Compression hemostasis device for cardiology department nursing

Abstract

The compression hemostasis device comprises a base, the base is provided with a fixed base and a hemostasis frame installed at the top of the base, the two sides of the bottom of the hemostasis frame extend into the base, and the bottom of an inner cavity of the base is fixedly connected with an anti-skid cushion block; the inflatable ball is provided with a cavity and a hose installed on the outer surface of the inflatable ball, the end, away from the inflatable ball, of the hose is communicated with an air bag, and the position, away from the hemostasis frame, of the air bag is fixedly connected with a lateral base plate. According to the compression hemostasis device for cardiology department nursing, the situation that a patient feels uncomfortable due to the fact that the extrusion force of the lateral base plate is too large is prevented, the protection plate has good stability on the base, the extrusion accuracy of an extrusion frame on a hemostasis position is conveniently improved, and the extrusion force can be adjusted through lifting of the extrusion frame on the displacement piece; and the situation that the extrusion force of the extrusion frame is too small to stop bleeding is avoided.

Description

Technical Field

[0001] This invention relates to the field of medical device technology, specifically to a compression hemostasis device for cardiology nursing. Background Technology

[0002] Cardiology, or cardiovascular medicine, is a clinical department set up by the general internal medicine department of hospitals at all levels to diagnose and treat cardiovascular diseases. The diseases treated include angina pectoris, hypertension, sudden death, arrhythmia, heart failure, premature beats, irregular heartbeats, myocardial infarction, cardiomyopathy, myocarditis, myocardial infarction, and other cardiovascular diseases. Compression hemostasis is often required when treating patients.

[0003] According to Chinese Patent No. CN113243961A, an intermittent compression hemostasis device for cardiology nursing comprises a hemostasis main body and a support mechanism. The hemostasis main body has a mounting ring fixedly connected internally, and a rubber spring frame movably connected to the outer surface of the mounting ring frame. A compression spring seat is movably connected internally to the rubber spring frame, and a pressure rod is movably connected to the side surface of the compression spring seat. The support mechanism includes a holding seat, and a winding strap is movably connected to the outer surface of the holding seat. It also includes a hemostasis mechanism, which includes a connecting disc. A first rotating rod is rotatably connected to the outer surface of the connecting disc, and a moving rod is movably connected to the outer surface of the first rotating rod. Through the indirect mutual compression of a first and second compression hemostasis seat, intermittent compression and buffering release can be applied to the wound to ensure normal blood supply, bringing convenience to the patient's treatment. However, it is difficult to adjust the position and force of the hemostasis during the process, which can easily affect the hemostasis effect. Furthermore, the device is prone to loosening during compression, reducing the quality of hemostasis. It is also difficult to adjust the contact force around the hemostasis position.

[0004] In summary, it is not easy to adjust the position and force of hemostasis during the hemostasis process, which can easily affect the hemostasis effect. Furthermore, the patient is prone to loosening the device during the compression process, which reduces the quality of hemostasis. It is also not easy to adjust the contact force of the device around the hemostasis position. Summary of the Invention

[0005] To address the shortcomings of existing technologies, the technical solution adopted by this invention is: a compression hemostasis device for cardiology nursing, comprising,

[0006] The base has a fixed base and a hemostat mounted on the top of the base. The bottom sides of the hemostat extend into the interior of the base, and an anti-slip pad is fixedly connected to the bottom of the inner cavity of the base.

[0007] An inflatable ball has a cavity and a hose installed on its outer surface. An air bladder is connected to the end of the hose away from the inflatable ball. A lateral pad is fixedly connected to the air bladder at a position away from the hemostatic frame. When the inflatable ball is pressed by a staff member, gas is supplied to the air bladder through the hose, causing the air bladder to expand and push the lateral pad against the patient. This ensures the stability of the patient's installation position and prevents the device from falling off or loosening. The gas content inside the air bladder can adjust the pressure of the lateral pad, preventing excessive pressure that could cause discomfort to the patient. Anti-slip pads on the base cooperate with the lateral pads. The uneven surface of the anti-slip pads in contact with the patient prevents the patient from easily loosening after fixation. The hemostatic frame includes:

[0008] A snap-fit ​​strip having a snap-fit ​​groove and a lifting member installed at the bottom of the snap-fit ​​strip, wherein a stop block is slidably connected to the side of the lifting member away from the airbag, and the stop block extends into the interior of the lifting member near the airbag.

