Hepatobiliary clinical surgery hemostasis device

Abstract

The invention provides a hepatobiliary clinical surgery hemostasis device, and belongs to the field of medical instruments. Comprising a mounting frame, binding belts are symmetrically arranged on the outer surface of the mounting frame, and a threaded rod is rotationally connected to the upper surface of the mounting frame in a penetrating mode. Inflammation diminishing and hemostasis liquid medicine can be slowly added into the first liquid storage barrel, the liquid medicine finally flows into the circular disinfection sponge through the multiple liquid outlet holes to soak the circular disinfection sponge, the liquid medicine makes contact with a wound through the circular disinfection sponge, healing and hemostasis of the wound are effectively promoted, and the wound disinfection effect is improved. Meanwhile, liquid medicine can be conveniently and quickly added, and compared with a traditional device which cannot directly add the liquid medicine to the wound and directly extrude a sponge soaked with the liquid medicine to the wound, the liquid medicine in the sponge is easily extruded out, a bed sheet is easily polluted, the liquid medicine cannot fully play a role, the wound hemostasis speed is low, and the wound hemostasis effect is poor. And liquid medicine can be added under the condition that the device is not dismounted.

Description

Technical Field

[0001] The present invention relates to the technical field of medical devices, and more specifically, to a hemostatic device for hepatobiliary clinical surgery. Background Art

[0002] Hepatobiliary surgery mainly studies major diseases that seriously threaten the health of Chinese people, such as hepatocellular carcinoma, hepatolithiasis, post-hepatitis cirrhosis, and acute liver failure caused by severe hepatitis. The above diseases all need to be treated together with surgery. When performing hepatobiliary surgery in a hospital, it is necessary to stop bleeding at the incision of the liver and gallbladder, and controlling bleeding is the key to affecting postoperative complications and mortality.

[0003] To solve the problem of wound hemostasis, there is a hemostatic device for general surgery with the authorization announcement number CN210931641U. This device presses the wound with a disinfected cotton and provides the pressure to press the disinfected cotton through an airbag. However, this device cannot add medicine to the pressed wound. Without adding medicine, the speed of hemostasis and healing is slow and the effect is poor. If adding liquid medicine, the whole device needs to be disassembled, which increases the steps and is rather troublesome. If adding alcohol to the sponge before pressing, it is easy for the alcohol to be squeezed out and flow. Summary of the Invention

[0004] Aiming at the problems existing in the prior art, the purpose of the present invention is to provide a hemostatic device for hepatobiliary clinical surgery.

[0005] To solve the above problems, the present invention adopts the following technical solutions:

[0006] A hemostatic device for hepatobiliary clinical surgery, including a mounting frame. The outer surface of the mounting frame is symmetrically provided with restraint belts. The upper surface of the mounting frame is rotatably connected through a threaded rod. The outer surface of the threaded rod is threadedly connected with an internally threaded sleeve. The bottom of the internally threaded sleeve is fixedly connected with a ring. The inside of the mounting frame is provided with a medicine adding component for convenient medicine application.

[0007] The medicine adding component includes a first liquid inlet pipe sliding on the upper surface of the mounting frame. The top of the first liquid inlet pipe is fixedly connected with a first liquid storage cylinder. The lower surface of the first liquid inlet pipe is rotatably connected with a hollow plate. The inner bottom of the hollow plate is evenly distributed with liquid outlet holes. The outer surface of the hollow plate is slidably sleeved with a first annular frame. The inner surface of the first annular frame is connected with a circular disinfected sponge.

[0008] Optionally, one side of the outer surface of the installation frame is fixedly connected with a limiting rod, and the limiting rod extends out of the interior of the installation frame and slides with each other. The restraint belts are two and are axially symmetrically distributed on the outer surface of the installation frame. Magic tapes are respectively arranged on the two restraint belts, and the two magic tapes are arranged on opposite faces. The first liquid inlet pipe is communicated with the interior of the first liquid storage cylinder and the hollow plate. A medicine injection port is fixedly connected to the upper surface of the first liquid storage cylinder. The upper surface of the circular disinfection sponge is attached to the lower surface of the hollow plate. A disassembly and assembly component is arranged on the inner surface of the ring.

