CN108096704B - Device and system for treating infertility and method for carrying out body fluid regulation and nerve channel regulation - Google Patents
Device and system for treating infertility and method for carrying out body fluid regulation and nerve channel regulation Download PDFInfo
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- CN108096704B CN108096704B CN201711283551.3A CN201711283551A CN108096704B CN 108096704 B CN108096704 B CN 108096704B CN 201711283551 A CN201711283551 A CN 201711283551A CN 108096704 B CN108096704 B CN 108096704B
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- A61N1/00—Electrotherapy; Circuits therefor
- A61N1/18—Applying electric currents by contact electrodes
- A61N1/32—Applying electric currents by contact electrodes alternating or intermittent currents
- A61N1/36—Applying electric currents by contact electrodes alternating or intermittent currents for stimulation
- A61N1/36014—External stimulators, e.g. with patch electrodes
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N7/00—Ultrasound therapy
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N7/00—Ultrasound therapy
- A61N2007/0004—Applications of ultrasound therapy
- A61N2007/0021—Neural system treatment
- A61N2007/0026—Stimulation of nerve tissue
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Abstract
The invention relates to the technical field of medical treatment, in particular to a device and a system for treating infertility and a method for regulating body fluid and regulating nerves and channels and collaterals. By adopting the system, the body fluid regulation and the nerve and meridian regulation are carried out, and the infertility problems caused by thin endometrium, low endometrial receptivity, premature ovarian failure and low ovarian reserve function are solved. Compared with the prior art, the invention has the advantages that: physical non-wound, no side effect and simple operation, can improve the body fluid circulation of human body, increase the blood supply of reproductive organs such as pelvic cavity, uterus and ovary, increase the nutrition supply and promote the generation of new vessels; the invention can also improve the human reproductive endocrine system, improve the hormone level, balance the internal environment, and effectively treat infertility problems such as thin endometrium, premature ovarian failure, low ovarian reserve function, IVF-ET pre-adjuvant therapy and the like.
Description
Technical Field
The invention relates to the technical field of medical treatment, in particular to a device and a system for treating infertility and a method for regulating body fluid and regulating nerves and channels and collaterals.
Background
In recent years, female infertility becomes a big problem in the medical field, mainly manifested by thin endometrium, low endometrial receptivity, premature ovarian failure, low ovarian reserve function and the like, even if the IVF _ ET technology is adopted, for the female with the overall reproductive function decline, the success rate is low from successful conception to successful delivery. The main treatment mode at present is drug treatment, but certain side effects exist in drug treatment. The physical therapy mode is the traditional Chinese medicine acupoint therapy, the acupuncture points, nerves and channels and collaterals are punctured by a simple hand needle or an electric needle for stimulation, but the accuracy requirement on the acupuncture point puncturing position is extremely high, the operation is not easy, and the clinical therapy effect cannot be guaranteed.
Disclosure of Invention
The invention aims to provide a device and a system for treating infertility and a method for carrying out body fluid regulation and nerve channel regulation. By adopting the system, the body fluid regulation and the nerve and meridian regulation are carried out, and the infertility problems caused by thin endometrium, low endometrial receptivity, premature ovarian failure and low ovarian reserve function are solved.
In order to achieve the above purpose, the embodiment of the present invention adopts the following technical solutions:
a device for treating infertility, comprising: a signal generator for generating an electrical stimulation signal and an ultrasound signal; an output port; the output port is electrically connected with the signal generator; an actuator; the actuator is configured for electrical connection to the output port; the main controller is electrically connected with the signal generator; the main controller is used for controlling the signal generator to send out an electrical stimulation signal and an ultrasonic signal and transmitting the electrical stimulation signal and the ultrasonic signal to the actuating mechanism through the output port; the executing mechanism can receive the signal sent by the main controller and execute corresponding operation.
In a preferred embodiment of the present invention, the output ports include a first output port, a second output port and a third output port, and the first output port, the second output port and the third output port are electrically connected to the main controller.
In a preferred embodiment of the invention, the actuator comprises a transcutaneous electrical stimulation electrode, an intracavity electrical stimulation probe and a focused ultrasound probe, the intracavity electrical stimulation probe being configured for electrical connection to the first output port; the focused ultrasound probe is configured for electrical connection to the second output port; the transcutaneous electrical stimulation electrode is configured for electrical connection to the third output port.
In a preferred embodiment of the invention, the intracavity electrical stimulation probe comprises a probe base body, an annular metal electrode plate, an arc spherical electrode plate, a first cable and a first plug port; the probe base body is cylindrical, and is made of plastic or medical silica gel; the top end of the probe base body comprises two hemispherical surfaces with equal diameters; the annular metal electrode plate is fixed on the whole body of the probe base body; the number of the annular metal electrode plates is even; the arc spherical electrode plates are fixed on two sides of the two hemispherical surfaces; the number of the arc-shaped electrode plates is 2; one end of a first cable is connected with the probe substrate, and the other end of the first cable is connected with the first plug port; the first connector port is configured to be electrically connected to the first output port, receive an electrical stimulation signal from the signal generator, and conduct the electrical stimulation signal to the annular metal electrode sheet and the arc-sphere electrode sheet.