[0009] The protective plate comprises a plate body and a displacement member mounted on top of the protective plate. A compression frame is fixedly connected to the top of the displacement member, and the bottom of the compression frame penetrates the displacement member and extends to its exterior. Inner support frames are fixedly connected to the top of the inner cavity of the protective plate on both sides of the compression frame. The protective plate is secured to a lifting member via snap-fit ​​strips, ensuring close contact between the protective plate and the lifting member. This facilitates sliding of the protective plate on the base after power is applied, providing excellent stability. The space between the protective plate and the base can be adjusted to prevent patients from being unable to insert themselves into the device. Furthermore, the lifting member has a stop block that allows for adjustable height of the internal movement. The device is reinforced to increase the load-bearing capacity of the lifting component, while the displacement component can move the compression frame on the protective plate. This allows the displacement component to adjust the hemostasis position on the patient, improving the accuracy of the compression frame. The lifting and lowering of the compression frame on the displacement component can also adjust the compression force, preventing insufficient compression force from achieving hemostasis and thus improving the hemostasis effect of the device. The bottom of the displacement component penetrates the protective plate and extends to the outside of the protective plate. The bottom of the inner support frame near the protective plate is slidably connected to the airbag. The protective plate near the base is fixedly connected to the lifting component. The hose near the airbag penetrates the protective plate and extends to the outside of the protective plate.

[0010] Preferably, the inner support frame includes an arc-shaped plate, and an auxiliary plate is fixedly connected to the outer surface of the arc-shaped plate. The auxiliary plate reinforces the arc-shaped plate, increasing the tightness of the arc-shaped plate's installation position. The arc-shaped plate can limit the airbag's position, thereby controlling the airbag's inflation height and preventing the airbag from insufficiently pushing the lateral pads during inflation. Simultaneously, the airbag's inflation supports the arc-shaped plate, increasing its contact area. A fixing shell is fixedly connected to the side of the arc-shaped plate away from the auxiliary plate. A support plate is fixedly connected at a position away from the curved plate. A contact reinforcement body is rotatably connected to the support plate at a position away from the fixed shell. The contact reinforcement body extends to the outside of the curved plate at a position away from the contact reinforcement body. The support plate can provide support inside the fixed shell, thereby increasing the load-bearing capacity of the fixed shell itself. When the contact reinforcement body is pushed by the lifting and lowering of the extrusion frame inside the fixed shell, it rotates, so that the contact reinforcement body contacts the support plate when rotating. This allows the support plate to limit the rotation range of the contact reinforcement body. As the contact reinforcement body rotates to contact the support plate, it can share the pressure on the support plate.

[0011] Preferably, the displacement component includes a displacement block, a limiting frame is fixedly connected to the bottom of the displacement block, a guide sleeve is connected to the bottom of the limiting frame, an assembly plate is fixedly connected to the outer surface of the guide sleeve, and a protective plate is connected to the displacement block and the assembly plate, so that the displacement block and the assembly plate can contact the protective plate at different positions, thereby increasing the ease of movement of the protective plate surface and preventing the displacement block from tilting or lifting when moving, thus ensuring that the extrusion frame can maintain a vertical state when extruding. The top of the assembly plate is fixedly connected to the limiting frame, and a stabilizing frame is fixedly connected to the top of the inner walls on both sides of the displacement block. The bottom of the stabilizing frame is fixedly connected to the limiting frame. The extrusion frame can be fixed through the movable space formed by the limiting frame and the guide sleeve, thus ensuring the ease of movement of the extrusion frame. Moreover, the cooperation between the limiting frame and the guide sleeve can maintain the distance between the displacement block and the assembly plate, thereby ensuring that the protective plate can have sufficient contact area with the displacement block and the assembly plate. The contact between the limiting frame and the assembly plate limits the installation position of the protective plate on the guide sleeve.

[0012] Preferably, the compression frame includes a top cover, a screw fixedly connected to the bottom of the top cover, and a mating sleeve rotatably connected to the outer surface of the screw. The bottom end of the screw passes through the mating sleeve and extends to the outside of the mating sleeve. The screw rotates under the drive of the top cover, causing it to descend within the mating sleeve during clockwise rotation. This allows the screw to maintain an adjustable length via the mating sleeve after rotation stops, enabling adjustment of the compression force at the hemostatic position. This avoids excessive or insufficient pressure causing patient discomfort and allows the patient's arm to be freed after adjustment, preventing prolonged use of the compression sleeve. When applying pressure to the hemostatic site, the bottom end of the screw is rotatably connected to a mounting base, and the bottom of the mounting base is fixedly connected to a compression plate. The top of the compression plate penetrates through the mounting base and extends into its interior. A replaceable hemostatic pad is provided on the surface of the compression plate, allowing the pad to be replaced after each use, thus avoiding contamination from repeated use. The compression plate moves with the screw on the mounting base, facilitating sufficient pressure on the patient. Furthermore, the compression plate is larger than the hemostatic site, allowing for precise pressure on the hemostatic area, thus preventing deviations in hemostasis.

[0013] Preferably, the contact enhancement body includes a limiting post, a connecting block fixedly connected to the outer surface of the limiting post, and a movable post rotatably connected to the middle left side of the connecting block. The connecting block rotates under the influence of the limiting post, and both ends of the limiting post are connected to the fixed shell, so that the connecting block can contact the support plate when it rotates, and the movable post can rotate on the connecting block after the connecting block stops rotating. This allows the connecting block to limit the rotation of the movable post, and the connection between the limiting post and the fixed shell can reinforce the fixed shell, thereby increasing the strength of the fixed shell itself. A connecting plate is fixedly connected to the movable post away from the connecting block, and a contact plate is fixedly connected to the side of the connecting plate away from the movable post. The contact plate rotates on the connecting plate via the movable post, which facilitates the movable post to adjust the connecting plate. This allows the contact plate to contact the movement of the mounting base, providing a positioning effect when the mounting base rises and preventing the screw from causing the mounting base to slide down.

