Wound hemostasis device for general surgery clinical operation

Abstract

The invention relates to the technical field of medical instruments, and particularly discloses a wound hemostasis device for general surgery clinical surgery, which comprises a base, and further comprises a hemostasis component arranged on the base and used for carrying out compression hemostasis on a wound of a patient; the regulation and control assembly is arranged on the hemostasis assembly, and the regulation and control assembly is used for regulating the compression force of the hemostasis assembly on the wound. The hemostasis device can be conveniently aligned to the wound of a patient through the hemostasis assembly, the compression hemostasis effect is prevented from being affected by the offset of the compression position, the compression force on the wound of the patient can be relieved every set time in the compression hemostasis process of the wound of the patient through the regulation and control assembly, and the hemostasis effect is improved. The compression hemostasis device can be used for preventing discomfort of a patient possibly caused by long-time compression on the wound, and can be used for adjusting the compression on the wound according to the hemostasis condition when the compression is relieved and if the errhysis condition occurs, so as to ensure compression hemostasis on the wound.

Description

Technical Field

[0001] The invention relates to the technical field of medical devices, in particular to a wound hemostasis device for general surgery clinical operations. Background Art

[0002] General surgery is ordinary surgery. In addition to general surgery, general comprehensive hospitals also have orthopedics, neurosurgery, cardiothoracic surgery, urology, etc. Some hospitals further divide general surgery into cervical and breast surgery, gastrointestinal surgery, hepatobiliary, pancreatic and spleen surgery, etc. Anorectal surgery, burn and plastic surgery, vascular surgery, pediatric surgery, transplant surgery, nutrition, etc. are all related to general surgery. During clinical surgery, the patient's wound needs to be stopped before and after the operation to avoid excessive blood loss.

[0003] When using compression hemostasis to stop bleeding, it may be difficult to adjust the wound position for different patients and wound locations, causing the compression position to shift and affecting the hemostasis effect. In addition, during the compression hemostasis process, the pressure on the wound position may not be adjusted in time according to the hemostasis situation. Long-term compression may cause discomfort to the patient. For this reason, we propose a wound hemostasis device for general surgery clinical surgery. Summary of the invention

[0004] The purpose of the present invention is to provide a wound hemostasis device for general surgery clinical surgery to solve the problem raised in the above background technology that during compression hemostasis, it may be difficult to adjust the position of the wound, causing the compression position to shift and affecting the hemostasis effect. In addition, during the process of compression hemostasis, the pressure on the wound position may not be adjusted in time according to the hemostasis situation, which may cause discomfort to the patient.

[0005] To achieve the above-mentioned purpose, the present invention provides the following technical solution: a wound hemostasis device for general surgery clinical operation, comprising: a base, a protective pad is fixed on the base,

[0006] It also includes: a hemostasis component, which is arranged on the base and is used to compress and stop bleeding on the patient's wound;

[0007] The regulating component is arranged on the hemostasis component and is used to adjust the pressure of the hemostasis component on the wound.

[0008] Among them, the hemostasis component includes a mounting part fixed to the base, a support column is fixed on the upper side of the mounting part, a rotating block is rotatably arranged on the support column, a connecting tube is fixed on one side of the rotating block, a connecting part is slidably arranged in the connecting tube, and a sliding groove adapted to the connecting part is symmetrically arranged in the connecting tube, and the connecting part slides up and down along the sliding groove.

[0009] Among them, a first motor is fixed on the upper side of the connecting cylinder, a screw threadedly connected to the connecting piece is fixed on the output end of the first motor, a pressure plate is fixed at the lower end of the connecting piece, a flexible pad is fixed on the lower side of the pressure plate, and a through groove matching the pressure plate is set through the mounting piece.

[0010] Among them, a connecting shell is fixedly provided on one side of the support column, a first electromagnetic block is fixedly provided in the connecting shell, an adsorption block which can be adsorbed with the first electromagnetic block is slidably provided in the connecting shell, a first spring is symmetrically fixedly provided between the adsorption block and the connecting shell, an insertion block which movably passes through the connecting shell is fixedly provided on the upper side of the adsorption block, a socket matching with the insertion block is provided on the lower side of the rotating block, and a first switch electrically connected with the first electromagnetic block is installed on one side of the rotating block.