In a preferred embodiment of the present invention, the focused ultrasound probe comprises a probe housing, a focused ceramic plate, a second cable and a second connector port; the focusing ceramic plate is fixed inside the probe shell, the second cable is electrically connected with the focusing ceramic plate, and the second plugging port is configured for being electrically connected with the second output port; the focusing ceramic chip is used for receiving the ultrasonic signal sent by the signal generator and outputting the ultrasonic signal after focusing.
In a preferred embodiment of the present invention, the apparatus further comprises a mobile control platform electrically connected to the main controller; the first output port, the second output port and the third output port are all arranged on the mobile control platform.
In the preferred embodiment of the present invention, the mobile control platform is electrically connected to the main controller through the assembly cable.
In a preferred embodiment of the invention, the device comprises an electrical stimulation signal generator and a focused ultrasound signal generator; the electrical stimulation signal generator comprises a low-frequency electrical stimulation module and a medium-frequency electrical stimulation module; the low-frequency electrical stimulation module and the medium-frequency electrical stimulation module are electrically connected to the assembly cable.
In a preferred embodiment of the present invention, the apparatus further comprises a display module and a power module, wherein the display module is electrically connected to the main controller; the power supply module is electrically connected with the main controller; the power supply module is used for converting a network power supply into a low-voltage direct-current power supply required by the work of the host.
A system for treating infertility, comprising the above-described device for treating infertility;
the frequency range of the ultrasonic stimulation signal is 0.8MHz-2.0MHz, the focusing depth is 9mm-35mm, the intensity is 0-2.5W/cm2, and continuous waves or pulse waves are output; the electrical stimulation signals comprise low-frequency electrical stimulation signals and medium-frequency electrical stimulation signals; wherein, the current frequency range of the low-frequency electric stimulation signal is 1-500Hz, the pulse width is 1-2000us, the current intensity is 0-100mA, and a bidirectional balanced wave, a unidirectional balanced wave, a sine wave or a sawtooth wave signal waveform is output; the current frequency range of the intermediate frequency electrical stimulation signal is 2000-5000Hz, the pulse width is 1-2000us, and the current intensity is 0-100mA, and a bidirectional balanced wave, a unidirectional balanced wave, a sine wave or a sawtooth wave signal waveform is output.
In a preferred embodiment of the present invention, the signal generator is electrically connected to the stimulation actuator, and the signal generator is capable of outputting a stimulation signal to the stimulation actuator; the stimulation executing mechanism comprises a percutaneous electrical stimulation electrode, an intracavity electrical stimulation probe and a focused ultrasound probe; the transcutaneous electric stimulation electrode is configured to receive the electric stimulation signal output by the signal generator and act on the surface of the human body; the intracavity electrical stimulation probe is configured to be used for receiving the electrical stimulation signal output by the signal generator and acting on the inner wall of the vagina and the cervix; the focused ultrasonic probe is configured to receive the focused ultrasonic stimulation signals output by the signal generator and act on the acupuncture points of the human body; wherein, the first stage of the percutaneous electric stimulation electrode receives and executes intermediate frequency electric stimulation; the second stage receives and executes low-frequency electrical stimulation; the intracavity electrical stimulation probe receives and executes low-frequency electrical stimulation; the focused ultrasound probe receives and executes the focused ultrasound stimulation signal.
A method for regulating body fluid by using the system for treating infertility, the percutaneous electric stimulation electrode comprises 10 electrodes; respectively attaching the positive electrode and the negative electrode of the first percutaneous electrical stimulation electrode to the upper skin surface of the peroneal artery on the back of the left calf and the right calf of the human body; attaching the positive electrode of the second percutaneous electrical stimulation electrode to the skin surface of the anterior superior iliac spine on the left side, and attaching the negative electrode to the skin surface of the upper layer of the femoral artery on the left side; attaching the positive electrode of the third percutaneous electrical stimulation electrode to the upper skin surface of the right anterior superior iliac spine, and attaching the negative electrode to the upper skin surface of the right femoral artery; attaching the negative electrode of the fourth percutaneous electrical stimulation electrode to the upper skin surface of the abdominal aorta, and attaching the positive electrode to the opposite skin surface of the back; the positive electrodes of the fifth to the eighth percutaneous electrical stimulation electrodes are attached to the surface of the skin on the pelvic cavity, and the negative electrodes are attached to the lumbosacral part of the back; respectively attaching the positive electrode and the negative electrode of the ninth percutaneous electrical stimulation electrode to the surface of the skin of the left groin; respectively attaching the positive electrode and the negative electrode of the tenth percutaneous electrical stimulation electrode to the surface of the skin of the right groin; and inserting the intra-cavity electrical stimulation probe into the vagina through the vaginal orifice to the cervix.
A method for regulating nerve channels and collaterals by using the system for treating infertility comprises a plurality of focused ultrasound probes; the focused ultrasound probe is fixed on uterus acupoint, Guanyuan acupoint, Tianshu acupoint, Zhongji acupoint, Shenshu acupoint, Mingmen acupoint, Yao sunshine acupoint and Sanyinjiao acupoint.
