Gynecological pelvic floor rehabilitation equipment

Abstract

The invention relates to the technical field of medical equipment, and particularly discloses gynecological pelvic floor rehabilitation equipment which comprises a therapeutic apparatus body and further comprises a stabilizing assembly arranged on the outer side of a probe and used for keeping the probe stable during treatment and protecting the probe when the probe is not treated; the adjusting assembly is arranged on the stabilizing assembly and the therapeutic apparatus body, and the adjusting assembly is used for adjusting the stimulation intensity of the probe. By means of the stabilizing assembly, when the probe is inserted into the vagina for treatment, the probe can be kept stable, the situation that the probe slides out of the body during treatment, and rehabilitation treatment on a patient is affected is prevented, after treatment is finished, the probe can be protected through the stabilizing assembly, the probe is prevented from being polluted possibly when the probe is not used for treatment, and the treatment effect is improved. Through the adjusting assembly, the stimulation intensity of the probe can be adjusted, so that the situation that the stimulation intensity of the probe is too high, so that a patient feels uncomfortable or painful, and rehabilitation treatment on the patient is affected is prevented.

Description

Technical Field

[0001] The present invention relates to the technical field of medical equipment, in particular to a gynecological pelvic floor rehabilitation device. Background Art

[0002] The pelvic floor rehabilitation therapy device is a therapeutic instrument with biofeedback and electrical stimulation. The instrument objectively evaluates the degree of damage to the patient's closed pelvic floor muscle groups through an intracavitary probe. Pelvic floor rehabilitation applies the principle of electric pulses, combines bioengineering technology and bioinformatics to develop personalized treatment techniques for patients, and uses electrical stimulation of different frequencies, pulse widths, and intensities for different patients to treat damaged pelvic floor nerves and muscles, increase pelvic floor sensation, muscle strength and elasticity, and restore floor function to normal.

[0003] When using the pelvic floor rehabilitation therapy device, the probe is usually inserted into the patient's vagina to treat the pelvic floor muscles through electrical stimulation. However, due to factors such as vaginal relaxation of the patient, the probe may slip out of the body during treatment, affecting the patient's rehabilitation treatment. Different patients may have different sensitivities to the electrical stimulation of the probe, which may cause the patient to feel discomfort or pain due to excessive stimulation intensity of the probe, which in turn affects the patient's rehabilitation treatment. For this reason, we propose a gynecological pelvic floor rehabilitation device. Summary of the invention

[0004] The object of the present invention is to provide a gynecological pelvic floor rehabilitation device to solve the problem raised in the above-mentioned background technology that when using the pelvic floor rehabilitation therapeutic device, the probe may slip out of the body during treatment, and the patient may also feel discomfort or pain due to the excessive stimulation intensity of the probe, thereby affecting the rehabilitation treatment of the patient.

[0005] To achieve the above object, the present invention provides the following technical solution: a gynecological pelvic floor rehabilitation device, comprising: a therapeutic device body, one side of the therapeutic device body is electrically connected to a probe, and the other side of the therapeutic device body is provided with an adjustment knob,

[0006] The device also includes: a stabilizing component, which is arranged on the outside of the probe and is used to keep the probe stable during treatment and to protect the probe when not treating;

[0007] An adjustment component is arranged on the stabilization component and the therapeutic device body, and is used to adjust the stimulation intensity of the probe.

[0008] Among them, the stabilizing component includes a placement rack fixedly arranged on one side of the therapeutic device body, a connecting block fixedly arranged on the lower side of the probe, connecting plates rotatably arranged on both sides of the connecting block, a protective cloth fixedly arranged between the two connecting plates, and a closing cover arranged on the upper side of the connecting plate.

[0009] A connecting rod is rotatably provided on one side of the closing cover, a fixing block is symmetrically fixedly provided on one side of the connecting plate close to the connecting rod, a pillar is rotatably provided between the two fixing blocks, and a first clamping ring adapted to the connecting rod is fixedly provided on the upper side of the pillar.

[0010] Among them, the first strap and the second strap are fixedly arranged on both sides of the connecting plate, the inner lower end of the closing cover is symmetrically fixed with a limit block, and the upper sides of the two connecting plates are provided with slots adapted to the limit blocks.

[0011] Among them, the adjustment component includes a mounting tube fixedly arranged on the lower side of the probe, a porcelain tube fixedly arranged on the inner side of the mounting tube, a resistance coil wound on the outer side of the porcelain tube, a metal sliding rod fixedly arranged on one side inside the mounting tube, and a sliding piece slidingly arranged with the metal sliding rod is slidably arranged on the outer side of the resistance coil.

