Female stress incontinence intervention device with feedback and automatic inflation functions

By using a device that monitors urethral pressure and body activity in real time, and constructs a closed-loop control system with sensors and an air pump, the problem of existing devices being unable to adjust support force in real time is solved, enabling precise and timely treatment and personalized management of stress urinary incontinence.

CN121196789APending Publication Date: 2025-12-26THE SECOND HOSPITAL OF TIANJIN MEDICAL UNIV
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Patent Information

Application Number
CN202511687381.X
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2025-11-18
Publication Date
2025-12-26

AI Technical Summary

Technical Problem

Existing physical intervention devices cannot sense the user's physical activity status in real time and cannot adjust the support force in time when abdominal pressure increases suddenly, resulting in poor treatment effect of stress urinary incontinence.

Method used

A female stress urinary incontinence intervention device with feedback automatic inflation function was designed. The device monitors the pressure around the urethra and the body's activity status in real time through pressure sensors and acceleration sensors. The controller and air pump realize the rapid inflation and deflation of the airbag, constructing a closed-loop control system to provide immediate urethral support.

Benefits of technology

It significantly improves the accuracy and timeliness of stress urinary incontinence treatment, providing a stable connection, fluid management, convenient maintenance, and comfortable wear, and enables remote monitoring and personalized treatment plan adjustments.

✦ Generated by Eureka AI based on patent content.

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Abstract

The invention discloses a female stress incontinence intervention device with a feedback automatic inflation function, and relates to the technical field of medical auxiliary instruments, the female stress incontinence intervention device comprises an intervention column main body, and the surface of the intervention column main body is sleeved with an air bag; according to the female stress incontinence intervention device with the feedback and automatic inflation functions, real-time monitoring and intelligent regulation and control of urethral pressure are achieved through the arrangement of the intervention column body, the air bag, the controller, the air pump and the electromagnetic valve, and a pressure sensor continuously collects pressure data of tissues around the urethra; the acceleration sensor sensitively senses the physical activity state of a user, when cough, jumping and other actions possibly causing urinary incontinence are detected, the controller immediately starts the air pump to rapidly inflate the air bag through the exhaust pipe, the urethra closing pressure is enhanced, and after the actions are finished, the electromagnetic valve is opened to enable the air bag to be exhausted through the exhaust pipe to recover. Therefore, a closed-loop control system integrating real-time monitoring, intelligent judgment and active intervention is constructed.
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Description

TECHNICAL FIELD

[0001] The present application relates to the technical field of medical auxiliary devices, in particular to a female stress urinary incontinence intervention device with feedback automatic inflation function. BACKGROUND

[0002] In recent years, as a representative of pelvic floor dysfunction, the treatment technology of female stress urinary incontinence has developed rapidly, covering various means from non-invasive pelvic floor muscle training, behavior therapy to invasive surgical treatment. With the continuous innovation of medical auxiliary device technology, physical intervention devices are increasingly widely used in the treatment of stress urinary incontinence, such as urethral support devices and vaginal cones. These devices enhance urethral closure pressure through different mechanisms and reduce involuntary urine leakage. However, although the existing physical intervention devices have improved the symptoms of patients to some extent, they still have significant technical limitations in dealing with complex and variable life scenarios.

[0003] The existing physical intervention devices generally lack real-time perception and dynamic response capability to the physical activity state of the user. In daily life scenarios, such as coughing, jumping or lifting heavy objects, which cause sudden increase in abdominal pressure, are common causes of stress urinary incontinence. However, the existing devices often cannot immediately adjust the support or resistance provided by them at the moment when these critical actions occur, in order to effectively resist the sudden increase in abdominal pressure. This lag results in the device being difficult to achieve the expected therapeutic effect in actual application, especially in emergency situations that require rapid response to prevent urinary incontinence. Therefore, the existing technology needs to be improved. SUMMARY

[0004] The purpose of the present application is to provide a female stress urinary incontinence intervention device with feedback automatic inflation function, in order to solve the problem that the existing physical intervention devices cannot perceive the physical activity state of the user in real time and actively and accurately intervene immediately when the action that causes the sudden increase in abdominal pressure occurs.

