Wearable cardiac pacemaker post-implantation compression hemostat

Abstract

The utility model relates to a wearable cardiac pacemaker after-implantation compression hemostat which comprises a front blocking back and a rear blocking back, the two sides of the front blocking back are fixedly connected with A fixing assemblies, the upper surface of the front blocking back is fixedly connected with a B fixing assembly, the front face of the front blocking back is provided with a groove, and the back face of the front blocking back is provided with an A fixing assembly and a B fixing assembly. A groove is formed in the fixing assembly A, a connecting assembly is fixedly connected to the interior of the groove, a pressurizing assembly is fixedly connected to the upper surface of the connecting assembly, the fixing assembly A comprises a bandage A, and one end of the bandage A is fixedly connected to one side of the front blocking back. By means of the connecting assembly, compression hemostasis can be conducted through a sandbag in the connecting assembly during hemostasis, operation is easy and convenient, when a wound needs to be checked, the connecting assembly can be rapidly detached, the wound can be rapidly watched, and by means of the arranged pressurizing assembly, when hemostasis compression is conducted on the wound, the pressurizing assembly can be controlled according to the needed force; and the pressurizing assembly compresses the wound to stop bleeding.

Description

Technical Field

[0001] The utility model relates to the technical field of medical devices, in particular to a compression hemostat for wearable cardiac pacemaker implantation. Background Art

[0002] A pacemaker is an electronic therapeutic instrument implanted in the body. It emits electrical pulses powered by a battery through a pulse generator, which are conducted through wire electrodes to stimulate the myocardium in contact with the electrodes, causing the heart to be excited and contracted, thereby achieving the purpose of treating heart dysfunction caused by certain arrhythmias. Since the first pacemaker was implanted in the human body in 1958, pacemaker manufacturing technology and processes have developed rapidly, and its functions have become increasingly perfect. While pacemakers have successfully treated slow arrhythmias and saved the lives of thousands of patients, pacemakers have also begun to be used to treat tachyarrhythmias and non-electrocardiologic diseases, such as preventing paroxysmal atrial tachyarrhythmias, carotid sinus syncope, and biventricular synchronous treatment of drug-refractory congestive heart failure.

[0003] Currently, salt bags / sand bags are commonly used to compress and stop bleeding. However, the process is limited by the patient's cooperation, body shape, subcutaneous fat thickness, body position changes, etc., which often causes the sand bags / salt bags to shift and slide, resulting in uneven force on the local surgical incision, excessive local compression leading to pressure injuries, or ineffective compression after displacement, resulting in subcutaneous bleeding and pocket infection, etc. Moreover, during compression, in order to ensure the compression effect, the patient's shoulder joints and arms are often completely unable to move, and the comfort level is also reduced. Utility Model Content

[0004] 1. Technical issues to be resolved

[0005] In order to solve the above-mentioned problems of the prior art, the utility model provides a wearable postoperative compression hemostat for pacemaker implantation to solve the problem of displacement and sliding of sandbags / salt bags, which may cause uneven force on the local surgical incision, excessive local compression force leading to pressure injury, or ineffective compression after displacement resulting in subcutaneous bleeding and pocket infection, etc. Moreover, during compression, in order to ensure the compression effect, the patient's shoulder joint and arm are often completely unable to move.

[0006] (II) Technical solution

[0007] In order to achieve the above purpose, the main technical solutions adopted by the utility model are:

[0008] A wearable cardiac pacemaker post-implantation compression hemostat comprises a front back shield and a rear back shield, both sides of the front back shield are fixedly connected with an A fixing component, the upper surface of the front back shield is fixedly connected with a B fixing component, the front side of the front back shield is provided with a groove, the interior of the groove is fixedly connected with a connecting component, and the upper surface of the connecting component is fixedly connected with a pressurizing component.

[0009] The A fixing assembly includes an A strap, one end of which is fixedly connected to one side of the front guard, and one side of the upper surface of the A strap is fixedly connected to an A Velcro.

[0010] The other side of the upper surface of the A strap is fixedly connected with the B Velcro, the outer surface of the A strap is sleeved with an A clip, and one end of the A clip is fixedly connected to one side of the rear guard.

[0011] The B fixing assembly includes a B strap, one end of which is fixedly connected to the upper surface of the front windshield, and one side of the upper surface of the B strap is fixedly connected to a C Velcro.

[0012] The other side of the upper surface of the B strap is fixedly connected with a D Velcro, and the outer surface of the B strap is sleeved with a B clip, and one end of the B clip is fixedly connected to the upper surface of the rear guard.

[0013] The connecting assembly comprises a chain, the outer surface of the chain is fixedly connected to the inside of the groove, the inner side wall of the chain is fixedly connected to a placement bag, and the inside of the chain is meshed with a zipper head.

[0014] The pressurizing component includes an air cushion, the bottom of which is fixedly connected to the upper surface of the connecting component, an air bag is fixedly connected inside the air cushion, an air intake pipe is fixedly connected to one side of the air cushion, and a squeezing ball is fixedly connected to one end of the air intake pipe.

