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 measures changes in the electrical characteristic to determine when the drug solution level falls below a predetermined threshold, and deactivates the device accordingly.

Abstract: A liquefied gas storage/delivery system and method that includes a liquefied gas storage system. The liquefied gas storage system includes a housing containing a storage vessel suited to contain a supply of liquefied gas, such as liquid oxygen (LOX). A rotatable turntable is provided on an exterior surface of the housing. An interface shaped to match the shape of at least a portion of a portable liquid storage/delivery device is provide in or on the turntable. A connector is disposed in the interface that couples to a corresponding connector on the portable liquid storage/delivery device. The two connectors are coupled by placing the portable liquid storage/delivery device in the interface and rotating the turntable.

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 drug delivery apparatus includes a mouthpiece portion having an internal conduit for delivering an aerosol including the drug to the patient. The internal conduit has an inlet end and a mouthpiece end that is structured to be received in the patient's mouth. The mouthpiece portion is structured to operate at a substantially fixed inhalation flow rate when the patient inhales through the mouthpiece end. The apparatus further includes an aerosol generator for generating the aerosol from a drug supply and injecting the aerosol into a first region within the mouthpiece portion located between an outlet of the aerosol generator and the inlet end of the conduit. The mouthpiece portion also includes a flow accelerating mechanism that causes a localized flow rate at the first region to be greater than the inhalation flow rate. A method is also provided that increases the local flow rate within the mouthpiece portion.

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.

Abstract: A system configured to monitor ambient illumination experienced by a subject. In one embodiment, the system comprises an illumination sensor, a timer, and a storage module. The illumination sensor is configured to monitor an intensity of ambient illumination within two or more wavelength ranges by generating one or more output signals that convey information related to the intensity of ambient illumination within the two or more wavelength ranges. The timer is configured to indicate the passage of periods of time. The storage module is configured to store information related to the intensity of ambient illumination within the two or more wavelength ranges, as conveyed by the one or more output signals, for individual periods of time. The system is portable to be carried by the subject.

Abstract: A patient interface that reliably and comfortably seals a user's face by providing an oral-nasal mask that includes an integrated nasal interface. The patient interface includes a seal member having an oral cushion portion configured to surround the user's mouth and a nasal interface portion that provides an interface with the user's nose. The seal member, including the oral cushion portion and the nasal interface portion, is a unitary member. Finally, the nasal interface portion remains below the bridge of the nose.

Abstract: Methods for noninvasively determining a pulmonary capillary blood flow or a cardiac output of a subject include determining data of the amount of gas exchanged between blood and gas in lungs of the subject, as well as data of an indicator of the content of the gas in blood of the subject. Such a determination may be made during two or more different states of ventilation. A geometric relationship is identified between data points, with any data points outlying the geometric relationship being disregarded. The remaining data points may be used to estimate or calculate a measure of pulmonary capillary blood flow or cardiac output. Systems that include elements that are configured to effect such methods are also disclosed.

Abstract: A therapy system adapted to treat a patient's ventilatory instability using a ventilatory therapy, a gas modulation therapy, or both. The algorithm implemented by the therapy system monitors the ventilatory instability, such as Cheyne Stokes Respiration (CSR), mixed apneas, CPAP emergent apneas, and complex sleep disordered breathing (CSDB) and treats the ventilatory instability. The algorithm also determine a reference point with respect to the ventilatory instability. The therapy delivery system initiate the treatment based on the reference point.

Abstract: A method of delivering a flow of gas to a patient's airway via a pressure generating system and a patient circuit. A controller receives a treatment set point from an input source and determines an adjusted treatment set point based on the treatment set point and a comfort feature function, which in one embodiment, is not based on a physiological condition of such a patient. In another embodiment, the controller provides a respiratory treatment therapy during a therapy session based on the treatment set point and the comfort feature, which is modified automatically during a therapy session without user intervention based on a comparison of the treatment set point to a treatment set point variable. The controller controls the operation of the pressure generating system based on the adjusted treatment set point or the combination of the treatment set point and the comfort feature.