[0005] In order to achieve the above-mentioned purpose, the present application provides the following technical solution: a female stress urinary incontinence intervention device with feedback automatic inflation function, comprising an intervention column body, a gas bag is sleeved on the surface of the intervention column body, a controller is installed on the inner wall of the intervention column body, a gas pump is installed on one side of the inner wall of the intervention column body, and the controller and the gas pump are electrically connected to each other;

[0006] An air inlet pipe is installed on the input end of the gas pump, an air outlet pipe is installed on the output end of the gas pump, the top end of the air outlet pipe is inserted into the inner wall of the gas bag, an exhaust pipe is installed on the surface of the air outlet pipe, and an electromagnetic valve is installed on the inner wall of the exhaust pipe.

[0007] Further, the front end of the intervention column body is provided with a fixing ring, the surface of the fixing ring is provided with a plurality of groups of pressure sensors, the inner wall of the fixing ring is provided with a transmitter, the inner wall of the transmitter is provided with an acceleration sensor, and the pressure sensor and the acceleration sensor are electrically connected with the transmitter.

[0008] Further, the tail end of the intervention column body is provided with a connecting rod, and the surfaces of the air inlet pipe and the exhaust pipe are inserted into the inner wall of the connecting rod, and the surface of the connecting rod is sleeved with adsorbing cotton.

[0009] Further, the inner wall of the connecting rod is provided with a mounting hole, and the inner wall of the mounting hole is threadedly connected with a threaded rod.

[0010] Further, one end of the threaded rod is provided with a limiting plate, and the surfaces of the air inlet pipe and the exhaust pipe are inserted into the inner wall of the limiting plate.

[0011] Further, the surface of the limiting plate is provided with a connecting soft belt.

[0012] Further, the front end of the fixing ring is provided with an arc-shaped plug-in block.

[0013] Further, the inner wall of the intervention column body is provided with a wireless communication module on one side of the controller, and the inner wall of the intervention column body is provided with a power management module on one side of the wireless communication module.

[0014] Further, the inner wall of the intervention column body is provided with a data recording module on one side of the power management module.

[0015] Compared with the prior art, the female stress urinary incontinence intervention device with feedback automatic inflation function provided by the present application realizes real-time monitoring and intelligent control of urethral pressure through the arrangement of the intervention column body, the air bag, the controller, the air pump, the air inlet pipe, the air outlet pipe, the exhaust pipe and the electromagnetic valve, wherein the pressure sensor continuously collects urethral tissue pressure data, the acceleration sensor sensitively perceives the body activity state of the user, when detecting actions such as coughing and jumping that may cause urinary incontinence, the controller immediately starts the air pump to quickly inflate the air bag through the air outlet pipe to enhance the urethral closure pressure, and after the action is completed, the electromagnetic valve is opened to make the air bag exhaust through the exhaust pipe to recover, thereby constructing a closed-loop control system integrating real-time monitoring, intelligent judgment and active intervention, and significantly improving the accuracy, timeliness and effectiveness of stress urinary incontinence treatment.

[0016] Through the setting of the connecting rod, the adsorbing cotton, the mounting hole, the threaded rod, the limiting plate, the connecting soft belt and the arc-shaped plug-in block, the structural design and wearing experience of the device are improved, wherein the connecting rod provides stable extension connection, the adsorbing cotton effectively absorbs local secretion to keep dry, the threaded rod forms an adjustable fixing structure with the limiting plate through the mounting hole, which not only restricts the trend of the air inlet pipe and the discharge pipe to prevent twisting, but also facilitates the replacement of the adsorbing cotton, the connecting soft belt provides a comfortable and adjustable wearing mode, and the arc-shaped plug-in block ensures accurate front positioning, so that stable connection, body fluid management, convenient maintenance and comfortable wearing of the device are realized, and the reliability, hygiene and user experience of use are significantly improved.

