Radial artery intervention postoperative puncture point hemostasis device

Abstract

The utility model belongs to the technical field of hemostasis tools, and particularly relates to a radial artery intervention postoperative puncture point hemostasis device which comprises a compression assembly, the compression assembly comprises a connecting frame and a hemostasis pad, the hemostasis pad is inserted into the inner side of the connecting frame, and a first adhesive tape is inserted into the top of the connecting frame. A first adhesive tape is inserted into the top of the connecting frame, a second adhesive tape is inserted into the top of the connecting frame, a third adhesive tape is inserted into the top of the connecting frame, an adhesive sticker is fixed to the bottom of one end of the first adhesive tape, and an elastic tape is fixedly connected to one end of the first adhesive tape. After the hemostatic pad is abutted against a puncture position, the hemostatic pad can be adhered to a wrist or a palm of a patient through the three adhesive tapes for fixation and compression hemostasis of the puncture position of the patient, and the adhesive tapes can be adhered to proper positions respectively according to specific conditions of the puncture position of the patient through the three adhesive tapes capable of rotating and adjusting. Convenience of adhesion operation is improved, the situation that fingers of a patient hinder adhesion of the hemostasis tool is avoided, and practicability is high.

Description

Technical Field

[0001] This utility model belongs to the field of hemostasis tool technology, specifically relating to a hemostasis device for the puncture point after radial artery intervention. Background Technology

[0002] After a patient undergoes radial artery interventional treatment, bleeding may occur at the puncture site, requiring hemostasis. Currently, tourniquets are typically used to apply pressure and stop the bleeding at the puncture site. However, this method is inconvenient, making it difficult to change the tourniquet. Furthermore, existing tourniquets need to be wrapped around the patient's hand or wrist, and when wrapped around the palm, the patient's fingers often interfere with the fixation of the tourniquet, thus affecting hemostasis.

[0003] Therefore, there is a need for a convenient, easy-to-replace, and highly practical device for stopping bleeding at the puncture site after radial artery interventional treatment. Utility Model Content

[0004] To address the aforementioned problems in the existing technology, this utility model provides a hemostasis device for the puncture point after radial artery intervention, which is convenient to operate, easy to care for, and highly practical.

[0005] To achieve the above objectives, this utility model provides the following technical solution: a hemostasis device for the puncture point after radial artery intervention, comprising a compression component, the compression component comprising a connecting frame and a hemostatic pad, the hemostatic pad being inserted into the inner side of the connecting frame, a first adhesive band being inserted into the top of the connecting frame, a second adhesive band being inserted into the top of the connecting frame, a third adhesive band being inserted into the top of the connecting frame, an adhesive patch being fixed to the bottom of one end of the first adhesive band, and an elastic band being fixedly connected to one end of the first adhesive band.

[0006] As a preferred technical solution of the radial artery interventional puncture point hemostasis device of this utility model, the top of the connecting frame is provided with a first slot, the bottom of the other end of the first adhesive band is fixed with a first insert ring, the first insert ring passes through the first adhesive band, and the first insert ring is inserted into the inner side of the first slot.

[0007] As a preferred technical solution of the radial artery interventional puncture point hemostasis device of this utility model, the top of the connecting frame is provided with a second slot, the second slot is located inside the first slot, one end of the second adhesive band is fixed with a second insert ring, the second insert ring passes through the second adhesive band, and the second insert ring is inserted into the inside of the second slot.

[0008] As a preferred technical solution of the radial artery interventional puncture point hemostasis device of this utility model, the top of the connecting frame is provided with a third slot, the third slot is located inside the second slot, one end of the third adhesive band is fixed with a third insert ring, the third insert ring passes through the third adhesive band, and the third insert ring is inserted into the inside of the third slot.

[0009] As a preferred technical solution of the radial artery interventional puncture site hemostasis device of this utility model, the second insertion ring penetrates the first insertion ring, and the third insertion ring penetrates the second insertion ring.

[0010] As a preferred technical solution of the radial artery interventional puncture point hemostasis device of this utility model, the length of the third insertion ring is greater than the length of the second insertion ring, and the length of the second insertion ring is greater than the length of the first insertion ring.

[0011] As a preferred technical solution of the radial artery interventional puncture point hemostasis device of this utility model, the first insertion ring, the second insertion ring and the third insertion ring are all made of elastic material.

