Artery puncture injury compressor
By designing and assembling an arterial puncture injury compressor with a rubber stent and tension adjustment components, the problem of traditional compressors being unable to adjust the compression tension and position is solved, achieving flexible hemostasis, reducing hematoma, and improving hemostasis effect and work efficiency.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-12-26
- Publication Date
- 2026-03-13
AI Technical Summary
Traditional arterial puncture compression devices cannot flexibly adjust the tightness and position of the compression, resulting in poor hemostasis, increasing the workload of medical staff, and posing risks of hematoma and vascular occlusion.
A compression device for arterial puncture injury is designed, which uses an assembled rubber stent and a tension adjustment component, combined with a compression component and a rope, to achieve flexible compression hemostasis at the puncture site. The tension adjustment component can be used to adjust the compression position and tightness.
It allows for flexible adjustment of the compression position and tightness, improving hemostasis, reducing hematoma formation, reducing the workload of medical staff, and improving work efficiency.
Smart Images
Figure CN223987892U_ABST
Abstract
Description
Technical Field
[0001] This utility model relates to the field of medical device technology, specifically an arterial puncture injury compression device. Background Technology
[0002] In modern medical practice, arterial puncture is a common diagnostic and treatment method, widely used in cardiovascular disease examinations, interventional surgeries, and hemodialysis. However, arterial puncture often carries the risk of bleeding and vascular injury. These complications can not only increase patient suffering but also affect surgical outcomes and subsequent recovery. Therefore, how to effectively and safely manage bleeding and vascular injury after arterial puncture has become an important issue in clinical medicine.
[0003] Traditionally, hemostasis and vascular protection after arterial puncture rely primarily on manual compression by medical staff. While this method is simple to perform, it has several drawbacks. First, manual compression makes it difficult to precisely control the pressure and duration, potentially leading to poor hemostasis or excessive pressure on the vessel, which can cause complications such as hematoma and vascular occlusion. Second, prolonged manual compression increases the workload and reduces efficiency for medical staff, especially in emergency or high-intensity work environments. Furthermore, traditional compression devices cannot flexibly adjust the pressure tightness according to different patients' needs, nor can they freely adjust the compression position, resulting in poor effectiveness. Utility Model Content
[0004] In order to overcome the shortcomings of the existing technology, the purpose of this utility model is to provide an arterial puncture injury compression device. By setting a tension adjustment component in conjunction with the compression component, better hemostasis and compression can be achieved, so as to solve the problems of traditional compression devices that cannot flexibly adjust the compression tension according to the needs of different patients, and cannot flexibly adjust the compression position, resulting in poor use effect.
[0005] To achieve the above objectives, this utility model provides the following technical solution:
[0006] An arterial puncture injury compression device includes an assembled rubber stent, and further includes: two assembled rubber stents are provided, the two assembled rubber stents are arranged at a certain angle, a compression component is provided on one side of the assembled rubber stent, and ropes are provided at both ends of the compression component. The ends of the ropes away from the compression component pass through the assembled rubber stents, and a tension adjustment component is provided externally between the assembled rubber stents.
[0007] As a preferred embodiment of this utility model, the compression component includes a cotton pad, with both ends of the cotton pad being fixedly connected to a rope.
[0008] As a preferred embodiment of this utility model, the tension adjustment component includes a flexible support, the end of which is fixedly connected to the end of the rope.
[0009] The present invention has the following advantages:
[0010] In actual use, the device is placed between the assembled rubber supports on the patient's neck or arm. Under the action of the compression components between the straps, it can achieve hemostasis by compressing the puncture site. At the same time, the tension adjustment component can flexibly adjust the position of the compression component and the tightness of the compression. After arterial puncture injury in a special position, mechanical compression hemostasis can be performed to reduce hematoma formation. It is more flexible to use and has a better hemostatic effect. Attached Figure Description
[0011] Figure 1 Schematic diagram of an arterial puncture injury compression device Figure 1 .
[0012] Figure 2 Schematic diagram of an arterial puncture injury compression device Figure 2 .
[0013] Figure 3 This is a top view schematic diagram of an arterial puncture injury compression device.
[0014] In the picture: 1. Assemble the rubber support; 2. Soft support; 3. Ropes and straps; 4. Cotton pad. Detailed Implementation
[0015] The preferred embodiments of the present invention will be described below with reference to the accompanying drawings. It should be understood that the preferred embodiments described herein are for illustration and explanation only and are not intended to limit the present invention.
[0016] Example 1, please refer to Figures 1-3 An arterial puncture injury compression device includes an assembled rubber stent 1, and further includes: two assembled rubber stents 1 are provided, the two assembled rubber stents 1 are fixedly fitted at a certain angle, a compression component is provided on one side of the assembled rubber stent 1, and ropes 3 are provided at both ends of the compression component. The end of the rope 3 away from the compression component passes through the assembled rubber stent 1, and a tension adjustment component is provided on the outside between the assembled rubber stents 1.
