CN218960830U - Pacemaker postoperative incision compression device - Google Patents
Pacemaker postoperative incision compression device Download PDFInfo
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- CN218960830U CN218960830U CN202222194731.7U CN202222194731U CN218960830U CN 218960830 U CN218960830 U CN 218960830U CN 202222194731 U CN202222194731 U CN 202222194731U CN 218960830 U CN218960830 U CN 218960830U
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- cloth
- belt
- strap
- compression device
- arm
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Abstract
The utility model discloses a pacemaker postoperative incision compression device which is characterized by comprising an I-shaped belt body, wherein the upper part of the belt body is provided with a shoulder belt extending leftwards and rightwards, the lower part of the belt body is provided with an arm belt extending leftwards and rightwards, the outside of the arm belt is provided with a restraint belt, the joint of the shoulder belt, the arm belt and the belt body is provided with a compression cloth, and the compression cloth is internally provided with a compression device. The pressing device is characterized in that triangular cover cloth is arranged on the pressing cloth, and a sand bag sleeve is arranged under the cover cloth. The three corners of the covering cloth are provided with buckles. The sand bag is sleeved with an opening for taking and placing the sand bag. The compression cloth and the cover cloth are made of transparent breathable materials, and are preferably hexagonal mesh fabrics. The restraint strap, the arm strap and the shoulder strap are made of flexible skin-friendly materials, and are preferably OK skin-friendly fabrics. The shoulder strap is characterized in that the two ends of the shoulder strap are provided with first connecting parts which are matched with each other, the two ends of the arm strap are provided with second connecting parts which are matched with each other, and the two ends of the restraint strap are provided with third connecting parts which are matched with each other.
Description
Technical Field
The technical scheme relates to a medical auxiliary tool, in particular to a pacemaker postoperative incision compression device.
Background
It is well known that permanent cardiac pacemaker implantation is widely used in the treatment of heart diseases such as bradycardia, heart failure, and malignant arrhythmia. Common complications after permanent cardiac pacemaker implantation include electrode displacement, capsular bag hematoma, capsular bag infection, subcutaneous blood stasis, and the like. Thus, pacemaker post-operative care is particularly important to reduce related complications. At present, a common method for hemostasis at the implantation incision of a pacemaker is to use a sand bag for hemostasis by compression, for example, a compression bag of 0.5-1.0 kg is commonly used for compressing the incision for 6-12 hours in clinic, and a patient is absolute in bed for 1-3 days, but the method is easy to shift and slide down the compression bag, so that postoperative complications such as bleeding, subcutaneous blood stasis, swelling of operative limbs and the like at the implantation incision of the pacemaker are caused, and the improper movement of the shoulder joint is also the main cause of electrode shift.
Through patent retrieval, the problem of oppression bag landing has been solved to some technical scheme, like chinese patent CN202021391707.7 permanent pacemaker bag oppression undershirt, has utilized wearing undershirt and fixed the oppression gasbag on the back of the body to oppress the incision, has avoided the landing of oppression equipment, but still has following problem: 1. the vest type device is worn by a patient, so that the patient is weak after the operation, the patient is inconvenient, and the condition of secondary injury of wounds, displacement of pacemakers and the like can be caused by the excessive limb movement; 2. because the pacemaker is generally arranged at the lower part of the left or right collarbone (most commonly on the left side), in order to avoid the influence of the stretching of the deltoid muscle of the arm on the pacemaker, the arm abduction activity is usually avoided as much as possible after operation, but part of patients are used to lift hands, and the patients can feel uninteresting to hold some objects by hands, so that the rehabilitation is influenced. Even part of patients stretch arms in the dream, seriously affecting postoperative recovery; 3. the study shows that the balloon is generally spherical after being inflated, the surface contacted with the incision is arc-shaped, and the contact surface is in point contact although the pressure is certain, so that the whole section can not be well pressed, and the crushing effect is poor.
