A hepatobiliary clinical surgical hemostasis device
By designing a hepatobiliary clinical surgical hemostasis device with dosing, disassembly and disinfection components, the problems of existing devices being unable to add liquid medicine and prone to infection are solved, rapid hemostasis and aseptic operation are achieved, and the efficiency and safety of wound healing are improved.
Patent Information
- Application Number
- CN202510343078.1
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Filing Date
- 2025-03-21
- Publication Date
- 2025-09-16
- Estimated Expiration
- 2045-03-21
AI Technical Summary
Existing hepatobiliary surgical hemostasis devices are unable to add drugs when compressing the wound, resulting in slow hemostasis and healing. Traditional methods are also prone to drug leakage and bacterial infection.
A hepatobiliary clinical surgical hemostasis device was designed, which includes a dosing component, a disassembly component and a disinfection component. The dosing component is used to slowly add liquid medicine into the disinfection sponge. The disassembly component facilitates the replacement of the disinfection sponge. The disinfection component keeps the device sterile to prevent bacterial growth.
It realizes the rapid addition of liquid medicine without removing the device, promotes wound healing, reduces the steps of replacing disinfected sponges, avoids liquid medicine flow and bacterial infection, and improves hemostasis efficiency and safety.
Smart Images

Figure CN120078471B_ABST
Abstract
Description
Technical Field
[0001] The present invention relates to the technical field of medical devices, and more particularly to a hepatobiliary clinical surgical hemostasis device. Background Art
[0002] Hepatobiliary surgery focuses on treating major diseases that pose a serious threat to the health of the Chinese people, including hepatocellular carcinoma, hepatolithiasis, post-hepatitis cirrhosis, and acute liver failure caused by severe hepatitis. All of these conditions require surgical treatment, and during hepatobiliary surgery in hospitals, hemostasis is essential for hepatobiliary incisions. Bleeding control is crucial for impacting postoperative complications and mortality.
[0003] In order to solve the problem of wound hemostasis, a general surgery hemostasis device with authorization announcement number CN210931641U is disclosed. The device compresses the wound with sterilized cotton and provides pressure to compress the sterilized cotton through an airbag. However, the device cannot add medicine to the compressed wound. Without adding medicine, the hemostasis and healing speed are slow and the effect is poor. If the medicine is added, the entire device needs to be disassembled, which increases the steps and is more troublesome. If alcohol is added to the sponge before compression, the alcohol is easily squeezed out and flows. Summary of the Invention
[0004] In view of the problems existing in the prior art, the purpose of the present invention is to provide a hepatobiliary clinical surgical hemostasis device.
[0005] In order to solve the above problems, the present invention adopts the following technical solutions:
[0006] A hepatobiliary clinical surgical hemostasis device, a hepatobiliary clinical surgical hemostasis device, includes a mounting frame, the outer surface of the mounting frame is symmetrically provided with restraints, the upper surface of the mounting frame is rotatably connected to a threaded rod, the outer surface of the threaded rod is threadedly connected to an internally threaded sleeve, the bottom of the internally threaded sleeve is fixedly connected to a ring, and the interior of the mounting frame is provided with a dosing component for convenient drug application.
[0007] 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 is evenly distributed with liquid outlet holes, the outer surface of the hollow plate is slidingly sleeved with a first annular frame, and the inner surface of the first annular frame is connected to a circular disinfection sponge.
[0008] Optionally, a limit rod is fixedly connected to one side of the outer surface of the mounting frame, and the limit rod extends out of the interior of the mounting frame and slides with each other, the two restraining straps are axially symmetrically distributed on the outer surface of the mounting frame, and the two restraining straps are respectively provided with Velcro, 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 to the 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.
[0009] Optionally, the disassembly and assembly assembly 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, the outer surface of the installation frame is slidably connected with a shielding door, and the inner surface of the installation frame is provided with a through groove.
[0010] Optionally, 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 provided on one side of the inner surface of the through slot, and a second magnet is provided on one side of the shielding door.
[0011] Optionally, a disinfection assembly is provided near the bottom of the inner surface of the mounting frame, and the disinfection assembly includes a rotating shaft rotating at the top edge of the mounting frame, a second annular frame rotating near the bottom of the inner surface of the mounting frame, and a first gear fixed to the outer surface of the threaded rod, the outer surface of the rotating shaft is fixedly connected to the second gear, the bottom of the rotating shaft is fixedly connected to the third gear, the upper surface edge of the second annular frame is fixedly connected to an annular rack, and the inner surface of the second annular frame is fixedly connected to an annular disinfection sponge.
