Tumor postoperative femoral artery compression hemostasis nursing device

Abstract

The invention relates to the technical field of femoral artery compression hemostasis nursing, and discloses a tumor postoperative femoral artery compression hemostasis nursing device which comprises a pressing frame, and a bandage component is arranged on the surface of the pressing frame; the bandage component comprises a center frame, the bottom of the center frame is fixedly connected with the top of a pressing frame, a through hole frame is arranged on the surface of the center frame, a cotton cushion is arranged below the pressing frame, an arc-shaped plate is inserted into the bottom of the cotton cushion, and a limiting hole is formed in the bottom of the arc-shaped plate. The cotton cushion is arranged at the top of the arc-shaped plate and makes contact with the legs of a patient, the comfort is improved, the legs of the patient can press the arc-shaped plate, the bandage is limited through the arc-shaped plate, and the stability of the bandage during hemostasis and compression is improved; the bandage penetrates through the through hole frame and is bonded and fixed through the magic tape, the pressing frame is fixed above the leg of the patient through the bandage, and after the pressing frame is placed, compression treatment can be conducted on the femoral artery of the patient through the compression component.

Description

Technical Field

[0001] This invention relates to the field of femoral artery compression hemostasis nursing technology, specifically a femoral artery compression hemostasis nursing device after tumor surgery. Background Technology

[0002] The femoral artery compression hemostat is a medical device used for hemostasis after vascular interventional procedures. It promotes wound healing by applying external mechanical pressure to the femoral artery puncture site. Originating in the 1980s, this device was first developed in the United States, France, Germany, Japan, and other countries to replace the traditional sandbag compression method. Currently, the usual procedure is to use a bandage to compress the femoral artery to stop bleeding. The bandage is used to wrap a cotton pad or other compression block around the puncture site of the femoral artery to prevent bleeding. However, the femoral artery is located deep in the groin, which is a joint movement area. When using a bandage to compress the femoral artery to stop bleeding, the pressure point of the bandage is prone to shift when the patient moves their leg, resulting in unstable compression effect. Summary of the Invention

[0003] The purpose of this invention is to provide a femoral artery compression hemostasis nursing device after tumor surgery to solve the problems mentioned in the background art.

[0004] To solve the above-mentioned technical problems, the present invention is achieved through the following technical solution: This invention relates to a femoral artery compression hemostasis nursing device after tumor surgery, comprising a compression frame, the surface of which is provided with a bandage component; The bandage component includes a central frame, the bottom of which is fixedly connected to the top of a pressing frame. A through-hole frame is provided on the surface of the central frame. A cotton pad is provided below the pressing frame, and an arc-shaped plate is inserted into the bottom of the cotton pad. A limiting hole is provided at the bottom of the arc-shaped plate. A bandage is provided on the surface of the pressing frame, with the top of the bandage penetrating the arc-shaped plate and extending to its outer end. The bottom of the bandage penetrates the limiting hole and extends to its outer end. An adjustment component is provided inside the central frame, and a compression component is provided at the end of the pressing frame.

[0005] Furthermore, the bandage is provided in two quantities, and the two bandages are symmetrically arranged around the central frame, with Velcro tape at the ends of the bandages.

[0006] Furthermore, the ends of the bandage are attached with Velcro tape, the bottom of the curved plate extends to the outer end of the bottom of the cotton pad, and the end of the cotton pad extends to the outer end of the curved plate.

[0007] Furthermore, the adjusting component includes a rotating disk, a threaded rod fixedly connected to the bottom of the rotating disk, a tripod rotatably connected to the bottom of the threaded rod, a movable plate slidably connected to the bottom of the inner wall of the central frame, a groove formed on the surface of the movable plate, a connecting plate fixedly connected to the end of the movable plate away from the groove, a through-hole frame fixedly connected to the end of the connecting plate away from the movable plate, and the bottom of the tripod hinged to the bottom of the inner wall of the groove.

[0008] Furthermore, there are two movable plates, which are symmetrically arranged around the tripod. The bottom of the threaded rod passes through the central frame and extends into the interior of the central frame. The surface of the threaded rod is threadedly connected to the inner wall of the central frame.

