A dual-point positioning compression hemostasis device

Abstract

This utility model belongs to the technical field of compression hemostasis devices, specifically relating to a dual-point positioning compression hemostasis device. It includes a fixing part, a first hemostasis part, and a second hemostasis part. The first hemostasis part includes a first positioning frame and a first pressing element; the first pressing element and the first positioning frame are detachably connected. The second hemostasis part includes a second positioning frame and a second pressing element; the second pressing element and the second positioning frame are detachably connected. Both ends of the fixing part are slidably connected to the first and second positioning frames, respectively. It also includes an adjustment part; both ends of the adjustment part are detachably connected to the first and second positioning frames, respectively. The first and second hemostasis parts provide precise compression hemostasis at skin puncture points and vascular puncture points, effectively preventing subcutaneous hematoma and fistula endothelial damage, thus extending the lifespan of the arteriovenous fistula. The states of the first and second hemostasis parts can be adjusted to regulate the pressure intensity, meeting the dual requirements of dual-point positioning and precise pressure control.

Description

Technical Field

[0001] This utility model belongs to the technical field of compression hemostasis devices, specifically relating to a dual-point positioning compression hemostasis device. Background Technology

[0002] Arteriovenous fistulas are the core vascular access for maintenance hemodialysis in patients with end-stage renal disease. After hemodialysis, precise compression of the fistula puncture site is required to stop bleeding. The core requirements are to achieve double-point alignment, controllable pressure, and continuous stability. It is necessary to avoid bleeding at the puncture site and prevent excessive compression from causing blood flow blockage and thrombosis in the fistula. At the same time, it is necessary to adapt to the narrow operating space of the wrist / forearm and the differences in arm size among different patients.

[0003] Currently, most arteriovenous fistula compression hemostasis devices used in clinical and home settings are single-pressure surfaces or simple bandage structures, lacking a dual-point positioning structure. The compression point is only aligned with the skin puncture point and does not cover the vascular puncture point, which can easily lead to subcutaneous hematoma and damage to the fistula endothelium, affecting the lifespan of the arteriovenous fistula. Utility Model Content

[0004] To address the aforementioned issues, this application discloses a dual-point positioning compression hemostasis device.

[0005] A dual-point positioning compression hemostasis device includes a fixing part, a first hemostasis part, and a second hemostasis part. The first hemostasis part includes a first positioning frame and a first pressing member; the first pressing member and the first positioning frame are detachably connected. The second hemostasis part includes a second positioning frame and a second pressing member; the second pressing member and the second positioning frame are detachably connected. One end of the fixing part is slidably connected to the first positioning frame, and the other end is slidably connected to the second positioning frame. The device also includes an adjustment part; one end of the adjustment part is detachably connected to the end of the first positioning frame away from the fixing part, and the other end is detachably connected to the end of the second positioning frame away from the fixing part.

[0006] Furthermore, the first pressing component includes a first pressure adjusting structure, a first connecting rod, a first support frame, and a first pressing structure; the outer wall of the first pressure adjusting structure is detachably connected to the first support frame; one end of the first connecting rod is fixedly connected to the first support frame, and the other end passes through the first adjusting structure; the first pressing structure is wrapped around the outer wall of the first connecting rod; one end of the first pressing component abuts against the first support frame, and the other end abuts against the first pressure adjusting structure.

[0007] Furthermore, the second pressing component includes a second pressure adjusting structure, a second connecting rod, a second support frame, and a second pressing structure; the outer wall of the second pressure adjusting structure is detachably connected to the second support frame; one end of the second connecting rod is fixedly connected to the second support frame, and the other end passes through the second adjusting structure; the second pressing structure is wrapped around the outer wall of the second connecting rod; one end of the second pressing component abuts against the second support frame, and the other end abuts against the second pressure adjusting structure.

[0008] Furthermore, the fixing part includes a first fixing strap and a second fixing strap; one end of the first fixing strap is detachably connected to the second fixing strap, and the other end is connected to the first support frame; the end of the second fixing strap away from the first fixing strap is connected to the second support frame.

