A post-implantation pacemaker wound compression hemostasis device

Abstract

The utility model relates to the field of medical equipment, disclose a kind of postoperative wound compression hemostasis device, including storage bag, first connecting belt and second connecting belt, storage bag has cavity, the cavity is used to put into salt bag or sandbag, first connecting part, second connecting part and third connecting part are formed on the storage bag;First connecting belt one end is set in the first connecting part, the other end is wound from the right side of chest to back, and with the third connecting part detachable connection, the third connecting part is located on shoulder part;Second connecting belt one end is set in the second connecting part, the other end is wound from the left side of chest to back, and with the first connecting belt detachable connection.The utility model is stored in storage bag by storing salt bag, cooperate the connecting mode of first connecting belt and second connecting belt, so that the salt bag in storage bag is fully contacted with the position of patient's wound, and is adhered to patient's wound, not easy to slip, keep sustained effective compression state, guarantee the effect of pressure hemostasis.

Description

Technical Field

[0001] This utility model relates to the field of medical equipment technology, and in particular to a device for compression and hemostasis of post-pacemaker wounds. Background Technology

[0002] Cardiac pacing surgery is a medical procedure used to treat arrhythmias by implanting a small pacemaker to help patients control their heart rhythm.

[0003] Following cardiac pacing surgery, local pressure is applied to the wound site to stop bleeding and effectively reduce the risk of postoperative wound bleeding and pocket hematoma. Currently, 0.5kg salt bags or sandbags are commonly used in clinical practice. However, these bags are often packaged in paper or plastic, are relatively rigid, and have upturned edges, making them unable to make close contact with the skin around the wound. Furthermore, they are prone to displacement or slippage during application, resulting in unsatisfactory hemostasis.

[0004] Therefore, existing technologies still need to be improved and developed. Utility Model Content

[0005] The technical problem to be solved by this utility model is to provide a pacemaker postoperative wound compression hemostasis device in view of the above-mentioned defects of the prior art. It aims to solve the problem that in the prior art, after cardiac pacing surgery, local compression hemostasis is performed on the patient's wound using paper or plastic packaging, which is relatively hard and has upturned edges. This makes it unable to make close contact with the skin around the patient's wound, and it is easy to shift or slip during the compression process, resulting in unsatisfactory compression hemostasis effect.

[0006] The technical solution adopted by this utility model to solve the technical problem is as follows:

[0007] A pacemaker postoperative wound compression hemostasis device, comprising:

[0008] A storage bag having a cavity for holding a salt bag, the storage bag having a first connecting portion, a second connecting portion and a third connecting portion formed thereon;

[0009] The first connecting strap has one end located at the first connecting part and the other end wrapped around from the right side of the chest to the back, and is detachably connected to the third connecting part, which is located on the shoulder.

[0010] The second connecting strap has one end located at the second connecting part and the other end wrapped around from the left side of the chest to the back, and is detachably connected to the first connecting strap.

[0011] The post-pacemaker wound compression hemostasis device includes a storage bag with an opening that communicates with the cavity, and a sealing structure for opening or closing the opening on the storage bag located at the opening.

[0012] The post-pacemaker wound compression hemostasis device, wherein the sealing structure includes any one of a zipper, Velcro, and self-sealing strip.

[0013] The post-pacemaker wound compression hemostasis device includes a storage bag with an anti-slip strip on the side near the chest, the anti-slip strip being offset from the opening, and the anti-slip strip having several abrasive particles.

[0014] The post-pacemaker wound compression hemostasis device includes a first pull ring on the first connecting part, which is detachably connected to one end of the first connecting band; a second pull ring on the second connecting part, which is detachably connected to one end of the second connecting band; and a third pull ring on the third connecting part, which is detachably connected to the other end of the first connecting band.

[0015] The post-pacemaker wound compression hemostasis device, wherein the cross-sectional shape of the storage bag includes any one of rectangle, triangle and circle.

[0016] The post-pacemaker wound compression hemostasis device, wherein the connection method between the third connecting part and the first connecting strap includes any one of buckle connection, Velcro connection and strap connection.

[0017] The post-pacemaker wound compression hemostasis device includes a sleeve at one end of the second connecting strap away from the second connecting portion. The sleeve is used for the first connecting strap to pass through, so that the second connecting strap is fixed to the first connecting strap.

