KR200442399Y1 - tourniquet - Google Patents

Abstract

The present invention is a tourniquet for bleeding bleeding region, the first belt is provided with a first binding portion at one end and the second binding portion at the other end; A third binding part detachably coupled to the first binding part and a fourth binding part detachably coupled to the second binding part are provided at both ends to surround the body part of the user where the bleeding part is located. Second belt; A hemostatic belt interconnected to a first connection part located at one side of the first fastening part of the first belt and a second connection part located at one side of the third fastening part of the second belt; And a pressing member mounted on the hemostatic belt and pressurizing the bleeding portion to bleed, and a third binding portion of the second belt is coupled to a first binding portion of the first belt to form a first coupling portion. It relates to a tourniquet characterized in that the length from the first connection portion to the second connection portion is equal to or shorter than the length of the hemostatic belt.

The tourniquet according to the present invention has an effect of increasing the hemostatic effect by allowing the pressurizing unit to easily change the pressure pressurizing the opening over time to an appropriate pressure appropriate to the bleeding degree of the patient.

Description

Tourniquet {Tourniquet}

The present invention relates to a tourniquet, and more particularly to a tourniquet capable of pressing the bleeding site of the patient to a suitable pressure.

In general, a medical procedure through a blood vessel of the human body, such as by inserting a catheter into the blood vessel or some other biological tissues, to easily administer the reagents, such as inside the human body, these instruments are perforated passage between the skin tissue and the vessel side After being inserted into the blood vessel through the blood vessel moves along a section of the blood vessel to perform a predetermined medical procedure.

When the catheter is extracted from the punctured part after the procedure using the catheter is completed, the blood in the blood vessel is ejected by pulsation such as a pulse, and the bleeding phenomenon occurs. Therefore, after the treatment treatment is completed, it is necessary to bleed the punctured part. For example, doctors and nurses perform hemostasis treatment by directly blocking the perforated area by hand or using a separate device capable of physical blockage and compression.

However, depending on the patient's situation, hemostasis usually takes from 30 minutes to 3 to 4 hours, so it is difficult for a weak female nurse to perform, and the strength of the acupressure is important, so expertise It was uneconomical for a male doctor to spend time bleeding because the male doctor needed it.

In order to solve this problem, in recent years, a belt member having a length that can cover a bleeding part and having a freely detachable velcro tape at both ends, and a gauze that is attached near the center of the inner surface of the belt member and presses the bleeding part to bleed The tourniquet to be configured has been proposed and used.

The tourniquet is to place the gauze in the bleeding position, and then fixed the gauze with a belt member so that the gauze pressurizes the bleeding site, so that the gauze is continuously pressed to the bleeding site to simplify the hemostasis that takes a long time. It is composed.

However, the conventional tourniquet simply wraps the bleeding portion with a belt member and presses it, and the pressurized degree is fixed by the Velcro fastener, and thus, it is inconvenient to finely adjust the pressurization degree over time.

In order to solve the problems of the prior art as described above, an object of the present invention is to finely adjust the degree of pressing the bleeding region by a predetermined intensity can be appropriately press the bleeding region according to the degree of bleeding of the patient to improve the hemostatic effect To provide a tourniquet to increase.

In order to achieve the above object, the present invention provides a tourniquet for bleeding a bleeding region, comprising: a first belt having a first binding portion at one end and a second binding portion at the other end; A third binding part detachably coupled to the first binding part and a fourth binding part detachably coupled to the second binding part are provided at both ends to surround the body part of the user where the bleeding part is located. Second belt; A hemostatic belt interconnected to a first connection part located at one side of the first fastening part of the first belt and a second connection part located at one side of the third fastening part of the second belt; And a pressing member mounted on the hemostatic belt and pressurizing the bleeding portion to bleed, and a third binding portion of the second belt is coupled to a first binding portion of the first belt to form a first coupling portion. It provides a tourniquet, characterized in that the length from the first connection portion to the second connection portion is the same as or shorter than the length of the hemostatic belt.

In addition, the tourniquet belt provides a tourniquet, characterized in that consisting of a stretchable material.

In addition, the fourth coupling portion of the second belt is coupled to one surface of the second binding portion of the first belt to form a second coupling portion, the second coupling portion to the support member that is tightly fixed to one side of the bleeding portion of the user It provides a tourniquet characterized in that the detachably coupled.