[0012] Optionally, the third gear is meshed with the annular rack, the second gear and the first gear are located at the same height, and the second gear and the first gear are meshed with each other.
[0013] Optionally, an adding component is fixedly connected to the edge of the upper surface of the mounting frame, and the adding component includes a second liquid storage cylinder fixed at the edge of the upper surface of the mounting 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 with 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.
[0014] Optionally, 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.
[0015] Optionally, 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 provided at the bottom of the connecting tube, and the second annular frame is made of metal iron.
[0016] Optionally, 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 movement of the C-shaped plate.
[0017] Compared with the prior art, the technical solution provided by the present invention has at least the following beneficial effects:
[0018] In the above scheme, by setting up a dosing component, anti-inflammatory and hemostatic liquid medicine is slowly added to the interior of the first liquid storage cylinder, and the liquid medicine eventually flows from multiple liquid outlets to the interior of the circular disinfection sponge, soaking the circular disinfection sponge, so that the liquid medicine contacts the wound through the circular disinfection sponge, effectively promoting wound healing and hemostasis, and facilitating the rapid addition of liquid medicine, avoiding the inability of traditional devices to directly add liquid medicine to the wound, and directly squeezing the sponge soaked with liquid medicine on the wound, which easily causes the liquid medicine inside the sponge to be squeezed out, not only easily causing contamination of the bed sheets, but also causing the liquid medicine to fail to fully play its role, and the wound hemostasis speed is slow. Liquid medicine can be added without dismantling the device.
[0019] By setting up a disassembly and assembly component, the first liquid storage cylinder is pulled upward to drive the hollow plate and the first annular frame upward as a whole through the first liquid inlet tube, driving the circular disinfection sponge to separate from the patient's wound, and the first annular frame is removed from the hollow plate as a whole. In this way, the circular disinfection sponge can be quickly replaced without removing the entire device, effectively improving the efficiency of replacing the circular disinfection sponge and reducing the steps of patients wearing and disassembling back and forth.
[0020] By setting up a disinfection component, when the threaded rod is rotated, the annular disinfection sponge is driven to rotate synchronously through a series of transmissions, which not only reduces the steps of rotating the annular disinfection sponge in the secondary operation, but also ensures that the interior of the installation frame is in a relatively sterile space, avoiding the growth of bacteria on the patient's skin, and preventing bacteria from infecting the wound and causing pain to the patient. BRIEF DESCRIPTION OF THE DRAWINGS
[0021] The accompanying drawings, which are incorporated herein and constitute a part of the specification, illustrate embodiments of the invention and, together with the description, further serve to explain the principles of the invention and to enable one skilled in the art to make and use the invention.
[0022] Figure 1 It is a schematic diagram of the three-dimensional structure of the present invention;
[0023] Figure 2 This 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 cut away Figure 1 ;
[0025] Figure 4 The installation frame of the present invention is cut away Figure 2 ;
[0026] Figure 5 It is a schematic diagram of the installation frame of the present invention;
[0027] Figure 6 This is a schematic cross-sectional view 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 This 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. Shield 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 describes in detail an expandable cancellous bone hollow screw with a pressurized structure provided by the present invention, with reference to the accompanying drawings and specific embodiments. It is also noted that, for the sake of completeness, the following embodiments are best and preferred embodiments, and those skilled in the art may employ alternative implementations for known techniques. Furthermore, the accompanying drawings are provided solely for the purpose of describing the embodiments in greater detail and are not intended to limit the present invention.
[0039] It should be noted that references in the specification to "one embodiment," "an embodiment," "exemplary embodiments," "some embodiments," etc. indicate that the described embodiments may include specific features, structures, or characteristics, but not necessarily every embodiment will include such specific features, structures, or characteristics. Furthermore, when specific features, structures, or characteristics are described in conjunction with an embodiment, it is within the knowledge of persons skilled in the relevant art to implement such features, structures, or characteristics in conjunction with other embodiments (whether or not explicitly described).
[0040] In general, terms can be understood, at least in part, from their use in context. For example, depending at least in part on the context, the term "one or more" as used herein can be used to describe any feature, structure, or characteristic in the singular sense, or can be used to describe a combination of features, structures, or characteristics in the plural sense. Additionally, the term "based on" can be understood as not necessarily intended to convey an exclusive set of factors, but can instead, depending at least in part on the context, allow for the presence of other factors that are not necessarily explicitly described.
[0041] It will be understood that the meanings of “on,” “over,” and “above” in the present invention should be interpreted in the broadest manner, so that “on” means not only “directly on” something but also includes the meaning of being “on” something with intervening features or layers, and “on” or “above” means not only “on” or “above” something but also includes the meaning of being “on” or “above” something with no intervening features or layers.