[0012] Among them, a mounting seat is fixedly provided on one side of the slide, a rotating rod adapted to the first clamping ring is rotatably provided on one side of the mounting seat, a second clamping ring adapted to the rotating rod is fixedly provided on the upper side of the mounting cylinder, a through groove adapted to the mounting seat is penetrated through one side of the mounting cylinder, and the mounting seat is slidably provided in the through groove.

[0013] A first magnetic block is fixedly arranged on one side of the mounting seat, a mounting block is symmetrically fixedly arranged on one side of the mounting tube close to the rotating rod, and a second magnetic block that is magnetically attracted to the first magnetic block is fixedly embedded on the lower side of one mounting block.

[0014] Among them, a pressure block is fixedly arranged on the other side of the mounting seat, and a button is installed on the lower side of the mounting block on the other side, and the positions of the pressure block and the button correspond to each other up and down.

[0015] Among them, a mounting plate is fixedly arranged on the lower side of the adjusting knob of the therapeutic device body, a motor is fixedly arranged on the upper side of the mounting plate, a mounting sleeve is fixedly arranged on one side of the adjusting knob, and the output shaft of the motor is fixedly arranged on the mounting sleeve.

[0016] The present invention has at least the following beneficial effects:

[0017] The present invention can maintain the stability of the probe when the probe is inserted into the vagina for treatment through the stabilizing component, so as to prevent the probe from slipping out of the body during treatment and affecting the patient's rehabilitation treatment. After the treatment, the probe can be protected by the stabilizing component to prevent the probe from being contaminated when it is not used for treatment. The stimulation intensity of the probe can be adjusted by the adjusting component to prevent the stimulation intensity of the probe from being too high, causing discomfort or pain to the patient and affecting the patient's rehabilitation treatment. BRIEF DESCRIPTION OF THE DRAWINGS

[0018] Figure 1 It is a schematic diagram of the front-view stereoscopic structure of the present invention;

[0019] Figure 2 It is a structural schematic diagram of the stabilizing component and the adjusting component when protecting the probe of the present invention;

[0020] Figure 3 It is a schematic diagram of the structure of the connecting plate of the present invention when it is unfolded;

[0021] Figure 4 It is a schematic diagram of the structure of the explosion of the closing cover and the connecting plate of the present invention;

[0022] Figure 5 For the present invention Figure 2 The enlarged structural diagram at B in the middle;

[0023] Figure 6 For the present invention Figure 2 The enlarged structural diagram at C in the middle;

[0024] Figure 7 It is a schematic diagram of the structure of the installation block, the first magnetic block and the pressing block explosion of the present invention;

[0025] Figure 8 For the present invention Figure 1 The enlarged structural diagram at A in the middle;

[0026] Fig. 9 It is a structural schematic diagram of the connection of the rotating rod after the connecting plate of the present invention is unfolded;

[0027] Fig.10 It is a structural schematic diagram of another viewing angle of the rotating rod connected after the connecting plate of the present invention is unfolded;

[0028] Fig.11 It is a schematic structural diagram of a cross-section of the installation tube of the present invention.

[0029] In the figure: 11, therapeutic instrument body; 12, probe; 13, adjustment knob; 2, stabilizing component; 21, placement rack; 22, connecting block; 23, connecting plate; 24, protective cloth; 25, closing cover; 26, connecting rod; 27, fixing block; 28, pillar; 29, first clamping ring; 210, first binding band; 211, limiting block; 212, slot; 213, second binding band; 3, adjusting component; 31, mounting tube; 32, porcelain tube; 33, resistance coil; 34, slide; 35, metal slide rod; 36, mounting seat; 37, rotating rod; 38, mounting plate; 39, motor; 310, mounting sleeve; 311, first magnetic block; 312, pressure block; 313, mounting block; 314, second magnetic block; 315, button; 316, second clamping ring; 317, through groove. DETAILED DESCRIPTION

[0030] The following will be combined with the drawings in the embodiments of the present invention to clearly and completely describe the technical solutions in the embodiments of the present invention. Obviously, the described embodiments are only part of the embodiments of the present invention, not all of the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the present invention.

[0031] Embodiment 1

[0032] See also Figures 1 to 11 The present invention provides a technical solution: a gynecological pelvic floor rehabilitation device, comprising: a therapeutic device body 11, a probe 12 is electrically connected to one side of the therapeutic device body 11, and an adjustment knob 13 is provided on the other side of the therapeutic device body 11.

