A system and method to match an interface to the face of a user for respiratory therapy. A facial image of the user is stored. Facial features based on the facial image are determined. A database stores facial profiles based on facial features and a corresponding plurality of interfaces. A database stores operational data of respiratory therapy devices with the plurality of corresponding interfaces. A selection engine is coupled to the databases. The selection engine is operative to select an interface for the user from the plurality of corresponding interfaces based on a desired outcome based on the stored operational data and the facial features. The collected data may also be employed to determine whether the selected interface is correctly fitted to the face of the user.
Disclosed are methods, systems, and devices for providing a personalized humidification level. A control system receives, from a first sensor, one or more environmental parameters regarding conditions of the environment. The control system receives, from a second sensor, one or more physiological parameters associated with a user within the environment. The control system determines an action associated with a desired change in the humidity within the environment based, at least in part, on the one or more environmental parameters and the one or more physiological parameters. The control system causes, at least in part, a performance of the action associated with the change in the humidity in the environment based, at least in part, on moisture outputted by a humidifier module. The methods and devices perform the same functionality as the control system.
A data gathering system (100) has at least one processor configured to perform a compression scheme for wireless transmission. The compression scheme may include amplitude reduction, where a difference between every two consecutive values of a plurality of values is computed and stored in an array. Additionally, the compression scheme may include bit packing, where outlier values are output in a first bit length, and remaining values are output in a second bit length, where the second bit length is determined so as to minimize a total memory cost for all values. Further, the system may store data recorded at different points in time in an array of data chunks, and wirelessly transmit the array of data chunks simultaneously.
A method for analyzing sounds made by an individual during a sleep session includes receiving audio data associated with the sleep session. The sleep session is divided into at least a plurality of primary segments. The method further includes determining, based at least in part on the audio data, whether one or more snoring sounds were made by the individual during each of at least two of the plurality of primary segments. The method further includes determining a snore score for each of a plurality of secondary segments of the sleep session. Each of the plurality of secondary segments contains two or more of the plurality of primary segments. The method further includes generating, based at least in part on the snore score for each of the plurality of secondary segments, a human-perceivable audio sample of at least one of the plurality of secondary segments.
A method includes receiving a flow rate signal associated with a user interface of a respiratory therapy device used by a user engaging in a sleep session. The method further includes identifying a plurality of cardiogenic oscillations from the flow rate signal. The method further includes determining consecutive peak distances based at least in part on the identified plurality of cardiogenic oscillations. The method further includes calculating heart rate information based on the consecutive peak distances.
A method for predicting a subjective comfort level of a user of a respiratory therapy system is disclosed as follows. Data associated with the user of the respiratory therapy system during a therapy session is received. At least one parameter associated with the user is determined based at least in part on a first portion of the received data. A comfort score is determined based at least in part on the determined at least one parameter. The comfort score is indicative of the subjective comfort level of the user of the respiratory therapy system during at least a portion of the therapy session.
A wireless communications enabled memory card (100) has a card interface (104) for wired communicating with a medical device. The memory card has a non-volatile memory (106) for storing therapy data provided by the medical device. The memory card may have a Wi-Fi transceiver (110) for joining a Wi-Fi network. The memory card may receive authentication information for joining the network from the medical device via the card interface or from a wireless device via a direct Wi-Fi connection. After joining the Wi-Fi network, the memory card may transmit the therapy data to a remote server (130).
G16H 10/65 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données spécifiques de patients, p.ex. pour des dossiers électroniques de patients stockées sur des supports d’enregistrement portables, p.ex. des cartes à puce, des étiquettes d’identification radio-fréquence [RFID] ou des CD
8.
SYSTEMS AND METHODS FOR LEAK DETECTION IN A RESPIRATORY THERAPY SYSTEM
Various implementations of the present disclosure are directed to systems and methods for leak detection in a respiratory therapy system using acoustic data. According to some implementations, a method includes receiving acoustic data associated with airflow caused by operation of a respiratory therapy system during a sleep session of a user. The method also includes analyzing at least a portion of the acoustic data to determine a value of a parameter associated with the at least a portion of the acoustic data. The method further includes determining an occurrence of a leak during the sleep session in response to the determined value of the parameter satisfying a condition.
A61M 16/16 - Dispositifs pour humidifier l'air à respirer
G16H 40/40 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour la gestion d’équipement ou de dispositifs médicaux, p.ex. pour planifier la maintenance ou les mises à jour
9.
SYSTEMS AND METHODS FOR DETECTING OCCLUSIONS IN HEADGEAR CONDUITS DURING RESPIRATORY THERAPY
A system and method detects an occlusion in a respiratory therapy system. The system and method includes determining an acoustic signature for a conduit of a headgear user interface. The determined acoustic signature is analyzed to identify an anomaly in the acoustic signature. In response to the determined acoustic signature being identified as anomalous, a determination is made if the identified anomaly relates to an occlusion of the conduit.
Certain aspects and features of the present disclosure relate to evaluating the sleep performance of a cohort of multiple individuals sleeping in a shared environment (e.g., a single bed, a single room, a set of adjacent rooms, or a single household). Individual or concerted sleep performance scores can be determined, as well as other sleep performance metrics. The evaluation of sleep performance for the entire cohort can be useful when one of the individuals is being treated (e.g., with a respiratory therapy device) for a sleep-related and/or respiratory disorder. Evaluation of the cohort can help identify actions that can be taken to improve the sleep performance of all individuals in the cohort. In some cases, parameters of a user's therapy device are adjusted based on the monitored sleep performance of another individual in the cohort.
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p.ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p.ex. bouche-à-bouche; Tubes trachéaux
G16H 40/67 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement à distance
G16H 10/20 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des essais ou des questionnaires cliniques électroniques
G16H 50/50 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour la simulation ou la modélisation des troubles médicaux
11.
SYSTEMS AND METHODS FOR DETERMINING MOVEMENT DURING RESPIRATORY THERAPY
The present disclosure relates to a method for determining movement of a user while using a respiratory therapy system is disclosed. Acoustic data associated with the user of the respiratory therapy system is received. The received acoustic data is analyzed. Based at least in part on the analyzed acoustic data, a movement event associated with the user is determined.
A61M 16/06 - Masques respiratoires ou pour l'anesthésie
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p.ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
12.
SYSTEMS FOR DETECTING A LEAK IN A RESPIRATORY THERAPY SYSTEM
A method for characterizing a leak in a respiratory therapy system comprises identifying a specific model of a user interface and a conduit of the respiratory therapy system. The method further comprises selecting one of a plurality of predefined pressure versus flow curves based on the identified user interface and conduit. The predefined pressure versus flow curve is associated with airflow characteristics of the respiratory therapy system when the identified user interface is coupled to the identified conduit. The method further comprises receiving pressure data and flow data associated with air flowing in the respiratory therapy system. The method further comprises comparing the pressure data and the flow data to the predefined pressure versus flow curve. The method further includes characterizing, based at least in part on the comparing, a leak in the respiratory therapy system that occurred during the use of the respiratory therapy system.
Systems and methods are disclosed for categorizing and/or characterizing a user interface. The systems and methods include generating acoustic data associated with an acoustic reflection of an acoustic signal, the acoustic reflection being indicative of, at least in part, one or more features of a user interface coupled to a respiratory therapy device via a conduit. The systems and methods further include analyzing the generated acoustic data. The systems and methods further include categorizing and/or characterizing the user interface based, at least in part, on the analyzed acoustic data.
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p.ex. bouche-à-bouche; Tubes trachéaux
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
14.
SYSTEMS AND METHODS FOR DETECTING RAINOUT IN A RESPIRATORY THERAPY SYSTEM
A method of detecting rainout in a respiratory therapy system that includes a conduit fluidly coupled to a user interface comprises generating, via at least one microphone, acoustic data representative of noise associated with the respiratory therapy system. The method further comprises analyzing the acoustic data to detect a presence of liquid in the respiratory therapy system. The method further comprises causing an action to be performed, based on the detected presence of the liquid.
A method includes receiving data associated with a sleep session of a user. The method also includes determining that the user is experiencing or has experienced an event based at least in part on the data. The method also includes causing pressurized air to be directed from a respiratory device to a multi-compartment bladder in response to determining that the user is experiencing or has experienced the event to aid in modifying a position of a head of the user.
A system includes a respiratory therapy system, a memory, and a control system. The respiratory therapy system includes a respiratory therapy device supplying pressurized air and a user interface coupled to the respiratory therapy device via a conduit. The user interface engages the individual and aids in directing the pressurized air to an airway of the individual. The system can be used to cause an acoustic signal to be directed into the airway of the individual, via the conduit and the user interface; generate acoustic data representative of one or more reflections of the acoustic signal caused by a portion of the airway of the individual, an obstruction within the airway of the individual, or both; analyze the acoustic data to determine a value of a parameter associated with the airway of the individual; and cause an action to be performed, based on the determined value of the parameter.
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p.ex. bouche-à-bouche; Tubes trachéaux
A61M 16/10 - Préparation de gaz ou vapeurs à respirer
G16H 40/67 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement à distance
17.
APPARATUS, SYSTEM, AND METHOD FOR PHYSIOLOGICAL SENSING IN VEHICLES
Methods and apparatus provide physiological movement detection, such as gesture, breathing, cardiac and/or gross motion, such as with sound, radio frequency and/or infrared generation, by electronic devices such as vehicular processing devices. The electronic device in a vehicle may, for example, be any of an audio entertainment system, a vehicle navigation system, and a semi-autonomous or autonomous vehicle operations control system. One or more processors of the device, may detect physiological movement by controlling producing sensing signal(s) in a cabin of a vehicle housing the electronic device. The processor(s) control sensing, with a sensor, reflected signal(s) from the cabin. The processor(s) derive a physiological movement signal with the sensing signal and reflected signal and generate an output based on an evaluation of the derived physiological movement signal. The output may control operations or provide an input to any of the entertainment system, navigation system, and vehicle operations control system.
A system and method for providing a unique signature for proprietary data. The proprietary data may be transmitted to multiple trusted parties. Each of the trusted parties will have proprietary data with a unique signature to that trusted party. The signature allows a user to determine the source of the proprietary data breach via the signature.
