Restraint tool for internal arteriovenous fistula patient in hemodialysis

Abstract

The utility model discloses a restraining tool for a hemodialysis internal arteriovenous fistula patient, and relates to the technical field of medical instruments. A limiting groove is formed in the rear side of the side wall of the restraint sleeve body, a first limiting belt, a second limiting belt and a strapping belt are arranged below the limiting groove, the two ends of the first limiting belt and the two ends of the second limiting belt are fixedly connected with the outer side wall of the restraint sleeve body, the strapping belt is located on the inner side of the first limiting belt, and the second limiting belt is located on the front side of the first limiting belt. An outer fixing belt is arranged on the inner side of the second limiting belt. When the restraint sleeve is used, the restraint sleeve body is arranged on the hand of a patient in a sleeving mode, the thumb of the patient is placed in the limiting groove, the strapping tape penetrates through the two auxiliary limiting tapes, and then the device and the hand of the patient are fixed; meanwhile, the external fixing band is fixedly connected with a bed body where the patient is located, so that the device and the hand of the patient are well limited, the device is prevented from moving in the using process, and internal arteriovenous fistula blocking of the front arm of the hemodialysis patient is avoided.

Description

Technical Field

[0001] This utility model relates to the field of medical device technology, and in particular to a restraint device for arteriovenous fistula patients undergoing hemodialysis. Background Technology

[0002] Arteriovenous fistulas (AVFs) in hemodialysis are vital vascular access points for maintaining the lives of hemodialysis patients. They surgically connect an artery and a vein, providing a stable and sufficient blood supply for dialysis treatment. However, during dialysis, the patient's hand movements can accidentally impact or compress the fistula site, potentially leading to serious complications such as thrombosis, stenosis, or occlusion. Therefore, to protect the integrity and function of the fistula, ensure the smooth progress of dialysis treatment, and improve patient comfort, the use of restraints to limit the patient's hand movement is crucial. Proper use of restraints can effectively reduce the adverse effects of the patient's hand on the fistula site, ensuring the safety and effectiveness of dialysis treatment.

[0003] However, existing glove-type restraints are all applied to the wrist, and the restraint position is too high, causing them to slide up and down during use, which can easily lead to occlusion of arteriovenous fistulas in the forearm of hemodialysis patients. Furthermore, most existing glove-type restraints are disposable, and the materials are not easy to sterilize and cannot be recycled. Additionally, existing glove-type restraints are designed with five fingers spread apart, making them inconvenient for patients with different hand shapes. Therefore, this application proposes a restraint device for hemodialysis patients with arteriovenous fistulas to solve the above problems. Utility Model Content

[0004] The purpose of this invention is to provide a restraint device for arteriovenous fistula patients undergoing hemodialysis, thereby solving the technical problems mentioned in the background art.

[0005] To achieve the above objectives, this utility model provides the following technical solution: a restraint device for arteriovenous fistula patients undergoing hemodialysis, comprising a restraint sleeve body, a limiting groove being formed on the rear side wall of the restraint sleeve body, a first limiting band, a second limiting band, and a binding band being provided below the limiting groove, both ends of the first limiting band and the second limiting band being fixedly connected to the outer side wall of the restraint sleeve body, the binding band being located inside the first limiting band, the second limiting band being located in front of the first limiting band, and an external fixing band being provided inside the second limiting band.

[0006] Preferably, two auxiliary limiting bands are fixedly connected to the outer side wall of the constraint sleeve body. Both auxiliary limiting bands are fixedly connected to the outer side wall of the constraint sleeve body, and the two auxiliary limiting bands are symmetrically arranged on both sides of the limiting groove.

[0007] Preferably, two pipe adjustment bands are fixedly connected to the side of the outer wall of the constraint sleeve body away from the auxiliary limiting band, and the two pipe adjustment bands are connected to the constraint sleeve body at the left and right sides of the limiting groove, respectively.

[0008] Preferably, the main body of the constraint sleeve is made of a soft material.

[0009] Compared with related technologies, the restraint device for hemodialysis arteriovenous fistula patients provided by this utility model has the following advantages:

[0010] Beneficial effects:

[0011] 1. This utility model provides a restraint device for hemodialysis patients with arteriovenous fistulas. In this solution, a limiting groove is provided on the main body of the restraint sleeve. When in use, the main body of the restraint sleeve is put on the patient's hand, and the patient's thumb is placed in the limiting groove. Then, the device and the position of the patient's hand are fixed by passing a strap through two auxiliary limiting straps. At the same time, the external fixing strap is used to fix the device to the bed where the patient is located, thereby playing a good limiting role for the device and the patient's hand, and also preventing the device from moving during use, thus preventing the arteriovenous fistula in the forearm of the hemodialysis patient from becoming blocked.

[0012] 2. This utility model provides a restraint device for patients with arteriovenous fistulas undergoing hemodialysis. The main body of the restraint sleeve adopts a tubular structure, and the four fingers of the finger part are connected, which can be adapted to different hand shapes, greatly improving the practicality of the device. At the same time, the device is equipped with a tube opening adjustment strap, which allows for adjustment of the size of the front port of the restraint sleeve main body through the connection of two tube opening adjustment straps, thereby improving the device's restraint effect on the patient's hand position. In addition, the binding strap, external fixation strap and restraint sleeve main body of this device are all detachable, which facilitates disinfection and sterilization, thereby enabling the device to be reused and reducing the economic burden on patients. Attached Figure Description

[0013] Figure 1 This is a three-dimensional structural diagram of the present invention;

[0014] Figure 2 This is another three-dimensional structural diagram of the present invention;

[0015] Figure 3 for Figure 2 Enlarged view of a portion of point A in the middle.

