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.

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: Securement arrangements for use in securing a patient interface to the skin of a patient include a substrate material having a first surface and an adhesive material disposed on the first surface. The locations of the adhesive material are varied so as to minimize repetitious adherence of the adhesive material to the patient during repeated applications.

Abstract: Methods and systems for recommending at least one patient interface device from among a plurality of patient interface devices for a patient. The methods and systems monitor an initial stress response of the patient upon being exposed to each of the potential patient interface devices of the plurality and from such monitoring select a device or devices that produce lesser stress responses.

Abstract: A respiratory interface system for use in delivering a flow of a positive pressure breathing gas to an airway of a patient that includes a patient interface device with a tubing assembly structured to be disposed on the head of the patient, a mask having a sealing element structured to sealingly engage about the airway of the patient, and an adaptor. The adapter includes a flange portion that extends generally radially outward from a central aperture and a hollow male connector extending from the flange portion and coupled with a correspondingly-shaped female connector of the tubing assembly or the mask. The mask is coupled to the tubing assembly via the adaptor, and the tubing assembly, the mask, and the adapter define a pathway structured to conduct the flow of the positive pressure breathing gas to the airway of the patient.

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 method of identifying a particular mask for a patient for use in delivering a flow of breathing gas to the patient includes capturing with a visual presentation and interaction component a plurality of images of the patient; receiving with the visual presentation and interaction component a number of responses from the patient to questions presented to the patient, eliminating one or more masks from a pool of potential masks for the patent based on at least one of the responses, utilizing at least some images of the plurality of images to determine the particular mask for the patient from the pool of potential masks, and identifying the particular mask to the patient.

Abstract: A cushion for use in providing a regimen of respiratory therapy to a patient includes a base that defines a main cavity therein an aperture for receiving a flow of breathing gas. A pair of nasal pillows each extend from the base, each having a cone-shaped head that tapers inward and upward from a base portion, that extends directly from the base, to a top opening. Each head is formed to engage an inner portion of a nare of the patient. Each head defines a passage extending between the main cavity and the top opening for further conveying the flow of breathing gas from the main cavity to a nasal passage of the patient. Each base portion includes an inner edge positioned near the center of the cushion that merges with the hollow base and an opposite outer edge spaced upward from an outer surface of the hollow base.

Abstract: A method of detecting stroke in a patient receiving a pressure support therapy includes: receiving data from one or more sensors structured to gather data related to patient respiration while receiving pressure support therapy from an airflow generator via a patient circuit; analyzing the data from the one or more sensors while pressure support therapy is provided to the patient; determining that the analyzed data from the one or more sensors is indicative of a patient experiencing respiratory changes indicative of a stroke; and responsive to said determining, triggering at least one alarm.

Abstract: A cushion for use in providing a regimen of respiratory therapy to a patient includes a base that defines a main cavity therein an aperture for receiving a flow of breathing gas. A pair of nasal pillows each extend from the base, each having a cone-shaped head that tapers inward and upward from a base portion, that extends directly from the base, to a top opening. Each head is formed to engage an inner portion of a nare of the patient. Each head defines a passage extending between the main cavity and the top opening for further conveying the flow of breathing gas from the main cavity to a nasal passage of the patient. Each base portion includes an inner edge positioned near the center of the cushion that merges with the hollow base and an opposite outer edge spaced upward from an outer surface of the hollow base.

Abstract: A headgear assembly includes a first arm member and a second arm member each having a first end and a second, opposing end. The first end of the first arm member has a structure sized and configured to engage a first rotation-resistant coupling of a frame in a manner which prohibits rotation of the first arm member with respect to the frame in a first plane in which the first arm member is located. The first end of the second arm member has a structure sized and configured to engage a second rotation-resistant coupling of the frame in a manner which prohibits rotation of the second arm member with respect to the frame in a second plane in which the second arm member is located. The assembly further includes a strap member coupled to the first and second arm members.

Abstract: An apparatus including a patient interface device formed from a flat substrate that is folded, wherein the patient interface device includes a plurality of seams where sections of the substrate are joined together, and wherein one or more of the plurality of seams form a shape that corresponds to a perimeter of a bottom side of a nose from a first alare corner of the nose to a tip of the nose to a second alare corner of the nose.

