Intracavity anti-adhesion balloon structure used after uterine cavity operation

By designing a postoperative intra-cavity anti-adhesion balloon structure with a contraction frame and a U-shaped frame, the risk of uterine cavity internal wall tear caused by balloon expansion in the prior art is solved, and the effect of effectively preventing adhesion is achieved, and the safety of surgery is improved.

CN222854429UActive Publication Date: 2025-05-13URUMQI MATERNAL & CHILD HEALTH HOSPITAL
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Patent Information

Application Number
CN202420430442.9
Authority / Receiving Office
CN · China
Patent Type
Utility models(China)
Current Assignee / Owner
Filing Date
2024-03-06
Publication Date
2025-05-13
Estimated Expiration
2034-03-06

AI Technical Summary

Technical Problem

When existing uterine cavity balloons expand and open, it may cause the entire inner wall of the uterine cavity to be opened outward, increasing the risk of torn surgery.

Method used

A balloon structure for anti-adhesion in the cavity after uterine cavity surgery is designed. The balloon is made of flexible material and has an inflatable cavity and a contraction frame inside. Through the setting of the U-shaped frame, the balloon can only expand left and right to avoid up and down, and ensure flat expansion.

Benefits of technology

By controlling the expansion direction of the balloon, the risk of tearing of the inner wall of the uterine cavity is avoided, and adhesion to the inner wall of the uterine cavity is effectively prevented, thereby improving the safety of the surgery.

✦ Generated by Eureka AI based on patent content.

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Abstract

The utility model provides an intracavitary anti-adhesion sacculus structure after a uterine cavity operation. A sacculus is made of flexible materials and is arranged in a flat shape, an inflation cavity is formed in the sacculus, the top end of a connecting pipe is inserted into the inflation cavity, the bottom end of the connecting pipe is connected with a valve, and a plurality of air outlet holes communicated with the inflation cavity are formed in the outer wall of the top end of the connecting pipe. The valve is opened, air in the inflation cavity is firstly pumped out, negative pressure is formed in the inflation cavity, the valve is closed, the balloon is wizened under the action of atmospheric pressure, the balloon is fed into an operation area by holding the connecting pipe with a hand, then the valve is opened, air is inflated from one end of the outer side of the valve, and the air penetrates through the connecting pipe to enter the inflation cavity. The wizened balloon is expanded and spread out to cover an operation area, and adhesion of the inner wall of the uterine cavity is prevented through the balloon.
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Description

Technical Field

[0001] The utility model relates to the technical field of instruments for introducing or retaining a medium, such as medicine, in a body cavity, and in particular to an intracavitary anti-adhesion balloon structure after uterine cavity surgery. Background Art

[0002] In the prior art, the post-operative intrauterine adhesion prevention device is an intrauterine balloon. When the common intrauterine balloon is used, water is often injected or air is inflated in the balloon to open the balloon to support the uterine cavity. However, when the existing balloon is inflated and opened, the balloon expands outward as a whole, causing the inner wall of the uterine cavity to open outward as a whole, resulting in the risk of the surgical area being torn. Therefore, a post-operative intrauterine adhesion prevention balloon structure is proposed. Utility Model Content

[0003] In order to solve at least one of the above-mentioned technical shortcomings, the utility model provides a post-operative intracavitary anti-adhesion balloon structure, including a balloon, the balloon is made of flexible material, the balloon is flat, an inflation cavity is provided inside the balloon, the top end of the connecting tube is inserted into the inflation cavity, the bottom end of the connecting tube is connected to a valve, and the top outer wall of the connecting tube is provided with a plurality of air outlet holes connected to the inflation cavity.

[0004] Furthermore, a shrinkage frame fixed on the connecting pipe is provided inside the inflation cavity.

[0005] Furthermore, a connecting horizontal block integrally connected to the inner wall of the inflation cavity is provided at the top end of the connecting pipe.

