Abstract: A hydroponic grow system includes: multiple grow containers; a reservoir; and a water pump, where an output of the water pump is coupled to an inlet of the reservoir and at least one outlet of the reservoir is coupled to an input of the water pump. A hydroponic grow container includes: a grow vessel; and an adaptable manifold coupled to the grow vessel. A hydroponic reservoir including: at least one inlet; at least one outlet; a return tank; and a distribution tank.

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

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

Abstract: Concurrent treatment of obstructive sleep apnea and hypertension in a patient, via a pressure generating system, includes providing a flow of treatment gas to an airway of a patient in accordance with an initial set of flow parameters with respect to an obstructive sleep apnea mode. Responsive to determining that the patient has achieved stable breathing while receiving the flow of treatment gas, the flow parameters are increased above the initial set of flow parameters with respect to a hyper-ventilation mode. The flow of treatment gas is then provided to the airway of the patient in accordance with the increased flow parameters for a predetermined period of time. The increased flow parameters are configured to bring the patient's breath into accordance with target patient breath parameters configured to inflate the patient's lungs beyond a threshold for activating pulmonary stretch receptors of the airway of the patient.

Abstract: Concurrent treatment of obstructive sleep apnea and hypertension in a patient, via a pressure generating device, includes providing a flow of treatment gas to an airway of a patient in accordance with an initial set of flow parameters with respect to an obstructive sleep apnea mode. Responsive to determining that the patient has achieved stable breathing while receiving the flow of treatment gas, the flow parameters are increased above the initial set of flow parameters with respect to a hyper-ventilation mode. The flow of treatment gas is then provided to the airway of the patient in accordance with the increased flow parameters for a predetermined period of time. The increased flow parameters are configured to bring the patient's breath into accordance with target patient breath parameters configured to inflate the patient's lungs beyond a threshold for activating pulmonary stretch receptors of the airway of the patient.

Abstract: Concurrent treatment of obstructive sleep apnea and hypertension in a patient, via a pressure generating device, includes providing a flow of treatment gas to an airway of a patient in accordance with an initial set of flow parameters with respect to an obstructive sleep apnea mode. Responsive to determining that the patient has achieved stable breathing while receiving the flow of treatment gas, the flow parameters are increased above the initial set of flow parameters with respect to a hyper-ventilation mode. The flow of treatment gas is then provided to the airway of the patient in accordance with the increased flow parameters for a predetermined period of time. The increased flow parameters are configured to bring the patient's breath into accordance with target patient breath parameters configured to inflate the patient's lungs beyond a threshold for activating pulmonary stretch receptors of the airway of the patient.

Abstract: The systems and methods disclosed herein provide an improved processor package to determine a connection type between the package and an external circuit and to optimize processor performance based on the connection type. As a non-limiting example, a processor package consistent with the present disclosure may include a central processing unit (CPU) die and a plurality of pins (including two connection detection pins) to connect the package to a motherboard. The CPU die may include connection determination logic and execution policy logic, implemented via processor code (“p-code”), as well as a more typical processor.

Abstract: The present invention relates to a method for re-synchronizing a breathing pattern of a patient (16) suffering from ataxic breathing, the method including the steps of monitoring the breathing pattern of the patient (16) during sleep; detecting whether the monitored breathing pattern includes an ataxic breathing episode; and if an ataxic breathing episode is detected, ventilating the patient (16) and eliminating a spontaneous breathing of the patient (16) for a predetermined first period of time (?t1) by providing a flow of breathing gas (14) to an airway of the patient (16) with a volume of the breathing gas (14) provided per minute being above an individual-related threshold value of the patient (16).

Abstract: There is provided a control unit (100) for use with a respiratory assist device (102) that assists a subject (104) with respiration. The control unit (100) configured to detect a time at which delivery of an inhalable therapy to the subject (104) is manually triggered on an inhalable therapy device (106). The control unit (100) is also configured to detect whether the subject (104) has fallen asleep and, on detecting that the subject (104) has fallen asleep, control the inhalable therapy device (106) to automatically trigger delivery of the inhalable therapy to the subject (104) at least a predefined length of time following the detected time at which delivery of the inhalable therapy to the subject (104) is manually triggered.