[0009] Optionally, the disassembly and assembly component includes a clamping plate fixed on the outer surface of the first liquid inlet pipe and a clamping groove opened on the inner surface of the ring. A shielding door is slidably connected to the outer surface of the installation frame. A through groove is opened on the inner surface of the installation frame.

[0010] Optionally, the clamping plate is located inside the clamping groove. The diameter of the first annular frame is smaller than the width of the through groove. A first magnet is arranged on one side of the inner surface of the through groove, and a second magnet is arranged on one side of the shielding door.

[0011] Optionally, a disinfection component is arranged near the bottom of the inner surface of the installation frame. The disinfection component includes a rotating shaft rotating at the edge of the inner top of the installation frame, a second annular frame rotating at the inner surface of the installation frame near the bottom, and a first gear fixed on the outer surface of the threaded rod. A second gear is fixedly connected to the outer surface of the rotating shaft. A third gear is fixedly connected to the bottom of the rotating shaft. An annular rack is fixedly connected to the edge of the upper surface of the second annular frame. An annular disinfection sponge is fixedly connected to the inner surface of the second annular frame.

[0012] Optionally, the third gear meshes with the annular rack. The second gear and the first gear are at the same height, and the second gear and the first gear mesh with each other.

[0013] Optionally, an adding component is fixedly connected to the edge of the upper surface of the installation frame. The adding component includes a second liquid storage cylinder fixed to the edge of the upper surface of the installation frame and an annular groove opened at the inner top of the second annular frame. A fixed cylinder is fixedly connected to the inner bottom of the second liquid storage cylinder. Second liquid inlet openings are axially symmetrically opened on the outer surface of the fixed cylinder. A second liquid inlet pipe is slidably sleeved inside the fixed cylinder. First liquid inlet openings are axially symmetrically opened near the top of the outer surface of the second liquid inlet pipe. A connecting cylinder is sleeved near the bottom of the outer surface of the second liquid inlet pipe.

[0014] Optionally, a cross bar is fixedly connected to the outer surface of the second liquid inlet pipe. Four wedge-shaped plates are evenly and fixedly connected to the upper surface of the second annular frame near the inner side. The inclined surface of the wedge-shaped plate slides with the cross bar.

[0015] Optionally, the bottom of the connecting cylinder extends through the annular groove into the interior of the second annular frame. The connecting cylinder and the annular groove slide relative to each other. A magnet ring is provided at the bottom of the connecting cylinder, and the second annular frame is made of metallic iron.

[0016] Optionally, C-shaped plates are symmetrically and fixedly connected to the inner bottom of the second annular frame, and the magnet ring is located above the C-shaped plates without hindering the circumferential movement of the C-shaped plates.

[0017] The technical solution provided by the present invention has at least the following beneficial effects compared with the prior art:

[0018] In the above solution, by providing a medicine adding assembly, anti-inflammatory and hemostatic liquid medicine is slowly added into the first liquid storage cylinder. Finally, the liquid medicine flows into the interior of the circular disinfection sponge through a plurality of liquid outlet holes, wetting the circular disinfection sponge, so that the liquid medicine contacts the wound through the circular disinfection sponge, effectively promoting the healing and hemostasis of the wound. At the same time, it is convenient to quickly add the liquid medicine, avoiding the situation that the traditional device cannot directly add the liquid medicine to the wound. Directly squeezing the sponge soaked with the liquid medicine on the wound easily causes the liquid medicine inside the sponge to be squeezed out, not only easily contaminating the bedsheet, but also causing the liquid medicine to not fully play its role, and the wound hemostasis speed is slow. The liquid medicine can be added without removing the device.

