Abstract: A patient interface packaging that includes an integrated sizing template. The packaging system includes a container having an inner chamber containing a patient interface device having a size contained within. The packaging further includes an outer exterior having an integral flap. The integral flap includes at least one opening therethrough forming a sizing template. The size of the opening corresponds to the size of the mask contained within the package so that the opening may be fitted to the nose region of a patient's to allow the user to determine an appropriate size patient interface device that matches his or her anatomical dimensions.

Abstract: A multi-chamber canister for a pressure swing absorption system within a general housing assembly. The chambers include a first molecular sieve chamber for receiving a first molecular sieve for separating air from the ambient environment into a concentrated gas and at least a second molecular sieve chamber disposed within the housing assembly for receiving a second molecular sieve for separating air from the ambient environment into a concentrated gas component. Furthermore, a supply chamber is disposed within the housing for receiving air from the ambient environment and for communicating air to either first or second molecular sieve chambers.

Abstract: The present invention provides a removably attachable compact desiccant cartridge that is useful in lowering the dew point of a medically useful gas, which is liquefied by a cryogenic device. The desiccant cartridge of the present invention comprises a gas feedstream inlet, a dehumidifying zone which comprises a desiccant material, and a dehumidified gas feedstream outlet. The present invention also provides a method for using the same.

Abstract: A trans-fill method and system comprising obtaining therapeutic gas from a therapeutic gas source, compressing the therapeutic gas from the therapeutic gas source in at least two stages to create an intermediate therapeutic gas stream and a high pressure therapeutic gas stream, supplying therapeutic gas to a patient from the intermediate therapeutic gas stream, and filling a cylinder with the therapeutic gas from the high pressure therapeutic gas stream substantially simultaneously with supplying therapeutic gas to the patient.

Abstract: A patient interface device that includes a support member sized and configured to span at least a portion of a patient's face while remaining below the patient's eyes responsive to the patient interface device being donned by such a patient. A sealing assembly is attached to the support member via a snap assembly associated with the support member and the sealing assembly. The snap assembly allows the sealing assembly to selectively attach to the support member.

Abstract: A patient interface device that includes a body portion comprising a pair of arms and a chin support. A first end portion of each arm in the pair of arms is coupled to an opposite end of the chin support. The chin support is adapted to be disposed under the mandible responsive to the patient interface device being donned by a user. At least one headgear attachment element is provided on each arm in the pair of arms. A circuit portion is provided at a second end portion of each arm in the pair of arm. A patient interface portion is coupled to the circuit portion.

Abstract: A computer-implemented method for tracking and monitoring a patient's compliance with a medical device usage prescription for a medical device is disclosed. This method and system includes the steps of: (a) providing a minimum medical device usage compliance value for the medical device for a predetermined compliance period; (b) providing the quantity of compliance periods in a measurement cycle; and (c) determining a compliance period value as the number of compliance periods in the measurement cycle in which an actual medical device usage value is at least equal to the minimum medical device usage compliance value. In another embodiment, the method also includes: providing a weighting factor, and applying the weighting factor to at least one actual medical device session usage value.

Abstract: A mask attachment assembly for use in attaching a mask in a sealed position on the user's face. The mask attachment assembly includes a panel member with a sleeve extending along the panel member, and one or more straps extending through and slidable within the sleeve. The strap includes a first attachment assembly on a first end of the strap for engaging a first engagement member on a first side of the mask, and a second attachment assembly on a second side of the strap for engaging a second engagement member on a second side of the mask. The strap is repositionable by releasing the attachment assemblies, sliding the strap through the sleeve of the panel and re-engaging the attachment assemblies. A patient interface device and a strap are also disclosed.

Abstract: A seal and a respiraoty mask having a seal adapted for confronting engagement with a surface of a user to form an interface therewith. The seal includes a first portion defined by a gel substance. In one embodiment, the seal includes a selectively formable substance adapted to be molded from a first pattern into a second pattern and to retain the second pattern responsive to being so molded. The seal and mask having the seal in this embodiment is tailored to patient by causing the formable portion of the seal to be placed in a malleable state, applying the seal to the patient while the formable portion is in the malleable state, and causing the formable portion to be placed in a fixed state to retain a shape generally conforming to the portion of the patient underlying the seal.

Abstract: A patient interface device that includes a frame sized and configured to span at least a portion of a patient's face while remaining below the patient's eyes when the patient interface device is donned by the patient. A support member is coupled to the frame such that the support member is moveable relative to the frame. A sealing assembly is attached to the support member. A pair of patient contacting members are operatively coupled to the frame and supporting the frame on a patient's face.

