Thyroid thermal ablation postoperative hemostasis compression device

Abstract

The invention provides a hemostasis compression device used after thyroid thermal ablation, and belongs to the technical field of medical instruments. Comprising a gasket body, the outer wall of the gasket body is fixedly connected with a hook-and-loop fastener son face and a hook-and-loop fastener mother face, a plurality of connecting pieces are arranged at the bottom of the gasket body, and connecting pieces are arranged on the sides, away from the gasket body, of the connecting pieces; the supporting assembly supports and fixes the neck and the head of a patient and is connected with the gasket, the connecting piece and the connecting piece. And the adjusting assembly is used for carrying out compression hemostasis on the surgical site and adjusting the supporting assembly. By arranging the supporting assembly and the adjusting assembly, the adjusting assembly can be matched with the supporting assembly to adjust the height of the compression device, so that the compression device adapts to neck heights of different patients, and the application range of the compression device is widened; the adjusting assembly can be matched with the supporting assembly to conduct compression hemostasis on the surgical part of the neck of the patient, so that automatic and precise continuous compression hemostasis is achieved, the hands of the patient and medical staff can be completely liberated, and postoperative recovery experience and nursing efficiency are improved.

Description

Technical Field

[0001] The present invention relates to the technical field of medical devices, and particularly relates to a hemostatic compression device after thyroid thermal ablation. Background Art

[0002] Thyroid thermal ablation is a minimally invasive treatment technique that precisely destroys thyroid diseased tissues through thermal energy such as radiofrequency, microwave, or laser, achieving the effect of shrinking or eliminating nodules and tumors.

[0003] After thyroid thermal ablation surgery, hemostasis needs to be performed on the patient's wound. In the prior art, the patient or medical staff needs to manually press the surgical site for 15 - 30 minutes to promote blood vessel closure and form thrombus for hemostasis through physical compression. However, during the pressing period, an appropriate pressure needs to be continuously maintained to avoid excessive pressure affecting the patient's breathing and too little pressure resulting in poor hemostasis effect. Such an operation not only increases the operation time of medical staff, occupies medical resources, but also easily causes problems of non-standard operation, and at the same time limits the patient's hand movement. Therefore, the present invention provides a hemostatic compression device after thyroid thermal ablation to meet the needs. Summary of the Invention

[0004] The technical problem to be solved by the present invention is to provide a hemostatic compression device after thyroid thermal ablation. By setting a support component and an adjustment component, the adjustment component can cooperate with the support component to compress and stop bleeding at the patient's neck surgical site, thus liberating medical staff and allowing them to perform other tasks. Through the above settings, the problem that the prior art requires medical staff to manually press for hemostasis and occupies medical resources can be solved.

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

[0006] A hemostatic compression device after thyroid thermal ablation, including a gasket, the outer wall of the gasket is fixedly connected with a hook surface and a loop surface of a magic tape, the bottom of the gasket is provided with a plurality of connecting pieces, and one side of the plurality of connecting pieces away from the gasket is provided with a connecting member; a support component that supports and fixes the patient's neck and head, and the support component is connected to the gasket, the connecting pieces, and the connecting member; an adjustment component that compresses and stops bleeding at the bleeding site and adjusts the support component, and the adjustment component is connected to the support component.

[0007] Optionally, the number of the support components is set to be multiple, and the multiple support components are fixedly connected to the outer wall of the gasket in sequence, and the adjustment component is arranged between two adjacent support components.

[0008] Optionally, the support assembly includes a first support piece fixedly connected to the outer wall of the gasket and a second support piece disposed on the outer wall of the connecting piece. A first connecting frame, a first weakening section, and a second connecting frame are sequentially arranged between the first support piece and the second support piece.

[0009] Optionally, the overall contours of the first connecting frame and the second connecting frame are in a "U" shape. The first connecting frame is fixedly connected to the outer wall of the first support piece, the second connecting frame is fixedly connected to the outer wall of the second support piece, and both the first connecting frame and the second connecting frame are fixedly connected to the first weakening section.

[0010] Optionally, a second weakening section is fixedly connected to the outer wall of the second connecting frame, and a U-shaped piece is fixedly connected to one end of the second weakening section away from the second connecting frame.