[0019] By providing a disassembly and assembly component, when pulling up the first liquid storage cylinder upward, the hollow plate and the first annular frame are driven to move upward as a whole through the first liquid inlet pipe, driving the circular disinfection sponge to separate from the patient's wound. The first annular frame as a whole is removed from the hollow plate, so that the circular disinfection sponge can be quickly replaced without removing the whole device, effectively improving the efficiency of replacing the circular disinfection sponge and reducing the steps of the patient wearing and disassembling back and forth.

[0020] By providing a disinfection component, when rotating the threaded rod, the annular disinfection sponge is driven to rotate synchronously through a series of transmissions. This can not only reduce the steps of rotating the annular disinfection sponge in the secondary operation, but also ensure a relatively sterile space inside the installation frame, avoiding the growth of bacteria on the patient's skin and preventing the bacteria from infecting the wound and causing pain to the patient. BRIEF DESCRIPTION OF THE DRAWINGS

[0021] The drawings incorporated herein and constituting a part of the specification illustrate embodiments of the present invention and, together with the specification, are further used to explain the principles of the present invention and enable those skilled in the relevant art to implement and use the present invention.

[0022] Figure 1 is a three-dimensional structural schematic diagram of the present invention;

[0023] Figure 2 is a schematic diagram of the interior of the installation frame of the present invention;

[0024] Figure 3 The installation frame of the present invention is a cross-sectional view Figure 1 ;

[0025] Figure 4 The installation frame of the present invention is a cross-sectional view Figure 2 ;

[0026] Figure 5 It is a schematic diagram of the installation frame of the present invention;

[0027] Figure 6 It is a schematic cross-sectional structural diagram of the dosing assembly of the present invention;

[0028] Figure 7 This is a schematic diagram of the structure of the added components of the present invention;

[0029] Figure 8 It is a schematic diagram of the added component structure of the present invention.

[0030] [Reference Signs]

[0031] 1. Mounting frame; 2. Tie straps; 3. Threaded rods;

[0032] 4. Dosing assembly; 41. First liquid inlet pipe; 42. First liquid storage cylinder; 43. Hollow plate; 44. Round disinfection sponge; 45. First annular frame;

[0033] 46. ​​disassembly and assembly components; 461. card plate; 462. card slot; 463. shielding door; 464. through slot; 47. liquid outlet;

[0034] 5. Disinfection assembly; 51. Rotating shaft; 52. First gear; 53. Second gear; 54. Ring rack; 55. Third gear; 56. Second ring frame;

[0035] 57. Adding component; 571. Second liquid inlet pipe; 572. Connecting cylinder; 573. Crossbar; 574. Second liquid storage cylinder; 575. Fixed cylinder; 576. First liquid inlet; 577. Second liquid inlet; 578. Annular groove; 579. Wedge plate; 58. Annular disinfection sponge;

[0036] 6. Internal threaded casing; 7. Ring.

[0037] As shown in the figure, in order to clearly implement the structure of the embodiment of the present invention, specific structures and devices are marked in the figure, but this is only for illustrative purposes and is not intended to limit the present invention to the specific structure, device and environment. According to specific needs, ordinary technicians in this field can adjust or modify these devices and environments. DETAILED DESCRIPTION

[0038] The following will describe in detail an expandable cancellous bone hollow screw with a pressurizing structure provided by the present invention in conjunction with the accompanying drawings and specific embodiments. At the same time, it should be noted here that in order to make the embodiments more detailed, the following embodiments are the best and preferred embodiments. For some well-known technologies, those skilled in the art can also adopt other alternative methods for implementation; moreover, the accompanying drawings are only for more specifically describing the embodiments and are not intended to specifically limit the present invention.

[0039] It should be noted that in the specification, references to "an embodiment", "embodiments", "exemplary embodiments", "some embodiments", etc. indicate that the described embodiments may include specific features, structures, or characteristics, but not necessarily every embodiment includes such specific features, structures, or characteristics. Additionally, when combining embodiments to describe a specific feature, structure, or characteristic, implementing such feature, structure, or characteristic in combination with other embodiments (whether explicitly described or not) should be within the knowledge of those skilled in the relevant art.