[0009] The beneficial effects of this utility model are:

[0010] The first and second hemostatic parts provide precise pressure to stop bleeding at the skin puncture point and vascular puncture point, respectively, effectively preventing subcutaneous hematoma and damage to the fistula lining, thus extending the lifespan of the arteriovenous fistula. The states of the first and second hemostatic parts can be adjusted to regulate the pressure, meeting the dual requirements of dual-point positioning and precise pressure control.

[0011] The first and second hemostatic parts are attached to the patient's body surface using the fixation part. Then, the adjustment part is used to adjust the lateral and longitudinal distances between the first and second hemostatic parts so that the first and second hemostatic parts are aligned with the skin puncture point and the blood vessel puncture point respectively, so as to apply precise pressure to the skin puncture point and the blood vessel puncture point. Attached Figure Description

[0012] Figure 1 A perspective view of a dual-point positioning compression hemostasis device that implements this utility model;

[0013] Figure 2 A top view of a dual-point positioning compression hemostasis device that implements this utility model;

[0014] Figure 3 for Figure 2 Sectional view along axis AA;

[0015] Figure 4 A front view of a dual-point positioning compression hemostasis device that implements this utility model;

[0016] In the figure, 1 is the fixing part; 2 is the first hemostatic part; 3 is the second hemostatic part; 4 is the adjusting part; 11 is the first fixing strap; 12 is the second fixing strap; 21 is the first positioning frame; 22 is the first pressing element; 23 is the first limiting element; 211 is the first fixing bracket; 212 is the first adjusting bracket; 213 is the first hemostatic bracket; 221 is the first pressure regulating structure; 222 is the first connecting rod; 223 is the first support frame; 224 is the first buffer structure; 225 is the first pressing structure; 31 is the second positioning frame; 32 is the second pressing element; 311 is the second adjusting bracket; 312 is the second fixing bracket. Detailed Implementation

[0017] To make the objectives, technical solutions, and advantages of this application clearer, the technical solutions of this application will be clearly and completely described below in conjunction with specific embodiments and corresponding drawings. Obviously, the described embodiments are only a part of the embodiments of this application, and not all of them. Based on the embodiments in this application, all other embodiments obtained by those skilled in the art without creative effort are within the scope of protection of this application.

[0018] In this document, “illustrative” means “serving as an example, illustration or description”, and any illustration or implementation described herein as “illustrative” should not be construed as a more preferred or advantageous technical solution.

[0019] To keep the drawings concise, only the parts relevant to this application are shown schematically in each drawing, and they do not represent the actual structure of the product. In addition, to make the drawings concise and easy to understand, in some drawings, only one of the components with the same structure or function is shown schematically, or only one of them is labeled.

[0020] In this document, it should be understood that the terms "longitudinal", "lateral", "up", "down", "front", "back", "inner", and "outer" indicate the orientation or positional relationship based on the orientation or positional relationship shown in the accompanying drawings. They are used only for the convenience of describing this utility model and simplifying the description, and do not indicate or imply that the device or component referred to must have a specific orientation, or be constructed and operated in a specific orientation. Therefore, they should not be construed as limitations on this utility model.

[0021] In this document, unless otherwise expressly specified and limited, the terms "first" and "second" are used for descriptive purposes only and should not be construed as indicating or implying relative importance; the terms "connection," "fixed," etc., should be interpreted broadly. For example, "connection" can be a fixed connection, a detachable connection, an integral connection, or an electrical connection; it can be a direct connection or an indirect connection through an intermediate medium. Those skilled in the art can understand the specific meaning of the above terms in this application according to the specific circumstances.