[0011] Optionally, an insertion piece and a slot are fixedly connected to the outer wall of the first support piece, and the insertion piece and the slot on adjacent first support pieces are inserted into each other.

[0012] Optionally, the adjustment assembly includes a connecting rod and a pressing member disposed on the outer wall of the first weakening section. A threaded cap is rotatably connected inside the connecting rod, and a threaded rod is threadedly connected inside the threaded cap.

[0013] Optionally, the threaded rod is rotatably connected inside the pressing member, and the threaded rod is inserted between the first weakening sections of two adjacent support assemblies.

[0014] Optionally, guiding members are symmetrically installed on the outer wall of the second support piece. The connecting member is disposed between the two guiding members, and a connecting rope is inserted into the connecting member. Both ends of the connecting rope are fixedly connected with connecting heads.

[0015] Optionally, a first collar, a second collar, and a hook are installed on the outer wall of the second support piece near the position of the hook-and-loop sub-surface and the hook-and-loop main surface. The connecting rope is sequentially inserted into the first collar and the second collar.

[0016] Compared with the prior art, the present invention has at least the following beneficial effects:

[0017] In the above solution, by providing the support assembly and the adjustment assembly, the adjustment assembly can cooperate with the support assembly to adjust the height of the compression device, so as to adapt to the neck heights of different patients, improve the adaptability range of the compression device, and enable the adjustment assembly to cooperate with the support assembly to compress and stop bleeding at the neck surgical site of the patient, thereby liberating medical staff and allowing them to perform other tasks.

[0018] By setting up the support component, the neck and head of the patient can be supported and fixed, preventing excessive movement of the patient's neck, which may cause bleeding at the surgical site and affect the patient's recovery. Moreover, the ice pack can be fixed to assist the patient's postoperative recovery and improve the recovery efficiency. BRIEF DESCRIPTION OF THE DRAWINGS

[0019] The accompanying 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.

[0020] Figure 1 Schematic diagram of the three-dimensional structure of the hemostatic compression device after thyroid thermal ablation from the first perspective;

[0021] Figure 2 Schematic diagram of the three-dimensional structure of the hemostatic compression device after thyroid thermal ablation from the second perspective;

[0022] Figure 3 For Figure 2 Enlarged three-dimensional structure schematic diagram of part A;

[0023] Figure 4 Schematic diagram of the enlarged three-dimensional structure of the gasket fit;

[0024] Figure 5 Schematic diagram of the three-dimensional structure of the first state of the support component cooperating with the adjustment component;

[0025] Figure 6 Schematic diagram of the three-dimensional structure of the second state of the support component cooperating with the adjustment component;

[0026] Figure 7 Schematic diagram of the deformed three-dimensional structure of the guide member cooperating with the adjustment component.

[0027] Reference numerals:

[0028] 1. Gasket; 2. Hook surface of the magic tape; 3. Loop surface of the magic tape; 4. Connecting piece; 5. Connecting member; 6. First support piece; 7. Second support piece; 8. First connecting frame; 9. First weakening section; 10. Second connecting frame; 11. Second weakening section; 12. U-shaped piece; 13. Insertion piece; 14. Slot; 15. Connecting rod; 16. Compression member; 17. Threaded cap; 18. Threaded rod; 19. Guide member; 20. Connecting rope; 21. Connecting head; 22. First collar; 23. Second collar; 24. Hook.

[0029] As shown in the figure, in order to clearly show the structure of the embodiments of the present invention, specific structures and devices are marked in the figure. However, this is only for illustrative purposes and is not intended to limit the present invention to this specific structure, device, and environment. Those of ordinary skill in the art can adjust or modify these devices and environments according to specific needs. Detailed Description of the Invention

[0030] The following will describe in detail a hemostatic compression device after thyroid thermal ablation provided by the present invention with reference to 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.

[0031] It should be noted that when referring to "an embodiment", "embodiments", "exemplary embodiments", "some embodiments", etc. in the specification, it indicates 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 specific features, structures, or characteristics, the implementation of such features, structures, or characteristics in combination with other embodiments (whether explicitly described or not) should be within the knowledge of those skilled in the relevant art.

