CN213665519U - Compression hemostasis device for puncture point after cardiac intervention - Google Patents

Compression hemostasis device for puncture point after cardiac intervention Download PDF

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Publication number
CN213665519U
CN213665519U CN202022513440.0U CN202022513440U CN213665519U CN 213665519 U CN213665519 U CN 213665519U CN 202022513440 U CN202022513440 U CN 202022513440U CN 213665519 U CN213665519 U CN 213665519U
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fixedly connected
device body
wall
groove
cardiac intervention
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李华
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Abstract

The utility model discloses a heart intervention postoperative puncture point hemostasis by compression device relates to medical instrument technical field, the device comprises a device body, the observation window has been seted up at the top middle part of device body, annular pressurized groove has been seted up all around at the bottom middle part of device body, the inside in annular pressurized groove is equipped with the pressurization gasbag, the bottom middle part of device body is equipped with soft glass, one side top fixedly connected with pressurized sleeve in annular pressurized groove, the opposite side top fixedly connected with blast pipe in annular pressurized groove, outer wall one side fixedly connected with fixed band of device body, the outer wall opposite side fixedly connected with clamping mechanism of device body. The utility model discloses, through setting up protection pad clamping mechanism and fixed band, avoided using the fixed influence that causes the patient of adhesive tape, simultaneously can be through the length of adjustment fixed band for the device can be applicable to different positions and different size patients' pressurization hemostasis.