Methods and devices provide physiological movement detection, such as gesture, breathing, cardiac and/or gross body motion, with active sound generation such as for an interactive audio device. The processor may evaluate, via a microphone coupled to the interactive audio device, a sensed audible verbal communication. The processor may control producing, via a speaker coupled to the processor, a sound signal in a user's vicinity. The processor may control sensing, via a microphone coupled to the processor, a reflected sound signal. This reflected sound signal is a reflection of the generated sound signal from the vicinity or user. The processor may process the reflected sound, such as by a demodulation technique, to derive a physiological movement signal. The processor may generate, in response to the sensed audible verbal communication, an output based on an evaluation of the derived physiological movement signal.
G08B 21/04 - Alarmes pour assurer la sécurité des personnes réagissant à la non-activité, p.ex. de personnes âgées
G06F 21/32 - Authentification de l’utilisateur par données biométriques, p.ex. empreintes digitales, balayages de l’iris ou empreintes vocales
G08B 5/22 - Systèmes de signalisation optique, p.ex. systèmes d'appel de personnes, indication à distance de l'occupation de sièges utilisant une transmission électromécanique
G08B 21/06 - Alarmes pour assurer la sécurité des personnes indiquant un état de sommeil, p.ex. alarmes contre l'assoupissement
G08B 21/22 - Alarmes de situation réagissant à la présence ou à l'absence de personnes
G08B 27/00 - Systèmes d'alarme dans lesquels la condition déclenchant l'alarme est signalée par une station centrale à plusieurs sous-stations
G10L 25/51 - Techniques d'analyses de la parole ou de la voix qui ne se limitent pas à un seul des groupes spécialement adaptées pour un usage particulier pour comparaison ou différentiation
G10L 25/78 - Détection de la présence ou de l’absence de signaux de voix
20.
SYSTEMS AND METHODS FOR IDENTIFYING USER BODY POSITION DURING RESPIRATORY THERAPY
A system for identifying a body position of a user of a respiratory therapy system includes a sensor, a memory, and a control system. The sensor is configured to generate airflow data associated with the user. The memory stores machine-readable instructions. The control system includes one or more processors configured to execute the machine-readable instructions to receive the airflow data associated with the user during a sleep session. The control system is further configured to determine one or more features associated with the airflow data, and identify the body position of the user during a first portion of the sleep session based at least in part on the determined one or more features. The control system is further configured to cause an action to be performed based at least in part on the identified body position of the user.
A method includes generating, using one or more sensors, data. The data includes (i) environmental data related to an environment of a user and (ii) physiological data associated with the user during a sleep session. Based at least in part on the physiological data, a comfort score associated with the user during the sleep session is determined. The comfort score is indicative of a comfort level of the user during at least a portion of the sleep session. Based at least in part on the determined comfort score, a setting of one or more devices associated with the environment of the user is adjusted.
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
G16H 10/60 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données spécifiques de patients, p.ex. pour des dossiers électroniques de patients
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
22.
SYSTEMS AND METHODS FOR DETERMINING A LENGTH AND/OR A DIAMETER OF A CONDUIT
A method includes generating acoustic data representative of at least one or more reflections of an acoustic signal. The one or more reflections are indicative of a length and/or a diameter of a conduit coupled to a respiratory therapy device. The method further includes analyzing the acoustic data to determine the length and/or diameter of the conduit. In some cases, analyzing the acoustic data includes determining a resonant frequency of the conduit, and determining the length of the conduit based at least in part on the resonant frequency. In some cases, analyzing the acoustic data includes comparing the acoustic data to predetermined sets of acoustic data that each correspond to a known length and/or diameter of the conduit, and selecting one of the predetermined sets of acoustic data that best matches the generated acoustic data. The selected set of acoustic data corresponds to the length and/or diameter of the conduit.
Automatic adjustment of an oral appliance, such as a mandibular repositioning device, is disclosed. Sensor data can be received from one or more sensors external to a user using the oral appliance. An adjustment associated with the oral appliance is determined using the sensor data, and an action can be taken to facilitate applying the determined adjustment. Such actions can include transmitting a signal to the oral appliance to effect the adjustment (e.g., using an actuator or onboard electrical stimulator), presenting adjustment parameters to help the user manually make the adjustment, activating actuators in an oral appliance storage receptacle the next time the oral appliance is stored, or other such actions. Adjustments can be made dynamically in real-time or asynchronously (e.g., between sleep sessions).
A61F 5/56 - Dispositifs pour prévenir le ronflement
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
A61N 1/36 - Application de courants électriques par électrodes de contact courants alternatifs ou intermittents pour stimuler, p.ex. stimulateurs cardiaques
24.
SYSTEMS AND METHODS FOR DETERMINING USAGE OF A RESPIRATORY THERAPY SYSTEM
A method includes generating, by a sensor, physiological data associated with a user during a sleep session. The method also includes processing, by an electronic device including one or more processors, the generated physiological data to distinguish between on-therapy data and off-therapy data. The on-therapy data is the generated physiological data while a respiratory therapy system is coupled to the user and supplies pressurized air to an airway of the user. The off-therapy data is the generated physiological data while the respiratory therapy system is not supplying pressurized air to the airway of the user. The method also includes determining, by the electronic device, a sleep measure based at least in part on the off-therapy data.
The disclosure provides methods for diagnosis or prediction of the likelihood of a subject experiencing obstructive sleep apnea, determined at least in part by measuring the degree of tongue fat in a subject using, e.g., thermal imaging, THz imaging or other multispectral imaging.
G06V 10/764 - Dispositions pour la reconnaissance ou la compréhension d’images ou de vidéos utilisant la reconnaissance de formes ou l’apprentissage automatique utilisant la classification, p.ex. des objets vidéo
G06V 10/143 - Détection ou éclairage à des longueurs d’onde différentes
26.
SYSTEMS AND METHODS FOR DIAGNOSING OPERATIONAL ISSUES IN A RESPIRATORY SYSTEM
The present disclosure relates to a method for diagnosing an operational issue in a respiratory therapy system. A command is received, via an external device, to begin diagnosing the operational issue in the respiratory therapy system. One or more sensors of the external device are caused to generate acoustic data, which is indicative of one or more sounds emanating from the respiratory therapy system. At least a portion of the generated acoustic data is analyzed to identify (i) a location of the operational issue in the respiratory therapy system, (ii) one or more causes of the operational issue in the respiratory therapy system, or (iii) both (i) and (ii).
Airflow parameters (e.g., flow rate and airflow pressure) of airflow generated by a flow generator of a respiratory therapy system can be measured during use and processed to automatically identify user interface and/or conduit identification information. This user interface and/or conduit identification information can be used to adjust settings of the respiratory therapy device, generate notifications (e.g., notifications of a detected change in user interface without concomitant, expected adjustment of settings of the respiratory therapy device), or otherwise facilitate respiratory therapy of the user or of other users. User interface and/or conduit identification information can be indicative of specific characteristics of the user interface and/or conduit (e.g., resonant frequencies, impedance, and the like), a style of the user interface (e.g., a face mask, nasal mask, or nasal pillow) and/or style of conduit, a specific manufacturer, a specific model, or other such identifiable information.
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
G16H 40/40 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour la gestion d’équipement ou de dispositifs médicaux, p.ex. pour planifier la maintenance ou les mises à jour
G16H 10/20 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des essais ou des questionnaires cliniques électroniques
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p.ex. bouche-à-bouche; Tubes trachéaux
A61M 16/06 - Masques respiratoires ou pour l'anesthésie
A method includes receiving first physiological data associated with a user. The method also includes determining a first emotion score associated with the user based at least in part on the first physiological data. The method also includes modifying one or more settings of a respiratory therapy system responsive to determining that the first emotion score satisfies a predetermined condition.
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p.ex. bouche-à-bouche; Tubes trachéaux
A61B 5/16 - Dispositifs pour la psychotechnie; Test des temps de réaction
A61B 5/0205 - Evaluation simultanée de l'état cardio-vasculaire et de l'état d'autres parties du corps, p.ex. de l'état cardiaque et respiratoire
A61M 21/02 - Autres dispositifs ou méthodes pour amener un changement dans l'état de conscience; Dispositifs pour provoquer ou arrêter le sommeil par des moyens mécaniques, optiques ou acoustiques, p.ex. pour mettre en état d'hypnose pour provoquer le sommeil ou la relaxation, p.ex. par stimulation directe des nerfs, par hypnose ou par analgésie
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
A system includes a respiratory therapy system, a memory device, and a control system. The respiratory therapy system includes a respiratory therapy device supplying pressurized air, and a user interface coupled to the respiratory therapy device via a conduit to direct the pressurized air to an airway of a user. The memory device stores machine-readable instructions. The control system includes a processor(s) to execute the machine-readable instructions to: generate data, during a current sleep session, associated with a user of a respiratory therapy system; analyze the generated data to determine a value of a first metric that is associated with a sleep disordered breathing (SDB) condition; analyze the generated data to determine a value of a second metric that is associated with a health condition other than the SDB condition; and based at least in part on the determined value of the second metric, cause an action to be performed.
A method of analyzing data related to use of a respiratory therapy system by a user comprises receiving a first type of data, determining a first value of a first parameter based at least in part on the first type of data, identifying a desired second type of data, transmitting a request for consent to receive the second type of data, and determining, based at least in part on the second type of data, a second value of the first parameter, a value of a second parameter, or both. The first type of data and the first parameter are related to the user's use of the respiratory therapy system. The identification of the second type of data is based at least in part on the first type of data, the first value of the first parameter, an accuracy of the first value of the first parameter, or any combination thereof.
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p.ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
G16H 10/60 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données spécifiques de patients, p.ex. pour des dossiers électroniques de patients
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
G16H 50/70 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour extraire des données médicales, p.ex. pour analyser les cas antérieurs d’autres patients
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
A61B 5/08 - Dispositifs de mesure pour examiner les organes respiratoires
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p.ex. tremblement de la tête ou des mains ou mobilité d'un membre
31.
