Radial artery hemostat capable of simultaneously compressing same-side ulnar arteries
By designing a radial artery hemostat that can simultaneously compress the ipsilateral ulnar artery, the problem of radial artery hemostats being unable to compress both the radial and ulnar arteries at the same time has been solved, achieving precise hemostasis and preventing radial artery occlusion, thus improving patients' treatment outcomes and quality of life.
Patent Information
- Application Number
- CN202422773068.5
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Priority Date
- 2024-11-06
- Filing Date
- 2024-11-14
- Publication Date
- 2025-11-21
- Estimated Expiration
- 2034-11-14
AI Technical Summary
Existing radial artery hemostats cannot simultaneously compress the radial artery and the ipsilateral ulnar artery, resulting in a high incidence of radial artery occlusion, which affects patients' treatment and quality of life, and there is a lack of preventive and treatment measures.
A radial artery hemostat is designed to simultaneously compress the ipsilateral ulnar artery. It employs a stacked radial artery and radial artery-side small airbags and ulnar artery-side airbags, connected to a one-way valve via an air tube, to achieve synchronous and precise compression of the radial and ulnar arteries. By independently separating straps A and B and adjusting the hook and loop straps, precise compression hemostasis of the radial and ulnar arteries can be achieved.
By simultaneously compressing the radial and ulnar arteries, the blood flow to the radial artery is increased, the incidence of occlusion is reduced, the rate of radial artery recanalization is improved, and patient comfort and quality of life are enhanced.
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Figure CN223569358U_ABST
Abstract
Description
TECHNICAL FIELD
[0001] The utility model relates to a hemostat, especially to a radial artery hemostat capable of simultaneously compressing the same side ulnar artery. BACKGROUND
[0002] Transradial access (TRA) is one of the most common accesses in interventional therapy. In the aspect of coronary intervention, the European Society of Cardiology suggests that transradial access should be used as the IA level indication for patients with acute coronary syndrome who receive interventional therapy. Similarly, the American Heart Association proposes that transradial access should be the default access for patients with acute coronary syndrome in the United States. At the same time, with the understanding of transradial access, more and more peripheral interventional therapies in the world begin to use TRA. In China, more and more interventional therapy centers begin to explore TRA in the aspects of hepatic arterial chemoembolization, hepatic arterial infusion chemotherapy, visceral aneurysm, interventional therapy for gynecological diseases, and gradually accumulate the clinical application experience of TRA in peripheral interventional therapy. TRA is gradually applied widely. Although compared with the traditional femoral artery access, transradial access can reduce the complications of the puncture point of patients, mortality, economic burden, shorten the hospitalization time, and increase the comfort of patients, but due to the fact that the radial artery is relatively thin, radial artery occlusion (RAO) is very likely to occur after puncture. RAO is the most common complication after transradial puncture catheterization, and its incidence is about 1% to 33%, which has an important impact on the treatment and quality of life of patients. On the one hand, after the occurrence of RAO, the patient loses the opportunity to perform interventional surgery through the same side radial artery in the future, such as the case of acute coronary syndrome patients who may not be able to use the radial artery for surgery when they are transferred for coronary artery bypass surgery; hepatic arterial chemoembolization, hepatic arterial infusion chemotherapy, etc. are periodic tumor interventional therapy methods, and after the occurrence of RAO, the patient cannot perform anti-tumor treatment through the radial artery. On the other hand, due to radial artery occlusion, some patients may have symptoms of hand ischemia, such as pain, numbness and limited activity, which affects the body function and quality of life. Therefore, the prevention of RAO is very important.
[0003] The appropriate radial artery compression hemostasis method and process is an important link to reduce the incidence of RAO. The Best Practices for Prevention of Radial Artery Occlusion After Transradial Diagnostic Angiography and Interventional Procedures - An International Consensus suggests that the same side ulnar artery should be compressed at the same time when the radial artery is compressed for hemostasis, so as to prevent the occurrence of RAO. In addition, after the occurrence of RAO, early compression of the same side ulnar artery can improve the recanalization rate of the radial artery. The guidelines point out that the lack of a special device for radial artery-ulnar artery double compression is one of the obstacles to using this simple and effective technique to prevent RAO.
