CN215690931U - Vagina mold - Google Patents

Abstract

The utility model provides a vaginal mold, which solves the problem that part of muscles are embedded into a through hole in the prior art, and simultaneously still ensures the cleanness of the whole vaginal mold and improves the comfort of the mold. In order to solve the technical problem, the utility model adopts a vaginal mold which comprises a handheld part and a supporting part, wherein the supporting part extends into a vagina to maintain the inner side of the vagina in an open state, the supporting part comprises a hollow columnar frame body, a drainage hole is formed in the top of the frame body, a clamping part is arranged at the tail end of the supporting part, and an annular cushion block is sleeved on the clamping part. After the technical scheme is adopted, the direction and the position of the drainage hole are adjusted, and a certain drainage effect on extravasated blood and secretion in the vagina can be better achieved. The original connecting part is eliminated, the connecting part is changed into the annular cushion block, and different patients can be matched at lower cost through the replaceable annular cushion block.

Description

Vagina mold

Technical Field

The utility model relates to medical equipment for gynecology, in particular to a vaginal mold for gynecology.

Background

After a gynecological patient receives a vaginal operation, such as a vaginal reconstruction operation or a vaginal extension operation, a vaginal mold needs to be placed to consolidate the operation effect. The applicant filed 2016 patent numbers: 201611184990.4 entitled vaginal mould for recovery. The vagina mold mainly improves the convenience and the comfort of the vagina mold, improves the cleanliness of the vagina mold, and reduces the possibility of infection in the use process.

The patented product is already put into the market and brings good effects. The product is mainly used for the recovery of patients without vagina and with uterus after vagina reconstruction surgery. However, in the process of using the vaginal wall muscle for patients, the situation that the vaginal wall muscle is embedded into the through hole on the surface of the plastic frame body occurs in practice because the operation is usually performed for young girls and the activity of the vaginal wall muscle is stronger after the operation. This can cause the mold to be removed, which can pull on the muscle and cause pain to the patient, and in severe cases can cause a wound that can result in intravaginal bleeding that can be detrimental to the patient's recovery. In this regard, the applicant has further improved the mold over the prior art so that its use is more conducive to patient recovery.

SUMMERY OF THE UTILITY MODEL

The utility model provides a vaginal mold, which solves the problem that part of muscles are embedded into a through hole in the prior art, and simultaneously still ensures the cleanness of the whole vaginal mold and improves the comfort of the mold.

In order to solve the technical problems, the utility model adopts the following technical scheme:

the utility model provides a vagina mould, includes handheld portion and supporting part, wherein the supporting part stretches into the vagina in with the vagina inboard maintain the state of strutting, the supporting part includes a hollow column framework, open at the framework top has a drainage hole, the supporting part end is equipped with joint portion, the cover is equipped with annular cushion in the joint portion, annular cushion diameter is greater than the diameter of column framework, column framework inboard is equipped with the internal thread, handheld portion top is equipped with the external screw thread that matches with the internal thread.

Preferably, the clamping portion is provided with a horizontally arranged convex ring, and the inner side of the annular cushion block is provided with a concave ring matched with the convex ring. The clamping mode enables the annular cushion block to rotate around the supporting part. Thus, when an external force is applied, the whole supporting part is not driven.

Preferably, the annular cushion block is sleeved with a resin bag, and the shape of the outer surface of the resin bag, particularly the outer surface of the lower surface of the resin bag, is matched with the structure of the inner side of the resin bag when the vaginal orifice is closed. Such a construction is primarily intended to improve the comfort of the entire mould.

Preferably, a plurality of diversion trenches parallel to the central axis of the support part are arranged on the outer side of the frame body. The structure is mainly used for avoiding that the frame body is adhered to the inner wall of the vagina after the extravasated blood on the outer side of the frame body is solidified, so that the support part is painful to take off.

Preferably, a spacing part of not less than 3cm is arranged between the actual holding position of the holding part and the external thread part. Such a construction ensures that the hand and the support remain at a certain distance during use, and reduces the likelihood of contamination, particularly at home.

Preferably, the bottom of the annular cushion block is sealed by a plastic cover body, a fixing column is arranged on the plastic cover body, and medical sponge is wound on the fixing column. For some patients with small bleeding and under the condition of timely replacement, the supporting part can be made into a closed form, so that secretion and extravasated blood are temporarily stored in the supporting part, and the cleanliness of the outer part of the frame body is ensured.

