Wound compression device
By designing a wound compression device including a connecting block, a pressing rod and a fixing belt, the problem of inconvenient wound compression and hemostasis after cardiac interventional treatment is solved, and flexible and convenient pressing and timing decompression functions are realized, which improves postoperative care efficiency.
Patent Information
- Application Number
- CN202420545005.1
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-03-20
- Publication Date
- 2025-02-07
- Estimated Expiration
- 2034-03-20
AI Technical Summary
After cardiac interventional treatment, the patient's postoperative wound compression and hemostasis operation is inconvenient, and the existing manual compression and bandaging methods have problems such as inconvenient operation and difficulty in controlling and reducing pressure.
A wound compression device is designed, including a connecting block, a pressing rod, a fixing disk, a piston cavity, a curved piston rod and a fixing belt. Through the combination of these components, flexible and convenient pressing operation and timing reduction functions are achieved.
This device allows medical staff to easily press and stop bleeding on the patient's puncture site, and flexibly control the pressing position by moving the connecting block and the cushion, simplifying the operation process and improving the efficiency of postoperative care.
Smart Images

Figure CN222426120U_ABST
Abstract
Description
Technical Field
[0001] The utility model relates to the technical field of medical auxiliary equipment, in particular to a wound compression device. Background Art
[0002] Cardiac intervention is a minimally invasive interventional procedure that can be used for the diagnosis and treatment of coronary heart disease. Coronary angiography can be used to determine whether coronary heart disease exists. If the degree of coronary artery vascular disease is relatively serious, balloon angioplasty, stent implantation, coronary artery atherectomy or thromboembolism can be performed to treat coronary heart disease. For structural heart diseases, including valvular heart disease and congenital heart disease, interventional surgery can also be used, including balloon angioplasty, valve replacement surgery and occlusion surgery. It is necessary to choose the appropriate indications. Interventional treatment has the characteristics of less trauma and faster recovery, which reduces the trauma of patients and is conducive to the early recovery of the disease. Cardiac intervention is mainly between internal medicine and surgery and is an invasive treatment. For example, coronary artery intervention is mainly used to place artificial stents in the narrowed part of the coronary artery to help relieve the symptoms of stenosis. For example, valve intervention can help treat patients with severe stenosis of the aortic valve, especially elderly patients who cannot undergo open-chest and replacement surgery, so interventional treatment can be chosen.
[0003] Cardiac interventional therapy is a new technology for diagnosing and treating cardiovascular diseases. It does not require thoracotomy. Under the guidance of imaging methods, the catheter is sent to the lesion site through puncture of surface blood vessels with the help of certain instruments. The heart disease is diagnosed and treated through specific cardiac catheter operation techniques. The compression and hemostasis effect at the radial artery or femoral artery puncture site after surgery directly affects the patient's recovery speed after surgery. Usually, hemostasis methods include manual compression and mechanical compression. Since patients receive heparinization treatment during and after surgery, the compression time needs to be extended. Currently, manual compression or bandaging and pressurization are often used for treatment. The manual compression process is long and the workload is large. The bandaging and pressurization method is inconvenient to operate, and it is inconvenient to control the decompression operation during use, which brings inconvenience to the patient's treatment. Utility Model Content
[0004] In view of the above situation, in order to overcome the defects of the prior art, the purpose of the present utility model is to provide a wound compression device, which effectively solves the problem that it is inconvenient for medical staff to operate the wound pressure hemostasis after interventional surgery.
[0005] The technical solution is as follows: the utility model comprises a connecting block, a pressing rod is slidably connected inside the connecting block, the lower end of the pressing rod passes through the connecting block and is provided with a pressing block, an upper end of the connecting block is fixed with an up-and-down axial fixing plate, a through groove is coaxially opened in the middle of the fixing plate and opens downward, the upper end of the pressing rod is inserted into the through groove, a C-shaped piston cavity is opened on the fixing plate, the left side of the piston cavity is connected with the through groove via a connecting hole, an arc-shaped piston rod is slidably connected inside the piston cavity, a pushing block in the up-and-down directions is provided on the upper left end of the piston rod, fixing columns are respectively provided at the left and right ends of the connecting block, fixing belts are respectively mounted on the two fixing columns, an arc-shaped supporting pad is provided under the connecting block, positioning grooves are respectively opened on the left and right sides of the supporting pad, and the free end of the fixing belt passes through the positioning grooves on its corresponding sides.