Description

Compression hemostasis device for puncture point after cardiac intervention
Technical Field
The utility model relates to the technical field of medical equipment, more specifically relate to a puncture point hemostasis by compression device after cardiac intervention.
Background
After the cardiac intervention, the conventionality requires that the patient lies in bed to have a rest, and the puncture position need pressurize and wrap 24 hours, because traditional tourniquet function singleness, medical personnel can't accurate control patient puncture position's pressurization, when pressurization is great or less, patient puncture position phenomenons such as bleeding can appear, cause the injury to the patient, medical personnel's work burden has also been increased simultaneously, need a cardiac intervention postoperative puncture point hemostasis by compression device in view of above defect, current cardiac intervention postoperative puncture point hemostasis by compression device, generally need glue the adhesive tape and fix on patient's skin, the adhesive tape contacts skin for a long time and causes skin itch easily, it is broken, a great deal of discomfort such as pain, be not convenient for simultaneously to adjust the pressurized pressure value of device, be unfavorable for the use of device.
Therefore, it is necessary to provide a compression hemostasis device for puncture site after cardiac intervention to solve the above problems.
SUMMERY OF THE UTILITY MODEL
Technical problem to be solved
The utility model aims to provide a: in order to solve current heart intervention postoperative point of puncture hemostasis by compression device, need glue the adhesive tape on patient's skin usually and fix, the adhesive tape contacts skin for a long time and causes a large amount of discomforts such as itch of skin, breakage, pain easily, is not convenient for adjust the device pressor pressure value simultaneously, is unfavorable for the problem of the use of device, the utility model provides a heart intervention postoperative point of puncture hemostasis by compression device.
(II) technical scheme
The utility model discloses a realize above-mentioned purpose and specifically adopt following technical scheme:
a puncture point compression hemostasis device after cardiac intervention comprises a device body, wherein an observation window is arranged in the middle of the top end of the device body, an annular pressurizing groove is formed in the periphery of the middle of the bottom end of the device body, a pressurizing air bag is arranged inside the annular pressurizing groove, a protective pad is fixedly connected with the periphery of the bottom of the device body, soft glass is arranged in the middle of the bottom end of the device body, a pressurizing sleeve is fixedly connected with the top of one side of the annular pressurizing groove, an inflation tube is fixedly connected with the top of one side of the outer wall of the pressurizing sleeve, an exhaust tube is fixedly connected with the top of the other side of the annular pressurizing groove, a solenoid valve is arranged in the middle of one side of the outer wall of the exhaust tube, a storage battery is fixedly connected with the inside of one side of the device body, an insulating base plate is fixedly connected between the, and the other side of the outer wall of the device body is fixedly connected with a clamping mechanism.
Furthermore, the bottom of the pressurizing sleeve and the bottom of the exhaust pipe both extend into the annular pressurizing groove and are communicated with the pressurizing air bag, and the tops of the inflation pipe and the exhaust pipe both extend out of the device body.
Furthermore, the top of the inner wall of the pressurizing sleeve is fixedly connected with a first spring, the bottom of the first spring is fixedly connected with a one-way ball valve, and one side of the top of the inner wall of the pressurizing sleeve is communicated with the bottom end of the inflation tube.
Furthermore, a clamping groove is formed in the electromagnetic valve, an electromagnet is fixedly connected to the middle of one side of the inner wall of one side, away from the exhaust pipe, of the clamping groove, the electromagnet is electrically connected with the storage battery, and a magnetic sliding block is connected to the other side of the clamping groove in a sliding mode.
Furthermore, the middle part of one side of the outer wall, away from the electromagnet, of the magnetic sliding block is fixedly connected with a baffle plate, one end of the baffle plate extends into the exhaust pipe, and the other side of the outer wall of the magnetic sliding block is fixedly connected with a second spring.
Furthermore, an L-shaped fixing groove is formed in the bottom of one side, away from the device body, of the outer wall of the clamping mechanism, a clamping sliding groove is formed in the top of the outer wall of one side of the L-shaped fixing groove, and one end of the fixing belt stretches into the L-shaped fixing groove and is connected with the L-shaped fixing groove in a sliding mode.
Further, the inside sliding connection who presss from both sides tight spout has the tight slider of clamp, the tight slider of clamp keeps away from outer wall one side middle part of L type fixed slot and offers threaded hole, the inside thread connection of threaded hole has the tight screw rod of clamp, the one end of the tight screw rod of clamp stretches out L type fixed slot and is connected rather than rotating.
Further, the protection pad is made of elastic breathable cotton materials, the soft glass is made of transparent soft materials, and the insulating base plate is made of insulating rubber materials.
(III) advantageous effects
The utility model has the advantages as follows:
1. the utility model discloses, through setting up protection pad clamping mechanism and fixed band, avoided using the fixed influence that causes the patient of adhesive tape, simultaneously can be through the length of adjustment fixed band for the device can be applicable to different positions and different size patients' pressurization hemostasis, has improved the suitability and the practicality of device.
2. The utility model discloses, through setting up pressurization gasbag, one-way ball valve, pressurization cover, gas tube, spring, blast pipe and solenoid valve, can fill the gas volume in the pressurization gasbag through control to the pressure that controlling means applyed, thereby blast pipe and solenoid valve can avoid device internal pressure too big to cause harmful effects to the patient, have improved the suitability of device.
3. The utility model discloses, through setting up soft glass, observation window, insulating backing plate and battery for the device is convenient for doctor and nurse and observes the hemostasis condition of patient's wound, and the battery has guaranteed simultaneously that the device can use anytime and anywhere, has improved the practicality of device.
Drawings
Fig. 1 is a schematic perspective view of the structure of the present invention;
FIG. 2 is a schematic sectional view of the structure of the present invention;
FIG. 3 is an enlarged cross-sectional view taken at A of FIG. 2 according to the present invention;
fig. 4 is an enlarged schematic sectional view of the clamping mechanism of the present invention.
