Pulse pressing hemostasis auxiliary device
By designing a pulse pressure hemostasis assist device including positioning, measuring and control components, the prior art tourniquet cannot adapt to patients of different body types, and effective hemostasis for patients of different body types is achieved.
Patent Information
- Application Number
- CN202510281704.9
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2025-03-11
- Publication Date
- 2025-05-13
AI Technical Summary
In the case where the existing electric pneumatic hemostatic device is too thin or too heavy, the diameter of the arms or legs is too small or too large, the contact surface of the tourniquet is enlarged or cannot fit the blood vessels, resulting in the inability to completely block the blood flow and thus the bleeding cannot be completely stopped.
A pulse pressure hemostasis auxiliary device is designed, including a bed body, an inflation box, a positioning assembly, a measurement assembly and a control assembly. The positioning component determines the fixed position of the tourniquet, the measuring component measures the patient's arm and leg circumference, and the control component adjusts the gas volume and pressure based on this information to ensure that the tourniquet can effectively block blood flow.
The device can adjust the contact surface and pressure of the tourniquet according to the patient's specific circumstances, avoid secondary damage and ensure complete hemostasis, and is suitable for patients of different body types.
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Figure CN119970142A_ABST
Abstract
Description
Technical Field
[0001] The invention relates to the technical field of pulse compression hemostasis, in particular to a pulse compression hemostasis auxiliary device. Background Art
[0002] During the operation, compression hemostasis is required. This method of hemostasis can block blood flow to the limbs during the operation, stop bleeding from the wound to the maximum extent, reduce the amount of bleeding during the operation, provide a bloodless field of view for the operation, and make the tendons, nerves and other microstructures clearly identifiable, thereby improving the accuracy and quality of the operation. Compression hemostasis requires the use of an electric pneumatic hemostat, which is often used in surgery, ICU, anesthesia, emergency department and other occasions, especially in limb surgery.
[0003] The electric pneumatic hemostatic device controls the air pressure in the pathway through a microcomputer, so that the cuff connected to the pathway changes accordingly, thereby exerting pressure on the limbs to control the blood flow in the limbs, thereby achieving the effect of stopping bleeding. However, if the patient is too thin, or the diameter of the patient's arms and legs is too small, the contact surface of the tourniquet will increase, and the use of standard pressure will cause secondary injury to the patient. If the patient is overweight, or the diameter of the patient's arms and legs is too large, and the subcutaneous fat is thick, the tourniquet may not be able to adhere to the blood vessels, and it cannot be ensured that the tourniquet can completely block the blood flow, resulting in failure to completely stop bleeding. For this reason, we propose a pulse pressure hemostasis auxiliary device. Summary of the invention
[0004] The purpose of the present invention is to provide a pulse compression hemostasis auxiliary device to solve the above-mentioned problems that the patient is too thin, or the diameter of the patient's arms and legs is too small, thereby increasing the contact area of the tourniquet, and the use of standard pressure may cause secondary injury to the patient; the patient is overweight, or the diameter of the patient's arms and legs is too large, and the subcutaneous fat is thick, the tourniquet may not be able to adhere to the blood vessels, and it cannot be ensured that the tourniquet can completely block the blood flow, thereby causing the problem of inability to completely stop bleeding.
[0005] To achieve the above object, the present invention provides the following technical solutions: a compression hemostasis auxiliary device, comprising: a bed and an inflatable box, one side of the bed is connected to the inflatable box, the inflatable box is connected to an air supply pipe, the other side of the air supply pipe is connected to a tourniquet, the air supply pipe delivers gas in the inflatable box to the tourniquet, and the tourniquet is fixed on the patient's limbs for hemostasis;
[0006] Also includes:
[0007] A positioning component is connected to one side of the inflation box and is connected to the infusion tube. The fixed position of the tourniquet is determined according to the extension position of the infusion tube.
