CN220938516U - Female pelvic floor muscle group stimulation and rehabilitation monitoring device - Google Patents
Female pelvic floor muscle group stimulation and rehabilitation monitoring device Download PDFInfo
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- CN220938516U CN220938516U CN202222530463.1U CN202222530463U CN220938516U CN 220938516 U CN220938516 U CN 220938516U CN 202222530463 U CN202222530463 U CN 202222530463U CN 220938516 U CN220938516 U CN 220938516U
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Abstract
The utility model relates to a female pelvic floor muscle group stimulation and rehabilitation monitoring device, which comprises a stimulation unit, a pressure sensing unit, a data processing unit and a variability main body, wherein the stimulation unit is connected with the pressure sensing unit; the variable main body is internally provided with a stimulation unit. The advantages are as follows: according to the stimulation and rehabilitation monitoring device for the pelvic floor muscle group of the female, on one hand, the contraction performance can be improved in a stimulation mode, on the other hand, the contraction performance of the pelvic floor muscle group can be accurately estimated by accurately monitoring the pressure distribution diagram of the pelvic floor muscle group in mechanical stimulation and non-mechanical stimulation, and further, the estimation and preliminary pathological analysis are realized, so that a scheme of rehabilitation of the pelvic floor muscle group is obtained, and the rehabilitation of the pelvic floor muscle group is promoted.
Description
Technical Field
The utility model relates to the technical field of medical equipment, in particular to a female pelvic floor muscle group stimulation and rehabilitation monitoring device.
Background
Female urinary incontinence is a common disorder in women, with prevalence approaching 50% currently being statistically global, about half of which is stress urinary incontinence (Stress Urinary Incontinence, SUI). Stress incontinence refers to urinary incontinence in which urine does not overflow autonomously from the external urethral orifice in the absence of bladder detrusor contraction when the bladder pressure is greater than the maximum urethral pressure, and often occurs when the abdominal pressure suddenly increases, for example: laughing, sneezing, coughing, etc. Postmenopausal populations are more prone to morbidity. Most of the pathogenesis is that the birth injury is caused during the delivery, the estrogen level is reduced after menopause, the pelvic floor soft tissue is relaxed, and the like. SUI was initially recognized as one of five major diseases affecting human health in the mid 90 s, known as "social cancer". Particularly in China, SUI is more and more valued with further aging of population. The incidence rate of organ prolapse in the pelvic floor of middle-aged and elderly women is high, and the development process and pathological reasons of the prolapse are not clear, so that proper methods and equipment are urgently needed to carry out systematic study on urinary incontinence and organ prolapse. With the crisis awareness of the gradual improvement and the aging of the physical life of people, people pay more and more attention to periodic physical examination. Early pressure and myoelectric tests were performed on pelvic floor organs such as bladder, vagina, uterus and rectum to provide reliable diagnosis before lesions developed to give early prophylactic and therapeutic measures.
The following drawbacks and deficiencies exist in the prior art with respect to improving the contractile performance of pelvic floor muscles:
The shrinkage performance detection of pelvic floor muscles in the prior art is still in the medical means of manual finger sensing exploration or traumatism of external force, the accuracy and the repeatability are poor, and summarized data or a physiological state model which is easy to count and judge pathological aberrations cannot be formed.
In view of the foregoing, there is a need for a device that can accurately evaluate the contractility of pelvic floor muscle groups, thereby performing evaluation and preliminary pathological analysis to promote the rehabilitation of pelvic floor muscle groups, but such a device has not been reported yet.
Disclosure of Invention
The utility model aims to provide a device capable of accurately evaluating the contractility of pelvic floor muscle groups, further realizing evaluation and preliminary pathological analysis and implementing pelvic floor muscle group rehabilitation.
In order to achieve the above purpose, the technical scheme adopted by the utility model is as follows:
A device for stimulating and rehabilitation monitoring of female pelvic floor muscles comprises a stimulating unit, a pressure sensing unit, a data processing unit and a variability main body; the variable main body is internally provided with a stimulation unit; the pressure sensing units are distributed on the periphery of the variability main body; the data processing unit is connected with the pressure sensing unit; the data processing unit gathers dynamic readings of each pressure sensing unit; the data processing unit is internally provided with a data processor; the data processor is used for processing the dynamic readings of the pressure sensing units and feeding back the pressure of the muscle groups, storing, transmitting or displaying the pressure change; the data processor is connected with a display; the display is internally provided with a sensing unit model; and the sensing unit model receives the processing signals of the data processor to form a pressure distribution map, and the pressure distribution map is displayed on the sensing unit model on the display.
