Abstract: A frame for use in an interface device for delivering a flow of treatment gas to the airway of a patient includes a first and second frame members, each having a first end structured to be coupled to a conduit supplying the flow of treatment gas and an opposite second end structured to be coupled to a sealing assembly. Each frame member has a passage defined therein which extends between the first end and the second end thereof. The first frame member is disposed on a first side of a reference plane which passes through the sealing assembly and the second frame member is disposed on a second side of the reference plane opposite the first side. At least one of the first frame member and the second frame member is biased toward the other of the first frame member and the second frame member.

Abstract: Concurrent treatment of obstructive sleep apnea and hypertension in a patient, via a pressure generating device, includes providing a flow of treatment gas to an airway of a patient in accordance with an initial set of flow parameters with respect to an obstructive sleep apnea mode. Responsive to determining that the patient has achieved stable breathing while receiving the flow of treatment gas, the flow parameters are increased above the initial set of flow parameters with respect to a hyper-ventilation mode. The flow of treatment gas is then provided to the airway of the patient in accordance with the increased flow parameters for a predetermined period of time. The increased flow parameters are configured to bring the patient's breath into accordance with target patient breath parameters configured to inflate the patient's lungs beyond a threshold for activating pulmonary stretch receptors of the airway of the patient.

Abstract: Concurrent treatment of obstructive sleep apnea and hypertension in a patient, via a pressure generating system, includes providing a flow of treatment gas to an airway of a patient in accordance with an initial set of flow parameters with respect to an obstructive sleep apnea mode. Responsive to determining that the patient has achieved stable breathing while receiving the flow of treatment gas, the flow parameters are increased above the initial set of flow parameters with respect to a hyper-ventilation mode. The flow of treatment gas is then provided to the airway of the patient in accordance with the increased flow parameters for a predetermined period of time. The increased flow parameters are configured to bring the patient's breath into accordance with target patient breath parameters configured to inflate the patient's lungs beyond a threshold for activating pulmonary stretch receptors of the airway of the patient.

Abstract: A pressure support device for providing pressure support therapy to a patient includes an airflow generator structured to generate pressure to provide pressure compensation to the patient via a patient circuit, one or more sensors structured to gather data related to effectiveness of the pressure compensation, and a processing unit structured to analyze outputs of the sensors while pressure support therapy is provided to the patient to determine if the pressure compensation provided to the patient is improper and to initiate action to confirm whether components of the patient circuit have been changed in response to determining that the pressure compensation provided to the patient is improper.

Abstract: A respiratory interface device is provided. The respiratory interface device includes a patient interface device, a patient circuit, and a pressure generating assembly. Pressure generating assembly includes a first pressure generating device and a second pressure generating device. Patient circuit includes a reduced conduit.

Abstract: A tubing assembly for use with a patient interface device includes a manifold portion structured to be coupled to a conduit carrying a flow of breathing gas and a number of tubular portions. Each tubular portion extends from the manifold portion to a distal end which is structured to be coupled to the patient interface device. Each tubular portion is structured to communicate the flow of breathing gas from the manifold portion to the patient interface device. Each tubular portion comprises an adjustment element which provides for a characteristic of the tubular portion to be selectively varied.

Abstract: Concurrent treatment of obstructive sleep apnea and hypertension in a patient, via a pressure generating device, includes providing a flow of treatment gas to an airway of a patient in accordance with an initial set of flow parameters with respect to an obstructive sleep apnea mode. Responsive to determining that the patient has achieved stable breathing while receiving the flow of treatment gas, the flow parameters are increased above the initial set of flow parameters with respect to a hyper-ventilation mode. The flow of treatment gas is then provided to the airway of the patient in accordance with the increased flow parameters for a predetermined period of time. The increased flow parameters are configured to bring the patient's breath into accordance with target patient breath parameters configured to inflate the patient's lungs beyond a threshold for activating pulmonary stretch receptors of the airway of the patient.

Abstract: A headgear for use with a patient interface for providing a flow of pressurized breathing gas to the airway of a patient includes a pair of wrapping panels positioned at a rear thereof. The wrapping panels prevent the tension in the neck of a patient that commonly results when non-wrapping headgear is tightened.

Abstract: An arrangement for exhausting gases from a cavity of a patient interface to an ambient environment, patient interface for use in providing a flow of treatment gas to the airway of a patient. The arrangement includes a body member that forms a portion of the patient interface between the cavity and the ambient environment. The body member includes: a number of inlets defined in a first side of the body member for receiving gases from the cavity; a number of outlets defined in a second side of the body member opposite the first side for provide for the exit of gases from the patient interface to the surrounding environment; and a number of high-drag passages defined in the body member extending laterally between an inlet of the number of inlets and an outlet of the number of outlets.

Abstract: A conduit (14A) for conducting a flow of breathing gas from a pressure generating device (4) to a cushion (10) of a patient interface device (8) includes a housing (22) that defines a passage (24) therethrough. The conduit further includes a first magnetic element (30A) disposed on a first side of the passage and a second magnetic element (32A) disposed on a second side of the passage opposite the first side. The first and second magnetic elements are positioned such that the magnetic fields produced by each magnetic element interact in a manner such that the first magnetic element and the second magnetic element are repelled away from each other in a manner which resists collapse of the passage.