SYSTEMS AND METHODS FOR DETECTING AN INTENTIONAL LEAK CHARACTERISTIC CURVE FOR A RESPIRATORY THERAPY SYSTEM
A plurality of flow rate values associated with pressurized air directed to an airway of a user of a respiratory therapy system is received. A plurality of pressure values associated with the pressurized air directed to the airway of the user is received. A first time associated with a first breath of the user and a second time associated with a second breath of the user are identified. The plurality of flow rate values is filtered based at least in part on the identified first time and the identified second time. The filtering produces a subset of the plurality of flow rate values. An intentional leak characteristic curve for the respiratory therapy system is determined using at least two of the subset of the plurality of flow rate values and the corresponding pressure values for said at least two of the subset of the plurality of flow rate values.
A method and system for determining a positional sleep disordered breathing (pSDB) status associated with a respiratory device user is disclosed. Airflow data associated with the user is received. The airflow data is analyzed to identify a first time period of suspected arousal and a second time period of suspected arousal. A first time section between the identified first time period and the identified second time period is determined. The airflow data associated with the determined first time section is analyzed to identify (i) an indication of one or more respiratory events and/or (ii) an indication of one or more therapy events. Based at least in part on the (i) identified indication of one or more respiratory events and/or (ii) identified indication of one or more therapy events, the pSDB status of the user is determined, where the pSDB status is indicative of whether or not the user has pSDB.
A method includes receiving a first value for each of a plurality of parameters, each of the first values being associated with a user and a first day. The method also includes receiving a second value for each of the plurality of parameters, each of the second values being associated with the user and a second day that is subsequent to the first day. The method also includes determining, for each of the plurality of parameters, a trend indication. The method also includes determining a base weight value for each of the plurality of parameters and multiple pairs of the plurality of parameters. The method also includes causing a message to be communicated to the user that is based at least in part on the determined base weight values.
An apparatus, system, and method monitors the motion, breathing, heart rate and sleep state of subjects, e.g., humans, in a convenient, non-invasive/non-contact, and low-cost fashion. More particularly, the motion, breathing, and heart rate signals are obtained through processing applied to a raw signal obtained in a non-contact fashion, typically using a radio-frequency sensor. Periods of sleep disturbed respiration, or central apnea can be detected through analysis of the respiratory signal. The mean heart rate, and derived information, such as the presence of cardiac arrhythmias can be determined from the cardiac signal. Motion estimates can be used to recognize disturbed sleep and periodic limb movements. The sleep state may be determined by applying a classifier model to the resulting streams of respiratory, cardiac and motion data. A means for display of the sleep state, respiratory, cardiac, and movement status may also be provided.
A61B 5/0205 - Evaluation simultanée de l'état cardio-vasculaire et de l'état d'autres parties du corps, p.ex. de l'état cardiaque et respiratoire
A61B 5/0507 - Détection, mesure ou enregistrement pour établir un diagnostic au moyen de courants électriques ou de champs magnétiques; Mesure utilisant des micro-ondes ou des ondes radio utilisant des micro-ondes ou des ondes térahertz
A61B 5/08 - Dispositifs de mesure pour examiner les organes respiratoires
A61B 5/113 - Mesure du mouvement du corps entier ou de parties de celui-ci, p.ex. tremblement de la tête ou des mains ou mobilité d'un membre se produisant au cours de la respiration
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p.ex. basé sur des systèmes experts médicaux
35.
SYSTEMS AND METHODS FOR GENERATING CUSTOM MESSAGES TO ENCOURAGE A BEHAVIORAL RESPONSE
A method for generating one or more custom messages for a user to aid in encouraging a behavioral response includes receiving physiological data associated with a user during a first time period, the first time period including at least one sleep session. The method further includes determining a first parameter associated with the user based on a first portion of the physiological data. The method further includes determining a second parameter associated with the user based on a second portion of the physiological data. The method further includes generating a custom message based on the determined first parameter and the determined second parameter to aid in encouraging a behavioral response, the custom message including information associated with the determined first parameter and information associated with the determined second parameter. The method further includes causing the custom message to be communicated to the user.
G16H 20/70 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mentales, p.ex. la thérapie psychologique ou le training autogène
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
A method includes causing first media content to be displayed on a display device, the first media content including a first prompt to perform a first activity. The method also includes receiving data associated with the user, the data including motion data associated with movement of the user and physiological data associated with the user. The method also includes determining whether the user is performing the first activity based at least in part on the physiological data, the motion data, or both. The method also includes determining a first physiological parameter associated with the user subsequent to the first prompt based at least in part on the physiological data associated with the user. The method also includes determining whether the first physiological parameter exceeds a predetermined threshold.
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
G06F 3/01 - Dispositions d'entrée ou dispositions d'entrée et de sortie combinées pour l'interaction entre l'utilisateur et le calculateur
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p.ex. tremblement de la tête ou des mains ou mobilité d'un membre
A61B 5/0205 - Evaluation simultanée de l'état cardio-vasculaire et de l'état d'autres parties du corps, p.ex. de l'état cardiaque et respiratoire
A61B 5/05 - Détection, mesure ou enregistrement pour établir un diagnostic au moyen de courants électriques ou de champs magnétiques; Mesure utilisant des micro-ondes ou des ondes radio
A processing system includes methods to promote sleep. The system may include a monitor such as a non-contact motion sensor from which sleep information may be determined. User sleep information, such as sleep stages, hypnograms, sleep scores, mind recharge scores and body scores, may be recorded, evaluated and/or displayed for a user. The system may further monitor ambient and/or environmental conditions corresponding to sleep sessions. Sleep advice may be generated based on the sleep information, user queries and/or environmental conditions from one or more sleep sessions. Communicated sleep advice may include content to promote good sleep habits and/or detect risky sleep conditions. In some versions of the system, any one or more of a bedside unit 3000 sensor module, a smart processing device, such as a smart phone or smart device 3002, and network servers may be implemented to perform the methodologies of the system.
A61M 21/02 - Autres dispositifs ou méthodes pour amener un changement dans l'état de conscience; Dispositifs pour provoquer ou arrêter le sommeil par des moyens mécaniques, optiques ou acoustiques, p.ex. pour mettre en état d'hypnose pour provoquer le sommeil ou la relaxation, p.ex. par stimulation directe des nerfs, par hypnose ou par analgésie
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
G10L 15/26 - Systèmes de synthèse de texte à partir de la parole
A method includes data associated with a sleep session of a user, including respiration data associated with the user during at least a portion of the sleep session and audio data reproducible as one or more sounds during at least a portion of the sleep session. The method also includes determining a respiration signal associated with the user during the sleep session based, at least in part, on at least a portion of the data. The method also includes identifying an event experienced by the user during the sleep session based, at least in part on, at least a portion of the data. The method also includes causing to be communicated to the user via a user device a graphical representation of a portion of the respiration signal and an event indication that aids in identifying the identified event within the graphical representation of the portion of the respiration signal.
Systems and methods for generating and presenting a multi-component health score are disclosed. The health score can be generated from a set of weighted component scores each associated with a particular component being evaluated. Each component score can be generated based on a combination of first physiological data collected during a sleep session, second physiological data collected during a duration adjacent a sleep session, and subjected feedback data associated with the sleep session. Dynamic adjustments of weightings and presentation in a format indicating the contribution of each component to the total health score can facilitate good habits and healthy practices.
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
G16H 50/70 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour extraire des données médicales, p.ex. pour analyser les cas antérieurs d’autres patients
G16H 10/60 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données spécifiques de patients, p.ex. pour des dossiers électroniques de patients
Radio frequency motion sensors may be configured for operation in a common vicinity so as to reduce interference. In some versions, interference may be reduced by timing and/or frequency synchronization. In some versions, a master radio frequency motion sensor may transmit a first radio frequency (RF) signal. A slave radio frequency motion sensor may determine a second radio frequency signal which minimizes interference with the first RF frequency. In some versions, interference may be reduced with additional transmission adjustments such as pulse width reduction or frequency and/or timing dithering differences. In some versions, apparatus may be configured with multiple sensors in a configuration to emit the radio frequency signals in different directions to mitigate interference between emitted pulses from the radio frequency motion sensors.
A61B 5/024 - Mesure du pouls ou des pulsations cardiaques
G01S 7/02 - DÉTERMINATION DE LA DIRECTION PAR RADIO; RADIO-NAVIGATION; DÉTERMINATION DE LA DISTANCE OU DE LA VITESSE EN UTILISANT DES ONDES RADIO; LOCALISATION OU DÉTECTION DE LA PRÉSENCE EN UTILISANT LA RÉFLEXION OU LA RERADIATION D'ONDES RADIO; DISPOSITIONS ANALOGUES UTILISANT D'AUTRES ONDES - Détails des systèmes correspondant aux groupes , , de systèmes selon le groupe
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
A61B 5/0507 - Détection, mesure ou enregistrement pour établir un diagnostic au moyen de courants électriques ou de champs magnétiques; Mesure utilisant des micro-ondes ou des ondes radio utilisant des micro-ondes ou des ondes térahertz
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p.ex. tremblement de la tête ou des mains ou mobilité d'un membre
G01S 7/41 - DÉTERMINATION DE LA DIRECTION PAR RADIO; RADIO-NAVIGATION; DÉTERMINATION DE LA DISTANCE OU DE LA VITESSE EN UTILISANT DES ONDES RADIO; LOCALISATION OU DÉTECTION DE LA PRÉSENCE EN UTILISANT LA RÉFLEXION OU LA RERADIATION D'ONDES RADIO; DISPOSITIONS ANALOGUES UTILISANT D'AUTRES ONDES - Détails des systèmes correspondant aux groupes , , de systèmes selon le groupe utilisant l'analyse du signal d'écho pour la caractérisation de la cible; Signature de cible; Surface équivalente de cible
G01S 13/87 - Combinaisons de plusieurs systèmes radar, p.ex. d'un radar primaire et d'un radar secondaire
G01S 13/88 - Radar ou systèmes analogues, spécialement adaptés pour des applications spécifiques
A61B 5/113 - Mesure du mouvement du corps entier ou de parties de celui-ci, p.ex. tremblement de la tête ou des mains ou mobilité d'un membre se produisant au cours de la respiration
G01S 13/56 - Discrimination entre objets fixes et mobiles ou entre objets se déplaçant à différentes vitesses pour la détection de présence
G01S 13/524 - Discrimination entre objets fixes et mobiles ou entre objets se déplaçant à différentes vitesses utilisant la transmission de trains discontinus d'ondes modulées par impulsions basée sur le décalage de phase ou de fréquence résultant du mouvement des objets, avec référence aux signaux transmis, p.ex. MTI cohérent
A61B 5/08 - Dispositifs de mesure pour examiner les organes respiratoires
41.
