Hemodialysis room nursing hemostasis device

Abstract

The invention discloses a hemodialysis room nursing hemostasis device which is characterized in that the two sides of a plastic plate are connected with one ends of bandages respectively, the other ends of the two bandages are detachably connected, a fixing plate is connected to the middle of the plastic plate, a positioning frame is fixed to one face of the fixing plate, and a pressing plate and a pressing bag are arranged in the positioning frame; one side of the pressing plate is connected with the fixing plate or the positioning frame, the other side of the pressing plate is detachably connected with the fixing plate, the pressing bag is arranged between the bottom of the pressing plate and the fixing plate, a through hole is formed in the area, surrounded by the positioning frame, of the fixing plate, and the size of the through hole is smaller than that of the positioning frame; after the pressing bag is inflated, the part, located at the position of the through hole, of the pressing bag penetrates through the through hole, an air inlet and outlet valve is connected to the pressing bag, and the air inlet and outlet valve is fixed to the pressing plate. The device is convenient to wear, whether the puncture port of a patient bleeding or not and the bleeding amount can be judged, and therefore the force borne by the puncture port can be set.

Description

Technical Field

[0001] The invention relates to a hemodialysis room nursing hemostasis device, belonging to the technical field of medical equipment. Background Art

[0002] At present, the most commonly used vascular access for hemodialysis patients is arteriovenous fistula. Because the fistula puncture needle is thick and the needle hole is large, it is difficult to stop bleeding from the puncture site after dialysis is completed. It is necessary to press the needle hole with fingers for about 20 minutes to stop the bleeding. Some patients need to press for a longer time to stop the bleeding.

[0003] After patients undergo hemodialysis, they usually use a hemostatic device to press and stop bleeding. Currently, the most common hemostatic device is a tourniquet with a certain degree of elasticity, which is tightened at the puncture site with Velcro to compress the blood vessels to stop bleeding. However, it is not convenient to adjust the pressure of conventional tourniquets, and the Velcro needs to be frequently opened for adjustment, which is inconvenient to use. In addition, the tourniquets in the prior art cannot observe whether the patient's puncture site is bleeding in time, and cannot make a relatively accurate and intuitive judgment of the pressure of the puncture site to stop bleeding.

[0004] Therefore, it is necessary to provide a new hemodialysis room care hemostasis device to solve the above technical problems. Summary of the invention

[0005] The technical problem to be solved by the present invention is: how to effectively compress the puncture site to stop bleeding, timely observe whether the patient's puncture site is bleeding, and accurately and intuitively judge the pressure of the puncture site to stop bleeding.

[0006] In order to solve the above technical problems, the technical solution of the present invention is to provide a hemodialysis room care hemostasis device, which is characterized in that it includes two sides of a plastic plate respectively connected to one end of a strap, the other ends of the two straps are detachably connected, a fixing plate is connected in the middle of the plastic plate, a positioning frame is fixed on one surface of the fixing plate, a pressing plate and a pressing bag are provided in the positioning frame, one side of the pressing plate is connected to the fixing plate or the positioning frame, and the other side of the pressing plate is detachably connected to the fixing plate, the pressing bag is arranged between the bottom of the pressing plate and the fixing plate, and a through hole is opened in the fixing plate in the area surrounded by the positioning frame, and the through hole is smaller than the size of the positioning frame; after the pressing bag is inflated, the part of the pressing bag located at the position of the through hole passes through the through hole, the pressing bag is connected to the inlet and exhaust valves, and the inlet and exhaust valves are both fixed on the pressing plate.

[0007] Preferably, a mounting hole is provided in the middle of the plastic plate, an annular groove is provided on the inner wall of the mounting hole, and the side edges of the fixing plate are all arranged in the annular groove.

