Control method and device based on respiratory rehabilitation equipment, equipment, medium and product

Abstract

The invention relates to a control method and device based on respiratory rehabilitation equipment, equipment, a medium and a product, and the method comprises the steps that in response to a first sampling signal output by a sampling device, a first physical sign parameter set, reflected by the first sampling signal, of a target object is determined; wherein the first physical sign parameter set comprises a plurality of first physical sign parameter values; and when the average value of the multiple first physical sign parameter values exceeds a first set range, working parameters of the auxiliary control device are adjusted.

Description

TECHNICAL FIELD

[0001] The present disclosure relates to the technical field of medical devices, and more particularly, to a control method, device, equipment, medium and product based on a respiratory rehabilitation device. BACKGROUND

[0002] With the development of intelligent medical devices, when patients have respiratory disorders, they can improve ventilation and oxygenation through mechanical ventilation (MV). However, measures related to MV, such as ventilator parameter settings, braking, and the use of sedative and analgesic drugs, can cause diaphragmatic muscle function to decline, affecting the respiratory function of patients and leading to a worse prognosis (such as an increased mortality rate). Currently, existing respiratory rehabilitation devices can include diaphragmatic nerve stimulation devices that can induce diaphragmatic muscle contraction to slow the rate of diaphragmatic muscle atrophy during mechanical ventilation, improve diaphragmatic muscle function, and improve the extubation rate and survival prognosis of patients. However, existing diaphragmatic nerve stimulation devices can only maintain fixed working parameters and cannot be synchronized with patient respiration, and it is unknown whether the stimulation intensity can cause effective diaphragmatic muscle contraction training. SUMMARY

[0003] One object of embodiments of the present disclosure is to provide a new technical solution for controlling a respiratory rehabilitation device.

[0004] According to a first aspect of the present disclosure, a control method based on a respiratory rehabilitation device is provided, the method comprising: The respiratory rehabilitation device comprises a sampling device, a control device, and an auxiliary control device, the sampling device and the auxiliary control device are respectively electrically connected to the control device, the execution subject of the method is the control device, and the method comprises: In response to a first sampling signal output by the sampling device, a first set of vital sign parameters of a target object reflected by the first sampling signal is determined; wherein the first set of vital sign parameters comprises a plurality of first vital sign parameter values; When the average value of the plurality of first vital sign parameter values exceeds a first set range, the working parameters of the auxiliary control device are adjusted.

[0005] Optionally, the first vital sign parameter values in the first set of vital sign parameters are of a set number, the first vital sign parameter values correspond to a first sampling time, and the difference between the first sampling times corresponding to the second vital sign parameter values and the third vital sign parameter values is associated with the respiratory rhythm of the target object; wherein the second vital sign parameter values and the third vital sign parameter values are vital sign parameter values close in time among the plurality of first vital sign parameter values.

[0006] Optionally, the first set of parameters of the target object reflected by the first sampling signal is determined in response to the first sampling signal output by the sampling device, comprising: a first sampling sequence corresponding to the first sampling signal and a fourth parameter value are determined in response to the first sampling signal output by the sampling device; a second sampling sequence within a second set range from the first sampling sequence is determined in the pre-stored set of parameter data; a first set of parameters is constructed according to the fourth parameter value and a fifth parameter value corresponding to the second sampling sequence.

[0007] Optionally, when the average of the first parameter values exceeds a first set range, the working parameters of the auxiliary control device are adjusted, comprising: when the average of the first parameter values is greater than the maximum value of the first set range, the working current of the auxiliary control device is reduced at a first set rate; when the average of the first parameter values is less than the minimum value of the first set range, the working current of the auxiliary control device is increased at a second set rate; wherein the first set rate is less than the second set rate.

[0008] Optionally, the auxiliary control device comprises a plurality of neck electrode pads and chest electrode pads; before the first set of parameters of the target object reflected by the first sampling signal is determined in response to the first sampling signal output by the sampling device, the method further comprises: a first electrical signal representing the esophageal pressure value and a second electrical signal representing the intragastric pressure value fed back by the sampling device are determined; the maximum difference in the difference between the esophageal pressure value and the intragastric pressure value and the neck electrode pad corresponding to the maximum difference are determined according to the first electrical signal and the second electrical signal; the neck electrode pad corresponding to the maximum difference and the chest electrode pad are activated.