SYSTEMS AND METHODS FOR DETECTING REM BEHAVIOR DISORDER
A method for monitoring a sleep session of an individual comprises receiving data associated with a current sleep session of the individual; analyzing at least a portion of the received data to identify one or more sleep stages experienced by the individual during the current sleep session, the one or more sleep stages including a light sleep stage, a deep sleep stage, a typical rapid eye movement (REM) stage, an atypical REM stage, a wake stage, or any combination thereof; and generating a summary of the current sleep session, the summary including (i) a number of atypical REM sleep stages experienced by the individual during the sleep current sleep session, (ii) a time spent in atypical REM sleep stages during the current sleep session, or (iii) both (i) and (ii).
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
A61B 5/08 - Dispositifs de mesure pour examiner les organes respiratoires
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p.ex. tremblement de la tête ou des mains ou mobilité d'un membre
G16H 40/67 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement à distance
G16H 10/60 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données spécifiques de patients, p.ex. pour des dossiers électroniques de patients
42.
SYSTEMS AND METHODS FOR DETERMINING MOVEMENT OF A CONDUIT
A system includes an electronic circuit, a memory, and a control system. The electronic circuit is coupled to a conduit. The conduit may be configured to deliver pressurized air. A portion of the electronic circuit has a first electrical property that is configured to change based at least in part on movement of the portion of the electronic circuit. The memory stores machine-readable instructions. The control system includes one or more processors configured to execute the machine-readable instructions. Data associated with the first electrical property of the electronic circuit is received. The received data is analyzed. Based at least in part on the analysis, it is determined that the first electrical property of the electronic circuit has changed. Responsive to the determination that the first electrical property of the electronic circuit has changed, it is determined that the conduit is moving or has moved.
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p.ex. bouche-à-bouche; Tubes trachéaux
G01R 27/02 - Mesure de résistances, de réactances, d'impédances réelles ou complexes, ou autres caractéristiques bipolaires qui en dérivent, p.ex. constante de temps
43.
SYSTEMS AND METHODS FOR MONITORING THE USE OF A RESPIRATORY THERAPY SYSTEM BY AN INDIVIDUAL WITH DIABETES
A method comprises receiving data associated with a diabetes treatment plan of the individual. The method further comprises receiving data associated with a respiratory therapy plan of the individual. The respiratory therapy plan is implementable by a respiratory therapy system during a sleep session. The method further comprises determining a potential interaction between the diabetes treatment plan of the individual and the respiratory therapy plan of the individual. The method further comprises, based on the interaction, updating the diabetes treatment plan of the individual.
G16H 20/00 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients
G16H 20/10 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des médicaments ou des médications, p.ex. pour s’assurer de l’administration correcte aux patients
44.
SYSTEMS AND METHODS FOR LOCATING USER INTERFACE LEAK
Detection of unintentional air leaks in a user interface (e.g., mask) of a respiratory therapy system (e.g., a positive air pressure device) is disclosed. One or more sensors (e.g., within a computing device, such as a smartphone) can be moved around relative to the user interface to determine a location and/or intensity of an air leak. The computing device can provide feedback regarding the location and/or intensity of the air leak to facilitate the user locating the air leak, and thus correcting the air leak. In some cases, augmented reality annotations can be overlaid on an image (e.g., live image) of the user wearing the user interface to identify the location of the air leak. The system can automatically detect the type of user interface being used and can provide tailored guidance for reducing the air leaks.
A method of predicting an unintentional leak in a respiratory system during a sleep session includes causing, during the sleep session, pressurized air to be delivered from a respiratory device to a user via a conduit coupled to a user interface. The method also includes receiving historical first data associated with pressurized air delivered from the respiratory device during one or more prior sleep sessions; receiving current first data associated with the pressurized air being delivered from the respiratory device during the sleep session; receiving historical second data associated with the user during one or more prior sleep sessions; and receiving, via one or more second sensors, current second data associated with the user during the current sleep session. The method determines, a likelihood that an unintentional leak in the respiratory system will occur within a predetermined amount of time.
A method includes receiving physiological data associated with a user during a sleep session. The method also includes determining a sleep-wake signal for the user during the sleep session based at least in part on the received physiological data. The method also includes determining one or more sleep-related parameters for the user during the sleep session based at least in part on the sleep-wake signal. The method also includes determining that the user experienced insomnia during the sleep session based at least in part on at least one of the one or more sleep-related parameters. The method also includes identifying a type for the insomnia experienced by the user based at least in part on the one or more sleep-related parameters.
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p.ex. bouche-à-bouche; Tubes trachéaux
G16H 40/67 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement à distance
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
47.
Systems and methods for identifying a user interface
The present disclosure relates to a method for identifying a user interface. Flow data associated with air flowing in a respiratory therapy system is received. Acoustic data associated with the respiratory therapy system is received. The received flow data and the received acoustic data are analyzed. Based at least in part on the analysis, a mask type for the user interface is determined.
Methods and apparatus provide monitoring of coughing and/or a sleep disordered breathing state of a person. One or more sensors may be configured for non-contact active and/or passive sensing. The processor(s) may extract respiratory effort signal(s) from one or more motion signals generated by active non-contact sensing with the sensor(s). The processor(s) may extract one or more energy band signals from an acoustic audio signal generated by passive non-contact sensing with the sensor(s). The processor(s) may assess the energy band signal(s) and/or the respiratory efforts signal(s) to generate intensity signal(s) representing sleep disorder breathing modulation. The processor(s) may classify feature(s) derived from the one or more intensity signals to generate measure(s) of coughing and/or sleep disordered breathing. The processor may evaluate sensing signal(s) to generate indication(s) of cough event(s) and/or cough type which may include generating an indication of a coronavirus disease or a coronavirus disease cough type.
A61B 5/113 - Mesure du mouvement du corps entier ou de parties de celui-ci, p.ex. tremblement de la tête ou des mains ou mobilité d'un membre se produisant au cours de la respiration
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
49.
SYSTEMS AND METHODS FOR PROMOTING A SLEEP STAGE OF A USER
System and methods are disclosed that promote a sleep stage of a user. The systems and methods determine a current sleep stage of a user during a sleep session, with the user using a respiratory therapy system during the sleep session. The systems and methods further predict an undesired sleep stage upcoming for the user during the sleep session based, at least in part, on (i) one or more user parameters, information from one or more previous sleep sessions, or a combination thereof, and (ii) the current sleep stage. The systems and methods adjust one or more control parameters of the respiratory therapy system, of one or more devices in an environment of the user, or of a combination thereof to promote a desired sleep stage of the user, thereby optimizing sleep of the user.
A61M 21/02 - Autres dispositifs ou méthodes pour amener un changement dans l'état de conscience; Dispositifs pour provoquer ou arrêter le sommeil par des moyens mécaniques, optiques ou acoustiques, p.ex. pour mettre en état d'hypnose pour provoquer le sommeil ou la relaxation, p.ex. par stimulation directe des nerfs, par hypnose ou par analgésie
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p.ex. bouche-à-bouche; Tubes trachéaux
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p.ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
G16H 40/67 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement à distance
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
50.
SYSTEMS AND METHODS FOR ANALYZING PHYSICAL FEATURES OF AN INDIVIDUAL
A method for analyzing physical features of an individual comprises directing an acoustic signal toward a mouth of the individual, receiving a reflected acoustic signal from the interior of the mouth of the individual, generating a structural profile of at least the interior of the mouth of the individual based at least in part on the reflected acoustic signal, and causing an action to be performed in response to generating the structural profile. The acoustic signal is configured to reflect off at least a portion of the interior of the mouth of the individual. The reflected acoustic signal is indicative of structural characteristics of the mouth of the individual. The structural profile can also be based on image data associated with the exterior of the head and neck of the individual, and image data associated with the interior of the mouth of the individual.
User alertness can be monitored and leveraged while the user is interacting with a computing device, such as a mobile device (e.g., a smartphone or tablet). By monitoring interaction data, an alertness inference of the user can be generated. The interaction data can include biometric data of the user (e.g., blink rate, eye focus, and breathing rate), inertia data of the device (e.g., swaying and orientation), and software-usage data of the device (e.g., button press speed and accuracy, app or action being used, and response times). The alertness inference can be a score measuring a degree of alertness of the user, from a deep sleep through fully alert. The alertness inference can be leveraged to automatically alert presentation of a message (e.g., notification) on the device, such as withholding presentation of the message or presenting it in different fashion (e.g., silently).
A wearable device can automatically switch between modes of collecting sensor data when a docking event is detected between the wearable device and a docking device. In a first mode (e.g., when undocked), data can be collected using a first sensor configuration (e.g., a first set of sensors operating using a first set of sensing parameters). In a second mode (e.g., when docked), data can be collected using a second sensor configuration, which can include the use of one or more different sensors and/or the use of one or more different sensing parameters. The first mode may prioritize battery life, whereas the second mode may prioritize sensor data fidelity, such as by increasing sampling rates, using different sensors, and the like. Sensor data from the first and second modes can be used individually (e.g., to calibrate the other) and/or together (e.g., to determine physiological parameters).
A61B 5/08 - Dispositifs de mesure pour examiner les organes respiratoires
A61B 5/1455 - Mesure des caractéristiques du sang in vivo, p.ex. de la concentration des gaz dans le sang, de la valeur du pH du sang en utilisant des capteurs optiques, p.ex. des oxymètres à photométrie spectrale
A61B 5/1495 - Mesure des caractéristiques du sang in vivo, p.ex. de la concentration des gaz dans le sang, de la valeur du pH du sang Étalonnage ou test des sondes in vivo
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
53.
SYSTEMS AND METHODS FOR ANALYZING SLEEP-RELATED PARAMETERS
A method includes receiving first data associated with a first sleep session of a user. The method also includes determining a first set of sleep-related parameters associated with the first sleep session of the user based at least in part on the first data. The method also includes receiving second data associated with a second sleep session of the user. The method also includes determining a second set of sleep-related parameters associated with the second sleep session of the user based at least in part on the second data. The method also includes receiving third data associated with a variable condition. The method also includes causing one or more indications associated with the variable condition and the first sleep session, the second sleep session, or both to be communicated to the user.