[0014] Preferably, the stabilizing frame includes a docking plate, a reset plate fixedly connected to the top of the docking plate, and a positioning arc plate fixedly connected to the top of the reset plate. The docking plate is reinforced by the reset plate on the positioning arc plate, and the docking plate, supported by the reset plate, can remain horizontal. This allows the docking plate to fix the limiting frame, increasing the contact area of ​​the limiting frame. Furthermore, the connection between the reset plate and the docking plate ensures that the docking plate remains horizontal after installation, preventing the docking plate from tilting and squeezing the reset plate on the limiting frame. The positioning arc plate is located near the reset plate. A partition plate is fixedly connected to the positioning arc plate. A clamping frame is fixedly connected to the right side of the positioning arc plate away from the partition plate. The clamping frame passes through the positioning arc plate and extends to the outside of the positioning arc plate near the partition plate. The clamping frame on the positioning arc plate clamps the partition plate while contacting the displacement block, thereby increasing the strength of the positioning arc plate itself and preventing the connection between the clamping frame and the displacement block from loosening. In addition, the clamping frame and the partition plate work together to reinforce the inside of the displacement block, thereby increasing the load-bearing capacity of the displacement block and preventing excessive wear on the surface of the displacement block.

[0015] Preferably, the mounting base includes a mounting frame, the top of which is connected to a movable sleeve, the bottom of which extends through the mounting frame, and a sliding disc slidably connected to the inner surface of the movable sleeve. The movable sleeve communicates with the mounting frame, allowing the sliding disc inside the movable sleeve to slide within a limited position. This allows the sliding disc to move within the movable sleeve under the pressure of the screw, increasing the stability of the screw's mounting position and preventing it from loosening and falling off. Simultaneously, the sliding disc increases the contact area inside the movable sleeve, preventing tilting at the connection point between the movable sleeve and the screw. Load-bearing blocks are fixedly connected to both sides of the bottom of the inner cavity of the mounting frame, and a support frame is fixedly connected to the top of the load-bearing blocks. The outer walls of the support frame are fixedly connected to the mounting frame. Supported by the load-bearing blocks inside the mounting frame, the support frame remains horizontal, allowing it to contact the sliding disc and limit its descent, preventing it from sliding out of the movable sleeve.

[0016] This invention provides a compression hemostasis device for use in cardiology nursing. It has the following beneficial effects:

[0017] 1. This compression hemostasis device for cardiology nursing includes an air bladder, a side pad, a protective plate, and a lifting component. Gas is delivered into the air bladder via a hose when the staff presses the air bladder, causing it to expand and push the side pad to compress the patient. This ensures the stability of the device's position and prevents it from falling off or loosening. It also prevents excessive pressure from the side pad that could cause discomfort. A locking strip secures the protective plate to the lifting component, ensuring tight contact and good stability of the protective plate on the base. This improves the accuracy of the compression device in stopping the hemostasis. Furthermore, the lifting and lowering of the compression device on the displacement component allows for adjustment of the compression force, preventing insufficient compression from achieving hemostasis.

[0018] 2. This compression hemostasis device for cardiology nursing connects to the mounting frame via a movable sleeve, allowing the sliding disc inside the movable sleeve to slide within a limited position. This prevents the screw from loosening and causing the compression point to fall off. The support frame inside the mounting frame is supported by a load-bearing block, ensuring it remains horizontal. This allows the support frame to contact the sliding disc, limiting its descent and preventing it from sliding out of the movable sleeve.

[0019] 3. This compression hemostasis device for cardiology nursing uses a reset plate to reinforce the docking plate on the positioning arc plate. The docking plate is supported by the reset plate and can remain horizontal, thereby fixing the limiting frame and increasing the contact area of ​​the limiting frame. The clamping frame on the positioning arc plate contacts the displacement block and clamps the partition plate, thereby increasing the strength of the positioning arc plate itself, preventing the connection between the clamping frame and the displacement block from becoming loose, and preventing excessive wear on the surface of the displacement block.

[0020] 4. This compression hemostasis device for cardiology nursing uses a connecting block that rotates under the influence of a limiting column. The two ends of the limiting column are connected to a fixed shell, allowing the connecting block to contact the support plate when it rotates. After the connecting block stops rotating, the movable column can rotate on the connecting block, thus limiting the rotation of the movable column. The contact plate rotates on the connecting plate via the movable column, facilitating the adjustment of the connecting plate by the movable column and enabling the contact plate to contact the movement of the mounting base.