[0018] The post-pacemaker wound compression hemostasis device, wherein the first connecting band is a first elastic connecting band and the second connecting band is a second elastic connecting band.

[0019] Beneficial effects:

[0020] This invention provides a pressure hemostasis device for post-pacemaker surgery wounds. A storage bag is placed against the wound on the left side of the patient's chest. A first connecting strap is used, with one end connected to a first connecting part on the storage bag, and the other end wrapped around the patient's right side of the chest to the back, then connected to a third connecting part. Finally, a second connecting strap is used, with one end connected to a second connecting part, and the other end wrapped around the patient's left side of the chest to the back, then connected to the first connecting strap. This design, by storing a saline bag or sandbag inside the storage bag and using the connection method of the first and second connecting straps, ensures that the saline bag or sandbag in the storage bag makes full contact with the wound after pacemaker surgery, adhering closely to the wound and preventing slippage. This maintains continuous and effective pressure on the wound after cardiac pacing surgery, ensuring effective pressure hemostasis. Attached Figure Description

[0021] Figure 1 This is a front view of the salt bag fixing device of this utility model;

[0022] Figure 2 This is a rear view of the salt bag fixing device of this utility model;

[0023] Figure 3 This is a rear view structural diagram of the storage bag of this utility model;

[0024] Figure 4 This is a structural diagram of another embodiment of the salt bag fixing device of this utility model.

[0025] In the picture:

[0026] 1. Model; 2. Storage bag; 2-1. Zipper; 2-2. First connecting part; 2-3. Second connecting part; 2-4. Third connecting part; 2-5. Buckle; 2-6. Anti-slip strip; 2-7. First pull ring; 2-8. Second pull ring; 2-9. Third pull ring; 3. First connecting strap; 4. Second connecting strap; 4-1. Sleeve opening. Detailed Implementation

[0027] The embodiments of this application are described in detail below. Examples of these embodiments are shown in the accompanying drawings, wherein the same or similar reference numerals denote the same or similar elements or elements having the same or similar functions throughout. The embodiments described below with reference to the accompanying drawings are exemplary and are only used to explain this application, and should not be construed as limiting this application.

[0028] In the description of this application, it should be understood that the terms "center," "longitudinal," "lateral," "upper," "lower," "front," "rear," "left," "right," "vertical," "horizontal," "top," "bottom," "inner," and "outer," etc., indicating orientation or positional relationships based on the orientation or positional relationships shown in the accompanying drawings, are used only for the convenience of describing this application 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 application. 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 one or more of that feature. In the description of this application, unless otherwise stated, "a plurality of" means two or more.

[0029] In the description of this application, it should be noted that, unless otherwise expressly specified and limited, the terms "installation," "connection," and "linking" should be interpreted broadly. For example, they can refer to a fixed connection, a detachable connection, or an integral connection; 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; and they can refer to the internal connection between two components. Those skilled in the art can understand the specific meaning of the above terms in this application based on the specific circumstances.

[0030] Please see Figures 1 to 2 As shown, this application provides a pacemaker postoperative wound compression hemostasis device, including a storage bag 2, a first connecting strap 3, and a second connecting strap 4. The storage bag 2 has a cavity for holding a salt pack or sandbag. The storage bag 2 has a first connecting portion 2-2, a second connecting portion 2-3, and a third connecting portion 2-4. One end of the first connecting strap 3 is disposed at the first connecting portion 2-2, and the other end is wrapped around from the right side of the chest to the back and detachably connected to the third connecting portion 2-4, which is located on the shoulder. One end of the second connecting strap 4 is disposed at the second connecting portion 2-3, and the other end is wrapped around from the left side of the chest to the back and detachably connected to the first connecting strap 3.

[0031] Specifically, this embodiment discloses a storage bag 2, which has an internal cavity for holding a salt bag or a sandbag. The salt bag refers to a bag for storing sea salt, i.e., a special medical salt bag. The shape of the salt bag is adapted to the shape of the cavity so that the sea salt bag can be placed inside the storage bag 2 and make full contact with all parts of the storage bag 2. The sandbag refers to a bag for storing fine sand, i.e., a special medical sandbag. The shape of the sandbag is also adapted to the shape of the cavity so that the sandbag can also be placed inside the storage bag 2 and make full contact with all parts of the storage bag 2. The storage bag 2 also has a first connecting part 2-2, a second connecting part 2-3, and a third connecting part 2-4. The first connecting part 2-2, the second connecting part 2-3, and the third connecting part 2-4 are used to form a cooperative relationship with the first connecting strap 3 and the second connecting strap 4, so that the saline pack of the storage bag 2 can fully contact the wound of the patient after pacemaker surgery, fit tightly, and not easily slip off. It can be understood that the first connecting part 2-2, the second connecting part 2-3, and the third connecting part 2-4 refer to the connection position and are not affected by the shape of the storage bag 2.