The invention has the beneficial effects that:
the invention provides a device and a system for treating infertility and a method for carrying out body fluid regulation and nerve channel regulation, wherein the method comprises the following steps:
compared with the prior art, the invention has the advantages that: physical non-wound, no side effect and simple operation, can improve the body fluid circulation of human body, increase the blood supply of reproductive organs such as pelvic cavity, uterus and ovary, increase the nutrition supply and promote the generation of new vessels; the invention can also improve the human reproductive endocrine system, improve the hormone level, balance the internal environment, and effectively treat infertility problems such as thin endometrium, premature ovarian failure, low ovarian reserve function, IVF-ET pre-adjuvant therapy and the like.
Drawings
In order to more clearly illustrate the technical solutions of the embodiments of the present invention, the drawings needed to be used in the embodiments will be briefly described below, it should be understood that the following drawings only illustrate some embodiments of the present invention and therefore should not be considered as limiting the scope, and for those skilled in the art, other related drawings can be obtained according to the drawings without inventive efforts.
FIG. 1 is a schematic structural diagram of an apparatus according to a first embodiment of the present invention;
FIG. 2 is a block diagram of an apparatus according to a first embodiment of the present invention;
FIG. 3 is a schematic diagram of the configuration and a first usage state of an intracavity electrical stimulation probe of the device provided by the first embodiment of the invention;
fig. 4 is a schematic structural diagram of a transcutaneous electrical stimulation electrode of the device provided by the first embodiment of the invention and a second use state diagram;
fig. 5 is a schematic structural diagram of a focused ultrasound probe of the apparatus according to the first embodiment of the present invention and a third usage state diagram;
FIG. 6 is a schematic diagram illustrating a usage status of a display module of the apparatus according to the first embodiment of the present invention;
fig. 7 is a fourth usage state diagram of the apparatus according to the first embodiment of the present invention.
Icon: 10-a host machine; 11-a master controller; 12-an electrical stimulation signal generator; 13-a focused ultrasound signal generator; 14-power module composition; 15-a cable line assembly; 20-a display module; 30-moving the control platform; 31-percutaneous electrical stimulation signal output port; 32-intracavity electrical stimulation probe signal output port; 33-focused ultrasound probe signal output port; 34-a display screen; 35-a knob; 40-transcutaneous electrical stimulation electrodes; 50-intracavity electrical stimulation probe; 51-probe base body; 52-ring-shaped electrode sheet; 53-arc spherical electrode slice; 54-a first cable line; 55-a first patch port; 60-focused ultrasound probe; 61-focusing ceramic wafer; 62-a probe housing; 63-a second cable line; 64-second connector port.
Detailed Description
In order to make the objects, technical solutions and advantages of the embodiments of the present invention clearer, the technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are some, but not all, embodiments of the present invention. The components of embodiments of the present invention generally described and illustrated in the figures herein may be arranged and designed in a wide variety of different configurations.
Thus, the following detailed description of the embodiments of the present invention, presented in the figures, is not intended to limit the scope of the invention, as claimed, but is merely representative of selected embodiments of the invention. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
It should be noted that: like reference numbers and letters refer to like items in the following figures, and thus, once an item is defined in one figure, it need not be further defined and explained in subsequent figures.
In the description of the embodiments of the present invention, it should be noted that the terms "upper", "inner", and the like refer to orientations or positional relationships based on the orientations or positional relationships shown in the drawings or orientations or positional relationships that are conventionally arranged when the products of the present invention are used, and are used only for convenience in describing the present invention and simplifying the description, but do not indicate or imply that the devices or elements referred to must have a specific orientation, be constructed in a specific orientation, and be operated, and thus, should not be construed as limiting the present invention.
In the description of the present invention, it should also be noted that, unless otherwise explicitly specified or limited, the terms "disposed," "mounted," "connected," and "connected" are to be construed broadly and may, for example, be fixedly connected, detachably connected, or integrally connected; they may be connected directly or indirectly through intervening media, or they may be interconnected between two elements. The specific meanings of the above terms in the present invention can be understood in specific cases to those skilled in the art.
As shown in fig. 1, the apparatus for treating infertility provided by the embodiment of the present invention includes a host 10, a display module 20, a mobile control platform 30, a transcutaneous electrical stimulation electrode 40, an intra-cavity electrical stimulation probe 50, and a focused ultrasound probe 60.
The main machine 10 is composed of a main controller 11, an electrical stimulation signal generator 12, a focused ultrasound signal generator 13 and a power module 14. Wherein the electrical stimulation signal generator 12 includes a low frequency electrical stimulation module and a medium frequency electrical stimulation module so as to be able to generate a multi-mode electrical stimulation signal. The focused ultrasound signal generator 13 is used to generate a multi-mode focused ultrasound excitation signal.