[0004] The radial artery hemostat in the prior art only has the function of pressing the radial artery to stop bleeding, and the comfort is improved by improving the material of the pressor, such as the patent with the application number 202320558621.6 which increases the functions of intelligent pressure detection and automatic pressure reduction to increase the patency of the radial artery, and the patents with the application numbers 202221950290.2 and 202211381276.X which further improve the hemostatic capacity of the radial artery hemostat. However, the effect of these in preventing radial artery occlusion is far from enough. And there is no radial artery hemostat that can press the ulnar artery on the same side at present in China, neither related products nor related patents. Content of the utility model
[0005] The radial artery hemostat provided by the utility model can press the radial artery and the ulnar artery on the same side at the same time to overcome the defects of the prior art.
[0006] In order to solve the above technical problems, the utility model provides the following technical scheme:
[0007] The utility model discloses a radial artery hemostat that can press the ulnar artery on the same side simultaneously, which is used to overcome the defects of the prior art that the radial artery hemostat cannot press the radial artery and the ulnar artery on the same side at the same time.
[0008] Further, the radial artery side big air bag is connected with the air guide pipe A, the radial artery side small air bag is connected with the air guide pipe B, the air guide pipe A and the air guide pipe B are combined into a total air guide pipe, and the total air guide pipe is connected with the one-way valve A.
[0009] Further, the inflation device inflates the radial artery side big air bag and the radial artery side small air bag at the same time through the one-way valve A, the total air guide pipe, the air guide pipe A and the air guide pipe B, and the directional extrusion of the radial artery side big air bag and the radial artery side small air bag can press at a fixed point to realize more accurate compression hemostasis of the radial artery.
[0010] Further, the ulnar artery side air bag is connected with the air guide pipe C, the air guide pipe C is connected with the one-way valve B, the inflation device inflates the ulnar artery side air bag through the one-way valve B and the air guide pipe C, and the radial artery is pressed at the same time.
[0011] Further, the bandage A and the bandage B are independent, the hook-and-loop fastener A and the hook-and-loop fastener C are bonded, and the hook-and-loop fastener B and the hook-and-loop fastener D are bonded, so that the wrist thickness of each patient and the radial artery and ulnar artery compression position can be adjusted.
[0012] Further, the bandage B is provided with a support plate with an arc, which is used to prevent the bandage A and the bandage B from being bonded to excessively press the whole wrist and affect blood circulation.
[0013] The radial artery and the ulnar artery are widely anastomosed together through the superficial palmar arch and the deep palmar arch of the palm part, and the palm part is supplied with blood together, the blood flow of the radial artery can be increased when the ipsilateral ulnar artery is pressed, so that the release of vasodilator medium (blood flow-mediated vasodilation) is increased, and the incidence of radial artery occlusion is reduced. BRIEF DESCRIPTION OF DRAWINGS
[0014] The accompanying drawings are used to provide a further understanding of the present application, and constitute a part of the specification, and are used to explain the present application together with embodiments of the present application, and do not constitute a limitation to the present application. In the drawings:
[0015] Fig. 1 It is a whole structure schematic view of the present application;
[0016] Fig. 2 It is a front view structure schematic view of the present application.
[0017] In the figure: 1, radial artery side large air bag; 2, radial artery side small air bag; 3, air guide pipe A; 4, air guide pipe B; 5, total air guide pipe; 6, one-way valve A; 7, radial artery side mark point; 8, ulnar artery side air bag; 9, air guide pipe C; 10, one-way valve B; 11, ulnar artery side mark point; 12, bandage A; 13, hook-and-loop fastener A; 14, hook-and-loop fastener B; 15, bandage B; 16, hook-and-loop fastener C; 17, hook-and-loop fastener D; 18, support plate. DETAILED DESCRIPTION
[0018] The preferred embodiments of the present application are described below in combination with the drawings, and it should be understood that the preferred embodiments described herein are only used to illustrate and explain the present application, and are not used to limit the present application.
[0019] Embodiment 1
[0020] As Figs. 1-2As shown, a radial artery hemostat that can simultaneously compress the ipsilateral ulnar artery, comprising a ulnar artery side air bag 8, and a radial artery side large air bag 1 and a radial artery side small air bag 2 arranged in a stack and connected with each other in the opposite direction, the ulnar artery side air bag 8 is arranged inside the band B15, the radial artery side small air bag 2 is arranged inside the band A12, the outer surface of the band B15 is provided with a ulnar artery side mark point 11, the outer surface of the band A12 is provided with a radial artery side mark point 7, the two ends of the band A12 are respectively provided with a touch fastener strip A13 and a touch fastener strip B14, and the two ends of the band B15 are respectively provided with a touch fastener strip C16 and a touch fastener strip D17.