[0009] Optionally, the chest electrode pad comprises a first chest electrode pad and a second chest electrode pad, a first part of the plurality of neck electrode pads and the first chest electrode pad form a first electrode pad group, a second part of the plurality of neck electrode pads and the second chest electrode pad form a second electrode pad group, the first electrode pad group corresponds to the left side of the target object, and the second electrode pad group corresponds to the right side of the target object; the maximum difference in the difference between the esophageal pressure value and the intragastric pressure value and the neck electrode pad corresponding to the maximum difference are determined according to the first electrical signal and the second electrical signal; a first maximum difference in a difference between the esophageal pressure value on the left side of the target object and the intragastric pressure value on the left side of the target object, and a first neck electrode piece corresponding to the first maximum difference; a second maximum difference in a difference between the esophageal pressure value on the right side of the target object and the intragastric pressure value on the right side of the target object, and a second neck electrode piece corresponding to the second maximum difference.

[0010] According to a second aspect of the present disclosure, a control device based on a respiratory rehabilitation device is further provided, comprising: a response module configured to determine a first set of vital sign parameters of a target object reflected by a first sampling signal output by the sampling device in response to the first sampling signal; wherein the first set of vital sign parameters comprises a plurality of first vital sign parameter values; an adjustment module configured to adjust a working parameter of the auxiliary control device when an average value of the plurality of first vital sign parameter values exceeds a first set range.

[0011] According to a fourth aspect of the present disclosure, a computer readable storage medium is further provided, and the computer readable storage medium stores a computer program, wherein the computer program is configured to execute the voice processing method when running.

[0012] According to a fifth aspect of the present disclosure, a computer program product is further provided, and the computer program product comprises a game program, and the game program is configured to enable a computer to execute the voice processing method when running.

[0013] According to a sixth aspect of the present disclosure, an electronic device is further provided, and the electronic device comprises a memory and a processor, wherein the memory stores a computer program, and the processor is configured to execute the voice processing method through the computer program.

[0014] An advantage of the present disclosure is that the control method based on a respiratory rehabilitation device provided by the present disclosure can determine a first set of vital sign parameters of a target object reflected by a first sampling signal output by a sampling device in response to the first sampling signal, and adjust a working parameter of an auxiliary control device when an average value of a plurality of first vital sign parameter values in the first set of vital sign parameters exceeds a first set range, thereby realizing a truly effective control device synchronized with breathing and according to diaphragm function feedback, and improving the effectiveness of the control device.

[0015] The features and advantages of embodiments of the present disclosure will become apparent from the following detailed description of exemplary embodiments of the present disclosure with reference to the drawings. BRIEF DESCRIPTION OF DRAWINGS

[0016] The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments of the present specification and, together with the description, serve to explain the principles of the embodiments of the present specification.

[0017] Figure 1 A hardware structure schematic diagram of an electronic device that can be used to implement a control method of a respiratory rehabilitation device according to an embodiment of the present disclosure is shown. Figure 2 A flowchart schematic diagram of a control method of a respiratory rehabilitation device according to some embodiments is shown. Figure 3 A component structure schematic diagram of a respiratory rehabilitation device according to some embodiments is shown. Figure 4 A structure schematic diagram of a neck electrode pad and a chest electrode pad according to an embodiment is shown. Figure 5 A schematic diagram of a first setting range according to an embodiment is shown. Figure 6 A structure schematic diagram of a control device of a respiratory rehabilitation device according to some embodiments is shown. Figure 7 A hardware structure schematic diagram of an electronic device according to some embodiments is shown. DETAILED DESCRIPTION

[0018] Various exemplary embodiments of the present specification will now be described in detail with reference to the accompanying drawings.

[0019] The following description of at least one exemplary embodiment is merely illustrative in nature and is in no way intended to limit the present specification, its application or uses, nor is this description intended to limit the definition of the expressions used.

[0020] It should be noted that similar reference numerals and letters refer to like items in the drawings and as a result, once an item is defined in one drawing, it need not be discussed further in subsequent drawings.

[0021] It should be noted that all actions of acquiring signals, information or data in the embodiments of the present disclosure are performed in compliance with the corresponding data protection regulations and policies of the country where the device is located, and with the authorization given by the corresponding device owner.

[0022] Transdiaphragmatic pressure (Pdi) Esophageal pressure (Pes) Introgastric pressure (Pgi) This disclosure provides a novel control scheme based on a respiratory rehabilitation device. It can determine whether the vital signs of the target object are within the normal range by using the first sampling signal output by the sampling device. If the vital signs are outside the normal range, the operating parameters of assisted ventilation are adjusted. This achieves a control device that is synchronized with breathing and based on feedback from diaphragmatic function, thereby improving the effectiveness of the control device.

