CN218572242U

CN218572242U - Hemostasis device for obstetrics and gynecology department

Info

Publication number: CN218572242U
Application number: CN202221871744.7U
Authority: CN
Inventors: 陆平
Original assignee: Individual
Current assignee: Individual
Priority date: 2022-07-08
Filing date: 2022-07-08
Publication date: 2023-03-07
Anticipated expiration: 2032-07-08

Abstract

The utility model relates to a hemostasis technique field especially relates to a hemostasis device of gynaecology and obstetrics, which comprises a pipe body, the tip and the surface of body are equipped with main sacculus and vice sacculus respectively, fill the water pipe and fill the water branch of branch of academic or vocational study respectively to main sacculus and the inside water injection of vice sacculus through the main sacculus in the body during use, the body surface is equipped with intercommunication A and intercommunication B respectively, vice sacculus inner circle wall intercommunication has one and the intercommunication arch that matches with intercommunication A and intercommunication B, can make vice sacculus and the vice sacculus of body fill the water pipe intercommunication when the intercommunication arch is inserted inside back of intercommunication A or intercommunication B to this can make the hemostasis by compression sacculus change into two kinds of different using-ways and use, thereby be convenient for make two sacculus all for the palace intracavity compress the hemostasis use or a sacculus in another palace intracavity compress the hemostasis use outside palace chamber by compression.

Description

Hemostasis device for obstetrics and gynecology department

Technical Field

The utility model relates to a hemostasis technical field especially relates to a gynaecology and obstetrics's hemostasis device.

Background

The saccule compression hemostasis is one of the hemostasis modes in obstetrics and gynecology department, and can treat various postpartum hemorrhage caused by uterine contraction and hypodynamia, preposed placenta, low placenta, implanted placenta, DIC after postpartum or middle-stage abortion and the like in natural delivery or cesarean section. The disposable uterine cavity compression balloon mainly comprises a main cuff, an auxiliary cuff, a guide and drainage tube, a drainage tube connector, a main cuff water filling pipe, a control valve, an auxiliary cuff water filling pipe and a one-way valve.

During the use through to main cuff and the inside aseptic liquid that injects of vice cuff for the palace chamber oppresses the sacculus and produces one kind by the hydrostatic pressure outside the palace intracavity to the palace chamber, and this pressure is greater than uterus pulse pressure, and lower extreme in the uterus is acted on directly after the sacculus water injection to and uterus artery entry, thereby reduce the blood flow who flows into the uterus effectively, and simultaneously, palace chamber oppression sacculus can stimulate the uterus and produce the secretion of endogenous prostaglandin, the induced uterus contracts.

The disposable uterine cavity compression hemostasis balloon has two use modes respectively corresponding to the two use modes when in use, one mode is that the main cuff is placed in the uterine cavity, and the auxiliary cuff is placed in the vagina and close to the position of the uterine cavity opening; the other is that the main cuff and the auxiliary cuff are both arranged in the uterine cavity, and the auxiliary cuff is close to the mouth of the uterine cavity in the uterine cavity, and the prior art does not have a better disposable uterine cavity compression hemostasis balloon which can combine the two balloon compression hemostasis using modes and adjust automatically for compression hemostasis. To this end, we propose a hemostatic device for obstetrics and gynecology department to solve the above problems.

SUMMERY OF THE UTILITY MODEL

The utility model aims at solving the problem that the prior art does not have a better disposable uterine cavity hemostasis by compression sacculus which can combine the two sacculus hemostasis by compression using modes and is adjusted by oneself to carry out hemostasis by compression, and providing a hemostasis device for obstetrics and gynecology.

In order to achieve the above purpose, the utility model adopts the following technical scheme:

the utility model provides a hemostasis device of gynaecology and obstetrics, includes the body, the tip and the surface of body are equipped with main sacculus and vice sacculus respectively, fill water pipe and vice sacculus water pipe branch of academic or vocational study respectively to main sacculus and the inside water injection of vice sacculus through main sacculus in the body during use, the body surface is equipped with intercommunication portion A and intercommunication portion B respectively, it is protruding that vice sacculus inner circle wall intercommunication has a intercommunication that matches with intercommunication portion A and intercommunication portion B, can make vice sacculus and the vice sacculus water pipe intercommunication in the body after the intercommunication is protruding to be inserted inside intercommunication portion A or intercommunication portion B.