Reference numerals: 1. a device body; 2. a pressurized air bag; 3. an annular pressurized groove; 4. soft glass; 5. a protective pad; 6. a one-way ball valve; 7. pressing the sleeve; 8. an inflation tube; 9. a first spring; 10. an observation window; 11. an exhaust pipe; 12. an electromagnetic valve; 13. a baffle plate; 14. a magnetic slider; 15. an electromagnet; 16. a card slot; 17. a second spring; 18. an L-shaped fixing groove; 19. a clamping mechanism; 20. fixing belts; 21. clamping the chute; 22. clamping the sliding block; 23. a threaded hole; 24. clamping the screw rod; 25. an insulating base plate; 26. and (4) a storage battery.
Detailed Description
The technical solutions in the embodiments of the present invention will be described clearly and completely with reference to the accompanying drawings in the embodiments of the present invention, and it is obvious that the described embodiments are only some embodiments of the present invention, not all embodiments. Based on the embodiments in the present invention, all other embodiments obtained by a person skilled in the art without creative work belong to the protection scope of the present invention.
Example 1
Referring to fig. 1-4, a puncture point compression hemostasis device after cardiac intervention comprises a device body 1, an observation window 10 is arranged in the middle of the top end of the device body 1, an annular pressurizing groove 3 is arranged around the middle of the bottom end of the device body 1, a pressurizing air bag 2 is arranged inside the annular pressurizing groove 3, a protective pad 5 is fixedly connected around the bottom of the device body 1, soft glass 4 is arranged in the middle of the bottom end of the device body 1, a pressurizing sleeve 7 is fixedly connected to the top of one side of the annular pressurizing groove 3, an inflation tube 8 is fixedly connected to the top of one side of the outer wall of the pressurizing sleeve 7, an exhaust tube 11 is fixedly connected to the top of the other side of the annular pressurizing groove 3, an electromagnetic valve 12 is arranged in the middle of one side of the outer wall of the exhaust tube 11, a storage battery 26 is fixedly connected to the inside of one side of the, a fixing belt 20 is fixedly connected to one side of the outer wall of the device body 1, and a clamping mechanism 19 is fixedly connected to the other side of the outer wall of the device body 1.
In this embodiment, through setting up soft glass 4, observation window 10, insulating backing plate 25 and battery 26 for the device is convenient for doctor and nurse and observes the hemostasis condition of patient's wound, and battery 26 has guaranteed simultaneously that the device can use anytime and anywhere, has improved the practicality of device.
Example 2
Referring to fig. 2-4, the present embodiment is further optimized based on embodiment 1, specifically, the bottom portions of the pressurizing sleeve 7 and the exhaust pipe 11 both extend into the annular pressurizing groove 3 and are communicated with the pressurizing airbag 2, and the top portions of the inflation pipe 8 and the exhaust pipe 11 both extend out of the device body 1.
Specifically, the top of the inner wall of the pressurizing sleeve 7 is fixedly connected with a first spring 9, the bottom of the first spring 9 is fixedly connected with a one-way ball valve 6, and one side of the top of the inner wall of the pressurizing sleeve 7 is communicated with the bottom end of an inflation tube 8.
Specifically, a clamping groove 16 is formed in the electromagnetic valve 12, an electromagnet 15 is fixedly connected to the middle of one side of the inner wall of the clamping groove 16, which is far away from the exhaust pipe 11, the electromagnet 15 is electrically connected with the storage battery 26, and a magnetic sliding block 14 is slidably connected to the other side of the clamping groove 16.
Specifically, the magnetic slider 14 is far away from the baffle 13 fixedly connected to the middle of one side of the outer wall of the electromagnet 15, one end of the baffle 13 extends into the exhaust pipe 11, and the other side of the outer wall of the magnetic slider 14 is fixedly connected to the second spring 17.
In this embodiment, through setting up pressurization gasbag 2, one-way ball valve 6, pressurization cover 7, gas tube 8, spring 9, blast pipe 11 and solenoid valve 12, can fill the gas volume in the pressurization gasbag 2 through the control to the pressure that controlling means applyed, thereby blast pipe 11 and solenoid valve 12 can avoid the device internal pressure too big to cause harmful effects to the patient, have improved the suitability of device.
Example 3
Referring to fig. 2, the present embodiment is optimized based on the embodiment 1 or 2, specifically, an L-shaped fixing groove 18 is formed at the bottom of the outer wall of the clamping mechanism 19 away from the device body 1, a clamping sliding groove 21 is formed at the top of the outer wall of the L-shaped fixing groove 18, and one end of the fixing strap 20 extends into and is slidably connected to the L-shaped fixing groove 18.
Specifically, the clamping sliding block 22 is slidably connected inside the clamping sliding groove 21, a threaded hole 23 is formed in the middle of one side, away from the outer wall of the L-shaped fixing groove 18, of the clamping sliding block 22, a clamping screw 24 is connected to the inner thread of the threaded hole 23, and one end of the clamping screw 24 extends out of the L-shaped fixing groove 18 and is rotatably connected with the L-shaped fixing groove.
Specifically, the protective pad 5 is made of an elastic breathable cotton material, the soft glass 4 is made of a transparent soft material, and the insulating pad plate 25 is made of an insulating rubber material.
In this embodiment, through setting up 5 clamping mechanism 19 of protection pad and fixed band 20, avoided using the fixed influence that causes the patient of adhesive tape, can be through the length of adjustment fixed band 20 simultaneously for the device can be applicable to different positions and different size patients' pressurization hemostasis, has improved the suitability and the practicality of device.
In summary, the following steps: the utility model discloses, avoided using the fixed influence that causes the patient of adhesive tape, simultaneously can be through the length of adjustment fixed band 20, make the device can be applicable to different positions and different size patients 'pressurization hemostasis, the suitability and the practicality of device have been improved, simultaneously can fill the gas volume in pressurization gasbag 2 through control, thereby the pressure that controlling means applyed, thereby blast pipe 11 and solenoid valve 12 can avoid the device internal pressure too big to cause harmful effects to the patient, the suitability of device has been improved, and be convenient for doctor and nurse to observe the hemostasis condition of patient's wound, battery 26 has guaranteed simultaneously that the device can use anytime and anywhere, the practicality of device has been improved.
Above, only be the preferred embodiment of the present invention, not be used for limiting the present invention, the patent protection scope of the present invention is based on the claims, all the structural changes equivalent to the content of the description and drawings of the present invention should be included in the protection scope of the present invention.

