Abstract: A respiratory component mounting assembly includes a first respiratory component, a second respiratory component and a mounting clip for mounting the second respiratory component to the first respiratory component. Each of the first and second respiratory components includes at least two spaced apart clip openings. The mounting clip has an intermediate portion and two spaced apart free ends connected to the intermediate portion. The intermediate portion of the mounting clip is received within both of the clip openings of the first respiratory component and the free ends of the mounting clip are received in the clip openings of the second respiratory component for releasably securing the first and second respiratory components together.

Abstract: A patient interface having a cushion for engagement with the face of a user, a shell having an extension with a forehead support connected to the extension. The forehead support has a hinge so that the forehead support can be deformed to conform to the user's forehead. The patient interface also has a pivotable coupling defined by a body and a coplanar conduit that extends radially from the body. The coupling also has a port that allows access within the cavity formed by the cushion so that the port and coupling may rotate together.

Abstract: A method for forming at least one opening in a receptacle comprises the steps of providing a receptacle having a cover with an exterior surface and an interior surface covering a cavity. A cutting mechanism is also provided having at least one blade. The cover is pierced with the blade, and the blade is moved through the cover to cut a portion of the cover and create an opening in the cover to provide access into the cavity. Further, the cut portion curls on top of the exterior surface as the opening is created.

Abstract: A blister pack for use with inhalation therapy inhalers comprises an elongate bottom element having an overlying top element defining a plurality of spaced top crowned areas containing powder or liquid medications or drugs.

Abstract: A cardiopulmonary resuscitation device that combines ventilation of a patient's lungs with chest compressions on the patient's sternum area. The device includes a self-inflating bag having an outlet port through which the content of the bag is forced when bag is compressed; target indicia on the bag to indicate the proper position of the bag on the patient's sternum area and to indicate the proper location on the bag for applying force to the top side thereof; a face mask for placement over the patient's mouth and nose; and a tube extending from the bag to the face mask. The device may include indicia for indicating the amount of pressure applied to the self-inflating bag, and a backboard including belt/motor structure for providing repeated and rapid chest compression and forced ventilation of the patient's lungs.

Abstract: Described herein are nasal respiratory devices, in particular, nasal respiratory devices configured to achieve positive end-expiratory pressure (PEEP) in a subject wearing the device. PEEP devices may have a threshold pressure for opening during expiration. In some variations, these devices have a threshold pressure for closing during expiration.

Abstract: Method and apparatus for controlling a ventilator are described. The invention can be used to control mechanical ventilators as well as respiratory assist devices such as CPAP machines. The apparatus receives input data indicative of patient's oxygen level. A controller determines PEEP, or CPAP, and FIO2, on the basis of data indicative of the patient's oxygen level. In an alternative embodiment, the apparatus further receives input data indicative of patient's carbon dioxide levels, respiratory elastance and airway resistance, and barometric pressure. The controller further utilizes the said input data to determine the optimal values of tidal volume and breathing frequency for a next breath of the patient, and uses the respiratory elastance and airway resistance data to determine any necessary adjustments in the I:E ratio. The controller also applies safety rules, detects and corrects artifacts, and generates warning signals when needed.

Abstract: Disclosed is a flow control device for a bronchial passageway. The device can includes a valve member that regulates fluid flow through the flow control device, a frame coupled to the valve member, and a membrane attached to the frame. At least a portion of the flow control device forms a seal with the interior wall of the bronchial passageway when the flow control device is implanted in the bronchial passageway. The membrane forms a fluid pathway from the seal into the valve member to direct fluid flowing through the bronchial passageway into the valve member.

Abstract: A swim and skin-dive snorkel for providing positive end-expiratory pressure for pressure-balanced exhalation. The snorkel may include inhalation and exhalation conduits. Air can be exhaled into a chamber and released when exhalation pressure within the chamber exceeds a threshold pressure. The threshold pressure that must be overcome to achieve exhalation may be balanced against the compressive forces of the ambient water pressure acting against the user's chest and lungs, which may greatly reduce the resting expiratory flow rate, the minute respiratory rate, and therefore the overall work of breathing. The exhalation pressure may be linearly matched to the ambient water pressure as a function of dive depth, thereby discouraging exhalation while diving. A purge valve may also be placed at the lower aspect of the snorkel.

Abstract: A cartridge for propellant-free administration of a liquid pharmaceutical composition by inhalation includes: an elongate displacing device including an upper end and a lower end, the lower end for at least partial insertion into a container; a cartridge chamber disposed at the lower end of the displacing device and operable store a pharmaceutical formulation, the cartridge chamber including at least one pierceably sealed opening; and a cannula guide extending from the upper end of the displacing device to the cartridge chamber, wherein insertion of a cannula through the guide pierces the sealed opening and releases the pharmaceutical formulation into a liquid solvent in the container to form the liquid pharmaceutical composition.