[0017] Through the setting of the wireless communication module, the power management module and the data recording module, the intelligentization and digitization level of the device are enhanced, wherein the wireless communication module realizes remote data interaction and instruction transmission with external equipment, the power management module provides efficient energy distribution and power consumption control, and the data recording module continuously records key data such as pressure curve and activity event in the treatment process, so that remote monitoring, intelligent endurance and digital treatment process management are realized, the device is upgraded from a pure mechanical intervention equipment to a complete digital health solution, and important basis is provided for efficacy evaluation and individualized treatment scheme adjustment. BRIEF DESCRIPTION OF DRAWINGS

[0018] In order to more clearly illustrate the technical solutions in the embodiments of the present application or the prior art, the drawings needed in the embodiments will be briefly introduced as follows. Obviously, the drawings in the following description are only some embodiments described in the present application, and other drawings can also be obtained by those skilled in the art according to these drawings.

[0019] Figure 1 One of the overall structure schematic diagram provided by the embodiment of the present application;

[0020] Figure 2 The second overall structure schematic diagram provided by the embodiment of the present application;

[0021] Figure 3 The adsorbing cotton structure schematic diagram provided by the embodiment of the present application;

[0022] Figure 4 The air pump structure schematic diagram provided by the embodiment of the present application;

[0023] Figure 5 The discharge pipe structure schematic diagram provided by the embodiment of the present application;

[0024] Figure 6 The acceleration sensor structure schematic diagram provided by the embodiment of the present application.

[0025] Explanation of reference signs:

[0026] 1, intervention column main body; 2, air bag; 3, controller; 4, air pump; 5, air inlet pipe; 6, exhaust pipe; 7, discharge pipe; 8, electromagnetic valve; 9, fixed ring; 10, pressure sensor; 11, transmitter; 12, acceleration sensor; 13, connecting rod; 14, adsorbed cotton; 15, mounting hole; 16, threaded rod; 17, limiting plate; 18, connecting soft belt; 19, arc-shaped plug-in block; 20, wireless communication module; 21, power management module; 22, data recording module. DETAILED DESCRIPTION

[0027] In order for those skilled in the art to better understand the technical solutions of the present application, the present application will be further described in detail below with reference to the drawings.

[0028] As shown in the accompanying Figure 1 to the accompanying Figure 6 drawings:

[0029] Example one:

[0030] The present application provides a kind of female stress urinary incontinence intervention device with feedback automatic inflation function, including intervention column main body 1, the surface of intervention column main body 1 is sleeved with air bag 2, the inner wall of intervention column main body 1 is installed with controller 3, the inner wall of intervention column main body 1 is installed with air pump 4 on the side of controller 3, and controller 3 and air pump 4 are electrically connected with each other;

[0031] The input end of air pump 4 is installed with air inlet pipe 5, the output end of air pump 4 is installed with exhaust pipe 6, and the top end of exhaust pipe 6 is inserted into the inner wall of air bag 2, the surface of exhaust pipe 6 is installed with discharge pipe 7, the inner wall of discharge pipe 7 is installed with electromagnetic valve 8, the front end of intervention column main body 1 is installed with fixed ring 9, the surface of fixed ring 9 is installed with multiple pressure sensors 10, the inner wall of fixed ring 9 is installed with transmitter 11, the inner wall of transmitter 11 is installed with acceleration sensor 12, and pressure sensor 10 and acceleration sensor 12 are electrically connected with each other between transmitter 11.

