Hemostatic wristband with blood leakage alarm function
Patent Information
- Application Number
- CN202520872218.X
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2025-05-06
- Publication Date
- 2026-09-01
- Estimated Expiration
- 2035-05-06
AI Technical Summary
[0005]本实用新型的目的是为了解决现有技术中存在上述渗血情况下不能够及时的进行发现以及反馈的缺点,而提出的一种具有漏血报警功能的止血腕带
[0015]本实用新型提出的一种具有漏血报警功能的止血腕带,有益效果在于:本实用新型通过固定结构能够方便快捷的将止血腕带固定在患者的内瘘穿刺部位,当检测单元接触到血液时能够对监测终端立即报警,提醒医护人员及时处理,并且一对弹性腕带之间通过多档调节的方式能够在一定范围内对不同粗细的手臂进行适配,此外,止血层在止血过程中吸附部分血液,那么通过连接结构能够在使用完毕后快捷的对止血层进行拆卸,使外面层进行消毒后能够达到重复使用的好处。
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Figure CN224699234U_ABST
Abstract
Description
Technical Field
[0001] This utility model relates to the field of wristband technology, and in particular to a hemostatic wristband with a blood leakage alarm function. Background Technology
[0002] Uremic patients are prone to bleeding due to platelet adhesion dysfunction, coagulation abnormalities, and the use of anticoagulants during hemodialysis. Bleeding from the puncture site of the arteriovenous fistula is a common complication, and bleeding caused by needle slippage is a serious complication. Timely detection and treatment of bleeding are key measures to reduce blood loss during dialysis and avoid serious adverse consequences.
[0003] Hemostasis measures are used to prevent bleeding from the fistula puncture site, thus avoiding serious adverse consequences. For example, Chinese Patent Publication No. CN213465188U discloses a pressure-quantified hemostatic wristband for dialysis, belonging to the field of medical device technology. It includes a casing with hemostatic bands on both sides, a replaceable compression bladder on the lower surface of the casing, and a rubber-made inverted frustum-shaped sealed bladder structure. A connecting conduit is located inside the casing, and a vent is located on the lower surface of the casing. The first interface of the connecting conduit communicates with the inner cavity of the compression bladder through the vent. A control valve is located on one side of the casing, communicating with a second interface of the connecting conduit. A pressure sensor is located inside the casing, communicating with a third interface of the connecting conduit. A sound sensor and a processing and display unit are also located inside the casing. A miniature blood pressure sensor is located on the hemostatic bands. This invention is convenient and highly user-friendly for clinical operation, enabling objective quantitative indicators to guide the entire process of compression hemostasis and release. It is reusable, has stable performance, and easy to replace easily damaged components, thus protecting and extending the lifespan of the fistula.
[0004] In practice, external pressure is used to prevent bleeding from the puncture site. However, due to platelet adhesion dysfunction, coagulation abnormalities, or other conditions, bleeding from the puncture site can still occur. Therefore, it is not possible to apply external pressure to the patient for an extended period of time to stop the bleeding. Consequently, bleeding may not be detected or reported in a timely manner, which can easily cause harm to the patient. Utility Model Content
[0005] The purpose of this invention is to address the shortcomings of existing technologies that cannot detect and report bleeding in a timely manner, and to propose a hemostatic wristband with a bleeding alarm function.
[0006] To achieve the above objectives, the present invention adopts the following technical solution:
[0007] Design a hemostatic wristband with a bleeding alarm function, including an outer layer and a hemostatic layer. The outer layer is fixed to the fistula puncture site on the arm by a fixing structure on both sides. The fixing structure includes a pair of elastic wristbands, which are fixed together by a snap-fit part at the free end, and an anti-dislodgement part to prevent accidental dislodgement.
[0008] The outer layer and the hemostatic layer are stacked together, and a sensing unit is provided between them. The outer layer and the hemostatic layer are detachably connected by a connecting structure.
[0009] Furthermore, the fixing structure also includes stepped grooves and annular portions. One of the elastic wristbands has an annular portion at its free end. The elastic wristband has several stepped grooves evenly distributed along its length in the middle. The other elastic wristband has a snap-fit portion and an anti-detachment groove on its inner and outer sides at its free end, respectively.