[0023] Figure 1 A schematic diagram of the hardware structure of an electronic device that can be used to implement a control method based on a respiratory rehabilitation device according to embodiments of the present disclosure is shown.

[0024] The electronic device 1000 can be a respiratory rehabilitation device or a device capable of controlling the operation of a respiratory rehabilitation device. The electronic device 1000 can be a respiratory rehabilitation device, a mobile phone, a PC, etc., and is not limited here.

[0025] like Figure 1 As shown, the electronic device 1000 may include a processor 1101, a memory 1102, an interface device 1103, a communication device 1104, an output device 1105, an input device 1106, etc. Figure 1 The hardware configuration shown is illustrative only and is not intended to limit this disclosure, its application, or its use.

[0026] The processor 1101 executes computer programs, which can be written using instruction sets of architectures such as x86, Arm, RISC, MIPS, and SSE. The memory 1102 includes, for example, ROM (Read-Only Memory), RAM (Random Access Memory), and non-volatile memory such as a hard disk. The interface device 1103 includes, for example, a USB interface, a network cable interface, and a headphone jack. The communication device 1104 is capable of wired or wireless communication. The communication device 1104 may include at least one short-range communication module, such as any module for short-range wireless communication based on short-range wireless communication protocols such as Hilink, WiFi (IEEE 802.11), Mesh, Bluetooth, ZigBee, Thread, Z-Wave, NFC, UWB, and LiFi. The communication device 1104 may also include a long-range communication module, such as any module for WLAN, GPRS, or 2G / 3G / 4G / 5G long-range communication. The output device 1105 may include, for example, an LCD screen or touch screen, and a speaker. Input device 1106 may include, for example, a touch screen, a keyboard, a microphone, various sensors, etc.

[0027] In this embodiment, the memory 1102 of the electronic device 1000 is configured to store a computer program for controlling the processor 1101 to perform the control method of the respiratory rehabilitation device according to any embodiment of the present disclosure.

[0028] Next, taking the electronic device 1000 as shown in Figure 1 the embodiment as an example, various embodiments of the control method of the respiratory rehabilitation device are described.

[0029] <Method Embodiment> Figure 2 The control method of the respiratory rehabilitation device according to some embodiments is shown, which can include the following steps S210 and S220: Step S210, in response to the first sampling signal output by the sampling device, determining a first set of vital parameter values of the target object reflected by the first sampling signal; wherein the first set of vital parameter values includes a plurality of first vital parameter values.

[0030] In this embodiment, the respiratory rehabilitation device can include a sampling device, a control device, and an auxiliary control device, and the sampling device and the auxiliary control device are respectively electrically connected with the control device. The control device can be the electronic device 1000 described above.

[0031] In some examples, as shown in Figure 3 , the auxiliary control device can include a chest electrode and a neck electrode, and the chest electrode can be attached to the intersection of the midline of the two clavicles and the second rib of the target object, so that the neck electrode and the chest electrode form a closed loop, and the auxiliary control device can improve the respiratory function of the user.

[0032] In this application, as shown in Figure 4 , the neck electrode is multiple, i.e. neck electrode A1-neck electrode A6, and the center position between neck electrode A3 and neck electrode A4 is taken as a marker point. As shown in Figure 1 , the marker point can be attached to the lower 1 / 3 of the outer edge of the sternocleidomastoid muscle of the target object, and placed horizontally close to the skin surface of the neck of the patient.

[0033] In this application, the electronic device 1000 may have two ports (port 1 and port 2). Port 1 is used to connect to a Pes gastric tube (double-lumen tube) for monitoring esophageal pressure (Pes) and introgastric pressure (Pgi). The electronic device 1000 can calculate the difference between the esophageal pressure value and the introgastric pressure value, i.e., the difference ΔPdi = Pgi - Pes. The aperture size of port 1 is matched with that of a conventional double-lumen Pes gastric tube. The Pes gastric tube (double-lumen tube) is used to measure the esophageal pressure and introgastric pressure of the subject. Port 2 is used to electrically connect to the electrode assembly for outputting electrical stimulation current.

[0034] In some embodiments, the first vital sign parameter value in the first set of vital sign parameters is a set quantity, the first vital sign parameter value corresponds to a first sampling time, and the difference between the first sampling time corresponding to the second vital sign parameter value and the third vital sign parameter value is associated with the respiratory rhythm of the target object; wherein, the second vital sign parameter value and the third vital sign parameter value are vital sign parameter values ​​with similar times among multiple first vital sign parameter values.