The main controller 11 receives the working instruction information and then controls the electrical stimulation signal generator 12 and the focused ultrasound signal generator 13 to generate and output signals. Wherein the electrical stimulation signal generator 12 comprises a low-frequency electrical stimulation module and a medium-frequency electrical stimulation module. The low-frequency electrical stimulation module outputs electrical stimulation current with the frequency range of 1-500Hz, the pulse width of 1-2000us and the current intensity of 0-100mA, and outputs bidirectional balanced waves and unidirectional balanced wavesSine wave, sawtooth wave, etc. The intermediate frequency electrical stimulation module outputs electrical stimulation current with the frequency of low frequency modulation intermediate frequency, the frequency range of 2000-5000Hz, the pulse width of 1-2000us and the current intensity of 0-100mA, and outputs signal waveforms such as bidirectional balanced waves, unidirectional balanced waves, sine waves, sawtooth waves and the like. The frequency range of the excitation signal output by the focused ultrasonic signal generator 13 is 0.8MHz-2.0MHz, the focusing depth is 9mm-35mm, and the intensity is 0-2.5W/cm2And outputs continuous wave and pulse wave.
Further, the actuator is configured for electrical connection to the output port. The actuators include a transcutaneous electrical stimulation electrode 40, an intra-luminal electrical stimulation probe 50, and a focused ultrasound probe 60.
As shown in fig. 2, the mobile control platform 30 is connected to the host 10 for output port extension and output intensity adjustment. The electrical stimulation signal and the focused ultrasound excitation signal generated by the host machine 10 are connected with the mobile control platform 30 through the cable assembly 15; the movement control platform 30 is provided with a third output port. The third output port is the transcutaneous electrical stimulation signal output port 31. The percutaneous electrical stimulation signal output port 31 is connected with the percutaneous electrical stimulation electrode 40 through a cable, and applies multiple modes of electrical stimulation output to a human body.
The first output port is the intracavity electrical stimulation probe signal output port 32. The intracavity electrical stimulation probe signal output port 32 is connected with the intracavity electrical stimulation probe 50 through a cable, and applies multiple modes of electrical stimulation output to the vaginal wall and the cervix in the cavity.
The second output port is the focused ultrasound probe signal output port 33. The focused ultrasonic probe signal output port 33 is connected with the focused ultrasonic probe 60 through a cable, and applies the ultrasonic signals of various modes to the acupuncture points of the human body. The display screen 34 is used for displaying the current electrical stimulation and ultrasound output energy, and each output channel port can be selected by dedicated software built in the display module 20, and the output energy is adjusted by the knob 35.
As shown in FIG. 3, an intracavity electrical stimulation probe 50 can be placed within the vagina for regulating the circulation of body fluids by electrical stimulation. The intracavity electrical stimulation probe 50 is composed of a probe base body 51, an annular electrode plate 52, an arc spherical electrode plate 53, a first cable 54 and a first plug port 55. The probe base body 51 is cylindrical in circumference, and the top end thereof is hemispherical with the same diameter as the cylinder. The annular electrode plates 52 are fixed on the whole body of the cylindrical probe base body 51, and 4, 6, 8 and the like are arranged on the annular metal electrode plates in a number which is a multiple of 2 in order to ensure enough electrical stimulation area of the inner wall of the vagina. The arc spherical electrode plates 53 are fixed on two sides of the hemispherical surface at the top end of the probe base body 51, and 2 arc spherical metal electrode plates are arranged. The top end of the intracavity electrical stimulation probe 50 is inserted into the vagina to the cervix through the vaginal orifice, the inner wall of the vagina is wrapped by the annular electrode plate 52 due to the cylindrical whole body, and the arc spherical electrode plates 53 on two sides of the hemispherical surface of the top end of the probe base body 51 are contacted with the cervix. The intracavity electrical stimulation probe 50 is connected with the intracavity electrical stimulation probe signal output port 32 on the mobile control platform 30 through a first cable 54 and a first socket port 55.