Preferably, the volume of the medical sponge is one third of that of the columnar frame body. Therefore, the sponge can basically fill the whole frame body after absorbing the extravasated blood and the secretion, and the extravasated blood and the secretion cannot be scattered to cause pollution after being taken out.

Preferably, a single-layer gauze is paved on the inner side wall of the hollow frame body. Therefore, the workload of cleaning the inner side of the frame body is reduced by replacing the gauze after use.

After the technical scheme is adopted, the utility model has the following advantages: mainly adjusts the direction and the position of the drainage hole, and can better play a certain drainage effect on extravasated blood and secretion in the vagina. The original connecting part is eliminated, the connecting part is changed into the annular cushion block, and different patients can be matched at lower cost through the replaceable annular cushion block.

Compared with the prior technical scheme, the utility model has great improvement on cleanliness and comfort. During the use process, the situation that the muscle on the vaginal wall is embedded into the drainage hole does not occur. The foreign body sensation at the vaginal opening can be effectively relieved. The use is more convenient and refreshing.

Drawings

The following further describes embodiments of the present invention with reference to the accompanying drawings:

fig. 1 is a schematic view of an overall exploded structure of a vaginal mold of the present invention.

Fig. 2 is a cross-sectional view taken at a-a in fig. 1.

FIG. 3 is a schematic view of the closed configuration of the annular cushion of the vaginal mold of the present invention.

Detailed Description

The utility model discloses a vaginal mold, which comprises a hand-held part 2 and a supporting part 1 as shown in figures 1 and 2, and unlike the previous design, the hand-held part 2 and the supporting part 1 are not connected by a connecting part, but the hand-held part 2 and the supporting part 1 are fixed by the direct matching of internal threads 9 and external threads 10. The end of the supporting part 1 is provided with a clamping part 5, the clamping part 5 is sleeved with an annular cushion block 3, the diameter of the annular cushion block 3 is larger than that of the columnar frame body, and thus when the handheld part 2 is connected with the supporting part 1, the annular cushion block 3 can also play a certain guiding role.

The supporting part 1 extends into the vagina to maintain the inner side of the vagina in an open state, the supporting part 1 comprises a hollow columnar frame body, and the top of the frame body is provided with a drainage hole 4, so that the vagina can be fully supported, and extravasated blood and secretion can be timely discharged when the vaginal dilator is used. A plurality of diversion trenches 6 parallel to the central axis of the supporting part 1 are arranged on the outer side of the frame body. And a spacing part of not less than 3cm is arranged between the actual handheld position of the handheld part 2 and the external thread 10 part.

The clamping portion 5 is provided with a horizontally arranged convex ring 7, and the inner side of the annular cushion block 3 is provided with a concave ring 8 matched with the convex ring 7. The outer side of the annular cushion block 3 is sleeved with a resin bag, and the shape of the outer surface of the resin bag is matched with the structure of the inner side of the resin bag when the vaginal orifice is closed.

Example 1: in using the present invention, a suitable resin pack is first customized to the previous shape of the inside of the vagina. After the resin sleeve is sheathed outside the annular cushion block 3, the annular cushion block 3 is arranged at the position of the clamping part 5 at the tail end of the supporting part 1. The annular cushion block 3 is matched with a convex ring 7 horizontally arranged on the inner side concave ring 8 and the clamping portion 5, so that the annular cushion block 3 can rotate by taking the supporting portion 1 as an axis and cannot be separated from the axis. This can be adapted to various situations. When the device is installed, the handheld part 2 is connected with the supporting part 1 through the internal thread 9 and the external thread 10, and the handheld part 2 can be taken out in a rotating mode after the supporting part 1 is sent into a proper position of a vagina of a user. At this time, the user is required to contract the vagina, so that the friction force between the vagina wall and the supporting part 1 is larger than that at the thread part, and the handheld part 2 can be conveniently detached. In the embodiment, the supporting part 1 is a hollow columnar frame, the top of the frame is provided with a drainage hole 4, and extravasated blood and secretion in the vagina flow out of the drainage hole 4, so the sanitary towel is required to be matched for absorption when in use. When in use, the whole supporting part 1 is completely immersed into the vagina, and the inconvenience to the life and work of a user is avoided.