Claims (8)

1. The utility model provides a puncture point hemostasis by compression device after cardiac intervention, includes device body (1), its characterized in that: the utility model discloses a device for the gas-liquid separation of the air-liquid separation of air-liquid separation, observation window (10) have been seted up at the top middle part of device body (1), annular pressurized groove (3) have been seted up all around to the bottom middle part of device body (1), the inside of annular pressurized groove (3) is equipped with pressurization gasbag (2), fixedly connected with protection pad (5) all around the bottom of device body (1), the bottom middle part of device body (1) is equipped with soft glass (4), one side top fixedly connected with pressurized cover (7) of annular pressurized groove (3), outer wall one side top fixedly connected with gas tube (8) of pressurized cover (7), opposite side top fixedly connected with blast pipe (11) of annular pressurized groove (3), outer wall one side middle part of blast pipe (11) is equipped with solenoid valve (12), the inside fixedly connected with battery (26) of one side of device body (1), fixedly connected with insulating The fixing device is characterized in that a fixing belt (20) is fixedly connected to one side of the outer wall of the device body (1), and a clamping mechanism (19) is fixedly connected to the other side of the outer wall of the device body (1).
2. A compression hemostasis device for puncture points after cardiac intervention according to claim 1, wherein: the bottom of the pressurizing sleeve (7) and the bottom of the exhaust pipe (11) both extend into the annular pressurizing groove (3) and are communicated with the pressurizing air bag (2), and the tops of the inflation pipe (8) and the exhaust pipe (11) both extend out of the device body (1).
3. A compression hemostasis device for puncture points after cardiac intervention according to claim 1, wherein: the inner wall top fixedly connected with first spring (9) of pressurization cover (7), the bottom fixedly connected with one-way ball valve (6) of first spring (9), inner wall top one side of pressurization cover (7) is linked together with the bottom of gas tube (8).
4. A compression hemostasis device for puncture points after cardiac intervention according to claim 1, wherein: the electromagnetic valve is characterized in that a clamping groove (16) is formed in the electromagnetic valve (12), an electromagnet (15) is fixedly connected to the middle of one side of the inner wall of one side, away from the exhaust pipe (11), of the clamping groove (16), the electromagnet (15) is electrically connected with a storage battery (26), and a magnetic sliding block (14) is connected to the other side of the clamping groove (16) in a sliding mode.
5. A compression hemostasis device for puncture points after cardiac intervention according to claim 4, wherein: the middle part of one side of the outer wall of the magnetic sliding block (14), which is far away from the electromagnet (15), is fixedly connected with a baffle plate (13), one end of the baffle plate (13) extends into the exhaust pipe (11), and the other side of the outer wall of the magnetic sliding block (14) is fixedly connected with a second spring (17).
6. A compression hemostasis device for puncture points after cardiac intervention according to claim 1, wherein: l type fixed slot (18) have been seted up to outer wall one side bottom that clamping mechanism (19) kept away from device body (1), tight spout (21) have been seted up to one side outer wall top of L type fixed slot (18), the one end of fixed band (20) stretches into L type fixed slot (18) and rather than sliding connection.
7. A compression hemostasis device for puncture points after cardiac intervention according to claim 6, wherein: the inside sliding connection who presss from both sides tight spout (21) has clamping slider (22), outer wall one side middle part that L type fixed slot (18) was kept away from in clamping slider (22) is seted up screw hole (23), the inside threaded connection of screw hole (23) has clamping screw (24), the one end of clamping screw (24) stretches out L type fixed slot (18) and is connected rather than rotating.
8. A compression hemostasis device for puncture points after cardiac intervention according to claim 1, wherein: the protective pad (5) is made of elastic breathable cotton material, the soft glass (4) is made of transparent soft material, and the insulating pad plate (25) is made of insulating rubber material.
CN202022513440.0U 2020-11-04 2020-11-04 Compression hemostasis device for puncture point after cardiac intervention Active CN213665519U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202022513440.0U CN213665519U (en) 2020-11-04 2020-11-04 Compression hemostasis device for puncture point after cardiac intervention

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202022513440.0U CN213665519U (en) 2020-11-04 2020-11-04 Compression hemostasis device for puncture point after cardiac intervention

Publications (1)

Publication Number Publication Date
CN213665519U true CN213665519U (en) 2021-07-13

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Application Number Title Priority Date Filing Date
CN202022513440.0U Active CN213665519U (en) 2020-11-04 2020-11-04 Compression hemostasis device for puncture point after cardiac intervention

Country Status (1)

Country Link
CN (1) CN213665519U (en)

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