[0032] In actual use, such as Figure 1 and Figure 2 As shown, this device is used on a human model 1. The storage bag 2 is fitted to the left side of the patient's chest, corresponding to the location of the heart wound. Then, a first connecting strap 3 is used. One end of the first connecting strap 3 is connected to the first connecting part 2-2 on the storage bag 2, and the other end is wrapped around the right side of the patient's chest to the patient's back, and then detachably connected to the third connecting part 2-4. There are various ways to detachably connect the other end of the first connecting strap 3 to the third connecting part 2-4, and no limitation is made in this embodiment. Since the third connecting part 2-4 is located on the patient's left shoulder, the vertical direction of the storage bag 2 is fixed by the first connecting strap 3. Finally, the second connecting strap 4 is used. One end of the second connecting strap 4 is connected to the second connecting part 2-3, and the other end is wrapped around from the left side of the patient's chest to the patient's back, and then detachably connected to the first connecting strap 3, so that the storage bag 2 is fixed in the horizontal direction. The vertical and horizontal directions of the storage bag 2 are locked by the cooperation of the first connecting strap 3 and the second connecting strap 4, so that the storage bag 2 is not easy to shift or slide down. At the same time, the tight force of the first connecting strap 3 and the second connecting strap 4 makes the storage bag 2 fit tightly against the position of the patient's wound, that is, the sandbag or salt bag inside fits tightly against the position of the patient's wound, which is suitable for use when the patient is lying flat or semi-recumbent.

[0033] In some embodiments, the first connecting strip 3 and the second connecting strip 4 are both rectangular strips, which are simple in structure and reliable in use.

[0034] It is worth noting that when the second connecting strap 4 is on the patient's back, the second connecting strap 4 and the first connecting strap 3 are connected in the middle of the patient's back, so that the first connecting strap 3 and the second connecting strap 4 form an intersecting shape on the patient's back. The second connecting strap 4 can also play a certain role in tightening the first connecting strap 3, thereby making the fixation of the first connecting strap 3 and the second connecting strap 4 more secure.

[0035] See Figure 1 As shown, in another embodiment of this application, the storage bag 2 is provided with an opening, the opening is in communication with the cavity, and the storage bag 2 located at the opening is provided with a closing structure for opening or closing the opening.

[0036] Specifically, the storage bag 2 has an opening that communicates with the cavity, allowing the salt packet to be placed inside. A sealing structure is provided at the corresponding position of the opening. The sealing structure is used to close or open the opening, making it easy to retrieve the salt packet from the storage bag 2. The sealing structure also prevents the salt packet from falling out of the storage bag 2. It is understandable that, since the inside of the storage bag 2 is in contact with the patient's chest, in order to avoid the sealing structure affecting the patient's comfort, the opening and the corresponding sealing structure are located on the side of the storage bag 2 away from the patient, ensuring the comfort of the storage bag 2.

[0037] Further, see Figure 1 As shown, in another embodiment of this application, the closure structure includes any one of a zipper 2-1, Velcro, and self-sealing strip.

[0038] Specifically, there are various types of closure structures, such as zipper closure structures (2-1), which are durable, aesthetically pleasing, and safe; Velcro closure structures, which are easy to operate, reusable, and safe; and self-sealing closure structures, which are good-sealable, low-cost, and reusable. All three structures can achieve smooth opening and closing, making it easy to open or close the storage bag 2, which is beneficial for packaging sea salt into the storage bag 2. Users can choose the corresponding closure structure to set at the opening position according to their actual needs. In this embodiment, the preferred closure structure is a zipper 2-1. Zipper 2-1 includes two chains, chain teeth, a slider, and a pull tab. The two chains are mounted on the storage bag 2 at the opening position, the slider is sleeved on the two chains, and the pull tab is mounted on the slider. When the user pulls the pull tab, the slider moves along the two chains formed by the chain teeth, and the slider causes the two chain teeth on the two chains to press into the grooves between them, thereby forming a tight closure. When the user pulls the pull tab in the opposite direction, the slider causes the two chain teeth on the two chains to separate, allowing the two chains to open. By adopting a zipper-type closure structure, the structure is simple, the opening and closing is relatively fast, and it is durable, resulting in a longer service life for the closure structure.