[0011] Among them, the regulating component includes an installation box fixed to the installation piece, a sliding rheostat is fixed in the installation box, a sliding block is fixed on the sliding piece of the sliding rheostat and is slidably set with the installation box, a guide groove adapted to the sliding block is provided on the inner side of the top end of the installation box, and the sliding block slides along the guide groove.

[0012] Among them, a second electromagnetic block is fixedly provided on the inner side of the installation box, a magnetic block that can repel the second electromagnetic block is fixedly embedded on one side of the sliding block, a second spring fixed to the installation box is fixed on one side of the sliding block, and mounting blocks fixed to the installation box are provided on both sides of the sliding block. A second switch is installed on one side of the mounting block close to the sliding block, and a third switch is installed on the other side of the mounting block close to the sliding block.

[0013] Among them, multiple layers of gauze are fixed on the lower side of the flexible pad, resistor patches are arranged between the flexible pad and the upper layer of gauze and between the two layers of gauze, and an isolation membrane is arranged between the two layers of gauze.

[0014] Among them, an air pump is fixedly provided on the upper side of the pressure plate, one end of the air pump is fixedly connected to a three-way pipe, both ends of the three-way pipe are fixedly connected to connecting pipes, the connecting pipes pass through the pressure plate and the flexible pad and face the resistor patch, and the other end of the air pump is fixedly connected to an air intake pipe.

[0015] A second motor is fixedly arranged on the upper side of the pressure plate, a transmission rod is fixedly arranged on the output end of the second motor, two blocks are fixedly arranged on the transmission rod, and one end of the isolation membrane is fixed to the transmission rod and located between the two blocks.

[0016] Among them, a pressure block is threadedly arranged on one side of the transmission rod and is slidably arranged with a pressure plate. A limiting groove adapted to the pressure block is arranged on the pressure plate. The pressure block limiting groove slides. A connecting block is fixedly arranged at equal intervals on one side of the pressure block on the pressure plate. A fourth switch is installed on the side of the connecting block close to the pressure block.

[0017] The present invention has at least the following beneficial effects:

[0018] The present invention uses a hemostatic component to compress and stop bleeding at the wound of the patient, and the hemostatic component can be conveniently adjusted for different patients and wound locations to align with the patient's wound to prevent the compression position from shifting and affecting the compression and hemostasis effect. The regulating component can be used to reduce the pressure on the patient's wound at set intervals during the process of compressing and stopping bleeding at the patient's wound to prevent discomfort to the patient caused by long-term compression on the wound. When the pressure is reduced, if bleeding occurs, the pressure on the wound can be adjusted according to the hemostasis situation to ensure compression and hemostasis of the wound. Therefore, the pressure on the wound of the hemostatic component can be adjusted by the regulating component, which is convenient for medical staff to use. BRIEF DESCRIPTION OF THE DRAWINGS

[0019] Figure 1 It is a three-dimensional structural schematic diagram of the present invention;

[0020] Figure 2 It is a schematic structural diagram of a cross-section of a connecting tube and a connecting piece of the present invention;

[0021] Figure 3 It is a schematic structural diagram of a cross-section of a connecting shell of the present invention;

[0022] Figure 4 It is a structural schematic diagram of the upper side regulating assembly of the pressing plate of the present invention;

[0023] Figure 5 It is a schematic structural diagram of a cross-section of the installation box of the present invention;

[0024] Figure 6 It is a schematic diagram of the structure in which the sliding block of the present invention is separated from the mounting blocks on both sides;

[0025] Figure 7 It is a schematic diagram of the structure of the explosion of the gauze, the resistor patch and the isolation film of the present invention;

[0026] Figure 8 It is a schematic structural diagram of the transmission rod connection of the present invention.

[0027] In the figure: 11, base; 12, protective pad; 2, hemostasis component; 21, mounting member; 22, support column; 23, rotating block; 24, connecting tube; 25, connecting member; 26, slide groove; 27, screw; 28, first motor; 29, pressing plate; 210, flexible pad; 211, connecting shell; 212, first electromagnetic block; 213, adsorption block; 214, first spring; 215, plug block; 216, first switch; 217, jack; 3, regulating component; 31, mounting box; 32, sliding block; 33 , sliding rheostat; 34, second electromagnetic block; 35, magnetic block; 36, second spring; 37, mounting block; 38, guide groove; 39, second switch; 310, third switch; 311, gauze; 312, resistor patch; 313, isolation membrane; 314, air pump; 315, connecting pipe; 316, air intake pipe; 317, second motor; 318, transmission rod; 319, stopper; 320, pressure block; 321, connecting block; 322, fourth switch; 323, limit groove; 324, three-way pipe. DETAILED DESCRIPTION

[0028] The following will be combined with the drawings in the embodiments of the present invention to clearly and completely describe the technical solutions in the embodiments of the present invention. Obviously, the described embodiments are only part of the embodiments of the present invention, not all of the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the present invention.