As a preferred embodiment, the stimulation unit is provided with a vibration source by at least one vibration motor.
As a preferred embodiment, the pressure sensing unit is at least one pressure sensing module arranged on the surface of the deformable body, wherein the pressure sensing module may be a flexible capsule-like or thin-layer pressure sensor, a pressure-sensitive patch, or a pressure-sensitive sleeve.
As a preferred technical scheme, the periphery of the pressure sensing unit is provided with a protective sleeve.
As a preferred technical solution, the pressure sensing unit includes a plurality of separate digital pressure sensors; the digital pressure sensor is designed corresponding to the distribution form of the pelvic floor muscle group of the human body.
As a preferred technical solution, the vibration direction of the stimulation unit includes two modes of axial vibration or radial vibration along the variability main body, and the axial vibration and the radial vibration can be stimulated simultaneously, or the axial vibration and the radial vibration can be stimulated separately.
As a preferable technical scheme, the handle part of the variability main body is provided with an inserting port; the plug interface is used for connecting the charging plug, the wireless antenna and the data line.
As a preferable technical scheme, the data processor is provided with a pressure accumulation module; the pressure accumulation module is used for measuring the accumulated maximum pressure and pressure distribution of surrounding tissues or muscle groups to the stimulation rod body after a certain period of time of in-place use.
As a preferable technical scheme, the stimulation unit is provided with a corresponding control board; the control panel is provided with parameters required by the stimulation unit, and the parameters comprise frequency, pulse width, intensity, on-off power ratio, wave rise and fall, time adjustment and other series parameters.
The utility model has the advantages that:
1. According to the stimulation and rehabilitation monitoring device for the pelvic floor muscle group of the female, on one hand, the contraction performance can be improved in a stimulation mode, on the other hand, the contraction performance of the pelvic floor muscle group can be accurately estimated by accurately monitoring the pressure distribution diagram of the pelvic floor muscle group in mechanical stimulation and non-mechanical stimulation, and further, the estimation and preliminary pathological analysis are realized, so that a scheme of rehabilitation of the pelvic floor muscle group is obtained, and the rehabilitation of the pelvic floor muscle group is promoted.
2. The stimulation unit is used for stimulating the pelvic floor muscle group nerves to cause reflex stimulation, and the contraction capacity of the pelvic floor muscle group is trained in a mechanical stimulation mode, so that the pelvic floor dysfunction is improved.
3. The device is provided with a pressure sensing unit, wherein the pressure sensing unit is used for acquiring bioelectric force of the pelvic floor muscle group in a contracted and relaxed state and providing basis for analyzing the contraction performance of the pelvic floor muscle group.
4. A data processing unit is provided, and a data processor is built in the data processing unit. The data processor has two functions, one of which is to process the dynamic readings of each pressure sensing unit and is used for feeding back the pressure of muscle groups, storing, transmitting or displaying the pressure change; on the other hand, data signals which are in one-to-one correspondence with the pressure sensing units and the sensing unit models are processed, and a pressure distribution diagram is formed and then displayed. Therefore, the contractility of the pelvic floor muscle group can be accurately estimated, and further, estimation and preliminary pathological analysis are realized.
5. The pressure sensors are separated, so that the sensors are independent, and mutual interference is avoided; secondly, the distribution positions conform to the physiological positions of pelvic floor muscle groups, and the contraction force of each pelvic floor muscle can be obtained.
6. The data processor is provided with a pressure accumulation module; the effect of this design is: the pressure accumulation module is used for measuring the accumulated maximum pressure and pressure distribution of surrounding tissues or muscle groups to the stimulation rod body after a certain period of time of in-place use.
7. A sensor cell model is provided by which the magnitude and pressure distribution of the pressure experienced by different locations is represented by different color changes after use.
Drawings
Fig. 1 is a schematic structural view of a device for stimulating and rehabilitation monitoring of female pelvic floor muscle groups according to the present utility model.
Fig. 2 is a main structure block diagram of a female pelvic floor muscle group stimulating and rehabilitation monitoring device of the utility model.
Fig. 3 is a schematic diagram of a female pelvic floor muscle group stimulation and rehabilitation monitoring device matched with a display according to the present utility model.
Fig. 4 is a schematic distribution diagram of the protective sleeve and the pressure sensing unit.
Fig. 5 is a schematic diagram of the axial and radial distribution of the stimulation unit in the deformable body.
Fig. 6 is a block diagram of the structure of the stimulation unit of the present utility model.
Fig. 7 is a schematic structural view of the variability body 4.
Detailed Description
The utility model is further described below with reference to examples and with reference to the accompanying drawings.