[0039] See Figure 3 As shown, in another embodiment of this application, the storage bag 2 is provided with an anti-slip strip 2-6 on the side near the chest. The anti-slip strip 2-6 is offset from the opening, and a plurality of abrasive particles are provided on the anti-slip strip 2-6.

[0040] Specifically, the side of the storage bag 2 closest to the chest refers to the inner side, which is equipped with anti-slip strips 2-6. Anti-slip strips 2-6 are rectangular strips of fabric that can be glued to the inner side of the storage bag 2 or sewn onto it. Several frosted particles are set on the fabric strips, which are made of polyethylene or polypropylene. These frosted particles are fixed to the fabric strips, forming anti-slip strips 2-6, which have a certain anti-slip effect. This makes it easier to generate friction when the storage bag 2 is attached to the patient's chest, making the storage bag 2 less prone to shaking and improving its firmness.

[0041] See Figure 4 As shown, in another embodiment of this application, a first pull ring 2-7 is provided on the first connecting part 2-2, and the first pull ring 2-7 is detachably connected to one end of the first connecting band 3; a second pull ring 2-8 is provided on the second connecting part 2-3, and the second pull ring 2-8 is detachably connected to one end of the second connecting band 4; a third pull ring 2-9 is provided on the third connecting part 2-4, and the third pull ring 2-9 is detachably connected to the other end of the first connecting band 3.

[0042] Specifically, a first pull ring 2-7 is provided on the first connecting part 2-2, and the first pull ring 2-7 is detachably connected to the left end of the first connecting band 3. A second pull ring 2-8 is provided on the second connecting part 2-3, and the second pull ring 2-8 is detachably connected to the left end of the second connecting band 4. A third pull ring 2-9 is provided on the third connecting part 2-4, and the third pull ring 2-9 is detachably connected to the right end of the first connecting band 3. It can be understood that there are various detachable connection methods, such as hook and loop fasteners or snap fasteners. In this embodiment, the detachable connection method adopts a hook and loop fastener structure. For example, the hook and loop fastener structure includes two hook and loop fasteners, which are provided on the left side of the first connecting band 3. The first connecting strap 3 is attached to two different positions, then wrapped around the first pull ring 2-7, and finally secured with two Velcro straps, thus achieving a detachable connection between the first connecting strap 3 and the first pull ring 2-7; the detachable connection between the second pull ring 2-8 and the left end of the second connecting strap 4 is achieved in the same way; the detachable connection between the third pull ring 2-9 and the right end of the first connecting strap 3 is also achieved in the same way; in this embodiment, by setting the first connecting strap 3 and the second connecting strap 4 to a detachable connection method, it is beneficial to remove the storage bag 2, the first connecting strap 3 and the second connecting strap 4 separately for cleaning and disinfection, which facilitates reuse, makes disinfection more thorough, and also reduces the cost of replacing the storage bag 2.

[0043] In some embodiments, an adhesive layer is provided inside the storage bag 2 for bonding salt packs or sandbags.

[0044] Specifically, since the storage bag 2 is equipped with a first pull ring 2-7, a second pull ring 2-8, and a third pull ring 2-9, and both the first connecting strap 3 and the second connecting strap 4 are detachable, an adhesive layer is provided inside the storage bag 2. The adhesive layer is glue, which covers one side of the cavity inside the storage bag 2. Then, the salt bag or sandbag is placed inside the cavity of the storage bag 2 and bonded with the glue, so that the salt bag or sandbag is completely fixed inside the storage bag 2. The storage bag 2 and the salt bag or the storage bag 2 and the sandbag are configured as disposable items. Both the first connecting strap 3 and the second connecting strap 4 are detachable and reusable, which is especially suitable for patients who exercise frequently, such as walking.

[0045] In another embodiment of this application, the storage bag 2 is a sweat-absorbing and breathable storage bag 2.

