CN221013385U - Compression assembly after cardiac pacemaker implantation - Google Patents
Compression assembly after cardiac pacemaker implantation Download PDFInfo
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- CN221013385U CN221013385U CN202322179513.0U CN202322179513U CN221013385U CN 221013385 U CN221013385 U CN 221013385U CN 202322179513 U CN202322179513 U CN 202322179513U CN 221013385 U CN221013385 U CN 221013385U
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- belt
- strap
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- restraint
- binder
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- 230000006835 compression Effects 0.000 title claims abstract description 70
- 238000007906 compression Methods 0.000 title claims abstract description 70
- 230000000747 cardiac effect Effects 0.000 title claims abstract description 32
- 238000002513 implantation Methods 0.000 title claims abstract description 20
- 239000011230 binding agent Substances 0.000 claims abstract description 35
- 230000000452 restraining effect Effects 0.000 claims abstract description 24
- 239000004576 sand Substances 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 9
- 230000002980 postoperative effect Effects 0.000 claims description 5
- 229920000742 Cotton Polymers 0.000 claims description 3
- 239000004744 fabric Substances 0.000 claims description 3
- 206010040007 Sense of oppression Diseases 0.000 abstract description 14
- 230000000474 nursing effect Effects 0.000 abstract description 7
- 230000009286 beneficial effect Effects 0.000 abstract description 4
- 230000003699 hair surface Effects 0.000 description 14
- 206010052428 Wound Diseases 0.000 description 7
- 208000027418 Wounds and injury Diseases 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 230000008569 process Effects 0.000 description 6
- 230000008859 change Effects 0.000 description 4
- 230000036541 health Effects 0.000 description 3
- 102100026827 Protein associated with UVRAG as autophagy enhancer Human genes 0.000 description 2
- 101710102978 Protein associated with UVRAG as autophagy enhancer Proteins 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000009940 knitting Methods 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 206010063659 Aversion Diseases 0.000 description 1
- 206010071504 Wound haematoma Diseases 0.000 description 1
- 206010051373 Wound haemorrhage Diseases 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 206010003119 arrhythmia Diseases 0.000 description 1
- 230000006793 arrhythmia Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
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- Orthopedics, Nursing, And Contraception (AREA)
Abstract
The utility model discloses a compression assembly after cardiac pacemaker implantation, which comprises: the device comprises a pressing block, a binding belt and a restraint belt, wherein the restraint belt is connected with the binding belt, the pressing block is arranged on the outer surface of the binding belt, and the pressing block is used for pressing and pressing an affected part of a patient when the patient lies on the front surface of the patient; one surface of the pressing block is provided with a thorn surface, one surface of the binding belt is provided with a round surface, and the pressing block and the binding belt can be connected with each other through the thorn surface and the round surface; the restraining strap is capable of restraining the binder strap; wherein, the oppression piece covers the surface of binder area locally, and the thorn hair face sets up in the upper and lower both ends of oppression piece one side, and the thorn hair face is the strip square structure, and the circle hair face covers on the surface of binder area completely, and the oppression piece still is equipped with the skirt, and skirt and binder area are connected with the magic subsides. The utility model can ensure that the sandbag is not easy to shift, is beneficial to sustainable nursing of wound compression and is more convenient to wear and release.
Description
Technical Field
The utility model relates to the technical field of clinical medical supplies, in particular to a compression assembly after cardiac pacemaker implantation.
Background
At present, permanent cardiac pacemaker implantation is a safe and effective treatment for slow arrhythmias. In the process of implanting the cardiac pacemaker into a human body, an operation incision is needed to be made at the chest, then the cardiac pacemaker is implanted, the operation incision is sutured, and a large number of blood vessels are distributed at the operation incision of the chest, so that the possibility of blood seepage exists. Therefore, in order to reduce the occurrence of complications such as postoperative wound hemorrhage and hematoma and accelerate the healing speed of an operation incision, the conventional sandbag compression after the operation is often required to be carried out on a patient with a cardiac pacemaker in the current clinical treatment.