Abstract: Sleep related conditions of a subject are monitored and/or diagnosed based on both sleep quality and apnea hypopnea index. A first sleep test is performed in which a sleep quality of the subject and an apnea-hypopnea index are determined. A determination is made as to whether results of the first sleep test meet a first condition based on both the sleep quality and apnea-hypopnea index of the subject associated with the first sleep test. Responsive to the results of the first sleep test failing to meet the first condition, a recommendation of a treatment for the subject is provided. An efficacy of the treatment is confirmed in a second sleep test involving the treatment by determining whether results of the second sleep test meet the first condition based on both the sleep quality and apnea-hypopnea index of the subject associated with the second sleep test.

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

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

Abstract: A hydroponic grow system includes: multiple grow containers; a reservoir; and a water pump, where an output of the water pump is coupled to an inlet of the reservoir and at least one outlet of the reservoir is coupled to an input of the water pump. A hydroponic grow container includes: a grow vessel; and an adaptable manifold coupled to the grow vessel. A hydroponic reservoir including: at least one inlet; at least one outlet; a return tank; and a distribution tank.

Abstract: The systems and methods disclosed herein provide an improved processor package to determine a connection type between the package and an external circuit and to optimize processor performance based on the connection type. As a non-limiting example, a processor package consistent with the present disclosure may include a central processing unit (CPU) die and a plurality of pins (including two connection detection pins) to connect the package to a motherboard. The CPU die may include connection determination logic and execution policy logic, implemented via processor code (“p-code”), as well as a more typical processor.

Abstract: Sleep related conditions of a subject are monitored and/or diagnosed based on both sleep quality and apnea hypopnea index. A first sleep test is performed in which a sleep quality of the subject and an apnea-hypopnea index are determined. A determination is made as to whether results of the first sleep test meet a first condition based on both the sleep quality and apnea-hypopnea index of the subject associated with the first sleep test. Responsive to the results of the first sleep test failing to meet the first condition, a recommendation of a treatment for the subject is provided. An efficacy of the treatment is confirmed in a second sleep test involving the treatment by determining whether results of the second sleep test meet the first condition based on both the sleep quality and apnea-hypopnea index of the subject associated with the second sleep test.

Abstract: A method for the concurrent treatment of obstructive sleep apnea and hypertension in a patient, the method comprises: a) providing a flow of treatment to an airway of the patient in accordance with an initial set of flow parameters; b) determining that the patient has achieved stable breathing while receiving the provided flow of treatment gas in accordance with the initial set of parameters; c) increasing the flow parameters; d) providing the flow of treatment gas to the airway of the patient in accordance with the increased flow parameters until it is determined that a predetermined period of time has elapsed; e) further increasing the flow parameters; and f) providing the flow of treatment gas to the airway of the patient in accordance with the further increased flow parameters for a predetermined time.

Abstract: The present invention relates to a method for re-synchronizing a breathing pattern of a patient (16) suffering from ataxic breathing, the method including the steps of monitoring the breathing pattern of the patient (16) during sleep; detecting whether the monitored breathing pattern includes an ataxic breathing episode; and if an ataxic breathing episode is detected, ventilating the patient (16) and eliminating a spontaneous breathing of the patient (16) for a predetermined first period of time (?t1) by providing a flow of breathing gas (14) to an airway of the patient (16) with a volume of the breathing gas (14) provided per minute being above an individual-related threshold value of the patient (16).

Abstract: A pressure support system includes a gas flow generator; a patient interface device structured to be secured to a patient; a gas delivery conduit structured to couple the gas flow generator to the patient interface device; and a passive noise system provided on at least one of the gas flow generator, the patient interface device, and the gas delivery conduit, the passive noise system being structured to utilize a flow of gas to alter a base audible output of the pressure support system.