[0017] In actual use, the device is placed between the assembled rubber brackets 1 and the compression components between the ropes 3 on the patient's neck or arm to achieve hemostasis at the puncture site. At the same time, the position of the compression components and the tightness of the compression can be flexibly adjusted by the tension adjustment components, thus achieving flexible use and better hemostasis effect.
[0018] Example 2, please refer to Figures 1-3 The compression component includes a cotton pad 4, with both ends of the cotton pad 4 fixedly connected to the rope 3. The cotton pad 4 can also be a gauze block. The tension adjustment component includes a soft support 2, with one end of the soft support 2 fixedly connected to the end of the rope 3. In actual use, the cotton pad 4 corresponds to the puncture position to achieve compression fit. At the same time, under the action of the soft support 2, the operator can move the cotton pad 4 between the ropes 3 through the soft support 2 to achieve flexible adjustment of the compression position. At the same time, under the action of the soft support 2, the tightness of the compression can also be adjusted, ensuring good compression hemostasis effect while ensuring compression comfort, resulting in better and more comfortable use.
[0019] In actual use, the device is placed between the assembled rubber supports 1 and the cotton pads 4 between the ropes 3 to achieve hemostasis by compressing the puncture site. At the same time, the position of the cotton pads 4 and the tightness of the compression can be flexibly adjusted by the soft supports 2, thus achieving flexible use and better hemostasis. The device is more flexible to operate and can achieve hemostasis and compression operations more efficiently and quickly, with better results. After arterial puncture injury in a special position, mechanical compression hemostasis can be performed to reduce hematoma formation.
[0020] All standard parts used in this invention can be purchased from the market, and irregularly shaped parts can be customized according to the description and drawings. The specific connection methods for each part all employ conventional methods such as bolts, rivets, and welding, which are mature technologies in the prior art. The machinery, parts, and equipment all use conventional models in the prior art, and the circuit connections also use conventional connection methods in the prior art, which will not be detailed here. Any content not described in detail in this specification belongs to the prior art known to those skilled in the art.
[0021] In the description of this utility model, the terms "first" and "second" are used for descriptive purposes only and should not be construed as indicating or implying relative importance or implicitly specifying the number of indicated technical features. Thus, a feature defined as "first" or "second" may explicitly or implicitly include one or more of that feature. "A plurality of" means two or more, unless otherwise explicitly specified.
[0022] In this utility model, unless otherwise explicitly specified and limited, the terms "installation," "connection," "joining," and "fixing," etc., should be interpreted broadly. For example, they can refer to a fixed connection, a detachable connection, or an integral part; they can refer to a mechanical connection or an electrical connection; they can refer to a direct connection or an indirect connection through an intermediate medium; they can refer to the internal communication of two components or the interaction between two components. Those skilled in the art can understand the specific meaning of the above terms in this utility model according to the specific circumstances.
[0023] In this utility model, unless otherwise explicitly specified and limited, "above" or "below" the second feature can mean that the first feature is in direct contact with the second feature, or that the first feature is in indirect contact with the second feature through an intermediate medium. Furthermore, "above," "on top of," and "over" the second feature can mean that the first feature is directly above or diagonally above the second feature, or simply that the first feature is at a higher horizontal level than the second feature. "Below," "below," and "under" the second feature can mean that the first feature is directly below or diagonally below the second feature, or simply that the first feature is at a lower horizontal level than the second feature.
[0024] In the description of this specification, the references to terms such as "one embodiment," "some embodiments," "example," "specific example," or "some examples," etc., indicate that a specific feature, structure, material, or characteristic described in connection with that embodiment or example is included in at least one embodiment or example of the present invention. In this specification, the illustrative expressions of the above terms do not necessarily refer to the same embodiment or example. Furthermore, the specific features, structures, materials, or characteristics described may be combined in any suitable manner in one or more embodiments or examples. Moreover, without contradiction, those skilled in the art can combine and integrate the different embodiments or examples described in this specification, as well as the features of different embodiments or examples.
[0025] The accompanying drawings of the embodiments disclosed in this utility model only involve the structures involved in the embodiments disclosed in this utility model. Other structures can refer to the general design. In the absence of conflict, the same embodiment and different embodiments of this utility model can be combined with each other.
[0026] Although the present invention 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 the present invention should be included within the protection scope of the present invention.
Claims
1. An arterial puncture injury compressor comprising an assembled rubber support (1), characterized in that, Also include: The assembly rubber support (1) is provided with two, two assembly rubber supports (1) are matched and arranged at a certain angle, one side of the assembly rubber support (1) is provided with a compression assembly, and the two ends of the compression assembly are provided with a rope belt (3), one end of the rope belt (3) away from the compression assembly is arranged through the assembly rubber support (1), and the outer part between the assembly rubber supports (1) is provided with a tightness adjusting assembly.
2. An arterial puncture site injury compressing device according to claim 1, wherein The compression assembly comprises a cotton pad (4), and the two ends of the cotton pad (4) are fixedly connected with the rope belts (3) respectively.
3. An arterial puncture site injury compressing device according to claim 2, wherein The tightness adjusting assembly comprises a soft support (2), and the end of the soft support (2) is fixedly connected with the end of the rope belt (3).