In addition, the support member includes a support body for receiving a wrist extending from the back of the hand and the hand of the user; A first fixing band fixing one side of the support body to the back of the hand; And a second fixing band for fixing the other side of the support body to the wrist, wherein the first coupling part is located at the bleeding part located at one side of the back of the hand, and the second coupling part is located at the center of the support body. It provides a tourniquet characterized in that it is located.

In addition, the fifth fastening portion is formed in the center of the support body, the first belt provides a tourniquet characterized in that the detachable position is located in the fifth binding portion of the support body.

In addition, the support body provides a tourniquet, characterized in that the receiving groove is formed in a position facing the head bone located on the wrist.

As described above, the tourniquet according to the present invention has an effect of increasing the hemostatic effect by allowing the pressurizing unit to easily change the pressure pressurizing the opening to an appropriate pressure according to the bleeding degree of the patient over time. .

Hereinafter, with reference to the accompanying drawings will be described in more detail the tourniquet according to a preferred embodiment of the present invention.

1 is a view showing the front of the tourniquet according to a preferred embodiment of the present invention, Figure 2 is a view showing the rear of the tourniquet according to a preferred embodiment of the present invention.

 1 and 2, the tourniquet for bleeding the opening through the tissue membrane according to a preferred embodiment of the present invention is the first belt 10, the second belt 20, the hemostatic belt 30, the pressing member 40 and the support member 50 is configured.

The first belt 10 is formed to be elongated in the longitudinal direction and is provided with first and second binding parts 11 and 12 at one end and the other end. The second belt 20 covers the body part of the user whose opening is positioned together with the first belt 10, and the third binding part 21 detachably coupled to the first binding part 11. ) And a fourth binding portion 22 detachably coupled to the second binding portion 12 are provided at both ends.

In one embodiment of the present invention, one surface of the first and second belts 10 and 20 is made of velcro tape, and the other surface of the first and second belts 10 and 20 is made of brushed back and detached to the velcro tape. The first, second, third, and fourth fasteners 11, 12, 21, and 22 may include a Velcro tape or brushed material that is detachably coupled to both ends of the first and second belts 10 and 20. It is configured to be Ricky.

When the first belt 10 and the second belt 20 are coupled to each other to surround the user's body part, the first belt 10 of the second belt 20 is attached to the first fastening portion 11 of the first belt 10. The three binding portions 21 are engaged to form the first coupling portion 25, and the fourth binding portion 22 of the second belt 20 is connected to the second binding portion 12 of the first belt 10. While engaging, the second coupling part 27 is formed.

The hemostatic belt 30 is made of elastic material such as rubber and latex, and has one side of the first fastening part 11 of the first belt 10 and the third fastening part 21 of the second belt 20. It is located interconnected on one side. In detail, one end of the hemostatic belt 30 in the longitudinal direction is fixedly coupled to the first connecting portion 13 provided at a position spaced from the one end of the first binding portion 11 in the center direction thereof, and the hemostatic belt 30 The other end of the longitudinal direction is fixedly coupled to the second connecting portion 23 provided at a position spaced in the center direction at one surface end of the third binding portion 21, wherein the length of the hemostatic belt 20 is the first It is configured to be equal to the length d1 (shown in FIG. 4A) from the connecting portion 13 to the second connecting portion 23.

The pressing member 40 is mounted on the hemostatic belt 30, and presses the opening when the first belt 10 and the second belt 20 wrap the opening, that is, the cuff having a bleeding portion, and the like. 42 and the pressurizing part 46 are included.

The main body 42 has a ring-shaped guiding portion 44 on both sides thereof, and the main body 42 is mounted on the hemostatic belt 30, and the pressing portion 46 is disposed on the upper surface of the main body 42, that is, in the opening direction. Is located.

Pressing portion 46 is to press the opening directly to hemostasis, this pressing portion 46 is a porous structure or similar structure such as sponge to achieve a smooth hemostatic action in a state in close contact with the opening while inducing blocking force and support force Can be molded.

On the other hand, depending on the degree of bleeding of the patient, the pressurizing portion 46 initially presses the opening strongly, and after a predetermined time, the pressurizing portion 46 may press the opening slightly weaker than the first time. In this case, in the related art, after releasing the connection of the conventional belt member to which the gauze was fixed, it was loosely connected again. However, the patient is often unable to know how much looseness, so you should seek help from a professional medical practitioner. Even if the patient knows the degree of loosening, disconnect and reconnect the conventional belt member with the patient's own power. Is very difficult.