[0021] The radial artery side large air bag 1 is connected with the air guide pipe A3, the radial artery side small air bag 2 is connected with the air guide pipe B4, the air guide pipe A3 and the air guide pipe B4 are combined into a total air guide pipe 5, and the total air guide pipe 5 is connected with the one-way valve A6.
[0022] The inflation device inflates the radial artery side large air bag 1 and the radial artery side small air bag 2 through the one-way valve A6, the total air guide pipe 5, the air guide pipe A3 and the air guide pipe B4, and the directional extrusion of the radial artery side large air bag 1 and the radial artery side small air bag 2 can point compression and realize more accurate compression hemostasis of the radial artery, and the point compression force point can be reflected in the radial artery side mark point 7, which can help positioning when the arterial catheter is removed.
[0023] The ulnar artery side air bag 8 is connected with the air guide pipe C9, the air guide pipe C9 is connected with the one-way valve B10, the inflation device inflates the ulnar artery side air bag 8 through the one-way valve B10 and the air guide pipe C9, and the force point of the ulnar artery side air bag 8 on the ulnar artery compression is reflected in the mark point B11, which can help positioning when selecting the compression point. It is realized that the radial artery is compressed at the same time, and the ipsilateral ulnar artery is compressed; or after stopping the compression of the radial artery, the ulnar artery is continuously compressed without changing, removing or increasing any compression equipment.
[0024] The band A12 and the band B15 are independently separated, the radial artery compression point is positioned by the radial artery side mark point 7, and the ulnar artery compression point is positioned by the ulnar artery side mark point 11, then the touch fastener strip A13 and the touch fastener strip C16 are adhered, and the touch fastener strip B14 and the touch fastener strip D17 are adhered, so that the two bands are adhered together and fixed through the touch fastener strips, so that the two bands can be adjusted according to the thickness of the wrist of each patient, the compression positions of the radial artery and the ulnar artery. Among them, the band B15 is a part of the arc support plate 18 at the ulnar artery position, which can prevent the pressure of the two bands on the whole wrist from being too large after being adhered, affecting blood circulation.
[0025] The large balloon-small balloon combined double balloon mode obliquely points to the radial artery, accurately compresses the radial artery, and prevents / treats RAO by increasing the single balloon to compress the ipsilateral ulnar artery.
[0026] Method one: when the radial artery catheter needs to be removed, first withdraw the sheath tube 2-3cm, align the radial artery side mark point of the hemostat with the puncture point, align the ulnar artery side mark point with the ulnar artery, fix the two belts together on the wrist through the Velcro belt; inject air into the radial artery side balloon with a syringe, so that the balloon expands, remove the radial artery sheath tube; inject air into the ulnar artery side balloon; slowly release the gas in the radial artery side balloon, at the same time, use the blood oxygen saturation meter to measure the change of blood oxygen saturation, so that it is maintained above 95%, at the same time, there is no bleeding, at this time, the radial artery is unobstructed, at the same time, the ulnar artery is also compressed, which increases the blood flow of the radial artery and prevents it from being occluded.
[0027] Method two: after the radial artery puncture point is completely hemostatic, release the gas in the radial artery side balloon, inject more gas into the ulnar artery measuring balloon, use the blood oxygen saturation meter to measure the blood oxygen saturation, if the blood oxygen saturation decreases to below 95% or cannot be measured, slowly release the gas in the ulnar artery side balloon until the blood oxygen saturation reaches above 95%, at this time, the ulnar artery side balloon still has gas, which can compress the ulnar artery, through increasing the blood supply of the radial artery, the occluded radial artery is unobstructed in a short time, at the same time, it does not affect the blood supply of the hand.
[0028] Method one and method two can be used in combination to achieve the two purposes of preventing and treating radial artery occlusion.