[0032] When in use, the core support structure of the intervention column body 1 provides a stable mounting base for the internal components; the air bag 2 fitted on the surface of the intervention column body 1 serves as a key functional component, and its inflation and deflation processes directly achieve controllable compression and release of the urethra; the built-in controller 3 serves as a central processing unit, responsible for receiving sensor signals and coordinating the workflow of the entire system; the air pump 4 working in conjunction with the controller 3 serves as a power source, which sucks in air through the air inlet pipe 5 and then accurately delivers the gas into the air bag 2 through the air outlet pipe 6 to complete the inflation operation; to ensure flexibility in use, the air outlet pipe 6 is also provided with a branched discharge pipe 7, and an electromagnetic valve 8 is installed inside the discharge pipe 7, and the quick deflation function of the air bag 2 is realized by controlling the opening and closing of the electromagnetic valve 8. In terms of monitoring systems, the pressure sensor 10 group at the front end of the fixed ring 9 can collect real-time tissue pressure data around the urethra, providing accurate pressure feedback for the controller 3; the transmitter 11 integrated inside the fixed ring 9 is responsible for efficiently transmitting the collected sensor data to the controller 3; It is particularly worth noting that the acceleration sensor 12 is also integrated inside the transmitter 11, which can sensitively perceive the body movement state of the user (such as coughing, jumping and other activities), and when detecting sudden actions that may trigger urinary incontinence, the system can immediately trigger the air pump 4 to perform rapid inflation compensation, thereby effectively enhancing the urethral closure pressure before urine leakage occurs, thereby forming a closed-loop control system that integrates real-time monitoring, intelligent feedback and active intervention, significantly improving the accuracy and effectiveness of the treatment of stress urinary incontinence.

[0033] Embodiment two:

[0034] This embodiment is basically the same as the previous embodiment, the difference is that the tail end of the intervention column body 1 is installed with a connecting rod 13, and the surfaces of the air inlet pipe 5 and the discharge pipe 7 are inserted through the inner wall of the connecting rod 13, the surface of the connecting rod 13 is fitted with adsorbing cotton 14, the inner wall of the connecting rod 13 is provided with a mounting hole 15, the inner wall of the mounting hole 15 is threadedly connected with a threaded rod 16, one end of the threaded rod 16 is installed with a limiting plate 17, and the surfaces of the air inlet pipe 5 and the discharge pipe 7 are inserted through the inner wall of the limiting plate 17, the surface of the limiting plate 17 is installed with a connecting soft belt 18, and the front end of the fixed ring 9 is installed with an arc-shaped insertion block 19.

[0035] In use, the device is provided with a stable and reliable extension connection structure through the adapter rod 13, ensuring close connection with external components or fixing devices. The adsorbent cotton 14 is tightly sleeved on the surface of the adapter rod 13, and its high water absorption and softness can effectively absorb the secretions or sweat generated during use, keeping the contact part dry and hygienic. The mounting hole 15 is precisely provided in the inner wall of the adapter rod 13, providing a standard interface reference for the fixation of subsequent components. The threaded rod 16 is firmly screwed into the mounting hole 15 to form an adjustable mechanical fixation structure, thereby facilitating the convenient replacement of the adsorbent cotton 14. The limiting plate 17 is fixed at the end of the threaded rod 16, and the precise hole in the inside of the limiting plate 17 allows the air inlet pipe 5 and the discharge pipe 7 to penetrate through and be orderly constrained through the limiting plate 17, effectively preventing the displacement or distortion of the pipeline during use. The connecting soft belt 18 is flexibly connected to the surface of the limiting plate 17, providing a comfortable and adjustable wearing method that can adapt to the body curves of different users, enhancing the wearing stability. The arc-shaped plug-in block 19 is neatly installed at the front end of the fixing ring 9, and its ergonomic arc-shaped design can smoothly plug-in with other components or fixing devices, ensuring the accuracy of the connection and improving the comfort of use, thereby jointly forming a comprehensive functional system that integrates stable connection, body fluid management, comfortable wearing and rapid positioning, significantly improving the overall use experience and reliability of the device.