[0008] A measuring component, which is connected to the tourniquet and is used to measure whether the patient's leg circumference and arm circumference are within a standard range;
[0009] The control component is connected to the inflation box and the control component is connected to the infusion tube. The control component controls the output gas volume according to the fixed position of the tourniquet and the measured arm circumference or leg circumference.
[0010] Among them, the positioning component includes a positioning box, which is connected to one side of the inflation box. A telescopic tube is connected inside the positioning box, and the telescopic tube is connected to the air pipe. A positioning piece is connected to the air pipe, and the positioning piece is used to adjust the telescopic tube.
[0011] Among them, the positioning part includes a motor 1, which is connected in the positioning box, a screw rod 1 is connected to the output shaft of the motor 1, a sliding rod is connected in the positioning box, an adjustment plate is connected to the screw rod 1 and the sliding rod, and the adjustment plate is connected to the telescopic tube, and a trigger part 1 is connected to the adjustment plate.
[0012] Among them, the trigger member 1 includes a connecting plate, the connecting plate is arranged on one side of the adjustment plate, and the connecting plate is connected to the air pipe. A tension sensor 1 is connected between the adjustment plate and the connecting plate, and a trigger key 1 is connected to one side of the positioning box.
[0013] The measuring component includes two rectangular boxes, which are respectively connected to the two ends of the tourniquet. Buckles are connected to the two rectangular boxes, and an adjusting piece is connected to one of the rectangular boxes, which is used to adjust the length of the tourniquet.
[0014] The adjusting member includes a second motor, which is connected in a rectangular box, an output shaft of the second motor is connected to a rotating shaft, a tourniquet is wound around the rotating shaft, and a second trigger member is connected to the rotating shaft.
[0015] Among them, the trigger component 2 includes gear 1, which is connected to the rotating shaft, and gear 2 is arranged in the rectangular box, and gear 1 is meshed with gear 2, gear 2 is connected to screw rod 2, screw rod 2 is connected to moving block 1, moving block 1 is connected to the trigger plate, and the rectangular box is connected to several trigger keys 2.
[0016] Among them, the control component includes a groove, the groove is opened in the inflation box, the groove is connected to an air storage box, the air storage box is connected to an extrusion plate, the extrusion plate is connected to a screw rod three, the screw rod three is connected to a driving part, a slide groove is opened in the air storage box, and the extrusion plate is connected to the slide groove, and a plurality of trigger keys three are connected in the slide groove.
[0017] Among them, the driving part includes motor three, which is connected in the inflation box, and the output shaft of motor three is connected to screw rod four, and moving block two and moving block three are connected to screw rod four, and moving block two and moving block three are both connected to fixed plates, and motor four and motor five are connected to the two fixed plates.
[0018] Among them, the output shaft of motor four is connected to worm gear one, the output shaft of motor five is connected to worm gear two, a worm is provided between worm gear one and worm gear two, and the worm is connected to lead screw three.
[0019] The present invention has at least the following beneficial effects: by setting a positioning component, a measuring component and a control component, the positioning component is connected to one side of the inflation box, and the positioning component is connected to the infusion tube, and the fixed position of the tourniquet is judged according to the extended position of the infusion tube, and then it can be judged whether the tourniquet is fixed on the arm or the leg, and the gas pressure is adjusted according to the fixed position of the tourniquet to prevent the same pressure on the fixed position of the arm and the leg, resulting in excessive hemostatic pressure and causing secondary injury to the patient, and to prevent the hemostatic pressure from being too low so that the tourniquet can completely block the blood flow, thereby causing incomplete hemostasis;
[0020] The measuring component is connected to the tourniquet. It is used to measure whether the patient's leg circumference and arm circumference are within the standard range, and then the contact surface between the tourniquet and the arm and leg can be adjusted according to the arm circumference and leg circumference to prevent the tourniquet contact surface from being too large. Using standard pressure will cause secondary injury to the patient. It is also used to prevent the patient's arms and legs from being too large in diameter and having thick subcutaneous fat, which will cause the tourniquet to fail to completely block blood flow and stop bleeding completely.