[0008] Preferably, the pressure bag is provided with hemostatic cotton on the side away from the pressure plate; the hemostatic cotton is arranged in the positioning frame and is located between the pressure bag and the fixed plate; after the pressure bag is inflated, the part of the pressure bag away from the side of the pressure plate and located at the through hole position pushes the part of the hemostatic cotton located at the through hole position out of the through hole.

[0009] Preferably, the pressure bag is also connected to a pressure sensor with a display screen, and the pressure sensor is fixed on the pressure plate.

[0010] Preferably, a first connecting strip and at least one connecting block are fixed on the top of the fixing plate, a first connecting strip is fixed to one side of the first connecting band, a second connecting strip is fixed to the other side of the first connecting strip, and the second connecting strip is fixed to the pressing plate; third connecting strips are symmetrically fixed to the pressing plate, each third connecting strip is fixedly connected to one side of the second connecting band, a connecting bolt that can rotate freely on the second connecting band is passed through the other side of the second connecting strip, and each connecting bolt is connected to its corresponding connecting block by a thread; the first connecting strip and the connecting block are respectively located on two opposite sides of the positioning frame, and the third connecting strip and the second connecting strip are respectively located on two opposite sides of the pressing plate; the number of the third connecting strip, the second connecting band, the connecting bolt and the connecting block are the same.

[0011] Preferably, the pressure bag is provided with a plurality of observation holes distributed in a ring shape, the observation holes penetrate the pressure bag, a plurality of annular mounting holes are opened on the fixed plate, a transparent plate is fixed in the mounting holes; the position and size of the transparent plate are adapted to the observation holes; the transparent plate and the observation holes are both located in the through hole area of ​​the fixed plate.

[0012] Preferably, the other ends of the two straps are detachably connected via Velcro.

[0013] Preferably, it also includes a support bar fixed to the other end of a binding strap, one side of the support bar is symmetrically fixedly connected to one end of the two connecting ropes, and at least two protective covers are fixed to the other end of the other binding strap, each protective cover is provided with a limit column, a take-up roller, and a brake block, one end of the limit column is fixed to the other binding strap, and the other end of the limit column is provided with a brake block that can only slide along the length direction of the limit column and cannot rotate, a spring is sleeved on the limit column, and both ends of the spring are respectively abutted against the other binding strap and one end of the brake block, the other end of one end of the brake block is meshed and connected with one end of the take-up roller, one end of the take-up roller rotates and is limited in the protective cover, the other end of the rotating column passes through the protective cover and is connected to the rotating knob, a sliding hole is opened on the take-up roller, and a rotating column that penetrates the sliding hole is slidably provided in the sliding hole, and the other end of the connecting rope is connected and wrapped around the outside of the take-up roller; when the rotating column pushes the brake block, the brake block is separated from the take-up roller.

[0014] Preferably, a cylindrical cavity with a non-circular cross-section is provided in the brake block, and a cylindrical block with a cross-section matching the cylindrical cavity in the brake block is provided at the other end of the limiting column, the height of the cylindrical block is smaller than the height of the cylindrical cavity, and the cylindrical block is arranged in the cylindrical cavity; the top of the brake block and the bottom of the take-up roller are fixed with ring-shaped wedge-shaped teeth distributed in an annular shape, and the brake block and the take-up roller are connected by multiple wedge-shaped teeth; a sliding groove is provided on the inner wall of the sliding hole, a sliding block is fixed on the outer side of the rotating column, and the slider is slidably arranged in the sliding groove.

[0015] Preferably, at least two guide rollers are symmetrically fixed on the other binding strap, the number of the guide rollers is the same as the number of the connecting ropes, and each connecting rope is arranged on a corresponding guide roller.

[0016] The device of the present invention is convenient to wear, and can judge whether the puncture site of the patient is bleeding and the amount of bleeding, so that the force applied to the puncture site can be set.

