A61B5/0826

CPAP SYSTEM

An apparatus for humidifying a flow of breathable gas includes a water reservoir and a water reservoir dock forming a cavity structured and arranged to receive the water reservoir in an operative position. The water reservoir comprises a reservoir base including a cavity structured to hold a volume of water, the reservoir base including a main body and a thermally conductive portion provided to the main body. The thermally conductive portion comprises a combined layered arrangement including a metal plate and a thin film, the thin film comprising a non-metallic material and including a wall thickness of less than about 1 mm. The thin film is adapted to form at least a bottom interior surface of the water reservoir exposed to the volume of water, and the metal plate is adapted to form a bottom exterior surface of the water reservoir.

Providing sleep therapy with a pressure therapy system

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.

SYSTEM AND METHOD FOR DETECTING VENTILATORY DEPRESSION AND FOR PROMPTING A PATIENT TO BREATHE

A system and method for prompting a patient experiencing ventilatory depression to breathe includes at least one sensor for detecting ventilatory depression by detecting inadequate breathing or lack of breathing in the patient. The system also includes one or more sensors for determining the type of breathing problem experienced by the patient. A sensor for detecting motion of the patient is used to determine whether the patient is moving. If inadequate or a lack of breathing is detected and the patient is not moving, the system provides verbal prompts or tactile stimuli to prompt the patient to breathe to improve patient ventilation.

Respiration device and method for a respiration device

The present invention relates to a method and a respiration device having a respiration unit for generating an airflow for the respiration and having a monitoring unit. The monitoring unit is used to detect a respiration parameter and to classify events in the respiration on the basis of monitoring of the respiration parameter. In this case, the monitoring unit is configured to carry out an event analysis to recognize an occurrence, which is characteristic for Cheyne-Stokes respiration, of chronologically successive events and for this purpose to ascertain the period length thereof and to compare them to one another and to register the presence of Cheyne-Stokes respiration when the compared period lengths each deviate by less than 40% from one another.

System and method for non-invasively determining an internal component of respiratory effort

A non-invasive method and system is provided for determining an internal component of respiratory effort of a subject in a respiratory study. Both a thoracic signal (T) and an abdomen signal (A) are obtained, which are indicators of a thoracic component and an abdominal component of the respiratory effort, respectively. A first parameter of a respiratory model is determined from the obtained thoracic signal (T) and the abdomen signal (A). The first parameter is an estimated parameter of the respiratory model that is not directly measured during the study. The internal component of the respiratory effort is determined based at least on the determined first parameter of the respiratory model. The first model parameter is determined based on the thorax signal (T) and the obtained abdomen signal (A) without an invasive measurement.

DEVICE, METHOD AND COMPUTER PROGRAM FOR ANALYZING SLEEP BREATHING USING RADAR
20230075040 · 2023-03-09 · ·

A device for analyzing sleep breathing using a radar includes a transceiver configured to transmit a radar signal toward a subject and receive the radar signal reflected from the subject; an average breathing signal calculation unit configured to calculate an average breathing signal of the subject based on the radar signal; a sleep breathing pattern information generation unit configured to generate sleep breathing pattern information of the subject by comparing the radar signal with the average breathing signal; and a sleep breathing event detection unit configured to detect a sleep breathing event based on the sleep breathing pattern information.

Obstructive sleep apnea treatment devices, systems and methods
11471685 · 2022-10-18 · ·

A method of treating a patient, comprising: sensing a biological parameter indicative of respiration; analyzing the biological parameter to identify a respiratory cycle; identifying an inspiratory phase of the respiratory cycle; and delivering stimulation to a hypoglossal nerve of the patient, wherein stimulation is delivered if a duration of the inspiratory phase of the respiratory cycle is greater than a predetermined portion of a duration of the entire respiratory cycle.

Method For Recognizing Abnormal Sleep Audio Clip, Electronic Device

A method for recognizing an abnormal sleep audio clip, includes: obtaining a plurality of initial audio clips collected by a sensor, and determining a target audio clip matching a preset sleep state from the initial audio clips; determining first snore information before the target audio clip and second snore information after the target audio clip based on the initial audio clips; determining a confidence value for the target audio clip based on the first snore information and the second snore information; and determining whether the target audio clip is the abnormal sleep audio clip based on the confidence value of the target audio clip.

Flow therapy system and method

A method of determining a duration of safe apnoea. Information is obtained relating to a respiratory indicator, and a duration of safe apnoea is determined from the obtained information. A respiratory therapy system has one or more patient interfaces. A processor is configured to determine a duration of safe apnoea based on obtained information relating to a respiratory indicator.

WEARABLE DEVICE FOR IDENTIFYING BREATHING STATE OF USER
20230128404 · 2023-04-27 ·

A wearable device is provided. The wearable device includes a memory configured to store instructions, at least one display having a display area, a frame configured to support the at least one display, the frame including a nose pad in contact with a part of a user's body wearing the wearable device, a photoplethysmography (PPG) sensor exposed through at least a portion of the frame in contact with other part of the user's body, at least one microphone disposed in the nose pad, and a processor. The processor, when executing the instructions, is configured to identify a breathing state of the user, based at least in part on first data acquired through the PPG sensor and second data acquired through the at least one microphone.