[0021] 5. This compression hemostasis device for cardiology nursing uses a screw that rotates under the drive of the top cover. When the screw rotates clockwise, it descends inside the mating sleeve. This allows the screw to maintain its adjustable length after rotation stops, and the compression force at the hemostasis position can be adjusted. This avoids the need for the patient to apply pressure to the hemostasis position for an extended period. The surface of the compression plate has a replaceable hemostatic pad, allowing the pad to be replaced after each use, thus preventing deviations in hemostasis.

[0022] 6. This compression hemostasis device for cardiology nursing uses a protective plate connected to a displacement block and an assembly plate, allowing the displacement block and assembly plate to contact the protective plate at different positions. This ensures that the compression frame remains vertical during compression. The movable space formed by the limiting frame and the guide sleeve can fix the compression frame, thus ensuring convenient movement of the compression frame. The contact between the limiting frame and the assembly plate limits its installation position on the guide sleeve.

[0023] 7. This compression hemostasis device for cardiology nursing connects an auxiliary plate to an arc-shaped plate, which reinforces the arc-shaped plate and avoids the problem that the lateral pad cannot be fully pushed when the airbag inflates. At the same time, the inflation of the airbag can support the arc-shaped plate, thereby increasing the contact area of ​​the arc-shaped plate. The support plate can provide support inside the fixed shell. When the contact enhancer rotates to contact the support plate, it can distribute the pressure on the support plate. Attached Figure Description

[0024] Figure 1 This is a schematic diagram of the overall structure of the present invention;

[0025] Figure 2 This is a schematic diagram of the hemostatic frame of the present invention;

[0026] Figure 3 This is a schematic diagram of the internal support frame of the present invention;

[0027] Figure 4 This is a schematic diagram of the displacement component of the present invention;

[0028] Figure 5 This is a schematic diagram of the extrusion frame of the present invention;

[0029] Figure 6 This is a schematic diagram of the structure of the contact enhancer of the present invention;

[0030] Figure 7 This is a schematic diagram of the structure of the stabilizing frame of the present invention;

[0031] Figure 8 This is a schematic diagram of the mounting base of the present invention.

[0032] In the diagram: 1. Base; 2. Side pad; 3. Anti-slip pad; 4. Airbag; 5. Hemostat; 51. Lifting component; 52. Connecting strip; 53. Stop block; 54. Inner support frame; 541. Arc plate; 542. Auxiliary plate; 543. Fixed shell; 544. Support plate; 545. Contact enhancer; 71. Connecting block; 72. Connecting plate; 73. Limiting post; 74. Movable post; 75. Contact plate; 55. Displacement component; 551. Displacement block; 552. Assembly plate; 553. Limiting bracket; 554. Guide sleeve; 555. Stabilizing bracket; 81. Divider plate; 82. Reset plate; 83. Docking plate; 84. Positioning arc plate; 85. Tightening bracket; 56. Extrusion bracket; 561. Top cover; 562. Screw; 563. Mating sleeve; 564. Mounting base; 91. Mounting frame; 92. Movable sleeve; 93. Bearing bracket; 94. Load-bearing block; 95. Sliding disc; 565. Extrusion plate; 57. Protective plate; 6. Hoses; 7. Inflatable ball. Detailed Implementation

[0033] The present invention will now be described in further detail with reference to the accompanying drawings and specific embodiments. The embodiments of the present invention are given for illustrative and descriptive purposes only, and are not intended to be exhaustive or to limit the invention to the forms disclosed. Many modifications and variations will be apparent to those skilled in the art. The embodiments were chosen and described to better illustrate the principles and practical application of the invention, and to enable those skilled in the art to understand the invention and design various embodiments with various modifications suitable for a particular purpose.

[0034] Example 1

[0035] Please see Figures 1-5 This invention provides a technical solution: a compression hemostasis device for cardiology nursing, comprising,

[0036] The base 1 has a fixed base and a hemostat 5 installed on the top of the base 1. The bottom sides of the hemostat 5 extend into the interior of the base 1. Anti-slip pads 3 are fixedly connected to the bottom of the inner cavity of the base 1.

[0037] An inflatable ball 7 has a cavity, and a hose 6 is installed on the outer surface of the inflatable ball 7. An air bladder 4 is connected to the end of the hose 6 away from the inflatable ball 7. A lateral pad 2 is fixedly connected to the air bladder 4 away from the hemostat 5. When the inflatable ball 7 is pressed by the operator, gas is supplied to the inside of the air bladder 4 through the hose 6, causing the air bladder 4 to expand and push the lateral pad 2 to compress the patient, thus ensuring the stability of the patient's installation position and preventing the device from falling off or loosening. The gas content inside the air bladder 4 can adjust the pressure of the lateral pad 2, preventing excessive pressure from causing discomfort to the patient. Anti-slip pads 3 on the base 1 cooperate with the lateral pad 2. The uneven surface of the anti-slip pads 3 in contact with the patient makes it less likely for the patient to loosen after fixation. The hemostat 5 includes:

[0038] The snap-fit ​​strip 52 has a snap-fit ​​groove, and a lifting member 51 is installed at the bottom of the snap-fit ​​strip 52. A stop block 53 is slidably connected to the side of the lifting member 51 away from the airbag 4. The stop block 53 extends into the interior of the lifting member 51 near the airbag 4.

