Abstract:
A patient interface comprises a frame, a headgear, a manifold and two nasal prongs. The frame may be recessed from the face of the patient, and preferably from the manifold so that the manifold may deform or move with respect to the face of the patient. The manifold may be further configured to be compliant in the direction of engagement with the patient's face, such as in the anterior direction. These features may allow the manifold to engage with the face of the patient, such as the upper lip, without exerting a significant pressure which may lead to patient discomfort. The manifold may also be configured to be rotatable with respect to the frame, for example by a grip feature which may be configured to be held in one hand for rotation.
Abstract:
The present technology relates to a kit comprising a device for providing breathing gas to a patient and a specific facing as well as to a method of setting the mode of operation of such a device.
Abstract:
The present technology relates to a pad for forming a seal forming structure against a user's skin for use with a patient interface, the pad comprising, a base layer, a fibre layer comprising a plurality of fibers for contacting a patient's skin, and a connection layer for connecting the fibers to the base material, wherein the base layer and/or the fibre layer is/are adapted to act as a reservoir for substances. Furthermore, it relates to a set of pads, a kit and a patient interface.
Abstract:
A respiratory apparatus for treating a patient with a respiratory disorder includes a blower configured to generate a supply of pressurized breathable gas. The blower includes a gas inlet and a gas outlet. The gas outlet is configured to deliver the generated supply of pressurized breathable gas to an outlet of the respiratory apparatus for delivery to the patient. The blower also includes an impeller configured to rotate to generate the supply of pressurized gas. The impeller has a single shroud with a plurality of blades extending from a surface of the shroud in an upstream direction relative to the direction of flow of the pressurized breathable gas. Each of the plurality of blades radiate outwards from a hub in the shroud. The hub is configured to receive a motor shaft. In addition, the outer diameter of the shroud varies between maximum portions with a maximum outer diameter and minimum portions with a minimum outer diameter.
Abstract:
It is discloses a patient interface comprising a seal forming portion, a pad, and a cushion. The seal forming portion may comprise a base surface and a plurality of fibers fixed to and extending away from said base surface for contacting a patient's skin. The cushion may comprise at least along a portion of the circumference a first structure having an elongate section joined with at least one end section oriented substantially perpendicular or at an angle to the elongate section. A first end A of the elongate section may be connected or connectable to a frame member. The end section may be provided at an opposing second end B of the elongate section. The pad may comprise a resilient foam material layer with the seal forming portion. The pad may be adapted to be connected to the cushion.
Abstract:
The technology provides for a cushion assembly or a tool for forming the cushion assembly for a patient interface delivery of a supply of pressurised air or breathable gas to an entrance of a patient's airways. The cushion assembly has an inferior surface and a mask connection portion, and includes a pad arranged on the inferior surface for sealingly contacting a wearer's face in use.
Abstract:
The present specification is directed to a seal forming structure for a patient interface for delivery of air to a patient's airway, wherein the seal forming structure comprises a first section of a thermoformable material and a second section of another material. The present specification is also directed to a patient interface comprising such a seal forming structure, wherein the patient interface further comprises a shell. The specification is also directed to methods for manufacturing such a patient interface.
Abstract:
It is discloses a patient interface 3000 comprising a seal forming portion 11, a pad 10, and a cushion 20. The seal forming portion 11 may comprise a base surface 111 and a plurality of fibers 112 fixed to and extending away from said base surface 111 for contacting a patient's skin. The cushion 20 may comprise at least along a portion of the circumference a first structure 22 having an elongate section 24 joined with at least one end section 26 oriented substantially perpendicular or at an angle to the elongate section 24. A first end A of the elongate section 24 may be connected or connectable to a frame member 30. The end section 26 may be provided at an opposing second end B of the elongate section 24. The pad 10 may comprise a resilient foam material layer with the seal forming portion 11. The pad 10 may be adapted to be connected to the cushion 20.