[0036] Example Three

[0037] This example is basically the same as the previous example, the difference is that the inner wall of the intervention column body 1 is installed with a wireless communication module 20 on one side of the controller 3, the inner wall of the intervention column body 1 is installed with a power management module 21 on one side of the wireless communication module 20, and the inner wall of the intervention column body 1 is installed with a data recording module 22 on one side of the power management module 21.

[0038] In use, through the setting of the wireless communication module 20, remote and wireless data interaction with external intelligent devices (such as smartphones, tablets or medical monitoring systems) is achieved. Users or medical staff can monitor the working status of the device in real time, receive key information such as pressure data and motion activity, and remotely send instructions such as adjusting the airbag pressure parameters, starting or stopping the intervention program through a customized application without physical connection, thereby greatly improving the convenience of use and the timeliness of medical intervention. Through the setting of the power management module 21, efficient, stable and intelligent energy supply is provided for the entire electronic system. This module is responsible for charging management, power distribution and power consumption control of the built-in battery, ensuring that each power-consuming unit such as the air pump, controller and sensor can obtain continuous and stable power supply. Its intelligent power management function can also automatically enter low-power mode when idle, significantly extending the single-charge use time of the device and ensuring the endurance of daily use. Through the setting of the data recording module 22, the device has important data acquisition and storage functions. This module can continuously record and store various key data during treatment, such as the start and end time of each use, airbag pressure curve, body activity events (such as the number and intensity of coughing and jumping) detected by the acceleration sensor, and use patterns. Historical data not only facilitates user review of treatment history, but also provides objective and accurate data support for doctors to assess efficacy, adjust and optimize individualized treatment plans, thereby forming the intelligent core of the device, realizing a modern medical experience of remote interaction, long-lasting endurance and data-driven decision-making, and upgrading it from a simple mechanical intervention device to a complete digital health management solution.

[0039] Application example:

[0040] As a common pelvic floor dysfunction, stress urinary incontinence has a high incidence in the female population, especially in women who have experienced multiple deliveries or are in the perimenopausal period. Its main clinical manifestation is involuntary urine leakage during activities that cause sudden abdominal pressure increase, such as coughing, sneezing, jumping or lifting heavy objects, which seriously affects the patient's quality of life, social interaction and mental health. Traditional conservative treatment methods such as pelvic floor muscle training have poor patient compliance, difficult movements to master and slow onset, while some existing physical intervention devices often have single functions and lack real-time feedback and self-adaptive adjustment capabilities, and cannot provide timely and effective urethral closure support in the moment of sudden abdominal pressure increase. Therefore, there is an urgent need for a device that can intelligently perceive the activity state of the user and actively and accurately intervene accordingly to fill the gap in the immediacy and intelligence of existing treatment methods.

[0041] Firstly, the patient easily and accurately positions the intervention column body 1 and its surface airbag 2 at the target location around the urethra by the guidance of the arc-shaped plug-in block 19 at the front end of the fixing ring and the corresponding fixed component during device wearing. Then, she wraps the connecting soft belt 18 around the fixed part and uses its adjustable feature to ensure that the device fits the body curve, providing a stable and comfortable wearing experience. After wearing the device, the adsorbing cotton 14 is in close contact with the skin, starting to continuously absorb the moisture or trace secretions that may be generated locally, maintaining local dryness and hygiene during use.

[0042] In daily use, the core intelligent system of the device begins to work comprehensively. The multiple sets of pressure sensors 10 located on the surface of the fixing ring 9 continuously monitor the initial tissue pressure around the urethra and send this baseline data to the controller 3 through the transmitter 11. At the same time, the acceleration sensor 12 integrated inside the transmitter 11 acts as a sharp motion detective, capturing the motion state and acceleration changes of the patient's body in three-dimensional space in real time. When the patient performs daily activities such as sudden coughing or preparing to stand up from a chair, the acceleration sensor 12 can instantly identify this characteristic body movement that will cause abdominal pressure to rise.