[0009] Furthermore, the top of the tripod is hinged, the end of the connecting plate away from the moving plate passes through the central frame and extends to the outer end of the central frame, and the end of the moving plate contacts the inner wall of the central frame.

[0010] Furthermore, the pressing component includes a limiting block, the top of which is fixedly connected to the bottom of the pressing frame. A semi-circular block is fixedly connected to the surface of the limiting block, a bracket is inserted into the surface of the limiting block, and an arc plate is fixedly connected to the bottom of the bracket. An arc-shaped adhesive tape is provided at the bottom of the arc plate, and Velcro tape is provided between the arc-shaped adhesive tape and the arc plate. The pressing frame has a sliding groove inside, and a fixing block is fixedly connected to the inner wall of the pressing frame. A positioning groove is opened inside the fixing block, and a through hole is opened at one end of the positioning groove that is close to the sliding groove. The top of the pressing frame... The part has a sliding hole, and a stabilizing block is slidably connected to the inner wall of the sliding groove. A lifting plate is fixedly connected to the bottom of the stabilizing block, and a pressing block is fixedly connected to the bottom of the lifting plate. A silicone pad is sleeved on the surface of the pressing block, and a telescopic plate is fixedly connected to the surface of the stabilizing block. A locking plate is fixedly connected to the end of the telescopic plate away from the stabilizing block, and a locking block is fixedly connected to the surface of the locking plate. A spring rod is fixedly connected to the end of the locking plate away from the locking block, and a pressure plate is fixedly connected to the top of the locking plate. A contact plate is fixedly connected to the top of the pressure plate, and multiple locking holes are opened inside the positioning groove.

[0011] Furthermore, there are two semicircular blocks, which are symmetrically arranged around the limiting block. The surface of the semicircular block is in contact with the inner wall of the bracket. The arc-shaped adhesive tape is bonded to the arc plate with Velcro. The bottom of the lifting plate passes through the pressing frame and extends to the bottom outer end of the pressing frame. The pressing block is located at the end of the pressing frame away from the limiting block. The sliding hole and the positioning groove are interconnected.

[0012] Furthermore, the plurality of the card holes are configured in two groups, and each group has the same number of card holes. The two groups of card holes are symmetrically arranged with the through hole as the center. The surface of the card plate is in contact with the inner wall of the positioning groove. The surface of the card block is inserted into the inner wall of the card hole. The end of the elastic rod away from the card plate is in contact with the inner wall of the positioning groove. The top of the pressure plate extends to the top outer end of the pressing frame through the sliding hole.

[0013] The present invention has the following beneficial effects: After the patient's leg is lowered, it will come into contact with the top of the cotton pad. The cotton pad is located on the top of the curved plate and contacts the patient's leg to improve comfort. The patient's leg will press down on the curved plate, which limits the bandage and improves the stability of the bandage during hemostasis. After the compression frame is placed above the patient's leg, the bandage passes through the through-hole frame and is fixed with Velcro tape. The compression frame is fixed above the patient's leg with the bandage. After the compression frame is placed, the compression component can be used to compress the patient's femoral artery, improving the convenience of using the compression frame.

[0014] When the center of the tripod of this invention moves, its ends push two moving plates to move away from each other. When the moving plates move, they push the through-hole frame away from the center frame through the connecting plate. This allows the through-hole frame to adjust the distance between the bandage and the compression frame, leaving space for medical staff to operate the puncture needle. After the compression frame is fixed, the medical staff can remove the puncture needle, improving convenience.

[0015] When the pressure force needs to be adjusted, the pressure plate is pushed to slide inside the sliding hole. When the pressure plate moves, it pushes the clamping plate to compress the elastic rod and pulls the telescopic plate to extend. When the clamping plate moves, it pushes the clamping block to separate from the inner wall of the clamping hole. At this time, the clamping plate can be pushed downward through the connection between the contact plate and the pressure plate. When the clamping plate moves downward, it pushes the stabilizing block downward through the telescopic plate. When the stabilizing block moves downward, it pushes the compression block to compress the patient's femoral artery through the lifting plate. After the force adjustment is completed, the clamping plate is pushed to move. When the clamping plate moves, it pushes the clamping block into the interior of the clamping hole to fix the clamping plate and prevent the compression block from loosening after the force adjustment is completed.