[0010] Furthermore, the free end of one of the elastic wristbands passes through the annular portion so that the snap-fit portion snaps into the stepped groove, and the snap-fit portion has a T-shaped cross-section.
[0011] Furthermore, the anti-slip part is an elastic structure, which is sleeved and slidably connected to the periphery of one of the elastic wristbands through a central through groove. The anti-slip part is also sleeved in the anti-slip groove by stretching and deformation to tighten the pair of elastic wristbands.
[0012] Furthermore, the connection structure includes a first Velcro strap, an avoidance groove at one end of the outer layer, the outer layer being located on the outside of the other end, and the first Velcro straps being fixedly connected to both sides of the avoidance groove, wherein the sensing unit is placed between the outer layer and the hemostatic layer through the avoidance groove.
[0013] Furthermore, it also includes a second Velcro, the hemostatic layer is located at the lower end, and the left and right sides of the upper end are fixedly connected with the second Velcro, and the second Velcro at the upper and lower ends is bonded to the corresponding first Velcro.
[0014] In this case, a pair of second Velcro straps cover the clearance groove by bending.
[0015] The present invention proposes a hemostatic wristband with a blood leakage alarm function. The advantages are as follows: the present invention can conveniently and quickly fix the hemostatic wristband to the patient's arteriovenous fistula puncture site through a fixing structure. When the detection unit comes into contact with blood, it can immediately alarm the monitoring terminal to remind medical staff to deal with it in time. In addition, the pair of elastic wristbands can be adjusted in multiple positions to adapt to arms of different thicknesses within a certain range. Furthermore, since the hemostatic layer absorbs some blood during the hemostasis process, the connecting structure allows the hemostatic layer to be quickly disassembled after use, so that the outer layer can be disinfected and reused. Attached Figure Description
[0016] Figure 1 This is a schematic diagram of the structure of this utility model;
[0017] Figure 2 This is an enlarged view of the anti-detachment structure of this utility model;
[0018] Figure 3 This is an exploded view of the present invention;
[0019] Figure 4 This is an enlarged view of the fixed structure of this utility model.
[0020] In the diagram: 1. Outer layer; 11. Avoidance groove; 2. Hemostatic layer; 3. Fixing structure; 31. Elastic wristband; 32. Snap-fit part; 33. Anti-detachment part; 34. Step groove; 35. Annular part; 36. Anti-detachment groove; 4. Sensing unit; 5. Connecting structure; 51. First Velcro; 52. Second Velcro. 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 of the present utility model. Obviously, the described embodiments are only some embodiments of the present utility model, and not all embodiments.
[0022] Reference Figure 1-4 A hemostatic wristband with a bleeding alarm function includes an outer layer 1 and a hemostatic layer 2. The outer layer 1 is fixed to the fistula puncture site on both sides by a fixing structure 3. The fixing structure 3 includes a pair of elastic wristbands 31. The pair of elastic wristbands 31 are fixed together by a snap-fit part 32 at the free end, and an anti-dislodgement part 33 prevents accidental dislodgement.
[0023] The outer layer 1 and the hemostatic layer 2 are stacked together, and a sensing unit 4 is provided between them. The outer layer 1 and the hemostatic layer 2 are detachably connected by a connecting structure 5.
[0024] In some embodiments, the outer layer 1 is a waterproof structure, which is integrally formed with the elastic wristbands 31 on both sides. The outer layer 1 and the hemostatic layer 2 are connected and fixed by the connecting structure 5. The hemostatic layer 2 comes into contact with blood during the hemostasis process and can be disassembled and replaced by the connecting structure 5. The outer layer 1 can be reused by disinfection.
[0025] Specifically, the hemostatic layer 2 can be made of medical hemostatic gauze and directly attached to the puncture hole of the fistula to achieve hemostasis.
[0026] Furthermore, the fixing structure 3 also includes stepped grooves 34 and annular portions 35. One of the elastic wristbands 31 has an annular portion 35 at its free end. The elastic wristband 31 has several stepped grooves 34 evenly distributed along its length in the middle. The other elastic wristband 31 has a snap-fit portion 32 and an anti-detachment groove 36 on its inner and outer sides at its free end, respectively.
[0027] Furthermore, the free end of one of the elastic wristbands 31 passes through the annular portion 35 so that the snap-fit portion 32 snaps into the stepped groove 34, and the snap-fit portion 32 has a T-shaped cross-section.