As shown in fig. 4, the transcutaneous electrical stimulation electrode 40 can be attached to the body surface of a human body, and regulates the circulation of the body fluid by electrical stimulation. The percutaneous electrical stimulation electrode 40 is attached according to the direction of blood vessels of a human body to regulate the body fluid of the human body. The percutaneous electric stimulation electrode 40 is connected with the percutaneous electric stimulation signal output port 31 on the mobile control platform 30 through a cable, and the serial number of the port is 1-10. The percutaneous electrical stimulation signal output port 1 is connected with a percutaneous electrical stimulation electrode 40, and the positive electrode and the negative electrode of the percutaneous electrical stimulation electrode 40 are respectively attached to the upper skin surface of the peroneal artery on the back of the left leg and the right leg; the percutaneous electrical stimulation signal output port 2 is connected with a percutaneous electrical stimulation electrode 40, the positive electrode of the percutaneous electrical stimulation electrode 40 is attached to the surface of the skin of the anterior superior iliac spine on the left side, and the negative electrode of the percutaneous electrical stimulation electrode 40 is attached to the surface of the upper skin of the femoral artery on the left side; the percutaneous electrical stimulation signal output port 3 is connected with a percutaneous electrical stimulation electrode 40, the positive electrode of the percutaneous electrical stimulation electrode 40 is attached to the surface of the upper skin of the anterior superior iliac spine on the right side, and the negative electrode of the percutaneous electrical stimulation electrode is attached to the surface of the upper skin of the femoral artery on the right side; the percutaneous electrical stimulation signal output port 4 is connected with a percutaneous electrical stimulation electrode 40, the negative electrode of the percutaneous electrical stimulation electrode 40 is attached to the upper skin surface of the abdominal aorta, and the positive electrode is attached to the opposite skin surface of the back; the percutaneous electrical stimulation signal output ports 5, 6, 7 and 8 are connected with a percutaneous electrical stimulation electrode 40, the positive pole of the percutaneous electrical stimulation electrode 40 is attached to the surface of the skin on the pelvic cavity, and the negative pole is attached to the lumbosacral part of the back; the percutaneous electrical stimulation signal output port 9 is connected with a percutaneous electrical stimulation electrode 40, and the positive electrode and the negative electrode of the percutaneous electrical stimulation electrode 40 are respectively attached to the skin surface of the left inguinal region; the percutaneous electrical stimulation signal output port 10 is connected with a percutaneous electrical stimulation electrode 40, and the positive pole and the negative pole of the percutaneous electrical stimulation electrode 40 are respectively attached to the skin surface of the right inguinal region. The top end of the intracavity electrical stimulation probe 50 is inserted into the vagina to the cervix through the vaginal orifice, the inner wall of the vagina is wrapped by the annular electrode plate 52 due to the cylindrical whole body, and the arc spherical electrode plates 53 on two sides of the hemispherical surface of the top end of the probe base body 51 are contacted with the cervix.
The percutaneous electric stimulation electrode 40 is used for carrying out body surface stimulation by modulating medium-frequency electric stimulation and low-frequency electric stimulation by low frequency, so that superficial and deep body fluid circulation is accelerated, integral metabolism is accelerated, pelvic blood supply is increased, and discharge of metabolic products of a reproductive system is accelerated. Meanwhile, the intracavity electrical stimulation probe 50 is combined, low-frequency electrical stimulation is adopted, and low-frequency electrical stimulation current stimulates the inner wall of a vagina through an annular electrode slice 52 arranged on the whole body of a cylindrical probe substrate 51 to drive muscle in a pelvic cavity to move, stimulate vascular smooth muscle in the pelvic cavity, reduce vascular resistance, increase pelvic cavity blood circulation and increase nutrition supply of reproductive system organs such as uterus, ovary and the like; the arc spherical electrode plates 53 arranged on two sides of the hemispherical surface at the top end of the probe substrate 51 electrically stimulate the cervix, thereby microstimulating the whole uterus and promoting the generation of uterine spiral arteriole neovascularization and endometrium vascularization.
As shown in fig. 5, the focused ultrasound probe 60 can be fixed at the acupuncture points of the human body to regulate the hypothalamus-pituitary-ovary axis through the neural meridians. The focused ultrasound probe 60 consists of a focused ceramic wafer 61, a probe shell 62, a second cable 63 and a second patch port 64. The focusing ceramic sheet 61 is fixed in the probe shell 62, the lead in the second cable 63 is connected with the anode and cathode of the focusing ceramic sheet 61, the second inserting port 64 is connected with the signal output port 33 of the focusing ultrasonic probe on the mobile control platform 30, the excitation signal generated by the focusing ultrasonic signal generator 13 in the host machine 10 excites the focusing ceramic sheet 61 to generate focusing ultrasonic output, the focusing depth is 9-35 mm, and the intensity is 0-2.5W/cm2。
The focusing ultrasonic probe 60 is selected according to different acupuncture point depths and fixed on the surface of the acupuncture point body of the human body to regulate the nerves and the channels of the human body. For example, acupuncture points related to reproductive function: uterus, Guanyuan, Tianshu, Zhongji, Shenshu, Mingmen, Yaoyangguang, Sanyinjiao, etc. Focused ultrasound with different parameters is conducted to acupuncture points of a human body through a coupling agent coated on the surface of the human body, and ultrasonic energy is converged on the acupuncture points, so that the difficulty of point selection in the traditional acupuncture operation is reduced. The mechanical effect and the thermal effect generated by the ultrasound stimulate the acupuncture points, and the reflected signals generated by the stimulation of the acupuncture points are transmitted to the central nervous system from peripheral nerves and nerve fibers to activate or regulate the functions of the hypothalamus-pituitary-ovary axis, thereby realizing the homeostasis and the balance of the internal environment of the reproductive system.
As shown in fig. 6, the display module 20 is used to monitor the treatment mode and status of the device. The display module 20 is equipped with dedicated application software for acquiring the operation of the user on the software interface, sending work instruction information to the main controller 11 according to the operation, and displaying the treatment state after work. The display module 20 is used for monitoring the treatment mode and status, and is controlled by a dedicated application software installed on the display module 20. The treatment mode setting comprises a simple body fluid regulation mode, a simple nerve channel and collateral regulation mode, a simultaneous body fluid and nerve channel and collateral regulation mode and a sequential body fluid and nerve channel and collateral regulation mode.