[0022] like Figure 1-4 The illustrated dual-point positioning compression hemostasis device includes a fixing part 1, a first hemostasis part 2, and a second hemostasis part 3. The first hemostasis part 2 includes a first positioning frame 21 and a first pressing element 22; the first pressing element 22 is detachably connected to the first positioning frame 21. The second hemostasis part 3 includes a second positioning frame 31 and a second pressing element 32; the second pressing element 32 is detachably connected to the second positioning frame 31. One end of the fixing part 1 is slidably connected to the first positioning frame 21, and the other end is slidably connected to the second positioning frame 31. It also includes an adjustment part 4; one end of the adjustment part 4 is detachably connected to the end of the first positioning frame 21 away from the fixing part 1, and the other end is detachably connected to the end of the second positioning frame 31 away from the fixing part 1. The first hemostasis part 2 and the second hemostasis part 3 provide precise compression hemostasis at skin puncture points and vascular puncture points, effectively preventing subcutaneous hematoma and fistula endothelial damage, and extending the lifespan of the arteriovenous fistula. The states of the first hemostatic part 2 and the second hemostatic part 3 can be adjusted separately to regulate the pressure, meeting the dual requirements of dual-point positioning and precise pressure control.

[0023] When in use, the fixing part 1 is used to attach the first hemostatic part 2 and the second hemostatic part 3 to the patient's body surface. Then, the adjusting part 4 is used to adjust the lateral and longitudinal distances between the first hemostatic part 2 and the second hemostatic part 3 so that the first hemostatic part 2 and the second hemostatic part 3 are respectively aligned with the skin puncture point and the blood vessel puncture point, so as to apply precise pressure to the skin puncture point and the blood vessel puncture point.

[0024] like Figure 1-3 As shown, the first pressing component 22 includes a first pressure adjusting structure 221, a first connecting rod 222, a first support frame 223, and a first pressing structure 225. The outer wall of the first pressure adjusting structure 221 is detachably connected to the first support frame 223. One end of the first connecting rod 222 is fixedly connected to the first support frame 223, and the other end passes through the first adjusting structure. The first pressing structure 225 is wrapped around the outer wall of the first connecting rod 222. One end of the first pressing component 22 abuts against the first support frame 223, and the other end abuts against the first pressure adjusting structure 221. In use, the first positioning frame 21 is aligned with the skin puncture point or blood vessel puncture point, and then the fixing part 1 is used to wear the first positioning frame 21 on the patient's body surface. Then, the first pressure adjusting structure 221 is rotated, and the first pressure adjusting structure 221 moves towards the patient's body surface, thereby compressing the first pressing structure 225, so that the first support frame 223 compresses the skin puncture point or blood vessel puncture point to stop bleeding.

[0025] Specifically, the first pressing structure 225 is a linear compression spring. According to the spring force formula, the pressure on the spring is proportional to the change in its length. Therefore, by measuring the deformation of the first pressing structure 225, the pressure exerted by the patient's skin on the first pressing structure 225 can be obtained. This pressure is the pressure exerted by the first support frame 223 on the skin puncture point or blood vessel puncture point. Based on this principle, a scale is set at the end of the first connecting rod 222 away from the first support frame 223. Based on the length of the first connecting rod 222 passing through the first adjustment structure, the pressure of the first support frame 223 on the skin puncture point or blood vessel puncture point under the current condition can be obtained.

[0026] Preferably, a first hemostatic bracket 213 is fixedly connected to the first positioning frame 21; the first hemostatic bracket 213 is threadedly connected to the first pressure regulating structure 221. Rotating the first pressure regulating structure 221 changes its position, thereby adjusting the pressure of the first pressing element 22 on the skin puncture point or blood vessel puncture point.

[0027] Furthermore, the first pressing component 22 also includes a first buffer structure 224; the first buffer structure 224 is detachably connected to the side of the first support frame 223 away from the first connecting rod 222. The first buffer structure 224 can be replaced by hand, and the main components can be sterilized at high temperatures, taking into account both disposable hygiene requirements and the economy of reuse, making it suitable for mass use in dialysis rooms and for patients' home use.

[0028] Specifically, the first buffer structure 224 includes an absorbent sponge.

[0029] In some embodiments of this application, the first hemostatic part 2 further includes a first limiting member 23; the first limiting member 23 is threadedly connected to the first pressure adjusting structure 221. The first limiting member 23 is located in the direction away from the patient from the first hemostatic frame. In use, the first pressure adjusting structure 221 is rotated to adjust the pressure of the first pressing member 22 on the patient. Then, the first limiting member 23 is tightened, causing the first limiting member 23 to press against the side wall of the first hemostatic frame, generating additional friction and preventing the first pressure adjusting structure 221 from loosening.