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p.ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
54.
System And Method For Mapping An Airway Obstruction
A method includes emitting an acoustic signal into an airway of a user. The method further includes, detecting an acoustic reflection of the acoustic signal caused by one or more physical features within the airway of the user. The method also includes analyzing acoustic data associated with the acoustic reflection. The method also further includes characterizing an occurrence of the physical obstruction in the airway of the user. The characterization is based, at least in part, on the analyzed acoustic data. The characterization is indicative of an apnea event or a hypopnea event in the user, wherein the apnea event comprises an obstructive apnea event, a central apnea event or a mixed apnea event, and further distinguishes between the occurrence of the obstructive apnea event, the central apnea event, the mixed apnea event or the hypopnea event in the user.
A method for generating a three-dimensional model of a head including at least a portion of a face, comprising: obtaining a distance image of the head using a distance-measuring device having an imaging position, the distance image comprising for each of a two- dimensional array of distance pixels, a respective distance value indicating a distance from the measuring position to a corresponding point in a field of view of the distance-measuring device, the distance image including a face portion corresponding to the at least a portion of a face; estimating the position, relative to the imaging position, of a longitudinal axis of the model of the head based on the at least one dimension; based on the longitudinal axis, generating the three dimensional model of the head based on the position of the longitudinal axis.
A user interface of a respiratory therapy system includes a strap assembly, a frame, a connector, and a sensor. The strap assembly is positioned about a head of a user when the user wears the user interface. The frame is physically and electrically connected to the strap assembly, and defines an aperture. The connector has a first end portion and second end portion. The first end portion of the connector can be positioned within the aperture of the frame such that the connector is physically and electrically connected to the frame. The sensor is coupled to the strap assembly or the frame such that the sensor abuts a target area of the user when the user wears the user interface.
A method includes (i) receiving data associated with a user during a sleep session; (ii) determining an alertness level of the user using a machine learning model that takes as input the received data; and (iii) generating a response to be communicated to the user based at least in part on the determined alertness level. The data associated with the user can be received from a respiratory therapy device configured to supply pressurized air to an airway of the user by way of a user interface coupled to the respiratory therapy device via a conduit, a sensor, or both the respiratory therapy device and the sensor.
A system includes a memory device storing machine-readable instructions and a control system including one or more processors configured to execute the machine-readable instructions to receive initial physiological data associated with a user, determine, based at least in part on initial physiological data, an initial sleepiness level for the user, prompt the user, via an electronic device, to perform a first activity, receive subsequent physiological data associated with the user, determine, based at least in part on the subsequent physiological data, a subsequent sleepiness level for the user, and determine a first activity score based at least in part on the initial sleepiness level and the subsequent sleepiness level, the first activity score being indicative of an effectiveness of the first activity in modifying the sleepiness of the user.
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
The present disclosure relates to a method for determining a mouth leak status associated with a user of a respiratory device is disclosed. Airflow data associated with the user of the respiratory device is received. The respiratory device is configured to supply pressurized air to an airway of the user during a therapy session. The airflow data includes pressure data. The airflow data associated with the user is analyzed. Based at least in part on the analysis, the mouth leak status associated with the user is determined. The mouth leak status is indicative of whether or not air is leaking from a mouth of the user.
A system has an electronic interface, one or more sensors, a memory, and a control system including one or more processors. The processors are configured to execute instructions for activating an edema test, automatically or in response to receiving a user request via the electronic interface. Upon activation, user instructions are provided to locate, via one or more of the sensors, a skin area in the subject for testing. A user is instructed to depress the skin area for causing a temporary indentation. One or more images of the temporary indentation are captured, via one or more of the sensors, over a period of time following the depression of the skin area by the user. The images are analyzed for characteristics of skin bounce-back, which represents rebounding of the skin area after the temporary indentation. An edema result is determined based on the characteristics of the skin bounce-back.
Devices, systems, and methods are disclosed. The devices, systems, and methods detect one or more parameters with respect to movement of a user, cardiac activity of the user, audio associated with the user, or a combination thereof during a sleep session of the user; process the one or more parameters to determine a sleep status of the user, the sleep status being at least one of awake, asleep, or a sleep stage; and calculate an apnea-hypopnea index for the user during the sleep session based, at least in part, on the sleep status.
A plurality of flow rate values associated with pressurized air directed to an airway of a user of a respiratory therapy system is received. A plurality of pressure values associated with the pressurized air directed to the airway of the user is received. A first time associated with a first breath of the user and a second time associated with a second breath of the user are identified. The plurality of flow rate values is filtered based at least in part on the identified first time and the identified second time. The filtering produces a subset of the plurality of flow rate values. An intentional leak characteristic curve for the respiratory therapy system is determined using at least two of the subset of the plurality of flow rate values and the corresponding pressure values for the at least two of the subset of the plurality of flow rate values.
An intelligent entrainment program can make use of received biometric sensor data to provide hyper-personalized guidance to entrain a user's respiration pattern towards a target respiration pattern. The entrainment program can be used for sleep-related therapy, such as to facilitate falling asleep, staying asleep, and/or waking up. Respiration information (e.g., respiration rate, time between breaths, maximal inspiration information, maximal expiration information, respiration rate variability, respiration morphology information, and the like) can be extracted from the biometric sensor data and used to establish a target respiration pattern. An entrainment signal can be determined from the target respiration pattern and then used to present an entrainment stimulus (e.g., via audio, visual, tactile, or other stimuli) to the user.
G16H 20/30 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies ou des activités physiques, p.ex. la physiothérapie, l’acupression ou les exercices
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p.ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p.ex. basé sur des systèmes experts médicaux
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
G16H 20/70 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mentales, p.ex. la thérapie psychologique ou le training autogène
64.
BIOFEEDBACK COGNITIVE BEHAVIORAL THERAPY FOR INSOMNIA
Intelligent systems and methods for facilitating insomnia therapy are disclosed. Sensor data (e.g., non-contact sensor data) can be used to determine physiological parameter(s), such as sleep-related physiological parameter(s), which can be used to generate a sleep disorder prediction. The sleep disorder prediction can be used, along with an identified sleep therapy plan, to generate and facilitate application of (e.g., present to a user or automatically apply) a sleep therapy recommendation. When sleep apnea is predicted in concert with an identified cognitive behavioral therapy for insomnia (CBTi) plan, a warning can be presented to the user to not engage in certain CBTi therapies. Sensor data can also be used to automatically update therapy parameter(s) of an ongoing sleep therapy plan, such as in realtime.
G16H 20/00 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients
65.
SYSTEMS AND METHODS FOR REDUCING INSOMNIA-RELATED SYMPTOMS
A system includes a memory storing a user profile for a user of the system and machine-readable instructions and a control system including one or more processors configured to execute the machine-readable instructions to receive physiological data associated with the user during a sleep session, determine, based at least in part on the received physiological data, a set of sleep-related parameters for the sleep session, subsequent to the sleep session, select one of the set of sleep-related parameters as a targeted parameter, the selection of the targeted parameter being based at least in part on the stored user profile, the set of sleep-related parameters, or both, and cause information to be communicated to the user via a user device, the information being indicative of the targeted parameter, a recommendation associated with improving the targeted parameter for the user in one or more subsequent sleep sessions, or both.
A61M 21/02 - Autres dispositifs ou méthodes pour amener un changement dans l'état de conscience; Dispositifs pour provoquer ou arrêter le sommeil par des moyens mécaniques, optiques ou acoustiques, p.ex. pour mettre en état d'hypnose pour provoquer le sommeil ou la relaxation, p.ex. par stimulation directe des nerfs, par hypnose ou par analgésie
A method includes receiving first physiological data associated with a user during a first sleep session. The method also includes receiving second physiological data associated with the user subsequent to the first sleep session and prior to a second sleep session. The method also includes determining a recommended bedtime for the user for the second sleep session based at least in part on the first physiological data, the second physiological data, or both. The method also includes causing an indication of the recommended bedtime for the second sleep session to be communicated to the user via a user device before the recommended bedtime.
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
G16H 20/70 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mentales, p.ex. la thérapie psychologique ou le training autogène
67.
SYSTEMS AND METHODS FOR GENERATING REMINDERS TO USE RESPIRATORY THERAPY SYSTEMS
A system includes a respiratory therapy device, a sensor, and a control system. The respiratory therapy device supplies pressurized air to an airway of a user during a plurality of sleep sessions. The sensor generates data including current data that is associated with a current sleep session of the plurality of sleep sessions and historical data that is associated with one or more prior sleep sessions of the plurality of sleep sessions. The control system includes one or more processors configured to execute machine-readable instructions to: analyze the historical data to determine a behavior pattern associated with the user; analyze the current data to determine a condition of the user interface in relation to the user; and generate an alarm based at least in part on the behavior pattern associated with the user and the condition of the user interface in relation to the user.
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p.ex. bouche-à-bouche; Tubes trachéaux
G16H 15/00 - TIC spécialement adaptées aux rapports médicaux, p.ex. leur création ou leur transmission
A61M 21/02 - Autres dispositifs ou méthodes pour amener un changement dans l'état de conscience; Dispositifs pour provoquer ou arrêter le sommeil par des moyens mécaniques, optiques ou acoustiques, p.ex. pour mettre en état d'hypnose pour provoquer le sommeil ou la relaxation, p.ex. par stimulation directe des nerfs, par hypnose ou par analgésie
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
G16H 10/60 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données spécifiques de patients, p.ex. pour des dossiers électroniques de patients
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
68.
SYSTEM AND METHODS FOR TRIGGERING SOUNDS TO MASK NOISE FROM RESPIRATORY SYSTEMS AND THEIR COMPONENTS
A system includes a respiratory device, a mask, a microphone, a speaker, and a control system. The respiratory device is configured to supply pressurized air. The mask is coupled to the respiratory device and configured to engage a user during a sleep session to aid in directing the supplied pressurized air to the user. The microphone is configured to generate audio data. The speaker is configured to emit sound. The control system is configured to analyze the audio data to determine if noise associated with air leaking from the mask is occurring. Responsive to (i) the analysis resulting in a determination that noise associated with air leaking from the mask is occurring, (ii) the respiratory device determining that air is leaking from the mask, or (iii) both, the speaker is caused to emit the sound to aid in masking the noise associated with the air leaking from the mask.