Abstract: Aircraft passengers who require a therapeutic oxygen supply independently of the prevailing cabin pressure, as distinguished from an emergency oxygen supply that depends on an inadequate cabin pressure, can breath therapeutic oxygen and/or emergency oxygen depending on the situation, through the same therapeutic oxygen masks. For this purpose a control accessible to the crew is used to connect a therapeutic oxygen supply to the emergency oxygen distribution system of the aircraft, whereby the source of oxygen is used either partially for therapeutic purposes or fully for emergency purposes.

Abstract: A universal headgear is easy to use and creates an effective seal between a patient interface device, such as gas delivery mask, and a patient. The headgear of the present invention includes a halo-like headband formed from an elastomeric material. The headband includes contoured panels that allow the device to fit most people without circumference length adjustment. The halo headband is designed to maintain a substantially frusto-conical shape when worn. The present invention preferably includes an adjustable crossover strap on the top connecting the contoured panels that is adapted to hold the halo headband in position. The headpiece further includes connecting straps to adjustably connect the headgear to a patient interface device. The present headgear fits a wide range of head sizes and shapes, is easy to use, and provides increased stability.

Abstract: A dosing device with an electromechanical interface is provided. The dosing device includes delivery means, a medium reservoir and an applicator, on the one hand, and a control unit and electrical energy store, on the other hand, in separate structural units. Guide means are provided for fitting one of the structural units into the other structural unit. The guide means has an electromechanical interface for coupling and/or uncoupling relative to the control unit and/or energy store without using tools.

Abstract: A nebulizer includes a piezoelectric transducer for aerosolizing a drug solution in a disposable cup module disposed above the transducer. Acoustic waves generated by the transducer propagate sequentially through transmitting medium, a first barrier, coupling medium, and a second barrier that forms part of the cup module, and into the interior of the cup module. The transducer at least partially comprises silver. The silver fluidly contacts the transmitting medium to discourage bacteria growth in the transmitting medium. The device includes electronics components that drive the transducer and measure an electrical characteristic associated with the transducer during operation. The electronics components measure changes in the electrical characteristic to determine when the drug solution level falls below a predetermined threshold, and deactivates the device accordingly.

Abstract: A powder inhaler for administering powder by inhalation, comprising: a flow path defined by a plurality of surfaces through which a stream of air is in use drawn on inhalation by a user; and dosing means (18) for providing a dose of powder to the flow path for entrainment in the stream of air; characterized in that the inhaler further comprises dislodging means for dislodging powder accumulated on a surface of the flow path downstream of the dosing means (18).

Abstract: A breathing mask shall has an inspiration valve (4) that can be replaced in a simple manner. The breathing valve (4) is designed for this purpose as a modular assembly unit that can be inserted into the breathing gas channel (3) from the outer side (10) of the mask.

Abstract: A modular capillary pump loop (CPL) cooling system and associated components. The modular CPL cooling system transfers heat from high-power circuit components, such as microprocessors disposed within computer chassis, to other locations within or external to the chassis, where the heat can be more easily removed. In various embodiments, the CPL cooling system includes one or more evaporators connected to one or more condensers via flexible liquid transport and vapor transport lines. A wicking structure, such as a volume of sintered copper, is disposed within each condenser. The wicking structure draws working fluid (e.g., water) in a liquid state into the evaporator based on a capillary mechanism and a pressure differential across a meniscus/vapor interface on an upper surface of the wicking structure. As the liquid meniscus is evaporated, additional fluid is drawn into the evaporator. The working fluid is then condensed back into a liquid in the condenser.

Abstract: A method and a CPAP apparatus for characterizing a plurality of different mask systems, e.g., masks and hoses, are provided. The CPAP apparatus can be calibrated for different mask systems and hoses by including sensors configured to measure flow and pressure at a flow generator of the CPAP apparatus. When the flow generator is fitted to a new mask system, or any changes are made to an existing mask system, mask or patient interface and/or hose, a method for calibrating the flow generator for the new mask system, mask and/or hose is provided.

Abstract: A method of providing concentrated oxygen product gas to a patient. The method comprises producing product gas by a vacuum swing adsorption (VSA) process with an oxygen concentrator comprising a plurality of separation columns connected to a vacuum source driven by a motor. Separated product gas is then pumped to a product reservoir. The pressure of the reservoir is monitored and used to adjust the speed of the motor based on the reservoir pressure. The separated gas is then delivered to the patient.

Abstract: In one embodiment, the invention provides a medical method for treating a person and comprises repeatedly compressing the person's chest. While repeatedly compressing the person's chest, the method further includes repeatedly delivering a positive pressure breath to the person and extracting respiratory gases from the person's airway using a vacuum following the positive pressure breath to create an intrathoracic vacuum to lower pressures in the thorax and to enhance blood flow back to the heart.