Referring to fig. 1 to 7, the device is applied to body fluid and nerve meridian regulation treatment. Specifically, the method comprises the following steps:
the method comprises the following steps: the mode in which body fluid is simultaneously performed with the neuro-meridian regulation is selected through the display module 20.
Step two: selecting a percutaneous electrical stimulation signal output port 1 to be connected with a percutaneous electrical stimulation electrode 40, and respectively attaching the positive pole and the negative pole of the percutaneous electrical stimulation electrode 40 to the upper skin surface of the peroneal artery on the back of the left leg and the right leg; the percutaneous electrical stimulation signal output port 2 is connected with a percutaneous electrical stimulation electrode 40, the positive electrode of the percutaneous electrical stimulation electrode 40 is attached to the surface of the skin of the anterior superior iliac spine on the left side, and the negative electrode of the percutaneous electrical stimulation electrode 40 is attached to the surface of the upper skin of the femoral artery on the left side; the percutaneous electrical stimulation signal output port 3 is connected with a percutaneous electrical stimulation electrode 40, the positive electrode of the percutaneous electrical stimulation electrode 40 is attached to the surface of the upper skin of the anterior superior iliac spine on the right side, and the negative electrode of the percutaneous electrical stimulation electrode is attached to the surface of the upper skin of the femoral artery on the right side; the percutaneous electrical stimulation signal output port 4 is connected with a percutaneous electrical stimulation electrode 40, the negative electrode of the percutaneous electrical stimulation electrode 40 is attached to the upper skin surface of the abdominal aorta, and the positive electrode is attached to the opposite skin surface of the back; the percutaneous electrical stimulation signal output ports 5, 6, 7 and 8 are connected with a percutaneous electrical stimulation electrode 40, the positive pole of the percutaneous electrical stimulation electrode 40 is attached to the surface of the skin on the pelvic cavity, and the negative pole is attached to the lumbosacral part of the back; the percutaneous electrical stimulation signal output port 9 is connected with a percutaneous electrical stimulation electrode 40, and the positive electrode and the negative electrode of the percutaneous electrical stimulation electrode 40 are respectively attached to the skin surface of the left inguinal region; the percutaneous electrical stimulation signal output port 10 is connected with a percutaneous electrical stimulation electrode 40, and the positive pole and the negative pole of the percutaneous electrical stimulation electrode 40 are respectively attached to the skin surface of the right inguinal region. The first-stage current parameter range of the percutaneous electrical stimulation signal output port 1-10 is as follows: modulating the intermediate frequency of 2000-5000Hz, the pulse width of 1-2000us, the pulse time of 0-10s, the interruption time of 0-10s, the working time of 0-30 minutes, the current intensity of 0-100mA, and the current waveform is one of signal waveforms such as bidirectional balanced wave, unidirectional balanced wave, sine wave, sawtooth wave and the like; the second stage current parameter range of the electrical stimulation signal output port 1-10 is as follows: low frequency 1-500Hz, pulse width 1-2000us, pulse time 0-20s, intermission time 0-20s, working time 0-30 minutes, current intensity 0-100mA, and current waveform is one of bidirectional balance wave, unidirectional balance wave, sine wave, sawtooth wave and other signal waveforms.
Step three: the signal output port 32 of the intracavity electrical stimulation probe is connected with the intracavity electrical stimulation probe 50, and the top end of the intracavity electrical stimulation probe 50 is inserted into the vagina to the cervix through the vaginal orifice. The ring-shaped electrode slice 52 of the intracavity electrical stimulation probe 50 performs the electrical stimulation on the inner wall of the vagina, and the current parameter range is as follows: low frequency 1-500Hz, pulse width 1-2000us, pulse time 0-20s, intermission time 0-20s, working time 0-30 minutes, current intensity 0-100mA, and current waveform is one of bidirectional balance wave, unidirectional balance wave, sine wave, sawtooth wave and other signal waveforms. The arc spherical electrode plate 53 at the top end of the intracavity electrical stimulation probe 50 performs electrical stimulation on the cervix, and the current parameter range is as follows: low frequency 1-10Hz, pulse width 1-2000us, pulse time 0-20s, intermission time 0-20s, working time 0-30 minutes, current intensity 0-30mA, and current waveform is one of bidirectional balance wave, unidirectional balance wave, sine wave, sawtooth wave and other signal waveforms.
Step four: the signal output port 33 of the selected focused ultrasound probe is connected with the focused ultrasound probe 60, and the focused ultrasound probe 60 is respectively fixed on the uterus acupoint, the Guanyuan acupoint, the Tianshu acupoint, the Zhongji acupoint, the Shenshu acupoint, the Mingmen acupoint, the Yaoyangguang acupoint and the Sanyinjiao acupoint. Focused ultrasound parameter range: the ultrasonic frequency range is 0.8MHz-2.0MHz, the radiation time is 0-20s, the interruption time is 0-20s, the focusing depth is 9mm-35mm, the intensity is 0-2.5W/cm2, and one of continuous wave and pulse wave is output.
Step five: the special software built in the display module 20 starts the treatment to regulate body fluid and nerve channels and collaterals, and treat infertility problems such as thin endometrium, premature ovarian failure, low ovarian reserve function, IVF-ET pre-adjuvant therapy and the like.
