CN118436398B - Cardiology compression hemostasis device - Google Patents

Abstract

The invention relates to the technical field of medical equipment, and discloses a pressing hemostasis device for a department of cardiology, which comprises a supporting table, wherein two sides of the supporting table are respectively and rotatably connected with a bending plate, one end of the bending plate, which is far away from the supporting table, is fixedly connected with a pressing plate, the device is placed at the joint of a patient, the pressing plate is pulled to bind the device, meanwhile, a hexagonal screw rod is screwed, the hexagonal screw rod is limited through a limiting rod arranged, and is subjected to thread arrangement of the hexagonal screw rod, the rotation of the hexagonal screw rod drives the threaded plate to fall, the threaded plate drives a connecting rod to fall, the connecting rod drives a circular plate to drive hemostatic cotton to fall, so that the hemostatic cotton presses and hemostasis is carried out on the joint of the patient, when the threaded plate falls, the threaded plate extrudes air pressure in a cylinder, the air pressure enters the inside a liquid discharge groove through the liquid discharge groove, and the air pressure carries out surface air injection on the joint of the patient through the liquid discharge groove, so that bacteria on the surface of the joint of the patient are prevented, and the risk of infection of the patient is reduced.

Description

Cardiology compression hemostasis device

Technical Field

The invention relates to the technical field of medical equipment, in particular to a cardiology compression hemostasis device.

Background Art

Cardiology, also known as cardiovascular medicine, is a clinical department set up by the general internal medicine department of hospitals at all levels for the diagnosis and treatment of cardiovascular and vascular diseases. The diseases treated include angina pectoris, hypertension, sudden death, arrhythmia, heart failure, premature beats, irregular heartbeat, myocardial infarction, cardiomyopathy, myocarditis, acute myocardial infarction and other cardiovascular diseases. The cardiology department will use nurses to independently complete the collection of dynamic and static blood. The most commonly used treatment method in the field of cardiology is to administer medication through vascular interventional guidewires or other unblocking treatments. However, interventional treatment also has certain defects, mainly that bleeding from the puncture end is prone to occur when the catheter guidewire is removed after treatment.

When the existing compression hemostasis device is in use, blood is sometimes drawn from the blood vessels at the arm joints. During this process, the hemostatic cotton needs to be pressed on the bleeding site and fixed. However, since the location of the blood drawing site may bend during long-term pressing, the fixation of the hemostatic cotton may be offset, thereby affecting the compression hemostasis effect of the device.

Summary of the invention

The object of the present invention is to provide a cardiology compression hemostasis device to solve the problems raised in the above-mentioned background technology.

To solve the above technical problems, the present invention is achieved through the following technical solutions:

The camming device of the present invention is a cardiology compression hemostasis device, comprising a support platform, two sides of the support platform are respectively rotatably connected with bent plates, one end of the bent plate away from the support platform is fixedly connected with a pressing plate, two sides of the bent plate are respectively fixedly connected with a rotation spring, one end of the rotation spring is fixedly connected to one side of the inner wall of the support platform, two sides of the top of the support platform are respectively provided with card grooves, the inner walls of the card grooves are sleeved with and rotatably connected with a pressing belt, and also include a pressing hemostasis mechanism, the pressing hemostasis mechanism includes a hexagonal screw rod that passes through the support platform and extends to the outside of the support platform, the bottom of the support platform is fixedly connected with a cylinder, and a plurality of limit rods are respectively fixedly connected around the bottom of the inner wall of the cylinder, the middle end of the outer wall of the limit rod is sleeved with and slidably connected with a threaded plate, the inner wall of the threaded plate is sleeved with and threadedly connected to the middle end of the outer wall of the hexagonal screw rod, and a disinfection component is provided at the bottom of the threaded plate.