Reference numerals and components referred to in the drawings are as follows:
1. Stimulation unit 2. Pressure sensing unit
3. Data processing unit 4. Variability subject
5. Data processor 6. Display
7. Protective sleeve 8. Pressure accumulation Module
9. Interface 10. Sensor unit model
11. Display 12. Protective sheath
For the purpose of making the objects, technical solutions and advantages of the embodiments of the present utility model more apparent, the technical solutions of the embodiments of the present utility model will be clearly and completely described below with reference to the accompanying drawings in the embodiments of the present utility model, and it is apparent that the described embodiments are some embodiments of the present utility model, but not all embodiments of the present utility model. All other embodiments, which can be made by those skilled in the art based on the embodiments of the utility model without making any inventive effort, are intended to be within the scope of the utility model.
For the purpose of facilitating an understanding of the embodiments of the present utility model, reference will now be made to the following description of specific embodiments, taken in conjunction with the accompanying drawings, which are not intended to limit the embodiments of the utility model.
In the description of the embodiments of the present utility model, it should be noted that, directions or positional relationships indicated by terms such as "axial", "radial", "one end", "the other end", "front", "rear", "middle portion", "inside", etc., are based on those shown in the drawings, are merely for convenience of description and simplification of description, and do not indicate or imply that the apparatus or element to be referred to must have a specific direction, be configured and operated in a specific direction, and thus should not be construed as limiting the present utility model; the terms "first gear," "second gear," and "third gear" are used for descriptive purposes only and are not to be construed as indicating or implying relative importance; furthermore, unless explicitly specified and limited otherwise, the terms "mounted," "connected," and "connected" are to be construed broadly, and may be either fixedly connected, detachably connected, or integrally connected, for example; can be mechanically or electrically connected; can be directly connected or indirectly connected through an intermediate medium, and can be communication between two elements. The specific meaning of the above terms in the present utility model will be understood in specific cases by those of ordinary skill in the art.
Example 1
Referring to fig. 1 and 2, fig. 1 is a schematic structural diagram of a device for stimulating and rehabilitation monitoring of female pelvic floor muscle group according to the present utility model. FIG. 2 is a block diagram of the main structure of a device for stimulating and rehabilitation monitoring of female pelvic floor muscle groups according to the present utility model; fig. 3 is a schematic diagram of a female pelvic floor muscle group stimulation and rehabilitation monitoring device matched with the display 116 according to the present utility model. A female pelvic floor muscle group stimulation and rehabilitation monitoring device; the device comprises a stimulation unit 1, a pressure sensing unit 2 and a data processing unit 3; the variability main body 4 is internally provided with a stimulation unit 1; the pressure sensing units 2 are distributed on the periphery of the variability main body 4; the data processing unit 3 is connected with the pressure sensing unit 2; the data processing unit 3 gathers dynamic readings of each pressure sensing unit 2; the data processing unit 3 is internally provided with a data processor 5; the data processor 5 is used for processing the dynamic readings of each pressure sensing unit 2 and feeding back the pressure of the muscle group, storing, transmitting or displaying the pressure change; the data processor 5 is connected with a display 116; the display 116 is internally provided with a sensing unit model 10; the sensor unit model 10 receives the processing signals from the data processor to form a pressure distribution map, which is displayed on the sensor unit model 10 on the display 116.
The stimulation unit 1 is provided with a vibration source by at least one vibration motor; the pressure sensing unit 2 is at least one pressure sensing module arranged on the surface of the deformable main body, wherein the pressure sensing module can be a flexible capsule-shaped or thin-layer pressure sensor, a pressure-sensitive patch and a pressure-sensitive sleeve.
Referring to fig. 4, fig. 4 is a schematic distribution diagram of the protective cover 127 and the pressure sensing unit 2. The outer circumference of the pressure sensing unit 2 is provided with a protective sleeve 127. The pressure sensing unit 2 comprises a plurality of separated digital pressure sensors; the digital pressure sensor is designed corresponding to the distribution form of the pelvic floor muscle group of the human body.
Referring to fig. 5, fig. 5 is a schematic diagram illustrating the axial and radial distribution of the stimulation unit 1 in the variable body 4.
The vibration direction of the stimulation unit 1 includes two modes of axial vibration or radial vibration along the variable main body 4, and the axial vibration and the radial vibration can be stimulated simultaneously, or the axial vibration and the radial vibration can be stimulated separately. The stimulation unit 1 is provided with a corresponding control board; the control panel is provided with parameters required by the stimulation unit 1, and the parameters comprise frequency, pulse width, intensity, on-off ratio, wave rise and fall, time adjustment and other series parameters.
