Surgical nursing hemostasis device

Abstract

The utility model discloses a surgical nursing hemostasis device, and particularly relates to the technical field of surgical nursing hemostasis, the surgical nursing hemostasis device comprises a bearing plate, the upper end of the bearing plate is in sliding connection with two limiting assemblies, the interiors of the two limiting assemblies are jointly and rotatably connected with a sliding ring, and the lower parts of the two limiting assemblies are fixedly connected with a sliding piece; the upper portion of the outer surface of the sliding ring is fixedly connected with an adjusting assembly, the lower portion of the adjusting assembly is fixedly connected with a pressing assembly, and the front side and the rear side of the upper end of the bearing plate are jointly and fixedly connected with a placing assembly. The surgical nursing hemostasis device can be matched with the first threaded rod and the sliding piece to adjust the front-back position of the sliding ring and the limiting assembly in the using process, a patient does not need to move back and forth, the pain feeling of the patient is improved, then the pressing assembly can be adjusted to be aligned with the hemostasis position through the adjusting assembly and the sliding ring, and the hemostasis effect is improved. The hemostasis position can be more directly pressed, the operation is simple and portable, and the practicability of the device is further improved.

Description

Technical Field

[0001] The utility model relates to the technical field of surgical nursing hemostasis, in particular to a surgical nursing hemostasis device. Background Art

[0002] At present, compression hemostasis is used for arterial bleeding. The artery near the wound is closed to temporarily stop the bleeding. Generally, local compression hemostasis is tried first. If the bleeding does not stop, the corresponding proximal artery needs to be pressurized. Now, in surgical nursing, temporary hemostasis treatment is required for the wound. When stopping bleeding at the wound of surgical patients, finger pressure hemostasis or tourniquet hemostasis is generally used for arm injury hemostasis. Existing nursing hemostasis devices mostly fix the arm with a cloth belt or a tourniquet, which can easily cause pain to the patient and is cumbersome to operate. Therefore, a surgical nursing hemostasis device is needed.

[0003] Chinese patent document CN219089486U discloses a surgical nursing hemostatic device, which includes at least one frame component, the frame component forms a limb fixing area, a hemostatic component is arranged inside the frame component, the hemostatic component forms a compression surface in the limb fixing area, which is used to intercept blood so that it cannot flow to the wound, the frame component is connected to the hemostatic component in a transmission manner, which is used to adjust the compression area inside the hemostatic component so that the hemostatic component fits the limb of the injured person, and a bandage component is arranged inside the hemostatic component, which is adapted to the hemostatic component and is used to form multi-point compression on the limb; the compression area inside the hemostatic component can be adjusted by the frame component, so that the above device is suitable for people of different weights, improves the adaptability of the device, and makes the hemostatic component compress around the limb of the injured person, cuts off the blood flow path, prevents blood from flowing to the wound, improves the protection of the health of the injured person, and increases the protectiveness of the above device, but the above patent document still has the following defects during use:

[0004] In the above patent document, when the device is used to fix the bleeding part of the injured limb, if the injured part does not completely correspond to the first compression band and the second compression band, it is necessary to rotate the entire device or the injured person rotates the limb to press the injured bleeding part to stop the bleeding. During the adjustment process, it is easy to touch the patient's wound and cause pain to the patient. Utility Model Content

[0005] The main purpose of the utility model is to provide a surgical nursing hemostasis device, which can effectively solve the problem of facilitating fine adjustment.

[0006] In order to achieve the above purpose, the technical solution adopted by the utility model is:

[0007] A surgical care hemostasis device comprises a receiving plate, wherein the upper end of the receiving plate is slidably connected to two limit assemblies, the two limit assemblies are internally rotatably connected to a slip ring, the lower parts of the two limit assemblies are fixedly connected to a sliding member, the upper part of the outer surface of the slip ring is fixedly connected to an adjustment assembly, the lower part of the adjustment assembly is fixedly connected to a pressing assembly, the upper front side and the upper rear side of the receiving plate are jointly fixedly connected to a placement assembly, and the lower part of the placement assembly is rotatably connected to a threaded rod 1.

[0008] Preferably, the limiting assembly comprises a fixing ring, a sliding groove is provided in the middle of one end of the fixing ring away from the adjusting assembly, and the sliding ring is rotatably connected to the two fixing rings.

[0009] Preferably, the placement assembly includes a placement plate, and the front side of the lower end and the rear side of the lower end of the placement plate are fixedly connected to a fixing plate.