[0016] Of course, any product implementing this invention does not necessarily need to achieve all of the advantages described above at the same time. Attached Figure Description

[0017] To more clearly illustrate the technical solutions of the embodiments of the present invention, the accompanying drawings used in the description of the embodiments will be briefly introduced below. Obviously, the drawings described below are only some embodiments of the present invention. For those skilled in the art, other drawings can be obtained based on these drawings without creative effort.

[0018] Figure 1 This is a schematic diagram of the overall structure of the present invention; Figure 2 This is a schematic diagram of the overall structure of the bandage component of the present invention; Figure 3 This is another structural schematic diagram of the bandage component of the present invention; Figure 4 This is a schematic diagram of the overall structure of the adjusting component of the present invention; Figure 5 This is a schematic diagram of another structure of the adjusting component of the present invention; Figure 6 This is a schematic diagram of the overall structure of the compression component of the present invention; Figure 7 This is a schematic diagram of another structure of the compression component of the present invention; Figure 8 This is a schematic cross-sectional view of the pressing frame of the present invention; Figure 9 For the present invention Figure 8 Enlarged schematic diagram of part A in the diagram.

[0019] The attached diagram lists the components represented by each number as follows: In the diagram: 1. Pressing frame; 2. Bandage component; 3. Adjusting component; 4. Compression component; 10. Center frame; 11. Through-hole frame; 12. Bandage; 13. Cotton pad; 14. Arc plate; 15. Limiting hole; 20. Rotating disc; 21. Threaded rod; 22. Groove; 23. Triangular frame; 24. Moving plate; 25. Connecting plate; 30. Limiting block; 31. Bracket; 32. Arc plate; 33. Semi-circular block; 34. Arc-shaped adhesive tape; 35. Silicone pad; 36. Contact plate; 37. Pressure plate; 38. Fixing block; 39. Compression block; 40. Slide groove; 41. Lifting plate; 42. Slide hole; 43. Positioning groove; 44. Elastic rod; 45. Locking hole; 46. Through hole; 47. Locking plate; 48. Locking block; 49. Stabilizing block; 50. Telescopic plate. Detailed Implementation

[0020] The technical solutions of the embodiments of the present invention will be clearly and completely described below with reference to the accompanying drawings. Obviously, the described embodiments are only some embodiments of the present invention, and not all embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those skilled in the art without creative effort are within the scope of protection of the present invention.

[0021] Please see Figures 1-9 As shown, the present invention is a femoral artery compression hemostasis nursing device after tumor surgery, including a compression frame 1, and a bandage component 2 is provided on the surface of the compression frame 1; The bandage component 2 includes a central frame 10, the bottom of which is fixedly connected to the top of the compression frame 1. A through-hole frame 11 is provided on the surface of the central frame 10. A cotton pad 13 is provided below the compression frame 1, and an arc-shaped plate 14 is inserted into the bottom of the cotton pad 13. A limiting hole 15 is provided at the bottom of the arc-shaped plate 14. A bandage 12 is provided on the surface of the compression frame 1. The top of the bandage 12 passes through the arc-shaped plate 14 and extends to the outer end of the arc-shaped plate 14, while the bottom of the bandage 12 passes through the limiting hole 15 and extends to the outer end of the limiting hole 15. After the patient's leg is lowered, the patient's leg will contact the top of the cotton pad 13. The cotton pad is located on the top of the arc-shaped plate 14. 13. Contact with the patient's leg to improve comfort. The patient's leg will press the arc plate 14. The arc plate 14 is used to limit the bandage 12, improving the stability of the bandage 12 during hemostasis and compression. After the compression frame 1 is placed above the patient's leg, the bandage 12 passes through the through hole frame 11 and is fixed by Velcro tape. The compression frame 1 is fixed above the patient's leg by the bandage 12. After the compression frame 1 is placed, the patient's femoral artery can be compressed by the compression component 4, improving the convenience of using the compression frame 1. The center frame 10 is provided with an adjustment component 3, and the end of the compression frame 1 is provided with a compression component 4.