Preferably, the tube body comprises a guide tube, a drainage tube joint, a main balloon water filling tube, a control valve, an auxiliary balloon water filling tube and a one-way valve.

Preferably, the main balloon is connected to the end of the main balloon water filling pipe, and the auxiliary balloon is communicated with the auxiliary balloon water filling pipe under the matching of the communicating part and the communicating protrusion, so that water can be conveniently filled into the main balloon and the auxiliary balloon through the main balloon water filling pipe and the auxiliary balloon water filling pipe respectively.

Preferably, the communicating part a and the communicating part B comprise communicating holes, and the communicating holes are covered with elastic sealing layers, when the communicating protrusions need to be inserted into the communicating part a or the communicating part B, a worker pricks the elastic sealing layers by using a pointed tool, then inserts the communicating protrusions into the communicating part a or the communicating part B, and meanwhile the elastic sealing layers extrude the communicating protrusions, so that the communicating protrusions are not easy to separate in the communicating holes.

Preferably, a liquid inlet hole communicated with the inside of the auxiliary balloon penetrates through the inside of the communicating bulge, so that liquid can conveniently enter the auxiliary balloon after entering the liquid inlet hole through the communicating hole.

Preferably, the inner wall of the communicating hole is provided with a clamping groove, and the surface of the communicating bulge is provided with a clamping ring matched with the clamping groove, so that the stability of the communicating bulge in the communicating hole is improved.

Compared with the prior art, the beneficial effects of the utility model are that:

1. this application can be convenient for change vice sacculus when using apart from the distance position of main sacculus to this makes the hemostasis by compression sacculus change into two kinds of different using-way and uses, thereby is convenient for make two sacculus all for the palace intracavity hemostasis by compression use or a sacculus in another hemostasis by compression use outside palace intracavity.

2. This application can be convenient for prevent that the intercommunication is protruding to break away from with the intercommunicating pore easily when using, improves the stability in use, is convenient for better annotate the liquid to vice sacculus inside.

Drawings

Fig. 1 is a use structure diagram of the hemostatic device of the obstetrics and gynecology department provided by the utility model, in which the main balloon and the auxiliary balloon are far away from each other;

FIG. 2 is a disassembled view of the auxiliary balloon and the tube body in FIG. 1;

fig. 3 is a use structure diagram of the main balloon and the auxiliary balloon of the hemostatic device for obstetrics and gynecology department provided by the utility model;

FIG. 4 is a disassembled view of the auxiliary balloon and the tube body in FIG. 3;

fig. 5 is a structural view of the secondary balloon of fig. 4.

In the figure: 1. a tube body; 2. a communicating hole A; 3. a communicating hole B; 4. a main balloon; 5. a secondary balloon; 6. and a communicating protrusion.

Detailed Description

In the description of the present invention, it is to be understood that the terms "center", "longitudinal", "lateral", "length", "width", "thickness", "upper", "lower", "front", "rear", "left", "right", "vertical", "horizontal", "top", "bottom", "inner", "outer", "clockwise", "counterclockwise", and the like indicate orientations or positional relationships based on the orientations or positional relationships shown in the drawings, and are only for convenience of description and for simplicity of description, but do not indicate or imply that the device or element referred to must have a particular orientation, be constructed and operated in a particular orientation, and therefore, should not be construed as limiting the present invention.

In the description of the present invention, "a plurality" means two or more unless specifically limited otherwise.

In the description of the present invention, it is to be noted that, unless otherwise explicitly specified or limited, the terms "mounted", "provided", "sleeved/connected", "connected", and the like are to be understood in a broad sense, such as "connected", which may be fixedly connected, detachably connected, or integrally connected; can be mechanically or electrically connected; they may be connected directly or indirectly through intervening media, or they may be interconnected between two elements. The specific meaning of the above terms in the present invention can be understood in specific cases to those skilled in the art.

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.