The present invention, in order to solve this problem, the first, second, third, fourth fastening portions 11, 12, 21, 22 of the first belt 10 and the second belt 20 are mutually coupled, the pressing portion When 46 is pressurizing the bleeding part of the patient, i.e., the opening, the length d1 from the first connection 13 to the second connection 23 is determined by the length d2 of the hemostatic belt 30 (Fig. 4). B) shorter than, so that the hemostatic belt 30 is partially folded. At this time, the length (d1) from the first connecting portion 13 to the second connecting portion 23 is to be predetermined by a medical professional. After that, when the pressing portion 46 has to press the opening weaker than the first time, when the first binding portion 11 and the third binding portion 21 are disconnected, the hemostatic belt folded As the 30 is opened, the pressing unit 46 weakly presses the opening by the extended length of the hemostatic belt 30.

In this way, simply disconnecting the first binding portion 11 and the third binding portion 21, the pressing portion 46 to press the strength to press the opening weaker than the first, and also the strength, Since only a predetermined weak adjustment can be made, there is an advantage that the pressure unit 46 can easily change the pressure pressurizing the opening to an appropriate pressure according to the bleeding degree of the patient over time.

The support member 50 is for supporting the body part when the first belt 10 and the second belt 20 are combined to surround the body part of the user, so that the user feels comfortable. For example, the support member 50 is positioned above the support body 52 to accommodate the back of the user's hand and the wrist extending from the back of the hand, and to secure the upper side of the support body 52 to the back of the hand. A first fixing band 54 and a second fixing band 56 positioned below the supporting body 52 to fix the lower side of the supporting body 52 to the wrist. In the center of the support body 52, a second coupling part 27 formed by coupling the first belt 10 and the second belt 20 is positioned. And when the back of the user's hand and wrist is accommodated in the front of the support body 52, the auxiliary support 53 is coupled to the back of the support body 52 to ensure that the support body 52 is firmly configured. In addition, when the user wears the support member 50 for a long time, the head bone protruding from the wrist does not feel pain by the support body 52 of the support member 50. A receiving groove 52a is formed at a position facing the head bone to be located, and the head bone is accommodated in the receiving groove 52a, so that the user can bleed the bleeding site in a more comfortable state.

And since the first fixing band 54 and the second fixing band 56 is used for fixing the support member 50 of the present invention to the body, the structure of the Velcro tape shape, or adjust the length of the strap You can use either a belt or a lanyard.

In addition, when the second coupling part 27 is positioned at the center of the support body 52, the fifth binding part is attached to the support body 52 such that the first belt 10 is detachably positioned at the support body 52. 58 is positioned, and the first belt 10 is coupled to the fifth fastening portion 58. This is to adjust the overall length of the first belt 10 according to the individual thickness variation of the wrist. When the first belt 10 and the fifth fastening unit 58 are coupled, the thickness of the wrist is thick. The fifth fastening portion 58 is coupled to a position near the end of the second fastening portion 12 of the first belt 10, and if the thickness of the wrist is thin, the second fastening portion 12 of the first belt 10 is formed. The fifth fastening portion 58 is coupled to a position far from the end of the c).

On the other hand, the first belt 10 and the fifth fastening portion 58 of the support body 52 are separated from each other according to the body portion, the support member 50 is omitted, the first belt 10 and the second belt Only 20 may be configured to wrap the body part and bleed the bleeding part of the user.

Hereinafter, with reference to the accompanying drawings will be described the operation of the tourniquet according to a preferred embodiment of the present invention.

3 is a view showing a state of use of the tourniquet according to a preferred embodiment of the present invention, Figure 4 is a view showing to explain the length of the tourniquet belt of the tourniquet according to a preferred embodiment of the present invention.

Referring to the drawings, the tourniquet according to a preferred embodiment of the present invention is to bleed the bleeding portion located in the wrist of the arm, that is, the opening, first, the support body 52 of the support member 50 to the back of the user's hand and wrist After positioning, the support body 52 is fixed to the back of the user's hand and wrist by using the first and second fixing bands 54 and 56. The support member 50 may be positioned in advance on the wrist and the back of the patient before the opening of the wrist by the needle or the like.

Thereafter, referring to FIG. 4A, the first and third fastening portions 11 and 21 of the first and second belts 10 and 20 are connected to each other so that the first coupling portion 25 is formed. At this time, the length d1 from the first connecting portion 13 to the second connecting portion 23 is shorter than the length of the hemostatic belt 30 (d2: shown in b of FIG. 4) so that the hemostatic belt 30 is partially. Fold it.