[0039] The protective plate 57 has a plate body and a displacement member 55 installed on the top of the protective plate 57. A pressing frame 56 is fixedly connected to the top of the displacement member 55, and the bottom of the pressing frame 56 penetrates through the displacement member 55 and extends to the outside of the displacement member 55. Inner support frames 54 are fixedly connected to the top of the inner cavity of the protective plate 57 on both sides of the pressing frame 56. The protective plate 57 is fixed to the lifting member 51 by a snap-fit ​​strip 52, ensuring close contact between the protective plate 57 and the lifting member 51. This facilitates the lifting member 51 driving the protective plate 57 to slide on the base 1 after being connected to electricity, giving the protective plate 57 good stability on the base 1. Simultaneously, it can provide support for the protective plate 57. The space between 7 and base 1 can be adjusted to prevent the patient from being unable to reach inside the device. The stop block 53 of the lifting member 51 can reinforce the height of its internal lifting, thereby increasing the bearing capacity of the lifting member 51. The displacement member 55 can drive the compression frame 56 to move on the protective plate 57, so that the displacement member 55 can adjust the hemostasis position of the patient, which can improve the accuracy of the compression frame 56 to the hemostasis position. The lifting and lowering of the compression frame 56 on the displacement member 55 can adjust the compression force, avoiding the situation where the compression force of the compression frame 56 is too small to stop the bleeding, thereby improving the hemostasis effect of the device.

[0040] The inner support frame 54 includes an arc-shaped plate 541, with an auxiliary plate 542 fixedly connected to its outer surface. The auxiliary plate 542 reinforces the arc-shaped plate 541, increasing the tightness of its installation position. This allows the arc-shaped plate 541 to limit the airbag 4, controlling its inflation height and preventing insufficient pushing of the lateral pad 2 during inflation. Simultaneously, the inflation of the airbag 4 supports the arc-shaped plate 541, increasing its contact area. A fixing shell 543 is fixedly connected to the side of the arc-shaped plate 541 away from the auxiliary plate 542. A support plate 544 is fixedly connected to the support plate 544, and an augmenting body 545 is rotatably connected to the support plate 544 at a position away from the fixed shell 543. The augmenting body 545 extends to the outside of the arc plate 541 at a position away from the augmenting body 544. The support plate 544 can provide support inside the fixed shell 543, thereby increasing the bearing capacity of the fixed shell 543 itself. When the augmenting body 545 is pushed by the lifting and lowering of the pressing frame 56 inside the fixed shell 543, it rotates, so that the augmenting body 545 contacts the support plate 544 when rotating. This allows the support plate 544 to limit the rotation range of the augmenting body 545. As the augmenting body 545 rotates to contact the support plate 544, it can share the pressure on the support plate 544.

[0041] The displacement component 55 includes a displacement block 551. A limiting frame 553 is fixedly connected to the bottom of the displacement block 551. A guide sleeve 554 is connected to the bottom of the limiting frame 553. An assembly plate 552 is fixedly connected to the outer surface of the guide sleeve 554. A protective plate 57 is connected to the assembly plate 552 via the displacement block 551, allowing the displacement block 551 and the assembly plate 552 to contact the protective plate 57 at different positions. This increases the ease of movement of the protective plate 57 surface and prevents the displacement block 551 from tilting or lifting during movement. This ensures that the extrusion frame 56 remains vertical during extrusion. The top of the assembly plate 552 is connected to the limiting frame 551. 3. Fixed connection: The top of the inner walls on both sides of the displacement block 551 is fixedly connected to a stabilizing frame 555. The bottom of the stabilizing frame 555 is fixedly connected to a limiting frame 553. The extrusion frame 56 can be fixed through the movable space formed by the limiting frame 553 and the guide sleeve 554, thereby ensuring the convenient movement of the extrusion frame 56. The limiting frame 553 and the guide sleeve 554 cooperate to maintain the distance between the displacement block 551 and the assembly plate 552, thereby ensuring that the protective plate 57 can fully contact the displacement block 551 and the assembly plate 552. The installation position of the protective plate 57 on the guide sleeve 554 is limited by the contact between the limiting frame 553 and the assembly plate 552.

[0042] The compression frame 56 includes a top cover 561, with a screw 562 fixedly connected to the bottom of the top cover 561. A mating sleeve 563 is rotatably connected to the outer surface of the screw 562. The bottom end of the screw 562 passes through the mating sleeve 563 and extends to the outside of the mating sleeve 563. The screw 562 rotates under the drive of the top cover 561, causing it to descend within the mating sleeve 563 during clockwise rotation. This allows the screw 562 to maintain its adjustable length after rotation stops, and to adjust the compression force at the hemostatic position. This avoids excessive or insufficient pressure causing patient discomfort and allows the patient's arm to be freed after adjustment, preventing prolonged use of the arm. When applying pressure to the hemostatic site, the bottom end of the screw 562 is rotatably connected to the mounting base 564, and the bottom of the mounting base 564 is fixedly connected to the compression plate 565. The top of the compression plate 565 penetrates through the mounting base 564 and extends into the interior of the mounting base 564. The surface of the compression plate 565 has a replaceable hemostatic pad, which allows the hemostatic pad to be replaced after each use, thus avoiding contamination caused by repeated use. The compression plate 565 moves on the mounting base 564 with the screw 562, making it easy for the compression plate 565 to fully compress the patient. The compression plate 565 is larger than the hemostatic site, which can press the hemostatic area, thus avoiding deviation in hemostasis.