A61M 21/02 - Autres dispositifs ou méthodes pour amener un changement dans l'état de conscience; Dispositifs pour provoquer ou arrêter le sommeil par des moyens mécaniques, optiques ou acoustiques, p.ex. pour mettre en état d'hypnose pour provoquer le sommeil ou la relaxation, p.ex. par stimulation directe des nerfs, par hypnose ou par analgésie
G10K 11/175 - Procédés ou dispositifs de protection contre le bruit ou les autres ondes acoustiques ou pour amortir ceux-ci, en général utilisant des effets d'interférence; Masquage du son
A61M 16/06 - Masques respiratoires ou pour l'anesthésie
H04R 1/02 - Boîtiers; Meubles; Montages à l'intérieur de ceux-ci
H04R 1/40 - Dispositions pour obtenir la fréquence désirée ou les caractéristiques directionnelles pour obtenir la caractéristique directionnelle désirée uniquement en combinant plusieurs transducteurs identiques
Various implementations of the present disclosure are directed to systems and methods for characterizing a conduit coupled to a respiratory therapy device in a respiratory therapy system. The method includes generating a first airflow from the respiratory therapy device to the conduit by operating a motor of the respiratory therapy device at a first revolutions per minute. The method further includes receiving a first airflow parameter data associated with the first airflow, wherein the first airflow parameter data has a first pair of two distinct airflow parameter values. The method further includes determining a first relationship between the first airflow parameter data and the conduit, and characterizing the conduit based on the first relationship.
A method includes receiving data associated with a sleep session of a user. The method also includes determining that the user is experiencing or has experienced an event based at least in part on the data. The method also includes causing pressurized air to be directed from a respiratory device to a multi-compartment bladder in response to determining that the user is experiencing or has experienced the event to aid in modifying a position of a head of the user.
A system for predicting adoption of a prescribed treatment plan by an individual includes a data repository, a memory storing instruction, and a control system to execute the instructions. The data repository is communicatively coupled to a network and includes a plurality of storage devices storing data. The control system receives at least a portion of the data stored in the data repository. The at least a portion of the data is associated with the individual. The control system uses the machine learning adoption prediction algorithm to process the received at least a portion of the data to determine a likelihood that the individual will adopt the prescribed treatment plan. Based at least in part on (i) the prescribed treatment plan and (ii) the determined likelihood that the individual will adopt the prescribed treatment plan, the control system generates a personalized treatment adoption plan for the individual.
G16H 10/60 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données spécifiques de patients, p.ex. pour des dossiers électroniques de patients
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p.ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
72.
SYSTEMS AND METHODS FOR DETERMINING A SLEEP STAGE OF AN INDIVIDUAL
A method of determining a sleep stage of an individual comprises identifying features associated with a current epoch of the sleep session, determining a plurality of sleep stage probabilities based on the features, identifying events experienced by the individual during the current epoch, and adjusting each of the plurality of sleep stage probabilities based on events experienced by the individual during the current epoch or a prior epoch, and/or a sleep stage previously determined for the prior epoch. The features include at least one feature associated with a flow of pressurized air from a respiratory therapy system used by the individual, at least one feature associated with a respiration rate of the individual, and/or at least one feature associated with a time of the sleep session. Each sleep stage probability corresponds to a respective one of a plurality of potential sleep stages during the current epoch of the sleep session.
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
A61B 5/369 - Modalités, c. à d. méthodes diagnostiques spécifiques Électroencéphalographie [EEG]
A61B 5/398 - Modalités, c. à d. méthodes diagnostiques spécifiques Électrorétinographie [ERG]
G16H 20/00 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients
G16H 30/00 - TIC spécialement adaptées au maniement ou au traitement d’images médicales
G16H 70/00 - TIC spécialement adaptées au maniement ou au traitement de références médicales
73.
Systems, methods and devices for smart humidification
Disclosed are methods, systems, and devices for providing a personalized humidification level. A control system receives, from a first sensor, one or more environmental parameters regarding conditions of the environment. The control system receives, from a second sensor, one or more physiological parameters associated with a user within the environment. The control system determines an action associated with a desired change in the humidity within the environment based, at least in part, on the one or more environmental parameters and the one or more physiological parameters. The control system causes, at least in part, a performance of the action associated with the change in the humidity in the environment based, at least in part, on moisture outputted by a humidifier module. The methods and devices perform the same functionality as the control system.
Methods and devices provide physiological movement detection with active sound generation. In some versions, a processor may detect breathing and/or gross body motion. The processor may control producing, via a speaker coupled to the processor, a sound signal in a user's vicinity. The processor may control sensing, via a microphone coupled to the processor, a reflected sound signal. This reflected sound signal is a reflection of the sound signal from the user. The processor may process the reflected sound, such as by a demodulation technique. The processor may detect breathing from the processed reflected sound signal. The sound signal may be produced as a series of tone pairs in a frame of slots or as a phase-continuous repeated waveform having changing frequencies (e.g., triangular or ramp sawtooth). Evaluation of detected movement information may determine sleep states or scoring, fatigue indications, subject recognition, chronic disease monitoring/prediction, and other output parameters.
A61B 5/08 - Dispositifs de mesure pour examiner les organes respiratoires
G16H 40/67 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement à distance
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p.ex. tremblement de la tête ou des mains ou mobilité d'un membre
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
75.
Systems and methods for insomnia screening and management
A method includes receiving physiological data associated with a user during a sleep session. The method also includes determining a sleep-wake signal for the user during the sleep session based at least in part on the received physiological data. The method also includes determining one or more sleep-related parameters for the user during the sleep session based at least in part on the sleep-wake signal. The method also includes determining that the user experienced insomnia during the sleep session based at least in part on at least one of the one or more sleep-related parameters. The method also includes identifying a type for the insomnia experienced by the user based at least in part on the one or more sleep-related parameters.
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p.ex. bouche-à-bouche; Tubes trachéaux
G16H 40/67 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement à distance
Systems and methods are provided for a multi-modal sleep system comprising a data processor for operating in a plurality of operating modes. The data processor may detect at least one sensor providing data to the data processor and determine a sensor type associated with each of the at least one sensor. The data processor may select a mode of operation based on the determined sensor type of the detected at least one sensor and of each of the at least one sensor. A first of the plurality of operating modes may be selected in response to determining that the at least one detected sensor includes a first sensor type or combination of sensor types. The data processor may be configured to receive data from the at least one detected sensor and process the received data according to the selected mode of operation to output a characterization of a user's sleep.
A method of modifying pressure settings of a respiratory therapy system comprises supplying pressurized air at a first pressure to a user during a current sleep session; determining a number and/or type of events experienced by the user during a first portion of the current sleep session; and modifying the pressure settings of the respiratory therapy system during a subsequent sleep session portion in response to the number and/or type of events satisfying a threshold. Modifying the pressure settings can include modifying the first pressure to be a modified first pressure for the subsequent sleep session portion, (ii) modifying a difference in pressure between the first pressure and a second pressure for the subsequent sleep session portion, (iii) modifying a rate of change from the first pressure to the second pressure for the subsequent sleep session portion, or (iv) any combination of (i)-(iii).
A method includes receiving, from a first sensor, first physiological data associated with a first sleep session of a user. The method also includes receiving, from a sensor, second physiological data associated with a first sleep session of a user. The method also includes determining a first set of sleep-related parameters associated with the first sleep session of the user based at least in part on the first physiological data. The method also includes determining a second set of sleep-related parameters associated with the first sleep session of the user based at least in part on the second physiological data. The method also includes calibrating the second sensor based at least in part on a comparison between the first set of sleep-related parameters and the second set of sleep-related parameters.
Method and apparatus obtain information about a patient and/or a respiratory therapy system that is configured to deliver respiratory therapy to the patient. The respiratory therapy system may include a flow generator configured to generate a supply of pressurized air along an air circuit to a patient interface. A sound signal representing a sound in the air circuit may be processed to obtain cepstrum data. A time series of delay estimates based on acoustic signatures of the cepstrum data may be generated. Each acoustic signature may represent a reflection of sound from a patient interface along the air circuit. Variation in the time series of delay estimates may be analysed. One or more output indicators based on the variation may be generated. The one or more output indicators may concern patient and/or system status.
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p.ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
G10L 25/24 - Techniques d'analyses de la parole ou de la voix qui ne se limitent pas à un seul des groupes caractérisées par le type de paramètres extraits les paramètres extraits étant le cepstre
G10L 25/63 - Techniques d'analyses de la parole ou de la voix qui ne se limitent pas à un seul des groupes spécialement adaptées pour un usage particulier pour comparaison ou différentiation pour estimer un état émotionnel
G10L 21/0224 - Traitement dans le domaine temporel
G10L 21/0308 - Séparation du signal de voix caractérisée par le type de mesure du paramètre, p.ex. techniques de corrélation, techniques de passage par zéro ou techniques prédictives
80.
SYSTEMS AND METHODS FOR CHARACTERIZING A USER INTERFACE OR A VENT USING ACOUSTIC DATA ASSOCIATED WITH THE VENT
Method wherein acoustic data associated with airflow caused by operation of a respiratory therapy system (120), which is configured to supply pressurized air to a user and includes a user interface (400) and a vent, is received (710), and wherein based at least in part on a portion of the received acoustic data, an acoustic signature associated with the vent (720) is determined, so that the user interface, the vent, or both can be identified (730).
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p.ex. tremblement de la tête ou des mains ou mobilité d'un membre
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p.ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
G16H 40/67 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement à distance
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p.ex. bouche-à-bouche; Tubes trachéaux
A61M 16/06 - Masques respiratoires ou pour l'anesthésie
A61M 16/20 - Valves spécialement adaptées aux dispositifs respiratoires médicaux
A61M 16/10 - Préparation de gaz ou vapeurs à respirer
81.