Abstract: A portable oxygen concentrator includes a reservoir adapted to store oxygen-enriched gas, a delivery valve adapted to communicate with the reservoir, a pressure sensor adapted to measure a reservoir pressure within the reservoir and to measure a pressure drop across the delivery valve, and an input device adapted to receive a pulse does setting. A controller coupled to the pressure sensor and monitors the reservoir pressure and the pressure drop across the delivery valve. The controller is also coupled to the delivery valve to selectively open the delivery valve for pulse durations based on the pulse dose setting to deliver pulses of gas from the reservoir to a user. The controller further adjusts the pulse durations based at least partially upon the reservoir pressure and the pressure drop across the delivery valve.

Abstract: A pressure support system and method of treating disordered breathing that optimizes the pressure delivered to the patient to treat the disordered breathing while minimizing the delivered pressure for patient comfort. The controller in the pressure support system operates as a set of prioritized control layers, wherein each control layer competes for control of the pressure generating system to implement a unique pressure control process. The pressure support system also controls the pressure provided to the patient based on the variability of the monitored data and a trend analysis of this data, including an indication of the skewness of the patient's inspiratory waveform.

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 system including methods and apparatus for treatment of a medical disorder such as obstructive sleep apnea or congestive heart failure. The system involves applying a gain to flow rate of pressurized gas delivered to a patient during inspiratory and/or expiratory phases of a respiratory cycle to deliver the pressurized gas in proportion to the respective gains during inspiration and/or expiration. A base pressure may be applied in addition to the gain-modified pressures and an elevated pressure profile may be employed to assist or control inspiration. The system may be fully automated responsive to feedback provided by a flow sensor that determines the estimated patient flow rate. A leak computer can be included to instantaneously calculate gas leakage from the system. The system may be utilized in connection with conventional continuous positive airway pressure treatments, such as CPAP or bi-level positive airway pressure equipment to effect various beneficial treatment applications.

Abstract: A system is provided for delivering a flow of breathing gas to an airway of a patient. The system includes a pressurizing flow module that generates a pressurized flow of breathing gas and a patient circuit coupled to the pressurizing flow module configured to communicate the flow of breathing gas to an airway of a patient. The system includes a sensor for monitoring a characteristic of a breathing pattern of the patient a controller that communicates with the sensor configured to increase a fraction of inspired carbon dioxide if the characteristic exceeds an upper threshold value and to provide servo-ventilation if the characteristic is less than a lower threshold value. The upper threshold value and the lower threshold value are changed based on the monitored characteristic of the breathing pattern of the patient.

Abstract: A compliance monitoring system and method in which a modular compliance monitor is selectively disposed in-line in a patient circuit of a pressure support system. The monitor includes a housing having an inlet and an outlet, each of which is selectively connectable to the patient circuit so that the flow of gas in the patient circuit also passes through a passage is provided through the housing. A sensor operatively coupled to the passage detects a parameter indicative of patient breathing. A processor disposed in the housing and receives the output of the sensor and determines, from the output of the sensor, whether the patient is breathing into the patient circuit, and outputs compliance data based on this determination.

Abstract: A magnetic coupling assembly for use in coupling portions of a gas delivery system. The magnetic coupling assembly includes a first member and a second member to be coupled together. The attractive forces between the first plurality of magnetic elements on the first member and a second plurality of magnetic elements on the second member join these members. The poles of magnetic elements in the first and second plurality of magnetic elements is opposite that of an adjacent magnetic element. The first and second members are easily detached from one another simply by rotating the first member relative to the second member such that the magnetic poles of the magnetic elements in each plurality of magnetic elements become unaligned, causing an weakening of the attractive forces.

Abstract: A portable oxygen concentrator includes a pair of sieve beds, a compressor for delivering air to the sieve beds, a reservoir receiving oxygen-enriched gas from the sieve beds, and an air manifold attached to the first ends of the sieve beds. A set of valves operate under the control of a controller for selectively opening and closing the valves to alternately charge and purge the sieve beds to deliver oxygen-enriched gas into the reservoir. In addition, an exhaust passage communicates with the plurality of sieve beds to deliver a flow of nitrogen evacuated from the sieve beds such that the flow of the nitrogen is directed at or across the controller to cool the controller.

Abstract: A multi-chamber canister for a pressure swing absorption system within a general housing assembly. The chambers include a first molecular sieve chamber for receiving a first molecular sieve for separating air from the ambient environment into a concentrated gas and at least a second molecular sieve chamber disposed within the housing assembly for receiving a second molecular sieve for separating air from the ambient environment into a concentrated gas component. Furthermore, a supply chamber is disposed within the housing for receiving air from the ambient environment and for communicating air to either first or second molecular sieve chambers.

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 catalytically active gel product is described consisting of a silica matrix which is amorphous to x-rays with uniform porosity, monomodal pore distribution and high surface area, within which one or more metal oxides possessing catalytic activity are dispersed. A process for preparing this catalytic gel is also described.