Furthermore, the disinfection assembly includes a plurality of connecting rods fixedly connected around the bottom of the threaded plate, one end of the connecting rod passes through the cylinder and extends to the outside of the cylinder, the bottom of the connecting rod is fixedly connected to a circular plate, a drainage groove is opened at the bottom center of the circular plate, the bottom of the circular plate is fixedly connected to hemostatic cotton, and a drainage pipe passes through and is connected to one side of the top of the connecting rod, and one end of the drainage pipe is connected to the top of the inner wall of the drainage groove.

Furthermore, an adjustment component is provided at the top of the bending plate, and the adjustment component includes a flexible spring plate fixedly connected to the top of the bending plate, the inner wall of the flexible spring plate is sleeved and slidably connected with a cross bar, the two ends of the cross bar are respectively fixedly connected with vertical blocks, the bottom of the vertical block is fixedly connected to the top of the support platform, and sliding grooves are respectively provided on both sides of the top of the support platform near the card slot.

Furthermore, one end of the flexible spring plate away from the bending plate is fixedly connected to a sliding block, the outer wall of the sliding block is sleeved and slidably connected to the inner wall of the sliding groove, the sliding block is fixedly connected to a first clamping plate near the top of the sliding groove, the tops of both ends of the first clamping plate are respectively fixedly connected to arc blocks, and one end of the arc block is fixedly connected to a bent rod.

Furthermore, the side wall of one end of the bent rod away from the arc block passes through and is slidably connected to a sliding rod, one end of the sliding rod is fixedly connected to a second clamping plate, the second clamping plate is fixedly connected to a side of the sliding rod close to a return spring, one end of the return spring is fixedly connected to one side of the bent rod, the return spring is arranged on the outside of the sliding rod, and a hexagonal bag is fixedly connected at the top center of the support platform.

Furthermore, a sealing assembly is provided at the bottom of the hexagonal capsule, and the sealing assembly includes a plurality of elastic tubes connected around the bottom of the hexagonal capsule, one end of the elastic tube passes through the support platform and extends to the interior of the cylinder, and the end of the elastic tube away from the hexagonal capsule is connected to a sealing ring, the bottom of the sealing ring is fixedly connected to the top of the threaded plate, and the threaded plate is fixedly connected to a limiting shell near the top of the sealing ring, and a plurality of negative pressure tubes are respectively connected around the outer wall of the top end of the cylinder.

Furthermore, a lifting block is sleeved on the middle end of the inner wall of the negative pressure tube and is slidably connected to it, an elastic rope is fixedly connected to the bottom of the lifting block, and a plurality of limit sleeves are fixedly connected to the four sides of the bottom of the cylinder, one end of the elastic rope passes through the limit sleeve and extends to the outside of the limit sleeve, and a rubber ball is fixedly connected to the end of the elastic rope away from the lifting block, and a rubber ring is sleeved on the outer wall of the rubber ball and is slidably connected to it.

Furthermore, a stabilizing component is provided on the outer wall of the rubber ring, and the stabilizing component includes a plurality of concave blocks fixedly connected around the outer wall of the rubber ring, a rotating rod is rotatably connected to one side of the inner wall of the concave block, a clamping rod passes through the middle end of one side of the outer wall of the rotating rod and is rotatably connected, and a plurality of square holes are respectively opened around the top of the circular plate.

Furthermore, both ends of the clamping rod are fixedly connected to both sides of the inner wall of the square hole, the bottom of the end of the rotating rod away from the concave block is fixedly connected to a rubber plate, the top of the rotating rod is fixedly connected to a three-pronged plate, both ends of one side of the three-pronged plate are respectively fixedly connected to pull ropes, and the end of the pull rope away from the three-pronged plate is fixedly connected to a flexible elastic strip.