[0015] A hole is provided on the upper surface of the air cushion, an air outlet pipe is fixedly connected inside the hole, and a rubber plug is inserted inside the air outlet pipe.

[0016] (III) Beneficial effects

[0017] The beneficial effects of the utility model are as follows: through the setting of the connecting component, when stopping bleeding, the sandbag in the connecting component can be used for compression to stop bleeding, the operation is simple and convenient, and when it is necessary to check the wound, the connecting component can be quickly disassembled to check the wound, and through the setting of the pressurizing component, when pressing the wound to stop bleeding, the pressurizing component can be controlled according to the required force to press the wound to stop bleeding. BRIEF DESCRIPTION OF THE DRAWINGS

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

[0019] Figure 2 This is a schematic diagram of the structure of the pressurizing component of the utility model;

[0020] Figure 3 This is a schematic diagram of the structure of the connection assembly of the utility model;

[0021] Figure 4This is a schematic diagram of the structure of the fixed component A of the utility model;

[0022] Figure 5 This is a schematic diagram of the structure of the B fixing component of the utility model.

[0023] [Description of Reference Numerals]

[0024] 1. Front back guard; 2. A fixing component; 201. A strap; 202. A Velcro; 203. B Velcro; 204. A snap ring; 3. Rear back guard; 4. B fixing component; 401. B strap; 402. C Velcro; 403. D Velcro; 404. B snap ring; 5. Connecting component; 501. Chain; 502. Storage bag; 503. Zipper head; 6. Pressurizing component; 601. Air cushion; 602. Air bag; 603. Inlet pipe; 604. Squeeze ball; 605. Exhaust pipe; 606. Rubber plug. DETAILED DESCRIPTION

[0025] In order to better explain the present invention and facilitate understanding, the present invention is described in detail below through specific implementation modes in conjunction with the accompanying drawings.

[0026] Please refer to Figures 1 to 5 As shown, the wearable postoperative compression hemostatic device for pacemaker implantation of the utility model comprises a front back shield 1 and a rear back shield 3, both sides of the front back shield 1 are fixedly connected with an A fixing component 2, the upper surface of the front back shield 1 is fixedly connected with a B fixing component 4, the front side of the front back shield 1 is provided with a groove, the interior of the groove is fixedly connected with a connecting component 5, and the upper surface of the connecting component 5 is fixedly connected with a pressurizing component 6. In the actual implementation process, the front back shield 1 is worn on the chest, the A strap 201 is inserted into the A clip 204, and the rear back shield 3 is carried on the back, then, according to the width of the person's body, the A strap 201 is placed in a suitable position and fixed with the A Velcro 202 and the B Velcro 203, then, the B strap 401 is inserted into the B clip 404, and according to the shoulder width of the person, the B strap 401 is placed in position, and the C Velcro 402 and the D Velcro 403 are used to fix it. 03 is used for fixation, and then the sandbag is placed in the placement bag 502, the zipper head 503 is pulled, the chain 501 is merged, and the sandbag is placed on the wound of the person to apply pressure to stop bleeding, and then the squeezing ball 604 is squeezed to take in air from the air inlet pipe 603, inflate the air bag 602, and use the air cushion 601 to pressurize the placement bag 502 and the wound, and then, when the gas needs to be released, the rubber plug 606 is pulled out and the gas is released from the air outlet pipe 605.

[0027] Optionally, the A fixing component 2 includes an A strap 201, one end of which is fixedly connected to one side of the front back 1, and one side of the upper surface of the A strap 201 is fixedly connected to an A Velcro 202. In the actual implementation process, the A Velcro 202 is attached to the B Velcro 203 to play a fixing role.

[0028] Optionally, the other side of the upper surface of the A strap 201 is fixedly connected with a B Velcro 203, and the outer surface of the A strap 201 is sleeved with an A snap ring 204, and one end of the A snap ring 204 is fixedly connected to one side of the rear guard 3. In actual implementation, the A strap 201 is placed in a suitable position according to the width of the person's body, and is fixed by the A Velcro 202 and the B Velcro 203.

[0029] Optionally, the B fixing assembly 4 includes a B strap 401, one end of which is fixedly connected to the upper surface of the front back 1, and one side of the upper surface of the B strap 401 is fixedly connected to a C Velcro 402. In the actual implementation process, the C Velcro 402 is attached to the D Velcro 403 to play a fixing role.

[0030] Optionally, the other side of the upper surface of the B strap 401 is fixedly connected with a D Velcro 403, and the outer surface of the B strap 401 is sleeved with a B clip 404, and one end of the B clip 404 is fixedly connected to the upper surface of the rear guard 3. In the actual implementation process, the B strap 401 is inserted into the B clip 404, and the B strap 401 is placed in a position according to the shoulder width of the person, and is fixed by the C Velcro 402 and the D Velcro 403.

