Adjustable wound fixing device after permanent pacemaker implantation

Abstract

The utility model discloses an adjustable wound fixing device after permanent pacemaker implantation, and relates to the technical field of wound fixing after permanent pacemaker implantation. The technical problem that an existing wound fixing device used after the permanent pacemaker operation does not have the function of limiting the arm abduction range, and wound recovery is likely to be affected is solved. According to the technical scheme, the adjustable wound fixing device after permanent pacemaker implantation comprises a fixing device body and further comprises a rear chest extension piece, a front chest extension piece, axilla belts, arm belts, a limiting assembly and a pressurizing assembly; according to the adjustable wound fixing device after implantation of the permanent pacemaker, arm abduction can be effectively prevented through the limiting assembly, a wound can be conveniently pressurized and fixed on the same day after implantation through the pressurizing assembly, bleeding is prevented, the device is provided with multiple adjusting structures, the flexibility is high, the applicability is wide, the arm movement range of a patient can be effectively limited, and the practicability is high. Therefore, the implantation effect of the permanent pacemaker is greatly guaranteed, and wound recovery is facilitated.

Description

Technical Field

[0001] The utility model relates to the technical field of wound fixation after permanent pacemaker implantation, in particular to an adjustable wound fixation device after permanent pacemaker implantation. Background Art

[0002] Permanent pacemakers can treat various serious arrhythmias that affect myocardial pump function. Its implantation generally uses the cephalic vein as the access point. The cephalic vein is located in the gap between the deltoid and pectoralis major muscles. After finding the cephalic vein, use a small sharp knife or ophthalmic eyelid to cut the vein, and then insert the endocardial electrode into the vein and push it forward. The wound fixation device is a key tool for postoperative recovery. However, in actual use, the existing wound fixation device for permanent pacemakers after surgery generally adopts a simple strap design. For some active patients, they tend to like to lift the arm on the wound side, which can easily cause wound bleeding or even electrode dislocation during the abduction movement, which seriously affects postoperative recovery. Utility Model Content

[0003] The purpose of the utility model is to provide an adjustable permanent pacemaker post-implantation wound fixation device to solve the problem in the above background technology that the existing permanent pacemaker post-implantation wound fixation device does not have the function of limiting the arm abduction range, which easily affects wound recovery.

[0004] To achieve the above-mentioned purpose, the utility model provides the following technical solutions: an adjustable permanent pacemaker post-implantation wound fixation device, comprising a fixation device body, and also comprising a rear chest extension piece, a front chest extension piece, an axillary band, an arm band, a restriction component, and a pressurizing component; the back of the fixation device body is connected to the rear chest extension piece, the front of the fixation device body is connected to the front chest extension piece, the right side of the rear chest extension piece is connected to the axillary band, the lower end of the fixation device body is provided with an arm band, the front of the front chest extension piece is provided with a restriction component, and the front of the fixation device body is provided with a pressurizing component.

[0005] Preferably, adjustable axillary straps and arm straps are provided to facilitate users to adjust the wearing according to personal needs. The limiting component provided can effectively prevent arm abduction, and the pressurizing component provided can facilitate pressurized fixation of the wound on the day after implantation to prevent bleeding.

[0006] Preferably, a first Velcro hook surface is fixed to the front end of the armpit strap, the first Velcro hook surface is adhesively connected to the first Velcro fleece surface, the first Velcro hook surface is fixed to the front of the front chest extension piece, and the first Velcro hook surface is adhered to the first Velcro fleece surface, so that the armpit strap can be fixed to the front chest extension piece, thereby achieving fixation of the armpit area.

[0007] Preferably, a second Velcro hook surface is fixed to the front end of the armband, the second Velcro hook surface is adhesively connected to the second Velcro fleece surface, the second Velcro hook surface is fixed to the front of the fixing device body, and the second Velcro hook surface is adhered to the second Velcro fleece surface, so that the armband can be fixed to the fixing device body, thereby achieving fixation of the arm part.

[0008] Preferably, the restriction component includes a chest rope, an adjustment hole, and a button. The front of the front chest extension piece is connected to the chest rope, and the front of the chest rope is provided with adjustment holes at equal intervals. The front of the fixing device body is provided with a button, which is buckled into the adjustment hole to facilitate the restriction of one arm to prevent the implanted arm on that side from performing abduction activities.

[0009] Preferably, the limiting component also includes scale lines, and scale lines are arranged in front of the chest strap, so that the user can mark and record them conveniently so as to make corresponding adjustments according to the patient's condition.

