Sleep breathing control method, device, system, equipment and medium

Abstract

The invention relates to the technical field of medical equipment, in particular to a sleep breathing control method, device, system, equipment and medium, and aims to obtain sleep-related data of a monitored object in a sleep period, judge whether the monitored object needs breathing control or not according to the sleep-related data, and control breathing of the monitored object if the monitored object needs breathing control. If yes, mode setting information of the breathing control system is determined, the mode setting information is used for indicating working modes of the breathing control system, the working modes comprise a CPAP ventilation mode, a BiPAP-T ventilation mode and an Auto BiPAP ventilation mode, and corresponding different control strategies are adopted for the monitored object according to the mode setting information of the breathing control system. It can be seen that according to the sleep related data, whether the monitored object needs to be subjected to breathing control or not is determined, and when the monitored object needs to be subjected to breathing control, accurate sleep breathing control can be conducted on the monitored object according to the mode setting information of the breathing control system, so that the treatment effect becomes better.

Description

Technical Field

[0001] The present invention relates to the technical field of medical equipment, and in particular to a sleep breathing control method, device, system, equipment and medium. Background Art

[0002] As people's life and work rhythms continue to accelerate, people's mental stress is also increasing. If these anxiety and tension are not effectively relieved, it will easily cause sleep disorders. Sleep disorders not only cause harm to the patient's body and mind, but also seriously affect the patient's life and work.

[0003] The existing technologies all use traditional home breathing control systems or drug treatments to control sleep breathing. However, these methods cannot accurately control sleep breathing for some serious sleep disorders caused by psychological tension and bipolar disorder, resulting in poor treatment effects. Therefore, how to accurately control the sleep breathing of patients to improve the treatment effect is a technical problem that needs to be solved urgently. Summary of the invention

[0004] Based on this, it is necessary to address the above technical problems and provide a sleep breathing control method, device, equipment and medium in the embodiments of the present invention to solve the problem that the prior art cannot perform accurate sleep breathing control, resulting in poor treatment effect.

[0005] A first aspect of an embodiment of the present application provides a sleep breathing control method, the sleep breathing control method comprising: Acquiring sleep-related data of the monitored subject during sleep, wherein the sleep-related data includes sleep oxygenation data and sleep turning data; Determining whether the monitored subject needs to perform breathing control according to the sleep-related data; If the monitored object needs to perform breathing control, determining mode setting information of the breathing control system, wherein the mode setting information is used to indicate the working mode of the breathing control system, and the working mode includes CPAP ventilation mode, BiPAP-T ventilation mode and Auto BiPAP ventilation mode; According to the mode setting information of the breathing control system, different corresponding control strategies are adopted for the monitored object.

[0006] A second aspect of an embodiment of the present application provides a sleep breathing control device, the sleep breathing control device comprising: An acquisition module, used to acquire sleep-related data of the monitored subject during sleep, wherein the sleep-related data includes sleep oxygenation data and sleep turning data; A judgment module, configured to judge whether the monitored object needs to perform breathing control according to the sleep-related data; A determination module, configured to determine the mode setting information of the breathing control system if the monitored object needs to perform breathing control, where the mode setting information is used to indicate the working mode of the breathing control system, and the working mode includes a CPAP ventilation mode, a BiPAP-T ventilation mode, and an Auto BiPAP ventilation mode; A control module, configured to adopt corresponding different control strategies for the monitored object according to the mode setting information of the breathing control system.

[0007] A third aspect of the embodiments of the present application provides a sleep disorder treatment system, characterized in that the sleep disorder treatment system includes a control system, a monitoring system, and a breathing control system; The control system is configured to obtain sleep-related data of the monitored object during sleep fed back by the monitoring system, where the sleep-related data includes sleep oxygenation data and sleep turning data; judge whether the monitored object needs to perform breathing control according to the sleep-related data; if the monitored object needs to perform breathing control, determine the mode setting information of the breathing control system, where the mode setting information is used to indicate the working mode of the breathing control system, and the working mode includes a CPAP ventilation mode, a BiPAP-T ventilation mode, and an Auto BiPAP ventilation mode; adopt corresponding different control strategies for the monitored object according to the mode setting information of the breathing control system.

[0008] In a fourth aspect, an electronic device is provided, including a memory, a processor, and a computer program stored in the memory and executable on the processor, where when the processor executes the computer program, the sleep breathing control method described in the first aspect is implemented.

[0009] In a fifth aspect, a computer-readable storage medium is provided, where the computer-readable storage medium stores a computer program, and when the computer program is executed by a processor, the sleep breathing control method described in the first aspect is implemented.

[0010] In summary, the present invention provides a sleep breathing control method, apparatus, system, device and medium, which obtain sleep-related data of a monitoring object during sleep. The sleep-related data includes sleep oxygenation data and sleep turning data. According to the sleep-related data, it is determined whether the monitoring object needs to perform breathing control. If the monitoring object needs to perform breathing control, the mode setting information of the breathing control system is determined. The mode setting information is used to indicate the working mode of the breathing control system, and the working modes include CPAP ventilation mode, BiPAP-T ventilation mode and Auto BiPAP ventilation mode. According to the mode setting information of the breathing control system, corresponding different control strategies are adopted for the monitoring object. It can be seen that through the present application, it is determined whether the monitoring object needs to perform breathing control according to the sleep-related data, and then when the monitoring object needs to perform breathing control, according to the mode setting information of the breathing control system, accurate sleep breathing control can be performed on the monitoring object, so that the treatment effect becomes better. BRIEF DESCRIPTION OF THE DRAWINGS

[0011] In order to more clearly illustrate the technical solutions of the embodiments of the present invention, the drawings required for the description of the embodiments of the present invention will be briefly introduced below. Obviously, the drawings in the following description are only some embodiments of the present invention, and those of ordinary skill in the art can obtain other drawings without creative efforts based on these drawings.

[0012] Figure 1 FIG. is a schematic structural diagram of a sleep disorder treatment system provided by an embodiment of the present invention; Figure 2 FIG. is a schematic flowchart of a sleep breathing control method provided by an embodiment of the present invention; Figure 3 FIG. is a schematic structural diagram of a sleep breathing control device provided by an embodiment of the present invention; Figure 4 FIG. is a schematic structural diagram of an electronic device provided by an embodiment of the present invention. DETAILED DESCRIPTION OF THE EMBODIMENTS

[0013] The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention. Obviously, the described embodiments are some, but not all, embodiments of the present invention. All other embodiments obtained by those of ordinary skill in the art without creative efforts based on the embodiments of the present invention belong to the protection scope of the present invention.

[0014] It should be understood that, as used in the specification of the present invention and the appended claims, the term "comprising" indicates the presence of the described features, integers, steps, operations, elements and / or components, but does not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components and / or their combinations.

[0015] It should also be understood that the term "and / or" used in the specification of the present invention and the appended claims refers to any combination and all possible combinations of one or more of the associated listed items, and includes these combinations.

[0016] As used in the specification of the present invention and the appended claims, the term "if" may be interpreted, depending on the context, as "when" or "once" or "in response to determining". Similarly, the phrase "if determined" or "if matched to [the described condition or event]" may be interpreted, depending on the context, as meaning "once determined" or "in response to determining" or "once matched to [the described condition or event]" or "in response to matching to [the described condition or event]".