Abstract: A headgear assembly includes a first arm member and a second arm member each having a first end and a second, opposing end. The first end of the first arm member has a structure sized and configured to engage a first rotation-resistant coupling of a frame in a manner which prohibits rotation of the first arm member with respect to the frame in a first plane in which the first arm member is located. The first end of the second arm member has a structure sized and configured to engage a second rotation-resistant coupling of the frame in a manner which prohibits rotation of the second arm member with respect to the frame in a second plane in which the second arm member is located. The assembly further includes a strap member coupled to the first and second arm members.

Abstract: A system for obtaining and providing enhanced PAP metrics of a patient's sleep period includes: a pressure support device for use in providing a flow of breathing gas to the patient; a processing unit; and a number of auxiliary devices in wireless communication with the processing unit. Each auxiliary device of the number of auxiliary devices is structured to detect and collect sleep-related data of the patient. The processing unit is programmed to: receive data obtained by a number of sensors of the pressure support device during operation of the pressure support device in providing the flow of breathing gas to the patient; receive supplemental data obtained by the number of auxiliary devices while the pressure support device is not providing the flow of breathing gas to the patient; and determine the enhanced PAP metrics of the sleep period of the patient utilizing the data and the supplemental data.

Abstract: The present disclosure pertains to a system configured to enhance deep sleep in a subject during positive airway pressure therapy. A pressure generator is configured to generate a pressurized flow of breathable gas for delivery to an airway of the subject. Sensors are configured to generate output signals conveying information related to breathing of the subject. One or more hardware processors are configured to cause the pressure generator to generate the pressurized flow of breathable gas in accordance with a positive airway pressure therapy regime based on the information in the output signals; determine sleep stages of the subject based on the information in the output signals; and responsive to the sleep stages indicating the subject is in deep sleep, cause the pressure generator to adjust the pressurized flow of breathable gas to deliver a stimulus to the subject, the stimulus configured to enhance deep sleep in the subject.

Abstract: An interface device is structured to be connected in fluid communication with a source of breathing gas and to provide a flow of breathing gas to the airways of a patient. The interface device includes a support (24), a deformable portion (28) situated on the support, and an interface portion (32) situated on the deformable portion and being structured to be engaged with the patient in the vicinity of the airways, with the deformable portion including a plurality of deformable elements (36) that form a lattice structure and that are connected with the support at a plurality of spaced apart points of connection (44) on the support. The interface device may be formed via an additive manufacturing process.

Abstract: A method of selecting or generating a design for a component of a patient interface device, the method including receiving a scan of at least a portion of a patient's face, receiving preference information about the patient, and generating a custom design or selecting a preexisting design for the component of the patient interface device based on the scan of at least a portion of the patient's face and the preference information, wherein a size or shape of the generated custom design for the component or selected preexisting design for the component is based on the preference information.

Abstract: A system for obtaining and providing enhanced PAP metrics of a patient's sleep period includes: a pressure support device for use in providing a flow of breathing gas to the patient; a processing unit; and a number of auxiliary devices in wireless communication with the processing unit. Each auxiliary device of the number of auxiliary devices is structured to detect and collect sleep-related data of the patient. The processing unit is programmed to: receive data obtained by a number of sensors of the pressure support device during operation of the pressure support device in providing the flow of breathing gas to the patient; receive supplemental data obtained by the number of auxiliary devices while the pressure support device is not providing the flow of breathing gas to the patient; and determine the enhanced PAP metrics of the sleep period of the patient utilizing the data and the supplemental data.

Abstract: A method for the concurrent treatment of obstructive sleep apnea and hypertension in a patient comprises providing a flow of treatment gas to the airway of the patient in accordance with a first set of flow parameters. Determining that the patient has achieved stable breathing while receiving the provided flow of treatment gas in accordance with the first set of parameters. Determining a set of target patient breath parameters from breath data collected from the patient. Adjusting the flow of treatment gas to a different set of flow parameters. Determining that the new patient breath data, collected from the patient, accords with the target patient breath parameters and providing the flow of treatment gas to the patient in accordance with the different set of flow parameters. The target patient breath parameters include a target tidal volume of the patient which is greater than a first tidal volume of the patient.

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.