Hemostatic balloon for uterine cavity

By setting a guide tube and a drainage tube in the uterine cavity hemostasis balloon and stamping with cleaning liquid, the problem of blood duct shrinkage caused by the introduction of plastic drawstrings in the prior art is solved, and effective serum blockage and rapid hemostasis are achieved.

CN222676323UActive Publication Date: 2025-03-28YUNNAN BAIYAO GRP CO LTD +1
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Patent Information

Application Number
CN202420489651.0
Authority / Receiving Office
CN · China
Patent Type
Utility models(China)
Current Assignee / Owner
Filing Date
2024-03-13
Publication Date
2025-03-28
Estimated Expiration
2034-03-13

AI Technical Summary

Technical Problem

When the existing hemostasis balloons used for uterine cavity clear up blocked blood stasis, the introduction of plastic drawstrings will narrow the blood tract and hinder the excretion of blood stasis.

Method used

A hemostasis balloon for uterine cavity is designed. By setting up a guide tube and a drainage tube, the cleaning fluid is provided by the liquid supply equipment, and the water pressure is controlled. The cleaning fluid is transported to the drainage tube through the guide tube, and the blood stasis at the blood induction mouth is stamped to prevent blockage.

Benefits of technology

While not affecting the blood flow, the blockage clearing function is realized, which is faster to use and improves work efficiency.

✦ Generated by Eureka AI based on patent content.

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Abstract

The utility model relates to the technical field of medical instruments, and provides a uterine cavity hemostasis balloon which comprises a main catheter, a first balloon body and a second balloon body, the first balloon body and the second balloon body are arranged at one end of the main catheter in a spaced mode, a drainage tube is arranged in the main catheter, one end of the drainage tube is provided with a blood guide opening, and the other end of the drainage tube is provided with a blood outlet. A first guide pipe and a second guide pipe are further arranged in the main guide pipe, one end of the first guide pipe and one end of the second guide pipe are both communicated with the drainage pipe, cleaning liquid can be transmitted into the drainage pipe through the first guide pipe and the second guide pipe, blockage of the blood guide opening is removed, the cleaning liquid is provided by liquid supply equipment, and the water pressure of the cleaning liquid is further controlled. Cleaning liquid is conveyed to the first guide pipe and the second guide pipe through the connecting pipe and conveyed to the drainage pipe through the first guide pipe and the second guide pipe, extravasated blood at the blood guide opening is stamped, the blood guide opening is prevented from being blocked, in the process, the blockage clearing function can be achieved while the blood guide flow is not affected, use is faster, and the working efficiency is improved.
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Description

Technical Field

[0001] The utility model relates to the technical field of medical devices, and more specifically to a hemostatic balloon for uterine cavity. Background Art

[0002] The uterine cavity is the space of the uterus, also called the uterus. The uterus is a single muscular organ. During normal delivery, the mother's body has a perfect self-hemostatic function, including strong contraction of the uterus to compress the capillaries in the placenta and fetal membrane detachment wound in the cavity. The body's coagulation system is activated and works together to play a hemostatic role. When the above two self-hemostatic functions are destroyed, excessive postpartum bleeding may occur. Intrauterine balloon compression is a conservative treatment method for postpartum hemorrhage. Water is injected into the balloon to make the balloon continue to expand, thereby forming a compression effect on the blood vessels at the bleeding site, thereby achieving the hemostatic function.

[0003] In the existing hemostasis technology, an anti-blocking structure is set up, and a plastic pull rope is used to pass through the guide tube and the inside of the blood guide groove in sequence and fixedly connected to one end of the retaining groove. When blood stasis blocks the blood guide groove, the retaining groove is inserted into the blood guide groove by pulling and pulling the plastic pull rope, and the blood stasis condensed in the blood guide groove is squeezed and broken, so that the blood stasis can flow into the inside of the main guide tube through the blood guide groove and be discharged from the blood drainage tube, thereby preventing the discharge of blood stasis from being blocked. However, in this process, the plastic pull rope runs through the inside of the blood guide groove. Although it can clear the blocked blood stasis, the introduction of the plastic pull rope also shrinks the blood guide groove, hindering the discharge of blood stasis. Utility Model Content

[0004] The technical problem to be solved by the utility model is to provide a hemostatic balloon for the uterine cavity which can effectively clear the blocked blood stasis and does not hinder the discharge of the blood stasis.