[0021] The control component is connected to the inflation box and the infusion tube. The control component controls the output gas volume according to the fixed position of the tourniquet and the measured arm circumference or leg circumference, thereby ensuring that the tourniquet can completely stop bleeding and preventing the tourniquet from causing excessive squeezing pressure and causing secondary injury to the patient. BRIEF DESCRIPTION OF THE DRAWINGS
[0022] Figure 1 It is a schematic diagram of the overall structure of the present invention;
[0023] Figure 2 This is a schematic diagram of the structure of the inflatable box of the present invention;
[0024] Figure 3 This is a schematic diagram of the structure of the positioning component of the present invention;
[0025] Figure 4 This is a schematic diagram of the positioning member structure of the present invention;
[0026] Figure 5 for Figure 4 A magnified schematic diagram of the middle A area;
[0027] Figure 6 This is a schematic diagram of the structure of the measuring component of the present invention;
[0028] Figure 7 for Figure 6 A magnified schematic diagram of the middle B area;
[0029] Figure 8This is a schematic diagram of the control component structure of the present invention;
[0030] Fig. 9 This is a schematic diagram of the structure of the driving member of the present invention;
[0031] Fig.10 It is a schematic diagram of the structure of the gas storage box of the present invention;
[0032] Fig.11 This is a schematic diagram of the structure of the trigger key 3 of the present invention;
[0033] Fig.12 for Fig.11 Enlarged schematic diagram of the middle C area;
[0034] Fig.13 It is a schematic diagram of the bed structure of the present invention.
[0035] In the figure: 1, bed; 2, inflatable box; 3, tourniquet; 4, air pipe; 411, trigger key 1; 5, positioning component; 51, positioning box; 6, measuring component; 61, rectangular box; 7, positioning piece; 8, telescopic tube; 9, motor 1; 10, screw rod 1; 11, slide rod; 12, adjustment plate; 13, connecting plate; 14, tension sensor 1; 15, motor 2; 16, gear 1; 17, rotating shaft; 18, gear 2; 19, tension sensor 2; 20 1. Moving block 1; 21. Trigger plate; 22. Screw rod 2; 23. Trigger key 2; 24. Control assembly; 241. Groove; 25. Driving member; 26. Gas storage box; 27. Motor 3; 28. Screw rod 4; 29. Fixed plate; 30. Motor 4; 31. Motor 5; 32. Worm gear 1; 33. Worm gear 2; 34. Worm; 35. Extrusion plate; 36. Screw rod 3; 38. Trigger key 3; 39. Electric telescopic rod; 40. Slide; 41. Weight measuring device. DETAILED DESCRIPTION
[0036] 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.
[0037] Embodiment 1
[0038] See also Figures 1 to 13 The present invention provides a technical solution: a compression hemostasis auxiliary device, comprising: a bed 1 and an air box 2, one side of the bed 1 is connected to the air box 2, the air box 2 is connected to an air pipe 4, the other side of the air pipe 4 is connected to a tourniquet 3, the air pipe 4 transports the gas in the air box 2 to the tourniquet 3, and the tourniquet 3 is fixed on the patient's limbs for hemostasis;
[0039] Also includes:
[0040] Positioning assembly 5, which is connected to one side of the inflatable box 2 and is connected to the infusion tube. The fixed position of the tourniquet 3 is determined according to the extended position of the infusion tube, and then it can be determined whether the tourniquet 3 is fixed to the arm or the leg. The gas pressure is adjusted according to the fixed position of the tourniquet 3 to prevent the same pressure on the fixed position of the arm and the leg, which causes excessive hemostatic pressure and causes secondary injury to the patient, and to prevent the hemostatic pressure from being too low so that the tourniquet 3 can completely block the blood flow, which causes inability to completely stop bleeding;
[0041] Measuring component 6, measuring component 6 is connected to the tourniquet 3, and is used to measure whether the patient's leg circumference and arm circumference are within the standard range, and then the contact surface between the tourniquet 3 and the arm and leg can be adjusted according to the arm circumference and leg circumference, to prevent the contact surface of the tourniquet 3 from being too large, and the use of standard pressure will cause secondary injury to the patient, and to prevent the patient's arms and legs from being too large in diameter and having thick subcutaneous fat, which will cause the tourniquet 3 to fail to completely block the blood flow and fail to completely stop bleeding;
[0042] The control component 24 is connected to the inflation box 2, and the control component 24 is connected to the infusion tube. The control component 24 controls the output gas volume according to the fixed position of the tourniquet 3 and the measured arm circumference or leg circumference, thereby ensuring that the tourniquet 3 can completely stop bleeding and preventing the extrusion pressure of the tourniquet 3 from being too large, causing secondary injury to the patient.