SYSTEMS AND METHODS FOR MANAGING BLOOD PRESSURE CONDITIONS OF A USER OF A RESPIRATORY THERAPY SYSTEM
Various implementations of the present disclosure are directed to systems and methods for managing blood pressure conditions of a user of a respiratory therapy system by controlling operational parameters associated with the respiratory therapy system. The method includes receiving cardiovascular data associated with a user of a respiratory therapy system during a sleep session and determining, based at least in part on the received cardiovascular data, a value of a first physiological parameter associated with the user. The method further includes determining whether the value of the first physiological parameter satisfies a first condition and in response to the first physiological parameter satisfying the first condition, determining a modification of an operational parameter associated with the respiratory therapy system.
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p.ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
A sensor for motion or gesture sensing may be configured to emit radio frequency signals such as for pulsed range gated sensing. The sensor may include a radio frequency transmitter configured to emit the pulses and a receiver configured to receive reflected ones of the emitted radio frequency signals. The received pulses may be processed by a motion channel and/or a gesture channel. The gesture channel may produce signals for further processing for identification of one or more different motion gestures such as by calculating and evaluating features from any of the amplitude, phase and frequency of the output signals of the gesture channel. The sensing apparatus may optionally serve as a monitor for evaluating user activities, such as by counting activities. The sensor may optionally serve as a user control interface for many different devices by generating control signal(s) based on identification of one or more different motion gestures.
G01S 7/41 - DÉTERMINATION DE LA DIRECTION PAR RADIO; RADIO-NAVIGATION; DÉTERMINATION DE LA DISTANCE OU DE LA VITESSE EN UTILISANT DES ONDES RADIO; LOCALISATION OU DÉTECTION DE LA PRÉSENCE EN UTILISANT LA RÉFLEXION OU LA RERADIATION D'ONDES RADIO; DISPOSITIONS ANALOGUES UTILISANT D'AUTRES ONDES - Détails des systèmes correspondant aux groupes , , de systèmes selon le groupe utilisant l'analyse du signal d'écho pour la caractérisation de la cible; Signature de cible; Surface équivalente de cible
G01S 13/56 - Discrimination entre objets fixes et mobiles ou entre objets se déplaçant à différentes vitesses pour la détection de présence
G01S 13/87 - Combinaisons de plusieurs systèmes radar, p.ex. d'un radar primaire et d'un radar secondaire
G01S 13/88 - Radar ou systèmes analogues, spécialement adaptés pour des applications spécifiques
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p.ex. tremblement de la tête ou des mains ou mobilité d'un membre
G06F 3/01 - Dispositions d'entrée ou dispositions d'entrée et de sortie combinées pour l'interaction entre l'utilisateur et le calculateur
A61B 5/113 - Mesure du mouvement du corps entier ou de parties de celui-ci, p.ex. tremblement de la tête ou des mains ou mobilité d'un membre se produisant au cours de la respiration
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
A61B 5/0507 - Détection, mesure ou enregistrement pour établir un diagnostic au moyen de courants électriques ou de champs magnétiques; Mesure utilisant des micro-ondes ou des ondes radio utilisant des micro-ondes ou des ondes térahertz
A61B 5/08 - Dispositifs de mesure pour examiner les organes respiratoires
A processing system includes methods to promote sleep. The system may include a monitor such as a non-contact motion sensor from which sleep information may be determined. User sleep information, such as sleep stages, hypnograms, sleep scores, mind recharge scores and body scores, may be recorded, evaluated and/or displayed for a user. The system may further monitor ambient and/or environmental conditions corresponding to sleep sessions. Sleep advice may be generated based on the sleep information, user queries and/or environmental conditions from one or more sleep sessions. Communicated sleep advice may include content to promote good sleep habits and/or detect risky sleep conditions. In some versions of the system, any one or more of a bedside unit 3000 sensor module, a smart processing device, such as a smart phone or smart device 3002, and network servers may be implemented to perform the methodologies of the system.
A61M 21/02 - Autres dispositifs ou méthodes pour amener un changement dans l'état de conscience; Dispositifs pour provoquer ou arrêter le sommeil par des moyens mécaniques, optiques ou acoustiques, p.ex. pour mettre en état d'hypnose pour provoquer le sommeil ou la relaxation, p.ex. par stimulation directe des nerfs, par hypnose ou par analgésie
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
G10L 15/26 - Systèmes de synthèse de texte à partir de la parole
H04R 29/00 - Dispositifs de contrôle; Dispositifs de tests
A61M 21/00 - Autres dispositifs ou méthodes pour amener un changement dans l'état de conscience; Dispositifs pour provoquer ou arrêter le sommeil par des moyens mécaniques, optiques ou acoustiques, p.ex. pour mettre en état d'hypnose
G10L 25/78 - Détection de la présence ou de l’absence de signaux de voix
G10L 15/22 - Procédures utilisées pendant le processus de reconnaissance de la parole, p.ex. dialogue homme-machine
Aspects of the of the disclosure relate to a non-contact physiological motion sensor and a monitor device that can incorporate use of the Doppler effect. A continuous wave of electromagnetic radiation can be transmitted toward one or more subjects and the Doppler-shifted received signals can be digitized and/or processed subsequently to extract information related to the cardiopulmonary motion in the one or more subjects. The extracted information can be used, for example, to determine apneic events and/or snoring events and/or to provide apnea or snoring therapy to subjects when used in conjunction with an apnea or snoring therapy device. In addition, methods of use are disclosed for sway cancellation, realization of cessation of breath, integration with multi-parameter patient monitoring systems, providing positive providing patient identification, or any combination thereof.
A61B 5/08 - Dispositifs de mesure pour examiner les organes respiratoires
A61H 23/02 - Massage par percussion ou vibration, p.ex. en utilisant une vibration ultrasonique; Massage par succion-vibration; Massage avec des membranes mobiles à entraînement électrique ou magnétique
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
A61H 21/00 - Dispositifs de massage pour les cavités du corps
A61N 1/36 - Application de courants électriques par électrodes de contact courants alternatifs ou intermittents pour stimuler, p.ex. stimulateurs cardiaques
G01S 7/00 - DÉTERMINATION DE LA DIRECTION PAR RADIO; RADIO-NAVIGATION; DÉTERMINATION DE LA DISTANCE OU DE LA VITESSE EN UTILISANT DES ONDES RADIO; LOCALISATION OU DÉTECTION DE LA PRÉSENCE EN UTILISANT LA RÉFLEXION OU LA RERADIATION D'ONDES RADIO; DISPOSITIONS ANALOGUES UTILISANT D'AUTRES ONDES - Détails des systèmes correspondant aux groupes , ,
G01S 13/50 - Systèmes de mesure basés sur le mouvement relatif à la cible
G01S 13/82 - Systèmes utilisant la reradiation d'ondes radio, p.ex. du type radar secondaire; Systèmes analogues dans lesquels des signaux de type continu sont transmis
G01S 13/87 - Combinaisons de plusieurs systèmes radar, p.ex. d'un radar primaire et d'un radar secondaire
G01S 13/88 - Radar ou systèmes analogues, spécialement adaptés pour des applications spécifiques
A61B 5/113 - Mesure du mouvement du corps entier ou de parties de celui-ci, p.ex. tremblement de la tête ou des mains ou mobilité d'un membre se produisant au cours de la respiration
A sleep monitoring system includes an ECG device (2) and a respiration inductance plethysmogram (3) which monitor cardiac activity and physical (ribcage) respiration respectively and feed representative signals to a digital data processor. Operations (5-9) process the beat interval data, while in a second thread, operations (20-24) independently process the amplitude modulation of the ECG data caused by the respiratory motion of the subject. The inductance plethysmogram device (3) provides an input to the processor which represents respiration as directly monitored independently of the ECG. Operations (30-34) process this direct respiration data independently and in parallel, in a third thread. All extracted features are fed to a classifier which in step (10) combines selected combinations of features to make decisions in real time.
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
A61B 5/024 - Mesure du pouls ou des pulsations cardiaques
A61B 5/113 - Mesure du mouvement du corps entier ou de parties de celui-ci, p.ex. tremblement de la tête ou des mains ou mobilité d'un membre se produisant au cours de la respiration
G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p.ex. basé sur des systèmes experts médicaux
86.
SYSTEM AND METHOD FOR CONTINUOUS ADJUSTMENT OF PERSONALIZED MASK SHAPE
A system and method to match an interface to the face of a user for respiratory therapy. A facial image of the user is stored. Facial features based on the facial image are determined. A database stores facial profiles based on facial features and a corresponding plurality of interfaces. A database stores operational data of respiratory therapy devices with the plurality of corresponding interfaces. A selection engine is coupled to the databases. The selection engine is operative to select an interface for the user from the plurality of corresponding interfaces based on a desired outcome based on the stored operational data and the facial features. The collected data may also be employed to determine whether the selected interface is correctly fitted to the face of the user.
G16H 20/30 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies ou des activités physiques, p.ex. la physiothérapie, l’acupression ou les exercices
G16H 40/40 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour la gestion d’équipement ou de dispositifs médicaux, p.ex. pour planifier la maintenance ou les mises à jour
G16H 40/60 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
A61B 5/107 - Mesure de dimensions corporelles, p.ex. la taille du corps entier ou de parties de celui-ci
A61M 16/06 - Masques respiratoires ou pour l'anesthésie
87.
SYSTEMS AND METHODS FOR ADJUSTING USER POSITION USING MULTI-COMPARTMENT BLADDERS
A system includes one or more sensors one or more sensors configured to generate data associated with a sleep session of a user. The system also includes a multi-compartment bladder configured to be positioned adjacent to a user during the sleep session. The system also includes a memory storing machine-readable instructions. The system also includes a control system including one or more processors configured to execute the machine-readable instructions to determine, based at least in part on the generated data associated with the sleep session, that the user is experiencing or has experienced an event and responsive to determining that the user is experiencing or has experienced the event, cause the multi-compartment bladder to be modified to aid in causing the user to move.
Various implementations of the present disclosure are directed to systems and methods for leak detection in a respiratory therapy system using acoustic data. According to some implementations, a method includes receiving acoustic data associated with airflow caused by operation of a respiratory therapy system during a sleep session of a user. The method also includes analyzing at least a portion of the acoustic data to determine a value of a parameter associated with the at least a portion of the acoustic data. The method further includes determining an occurrence of a leak during the sleep session in response to the determined value of the parameter satisfying a condition.