[0017] In addition, in the description of the specification of the present invention and the appended claims, the terms "first", "second", "third", etc. are only used for distinguishing descriptions and should not be construed as indicating or implying relative importance.

[0018] Reference to "one embodiment" or "some embodiments" or the like described in the specification of the present invention means that a specific feature, structure or characteristic described in connection with that embodiment is included in one or more embodiments of the present invention. Thus, statements such as "in one embodiment", "in some embodiments", "in other some embodiments", "in still other embodiments" and the like that appear in different places in this specification do not necessarily all refer to the same embodiment, but mean "one or more but not all embodiments", unless otherwise specifically emphasized in other ways. The terms "comprising", "including", "having" and their variants all mean "including but not limited to", unless otherwise specifically emphasized in other ways.

[0019] It should be understood that the magnitudes of the sequence numbers of the steps in the following embodiments do not mean the order of execution is prior or posterior, and the order of execution of each process should be determined by its function and internal logic, and should not constitute any limitation to the implementation process of the embodiments of the present invention.

[0020] In order to illustrate the technical solutions of the present invention, the following specific embodiments are used for illustration.

[0021] See Figure 1 , which is a schematic structural diagram of a sleep disorder treatment system provided by an embodiment of the present invention. The sleep disorder treatment system includes a control system, a monitoring system and a respiratory control system.

[0022] In a specific embodiment, the control system is used to obtain sleep-related data of a monitored object during sleep fed back by a monitoring system. The sleep-related data includes sleep oxygenation data and sleep turning data. According to the sleep-related data, it is determined whether the monitored object needs to perform respiratory control. If the monitored object needs to perform respiratory control, the mode setting information of the respiratory control system is determined. The mode setting information is used to indicate the working mode of the respiratory control system, and the working modes include CPAP ventilation mode, BiPAP-T ventilation mode, and Auto BiPAP ventilation mode. According to the mode setting information of the respiratory control system, different corresponding control strategies are adopted for the monitored object.

[0023] In the embodiment of the present application, the monitoring system collects sleep-related data of the monitored object during sleep. The monitoring system consists of a blood oxygen module and a sleep blanket. The blood oxygen module monitors the sleep oxygenation data in the sleep state to ensure that respiratory control can ensure sufficient air supply as much as possible and ensure normal blood oxygen saturation during sleep. The oxygenation data includes blood oxygen saturation, partial pressure of oxygen, oxygenation index, respiratory rate, tidal volume, and ventilation / perfusion ratio, etc. Among them, blood oxygen saturation reflects the degree of combination of hemoglobin in red blood cells in the blood with oxygen; partial pressure of oxygen reflects the tension generated by physically dissolved oxygen molecules in the blood; the oxygenation index is used to evaluate the oxygenation ability of the lungs and is calculated by dividing the arterial partial pressure of oxygen (PaO2) by the inspired oxygen concentration (FiO2); respiratory rate, tidal volume, and ventilation / perfusion ratio: Although these parameters do not directly reflect the oxygenation situation, their abnormalities can affect the oxygenation process. For example, too fast or too slow respiratory rate, insufficient or excessive tidal volume, and imbalance of ventilation / perfusion ratio may all lead to poor oxygenation. The sleep turning data of the user in the sleep state is monitored through the pressure sensor inside the sleep blanket, so as to indirectly achieve the purpose of monitoring sleep quality. The monitoring system and the respiratory control system are respectively connected to the control system through the wireless Bluetooth method, so as to receive the sleep-related data of the monitored object collected by the monitoring system during sleep. Then, according to the sleep-related data, it is determined whether the monitored object needs to perform respiratory control. If the monitored object needs to perform respiratory control, the most suitable working mode of the respiratory control system is selected, and sleep respiratory control is performed on the monitored object.

[0024] In the embodiments of the present application, the working modes of the respiratory control system include the CPAP ventilation mode, the BiPAP-T ventilation mode, and the Auto BiPAP ventilation mode. Among them, the CPAP ventilation mode refers to continuous positive airway pressure ventilation, which delivers a certain pressure of airflow into the airway during the respiratory cycle through a specific device to keep the airway open and prevent airway collapse; the BiPAP-T ventilation mode refers to the time control mode in bilevel positive airway pressure ventilation (BiPAP), which performs inhalation-exhalation phase conversion according to a preset time constant (or frequency) and works according to strict parameters such as the respiratory rate and inhalation-exhalation time set by the user, without relying on the patient's spontaneous breathing trigger. When the patient's breathing is weak and unable to breathe spontaneously, the machine drives the patient to breathe; the Auto BiPAP ventilation mode is automatic bilevel positive airway pressure ventilation, which is a device technology commonly used to treat diseases such as sleep apnea and respiratory insufficiency. By adjusting the inspiratory positive airway pressure (IPAP) and the expiratory positive airway pressure (EPAP), when the patient inhales, the machine provides a higher IPAP to assist in inhaling more air; when exhaling, a lower EPAP is given to prevent airway collapse and ensure smooth breathing. It can be seen that by selecting the most suitable ventilation mode and adjusting the settings in real time through the above steps, personalized treatment can be provided to meet the specific needs of different patients, thereby improving sleep quality and treatment effect.

[0025] See Figure 2 , which is a schematic flowchart of a sleep respiratory control method provided by an embodiment of the present invention. As Figure 2 shown, the sleep respiratory control method can be implemented through the following steps.

[0026] S201: Obtain sleep-related data of the monitoring object during sleep, where the sleep-related data includes sleep oxygenation data and sleep turning data.

[0027] In step S201, multi-modal raw data is acquired based on the monitoring system in the wearable device of the monitoring object. For example, the multi-modal raw data is acquired through a pulse wave sensor, a galvanic skin sensor, an acceleration sensor, an angular velocity sensor, a GPS sensor, a blood oxygen sensor, a blood pressure sensor, a voice sensor, etc. Then, data extraction is performed on the multi-modal raw data to obtain sleep-related data of the monitoring object during sleep. The monitoring system consists of a blood oxygen module and a sleep blanket. The blood oxygen module can monitor sleep oxygenation data in the sleep state to ensure that the respiratory control can ensure sufficient air supply as much as possible and ensure normal blood oxygen saturation during sleep. The oxygenation data includes blood oxygen saturation, partial pressure of oxygen, oxygenation index, respiratory rate, tidal volume, and ventilation / perfusion ratio, etc. Among them, blood oxygen saturation reflects the degree of binding of hemoglobin in red blood cells in the blood to oxygen; partial pressure of oxygen reflects the tension generated by physically dissolved oxygen molecules in the blood; the oxygenation index is used to evaluate the oxygenation ability of the lungs and is calculated by dividing the arterial partial pressure of oxygen (PaO2) by the inspired oxygen concentration (FiO2); respiratory rate, tidal volume, and ventilation / perfusion ratio: Although these parameters do not directly reflect the oxygenation situation, their abnormalities can affect the oxygenation process. For example, too fast or too slow respiratory rate, insufficient or excessive tidal volume, and imbalance of ventilation / perfusion ratio may all lead to poor oxygenation. The sleep turning data of the user in the sleep state is monitored through the pressure sensor inside the sleep blanket, thereby indirectly achieving the purpose of monitoring sleep quality. Since the monitoring system is connected to the control system through wireless Bluetooth, the control system receives the sleep-related data collected by the monitoring system during the sleep period of the monitoring object. Among them, the sleep-related data refers to various types of data related to the sleep status of the user, and each category of sleep-related data can be used as a consideration factor when identifying sleep disorders. In this embodiment, the sleep-related data includes sleep oxygenation data and sleep turning data in different dimensions and different forms.