[0010] Preferably, the two fixing plates are rotatably connected to the threaded rod, the two fixing plates are fixedly connected to the receiving plate, the sliding member is slidably connected to the receiving plate, and the threaded rod passes through the sliding member and is threadedly connected to the sliding member.

[0011] Preferably, the adjustment assembly includes a sliding frame, the upper end of the sliding frame is threadedly connected to a threaded rod 2, the lower side of the front end and the lower side of the rear end of the sliding frame are fixedly connected to a fixing column, the upper outer surface of the threaded rod 2 is threadedly connected to a pressing plate, and the front side and the rear side of the lower end of the pressing plate are fixedly connected to a sliding rod.

[0012] Preferably, the sliding frame is rotatably connected to the two fixing rings, the two sliding rods are slidably connected to the sliding frame, and the fixing column is slidably connected to the sliding groove.

[0013] Preferably, the pressing assembly comprises an arc-shaped plate, a plurality of springs are fixedly connected to the outer side of the lower end of the arc-shaped plate, and the lower ends of the plurality of springs are fixedly connected to cushions.

[0014] Preferably, the sliding rod is fixedly connected to the arc plate.

[0015] Compared with the prior art, the utility model has the following beneficial effects:

[0016] 1. During use, the utility model can cooperate with the threaded rod and the sliding part to adjust the front and rear positions of the slip ring and the limit assembly, without the patient moving back and forth, which increases the patient's pain. Then, the pressing assembly can be adjusted to align with the hemostasis position in conjunction with the adjustment assembly and the slip ring, so that the hemostasis position can be pressed more directly. The operation is simple and portable, which further improves the practicality of the device.

[0017] 2. During use, the utility model directly pulls the pressing plate to rotate the slip ring to cooperate with the limit assembly to make the slip ring more stable when rotating. When the position is adjusted, the fixing column is pressed to fix the corresponding positions of the limit assembly and the slip ring at this time, and then the threaded rod 2 is rotated downward to drive the pressing plate, and then the sliding rod is driven to press the pressing assembly to stop bleeding from the wound. In this process, the patient places his arm on the placement board without moving, so as to avoid increased pain when moving. BRIEF DESCRIPTION OF THE DRAWINGS

[0018] Figure 1 It is a schematic diagram of the overall structure of the utility model;

[0019] Figure 2 It is a schematic diagram of the overall structure of the sliding member of the utility model;

[0020] Figure 3 This is a schematic diagram of the overall structure of the adjustment component of the utility model;

[0021] Figure 4 For the utility model Figure 3 The enlarged schematic diagram at A in the middle;

[0022] Figure 5 It is a schematic diagram of the overall structure of the limit assembly of the utility model.

[0023] In the figure: 1. Adjustment component; 2. Limiting component; 3. Slip ring; 4. Pressing component; 5. Placing component; 6. Threaded rod one; 7. Receiving plate; 8. Sliding member; 51. Placing plate; 52. Fixed plate; 11. Threaded rod two; 12. Pressing plate; 13. Sliding frame; 14. Sliding rod; 15. Fixed column; 41. Arc plate; 42. Spring; 43. Cushion; 21. Fixed ring; 22. Slide groove. DETAILED DESCRIPTION

[0024] In order to make the technical means, creative features, objectives and effects achieved by the present invention easy to understand, the present invention is further described below in conjunction with specific implementation methods.

[0025] like Figure 1-5As shown, a surgical care hemostasis device includes a receiving plate 7, and two limit assemblies 2 are slidably connected to the upper end of the receiving plate 7, and a slip ring 3 is clamped to keep the slip ring 3 stable during rotation. The two limit assemblies 2 are rotatably connected inside with the slip ring 3 to make slight adjustments to the position to be pressed by the pressing assembly 4. The two limit assemblies 2 are fixedly connected with a sliding member 8 at the lower part to adjust the pressing position of the pressing assembly 4. The upper part of the outer surface of the slip ring 3 is fixedly connected with an adjusting assembly 1 to ensure that the wound is pressed as firmly as possible. The lower part of the adjusting assembly 1 is fixedly connected with the pressing assembly 4. The front side and the rear side of the upper end of the receiving plate 7 are fixedly connected with a placing assembly 5. The patient places his arm on the upper part of the placing assembly 5 to facilitate pressing and stopping bleeding. The lower part of the placing assembly 5 is rotatably connected with a threaded rod 6.