In addition, in the seventh edition of national higher school textbooks, national health committee 'fourteen five' planning textbooks, internal medicine nursing, also mention is made:
wound care and observation: the wound of the implantable pacer is locally pressurized by a sand bag for 6 hours, and the pressure is released for 5 minutes or the local pressure is wrapped every 2 hours. The skin at the incision is kept clean and dry, sterile dressing change is performed strictly, the dressing change is performed 1 time in 24 hours after operation, and the dressing change can be performed 1 time in 2-3 days without abnormality. Temporary pacemakers change dressings daily to prevent infection.
In summary, the requirement on portability required for the sandbag compression release of an implantable or temporary pacer is high, and in the prior art, conventional sandbag compression is easily displaced, which is unfavorable for sustainable nursing of wound compression, and is often in the form of a constraint garment or patient's gown, which is inconvenient to wear and release.
Disclosure of utility model
Aiming at the problems in the prior art, the utility model provides a compression assembly for a cardiac pacemaker after implantation operation, and after the compression assembly is used, a sand bag is not easy to shift, so that sustainable nursing of wound compression is facilitated, and wearing and releasing are more convenient.
In order to solve the technical problems, the utility model adopts the following technical scheme:
the application provides a compression assembly after cardiac pacemaker implantation, which comprises: the device comprises a pressing block, a binding belt and a restraint belt, wherein the restraint belt is connected with the binding belt, the pressing block is arranged on the outer surface of the binding belt, and the pressing block is used for pressing and pressing an affected part of a patient when the patient lies on the front surface of the patient; one surface of the pressing block is provided with a bristle surface, one surface of the binding belt is provided with a round bristle surface, and the pressing block and the binding belt can be connected with each other through the bristle surface and the round bristle surface; the restraining strap is configured to restrain the binder strap;
The compression block partially covers the outer surface of the binder band, the bristle surface is arranged at the upper end and the lower end of one surface of the compression block, the bristle surface is in a strip-shaped square structure, and the round bristle surface completely covers the outer surface of the binder band;
the compression block is also provided with a skirt part, and the skirt part is connected with the binder belt through a magic tape;
Above-mentioned scheme's design for the oppression piece can firmly bond on the binder, through the skirt of oppression piece and the design that the binder bonds, further strengthen its bonding firmness, make it be difficult for taking place to shift, do benefit to the sustainable nursing of wound oppression, through the design of binder and restraint strap, avoided traditional restraint clothing or patient's gown to bring integral dress and remove inconvenient problem, small, simple structure, the cover face is little, dress and remove more conveniently.
The utility model aims to solve the technical problems, and adopts the following further technical scheme:
Optionally, the cardiac pacemaker post-operation compression assembly, wherein the constraining bands comprise a first constraining band and a second constraining band, the constraining bands comprise a first binding band and a second binding band, when the first binding band and the second binding band are tiled, sides of the first binding band and the second binding band close to each other are fixedly connected through the first constraining band, and sides of the first binding band and the second binding band far away from each other are movably connected through the second constraining band;
By the design of the scheme, when the pressing assembly binds and tightens the affected part, only one part is movably connected, and the other parts are fixedly connected, so that the pressing assembly is convenient to clinically wear and release.
Optionally, the above-mentioned cardiac pacemaker post-operation pressing assembly, further, when the sides of the first binding band and the second binding band away from each other are movably connected through the second binding band, one end of the second binding band is fixedly connected with the first binding band, and the other end of the second binding band is detachably connected with the second binding band through a magic tape; or, one end of the second restraint strap is detachably connected with the first binding strap through the magic tape, and the other end of the second restraint strap is fixedly connected with the second binding strap.
Optionally, above-mentioned cardiac pacemaker is placed postoperative and is oppressed subassembly, still further, first restraint strap with the second restraint strap all sets up three at least, and the quantity of restraint strap sets up, can increase the health and retrain the pressurized area, improves local compression uncomfortable, does not influence pleasing to the eye simultaneously.
Optionally, the cardiac pacemaker post-implantation compression assembly is characterized in that the compression block is a sand bag filled with sand grains, and the sand bag is made of cotton-flax material, cotton cloth material or canvas material;
By the design of the scheme, the sand bag is firm and durable, has good air permeability and is beneficial to recovery of an affected part.