The present invention has the following beneficial effects:

(1) In the present invention, the device is placed on the patient's joint, the pressing belt is pulled to bind the device, and the hexagonal screw is twisted at the same time. Not only is the limit rod set to limit the position, but also the thread setting of the hexagonal screw drives the threaded plate to fall, the threaded plate drives the connecting rod to fall, the connecting rod drives the circular plate to fall, and the circular plate drives the hemostatic cotton to fall, so that the hemostatic cotton presses the patient's joint to stop bleeding. When the threaded plate falls, the threaded plate displaces the air pressure inside the cylinder, and the air pressure enters the inside of the drainage trough through the drainage pipe. The air pressure sprays the surface of the patient's joint through the drainage trough to prevent bacteria on the surface of the patient's joint, thereby reducing the risk of infection for the patient. When the threaded plate continues to fall, the threaded plate squeezes the disinfectant water at the bottom of the inner wall of the cylinder into the inside of the drainage trough through the drainage pipe, so that the disinfectant water infects the hemostatic cotton through the drainage trough, thereby disinfecting the patient's joint, further reducing the risk of infection for the patient.

(2) According to the present invention, when the threaded plate falls, negative pressure is generated in the area of the cylinder at the sealing ring position. The negative pressure enters the negative pressure tube through the cylinder, and the negative pressure causes the lifting block to move upward. The lifting block drives the elastic rope to move upward, and is limited by the limit sleeve. The elastic rope drives the rubber ball to rise vertically, and the rubber ball drives the rubber ring to move upward. During the upward movement of the rubber ring, the hemostatic cotton is squeezed, so that the area of the hemostatic cotton soaked by the disinfectant water becomes smaller, preventing the disinfectant water from spreading around the hemostatic cotton, so that the disinfectant water can pass through the hemostatic cotton to disinfect the patient's joints, ensuring that the disinfectant water accurately reaches the patient's joints.

(3) In the present invention, when the rubber ring rises, the rubber ring drives the concave block to rise, and the concave block drives the rotating rod to rise. When one end of the rotating rod rises, the other end of the rotating rod drops in the opposite direction. The other end of the rotating rod drives the rubber plate to drop, so that the rubber plate presses down the outside of the hemostatic cotton. The outside of the hemostatic cotton is pressed down, which can enhance the pressure of the hemostatic cotton on the blood around the patient's joints and enhance the hemostatic effect of the hemostatic cotton on the patient's joints. In addition, the rubber plate can drive the three-pronged plate to fall, and the three-pronged plate drives the pull rope to move When the pull rope moves, the pull rope is stretched, and the pull rope drives the flexible elastic strip to deform. During the deformation of the flexible elastic strip, a thrust can be applied to the outer wall of the elastic rope. The elastic rope is affected by the thrust, which can enhance the squeezing effect of the rubber ring on the hemostatic cotton, thereby further enhancing the disinfection effect of the hemostatic cotton. When the rotating rod is close to one end of the concave block and rotates around the clamping rod, the rotating rod drives the concave block to squeeze the rubber ring. When the four concave blocks squeeze the rubber ring, the rubber ring will further reduce the infection range of the disinfectant water of the hemostatic cotton, thereby further enhancing the hemostatic effect of the hemostatic cotton.

(4) In the present invention, when the device is installed on the patient's joint, during the long-term pressing process, the angle of the patient's joint may change, causing the bent plate to rotate around the support platform, and the bent plate drives the flexible spring plate to rotate. Limited by the vertical block, the flexible spring plate can drive the sliding block to move inside the slide groove, and the sliding block drives the first clamping plate to move. The two groups of first clamping plates are close to each other, thereby clamping the hexagonal capsule, enhancing the stabilization effect of the device and enhancing the pressing effect of the patient. When the angle of the patient's joint moves in the opposite direction, the first clamping plate drives the arc block to move, and the arc block with The movable bending rod moves, the bending rod drives the sliding rod to move, the sliding rod drives the second clamping plate to move, and the two groups of second clamping plates approach each other to clamp the hexagonal capsule, further enhancing the stabilization effect of the device and the pressing effect on the patient's joints. When the hexagonal capsule is squeezed, the internal airflow enters the interior of the sealing ring through the elastic tube to expand the sealing ring. During the expansion of the sealing ring, the threaded connection between the hexagonal screw and the threaded plate is sealed to prevent pressure relief inside the cylinder, further enhancing the generation of negative pressure inside the cylinder, and indirectly enhancing the hemostatic effect of the hemostatic cotton.