[0022] There are two bandages 12, which are symmetrically arranged around the central frame 10. The ends of the bandages 12 are provided with Velcro tape.

[0023] The ends of the bandage 12 are glued together with Velcro tape. The bottom of the curved plate 14 extends to the outer end of the bottom of the cotton pad 13, and the end of the cotton pad 13 extends to the outer end of the curved plate 14.

[0024] The adjusting component 3 includes a rotating disk 20, with a threaded rod 21 fixedly connected to the bottom of the rotating disk 20. A tripod 23 is rotatably connected to the bottom of the threaded rod 21. A movable plate 24 is slidably connected to the bottom of the inner wall of the central frame 10. A groove 22 is provided on the surface of the movable plate 24. A connecting plate 25 is fixedly connected to the end of the movable plate 24 away from the groove 22. The end of the connecting plate 25 away from the movable plate 24 is fixedly connected to the through-hole frame 11. The bottom of the tripod 23 is hinged to the bottom of the inner wall of the groove 22. When the center of the tripod 23 moves, its end will push the two movable plates 24 to move away from each other. When the movable plate 24 moves, it pushes the through-hole frame 11 to move away from the central frame 10 through the connecting plate 25. Thus, the distance between the bandage 12 and the pressure frame 1 is adjusted by the through-hole frame 11, leaving space for medical staff to operate the puncture needle, so that the medical staff can remove the puncture needle after the pressure frame 1 is fixed, thus improving convenience.

[0025] There are two movable plates 24, which are symmetrically arranged with the tripod 23 as the center. The bottom of the threaded rod 21 passes through the central frame 10 and extends into the interior of the central frame 10. The surface of the threaded rod 21 is threadedly connected to the inner wall of the central frame 10.

[0026] The top of the tripod 23 is hinged, and the end of the connecting plate 25 away from the moving plate 24 passes through the central frame 10 and extends to the outer end of the central frame 10. The end of the moving plate 24 contacts the inner wall of the central frame 10.

[0027] The pressing component 4 includes a limiting block 30, the top of which is fixedly connected to the bottom of the pressing frame 1. A semi-circular block 33 is fixedly connected to the surface of the limiting block 30, and a bracket 31 is inserted into the surface of the limiting block 30. An arc plate 32 is fixedly connected to the bottom of the bracket 31. An arc-shaped adhesive tape 34 is provided at the bottom of the arc plate 32, and Velcro tape is provided between the arc-shaped adhesive tape 34 and the arc plate 32. A sliding groove 40 is provided inside the pressing frame 1, and a fixing block 38 is fixedly connected to the inner wall of the pressing frame 1. A positioning function is provided inside the fixing block 38. The positioning groove 43 and the sliding groove 40 are close to each other and have a through hole 46 at one end. The top of the pressing frame 1 has a sliding hole 42. A stabilizing block 49 is slidably connected to the inner wall of the sliding groove 40. A lifting plate 41 is fixedly connected to the bottom of the stabilizing block 49. A pressing block 39 is fixedly connected to the bottom of the lifting plate 41. A silicone pad 35 is fitted onto the surface of the pressing block 39. A telescopic plate 50 is fixedly connected to the surface of the stabilizing block 49. A locking plate 47 is fixedly connected to the end of the telescopic plate 50 away from the stabilizing block 49. A locking plate 47 is fixedly connected to the surface of the locking plate 47. Block 48, a spring rod 44 is fixedly connected to the end of the clamping plate 47 away from the clamping block 48, a pressure plate 37 is fixedly connected to the top of the clamping plate 47, and a contact plate 36 is fixedly connected to the top of the pressure plate 37. Multiple locking holes 45 are provided inside the positioning groove 43. When the pressure force needs to be adjusted, the pressure plate 37 is pushed to slide inside the sliding hole 42. When the pressure plate 37 moves, it pushes the clamping plate 47 to compress the spring rod 44 and retract it, pulling the telescopic plate 50 to extend. When the clamping plate 47 moves, it pushes the inner wall of the clamping block 48 against the locking hole 45. Separation is achieved, at which point the contact plate 36 and pressure plate 37 can be connected to push the clamping plate 47 downward. When the clamping plate 47 moves downward, the telescopic plate 50 pushes the stabilizing block 49 downward. When the stabilizing block 49 moves downward, the lifting plate 41 pushes the compression block 39 to compress the patient's femoral artery. After the force adjustment is completed, the clamping plate 47 is pushed to move. When the clamping plate 47 moves, it pushes the clamping block 48 into the clamping hole 45 to fix the clamping plate 47, preventing the compression block 39 from loosening after the force adjustment is completed.