[0028] More specifically, the anti-slip part 33 is an elastic structure, which is sleeved and slidably connected to the periphery of one of the elastic wristbands 31 through a central through groove. The anti-slip part 33 is also sleeved in the anti-slip groove 36 by stretching and deformation to tighten the pair of elastic wristbands 31.
[0029] In this embodiment, the specific structure of the fixing structure 3 can refer to the fixing structure of a wristwatch strap in the prior art;
[0030] In specific operation, the elastic wristband 31 and the anti-detachment part 33 are preferably made of materials with deformation capabilities such as rubber and silicone. One of the elastic wristbands 31 passes through the ring part 35 and is attached to the other elastic wristband 31. The snap-fit part 32 is snapped into the stepped groove 34 to achieve the purpose of fixing the elastic wristbands 31 on both sides and tightening the hemostatic wristband. At this time, the hemostatic layer 2 is tightly attached to the puncture hole.
[0031] Specifically, the stepped groove 34 prevents the end protrusion of the locking part 32 from touching the patient's arm and causing discomfort;
[0032] Furthermore, the anti-slip part 33 is sleeved around one of the elastic wristbands 31 and the anti-slip groove 36 by stretching and deforming, and after restoring the deformation, it achieves the purpose of tightening a pair of elastic wristbands 31. At this time, the snap-fit part 32 cannot easily disengage from the stepped groove 34, thus achieving the anti-slip function.
[0033] In general, the connection structure 5 includes a first Velcro 51, one end of the outer layer 1 is provided with an avoidance groove 11, the outer layer 1 is located on the outside of the other end, and the first Velcro 51 is fixedly connected to both sides of the avoidance groove 11. The sensing unit 4 is placed between the outer layer 1 and the hemostatic layer 2 through the avoidance groove 11.
[0034] Finally, it also includes a second Velcro 52. The hemostatic layer 2 is located at the lower end, and the left and right sides at the upper end are fixedly connected with the second Velcro 52. The second Velcro 52 at the upper and lower ends is bonded to the corresponding first Velcro 51.
[0035] In this case, a pair of second Velcro straps 52 cover the clearance groove 11 by bending.
[0036] It should be added that the sensing unit 4 is a blood oxygen monitoring probe or a water immersion sensor in the prior art. The sensor is electrically connected to monitoring equipment such as a monitor to detect and alarm the bleeding reaction.
[0037] It is worth mentioning that the first hook and loop fastener 51 and the second hook and loop fastener 52 are the adhesive side and the hook side, respectively, and they are connected and fixed to the outer layer 1 and the hemostatic layer 2 by mutual adhesion.
[0038] When the pair of second Velcro straps 52 are bent to cover the avoidance groove 11 and the elastic wristbands 31 on both sides are closed and tightened, they can cooperate with the human arm to close the openings on both sides between the outer layer 1 and the hemostatic layer 2, thereby achieving the function of stopping and fixing the sensing unit 4.
[0039] Of course, the detection surface of the sensing unit 4 needs to be set to face the hemostatic layer 2.
[0040] Working method: During operation, the sensing unit 4 is located between the outer layer 1 and the hemostatic layer 2 through the clearance groove 11, and the second Velcro 52 at the upper and lower ends are bonded to the corresponding first Velcro 51 to achieve the function of connecting and fixing the outer layer 1 and the hemostatic layer 2.
[0041] The hemostatic layer 2 is attached to the puncture site of the fistula. When the two elastic wristbands 31 are closed, they are used in conjunction with a pair of second Velcro straps 52 to fix the sensing unit 4. One of the elastic wristbands 31 passes through the annular part 35 and is attached to the other elastic wristband 31. The snap-fit part 32 is snapped into the stepped groove 34. The anti-dislodgement part 33 is stretched and deformed and sleeved around one of the elastic wristbands 31 and the anti-dislodgement groove 36. After the deformation is restored, it achieves the purpose of tightening the pair of elastic wristbands 31. At this time, the snap-fit part 32 cannot easily disengage from the stepped groove 34, thus achieving the anti-dislodgement function.