Of course, any product implementing the present invention does not necessarily need to achieve all of the above-mentioned advantages at the same time.

BRIEF DESCRIPTION OF THE DRAWINGS

In order to more clearly illustrate the technical solutions of the embodiments of the present invention, the accompanying drawings required for describing the embodiments will be briefly introduced below. Obviously, the accompanying drawings described below are only some embodiments of the present invention. For ordinary technicians in this field, other accompanying drawings can be obtained based on these accompanying drawings without paying creative work.

FIG1 is a schematic diagram of the overall top view of the structure of the present invention;

FIG2 is a schematic diagram of the overall half-section structure of the present invention;

FIG3 is a schematic diagram of a partial top view of an exploded structure of the present invention;

FIG4 is a schematic diagram of a half-section side structure of a disinfection assembly according to the present invention;

FIG5 is a schematic diagram of the internal half-section side structure of the present invention;

FIG6 is a schematic diagram of an internal explosion structure of the present invention;

FIG7 is an enlarged view of A in FIG3 of the present invention;

FIG8 is an enlarged view of B in FIG4 of the present invention.

In the accompanying drawings, the components represented by the reference numerals are listed as follows:

In the figure: 1, support platform; 2, bending plate; 3, pressing plate; 4, rotating spring; 5, slot; 6, pressing belt; 7, pressing hemostasis mechanism; 71, hexagonal screw; 72, cylinder; 73, limit rod; 74, threaded plate; 75, disinfection component; 76, adjustment component; 77, sealing component; 78, stabilizing component; 751, connecting rod; 752, round plate; 753, drainage trough; 754, hemostatic cotton; 755, drainage pipe; 761, flexible spring plate; 762, vertical block; 763, horizontal bar; 764, sliding block; 765, slide groove; 766, first Clamping plate; 767, arc block; 768, bent rod; 769, sliding rod; 7610, return spring; 7611, second clamping plate; 7612, hexagonal bag; 771, elastic tube; 772, limit shell; 773, sealing ring; 774, negative pressure tube; 775, lifting block; 776, elastic rope; 777, limit sleeve block; 778, rubber ball; 779, rubber ring; 781, concave block; 782, rotating rod; 783, clamping rod; 784, square hole; 785, three-pronged plate; 786, rubber plate; 787, pull rope; 788, flexible elastic strip.

DETAILED DESCRIPTION

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.

Please refer to Figures 1 to 8, the present invention is a cardiology compression hemostasis device, including a support platform 1, two sides of the support platform 1 are rotatably connected with bent plates 2, one end of the bent plate 2 away from the support platform 1 is fixedly connected with a pressing plate 3, and two sides of the bent plate 2 are fixedly connected with a rotation spring 4, the purpose of this arrangement is to facilitate resetting, one end of the rotation spring 4 is fixedly connected to one side of the inner wall of the support platform 1, and two sides of the top of the support platform 1 are respectively provided with a card slot 5, and the inner wall of the card slot 5 is sleeved and rotatably connected with a pressing belt 6, and also includes;

The pressing hemostasis mechanism 7 includes a hexagonal screw 71 which passes through the support platform 1 and extends to the outside of the support platform 1. A cylinder 72 is fixedly connected to the bottom of the support platform 1. A plurality of limit rods 73 are fixedly connected to the bottom of the inner wall of the cylinder 72. The purpose of this arrangement is to enable the threaded plate 74 to be raised and lowered. A threaded plate 74 is sleeved and slidably connected to the middle end of the outer wall of the limit rod 73. The inner wall of the threaded plate 74 is sleeved and threadedly connected to the middle end of the outer wall of the hexagonal screw 71. A disinfection component 75 is provided at the bottom of the threaded plate 74.