[0028] In this embodiment, by obtaining the sleep-related data of the monitoring object during sleep, the mode setting information of a more reasonable respiratory control system can be determined subsequently, so as to perform more accurate sleep respiratory control and improve the user experience.

[0029] S202: According to the sleep-related data, determine whether the monitoring object needs respiratory control.

[0030] In step S202, the control system compares the collected sleep data with a preset threshold or algorithm to determine whether the monitored object has a risk of respiratory disorders, such as hypoxemia or obstructive sleep apnea (OSA). If the data indicates that the monitored object has a respiratory problem, the system will trigger a respiratory control process, that is, determine that the monitored object needs respiratory control. If the monitored object does not have a risk of respiratory disorders, it is determined that the monitored object does not need respiratory control and does not execute the steps of this sleep respiratory control method.

[0031] In an embodiment of the invention, determining whether a monitored object needs respiratory control based on sleep-related data includes: Comparing the sleep-related data with a preset sleep recognition index, where the sleep recognition index includes an index category related to sleep disorders and an index score used to characterize the degree of association between each index category and sleep disorders; When the sleep-related data is the same as the index score, or the difference between the sleep-related data and the index score is less than a predetermined threshold, it is determined that the monitored object needs respiratory control.

[0032] Specifically, the sleep recognition index includes an index category related to sleep disorders and an index score used to characterize the degree of association between each index category and sleep disorders, that is, the index category is consistent with the category of the above sleep-related data, and the index score can be used as the influence threshold of each index category on sleep disorders. It should be noted that the preset sleep recognition index can be specifically set according to the actual situation, and this application does not make any limitations in this regard. For any two different types of mental disorders (such as sleep disorders and anxiety disorders), their corresponding index categories can be the same or partially the same (partially the same means that some mental disorders are more prominent in some index categories and have a higher degree of association with the index category, while another mental disorder has no association with this index category. For example, the sleep oxygenation data has a higher degree of association with sleep disorders, but has basically no association with anxiety disorders, depressive mood disorders or bipolar disorder). In the case where the index categories are the same or partially the same, there is at least one or more identical index categories corresponding to different index scores, that is, the degree of association between the same index category and different types of mental disorders is different. For example, for the index categories related to sleep disorders are sleep oxygenation index and sleep turning index. However, the association between sleep disorders and the above sleep index is significantly higher than the association between anxiety disorders and sleep index. Therefore, when the sleep-related data is the same as the index score, or the difference between the sleep-related data and the index score is less than a predetermined threshold, it is determined that the monitored object needs respiratory control.

[0033] Moreover, when identifying different types of mental disorders, the required precision for the same index category is different. Therefore, different indexes in the same index category need to be selected.

[0034] This application compares each sleep-related data with a preset sleep recognition index. Specifically, it refers to comparing the above-mentioned sleep-related data with the index scores, that is, comparing all sleep-related data with the index scores of their corresponding index categories respectively. When the sleep-related data is the same as the above index scores, or the difference between the sleep-related data and the index scores is less than a predetermined threshold, it is determined that the monitored object needs to perform respiratory control. Through the above steps, sleep-related data in different forms or dimensions, such as sleep oxygenation data and sleep turning data, are all considered as factors when identifying sleep disorders. This makes the respiratory control process of the monitored object not only consider the influence of a single factor or the same type of factors such as the physical or physiological condition, but also consider the influence of multiple types of factors related to sleep quality in different dimensions and different forms, making full use of the different degrees of association between different types of factors and different sleep disorders, so that the subsequent respiratory control results of the monitored object can be more effective, improving the accuracy and efficiency of sleep respiratory control.

[0035] S203: If the monitored object needs to perform respiratory control, determine the mode setting information of the respiratory control system, where the mode setting information is used to indicate the working mode of the respiratory control system, and the working mode includes CPAP ventilation mode, BiPAP-T ventilation mode, and Auto BiPAP ventilation mode.

[0036] In step S203, when the monitored object needs to perform respiratory control, since the respiratory control system is connected to the control system through wireless Bluetooth, the control system can obtain the mode setting information of the respiratory control system for informing the control system which mode it is currently working in. The mode setting information is usually used to guide the respiratory control system to perform specific tasks or operations to ensure that the respiratory control system performs sleep respiratory control according to the user's needs. And the working modes of the respiratory control system in this application include CPAP ventilation mode, BiPAP-T ventilation mode, and Auto BiPAP ventilation mode, so as to select the most suitable working mode of the respiratory control system for the monitored object to perform sleep respiratory control subsequently.

[0037] Among them, the CPAP ventilation mode refers to continuous positive airway pressure ventilation, which delivers a certain pressure of airflow into the airway during the respiratory cycle through a specific device to keep the airway open and prevent airway collapse; the BiPAP-T ventilation mode refers to the time control mode in bilevel positive airway pressure ventilation (BiPAP), which performs inspiration-expiration phase conversion according to the preset time constant (or frequency), works according to strict parameters such as the respiratory rate and inspiratory and expiratory times set by the user, does not rely on the patient's spontaneous breathing trigger, and drives the patient's breathing by the machine when the patient's breathing is weak and unable to breathe spontaneously; the Auto BiPAP ventilation mode is automatic bilevel positive airway pressure ventilation, which is a device technology commonly used to treat conditions such as sleep apnea and respiratory insufficiency. By adjusting the inspiratory positive airway pressure (IPAP) and expiratory positive airway pressure (EPAP), when the patient inhales, the machine provides a higher IPAP to assist in inhaling more air; when exhaling, a lower EPAP is given to prevent airway collapse and ensure smooth breathing. It can be seen that by selecting the most suitable ventilation mode and adjusting the settings in real time through the above steps, personalized treatment can be provided to meet the specific needs of different patients, thereby improving the sleep quality and enhancing the treatment effect.

[0038] S204: According to the mode setting information of the respiratory control system, different corresponding control strategies are adopted for the monitored object.

[0039] In step S204, since the mode setting information of the respiratory control system is used to indicate the working mode of the respiratory control system, and this working mode includes the CPAP ventilation mode, the BiPAP-T ventilation mode, and the Auto BiPAP ventilation mode, different corresponding control strategies are adopted for the monitored object in different ventilation working modes, so as to meet the specific needs of different patients, improve the sleep quality, and enhance the treatment effect. For example, in the CPAP ventilation mode, the ventilator provides continuous positive airway pressure for the monitored object, and the pressure level is adjusted according to the severity of the monitored object's sleep apnea and comfort. The respiratory rate, tidal volume and other parameters of the monitored object are monitored in real time to ensure the treatment effect; in the BiPAP-T ventilation mode, different pressure levels are provided when the monitored object inhales and exhales. The inspiratory pressure is higher, which helps to overcome the airway resistance and increase the tidal volume, and the expiratory pressure is lower, which helps to reduce the residual volume in the lungs at the end of exhalation. The inspiratory and expiratory pressure levels are dynamically adjusted according to the respiratory effort degree and comfort of the monitored object; in the Auto BiPAP ventilation mode, the inspiratory and expiratory pressure levels are automatically adjusted according to the real-time respiratory parameters and blood gas analysis results of the monitored object, that is, when the patient's breathing is stable, a lower pressure level is maintained; when the patient has apnea or hypoventilation, the pressure is rapidly increased to provide support.