[0006] The utility model has an ingenious structure and is easy to use. It is convenient for medical staff to press and stop bleeding on the puncture site of the patient after interventional treatment, and is also helpful for medical staff to control the pressing site. By moving the connecting block and the supporting pad, the pressing operation positioning is more flexible and convenient, which is convenient for medical staff to operate, and makes the initial positioning of the connecting block more stable. At the same time, only the push block needs to be turned to complete the compression of the patient's puncture site, and after maintaining it for a period of time, it is convenient for medical staff to perform timed decompression operations, which is beneficial to postoperative care of patients and convenient for medical staff to use. This utility model has a simple structure, is easy to operate, has a novel conception, and is highly practical. BRIEF DESCRIPTION OF THE DRAWINGS
[0007] Figure 1 It is an axonometric drawing of the utility model.
[0008] Figure 2 It is a full cutaway front view of the utility model.
[0009] Figure 3 It is a partially cutaway main axonometric drawing of the utility model.
[0010] Figure 4 It is a partially cutaway top view of the utility model.
[0011] Figure 5 It is a top view of the utility model. DETAILED DESCRIPTION
[0012] The specific implementation of the utility model is further described in detail below with reference to the accompanying drawings.
[0013] Depend on Figures 1 to 5It is given, including a connecting block 1, a pressing rod 2 is slidably connected inside the connecting block 1, the lower end of the pressing rod 2 passes through the connecting block 1 and is provided with a pressing block 3, an upper end of the connecting block 1 is fixed with an up and down axial fixing plate 4, a through groove 5 with an opening facing downward is coaxially opened in the middle of the fixing plate 4, the upper end of the pressing rod 2 is inserted into the through groove 5, a C-shaped piston chamber 6 is opened on the fixing plate 4, the left side of the piston chamber 6 is connected with the through groove 5 via a connecting hole 7, an arc-shaped piston rod 8 is slidably connected in the piston chamber 6, a push block 9 in the up and down directions is provided on the upper left end of the piston rod 8, fixing columns 10 are respectively provided at the left and right ends of the connecting block 1, fixing belts 11 are respectively mounted on the two fixing columns 10, an arc-shaped supporting pad 12 is provided at the bottom of the connecting block 1, positioning grooves 13 are respectively opened on the left and right sides of the supporting pad 12, and the free end of the fixing belt 11 passes through the positioning groove 13 on its corresponding side.
[0014] In order to facilitate the resetting of the piston rod 8 , the rear end of the piston rod 8 is connected to the left end of the piston chamber 6 via an arc spring 14 .
[0015] In order to facilitate the movement of the piston rod 8 , the fixed plate 4 is provided with an arc-shaped clearance groove 15 with an opening facing upwards. The lower end of the clearance groove 15 is communicated with the piston cavity 6 , and the push block 9 is located in the clearance groove 15 .
[0016] In order to facilitate limiting the position of the piston rod 8, the fixed disk 4 is provided with a plurality of slots 16 evenly distributed along its circumferential direction and connected to the piston chamber 6, and the piston rod 8 is provided with a rectangular slot 17, in which a block 18 that can be inserted into the slot 16 is slidably connected.
[0017] In order to facilitate the movement of the block 18, the front end of the block 18 is connected to the rectangular groove 17 via a U-shaped elastic sheet 19, and the rear end face of the block 18 is an inclined surface tilted forward on the right side. A moving groove 20 with an opening facing upward and connected to the right end of the rectangular groove 17 is provided on the piston rod 8. A lever 21 fixedly connected to the block 18 is slidably connected in the moving groove 20, and the upper end of the lever 21 extends out of the moving groove 20.
[0018] In order to facilitate the use of the fixing belt 11, a Velcro is provided at the free end of the fixing belt 11, and a Velcro mother tape which can be bonded to the Velcro is provided on the upper side of the fixing belt 11.