[0040] Generally, terms can be understood at least in part from their use in context. For example, at least in part depending on the context, the term "one or more" as used herein can be used to describe any feature, structure, or characteristic in a singular sense, or can be used to describe a combination of features, structures, or characteristics in a plural sense. Additionally, the term "based on" can be understood as not necessarily intended to convey a set of exclusive factors, but rather can alternatively, at least in part depending on the context, allow for the existence of other factors that may not be explicitly described.

[0041] It can be understood that the meanings of "on...", "above...", and "over..." in the present invention should be interpreted in the broadest manner, such that "on..." not only means "directly on" something, but also includes the meaning of being "on" something with intervening features or layers therebetween, and "above..." or "over..." not only means "above" or "over" something, but also can include the meaning of being "above" or "over" something with no intervening features or layers therebetween.

[0042] In addition, spatial relative terms such as "under...", "below...", "lower", "above...", "upper", etc. are used herein for convenience of description to describe the relationship between one element or feature and another or more elements or features, as shown in the accompanying drawings. Spatial relative terms are intended to cover different orientations in the use or operation of the device other than the orientation depicted in the accompanying drawings. The device can be oriented in other ways, and the spatial relative descriptive terms used herein can be correspondingly interpreted similarly.

[0043] As Figures 1 to 8As shown in the figure, an embodiment of the present invention provides a hemostatic device for hepatobiliary clinical surgery, which includes a mounting frame 1. Symmetrically arranged on the outer surface of the mounting frame 1 are restraint straps 2. Rotatably connected through the upper surface of the mounting frame 1 is a threaded rod 3. Threadedly connected to the outer surface of the threaded rod 3 is an internally threaded sleeve 6. Fixedly connected to the bottom of the internally threaded sleeve 6 is a circular ring 7. Inside the mounting frame 1 is a medicine adding assembly 4 for facilitating medicine application.

[0044] As Figures 2 to 6 shown, the medicine adding assembly 4 includes a first liquid inlet pipe 41 sliding on the upper surface of the mounting frame 1. Fixedly connected to the top of the first liquid inlet pipe 41 is a first liquid storage cylinder 42. Rotatably connected to the lower surface of the first liquid inlet pipe 41 is a hollow plate 43. Evenly distributed on the inner bottom of the hollow plate 43 are liquid outlet holes 47. Slidingly sleeved on the outer surface of the hollow plate 43 is a first annular frame 45. Connected to the inner surface of the first annular frame 45 is a circular disinfection sponge 44.

[0045] Fixedly connected to one side of the outer surface of the mounting frame 1 is a limiting rod, and the limiting rod extends out of the inside of the mounting frame 1 and slides mutually. The restraint straps 2 are two and are symmetrically distributed on the outer surface of the mounting frame 1. Magic tapes are respectively arranged on the two restraint straps 2, and the two magic tapes are arranged on opposite faces. The first liquid inlet pipe 41 communicates with the inside of the first liquid storage cylinder 42 and the hollow plate 43. Fixedly connected to the upper surface of the first liquid storage cylinder 42 is a medicine injection port. The upper surface of the circular disinfection sponge 44 is in mutual contact with the lower surface of the hollow plate 43. Arranged on the inner surface of the circular ring 7 is a disassembly and assembly component 46.