[0012] Compared with the prior art, the beneficial effects of this utility model are:

[0013] In use, this invention utilizes a compression component, a first adhesive band, a second adhesive band, and a third adhesive band. The compression component consists of a connecting frame and a hemostatic pad. When stopping bleeding at the radial artery puncture site, the hemostatic pad is inserted into the inner side of the connecting frame. Then, one end of each of the first, second, and third adhesive bands is inserted into the top of the connecting frame. After the hemostatic pad is placed against the puncture site, it can be fixed to the patient's wrist or palm using the three adhesive bands, achieving compression hemostasis at the puncture site. The three adjustable adhesive bands can be adjusted to the appropriate position according to the specific condition of the puncture site, improving the convenience of the adhesion operation and preventing the patient's fingers from obstructing the adhesion of the hemostatic tool. It is highly practical.

[0014] Furthermore, the first adhesive band is equipped with an elastic band, and the second and third adhesive bands are also equipped with elastic band structures. When it is necessary to replace the hemostatic pad, the connecting frame can be pulled up to stretch the elastic band, making it easy to remove the hemostatic pad inside the connecting frame for replacement, which is convenient to operate. Attached Figure Description

[0015] The accompanying drawings are provided to further illustrate the present invention and form part of the specification. They are used together with the embodiments of the present invention to explain the present invention, but do not constitute a limitation thereof. In the drawings:

[0016] Figure 1 This is a schematic diagram of the overall structure of this utility model;

[0017] Figure 2 This is a three-dimensional sectional view of the present invention;

[0018] Figure 3 This is a three-dimensional schematic diagram of the compression component of this utility model;

[0019] Figure 4 This is a schematic diagram of the first adhesive band, the second adhesive band, and the third adhesive band of this utility model.

[0020] In the diagram: 1. Compression component; 11. Connecting frame; 111. First slot; 112. Second slot; 113. Third slot; 12. Hemostatic pad; 2. First adhesive band; 21. First insert ring; 22. Adhesive patch; 23. Elastic band; 3. Second adhesive band; 31. Second insert ring; 4. Third adhesive band; 41. Third insert ring. Detailed Implementation

[0021] The technical solutions of the present utility model will be clearly and completely described below with reference to the accompanying drawings of the embodiments. Obviously, the described embodiments are only some embodiments of the present utility model, and not all embodiments. Based on the embodiments of the present utility model, all other embodiments obtained by those of ordinary skill in the art without creative effort are within the protection scope of the present utility model.

[0022] Example

[0023] Please see Figure 1-4 This utility model provides the following technical solution: a hemostasis device for the puncture point after radial artery intervention, including a compression component 1. The compression component 1 includes a connecting frame 11 and a hemostatic pad 12. The hemostatic pad 12 is inserted into the inner side of the connecting frame 11. The hemostatic pad 12 is made of existing hemostatic materials. A first adhesive band 2, a second adhesive band 3, and a third adhesive band 4 are inserted into the top of the connecting frame 11. The adhesive bands can be adhered to the patient's wrist or palm for fixation. An adhesive sticker 22, which is made of an adhesive material, is fixed to the bottom of one end of the first adhesive band 2, ensuring stable adhesion. (See attached drawing.) Figure 2 Appendix Figure 3 and attached Figure 4The top of the connecting frame 11 is provided with a first slot 111, and the bottom of the other end of the first adhesive strip 2 is fixed with a first insert ring 21, which passes through the first adhesive strip 2 and is inserted into the inner side of the first slot 111; the top of the connecting frame 11 is provided with a second slot 112, which is located inside the first slot 111, and the bottom of one end of the second adhesive strip 3 is fixed with a second insert ring 31, which passes through the second adhesive strip 3 and is inserted into the inner side of the second slot 112; the connecting frame 11's... The top is provided with a third slot 113, which is located inside the second slot 112. A third insert ring 41 is fixed to the bottom of one end of the third adhesive strip 4. The third insert ring 41 passes through the third adhesive strip 4 and is inserted into the inside of the third slot 113. The insertion method is convenient for disassembly and assembly. In use, multiple adhesive strips are inserted into the top of the connecting frame 11. The connecting frame 11 can be fixed by multiple adhesive strips, thereby stably pressing the hemostatic pad 12 against the patient's puncture site for hemostasis. The structure is simple and the operation is convenient.