[0042] Additionally, spatially relative terms such as "below," "beneath," "lower," "above," and "upper" may be used herein for descriptive convenience to describe the relationship of one element or feature to another element or features, as illustrated in the accompanying drawings. Spatially relative terms are intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the accompanying drawings. The device may be oriented in other ways, and the spatially relative descriptors used herein should be similarly interpreted accordingly.
[0043] like Figures 1 to 8As shown, an embodiment of the present invention provides a hepatobiliary clinical surgical hemostasis device, including a mounting frame 1, the outer surface of the mounting frame 1 is symmetrically provided with a restraining belt 2, the upper surface of the mounting frame 1 is rotatably connected with a threaded rod 3, the outer surface of the threaded rod 3 is threadedly connected with an internal threaded sleeve 6, the bottom of the internal threaded sleeve 6 is fixedly connected with a ring 7, and the interior of the mounting frame 1 is provided with a dosing component 4 for convenient drug application.
[0044] like Figures 2 to 6 As shown, the dosing component 4 includes a first liquid inlet pipe 41 sliding on the upper surface of the mounting frame 1, the top of the first liquid inlet pipe 41 is fixedly connected to a first liquid storage cylinder 42, the lower surface of the first liquid inlet pipe 41 is rotatably connected to a hollow plate 43, the inner bottom of the hollow plate 43 is evenly distributed with liquid outlet holes 47, the outer surface of the hollow plate 43 is slidingly sleeved with a first annular frame 45, and the inner surface of the first annular frame 45 is connected to a circular disinfection sponge 44.
[0045] A limiting rod is fixedly connected to one side of the outer surface of the mounting frame 1, and the limiting rod extends out of the interior of the mounting frame 1 and slides with each other. The two restraints 2 are axially symmetrically distributed on the outer surface of the mounting frame 1. Velcro is provided on each of the two restraints 2, and the two Velcros are arranged on opposite surfaces. The first liquid inlet pipe 41 is connected to the first liquid storage cylinder 42 and the interior of the hollow plate 43. The upper surface of the first liquid storage cylinder 42 is fixedly connected to the injection port. The upper surface of the circular disinfection sponge 44 is in contact with the lower surface of the hollow plate 43. The inner surface of the ring 7 is provided with a disassembly and assembly component 46.
[0046] When stopping bleeding from a wound, it is necessary to buckle the mounting frame 1 around the wound and wrap the two binding belts 2 around the patient's body to effectively fix the mounting frame 1. After fixing, the threaded rod 3 is rotated to drive the internal threaded sleeve 6 and the circular ring 7 to move downward as a whole through the action of the thread. Under the action of the limiting rod, the circular ring 7 can ensure vertical and stable movement. Buckle the circular ring 7 around the wound. The circular ring 7 can compress the surrounding blood vessels and slow down the blood flow. The movement of the circular ring 7 also drives the first annular frame 45 to move downward as a whole, so that the circular disinfection sponge 44 can be in close contact with the wound. At this time, the interior of the first liquid storage cylinder 42 is slowly added with anti-inflammatory and antiseptic liquids. The blood-removing medicine liquid enters the interior of the first liquid inlet pipe 41 through the first liquid storage cylinder 42, and the medicine liquid enters the interior of the hollow plate 43 through the first liquid inlet pipe 41, and then flows to the interior of the circular disinfection sponge 44 through multiple liquid outlet holes 47, soaking the circular disinfection sponge 44, so that the medicine liquid contacts the wound through the circular disinfection sponge 44, effectively promoting wound healing and hemostasis, and facilitating rapid addition of medicine liquid, avoiding the inability of traditional devices to directly add medicine liquid to the wound, and directly squeezing the sponge soaked with medicine liquid on the wound, which easily causes the medicine liquid inside the sponge to be squeezed out, not only easily causing pollution to the bed sheet, but also causing the medicine liquid to be unable to fully play its role, and the wound hemostasis speed is slow.
[0047] like Figures 4 to 6 As 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 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 slot 462 . The diameter of the first annular frame 45 is smaller than the width of the through slot 464 . A first magnet is provided on one side of the inner surface of the through slot 464 , and a second magnet is provided on one side of the shielding door 463 .