The disinfection assembly 75 includes a plurality of connecting rods 751 fixedly connected around the bottom of the threaded plate 74. One end of the connecting rod 751 passes through the cylinder 72 and extends to the outside of the cylinder 72. The bottom of the connecting rod 751 is fixedly connected to a circular plate 752. A drainage groove 753 is provided at the bottom center of the circular plate 752. The purpose of this arrangement is to facilitate the discharge of disinfectant water. A hemostatic cotton 754 is fixedly connected to the bottom of the circular plate 752. A drainage pipe 755 passes through and is connected to one side of the top end of the connecting rod 751. One end of the drainage pipe 755 is connected to the top of the inner wall of the drainage groove 753.

An adjustment component 76 is provided at the top of the bending plate 2, and the adjustment component 76 includes a flexible spring plate 761 fixedly connected to the top of the bending plate 2. The purpose of this arrangement is that the flexible spring plate 761 has the property of elastic deformation. The inner wall of the flexible spring plate 761 is sleeved and slidably connected with a cross bar 763, and the two ends of the cross bar 763 are respectively fixedly connected with vertical blocks 762. The bottom of the vertical block 762 is fixedly connected to the top of the support platform 1, and sliding grooves 765 are respectively provided on both sides of the top of the support platform 1 near the card slot 5.

The end of the flexible spring plate 761 away from the bending plate 2 is fixedly connected to a sliding block 764, the outer wall of the sliding block 764 is sleeved and slidably connected to the inner wall of the sliding groove 765, the sliding block 764 is fixedly connected to a first clamping plate 766 near the top of the sliding groove 765, the tops of both ends of the first clamping plate 766 are respectively fixedly connected to arc blocks 767, and one end of the arc block 767 is fixedly connected to a bending rod 768.

The side wall of one end of the bent rod 768 away from the arc block 767 passes through and is slidably connected to a sliding rod 769, one end of the sliding rod 769 is fixedly connected to a second clamping plate 7611, and the side of the second clamping plate 7611 close to the sliding rod 769 is fixedly connected to a return spring 7610. The purpose of this arrangement is to enable the second clamping plate 7611 to always be in contact with the outer wall of the hexagonal bag 7612, one end of the return spring 7610 is fixedly connected to one side of the bent rod 768, and the return spring 7610 is arranged on the outside of the sliding rod 769, and the hexagonal bag 7612 is fixedly connected at the top center of the support platform 1.

A sealing assembly 77 is provided at the bottom of the hexagonal capsule 7612. The sealing assembly 77 includes a plurality of elastic tubes 771 connected around the bottom of the hexagonal capsule 7612. The purpose of this arrangement is to enable stretching. One end of the elastic tube 771 passes through the support platform 1 and extends to the interior of the cylinder 72. The end of the elastic tube 771 away from the hexagonal capsule 7612 is connected to a sealing ring 773. The purpose of this arrangement is to have a sealing effect. The bottom of the sealing ring 773 is fixedly connected to the top of the threaded plate 74. The threaded plate 74 is fixedly connected to a limiting shell 772 near the top of the sealing ring 773. The top outer wall of the cylinder 72 is respectively connected with a plurality of negative pressure tubes 774.

A lifting block 775 is sleeved and slidably connected to the middle end of the inner wall of the negative pressure tube 774, and an elastic rope 776 is fixedly connected to the bottom of the lifting block 775. A plurality of limit sleeves 777 are fixedly connected to the four sides of the bottom of the cylinder 72. One end of the elastic rope 776 passes through the limit sleeve 777 and extends to the outside of the limit sleeve 777. A rubber ball 778 is fixedly connected to the end of the elastic rope 776 away from the lifting block 775, and a rubber ring 779 is sleeved and slidably connected to the outer wall of the rubber ball 778.