[0046] Specifically, the sweat-absorbing and breathable storage bag 2 refers to the storage bag 2 being made of a sweat-absorbing and breathable material, such as cotton, cotton-polyester blend, linen, wool, polyester, nylon, spandex, and synthetic fiber materials with sweat-absorbing and breathable properties. In this embodiment, the storage bag 2 is preferably made of a cotton-polyester blend, combining the comfort and breathability of cotton with the quick-drying function of polyester, making the storage bag 2 more durable, effectively extending its service life, and improving product quality.

[0047] See Figure 1 and Figure 3 As shown, in another embodiment of this application, the cross-sectional shape of the storage bag 2 includes any one of a rectangle, a triangle, and a circle.

[0048] Specifically, the cross-sectional shape of the storage bag 2 includes three types: rectangle, triangle, and circle. Users can choose to manufacture the storage bag 2 of the corresponding shape according to their actual needs. In this embodiment, the storage bag 2 is preferably triangular, which helps to reduce the overall area of ​​the storage bag 2, thereby reducing the material used in manufacturing the storage bag 2 and effectively reducing costs. In other embodiments, the first connecting part 2-2, the second connecting part 2-3, and the third connecting part 2-4 of the triangular storage bag 2 are respectively located at the three corners of the triangular storage bag 2. Setting the three corners of the triangular storage bag 2 to be flat not only facilitates the connection and installation of the first connecting strap 3, the second connecting strap 4, and the buckle 2-5, but also contributes to the aesthetics of the device and improves the appearance of the product.

[0049] See Figure 1 and Figure 2As shown, in another embodiment of this application, the connection method between the third connecting part 2-4 and the first connecting strap 3 includes any one of buckle 2-5 connection, Velcro connection and strap connection.

[0050] Specifically, the third connecting part 2-4 is detachably connected to the first connecting strap 3, allowing the first connecting strap 3 to be easily opened and secured, facilitating the patient's donning and doffing of the device. The connection method between the third connecting part 2-4 and the first connecting strap 3 includes any one of the following: buckle 2-5 connection, Velcro connection, and strap connection. Buckle 2-5 connection offers advantages such as speed, convenience, safety, and durability; Velcro connection offers advantages such as ease of operation, reusability, and good adaptability; and strap connection offers advantages such as high flexibility, low cost, and simple reliability. Figures 1 to 2 As shown, in this embodiment, the preferred connection method is a buckle 2-5 connection. The third connecting part 2-4 is provided with a first buckle 2-5. The end of the first connecting band 3 facing away from the first connecting part 2-2 is equipped with a second buckle 2-5 that is compatible with the first buckle 2-5. The first buckle 2-5 and the second buckle 2-5 are connected, thereby connecting the third connecting part 2-4 and the first connecting band 3. The structure is simple and easy to use. It can be understood that the first buckle 2-5 and the second buckle 2-5 are both existing bag buckles 2-5.

[0051] See Figures 1 to 2 As shown, in another embodiment of this application, the end of the second connecting strap 4 opposite to the second connecting portion 2-3 is provided with a sleeve 4-1, which is used for the first connecting strap 3 to pass through so that the second connecting strap 4 is fixed on the first connecting strap 3.

[0052] Specifically, the end of the second connecting strip 4 opposite to the second connecting part 2-3 has a sleeve 4-1, which is used for the first connecting strip 3 to pass through, so that the second connecting strip 4 can be directly connected to the first connecting strip 3. The structure is simple, reliable, and easy to fix. More specifically, the end of the second connecting strip 4 is wrapped around and attached to the second connecting strip 4 to form the sleeve 4-1.

[0053] In another embodiment of this application, the first connecting strip 3 is a first elastic connecting strip, and the second connecting strip 4 is a second elastic connecting strip.

[0054] Specifically, the first connecting strap 3 is a first elastic connecting strap, which refers to a strap made of elastic material, possessing a certain degree of elasticity, comfort, and durability. The elastic material is made of elastic fiber (such as spandex). Similarly, the second connecting strap 4 is a second elastic connecting strap, which is also a strap made of elastic material. The first connecting strap 3 and the second connecting strap 4 are made of the same elastic material, namely spandex, making production and manufacturing more convenient. In this embodiment, the tightness of the first connecting strap 3 and the second connecting strap 4 can be changed through simple adjustment to ensure optimal fit and support. At the same time, due to the elasticity of the first connecting strap 3 and the second connecting strap 4, this device can also be adapted to different patients, thereby increasing its applicability.