[0043] The positioning assembly 5 includes a positioning box 51, which is connected to one side of the inflation box 2. A telescopic tube 8 is connected inside the positioning box 51. The telescopic tube 8 can be protected by setting the positioning box 51, thereby extending the service life of the telescopic tube 8. The telescopic tube 8 is connected to the air pipe 4. The telescopic tube 8 is a PC hose. The length of the air pipe 4 can be adjusted by adjusting the telescopic tube 8. A positioning member 7 is connected to the air pipe 4. The positioning member 7 is used to adjust the telescopic tube 8. The position of the telescopic tube 8 is adjusted by setting the positioning member 7, and the fixed position of the tourniquet 3 can be determined according to the position of the telescopic tube 8. The squeezing pressure of the tourniquet 3 on the arm and the leg is different, and the squeezing pressure of the tourniquet 3 can be adjusted according to the fixed position of the tourniquet 3.
[0044] The positioning member 7 includes a motor 9, which is connected to the positioning box 51. A screw rod 10 is connected to the output shaft of the motor 9. A slide rod 11 is connected to the positioning box 51. An adjusting plate 12 is connected to the screw rod 10 and the slide rod 11. The adjusting plate 12 is connected to the telescopic tube 8. A trigger member 1 is connected to the adjusting plate 12. When the arm needs to be fixed, the air pipe 4 needs to be pulled out to trigger the motor 9. The motor 9 can drive the screw rod 10 to rotate. The rotation of the screw rod 10 can drive the adjusting plate 12 to move laterally, and then the adjusting plate 12 can drive the telescopic shaft to extend and retract, so that the air pipe 4 can be adjusted to fix the legs and arms.
[0045] The trigger member 1 includes a connecting plate 13, which is arranged on one side of the adjusting plate 12 and connected to the air supply pipe 4. A tension sensor 14 is connected between the adjusting plate 12 and the connecting plate 13. The tension sensor 14 can be fixed by setting the connecting plate 13 and the adjusting plate 12. When the patient's arm needs to be fixed, the air supply pipe 4 is stretched, and then the air supply pipe 4 stretches the connecting plate 13. The tension sensor 14 can sense the tension of the connecting plate 13. When the connecting plate 13 When the pulling force exceeds the standard value, the motor 9 is started, and the fixed position of the tourniquet 3 can be determined. A trigger key 411 is connected to one side of the positioning box 51. When the adjustment plate 12 does not press the trigger key 411, it can be determined that the tourniquet 3 is fixed to the patient's leg, so that the pressure of the tourniquet 3 is within the standard value of the pressure borne by the leg. When the adjustment plate 12 moves to press the trigger key 411, it can be determined that the tourniquet 3 is fixed to the patient's arm, and the pressure of the tourniquet 3 is within the standard value of the pressure borne by the arm.
[0046] The measuring component 6 includes two rectangular boxes 61, and the two rectangular boxes 61 are respectively connected to the two ends of the tourniquet 3. Buckles are connected to the two rectangular boxes 61. The tourniquet 3 can be clamped by setting the buckles, so that the tourniquet 3 can be fixed on the patient's arms and legs. An adjusting piece is connected to one of the rectangular boxes 61. The adjusting piece can be protected by setting the rectangular box 61, so as to extend the service life of the adjusting piece. The adjusting piece is used to adjust the length of the tourniquet 3. The adjusting piece can drive the length of the tourniquet 3 to be adjusted, so as to judge the patient's arm circumference and leg circumference, and then the squeezing force of the tourniquet 3 can be adjusted according to the arm circumference and leg circumference.