Abstract: A pressure support system that delivers a flow of gas to a patient's airway via a pressure generating system and a patient circuit. A controller receives a treatment set point from an input source and determines an adjusted treatment set point based on the treatment set point and a comfort feature function, which in one embodiment, is not based on a physiological condition of such a patient. In another embodiment, the controller provides a respiratory treatment therapy during a therapy session based on the treatment set point and the comfort feature, which is modified automatically during a therapy session without user intervention based on a comparison of the treatment set point to a treatment set point variable. The controller controls the operation of the pressure generating system based on the adjusted treatment set point or the combination of the treatment set point and the comfort feature.

Abstract: A patient interface device includes a support member, a sealing assembly attached to the support member, and a pair of contacting members. The contacting members are coupled to the support member on each side of the sealing assembly. The contacting members are each configured and arranged to contact the user over a limited contacting region, which corresponds to a junction of the oribicularis oris facial muscle, the zygomaticus facial muscle, and the risorius facial muscle.

Abstract: A system and method for delivering a flow of breathing gas to an airway of a patient. The system monitors a characteristic that varies based on variations of the flow of the breathing gas and determines a Target Flow for the gas to be delivered to the patient based on the monitored characteristic. The Target Flow is set to a level sufficient to treat Cheyne-Stokes respiration or a sleep disordered breathing event. The system also alters the Target Flow based on a determination that the patient is experiencing a sleep disordered breathing event. The system further determines a pressure relief component and controls the flow of gas delivered to the patient based on the Target Flow and the pressure relief component.

Abstract: Condensation management techniques for a gas flow delivery system. The techniques include providing a radiant barrier associated with patient circuit and/or a patient interface, providing a water trap and/or an absorbent insert in the patient interface device, or a combination of these techniques. The radiant barrier prevents condensation from forming in the patient circuit and/or the patient interface. The water trap and absorbent insert in the patient interface control condensation that reaches or forms in the interior of the patient interface to prevent it from interfering the user of the gas delivery system.

Abstract: A portable oxygen concentrator includes a pressure swing absorption system defined by a relatively rigid housing adapted to generate a flow of oxygen enriched gas and a battery adapted to provide power to the pressure swing absorption system. The oxygen concentrator has a total weight of less than about 10 lbs, has a maximum flow of 100% O2 equivalent gas of about 0.9 lpm, has a total volume less than about 800 in3, and gas a battery life of at least about 8 hours. The present invention also using a liquefaction or transfill system in combination with such an oxygen concentrator.

Abstract: A method for selecting a device adapted to treat disordered breathing includes determining a number of characteristics associated with at least a portion of the airway of a patient, comparing each of at least some of the number of characteristics to a corresponding threshold, and selecting such a device in response to the comparison. An alternative method for selecting a device adapted to treat disordered breathing includes delivering a flow of breathing gas to the airway of a patient, determining a minimum effective therapeutic pressure associated with such patient, and selecting, relative to the minimum effective therapeutic pressure, an oral appliance or one of a number of patient interface devices.

Abstract: A respiratory mask is provided having an outer shell coupled to a cushion for the delivery of a gas to a user. The cushion of the respiratory mask has at least one pleat disposed in the cushion in order to provide varying degrees of flexibility and support about the cushion.

Abstract: A patient interface device includes a support member, a sealing assembly attached to the support member, and a pair of contacting members. The contacting members are coupled to the support member on each side of the sealing assembly. The contacting members are each configured and arranged to contact the user over a limited contacting region, which corresponds to a junction of the orbicularis oris facial muscle, the zygomaticus facial muscle, and the risorius facial muscle.

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 mainstream gas monitoring method includes a using a mainstream airway adapter and a gas sensing assembly associated with the mainstream airway adapter to measure an analyte of a gas flow through the adapter. A gas sensing portion outputs a signal indicative of the analyte in a gas flow in the mainstream airway adapter. A processing portion receives the signal from the gas sensing portion and determines an amount of the analyte in the gas flow based on the signal from the gas sensing portion. The processing portion also compensates for volumetric differences between the gas flow during inspiration and the gas flow during expiration to maximize the accuracy in the measurements.