[0024] Reference Figure 2 and Figure 3 As shown, specifically, the second insertion ring 31 penetrates the first insertion ring 21, and the third insertion ring 41 penetrates the second insertion ring 31; the length of the third insertion ring 41 is greater than the length of the second insertion ring 31, and the length of the second insertion ring 31 is greater than the length of the first insertion ring 21; the first insertion ring 21, the second insertion ring 31, and the third insertion ring 41 are all made of elastic material. The elastic material ensures stable insertion of the insertion rings without affecting their rotation. This solution uses rotatable adhesive bands to adhere and fix the hemostatic pad 12. Depending on the specific situation of the patient's puncture site, the adhesive bands can be rotated to adhere multiple adhesive bands to appropriate positions, avoiding the situation where the patient's fingers easily interfere with the adhesion and fixation of the hemostatic tool during routine operations, thus improving the practicality of the hemostatic tool.

[0025] Reference Figure 1 As shown, specifically, one end of the first adhesive band 2 is fixedly connected to an elastic band 23. The elastic band 23 can stretch the adhesive band without affecting its fixation. In this solution, when the hemostatic pad 12 needs to be replaced, the connecting frame 11 can be pulled upward to stretch the elastic band 23, and then the hemostatic pad 12 can be easily disassembled and replaced.

[0026] The working principle and usage process of this utility model are as follows: When performing hemostasis at the puncture site after radial artery interventional treatment, the hemostatic pad 12 is inserted into the inner side of the connecting frame 11. Then, one end of the first adhesive band 2, the second adhesive band 3, and the third adhesive band 4 are all inserted into the top of the connecting frame 11. Then, according to the position of the puncture site on the patient's hand, the three adhesive bands are rotated to adhere the ends of the adhesive bands to the appropriate position on the patient's hand, so that the hemostatic pad 12 is pressed against the puncture site, making the adhesion operation more convenient and more stable, and highly practical.

[0027] Finally, it should be noted that the above description is merely a preferred embodiment of this utility model and is not intended to limit the utility model. Although the utility model has been described in detail with reference to the foregoing embodiments, those skilled in the art can still modify the technical solutions described in the foregoing embodiments or make equivalent substitutions for some of the technical features. Any modifications, equivalent substitutions, improvements, etc., made within the spirit and principles of this utility model should be included within the protection scope of this utility model.

Claims

1. A radial artery post intervention access site hemostasis device comprising a compression assembly (1), characterized in that: The compression assembly (1) comprises a connecting frame (11) and a hemostatic pad (12), the inner side of the connecting frame (11) is inserted with the hemostatic pad (12), the top of the connecting frame (11) is inserted with a first adhesive tape (2), the top of the connecting frame (11) is inserted with a second adhesive tape (3), the top of the connecting frame (11) is inserted with a third adhesive tape (4), one end of the first adhesive tape (2) is fixedly provided with an adhesive patch (22) at the bottom, one end of the first adhesive tape (2) is fixedly connected with an elastic band (23), the top of the connecting frame (11) is provided with a first insertion slot (111), the other end of the first adhesive tape (2) is fixedly provided with a first insertion ring (21) at the bottom, the first insertion ring (21) penetrates through the first adhesive tape (2), and the first insertion ring (21) is inserted into the inner side of the first insertion slot (111); the top of the connecting frame (11) is provided with a second insertion slot (112), the second insertion slot (112) is located on the inner side of the first insertion slot (111), one end of the second adhesive tape (3) is fixedly provided with a second insertion ring (31) at the bottom, the second insertion ring (31) penetrates through the second adhesive tape (3), and the second insertion ring (31) is inserted into the inner side of the second insertion slot (112); the top of the connecting frame (11) is provided with a third insertion slot (113), the third insertion slot (113) is located on the inner side of the second insertion slot (112), one end of the third adhesive tape (4) is fixedly provided with a third insertion ring (41) at the bottom, the third insertion ring (41) penetrates through the third adhesive tape (4), and the third insertion ring (41) is inserted into the inner side of the third insertion slot (113).

2. The radial artery post-procedure access site hemostasis device of claim 1, wherein: The second insertion ring (31) penetrates through the first insertion ring (21), and the third insertion ring (41) penetrates through the second insertion ring (31).

3. The radial artery post-interventional access site hemostasis device according to claim 2, wherein: The length of the third insertion ring (41) is greater than that of the second insertion ring (31), and the length of the second insertion ring (31) is greater than that of the first insertion ring (21).

4. The radial artery post-interventional access site hemostasis device according to claim 3, wherein: The first insertion ring (21), the second insertion ring (31) and the third insertion ring (41) are all made of elastic material.

Images