[0010] Preferably, the pressurization component includes a placement bag, a zipper, and a sandbag. The placement bag is arranged in front of the fixing device body, the zipper is installed in front of the placement bag, and the inner side of the placement bag is connected to the sandbag. The opening and closing of the zipper facilitates the postoperative fixation of the sandbag to achieve pressurization treatment of the wound.

[0011] Preferably, a side pocket is provided on the left side of the fixing device body. By providing a side pocket on the side of the arm, the user can place the pacemaker information card there, thereby facilitating medical staff to quickly understand the situation.

[0012] Compared with the prior art, the beneficial effects of the utility model are:

[0013] 1. The adjustable permanent pacemaker post-implantation wound fixation device is convenient for users to adjust the wear according to personal needs by setting adjustable axillary straps and arm straps. It can also effectively prevent arm abduction through the restriction component, and pressurize the wound to prevent bleeding on the day after implantation through the pressurization component. Compared with traditional protection methods, the device has multiple adjustment structures, which is not only highly flexible and widely applicable, but also can effectively limit the range of motion of the patient's arm, thereby greatly ensuring the implantation effect of the permanent pacemaker and helping the recovery of the wound;

[0014] 2. The adjustable permanent pacemaker post-implantation wound fixation device has a chest rope in front of the fixation device body, and uses multiple adjustment holes to adjust the width according to the individual conditions of the patient. In addition, scale lines are provided on the surface of the chest rope, which is not only convenient for users to mark, but also can limit the excessive abduction of the upper arm on the implanted pacemaker side within six months after the permanent pacemaker is implanted, thereby avoiding electrode displacement. BRIEF DESCRIPTION OF THE DRAWINGS

[0015] Figure 1 The three-dimensional structure of the utility model is shown in FIG. Figure 1 ;

[0016] Figure 2 The three-dimensional structure of the utility model is shown in FIG. Figure 2 ;

[0017] Figure 3 This is a partial enlarged structural diagram of the utility model. Figure 1 ;

[0018] Figure 4 This is a partial enlarged structural diagram of the utility model. Figure 2 .

[0019] In the figure: 1. fixing device body; 2. rear chest extension piece; 3. front chest extension piece; 4. armpit strap; 5. first Velcro hook surface; 6. first Velcro fleece surface; 7. arm strap; 8. second Velcro hook surface; 9. second Velcro fleece surface; 10. restriction component; 11. pressurization component; 12. side pocket; 1001. chest rope; 1002. adjustment hole; 1003. button; 1004. scale line; 1101. placement bag; 1102. zipper; 1103. sandbag. DETAILED DESCRIPTION

[0020] See also Figure 1-3 The utility model provides a technical solution: an adjustable permanent pacemaker post-implantation wound fixation device, comprising a fixing device body 1, and also comprising a rear chest extension piece 2, a front chest extension piece 3, an axillary band 4, an armband 7, a limiting component 10, and a pressurizing component 11; the back of the fixing device body 1 is connected to the rear chest extension piece 2, the front of the fixing device body 1 is connected to the front chest extension piece 3, the right side of the rear chest extension piece 2 is connected to the axillary band 4, the lower end of the fixing device body 1 is provided with the armband 7, the front of the front chest extension piece 3 is provided with the limiting component 10, and the front of the fixing device body 1 is provided with the pressurizing component 11. By arranging the adjustable axillary band 4 and the armband 7, it is convenient for users to adjust the wearing according to personal needs, and the limiting component 10 can effectively prevent the arm from abduction, and by arranging The pressure-applying component 11 is convenient for applying pressure and fixing the wound on the day after the implantation to prevent bleeding. The front end of the axillary band 4 is fixed with a first Velcro hook surface 5, which is bonded and connected to the first Velcro fleece surface 6. The first Velcro hook surface 5 is fixed to the front of the front chest extension piece 3. The first Velcro hook surface 5 is adhered to the first Velcro fleece surface 6, so that the axillary band 4 can be fixed to the front chest extension piece 3, thereby achieving fixation of the armpit area. The front end of the armband 7 is fixed with a second Velcro hook surface 8, which is bonded and connected to the second Velcro fleece surface 9. The second Velcro hook surface 8 is fixed to the front of the fixing device body 1, and the armband 7 can be fixed to the fixing device body 1 by the second Velcro hook surface 8 being adhered to the second Velcro fleece surface 9, thereby achieving fixation of the arm area.