Subsequently, the other surface of the second binding unit 12 is connected to the support body 52, and then one surface and the fourth binding unit 22 of the second binding unit 12 of the first and second belts 10 and 20 are connected. Are connected to each other, the pressing portion 46 of the pressing member 40 presses the opening to start the hemostasis.

After that, referring to FIG. 4B, when the pressing part 46 has to press the opening loosely than the first time after a predetermined time, the first binding part 11 and the third binding part 21 are closed. By releasing the connection, the folded length d2 of the hemostatic belt 30 is extended, so that the pressing portion 46 loosely presses the opening.

As described so far, the tourniquet of the present invention is the first to determine the strength of the pressing portion 46 to press the opening simply by releasing the connection between the first binding portion 11 and the third binding portion 21. It is possible to press more lightly, and the strength can also be adjusted only weakly as predetermined, so that the pressure of the pressurizing portion 46 to pressurize the opening over time can be easily at an appropriate pressure according to the degree of bleeding of the patient. There is an advantage to change. There is an advantage.

Meanwhile, in one embodiment of the present invention, one surface of the first and second belts 10 and 20 is formed of a Velcro tape and the other surface is brushed, but the present invention is not limited thereto. Only the 3, 4 binding parts 11, 12, 21, 22 may be comprised by means which mutually detachably couple | bonds, ie, a Velcro tape, a napping, or an adhesive.

Although the present invention has been described in detail in the above embodiments, it will be apparent to those skilled in the art that various modifications and changes are possible within the technical spirit of the present invention, and such modifications and modifications belong to the appended utility model registration claims.

1 is a view showing the front of the tourniquet according to a preferred embodiment of the present invention.

2 is a view showing the rear of the tourniquet according to a preferred embodiment of the present invention.

3 is a view showing a state of use of the tourniquet according to a preferred embodiment of the present invention.

Figure 4 is a view showing for explaining the length of the tourniquet belt of the tourniquet according to a preferred embodiment of the present invention.

<Explanation of symbols for the main parts of the drawings>

10: first belt 11: first binding portion

12: 2nd binding part 13: 1st connection part

20: second belt 21: third binding portion

22: fourth binding portion 23: second connecting portion

25: first coupling portion 27: second coupling portion

30: hemostatic belt 40: pressing member

42: main body 44: guiding part

46: pressure portion 50: support member

52: support body 52a: guide groove

53: auxiliary support 54: first fixing band

56: second fixing band 58: fifth binding portion

Claims (6)

In tourniquet for bleeding bleeding area, A first belt having a first binding portion at one end and a second binding portion at the other end; A third binding part detachably coupled to the first binding part and a fourth binding part detachably coupled to the second binding part are provided at both ends to surround the body part of the user where the bleeding part is located. Second belt; A hemostatic belt interconnected to a first connection part located at one side of the first fastening part of the first belt and a second connection part located at one side of the third fastening part of the second belt; And It is mounted on the hemostatic belt, and includes a pressing member for pressing the bleeding site to hemostatic, The third binding part of the second belt is coupled to the first binding part of the first belt to form a first coupling part, wherein the length from the first connection part to the second connection part is equal to or shorter than the length of the hemostatic belt. Tourniquet characterized in that. The method of claim 1, The tourniquet is characterized in that the tourniquet is composed of a stretchable material. The method of claim 1, The fourth binding part of the second belt is coupled to one surface of the second binding part of the first belt to form a second coupling part, Tourniquet characterized in that the second coupling portion is detachably coupled to the support member that is tightly fixed to one side of the bleeding portion of the user. The method of claim 3, wherein The support member is: A support body for receiving a user's back of the hand and a wrist extending from the back of the hand; A first fixing band fixing one side of the support body to the back of the hand; And A second fixing band for fixing the other side of the support body to the wrist, Tourniquet characterized in that the first coupling portion is located in the bleeding portion located on one side of the back of the hand, the second coupling portion is located in the center of the support body. The method of claim 4, wherein A tourniquet characterized in that a fifth binding portion is formed in the center of the support body, so that the first belt is detachably positioned at the fifth binding portion of the support body. The method of claim 4, wherein Tourniquet characterized in that the receiving groove is formed in a position facing the head bone located on the wrist in the support body.

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