Referring to fig. 1-5, a hemostasis device for obstetrics and gynecology department comprises a tube body 1, wherein a main balloon 4 and an auxiliary balloon 5 are respectively arranged at the end part and the surface of the tube body 1, water is respectively injected into the main balloon 4 and the auxiliary balloon 5 through a main balloon water filling pipe and an auxiliary balloon water filling pipe in the tube body 1 during use, a communicating part A2 and a communicating part B3 are respectively arranged on the surface of the tube body 1, a communicating protrusion 6 matched with the communicating part A2 and the communicating part B3 is communicated with the inner ring wall of the auxiliary balloon 5, and the auxiliary balloon 5 can be communicated with the auxiliary balloon water filling pipe in the tube body 1 after the communicating protrusion 6 is inserted into the communicating part A2 or the communicating part B3.

Referring to fig. 1-5, a hemostasis device for obstetrics and gynecology department, a tube body 1 in the prior art comprises a guide tube, a drainage tube connector, a main balloon water filling tube, a control valve, an auxiliary balloon water filling tube and a one-way valve, wherein the main balloon 4 is connected to the end part of the main balloon water filling tube, the auxiliary balloon 5 is communicated with the auxiliary balloon water filling tube under the matching of a communicating part and a communicating bulge 6, so that water can be respectively filled into the main balloon 4 and the auxiliary balloon 5 through the main balloon water filling tube and the auxiliary balloon water filling tube, and the one-way valve prevents liquid from leaking out.

Referring to fig. 1-5, a hemostatic device for obstetrics and gynecology department, the communicating part A2 and the communicating part B3 include communicating holes, and the communicating holes are covered with an elastic sealing layer, when the communicating protrusion 6 needs to be inserted into the communicating part A2 or the communicating part B3, a worker punctures the elastic sealing layer by using a pointed tool, then inserts the communicating protrusion 6 into the elastic sealing layer to the communicating part A2 or the communicating part B3, and simultaneously the elastic sealing layer extrudes the communicating protrusion 6, so that the communicating protrusion 6 is not easy to separate in the communicating holes.

Referring to fig. 1-5, a hemostatic device for obstetrics and gynecology department, wherein a liquid inlet hole communicated with the inside of the auxiliary balloon 5 is arranged in the communicating bulge 6 in a penetrating way, and when the communicating bulge 6 is positioned in the communicating hole, liquid can conveniently enter the liquid inlet hole through the communicating hole and then enter the auxiliary balloon 5.

Referring to fig. 1-5, a hemostatic device for obstetrics and gynecology department, the surface of the communicating bulge 6 is provided with a snap ring matched with the snap groove, when the communicating bulge 6 is positioned in the intercommunicating pore, the snap ring on the surface of the communicating bulge 6 is clamped with the snap groove arranged on the inner wall of the intercommunicating pore, so as to improve the stability of the communicating bulge 6 in the intercommunicating pore, and the elastic sealing layer is matched to extrude the communicating bulge 6 to ensure that the connecting stability in use is better.

Referring to fig. 1-5, a hemostatic device for obstetrics and gynecology department, when needing to change the compression hemostatic balloon into two different using modes, as follows:

two sacculus all can be located the palace intracavity and carry out hemostasis by compression and use: the medical staff takes the compression hemostasis balloon out of the sterile sealing bag, no liquid is injected into the balloon in an initial state, the medical staff pricks through an elastic sealing layer in the communicating hole B3 by using a pointed tool, then pulls and moves the auxiliary balloon 5 on the surface of the tube body 1, so that the auxiliary balloon 5 covers the communicating hole B3, the communicating protrusion 6 corresponds to the communicating hole B3, then the medical staff slowly corrects the communicating protrusion 6 from a transverse state by hands, so that the communicating protrusion 6 stands up, then the nursing staff presses the communicating protrusion 6 by fingers and presses the communicating protrusion 6 to penetrate the elastic sealing layer to be located in the communicating hole B3, meanwhile, a clamping ring on the surface of the communicating protrusion 6 is clamped with a clamping groove formed in the inner wall of the communicating hole, the main balloon 4 is close to the auxiliary balloon 5, and then the medical staff can place the main balloon 4 and the auxiliary balloon 5 into a uterine cavity of a patient and inject water into the main balloon 4 and the auxiliary balloon 5, so that the main balloon 4 and the auxiliary balloon 5 expand in the uterine cavity of the uterine cavity, and the main balloon 4 and the auxiliary balloon 5 are fixed in the cavity wall of the uterine cavity to compress the hemostasis balloon for compressing cavity;