[0043] In use, the patient inserts their arm into the space between the protective plate 57 and the base 1 and contacts the anti-slip pad 3. Then, the lifting component 51 lowers the protective plate 57 via the locking strip 52, and the adjusting stop block 53 tightens the lifting component 51. The operator presses the inflatable ball 7, so that the air generated by the inflatable ball 7 is delivered to the inside of the airbag 4 through the hose 6, so that the airbag 4 can expand after inflation and push the lateral pad 2 to squeeze the patient. The moving displacement block 551 moves the assembly plate 552 in the same direction via the limiting frame 553 and the guide sleeve 554. After the movement stops, the top cover 561 drives the screw 562 to rotate clockwise inside the mating sleeve 563, causing the screw 562 to descend via the mounting base 564 and compress the compression plate 565 to stop bleeding. Conversely, the top cover 561 rises counterclockwise via the screw 562 inside the mating sleeve 563, causing the compression plate 565 to gradually move away from the patient. Meanwhile, the arc plate 541 is mounted on the protective plate 57 via the auxiliary plate 542, and the fixing shell 543 on the arc plate 541 contacts the contact block 545.

[0044] Example 2:

[0045] Please see Figures 6-8Based on Embodiment 1, the present invention provides a technical solution: the contact enhancement body 545 includes a limiting post 73, a connecting block 71 fixedly connected to the outer surface of the limiting post 73, and a movable post 74 rotatably connected to the middle left side of the connecting block 71. The connecting block 71 rotates under the drive of the limiting post 73, and both ends of the limiting post 73 are connected to the fixed shell 543, so that the connecting block 71 can contact the support plate 544 when it rotates, and the movable post 74 can rotate on the connecting block 71 after the connecting block 71 stops rotating, so that the connecting block 71 can limit the rotation of the movable post 74, and the limiting post 73 and the fixed shell 543 are connected to the fixed shell 543. The connection of shell 543 can reinforce the fixed shell 543, thereby increasing the strength of the fixed shell 543 itself. A connecting plate 72 is fixedly connected to the movable column 74 away from the connecting block 71. A contact plate 75 is fixedly connected to the side of the connecting plate 72 away from the movable column 74. The contact plate 75 rotates on the connecting plate 72 via the movable column 74, which facilitates the adjustment of the connecting plate 72 by the movable column 74. This allows the contact plate 75 to contact the movement of the mounting base 564, which facilitates the positioning effect when the mounting base 564 rises, and prevents the screw 562 from causing the mounting base 564 to slide down.

[0046] The stabilizing frame 555 includes a docking plate 83, a reset plate 82 fixedly connected to the top of the docking plate 83, and a positioning arc plate 84 fixedly connected to the top of the reset plate 82. The reset plate 82 reinforces the docking plate 83 on the positioning arc plate 84, and the docking plate 83, supported by the reset plate 82, remains horizontal. This allows the limiting frame 553 to be fixed, increasing the contact area of ​​the limiting frame 553. The connection between the reset plate 82 and the docking plate 83 ensures that the docking plate 83 remains horizontal after installation, preventing the docking plate 83 from tilting and pressing against the reset plate 82 on the limiting frame 553. The positioning arc plate 84 is located near the reset plate 82. A partition plate 81 is fixedly connected to the positioning arc plate 84. A clamping frame 85 is fixedly connected to the right side of the positioning arc plate 84 away from the partition plate 81. The clamping frame 85 passes through the positioning arc plate 84 near the partition plate 81 and extends to the outside of the positioning arc plate 84. When the clamping frame 85 on the positioning arc plate 84 contacts the displacement block 551, it clamps the partition plate 81, thereby increasing the strength of the positioning arc plate 84 itself and preventing the connection between the clamping frame 85 and the displacement block 551 from becoming loose. In addition, the clamping frame 85 cooperates with the partition plate 81 to reinforce the inside of the displacement block 551, thereby increasing the bearing capacity of the displacement block 551 itself and preventing excessive wear on the surface of the displacement block 551.