[0049] Although the circular disinfection sponge 44 soaked in liquid medicine can accelerate the hemostasis of the wound when applied to the wound, blood and exudate will still flow out. The circular disinfection sponge 44 staying in the wound for a long time is easy to absorb blood, exudate, etc., becoming a breeding ground for bacteria, increasing the probability of local infection. Failure to replace it in time may aggravate the infection and affect the healing process. After using it 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. At this time, rotate the first liquid storage cylinder 42 to drive the card plate 461 to rotate synchronously. The card plate 461 is completely removed from the inside of the card groove 462. Pull the first liquid storage cylinder 42 upward and drive the hollow plate 43 and the first annular frame 45 upward as a whole 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 When the wound is in the hands of a wound specialist, the first container 42 is moved downwards to allow the new container 42 to be moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound. The container 42 is then moved back into contact with the wound.
[0050] like Figures 2 to 4As shown, a disinfection component 5 is provided near the bottom of the inner surface of the mounting frame 1, and the disinfection component 5 includes a rotating shaft 51 rotating at the top edge of the mounting frame 1 and a second annular frame 56 rotating near the bottom of the inner surface of the mounting frame 1 and a first gear 52 fixed to the outer surface of the threaded rod 3. The outer surface of the rotating shaft 51 is fixedly connected to the second gear 53, the bottom of the rotating shaft 51 is fixedly connected to the third gear 55, the upper surface edge of the second annular frame 56 is fixedly connected to an annular rack 54, and the inner surface of the second annular frame 56 is fixedly connected to an annular disinfection sponge 58.
[0051] The third gear 55 is meshed with the annular rack 54 . The second gear 53 and the first gear 52 are located at the same height and are meshed with each other.
[0052] When the patient wears the mounting frame 1, the threaded rod 3 is rotated to drive the ring 7 and the circular disinfection sponge 44 to move toward the wound. At this time, the first gear 52 rotates synchronously with the threaded rod 3, and the transmission of the second gear 53 drives the rotating shaft 51 to rotate. The rotating shaft 51 drives the annular rack 54 to rotate through the third gear 55, and the annular rack 54 drives the second annular frame 56 to rotate inside the mounting frame 1, so that the annular disinfection sponge 58 can disinfect the skin around the wound. When the threaded rod 3 is rotated, the annular disinfection sponge 58 is driven to rotate synchronously through a series of transmissions, which not only reduces the steps of the secondary operation of rotating the annular disinfection sponge 58, but also ensures that the inside of the mounting frame 1 is in a relatively sterile space, avoiding the growth of bacteria on the patient's skin, and avoiding bacteria from infecting the wound and causing pain to the patient.
[0053] like Figure 4 、 Figure 7 and Figure 8 As shown, an adding component 57 is fixedly connected to the edge of the upper surface of the mounting frame 1, and the adding component 57 includes a second liquid storage cylinder 574 fixed at the edge of the upper surface of the mounting frame 1 and an annular groove 578 opened at the top of the second annular frame 56, and a fixed cylinder 575 is fixedly connected to the bottom of the second liquid storage cylinder 574. A second liquid inlet 577 is axially symmetrically provided on the outer surface of the fixed cylinder 575, and a second liquid inlet pipe 571 is provided on the internal sliding sleeve of the fixed cylinder 575. A first liquid inlet 576 is axially symmetrically provided on the outer surface of the second liquid inlet pipe 571 near the top, and a connecting cylinder 572 is provided 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, and four wedge plates 579 are evenly fixedly connected to the inner side of the upper surface of the second annular frame 56. The inclined surfaces of the wedge plates 579 slide 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 material of the second annular frame 56 is 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 as not to hinder the circular motion of the C-shaped plate.
[0057] The disinfection effect of the annular disinfection sponge 58 is low if the alcohol inside 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 and the cross bar 573 slide against each other, forcing the cross bar 573 to move upward, driving the second liquid inlet pipe 571 to move upward, and driving the first liquid inlet 576 to move upward. The second liquid inlet 577 is close to each other. When the first liquid inlet 576 and the second liquid inlet 577 coincide with each other, the alcohol inside the second liquid storage cylinder 574 enters the interior of the second liquid inlet pipe 571, and in turn passes through the connecting cylinder 572 into the interior of the annular disinfection sponge 58, soaking 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 pipe 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 in a quantitative and uniform manner, and avoid excessive addition of alcohol at one time, causing alcohol to flow.