[0055] See Figure 1 and Figure 2 As shown, in another embodiment of this application, the storage bag 2 is located on the left side of the patient's chest, close to the heart, i.e., in contact with the wound. The length of the first connecting strap 3 is greater than the length of the second connecting strap 4, so that the first connecting strap 3 can be wrapped around the patient's back and connected to the third connecting part 2-4. Since the second connecting strap 4 only needs to be fixed on the first connecting strap 3, when the length of the first connecting strap 3 is greater than the length of the second connecting strap 4, the user can reasonably reduce the manufacturing material of the second connecting strap 4, thereby further reducing the manufacturing cost of this device.

[0056] In summary, this utility model provides a device for compression hemostasis of a pacemaker-induced surgical wound. First, the storage bag is placed against the patient's left chest, at the location of the pacemaker wound, allowing the salt pack or sandbag inside the bag to effectively compress and stop the bleeding. Then, the first connecting strap on the storage bag is wrapped around the patient's right side of the chest to the back and connected to the third connecting part. Since the third connecting part is located on the patient's left shoulder, the vertical direction of the storage bag is fixed. Finally, the second connecting strap on the storage bag is wrapped around the patient's left side of the chest to the back, and the end of the second connecting strap is inserted into the first connecting strap, creating a cross-fixing effect on the patient's back. The combined use of the first and second connecting straps and the storage bag ensures that the storage bag is fixed both vertically and horizontally, preventing the salt pack or sandbag from shifting due to weight and ensuring full contact with the patient's wound after pacemaker surgery, thus avoiding affecting the compression effect of the salt pack or sandbag on the wound.

[0057] It should be understood that the application of this utility model is not limited to the examples above. Those skilled in the art can make improvements or modifications based on the above description, and all such improvements and modifications should fall within the protection scope of the appended claims.

Claims

1. A device for compression hemostasis of a post-pacemaker wound, characterized in that, include: A storage bag having a cavity for holding salt bags or sandbags, and the storage bag having a first connecting part, a second connecting part and a third connecting part; The first connecting strap has one end located at the first connecting part and the other end wrapped around from the right side of the chest to the back, and is detachably connected to the third connecting part, which is located on the shoulder. The second connecting strap has one end located at the second connecting part and the other end wrapped around from the left side of the chest to the back, and is detachably connected to the first connecting strap.

2. The pacemaker postoperative wound compression hemostasis device according to claim 1, characterized in that, The storage bag has an opening that communicates with the cavity, and the storage bag located at the opening has a closing structure for opening or closing the opening.

3. The pacemaker postoperative wound compression hemostasis device according to claim 2, characterized in that, The closure structure includes any one of zippers, Velcro, and self-sealing strips.

4. The pacemaker postoperative wound compression hemostasis device according to claim 3, characterized in that, The storage bag is provided with an anti-slip strip on the side near the chest, the anti-slip strip is offset from the opening, and the anti-slip strip is provided with a number of abrasive particles.

5. A pacemaker postoperative wound compression hemostasis device according to claim 1, characterized in that, The first connecting part is provided with a first pull ring, which is detachably connected to one end of the first connecting strip. The second connecting part is provided with a second pull ring, which is detachably connected to one end of the second connecting strip. The third connecting part is provided with a third pull ring, which is detachably connected to the other end of the first connecting strip.

6. A pacemaker postoperative wound compression hemostasis device according to claim 1, characterized in that, The cross-sectional shape of the storage bag includes any one of rectangle, triangle and circle.

7. A pacemaker postoperative wound compression hemostasis device according to claim 1, characterized in that, The connection method between the third connecting part and the first connecting strip includes any one of buckle connection, Velcro connection and strap connection.

8. A pacemaker postoperative wound compression hemostasis device according to claim 1, characterized in that, The second connecting strip has a sleeve at one end opposite to the second connecting part, the sleeve being used for the first connecting strip to pass through, so that the second connecting strip is fixed on the first connecting strip.

9. A pacemaker postoperative wound compression hemostasis device according to claim 1, characterized in that, The first connecting strip is a first elastic connecting strip, and the second connecting strip is a second elastic connecting strip.

Images