one saccule is used for compression hemostasis in the uterine cavity and the other saccule is used for compression hemostasis outside the uterine cavity: two sacculus all can be located the palace intracavity and carry out hemostasis by compression and use: medical personnel tear the sterile sealing bag and take out the compression hemostasis balloon from the sterile sealing bag, liquid is not injected into the balloon in an initial state, the medical personnel prick through an elastic sealing layer in the communicating hole A2 by using a pointed tool, then the auxiliary balloon 5 is pulled and moved on the surface of the tube body 1, the auxiliary balloon 5 covers the position of the communicating hole A2, the communicating protrusion 6 corresponds to the communicating hole A2, then the medical personnel slowly straightens the communicating protrusion 6 from a transverse state by using hands to enable the communicating protrusion 6 to stand up, then the nursing personnel press the communicating protrusion 6 by using fingers and press the communicating protrusion 6 to penetrate through the elastic sealing layer to be positioned in the communicating hole A2, a clamping ring on the surface of the communicating protrusion 6 is clamped with a clamping groove arranged on the inner wall of the communicating hole, the main balloon 4 is far away from the auxiliary balloon 5, then the main balloon 4 can be placed into the uterine cavity of the patient by the medical personnel, the auxiliary balloon 5 is positioned at the position of the opening in the vagina, water is injected into the main balloon 4 and the auxiliary balloon 5, so that the wall 4 of the uterine cavity is expanded inside and outside the uterine cavity of the patient, the main balloon is expanded in the vagina, and the auxiliary balloon 4 is fixed at the position of the uterine cavity to compress the uterine cavity and the uterine cavity to carry out the uterine cavity.

The above embodiments are preferred embodiments of the present invention, but the present invention is not limited to the above embodiments, and any other changes, modifications, substitutions, combinations, and simplifications which do not depart from the spirit and principle of the present invention should be equivalent replacement modes, and all should be included in the protection scope of the present invention.

In the description of the present invention, it is to be understood that the terms indicating orientation or positional relationship are based on the orientation or positional relationship shown in the drawings, and are only for convenience of description and simplification of description, and do not indicate or imply that the equipment or elements referred to must have a specific orientation, be constructed and operated in a specific orientation, and thus, should not be construed as limiting the present invention.

Claims

1. The utility model provides a hemostasis device of gynaecology and obstetrics, includes body (1), its characterized in that, the tip and the surface of body (1) are equipped with main sacculus (4) and vice sacculus (5) respectively, body (1) surface is equipped with intercommunication portion A (2) and intercommunication portion B (3) respectively, the intercommunication of vice sacculus (5) inner circle wall has one and intercommunication portion A (2) and intercommunication portion B (3) the protruding (6) of intercommunication that match.

2. A hemostatic device according to claim 1, wherein the tube (1) comprises a guide tube, a drainage tube connector, a main balloon water-filling tube, a control valve, a secondary balloon water-filling tube and a one-way valve.

3. A hemostatic device according to claim 1, wherein the main balloon (4) is connected to the end of the main balloon water-filling tube, and the auxiliary balloon (5) is connected to the auxiliary balloon water-filling tube by the connection part and the connection protrusion (6).

4. A hemostatic device according to claim 1, wherein the communication part a (2) and the communication part B (3) comprise communication holes, and the communication holes are covered with an elastic sealing layer.

5. A hemostatic device according to claim 1, wherein a liquid inlet hole communicated with the inside of the secondary balloon (5) is arranged inside the communicating bulge (6) in a penetrating way.

6. The hemostatic device for department of obstetrics and gynecology as claimed in claim 4, wherein the inner wall of the communicating hole is provided with a clamping groove, and the surface of the communicating bulge (6) is provided with a clamping ring matched with the clamping groove.