[0043] The key dynamic information is immediately transmitted to the controller 3. The controller 3, as the brain of the system, combines the real-time pressure data provided by the pressure sensor 10 and the preset safe pressure parameters to perform high-speed calculation and judgment. Once it is confirmed that intervention is needed, the controller 3 immediately issues an instruction to the air pump 4. The air pump 4 is then started, inhaling air through the air inlet pipe 5 and pumping a certain amount of gas into the airbag 2 through the air outlet pipe 6, causing the airbag 2 to moderately expand in a very short time, thereby strengthening the support force on the urethra and compensating for the possible incomplete closure of the urethra due to the sudden increase in abdominal pressure.

[0044] When the coughing action ends, the abdominal pressure returns to normal, the acceleration sensor 12 detects that the body activity tends to be stable, the controller 3 will instruct the electromagnetic valve 8 to open. At this time, the excess gas in the airbag 2 is discharged through the exhaust pipe 7, so that the airbag 2 returns to the initial low pressure state, avoiding unnecessary long-term compression of the urethra. Throughout the intervention process, the wireless communication module 20 enables the patient's smartphone to maintain connection with the device, and the patient can intuitively view the current pressure state, historical activity record and operation log of the device on the mobile phone application, and remotely fine-tune the basic parameters as needed according to the doctor's authorization. The power management module 21 efficiently manages the battery energy in the background, ensuring that all electronic components, especially the air pump 4 which requires instantaneous large current drive, can obtain stable power, and ensure that the device will not be interrupted due to power problems during long-term use throughout the day. The data recording module 22 silently records the time of each intervention event, the corresponding activity type (judged by the acceleration sensor 12), the airbag pressure change curve and other detailed data, forming a complete personal treatment log. This log provides extremely objective and accurate data basis for doctors to assess treatment effect, understand the correlation between patient's daily activity pattern and urinary incontinence, and further individualize the treatment plan when the patient is reexamined.

[0045] Working principle: When the device is initially worn, the intervention column body 1 acts as the core support structure to bear various functional components, and the air bag 2 on its surface is in a deflated low-profile state to facilitate placement; after wearing, the multiple sets of pressure sensors 10 on the surface of the fixing ring 9 begin to continuously monitor the tissue basal pressure around the urethra, and send the pressure data to the controller 3 in real time through the transmitter 11; at the same time, the acceleration sensor 12 integrated in the transmitter 11 synchronously monitors the motion state of the user's body, and real-time senses specific acceleration changes such as coughing, jumping and other actions that can cause sudden increase in abdominal pressure; when the acceleration sensor 12 detects a sudden action indicating the risk of urinary incontinence, it immediately transmits the signal to the controller 3 through the transmitter 11, and the controller 3 immediately makes a comprehensive judgment in combination with the real-time pressure data fed back by the pressure sensor 10, and immediately issues an instruction to the air pump 4 if it is judged to intervene; after the air pump 4 is started, it inhales air through the air inlet pipe 5, and pumps compressed air into the air bag 2 through the air outlet pipe 6, so that the air bag 2 rapidly expands to increase the closing pressure on the urethra, effectively resisting the risk of urine leakage caused by increased abdominal pressure; after the intervention action is completed, the controller 3 restores to be stable according to the signal of the acceleration sensor 12 and the continuous feedback of the pressure sensor 10, and controls the electromagnetic valve 8 installed on the discharge pipe 7 of the branch pipeline of the air outlet pipe 6 to be opened, so that the gas in the air bag 2 is orderly discharged, and the pressure returns to a comfortable basic level; in order to ensure stable and comfortable wearing, the device provides extension connection through the connecting rod 13, the adsorbing cotton 14 on the surface of which absorbs local moisture, and the threaded rod 16 screwed in the mounting hole 15 drives the limiting plate 17 to constrain and limit the air inlet pipe 5 and the discharge pipe 7 penetrating through the inside thereof, and the connecting soft belt 18 provides flexible body fixation, and the arc-shaped plug-in block 19 ensures accurate front positioning; the intelligent operation of the whole system relies on the built-in wireless communication module 20 to realize remote monitoring and instruction interaction with external equipment, the power management module 21 provides efficient and stable energy management and distribution for all power-consuming units such as the air pump 4, the controller 3, the sensor, etc., and the data recording module 22 continuously records key treatment data including pressure curve, activity event and intervention record, thereby jointly forming a closed-loop automatic control system integrating real-time physiological signal monitoring, intelligent decision-making, active physical intervention and data management.