Abstract: A tubing assembly for use with a patient interface device includes a manifold portion structured to be coupled to a conduit carrying a flow of breathing gas and a number of tubular portions. Each tubular portion extends from the manifold portion to a distal end which is structured to be coupled to the patient interface device. Each tubular portion is structured to communicate the flow of breathing gas from the manifold portion to the patient interface device. Each tubular portion comprises an adjustment element which provides for a characteristic of the tubular portion to be selectively varied.

Abstract: A cradle style cushion includes a central sealing body portion including a front wall, a rear wall, a top wall and a bottom wall. The top wall includes a central sealing surface, a first stabilizing surface and a second stabilizing surface, the first and second stabilizing surfaces each extending upwardly and outwardly with respect to the central sealing surface and a top edge of the front wall and being structured to wrap around and engage an outside of the nostrils when the patient interface device is donned by the patient, wherein the first stabilizing surface includes a first front side edge portion and the second stabilizing surface includes a second front side edge portion, and wherein the top edge of the front wall, the first front side edge portion and the second front side edge portion together define a front opening of the central sealing body portion.

Abstract: A respiratory interface device is provided that includes a cushion and a faceplate. The cushion is structured to be coupled to the faceplate. The faceplate includes a peripheral end and a number of custom features. The cushion is coupled to the faceplate adjacent the faceplate peripheral end.

Abstract: An advice system employs a genetic analysis of a patient to identify one or more characteristics of the patient. The advice system employs the characteristics to identify one or more attributes of a medical device that would desirably exist in a medical device that is to be prescribed for the patient. The advice system then identifies from the one or more attributes one or more medical devices from among a plurality of medical devices whose features at least in part meet the one or more attributes. The advice system then outputs a recommendation of the one or more medical devices. The system employs known genes that are expressive of certain traits in a person, with the known traits being interpreted or evaluated in terms of characteristics that are relevant in selecting a medical device from among a plurality of medical devices, such as patient interface devices or other devices.

Abstract: A nasal portion is for a patient interface device of an airway pressure support system. The airway pressure support system includes a gas flow generator. The gas flow generator is configured to generate a flow of breathing gas to be delivered to an airway of a patient. The patient interface device is in fluid communication with the gas flow generator. The nasal portion includes an extension portion configured to be in fluid communication with the gas flow generator, and a cap member provided on the extension portion. The extension portion and the cap member each move between first and second positions, the cap member moving independently with respect to the extension portion when the extension portion and the cap member move between the first and second positions.

Abstract: A cushion is for use in a pressure support system for delivering a flow of breathing gas to an airway of a patient. The cushion includes a body having a first end and a second end located opposite the first end. The body defines a space therein. The cushion further includes a sealing portion defining a single opening into the space. The single opening is adapted to surround both a first nostril and a second nostril of a patient. The sealing portion is located between the first end and the second end. The sealing portion includes a first protruding portion and a second protruding portion each extending outwardly from the body and being adapted to sealingly engage against an interior surface of a corresponding one of the first nostril and the second nostril.

Abstract: A customized mask is manufactured by the process of: generating surface geometry data of a face of a patient, the surface geometry data corresponding to and representing a surface geometry of the face of the patient; generating original cushion geometry data using the surface geometry data; generating modified cushion geometry data using the original cushion geometry data; producing a rigid support member using the modified cushion geometry data such that it is shaped according to the modified cushion geometry data, the support member being made of a unitary material; and coupling a sealing flap to the support member, the sealing flap being structured to engage the face of the patient.

Abstract: A system including a user information database structured to store first information corresponding to a consumer and a first fit score corresponding to a current product associated with the consumer, a product information database structured to store second information corresponding to a new product, a communication unit structured to communicate with a user device, and a processing unit including a fit score determination module structured to determine a second fit score of the new product based on the first information and the second information, to determine if the second fit score is greater than the first fit score, and to control the communication unit to push a notification to the user device in response to determining that the second fit score is greater than the first fit score.

Abstract: An electronic apparatus including an adjustment determination unit structured to receive patient interface device information for a patient interface device including one or more adjustable features and a 3-D model of a patient's face, and to calculate adjustment information for the patient interface device corresponding to the patient's face using the patient interface device information and the 3-D model of the patient's face and an output unit structured to output the adjustment information.

Abstract: A system for capturing a 3D image of a subject includes a detection device which is structured to capture images of the subject and surrounding environment, a projection device which is structured to provide a source of structured light, and a processing unit in communication with the detection device and the projection device. The processing unit is programmed to: analyze an image of the subject captured by the detection device; modify one or more of: the output of the projection device or the intensity of a source of environmental lighting illuminating the subject based on the analysis of the image; and capture a 3D image of the subject with the detection device and the projection device using the modified one or more of the output of the projection device or the intensity of the source of environmental lighting illuminating the subject.