It should be understood that the above-described embodiments of the present invention are merely examples for clearly illustrating the present invention, and are not intended to limit the embodiments of the present invention. Other variations and modifications will be apparent to persons skilled in the art in light of the above description. And are neither required nor exhaustive of all embodiments. Any modification, equivalent replacement, and improvement made within the spirit and principle of the present invention should be included in the protection scope of the claims of the present invention.
Claims (11)
1. A device for treating infertility, comprising:
a signal generator for generating an electrical stimulation signal and an ultrasonic stimulation signal;
an output port; the output port is electrically connected with the signal generator;
a stimulation actuator; the stimulation actuator is configured for electrical connection to the output port; the main controller is electrically connected with the signal generator;
the main controller is used for controlling the signal generator to send out the electrical stimulation signal and the ultrasonic stimulation signal and conducting the electrical stimulation signal and the ultrasonic stimulation signal to the stimulation execution mechanism through the output port; the stimulation executing mechanism can receive the signal sent by the main controller and execute corresponding operation;
the stimulation executing mechanism comprises an intracavity electrical stimulation probe; the intracavity electrical stimulation probe comprises a probe base body and an arc spherical electrode slice; the whole body of the probe base body is cylindrical; the top end of the probe base body comprises two hemispherical surfaces with equal diameters; the arc spherical electrode plates are fixed on two sides of the two hemispherical surfaces; the number of the arc-shaped electrode plates is 2.
2. The device for treating infertility according to claim 1,
the output ports include a first output port, a second output port and a third output port, and the first output port, the second output port and the third output port are electrically connected to the main controller.
3. The device for treating infertility according to claim 2,
the stimulation actuator further comprises a transcutaneous electrical stimulation electrode and a focused ultrasound probe, the intracavity electrical stimulation probe configured for electrical connection to the first output port; the focused ultrasound probe is configured for electrical connection to the second output port; the transcutaneous electrical stimulation electrode is configured for electrical connection to the third output port.
4. The device for treating infertility according to claim 3,
the intracavity electrical stimulation probe also comprises an annular metal electrode plate, a first cable and a first plug port;
the probe substrate is made of plastic or medical silica gel;
the annular metal electrode plate is fixed on the whole body of the probe base body; the number of the annular metal electrode plates is even;
one end of the first cable is connected to the probe base body, and the other end of the first cable is connected to the first plug port;
the first connector port is configured to be electrically connected to the first output port, receive an electrical stimulation signal from the signal generator, and conduct the electrical stimulation signal to the annular metal electrode sheet and the arc-sphere electrode sheet.
5. The device for treating infertility according to claim 3,
the focusing ultrasonic probe comprises a probe shell, a focusing ceramic sheet, a second cable and a second plugging port;
the focusing ceramic plate is fixed inside the probe shell, the second cable is electrically connected to the focusing ceramic plate, and the second patch port is configured to be electrically connected to the second output port;
the focusing ceramic chip is used for receiving the ultrasonic stimulation signal sent by the signal generator and outputting the ultrasonic stimulation signal after focusing.
6. The device for treating infertility according to claim 2,
the device for treating infertility further comprises a mobile control platform, wherein the mobile control platform is electrically connected to the main controller; the first output port, the second output port and the third output port are all arranged on the mobile control platform.
7. The device of claim 6, wherein the mobile control platform is electrically connected to the main controller via an assembly cable.
8. The device for treating infertility according to claim 7,
the device for treating infertility comprises an electrical stimulation signal generator and a focused ultrasound stimulation signal generator;
the electrical stimulation signal generator comprises a low-frequency electrical stimulation module and a medium-frequency electrical stimulation module;
the low-frequency electrical stimulation module and the medium-frequency electrical stimulation module are electrically connected to the assembly cable.
9. The device for treating infertility according to claim 1,
the device for treating infertility further comprises a display module and a power supply module, wherein the display module is electrically connected to the main controller; the power supply module is electrically connected with the main controller; and the power supply module is used for converting a network power supply into a low-voltage direct-current power supply required by the work of the host.
10. A system for treating infertility, comprising the device for treating infertility according to claim 1;
the frequency range of the ultrasonic stimulation signal is 0.8MHz-2.0MHz, the focusing depth is 9mm-35mm, the intensity is 0-2.5W/cm2,
outputting continuous waves or pulse waves;
the electrical stimulation signals comprise low-frequency electrical stimulation signals and medium-frequency electrical stimulation signals;
wherein, the current frequency range of the low-frequency electric stimulation signal is 1-500Hz, the pulse width is 1-2000us, and the current intensity is 0-100mA, and a bidirectional balanced wave, a unidirectional balanced wave, a sine wave or a sawtooth wave signal waveform is output;
the current frequency range of the intermediate frequency electrical stimulation signal is 2000-5000Hz, the pulse width is 1-2000us, and the current intensity is 0-100mA, and a bidirectional balanced wave, a unidirectional balanced wave, a sine wave or a sawtooth wave signal waveform is output.
