Abstract: A dilator assembly for percutaneous dilatational tracheostomy includes a dilator element having a wall and a proximal end part extending into a distal tip part via an intermediate part. The wall has a substantially U-shaped cross section defining a dilator opening. The assembly extends towards the distal tip part. The dilator assembly is part of a tracheostomy device. The device has a first branch for arranging inside the trachea, and a second branch co-operative with the first branch. The first branch has a first end and a receiving member while the opposing second end has a first coupling part. The second branch has a first end with a guide for a neck penetration member and an opposing second end with a second coupling part for coupling with the first coupling part of the first branch. The first and second branches are detachably coupled together at their respective second ends.

Abstract: Embodiments of the present invention include an insertion aid device with a handle, a tongue depressor, a tracheal suction catheter guide, and a guide with a recess formed by a pair of prongs. The guide may be configured to accommodate the cross-sectional shape of a tracheal suction catheter, a nasogastric tube, or an orogastric tube. The tracheal suction catheter guide may include a connection port configured to couple to an in-line suction catheter. A light source may be included with the insertion aid device.

Abstract: A humidifier for use with a pressure support system. The humidifier includes a body having an inlet, a fluid holding chamber, and an outlet. The inlet is positioned upstream and in fluid communication with the fluid holding chamber. The outlet is positioned downstream of and in fluid communication with the fluid holding chamber. A back-flow preventing valve is positioned upstream of the fluid chamber. The back-flow preventing valve is movable between an open position, in which the inlet is unblocked, and a closed position in which the inlet is blocked. In the closed position, the back-flow preventing valve prevents fluid, fluid vapor, or both from entering the pressure support via the inlet to the humidifier.

Abstract: A positive airway pressure apparatus is automatically adjusting. Pressure increases in response to apnea events when the apparatus is in one or more responsive states. Pressure does not increase in response to apnea events when the apparatus is in a non-responsive state. The apparatus switches between responsive and nonresponsive states depending upon any of a number of different criteria that help differentiate between open airway apnea events and closed airway apnea events.

Abstract: A nasal interface including a hard base and a soft pad portion with angled butterfly wing portions. The soft pad portion is connected to the hard base portion, and in some arrangements, can be removed from the hard base portion. The soft pad portion includes a bellows positioned between a lower boarder and the butterfly wings.

Abstract: For use in premature babies and infants, in particular for administering surfactant to the lungs, the inhalation therapy device described herein comprises an aerosol generating device 1, a respiratory air flow generating means 3 and a nebulising chamber 5 into which the generated liquid droplets 2 and the respiratory air flow 4 are supplied. The nebulising chamber 5 comprises a tapering area 52 which ends in a tubular intubation means 6. The intubation means 6 is designed such that the intubation end 6b can be positioned in such a manner that the liquid droplet/respiratory air mixture conveyed via the intubation means is released behind those areas of the respiratory tract that filter out to a great extent the liquid droplets from the mixture.

Abstract: A filtering face-piece respirator 10 that has a harness 14 and a mask body 12. The mask body 12 includes a support structure 16 and a filtering structure 18. The support structure 16 contains an auxetic mesh 20 that has been molded into an intended cup-shape configuration, and the filtering structure 18 contains a filtration layer 42 for removing contaminants from the ambient air. The use of an auxetic mesh 20 in the support structure 16 provides more uniformly-sized openings 26 in the mesh 20 and reduces opportunities for mesh overlapping and mesh distortion.

Abstract: The present specification discloses a ventilator system that can be manufactured quickly with minimal skill requirements and rapidly deployed in response to epidemic respiratory disease conditions. In one embodiment, the ventilator, having a minimal number of controls, is used to give ventilation or mechanical breathing to a patient suffering ARDS. The mechanical ventilation is based on pressure control and has variable pressure, breathing rate, and oxygenation. Preferably, the ventilator is rapidly deployable, easy and intuitive to operate, and capable of sustaining at least 75% of epidemic respiratory distress victims who require assisted ventilation until resuming normal breathing.

Abstract: A powder inhaler comprising: a body (10) that is provided with a dispenser orifice; at least one reservoir containing a dose of powder for dispensing; reservoir-opening means for opening a reservoir on each actuation; and a dispersion chamber (70) including an outlet (720) that is connected to said dispenser orifice, and an inlet (710) that is connected to said opening means and that receives the dose of powder from said open reservoir, said dispersion chamber (70) containing at least one movable element (75), such as a ball; the inhaler being characterized in that said dispersion chamber (70) includes a ball path (730) having a width that decreases from said inlet (710) in the direction of displacement of said at least one ball (75).

Abstract: The present invention provides a method and apparatus for providing continuous positive airway pressure for treating sleep apnea. The method comprises the steps of providing a breathing gas flow to a subject, measuring a respiratory characteristic of the subject, determining or estimating a preferable breathing gas flow for the subject based on wavelet analysis utilizing in part the respiratory characteristic of the subject, and preferably adjusting the breathing gas flow if the determined or estimated preferable breathing gas flow is different. This method and apparatus can be used in a number of applications including both clinical and home use in the form of CPAP for the treatment of sleep apnea or less preferably as a ventilator to assist in patient breathing.