Referring to fig. 6, fig. 6 is a block diagram of the stimulation unit 1 according to the present utility model. The data processor 5 is provided with a pressure accumulation module 8; the pressure accumulation module 8 is used for measuring the accumulated maximum pressure and pressure distribution of surrounding tissues or muscle groups to the stimulation rod body after a certain period of time.
Referring to fig. 7, fig. 7 is a schematic structural view of the variable body 4. The handle part of the variability main body 4 is provided with a plug-in port 9; the plug interface 9 is used for connecting a charging plug, a wireless antenna and a data line.
It should be noted that:
The device comprises a stimulation unit 1, wherein the stimulation unit 1 is used for stimulating pelvic floor muscle group nerves to cause reflex stimulation and improve pelvic floor dysfunction.
The device comprises a pressure sensing unit 2, wherein the pressure sensing unit 2 is used for acquiring biological elasticity of the pelvic floor muscle group in a contracted state and a relaxed state, and providing a basis for analyzing the contraction performance of the pelvic floor muscle group.
The device comprises a data processing unit 3, and dynamic readings of the digital sensors can be obtained in real time through the data processing unit 3.
The device comprises a deformable body 4; the deformable body 4 is used as a carrier of the stimulation unit 1 and the sensing unit, and is convenient to be placed into the vagina to reach the position of the pelvic floor muscle group in a use state.
The data processing unit 3 is internally provided with a data processor 5. The data processor 5 has two functions, one of which is to process the dynamic readings of each pressure sensing unit 2 for feeding back the muscle group pressure, storing, transmitting or displaying the pressure change; on the other hand, the data signals of the pressure sensor unit 2 and the sensor unit model 10, which are in one-to-one correspondence, are processed to form a pressure distribution map, and then displayed. Therefore, the contractility of the pelvic floor muscle group can be accurately estimated, and further, estimation and preliminary pathological analysis are realized.
The stimulation unit 1 is provided with a vibration source by at least one vibration motor. Thus, vibration power is provided for the stimulation unit 1, and the stimulation power requirement of the stimulation unit 1 on pelvic floor muscle groups is met.
The pressure sensing unit 2 is at least one pressure sensing module arranged on the surface of the deformable body 4, wherein the pressure sensing module can be a flexible capsule-shaped or thin-layer pressure sensor, a pressure-sensitive patch or a pressure-sensitive sleeve. The effect of this design is: the requirements of collecting contraction force of each pelvic floor muscle block can be met according to the requirements; secondly, through setting up the sensor of multiple structural style, sensitivity is high, and the interference factor of acquisition data is little.
The outer circumference of the pressure sensing unit 2 is provided with a protective sleeve 127. The effect of this design is: by providing the protective sleeve 127, replacement is facilitated, while user hygiene is ensured, and related infections caused by placement in the vagina are avoided.
The pressure sensing unit 2 comprises a plurality of separated digital pressure sensors; the digital pressure sensor is designed corresponding to the distribution form of the pelvic floor muscle group of the human body. The pressure sensors are separated, so that the sensors are independent, and mutual interference is avoided; secondly, the distribution positions conform to the physiological positions of pelvic floor muscle groups, and the contraction force of each pelvic floor muscle can be obtained.
The vibration direction of the stimulation unit 1 includes two modes of axial vibration or radial vibration along the variable main body 4, and the axial vibration and the radial vibration can be stimulated simultaneously, or the axial vibration and the radial vibration can be stimulated separately. The effect of this design is: the multi-dimensional stimulation can be realized, and the extrusion performance of the pelvic floor muscle group can be evaluated conveniently.
The handle part of the variability main body 4 is provided with a plug-in port 9; the plug interface 9 is used for connecting a charging plug, a wireless antenna and a data line. The effect of this design is: charging is convenient for, and each circuit can be connected simultaneously to be stored, so that disorder winding is avoided.
The data processor 5 is provided with a pressure accumulation module 8; the effect of this design is: the pressure accumulation module 8 is used for measuring the accumulated maximum pressure and pressure distribution of surrounding tissues or muscle groups to the stimulation rod body after a certain period of time.
The stimulation unit 1 is provided with a corresponding control board; the control panel is provided with parameters required by the stimulation unit 1, and the parameters comprise frequency, pulse width, intensity, on-off ratio, wave rise and fall, time adjustment and other series parameters. The effect of this design is: by setting various parameters of the control panel, the variable main body 4 can stimulate the pelvic floor muscle group to different degrees, so that the mechanical stimulation is satisfied, and the contraction performance of the pelvic floor muscle group is improved.