[0028] There are two semicircular blocks 33, which are symmetrically arranged with the limiting block 30 as the center. The surface of the semicircular block 33 is in contact with the inner wall of the bracket 31. The arc-shaped adhesive tape 34 is bonded to the arc plate 32 by magic tape. The bottom of the lifting plate 41 passes through the pressing frame 1 and extends to the bottom outer end of the pressing frame 1. The pressing block 39 is located at the end of the pressing frame 1 away from the limiting block 30. The sliding hole 42 and the positioning groove 43 are interconnected.

[0029] Multiple locking holes 45 are set in two groups, and the number of each group is the same. The two groups of locking holes 45 are symmetrically arranged with the through hole 46 as the center. The surface of the locking plate 47 is in contact with the inner wall of the positioning groove 43. The surface of the locking block 48 is inserted into the inner wall of the locking hole 45. The end of the elastic rod 44 away from the locking plate 47 is in contact with the inner wall of the positioning groove 43. The top of the pressure plate 37 extends to the top outer end of the pressing frame 1 through the sliding hole 42.

[0030] When using this device to perform femoral artery compression hemostasis on post-tumor surgery patients, medical staff raise the patient's thigh to a certain height and place the arc-shaped plate 14 under the patient's thigh, with the arc-shaped plate 14 positioned at the root of the thigh. The bandage 12 is fixed to the limiting hole 15 with Velcro tape. After lowering the patient's leg, the patient's leg will come into contact with the top of the cotton pad 13. The cotton pad 13 on the top of the arc-shaped plate 14 contacts the patient's leg, improving comfort. The patient's leg will press down on the arc-shaped plate 14, using the arc-shaped plate 14 to limit the bandage 12 and improve the stability of the bandage 12 during hemostasis. After placing the compression frame 1 above the patient's leg, the bandage 12 passes through the through-hole frame 11 and is fixed with Velcro tape. The compression frame 1 is fixed above the patient's leg using the bandage 12. After the compression frame 1 is placed, the patient's femoral artery can be compressed by the compression component 4, improving the convenience of using the compression frame 1. When the compression frame 1 is installed, medical staff can turn the rotating disk 20 to rotate. The threaded rod 21 moves towards the interior of the central frame 10 as the rotating disk 20 rotates. When the threaded rod 21 moves downward, it pushes the center of the tripod 23 downward. When the center of the tripod 23 moves, its end pushes the two moving plates 24 to move away from each other. When the moving plates 24 move, they push the through-hole frame 11 away from the central frame 10 through the connecting plate 25. Thus, the distance between the bandage 12 and the compression frame 1 is adjusted by the through-hole frame 11, leaving space for medical staff to operate the puncture needle. After the compression frame 1 is fixed, the medical staff can remove the puncture needle, which improves convenience. The silicone pad 35 is placed over the surface of the compression block 39. When the compression frame 1 is fixed, medical staff need to place the silicone pad 35 directly above the vascular puncture needle to apply pressure to the patient's puncture site, preventing excessive bleeding after the needle is removed. After the silicone pad 35 is positioned, the arc-shaped adhesive tape 34 is attached to the patient's leg above the patient's leg using the adhesive at the bottom. The arc-shaped adhesive tape 34 is used to fix the compression frame 1, improving the stability of the compression frame 1 during hemostasis. When the pressure force needs to be adjusted, the pressure plate 37 is pushed to slide inside the sliding hole 42. When the pressure plate 37 moves, it pushes the locking plate 47 to compress the elastic rod 44 and pulls the telescopic plate 50 to extend. When the locking plate 47 moves, it pushes the locking block 48 to separate from the inner wall of the locking hole 45. At this time, the locking plate 47 can be pushed downward through the connection between the contact plate 36 and the pressure plate 37. When the locking plate 47 moves downward, it pushes the stabilizing block 49 downward through the telescopic plate 50. When moving downwards, the lifting plate 41 pushes the compression block 39 to compress the patient's femoral artery. After the force adjustment is completed, the locking plate 47 is pushed to move. When the locking plate 47 moves, it pushes the locking block 48 into the locking hole 45 to fix the locking plate 47, preventing the compression block 39 from loosening after the force adjustment is completed. The locking plate 47 is attached to the inside of the positioning groove 43 under the pressure of the elastic rod 44, improving the stability between the locking block 48 and the locking hole 45. When the compression block 39 is adjusted, the pressing frame 1 will rotate inside the support 31 with the limiting block 30 as the fulcrum, further improving the stability of the pressing frame 1 during hemostasis. The compression force of the compression block 39 is adjusted by pressing the pressure plate 37, improving the convenience of adjustment. The arc-shaped adhesive tape 34 is attached to the bottom of the arc plate 32 with magic tape, making it easy to replace the arc-shaped adhesive tape 34. The silicone pad 35 is directly covered on the surface of the compression block 39. When replacing, the silicone pad 35 can be directly removed, improving the convenience of replacement.

