Compression hemostasis device for post-thyroid nodule puncture ablation

Abstract

The utility model relates to a kind of compression hemostasis device for thyroid puncture ablation after operation, including compression frame, frame body adjusting and fixing assembly, hemostasis compression pack and compression adjusting assembly;Compression frame is equipped with the compression area for compression operation area, and the adjusting end of frame body adjusting and fixing assembly is connected with compression frame;Compression adjusting assembly can be adjusted and set on compression frame, and hemostasis compression pack is detachably set on compression adjusting assembly and corresponds with the compression area of compression frame.Precise compression is carried out to thyroid puncture ablation operation area using compression frame, and hemostasis compression pack is used to compress and hemostasis operation area;Compression frame can be sleeved on neck by frame body adjusting and fixing assembly and be adjusted, liberate patient's both hands, facilitate patient postoperative activity, and adjustable compression strength, at the same time, the compression strength of hemostasis compression pack can also be adjusted by compression adjusting assembly, and hemostasis compression pack is detachably connected on compression adjusting assembly, and it is also convenient to replace hemostasis compression pack.

Description

Technical Field

[0001] This utility model relates to the field of medical supplies technology, and in particular to a compression hemostasis device for use after thyroid puncture ablation. Background Technology

[0002] After a thyroid biopsy, pressure is applied to the puncture site to stop bleeding. Currently, the common method of pressure hemostasis after thyroid biopsy is to apply an ice pack to the surgical area for cold compresses. While this method effectively stops bleeding at the surgical site, it requires the patient to manually hold the ice pack, making it difficult for them to perform other activities or maintain precise pressure on the surgical area throughout the procedure. Furthermore, it may cause pressure on other areas of the neck outside the surgical area. Summary of the Invention

[0003] The problem this invention aims to solve is to provide a compression hemostasis device for use after thyroid biopsy ablation. This device can accurately apply pressure to the surgical area for hemostasis and facilitates postoperative movement for the patient. The technical solution adopted is as follows: A compression hemostasis device for use after thyroid puncture ablation, characterized in that: it includes a compression frame, a frame adjustment and fixing component, a hemostatic compression pack, and a compression adjustment component; the compression frame has a compression area for compressing the surgical area, and the compression frame is connected to the adjustment end of the frame adjustment and fixing component; the compression adjustment component is adjustablely mounted on the compression frame, and the hemostatic compression pack is detachably mounted on the compression adjustment component and corresponds to the compression area of ​​the compression frame.

[0004] The aforementioned compression frame is used to enclose the thyroid ablation procedure area. After aligning the compression area with the procedure area, it is secured to the neck using the frame's adjustment and fixation components, and the tightness is adjusted accordingly. The aforementioned hemostatic compression pack is used to apply pressure to the defined compression area to stop bleeding. After aligning the hemostatic compression pack with the defined procedure area, the tightness of the pressure is adjusted using the pressure adjustment components. The hemostatic compression pack can be an ice pack or a cloth bag containing hemostatic ingredients. The hemostatic compression pack features detachable connections for easy replacement at any time.

[0005] As a preferred embodiment of this utility model, the compression frame includes a closed frame body, and two constraint strips are provided on the rear side of the frame body. The two constraint strips are connected in parallel along the vertical direction between the upper side and the lower side of the frame body. The upper side, the lower side, and the two constraint strips together form the compression area. The frame body can be a square frame, a rounded quadrilateral frame, a circular frame, an elliptical frame, etc.

[0006] As a further preferred solution of the present utility model, the compression adjustment assembly comprises an adjustment strap and a tightness adjustment member; the middle part of the adjustment strap passes through the two constraint strips in sequence, and both ends of the adjustment strap are adjustably connected through the tightness adjustment member; the hemostatic compression pack is detachably attached to the middle part of the adjustment strap. The adjustment strap is used to align the hemostatic compression pack with the compression area of the frame, and the tightness is adjusted by the tightness adjustment member, so that the hemostatic compression pack can compress the compression area.

[0007] As a still further preferred solution of the present utility model, the tightness adjustment member is an adjustment buckle, a hook and loop fastener, or matched multiple rows of buckles. The adjustment buckle can be a day-shaped buckle, which is a common metal member for adjusting straps, and its shape is similar to the Chinese character "ri (day)". This day-shaped buckle can easily adjust the length of the strap, and ensure the strap remains stable after adjustment through the buckle design; a side-release buckle can also be used, which is a simple and effective strap adjustment method. It usually consists of a slot and an insertion piece, and the length of the strap is adjusted by inserting the insertion piece into the slot. Through the tightness adjustment member, the length of the adjustment strap located at the rear side of the two constraint strips is adjusted, so that the adjustment strap (including the front side and the rear side) between the two constraint strips is flattened and tensioned, which forces the hemostatic compression pack to move forward, thereby enabling the hemostatic compression pack to compress the surgical area.