[0047] The adjusting member includes a second motor 15, which is connected in a rectangular box 61. A rotating shaft 17 is connected to the output shaft of the second motor 15, and the tourniquet 3 is wound around the rotating shaft 17. A trigger member 2 is connected to the rotating shaft 17. When the arm circumference or leg circumference is less than the standard value, the tension sensor 2 19 is less than the standard value, and the second motor 15 drives the rotating shaft 17 to rotate forward, and the rotating shaft 17 can drive the tourniquet 3 to rotate forward. A tension sensor 2 19 is connected in another rectangular box 61. When the tension sensor 2 19 returns to the standard value, the rotating shaft 17 stops rotating. When the arm circumference or leg circumference is greater than the standard value, the tension sensor 2 19 is greater than the standard value, and the second motor 15 drives the rotating shaft 17 to rotate in the opposite direction, and the rotating shaft 17 can drive the tourniquet 3 to rotate in the opposite direction. When the tension sensor 2 19 returns to the standard value, the rotating shaft 17 stops rotating, thereby ensuring that the tourniquet 3 can be fixed on the arm or leg according to the arm circumference and leg circumference.
[0048] The trigger member 2 includes a gear 16, which is connected to the rotating shaft 17. A gear 2 18 is arranged in the rectangular box 61, and the gear 16 is meshed with the gear 2 18. The gear 2 18 is connected to a screw rod 22, and the screw rod 22 is connected to a moving block 20, and the moving block 20 is connected to a trigger plate 21. A plurality of trigger keys 23 are connected to the rectangular box 61, and the plurality of trigger keys 23 can control the gas delivery volume, and the gas delivery volume can be controlled according to the arm circumference and the leg circumference. The positive rotation of the rotating shaft 17 can drive the gear 16 to rotate forward, and the positive rotation of the gear 16 can drive the gear 2 18 to rotate in the reverse direction, so that the gear 2 18 can drive the screw rod 22 to rotate in the opposite direction, and the reverse rotation of the screw rod 22 can drive the trigger plate 21 to move downward, and then the trigger plate 21 can squeeze the trigger key 23, reduce the gas supply, and then reduce the extrusion force of the tourniquet 3; the reverse rotation of the rotating shaft 17 can drive the gear 16 to rotate in the opposite direction, and the reverse rotation of the gear 16 can drive the gear 2 18 to rotate forward, and then the gear 2 18 can drive the screw rod 22 to rotate forward, and the forward rotation of the screw rod 22 can drive the trigger plate 21 to move upward, and then the trigger plate 21 can squeeze the trigger key 23, increase the gas supply, and then increase the extrusion force of the tourniquet 3.
[0049] The control component 24 includes a groove 241, which is provided in the inflatable box 2, and the groove 241 is connected to the gas storage box 26, and the gas storage box 26 is connected to the extrusion plate 35, and the extrusion plate 35 is connected to the screw rod 36, and the screw rod 36 is connected to the driving member 25, and a slide groove 40 is provided in the gas storage box 26, and the extrusion plate 35 is connected to the slide groove 40, and a plurality of trigger keys 38 are connected in the slide groove 40, and the plurality of trigger keys 38 are connected to the electric telescopic rod 39, and the trigger keys 38 are connected to the electric telescopic rod 39 according to the arm circumference and leg circumference of the patient. The second 23 can start the electric telescopic rod 392 at different positions, thereby extending the trigger button 38. When the extrusion plate 35 moves downward, the extrusion plate 35 squeezes the trigger button 38 to close the driving member 25. By setting the groove 241, the gas storage box 26 and the driving member 25 can be protected, thereby extending the service life of the gas storage box 26 and the driving member 25. The gas storage box 26 can store gas, and the rotation of the screw rod 36 can drive the extrusion plate 35 to move vertically, thereby controlling the extrusion force of the tourniquet 3.