[0046] When hemostasis is performed on a wound, it is necessary to buckle the mounting frame 1 around the wound and fix the mounting frame 1 effectively by winding the two restraint straps 2 around the patient's body. After the fixation is completed, then rotate the threaded rod 3. Driven by the thread, the internally threaded sleeve 6 and the circular ring 7 as a whole move downward. Under the action of the limiting rod, the circular ring 7 can ensure vertical and stable movement. Buckle the circular ring 7 around the periphery close to the wound. The circular ring 7 can compress the surrounding blood vessels and slow down the blood flow rate. The movement of the circular ring 7 simultaneously drives the first annular frame 45 as a whole to move downward, so that the circular disinfection sponge 44 can be in close contact with the wound. At this time, slowly add anti-inflammatory and hemostatic liquid medicine into the inside of the first liquid storage cylinder 42. The liquid medicine enters the inside of the first liquid inlet pipe 41 through the first liquid storage cylinder 42, enters the inside of the hollow plate 43 through the first liquid inlet pipe 41, and then flows into the inside of the circular disinfection sponge 44 through the plurality of liquid outlet holes 47 to wet the circular disinfection sponge 44, so that the liquid medicine contacts the wound through the circular disinfection sponge 44, effectively promoting the healing and hemostasis of the wound, and at the same time facilitating the rapid addition of the liquid medicine, avoiding that the traditional device cannot directly add the liquid medicine to the wound, directly squeezing the sponge soaked with the liquid medicine on the wound, which is likely to cause the liquid medicine inside the sponge to be squeezed out, not only easily polluting the bedsheet, but also causing the liquid medicine to not fully play its role and the wound hemostasis speed to be slow.

[0047] As Figures 4 to 6 shown, the disassembly and assembly component 46 includes a clamping plate 461 fixed on the outer surface of the first liquid inlet pipe 41 and a clamping groove 462 opened on the inner surface of the circular ring 7. A shielding door 463 is slidably connected to the outer surface of the installation frame 1, and a through groove 464 is opened on the inner surface of the installation frame 1.

[0048] The clamping plate 461 is located inside the clamping groove 462. The diameter of the first annular frame 45 is smaller than the width of the through groove 464. A first magnet is provided on one side of the inner surface of the through groove 464, and a second magnet is provided on one side of the shielding door 463.

[0049] Although the circular disinfection sponge 44 soaked with the liquid medicine applied to the wound can accelerate the hemostasis of the wound, there will still be a situation where blood and exudate flow out. The circular disinfection sponge 44 staying on the wound for a long time is likely to adsorb blood, exudate, etc., becoming a breeding ground for bacteria, increasing the probability of local infection. If not replaced in time, it may aggravate the infection and affect the healing process. After using for a period of time, the circular disinfection sponge 44 needs to be replaced in time. At this time, push the shielding door 463 to slide on the outer surface of the installation frame 1 to fully expand the through groove 464. Then rotate the first liquid storage cylinder 42 to drive the clamping plate 461 to rotate synchronously. The clamping plate 461 is completely removed from the inside of the clamping groove 462. Pull up the first liquid storage cylinder 42 to drive the hollow plate 43 and the first annular frame 45 as a whole upward through the first liquid inlet pipe 41, driving the circular disinfection sponge 44 to separate from the patient's wound. When the first annular frame 45 is completely removed from the inside of the circular ring 7, pull the first annular frame 45 to slide outside the hollow plate 43, remove the first annular frame 45 as a whole from the hollow plate 43, take out the first annular frame 45 from the inside of the through groove 464, reinstall the new circular disinfection sponge 44 and the first annular frame 45, put the new first annular frame 45 back on the outside of the hollow plate 43, then push the first liquid storage cylinder 42 downward so that the hollow plate 43 drives the new circular disinfection sponge 44 to contact the wound again, and then rotate the first liquid storage cylinder 42 in the reverse direction to drive the clamping plate 461 to move back into the inside of the clamping groove 462 through the first liquid inlet pipe 41 to complete the installation. At this time, liquid medicine can be added to the inside of the first liquid storage cylinder 42 to further accelerate the healing of the wound. Thus, the circular disinfection sponge 44 can be quickly replaced without removing the whole device, effectively improving the efficiency of replacing the circular disinfection sponge 44 and reducing the steps of the patient wearing and disassembling back and forth.

[0050] As Figures 2 to 4As shown in the figure, a disinfection component 5 is provided near the bottom of the inner surface of the installation frame 1. The disinfection component 5 includes a rotating shaft 51 rotating at the top edge inside the installation frame 1, a second annular frame 56 rotating on the inner surface near the bottom of the installation frame 1, and a first gear 52 fixed on the outer surface of the threaded rod 3. A second gear 53 is fixedly connected to the outer surface of the rotating shaft 51, a third gear 55 is fixedly connected to the bottom of the rotating shaft 51, a ring rack 54 is fixedly connected to the edge of the upper surface of the second annular frame 56, and a ring-shaped disinfection sponge 58 is fixedly connected to the inner surface of the second annular frame 56.