Optionally, the postoperative oppression subassembly is placed to above-mentioned cardiac pacemaker, wherein, restraint strap is flat woven elastic cord, knitting elastic cord or knitting elastic cord, can improve the tightening effect of binder belt for oppression subassembly better oppression in the health affected part.
Optionally, the cardiac pacemaker implantation postoperative compression assembly, wherein the bandwidth of the restraint strap is 0.5-3 cm, the bandwidth is preferably 2cm, and the two sides of the body are not pulled, so that the appearance is not affected.
Optionally, the cardiac pacemaker post-surgical compression assembly described above wherein the binder band is elastic; and/or the restraint strap has elasticity, so that the whole compression assembly can be more restrained and firmly restrained on the affected part of the body through the design.
The utility model has the beneficial effects that:
The binding belt and the binding belt are connected with each other, the compression block is arranged on the outer surface of the binding belt, when a patient lies on the front side of the binding belt, the compression block is used for pressing and compressing an affected part of the patient, the thorn hair surface is arranged on one surface of the compression block, the round hair surface is arranged on one surface of the binding belt, the compression block is connected with the binding belt through the thorn hair surface and the round hair surface, the compression block partially covers the outer surface of the binding belt, the thorn hair surface is arranged at the upper end and the lower end of one surface of the compression block, the thorn hair surface is in a strip-shaped square structure, the round hair surface completely covers the outer surface of the binding belt, the skirt part is connected with the binding belt through a magic tape, the compression block can be stably connected to the binding belt, the compression block is not easy to shift when the compression block is used, and the upper thorn hair surface and the lower thorn hair surface of the binding belt are in an adhesion design with the round hair surface of the binding belt, and the outer surface of the compression block partially covers the outer surface of the binding belt, so that the medical staff can conveniently and intermittently release the compression block, and the sustainable nursing of a wound is facilitated; in addition, through dismantling each other with the binder belt and being connected, realize that the patient is to the dress of oppression subassembly and remove, compare with traditional constraint clothing, saved the loaded down with trivial details of whole dress, more conveniently drew and remove, efficiency is higher.
The foregoing description is only an overview of the present utility model, and is intended to provide a better understanding of the present utility model, as it is embodied in the following description, with reference to the preferred embodiments of the present utility model and the accompanying drawings.
Drawings
Fig. 1 is a schematic view showing a compression assembly of the present utility model after a cardiac pacemaker implantation;
fig. 2 is a schematic perspective view of a compression assembly after a cardiac pacemaker implantation according to the present utility model;
the parts in the drawings are marked as follows:
Compression block 1, barbed surface 11, skirt 12, binder strip 2, round surface 21, first binder strip 22, second binder strip 23, restraining strip 3, first restraining strip 31, and second restraining strip 32.
Description of the embodiments
The following specific embodiments of the utility model are described in order to provide those skilled in the art with an understanding of the present disclosure. The utility model may be embodied in other different forms, i.e., modified and changed without departing from the scope of the utility model.
Examples
The application provides a compression assembly after cardiac pacemaker implantation, as shown in fig. 1 and 2, the compression assembly comprises a compression block 1, a binding belt 2 and a restraint belt 3, wherein the restraint belt 3 is connected with the binding belt 2, the compression block 1 is arranged on the outer surface of the binding belt 2, and when a patient lies on the front, the compression block 1 is used for compressing and pressing the affected part of the patient; a bristle surface 11 is arranged on one surface of the pressing block 1, a round bristle surface 21 is arranged on one surface of the binder belt 2, and the pressing block 1 and the binder belt 2 can be connected with each other through the bristle surface 11 and the round bristle surface 21; the restraining strap 3 is capable of restraining the binder strap 2;
Wherein, the compression block 1 partially covers the outer surface of the binder 2, the bristle surface 11 is arranged at the upper and lower ends of one surface of the compression block 1, the bristle surface 11 is in a strip square structure, and the round bristle surface 21 completely covers the outer surface of the binder 2;
the compression block 1 is also provided with a skirt 12, and the skirt 12 is connected with the binder strip 2 through a magic tape.