[0032] Generally, terms can be understood, at least in part, from their use in the context. For example, at least in part depending on the context, the term "one or more" 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, at least in part depending on the context, allowing for the existence of other factors that may not be explicitly described.

[0033] 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 intermediate 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 intermediate features or layers therebetween.

[0034] In addition, spatial relative terms such as "under", "below", "lower", "above", "upper", etc. may be used herein for convenience of description to describe the relationship of one element or feature to another or multiple other elements or features, as shown in the drawings. The spatial relative terms are intended to cover different orientations in the use or operation of the device in addition to the orientation depicted in the drawings. The device may be oriented in other ways, and the spatial relative descriptors used herein may be interpreted correspondingly.

[0035] As Figures 1 to 7 shown, an embodiment of the present invention provides a hemostatic compression device after thyroid thermal ablation, including a gasket 1. The outer wall of the gasket 1 is fixedly connected with a hook surface 2 of a magic tape. A loop surface 3 of the magic tape is pasted on the hook surface 2 of the magic tape. The hook surface 2 of the magic tape and the loop surface 3 of the magic tape are prior arts, so the usage method will not be elaborated too much. A plurality of connecting pieces 4 are arranged at the bottom of the gasket 1. As Figure 3 shown, a connecting member 5 is arranged on one side of the plurality of connecting pieces 4 away from the gasket 1. The gasket 1, the connecting pieces 4, and the connecting member 5 are integrally formed of transparent silica gel material. The transparent silica gel material facilitates medical staff to observe the neck edema of the patient; the support assembly is used to support and fix the patient's neck and head. The support assembly is connected to the gasket 1, the connecting pieces 4, and the connecting member 5. By providing the support assembly, the patient's neck and head can be supported and fixed, avoiding excessive movement of the patient's neck, resulting in bleeding at the patient's surgical site and affecting the patient's recovery. Moreover, an ice pack can be fixed to assist the patient's postoperative recovery and improve the patient's recovery efficiency; the adjustment assembly is used to compress and stop bleeding at the bleeding site and adjust the support assembly. The adjustment assembly is connected to the support assembly. The number of support assemblies is set to be multiple. The multiple support assemblies are fixedly connected to the outer wall of the gasket 1 in sequence. The adjustment assembly is arranged between two adjacent support assemblies. The support assembly and the adjustment assembly are made of metal material. By providing the adjustment assembly, the adjustment assembly can cooperate with the support assembly to adjust the height of the compression device, so as to adapt to the neck heights of different patients and improve the adaptation range of the compression device. The adjustment assembly can cooperate with the support assembly to compress and stop bleeding at the patient's neck surgical site, thus liberating medical staff to perform other tasks.

[0036] In this embodiment, as Figure 1 , Figure 5 , Figure 6 , Figure 7As shown, the support assembly includes a first support piece 6 fixedly connected to the outer wall of the gasket 1 and a second support piece 7 provided on the outer wall of the connecting piece 4. A first connecting frame 8, a first weakening section 9, and a second connecting frame 10 are sequentially arranged between the first support piece 6 and the second support piece 7. The overall contours of the first connecting frame 8 and the second connecting frame 10 are in a "U" shape. The first connecting frame 8 is fixedly connected to the outer wall of the first support piece 6, and the second connecting frame 10 is fixedly connected to the outer wall of the second support piece 7. Both the first connecting frame 8 and the second connecting frame 10 are fixedly connected to the first weakening section 9. A second weakening section 11 is fixedly connected to the outer wall of the second connecting frame 10, and a U-shaped piece 12 is fixedly connected to one end of the second weakening section 11 away from the second connecting frame 10. An insertion piece 13 and a slot 14 are fixedly connected to the outer wall of the first support piece 6. The insertion piece 13 and the slot 14 on adjacent first support pieces 6 are inserted into each other. By providing the insertion piece 13 and the slot 14, adjacent support assemblies can be inserted and clamped together through the insertion piece 13 and the slot 14, so that when medical staff presses the first support piece 6, all support assemblies will deform and descend synchronously. The adjustment assembly includes a connecting rod 15 and a pressing member 16 provided on the outer wall of the first weakening section 9. Anti-slip lines are provided on one side of the connecting rod 15 away from the pressing member 16. The length of the connecting rod 15 is greater than the gap between the U-shaped pieces 12, so that the connecting rod 15 can be inserted into the interior of the U-shaped piece 12 in the vertical state. In the horizontal state, the anti-slip lines on the connecting rod 15 will be blocked by the side of the U-shaped piece 12 close to the gasket 1. A threaded cap 17 is rotatably connected to the interior of the connecting rod 15. A threaded rod 18 is threadedly connected to the interior of the threaded cap 17. The threaded rod 18 is rotatably connected to the interior of the pressing member 16. The rotational connection between the threaded rod 18 and the pressing member 16 is an interference fit, so that sufficient force is required for the threaded rod 18 to rotate relative to the pressing member 16, avoiding unnecessary displacement between the threaded rod 18 and the pressing member 16 and affecting normal use. The threaded rod 18 is inserted between the first weakening sections 9 of two adjacent support assemblies.

[0037] When medical staff needs to adjust the overall height of the compression device according to the patient's neck, the medical staff can press the top of the compression device, so that the first support piece 6 at the top of the support assembly is stressed and descends. Then, the first support piece 6 transmits the pressure to the first weakening section 9 through the first connecting frame 8. Since the first weakening section 9 is a weakened setting, the support assembly deforms at the position where the first weakening section 9 is located (as Figure 7As shown in the figure, the distance between the first support piece 6 and the second support piece 7 of the support assembly is changed until the distance between the first support piece 6 and the second support piece 7 is adapted to the height of the patient's neck. Then the medical staff can stop pressing down further and let the support assembly maintain this height. Then the medical staff can rotate the threaded cap 17 so that the threaded cap 17 rotates spirally along the outer wall of the threaded rod 18, and further make the threaded cap 17 drive the connecting rod 15 to move towards the pressing member 16 until the connecting rod 15 and the pressing member 16 respectively abut against the first weakened section 9 and the joints of the first connecting frame 8 and the second connecting frame 10 and then stop. At this time, the height of the support assembly is fixed by the adjusting assembly, and the height of the pressing device is adapted to the height of the patient's neck. The medical staff can stop pressing the pressing device to achieve the effect of adjusting the height of the pressing device according to the height of the patient's neck and improve the applicable range of the pressing device.

[0038] Further, after the medical staff adjusts the height of the pressing device, the medical staff can surround the pressing device around the patient's neck, and then attach and fix the pressing device to the patient's neck through the hook surface 2 and the loop surface 3 of the magic tape, so as to support and limit the head and neck of the patient after thyroid thermal ablation, and avoid excessive movement of the patient's neck, resulting in rebleeding of the wound after hemostasis in the thyroid thermal ablation surgery and affecting the patient's recovery.

[0039] When the patient needs cold compress, the medical staff can insert the ice pack into the support device, so that the ice pack or the hot water bag is fixed between the U-shaped piece 12 and the gasket 1 (as Figure 1 shown), and let the ice perform cold compress on the patient's neck through the gasket 1. Within 24 hours after the thyroid thermal ablation surgery, cold compress can relieve the pain of the wound, shrink blood vessels, reduce blood exudation, thereby reducing the edema of the patient's neck and improving the patient's recovery effect. Moreover, the weight of the ice pack will be transmitted to the second support piece 7 through the U-shaped piece 12, the second weakened section 11 and the second connecting frame 10, and the second support piece 7 will transmit the weight to the patient's shoulder part through the connecting piece 4, avoiding the weight of the ice pack pressing on the patient's neck and affecting the patient's breathing.

[0040] Furthermore, when medical staff need to apply compressive hemostasis to a patient after thyroid thermal ablation surgery, first cover the surgical site on the patient's neck with a gauze, then the medical staff wrap the compression device around the patient's neck, align the U-shaped piece 12 of one of the support components with the surgical site, and fix the compression device to the patient's neck through the hook surface 2 and the loop surface 3 of the magic tape to preliminarily fix the gauze at the surgical site on the patient's neck. Then remove one adjustment component from the compression device (there are multiple adjustment components on the compression device), and rotate the compression piece 16 by ninety degrees so that the compression piece 16 is perpendicular to the threaded rod 18. Then the medical staff rotate the threaded nut 17 until the threaded nut 17 drives the connecting rod 15 to move along the threaded rod 18 towards the compression piece 16 until it reaches the end of the thread of the threaded rod 18 and stops. At this time, the medical staff can insert the deformed adjustment component between the U-shaped piece 12 aligned with the surgical site on the patient's neck and the gasket 1, so that the connecting rod 15 abuts against the side of the U-shaped piece 12 close to the gasket 1. Finally, the medical staff apply a force away from the patient's neck to the threaded nut 17 and rotate the threaded nut 17 in the reverse direction, so that the threaded nut 17 drives the side of the connecting rod 15 with anti-slip lines to fit against the U-shaped piece 12 to increase the friction, preventing the connecting rod 15 from being driven to rotate together with the threaded nut 17 when the threaded nut 17 rotates along the thread of the threaded rod 18, resulting in the connecting rod 15 being unable to be stuck between the U-shaped pieces 12 to limit the adjustment component. As the threaded nut 17 rotates in the reverse direction, the threaded nut 17 will gradually move away from the compression piece 16 along the thread of the threaded rod 18, so that the threaded nut 17 drives the connecting rod 15 away from the compression piece 16, and further increases the distance between the connecting rod 15 and the compression piece 16. Since the connecting rod 15 is blocked by the U-shaped piece 12, the compression piece 16 will move relatively towards the bleeding site on the patient's neck until the compression piece 16 stops applying compressive hemostasis to the bleeding position on the patient's neck.

[0041] In this embodiment, as Figure 3As shown, guide members 19 are symmetrically installed on the outer wall of the second support piece 7. The connecting piece 5 is arranged between the two guide members 19. The length of the connecting piece 5 is the same as the distance between the two guide members 19, so that the part of the connecting piece 5 connected to the bulging part of the connecting rope 20 can slide along between the two guide members 19, ensuring the direction when the connecting piece 5 pulls the connecting piece 4 to move. The connecting rope 20 is inserted into the connecting piece 5. Both ends of the connecting rope 20 are fixedly connected with connecting heads 21. On the outer wall of the second support piece 7 near the positions of the hook-and-loop fastener sub-surface 2 and the hook-and-loop fastener mother-surface 3, a first collar 22, a second collar 23 and a hook 24 are installed. The number of hooks 24 is set to be multiple, and they are fixedly connected to one side of the second support piece 7 at equal intervals in sequence. The connecting rope 20 is inserted into the first collar 22 and the second collar 23 in sequence. When the medical staff adjusts the height of the compression device according to the height of the patient's neck, the medical staff can pull a section of the connecting rope 20 between the first collar 22 and the second collar 23 and put this section of the connecting rope 20 on the hook 24, so that the connecting rope 20 pulls the connecting piece 5 to move along the guide member 19 towards the direction of the second connecting frame 10, and then the connecting piece 5 drives the connecting piece 4 to move, so that the redundant connecting piece 4 after the compression device is deformed is pulled by the connecting rope 20 through the connecting piece 5 and stored on the side of the second support piece 7 connecting the guide member 19, avoiding the situation that the redundant connecting piece 4 after the compression device is deformed has nowhere to be placed and accumulates on the patient's neck, affecting the comfort of the patient's neck and reducing the comfort of the compression device.

[0042] The working principle of the technical solution provided by the present invention is as follows: When the medical staff stops bleeding at the surgical site of the patient's neck, first cover the bleeding site of the patient's neck with a gauze, and then the medical staff surround the compression device around the patient's neck, align the U-shaped piece 12 of one of the support components with the surgical site, and fix the compression device on the patient's neck through the hook-and-loop fastener sub-surface 2 and the hook-and-loop fastener mother-surface 3 to preliminarily fix the gauze at the surgical site of the patient's neck. Then, adjust one of the adjustment components to the second state (as Figure 6 shown), insert the adjustment component in the second state between the U-shaped piece 12 aligned with the bleeding position of the patient's neck and the gasket 1, and finally the medical staff rotate the threaded cap 17, and finally make the compression member 16 compress and stop bleeding at the surgical site of the patient's neck, so as to achieve the effect of compressing and stopping bleeding at the surgical site of the patient, avoid manual compression and hemostasis by the medical staff, reduce the operation time of the medical staff, enable the medical staff to have time for other work, and avoid the occurrence of non-standard operations.