11. The system for treating infertility according to claim 10,
the signal generator is electrically connected with the stimulation executing mechanism and can output stimulation signals to the stimulation executing mechanism;
the stimulation executing mechanism comprises a percutaneous electrical stimulation electrode, an intracavity electrical stimulation probe and a focused ultrasound probe;
the transcutaneous electric stimulation electrode is configured to receive the electric stimulation signal output by the signal generator and act on the surface of the human body;
the intracavity electrical stimulation probe is configured to receive the electrical stimulation signal output by the signal generator and act on the inner wall of the vagina and the cervix;
the focused ultrasonic probe is configured to receive the focused ultrasonic stimulation signal output by the signal generator and act on a human body acupuncture point;
wherein the transcutaneous electrical stimulation electrode first stage receives and performs the medium frequency electrical stimulation; a second stage receiving and executing the low-frequency electrical stimulation;
the intracavity electrical stimulation probe receives and executes the low-frequency electrical stimulation;
the focused ultrasound probe receives and executes the focused ultrasound stimulation signal.
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| CN201711283551.3A CN108096704B (en) | 2017-12-07 | 2017-12-07 | Device and system for treating infertility and method for carrying out body fluid regulation and nerve channel regulation |
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| CN109011143A (en) * | 2018-06-21 | 2018-12-18 | 南京麦澜德医疗科技有限公司 | Vaginal electrode and preparation method thereof and diagnosis and treatment instrument |
| CN114917124B (en) * | 2022-04-24 | 2024-09-03 | 天津威力恒科技有限公司 | Palace abdomen body acupoint therapeutic apparatus and control method thereof |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN2848126Y (en) * | 2005-12-15 | 2006-12-20 | 广州市杉山医疗器械实业有限公司 | Vagina and anus probe |
| CN102481450A (en) * | 2009-04-07 | 2012-05-30 | 威斯特天主教保健中心 | Uterine electrical stimulation system and method |
| CN102871659A (en) * | 2012-11-05 | 2013-01-16 | 杨东 | Vagina electrode |
| CN104582565A (en) * | 2012-06-09 | 2015-04-29 | 费姆脉冲有限责任公司 | Devices and methods for stimulating nerves |
| CN106964066A (en) * | 2015-12-28 | 2017-07-21 | 烟台万适美医疗科技有限公司 | Wearable electronic pelvic girdle |
| CN107049342A (en) * | 2017-05-18 | 2017-08-18 | 孙大明 | A kind of female pelvic Function detection is popped one's head in treatment |
| CN107096128A (en) * | 2017-05-27 | 2017-08-29 | 烟台万适美医疗科技有限公司 | Puerpera uses deformable transvaginal probe |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101015725A (en) * | 2007-02-16 | 2007-08-15 | 福州大学 | Wearable physiotherapeutic instrument |
| WO2011150576A1 (en) * | 2010-06-04 | 2011-12-08 | 广州市杉山医疗器械实业有限公司 | Device for infertility treatment |
| CN201959420U (en) * | 2010-06-04 | 2011-09-07 | 广州市杉山医疗器械实业有限公司 | Device used for treating infertility |
| CN103566490B (en) * | 2012-07-27 | 2016-08-03 | 重庆海扶医疗科技股份有限公司 | postpartum rehabilitation device |
| WO2014164438A1 (en) * | 2013-03-11 | 2014-10-09 | Ohio State Innovation Foundation | Devices and systems for treating obstetric and gynecological disorders |
| PL228476B1 (en) * | 2013-11-13 | 2018-04-30 | Univ Medyczny Im Piastow Slaskich We Wroclawiu | Device for transdermal therapeutical electrostimulation |
| US9713565B2 (en) * | 2014-06-20 | 2017-07-25 | Chongqing Peninsula Medical Technology Co., Ltd. | Virginal rejuvenation apparatus and method |
| CN205433686U (en) * | 2016-03-02 | 2016-08-10 | 南京麦澜德医疗科技有限公司 | Disposable vagina electrode |
-
2017
- 2017-12-07 CN CN201711283551.3A patent/CN108096704B/en active Active
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN2848126Y (en) * | 2005-12-15 | 2006-12-20 | 广州市杉山医疗器械实业有限公司 | Vagina and anus probe |
| CN102481450A (en) * | 2009-04-07 | 2012-05-30 | 威斯特天主教保健中心 | Uterine electrical stimulation system and method |
| CN104582565A (en) * | 2012-06-09 | 2015-04-29 | 费姆脉冲有限责任公司 | Devices and methods for stimulating nerves |
| CN102871659A (en) * | 2012-11-05 | 2013-01-16 | 杨东 | Vagina electrode |
| CN106964066A (en) * | 2015-12-28 | 2017-07-21 | 烟台万适美医疗科技有限公司 | Wearable electronic pelvic girdle |
| CN107049342A (en) * | 2017-05-18 | 2017-08-18 | 孙大明 | A kind of female pelvic Function detection is popped one's head in treatment |
| CN107096128A (en) * | 2017-05-27 | 2017-08-29 | 烟台万适美医疗科技有限公司 | Puerpera uses deformable transvaginal probe |
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|---|---|
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