Above-mentioned embodiment for the oppression piece can firmly bond on the binder, through the design that skirt and binder of oppression piece bond, further strengthen its bonding firmness, make it be difficult for taking place the aversion more, do benefit to the sustainable nursing of wound oppression, through the design of binder and restraint belt, avoided the integral dress that traditional restraint clothing or patient's gown brought with remove inconvenient problem, small, simple structure covers the face little, dress and remove more conveniently.
In this embodiment, the restraining strip 3 includes a first restraining strip 31 and a second restraining strip 32, the strap 2 includes a first strap 22 and a second strap 23, when the first strap 22 and the second strap 23 are laid flat, the sides of the first strap 22 and the second strap 23 close to each other are fixedly connected by the first restraining strip 31, and the sides of the first strap 22 and the second strap 23 far from each other are movably connected by the second restraining strip 32.
Above-mentioned embodiment for the oppression subassembly is when binding up and tighten the affected part, and only one is swing joint, and the other is fixed connection, makes its clinical dress and release very convenient.
In this embodiment, it is further preferred that, when the sides of the first binding band 22 and the second binding band 23 away from each other are movably connected by the second binding band 32, one end of the second binding band 32 is fixedly connected to the first binding band 22, and the other end of the second binding band 32 is detachably connected to the second binding band 23 by a velcro; or, one end of the second restraining strip 32 is detachably connected with the first binding strip 22 through a magic tape, and the other end of the second restraining strip 32 is fixedly connected with the second binding strip 23.
In this embodiment, it is further preferable that at least three first restraining belts 31 and at least three second restraining belts 32 are provided.
According to the embodiment, the number of the restraint belts is set, so that the body restraint compression area can be increased, the local compression discomfort is improved, and the appearance is not influenced.
In this embodiment, the compression block 1 is a sand bag filled with sand grains, and the sand bag is made of cotton-flax material, cotton cloth material or canvas material.
The embodiment ensures that the sand bag is firm and durable, has good air permeability and is beneficial to recovery of the affected part.
In this embodiment, the restraining band 3 is a flat woven elastic band, a knitted elastic band or a knitted elastic band, preferably a knitted elastic band, and is more comfortable to wear.
According to the embodiment, the tightening effect of the binder belt can be improved, so that the pressing assembly can be pressed on an affected part of a human body better.
In this embodiment, the bandwidth of the constraint belt 3 is 0.5-3 cm, and the preferred bandwidth is 2 cm.
In the embodiment, the bandwidth is preferably 2cm, the two sides of the body are not tied, the appearance is not affected, and the discomfort of the binding and tightening part of the body is improved and relieved.
In this embodiment, the binder 2 has elasticity; and/or the restraining strip 3 has elasticity.
The above embodiment enables the whole compression assembly to be more tethered and more firmly tethered to the affected part of the body through the above design.
The working process and working principle of the utility model are as follows:
Compression assembly donning process: firstly, the compression assembly is unfolded and spread on a sickbed, the cardiac pacemaker is placed in a patient and is flatly laid on a second binding belt of the compression assembly, the integral position of the compression assembly is adjusted until the second binding belt is positioned below the cardiac pacemaker placed on an affected part, then, one hand of medical staff stretches the first binding belt with force and folds back to cover the cardiac pacemaker placed on the affected part, the first binding belt is in a tight stretching state, the other hand stretches and folds back the second binding belt with force and is bonded with a round hair surface on the first binding belt through a magic tape at one end of the second binding belt, and finally, the compression block is bonded on the first binding belt, and the method specifically comprises the following steps: the thorn hair surface of the pressing block is adhered to the round hair surface of the first binding belt, so that the pressing block is connected to the first binding belt to press and press the affected part of a patient;
The wearing process of the pressing assembly is clinically and repeatedly measured and calculated, and the wearing action can be completed within 2-3 minutes;
The compression assembly release process: firstly, placing a cardiac pacemaker on a sickbed, separating a compression block and a skirt part of the compression block from a first binding belt, then stabilizing the first binding belt by one hand of a medical staff, slowly retracting the first binding belt and the first binding belt, slowly separating a second binding belt from a round hair surface on the first binding belt by the other hand until the first binding belt and the first binding belt are completely released after the second binding belt and the first binding belt are completely separated, and finally drawing out a compression assembly from the back of the patient and folding and storing the compression assembly;
the pressing component release process is clinically and repeatedly measured and calculated, and the release action can be completed within about 1 minute.