[0026] To avoid patient movement and secondary injury, such as Figure 2 As shown, the placement assembly 5 includes a placement plate 51, and a fixing plate 52 is fixedly connected to the front side and the rear side of the lower end of the placement plate 51;

[0027] For further information, see Figure 2 , the two fixed plates 52 are rotatably connected to the threaded rod 16, the two fixed plates 52 are fixedly connected to the receiving plate 7, the sliding member 8 is slidably connected to the receiving plate 7, and the threaded rod 16 penetrates the sliding member 8 and is threadedly connected to the sliding member 8;

[0028] When the patient passes his arm through the slip ring 3 and places it on the upper end of the placement plate 51, the threaded rod 6 can be rotated at this time, and the two fixed plates 52 can be cooperated to make the threaded rod 6 rotate in place, driving the sliding member 8 to move back and forth along the path of the threaded rod 6. The sliding member 8 can drive the limiting component 2 and the slip ring 3 to move back and forth, and the pressing component 4 is observed to adjust the corresponding hemostasis position of the patient until the pressing component 4 corresponds to the hemostasis position, completing the first pressing position adjustment, avoiding the patient from dragging his arm for adjustment, and reducing the patient's pressure during the treatment process.

[0029] In order to ensure that the wound is pressed as completely as possible and improve the hemostasis effect, Figure 3-5 As shown, the limit assembly 2 includes a fixed ring 21, a sliding groove 22 is provided in the middle of one end of the fixed ring 21 away from the adjustment assembly 1, and the slip ring 3 is rotatably connected to both fixed rings 21;

[0030] For further information, see Figure 4 The adjustment assembly 1 includes a sliding frame 13, the upper end of the sliding frame 13 is threadedly connected to a threaded rod 11, the lower side of the front end and the lower side of the rear end of the sliding frame 13 are fixedly connected to a fixing column 15, the upper part of the outer surface of the threaded rod 11 is threadedly connected to a pressing plate 12, and the front side and the rear side of the lower end of the pressing plate 12 are fixedly connected to a sliding rod 14;

[0031] For further information, see Figure 4, the sliding frame 13 is rotatably connected to the two fixing rings 21, the two sliding rods 14 are slidably connected to the sliding frame 13, and the fixing column 15 is slidably connected to the sliding groove 22;

[0032] For further information, see Figure 4 The pressing assembly 4 includes an arc-shaped plate 41, a plurality of springs 42 are fixedly connected to the outer side of the lower end of the arc-shaped plate 41, and a plurality of springs 42 are fixedly connected to the lower ends of the cushions 43;

[0033] For further information, see Figure 4 , the slide bar 14 is fixedly connected to the arc plate 41;

[0034] Then, a secondary adjustment is performed to ensure that the wound is completely covered by the pressing component 4 to stop bleeding as much as possible. The medical staff can pull the pressing plate 12 to rotate the adjustment component 1 as a whole along the trajectory of the fixing ring 21. During the rotation of the adjustment component 1, the hemostasis position corresponding to the pressing component 4 is observed. When the pressing component 4 completely corresponds to the hemostasis position, the fixing column 15 is pressed and inserted into the inner surface of the slide groove 22 to fix the position of the limit component 2 and the slip ring 3.

[0035] Then, the threaded rod 11 is rotated to drive the pressing plate 12 to move downward. During the movement, the pressing plate 12 drives the sliding rods 14 on both sides to slide downward. When the hemostatic cotton at the lower end of the cushion 43 touches the skin, the threaded rod 11 is continued to be rotated, and in conjunction with a number of springs 42, when part of the position has touched the skin, the arc plate 41 can continue to move downward until the cushion 43 is completely in contact with the skin, pressing to stop bleeding, and the threaded rod 11 is stopped to complete the hemostasis.