[0029] Embodiment 1

[0030] See also Figures 1 to 8 The present invention provides a technical solution: a wound hemostasis device for general surgery clinical operation, comprising: a base 11, a protective pad 12 is fixed on the base 11,

[0031] It also includes: a hemostasis component 2, which is arranged on the base 11 and is used to compress and stop bleeding on the patient's wound;

[0032] The regulating component 3 is arranged on the hemostasis component 2, and is used to adjust the pressure of the hemostasis component 2 on the wound.

[0033] When stopping bleeding at the wound of the patient, the patient's wound area that needs compression and hemostasis is placed on the protective pad 12 on the base 11, and the wound area of ​​the patient is compressed and hemostatically controlled through the hemostatic component 2. For different patients and wound locations, the hemostatic component 2 can be conveniently adjusted to align with the patient's wound to prevent the compression position from shifting and affecting the compression and hemostasis effect. Through the regulating component 3, during the process of compressing and stopping bleeding at the patient's wound, the pressure on the patient's wound can be reduced at set intervals to prevent the patient's discomfort caused by long-term compression on the wound. When the pressure is reduced, if bleeding occurs, the pressure on the wound can be adjusted according to the hemostasis situation to ensure compression and hemostasis of the wound. Therefore, the pressure of the hemostatic component 2 on the wound can be adjusted through the regulating component 3, which is convenient for medical staff to use.

[0034] Embodiment 2

[0035] The hemostasis component 2 includes a mounting member 21 fixed to the base 11, a support column 22 is fixed to the upper side of the mounting member 21, a rotating block 23 is rotatably arranged on the supporting column 22, a connecting tube 24 is fixed to one side of the rotating block 23, a connecting member 25 is slidably arranged in the connecting tube 24, the connecting member 25 can slide downward to pass through the connecting tube 24, a sliding groove 26 adapted to the connecting member 25 is symmetrically arranged in the connecting tube 24, the connecting member 25 slides up and down along the sliding groove 26, and can guide and limit the sliding of the connecting member 25 in the connecting tube 24;

[0036] A first motor 28 is fixedly disposed on the upper side of the connecting tube 24, a screw 27 threadedly connected to the connecting member 25 is fixedly disposed on the output end of the first motor 28, a pressing plate 29 is fixedly disposed on the lower end of the connecting member 25, a flexible pad 210 is fixedly disposed on the lower side of the pressing plate 29 to increase the comfort during compression, and a through slot matching the pressing plate 29 is provided through the mounting member 21, so that the pressing plate 29 can pass downward through the mounting member 21 to compress the wound position of the patient to stop bleeding;

[0037] A connection shell 211 is fixedly provided on one side of the support column 22, a first electromagnetic block 212 is fixedly provided in the connection shell 211, an adsorption block 213 which can be adsorbed with the first electromagnetic block 212 is slidably provided in the connection shell 211, a first spring 214 is symmetrically fixedly provided between the adsorption block 213 and the connection shell 211, an insertion block 215 which movably penetrates the connection shell 211 is fixedly provided on the upper side of the adsorption block 213, a socket 217 which matches with the insertion block 215 is provided on the lower side of the rotating block 23, and a first switch 216 which is electrically connected with the first electromagnetic block 212 is installed on one side of the rotating block 23;