[0051] The third gear 55 meshes with the ring rack 54, the second gear 53 and the first gear 52 are at the same height, and the second gear 53 meshes with the first gear 52.

[0052] When the patient wears the installation frame 1 and rotates the threaded rod 3 to drive the ring 7 and the circular disinfection sponge 44 to move towards the wound, at this time, the first gear 52 rotates synchronously with the threaded rod 3. Through the transmission of the second gear 53, the rotating shaft 51 is driven to rotate. The rotating shaft 51 drives the ring rack 54 to rotate through the third gear 55, and the ring rack 54 drives the second annular frame 56 to rotate inside the installation frame 1. Thus, the ring-shaped disinfection sponge 58 can disinfect the skin around the wound. When rotating the threaded rod 3, through a series of transmissions, the ring-shaped disinfection sponge 58 is driven to rotate synchronously. This can not only reduce the steps of rotating the ring-shaped disinfection sponge 58 in the secondary operation, but also ensure that the space inside the installation frame 1 is relatively sterile, avoid the breeding of bacteria on the patient's skin, and prevent the bacteria from infecting the wound and causing pain to the patient.

[0053] As Figure 4 、 Figure 7 and Figure 8 shown, an adding component 57 is fixedly connected to the edge of the upper surface of the installation frame 1. The adding component 57 includes a second liquid storage cylinder 574 fixedly connected to the edge of the upper surface of the installation frame 1 and an annular groove 578 opened at the top inside the second annular frame 56. A fixed cylinder 575 is fixedly connected to the bottom inside the second liquid storage cylinder 574. Second liquid inlet openings 577 are axially symmetrically opened on the outer surface of the fixed cylinder 575. A second liquid inlet pipe 571 is slidably sleeved inside the fixed cylinder 575. First liquid inlet openings 576 are axially symmetrically opened on the outer surface of the second liquid inlet pipe 571 near the top. A connecting cylinder 572 is sleeved on the outer surface of the second liquid inlet pipe 571 near the bottom.

[0054] A cross bar 573 is fixedly connected to the outer surface of the second liquid inlet pipe 571. Four wedge-shaped plates 579 are evenly and fixedly connected to the upper surface of the second annular frame 56 near the inner side. The inclined surface of the wedge-shaped plate 579 slides with the cross bar 573.

[0055] The bottom of the connecting tube 572 passes through the annular groove 578 and extends to the inside of the second annular frame 56. The connecting tube 572 and the annular groove 578 slide against each other. A magnet ring is provided at the bottom of the connecting tube 572. The second annular frame 56 is made of metal iron.

[0056] A C-shaped plate is symmetrically fixedly connected to the bottom of the second annular frame 56, and the magnet ring is located above the C-shaped plate so that the magnet ring does not hinder the circular motion of the C-shaped plate.

[0057] The disinfection effect of the annular disinfection sponge 58 is low if the alcohol contained in the annular disinfection sponge 58 is used for disinfection. The alcohol is volatile, which further limits the disinfection effect of the annular disinfection sponge 58. Therefore, before wearing, a certain amount of alcohol is added to the inside of the second liquid storage cylinder 574. When the threaded rod 3 is rotated, the second annular frame 56 and the annular disinfection sponge 58 are rotated through transmission. At the same time, the second annular frame 56 drives the four wedge plates 579 to move in a synchronous circular motion. When the wedge plates 579 contact the cross bar 573, the inclined surfaces of the wedge plates 579 slide against the cross bar 573, forcing the cross bar 573 to move upward, driving the second liquid inlet pipe 571 to move upward, and driving the first liquid inlet port 576 to move upward. The second liquid inlet 577 is close to the first liquid inlet 576 and the second liquid inlet 577. When the first liquid inlet 576 and the second liquid inlet 577 overlap, the alcohol inside the second liquid storage cylinder 574 enters into the second liquid inlet tube 571, and in turn passes through the connecting cylinder 572 into the annular disinfection sponge 58 to soak the annular disinfection sponge 58, so that the annular disinfection sponge 58 can fully disinfect the patient's skin. When the wedge plate 579 moves out of the cross bar 573, the second liquid inlet tube 571 moves downward, so that the first liquid inlet 576 and the second liquid inlet 577 are staggered, so that the alcohol no longer flows out, which can ensure that the alcohol is added quantitatively and evenly, and avoid adding too much alcohol at one time, causing the alcohol to flow.