[0017] Compared with the prior art, the hemodialysis room care hemostasis device provided by the present invention specifically has at least one of the following

[0018] Beneficial effects:

[0019] The entire hemostatic device can be quickly and conveniently fixed by the plastic plate and the binding strap. The first connecting strip, the first connecting strap, the second connecting strip, the second connecting strap, the connecting bolt and the connecting block cooperate to facilitate the opening and closing of the pressure plate and the pressure bag, so that the hemostatic cotton can be easily replaced, thereby improving the replacement efficiency of the hemostatic cotton; the pressure bag can be inflated and deflated by the air inlet and exhaust valve, so that the pressure on the patient's wound can be adjusted, and at the same time, the pressure value of the patient's wound can be intuitively displayed by the pressure sensor; by cooperating with the mounting hole, the transparent plate and the observation hole, it is possible to observe at any time whether there is blood stain on the hemostatic cotton, so as to judge whether the patient's wound is bleeding and the amount of bleeding at any time, and at the same time, the pressure on the patient's wound can be adjusted according to whether the patient's wound is bleeding and the amount of bleeding, thereby improving the healing efficiency of the patient's wound. BRIEF DESCRIPTION OF THE DRAWINGS

[0020] Figure 1 This is a schematic structural diagram of a hemodialysis room care hemostasis device in Example 1;

[0021] Figure 2 for Figure 1 A schematic diagram of the structure from another perspective;

[0022] Figure 3 for Figure 1 Schematic diagram of the connection structure between the middle plastic plate and the strap;

[0023] Figure 4 for Figure 1 Schematic diagram of the structure after removing the plastic plate and straps;

[0024] Figure 5 for Figure 4 Schematic diagram of the structure after removing the fixing plate and the positioning frame;

[0025] Figure 6 for Figure 5 Schematic diagram of the structure after removing the pressure plate;

[0026] Figure 7 for Figure 6 Schematic diagram of the structure of the medium pressure bag;

[0027] Figure 8 for Figure 7 A schematic cross-sectional view of the structure from another perspective is shown;

[0028] Fig. 9 This is a schematic diagram of a hemodialysis room care hemostasis device in Example 2;

[0029] Fig.10 for Fig. 9 A schematic diagram of the structure after all structures in the first embodiment are removed;

[0030] Fig.11 for Fig.10 Schematic diagram of the middle protective cover and its internal structure;

[0031] Fig.12 for Fig.11 Schematic diagram of the structure after removing the protective cover;

[0032] Fig.13 for Fig.11 Schematic diagram of the cross-sectional structure from another perspective. DETAILED DESCRIPTION

[0033] In order to make the present invention more clearly understood, preferred embodiments are described in detail below with reference to the accompanying drawings.

[0034] Example 1

[0035] The present invention provides a hemodialysis room nursing hemostasis device, such as Figure 1 , Figure 2 As shown, it includes a plastic plate 1, one end of a strap 2 is fixedly installed on both sides of the plastic plate 1, and the other ends of the two straps 2 are detachably connected (in this embodiment, the two straps 2 are detachably connected by Velcro), and a fixing plate 4 is fixedly installed inside the plastic plate 1. Figure 4 As shown, a positioning frame 5 is fixed on one side of the fixing plate 4, and a pressing plate 6 is arranged inside the positioning frame 5. One side of the pressing plate 6 is connected to the fixing plate 4 or the positioning frame 5, and the other side of the pressing plate 6 (the side opposite to the fixing plate 4 or the positioning frame 5) is detachably connected to the fixing plate 4, as shown in FIG. Figure 5 As shown, a pressure bag 18 is fixedly installed at the bottom of the pressing plate 6, and the pressure bag 18 is arranged in the positioning frame 5 and between the bottom of the pressing plate 6 and the fixed plate 4. A hemostatic cotton 21 is arranged on the side of the pressure bag 18 away from the pressing plate 6. The area of ​​the hemostatic cotton 21 is set to be smaller than the area of ​​the pressing plate 6, which can facilitate the replacement of the hemostatic cotton 21.