[0031] The preferred embodiments of the present invention disclosed above are merely illustrative of the invention. These preferred embodiments do not exhaustively describe all details, nor do they limit the invention to the specific implementations described. Clearly, many modifications and variations can be made based on the content of this specification. This specification selects and specifically describes these embodiments to better explain the principles and practical applications of the invention, thereby enabling those skilled in the art to better understand and utilize the invention. The invention is limited only by the claims and their full scope and equivalents.

Claims

1. A femoral artery compression hemostasis nursing device after tumor surgery, comprising a compression frame (1), characterized in that, The surface of the pressing frame (1) is provided with a bandage component (2); The bandage component (2) includes a central frame (10), the bottom of which is fixedly connected to the top of the pressing frame (1). A through-hole frame (11) is provided on the surface of the central frame (10). A cotton pad (13) is provided below the pressing frame (1). An arc plate (14) is inserted into the bottom of the cotton pad (13). A limiting hole (15) is provided at the bottom of the arc plate (14). A bandage (12) is provided on the surface of the pressing frame (1). The top of the bandage (12) passes through the arc plate (14) and extends to the outer end of the arc plate (14). The bottom of the bandage (12) passes through the limiting hole (15) and extends to the outer end of the limiting hole (15). An adjustment component (3) is provided inside the central frame (10). A compression component (4) is provided at the end of the pressing frame (1).

2. The femoral artery compression hemostasis nursing device according to claim 1, characterized in that: The number of bandages (12) is set to two, and the two bandages (12) are symmetrically arranged with the central frame (10) as the center. The ends of the bandages (12) are provided with magic tape.

3. The femoral artery compression hemostasis nursing device according to claim 2, characterized in that: The ends of the bandage (12) are glued together with Velcro, the bottom of the arc plate (14) extends to the bottom outer end of the cotton pad (13), and the end of the cotton pad (13) extends to the outer end of the arc plate (14).

4. The femoral artery compression hemostasis nursing device according to claim 3, characterized in that: The adjusting component (3) includes a rotating disk (20), a threaded rod (21) is fixedly connected to the bottom of the rotating disk (20), a tripod (23) is rotatably connected to the bottom of the threaded rod (21), a movable plate (24) is slidably connected to the bottom of the inner wall of the center frame (10), a groove (22) is provided on the surface of the movable plate (24), a connecting plate (25) is fixedly connected to the end of the movable plate (24) away from the groove (22), the end of the connecting plate (25) away from the movable plate (24) is fixedly connected to the through hole frame (11), and the bottom of the tripod (23) is hinged to the bottom of the inner wall of the groove (22).