[0019] When the utility model is used, the support pad 12 is placed in the opposite direction of the patient's puncture site, and then the pressing block 3 on the connecting block 1 is fitted with the patient's puncture site. At this time, the fixing belt 11 is passed around the positioning groove 13 of the support pad 12, and then the Velcro child tape is bonded with the Velcro mother tape to preliminarily position the support pad 12 and the connecting block 1 on the patient's limb;
[0020] The medical staff rotates the push block 9 counterclockwise, and the push block 9 moves along the yield groove 15, and drives the piston rod 8 to move counterclockwise. The piston rod 8 pushes the gas in the piston chamber 6 to flow into the through groove 5 through the connecting hole 7, and pushes the pressing rod 2 to move downward. The pressing rod 2 pushes the pressing block 3 to compress the patient's puncture point to stop bleeding;
[0021] During the sliding process of the piston rod 8, the piston rod 8 drives the synchronous movement, and since the rear side of the clamping block 18 is an inclined surface, the clamping block 18 is a unidirectional limit for the piston rod 8. When the piston rod 8 squeezes the arc spring 14 to the limit position, the clamping block 18 is inserted into the clamping groove 16;
[0022] When the patient needs to perform a decompression operation, the lever 21 is pushed forward, and the lever 21 drives the block 18 to move out of the slot 16 and squeeze the elastic sheet 19. Then the lever 21 is released, and under the action of the arc spring 14 and the elastic sheet 19, the block 18 is inserted into the adjacent slot 16 to perform a decompression operation. Through the above process, the patient is gradually decompressed.
[0023] The utility model has an ingenious structure and is easy to use. By arranging the connecting block, the fixing belt, the supporting pad, the pressing block and the pressing rod, it is convenient for medical staff to press and stop bleeding on the puncture site after the patient's interventional treatment, and it is also convenient for medical staff to control the pressing site. By moving the connecting block and the supporting pad, the pressing operation positioning is more flexible and convenient, which is convenient for medical staff to operate, and makes the initial positioning of the connecting block more stable. At the same time, a piston rod, a piston cavity, a fixing plate, a through groove and a connecting groove are provided. Only by toggling the pushing block can the compression of the patient's puncture site be completed, and after maintaining it for a period of time, it is convenient for medical staff to perform a timed decompression operation, which is beneficial to postoperative care of the patient and convenient for medical staff to use. The utility model has a simple structure, is easy to operate, has a novel conception and is highly practical.
Claims
1. A wound compression device, comprising a connecting block (1), characterized in that: A pressing rod (2) is slidably connected in the connecting block (1). The lower end of the pressing rod (2) passes through the connecting block (1) and is provided with a pressing block (3). A fixing plate (4) is fixed to the upper end of the connecting block (1) in an up-and-down axial direction. A through groove (5) with an opening facing downward is coaxially opened in the middle of the fixing plate (4). The upper end of the pressing rod (2) is inserted into the through groove (5). A C-shaped piston cavity (6) is opened on the fixing plate (4). The left side of the piston cavity (6) is connected to the through groove (5) via a connecting hole (7). An arc-shaped piston rod (8) is slidably connected in the piston cavity (6). A push block (9) is provided in an up-and-down direction on the upper side of the left end of the piston rod (8). Fixed columns (10) are respectively provided at the left and right ends of the connecting block (1). Fixed belts (11) are respectively mounted on the two fixed columns (10). An arc-shaped support pad (12) is provided below the connecting block (1). Positioning grooves (13) are respectively opened on the left and right sides of the support pad (12). The free end of the fixing belt (11) passes through the positioning groove (13) on the corresponding side.
2. A wound compression device according to claim 1, characterized in that: The rear end of the piston rod (8) is connected to the left end of the piston chamber (6) via an arc spring (14).
3. A wound compression device according to claim 1, characterized in that: The fixed plate (4) is provided with an arc-shaped clearance groove (15) with an opening facing upwards, the lower end of the clearance groove (15) is communicated with the piston cavity (6), and the push block (9) is located in the clearance groove (15).
4. A wound compression device according to claim 1, characterized in that: The fixed disk (4) is provided with a plurality of slots (16) evenly distributed along its circumferential direction and connected to the piston chamber (6); the piston rod (8) is provided with a rectangular slot (17), and a block (18) which can be inserted into the slot (16) is slidably connected in the rectangular slot (17).
5. A wound compression device according to claim 4, characterized in that: The front end of the clamping block (18) is connected to the rectangular groove (17) via a U-shaped elastic sheet (19); the rear end surface of the clamping block (18) is an inclined surface inclined forward on the right side; the piston rod (8) is provided with a movable groove (20) with an opening facing upward and connected to the right end of the rectangular groove (17); a shifting rod (21) fixedly connected to the clamping block (18) is slidably connected in the movable groove (20); and the upper end of the shifting rod (21) extends out of the movable groove (20).
6. A wound compression device according to claim 1, characterized in that: The free end of the fixing belt (11) is provided with a Velcro tape, and the upper side of the fixing belt (11) is provided with a Velcro tape that can be bonded to the Velcro tape.