[0035] In this embodiment, the first sampling time corresponding to the first vital sign parameter value can be a value collected based on the spontaneous breathing rhythm of the target object, rather than a fixed value. The capture of the spontaneous breathing rhythm can begin at the point when esophageal pressure decreases, so as to synchronize with respiration.

[0036] In this embodiment, the quantity can be 3, 5, or 10, etc., and is not limited here.

[0037] In some examples, the first sampling time corresponding to vital sign parameter value X2 is 5s, the first sampling time corresponding to vital sign parameter value X3 is 8s, and the first sampling time corresponding to vital sign parameter value X4 is 13s. Vital sign parameter values ​​X2 and X3 can be considered as vital sign parameter values ​​with similar times among multiple first vital sign parameter values, and vital sign parameter values ​​X3 and X4 can be considered as vital sign parameter values ​​with similar times among multiple first vital sign parameter values. The difference between the first sampling times corresponding to vital sign parameter values ​​X2 and X3 is 3s, and the difference between the first sampling times corresponding to vital sign parameter values ​​X3 and X4 is 5s.

[0038] In some embodiments, step S210 may include the following steps S310 to S330: Step S310: In response to the first sampling signal output by the sampling device, determine the first sampling order and the fourth vital sign parameter value corresponding to the first sampling signal.

[0039] In the embodiment, the control device can collect the current value of the first sampling signal at non-fixed interval time after the respiratory rehabilitation device is started, for example, the first sampling signal value is collected for the first time at 2s, the first sampling signal value is collected for the second time at 4s, and the first sampling signal value is collected for the third time at 6s, and then the Nth time and the first sampling signal value corresponding to the Nth time can be determined, that is, the first sampling order and the fourth physical parameter value.

[0040] In step S320, the second sampling order within the second set range from the first sampling order is determined in the pre-stored physical data set.

[0041] In the embodiment, the second set range is, for example, 1-4 or 1-6, and the like, without limitation.

[0042] In some examples, the second set range is 1-4, and the first sampling order is the fifth time, and then the second sampling order can be the first time, the second time, the third time, and the fourth time.

[0043] In step S330, the first physical parameter set is constructed according to the fourth physical parameter value and the fifth physical parameter value corresponding to the second sampling order.

[0044] In some examples, the second set range is 1-4, and the first sampling order is the fifth time, and then the second sampling order can be the first time, the second time, the third time, and the fourth time, and then the first physical parameter set can be [(1, △Pdi1), (2, △Pdi2), (3, △Pdi3), (4, △Pdi4), (5, △Pdi5)]. In step S220, when the average value of the plurality of first physical parameter values exceeds the first set range, the working parameter of the auxiliary control device is adjusted.

[0045] In some examples, the set number is 5, and the average value of the plurality of first physical parameter values can be determined by the following expression: wherein, is the average value of the plurality of first physical parameter values, is the latest physical parameter value in the plurality of first physical parameter values.

[0046] In this embodiment, the control device can respond to the first sampling signal output by the sampling device, determine the first set of vital signs parameters of the target object reflected by the first sampling signal, and adjust the working parameters of the auxiliary control device when the average value of multiple first vital signs parameter values ​​in the first set of vital signs parameters exceeds a first set range, thereby realizing a control device that is synchronized with breathing and based on feedback from diaphragmatic function, thereby improving the effectiveness of the control device.

[0047] In some embodiments, step S220 may include the following steps S410 and S420: Step S410: When the average value of multiple first vital signs parameters is greater than the maximum value of the first set range, the operating current of the auxiliary control device is reduced according to the first set rate.

[0048] Step S420: When the average value of multiple first vital signs parameters is less than the minimum value of the first set range, the operating current of the auxiliary control device is increased according to the second set rate; wherein the first set rate is less than the second set rate.

[0049] In some examples, such as Figure 5 As shown, after the control device can determine and memorize the optimal stimulation position, PNS treatment is performed with initial parameters (stimulation intensity 10mA, frequency 40Hz, pulse width 0.2ms). After 5 stimulation cycles, the control device automatically calculates the average ΔPdi. When the average ΔPdi < 6cmH2O, the intensity is iterated by increasing the working current by 3mA until ΔPdi is between 6-9cmH2O; when ΔPdi > 9cmH2O, the intensity is iterated by decreasing the working current by 1mA until ΔPdi is between 6-9cmH2O. The first set range is [6cmH2O, 9cmH2O].

[0050] In some examples, the relationship between the average value of multiple first vital sign parameters and the first set range is expressed as follows: Wherein, the minimum value of the first set range is 'a', and the maximum value of the first set range is 'b'. It is the average of multiple primary vital sign parameters. The latest value among multiple primary vital sign parameters. The next time corresponding to the latest value of the primary vital sign parameter among multiple primary vital sign parameter values.