Disclosure of Invention
The utility model aims to overcome the defects of the prior art, and provides the pacemaker postoperative incision compression device which can assist in compressing incisions after a permanent cardiac pacemaker implantation operation and effectively reduce complications after the pacemaker operation. The specific scheme is as follows:
the utility model provides a pacemaker postoperative incision compression device, characterized by includes the band body of I-shaped, and band body upper portion is for the baldric of extension about, and band body lower part is the arm area of extension about, and the arm area out-of-band is equipped with restraint strap, and baldric, arm area and band body junction are equipped with the oppression cloth, are equipped with the oppression device in the oppression cloth.
The pressing device is characterized in that triangular cover cloth is arranged on the pressing cloth, and a sand bag sleeve is arranged under the cover cloth. The three corners of the covering cloth are provided with buckles.
The sand bag is sleeved with an opening for taking and placing the sand bag.
The compression cloth and the cover cloth are made of transparent breathable materials, and are preferably hexagonal mesh fabrics.
The restraint strap, the arm strap and the shoulder strap are made of flexible skin-friendly materials, and are preferably OK skin-friendly fabrics.
The shoulder strap is characterized in that the two ends of the shoulder strap are provided with first connecting parts which are matched with each other, the two ends of the arm strap are provided with second connecting parts which are matched with each other, and the two ends of the restraint strap are provided with third connecting parts which are matched with each other.
The first, second and third connecting parts are mutually matched magic tapes or snap fasteners.
The application mode of the technical scheme is as shown in the accompanying figure 1: 1. the belt body is tightly attached to the left shoulder of a human body, the arm belt is wound on the upper arm and fixed through the end magic tape, the shoulder belt is wound on the back and the right armpit from the left shoulder and fixed through the end magic tape, and the restraint belt is wound on the back and the right armpit and fixed through the end magic tape; 2. preparing 0.5-1 kg of sand bags according to the requirement, opening the cover cloth, filling the sand bags into the sand bag cover, and fastening the cover cloth through the ring buckle to press the notch.
The technical scheme has the following effects:
1. compared with the common sand bag compression, the device has the advantages that the compression position is locked by the arm belt and the shoulder belt, so that the sand bag is prevented from sliding off; compared with the vest type compression device in the prior art, the vest type compression device is more convenient to put on and take off, a patient needs to carry out a series of actions such as dressing and wearing hands, and the patient just after the operation is usually weak and is not easy to stretch greatly. The device can fix the shoulder belt and the restraint belt through the back of the patient only by slightly lifting the back of the patient by medical staff, thereby greatly reducing the activity amplitude of the patient and preventing the pacemaker from sliding caused by wound tearing and muscle stretching;
2. the device takes the left shoulder as a stress point, the arm belt is wound on the upper arm, the shoulder belt is wound on the chest and shoulder, and the stress is stable and does not displace, so that the compression device is always positioned at the incision. Meanwhile, the arm belt, the shoulder belt and the restraint belt can also be adjusted to adapt to patients with different sizes through the positions of the magic tape;
3. the device restrains the left arm through the restraint strap, well fixes the shoulder joint, prevents that patient from shifting the pacemaker because of shoulder joint abduction leads to. Especially, partial patients can turn over and stretch and lift the arms during sleeping, so that the restraint strap can well solve the problem;
4. clinical observation shows that if the air bag is pressed, the air bag is generally spherical after being inflated, the surface contacted with the incision is an arc surface, the contact surface is small, and the crushing effect is poor. The device adopts the sand bag and the sand bag sleeve, because the sand bag has fluidity, the whole incision surface can be naturally covered under the action of gravity, the contact surface is enlarged, and the crushing effect is obviously better;
5. the detachable sandbag is designed to facilitate the replacement of the sandbag by medical staff to adjust the weight of the sandbag and to sterilize the sandbag;
6. because the compression cloth and the covering cloth are made of transparent materials, such as hexagonal mesh cloth, the medical staff can observe and change the medicine on the affected part conveniently. The triangle formed by the pressing cloth and the cover cloth covers the incision skin of the pacemaker implantation site completely, and the hexagonal mesh cloth facilitates observation of the dressing condition of the pacemaker incision site;
7. since most pacemaker incisions are positioned on the left side of a patient, the technical scheme and the drawing are described with the incisions on the left side, and if part of the pacemaker incisions are positioned on the right side, the compression device of the technical scheme is only required to be symmetrically arranged.
