Multifunctional postoperative flushing mold for cervical cancer
Patent Information
- Application Number
- CN202421617768.9
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-07-09
- Publication Date
- 2025-05-23
- Estimated Expiration
- 2034-07-09
AI Technical Summary
After cervical cancer surgery, the prior art can easily cause discomfort and pain when rinsing vaginal wounds, and frequent rinsing will cause discomfort in the insertion of vaginal foreign objects.
A multifunctional postoperative cervical cancer rinsing mold is designed, including a latex plug head nozzle and a temperature and humidity detection probe. The latex plug head nozzle and isolation film are combined to achieve drug delivery, avoiding direct contact between the pipe and the inner wall of the vagina and reducing pain.
The mold can detect the temperature and humidity of the vaginal wound in real time, and through the cooperation of the latex filler nozzle and isolation film, it reduces the pain in the patient's wound, reduces the discomfort of vaginal foreign objects, and improves the comfort of rinsing.
Smart Images

Figure CN222889239U_ABST
Abstract
Description
Technical Field
[0001] The utility model belongs to the technical field of vaginal washing, and in particular relates to a multifunctional washing mould after cervical cancer surgery. Background Art
[0002] After cervical cancer surgery, a wound will be left in the patient's vagina. During the recovery period, the vagina needs to be flushed and cleaned with liquid medicine. Currently, when flushing the vagina, the flushing device pipe is directly inserted into the patient's vagina and liquid medicine is injected to flush the wound in the vagina. Each time the flushing is performed, the flushing device pipe will cause friction and compression to the patient's vaginal wall and even the wound in the vagina, which will cause discomfort to the patient. In addition, the wound in the vagina needs to be flushed frequently in the early stage after the operation. Currently, directly using a flushing device to flush the wound will frequently cause vaginal pain in the patient, which is inconvenient to use. Utility Model Content
[0003] The utility model provides a multifunctional post-operative washing mold for cervical cancer, which has the characteristics of being able to wash the vaginal wound without extending a washing pipe into the vagina, thereby reducing the pain of the patient's wound.
[0004] The utility model provides the following technical solutions: a multifunctional cervical cancer postoperative flushing mold, comprising a latex packing head nozzle and a temperature and humidity detection probe, a drug flushing hole is opened at the top of the latex packing head nozzle, an isolation film is fixedly connected to the bottom of the latex packing head nozzle, the latex packing head nozzle and one side of the isolation film have side supporting strips, a film connecting sleeve is provided on the outer side of the side supporting strip, the film connecting sleeve located on one side of the latex packing head nozzle is fixedly connected to the latex packing head nozzle, and the film connecting sleeve located on one side of the isolation film is fixedly connected to the isolation film.
[0005] Among them, a yield installation groove is opened at the top end of the latex filling head nozzle, the temperature and humidity detection probe is fixedly connected to the inner wall of the yield installation groove, and an inclined guide groove is opened at the bottom end of the latex filling head nozzle.
[0006] Wherein, the side wall of the isolation film is fixedly connected with an adhesive positioning sticker, and the bottom end of the isolation film is fixedly connected with a latex expansion ring.
[0007] Among them, an inserted support rod is detachably connected to the latex filling head nozzle, and the diameter of the inserted support rod matches the inner diameter of the latex filling head nozzle.
[0008] Among them, the outer wall of the latex filling head nozzle is fixedly connected with a clamping and positioning airbag, the top end of the clamping and positioning airbag is inclined toward the center, and the bottom end of the clamping and positioning airbag is horizontal.
[0009] The beneficial effects of the utility model are:
[0010] 1. With the help of a latex packing head nozzle, a temperature and humidity detection probe and an isolation film placed in the patient's vagina, the temperature and humidity of the patient's wound area can be detected in real time, so that the staff can judge the recovery of the patient's wound.
[0011] 2. With the help of the latex packing head nozzle and the isolation film, the drug delivery is achieved, so that personnel do not need to reach into the vagina through the pipe to flush the vaginal wound. The pipe will not directly contact and rub against the inner wall of the patient's vagina, reducing the pain of the patient's wound. The latex packing head nozzle and the isolation film cooperate to form a delivery pipeline. The latex packing head nozzle can play a positioning role. At the same time, the isolation film with a larger length can correspond to the position of the muscle groups around the patient's vagina, will not hinder the contraction of the muscle groups, will not cause overflow of vaginal excrement, and can effectively reduce the discomfort of foreign objects inserted into the patient's vagina. The side support strips and the film connecting sleeve can support the isolation film with the help of the temperature and humidity detection probe to prevent the isolation film from folding or even shrinking in the patient's vagina.