[0046] The foregoing merely describes certain exemplary embodiments of the present application by way of illustration, and it is needless to say that those skilled in the art can modify the described embodiments in various ways without departing from the spirit and scope of the present application. Therefore, the above drawings and descriptions are illustrative in nature and should not be construed as limiting the scope of protection of the claims of the present application.

Claims

1. A female stress urinary incontinence intervention device with a feedback automatic inflation function, comprising an intervention column body (1), characterized in that, The surface of the intervention column body (1) is sleeved with an air bag (2), the inner wall of the intervention column body (1) is provided with a controller (3), the inner wall of the intervention column body (1) is provided with an air pump (4) on the side of the controller (3), and the controller (3) and the air pump (4) are electrically connected with each other. The input end of the air pump (4) is provided with an air inlet pipe (5), the output end of the air pump (4) is provided with an air outlet pipe (6), the top end of the air outlet pipe (6) is inserted into the inner wall of the air bag (2), and the surface of the air outlet pipe (6) is provided with an exhaust pipe (7), and the inner wall of the exhaust pipe (7) is provided with an electromagnetic valve (8).

2. A female stress urinary incontinence intervention device with a feedback automatic inflation function according to claim 1, characterized in that, The front end of the intervention column body (1) is provided with a fixing ring (9), the surface of the fixing ring (9) is provided with a plurality of pressure sensors (10), the inner wall of the fixing ring (9) is provided with a transmitter (11), the inner wall of the transmitter (11) is provided with an acceleration sensor (12), and the pressure sensor (10) and the acceleration sensor (12) are electrically connected with the transmitter (11).

3. The female stress urinary incontinence intervention device with automatic inflation function according to claim 1, characterized in that, The tail end of the intervention column body (1) is provided with a connecting rod (13), and the surfaces of the air inlet pipe (5) and the exhaust pipe (7) are inserted into the inner wall of the connecting rod (13) in penetrating mode, and the surface of the connecting rod (13) is sleeved with adsorbing cotton (14).

4. A female stress urinary incontinence intervention device with a feedback automatic inflation function according to claim 3, characterized in that, The inner wall of the connecting rod (13) is provided with a mounting hole (15), and the inner wall of the mounting hole (15) is threadedly connected with a threaded rod (16).

5. A female stress urinary incontinence intervention device with a feedback automatic inflation function according to claim 4, characterized in that, One end of the threaded rod (16) is provided with a limiting plate (17), and the surfaces of the air inlet pipe (5) and the exhaust pipe (7) are inserted into the inner wall of the limiting plate (17) in penetrating mode.

6. A female stress urinary incontinence intervention device with a feedback automatic inflation function according to claim 5, characterized in that, The surface of the limiting plate (17) is provided with a connecting soft belt (18).

7. The female stress urinary incontinence intervention device with automatic inflation function according to claim 2, characterized in that, The front end of the fixing ring (9) is provided with an arc-shaped insertion block (19).

8. The female stress urinary incontinence intervention device with automatic inflation function according to claim 1, characterized in that, The inner wall of the intervention column body (1) is provided with a wireless communication module (20) on the side of the controller (3), and the inner wall of the intervention column body (1) is provided with a power management module (21) on the side of the wireless communication module (20).

9. A female stress urinary incontinence intervention device with a feedback auto- inflation function according to claim 8, characterized in that, The inner wall of the intervention column body (1) is provided with a data recording module (22) on the side of the power management module (21).