[0050] The driving member 25 includes a motor three 27, which is connected to the inflation box 2. A screw rod four 28 is connected to the output shaft of the motor three 27, and a moving block two and a moving block three are connected to the screw rod four 28. Both the moving block two and the moving block three are connected to a fixed plate 29, and the two fixed plates 29 are connected to a motor four 30 and a motor five 31. When stopping bleeding on the arm, the motor three 27 drives the screw rod four 28 to rotate forward, thereby driving the moving block two and the moving block three to move to the right. When stopping bleeding on the leg, the motor three 27 drives the screw rod four 28 to rotate reversely, thereby driving the moving block two and the moving block three to move to the left, thereby driving the motor four 30 and the motor five 31 to move.
[0051] The output shaft of the motor 4 30 is connected with a worm gear 1 32, and the motor 4 30 can drive the worm gear 1 32 to rotate. The output shaft of the motor 5 31 is connected with a worm gear 2 33, and the motor 5 31 can drive the worm gear 2 33 to rotate. A worm 34 is arranged between the worm gear 1 32 and the worm gear 2 33. The worm gear teeth of the worm gear 2 33 are more than those of the worm gear 1 32. The different worm gear teeth can control the rotation speed of the worm gear 34, and then control the speed at which the extrusion plate 35 moves downward. The worm gear 34 and the lead screw 3 are connected to each other. 36 are connected, the motor three 27 drives the screw four 28 to rotate forward, thereby driving the moving block two and the moving block three to move rightward, thereby making the worm gear one 32 mesh with the worm 34, and then the worm 34 drives the screw to rotate, so that the extrusion plate 35 moves downward, and the motor three 27 drives the screw four 28 to rotate in the opposite direction, thereby driving the moving block two and the moving block three to move leftward, thereby making the worm gear two 33 mesh with the worm 34, so that the extrusion plate 35 moves downward quickly, thereby increasing the output gas.
[0052] Embodiment 2
[0053] A weight measuring device 41 is provided on the bed 1. By setting up the weight measuring device 41, the patient's weight can be measured, and then the hemostatic pressure that the patient can withstand can be determined. When the weight measuring device 41 monitors that the patient's weight is higher than the standard value, it is used in conjunction with the squeezing plate 35 to increase the squeezing pressure of the tourniquet 3, thereby preventing the subcutaneous fat from being thick, resulting in the tourniquet 3 being unable to completely block the blood flow and unable to completely stop the bleeding. When the weight measuring device 41 monitors that the patient's weight is lower than the standard value, it is used in conjunction with the squeezing plate 35 to reduce the squeezing pressure of the tourniquet 3, thereby preventing the pressure of the tourniquet 3 from remaining unchanged, causing secondary injury to the patient.
[0054] 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.
[0055] 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 pulse compression hemostasis auxiliary device, comprising: A bed (1) and an air box (2), wherein one side of the bed (1) is connected to the air box (2), the air box (2) is connected to an air supply pipe (4), the other side of the air supply pipe (4) is connected to a tourniquet (3), the air supply pipe (4) delivers gas in the air box (2) to the tourniquet (3), and the tourniquet (3) is fixed on the patient's limbs to stop bleeding; It is characterized by: also including: A positioning component (5), the positioning component (5) is connected to one side of the inflation box (2), and the positioning component (5) is connected to the infusion tube, and the fixed position of the tourniquet (3) is determined according to the extension position of the infusion tube; A measuring component (6), the measuring component (6) is connected to the tourniquet (3), and the measuring component (6) is used to measure whether the patient's leg circumference and arm circumference are within a standard range; A control component (24) is connected to the inflation box (2) and is connected to the infusion tube. The control component (24) controls the output gas volume according to the fixed position of the tourniquet (3) and the measured arm circumference or leg circumference.