[0058] The workflow of the technical solution provided by the present invention is as follows:

[0059] First, buckle the installation frame 1 around the wound, and wind the two restraint straps 2 around the patient's body to effectively fix the installation frame 1. After the fixation is completed, rotate the threaded rod 3 to drive the first gear 52 to rotate at the same time. Through transmission, the annular disinfection sponge 58 is driven to rotate to disinfect the skin around the wound. In cooperation with the components of the adding assembly 57, the alcohol in the second liquid storage cylinder 574 is quantitatively and evenly added into the annular disinfection sponge 58. Driven by the thread, the inner threaded sleeve 6 and the circular ring 7 are moved downward as a whole, and the anti-inflammatory and hemostatic liquid medicine is slowly added into the first liquid storage cylinder 42. The liquid medicine enters the inside of the first liquid inlet pipe 41 through the first liquid storage cylinder 42, and the liquid medicine enters the inside of the hollow plate 43 through the first liquid inlet pipe 41, and then flows to the inside of the circular disinfection sponge 44 through a plurality of liquid outlet holes 47 to wet the circular disinfection sponge 44, so that the liquid medicine contacts the wound through the circular disinfection sponge 44, effectively promoting the healing and anti-inflammation of the wound;

[0060] Rotate the first liquid storage cylinder 42 to drive the clamping plate 461 to completely move out of the inside of the clamping groove 462. Pull the first liquid storage cylinder 42 upward to drive the hollow plate 43 and the first annular frame 45 to move upward as a whole, driving the circular disinfection sponge 44 to separate from the patient's wound. When the first annular frame 45 completely moves out of the inside of the circular ring 7, pull the first annular frame 45 to slide outside the hollow plate 43 and remove the first annular frame 45 as a whole from the hollow plate 43 for replacement.

[0061] The present invention covers any substitutions, modifications, equivalent methods and solutions made on the essence and scope of the present invention. In order to enable the public to have a thorough understanding of the present invention, specific details are described in detail in the following preferred embodiments of the present invention. However, those skilled in the art can fully understand the present invention without these detailed descriptions. In addition, in order to avoid unnecessary confusion to the essence of the present invention, well-known methods, processes, procedures, components and circuits are not described in detail.

[0062] The above are only the preferred embodiments of the present invention. It should be noted that for those of ordinary skill in the art, without departing from the principle of the present invention, several improvements and refinements can be made, and these improvements and refinements should also be regarded as the protection scope of the present invention.

Claims

1. A hepatobiliary clinical surgical hemostasis device, comprising a mounting frame, the outer surface of which is symmetrically provided with restraints, a threaded rod rotatably connected to the upper surface of the mounting frame, an inner threaded sleeve threadedly connected to the outer surface of the threaded rod, and a ring fixedly connected to the bottom of the inner threaded sleeve; It is characterized in that The interior of the installation frame is provided with a medicine adding component for convenient medicine feeding; The dosing component includes a first liquid inlet pipe sliding on the upper surface of the mounting frame, the top of the first liquid inlet pipe is fixedly connected to a first liquid storage cylinder, the lower surface of the first liquid inlet pipe is rotatably connected to a hollow plate, the inner bottom of the hollow plate has liquid outlet holes evenly distributed, the outer surface of the hollow plate is slidably sleeved with a first annular frame, and the inner surface of the first annular frame is connected to a circular disinfection sponge.