Abstract: An aerosolization system includes a squeezable container having a resilient container body. The container is configured to deliver a unit dosage of a liquid when squeezed a single time. The system also includes an aerosolizer that is constructed of a housing defining a mouthpiece, and an aerosol generator disposed in the housing. The aerosol generator includes a vibratable membrane having a front face and a rear face, and a vibratable element used to vibrate the membrane. Further, the housing includes an opening that is adapted to receive a unit dosage of the liquid from the container. The opening provides a liquid path to the rear face of the vibratable membrane.

Abstract: Described are methods for safer nitric oxide delivery, as well as apparatuses for performing these methods. The methods may include detecting the presence or absence of a nasal cannula, and stopping the delivery of nitric oxide or providing an alert if the cannula is disconnected. The methods may also include purging the nasal cannula if it is reconnected after a disconnection or if it is replaced by a new cannula. Other methods pertain to automatic purging of the delivery conduit if the elapsed time between successive deliveries of therapeutic gas exceeds a predetermined period of time.

Abstract: This invention relates to a new technology that enables administration of Cannabis to patients for medical purposes. In one embodiment, this invention is a component of a system of technologies, processes and concepts that creates a new method of producing, delivering, administering and regulating the use of medical cannabis.

Abstract: A ventilator circuit for use in administering medication to a patient includes a housing, a one-way inhalation valve and a one-way exhalation valve. A metered does inhaler receptacle is in fluid flow communication with an interior space of the housing holding chamber. An exhaust conduit communicates between input and output passageways disposed on opposite sides of the interior space.

Abstract: A breathing assistance apparatus and method of controlling a breathing assistance apparatus is disclosed. Particularly, the breathing assistance apparatus is controlled such that it has a drying cycle to enable drying of the tubing that supplies gases to a user and prevent the harboring of pathogens within the tube. The drying cycle is preferably operated automatically by internal controllers in the apparatus. However, it may be manually activated by pressing a button on the apparatus. The drying cycle is preferably activated at the end of a user's treatment session.

Abstract: A powder inhaler includes: a housing having a port; a storage member located in the housing for storing a powder medicament; and a medicament-delivery member provided in the housing. The medicament-delivery member includes at least one concave portion for receiving medicament, and is capable of taking, relative to the storage member, a receiving position wherein the concave portion receives a predetermined amount of powder medicament from the storage member, and an inhalation position wherein the powder medicament can be inhaled through the admission port; and a stirring member for stirring the powder medicament stored in the storage member. An operation button is provided in the housing and is capable of moving between the initial position and a depressed position, while the operation button reciprocates between the initial position and the depressed position, the concave portion in the medicament-delivery member moves from the receiving position to the inhalation position and the stirring member operates.

Abstract: An inhaler (1) for dispensing doses of medicament from a container under user activation includes a body (7) which includes a mouthpiece (5) through which the medicament is dispensed and a cap (2) which can be place in a position to substantially occlude the mouthpiece (5). The cap (2) is attached to the body (7) by a strap (3) which pivots from the body (7), the cap (2) being arranged to slide on the strap (3) such that the cap (2) must translate away from the mouthpiece (5) prior to the pivoting of the strap (3).

Abstract: A method for improving the cardiac output of a patient who is suffering from pulseless electrical activity or shock and yet still displays some myocardial wall motion including sensing myocardial activity to determine the presence of residual left ventricular pump function having a contraction or ejection phase and a filling or relaxation phase. In such cases, a compressive force is repeatedly applied to the chest based on the sensed myocardial activity such that the compressive force is applied during at least some of the ejection phases and is ceased during at least some of the relaxation phases to permit residual cardiac filling, thereby enhancing cardiac output and organ perfusion. Also incorporated may be a logic circuit capable of utilizing multiple sensing modalities and optimizing the synchronization pattern between multiple phasic therapeutic modalities and myocardial residual mechanical function.

Abstract: The invention is an apparatus that blocks out light and improves breathing. The apparatus includes a sleep mask with an integral nasal dilation system. The nasal dilation system includes a nasal element mounted with on the nose section of the mask, where the nasal element in one version has a channel through which a band can move substantially orthogonal to the wearer's nose. Sidewalls center the band, and inward folded cuffs retain the band. The band encircles the wearer's head between the mask straps. It is threaded through the slideway and can slide therein equalizing side-to-side forces. The band is elastic and when stretched it generates an opposing force. Pressure is exerted on the nose by using the band in a stretched state. The extended band creates pressure on the slideway, which causes the nose section to press against the nostrils causing them to distend, which in turn dilates the nasal passages, and breathing is improved.

Abstract: A patient interface assembly that includes a first conduit, a second conduit, and a patient interface coupled to the first conduit and the second conduit. The first and second conduits each include a first end that is disposed proximate to a top of a head of a user, and a second end that is disposed proximate to an airway of such a user when the patient interface assembly is being worn by the user. The first and second conduits also each include a central portion that extends along the sides of a face between the user's eye and an ear a head strap is coupled between the first and second conduit, and a patient interface is coupled to the second ends of the first and second conduits.