[0040] In an embodiment of the invention, according to the mode setting information of the respiratory control system, different corresponding control strategies are adopted for the monitored object, including: When it is determined according to the mode setting information that the respiratory control system is in the CPAP ventilation mode, the initial ventilation parameters of the CPAP ventilation mode are obtained, and the fan is driven to start working according to a preset pressure value; According to the initial ventilation parameters of the CPAP ventilation mode, it is judged whether the monitored object stops treatment; If the monitored object does not stop treatment, it is judged whether the pressure generated by the fan reaches the preset pressure value; If the pressure generated by the fan does not reach the preset pressure value, the driving PWM signal of the fan is adjusted according to the difference between the pressure generated by the fan and the preset pressure value, so as to gradually approach and reach the preset pressure value.

[0041] Specifically, when the control system determines that the respiratory control system is in the CPAP ventilation mode according to the mode setting information, it will first obtain the initial ventilation parameters in the CPAP ventilation mode from a preset parameter library. These parameters usually include the basic pressure value of CPAP (such as 4 - 5 cmH2O), as well as other related settings that may be involved, such as respiratory rate, tidal volume, flow rate, etc. (although in the CPAP mode, these parameters may not be the main adjustment objects, but still need to be monitored to ensure patient safety). According to the obtained initial ventilation parameters of the CPAP ventilation mode, especially the preset pressure value, the control system drives the fan to start working, delivering a constant positive pressure to the patient's airway. At the same time, the control system continuously monitors the patient's treatment status, including whether to continue treatment, changes in respiratory parameters, etc. If the patient does not stop treatment, the control system then detects the actual pressure value generated by the fan in real time, judges whether the actual pressure value generated by the fan reaches the preset pressure value. If the actual pressure value generated by the fan does not reach the preset pressure value, the difference between the actual pressure value and the preset pressure value is calculated, and then the driving PWM signal of the fan is adjusted according to the size of the difference. The adjustment of this PWM signal can change the speed of the fan, so as to gradually approach and reach the preset pressure value. Through the above steps, the pressure generated by the fan can be accurately adjusted to always maintain near the preset pressure value, which helps to ensure the stability of the treatment effect, reduce discomfort or risks that may be brought by pressure fluctuations, and thus improve the treatment effect.

[0042] In an embodiment of the invention, according to the mode setting information of the respiratory control system, different corresponding control strategies are adopted for the monitored object, and also include: When it is determined according to the mode setting information that the respiratory control system is in the BiPAP-T ventilation mode, the initial ventilation parameters of the BiPAP-T ventilation mode are obtained; Judge whether the monitored object stops treatment according to the initial ventilation parameters of the BiPAP-T ventilation mode; If the monitored object does not stop treatment, calculate the first respiratory parameter of the monitored object within a preset time according to the initial ventilation parameters of the BiPAP-T ventilation mode; Judge whether the first respiratory parameter meets the inspiratory trigger condition; If the first respiratory parameter meets the inspiratory trigger condition, the monitored object enters the inspiratory state and inspiratory pressure is given; If the first respiratory parameter does not meet the inspiratory trigger condition, judge whether the first respiratory parameter meets the expiratory trigger condition; If the first respiratory parameter meets the expiratory trigger condition, the monitored object enters the expiratory state and expiratory pressure is given; If the first respiratory parameter does not meet the expiratory trigger condition, judge whether the monitored object is in the inspiratory state; If the monitored object is in the inspiratory state, adjust the fan drive PWM signal according to the difference between the pressure generated by the fan and the preset pressure value to gradually approach and reach the preset pressure value, and judge whether the monitored object has finished inhaling; If the monitored object has finished inhaling, continue to execute the judgment process of the expiratory trigger condition; If the monitored object is not in the inspiratory state, judge whether the monitored object is in the expiratory state; If the monitored object is in the expiratory state, adjust the fan drive PWM signal according to the difference between the pressure generated by the fan and the preset pressure value to gradually approach and reach the preset pressure value, and judge whether the monitored object meets the spontaneous breathing condition; If the monitored object meets the spontaneous breathing condition, continue to execute the judgment process of the inspiratory trigger condition; If the monitored object does not meet the spontaneous breathing condition, judge whether the monitored object has finished exhaling; If the monitored object has finished exhaling, continue to execute the judgment process of the inspiratory trigger condition.

[0043] Specifically, when the control system determines that the respiratory control system is in the BiPAP-T ventilation mode according to the mode setting information, it first obtains the initial ventilation parameters for this BiPAP-T ventilation mode from the preset parameter library. These parameters usually include the base pressure value of BiPAP-T (such as 4 - 5 cmH2O), as well as other relevant settings that may be involved, such as respiratory rate, tidal volume, flow rate, etc. (although in the CPAP mode, these parameters may not be the main adjustment objects, but still need to be monitored to ensure patient safety). According to the obtained initial ventilation parameters of the BiPAP-T ventilation mode, monitor the patient's treatment status, including whether to continue treatment, changes in respiratory parameters, etc. If the patient does not stop treatment, within the preset time, calculate the first respiratory parameter of the monitored object according to the initial ventilation parameters of the BiPAP-T ventilation mode. Thereafter, determine whether the first respiratory parameter meets the inspiratory trigger condition or the expiratory trigger condition. If the inspiratory trigger condition is met, the monitored object enters the inspiratory state, and the system gives the inspiratory pressure (IPAP). If the expiratory trigger condition is met, the monitored object enters the expiratory state, and the system gives the expiratory pressure (EPAP). If neither the inspiratory trigger condition nor the expiratory trigger condition is met, determine whether the monitored object is in the inspiratory state or the expiratory state. When the monitored object is in the inspiratory state or the expiratory state, perform corresponding processing according to the current state (inspiration or expiration). In the inspiratory or expiratory state, the control system continuously monitors the pressure generated by the blower and compares it with the preset pressure value (IPAP or EPAP), and adjusts the blower drive PWM signal according to the difference to gradually approach and reach the preset pressure value, and then determine whether the monitored object's inspiration or expiration ends. If the inspiration ends, enter the judgment process of the expiratory trigger condition. If the expiration ends, enter the judgment process of the inspiratory trigger condition, and determine whether the monitored object meets the condition of spontaneous breathing (that is, the breathing is stable and no additional ventilation support is required). If the monitored object meets the spontaneous breathing condition, continue to execute the judgment process of the inspiratory trigger condition. If the spontaneous breathing condition is not met, continue to execute the judgment process of the inspiratory trigger condition after the expiration ends. Through the above steps, it is possible to accurately give the inspiratory pressure and the expiratory pressure according to the real-time respiratory state of the monitored object, thereby providing personalized ventilation support. Furthermore, by monitoring the patient's spontaneous breathing condition, it is possible to reduce the ventilation support at an appropriate time, promote the recovery of the patient's spontaneous breathing function, and thus improve the treatment effect.