[0008] The aforementioned "front" refers to being close to the patient's surgical area, and the aforementioned "rear" refers to being far away from the patient's surgical area.

[0009] As a still further preferred solution of the present utility model, the hemostatic compression pack is attached to the middle part of the adjustment strap through a hook and loop fastener or a non-drying adhesive.

[0010] As a preferred solution of the present utility model, the frame adjustment and fixing assembly comprises a first connecting strap and a second connecting strap, the fixed ends of the first connecting strap and the second connecting strap are respectively fixedly connected with the left side edge of the frame and the right side edge of the frame, and the connecting ends of the first connecting strap and the second connecting strap are correspondingly and adjustably connected. By adopting the mode in which the first connecting strap and the second connecting strap are adjustably connected with each other, after the frame surrounds the surgical area, the connecting ends of the first connecting strap and the second connecting strap are connected correspondingly, so as to prevent the connection part of the first connecting strap and the second connecting strap from being close to the surgical area.

[0011] As a further preferred solution of the present utility model, both the first connecting strap and the second connecting strap are elastic straps; the connecting ends of the first connecting strap and the second connecting strap are provided with matched connecting members. The first connecting strap and the second connecting strap adopt elastic straps, which are suitable for patients with different neck circumferences.

[0012] As a still further preferred solution of the present utility model, the connecting member is a hook and loop fastener or matched multiple rows of snaps.

[0013] Compared with the prior art, the present utility model has the following advantages: This invention relates to a compression hemostasis device for thyroid ablation procedures. A compression frame precisely compresses the ablation site, and a hemostatic compression pack is used to apply pressure to stop bleeding. The compression frame can be adjusted and fitted onto the neck via an adjustable fixing component, freeing the patient's hands and facilitating postoperative movement. The compression intensity can also be adjusted to avoid compressing other parts of the neck, making the patient more comfortable. Simultaneously, the compression intensity of the hemostatic compression pack can be adjusted via the compression adjustment component, and the pack is detachably connected to the adjustment component for easy replacement. Attached Figure Description

[0014] Figure 1 This is a schematic diagram of the preferred embodiment of the present invention; Figure 2 for Figure 1 Exploded view; Figure 3 for Figure 2 Top view; The labels are as follows: 1-compression frame, 101-upper frame edge, 102-left frame edge, 103-lower frame edge, 104-right frame edge, 105-constraint strip; 2-frame adjustment and fixing component, 201-first connecting strap, 202-second connecting strap, 203-connector; 3-hemostatic compression pack, 4-compression adjustment component, 401-adjustment strap, 402-tightness adjustment component. Detailed Implementation

[0015] The following description, in conjunction with the accompanying drawings and preferred embodiments of the present invention, will provide further details.

[0016] like Figure 1 and Figure 2As shown, a compression hemostasis device for use after thyroid ablation includes a compression frame 1, a frame adjustment and fixation component 2, a hemostatic compression pack 3, and a compression adjustment component 4. The compression frame 1 includes a closed frame formed by sequentially connecting an upper frame edge 101, a left frame edge 102, a lower frame edge 103, and a right frame edge 104. Two constraint strips 105 are provided on the frame, and the two constraint strips 105 are connected parallel to each other in the vertical direction between the upper frame edge 101 and the lower frame edge 103. The upper frame edge 101, the lower frame edge 103, and the two constraint strips 105 together form a compression area for compressing the surgical site. The frame adjustment and fixation component 2 includes a first connecting strap 201 and a second connecting strap 202. In this embodiment, the first connecting strap 201 and the second connecting strap 202 are elastic straps to accommodate patients with different neck circumferences. The fixed end of the first connecting strap 201 is connected to the left frame edge 102, and the fixed end of the second connecting strap 202 is connected to the right frame edge 104. The first connecting strap 201 and the second connecting strap 202 are connected together, and the connecting ends are provided with matching connectors 203. In this embodiment, the connectors 203 are Velcro.