A method for predicting a subjective comfort level of a user of a respiratory therapy system is disclosed as follows. Data associated with the user of the respiratory therapy system during a therapy session is received. At least one parameter associated with the user is determined based at least in part on a first portion of the received data. A comfort score is determined based at least in part on the determined at least one parameter. The comfort score is indicative of the subjective comfort level of the user of the respiratory therapy system during at least a portion of the therapy session.
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p.ex. tremblement de la tête ou des mains ou mobilité d'un membre
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p.ex. bouche-à-bouche; Tubes trachéaux
G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p.ex. basé sur des systèmes experts médicaux
The disclosure provides methods for diagnosis or prediction of the likelihood of a subject experiencing obstructive sleep apnea, determined at least in part by measuring the degree of tongue fat in a subject using, e.g., thermal imaging, THz imaging or other multispectral imaging.
A61B 5/0507 - Détection, mesure ou enregistrement pour établir un diagnostic au moyen de courants électriques ou de champs magnétiques; Mesure utilisant des micro-ondes ou des ondes radio utilisant des micro-ondes ou des ondes térahertz
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p.ex. basé sur des systèmes experts médicaux
91.
SYSTEMS AND METHODS FOR DETECTING OCCLUSIONS IN HEADGEAR CONDUITS DURING RESPIRATORY THERAPY
A system and method detects an occlusion in a respiratory therapy system. The system and method includes determining an acoustic signature for a conduit of a headgear user interface. The determined acoustic signature is analyzed to identify an anomaly in the acoustic signature. In response to the determined acoustic signature being identified as anomalous, a determination is made if the identified anomaly relates to an occlusion of the conduit.
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p.ex. bouche-à-bouche; Tubes trachéaux
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
A61B 8/08 - Détection de mouvements ou de changements organiques, p.ex. tumeurs, kystes, gonflements
A61M 16/06 - Masques respiratoires ou pour l'anesthésie
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p.ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p.ex. basé sur des systèmes experts médicaux
92.
SYSTEMS AND METHODS FOR DETECTING RAINOUT IN A RESPIRATORY THERAPY SYSTEM
A method of detecting rainout in a respiratory therapy system that includes a conduit fluidly coupled to a user interface comprises generating, via at least one microphone, acoustic data representative of noise associated with the respiratory therapy system. The method further comprises analyzing the acoustic data to detect a presence of liquid in the respiratory therapy system. The method further comprises causing an action to be performed, based on the detected presence of the liquid.
A method for canceling noises generated by a respiratory system that is configured to supply pressurized air to a user during a sleep session comprises generating sound data using a microphone; generating, using or one or more sensors, respiration data associated with respiration of the user of the respiratory system; analyzing the sound data to determine if noise associated with operation of the respiratory system is occurring; and causing a speaker to emit sound waves based at least in part on (i) the sound data, (ii) the respiration data, (iii) data related to the operation of the respiratory system, or (iv) any combination of (i), (ii), and (iii), the emitted sound waves being configured to acoustically cancel at least a portion of the noise associated with operation of the respiratory system.
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
A61M 16/00 - Dispositifs pour agir sur le système respiratoire des patients par un traitement au gaz, p.ex. bouche-à-bouche; Tubes trachéaux
G16H 20/40 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des thérapies mécaniques, la radiothérapie ou des thérapies invasives, p.ex. la chirurgie, la thérapie laser, la dialyse ou l’acuponcture
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
A61B 5/024 - Mesure du pouls ou des pulsations cardiaques
A61B 5/08 - Dispositifs de mesure pour examiner les organes respiratoires
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p.ex. tremblement de la tête ou des mains ou mobilité d'un membre
A61M 16/16 - Dispositifs pour humidifier l'air à respirer
Certain aspects and features of the present disclosure relate to evaluating the sleep performance of a cohort of multiple individuals sleeping in a shared environment (e.g., a single bed, a single room, a set of adjacent rooms, or a single household). Individual or concerted sleep performance scores can be determined, as well as other sleep performance metrics. The evaluation of sleep performance for the entire cohort can be useful when one of the individuals is being treated (e.g., with a respiratory therapy device) for a sleep-related and/or respiratory disorder. Evaluation of the cohort can help identify actions that can be taken to improve the sleep performance of all individuals in the cohort. In some cases, parameters of a user's therapy device are adjusted based on the monitored sleep performance of another individual in the cohort.
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
G16H 50/50 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour la simulation ou la modélisation des troubles médicaux
95.
SYSTEMS AND METHODS FOR IDENTIFYING USER BODY POSITION DURING RESPIRATORY THERAPY
A system for identifying a body position of a user of a respiratory therapy system includes a sensor, a memory, and a control system. The sensor is configured to generate airflow data associated with the user. The memory stores machine-readable instructions. The control system includes one or more processors configured to execute the machine-readable instructions to receive the airflow data associated with the user during a sleep session. The control system is further configured to determine one or more features associated with the airflow data, and identify the body position of the user during a first portion of the sleep session based at least in part on the determined one or more features. The control system is further configured to cause an action to be performed based at least in part on the identified body position of the user.
A61B 5/0205 - Evaluation simultanée de l'état cardio-vasculaire et de l'état d'autres parties du corps, p.ex. de l'état cardiaque et respiratoire
A61B 5/1455 - Mesure des caractéristiques du sang in vivo, p.ex. de la concentration des gaz dans le sang, de la valeur du pH du sang en utilisant des capteurs optiques, p.ex. des oxymètres à photométrie spectrale
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
96.
SYSTEMS AND METHODS FOR MONITORING A COMFORT LEVEL OF AN INDIVIDUAL
A method includes generating, using one or more sensors, data. The data includes (i) environmental data related to an environment of a user and (ii) physiological data associated with the user during a sleep session. Based at least in part on the physiological data, a comfort score associated with the user during the sleep session is determined. The comfort score is indicative of a comfort level of the user during at least a portion of the sleep session. Based at least in part on the determined comfort score, a setting of one or more devices associated with the environment of the user is adjusted.
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
G16H 40/67 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement à distance
G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p.ex. basé sur des systèmes experts médicaux
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicales; TIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
Sleep performance scores can be generated for an individual receiving respiratory therapy. Sensor data can be obtained from one or more sensors while the user is sleeping and using a respiratory therapy system. The sensor data can be used to determine one or more usage variables associated with use of the respiratory therapy system, as well as sleep stage information indicative of the stages of sleep undergone by the user while sleeping. A sleep performance score can be calculated using the one or more usage variables and the sleep stage information. In some cases, the sleep stage information can be used to apply weightings to one, some, or all of the one or more usage variables. The sleep performance score can indicate compliance, efficacy, quality, and/or general use of the respiratory therapy system, taking into account the relationship between sleep stage and use of the respiratory therapy system.
A method includes generating acoustic data representative of at least one or more reflections of an acoustic signal. The one or more reflections are indicative of a length and/or a diameter of a conduit coupled to a respiratory therapy device. The method further includes analyzing the acoustic data to determine the length and/or diameter of the conduit. In some cases, analyzing the acoustic data includes determining a resonant frequency of the conduit, and determining the length of the conduit based at least in part on the resonant frequency. In some cases, analyzing the acoustic data includes comparing the acoustic data to predetermined sets of acoustic data that each correspond to a known length and/or diameter of the conduit, and selecting one of the predetermined sets of acoustic data that best matches the generated acoustic data. The selected set of acoustic data corresponds to the length and/or diameter of the conduit.
A system includes a respiratory device, a mask, a microphone, a speaker, and a control system. The respiratory device is configured to supply pressurized air. The mask is coupled to the respiratory device and configured to engage a user during a sleep session to aid in directing the supplied pressurized air to the user. The microphone is configured to generate audio data. The speaker is configured to emit sound. The control system is configured to analyze the audio data to determine if noise associated with air leaking from the mask is occurring. Responsive to (i) the analysis resulting in a determination that noise associated with air leaking from the mask is occurring, (ii) the respiratory device determining that air is leaking from the mask, or (iii) both, the speaker is caused to emit the sound to aid in masking the noise associated with the air leaking from the mask.
A61M 21/02 - Autres dispositifs ou méthodes pour amener un changement dans l'état de conscience; Dispositifs pour provoquer ou arrêter le sommeil par des moyens mécaniques, optiques ou acoustiques, p.ex. pour mettre en état d'hypnose pour provoquer le sommeil ou la relaxation, p.ex. par stimulation directe des nerfs, par hypnose ou par analgésie
G10K 11/175 - Procédés ou dispositifs de protection contre le bruit ou les autres ondes acoustiques ou pour amortir ceux-ci, en général utilisant des effets d'interférence; Masquage du son
H04R 1/40 - Dispositions pour obtenir la fréquence désirée ou les caractéristiques directionnelles pour obtenir la caractéristique directionnelle désirée uniquement en combinant plusieurs transducteurs identiques
H04R 1/02 - Boîtiers; Meubles; Montages à l'intérieur de ceux-ci
A61M 16/06 - Masques respiratoires ou pour l'anesthésie
A61M 21/00 - Autres dispositifs ou méthodes pour amener un changement dans l'état de conscience; Dispositifs pour provoquer ou arrêter le sommeil par des moyens mécaniques, optiques ou acoustiques, p.ex. pour mettre en état d'hypnose
Airflow parameters (e.g., flow rate and airflow pressure) of airflow generated by a flow generator of a respiratory therapy system can be measured during use and processed to automatically identify user interface and/or conduit identification information. This user interface and/or conduit identification information can be used to adjust settings of the respiratory therapy device, generate notifications (e.g., notifications of a detected change in user interface without concomitant, expected adjustment of settings of the respiratory therapy device), or otherwise facilitate respiratory therapy of the user or of other users. User interface and/or conduit identification information can be indicative of specific characteristics of the user interface and/or conduit (e.g., resonant frequencies, impedance, and the like), a style of the user interface (e.g., a face mask, nasal mask, or nasal pillow) and/or style of conduit, a specific manufacturer, a specific model, or other such identifiable information.
G16H 40/63 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement local
G16H 40/60 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santé; TIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux
