A contrast medium auxiliary injection device
By designing a contrast agent-assisted bouncing device for angiography, the problem of contrast agent leakage caused by high-pressure injection is solved, and the control and stable bouncing of contrast agent flow is achieved, which improves the safety and effect of the injection process.
Patent Information
- Application Number
- CN202420448474.1
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-03-08
- Publication Date
- 2025-04-08
- Estimated Expiration
- 2034-03-08
AI Technical Summary
During angiography, high-pressure injection of contrast agent can easily lead to leakage of contrast agent, causing local swelling, pain, congestion or more severe tissue necrosis and dysfunction.
A contrast agent-assisted bouncing device is designed, including a work table, a fixing assembly, a transmission assembly and a needle tube assembly. By setting a restraint and a transmission assembly, control and stable bouncing of the contrast agent flow rate are achieved.
Effectively control the flow of contrast agent, reduce the risk of leakage, improve the stability and safety of the injection process, and avoid local damage and functional dysfunction.
Smart Images

Figure CN222723419U_ABST
Abstract
Description
Technical Field
[0001] The utility model relates to the technical field of medical equipment, in particular to a contrast agent auxiliary injection device. Background Art
[0002] In angiography, vascular contrast agents need to be injected into blood vessels. At present, the contrast agent injection method uses high pressure. Due to the high pressure and fast speed of high-pressure injection of contrast agents, coupled with the patient's own vascular factors, it is easy to cause the contrast agent to leak out of the blood vessels. If not handled in time or improperly, local swelling, pain, and congestion may occur in mild cases; in severe cases, surrounding subcutaneous tissue necrosis may occur, and even functional disorders may occur, which will increase the pain of the patient. Therefore, the flow of contrast agents needs to be controlled. Utility Model Content
[0003] The utility model aims to overcome the deficiencies in the prior art and provides a contrast agent auxiliary injection device, which controls the flow of the contrast agent by arranging a syringe for binding a needle tube and being able to push evenly.
[0004] In order to achieve the above-mentioned purpose of the utility model, the utility model provides the following technical solutions: a contrast agent auxiliary injection device, including a workbench, on which a fixing component and a transmission component are arranged, the fixing component is arranged in the output end direction of the transmission component, the fixing component is detachably connected to a needle tube component, a hand pressing component is arranged in the needle tube component, and the output end of the transmission component abuts against the hand pressing component.
[0005] Furthermore, the fixing assembly includes a placement piece, which is disposed on a workbench, and the needle tube assembly includes a syringe, which is disposed on the placement piece.
[0006] Furthermore, the fixing assembly includes a restraining member, the restraining member has two oppositely arranged frame structures, the syringe is provided with a through hole, one end of the through hole is provided with a finger pressure part, and the finger pressure part is detachably arranged in the frame structure of the restraining member.
[0007] Furthermore, a terminal is provided at the other end of the through hole, and the terminal is detachably connected to an infusion tube, and the infusion tube is connected to a heating component.
[0008] Furthermore, a hand-pressing assembly is provided in the syringe, and the hand-pressing assembly includes a push rod, and the push rod is provided with an output end and an extrusion end, the output end of the push rod is arranged inside the syringe, the output end of the push rod is provided with a seal, and the seal is provided with a pushing end, and the output end of the pushing end is adapted to the end.
[0009] Furthermore, a pressing piece is arranged at the extrusion end of the push rod, and the pressing piece is used to abut against the output end of the transmission component.
[0010] Furthermore, the transmission component includes a base, a control button for controlling the pushing device is arranged on the base, a pushing device is arranged at one end of the base facing the fixing component, and a pushing block is arranged at the output end of the pushing device.
[0011] Furthermore, the pushing block is provided with a sliding block, the workbench is provided with a sliding groove, and the sliding block is slidably arranged in the sliding groove.
[0012] Furthermore, the sealing member is hermetically connected to the syringe barrel.
[0013] Furthermore, the frame structure of the binding member is a "C"-shaped structure, the diameter of the input end of the heating component is larger than the diameter of the output end of the heating component, a needle for acting on the patient is arranged at the output end of the heating component, the output end of the pushing device is arranged at the center of the pushing block, and the centers of the output end of the pushing block and the pressing piece are located at the same position.
[0014] Compared with the prior art, the beneficial effects of the present utility model are as follows:
[0015] 1: First, fill the inside of the syringe assembly with contrast agent, then place the syringe assembly on the fixing component to fix the syringe assembly, so that the pressing hand assembly on the syringe assembly is located on the output end of the transmission component. After adjusting the pushing speed of the transmission component to a fixed value, pressing the control button of the transmission component can realize the use of the rotating component. First, abut the output end of the transmission component against the pressing hand assembly. When controlling the output of the transmission component, the transmission component pushes the pressing hand assembly, so that the contrast agent in the syringe assembly is extruded and flows out from the output end of the syringe assembly.
[0016] 2: The finger pressing part is detachably arranged in the frame structure of the binding member. Even though the situation of slipping is avoided, a large displacement still occurs when in use. The binding member is used to secondarily constrain the finger pressing part, and further constrains the syringe assembly, making it more stable during use.
[0017] 3: The output end of the pushing end is adapted to the end, and the output end of the syringe barrel is the same as the end of the pressing hand assembly, so that during use, the contrast agent can be almost completely pushed out, avoiding waste of the contrast agent. Description of the Drawings
[0018] Figure 1 It is a schematic structural diagram of one embodiment of a contrast agent assisted injection device of the present application;
[0019] Figure 2This is a schematic diagram of a needle assembly of one embodiment of a contrast agent auxiliary injection device of the present application;
[0020] Figure 3 A schematic diagram of a workbench of one embodiment of a contrast agent auxiliary injection device of the present application;
[0021] Indications in the figure: 1-workbench, 2-placing piece, 3-restraint piece, 4-pushing block, 5-pushing device, 7-seat, 8-syringe, 9-finger pressure part, 10-push rod, 11-pressing sheet, 12-end, 13-infusion tube, 14-heating component, 16-pushing end, 17-sealing piece, 18-sliding block. DETAILED DESCRIPTION
[0022] To make the purpose, technical solution and advantages of the embodiment of the utility model clearer, the technical solution in the embodiment of the utility model will be described clearly and completely in conjunction with the accompanying drawings. Obviously, the described embodiment is a part of the embodiment of the utility model, not all of the embodiments.
[0023] Therefore, the following detailed description of the embodiments of the present invention is not intended to limit the scope of the present invention to be protected, but merely represents some embodiments of the present invention. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the present invention.
[0024] It should be noted that, in the absence of conflict, the embodiments of the present invention and the features and technical solutions in the embodiments may be combined with each other.
[0025] It should be noted that similar reference numerals and letters denote similar items in the following drawings, and therefore, once an item is defined in one drawing, further definition and explanation thereof is not required in subsequent drawings.
[0026] In the description of the present utility model, it should be noted that the terms "upper", "lower", etc. indicate the orientation or position relationship based on the orientation or position relationship shown in the drawings, or the orientation or position relationship in which the utility model product is usually placed when in use, or the orientation or position relationship commonly understood by those skilled in the art. Such terms are only for the convenience of describing the present utility model and simplifying the description, and do not indicate or imply that the device or element referred to must have a specific orientation, be constructed and operated in a specific orientation, and therefore cannot be understood as a limitation on the present utility model. In addition, the terms "first", "second", etc. are only used to distinguish the description, and cannot be understood as indicating or implying relative importance.
[0027] Example 1: See Figures 1 to 3 As shown,
[0028] A contrast agent auxiliary injection device provided in the present embodiment includes a workbench 1, on which a fixing component and a transmission component are arranged. The fixing component is arranged in the direction of the output end of the transmission component. The fixing component is detachably connected with a needle tube component. A hand pressing component is arranged in the needle tube component. The output end of the transmission component abuts against the hand pressing component. During use, the inside of the needle tube component is first filled with contrast agent, and then the needle tube component is placed on the fixing component to fix the needle tube component so that the hand pressing component on the needle tube component is located on the output end of the transmission component. After the pushing speed of the transmission component is adjusted to a fixed value, the control button of the transmission component can be pressed to realize the use of the rotating component. The output end of the transmission component is first abutted against the hand pressing component. When the transmission component is controlled to output, the transmission component pushes the hand pressing component to squeeze the contrast agent in the needle tube component and flow out from the output end of the needle tube component.
[0029] Furthermore, the fixing assembly includes a placement piece 2, which is disposed on the workbench 1. The needle tube assembly includes a syringe 8, which is disposed on the placement piece 2. The placement piece 2 is used to prevent the needle tube assembly from slipping. Since the needle tube assembly is round, the needle tube assembly is prevented from slipping during use.
[0030] Furthermore, the fixing assembly includes a restraining member 3, the restraining member 3 has two frame structures arranged opposite to each other, the syringe 8 is provided with a through hole, one end of the through hole is provided with a finger pressure part 9, and the finger pressure part 9 is detachably arranged in the frame structure of the restraining member 3. Even if slipping is avoided, a large displacement will still occur when the needle is placed in use. The restraining member 3 is used to perform a second constraint on the finger pressure part 9, thereby further constraining the needle tube assembly, making it more stable during use.
[0031] Furthermore, the other end of the through hole is provided with an end cap 12, and the end cap 12 is detachably connected to an infusion tube 13, and the infusion tube 13 is connected to a heating component 14. The contrast agent is input into the syringe 8 through the end cap 12, and then injected into the heating component through the hand pressing component for heating, and then input into the patient's body through the heating end.
[0032] Furthermore, a hand-pressing assembly is provided in the syringe 8, and the hand-pressing assembly includes a push rod 10. The push rod 10 is provided with an output end and an extrusion end. The output end of the push rod 10 is provided inside the syringe 8. The output end of the push rod 10 is provided with a seal 17. The seal 17 is provided with a pushing end 16. The output end of the pushing end 16 is adapted to the end 12. The output end of the syringe 8 is the same as the end of the hand-pressing assembly, so that during use, the contrast agent can be almost completely pushed out to avoid wasting the contrast agent.
[0033] Furthermore, a pressing piece 11 is provided at the extrusion end of the push rod 10. The pressing piece 11 is used to abut against the output end of the transmission component, so that when the transmission component is started, the transmission component can push the pressing piece 11 to move, thereby achieving the purpose of delivering the contrast agent.
[0034] Furthermore, the transmission component includes a base 7. A control button for controlling the pushing device 5 is provided on the base 7. A pushing device 5 is provided at one end of the base 7 facing the fixing component. A pushing block 4 is provided at the output end of the pushing device 5. When the control button is pressed, the pushing device 5 starts to move at a constant speed, pushing the pressing hand component to push out the contrast agent. When the control button is no longer pressed, the pushing device stops operating, thus making the operation convenient.
[0035] Furthermore, a sliding block 18 is provided on the pushing block 4, and a sliding groove is provided on the workbench 1. The sliding block 18 is slidably arranged in the sliding groove. During use, when the pushing block 4 pushes the pressing hand component, if there is a large deviation, it is easy to damage the equipment. After the sliding block 18 is provided on the pushing block 4, the sliding block 18 can restrict the direction of the pushing block 4, avoiding the situation of deviation during pushing and causing damage, and at the same time increasing the stability of the structure.
[0036] Furthermore, the seal 17 is hermetically connected to the syringe 8, avoiding the leakage of the contrast agent during use and improving the utilization efficiency of the contrast agent.
[0037] Furthermore, the frame structure of the restraint 3 is a "C" - shaped structure. The diameter of the input end of the heating component 14 is larger than the diameter of the output end of the heating component 14. A needle for acting on the patient is provided at the output end of the heating component 14. The output end of the pushing device 5 is arranged at the center of the pushing block 4. The centers of the output end of the pushing block 4 and the pressing piece 11 are located at the same position. The restraint 3 adopts a square - frame structure, which can well restrain the syringe assembly, making the pushing process more stable. The diameter of the input end of the heating component 14 is larger than the diameter of the output end of the heating component 14. Since the liquid input volume is the same, the flow rate at the output end of the heating component 14 is greater than the flow rate at the input end of the heating component 14, avoiding the situation of small air bubbles inside the contrast agent.
[0038] The above - mentioned embodiments are only used to illustrate the present invention rather than to limit the technical solutions described in the present invention. Although this specification has described the present invention in detail with reference to the above - mentioned respective embodiments, the present invention is not limited to the above - mentioned specific embodiments. Therefore, any modification or equivalent replacement to the present invention; and all technical solutions and their improvements that do not depart from the spirit and scope of the present invention are covered by the scope of the claims of the present invention.
Claims
1. A contrast agent auxiliary injection device, comprising a workbench (1), characterized in that: A fixed component and a transmission component are provided on the workbench (1). The fixed component is arranged in the output direction of the transmission component. The fixed component is detachably connected to a syringe component. A pressing component is arranged in the syringe component. The output end of the transmission component abuts against the pressing component.
2. A contrast agent auxiliary injection device according to claim 1, characterized in that: The fixed component includes a placing member (2). The placing member (2) is arranged on the workbench (1). The syringe component includes a syringe barrel (8). The syringe barrel (8) is arranged on the placing member (2).
3. A contrast agent auxiliary injection device according to claim 2, characterized in that: The fixed component includes a binding member (3). The binding member (3) has two oppositely arranged frame structures. The syringe barrel (8) is provided with a through hole. One end of the through hole is provided with a finger pressing portion (9). The finger pressing portion (9) is detachably arranged in the frame structure of the binding member (3).
4. A contrast agent auxiliary injection device according to claim 3, characterized in that: The other end of the through hole is provided with a head (12). The head (12) is detachably connected to an infusion tube (13). The infusion tube (13) is connected to a heating component (14).
5. A contrast agent auxiliary injection device according to claim 4, characterized in that: A pressing component is arranged in the syringe barrel (8). The pressing component includes a push rod (10). The push rod (10) is provided with an output end and a pressing end. The output end of the push rod (10) is arranged inside the syringe barrel (8). A sealing member (17) is arranged at the output end of the push rod (10). The sealing member (17) is provided with a pushing head (16). The output end of the pushing head (16) is adapted to the head (12).
6. A contrast agent auxiliary injection device according to claim 5, characterized in that: A pressing piece (11) is arranged at the pressing end of the push rod (10). The pressing piece (11) is used to abut against the output end of the transmission component.
7. A contrast agent auxiliary injection device according to claim 6, characterized in that: The transmission component includes a base (7). A control button for controlling a pushing device (5) is arranged on the base (7). A pushing device (5) is arranged at one end of the base (7) facing the fixed component. A pushing block (4) is arranged at the output end of the pushing device (5).
8. A contrast agent auxiliary injection device according to claim 7, characterized in that: The pushing block (4) is provided with a sliding block (18). The workbench (1) is provided with a sliding groove. The sliding block (18) is slidably arranged in the sliding groove.
9. The contrast agent auxiliary injection device according to claim 5, characterized in that: The sealing member (17) is sealingly connected to the syringe barrel (8).
10. A contrast agent auxiliary injection device according to any one of claims 3 to 9, characterized in that: The frame structure of the binding member (3) is a "C"-shaped structure. The input end diameter of the heating component (14) is larger than the output end diameter of the heating component (14). A needle for acting on a patient is arranged at the output end of the heating component (14). The output end of the pushing device (5) is arranged at the center of the pushing block (4). The centers of the output end of the pushing block (4) and the pressing piece (11) are located at the same position.