[0051] In other words, by iteratively increasing or decreasing the intensity of stimulation, electrical stimulation of the diaphragm of the target object can be achieved to ensure that the target object's ΔPdi [6cmH2O, 9cmH2O].

[0052] In some examples, the control device has an automatic stimulation mode and a manual stimulation mode. In the automatic stimulation mode, the optimal stimulation intensity is automatically adjusted by the △Pdi feedback, and the MV patient can use it in the control ventilation mode, the assist ventilation mode and the spontaneous breathing mode. In the full control ventilation mode, the data transmitted by the ventilator and the respiratory rehabilitation device cable is used to capture the time trigger of pressure change, and the stimulation is performed at a frequency synchronized with the respiration, and the stimulation intensity is automatically adjusted by the △Pdi feedback. In the assist ventilation and spontaneous breathing mode, the stimulation is performed according to the trigger threshold of 0.5 cmH2O of the Pes drop, and the stimulation intensity is automatically adjusted by the △Pdi feedback. In the manual stimulation mode, the assist pressure monitoring function is closed, the stimulation intensity parameter is manually set, and the automatic adjustment function of the △Pdi feedback is not available in this mode, and the treatment is performed at the set stimulation intensity. The function of automatically titrating the optimal stimulation position of the system is still retained.

[0053] In some embodiments, the auxiliary control device includes a plurality of neck electrode pads and chest electrode pads, and before the step S210, the method further includes the following steps S510 to S530: Step S510, determining the first electric signal representing the esophageal pressure value and the second electric signal representing the intragastric pressure value fed back by the sampling device.

[0054] In this embodiment, the first electric signal can reflect the esophageal pressure Pes, and the second electric signal can reflect the intragastric pressure value Pgi.

[0055] Step S520, determining the maximum difference in the difference between the esophageal pressure value and the intragastric pressure value and the neck electrode pad corresponding to the maximum difference according to the first electric signal and the second electric signal.

[0056] Step S530, controlling the neck electrode pad and the chest electrode pad corresponding to the maximum difference to start.

[0057] In other words, by the first electric signal and the second electric signal fed back by the sampling device, the maximum difference in the difference between the esophageal pressure value and the intragastric pressure value and the neck electrode pad corresponding to the maximum difference are determined, so that the neck electrode pad corresponding to the maximum difference is the optimal stimulation position, and the control device can perform electric stimulation on the target object through the neck electrode pad and the chest electrode pad corresponding to the maximum difference, thereby improving the electric stimulation effect of the respiratory rehabilitation device.

[0058] In some embodiments, to electrically stimulate the diaphragm on both sides of the target object, the chest electrode pads may include a first chest electrode pad and a second chest electrode pad. A first portion of a plurality of neck electrode pads and the first chest electrode pad constitute a first electrode pad group, and a second portion of a plurality of neck electrode pads and the second chest electrode pad constitute a second electrode pad group. The first electrode pad group corresponds to the left side of the target object, and the second electrode pad group corresponds to the right side of the target object. Step S520 may include the following steps S610 and S620: Step S610: Based on the first maximum difference between the esophageal pressure value on the left side of the target object and the gastric pressure value on the left side of the target object, and the first neck electrode corresponding to the first maximum difference.

[0059] Step S620: Based on the second maximum difference between the esophageal pressure value on the right side of the target object and the gastric pressure value on the right side of the target object, and the second neck electrode corresponding to the second maximum difference.

[0060] In this application, such as Figure 4 As shown, after the first and second electrode groups are firmly attached, the control device can initiate the treatment program, first performing the right and left stimulation location positioning program: First, the electrodes in the second part and the second chest electrode group are tested sequentially with electrical stimulation at a stimulation intensity of 10mA, a frequency of 40Hz, and a pulse width of 0.2ms. If there is no spontaneous breathing, the test is performed according to the airway pressure change capture time trigger point. If there is spontaneous breathing, the control device controls the neck electrode in the second part to decrease Pes by 0.5cmH2O to trigger stimulation; each small electrode is stimulated 5 times, and the value of the last ΔPdi is recorded. The test order is as follows: right inner ①, inner ②, inner ③, inner ④, inner ⑤, inner ⑥, and the recorded values ​​are ΔPdi respectively. ① , △Pdi ② , △Pdi ③ , △Pdi ④ , △Pdi ⑤ , △Pdi ⑥ The second largest difference among six ΔPdi values ​​is compared, and the electrode position of the second neck electrode corresponding to the second largest difference is the optimal stimulation position on the right side. Similarly, the control device locates the optimal stimulation position on the left side, determining that the electrode position of the first neck electrode corresponding to the first largest difference is the optimal stimulation position on the left side. The optimal stimulation positions on the right and left sides can be asymmetrical, using different electrode sequences. After the optimal positioning procedure is completed, the control device can proceed to the stimulation intensity titration procedure.