[0006] Furthermore, the shrinkage skeleton includes two fixed blocks fixed to the outer wall of the middle part of the connecting tube, the fixed blocks are located inside the inflation chamber, and at least one rotating hole is provided on the fixed blocks. A U-shaped skeleton is provided inside the rotating hole, and the two ends of the U-shaped skeleton are respectively connected to the top wall and the bottom wall of the inflation chamber, and the middle part of the U-shaped skeleton is rotatably connected to the rotating hole.

[0007] Furthermore, the top wall and the bottom wall of the inflation cavity are both concave and have a plurality of contraction grooves.

[0008] Furthermore, the balloon is made of medical silicone material.

[0009] Furthermore, an air pump is provided for inflating the air chamber. Beneficial Effects

[0010] Open the valve, first extract the gas inside the inflation cavity to form a negative pressure inside the inflation cavity, close the valve, and deflate the balloon under the action of atmospheric pressure. Send the balloon to the surgical area by holding the connecting tube. Open the valve again, and fill the gas from the outer end of the valve. The gas passes through the connecting tube into the inflation cavity, causing the deflated balloon to expand and spread out to cover the surgical area, thereby preventing adhesion to the inner wall of the uterine cavity.

[0011] When limiting the shape of the balloon, when the interior of the inflation cavity is inflated with gas, the balloon will expand under the action of air pressure, passing through the two ends of the U-shaped skeleton, so that the balloon cannot expand in the upper and lower planes, and the balloon can only expand to the left and right sides, so that the balloon is spread out flat. When expanding to the left and right, the middle part of the U-shaped skeleton rotates inside the rotating hole.

[0012] The realization of the purpose, functional features and advantages of the present invention will be further described in conjunction with embodiments and with reference to the accompanying drawings. BRIEF DESCRIPTION OF THE DRAWINGS

[0013] Figure 1 It is an axonometric drawing of the utility model as a whole.

[0014] Figure 2 It is a cross-sectional view of the balloon of the utility model.

[0015] Figure 3 It is an axonometric view of the shrinkage frame of the utility model.

[0016] Figure 4 It is an axonometric view of the connecting pipe of the utility model.

[0017] Figure 5 It is an axonometric drawing of the U-shaped frame of the utility model.

[0018] exist Figures 1 to 5 , the correspondence between the component names or lines and the figure numbers is: balloon 1, inflation cavity 101, contraction groove 102, connecting tube 2, air outlet 201, connecting horizontal block 202, valve 3, contraction skeleton 4, fixing block 401, rotation hole 402, U-shaped skeleton 403. DETAILED DESCRIPTION

[0019] Please refer to Figures 1 to 5 ;

[0020] This embodiment provides a postoperative intracavitary anti-adhesion balloon structure. Figure 1 and Figure 2 , including a balloon 1, the balloon 1 is made of a flexible material, the balloon 1 is flat, an inflation cavity 101 is arranged inside the balloon 1, the top end of the connecting tube 2 is inserted into the inflation cavity 101, the bottom end of the connecting tube 2 is connected with a valve 3, and the top outer wall of the connecting tube 2 is provided with a plurality of air outlet holes 201 connected to the inflation cavity 101;

[0021] In the specific implementation, the valve 3 is opened, and the gas inside the inflation cavity 101 is firstly extracted to form a negative pressure inside the inflation cavity 101, and the valve 3 is closed to make the balloon 1 deflate under the action of atmospheric pressure, and the balloon 1 is delivered to the operation area by holding the connecting tube 2, and the valve 3 is opened again, and the gas is filled from the outer end of the valve 3, and the gas passes through the connecting tube 2 and enters the inflation cavity 101, so that the deflated balloon 1 is expanded and spread out to cover the operation area, and the balloon 1 is prevented from adhering to the inner wall of the uterine cavity;

[0022] That is, reduce, insert, and enlarge for use.