[0005] The technical solution adopted by the utility model to solve its technical problems is:

[0006] A hemostatic balloon for uterine cavity, the hemostatic balloon comprises a main catheter, a balloon body 1 and a balloon body 2 which are arranged at intervals at one end of the main catheter, a drainage tube is arranged in the main catheter, a blood drainage port is arranged at one end of the drainage tube, a guide tube 1 and a guide tube 2 are also arranged in the main catheter, one end of the guide tube 1 and the guide tube 2 are both connected to the drainage tube, a cleaning liquid can be transferred to the drainage tube through the guide tube 1 and the guide tube 2, and the blood drainage port can be cleared.

[0007] Furthermore, a first connecting pipe and a second connecting pipe are provided in the main conduit, and an inner wall of one end of the main conduit is sealedly connected to an outer wall of the drainage pipe.

[0008] Furthermore, one end of the first connecting tube passes through the tube wall of the main tube and is connected to the balloon body, and the other end of the first connecting tube is connected to an energy supply device.

[0009] Furthermore, one end of the second connecting tube passes through the tube wall of the main tube and is connected to the balloon body, and the other end of the second connecting tube is connected to the energy supply device.

[0010] Furthermore, a first pipe clamp and a second pipe clamp are respectively provided on the first connecting pipe and the second connecting pipe.

[0011] Furthermore, one end of the guide tube 1 and the guide tube 2 are both connected to a connecting tube, and the other end of the connecting tube is connected to a liquid supply device.

[0012] The beneficial effects of the utility model are:

[0013] By setting guide tube one and guide tube two, cleaning liquid is provided by liquid supply equipment, and the water pressure of the cleaning liquid is further controlled. The cleaning liquid is transported to guide tube one and guide tube two through the connecting tube, and then transported to the drainage tube by guide tube one and guide tube two, so as to press the blood congestion at the blood drainage port to prevent the blood drainage port from being blocked. In this process, the function of clearing blockage can be realized without affecting the blood drainage flow, which makes it quicker to use and improves work efficiency. BRIEF DESCRIPTION OF THE DRAWINGS

[0014] The utility model is further described below in conjunction with the accompanying drawings and embodiments.

[0015] In the figure:

[0016] Figure 1 This is a front view of the hemostatic balloon of the utility model;

[0017] Figure 2 It is a schematic diagram of the three-dimensional structure of the hemostatic balloon in the utility model;

[0018] Figure 3 It is a left view of the hemostatic balloon in the utility model;

[0019] Figure 4 for Figure 1 A cross-sectional view cut along the AA direction;

[0020] Figure 5 for Figure 3 A cross-sectional view taken along the BB direction;

[0021] Figure 6 for Figure 4 Enlarged view of area C in the middle;

[0022] Among them, 10, main guide tube; 11, balloon body one; 12, balloon body two; 13, first connecting tube; 14, second connecting tube; 15, drainage tube; 16, guide tube one; 17, guide tube two; 18, blood inlet; 19, connecting tube; 20, tube clamp one; 21, tube clamp two; 22, liquid collection belt. DETAILED DESCRIPTION

[0023] Now the utility model is described in detail with reference to the accompanying drawings. This figure is a simplified schematic diagram, which only illustrates the basic structure of the utility model in a schematic manner, so it only shows the components related to the utility model.