[0044] In an embodiment of the invention, according to the mode setting information of the respiratory control system, different control strategies are adopted for the monitored object, and it further includes: When it is determined that the respiratory control system is in the Auto BiPAP ventilation mode according to the mode setting information, obtain the initial ventilation parameters of the Auto BiPAP ventilation mode; Based on the initial ventilation parameters of the Auto BiPAP ventilation mode, determine whether the monitored object stops treatment; If the monitored object does not stop treatment, calculate the second respiratory parameter of the monitored object within a preset time according to the initial ventilation parameters of the Auto BiPAP ventilation mode; Perform respiratory recognition on the second respiratory parameter to determine whether the monitored object meets the condition of spontaneous breathing; If the monitored object meets the condition of spontaneous breathing, determine whether the second respiratory parameter meets the inspiratory trigger condition; If the second respiratory parameter meets the inspiratory trigger condition, the monitored object enters the inspiratory state and inspiratory pressure is given; If the second respiratory parameter does not meet the inspiratory trigger condition, determine whether the second respiratory parameter meets the expiratory trigger condition; If the second respiratory parameter meets the expiratory trigger condition, the monitored object enters the expiratory state and expiratory pressure is given; If the second respiratory parameter does not meet the expiratory trigger condition, determine whether the monitored object is in the inspiratory state; If the monitored object is in the inspiratory state, adjust the fan drive PWM signal according to the difference between the pressure generated by the fan and the preset pressure value to gradually approach and reach the preset pressure value, and determine whether the monitored object finishes inspiration; If the monitored object finishes inspiration, continue to execute the judgment process of the expiratory trigger condition; If the monitored object is not in the inspiratory state, determine whether the monitored object is in the expiratory state; If the monitored object is in the expiratory state, adjust the fan drive PWM signal according to the difference between the pressure generated by the fan and the preset pressure value to gradually approach and reach the preset pressure value, and determine whether the monitored object meets the condition of spontaneous breathing; If the monitored object meets the condition of spontaneous breathing, continue to execute the judgment process of the inspiratory trigger condition; If the monitored object does not meet the condition of spontaneous breathing, determine whether the monitored object finishes expiration; If the monitored object finishes expiration, continue to execute the judgment process of the respiratory recognition.

[0045] Specifically, when the control system determines that the respiratory control system is in the Auto BiPAP ventilation mode according to the mode setting information, it will first obtain the initial ventilation parameters in the Auto BiPAP ventilation mode from the preset parameter library. These parameters usually include the base pressure value of Auto BiPAP (such as 4 - 5 cmH2O), as well as other related settings that may be involved, such as respiratory rate, tidal volume, flow rate, etc. (although in the CPAP mode, these parameters may not be the main adjustment objects, but still need to be monitored to ensure patient safety). According to the obtained initial ventilation parameters of the Auto BiPAP ventilation mode, monitor the treatment status of the patient, including whether to continue treatment, changes in respiratory parameters, etc. If the patient does not stop treatment, within the preset time, calculate the second respiratory parameters of the monitored object according to the initial ventilation parameters of the Auto BiPAP ventilation mode, perform respiratory recognition on the second respiratory parameters, and determine whether the monitored object meets the condition of spontaneous breathing. If it meets the condition of spontaneous breathing, then determine whether the second respiratory parameters meet the inspiratory trigger condition or the expiratory trigger condition. If the inspiratory trigger condition is met, the monitored object enters the inspiratory state, and the system gives the inspiratory pressure (IPAP). If the expiratory trigger condition is met, the monitored object enters the expiratory state, and the system gives the expiratory pressure (EPAP). If neither the inspiratory trigger condition nor the expiratory trigger condition is met, then determine whether the monitored object is in the inspiratory state or the expiratory state. When the monitored object is in the inspiratory state or the expiratory state, perform corresponding processing according to the current state (inspiration or expiration). In the inspiratory or expiratory state, the control system continuously monitors the pressure generated by the blower and compares it with the preset pressure value (IPAP or EPAP), and adjusts the blower drive PWM signal according to the difference to gradually approach and reach the preset pressure value, and then determine whether the monitored object's inspiration or expiration ends. If the inspiration ends, enter the judgment process of the expiratory trigger condition. If the expiration ends, enter the judgment process of the inspiratory trigger condition, and determine whether the monitored object meets the condition of spontaneous breathing (that is, stable breathing and no need for additional ventilation support). If the monitored object meets the condition of spontaneous breathing, continue to execute the judgment process of the inspiratory trigger condition. If it does not meet the condition of spontaneous breathing, continue to execute the judgment process of respiratory recognition after expiration. Through the above steps, the Auto BiPAP ventilation mode can provide personalized treatment plans according to the individual differences and respiratory needs of the monitored object, and realizes the automatic operation of the respiratory control system, reduces manual intervention, improves the treatment efficiency and accuracy, and thus improves the treatment effect.

[0046] In an embodiment of the invention, according to the mode setting information of the respiratory control system, different control strategies are adopted for the monitored object, and it further includes: If the monitored object does not meet the condition of spontaneous breathing, then determine whether the monitored object has been asphyxiated for too long; If the monitored object has been in asphyxia for too long, determine whether the number of asphyxia times of the monitored object reaches a preset threshold; If the number of asphyxia times of the monitored object reaches the preset threshold, switch the mode setting information of the respiratory control system to the BiPAP-T ventilation mode; If the number of asphyxia times of the monitored object does not reach the preset threshold, continue to execute the judgment process of the inhalation trigger condition.

[0047] Specifically, when the monitored object does not meet the conditions for spontaneous breathing, the control system starts to monitor whether the monitored object is in an asphyxiated state. Among them, the asphyxiated state can be determined by detecting abnormalities in respiratory parameters such as respiratory rate and tidal volume. For example, the respiratory rate is extremely low or the tidal volume is extremely small. If the monitored object is determined to be in an asphyxiated state, the control system starts timing and records the asphyxiation duration. A threshold for the asphyxiation duration is preset to determine whether the asphyxiation is too long, which can be set according to the actual situation, and the present application does not make any limitations in this regard. If the monitored object is in a state of excessive asphyxiation, the control system starts to count the number of asphyxia times. After each asphyxiation event ends, the number of asphyxia times is updated. If the number of asphyxia times of the monitored object reaches the preset threshold, the control system believes that the patient has a serious respiratory disorder and needs more aggressive ventilation support. At this time, the control system switches the mode setting information of the respiratory control system to the BiPAP-T ventilation mode to provide higher ventilation pressure and more flexible ventilation support. If the number of asphyxia times of the monitored object does not reach the preset threshold, the control system continues to execute the judgment process of the inhalation trigger condition and continuously monitors the respiratory state of the patient. Through the above steps, it is possible to determine whether to switch the ventilation mode according to the number of asphyxia times and the asphyxiation duration of the patient, which reflects the principle of personalized treatment, and realizes automatic monitoring and ventilation mode switching, reduces the manual intervention of medical staff, and improves the treatment efficiency and accuracy.