[0017] like Figure 1 and Figure 2 As shown, the compression adjustment assembly 4 includes an adjustment belt 401 and a tension adjustment member 402. Two constraint strips 105 pass through the middle of the adjustment belt 401 in sequence. The two ends of the adjustment belt 401 are adjustablely connected by the tension adjustment member 402. The hemostatic compression pack 3 is detachably attached to the middle of the adjustment belt 401 and corresponds to the compression area of ​​the compression frame 1. In this embodiment, the tension adjustment member 402 adopts a D-ring buckle, and the hemostatic compression pack 3 is attached to the middle of the adjustment belt 401 with an adhesive backing. Before use, first pass the adjusting strap 401 through the two restraint strips 105 on the compression frame 1, so that the hemostatic compression pack 3 is aligned with the compression area of ​​the compression frame 1. Then, use the tension adjusting piece 402 (D-ring buckle) to pre-fix the adjusting strap 401 to the compression frame 1. Next, align the compression area of ​​the compression frame 1 with the surgical area. Then, connect the first connecting strap 201 and the second connecting strap 202 with the connector 203 (V-fastener) to fix the compression frame 1 on the patient's neck. Adjust the tightness of the compression with the connector 203 (V-fastener) to avoid compressing other parts of the neck and make the patient more comfortable. Finally, adjust the tension adjusting piece 402 (D-ring buckle) again to adjust the length of the adjusting strap 401 located behind the two restraint strips 105, so that the adjusting strap 401 between the two restraint strips 105 (including the front and back sides) is flattened and tightened, which forces the hemostatic compression pack 3 to move forward, so that the hemostatic compression pack 3 can press on the surgical area.

[0018] In other embodiments, the connector 203 may also use matching multi-row snap fasteners, hook and loop fasteners, etc., and the tension adjustment component 402 may also use snap fasteners, multi-row hook and loop fasteners, Velcro, etc. Velcro or multi-row hook and loop fasteners need to be set at both ends of the adjustment band 401. In this case, the adjustment band 401 should not be too long, and should be set to an appropriate length, generally slightly longer than twice the distance between the two constraint strips 105.

[0019] Furthermore, it should be noted that the names of the various parts of the specific embodiments described in this specification may differ. All equivalent or simple variations made to the structure, features, and principles described in this utility model patent concept are included within the protection scope of this utility model patent. Those skilled in the art to which this utility model pertains may make various modifications or additions to the described specific embodiments or use similar methods to replace them, as long as they do not deviate from the structure of this utility model or exceed the scope defined in these claims, they should all fall within the protection scope of this utility model.

Claims

1. A compression hemostasis device for use after thyroid biopsy ablation, characterized in that: It includes a compression frame, a frame adjustment and fixation assembly, a hemostatic compression pack, and a compression adjustment assembly; the compression frame has a compression area for compressing the surgical site, and the compression frame is connected to the adjustment end of the frame adjustment and fixation assembly. The pressure adjustment component is adjustablely mounted on the pressure frame, and the hemostatic pressure pack is detachably mounted on the pressure adjustment component and corresponds to the pressure area of ​​the pressure frame.

2. The compression hemostasis device for thyroid puncture ablation as described in claim 1, characterized in that: The compression frame includes a closed frame, and two constraint strips are provided on the rear side of the frame. The two constraint strips are connected in parallel in the vertical direction between the upper side and the lower side of the frame. The upper side, the lower side, and the two constraint strips together form the compression area.

3. The compression hemostasis device for thyroid puncture ablation as described in claim 2, characterized in that: The compression adjustment assembly includes an adjustment belt and a tension adjustment component; the middle part of the adjustment belt passes through the two constraint strips in sequence, and the two ends of the adjustment belt are adjustablely connected by the tension adjustment component; the hemostatic compression pack is detachably attached to the middle part of the adjustment belt.

4. The compression hemostasis device for thyroid puncture ablation as described in claim 3, characterized in that: The tension adjustment element is an adjustment buckle, Velcro, or a matching multi-row buckle.

5. The compression hemostasis device for thyroid puncture ablation according to claim 3, characterized in that: The hemostatic compression pack is attached to the middle of the adjustment band via Velcro or adhesive tape.

6. The compression hemostasis device according to claim 1 for use after thyroid puncture ablation, characterized in that: The frame adjustment and fixing assembly includes a first connecting strap and a second connecting strap. The fixed ends of the first connecting strap and the second connecting strap are fixedly connected to the left side and the right side of the frame, respectively. The connecting ends of the first connecting strap and the second connecting strap are correspondingly adjustable.

7. The compression hemostasis device according to claim 6 for use after thyroid puncture ablation, characterized in that: Both the first connecting strip and the second connecting strip are elastic strips; the connecting ends of the first connecting strip and the second connecting strip are provided with matching connectors.

8. The compression hemostasis device according to claim 7 for use after thyroid puncture ablation, characterized in that: The connector is a Velcro fastener or a matching multi-row snap fastener.

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