[0016] In the diagram: 1. Constraint sleeve body; 2. Limiting groove; 3. Auxiliary limiting band; 4. Bundling band; 5. External fixing band; 6. Limiting band one; 7. Limiting band two; 8. Pipe opening adjustment band. Detailed Implementation

[0017] The technical solutions of the present utility model will be clearly and completely described below with reference to the accompanying drawings of the embodiments of the present utility model. Obviously, the described embodiments are only some embodiments of the present utility model, and not all embodiments. All other embodiments obtained by those skilled in the art based on the embodiments of the present utility model without creative effort are within the protection scope of the present utility model.

[0018] Please see Figure 1-3 This utility model provides a technical solution: a restraint device for hemodialysis patients with arteriovenous fistulas, including a restraint sleeve body 1. A limiting groove 2 is opened on the rear side of the side wall of the restraint sleeve body 1. A first limiting band 6, a second limiting band 7, and a binding band 4 are arranged below the limiting groove 2. Both ends of the first limiting band 6 and the second limiting band 7 are fixedly connected to the outer side wall of the restraint sleeve body 1. The binding band 4 is located inside the first limiting band 6, and the second limiting band 7 is located in front of the first limiting band 6. An external fixing band 5 is arranged inside the second limiting band 7. The device is bound to the patient's hand using the binding band 4, and then fixedly connected to the patient's bed using the external fixing band 5. This provides a good restraint effect on the device and the patient's hand, and also prevents the device from moving during use, thus preventing the arteriovenous fistula in the forearm of the hemodialysis patient from becoming blocked.

[0019] Two auxiliary limiting straps 3 are fixedly connected to the outer side wall of the restraint sleeve body 1. Both auxiliary limiting straps 3 are fixedly connected to the outer side wall of the restraint sleeve body 1, and the two auxiliary limiting straps 3 are symmetrically arranged on both sides of the limiting groove 2. When in use, the binding strap 4 is used to pass through the two auxiliary limiting straps 3 in sequence and tighten them to the rear port of the limiting groove 2. The binding strap 4 is located at the patient's wrist, thereby ensuring that the device is firmly bound to the patient's hand.

[0020] Two tube adjustment bands 8 are fixedly connected to the side of the outer wall of the restraint sleeve body 1 away from the auxiliary limiting band 3. The two tube adjustment bands 8 are connected to the restraint sleeve body 1 at the left and right sides of the limiting groove 2 respectively. The size of the front port of the restraint sleeve body 1 is adjusted by the two tube adjustment bands 8, thereby improving the limiting effect of the device on the position of the patient's hand.

[0021] The main body of the restraint sleeve 1 is made of soft material, which improves the comfort of using the device.

[0022] Working Principle: During use, the restraint sleeve body 1 is placed over the patient's hand, with the patient's thumb positioned within the limiting groove 2. The binding strap 4 is then passed sequentially through two auxiliary limiting straps 3 and secured to the rear end of the limiting groove 2. The binding strap 4 is positioned at the patient's wrist, ensuring the device is firmly bound to the patient's hand. The patient's other four fingers protrude from the front end of the restraint sleeve body 1. The size of the front end of the restraint sleeve body 1 is adjusted using two adjusting straps 8, thereby improving the device's restraint effect on the patient's hand. Simultaneously, the external fixation strap 5 is used to securely connect to the patient's bed, effectively restraining both the device and the patient's hand and preventing movement of the device during use, thus avoiding arteriovenous fistula occlusion in the forearm of hemodialysis patients. The binding strap 4, external fixation strap 5, and restraint sleeve body 1 are all detachable, facilitating subsequent cleaning and enabling device reuse. The use of a soft material for the restraint sleeve body 1 enhances user comfort.

Claims

1. A restraint for a patient with an arteriovenous fistula for haemodialysis, comprising a restraint sleeve body (1), characterised in that: The constraint sleeve body (1) is provided with a limiting groove (2) on the rear side of the side wall, a limiting band one (6), a limiting band two (7) and a binding band (4) are arranged below the limiting groove (2), the limiting band one (6) and the limiting band two (7) are fixedly connected with the outer side wall of the constraint sleeve body (1), the binding band (4) is located on the inner side of the limiting band one (6), the limiting band two (7) is located on the front side of the limiting band one (6), and the inner side of the limiting band two (7) is provided with an outer fixing band (5).

2. The patient restraint for hemodialysis arteriovenous fistula patients of claim 1, wherein: The outer side wall of the constraint sleeve body (1) is fixedly connected with two auxiliary limiting bands (3), the two auxiliary limiting bands (3) are fixedly connected with the outer side wall of the constraint sleeve body (1), and the two auxiliary limiting bands (3) are symmetrically arranged on the two sides of the limiting groove (2).

3. The patient restraint for hemodialysis arteriovenous fistula patients of claim 2, wherein: The outer side wall of the constraint sleeve body (1) is fixedly connected with two pipe opening adjusting bands (8) away from the auxiliary limiting bands (3), and the two pipe opening adjusting bands (8) are respectively located on the left and right sides of the limiting groove (2).

4. The hemodialysis arteriovenous fistula patient restraint of claim 1, wherein: The constraint sleeve body (1) is made of soft material.

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