Intrauterine adhesion therapeutic apparatus
By designing a uterine adhesion treatment device that can continuously anesthetize and inject drugs, the pain caused by hysteroscopic surgery in the prior art and the problem of inability to repair the endometrium is solved, and the effect of postoperative analgesia and endometrial repair is achieved.
Patent Information
- Application Number
- CN202510106297.8
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2025-01-23
- Publication Date
- 2025-04-11
- Estimated Expiration
- Not applicable · inactive patent
AI Technical Summary
Prior Art When indwelling balloon stents under hysteroscopy to treat postoperative uterine adhesions, patients are often unbearable due to the pain caused by surgical procedures and tumour pressure, and cannot repair the endometrium by injecting agents.
A uterine adhesion treatment device was designed to continuously anesthetize the nerves of the cervix and vagina through drugs to achieve postoperative analgesia, and at the same time it has the function of injecting drugs, which opens the uterine cavity through the uterine ring to prevent postoperative adhesion recurrence.
The continuous postoperative analgesia and further repair of the endometrium were achieved, reducing the risk of recurrence of uterine adhesions.
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Figure CN119791922A_ABST
Abstract
Description
Technical Field
[0001] The invention relates to a therapeutic device for intrauterine adhesion, belonging to the technical field of medical devices. Background Art
[0002] Any factors that cause endometrial damage can cause intrauterine adhesions. About 91% of intrauterine adhesions are related to pregnancy, which is common after artificial abortion or spontaneous abortion curettage. About 9% of intrauterine adhesions are caused by non-pregnancy, such as endometrial tuberculosis, myomectomy, diagnostic curettage, etc.
[0003] In recent years, hysteroscopic indwelling balloon stents have become a widely used treatment method for preventing postoperative intrauterine adhesions. However, during the operation, the pressure on the uterus, uterine dilation, curettage, clamping and other operations, as well as the compression of the uterine wall by the expansion balloon, cause unbearable pain to the patient, and there is a relatively severe postoperative pain; at the same time, in the existing technology, intrauterine adhesion treatment devices are placed in the uterus to reduce or avoid postoperative intrauterine adhesions, but there is no way to further repair the endometrium by injecting drugs. Summary of the invention
[0004] In order to solve the above problems existing in the prior art, the present invention provides a device for treating intrauterine adhesions, which can continuously anesthetize the nerves of the cervix and pudendum through drugs, thereby achieving the effect of postoperative analgesia. At the same time, the required drugs can be injected through the device for further treatment.
[0005] The technical solution of the present invention is as follows:
[0006] A device for treating intrauterine adhesions comprises two skeleton layers, wherein the two skeleton layers are symmetrically arranged to form a uterine-shaped ring, and the shape of the uterine-shaped ring is a bionic uterine structure; the skeleton layers comprise a first support member and a second support member, wherein the first support member and the second support member are hingedly arranged, and a longitudinal rod is hinged at the top of the two skeleton layers; the device for treating intrauterine adhesions further comprises an outer sleeve, and a connecting tube is fixedly arranged at the bottom of the outer sleeve, and the bottom ends of the two skeleton layers are hinged to the connecting tube, and the outer sleeve is slidably sleeved on the outside of the longitudinal rod; the bottom of the longitudinal rod is opened, and the bottom of the longitudinal rod is provided with an internal thread, and the longitudinal rod is connected to a booster rod via the internal thread.
[0007] The interior of the longitudinal rod is divided into a drug immersion part and a drug spraying part, the drug immersion part is arranged above the drug spraying part, and the drug immersion part and the drug spraying part are separated by a first one-way valve; the drug immersion part is adsorbed with tetracaine slurry; the longitudinal rod is provided with a plurality of circumferentially distributed through holes, the outer sleeve is provided with a drug delivery hole, the inner wall of the outer sleeve is provided with a connecting tube, one end of the connecting tube corresponds to the drug delivery hole, and the other end of the connecting tube matches the through hole.
[0008] The medicine soaking part includes an inner porous hydrogel structure and a cotton layer structure wrapped in an outer layer of the porous hydrogel structure.
[0009] Wherein, a second one-way valve is arranged at the bottom of the longitudinal rod above the internal thread.
[0010] Among them, a plurality of T-shaped slot holes are circumferentially arranged on the outer wall at the bottom of the longitudinal rod, and the intrauterine adhesion treatment device also includes a hand-held rod, and the inner wall of the hand-held rod is provided with a T-shaped protrusion that fits the T-shaped slot hole; a limit stop ring is fixedly arranged on the side wall of the booster rod, and the top of the limit stop ring abuts against the bottom of the hand-held rod.