Drawings
FIG. 1 is a schematic view of the use state structure of the present utility model;
FIG. 2 is a schematic view showing the structure of the embodiment 1 of the present utility model in the unfolded state;
fig. 3 is a schematic view showing the structure of embodiment 1 of the present utility model in the developed state.
Reference numerals illustrate: 1 sand bag cover, 2 cover cloth, 3 compression cloth, 4 arm band, 4-1 second connecting part, 5 restraint band, 5-1 third connecting part, 6 shoulder strap, 6-1 first connecting part and 7 band body.
Detailed Description
The pressing device is characterized in that triangular cover cloth 2 is arranged on the pressing cloth 3, and a sandbag cover 1 is arranged under the cover cloth. The three corners of the covering cloth are provided with buckles.
The sand bag is sleeved with an opening for taking and placing the sand bag.
The compression cloth and the cover cloth are hexagonal mesh cloth.
The restraint strap, the arm strap and the shoulder strap are OK skin-friendly fabrics.
The shoulder strap is characterized in that two ends of the shoulder strap are provided with first connecting parts 6-1 which are matched with each other, two ends of the arm strap are provided with second connecting parts 4-1 which are matched with each other, and two ends of the restraint strap are provided with third connecting parts 5-1 which are matched with each other.
The first, second and third connecting parts are mutually matched magic tapes.
The pressing device is characterized in that triangular cover cloth is arranged on the pressing cloth, and a sand bag sleeve is arranged under the cover cloth. The three corners of the covering cloth are provided with buckles.
The sand bag is sleeved with an opening for taking and placing the sand bag.
The compression cloth and the cover cloth are hexagonal mesh cloth.
The restraint strap, the arm strap and the shoulder strap are OK skin-friendly fabrics.
The shoulder strap is characterized in that the two ends of the shoulder strap are provided with first connecting parts which are matched with each other, the two ends of the arm strap are provided with second connecting parts which are matched with each other, and the two ends of the restraint strap are provided with third connecting parts which are matched with each other.
The first, second and third connecting parts are mutually matched magic tapes.
The restraint strap is longer at one end of the shoulder strap away from the compression device, so that the restraint strap can be used for bypassing the whole back, and the connecting position of the restraint strap and the shoulder strap is positioned in front of the chest of a patient, so that the patient can wear and take off the restraint strap more conveniently.
Claims (6)
1. The utility model provides a pacemaker postoperative incision compression device, characterized by includes the I-shaped area body, takes body upper portion to be the baldric of extending about, and the area body lower part is the armband of extending about, and the armband is equipped with restraint area outside the band, and baldric, armband and area body junction are equipped with the oppression cloth, are equipped with compression device in the oppression cloth, baldric both ends be equipped with the first connecting portion of mutually supporting, armband both ends be equipped with the second connecting portion of mutually supporting, restraint area both ends be equipped with the third connecting portion of mutually supporting.
2. The device according to claim 1, wherein the pressing device is a triangular cover cloth arranged on the pressing cloth, a sand bag cover is arranged under the cover cloth, and an opening is arranged on the sand bag cover.
3. The pacemaker post-operative incision compression device of claim 2 wherein three corners of the drape are provided with loops.
4. The pacemaker post-operative incision compression device of claim 2 wherein the compression cloth and drape are hexagonal mesh.
5. The pacemaker post-operative incision compression device of claim 1 wherein the constraining bands, armbands, shoulder straps are OK skin friendly fabric.
6. The pacemaker post-operative incision compression device according to claim 1, wherein the first, second and third connecting portions are velcro or snap fasteners that cooperate with each other.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202222194731.7U CN218960830U (en) | 2022-08-21 | 2022-08-21 | Pacemaker postoperative incision compression device |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202222194731.7U CN218960830U (en) | 2022-08-21 | 2022-08-21 | Pacemaker postoperative incision compression device |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN218960830U true CN218960830U (en) | 2023-05-05 |
Family
ID=86156286
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202222194731.7U Active CN218960830U (en) | 2022-08-21 | 2022-08-21 | Pacemaker postoperative incision compression device |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN218960830U (en) |
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2022
- 2022-08-21 CN CN202222194731.7U patent/CN218960830U/en active Active
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