When taking out, the hand-held part 2 is only required to be screwed back again to be connected with the supporting part 1. The support part 1 is slowly drawn out after the screw-thread fit. Usually, the supporting part 1 needs to be taken out, cleaned and replaced after the physical strength is continuously used for 8 hours, so that a large amount of hematocele and secretion are prevented from remaining in the columnar frame.

The supporting part 1 can be soaked and cleaned independently, only the resin bag on the annular cushion block 3 is contacted with the inner wall of the vagina, and the resin bag can be detached and cleaned independently.

This embodiment is the most common one.

Another embodiment is shown in fig. 3, which is a vaginal mold, the main structure of which is the same as the previous embodiment, except that the bottom of the annular cushion block 3 is sealed by a plastic cover 12, the plastic cover 12 is provided with a fixing column 11, and the fixing column 11 is wound with medical sponge. The volume of the medical sponge is one third of that of the columnar frame body. Such a configuration is primarily directed to those patients with low bleeding volume and secretions. Stagnant blood and secretions are stored by a closed hollow cylindrical frame.

When in use, the plastic cover body 12 with the fixing posts 11 is closed after the supporting part 1 is completely placed into the vagina. When taking out, the plastic cover 12 with the fixing post 11 needs to be taken down separately. Therefore, this embodiment is slightly more troublesome than example 1 in taking out, and it is necessary to avoid contamination when removing the plastic lid 12. Such embodiments are not suitable for immediate use immediately after surgery, and medical personnel typically recommend that the user be used 7 days after surgery with significantly reduced congestion and secretions. The embodiment has the advantage that the sanitary towel does not need to be additionally matched with a sanitary towel for use, and is more refreshing particularly in summer. Such an embodiment suggests replacing the support 1 and replacing the medical sponge on the corresponding fixing post 11 once for 4 hours.

In the present embodiment, a single layer of gauze is laid on the hollow inner side wall of the frame of the support portion 1 to prevent the extravasated blood from fully solidifying on the inner side wall of the frame. The single-layer gauze is required to be replaced when taken out at every time, so that the cleaning work of the inner side wall of the frame body is facilitated.

Other embodiments of the present invention than the preferred embodiments described above will be apparent to those skilled in the art from the present invention, and various changes and modifications can be made therein without departing from the spirit of the present invention as defined in the appended claims.

Claims (8)

1. The utility model provides a vagina mould, includes handheld portion and supporting part, wherein the supporting part stretches into the vagina in with the vagina inboard maintain the state of strutting, its characterized in that, the supporting part includes a hollow column framework, open at the framework top has a drainage hole, the supporting part end is equipped with joint portion, the cover is equipped with annular cushion in the joint portion, annular cushion diameter is greater than the diameter of column framework, column framework inboard is equipped with the internal thread, handheld portion top is equipped with the external screw thread that matches with the internal thread.

2. A vaginal mold as claimed in claim 1 wherein: the clamping portion is provided with a horizontally arranged convex ring, and the inner side of the annular cushion block is provided with a concave ring matched with the convex ring.

3. A vaginal mold as claimed in claim 2, wherein: the outer side of the annular cushion block is sleeved with a resin bag, and the shape of the outer surface of the resin bag is matched with the structure of the inner side of the resin bag when the vaginal orifice is closed.

4. A vaginal mold as claimed in claim 1 wherein: and a plurality of diversion trenches parallel to the central axis of the supporting part are arranged on the outer side of the frame body.

5. A vaginal mold as claimed in claim 1 wherein: and a spacing part of not less than 3cm is arranged between the actual handheld position of the handheld part and the external thread part.

6. A vaginal mold as claimed in claim 1 wherein: the bottom of the annular cushion block is sealed by a plastic cover body, a fixing column is arranged on the plastic cover body, and medical sponge is wound on the fixing column.

7. A vaginal mold as claimed in claim 6, wherein: the volume of the medical sponge is one third of that of the columnar frame body.

8. A vaginal mold as claimed in any one of claims 1 or 6 wherein: and a single-layer gauze is paved on the inner side wall of the hollow frame body.

Images