[0036] The working principle of the utility model is:

[0037] When the patient passes his arm through the slip ring 3 and places it on the upper end of the placement plate 51, the threaded rod 6 can be rotated at this time, and the two fixed plates 52 can be cooperated to make the threaded rod 6 rotate in place, driving the sliding member 8 to move forward and backward along the path of the threaded rod 6, and the sliding member 8 can drive the limit assembly 2 and the slip ring 3 to move forward and backward, and the pressing assembly 4 is observed to adjust the hemostasis position of the patient, until the pressing assembly 4 corresponds to the hemostasis position, and the first pressing position adjustment is completed, so as to avoid the patient dragging the arm for adjustment and reduce the pressure on the patient during the treatment process;

[0038] Then, a secondary adjustment is performed to ensure that the wound is completely covered by the pressing component 4 to stop bleeding as much as possible. The medical staff can pull the pressing plate 12 to rotate the adjustment component 1 as a whole along the trajectory of the fixing ring 21. During the rotation of the adjustment component 1, the hemostasis position corresponding to the pressing component 4 is observed. When the pressing component 4 completely corresponds to the hemostasis position, the fixing column 15 is pressed and inserted into the inner surface of the slide groove 22 to fix the position of the limit component 2 and the slip ring 3.

[0039] Then, the threaded rod 11 is rotated to drive the pressing plate 12 to move downward. During the movement, the pressing plate 12 drives the sliding rods 14 on both sides to slide downward. When the hemostatic cotton at the lower end of the cushion 43 touches the skin, the threaded rod 11 is continued to be rotated, and in conjunction with a number of springs 42, when part of the position has touched the skin, the arc plate 41 can continue to move downward until the cushion 43 is completely in contact with the skin, pressing to stop bleeding, and the threaded rod 11 is stopped to complete the hemostasis.

[0040] The above shows and describes the basic principle and main features of the utility model and the advantages of the utility model. Those skilled in the art should understand that the utility model is not limited by the above embodiments. The above embodiments and descriptions are only for explaining the principle of the utility model. Without departing from the spirit and scope of the utility model, the utility model may have various changes and improvements, which fall within the scope of the utility model to be protected. The scope of protection claimed by the utility model is defined by the attached claims and their equivalents.

Claims

1. A surgical nursing hemostasis device, comprising a receiving plate (7), characterized in that: The upper end of the receiving plate (7) is slidably connected to two limit assemblies (2), the two limit assemblies (2) are internally connected to a slip ring (3) for rotation, the lower parts of the two limit assemblies (2) are fixedly connected to a sliding member (8), the upper part of the outer surface of the slip ring (3) is fixedly connected to an adjustment assembly (1), the lower part of the adjustment assembly (1) is fixedly connected to a pressing assembly (4), the upper front side and the upper rear side of the receiving plate (7) are fixedly connected to a placement assembly (5), and the lower part of the placement assembly (5) is rotationally connected to a threaded rod (6).

2. A surgical care hemostasis device according to claim 1, characterized in that: The limiting assembly (2) comprises a fixing ring (21), a sliding groove (22) is provided in the middle of one end of the fixing ring (21) away from the adjusting assembly (1), and the sliding ring (3) is rotatably connected to both fixing rings (21).

3. A surgical care hemostasis device according to claim 1, characterized in that: The placing assembly (5) comprises a placing plate (51), and a fixing plate (52) is fixedly connected to the front side and the rear side of the lower end of the placing plate (51).

4. A surgical care hemostasis device according to claim 3, characterized in that: The two fixing plates (52) are rotatably connected to the threaded rod (6), the two fixing plates (52) are fixedly connected to the receiving plate (7), the sliding member (8) is slidably connected to the receiving plate (7), and the threaded rod (6) passes through the sliding member (8) and is threadedly connected to the sliding member (8).

5. A surgical care hemostasis device according to claim 2, characterized in that: The adjustment assembly (1) comprises a sliding frame (13), the upper end of the sliding frame (13) is threadedly connected to a second threaded rod (11), the lower side of the front end and the lower side of the rear end of the sliding frame (13) are fixedly connected to a fixing column (15), the upper part of the outer surface of the second threaded rod (11) is threadedly connected to a pressing plate (12), and the front side and the rear side of the lower end of the pressing plate (12) are fixedly connected to a sliding rod (14).

6. A surgical care hemostasis device according to claim 5, characterized in that: The sliding frame (13) is rotatably connected to the two fixing rings (21), the two sliding rods (14) are slidably connected to the sliding frame (13), and the fixing column (15) is slidably connected to the sliding groove (22).

7. A surgical care hemostasis device according to claim 5, characterized in that: The pressing assembly (4) comprises an arc-shaped plate (41), a plurality of springs (42) are fixedly connected to the outer side of the lower end of the arc-shaped plate (41), and the lower ends of the plurality of springs (42) are fixedly connected to a soft pad (43).

8. A surgical care hemostasis device according to claim 7, characterized in that: The sliding rod (14) is fixedly connected to the arc-shaped plate (41).

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