[0012] The parts not involved in the device are the same as those in the prior art or can be implemented by using the prior art. BRIEF DESCRIPTION OF THE DRAWINGS
[0013] Figure 1 It is a schematic diagram of the structure of the utility model;
[0014] Figure 2 It is a schematic diagram of the motion state of the insertion type delivery pipe in the utility model;
[0015] Figure 3 It is a schematic diagram of the structure of the clamping and positioning airbag in the utility model.
[0016] In the figure: 1. Latex filling head nozzle; 11. Drug flushing hole; 12. Yield installation groove; 13. Inclined guide groove; 2. Temperature and humidity detection probe; 3. Isolation film; 31. Adhesive positioning sticker; 32. Latex expansion ring; 4. Side support strip; 41. Film connecting sleeve; 5. Insert support rod; 6. Clamping positioning airbag. DETAILED DESCRIPTION
[0017] See also Figure 1-Figure 3 The utility model provides the following technical solutions: a multifunctional cervical cancer postoperative flushing mold, including a latex packing head nozzle 1 and a temperature and humidity detection probe 2, a drug flushing hole 11 is opened at the top of the latex packing head nozzle 1, and an isolation film 3 is fixedly connected to the bottom of the latex packing head nozzle 1, and the latex packing head nozzle 1 and the isolation film 3 have a side support strip 4 on one side, and a film connecting sleeve 41 is provided on the outer side of the side support strip 4, and the film connecting sleeve 41 located on one side of the latex packing head nozzle 1 is fixedly connected to the latex packing head nozzle 1, and the film connecting sleeve 41 located on one side of the isolation film 3 is fixedly connected to the isolation film 3.
[0018] In the present embodiment: when the patient performs the initial vaginal flushing after undergoing cervical cancer surgery, the staff inserts the insertable support rod 5 into the cavity of the latex packing head nozzle 1, and then the staff inserts the latex packing head nozzle 1 and the isolation film 3 into the patient's vagina, and then the staff pulls out the insertable support rod 5 from the latex packing head nozzle 1 and the isolation film 3, and then the staff holds the drug flushing pipeline and extends it into the exposed part of the tail of the isolation film 3, and supports and expands the isolation film 3 by delivering liquid medicine into the isolation film 3, so that after the pipeline is unobstructed, liquid medicine can be delivered into the vagina to flush the vaginal wound, and the latex packing head nozzle 1 and the isolation film 3 cooperate to play a drug delivery role, so that personnel do not need to extend the pipeline into the vagina to flush the vaginal wound, and the pipeline will not directly contact and rub against the inner wall of the patient's vagina, thereby reducing the pain of the patient's wound, and the latex packing head nozzle 1 and the isolation film 3 cooperate to form a delivery pipeline, and the latex packing head nozzle 1 can play a positioning role, while the isolation film 3 with a larger length ratio can correspond to the position of the muscle groups around the patient's vagina. After the liquid medicine in the isolation film 3 is discharged, the muscle group can contract to squeeze the isolation film 3, so that the isolation film 3 is closed, which will not hinder the contraction of the muscle group, will not cause the overflow of vaginal excrement, and can effectively reduce the discomfort of the patient's vaginal foreign body insertion. The side support strips 4 and the film connecting sleeve 41 can support the isolation film 3 with the help of the temperature and humidity detection probe 2 to prevent the isolation film 3 from folding or even shrinking in the patient's vagina. The side support strips 4 are made of highly elastic materials and can maintain a vertical state under a small diameter to support the isolation film 3. The mold is used during the patient's bed rest after surgery. When the patient uses it, the staff should instruct the patient to reduce the movement of the lower limbs as much as possible. After the wound recovers, the mold should be taken out of the patient's vagina as a whole, and the vagina should be directly flushed using the flushing pipe instead. With the help of the latex packing head nozzle 1, the temperature and humidity detection probe 2 and the isolation film 3 are placed in the patient's vagina for retention, the temperature and humidity of the patient's wound site can be detected in real time. The temperature and humidity detection probe 2 can be connected to an external device through a signal to facilitate the staff to judge the recovery of the patient's wound.
[0019] A yielding installation groove 12 is provided at the top of the latex filling head nozzle 1, and the temperature and humidity detection probe 2 is fixedly connected to the inner wall of the yielding installation groove 12, and an inclined guide groove 13 is provided at the bottom of the latex filling head nozzle 1; by setting the yielding installation groove 12, a holding space can be provided for the temperature and humidity detection probe 2, and the temperature and humidity detection probe 2 is wrapped by the latex filling head nozzle 1, and the temperature and humidity detection probe 2 is protected by means of the latex filling head nozzle 1, thereby improving the stability of the connection between the yielding installation groove 12 and the latex filling head nozzle 1, and by setting the inclined guide groove 13, the inserted support rod 5 can be guided, so that the inserted support rod 5 can be more smoothly inserted into the cavity inside the latex filling head nozzle 1.