The device is placed on the patient's joint, and the pressing belt 6 is pulled to bind the device. At the same time, the hexagonal screw 71 is twisted. It is not only limited by the limit rod 73, but also affected by the thread setting of the hexagonal screw 71. The rotation of the hexagonal screw 71 drives the threaded plate 74 to fall, and the threaded plate 74 drives the connecting rod 751 to fall. The connecting rod 751 drives the circular plate 752 to fall, and the circular plate 752 drives the hemostatic cotton 754 to fall, so that the hemostatic cotton 754 presses the patient's joint to stop bleeding. When the threaded plate 74 falls, the threaded plate 74 presses the cylinder The air pressure inside cylinder 72 is expelled, and the air pressure enters the interior of drainage groove 753 through drainage pipe 755. The air pressure sprays the surface of the patient's joints through drainage groove 753 to prevent bacteria on the surface of the patient's joints, thereby reducing the risk of infection for the patient. When threaded plate 74 continues to fall, threaded plate 74 squeezes the disinfectant water at the bottom of the inner wall of cylinder 72 into the interior of drainage groove 753 through drainage pipe 755, so that the disinfectant water infects the hemostatic cotton 754 through drainage groove 753, thereby disinfecting the patient's joints, further reducing the risk of infection for the patient.

When the threaded plate 74 falls, negative pressure is generated in the area inside the cylinder 72 at the position of the sealing ring 773. The negative pressure enters the interior of the negative pressure tube 774 through the cylinder 72, and the negative pressure causes the lifting block 775 to rise. The lifting block 775 drives the elastic rope 776 to move upward, and is limited by the limiting sleeve 777. The elastic rope 776 drives the rubber ball 778 to rise vertically, and the rubber ball 778 drives the rubber ring 779 to move upward. During the upward movement of the rubber ring 779, the hemostatic cotton 754 is squeezed to reduce the area of the hemostatic cotton 754 soaked by the disinfectant, thereby preventing the disinfectant from spreading around the hemostatic cotton 754, so that the disinfectant can pass through the hemostatic cotton 754 to disinfect the patient's joints, ensuring that the disinfectant reaches the patient's joints accurately.

A stabilizing assembly 78 is provided on the outer wall of the rubber ring 779, and the stabilizing assembly 78 includes a plurality of concave blocks 781 fixedly connected to the outer wall of the rubber ring 779, a rotating rod 782 is rotatably connected to one side of the inner wall of the concave block 781, a clamping rod 783 passes through the middle end of one side of the outer wall of the rotating rod 782 and is rotatably connected, and a plurality of square holes 784 are respectively opened around the top of the circular plate 752.

Both ends of the clamping rod 783 are fixedly connected to the inner walls of the square hole 784. The bottom of the end of the rotating rod 782 away from the concave block 781 is fixedly connected to a rubber plate 786. The top of the rotating rod 782 is fixedly connected to a three-pronged plate 785. Both ends of one side of the three-pronged plate 785 are respectively fixedly connected to a pull rope 787. The end of the pull rope 787 away from the three-pronged plate 785 is fixedly connected to a flexible elastic strip 788. The purpose of this arrangement is to enable deformation.

When in use, when the rubber ring 779 rises, the rubber ring 779 drives the concave block 781 to rise, and the concave block 781 drives the rotating rod 782 to rise. When one end of the rotating rod 782 rises, the other end falls in the opposite direction. The other end of the rotating rod 782 drives the rubber plate 786 to fall, so that the rubber plate 786 presses down the outside of the hemostatic cotton 754. The outside of the hemostatic cotton 754 is pressed downward, which can enhance the pressure of the hemostatic cotton 754 on the blood around the patient's joints, and enhance the hemostatic effect of the hemostatic cotton 754 on the patient's joints. In addition, the rubber plate 786 can drive the three-pronged plate 785 to fall, and the three-pronged plate 785 drives the pull rope 787 to move. 87 is stretched, and the pull rope 787 drives the flexible elastic strip 788 to deform. During the deformation of the flexible elastic strip 788, a thrust can be applied to the outer wall of the elastic rope 776. The elastic rope 776 is affected by the thrust, which can enhance the squeezing effect of the rubber ring 779 on the hemostatic cotton 754, further enhancing the disinfection effect of the hemostatic cotton 754. When the rotating rod 782 is close to one end of the concave block 781 and rotates around the clamping rod 783, the rotating rod 782 will drive the concave block 781 to squeeze the rubber ring 779. When the four concave blocks 781 squeeze the rubber ring 779, the rubber ring 779 will further reduce the disinfection range of the hemostatic cotton 754, further enhancing the hemostatic effect of the hemostatic cotton 754.

