure is arranged to cooperate with a frame to contact with the skin of a patient. The interfacing structure includes a clip portion joined to a cushioning component. The frame is more rigid than the clip portion and the clip portion is more rigid than the cushioning component.

Abstract: A respiratory device having a respiratory gas source, a control unit and a connecting device for connecting to a respiratory mask. The control unit is connected to a sensor for detecting a measurement parameter. The control unit has a step generator for specifying a stepped modification of the pressure that is generated by the respiratory gas source. The sensor measures a signal that corresponds to the pressure distribution and is coupled to an analyzer that evaluates the temporal distribution of an analysis signal that is dependent on the measuring signal. The step generator increases the pressure by a pressure step in a respiratory cycle that follows the measuring evaluation, if the analyzer determines a deviation of the analysis signal from a limit value after a predeterminable time limit has elapsed following the pressure increase. The deviation must exceed a predeterminable minimum differential in order to trigger a pressure increase.

Abstract: An interface for positive pressure therapy includes a mask assembly, a headgear assembly and a connection port assembly. The mask assembly comprises a seal member that has an upper portion movably connected to an integrated lower portion, wherein the upper portion rolls during hinging movement of the upper portion relative to the lower portion. The headgear assembly allows connection to the mask assembly in a direction substantially normal to a direction of strap tension. The connection port assembly includes a swivel elbow with a valve member that controls flow through a port that opens toward the user.

Abstract: A patient interface device includes a frame member and a cushion having a main body, a sealing portion, and first and second posts extending from the main body. The frame member defines a first orifice and a second orifice. The first post of the cushion is rotateably received within the first orifice and the second post is rotateably received within the second orifice in a manner that permits the cushion to rotate relative to the frame member.

Abstract: Systems and methods for compensating for leaks in a ventilation system based on data obtained during periods within a breath in which the patient is neither inhaling nor exhaling. The methods and systems described herein more accurately and quickly identify changes in leakage. This information is then to estimate leakage later in the same breath or in subsequent breaths to calculate a more accurate estimate of instantaneous leakage based on current conditions. The estimated leakage is then used to compensate for the leak flow rates, reduce the patient's work of breathing and increase the patient's comfort (patient-ventilator breath phase transition synchrony).

Abstract: A surgical mask for administering and/or scavenging medical gases includes a nasal mask and an oral mask that envelops the nasal mask. The nasal mask is secured to the oral mask and may be removable from it.

Abstract: A buckle assembly for a respiratory mask comprises a female part and a male part. The female part includes top and bottom walls and a curved vertical wall. The top wall is formed with a top pivot hole and a top guiding groove. The bottom wall is formed with a bottom pivot hole and a bottom guiding groove. The male part includes a hook section that has a free end formed with top and bottom pivot protrusions that are slidable respectively along the top and bottom guiding grooves into the top and bottom pivot holes, respectively, so as to bring the male part to pivot relative to the female part between a first angular position and a second angular position in which the curved vertical wall and the hook section hook to each other.

Abstract: A method for controlling mechanical lung ventilation is described. The method may include supplying a breathing gas to an airway of a patient in an intermittent way such that a plurality of respiratory cycles are formed; measuring a volume received by the patient in one or more respiratory cycles of the plurality of respiratory cycles; comparing the measured volume of each of the one or more respiratory cycles with a user defined target volume; attributing a classifying score to each of the one or more respiratory cycles based at least partially on a deviation between the measured volume and the user defined target volume; summing the classifying scores and dividing the result by a sample size of the one or more respiratory cycles; attributing a pressure step value based at least partially on the division result; and adding the pressure step value to a present pressure.

Abstract: A respiratory mask for continuous positive airway pressure treatment includes a cushion adapted to be positioned against the face of a patient. The cushion is configured in a gasket arrangement around an entrance to the airways of the patient. The cushion is constructed from a polyurethane foam and has a thickness of greater than about 5 mm.

Abstract: A nCPAP device includes an net configured for receiving a single gas jet flow. The single gas jet flow supplies gas for both nares. The device also includes a flow splitter configured for proportionally splitting said gas jet flow into two channels for the both nares according to one or more of nave anatomy and flow path resistance.

Abstract: Pressure indicator comprising a base, a deformable membrane fixed to the base in a fluid-tight manner according to a closed contour, and a body fixed to the base, delimiting a hollow volume covering the deformable membrane on the side opposite the base, while encompassing at least the closed contour, at least one inlet for a fluid the pressure of which is to be measured in a pressure range, wherein the deformable membrane is such that the expansion thereof for said pressure range is sufficient to be visible to the naked eye and to allow a direct display indicative of the pressure, in that the base is drilled with at least one first hole a first end of which emerges between the deformable membrane and the base in the closed contour, in that the body is drilled with at least one second hole a first end of which emerges into said hollow volume, in that the other end of the first hole is linked to the inlet respectively to the open air, in that the other end of the second hole is linked to the open air, respectiv

Abstract: A carrying system is provided for use with breathing apparatus. The carrying system includes a backplate and a plurality of straps adapted to hold the backplate on the back of a user when the carrying system is worn. The backplate includes at least one plate of a plastics material. The at least one plate having a predetermined shape and the at least one plate being adapted to provide impact protection to a user during use by at least partially absorbing and/or dispersing impact forces, and to deform resiliency in response to external forces imposed by bending and/or twisting of a user during use and return substantially to its predetermined shape when not subjected to an external force.

Abstract: An airway device (14), that is used to maintain a clear airway in a patient, e.g. for artificial ventilation during surgery, comprises an inflatable cuff (26), which is inflated when in position in a patient's airway (24). The inflated cuff (26) provides a seal to maintain the device (14) in position in a patient's airway (24), and to prevent leakage of infected oropharangeal secretions into the patient's lungs. A method and apparatus (10) for monitoring: leaks in the pressure system of the device (14) that includes the cuff (26); blockage in the pressure system, and/or malpositioning of the airway device (14) during use.

Abstract: Reinforced filter media are prepared by adhering discrete, non-intersecting strands of thermoplastic or thermoset materials to the filter media web. The filter media may be a fabric, a nonwoven web or a filtering foam. The reinforced filter media can be used to prepare respirators, including flat-fold respirators or molded respirators.