[0031] Optionally, the connection assembly 5 includes a chain 501, the outer surface of the chain 501 is fixedly connected to the inside of the groove, the inner wall of the chain 501 is fixedly connected to a placement bag 502, and the inside of the chain 501 is meshed with a zipper head 503. In actual implementation, a sandbag is placed in the placement bag 502, the zipper head 503 is pulled, the chain 501 is merged, and the sandbag is placed on the wound of the person to perform compression and hemostasis.

[0032] Optionally, the pressurizing component 6 includes an air cushion 601, the bottom of the air cushion 601 is fixedly connected to the upper surface of the connecting component 5, an air bag 602 is fixedly connected inside the air cushion 601, an air inlet pipe 603 is fixedly connected to one side of the air cushion 601, and a squeezing ball 604 is fixedly connected to one end of the air inlet pipe 603. In the actual implementation process, the squeezing ball 604 is squeezed to let air in from the air inlet pipe 603, and the air bag 602 is inflated, and the air cushion 601 is used to pressurize the placement bag 502 and the wound.

[0033] Optionally, a hole is formed on the upper surface of the air cushion 601, and an air outlet pipe 605 is fixedly connected to the inside of the hole, and a rubber plug 606 is inserted into the inside of the air outlet pipe 605. In the actual implementation process, when the gas needs to be released, the rubber plug 606 is pulled out and the gas is released from the air outlet pipe 605.

[0034] The above shows and describes the basic principle, main features and advantages of the utility model, and the standard parts used in the utility model can be purchased from the market, special-shaped parts can be customized according to the description and the drawings, and the specific connection methods of each part adopt mature conventional means such as bolts, rivets, welding, etc. in the prior art. Machinery, parts and equipment all adopt conventional models in the prior art, and the circuit connection adopts the conventional connection method in the prior art, which will not be described in detail here.

[0035] The above description is only an embodiment of the present invention, and does not limit the patent scope of the present invention. Any equivalent transformations made using the contents of the specification and drawings of the present invention, or directly or indirectly applied in the relevant technical field, are also included in the patent protection scope of the present invention.

Claims

1. A wearable cardiac pacemaker post-implantation compression hemostat, comprising a front back guard (1) and a rear back guard (3), characterized in that: Both sides of the front guard back (1) are fixedly connected to a fixing component A (2), the upper surface of the front guard back (1) is fixedly connected to a fixing component B (4), a groove is provided on the front side of the front guard back (1), a connecting component (5) is fixedly connected inside the groove, and a pressurizing component (6) is fixedly connected to the upper surface of the connecting component (5).

2. A wearable cardiac pacemaker post-implantation compression hemostatic device according to claim 1, characterized in that: The A fixing assembly (2) comprises an A binding strap (201), one end of the A binding strap (201) is fixedly connected to one side of the front guard (1), and one side of the upper surface of the A binding strap (201) is fixedly connected to an A Velcro (202).

3. A wearable cardiac pacemaker post-implantation compression hemostatic device according to claim 2, characterized in that: The other side of the upper surface of the A binding strap (201) is fixedly connected to a B Velcro (203), the outer surface of the A binding strap (201) is sleeved with an A clip (204), and one end of the A clip (204) is fixedly connected to one side of the rear guard (3).

4. A wearable cardiac pacemaker post-implantation compression hemostatic device according to claim 1, characterized in that: The B fixing assembly (4) comprises a B strap (401), one end of the B strap (401) is fixedly connected to the upper surface of the front guard (1), and one side of the upper surface of the B strap (401) is fixedly connected to a C Velcro (402).

5. A wearable cardiac pacemaker post-implantation compression hemostatic device according to claim 4, characterized in that: The other side of the upper surface of the B binding strap (401) is fixedly connected to a D Velcro (403), the outer surface of the B binding strap (401) is sleeved with a B clip (404), and one end of the B clip (404) is fixedly connected to the upper surface of the rear guard (3).

6. A wearable cardiac pacemaker post-implantation compression hemostatic device according to claim 1, characterized in that: The connection assembly (5) comprises a chain (501), the outer surface of the chain (501) is fixedly connected to the inside of the groove, the inner side wall of the chain (501) is fixedly connected to a placement bag (502), and the inside of the chain (501) is meshed with a zipper head (503).

7. The wearable cardiac pacemaker post-implantation compression hemostatic device according to claim 1, characterized in that: The pressurizing component (6) comprises an air cushion (601), the bottom of the air cushion (601) being fixedly connected to the upper surface of the connecting component (5), the interior of the air cushion (601) being fixedly connected to an air bag (602), one side of the air cushion (601) being fixedly connected to an air intake pipe (603), and one end of the air intake pipe (603) being fixedly connected to a squeezing ball (604).

8. A wearable cardiac pacemaker post-implantation compression hemostatic device according to claim 7, characterized in that: The upper surface of the air cushion (601) is provided with a hole, the interior of the hole is fixedly connected to an air outlet pipe (605), and the interior of the air outlet pipe (605) is plugged with a rubber plug (606).

Images