[0047] The mounting base 564 includes a mounting frame 91, with a movable sleeve 92 connected to the top of the mounting frame 91. The bottom of the movable sleeve 92 passes through the mounting frame 91, and a sliding disc 95 is slidably connected to the inner surface of the movable sleeve 92. The connection between the movable sleeve 92 and the mounting frame 91 allows the sliding disc 95 inside the movable sleeve 92 to slide within a limited position. This allows the sliding disc 95 to move within the movable sleeve 92 under the pressure of the screw 562, increasing the stability of the screw 562's mounting position and preventing it from loosening and falling off. Simultaneously, the sliding disc 95 can increase the stability of the movable sleeve 92. 2. The internal contact area prevents the connection position between the movable sleeve 92 and the screw 562 from tilting. The bottom two sides of the inner cavity of the mounting frame 91 are fixedly connected to the load-bearing blocks 94, and the top of the load-bearing blocks 94 is fixedly connected to the support frame 93. The outer walls of the two sides of the support frame 93 are fixedly connected to the mounting frame 91. The support frame 93 is supported by the load-bearing blocks 94 inside the mounting frame 91, so that the support frame 93 can remain horizontal under the support of the load-bearing blocks 94. Thus, the support frame 93 can contact the sliding plate 95, thereby limiting the range of descent of the sliding plate 95 and preventing the sliding plate 95 from sliding out of the inside of the movable sleeve 92.

[0048] In use, the screw 562 contacts the sliding disc 95 inside the movable sleeve 92, and as the sliding disc 95 slides inside the movable sleeve 92 when the compression plate 565 contacts the patient, it gradually contacts the support frame 93, so that the support frame 93 is supported by the load-bearing block 94. When the mounting frame 91 moves with the screw 562, it contacts the contact plate 75 on the connecting plate 72, so that the contact plate 75 is subjected to pressure and rotates on the movable column 74 via the connecting plate 72. Thus, the movable column 74 drives the connecting block 71 to rotate on the fixed shell 543 with the limiting column 73. As the connecting block 71 rotates, it contacts the support plate 544. The clamping frame 85 and the partition plate 81 fix the positioning arc plate 84 inside the displacement block 551, and the reset plate 82 on the positioning arc plate 84 is engaged with the limiting frame 553 via the docking plate 83.

[0049] Example 3:

[0050] Please see Figures 1-8 Based on Embodiments 1 and 2, the present invention provides a technical solution: a method of using a compression hemostasis device for cardiology nursing, step one: the protective plate 57 and the base 1 are installed on the patient, the lifting member 51 is driven by electricity, the protective plate 57 is raised and lowered on the base 1 via the snap-fit ​​strip 52, the staff squeezes the inflation ball 7, so that the inflation ball 7 generates air and is delivered to the inside of the airbag 4 through the hose 6.

[0051] Step 2: As the airbag 4 receives air and expands on the base 1, it pushes the lateral pad 2, causing the lateral pad 2 to come into contact with the patient. The arc plate 541 is installed on the protective plate 57 via the auxiliary plate 542, while the two ends of the limiting post 73 are installed on the fixed shell 543.

[0052] Step 3: The displacement block 551 moves on the protective plate 57 as pushed by the staff, and the movement of the displacement block 551 drives the assembly plate 552 to move together on the protective plate 57 via the limit frame 553, so that the connecting cavity formed by the limit frame 553 and the guide sleeve 554 can be fitted with the sleeve 563 for installation.

[0053] Step 4: The operator drives the screw 562 to rotate clockwise through the top cover 561 and descends inside the mating sleeve 563. As the screw 562 descends, it rotates inside the movable sleeve 92 and contacts the movable plate 95. As the mounting frame 91 descends with the screw 562, it reaches the compression plate 565 on the patient and compresses the hemostasis position.

[0054] Step 5: The sliding cavity formed by the mounting frame 91 and the movable sleeve 92 allows the sliding disk 95 to move. The sliding disk 95 moves inside the movable sleeve 92 under the pressure of the screw 562 until it contacts the support frame 93. The load-bearing block 94 supports the support frame 93 inside the mounting frame 91 and rises inside the mating sleeve 563 as the top cover 561 drives the screw 562 to rotate counterclockwise.

[0055] Step 6: The clamping frame 85 supports the displacement block 551 by contacting the positioning arc plate 84 and the docking plate 83. The reset plate 82 is connected to the positioning arc plate 84 and the docking plate 83, so that the docking plate 83 is connected to the limit frame 553. The displacement block 551 and the assembly plate 552 contact the protective plate 57 at different positions.

[0056] Obviously, the described embodiments are only a part of the embodiments of the present invention, and not all of them. All other embodiments obtained by those skilled in the art and related fields based on the embodiments of the present invention without inventive effort should fall within the scope of protection of the present invention. Structures, devices, and operating methods not specifically described and explained in the present invention, unless otherwise specified or limited, shall be implemented according to conventional means in the art.