The device for stimulating and rehabilitation monitoring of the female pelvic floor muscle group obtains relevant contraction performance through pressure distribution of the pelvic floor muscle group before and after the machine. Specifically: when the pelvic floor muscle group is in a non-stimulated state, the pressure sensors distributed on the surface of the variable body 4 record the pressure exerted by the peripheral muscle group and organs on the pelvic floor muscle group when the patient exercises himself or herself in a non-mechanical stimulation state. The pressure distribution of the peripheral muscle groups and organs can be obtained according to the digital sensors distributed at different positions, and the contraction performance improvement/enhancement progress condition of the muscle groups and related organs can be obtained by comparing the pressure distribution of different stimulation periods or treatment periods, so that the basis is provided for the next recovery.
A sensor unit model 10 is provided, and the magnitude and pressure distribution of the pressure applied to different portions are represented by different color changes after use of the sensor unit model 10.
The pressure sensing unit 2 of the utility model is composed of a plurality of digital pressure sensors, and a plurality of separated digital pressure sensors are distributed on the surface of the variability main body 4, so that the extrusion capacity of surrounding tissues or muscle groups to the stimulation rod body can be dynamically measured in real time, and the accumulated maximum pressure and pressure distribution of the surrounding tissues or muscle groups to the stimulation rod body can be measured after a certain time of in-place use.
The foregoing is merely a preferred embodiment of the present utility model and it should be noted that modifications and additions to the present utility model may be made by those skilled in the art without departing from the principles of the present utility model and such modifications and additions are to be considered as well as within the scope of the present utility model.
Claims (8)
1. The device is characterized by comprising a stimulation unit, a pressure sensing unit, a data processing unit and a variability main body; the variable main body is internally provided with a stimulation unit; the pressure sensing units are distributed on the periphery of the variability main body; the data processing unit is connected with the pressure sensing unit; the data processing unit gathers dynamic readings of each pressure sensing unit; the data processing unit is internally provided with a data processor; the data processor is used for processing the dynamic readings of the pressure sensing units and feeding back the pressure of the muscle groups, storing, transmitting or displaying the pressure change; the data processor is connected with a display; the display is internally provided with a sensing unit model; and the sensing unit model receives the processing signals of the data processor to form a pressure distribution map, and the pressure distribution map is displayed on the sensing unit model on the display.
2. The device of claim 1, wherein the pressure sensing unit is at least one pressure sensing module disposed on the surface of the deformable body, wherein the pressure sensing module is a flexible capsule or sheet pressure sensor, a pressure sensitive patch, or a pressure sensitive sleeve.
3. The device for stimulating and rehabilitating the pelvic floor muscle according to claim 2, wherein the outer periphery of the pressure sensing unit is provided with a protective sleeve.
4. The device for stimulating and rehabilitating the pelvic floor muscle according to claim 1, wherein the pressure sensor unit comprises a plurality of separate digital pressure sensors; the digital pressure sensor is designed corresponding to the distribution form of the pelvic floor muscle group of the human body.
5. The device according to claim 1, wherein the vibration direction of the stimulation unit includes two modes of axial vibration or radial vibration along the variability main body, and the axial vibration and the radial vibration can be stimulated simultaneously or the axial vibration and the radial vibration can be stimulated separately.
6. The device for stimulating and rehabilitating the pelvic floor muscle according to claim 3, wherein the handle portion of the deformable body is provided with an interface; the plug interface is used for connecting the charging plug, the wireless antenna and the data line.
7. The device for stimulating and rehabilitating the pelvic floor muscle according to claim 5, wherein the data processor is provided with a pressure accumulating module; the pressure accumulation module is used for measuring the accumulated maximum pressure and pressure distribution of surrounding tissues or muscle groups to the stimulation rod body after a certain period of time of in-place use.
8. The device for stimulating and rehabilitating the pelvic floor muscle according to any one of claims 1 to 6, wherein the stimulating unit is provided with a corresponding control board; the control panel is provided with parameters required by the stimulation unit, and the parameters comprise frequency, pulse width, intensity, on-off power ratio, wave rise and fall and time adjustment series parameters.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202222530463.1U CN220938516U (en) | 2022-09-24 | 2022-09-24 | Female pelvic floor muscle group stimulation and rehabilitation monitoring device |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202222530463.1U CN220938516U (en) | 2022-09-24 | 2022-09-24 | Female pelvic floor muscle group stimulation and rehabilitation monitoring device |
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| CN220938516U true CN220938516U (en) | 2024-05-14 |
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| CN202222530463.1U Active CN220938516U (en) | 2022-09-24 | 2022-09-24 | Female pelvic floor muscle group stimulation and rehabilitation monitoring device |
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| CN (1) | CN220938516U (en) |
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