Abstract: A methodology and apparatus for determining ventilator settings including an end expiratory pressure setting, pressure swing, resistive unloading and target ventilation for delivering ventilatory support based upon generalized patient ventilation characteristics and/or disease classifications. An apparatus may be programmed with the instructions to accomplish the methodology interactively by prompting the user/physician during setup and calculating settings based upon measurements or input responses. Pre-assigned values associated with ventilation characteristics or disease classifications may be combined with a base pressure value or measured values to provide patient customized settings or adjustments to determine pressure levels for the delivery of ventilatory support.

Abstract: A method, such as in a controller associated with a respiratory therapy device, determines whether high flow therapy is being used by a patient. The method may include determining whether a property of a flow of air being delivered by a respiratory therapy device along an air circuit to an unsealed patient interface contains a significant oscillation within a breathing rate frequency band. The method may also include generating, dependent on the determination, an indication of whether high flow therapy is being used by the patient.

Abstract: A backspill prevention apparatus prevents water from a humidifier portion of a positive airway pressure (PAP) device from reaching a blower motor of a PAP device. The backspill prevention apparatus can include a variety of different devices, and is placed somewhere along an air passageway between a blower motor and a humidifier portion of a PAP device.

Abstract: Headgear for a respiratory mask includes a strap arrangement comprising front strap portions adapted to be disposed over a patient's cheeks and each having a connector adapted for attachment to an airway interfacing portion, and a cover provided to each front strap portion and structured to at least partially encapsulate the front strap portion. The cover includes side portions adapted to be wrapped around the front strap portion and releasably fastened to one another.

Abstract: The present technology relates to methods and apparatus to provide ventilation to patients. In particular, the present technology relates to changing ventilator parameters to match changing patient metabolic demand.

Abstract: A system for therapy may include a mask (200) for a patient having a frame, cushion, forehead support and a light (100). The mask is connectable to a respiratory treatment apparatus, such as a flow generator, to receive breathable gas for a respiratory therapy. The light may also be connected to the power system and/or control system of the apparatus. A light may also be included in a module, such as a docking station, for a respiratory treatment apparatus. The lights may be controlled by one or more processors, and may be responsive to detected conditions, to assist with therapy. For example, the light may be turned on at a predetermined time or may be synchronized with the patient's sleep state, to assist in waking up the patient or re-setting the patient's circadian rhythm. Other components, such as sound and aroma generators of the system, may also be controlled for such therapies.

Abstract: A ventilator device delivers ventilatory support to a patient in a back up timed mode when patient respiration is not detected or a spontaneous mode when patient respiration is detected. The timing threshold governing the back-up mode is chosen to deviate from normal expected respiration time for the patient to promote patient initiated ventilation in the spontaneous mode but permit back-up ventilation in the event of apnea. Automated adjustments to the timing threshold during the timed mode are made from the less vigilant timing threshold to a more vigilant threshold at or near a timing of normal expected breathing of the patient. Such adjustments may be made from a minimum to a maximum vigilance timing settings or incrementally there between as a function of time in the timed mode which is preferably the number of delivered machine breaths.

Abstract: An apparatus for improving patient comfort during CPAP therapy includes a venting arrangement arranged to reduce expiratory pressure. A mask system for providing CPAP therapy to a patient includes a mask; a flow generator to provide a flow of pressurized breathable gas; a tube to connect the mask to the flow generator; and a venting arrangement arranged to reduce expiratory pressure.

Abstract: A cushion for a patient interface includes an outer membrane providing a sealing structure adapted to form a seal with the patient's face in use and an underlying membrane generally spaced away from the outer membrane. The underlying membrane provides a support structure for the outer membrane. The outer membrane and the underlying membrane each have an inner edge which defines an aperture to receive the patient's nose in use. The underlying membrane is segmented along its inner edge.

Abstract: A fastenable air delivery conduit includes a body portion having a supply end and a delivery end and a fastener that substantially extends from the supply end to the delivery end. The fastener, when engaged, forms the body portion into a fastened configuration, and when disengaged, forms the body portion into an unfastened configuration. The body portion defines a longitudinal axis when in the fastened configuration, and the fastener extends from the source end to the delivery end of the body portion at an angle that is non-parallel with the longitudinal axis of the conduit.

Abstract: Methods and apparatus for detection and treatment of respiratory disorders using implanted devices are described. In one form, afferent nerves are electrically or electro-mechanically stimulated to increase the tone of upper airway muscles. Detection of respiratory disorders is carried out using electrodes implanted in sub-pectoral regions. Open and closed airway apneas are distinguished using a combination of acoustic detectors and electrical transducers.

Abstract: An impeller includes a top shroud, a bottom shroud, and a plurality of vanes extending from the top shroud to the bottom shroud. The top and bottom shrouds are generally planar, and a lower edge of each vane tapers from an outer edge of the bottom shroud to a transverse tip edge thereof.

Abstract: A seal is provided for a chassis assembly of a flow generator configured to provide a flow of breathable gas. The chassis assembly includes an upper chassis and a lower chassis. The seal includes a blower receptacle sealing portion configured to seal a blower receptacle of the chassis assembly configured to receive a blower configured to generate the flow of breathable gas; a flow sensor sealing portion configured to seal a flow sensor provided in the chassis assembly and configured to measure the flow of breathable gas; a blower mount configured to receive a portion of the blower and mount the blower to the seal; and a blower mount suspension configured to connect the blower mount to the blower receptacle sealing portion, wherein in an assembled condition the seal and the chassis assembly define a flow path from an inlet of the chassis assembly to the blower receptacle of the chassis assembly to an outlet of the chassis assembly.

Abstract: A respiratory mask assembly includes a rigid mask frame and a cushion. A clip secures the cushion to the frame.

Abstract: According to certain example embodiments of this invention, there is provided an apparatus for treatment of a patient with both sleep-disordered breathing and diabetes. A PAP device may be configured to provide a supply of pressurized breathable gas. At least one glycemia sensor also may be provided. A controller may be operable to receive a signal from the at least one glycemia detector and may be further operable to analyze the signal for an indication of a glycemia abnormality (e.g., hypoglycemia, hyperglycemia, diabetic coma, etc.). Optionally, when the signal indicates that the patient is experiencing a diabetic event, an alert may be generated and/or a drug delivery unit may administer an appropriate treatment to the patient.

Abstract: A CPAP device includes a flow generator including an outlet, a humidifier including an inlet, and an adaptor connector between the outlet of the flow generator and the inlet of the humidifier. The connector includes a flexible and conformable sealing portion that is movable to accommodate misalignment.