The foregoing description is only illustrative of the present utility model and is not to be construed as limiting the scope of the utility model, and all equivalent structures made by the description of the utility model and the accompanying drawings, or direct or indirect application in other related technical fields, are equally included in the scope of the utility model.
Claims (8)
1. A cardiac pacemaker post-implantation compression assembly comprising: the device comprises a pressing block (1), a binding belt (2) and a restraint belt (3), wherein the restraint belt (3) is connected with the binding belt (2), the pressing block (1) is arranged on the outer surface of the binding belt (2), and when a patient lies on the front side, the pressing block (1) is used for pressing and pressing the affected part of the patient; one surface of the pressing block (1) is provided with a bristle surface (11), one surface of the binder belt (2) is provided with a round bristle surface (21), and the pressing block (1) and the binder belt (2) can be connected with each other through the bristle surface (11) and the round bristle surface (21); -the restraining strap (3) being able to restrain the binder strap (2);
The compression block (1) partially covers the outer surface of the binder belt (2), the bristle surface (11) is arranged at the upper end and the lower end of one surface of the compression block (1), the bristle surface (11) is of a strip-shaped square structure, and the round bristle surface (21) completely covers the outer surface of the binder belt (2);
The compression block (1) is also provided with a skirt (12), and the skirt (12) is connected with the binder belt (2) through a magic tape.
2. A cardiac pacemaker post-implantation compression assembly according to claim 1 wherein: the restraint strap (3) comprises a first restraint strap (31) and a second restraint strap (32), the binding strap (2) comprises a first binding strap (22) and a second binding strap (23), when the first binding strap (22) and the second binding strap (23) are tiled, the first binding strap (22) and the second binding strap (23) are close to each other and fixedly connected through the first restraint strap (31), and the first binding strap (22) and the second binding strap (23) are far away from each other and are movably connected through the second restraint strap (32).
3. A cardiac pacemaker post-implantation compression assembly according to claim 2 wherein: when the sides, far away from each other, of the first binding belt (22) and the second binding belt (23) are movably connected through the second restraining belt (32), one end of the second restraining belt (32) is fixedly connected with the first binding belt (22), and the other end of the second restraining belt (32) is detachably connected with the second binding belt (23) through a magic tape; or, one end of the second restraint strap (32) is detachably connected with the first binding strap (22) through a magic tape, and the other end of the second restraint strap (32) is fixedly connected with the second binding strap (23).
4. A cardiac pacemaker post-implantation compression assembly according to claim 2 wherein: at least three first restraint belts (31) and at least three second restraint belts (32) are arranged.
5. A cardiac pacemaker post-implantation compression assembly according to claim 1 wherein: the compressing block (1) is a sand bag filled with sand grains, and the sand bag is made of cotton-flax materials, cotton cloth materials or canvas materials.
6. A cardiac pacemaker post-implantation compression assembly according to claim 1 wherein: the restraint belt (3) is a flat woven elastic belt, a knitted elastic belt or a knitted elastic belt.
7. A cardiac pacemaker post-implantation compression assembly according to claim 6 wherein: the bandwidth of the restraint strap (3) is 0.5-3 cm.
8. A cardiac pacemaker implantation post-operative compression assembly as claimed in claim 1 wherein: the binder strip (2) has elasticity; and/or the restraining strip (3) has elasticity.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202322179513.0U CN221013385U (en) | 2023-08-11 | 2023-08-11 | Compression assembly after cardiac pacemaker implantation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202322179513.0U CN221013385U (en) | 2023-08-11 | 2023-08-11 | Compression assembly after cardiac pacemaker implantation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN221013385U true CN221013385U (en) | 2024-05-28 |
Family
ID=91167235
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202322179513.0U Active CN221013385U (en) | 2023-08-11 | 2023-08-11 | Compression assembly after cardiac pacemaker implantation |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN221013385U (en) |
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2023
- 2023-08-11 CN CN202322179513.0U patent/CN221013385U/en active Active
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