CN219021377U - Hemostasis compression device - Google Patents
Hemostasis compression device Download PDFInfo
- Publication number
- CN219021377U CN219021377U CN202222516882.XU CN202222516882U CN219021377U CN 219021377 U CN219021377 U CN 219021377U CN 202222516882 U CN202222516882 U CN 202222516882U CN 219021377 U CN219021377 U CN 219021377U
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- Prior art keywords
- bandage
- compression device
- backup pad
- pressure
- hemostasis
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
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Abstract
The utility model provides a hemostasis compression device, includes backup pad, bandage and aerating device, the bandage is left single open-ended U style of calligraphy, the bandage is equipped with the recess from left to right, the backup pad setting is in the recess and with bandage fixed connection, the bottom of backup pad be equipped with to the inside sunken trench of backup pad. The hemostasis compression device is provided with the baroreceptors, and can monitor the pressure of the compression point in real time by matching with the display, so that the phenomenon that hemostasis is impossible or blood flow is unsmooth, and finger paralysis caused by insufficient pressure or overlarge pressure is avoided; the wider bandages and the slot positions all play a role in avoiding the phenomenon of air bag displacement; the timing device is added to limit the pressing time, so that adverse reaction caused by too short or too long pressing time is prevented.
Description
Technical Field
The utility model relates to the field of medical instruments, in particular to a hemostasis compression device.
Background
The arteria carotis puncture is an operation between internal medicine and surgical treatment, is an emerging subject, and belongs to interventional treatment together with arteria cruris puncture and carotid artery puncture. In the operation, the puncture point needs to be stopped, and a method of manual finger pressure and bandaging is adopted in the early stage, the method is an empirical hemostasis method, the pressure feeling is completely dependent on the experience of doctors, the pressure of the compression point cannot be intuitively known, the pressure is too small, and bleeding is easy; excessive pressure is easy to cause unsmooth blood flow and numbness of fingers; the inflatable compression method is characterized in that a bandage is used for binding the radial artery, an air bag is placed between a compression point and the bandage, the air bag is inflated, the air bag bulges to compress and stop bleeding, but when the air bag is inflated clinically, the air bag is easy to slide from two sides due to the fact that the bandage is too narrow, and the hemostatic effect is affected; for novice, it is difficult to grasp the time of compression, the time is short, the hemostasis effect is not achieved, and the time is long, so that the unsmooth blood circulation is easily caused.
Disclosure of Invention
The utility model aims to solve the defects in the prior art and provides a hemostasis-compression device; the hemostasis compression device is provided with the baroreceptors, and can monitor the pressure of the compression point in real time by matching with the display, so that the phenomenon that hemostasis is impossible or blood flow is unsmooth, and finger paralysis caused by insufficient pressure or overlarge pressure is avoided; the wider bandages and the slot positions all play a role in avoiding the phenomenon of air bag displacement; the timing device is added to limit the pressing time, so that adverse reaction caused by too short or too long pressing time is prevented.
In order to achieve the above purpose, the utility model adopts the following technical scheme: the utility model provides a hemostasis compression device, includes backup pad, bandage and aerating device, the bandage is left single open-ended U style of calligraphy, the bandage is equipped with the recess from left to right, the backup pad setting is in the recess and with bandage fixed connection, the bottom of backup pad be equipped with to the inside sunken trench of backup pad.
Preferably, the width of the support plate is the same as the width of the groove.
Preferably, the air charging device comprises an air bag, an air pipe, an air release valve and an air charging ball, wherein two ends of the air pipe are respectively connected with the air bag and the air charging ball in a communication mode, and the air release valve is connected to the outer wall of the air pipe in a communication mode and is close to the air charging ball.
Preferably, the support plate comprises a body, a display and a baroreceptor, the display is arranged on the upper surface of the support plate, the baroreceptor is arranged on the lower surface of the support plate and is positioned in the groove, and the baroreceptor is connected with the display in a circuit manner.
Preferably, the supporting plate further comprises a timing button and a buzzer, the timing button and the buzzer are both arranged on the upper surface of the supporting plate, and the timing button is in circuit connection with the buzzer.
Preferably, the length of the groove is 40cm.
Preferably, the upper surface of the bandage is fixedly provided with a magic tape head, and the lower surface of the bandage is provided with a magic tape hair head.
Preferably, the length of the bandage is 50cm and the width is 20cm.