[0020] The side wall of the isolation film 3 is fixedly connected with an adhesive positioning sticker 31, and the bottom end of the isolation film 3 is fixedly connected with a latex expansion ring 32; by setting the adhesive positioning sticker 31, the exposed part of the tail of the isolation film 3 can be fixed. When in use, the staff will adhere the adhesive positioning sticker 31 to the patient's skin, and the latex expansion ring 32 can expand the tail of the isolation film 3, so that the staff can easily insert the flushing pipe into the isolation film 3. After the staff inserts the flushing pipe into the isolation film 3, the elastic force of the latex expansion ring 32 itself can shrink and wrap the isolation film 3 around the outer wall of the flushing pipe to prevent the flushing solution from flowing back.
[0021] An insertable support rod 5 is detachably connected to the latex packing head nozzle 1, and the diameter of the insertable support rod 5 matches the inner diameter of the latex packing head nozzle 1. By providing the insertable support rod 5, it is convenient for the staff to insert the latex packing head nozzle 1 and the isolation film 3 into the patient's vagina.
[0022] The outer wall of the latex packing head nozzle 1 is fixedly connected with a clamping positioning airbag 6, the top of the clamping positioning airbag 6 is inclined toward the center, and the bottom of the clamping positioning airbag 6 is horizontal; the latex packing head nozzle 1 and the clamping positioning airbag 6 correspond to the position of the soft flesh in the patient's vagina, and when the vagina contracts, the clamping latex packing head nozzle 1 and the clamping positioning airbag 6 play a positioning role to prevent the latex packing head nozzle 1 from moving significantly in the patient's vagina.
[0023] The working principle and use process of the utility model are as follows: when the patient performs the initial flushing of the vagina after undergoing cervical cancer surgery, the staff inserts the insertable support rod 5 into the cavity inside the latex packing head nozzle 1, and then the staff inserts the latex packing head nozzle 1 and the isolation film 3 into the patient's vagina, and then the staff pulls out the insertable support rod 5 from the latex packing head nozzle 1 and the isolation film 3, and then the staff holds the drug flushing pipeline and extends it into the exposed part of the rear end of the isolation film 3, and supports and expands the isolation film 3 by delivering the drug solution into the isolation film 3, so that the pipeline can be unobstructed after it is cleared. The drug solution is delivered into the vagina to flush the vaginal wound. The latex packing head nozzle 1 and the isolation film 3 cooperate to play the role of drug delivery, so that personnel do not need to reach into the vagina through a pipe to flush the vaginal wound. After the drug solution in the isolation film 3 is discharged, the muscle group can contract to squeeze the isolation film 3, so that the isolation film 3 is closed, which will not hinder the contraction of the muscle group, will not cause the overflow of vaginal excrement, and can effectively reduce the patient's discomfort caused by the insertion of foreign objects into the vagina. After the wound recovers, the entire mold should be removed from the patient's vagina, and the vagina should be directly flushed using a flushing pipe instead.
Claims
1. A multifunctional postoperative washing mold for cervical cancer, comprising a latex filling head nozzle (1) and a temperature and humidity detection probe (2), characterized in that: The top of the latex plugging head nozzle (1) is provided with a drug flushing hole (11), and the bottom of the latex plugging head nozzle (1) is fixedly connected with an isolation film (3). The latex plugging head nozzle (1) and one side of the isolation film (3) have a side support strip (4), and the outer side of the side support strip (4) is provided with a film connecting sleeve (41). The film connecting sleeve (41) located on one side of the latex plugging head nozzle (1) is fixedly connected to the latex plugging head nozzle (1), and the film connecting sleeve (41) located on one side of the isolation film (3) is fixedly connected to the isolation film (3).
2. The multifunctional postoperative washing mold for cervical cancer according to claim 1, characterized in that: The top end of the latex plugging head nozzle (1) is provided with a clearance installation groove (12), the temperature and humidity detection probe (2) is fixedly connected to the inner wall of the clearance installation groove (12), and the bottom end of the latex plugging head nozzle (1) is provided with an inclined guide groove (13).
3. The multifunctional postoperative washing mold for cervical cancer according to claim 1, characterized in that: The side wall of the isolation film (3) is fixedly connected with an adhesive positioning sticker (31), and the bottom end of the isolation film (3) is fixedly connected with a latex expansion ring (32).
4. The multifunctional postoperative washing mold for cervical cancer according to claim 1, characterized in that: An insertable support rod (5) is detachably connected to the latex plugging head nozzle (1), and the diameter of the insertable support rod (5) matches the inner diameter of the latex plugging head nozzle (1).
5. The multifunctional post-operative washing mold for cervical cancer according to claim 1, characterized in that: The outer wall of the latex filling head nozzle (1) is fixedly connected with a clamping and positioning airbag (6), the top end of the clamping and positioning airbag (6) is inclined toward the center, and the bottom end of the clamping and positioning airbag (6) is horizontal.