[0048] In summary, the present invention provides a sleep breathing control method, device, system, equipment and medium, which obtains sleep-related data of a monitored object during sleep. Among them, the sleep-related data includes sleep oxygenation data and sleep turning data. According to the sleep-related data, it is judged whether the monitored object needs to perform respiratory control. If the monitored object needs to perform respiratory control, the mode setting information of the respiratory control system is determined. Among them, the mode setting information is used to indicate the working mode of the respiratory control system, and the working modes include CPAP ventilation mode, BiPAP-T ventilation mode and Auto BiPAP ventilation mode. According to the mode setting information of the respiratory control system, different corresponding control strategies are adopted for the monitored object. It can be seen that the present application determines whether the monitored object needs to perform respiratory control according to the sleep-related data, and then when the monitored object needs to perform respiratory control, according to the mode setting information of the respiratory control system, so that accurate sleep breathing control can be performed on the monitored object, making the treatment effect better.

[0049] Please refer to Figure 3 , Figure 3 which is a schematic structural diagram of the sleep apnea control device provided by an embodiment of the present invention. The sleep apnea control device corresponds one-to-one with the sleep apnea control method in the above embodiment. Specifically, please refer to Figure 2 and Figure 2 the relevant descriptions in the corresponding embodiments. For the sake of convenience of description, only the parts related to this embodiment are shown. Refer to Figure 3 , the sleep apnea control device 30 includes: an acquisition module 31, a judgment module 32, a determination module 33, and a control module 34.

[0050] The acquisition module 31 is configured to acquire sleep-related data of a monitored object during sleep, where the sleep-related data includes sleep oxygenation data and sleep turning data; The judgment module 32 is configured to judge whether the monitored object needs to perform breathing control according to the sleep-related data; The determination module 33 is configured to determine the mode setting information of the breathing control system if the monitored object needs to perform breathing control, where the mode setting information is used to indicate the working mode of the breathing control system, and the working mode includes a CPAP ventilation mode, a BiPAP-T ventilation mode, and an Auto BiPAP ventilation mode; The control module 34 is configured to adopt corresponding different control strategies for the monitored object according to the mode setting information of the breathing control system.

[0051] Optionally, the above-mentioned judgment module 32 is specifically configured to: Compare the sleep-related data with a preset sleep recognition index, where the sleep recognition index includes an index category related to sleep disorders and an index score used to characterize the degree of association between each index category and sleep disorders; When the sleep-related data is the same as the index score, or the difference between the sleep-related data and the index score is less than a predetermined threshold, it is determined that the monitored object needs to perform breathing control.

[0052] Optionally, the above-mentioned calculation module 32 is specifically configured to: Calculate the time-sharing ratio of each of the cooperative applications in each time period according to the daily active user data; Compare the time-sharing ratio of each of the cooperative applications in each time period with the actual completion situation to obtain a comparison result, where the actual completion situation is used to represent the actual completion situation of pushing advertisement content by each of the cooperative applications in each time period; Allocate push weights for each of the cooperative applications according to the comparison result by using a preset algorithm.

[0053] Optionally, the above control module 34 is specifically configured to: When it is determined according to the mode setting information that the respiratory control system is in the CPAP ventilation mode, obtain the initial ventilation parameters of the CPAP ventilation mode, and drive the fan to start working according to a preset pressure value; Judge whether the monitored object stops treatment according to the initial ventilation parameters of the CPAP ventilation mode; If the monitored object does not stop treatment, judge whether the pressure generated by the fan reaches the preset pressure value; If the pressure generated by the fan does not reach the preset pressure value, adjust the fan drive PWM signal according to the difference between the pressure generated by the fan and the preset pressure value, so as to gradually approach and reach the preset pressure value.

[0054] Optionally, the above control module 34 is further configured to: When it is determined according to the mode setting information that the respiratory control system is in the BiPAP-T ventilation mode, obtain the initial ventilation parameters of the BiPAP-T ventilation mode; Judge whether the monitored object stops treatment according to the initial ventilation parameters of the BiPAP-T ventilation mode; If the monitored object does not stop treatment, calculate the first respiratory parameter of the monitored object within a preset time according to the initial ventilation parameters of the BiPAP-T ventilation mode; Judge whether the first respiratory parameter meets the inhalation trigger condition; If the first respiratory parameter meets the inhalation trigger condition, the monitored object enters the inhalation state and is given an inhalation pressure; If the first respiratory parameter does not meet the inhalation trigger condition, judge whether the first respiratory parameter meets the exhalation trigger condition; If the first respiratory parameter meets the exhalation trigger condition, the monitored object enters the exhalation state and is given an exhalation pressure; If the first respiratory parameter does not meet the exhalation trigger condition, judge whether the monitored object is in the inhalation state; If the monitored object is in the inhalation state, adjust the fan drive PWM signal according to the difference between the pressure generated by the fan and the preset pressure value, so as to gradually approach and reach the preset pressure value, and judge whether the monitored object has finished inhaling; If the monitored object has finished inhaling, continue to execute the judgment process of the exhalation trigger condition; If the monitored object is not in the inhalation state, judge whether the monitored object is in the exhalation state; If the monitoring object is in an exhalation state, then according to the difference between the pressure generated by the blower and a preset pressure value, adjust the blower drive PWM signal to gradually approach and reach the preset pressure value, and determine whether the monitoring object satisfies spontaneous breathing; If the monitoring object satisfies spontaneous breathing, then continue to execute the judgment process of the inhalation trigger condition; If the monitoring object does not satisfy spontaneous breathing, then determine whether the monitoring object has ended exhalation; If the monitoring object has ended exhalation, then continue to execute the judgment process of the inhalation trigger condition..

[0055] Optionally, the above control module 34 is further configured to: When it is determined according to the mode setting information that the respiratory control system is in the Auto BiPAP ventilation mode, obtain the initial ventilation parameters of the Auto BiPAP ventilation mode; According to the initial ventilation parameters of the Auto BiPAP ventilation mode, determine whether the monitoring object has stopped treatment; If the monitoring object has not stopped treatment, then calculate a second respiratory parameter of the monitoring object within a preset time according to the initial ventilation parameters of the Auto BiPAP ventilation mode; Perform respiratory recognition on the second respiratory parameter to determine whether the monitoring object satisfies spontaneous breathing; If the monitoring object satisfies spontaneous breathing, then determine whether the second respiratory parameter satisfies the inhalation trigger condition; If the second respiratory parameter satisfies the inhalation trigger condition, then the monitoring object enters an inhalation state and an inhalation pressure is given; If the second respiratory parameter does not satisfy the inhalation trigger condition, then determine whether the second respiratory parameter satisfies the exhalation trigger condition; If the second respiratory parameter satisfies the exhalation trigger condition, then the monitoring object enters an exhalation state and an exhalation pressure is given; If the second respiratory parameter does not satisfy the exhalation trigger condition, then determine whether the monitoring object is in an inhalation state; If the monitoring object is in an inhalation state, then according to the difference between the pressure generated by the blower and a preset pressure value, adjust the blower drive PWM signal to gradually approach and reach the preset pressure value, and determine whether the monitoring object has ended inhalation; If the monitoring object has ended inhalation, then continue to execute the judgment process of the exhalation trigger condition; If the monitoring object is not in an inhalation state, then determine whether the monitoring object is in an exhalation state; If the monitored object is in an exhalation state, adjust the blower drive PWM signal according to the difference between the pressure generated by the blower and a preset pressure value, so as to gradually approach and reach the preset pressure value, and determine whether the monitored object satisfies spontaneous breathing; If the monitored object satisfies spontaneous breathing, continue to execute the judgment process of the inspiration trigger condition; If the monitored object does not satisfy spontaneous breathing, determine whether the monitored object has ended exhalation; If the monitored object has ended exhalation, continue to execute the judgment process of the respiration recognition;