[0043] The present invention covers any alternatives, modifications, equivalent methods, and solutions made within the spirit and scope of the present invention. For 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, and those skilled in the art can fully understand the present invention without the description of these details. In addition, well-known methods, processes, procedures, components, and circuits are not described in detail to avoid unnecessary confusion about the essence of the present invention.

[0044] The above are only the preferred embodiments of the present invention. It should be noted that for those of ordinary skill in the art, several improvements and refinements can be made without departing from the principle of the present invention, and these improvements and refinements should also be regarded as the protection scope of the present invention.

Claims

1. A hemostatic compression device after thyroid thermal ablation, including a gasket, characterized in that, The outer wall of the gasket is fixedly connected with a hook-and-loop fastener surface and a hook-and-loop fastener mother surface. A plurality of connecting pieces are arranged at the bottom of the gasket. One side of the plurality of connecting pieces away from the gasket is provided with a connecting member; A support assembly that supports and fixes the patient's neck and head, and the support assembly is connected to the gasket, the connecting piece and the connecting member; An adjustment assembly that compresses and stops bleeding at the bleeding site and adjusts the height of the support assembly, and the adjustment assembly is connected to the support assembly.

2. The thyroid thermal ablation postoperative hemostatic compression device according to claim 1, characterized in that The number of the support assemblies is set to be multiple, and the multiple support assemblies are fixedly connected to the outer wall of the gasket in sequence, and the adjustment assembly is arranged between two adjacent support assemblies.

3. The thyroid thermal ablation postoperative hemostasis compression device according to claim 1, characterized in that, The support assembly includes a first support piece fixedly connected to the outer wall of the gasket and a second support piece arranged on the outer wall of the connecting piece. A first connecting frame, a first weakening section and a second connecting frame are sequentially arranged between the first support piece and the second support piece.

4. The thyroid thermal ablation postoperative hemostatic compression device according to claim 3, wherein, The overall contours of the first connecting frame and the second connecting frame are in a "U" shape. The first connecting frame is fixedly connected to the outer wall of the first support piece, the second connecting frame is fixedly connected to the outer wall of the second support piece, and both the first connecting frame and the second connecting frame are fixedly connected to the first weakening section.

5. The thyroid thermal ablation postoperative hemostatic compression device according to claim 3, characterized in that, A second weakening section is fixedly connected to the outer wall of the second connecting frame, and a U-shaped piece is fixedly connected to one end of the second weakening section away from the second connecting frame.

6. The thyroid thermal ablation postoperative hemostasis compression device according to claim 3, wherein An insertion piece and a slot are fixedly connected to the outer wall of the first support piece, and the insertion pieces and slots of adjacent first support pieces are inserted into each other.

7. The thyroid thermal ablation postoperative hemostatic compression device according to claim 1, wherein The adjustment assembly includes a connecting rod and a pressing member arranged on the outer wall of the first weakening section. A threaded cap is rotatably connected inside the connecting rod, and a threaded rod is connected to the inside of the threaded cap through threads.

8. The thyroid thermal ablation postoperative hemostasis compression device according to claim 7, wherein The threaded rod is rotatably connected inside the pressing member, and the threaded rod is inserted between the first weakening sections of two adjacent support assemblies.

9. The thyroid thermal ablation postoperative hemostatic compression device according to claim 3, characterized in that, Guide members are symmetrically installed on the outer wall of the second support piece. The connecting member is arranged between the two guide members. A connecting rope is inserted into the connecting member, and both ends of the connecting rope are fixedly connected with connecting heads.

10. The thyroid thermal ablation postoperative hemostatic compression device according to claim 9, characterized in that, A first collar, a second collar and a hook are installed on the outer wall of the second support piece near the hook-and-loop fastener surface and the hook-and-loop fastener mother surface, and the connecting rope is sequentially inserted into the first collar and the second collar.

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