[0023] For further reference, Figure 3 , a shrinkage frame 4 fixed on the connecting pipe 2 is provided inside the inflation cavity 101;

[0024] In a specific implementation, the expansion direction of the balloon 1 is positioned by setting the contraction skeleton 4, so that the balloon 1 can be expanded in a preset shape when being inflated.

[0025] For further reference, Figure 3 and Figure 4 The top end of the connecting pipe 2 is provided with a connecting horizontal block 202 integrally connected with the inner wall of the inflation chamber 101;

[0026] In specific implementation, when the balloon 1 is inserted, force is applied to the end of the balloon 1 through the connecting cross block 202 to facilitate the insertion of the balloon 1.

[0027] For further reference, Figures 3 to 5 The shrinkage frame 4 includes two fixed blocks 401 fixed to the outer wall of the middle part of the connecting tube 2. The fixed blocks 401 are located inside the inflation chamber 101. At least one rotation hole 402 is provided on the fixed blocks 401. The inside of the rotation hole 402 is provided with a U-shaped frame 403. The two ends of the U-shaped frame 403 are respectively connected to the top wall and the bottom wall of the inflation chamber 101. The middle part of the U-shaped frame 403 is rotatably connected to the rotation hole 402.

[0028] In a specific implementation, when the shape of the balloon 1 is limited, when the interior of the inflation chamber 101 is inflated with gas, the balloon 1 will expand under the action of air pressure, and through the two ends of the U-shaped skeleton 403, the balloon 1 cannot expand in the directions of the upper and lower planes, so that the balloon 1 can only expand to the left and right sides, so that the balloon 1 is spread out flat. When expanding to the left and right, the middle part of the U-shaped skeleton 403 rotates inside the rotating hole 402.

[0029] For further reference, Figure 2 The top wall and the bottom wall of the inflation cavity 101 are both concave and have a plurality of contraction grooves 102;

[0030] In a specific implementation, by setting the contraction groove 102 , when the gas inside the inflation cavity 101 is exhausted, the outer wall of the balloon 1 can be folded at the position of the contraction groove 101 to facilitate the contraction of the balloon 1 .

[0031] Furthermore, the balloon 1 is made of medical silicone material.

[0032] Furthermore, an air pump is provided for inflating the air chamber 101;

[0033] During specific implementation, inflation is performed by an air pump.

Claims

1. A post-operative intracavitary anti-adhesion balloon structure, comprising a balloon (1), characterized in that: The balloon (1) is made of a flexible material and is arranged in a flat shape. An inflation chamber (101) is arranged inside the balloon (1). The top end of the connecting tube (2) is inserted into the inflation chamber (101). The bottom end of the connecting tube (2) is connected to a valve (3). The top outer wall of the connecting tube (2) is provided with a plurality of air outlet holes (201) connected to the inflation chamber (101). The inflation chamber (101) is provided with a contraction frame (4) fixed to the connecting tube (2). The top end of the connecting tube (2) is provided with a valve (3) connected to the inner wall of the inflation chamber (101). An integrated connecting horizontal block (202); the contraction frame (4) comprises two fixed blocks (401) fixed to the outer wall of the middle part of the connecting tube (2); the fixed blocks (401) are located inside the inflation chamber (101); at least one rotating hole (402) is provided on the fixed blocks (401); a U-shaped frame (403) is provided inside the rotating hole (402); two ends of the U-shaped frame (403) are respectively connected to the top wall and the bottom wall of the inflation chamber (101); and the middle part of the U-shaped frame (403) is rotatably connected to the rotating hole (402).

2. According to claim 1, a post-hysterectomy intracavitary anti-adhesion balloon structure, characterized in that: The top wall and the bottom wall of the inflation cavity (101) are both concave and provided with a plurality of contraction grooves (102).

3. According to claim 2, a post-hysterectomy intracavitary anti-adhesion balloon structure, characterized in that: The balloon (1) is made of medical silicone material.

4. The post-operative intrauterine anti-adhesion balloon structure according to claim 3, characterized in that: An air pump is also provided for inflating the air chamber (101).