[0011] Wherein, the intrauterine adhesion treatment device also includes a pressure syringe and a drug delivery device, one end of the pressure syringe and the drug delivery device are both detachably connected to a connecting catheter, and the connecting catheter is connected to the inside of the longitudinal rod through the second one-way valve.
[0012] The palace-shaped ring is provided with an outer coating, which is made of a mixture of silica gel and nano-paper material containing chitosan, and a plurality of release holes are arranged on the outer coating.
[0013] Wherein, the palace ring is made of polypropylene (pp) material.
[0014] Wherein, a pull rope is also provided on the top of the longitudinal rod, and the pull rope is a nylon line.
[0015] Wherein, the first one-way valve and the second one-way valve have built-in spring-top plug valves.
[0016] The present invention has the following beneficial effects:
[0017] This device combines the drug soaking part and the drug spraying part with the uterine ring, so that the device has three functions at the same time. The tetracaine hydrochloride slurry arranged inside the drug soaking part can continuously anesthetize the nerves of the cervix and pudendum of the patient, thereby achieving the effect of postoperative analgesia; the uterine ring can open the patient's internal uterine cavity to avoid the recurrence of uterine cavity adhesions that may still occur after the operation, and the drug solution required for treatment can be injected into the interior through the drug spraying part, so that the postoperative treatment effect is further enhanced. BRIEF DESCRIPTION OF THE DRAWINGS
[0018] Figure 1 It is a schematic diagram of the folding structure of the present invention;
[0019] Figure 2 It is a schematic diagram of the structure of the present invention;
[0020] Figure 3 This is a top view of a half section of the connection between the hand-held rod and the longitudinal rod of the present invention.
[0021] The reference numerals in the figure represent:
[0022] 1. Skeleton layer; 2. Longitudinal rod; 3. Outer sleeve; 4. Booster rod; 5. Hand-held rod; 11. First support member; 12. Second support member; 21. Drug immersion unit; 22. Drug spraying unit; 23. First one-way valve; 24. Porous hydrogel structure; 25. Cotton layer structure; 26. Second one-way valve; 27. T-shaped slot hole; 28. Pull rope; 31. Connecting pipe; 32. Dosing hole; 33. Connecting pipe; 41. Limiting ring; 51. T-shaped protrusion. DETAILED DESCRIPTION
[0023] The present invention will be described in detail below with reference to the accompanying drawings and specific embodiments.
[0024] See also Figures 1 to 3 , the invention provides a technical solution:
[0025] A device for treating intrauterine adhesions comprises two skeleton layers 1, which are symmetrically arranged to form a uterine-shaped ring, and the shape of the uterine-shaped ring is a bionic uterine structure; the material is selected from polypropylene (PP) material, the skeleton layer 1 comprises a first support member 11 and a second support member 12, the first support member 11 and the second support member 12 are hingedly arranged, and a longitudinal rod 2 is hinged at the top of the two skeleton layers 1; the device for treating intrauterine adhesions also comprises an outer sleeve 3, a connecting tube 31 is fixedly arranged at the bottom of the outer sleeve 3, the bottom ends of the two skeleton layers 1 are hinged to the connecting tube 31, and the outer sleeve 3 is slidably sleeved on the outside of the longitudinal rod 2; the bottom of the longitudinal rod 2 is opened, and the bottom of the longitudinal rod 2 is provided with an internal thread, and the longitudinal rod 2 is connected to a booster rod 4 through the internal thread.
[0026] like Figure 1 As shown, when the longitudinal rod 2 slides downward, the first support member 11 and the second support member 12 are hinged and thus contracted to form a contracted shape that is easier to enter the uterus, so as to reduce the patient's discomfort. After entering the uterine cavity, the longitudinal rod 2 is pushed to slide upward by the booster rod 4. At this time, the first support member 11 and the second support member 12 are unfolded into a supporting shape, which can completely support the uterine cavity and effectively prevent the recurrence of intrauterine adhesions.