2. The hepatobiliary clinical surgical hemostasis device according to claim 1, characterized in that: A limiting rod is fixedly connected to one side of the outer surface of the installation frame, and the limiting rod extends out of the interior of the installation frame and slides with each other. The two restraining belts are axially symmetrically distributed on the outer surface of the installation frame. Velcro is respectively provided on the two restraining belts, and the two Velcros are arranged on opposite surfaces. The first liquid inlet pipe is connected to the first liquid storage cylinder and the interior of the hollow plate. The upper surface of the first liquid storage cylinder is fixedly connected with a medicine injection port, the upper surface of the circular disinfection sponge is in contact with the lower surface of the hollow plate, and the inner surface of the ring is provided with a disassembly and assembly component.

3. The hepatobiliary clinical surgical hemostasis device according to claim 2, characterized in that: The disassembly and assembly assembly comprises a clamping plate fixed on the outer surface of the first liquid inlet pipe and a clamping groove arranged on the inner surface of the circular ring; a shielding door is slidably connected to the outer surface of the installation frame, and a through groove is arranged on the inner surface of the installation frame.

4. The hepatobiliary clinical surgical hemostasis device according to claim 3, characterized in that: The card plate is located inside the card slot, the diameter of the first annular frame is smaller than the width of the through slot, a first magnet is arranged on one side of the inner surface of the through slot, and a second magnet is arranged on one side of the shielding door.

5. The hepatobiliary clinical surgical hemostasis device according to claim 4, characterized in that: A disinfection component is arranged near the bottom of the inner surface of the installation frame, and the disinfection component includes a rotating shaft rotating at the top edge of the installation frame, a second annular frame rotating near the bottom of the inner surface of the installation frame, and a first gear fixed to the outer surface of the threaded rod, a second gear is fixedly connected to the outer surface of the rotating shaft, a third gear is fixedly connected to the bottom of the rotating shaft, an annular rack is fixedly connected to the edge of the upper surface of the second annular frame, and an annular disinfection sponge is fixedly connected to the inner surface of the second annular frame.

6. The hepatobiliary clinical surgical hemostasis device according to claim 5, characterized in that: The third gear is meshed with the annular rack, the second gear is located at the same height as the first gear, and the second gear is meshed with the first gear.

7. The hepatobiliary clinical surgical hemostasis device according to claim 6, characterized in that: An adding component is fixedly connected to the edge of the upper surface of the installation frame, and the adding component includes a second liquid storage cylinder fixed at the edge of the upper surface of the installation frame and an annular groove opened at the top of the second annular frame, a fixed cylinder is fixedly connected to the bottom of the second liquid storage cylinder, a second liquid inlet is axially symmetrically opened on the outer surface of the fixed cylinder, a second liquid inlet pipe is provided in an internal sliding sleeve of the fixed cylinder, a first liquid inlet is axially symmetrically opened on the outer surface of the second liquid inlet pipe near the top, and a connecting cylinder is provided on the outer surface of the second liquid inlet pipe near the bottom.

8. The hepatobiliary clinical surgical hemostasis device according to claim 7, characterized in that: A cross bar is fixedly connected to the outer surface of the second liquid inlet pipe, and four wedge plates are evenly fixedly connected to the upper surface of the second annular frame near the inner side, and the inclined surfaces of the wedge plates slide with the cross bar.

9. The hepatobiliary clinical surgical hemostasis device according to claim 8, characterized in that: The bottom of the connecting tube passes through the annular groove and extends to the inside of the second annular frame. The connecting tube and the annular groove slide against each other. A magnet ring is arranged at the bottom of the connecting tube. The second annular frame is made of metal iron.

10. The hepatobiliary clinical surgical hemostasis device according to claim 9, characterized in that: A C-shaped plate is symmetrically fixedly connected to the bottom of the second annular frame, and the magnet ring is located above the C-shaped plate so that the magnet ring does not hinder the circular motion of the C-shaped plate.

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