[0036] In this embodiment, the hemostatic cotton 21 is arranged in the positioning frame 5 and between the pressure bag 18 and the fixing plate 4. A through hole is provided on the fixing plate 4 at the middle position of the area surrounded by the positioning frame 5, and the through hole is smaller than the size of the positioning frame 5. After the pressure bag 18 is inflated, the part of the pressure bag 18 away from the side of the pressure plate 6 and located at the position of the through hole passes through the through hole, thereby pushing the part of the hemostatic cotton 21 also located at the position of the through hole out of the through hole.

[0037] like Figure 5 As shown, the pressure bag 18 is fixedly mounted with an inlet and outlet valve 13 and a pressure sensor 12, and the pressure sensor 12 and the inlet and outlet valve 13 are both fixedly mounted on the pressure plate 6. Among them, the pressure sensor 12 itself has a display screen that can display the value of the currently measured pressure.

[0038] like Figure 4 As shown, a first connecting strip 7 is fixedly mounted on the top of the fixing plate 4, a first connecting belt 8 is fixedly mounted on the first connecting strip 7, a second connecting strip 9 is fixedly mounted on the side of the first connecting belt 8 away from the first connecting strip 7, and the second connecting strip 9 is fixedly mounted on the pressing plate 6. The height of the first connecting strip 7 matches the height of the positioning frame 5.

[0039] like Figure 4 As shown, the pressure plate 6 is symmetrically fixedly installed with two third connecting strips 14, the third connecting strips 14 are fixedly installed with second connecting belts 15, and the second connecting belts 15 are rotatably installed with connecting bolts 16, and the fixing plate 4 is symmetrically fixedly installed with two connecting blocks 17, one side of the connecting bolts 16 extends into the connecting block 17 and is threadedly connected with the connecting block 17. (Wherein, the number of the third connecting strips 14, the second connecting belts 15, the connecting bolts 16, and the connecting blocks 17 is the same, and there is at least one of each)

[0040] like Figure 3 As shown, a mounting hole is provided on the top of the plastic plate 1 , an annular groove 3 is provided on the inner wall of the mounting hole, and the sides of the fixing plate 4 are fixedly installed in the annular groove 3 .

[0041] like Figure 6 As shown, a fixing hole 20 is opened on one side of the pressure bag 18 close to the pressure plate 6 , and the pressure sensor 12 is fixedly installed in the fixing hole 20 .

[0042] The pressure bag 18 is provided with a plurality of observation holes 19 distributed in an annular shape, and the observation holes 19 penetrate the upper and lower ends of the pressure bag 18, but the observation holes 19 are separated from the inside of the pressure bag 18 and are not connected. The fixed plate 4 is provided with a plurality of mounting holes 10 in an annular shape, and a transparent plate 11 is fixedly mounted in the mounting holes 10, and the position and size of the transparent plate 11 and the observation holes 19 are adapted. The transparent plate 11 and the observation holes 19 are both located in the through hole area of ​​the fixed plate 4.

[0043] The working principle of the hemodialysis room care hemostasis device provided by the present invention is as follows:

[0044] When in use, after the patient has finished dialysis, the hemostatic cotton 21 of the device of the present invention is first spread on the patient's wound, and then the Velcro on the two straps 2 on both sides of the plastic plate 1 is used to fix the entire device of the present invention to the patient's wound (i.e., on the wrist), and then the air inlet and outlet valve 13 is connected to the inflation device (for example, an inflation pump) through a pipeline, and can also be connected to the hospital's oxygen supply pipeline to inflate the pressure bag 18. During the inflation process, the pressure in the pressure bag 18 is directly displayed by the pressure sensor 12, so that the pressure on the patient's wound can be judged. The inflated pressure bag 18 squeezes the patient's wound through the hemostatic cotton 21, so as to ensure the normal healing of the patient's wound;

[0045] During the wound healing process, the transparent plate 11 and the observation hole 19 can timely detect whether there is bleeding in the wound of the patient, and the pressure value of the wound of the patient can be adjusted according to the amount of bleeding in the wound of the patient; thus, the pressure bag 18 can be exhausted or inflated, so that the appropriate pressure intensity can be set according to the individual differences of different patients to stop bleeding;

[0046] When the hemostatic cotton 21 needs to be replaced during the healing process of the patient's wound to ensure the cleanliness of the patient's wound and avoid infection of the patient's wound, first, the pressure bag 18 is deflated through the air inlet and outlet valves 13, and then the connecting bolt 16 is rotated until the connecting bolt 16 is removed from the connecting block 17. At this time, the two second connecting belts 15 are pulled to move, and the second connecting belts 15 drive the pressure plate 6 and the pressure bag 18 to move out of the positioning frame 5. At this time, the old hemostatic cotton 21 can be removed, and then replaced with a new hemostatic cotton 21, and then the above steps are reversed to complete the replacement of the hemostatic cotton 21.

[0047] In another embodiment, the hemostatic cotton 21 in the device of the present invention is eliminated, and after the hemostatic cotton 21 is spread on the patient's wound, the device of the present invention is used to press the hemostatic cotton 21 on the patient's wound through the pressure bag 18 protruding from the through hole.

[0048] Example 2

[0049] In this embodiment, the present invention provides a hemodialysis room care hemostasis device, such as Figure 9-13As shown, it also includes a support bar 22 fixedly installed at one end of one of the straps 2, one end of two connecting ropes 23 are symmetrically fixedly installed on one side of the support bar 22, a limiting column 26, a protective cover 25 sleeved on the outside of the limiting column 26 and one end of a spring 30 are fixedly installed on the other strap 2, a brake block 27 is provided on the outer sliding sleeve of the limiting column 26, a take-up roller 28 is provided on the top of the brake block 27, the take-up roller 28 is rotatably installed in the protective cover 25, and a limiting groove matching the take-up roller 28 is provided in the protective cover 25, so that the take-up roller 28 can only rotate in the protective cover 25 and cannot slide up and down. The brake block 27 is meshed with the take-up roller 28, and a rotating column 29 is slidably installed in the take-up roller 28. The bottom end of the rotating column 29 contacts the brake block 27, and the top of the rotating column 29 extends to the protective cover 25 and is fixedly installed with a rotating knob. The spring 30 is sleeved on the outside of the limit column 26, and the other end of the spring 30 is fixedly installed on the bottom of the brake block 27. The top of the brake block 27 and the bottom of the take-up roller 28 are both fixedly installed with ring-shaped wedge-shaped teeth. The brake block 27 and the take-up roller 28 are connected by a plurality of wedge-shaped teeth, and the other end of the connecting rope 23 is fixedly wound around the outside of the take-up roller 28.

[0050] Two guide rollers 24 are symmetrically fixedly mounted on the other binding belt 2 , and the connecting rope 23 is connected to the guide rollers 24 .

[0051] like Fig.13 As shown, a cylindrical cavity 32 with a non-circular cross section is provided in the brake block 27, and a cylindrical block 31 with a cross section matching the cylindrical cavity 32 in the brake block 27 is provided at the other end of the limiting column 26. The cylindrical block 31 is arranged in the cylindrical cavity 32, and the height of the cylindrical block 31 is less than the height of the cylindrical cavity 32, so that there is a sliding space for the cylindrical block 31 in the cylindrical cavity 32. In this embodiment, the non-circular cylindrical cavity 32 in the brake block 27 is a square cavity, and the cylindrical block 31 at the other end of the limiting column 26 is a square block.

[0052] The take-up roller 28 is provided with a sliding hole, the rotating column 29 passes through the sliding hole, the inner wall of the sliding hole is provided with a sliding groove 34 , the outer side of the rotating column 29 is fixedly installed with a sliding block 33 , and the slider 33 is slidably installed in the sliding groove 34 .

[0053] In this embodiment, the bandage 2 is made of plastic material. When the entire hemostatic device needs to be installed, the entire device is firstly put on the patient, and then the hemostatic cotton 21 is spread on the patient's wound. Then the hemostatic device of the present invention is moved to make the pressure bag 18 face the hemostatic cotton 21, and then the rotating column 29 is rotated. The rotating column 29 drives the take-up roller 28 to rotate, so that the take-up roller 28 takes up the connecting rope 23. In the above process, since the wedge-shaped teeth are arranged between the brake block 27 and the take-up roller 28, when the take-up roller 28 rotates, the rotation of the take-up roller 28 causes the brake block 2 7 is continuously moved downward to engage, thereby ensuring the normal winding of the wire-receiving roller 28, until the bandage 2 and the plastic plate 1 are in contact with the patient's skin, at which time the fixing work of the entire hemostatic device is completed; when the entire device needs to be removed from the patient, it is only necessary to push down the rotating column 29, and the rotating column 29 pushes the brake block 27 to move downward on the outside of the limiting column 26 until the wedge-shaped teeth on the brake block 27 are out of contact with the wedge-shaped teeth on the wire-receiving roller 28, at which time the rotating column 29 can be rotated in the opposite direction, so that the connecting rope 23 can be loosened, until the entire device can be removed from the patient.

[0054] The above structure in this embodiment can replace the fastening method of Example 1 in which the two straps 2 are detachably connected by Velcro.

Claims

1. A hemodialysis room care hemostasis device, characterized in that: The invention comprises two sides of a plastic plate (1) connected to one end of a strap (2) respectively, the other ends of the two straps (2) are detachably connected, a fixing plate (4) is connected in the middle of the plastic plate (1), a positioning frame (5) is fixed on one surface of the fixing plate (4), a pressing plate (6) and a pressing bag (18) are arranged in the positioning frame (5), one side of the pressing plate (6) is connected to the fixing plate (4) or the positioning frame (5), the other side of the pressing plate (6) is detachably connected to the fixing plate (4), the pressing bag (18) is arranged between the bottom of the pressing plate (6) and the fixing plate (4), a through hole is opened in the fixing plate (4) in the area surrounded by the positioning frame (5), and the through hole is smaller than the size of the positioning frame (5); after the pressing bag (18) is inflated, the part of the pressing bag (18) located at the position of the through hole passes through the through hole, the pressing bag (18) is connected to the inlet and outlet valves (13), and the inlet and outlet valves (13) are fixed on the pressing plate (6).

2. A hemodialysis room care hemostasis device as claimed in claim 1, characterized in that: The plastic plate (1) is provided with a mounting hole in the middle, an annular groove (3) is provided on the inner wall of the mounting hole, and the side edges of the fixing plate (4) are all arranged in the annular groove (3).

3. A hemodialysis room care hemostasis device as claimed in claim 1, characterized in that: A hemostatic cotton (21) is provided on the side of the pressure bag (18) away from the pressure plate (6); the hemostatic cotton (21) is arranged in the positioning frame (5) and is located between the pressure bag (18) and the fixing plate (4); after the pressure bag (18) is inflated, the portion of the pressure bag (18) away from the side of the pressure plate (6) and located at the through hole position pushes the portion of the hemostatic cotton (21) located at the through hole position out of the through hole.

4. A hemodialysis room care hemostasis device as claimed in claim 1, characterized in that: The pressure bag (18) is also connected to a pressure sensor (12) with a display screen, and the pressure sensor (12) is fixed on the pressure plate (6).