[0027] At the same time, the interior of the longitudinal rod 2 is divided into a drug soaking part 21 and a drug spraying part 22. The drug soaking part 21 is used to fill and spray anesthetic drugs to relieve the patient's pain, and the drug spraying part 22 is used to spray therapeutic liquid to assist in treatment. The drug soaking part 21 is arranged above the drug spraying part 22, and the drug soaking part 21 and the drug spraying part 22 are separated by a first one-way valve 23; the drug soaking part 21 is adsorbed with tetracaine syrup, and tetracaine hydrochloride syrup (linin glue) is a commonly used local anesthetic with strong penetrating power and good diffusion. It can penetrate the mucosa and is clinically used for mucosal surface anesthesia for catheterization, cystoscopy, and gastroscopy; its analgesic effect is rapid, quick onset, and long duration; the longitudinal rod 2 is provided with a number of circular The outer sleeve 3 is provided with a drug delivery hole 32, and the inner wall of the outer sleeve 3 is provided with a connecting tube 33, one end of the connecting tube 33 corresponds to the drug delivery hole 32, and the other end of the connecting tube 33 matches the through hole; the diameter of the drug delivery hole 32 is 0.5mm~3mm, preferably 1mm~2mm, which is used to effectively release the drug; further, when the device is in the expanded state, the axes of the connecting tube 33, the drug delivery hole 32 and the through hole are on the same horizontal line, which can ensure the outflow of the drug solution. At the same time, the connecting tube 33 and the through hole may be slightly not on the same axis, but it does not affect the overall situation, and the connecting tube 33 can be made slightly larger than the through hole.
[0028] The drug soaking part 21 includes an inner porous hydrogel structure 24 and a cotton layer structure 25 wrapped in the outer layer of the porous hydrogel structure 24, so as to realize a multi-level slow drug release function.
[0029] A second one-way valve 26 is provided at the bottom of the longitudinal rod 2, above the internal thread; the first one-way valve 23 and the second one-way valve 26 are used to prevent the drug solution from flowing back out, and gas can be injected to achieve pressurization, thereby causing the internal drug body to reach the human body through the drug delivery hole 32, and slowly and long-term release, so as to achieve the effect of postoperative analgesia and treatment.
[0030] A plurality of T-shaped slots 27 are circumferentially arranged on the outer wall at the bottom of the longitudinal rod 2. The intrauterine adhesion therapeutic device also includes a hand-held rod 5, and the inner wall of the hand-held rod 5 is provided with a T-shaped protrusion 51 that fits the T-shaped slot 27; a limit stop ring 41 is fixedly arranged on the side wall of the booster rod 4, and the top of the limit stop ring 41 abuts against the bottom of the hand-held rod 5; specifically, during use, the hand-held rod 5 is connected by inserting the T-shaped protrusion 51 through the T-shaped slot 27 at the bottom of the longitudinal rod 2, and then the booster rod 4 is threadedly connected, and then pushed into the uterine cavity, and after the injection of the drug is completed, by holding the hand-held rod 5, The booster rod 4 can be rotated to separate the booster rod 4 from the longitudinal rod 2, so as to avoid the tingling sensation caused by stimulating the patient's uterine cavity by only rotating the booster rod 4; and after the booster rod 4 is disassembled, the hand-held rod 5 loses the limit of the bottom limit baffle ring 41 and can be slid out, so that the rest of the device can be left in the patient's body for continuous treatment; at the same time, a pull rope 28 is provided on the top and bottom of the longitudinal rod 2, and the pull rope 28 is a nylon line; when the device needs to be dragged out at the end, the treatment device remaining in the patient's body can be pulled out by pulling the pull rope 28.
[0031] The intrauterine adhesion treatment device also includes a pressure injector and a drug delivery device. One end of the pressure injector and the drug delivery device are both detachably connected to a connecting catheter, and the connecting catheter is connected to the interior of the longitudinal rod 2 through a second one-way valve 26 .
[0032] When in use, the medicine is injected from the second one-way valve 26 through the pressure syringe and the injection needle of the drug delivery device and pressurized at the same time, so that the medicine is sprayed out from the drug delivery hole 32 and reaches the human body, and is slowly and long-actingly released to achieve the effect of postoperative analgesia.
[0033] The uterine ring is covered with an outer layer membrane, which is made of a mixture of silica gel and nano-paper containing chitosan, and is provided with a number of release holes; medical chitosan can further enhance the anti-adhesion effect of the device, and at the same time, the outer layer membrane can be further expanded by bulging under the internal air pressure to avoid adhesion in the uterine cavity.
[0034] The first one-way valve 23 and the second one-way valve 26 are built-in spring-loaded plug valves.