[0042] Finally, when bleeding occurs from the puncture, the hemostatic layer 2 plays a role in stopping the bleeding. When the amount of bleeding is large, the blood penetrates into the interior of the hemostatic layer 2. After the sensing unit 4 detects the blood, it issues an alarm to the monitoring equipment.
[0043] Although embodiments of the present invention have been shown and described above, it is understood that the above embodiments are exemplary and should not be construed as limiting the present invention. Those skilled in the art can make changes, modifications, substitutions and variations to the above embodiments within the scope of the present invention.
[0044] In the description of this specification, it should be understood that the terms "center", "longitudinal", "lateral", "length", "width", "thickness", "upper", "lower", "front", "rear", "left", "right", "vertical", "horizontal", "top", "bottom", "inner", "outer", "clockwise", "counterclockwise", "axial", "radial", "circumferential", etc., indicating the orientation or positional relationship based on the orientation or positional relationship shown in the accompanying drawings, are only for the convenience of describing the technical solution of this patent and simplifying the description, and do not indicate or imply that the device or element referred to must have a specific orientation, or be constructed and operated in a specific orientation, and therefore should not be construed as a limitation on this patent application.
[0045] Furthermore, 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 at least one of that feature. In the description of this patent application, "a plurality of" means at least two, such as two, three, etc., unless otherwise explicitly specified.
[0046] In this specification, unless otherwise expressly 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, unless otherwise expressly limited. Those skilled in the art can understand the specific meaning of the above terms in this specification according to the specific circumstances.
[0047] In this specification, unless otherwise expressly specified and limited, "above" or "below" the second feature can mean that the first and second features are in direct contact, or that the first and second features are in indirect contact through an intermediate medium. Furthermore, "above," "over," and "on top" of 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.
[0048] 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.
Claims
1. A hemostatic wristband with a blood leakage alarm function, comprising an outer layer (1) and a hemostatic layer (2), characterized in that: The outer layer (1) is fixed to the fistula puncture site on both sides by the fixing structure (3) on both sides. The fixing structure (3) includes a pair of elastic wristbands (31). The pair of elastic wristbands (31) are fixed together by the snap-fit part (32) at the free end, and the anti-dislodgement part (33) prevents accidental dislodgement. The outer layer (1) and the hemostatic layer (2) are stacked together, and a sensing unit (4) is provided between them. The outer layer (1) and the hemostatic layer (2) are detachably connected by a connecting structure (5).
2. The hemostatic wristband according to claim 1, characterized in that: The fixing structure (3) further includes a stepped groove (34) and an annular portion (35). The free end of one of the elastic wristbands (31) is provided with the annular portion (35). The elastic wristband (31) has several stepped grooves (34) evenly distributed along its length in the middle. The inner and outer sides of the free end of the other elastic wristband (31) are respectively provided with the snap-fit portion (32) and the anti-detachment groove (36).
3. The hemostatic wristband according to claim 2, characterized in that: One of the elastic wristbands (31) has its free end inserted through the annular portion (35) so that the snap-fit portion (32) snaps into the stepped groove (34), and the snap-fit portion (32) has a T-shaped cross-section.
4. The hemostatic wristband according to claim 3, characterized in that: The anti-slip part (33) is an elastic structure, which is sleeved and slidably connected to the periphery of one of the elastic wristbands (31) through a central through groove. The anti-slip part (33) is also sleeved in the anti-slip groove (36) by stretching and deformation to tighten the pair of elastic wristbands (31).
5. The hemostatic wristband according to claim 1, characterized in that: The connection structure (5) includes a first Velcro (51), one end of the outer layer (1) is provided with an avoidance groove (11), the outer layer (1) is located on the outside of the other end, and the first Velcro (51) is fixedly connected to both sides of the avoidance groove (11). The sensing unit (4) is placed between the outer layer (1) and the hemostatic layer (2) through the avoidance groove (11).
6. The hemostatic wristband according to claim 5, characterized in that: It also includes a second Velcro (52), the hemostatic layer (2) is located at the lower end, and the left and right sides of the upper end are fixedly connected with the second Velcro (52), and the second Velcro (52) at the upper and lower ends are bonded to the corresponding first Velcro (51). In this case, a pair of second Velcro straps (52) cover the clearance groove (11) by bending.
Citation Information
Patent Citations
Pressure quantification hemostasis wristband for dialysis
CN213465188U