[0061] In other words, by entering the stimulation intensity titration procedure at the optimal stimulation positions on the right and left sides, electrical stimulation of the diaphragm on both sides of the target object can be achieved.

[0062] <Device Embodiments> Figure 6 A constituent structure schematic diagram of a control device based on a respiratory rehabilitation device according to an embodiment of the present disclosure is shown. As shown in the figure, the control device based on the respiratory rehabilitation device 600 comprises: Figure 6 A response module 610, configured to determine a first set of vital sign parameters of a target object reflected by a first sampling signal output by a sampling device in response to the first sampling signal; wherein the first set of vital sign parameters comprises a plurality of first vital sign parameter values; An adjustment module 620, configured to adjust a working parameter of an auxiliary control device when an average value of the plurality of first vital sign parameter values is out of a first set range.

[0063] In some embodiments, the response module 610 is further configured to determine a first sampling sequence corresponding to the first sampling signal and a fourth vital sign parameter value in response to the first sampling signal output by the sampling device; determine a second sampling sequence in the pre-stored set of vital sign data, which has a difference value within a second set range with the first sampling sequence; and construct the first set of vital sign parameters according to the fourth vital sign parameter value and a fifth vital sign parameter value corresponding to the second sampling sequence.

[0064] In some embodiments, the adjustment module 620 is further configured to decrease a working current of the auxiliary control device at a first set rate when the average value of the plurality of first vital sign parameter values is greater than a maximum value of the first set range; and increase the working current of the auxiliary control device at a second set rate when the average value of the plurality of first vital sign parameter values is less than a minimum value of the first set range; wherein the first set rate is less than the second set rate.

[0065] In some embodiments, the control device based on the respiratory rehabilitation device 600 further comprises a control module configured to determine a first electrical signal representing an esophageal pressure value and a second electrical signal representing an intragastric pressure value fed back by the sampling device; and control a neck electrode patch and a chest electrode patch corresponding to a maximum difference in a difference between the esophageal pressure value and the intragastric pressure value and the neck electrode patch corresponding to the maximum difference to be activated.

[0066] In some embodiments, the control module is further configured to determine a first maximum difference in a difference between a left esophageal pressure value of the target object and a left intragastric pressure value of the target object and a first neck electrode patch corresponding to the first maximum difference; and determine a second maximum difference in a difference between a right esophageal pressure value of the target object and a right intragastric pressure value of the target object and a second neck electrode patch corresponding to the second maximum difference.

[0067] <Device Embodiments> Figure 7 ​A hardware structure diagram of an electronic device according to another embodiment is shown. As shown in the figure, the electronic device 700 includes a processor 710 and a memory 720 for storing a computer program for controlling the processor 710 to operate to control the electronic device 700 to perform the control method based on the respiratory rehabilitation device according to any embodiment of the present disclosure. Figure 7

[0068] The embodiments of the present disclosure further provide a computer readable storage medium storing a computer program, which, when executed by a processor, implements the control method based on the respiratory rehabilitation device according to any embodiment of the present disclosure.

[0069] Each of the embodiments in the specification is described in a progressive manner, and the same or similar parts between the embodiments can be referred to each other. Each of the embodiments focuses on the difference from other embodiments. In particular, the device and equipment embodiments are basically similar to the method embodiments, and thus the description is relatively simple, and the relevant parts can be referred to the part of the method embodiment.

[0070] The above describes specific embodiments of the present specification. Other embodiments are within the scope of the appended claims. In some cases, the actions or steps recited in the claims can be performed in an order different than the order in which they are recited in the embodiments and still achieve desirable results. In addition, the processes depicted in the figures do not necessarily require the particular order shown, or sequential order, to achieve the desired results. In certain implementations, multitasking and parallel processing can be advantageous or necessary.

[0071] The embodiments of the present specification can be devices, methods and / or computer program products. The computer program product can include a computer readable storage medium on which a computer readable program instruction for causing a processor to implement various aspects of the embodiments of the present specification is loaded.