[0030] The structure of the second pressing member 32 is the same as that of the first pressing member 22. For example... Figure 1-3As shown, the second pressing component 32 includes a second pressure adjusting structure, a second connecting rod, a second support frame, and a second pressing structure. The outer wall of the second pressure adjusting structure is detachably connected to the second support frame. One end of the second connecting rod is fixedly connected to the second support frame, and the other end passes through the second adjusting structure. The second pressing structure is wrapped around the outer wall of the second connecting rod. One end of the second pressing component 32 abuts against the second support frame, and the other end abuts against the second pressure adjusting structure. In use, the second positioning frame 31 is aligned with the skin puncture point or blood vessel puncture point, and then the fixing part 1 is used to wear the second positioning frame 31 on the patient's body surface. Then, the second pressure adjusting structure is rotated, and the second pressure adjusting structure moves towards the patient's body surface, thereby compressing the second pressing structure, so that the second support frame compresses the skin puncture point or blood vessel puncture point to stop bleeding.

[0031] Specifically, the second pressing structure is a linear compression spring. According to the spring force formula, the pressure on a spring is directly proportional to its length change. Therefore, by measuring the deformation of the second pressing structure, the pressure exerted by the patient's skin on it can be determined. This pressure is the pressure exerted by the second support frame on the skin puncture point or blood vessel puncture point. Based on this principle, a scale is set at the end of the second connecting rod away from the second support frame. By measuring the length of the second connecting rod passing through the second adjustment structure, the pressure of the second support frame on the skin puncture point or blood vessel puncture point under the current condition can be determined.

[0032] Preferably, a second hemostatic bracket is fixedly connected to the second positioning frame 31; the second hemostatic bracket is threadedly connected to the second pressure regulating structure. Rotating the second pressure regulating structure changes its position, thereby adjusting the pressure of the second pressing element 32 on the skin puncture point or blood vessel puncture point.

[0033] Furthermore, the second pressing component 32 also includes a second buffer structure; the second buffer structure is detachably connected to the side of the second support frame away from the second connecting rod. The second buffer structure can be replaced by hand, and the main components can be sterilized at high temperatures, taking into account both disposable hygiene requirements and the economy of reusability, making it suitable for mass use in dialysis rooms and for patients' home use.

[0034] Specifically, the second buffer structure includes an absorbent sponge.

[0035] In some embodiments of this application, the second hemostatic part 3 further includes a second limiting member; the second limiting member is threadedly connected to the second pressure adjusting structure. The second limiting member is located in the direction away from the patient from the second hemostatic frame. In use, the second pressure adjusting structure is rotated to adjust the pressure of the second pressing member 32 on the patient. Then, the second limiting member is tightened so that the second limiting member presses against the side wall of the second hemostatic frame, generating additional frictional force to prevent the second pressure adjusting structure from loosening.

[0036] like Figure 1-4As shown, the fixing part 1 includes a first fixing strap 11 and a second fixing strap 12; one end of the first fixing strap 11 is detachably connected to the second fixing strap 12, and the other end is connected to the first positioning frame 21; the end of the second fixing strap 12 away from the first fixing strap 11 is connected to the second positioning frame 31. The fixing part 1, the first hemostatic part 2, the second hemostatic part 3, and the adjusting part 4 form a ring-shaped structure. By adjusting the total length of the first fixing strap 11 and the second fixing strap 12, the size of this ring-shaped structure can be adjusted, thereby allowing this ring-shaped structure to be worn on the patient's body surface.

[0037] The first positioning frame 21 has a first fixed bracket 211 at one end and a first adjusting bracket 212 at the other end; the first fixed bracket 211 is connected to the fixing part 1; the first adjusting bracket 212 is connected to the adjusting part 4. The second positioning frame 31 has a second fixed bracket 312 at one end and a second adjusting bracket 311 at the other end; the second fixed bracket 312 is connected to the fixing part 1; the second adjusting bracket 311 is connected to the adjusting part 4.