[0033] The device further comprises: a stabilizing component 2, which is arranged outside the probe 12 and is used to keep the probe 12 stable during treatment and to protect the probe 12 when not treating;

[0034] The adjusting component 3 is arranged on the stabilizing component 2 and the therapeutic device body 11 , and is used to adjust the stimulation intensity of the probe 12 .

[0035] When the pelvic floor rehabilitation therapy instrument body 11 is in use, the probe 12 is inserted into the patient's vagina to treat the pelvic floor muscles through electrical stimulation. The stabilizing component 2 can keep the probe 12 stable when the probe 12 is inserted into the vagina for treatment to prevent the probe 12 from slipping out of the body during treatment and affecting the patient's rehabilitation treatment. After the treatment, the stabilizing component 2 can protect the probe 12 to prevent the probe 12 from being contaminated when it is not used for treatment. The adjusting component 3 can adjust the stimulation intensity of the probe 12 to prevent the stimulation intensity of the probe 12 from being too high, causing discomfort or pain to the patient and affecting the patient's rehabilitation treatment.

[0036] Embodiment 2

[0037] The stabilizing component 2 includes a placement frame 21 fixedly arranged on one side of the therapeutic device body 11. When the probe 12 is not used for treatment, the probe 12 is protected by the stabilizing component 2 and placed on the placement frame 21. A slot is arranged on one side of the placement frame 21, and a connecting line connected to the probe 12 can pass through the slot to place the probe 12 on the placement frame 21. A connecting block 22 is fixedly arranged on the lower side of the probe 12, and connecting plates 23 are rotatably arranged on both sides of the connecting block 22. A protective cloth 24 is fixedly arranged between the two connecting plates 23, and a closing cover 25 is arranged on the upper side of the connecting plate 23.

[0038] A connecting rod 26 is rotatably provided on one side of the closing cover 25, a fixing block 27 is symmetrically fixedly provided on one side of the connecting plate 23 close to the connecting rod 26, a pillar 28 is rotatably provided between the two fixing blocks 27, a first clamping ring 29 adapted to the connecting rod 26 is fixedly provided on the upper side of the pillar 28, and the first clamping ring 29 is made of elastic material to facilitate the engagement, fixation and disassembly with the connecting rod 26. When the probe 12 is not in use, the connecting rod 26 is engaged and fixed with the first clamping ring 29.

[0039] The first strap 210 and the second strap 213 are fixedly provided on both sides of the connecting plate 23, and the hook surface and the fur surface of the Velcro are fixed on the opposite sides of the first strap 210 and the second strap 213, respectively. When the probe 12 is used, the connecting rod 26 is rotated to disengage the connecting rod 26 from the first clamping ring 29, and then the closing cover 25 is removed upward, and the connecting plates 23 on both sides are rotated and unfolded to both sides, so that the probe 12 can be exposed. During treatment, the probe 12 is inserted into the patient's vagina, and the first strap 210 and the second strap 213 on the connecting plates 23 unfolded on both sides are respectively tied to the patient's legs on both sides, and the hook surface and the fur surface on the first strap 210 and the second strap 213 are adhered and fixed to each other, so that the probe 12 can be kept stable during treatment, and the probe 12 can be prevented from slipping out of the body during treatment, which affects the patient's rehabilitation treatment;

[0040] A limit block 211 is symmetrically fixed on the inner lower end of the closing cover 25, and a slot 212 adapted to the limit block 211 is opened on the upper side of the two connecting plates 23. After the treatment is completed, the first strap 210 and the second strap 213 are released, the probe 12 is taken out and disinfected, and the connecting plates 23 on both sides are rotated to a vertical position so that the protective cloth 24 can be folded and retracted between the two connecting plates 23, and the closing cover 25 is inserted downwardly on the outside of the two connecting plates 23, and the limit blocks 211 on both sides are respectively inserted into the slots 212 of the connecting plates 23 on both sides to limit the rotation of the connecting plates 23, and then the connecting rod 26 is rotated so that the connecting rod 26 is engaged in the first clamping ring 29, so that the closing cover 25 can be restricted, and then the probe 12 can be protected by the connecting plate 23, the protective cloth 24 and the closing cover 25 to prevent a large contamination of the probe 12 when not in use.