[0038] When in use, the first switch 216 is pressed to energize the first electromagnetic block 212, thereby generating an adsorption force on the adsorption block 213, so that the plug block 215 moves downward out of the socket 217, the first spring 214 is stretched, and the rotating block 23 is rotated to one side, so that the pressure plate 29 moves out of the top of the through slot on the mounting member 21, and then the first switch 216 can be released. After preliminary treatment of the patient's wound, the patient's wound that needs compression and hemostasis is placed on the protective pad 12 on the base 11. The position of the base 11 can be adjusted so that the patient's wound position is below the through slot on the mounting member 21, that is, it corresponds to the position of the through slot on the mounting member 21 up and down. Then, the rotating block 23 is rotated in the opposite direction. The upper side of the plug block 215 is provided with an inclined surface, and during the reverse rotation of the rotating block 23, the inclined surface of the plug block 215 can be pressed. , so that the plug block 215 moves down, and after the socket 217 on the lower side of the rotating block 23 corresponds to the position of the plug block 215, under the elastic force of the first spring 214, the plug block 215 moves up and is inserted into the socket 217, so that the rotating block 23 can be fixed, and the pressure plate 29 is kept corresponding to the position of the through slot on the mounting member 21, that is, the pressure plate 29 can be aligned downward with the patient's wound, so that when the pressure plate 29 moves down to compress the wound to stop bleeding, the pressure position can be prevented from being offset, thereby affecting the effect of compressing and stopping bleeding; then, the first motor 28 is controlled to start, and the first motor 28 drives the screw rod 27 to rotate, so that the connecting member 25 moves downward along the slide groove 26, so that the pressure plate 29 and the flexible pad 210 can be driven to pass through the through slot on the mounting member 21 and move downward, so as to compress the patient's wound position to stop bleeding.

[0039] Embodiment 3

[0040] The regulating component 3 includes a mounting box 31 fixedly mounted on the mounting member 21, a sliding rheostat 33 fixedly mounted in the mounting box 31, the sliding rheostat 33 is electrically connected to the first motor 28 and the air pump 314, the sliding rheostat 33 is located on a side of the sliding piece away from the second electromagnetic block 34, and the coil resistance is connected to the circuit, a sliding block 32 slidingly mounted on the mounting box 31 is fixedly mounted on the sliding piece of the sliding rheostat 33, a guide groove 38 adapted to the sliding block 32 is arranged on the inner side of the top end of the mounting box 31, the sliding block 32 slides along the guide groove 38, and the cross section of the guide groove 38 is arranged to be trapezoidal, which can guide the sliding of the sliding block 32;

[0041] A second electromagnetic block 34 is fixedly arranged on the inner side of the installation box 31, a magnetic block 35 which can repel the second electromagnetic block 34 is fixedly arranged on one side of the sliding block 32, a second spring 36 fixedly arranged on the installation box 31 is fixedly arranged on one side of the sliding block 32, and installation blocks 37 fixedly arranged on the installation box 31 are arranged on both sides of the sliding block 32, a second switch 39 is installed on one side of the installation block 37 close to the sliding block 32, and the second switch 39 is electrically connected to the first motor 28, and a third switch 310 is installed on the other side of the installation block 37 close to the sliding block 32, and the third switch 310 is electrically connected to the air pump 314, and inclined surfaces are arranged on both sides of the sliding block 32 to facilitate the reset and pressing of the second switch 39 and the third switch 310;

[0042] A plurality of layers of gauze 311 are fixed to the lower side of the flexible pad 210. A resistor patch 312 is arranged between the flexible pad 210 and the upper layer of gauze 311 and between the two layers of gauze 311. The resistor patch 312 is a sensor array patch made of a flexible printed circuit board and is composed of a plurality of resistors and connecting wires. The plurality of resistors are arranged in series through metal wires to form a series resistor network. When blood seeps out of the wound, the resistance value of the series resistor network of the resistor patch 312 will change, so that the bleeding situation can be monitored. An isolation membrane 31 is arranged between the two layers of gauze 311. 3. Two isolation films 313 isolate the upper and lower resistor patches 312 respectively, so that when the lower resistor patch 312 detects bleeding, the isolation film 313 can isolate the blood to prevent the blood from seeping into the upper resistor patch 312 and affecting the subsequent use of the upper resistor patch 312. The three resistor patches 312 are electrically connected to the three fourth switches 322 respectively, and are all electrically connected to the second electromagnetic block 34. Initially, the pressing block 320 presses the first fourth switch 322, and the bottom resistor patch 312 is connected to the second electromagnetic block 34.