2. The hemostasis auxiliary device according to claim 1, characterized in that: The positioning assembly (5) comprises a positioning box (51), the positioning box (51) being connected to one side of the inflation box (2), a telescopic tube (8) being connected inside the positioning box (51), and the telescopic tube (8) being connected to the air supply pipe (4), a positioning member (7) being connected to the air supply pipe (4), and the positioning member (7) being used to adjust the telescopic tube (8).
3. The hemostasis auxiliary device according to claim 2, characterized in that: The positioning member (7) comprises a motor (9), the motor (9) being connected in a positioning box (51), a screw rod (10) being connected to an output shaft of the motor (9), a slide rod (11) being connected in the positioning box (51), an adjustment plate (12) being connected to the screw rod (10) and the slide rod (11), and the adjustment plate (12) being connected to a telescopic tube (8), and a trigger member (1) being connected to the adjustment plate (12).
4. The hemostasis auxiliary device according to claim 3, characterized in that: The trigger member 1 comprises a connecting plate (13), the connecting plate (13) being arranged on one side of the adjusting plate (12), and the connecting plate (13) being connected to the gas pipe (4), a tension sensor 1 (14) being connected between the adjusting plate (12) and the connecting plate (13), and a trigger key 1 (411) being connected to one side of the positioning box (51).
5. The hemostasis auxiliary device according to claim 1, characterized in that: The measuring assembly (6) comprises two rectangular boxes (61), the two rectangular boxes (61) being connected to two ends of the tourniquet (3) respectively, buckles being connected to the two rectangular boxes (61), an adjusting member being connected inside one of the rectangular boxes (61), the adjusting member being used to adjust the length of the tourniquet (3).
6. The hemostasis auxiliary device according to claim 5, characterized in that: The adjusting member comprises a second motor (15), the second motor (15) is connected in a rectangular box (61), the output shaft of the second motor (15) is connected to a rotating shaft (17), the tourniquet (3) is wound around the rotating shaft (17), and the rotating shaft (17) is connected to a second trigger member.
7. The hemostasis auxiliary device according to claim 6, characterized in that: The trigger member 2 comprises a gear 1 (16), the gear 1 (16) being connected to a rotating shaft (17), a gear 2 (18) being arranged inside the rectangular box (61), the gear 1 (16) being meshed with the gear 2 (18), a screw rod 2 (22) being connected to the gear 2 (18), a moving block 1 (20) being connected to the screw rod 2 (22), a trigger plate (21) being connected to the moving block 1 (20), and a plurality of trigger keys 2 (23) being connected to the rectangular box (61).
8. The hemostasis auxiliary device according to claim 1, characterized in that: The control component (24) comprises a groove (241), wherein the groove (241) is provided in the inflation box (2), wherein the groove (241) is connected to an air storage box (26), wherein the air storage box (26) is connected to an extrusion plate (35), wherein the extrusion plate (35) is connected to a screw rod three (36), wherein the screw rod three (36) is connected to a driving member (25), wherein a slide groove (40) is provided in the air storage box (26), wherein the extrusion plate (35) is connected to the slide groove (40), wherein a plurality of trigger keys three (38) are connected to the slide groove (40).
9. The hemostasis auxiliary device according to claim 8, characterized in that: The driving member (25) comprises a motor three (27), the motor three (27) is connected in the inflation box (2), the output shaft of the motor three (27) is connected to a screw rod four (28), the screw rod four (28) is connected to a moving block two and a moving block three, the moving block two and the moving block three are both connected to a fixed plate (29), and the two fixed plates (29) are connected to a motor four (30) and a motor five (31).
10. The hemostasis auxiliary device according to claim 9, characterized in that: The output shaft of the motor four (30) is connected to a worm gear one (32), the output shaft of the motor five (31) is connected to a worm gear two (33), a worm (34) is provided between the worm gear one (32) and the worm gear two (33), and the worm (34) is connected to a screw rod three (36).
Citation Information
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