Claims

1. A compression hemostasis device for cardiology nursing, comprising, The base (1) has a fixed base and a hemostat (5) installed on the top of the base (1). The bottom sides of the hemostat (5) extend into the interior of the base (1). Anti-slip pads (3) are fixedly connected to the bottom of the inner cavity of the base (1). An inflatable ball (7) having a cavity, and a hose (6) installed on the outer surface of the inflatable ball (7), the end of the hose (6) away from the inflatable ball (7) being connected to an airbag (4), and a lateral pad (2) being fixedly connected to the airbag (4) away from the hemostat (5), characterized in that: The hemostatic frame (5) includes: A snap-fit ​​strip (52) having a snap-fit ​​groove, and a lifting member (51) installed at the bottom of the snap-fit ​​strip (52), wherein a stop block (53) is slidably connected to the side of the lifting member (51) away from the airbag (4), and the stop block (53) extends into the interior of the lifting member (51) near the airbag (4): The protective plate (57) has a plate body and a displacement member (55) installed on the top of the protective plate (57). The top of the displacement member (55) is fixedly connected to an extrusion frame (56). The bottom of the extrusion frame (56) passes through the displacement member (55) and extends to the outside of the displacement member (55). The top of the inner cavity of the protective plate (57) is fixedly connected to the two sides of the extrusion frame (56) with an inner support frame (54).

2. The construction method for a pipe or pipe gallery joint according to claim 1, characterized in that: The inner support frame (54) includes an arc-shaped plate (541), an auxiliary plate (542) is fixedly connected to the outer surface of the arc-shaped plate (541), a fixed shell (543) is fixedly connected to the side of the arc-shaped plate (541) away from the auxiliary plate (542), a support plate (544) is fixedly connected to the fixed shell (543) away from the arc-shaped plate (541), a contact enhancer (545) is rotatably connected to the support plate (544) away from the fixed shell (543), and the contact enhancer (545) extends to the outside of the arc-shaped plate (541) away from the contact enhancer (545).

3. The compression hemostasis device for cardiology nursing according to claim 1, characterized in that: The displacement component (55) includes a displacement block (551), a limiting frame (553) is fixedly connected to the bottom of the displacement block (551), a guide sleeve (554) is connected to the bottom of the limiting frame (553), an assembly plate (552) is fixedly connected to the outer surface of the guide sleeve (554), the top of the assembly plate (552) is fixedly connected to the limiting frame (553), and a stabilizing frame (555) is fixedly connected to the top of the inner walls on both sides of the displacement block (551), and the bottom of the stabilizing frame (555) is fixedly connected to the limiting frame (553).

4. The compression hemostasis device for cardiology nursing according to claim 1, characterized in that: The extrusion frame (56) includes a top cover (561), a screw (562) is fixedly connected to the bottom of the top cover (561), a mating sleeve (563) is rotatably connected to the outer surface of the screw (562), the bottom end of the screw (562) passes through the mating sleeve (563) and extends to the outside of the mating sleeve (563), a mounting base (564) is rotatably connected to the bottom end of the screw (562), an extrusion plate (565) is fixedly connected to the bottom of the mounting base (564), and the top of the extrusion plate (565) passes through the mounting base (564) and extends to the inside of the mounting base (564).

5. A compression hemostatic device for cardiology nursing according to claim 2, characterized in that: The contact enhancement body (545) includes a limiting post (73), a connecting block (71) is fixedly connected to the outer surface of the limiting post (73), a movable post (74) is rotatably connected to the middle left side of the connecting block (71), a connecting plate (72) is fixedly connected to the movable post (74) away from the connecting block (71), and a contact plate (75) is fixedly connected to the side of the connecting plate (72) away from the movable post (74).

6. A compression hemostatic device for cardiology nursing according to claim 3, characterized in that: The stabilizing frame (555) includes a docking plate (83), a reset plate (82) is fixedly connected to the top of the docking plate (83), a positioning arc plate (84) is fixedly connected to the top of the reset plate (82), a partition plate (81) is fixedly connected to the positioning arc plate (84) near the reset plate (82), a clamping frame (85) is fixedly connected to the right side of the positioning arc plate (84) away from the partition plate (81), and the clamping frame (85) near the partition plate (81) penetrates the positioning arc plate (84) and extends to the outside of the positioning arc plate (84).

7. A compression hemostatic device for cardiology nursing according to claim 4, characterized in that: The mounting base (564) includes a mounting frame (91), the top of which is connected to a movable sleeve (92), the bottom of which passes through the mounting frame (91), a sliding disc (95) is slidably connected to the inner surface of the movable sleeve (92), a load-bearing block (94) is fixedly connected to both sides of the bottom of the inner cavity of the mounting frame (91), a support frame (93) is fixedly connected to the top of the load-bearing block (94), and the outer walls of both sides of the support frame (93) are fixedly connected to the mounting frame (91).

8. A compression hemostatic device for cardiology nursing according to claim 1, characterized in that: The bottom of the displacement member (55) penetrates through the protective plate (57) and extends to the outside of the protective plate (57), and the bottom of the inner support (54) near the protective plate (57) is slidably connected to the airbag (4).

9. A compression hemostatic device for cardiology nursing according to claim 1, characterized in that: The protective plate (57) is fixedly connected to the lifting member (51) near the base (1), and the hose (6) passes through the protective plate (57) near the airbag (4) and extends to the outside of the protective plate (57).

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