Compared with the prior art, the utility model has the beneficial effects that: the hemostasis compression device is provided with the baroreceptors, and can monitor the pressure of the compression point in real time by matching with the display, so that the phenomenon that hemostasis is impossible or blood flow is unsmooth, and finger paralysis caused by insufficient pressure or overlarge pressure is avoided; the wider bandages and the slot positions all play a role in avoiding the phenomenon of air bag displacement; the timing device is added to limit the pressing time, so that adverse reaction caused by too short or too long pressing time is prevented.
Drawings
Fig. 1 is a top view of a hemostatic compression device according to the utility model;
fig. 2 is a front view of a hemostatic compression device according to the utility model in a wound form;
fig. 3 is a schematic structural view of an inflator of a hemostatic compression device according to the present utility model.
Detailed Description
For a further understanding of the objects, construction, features, and functions of the utility model, reference should be made to the following detailed description of the preferred embodiments.
Referring to fig. 1-3, the hemostatic compression device according to an embodiment of the present utility model includes a support plate 1, a bandage 2 and an air-filling device 3, wherein the bandage 2 is U-shaped with a single opening on the left, the bandage 2 is provided with a groove 21 from left to right, the support plate 1 is disposed in the groove 21 and fixedly connected with the bandage 2, and a groove 11 recessed toward the inside of the support plate 1 is disposed at the bottom of the support plate 1. The slot 11 is used for positioning the placement position of the inflator 3, and also plays a role in preventing displacement of the inflator 3 when inflated.
Preferably, the width of the support plate 1 is the same as the width of the recess 21. The support plate 1 can be wound and fixed on the arm of a patient through the bandage 2, and the same width can ensure that the support plate 1 can be tightly pressed when the bandage 2 is wound.
Preferably, the inflator 3 comprises an air bag 31, an air pipe 32, an air release valve 33 and an inflation ball 34, wherein two ends of the air pipe 32 are respectively communicated with the air bag 31 and the inflation ball 34, and the air release valve 33 is connected to the outer wall of the air pipe 32 in a communicating way and is close to the inflation ball 34. The inflation device 3 is the same as the inflation device of a common mercury sphygmomanometer in principle, and the inflation balloon 34 is pressed to inflate the airbag 31, and the deflation valve 33 is unscrewed after the use is completed, so that the inflation can be performed.
Preferably, the support plate 1 comprises a body 12, a display 13 and a baroreceptor 16, the display 13 being arranged on the upper surface of the support plate 1, the baroreceptor 16 being arranged on the lower surface of the support plate 1 and being located in the slot 11, the baroreceptor 16 being in electrical connection with the display 13. The baroreceptors 16 can monitor the pressure of the air bags 31 positioned in the tank 11 during use, display real-time pressure feedback to doctors through the display 13, and the doctors can judge whether the pressure is proper or not through the pressure value displayed by the display 13, so that the optimal pressure is achieved, and adverse reactions caused by insufficient or overlarge pressure are effectively avoided.
Preferably, the support plate 1 further comprises a timing button 14 and a buzzer 15, the timing button 14 and the buzzer 15 are arranged on the upper surface of the support plate 1, and the timing button 14 is in circuit connection with the buzzer 15. The pressing time is set by the timing button 14, generally about one minute, and the buzzer 15 sounds after the time arrives, so that the doctor is reminded that the pressing time arrives, and the air bag 31 can be deflated, the pressing is finished, and adverse reactions caused by insufficient pressing time or overlong pressing time are prevented.
Preferably, the length of the recess 21 is 40cm. The dimension of the wrist of the adult is about 20cm, and the grooves 21 with the length of 40cm can ensure at least two windings during winding, so that the stability of the supporting plate 1 is improved.
Preferably, the upper surface of the bandage 2 is fixedly provided with a hook and loop fastener head 22, and the lower surface of the bandage 2 is provided with a hook and loop fastener head 23. The bandage 2 is fixed through the hook and loop fastener thorn head 22 and the hook and loop fastener hair head 23, and the hook and loop fastener hair head 23 is arranged on one side of the skin, so that the comfort level is improved and the buffering effect is also achieved.
Preferably, the bandage 2 has a length of 50cm and a width of 20cm. The part of the bandage 2 which is 10cm longer than the groove 21 can increase the attaching area of the magic tape, further improve the winding and fixing stability, and the width of 20cm can prevent the air bag 31 from shifting.