When the device is installed on the patient's joint, during the long-term pressing process, the angle of the patient's joint may change, causing the bent plate 2 to rotate around the support platform 1, and the bent plate 2 drives the flexible spring plate 761 to rotate. Limited by the vertical block 762, the flexible spring plate 761 can drive the sliding block 764 to move inside the sliding groove 765, and the sliding block 764 drives the first clamping plate 766 to move. The two groups of first clamping plates 766 approach each other, thereby clamping the hexagonal capsule 7612, enhancing the stabilization effect of the device and enhancing the pressing effect of the patient. When the angle of the patient's joint moves in the opposite direction, the first clamping plate 766 drives the arc block 767 to move, and the arc block 767 drives the bent rod 768 to move. The bending rod 768 drives the sliding rod 769 to move, and the sliding rod 769 drives the second clamping plate 7611 to move. The two groups of second clamping plates 7611 move close to each other, and can clamp the hexagonal capsule 7612, further enhancing the stabilization effect of the device and the pressing effect on the patient's joints. When the hexagonal capsule 7612 is squeezed, the internal airflow enters the interior of the sealing ring 773 through the elastic tube 771, causing the sealing ring 773 to expand. During the expansion of the sealing ring 773, the threaded connection between the hexagonal screw rod 71 and the threaded plate 74 is sealed to prevent pressure relief inside the cylinder 72, further enhancing the generation of negative pressure inside the cylinder 72, and indirectly enhancing the hemostatic effect of the hemostatic cotton 754.

The preferred embodiments of the present invention disclosed above are only used to help illustrate the present invention. The preferred embodiments do not describe all the details in detail, nor do they limit the invention to the specific implementation methods described. Obviously, many modifications and changes can be made according to the content of this specification. This specification selects and specifically describes these embodiments in order to better explain the principles and practical applications of the present invention, so that those skilled in the art can understand and use the present invention well. The present invention is limited only by the claims and their full scope and equivalents.

Claims (4)