[0056] Optionally, the above control module 34 is further configured to: If the monitored object does not satisfy spontaneous breathing, determine whether the monitored object has been asphyxiated for too long; If the monitored object has been asphyxiated for too long, determine whether the number of asphyxiations of the monitored object has reached a preset threshold; If the number of asphyxiations of the monitored object has reached the preset threshold, switch the mode setting information of the respiration control system to the BiPAP-T ventilation mode; If the number of asphyxiations of the monitored object has not reached the preset threshold, continue to execute the judgment process of the inspiration trigger condition.

[0057] It should be noted that for the information interaction, execution process, etc. between the above units, since they are based on the same concept as the method embodiment of the present invention, their specific functions and the technical effects brought thereby can be specifically referred to in the method embodiment part, and will not be elaborated here.

[0058] Figure 4 It is a schematic structural diagram of an electronic device provided by an embodiment of the present invention. As Figure 4 shown, the electronic device of this embodiment includes: at least one processor ( Figure 4 only one is shown in the figure), a memory, and a computer program stored in the memory and executable on at least one processor. When the processor executes the computer program, it implements the steps in any of the above embodiments of the sleep respiration control method.

[0059] The electronic device may include, but is not limited to, a processor and a memory. Those skilled in the art can understand that Figure 4 this is only an example of an electronic device and does not constitute a limitation on the electronic device. The electronic device may include more or fewer components than shown in the figure, or combine certain components, or different components. For example, it may also include a network interface, a display screen, and an input system, etc.

[0060] In one embodiment, a computer-readable storage medium is provided. When the instructions in the computer-readable storage medium are executed by a processor in an electronic device, the electronic device can execute each step of any embodiment of a sleep apnea control method disclosed in the present invention, which will not be repeated here. The computer-readable storage medium can be non-volatile or volatile.

[0061] The so-called processor can be a CPU, and the processor can also be other general-purpose processors, digital signal processors (DSPs), application specific integrated circuits (ASICs), field-programmable gate arrays (FPGAs), or other programmable logic devices, discrete gate or transistor logic devices, discrete hardware components, etc. The general-purpose processor can be a microprocessor or the processor can also be any conventional processor, etc.

[0062] The memory includes a readable storage medium, an internal memory, etc. Among them, the internal memory can be the memory of the electronic device, and the internal memory provides an environment for the operation of the operating system and computer-readable instructions in the readable storage medium. The readable storage medium can be the hard disk of the electronic device, and in some other embodiments, it can also be an external storage device of the electronic device. For example, a plug-in hard disk, a smart media card (SMC), a secure digital (SD) card, a flash card, etc. equipped on the electronic device. Further, the memory can also include both the internal storage unit and the external storage device of the electronic device. The memory is used to store the operating system, cooperative applications, a boot loader, data, and other programs, such as the program code of a computer program. The memory can also be used to temporarily store data that has been output or will be output.

[0063] Those of ordinary skill in the art can understand that all or part of the processes in the methods of the above embodiments can be completed by instructing relevant hardware through a computer program. This computer program can be stored in a non-volatile computer-readable storage medium. When the computer program is executed, it can include the processes of the embodiments of the above methods. Among them, any reference to a memory, storage, database, or other medium used in the embodiments provided in the present application can include non-volatile and / or volatile memories. Non-volatile memory can include read-only memory (ROM), programmable ROM (PROM), electrically programmable ROM (EPROM), electrically erasable programmable ROM (EEPROM), or flash memory. Volatile memory can include random access memory (RAM) or an external cache. By way of illustration and not limitation, RAM is available in various forms, such as static RAM (SRAM), dynamic RAM (DRAM), synchronous DRAM (SDRAM), double data rate SDRAM (DDR SDRAM), enhanced SDRAM (ESDRAM), synchronous link DRAM (SLDRAM), Rambus direct RAM (RDRAM), direct memory bus dynamic RAM (DRDRAM), and Rambus dynamic RAM (RDRAM), etc.

[0064] Those skilled in the art can clearly understand that, for the convenience and brevity of description, only the above division of each functional unit and module is used as an example. In actual applications, the above functions can be allocated to different functional units and modules according to needs, that is, the internal structure of the system is divided into different functional units or modules to complete all or part of the functions described above. Each functional unit and module in the embodiments can be integrated in a processing unit, or each unit can exist physically alone, or two or more units can be integrated in one unit. The above integrated unit can be implemented in the form of hardware or in the form of a software functional unit. In addition, the specific names of each functional unit and module are only for the convenience of mutual distinction and do not limit the protection scope of the present invention. The specific working processes of the units and modules in the above system can refer to the corresponding processes in the foregoing method embodiments and will not be elaborated herein. If the integrated unit is implemented in the form of a software functional unit and sold or used as an independent product, it can be stored in a computer-readable storage medium.

[0065] The above-described embodiments are only used to illustrate the technical solutions of the present invention, rather than to limit it; although the present invention has been described in detail with reference to the foregoing embodiments, those of ordinary skill in the art should understand that: they can still modify the technical solutions described in the foregoing embodiments, or perform equivalent replacements on some of the technical features; and these modifications or replacements do not cause the essence of the corresponding technical solutions to deviate from the spirit and scope of the technical solutions of the embodiments of the present invention, and should all be included within the protection scope of the present invention.

Claims

1. A sleep breathing control method, characterized in that: include: Acquiring sleep-related data of the monitored subject during sleep, wherein the sleep-related data includes sleep oxygenation data and sleep turning data; Determining whether the monitored subject needs to perform breathing control according to the sleep-related data; If the monitored object needs to perform breathing control, determining mode setting information of the breathing control system, wherein the mode setting information is used to indicate the working mode of the breathing control system, and the working mode includes CPAP ventilation mode, BiPAP-T ventilation mode and Auto BiPAP ventilation mode; According to the mode setting information of the breathing control system, different corresponding control strategies are adopted for the monitored object.

2. The sleep breathing control method according to claim 1, characterized in that: The step of determining whether the monitored subject needs to perform breathing control according to the sleep-related data includes: Comparing the sleep-related data with preset sleep identification indicators, wherein the sleep identification indicators include indicator categories related to sleep disorders and indicator scores used to characterize the degree of association between each indicator category and the sleep disorder; When the sleep-related data is the same as the index score, or the difference between the sleep-related data and the index score is less than a predetermined threshold, it is determined that the monitored object needs to perform breathing control.