By the above, when the hemostatic compression device is used, a compression point is selected, the groove 11 of the supporting plate 1 is aligned with the compression point, the supporting plate 1 and the bandage 2 are placed on an arm together, then the air bag 31 in the inflatable device 3 is plugged between the groove 11 and the compression point, the hook-and-loop fastener head 22 and the hook-and-loop fastener head 23 are mutually matched to wind the bandage 2, so that the supporting plate 1 is fixed on the arm of a patient, the hook-and-loop fastener is wound for at least two circles, the stability is improved, a doctor repeatedly presses the inflatable ball 34 to inflate the air bag 31, the air bag 31 is inflated to press the compression point and the baroreceptor 16, because the air bag 31 is spherical, the pressure at the surface of the air bag 31 is the same, namely, the pressure born by the baroreceptor 16 is the same as the compression point, the pressure is fed back in real time and displayed on the display 13, and the doctor judges the magnitude of the pressure born by the compression point through observing the numerical value of the display, so that the doctor adjusts the pressure to a proper pressure; after the pressure is proper, the time is usually one minute by timing the button 14, the buzzer 15 sounds after the time is up, and the doctor can unscrew the air release valve 33 to release the air bag 31 to release the bandage 2 to stop the compression hemostasis when the compression time is up. The hemostasis compression device is provided with the baroreceptors, and can monitor the pressure of the compression point in real time by matching with the display, so that the phenomenon that hemostasis is impossible or blood flow is unsmooth, and finger paralysis caused by insufficient pressure or overlarge pressure is avoided; the wider bandages and the slot positions all play a role in avoiding the phenomenon of air bag displacement; the timing device is added to limit the pressing time, so that adverse reaction caused by too short or too long pressing time is prevented.
Claims (8)
1. A hemostatic compression device, characterized in that: including backup pad (1), bandage (2) and aerating device (3), bandage (2) are left single open-ended U style of calligraphy, bandage (2) are equipped with recess (21) from left to right, backup pad (1) set up in recess (21) and with bandage (2) fixed connection, the bottom of backup pad (1) be equipped with to inside sunken trench (11) of backup pad (1).
2. A hemostatic compression device according to claim 1 wherein: the width of the supporting plate (1) is the same as the width of the groove (21).
3. A hemostatic compression device according to claim 1 wherein: the inflatable device (3) comprises an air bag (31), an air pipe (32), an air release valve (33) and an inflatable ball (34), wherein two ends of the air pipe (32) are respectively connected with the air bag (31) and the inflatable ball (34) in a communication mode, and the air release valve (33) is connected to the outer wall of the air pipe (32) in a communication mode and is close to the inflatable ball (34).
4. A hemostatic compression device according to claim 1 wherein: the support plate (1) comprises a body (12), a display (13) and a baroreceptor (16), wherein the display (13) is arranged on the upper surface of the support plate (1), the baroreceptor (16) is arranged on the lower surface of the support plate (1) and is positioned in the groove (11), and the baroreceptor (16) is in circuit connection with the display (13).
5. A hemostatic compression device according to claim 1 wherein: the supporting plate (1) further comprises a timing button (14) and a buzzer (15), the timing button (14) and the buzzer (15) are both arranged on the upper surface of the supporting plate (1), and the timing button (14) is in circuit connection with the buzzer (15).
6. A hemostatic compression device according to claim 1 wherein: the length of the groove (21) is 40cm.
7. A hemostatic compression device according to claim 1 wherein: the upper surface of the bandage (2) is fixedly provided with a magic tape head (22), and the lower surface of the bandage (2) is provided with a magic tape hair head (23).
8. A hemostatic compression device according to claim 1 wherein: the length of the bandage (2) is 50cm, and the width is 20cm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202222516882.XU CN219021377U (en) | 2022-09-22 | 2022-09-22 | Hemostasis compression device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202222516882.XU CN219021377U (en) | 2022-09-22 | 2022-09-22 | Hemostasis compression device |
Publications (1)
Publication Number | Publication Date |
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CN219021377U true CN219021377U (en) | 2023-05-16 |
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ID=86276276
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202222516882.XU Active CN219021377U (en) | 2022-09-22 | 2022-09-22 | Hemostasis compression device |
Country Status (1)
Country | Link |
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CN (1) | CN219021377U (en) |
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2022
- 2022-09-22 CN CN202222516882.XU patent/CN219021377U/en active Active
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