5. The femoral artery compression hemostasis nursing device according to claim 4, characterized in that: The number of the movable plates (24) is set to two, and the two movable plates (24) are symmetrically arranged with the tripod (23) as the center. The bottom of the threaded rod (21) passes through the central frame (10) and extends into the interior of the central frame (10). The surface of the threaded rod (21) is threadedly connected to the inner wall of the central frame (10).

6. The femoral artery compression hemostasis nursing device according to claim 5, characterized in that: The top of the tripod (23) is hinged, and the end of the connecting plate (25) away from the moving plate (24) passes through the central frame (10) and extends to the outer end of the central frame (10). The end of the moving plate (24) contacts the inner wall of the central frame (10).

7. The femoral artery compression hemostasis nursing device according to claim 6, characterized in that: The pressing component (4) includes a limiting block (30), the top of which is fixedly connected to the bottom of the pressing frame (1), a semi-circular block (33) is fixedly connected to the surface of the limiting block (30), a bracket (31) is inserted into the surface of the limiting block (30), an arc plate (32) is fixedly connected to the bottom of the bracket (31), an arc-shaped adhesive tape (34) is provided at the bottom of the arc plate (32), and a magic tape is provided between the arc-shaped adhesive tape (34) and the arc plate (32). The pressing frame (1) has a sliding groove (40) inside, a fixing block (38) is fixedly connected to the inner wall of the pressing frame (1), a positioning groove (43) is opened inside the fixing block (38), a through hole (46) is opened at one end of the positioning groove (43) and the sliding groove (40) that are close to each other, and a sliding hole (46) is opened at the top of the pressing frame (1). 42) A stabilizing block (49) is slidably connected to the inner wall of the chute (40). A lifting plate (41) is fixedly connected to the bottom of the stabilizing block (49). A pressing block (39) is fixedly connected to the bottom of the lifting plate (41). A silicone pad (35) is sleeved on the surface of the pressing block (39). A telescopic plate (50) is fixedly connected to the surface of the stabilizing block (49). A clamping plate (47) is fixedly connected to the end of the telescopic plate (50) away from the stabilizing block (49). A clamping block (48) is fixedly connected to the surface of the clamping plate (47). A spring rod (44) is fixedly connected to the end of the clamping plate (47) away from the clamping block (48). A pressure plate (37) is fixedly connected to the top of the clamping plate (47). A contact plate (36) is fixedly connected to the top of the pressure plate (37). Multiple clamping holes (45) are opened inside the positioning groove (43).

8. The femoral artery compression hemostasis nursing device according to claim 7, characterized in that: There are two semicircular blocks (33), and the two semicircular blocks (33) are symmetrically arranged with the limiting block (30) as the center. The surface of the semicircular block (33) is in contact with the inner wall of the bracket (31). The arc-shaped adhesive tape (34) is bonded to the arc plate (32) by magic tape. The bottom of the lifting plate (41) passes through the pressing frame (1) and extends to the bottom outer end of the pressing frame (1). The pressing block (39) is located at the end of the pressing frame (1) away from the limiting block (30). The sliding hole (42) and the positioning groove (43) are interconnected.

9. A postoperative femoral artery compression hemostasis nursing device according to claim 8, characterized in that: The multiple card holes (45) are set in two groups, and the number of each group is the same. The two groups of card holes (45) are symmetrically arranged with the through hole (46) as the center. The surface of the card plate (47) is in contact with the inner wall of the positioning groove (43). The surface of the card block (48) is inserted into the inner wall of the card hole (45). The end of the elastic rod (44) away from the card plate (47) is in contact with the inner wall of the positioning groove (43). The top of the pressure plate (37) extends to the top outer end of the pressing frame (1) through the sliding hole (42).

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