[0038] The adjusting part 4 is a strap that can be detachably connected at both ends. The adjusting part 4 passes around the first adjusting bracket 212 and the second adjusting bracket 311 to form a ring. By adjusting the length of this ring, the lateral distance between the first hemostatic part 2 and the second hemostatic part 3 can be adjusted. By changing the position of this ring structure on the first adjusting bracket 212 and the second adjusting bracket 311, the longitudinal distance between the first hemostatic part 2 and the second hemostatic part 3 can be adjusted.

[0039] The above are merely specific embodiments of this application. Under the guidance of the above teachings, those skilled in the art can make other improvements or modifications based on the above embodiments. Those skilled in the art should understand that the above specific description is only to better explain the purpose of this application, and the scope of protection of this application should be determined by the scope of the claims.

Claims

1. A dual-point positioning compression hemostasis device, comprising a fixing part, a first hemostasis part, and a second hemostasis part, characterized in that, The first hemostatic part includes a first positioning frame and a first pressing member; the first pressing member and the first positioning frame are detachably connected; the second hemostatic part includes a second positioning frame and a second pressing member; the second pressing member and the second positioning frame are detachably connected; one end of the fixing part is slidably connected to the first positioning frame, and the other end is slidably connected to the second positioning frame; it also includes an adjustment part; one end of the adjustment part is detachably connected to the end of the first positioning frame away from the fixing part, and the other end is detachably connected to the end of the second positioning frame away from the fixing part.

2. The dual-point positioning compression hemostasis device according to claim 1, characterized in that, The first pressing component includes a first pressure adjusting structure, a first connecting rod, a first support frame, and a first pressing structure; the outer wall of the first pressure adjusting structure is detachably connected to the first support frame; one end of the first connecting rod is fixedly connected to the first support frame, and the other end passes through the first adjusting structure; the first pressing structure is wrapped around the outer wall of the first connecting rod; one end of the first pressing component abuts against the first support frame, and the other end abuts against the first pressure adjusting structure.

3. The dual-point positioning compression hemostasis device according to claim 2, characterized in that, The first pressing component further includes a first buffer structure; the first buffer structure is detachably connected to the side of the first support frame away from the first connecting rod.

4. The dual-point positioning compression hemostasis device according to claim 1, characterized in that, The second pressing component includes a second pressure adjusting structure, a second connecting rod, a second support frame, and a second pressing structure; the outer wall of the second pressure adjusting structure is detachably connected to the second support frame; one end of the second connecting rod is fixedly connected to the second support frame, and the other end passes through the second adjusting structure; the second pressing structure is wrapped around the outer wall of the second connecting rod; one end of the second pressing component abuts against the second support frame, and the other end abuts against the second pressure adjusting structure.

5. The dual-point positioning compression hemostasis device according to claim 4, characterized in that, The second pressing component also includes a second buffer structure; the second buffer structure is detachably connected to the side of the second support frame away from the second connecting rod.

6. The dual-point positioning compression hemostasis device according to claim 1, characterized in that, The fixing part includes a first fixing strap and a second fixing strap; one end of the first fixing strap is detachably connected to the second fixing strap, and the other end is connected to the first positioning frame; the end of the second fixing strap away from the first fixing strap is connected to the second positioning frame.

7. The dual-point positioning compression hemostasis device according to claim 1, characterized in that, One end of the first positioning frame is provided with a first fixed bracket, and the other end is provided with a first adjusting bracket; the first fixed bracket is connected to the fixing part; the first adjusting bracket is connected to the adjusting part.

8. The dual-point positioning compression hemostasis device according to claim 1, characterized in that, The second positioning frame has a second fixed bracket at one end and a second adjusting bracket at the other end; the second fixed bracket is connected to the fixing part; the second adjusting bracket is connected to the adjusting part.

9. A dual-point positioning compression hemostasis device according to claim 1, characterized in that, A first hemostatic bracket is fixedly connected to the first positioning frame; the first hemostatic bracket is detachably connected to the first pressing member.

10. A dual-point positioning compression hemostasis device according to claim 1, characterized in that, A second hemostatic bracket is fixedly connected to the second positioning frame; the second hemostatic bracket is detachably connected to the second pressing member.

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