[0072] ​Computer readable storage media can be tangible storage media which can retain and store instructions for use by an instruction execution device. Computer readable storage media can be, for example, but is not limited to, an electronic storage device, a magnetic storage device, an optical storage device, an electromagnetic storage device, a semiconductor storage device, or any suitable combination of the foregoing. More specific examples (a non-exhaustive list) of computer readable storage media include the following: a portable computer diskette, a hard disk, a random access memory (RAM), a read-only memory (ROM), an erasable programmable read-only memory (EPROM or Flash memory), a static random access memory (SRAM), a portable compact disc read-only memory (CD-ROM), a digital versatile disk (DVD), a memory stick, a floppy disk, a mechanically encoded device such as punch-cards or raised structures in a groove having instructions recorded thereon, and any suitable combination of the foregoing. A computer readable storage medium, as used herein, is not to be construed as being transitory signals per se, such as radio waves or other freely propagating electromagnetic waves, electromagnetic waves propagating through a waveguide or other transmission media (e.g., light pulses passing through a fiber-optic cable), or electrical signals transmitted through a wire.

[0073] Computer readable program instructions described herein can be downloaded to respective computing / processing devices from a computer readable storage medium or to an external computer or external storage device via a network, for example, the Internet, a local area network, a wide area network and / or a wireless network. The network can comprise copper transmission cables, optical transmission fibers, wireless transmission, routers, firewalls, switches, gateway computers and / or edge servers. A network adapter card or network interface in each computing / processing device receives computer readable program instructions from the network and forwards the computer readable program instructions for storage in a computer readable storage medium within the respective computing / processing device.

[0074] Computer readable program instructions for carrying out embodiments of the present specification can be assembly instructions, instruction-set-architecture (ISA) instructions, machine instructions, machine dependent instructions, microcode, firmware instructions, state-setting data, or source or object code, in any combination of one or more programming languages including an object-oriented programming language such as Smalltalk, C++ or the like, and conventional procedural programming languages such as the "C" programming language or similar programming languages. The computer readable program instructions can execute entirely on a user's computer, partly on the user's computer, as a stand-alone software package, partly on the user's computer and partly on a remote computer or entirely on the remote computer or server. In the latter scenario, the remote computer can be connected to the user's computer through any type of network, including a local area network (LAN) or a wide area network (WAN), or the connection can be made to an external computer (for example, through the Internet using an Internet Service Provider). In some embodiments, electronic circuitry including, for example, programmable logic circuitry, field-programmable gate array (FPGA), or programmable logic array (PLA) can execute the computer readable program instructions by utilizing state information of the computer readable program instructions to personalize the electronic circuitry, in order to perform aspects of the present specification.

[0075] Various aspects of the embodiments of the present specification can be described in the general context of methods and / or apparatuses (devices) of the present specification, referring to the flowcharts and / or block diagrams of the methods, apparatuses (devices) and computer program products according to the embodiments of the present specification. It will be understood that each block of the flowcharts and / or block diagrams, and combinations of blocks in the flowcharts and / or block diagrams, can be implemented by computer readable program instructions.

[0076] These computer readable program instructions can be provided to a processor of a general purpose computer, special purpose computer, or other programmable data processing apparatus to produce a machine, such that the instructions, which execute via the processor of the computer or other programmable data processing apparatus, create means for implementing the functions / acts specified in the flowcharts and / or block diagrams of the methods, apparatuses (devices) and computer program products according to the embodiments of the present specification. These computer readable program instructions can also be stored in a computer readable storage medium that can direct a computer, a programmable data processing apparatus, and / or other devices to function in a particular manner, such that the computer readable medium having instructions stored therein comprises an article of manufacture including instructions which implement aspects of the function / act specified in the flowcharts and / or block diagrams of the methods, apparatuses (devices) and computer program products according to the embodiments of the present specification.

[0077] The computer readable program instructions can also be loaded onto a computer, other programmable data processing apparatus, or other device to cause a series of operational steps to be performed on the computer, other programmable apparatus or other device to produce a computer implemented process, such that the instructions which execute on the computer, other programmable data processing apparatus, or other device implement the functions / acts specified in the flowchart and / or block diagram block or blocks.

[0078] The computer readable program instructions can also be loaded onto a computer, other programmable data processing apparatus, or other device to cause a series of operational steps to be performed on the computer, other programmable apparatus or other device to produce a computer implemented process, such that the instructions which execute on the computer, other programmable data processing apparatus, or other device implement the functions / acts specified in the flowchart and / or block diagram block or blocks.