[0043] In the process of compressing and stopping bleeding on the patient's wound by the hemostasis component 2, at regular intervals, the first motor 28 will drive the screw 27 to rotate in the opposite direction, so that the connecting member 25 drives the pressure plate 29 to move up a certain distance, so as to gradually reduce the pressure on the patient's wound and prevent the discomfort of the patient caused by long-term pressure on the wound; after the pressure on the wound is reduced, if bleeding occurs, the blood will penetrate through the lower gauze 311 to the bottom layer of the resistor patch 312, so that the resistance value of the resistor network of the resistor patch 312 is reduced, so that the magnetism of the second electromagnetic block 34 is increased, and the repulsive effect on the magnetic block 35 is increased, so that the sliding block 32 moves away from the second electromagnetic block 34, and the second spring 36 is compressed, so that the sliding block 32 no longer presses the second switch 39, so that the first motor 28 drives the screw 27 to rotate forward for a certain distance. The time for the pressure plate 29 to move downward is to increase the pressure on the wound and prevent blood from seeping out. The sliding block 32 can also drive the sliding piece of the sliding rheostat 33 to move away from the second electromagnetic block 34, so that the resistance value of the sliding rheostat 33 connected to the circuit is reduced, and the torque of the first motor 28 is increased. When there is a lot of bleeding, the resistance value of the resistance network of the resistor patch 312 is reduced more, so that the second electromagnetic block 34 has a greater repulsive effect on the magnetic block 35, and the sliding block 32 moves away from the second electromagnetic block 34 more, which can increase the torque of the first motor 28. Therefore, when the amount of bleeding is large, when the first motor 28 drives the screw 27 to rotate forward for a certain period of time, the first motor 28 can drive the screw 27 to rotate forward for a large number of circles, so that the pressure on the wound is increased more, so as to ensure the compression and hemostasis effect.

[0044] An air pump 314 is fixedly arranged on the upper side of the pressing plate 29. One end of the air pump 314 is fixedly connected to a three-way pipe 324. Both ends of the three-way pipe 324 are fixedly connected to connecting pipes 315. The connecting pipes 315 penetrate the pressing plate 29 and the flexible pad 210 and face the resistor patch 312. The connecting pipes 315 can be set as rubber hoses. The other end of the air pump 314 is fixedly connected to an air inlet pipe 316. A filter is arranged at the end of the air inlet pipe 316 to filter and purify the gas to prevent the gas from being blown toward the resistor patch 312 and possibly infecting the wound.

[0045] After the pressure on the wound is relieved, if bleeding occurs, the movement of the sliding block 32 away from the second electromagnetic block 34 can also release the pressure on the third switch 310, so that the air pump 314 works and the gas is blown out through the three-way pipe 324 and the connecting pipes 315 on both sides, so as to blow the gas to the resistor patch 312 from both sides, dry the blood on the resistor patch 312, accelerate the coagulation of the blood on the resistor patch 312, and prevent the use of the subsequent upper resistor patch 312 from being affected. As the blood on the resistor patch 312 coagulates, the resistance value of the resistor network on the resistor patch 312 will increase, so that the repulsive effect of the second electromagnetic block 34 on the magnetic block 35 is reduced, and under the elastic force of the second spring 36 Under the condition that the sliding block 32 moves close to the second electromagnetic block 34, when the sliding block 32 presses the third switch 310 again, the air pump 314 stops working, and the sliding rheostat 33 is connected to the air pump 314. Similarly, when a lot of blood seeps out, the power of the air pump 314 can be increased to speed up the coagulation of the more seeped blood; the third switch 310 can be set as a delay switch. When the sliding block 32 releases the pressing effect on the third switch 310, the delayed operation of the air pump 314 can ensure that the resistance patch 312 detects the blood seepage. When the sliding block 32 moves close to the second electromagnetic block 34 and presses the third switch 310 again, the delayed stop of the air pump 314 can ensure the coagulation of the blood on the resistance patch 312.