[0058] The workflow of the technical solution provided by the present invention is as follows:
[0059] First, buckle the mounting frame 1 around the wound and wrap it around the patient's body with two restraints 2 to effectively fix the mounting frame 1. After fixation, rotate the threaded rod 3 to drive the first gear 52 to rotate at the same time, and drive the annular disinfection sponge 58 to rotate through the transmission to disinfect the skin around the wound. Cooperate with the components of the adding assembly 57 so that the alcohol inside the second liquid storage cylinder 574 is quantitatively and evenly added to the annular disinfection sponge 58. The internal threaded sleeve 6 and the circular ring 7 are driven downward as a whole by the action of the thread. Then, the interior of the first liquid storage cylinder 42 is slowly added with anti-inflammatory and hemostatic liquid. The liquid enters the interior of the first liquid inlet pipe 41 through the first liquid storage cylinder 42. The liquid enters the interior of the hollow plate 43 through the first liquid inlet pipe 41, and then flows to the interior of the circular disinfection sponge 44 through the multiple liquid outlet holes 47, soaking the circular disinfection sponge 44 so that the liquid contacts the wound through the circular disinfection sponge 44, effectively promoting wound healing and anti-inflammation.
[0060] Rotate the first liquid storage cylinder 42 to drive the card plate 461 to move completely out of the card slot 462, pull the first liquid storage cylinder 42 upward to drive the hollow plate 43 and the first annular frame 45 upward as a whole through the first liquid inlet pipe 41, and drive the circular disinfection sponge 44 to separate from the patient's wound. When the first annular frame 45 is completely moved out of the inside of the ring 7, pull the first annular frame 45 to slide on the outside of the hollow plate 43, and remove the first annular frame 45 as a whole from the hollow plate 43 and replace it.
[0061] The present invention encompasses any alternatives, modifications, equivalents, and solutions that fall within the spirit and scope of the present invention. To provide a thorough understanding of the present invention, specific details are described in detail below in connection with the preferred embodiments of the present invention, but those skilled in the art will be able to fully understand the present invention without these detailed descriptions. Furthermore, to avoid unnecessary confusion regarding the essence of the present invention, well-known methods, processes, procedures, components, and circuits have not been described in detail.
[0062] The above is only a preferred embodiment of the present invention. It should be pointed out that for ordinary technicians in this technical field, several improvements and modifications can be made without departing from the principles of the present invention. These improvements and modifications should also be regarded as within the scope of protection 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 internally threaded sleeve threadedly connected to the outer surface of the threaded rod, and a circular ring fixedly connected to the bottom of the internally threaded sleeve; It is characterized by: The interior of the installation frame is provided with a medicine adding component for convenient medicine addition; The dosing assembly 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 covered with a first annular frame, and the inner surface of the first annular frame is connected to a circular disinfection sponge; 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 to the injection port. The upper surface of the circular disinfection sponge is in contact with the lower surface of the hollow plate. The inner surface of the ring is provided with a disassembly assembly component. The disassembly and assembly assembly includes a clamping plate fixed to the outer surface of the first liquid inlet pipe and a clamping groove provided 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 provided on the inner surface of the installation frame; A disinfection assembly is provided on the inner surface of the mounting frame near the bottom, and the disinfection assembly includes a rotating shaft rotating at the top edge of the mounting frame and a second annular frame rotating on the inner surface of the mounting frame near the bottom, and a first gear fixed to the outer surface of the threaded rod, the outer surface of the rotating shaft is fixedly connected to the second gear, the bottom of the rotating shaft is fixedly connected to the third gear, 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; The third gear is meshed with the annular rack, the second gear and the first gear are located at the same height, and the second gear and the first gear are meshed with each other.
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 restraints are symmetrically distributed on the outer surface of the installation frame. Velcro is provided on each of the two restraints, and the two Velcros are provided on opposite surfaces.
3. The hepatobiliary clinical surgical hemostasis device according to claim 1, 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 provided on one side of the inner surface of the through slot, and a second magnet is provided on one side of the shielding door.
4. The hepatobiliary clinical surgical hemostasis device according to claim 1, characterized in that: An adding component is fixedly connected to the edge of the upper surface of the mounting frame, and the adding component includes a second liquid storage cylinder fixed at the edge of the upper surface of the mounting 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 for 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.
5. The hepatobiliary clinical surgical hemostasis device according to claim 4, characterized in that: The outer surface of the second liquid inlet pipe is fixedly connected with a cross bar, and the upper surface of the second annular frame is evenly fixedly connected with four wedge plates near the inner side, and the inclined surfaces of the wedge plates slide with the cross bar.
6. The hepatobiliary clinical surgical hemostasis device according to claim 5, 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 with each other. A magnet ring is provided at the bottom of the connecting tube. The second annular frame is made of metal iron.
7. The hepatobiliary clinical surgical hemostasis device according to claim 6, 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 as not to hinder the circular motion of the C-shaped plate.
Citation Information
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