[0021] See also Figure 2-4 In this embodiment, the limiting component 10 includes a chest rope 1001, an adjustment hole 1002, and a button 1003. The front of the front chest extension piece 3 is connected with the chest rope 1001, and the front of the chest rope 1001 is provided with adjustment holes 1002 at equal intervals. The front of the fixing device body 1 is provided with a button 1003, and the button 1003 is buckled into the adjustment hole 1002 to facilitate the restriction of one arm to prevent the implanted arm on the side from performing abduction activities. The limiting component 10 also includes a scale line 1004, and the front of the chest rope 1001 is provided with a scale line 1004, and the scale line 1004 is convenient for the user to mark and mark The pressurizing component 11 includes a placement bag 1101, a zipper 1102, and a sandbag 1103. The placement bag 1101 is arranged in front of the fixing device body 1. The zipper 1102 is installed in front of the placement bag 1101. The inner side of the placement bag 1101 is connected with the sandbag 1103. The zipper 1102 is opened and closed to facilitate the postoperative fixation of the sandbag 1103 to achieve pressurization treatment of the wound. The left side of the fixing device body 1 is provided with a side pocket 12. The side pocket 12 is provided on the side of the arm to facilitate the user to place the pacemaker information card, so as to facilitate medical staff to quickly understand the situation.

[0022] When using the adjustable permanent pacemaker post-implantation wound fixation device of the present technical solution, firstly, put the fixing device body 1 on the upper arm on the pacemaker implanted side, then stick the first Velcro hook surface 5 on the first Velcro fleece surface 6, and the axillary band 4 can be fixed on the front chest extension piece 3, and then stick the second Velcro hook surface 8 on the second Velcro fleece surface 9, and the armband 7 can be fixed on the fixing device body 1, thereby achieving the fixation of the device.

[0023] Then, grab the end of the chest rope 1001 and buckle the corresponding adjustment hole 1002 onto the button 1003 as needed, so as to restrict one arm. Finally, put the sandbag 1103 into the accommodation bag 1101 and close the zipper 1102 to fix the sandbag 1103.

[0024] Through the above steps, the axillary strap 4 and the armband 7 are first used to facilitate the user to wear the fixing device body 1 according to personal needs, and then the limiting component 10 can effectively prevent the arm from being abducted, and finally the pressurizing component 11 can achieve pressure hemostasis on the wound to facilitate wound recovery.

[0025] Although embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that various changes, modifications, substitutions and variations may be made to the embodiments without departing from the principles and spirit of the present invention, and that the scope of the present invention is defined by the appended claims and their equivalents.

Claims

1. An adjustable permanent pacemaker post-implantation wound fixation device, comprising a fixation device body (1), characterized in that: The invention also comprises a rear chest extension piece (2), a front chest extension piece (3), an axillary band (4), an armband (7), a limiting component (10), and a pressurizing component (11); the rear side of the fixing device body (1) is connected to the rear chest extension piece (2), the front side of the fixing device body (1) is connected to the front chest extension piece (3), the right side of the rear chest extension piece (2) is connected to the axillary band (4), the lower end of the fixing device body (1) is provided with an armband (7), the front side of the front chest extension piece (3) is provided with a limiting component (10), and the front side of the fixing device body (1) is provided with a pressurizing component (11).

2. The adjustable permanent pacemaker post-implantation wound fixation device according to claim 1, characterized in that: A first Velcro hook surface (5) is fixed to the front end of the axillary strap (4), the first Velcro hook surface (5) is bonded and connected to the first Velcro fleece surface (6), and the first Velcro hook surface (5) is fixed to the front of the front chest extension piece (3).

3. The adjustable permanent pacemaker post-implantation wound fixation device according to claim 1, characterized in that: A second Velcro hook surface (8) is fixed to the front end of the armband (7), the second Velcro hook surface (8) is bonded and connected to the second Velcro fleece surface (9), and the second Velcro hook surface (8) is fixed to the front of the fixing device body (1).

4. The adjustable permanent pacemaker post-implantation wound fixation device according to claim 1, characterized in that: The limiting component (10) comprises a chest rope (1001), an adjustment hole (1002), and a button (1003); the front of the front chest extension piece (3) is connected to the chest rope (1001); the front of the chest rope (1001) is provided with adjustment holes (1002) at equal intervals; and the front of the fixing device body (1) is provided with a button (1003).

5. The adjustable permanent pacemaker post-implantation wound fixation device according to claim 4, characterized in that: The limiting component (10) further comprises a scale line (1004), and the scale line (1004) is arranged in front of the chest rope (1001).

6. The adjustable permanent pacemaker post-implantation wound fixation device according to claim 1, characterized in that: The pressurizing component (11) comprises a placement bag (1101), a zipper (1102), and a sandbag (1103). The placement bag (1101) is arranged in front of the fixing device body (1), the zipper (1102) is installed in front of the placement bag (1101), and the sandbag (1103) is connected to the inner side of the placement bag (1101).

7. The adjustable permanent pacemaker post-implantation wound fixation device according to claim 1, characterized in that: A side pocket (12) is provided on the left side of the fixing device body (1).

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