[0024] Reference Figures 1 to 6 As shown, a hemostatic balloon for uterine cavity includes a main catheter 10, a balloon body 11 and a balloon body 2 12 which are spaced apart at one end of the main catheter 10, a drainage tube 15, a first connecting tube 13, and a second connecting tube 14 are arranged in the main catheter 10, the inner wall of one end of the main catheter 10 is sealedly connected to the outer wall of the drainage tube 15, and a blood drainage port 18 is arranged at one end of the drainage tube 15.

[0025] The other end of the drainage tube 15 is connected to a negative pressure pump, and the other end of the negative pressure pump is connected to a liquid collecting belt 22. By starting the negative pressure pump, the blood congestion in the uterus is drawn out by the drainage tube 15 and then collected by the liquid collecting belt 22. In this embodiment, scale lines are provided on the liquid collecting belt 22, so that the patient's bleeding volume can be clearly understood in preparation for subsequent rescue work.

[0026] One end of the first connecting tube 13 passes through the wall of the main catheter 10 and is connected to the balloon body 11. The other end of the first connecting tube 13 is connected to the energy supply device, and physiological saline or gas can be provided by the energy supply device and transported to the balloon body 11 by the first connecting tube 13. After the balloon body 11 expands, it fits against the inner wall of the uterus to compress the bleeding area of ​​the inner wall of the uterus to stop bleeding.

[0027] One end of the second connecting tube 14 passes through the wall of the main catheter 10 and is connected to the balloon body 12. The other end of the second connecting tube 14 is connected to the energy supply device, and physiological saline or gas can be provided by the energy supply device and transported to the balloon body 12 by the second connecting tube 14. After the balloon body 12 is expanded, it fits against the patient's cervix to increase the stability of the balloon body 11.

[0028] The first connecting tube 13 and the second connecting tube 14 are respectively provided with a tube clamp 1 20 and a tube clamp 2 21. In this embodiment, by providing the tube clamp 1 20 and the tube clamp 2 21, when the physiological saline or gas in the balloon body 11 and the balloon body 2 12 is perfused to an appropriate degree, the perfusion will be stopped. At this time, the medical staff will move the tube clamp 1 20 and the tube clamp 2 21 to seal the first connecting tube 13 and the second connecting tube 14 through the tube clamp 1 20 and the tube clamp 2 21 to prevent the medium in the balloon body 11 and the balloon body 2 12 from leaking.

[0029] A guide tube 16 and a guide tube 2 17 are also provided in the main conduit 10. One ends of the guide tube 16 and the guide tube 2 17 are both connected to the drainage tube 15, and the other ends of the guide tube 16 and the guide tube 2 17 are both connected to a connecting tube 19. The other end of the connecting tube 19 is connected to a liquid supply device, which provides a cleaning liquid and further controls the water pressure of the cleaning liquid. The cleaning liquid is transported to the guide tube 16 and the guide tube 2 17 through the connecting tube 19, and then transported to the drainage tube 15 by the guide tube 16 and the guide tube 2 17 to punch the blood congestion at the blood outlet 18 to prevent the blood outlet 18 from being blocked.

[0030] The working principle of this utility model:

[0031] One end of the first connecting tube 13 and the second connecting tube 14 are both connected to the energy supply device, and physiological saline or gas is provided by the energy supply device and transported to the balloon body 11 through the first connecting tube 13. After the balloon body 11 expands, it fits against the inner wall of the uterus to compress and stop bleeding at the bleeding site of the inner wall of the uterus; and transported to the balloon body 2 12 through the second connecting tube 14. After the balloon body 2 12 expands, it fits against the patient's cervix to increase the stability of the balloon body 11.

[0032] When the physiological saline or gas in the balloon body 11 and the balloon body 2 12 is infused to an appropriate degree, the infusion will be stopped. At this time, the medical staff will move the tube clamp 1 20 and the tube clamp 2 21 to seal the first connecting tube 13 and the second connecting tube 14 through the tube clamp 1 20 and the tube clamp 2 21 to prevent the medium in the balloon body 11 and the balloon body 2 12 from leaking.