1. A cardiology compression hemostasis device, comprising a support platform (1), characterized in that: bent plates (2) are rotatably connected to the two sides of the support platform (1), one end of the bent plate (2) away from the support platform (1) is fixedly connected to a compression plate (3), and rotation springs (4) are fixedly connected to the two sides of the bent plate (2), one end of the rotation spring (4) is fixedly connected to one side of the inner wall of the support platform (1), and the top of the support platform (1) is respectively provided with a card slot (5), and the inner wall of the card slot (5) is sleeved and rotatably connected with a compression belt (6), and further comprising; A pressing hemostasis mechanism (7), the pressing hemostasis mechanism (7) comprising a hexagonal screw (71) penetrating the support platform (1) and extending to the outside of the support platform (1), the bottom of the support platform (1) being fixedly connected to a cylinder (72), the inner wall bottom of the cylinder (72) being fixedly connected to a plurality of limit rods (73) respectively, the middle end of the outer wall of the limit rod (73) being sleeved and slidably connected to a threaded plate (74), the inner wall of the threaded plate (74) being sleeved and threadedly connected to the middle end of the outer wall of the hexagonal screw (71), and the bottom of the threaded plate (74) being provided with a disinfection component (75); The disinfection assembly (75) comprises a plurality of connecting rods (751) fixedly connected to the bottom of the threaded plate (74), one end of the connecting rod (751) passes through the cylinder (72) and extends to the outside of the cylinder (72), the bottom of the connecting rod (751) is fixedly connected to a circular plate (752), the bottom center of the circular plate (752) is provided with a drainage groove (753), the bottom of the circular plate (752) is fixedly connected to a hemostatic cotton (754), and one side of the top end of the connecting rod (751) passes through and is connected to a drainage pipe (755), and one end of the drainage pipe (755) is connected to the top of the inner wall of the drainage groove (753); An adjustment component (76) is provided at the top of the bent plate (2), and the adjustment component (76) comprises a flexible spring plate (761) fixedly connected to the top of the bent plate (2); a cross bar (763) is sleeved on the inner wall of the flexible spring plate (761) and slidably connected thereto; vertical blocks (762) are respectively fixedly connected at both ends of the cross bar (763); the bottom of the vertical block (762) is fixedly connected to the top of the support platform (1); and sliding grooves (765) are respectively provided on both sides of the top of the support platform (1) near the card slot (5); The end of the flexible spring plate (761) away from the bent plate (2) is fixedly connected to a sliding block (764); the outer wall of the sliding block (764) is sleeved and slidably connected to the inner wall of the slide groove (765); the top of the sliding block (764) close to the slide groove (765) is fixedly connected to a first clamping plate (766); the tops of both ends of the first clamping plate (766) are respectively fixedly connected to arc blocks (767); one end of the arc block (767) is fixedly connected to a bent rod (768); A sliding rod (769) is slidably connected to the side wall of one end of the bent rod (768) away from the arc block (767); one end of the sliding rod (769) is fixedly connected to a second clamping plate (7611); a side of the second clamping plate (7611) close to the sliding rod (769) is fixedly connected to a return spring (7610); one end of the return spring (7610) is fixedly connected to one side of the bent rod (768); the return spring (7610) is arranged outside the sliding rod (769); and a hexagonal capsule (7612) is fixedly connected to the top center of the support platform (1); A sealing assembly (77) is provided at the bottom of the hexagonal capsule (7612), and the sealing assembly (77) comprises a plurality of elastic tubes (771) connected around the bottom of the hexagonal capsule (7612), one end of the elastic tube (771) passes through the support platform (1) and extends to the interior of the cylinder (72), and one end of the elastic tube (771) away from the hexagonal capsule (7612) is connected to a sealing ring (773), the bottom of the sealing ring (773) is fixedly connected to the top of the threaded plate (74), and the threaded plate (74) is fixedly connected to the limiting shell (772) near the top of the sealing ring (773), and the outer wall of the top end of the cylinder (72) is respectively connected to a plurality of negative pressure tubes (774). 2. The cardiology compression hemostasis device according to claim 1 is characterized in that: a lifting block (775) is sleeved and slidably connected to the middle end of the inner wall of the negative pressure tube (774), the bottom of the lifting block (775) is fixedly connected to an elastic rope (776), and a plurality of limiting sleeves (777) are fixedly connected to the four sides of the bottom of the cylinder (72), one end of the elastic rope (776) passes through the limiting sleeve (777) and extends to the outside of the limiting sleeve (777), and the end of the elastic rope (776) away from the lifting block (775) is fixedly connected to a rubber ball (778), and the outer wall of the rubber ball (778) is sleeved and slidably connected to a rubber ring (779). 3. The cardiology compression hemostasis device according to claim 2 is characterized in that: the outer wall of the rubber ring (779) is provided with a stabilizing component (78), and the stabilizing component (78) includes a plurality of concave blocks (781) fixedly connected to the outer wall of the rubber ring (779) around, and a rotating rod (782) is rotatably connected to one side of the inner wall of the concave block (781), and a clamping rod (783) passes through and is rotatably connected to the middle end of one side of the outer wall of the rotating rod (782), and a plurality of square holes (784) are respectively opened around the top of the circular plate (752). 4. The cardiology compression hemostasis device according to claim 3 is characterized in that: both ends of the clamping rod (783) are fixedly connected to the two sides of the inner wall of the square hole (784), the bottom of the end of the rotating rod (782) away from the concave block (781) is fixedly connected to a rubber plate (786), the top of the rotating rod (782) is fixedly connected to a three-pronged plate (785), one end of the three-pronged plate (785) is fixedly connected to a pull rope (787) respectively, and the end of the pull rope (787) away from the three-pronged plate (785) is fixedly connected to a flexible elastic strip (788).