[0035] The working principle of the above-mentioned intrauterine adhesion treatment device is as follows:
[0036] First, if Figure 1 As shown, the whole device is in a contracted state, and then the device is pushed into the uterine cavity and the booster rod 4 is pushed to make the device in a contracted state. Figure 2 The expanded state shown in the figure is then pushed inward by an external pressure syringe and a drug delivery device to push the liquid medicine and input air pressure, so that the liquid medicine and tetracaine hydrochloride slurry are pushed out through the through hole, thereby achieving the purpose of treatment and analgesia.
[0037] The above descriptions are merely embodiments of the present invention and are not intended to limit the patent scope of the present invention. Any equivalent structure or equivalent process transformation made using the contents of the present invention specification and drawings, or directly or indirectly applied in other related technical fields, are also included in the patent protection scope of the present invention.
Claims
1. A device for treating intrauterine adhesions, characterized in that: The invention comprises two skeleton layers (1), wherein the two skeleton layers (1) are symmetrically arranged to form a uterine ring, and the shape of the uterine ring is a bionic uterine structure; the skeleton layer (1) comprises a first support member (11) and a second support member (12), wherein the first support member (11) and the second support member (12) are hingedly arranged, and a longitudinal rod (2) is hingedly arranged at the top of the two skeleton layers (1); the intrauterine adhesion treatment device also comprises an outer sleeve (3), and a connecting tube (31) is fixedly arranged at the bottom of the outer sleeve (3), and the bottom ends of the two skeleton layers (1) are hingedly connected to the connecting tube (31), and the outer sleeve (3) is slidably sleeved on the outside of the longitudinal rod (2); the bottom of the longitudinal rod (2) is opened, and the bottom of the longitudinal rod (2) is provided with an internal thread, and the longitudinal rod (2) is connected to a booster rod (4) through the internal thread.
2. A device for treating intrauterine adhesions as claimed in claim 1, characterized in that: The interior of the longitudinal rod (2) is divided into a drug soaking section (21) and a drug spraying section (22), the drug soaking section (21) is arranged above the drug spraying section (22), and the drug soaking section (21) and the drug spraying section (22) are separated by a first one-way valve (23); the drug soaking section (21) is adsorbed with tetracaine slurry; the longitudinal rod (2) is provided with a plurality of circumferentially distributed through holes, the outer sleeve (3) is provided with a drug delivery hole (32), and the inner wall of the outer sleeve (3) is provided with a connecting pipe (33), one end of the connecting pipe (33) corresponds to the drug delivery hole (32), and the other end of the connecting pipe (33) matches the through hole.
3. A device for treating intrauterine adhesions as claimed in claim 2, characterized in that: The medicine soaking part (21) comprises an inner porous hydrogel structure (24) and a cotton layer structure (25) wrapped around the outer layer of the porous hydrogel structure (24).
4. A device for treating intrauterine adhesions as claimed in claim 3, characterized in that: A second one-way valve (26) is arranged at the bottom of the longitudinal rod (2) above the internal thread.
5. The intrauterine adhesion treatment device according to claim 1, characterized in that: The outer wall at the bottom of the longitudinal rod (2) is circumferentially provided with a plurality of T-shaped slot holes (27); the intrauterine adhesion treatment device further comprises a hand-held rod (5); the inner wall of the hand-held rod (5) is provided with a T-shaped protrusion (51) that fits the T-shaped slot hole (27); a limit stop ring (41) is fixedly provided on the side wall of the booster rod (4); the top of the limit stop ring (41) abuts against the bottom of the hand-held rod (5).
6. A device for treating intrauterine adhesions as claimed in claim 4, characterized in that: The intrauterine adhesion treatment device also includes a pressure injector and a drug delivery device. One end of the pressure injector and the drug delivery device are both detachably connected to a connecting catheter, and the connecting catheter is connected to the interior of the longitudinal rod (2) through the second one-way valve (26).
7. The intrauterine adhesion treatment device according to claim 1, characterized in that: The palace-shaped ring is provided with an outer coating, which is made of a mixture of silica gel and nano-paper material containing chitosan, and a plurality of release holes are arranged on the outer coating.
8. The intrauterine adhesion treatment device according to claim 1, characterized in that: The palace ring is made of polypropylene (pp) material.
9. The intrauterine adhesion treatment device according to claim 1, characterized in that: A pull rope (28) is also provided on the top of the longitudinal rod (2), and the pull rope (28) is a nylon line.
10. The intrauterine adhesion treatment device according to claim 4, characterized in that: The first one-way valve (23) and the second one-way valve (26) are built-in spring-loaded plug valves.
Citation Information
Cited By
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