[0033] The other ends of guide tube 16 and guide tube 2 17 are connected to connecting tube 19, and the other ends of connecting tube 19 are connected to a liquid supply device, which provides cleaning liquid and further controls the water pressure of the cleaning liquid. The cleaning liquid is transported to guide tube 16 and guide tube 2 17 through connecting tube 19, and then transported to drainage tube 15 by guide tube 16 and guide tube 2 17 to punch out the blood congestion at the blood outlet 18 to prevent the blood outlet 18 from being blocked.

[0034] The drainage tube 15 drains the blood in the uterus and then collects it through the collection belt 22.

[0035] Beneficial effects of the utility model:

[0036] By setting up guide tube 16 and guide tube 2 17, cleaning liquid is provided by a liquid supply device, and the water pressure of the cleaning liquid is further controlled. The cleaning liquid is transported to guide tube 16 and guide tube 2 17 through connecting tube 19, and then transported to drainage tube 15 by guide tube 16 and guide tube 2 17 to press the blood congestion at the blood drawing port 18 to prevent the blood drawing port 18 from being blocked. In this process, the function of clearing blockage can be achieved without affecting the blood drawing flow rate, which makes it quicker to use and improves work efficiency.

[0037] It should be noted that the terms used herein are only for describing specific embodiments and are not intended to limit the exemplary embodiments according to the present application. As used herein, unless the context clearly indicates otherwise, the singular form is also intended to include the plural form. In addition, it should be understood that when the terms "comprise" and / or "include" are used in this specification, it indicates the presence of features, steps, operations, devices, components and / or combinations thereof.

[0038] It should be noted that the terms "first", "second", etc. in the specification and claims of the present application and the above-mentioned drawings are used to distinguish similar objects, and are not necessarily used to describe a specific order or sequence. It should be understood that the numbers used in this way can be interchanged where appropriate, so that the embodiments of the present application described herein can be implemented in an order other than those illustrated or described herein.

[0039] Based on the above ideal embodiments of the utility model, the relevant staff can make various changes and modifications without departing from the scope of the utility model through the above description. The technical scope of this utility model is not limited to the contents of the specification, and its technical scope must be determined according to the scope of the claims.

Claims

1. A hemostatic balloon for uterine cavity, characterized in that: The hemostatic balloon includes a main catheter, a balloon body 1 and a balloon body 2 which are spaced apart at one end of the main catheter, a drainage tube is arranged in the main catheter, a blood drainage port is arranged at one end of the drainage tube, a guide tube 1 and a guide tube 2 are also arranged in the main catheter, one end of the guide tube 1 and the guide tube 2 are both connected to the drainage tube, a cleaning liquid can be transferred to the drainage tube through the guide tube 1 and the guide tube 2, and the blood drainage port can be cleared.

2. A hemostatic balloon for uterine cavity according to claim 1, characterized in that: A first connecting pipe and a second connecting pipe are also provided in the main conduit, and an inner wall of one end of the main conduit is sealedly connected to an outer wall of the drainage pipe.

3. The intrauterine hemostatic balloon according to claim 2, characterized in that: One end of the first connecting tube penetrates through the tube wall of the main tube and is communicated with the balloon body, and the other end of the first connecting tube is communicated with an energy supply device.

4. The intrauterine hemostatic balloon according to claim 2, characterized in that: One end of the second connecting tube passes through the tube wall of the main tube and is communicated with the balloon main body. The other end of the second connecting tube is connected to the energy supply device.

5. The intrauterine hemostatic balloon according to claim 2, characterized in that: The first connecting pipe and the second connecting pipe are respectively provided with a first pipe clamp and a second pipe clamp.

6. The intrauterine hemostatic balloon according to claim 1, characterized in that: One end of the guide tube 1 and the guide tube 2 are both connected to a connecting tube, and the other end of the connecting tube is connected to a liquid supply device.