[0041] Embodiment 3

[0042] The adjustment component 3 includes a mounting tube 31 fixedly arranged on the lower side of the probe 12. The mounting tube 31 can also be used as a handle for taking the probe 12 and using it to facilitate the taking, placing and using of the probe 12. A porcelain tube 32 is fixedly arranged on the inner side of the mounting tube 31, and a resistance coil 33 is wound around the outer side of the porcelain tube 32. A metal slide bar 35 is fixedly arranged on one side inside the mounting tube 31. A slide plate 34 slidably arranged with the metal slide bar 35 is slidably arranged on the outer side of the resistance coil 33. The upper side of the resistance coil 33 is electrically connected to the probe 12 through a connecting line, and the lower side of the metal slide bar 35 is electrically connected to the therapeutic device body 11 through a connecting line, and the adjustment knob 13 is connected in the circuit. By rotating the adjustment knob 13, the stimulation intensity of the probe 12 can be adjusted, and the metal slide bar 35 can guide the sliding of the slide plate 34.

[0043] A mounting seat 36 is fixedly provided on one side of the slide 34, and a rotating rod 37 compatible with the first snap ring 29 is rotatably provided on one side of the mounting seat 36. The rotating rod 37 can be mutually engaged and fixed with the first snap ring 29. A second snap ring 316 compatible with the rotating rod 37 is fixedly provided on the upper side of the mounting tube 31. The second snap ring 316 is made of elastic material. When the probe 12 is not in use, the rotating rod 37 is engaged and fixed on the second snap ring 316 to limit the rotation of the rotating rod 37. When the connecting plates 23 on both sides are rotated and unfolded, the rotating rod 37 can be rotated and engaged with the first snap ring 29. As the connecting plates 23 are rotated and unfolded, the rotating rod 37 is rotated and engaged with the first snap ring 29, so that the first snap ring 29 and the rotating rod 37 are mutually engaged and fixed. A through groove 317 compatible with the mounting seat 36 is penetrated on one side of the mounting tube 31, and the mounting seat 36 is slidably arranged in the through groove 317.

[0044] A first magnetic block 311 is fixedly provided on one side of the mounting seat 36, and a mounting block 313 is symmetrically fixedly provided on one side of the mounting tube 31 close to the rotating rod 37. A second magnetic block 314 which is magnetically attracted to the first magnetic block 311 is fixedly embedded on the lower side of the mounting block 313 on one side. Initially, the first magnetic block 311 abuts against the second magnetic block 314, and the initial positions of the mounting seat 36 and the slide 34 are maintained by the magnetic attraction between the first magnetic block 311 and the second magnetic block 314.

[0045] A pressure block 312 is fixedly provided on the other side of the mounting seat 36, and a button 315 is installed on the lower side of the mounting block 313 on the other side. The button 315 is electrically connected to the motor 39, and the positions of the pressure block 312 and the button 315 correspond to each other. Initially, the first magnetic block 311 and the second magnetic block 314 are in conflict with each other, and at the same time, the pressure block 312 can press the button 315, so that the circuit between the button 315 and the motor 39 is connected.

[0046] The therapeutic apparatus body 11 is fixedly provided with a mounting plate 38 at the lower side of the adjusting knob 13, a motor 39 is fixedly provided at the upper side of the mounting plate 38, a mounting sleeve 310 is fixedly provided at one side of the adjusting knob 13, and the output shaft of the motor 39 is fixedly provided with the mounting sleeve 310. When the probe 12 is inserted into the vagina for treatment, the motor 39 is powered on by turning on the switch, and the output shaft of the motor 39 drives the mounting sleeve 310 and the adjusting knob 13 to rotate slowly to gradually increase the stimulation intensity of the probe 12. When the stimulation intensity of the probe 12 is large, the patient's legs tend to move toward each other, causing the connecting plates 23 on both sides to rotate toward each other, so that the mounting seat 36 can be moved downward along the through slot 317 through the rotating rod 37. The first magnetic block 311 slides away from the second magnetic block 314, and the pressing block 312 moves downward synchronously and no longer presses the button 315, so that the button 315 is disconnected, and the motor 39 no longer drives the adjusting knob 13 to continue to rotate, so as to prevent the stimulation intensity of the probe 12 from continuing to increase. At the same time, the downward movement of the mounting seat 36 will drive the downward movement of the slide 34, thereby increasing the resistance of the resistance coil 33 in the connecting circuit connected to the circuit, and reducing the current in the connecting circuit, thereby reducing the stimulation intensity of the probe 12 and adjusting the stimulation intensity of the probe 12 to a suitable state, so as to facilitate the adjustment of the stimulation intensity of the probe 12, and prevent the stimulation intensity of the probe 12 from being too high, causing discomfort or pain to the patient, thereby affecting the rehabilitation treatment of the patient.

[0047] It should be noted that, in this article, relational terms such as first and second, etc. are only used to distinguish one entity or operation from another entity or operation, and do not necessarily require or imply any such actual relationship or order between these entities or operations. Moreover, the terms "include", "comprise" or any other variants thereof are intended to cover non-exclusive inclusion, so that a process, method, article or device including a series of elements includes not only those elements, but also other elements not explicitly listed, or also includes elements inherent to such process, method, article or device.