[0079] The above-described embodiments of the present specification have been described, the above-described description is exemplary, not exhaustive, and is not limited to the disclosed embodiments. Many modifications and changes are obvious to those skilled in the art without departing from the scope of the described embodiments. The selection of the terms used herein is intended to best explain the principles of the embodiments, practical application or improvement of the technology in the market, or to enable other ordinary skilled persons in the art to understand the embodiments disclosed herein.

Claims

1. A control method for a respiratory rehabilitation device, wherein, The respiratory rehabilitation device comprises a sampling device, a control device and an auxiliary control device, the sampling device and the auxiliary control device are electrically connected with the control device respectively, the execution subject of the method is the control device, and the method comprises: In response to the first sampling signal output by the sampling device, a first set of vital sign parameters of a target object reflected by the first sampling signal is determined; wherein the first set of vital sign parameters comprises a plurality of first vital sign parameter values; When the average value of the plurality of first vital sign parameter values exceeds a first set range, the working parameter of the auxiliary control device is adjusted.

2. The method of claim 1, wherein, The first vital sign parameter values in the first set of vital sign parameters are of a set number, the first vital sign parameter values correspond to a first sampling time, and the difference between the second vital sign parameter values and the third vital sign parameter values corresponding to the first sampling time is related to the respiratory rhythm of the target object; wherein the second vital sign parameter values and the third vital sign parameter values are vital sign parameter values close in time in the plurality of first vital sign parameter values.

3. The method of claim 1, wherein, The response to the first sampling signal output by the sampling device to determine the first set of vital sign parameters of the target object reflected by the first sampling signal comprises: In response to the first sampling signal output by the sampling device, the first sampling sequence corresponding to the first sampling signal and the fourth vital sign parameter value are determined; In the pre-stored set of vital sign data, the second sampling sequence whose difference from the first sampling sequence is within a second set range is determined; According to the fourth vital sign parameter value and the fifth vital sign parameter value corresponding to the second sampling sequence, a first set of vital sign parameters is constructed.

4. The method of claim 1, wherein, When the average value of the plurality of first vital sign parameter values is greater than the maximum value of the first set range, the working current of the auxiliary control device is reduced at a first set rate; When the average value of the plurality of first vital sign parameter values is less than the minimum value of the first set range, the working current of the auxiliary control device is increased at a second set rate; Wherein, the first set rate is less than the second set rate. The auxiliary control device comprises a plurality of neck electrode pieces and chest electrode pieces; before the response to the first sampling signal output by the sampling device to determine the first set of vital sign parameters of the target object reflected by the first sampling signal, the method further comprises:

5. The method of claim 1, wherein, Determine the first electric signal representing the esophageal pressure value and the second electric signal representing the intragastric pressure value fed back by the sampling device; According to the first electric signal and the second electric signal, the maximum difference in the difference between the esophageal pressure value and the intragastric pressure value and the neck electrode piece corresponding to the maximum difference are determined; The maximum difference corresponding neck electrode piece and the chest electrode piece are controlled to start. ​ 6. The method of claim 5, wherein, The chest electrode patch comprises a first chest electrode patch and a second chest electrode patch, a first part of the plurality of neck electrode patches and the first chest electrode patch form a first electrode patch group, a second part of the plurality of neck electrode patches and the second chest electrode patch form a second electrode patch group, the first electrode patch group corresponds to the left side of the target object, and the second electrode patch group corresponds to the right side of the target object. The maximum difference between the difference between the esophageal pressure value and the intragastric pressure value and the neck electrode patch corresponding to the maximum difference comprises: According to the first maximum difference between the difference between the esophageal pressure value on the left side of the target object and the intragastric pressure value on the left side of the target object and the first neck electrode patch corresponding to the first maximum difference; According to the second maximum difference between the difference between the esophageal pressure value on the right side of the target object and the intragastric pressure value on the right side of the target object and the second neck electrode patch corresponding to the second maximum difference.

7. A control device based on a respiratory rehabilitation device, comprising: a response module configured to determine a first set of physical parameters of a target object in response to a first sampling signal output by the sampling device, wherein the first set of physical parameters comprises a plurality of first physical parameter values; an adjustment module configured to adjust a working parameter of the auxiliary control device when an average value of the plurality of first physical parameter values exceeds a first set range.

8. An electronic device, comprising: comprising a memory and a processor, the memory being configured to store a computer program, and the processor being configured to execute the method steps according to any one of claims 1 to 6 under control of the computer program.

9. A computer-readable storage medium including a stored computer program, wherein, The computer program is executed to perform the method steps of any one of claims 1 to 6.

10. A computer program product, characterised in that, comprising a computer program, the computer program being executed by a processor to implement the method of any one of claims 1 to 6. ​

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