[0046] A second motor 317 is fixedly provided on the upper side of the pressing plate 29, a transmission rod 318 is fixedly provided on the output end of the second motor 317, two blocks 319 are fixedly provided on the transmission rod 318, one end of the isolation film 313 is fixed to the transmission rod 318 and is located between the two blocks 319, the length of the upper isolation film 313 is greater than the length of the lower isolation film 313, after the lower isolation film 313 is rolled up and separated from the resistor patch 312, the upper isolation film 313 will not separate from the resistor patch 312, so as to continue to isolate the two upper resistor patches 312, A pressing block 320 is threadedly provided on one side of the transmission rod 318 and is slidably provided with the pressing plate 29. A limiting groove 323 adapted to the pressing block 320 is provided on the pressing plate 29. The limiting groove 323 of the pressing block 320 slides, which can guide and limit the pressing block 320. A connecting block 321 is fixedly provided at equal intervals on one side of the pressing block 320 of the pressing plate 29. A fourth switch 322 is installed on one side of the connecting block 321 close to the pressing block 320. An inclined surface is provided on one side of the pressing block 320 close to the connecting block 321 to facilitate the pressing of the fourth switch 322.

[0047] When the blood on the bottom layer of the resistor patch 312 coagulates, the sliding block 32 presses the third switch 310 again, which can make the second motor 317 work for a certain period of time, and the second motor 317 drives the transmission rod 318 to rotate, and the two isolation films 313 are rolled up and rolled up between the two stoppers 319, so that the lower isolation film 313 is separated from the resistor patch 312, so that when the set time is reached again in the future, the first motor 28 drives the screw rod 27 to reverse, and when the pressure on the wound is reduced, if bleeding occurs, the blood can seep into the resistor patch 312 at the middle position, and the bleeding is detected by the resistor patch 312 at the middle position; at the same time, the second motor 317 drives the transmission rod 318 to rotate, which can make the pressing block 320 move away from the second motor 317 along the limiting groove 323, and after the second motor 317 stops working after reaching the working time, the pressing block 320 can move to the connecting block 321 at the middle position, and press the first connecting block 321 on one side of the connecting block 321 at the middle position. The fourth switch 322 connects the resistor patch 312 in the middle position to the second electromagnetic block 34, so as to detect the hemostasis through the resistor patch 312 in the middle position. Similarly, the upper isolation film 313 can be rolled up later to separate from the resistor patch 312, so that blood can seep to the uppermost resistor patch 312. At the same time, the pressing block 320 can continue to move away from the second motor 317 and press the fourth switch 322 on one side of the third connecting block 321, so that the uppermost resistor patch The sheet 312 is connected to the second electromagnetic block 34 to detect the hemostasis situation through the uppermost resistor patch 312; when the screw 27 is initially driven to rotate by the first motor 28, the connecting piece 25 drives the pressure plate 29 to move downward to compress the wound position for hemostasis. If the hemostasis pressure is insufficient and bleeding occurs at the wound, the bleeding situation can be detected by the lowermost resistor patch 312, and the pressure of the hemostasis component 2 on the wound can also be adjusted to ensure the effect of compression hemostasis.

[0048] It should be noted that, in this article, relational terms such as first and second, etc. are only used to distinguish one entity or operation from another entity or operation, and do not necessarily require or imply any such actual relationship or order between these entities or operations. Moreover, the terms "include", "comprise" or any other variants thereof are intended to cover non-exclusive inclusion, so that a process, method, article or device including a series of elements includes not only those elements, but also other elements not explicitly listed, or also includes elements inherent to such process, method, article or device.

[0049] Although embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that various changes, modifications, substitutions and variations may be made to the embodiments without departing from the principles and spirit of the present invention, and that the scope of the present invention is defined by the appended claims and their equivalents.

Claims

1. A wound hemostasis device for general surgery clinical operation, comprising: A base (11), a protective pad (12) being fixed on the base (11), It is characterized in that it also comprises: a hemostasis component (2), wherein the hemostasis component (2) is arranged on the base (11), and the hemostasis component (2) is used to compress the wound of the patient to stop bleeding; A regulating component (3), wherein the regulating component (3) is arranged on the hemostasis component (2), and the regulating component (3) is used to adjust the pressure of the hemostasis component (2) on the wound.

2. The wound hemostasis device for general surgery clinical operation according to claim 1, characterized in that: The hemostasis component (2) comprises a mounting member (21) fixed to the base (11), a support column (22) fixedly arranged on the upper side of the mounting member (21), a rotating block (23) rotatably arranged on the support column (22), a connecting tube (24) fixedly arranged on one side of the rotating block (23), a connecting member (25) slidably arranged in the connecting tube (24), a sliding groove (26) adapted to the connecting member (25) symmetrically arranged in the connecting tube (24), and the connecting member (25) slides up and down along the sliding groove (26).