[0048] Although embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that various changes, modifications, substitutions and variations may be made to the embodiments without departing from the principles and spirit of the present invention, and that the scope of the present invention is defined by the appended claims and their equivalents.

Claims

1. A gynecological pelvic floor rehabilitation device, comprising: A therapeutic device body (11), one side of the therapeutic device body (11) is electrically connected to a probe (12), and the other side of the therapeutic device body (11) is provided with an adjustment knob (13). The invention is characterized in that it also comprises: a stabilizing component (2), wherein the stabilizing component (2) is arranged on the outside of the probe (12), and the stabilizing component (2) is used to keep the probe (12) stable during treatment and to protect the probe (12) when not treating; An adjustment component (3), wherein the adjustment component (3) is arranged on the stabilization component (2) and the therapeutic device body (11), and the adjustment component (3) is used to adjust the stimulation intensity of the probe (12).

2. The gynecological pelvic floor rehabilitation device according to claim 1, characterized in that: The stabilizing component (2) comprises a placement frame (21) fixedly arranged on one side of the therapeutic device body (11); a connecting block (22) is fixedly arranged on the lower side of the probe (12); connecting plates (23) are rotatably arranged on both sides of the connecting block (22); a protective cloth (24) is fixedly arranged between the two connecting plates (23); and a closing cover (25) is arranged on the upper side of the connecting plate (23).

3. The gynecological pelvic floor rehabilitation device according to claim 2, characterized in that: A connecting rod (26) is rotatably provided on one side of the closing cover (25), a fixing block (27) is symmetrically fixedly provided on one side of the connecting plate (23) close to the connecting rod (26), a supporting column (28) is rotatably provided between the two fixing blocks (27), and a first clamping ring (29) adapted to the connecting rod (26) is fixedly provided on the upper side of the supporting column (28).

4. The gynecological pelvic floor rehabilitation device according to claim 3, characterized in that: A first binding strap (210) and a second binding strap (213) are fixedly arranged on both sides of the connecting plate (23), a limit block (211) is symmetrically fixedly arranged on the inner lower end of the closing cover (25), and a slot (212) adapted to the limit block (211) is provided on the upper sides of the two connecting plates (23).

5. The gynecological pelvic floor rehabilitation device according to claim 1, characterized in that: The adjustment component (3) comprises a mounting tube (31) fixedly arranged at the lower side of the probe (12), a porcelain tube (32) fixedly arranged on the inner side of the mounting tube (31), a resistance coil (33) wound around the outer side of the porcelain tube (32), a metal slide rod (35) fixedly arranged on one side inside the mounting tube (31), and a slide sheet (34) slidably arranged on the outer side of the resistance coil (33) and slidably arranged with the metal slide rod (35).

6. The gynecological pelvic floor rehabilitation device according to claim 5, characterized in that: A mounting seat (36) is fixedly provided on one side of the slide (34); a rotating rod (37) adapted to the first retaining ring (29) is rotatably provided on one side of the mounting seat (36); a second retaining ring (316) adapted to the rotating rod (37) is fixedly provided on the upper side of the mounting tube (31); a through groove (317) adapted to the mounting seat (36) is penetrated through one side of the mounting tube (31); and the mounting seat (36) is slidably provided in the through groove (317).

7. The gynecological pelvic floor rehabilitation device according to claim 6, characterized in that: A first magnetic block (311) is fixedly provided on one side of the mounting seat (36), a mounting block (313) is symmetrically fixedly provided on one side of the mounting cylinder (31) close to the rotating rod (37), and a second magnetic block (314) magnetically attracted to the first magnetic block (311) is fixedly embedded on the lower side of the mounting block (313) on one side.

8. The gynecological pelvic floor rehabilitation device according to claim 7, characterized in that: A pressing block (312) is fixedly arranged on the other side of the mounting seat (36), and a button (315) is installed on the lower side of the mounting block (313) on the other side, and the positions of the pressing block (312) and the button (315) correspond to each other in vertical direction.

9. The gynecological pelvic floor rehabilitation device according to claim 8, characterized in that: The therapeutic apparatus body (11) is fixedly provided with a mounting plate (38) at the lower side of the adjusting knob (13), a motor (39) is fixedly provided at the upper side of the mounting plate (38), a mounting sleeve (310) is fixedly provided at one side of the adjusting knob (13), and an output shaft of the motor (39) is fixedly provided with the mounting sleeve (310).

Images