[0029] It should be noted that the above only describes preferred embodiments of the present application and is not intended to limit the present application, although the present application has been described in detail with reference to the foregoing embodiments, those skilled in the art can still modify the technical solutions recorded in the foregoing embodiments or make equivalent replacement for some technical features. Any modification, equivalent replacement, improvement, etc. made within the spirit and principle of the present application shall be included in the protection scope of the present application, the terms used in the description of the present application are only for describing the specific embodiments and are not intended to limit the exemplary embodiments according to the present application. In order to facilitate description, the sizes of the parts shown in the drawings are not drawn in accordance with the actual proportional relationship. The known technology, methods and devices of the related field may not be discussed in detail, but under appropriate circumstances, the technology, methods and devices should be regarded as part of the authorized description. In all examples shown and discussed here, any specific value should be interpreted as only exemplary, not as a limitation. Therefore, other examples of exemplary embodiments can have different values. It should be noted that similar reference numerals and letters represent similar items in the following drawings, therefore, once an item is defined in one drawing, it does not need to be further discussed in subsequent drawings.
[0030] It should be noted that the terms "first", "second" and the like in the description and in the claims of the present application are used for distinguishing between similar objects and not necessarily for describing a specific sequential or chronological order. It is to be understood that the data so distinguished can occur in any sequence. Hence, without departing from the scope of the present application, the data used in "first", "second", etc. can be interchanged with each other. The terms "and / or" and / or "or" as used herein link together alternative language alternatives and are understood to mean that at least one of the alternatives is present and that the alternatives are to be taken together. The term "comprises the possibility of comprising additional elements or steps not listed after the term comprises.
[0031] It should be noted that the terms "front", "rear", "upper", "lower", "left", "right", "horizontal", "vertical", "top", "bottom", and the like as used in this description and in the claims shall relate to the application as it is shown in the drawings and shall not be construed to limit the application to a particular orientation or configuration, unless otherwise noted. The terms "inner", "outer" refer to the inner and outer contours of the components themselves.
Claims
1. A radial artery tourniquet capable of simultaneously compressing ipsilateral saphenous arteries, characterized in that, The application relates to a wrist compression device, which comprises a ulnar artery side gas bag, a radial artery side large gas bag and a radial artery side small gas bag arranged in a stack and communicated with each other, the ulnar artery side gas bag is arranged in the inner side of a belt B, the radial artery side large gas bag and the radial artery side small gas bag are arranged in the inner side of a belt A, the outer surface of the belt B is provided with a ulnar artery side mark point, the outer surface of the belt A is provided with a radial artery side mark point, the two ends of the belt A are respectively provided with a touch fastener A and a touch fastener B, and the two ends of the belt B are respectively provided with a touch fastener C and a touch fastener D.
2. The radial artery tourniquet capable of simultaneously compressing ipsilateral femoral arteries according to claim 1, wherein, The radial artery side large gas bag is connected with a gas guide pipe A, the radial artery side small gas bag is connected with a gas guide pipe B, the gas guide pipe A and the gas guide pipe B are combined into a total gas guide pipe, and the total gas guide pipe is connected with a one-way valve A.
3. The radial artery tourniquet of claim 2, wherein, An inflation device inflates the radial artery side large gas bag and the radial artery side small gas bag through the one-way valve A, the total gas guide pipe, the gas guide pipe A and the gas guide pipe B, and the directional extrusion of the radial artery side large gas bag and the radial artery side small gas bag can realize pinpoint compression and more accurate compression hemostasis of the radial artery.
4. The radial artery tourniquet of claim 1, wherein, The ulnar artery side gas bag is connected with a gas guide pipe C, the gas guide pipe C is connected with a one-way valve B, the inflation device inflates the ulnar artery side gas bag through the one-way valve B and the gas guide pipe C, and the ulnar artery side gas bag can be inflated while the radial artery is compressed.
5. The radial artery tourniquet of claim 1, wherein, The belt A and the belt B are independently separated, the touch fastener A is adhered to the touch fastener C, the touch fastener B is adhered to the touch fastener D, and the device can be adjusted according to the thickness of the wrist of each patient and the compression positions of the radial artery and the ulnar artery.
6. The radial artery tourniquet of claim 1, wherein, The belt B is provided with a supporting plate with an arc, and the supporting plate is used for preventing the pressure of the belt A and the belt B on the whole wrist from being too large after being adhered and affecting blood circulation.
Citation Information
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An intelligent electronic radial artery hemostat with precise alarm function
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