3. The wound hemostasis device for general surgery clinical operation according to claim 2, characterized in that: A first motor (28) is fixedly arranged on the upper side of the connecting tube (24); a screw (27) threadedly connected to the connecting member (25) is fixedly arranged at the output end of the first motor (28); a pressure plate (29) is fixedly arranged at the lower end of the connecting member (25); a flexible pad (210) is fixedly arranged on the lower side of the pressure plate (29); and a through groove matching the pressure plate (29) is penetrated through the mounting member (21).

4. The wound hemostasis device for general surgery clinical operation according to claim 2, characterized in that: A connecting shell (211) is fixedly provided on one side of the support column (22), a first electromagnetic block (212) is fixedly provided in the connecting shell (211), an adsorption block (213) which can be adsorbed with the first electromagnetic block (212) is slidably provided in the connecting shell (211), a first spring (214) is symmetrically fixedly provided between the adsorption block (213) and the connecting shell (211), an insert block (215) which movably passes through the connecting shell (211) is fixedly provided on the upper side of the adsorption block (213), a socket (217) which matches with the insert block (215) is provided on the lower side of the rotating block (23), and a first switch (216) which is electrically connected with the first electromagnetic block (212) is installed on one side of the rotating block (23).

5. The wound hemostasis device for general surgery clinical operation according to claim 3, characterized in that: The regulating component (3) comprises a mounting box (31) fixedly mounted on the mounting member (21); a sliding rheostat (33) is fixedly mounted in the mounting box (31); a sliding block (32) is fixedly mounted on a sliding plate of the sliding rheostat (33) and is slidably mounted on the mounting box (31); a guide groove (38) adapted to the sliding block (32) is arranged on the inner side of the top end of the mounting box (31); and the sliding block (32) slides along the guide groove (38).

6. The wound hemostasis device for general surgery clinical operation according to claim 5, characterized in that: A second electromagnetic block (34) is fixedly arranged on the inner side of the installation box (31); a magnetic block (35) capable of repelling the second electromagnetic block (34) is fixedly arranged on one side of the sliding block (32); a second spring (36) fixedly arranged on the installation box (31) is fixedly arranged on one side of the sliding block (32); installation blocks (37) fixedly arranged on the installation box (31) are arranged on both sides of the sliding block (32); a second switch (39) is installed on one side of the installation block (37) close to the sliding block (32); and a third switch (310) is installed on the other side of the installation block (37) close to the sliding block (32).

7. The wound hemostasis device for general surgery clinical operation according to claim 6, characterized in that: A plurality of layers of gauze (311) are fixed to the lower side of the flexible pad (210), a resistor patch (312) is arranged between the flexible pad (210) and the upper layer of gauze (311) and between the two layers of gauze (311), and an isolation membrane (313) is arranged between the two layers of gauze (311).

8. The wound hemostasis device for general surgery clinical operation according to claim 7, characterized in that: An air pump (314) is fixedly provided on the upper side of the pressing plate (29); one end of the air pump (314) is fixedly connected to a three-way pipe (324); both ends of the three-way pipe (324) are fixedly connected to connecting pipes (315); the connecting pipes (315) penetrate the pressing plate (29) and the flexible pad (210) and face the resistor patch (312); the other end of the air pump (314) is fixedly connected to an air inlet pipe (316).

9. The wound hemostasis device for general surgery clinical operation according to claim 7, characterized in that: A second motor (317) is fixedly provided on the upper side of the pressure plate (29), a transmission rod (318) is fixedly provided on the output end of the second motor (317), two blocks (319) are fixedly provided on the transmission rod (318), and one end of the isolation membrane (313) is fixed to the transmission rod (318) and is located between the two blocks (319).

10. The wound hemostasis device for general surgery clinical operation according to claim 9, characterized in that: A pressure block (320) is threadedly provided on one side of the transmission rod (318) and is slidably provided with the pressure plate (29); a limiting groove (323) adapted to the pressure block (320) is provided on the pressure plate (29); the pressure block (320) slides in the limiting groove (323); a connecting block (321) is fixedly provided at equal intervals on one side of the pressure block (320) of the pressure plate (29); a fourth switch (322) is installed on the side of the connecting block (321) close to the pressure block (320).

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