3. The sleep breathing control method according to claim 1, characterized in that: The adopting of different corresponding control strategies for the monitored object according to the mode setting information of the respiratory control system includes: When it is determined according to the mode setting information that the respiratory control system is in CPAP ventilation mode, initial ventilation parameters of the CPAP ventilation mode are obtained, and the fan is driven to start working according to a preset pressure value; Determining whether the monitored subject should stop treatment according to the initial ventilation parameters of the CPAP ventilation mode; If the monitored subject does not stop treatment, determining whether the pressure generated by the blower reaches the preset pressure value; If the pressure generated by the fan does not reach the preset pressure value, the fan driving PWM signal is adjusted according to the difference between the pressure generated by the fan and the preset pressure value to gradually approach and reach the preset pressure value.

4. The sleep breathing control method according to claim 1, characterized in that: The adopting of different control strategies for the monitored object according to the mode setting information of the respiratory control system also includes: When it is determined according to the mode setting information that the respiratory control system is in BiPAP-T ventilation mode, initial ventilation parameters of the BiPAP-T ventilation mode are acquired; Determining whether the monitored subject should stop treatment according to the initial ventilation parameters of the BiPAP-T ventilation mode; If the monitored subject does not stop treatment, a first respiratory parameter of the monitored subject within a preset time is calculated based on the initial ventilation parameter of the BiPAP-T ventilation mode; Determining whether the first breathing parameter satisfies an inhalation trigger condition; If the first breathing parameter meets the inhalation trigger condition, the monitored object enters the inhalation state and is given an inhalation pressure; If the first breathing parameter does not meet the inhalation trigger condition, determining whether the first breathing parameter meets the exhalation trigger condition; If the first breathing parameter meets the exhalation trigger condition, the monitored object enters the exhalation state and is given exhalation pressure; If the first breathing parameter does not meet the exhalation trigger condition, determining whether the monitored subject is in an inhalation state; If the monitored object is in an inhalation state, the fan driving PWM signal is adjusted according to the difference between the pressure generated by the fan and the preset pressure value to gradually approach and reach the preset pressure value, and it is determined whether the monitored object has finished inhaling; If the monitored subject finishes inhaling, the exhalation trigger condition judgment process continues to be executed; If the monitored object is not in an inhalation state, determining whether the monitored object is in an exhalation state; If the monitored object is in an exhalation state, the fan driving PWM signal is adjusted according to the difference between the pressure generated by the fan and the preset pressure value to gradually approach and reach the preset pressure value, and it is determined whether the monitored object meets the spontaneous breathing condition; If the monitored object meets the condition of spontaneous breathing, the judgment process of the inhalation trigger condition is continued; If the monitored subject does not meet the condition of spontaneous breathing, determining whether the monitored subject has finished exhaling; If the monitored subject finishes exhaling, the judgment process of the inhalation trigger condition continues to be executed.

5. The sleep breathing control method according to claim 1, characterized in that: The adopting of different control strategies for the monitored object according to the mode setting information of the respiratory control system also includes: When it is determined according to the mode setting information that the respiratory control system is in the Auto BiPAP ventilation mode, initial ventilation parameters of the Auto BiPAP ventilation mode are acquired; Determining whether the monitored subject should stop treatment according to the initial ventilation parameters of the Auto BiPAP ventilation mode; If the monitored subject does not stop treatment, a second respiratory parameter of the monitored subject within a preset time is calculated based on the initial ventilation parameter of the Auto BiPAP ventilation mode; Performing breathing recognition on the second breathing parameter to determine whether the monitored object meets the requirement of spontaneous breathing; If the monitored object meets the condition of spontaneous breathing, determining whether the second breathing parameter meets the inhalation trigger condition; If the second breathing parameter satisfies the inhalation trigger condition, the monitored subject enters an inhalation state and is given an inhalation pressure; If the second breathing parameter does not meet the inhalation trigger condition, determining whether the second breathing parameter meets the exhalation trigger condition; If the second breathing parameter meets the exhalation trigger condition, the monitored subject enters the exhalation state and is given exhalation pressure; If the second breathing parameter does not meet the exhalation trigger condition, determining whether the monitored subject is in an inhalation state; If the monitored object is in an inhalation state, the fan driving PWM signal is adjusted according to the difference between the pressure generated by the fan and the preset pressure value to gradually approach and reach the preset pressure value, and it is determined whether the monitored object has finished inhaling; If the monitored subject finishes inhaling, the exhalation trigger condition judgment process continues to be executed; If the monitored object is not in an inhalation state, determining whether the monitored object is in an exhalation state; If the monitored object is in an exhalation state, the fan driving PWM signal is adjusted according to the difference between the pressure generated by the fan and the preset pressure value to gradually approach and reach the preset pressure value, and it is determined whether the monitored object meets the spontaneous breathing condition; If the monitored object meets the condition of spontaneous breathing, the judgment process of the inhalation trigger condition is continued; If the monitored subject does not meet the condition of spontaneous breathing, determining whether the monitored subject has finished exhaling; If the monitored object finishes exhaling, the judgment process of the breathing recognition continues to be executed.

6. The sleep breathing control method according to claim 5, characterized in that: The adopting of different control strategies for the monitored object according to the mode setting information of the respiratory control system also includes: If the monitored subject does not meet the requirement of spontaneous breathing, determining whether the monitored subject is in a state of suffocation for too long; If the monitored subject is in suffocation for too long, determining whether the number of suffocation times of the monitored subject reaches a preset threshold; If the number of apnea of ​​the monitored subject reaches a preset threshold, the mode setting information of the respiratory control system is switched to the BiPAP-T ventilation mode; If the number of suffocation times of the monitored object does not reach the preset threshold, the judgment process of the inhalation trigger condition continues to be executed.

7. A sleep breathing control device, characterized in that: include: An acquisition module, used to acquire sleep-related data of the monitored subject during sleep, wherein the sleep-related data includes sleep oxygenation data and sleep turning data; A judgment module, used for judging whether the monitored subject needs to perform breathing control according to the sleep-related data; a determination module, configured to determine mode setting information of a respiratory control system if the monitored subject needs to perform respiratory control, wherein the mode setting information is used to indicate a working mode of the respiratory control system, and the working modes include a CPAP ventilation mode, a BiPAP-T ventilation mode, and an Auto BiPAP ventilation mode; The control module is used to adopt different corresponding control strategies for the monitored object according to the mode setting information of the respiratory control system.

8. A sleep disorder treatment system, characterized in that: The sleep disorder treatment system includes a control system, a monitoring system and a breathing control system; The control system is used to obtain sleep-related data of the monitored object during sleep as fed back by the monitoring system, wherein the sleep-related data includes sleep oxygenation data and sleep turning data; based on the sleep-related data, determine whether the monitored object needs to perform respiratory control; if the monitored object needs to perform respiratory control, determine the mode setting information of the respiratory control system, wherein the mode setting information is used to indicate the working mode of the respiratory control system, and the working modes include CPAP ventilation mode, BiPAP-T ventilation mode and Auto BiPAP ventilation mode; based on the mode setting information of the respiratory control system, adopt corresponding different control strategies for the monitored object.

9. An electronic device comprising a memory, a processor, and a computer program stored in the memory and executable on the processor, characterized in that: When the processor executes the computer program, the sleep breathing control method according to any one of claims 1 to 6 is implemented.

10. A computer-readable storage medium storing a computer program, characterized in that: When the computer program is executed by a processor, the sleep breathing control method according to any one of claims 1 to 6 is implemented.

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