5. The hemodialysis room care hemostasis device according to claim 1, characterized in that: A first connecting strip (7) and at least one connecting block (17) are fixed on the top of the fixing plate (4); a first connecting strip (8) is fixed on one side of the first connecting strip (7); a second connecting strip (9) is fixed on the other side of the first connecting strip (8); the second connecting strip (9) is fixed on the pressing plate (6); third connecting strips (14) are symmetrically fixed on the pressing plate (6); each third connecting strip (14) is fixedly connected to one side of a second connecting strip (15); a connecting bolt (16) that can rotate freely on the second connecting strip (15) is passed through the other side of the second connecting strip (15); each connecting bolt (16) is connected to its corresponding connecting block (17) by a thread; the first connecting strip (7) and the connecting block (17) are respectively located on two opposite sides of the positioning frame (5); the third connecting strip (14) and the second connecting strip (9) are respectively located on two opposite sides of the pressing plate (6); the number of the third connecting strips (14), the second connecting strips (15), the connecting bolts (16) and the connecting blocks (17) are the same.

6. The hemodialysis room care hemostasis device according to claim 1, characterized in that: The pressure bag (18) is provided with a plurality of observation holes (19) distributed in an annular shape, the observation holes (19) penetrate the pressure bag (18), the fixed plate (4) is provided with a plurality of mounting holes (10) in an annular shape, a transparent plate (11) is fixed in the mounting holes (10); the transparent plate (11) and the observation holes (19) are adapted in position and size; the transparent plate (11) and the observation holes (19) are both located in the through hole area of ​​the fixed plate (4).

7. The hemodialysis room care hemostasis device according to claim 1, characterized in that: The other ends of the two binding straps (2) are detachably connected via Velcro.

8. The hemodialysis room care hemostasis device according to claim 1, characterized in that: The invention also comprises a support bar (22) fixed to the other end of one binding strap (2), one side of the support bar (22) being symmetrically fixedly connected to one end of two connecting ropes (23), at least two protective covers (25) being fixed to the other end of the other binding strap (2), each protective cover (25) being provided with a limit column (26), a wire take-up roller (28) and a brake block (27), one end of the limit column (26) being fixed to the other binding strap (2), the other end of the limit column (26) being provided with a brake block (27) which can only slide along the length direction of the limit column (26) and cannot rotate, a spring (30) being sleeved on the limit column (26), and the spring (30) being provided with a spring on both sides. The ends are respectively abutted against another binding belt (2) and one end of a brake block (27); the other end of one end of the brake block (27) is meshedly connected with one end of a take-up roller (28); one end of the take-up roller (28) is rotated and limited in the protective cover (25); the other end of the rotating column (29) passes through the protective cover (25) and is connected to the rotating knob; a sliding hole is opened on the take-up roller (28); a rotating column (29) passing through the sliding hole is slidably provided in the sliding hole; the other end of the connecting rope (23) is connected and wound around the outside of the take-up roller (28); when the rotating column (29) pushes the brake block (27), the brake block (27) is separated from the take-up roller (28).

9. A hemodialysis room care hemostasis device as claimed in claim 8, characterized in that: The brake block (27) is provided with a cylindrical cavity (32) with a non-circular cross section, and the other end of the limiting column (26) is provided with a cylindrical block (31) with a cross section matching the cylindrical cavity (32) in the brake block (27), the height of the cylindrical block (31) is less than the height of the cylindrical cavity (32), and the cylindrical block (31) is arranged in the cylindrical cavity (32); the top of the brake block (27) and the bottom of the take-up roller (28) are both fixed with ring-shaped wedge-shaped teeth, and the brake block (27) and the take-up roller (28) are connected by a plurality of wedge-shaped teeth; a sliding groove (34) is provided on the inner wall of the sliding hole, and a sliding block (33) is fixed on the outer side of the rotating column (29), and the slider (33) is slidably arranged in the sliding groove (34).

10. The hemodialysis room care hemostasis device according to claim 8, characterized in that: At least two guide rollers (24) are symmetrically fixed on the other binding belt (2), the number of the guide rollers (24) is the same as the number of the connecting ropes (23), and each connecting rope (23) is arranged on a corresponding guide roller (24).

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