KR20170046527A

KR20170046527A - Miniscapel niddle

Info

Publication number: KR20170046527A
Application number: KR1020150146978A
Authority: KR
Inventors: 김재수; 이건목
Original assignee: 대구한의대학교산학협력단
Priority date: 2015-10-21
Filing date: 2015-10-21
Publication date: 2017-05-02
Also published as: KR101805763B1

Abstract

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a needle having a function of a needle and a scalpel (knife) used in one direction. [0012] According to the present invention, there is provided a dovetail having corners, slopes, and inclinations of corners, the ends of which have a chiseled shape, wherein the stagnation is formed with a channel therein, And the connecting member is inserted into the end side of the grip member and is coupled to the stagnation member. The act of performing the doorknob according to the present invention can simplify the procedure and alleviate the burden on the patient during the procedure.

Description

Brush {MINISCAPEL NIDDLE}

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a needle having a function of a needle and a scalpel (knife) used in one direction.

In general, a suture is also called a needle, and is used to relieve pain caused by damage to a soft tissue by surgically removing, dissecting or cutting soft tissues in one direction.

Figure 1 shows the shape of a conventional donut. The corners of the dovetail 10 are divided into a needle point 11, a recess 12 and a needle 13, and the tip of the needle 13 is sharpened like a chisel. Such a needle can perform the function of needle and scalpel at the same time with the origin of the needle and the needle in the 九针 of the emperor 's inner bore.

On the other hand, in many cases, injection therapy for injecting medicine or other injection liquid or inserting a thread into the human body is performed at the same time in the case of using the doorknob, but in the conventional case, a separate needle Is repeatedly inserted into the affected area, so that the operation is troublesome and causes pain in the patient.

SUMMARY OF THE INVENTION The present invention provides a donor that can simultaneously perform salvage therapy and / or acupuncture.

The inventor of the present invention has devised a method of forming a channel in a stagnation of a needle and basically having a member that can be coupled to a syringe in a process of researching and developing the shape of a needle, And it has come to the present invention by effectively embodying it in accordance with the purpose of the treatment. The gist of the present invention regarding the recognition of the above-mentioned problems and the solution means based on the above is as follows.

(1) A needle-shaped needle having an acupuncture point, a stagnation and an acupuncture point, wherein the end of the acupuncture point has a chisel-like shape, wherein the recess is formed with a channel therein, and a connecting member To the end.

(2) The percussion instrument of (1), wherein a gripping member is provided in the engagement and the connecting member is inserted into the end of the gripping member and is coupled to the recess.

(3) The plug of (1) or (2) above, further comprising a plug coupled to the connecting member.

(4) The percolation needle of (1) or (2), wherein the channel communicates with the tip side of the needle.

(5) The needle of (1) or (2), wherein a hook is formed on a side surface of the needle.

(6) The doorknob of (5), wherein the hook is curved inward of the cone.

(7) The percolation needle of (1) or (2), wherein the inner diameter of the channel is 1/2 to 3/4 of the outer diameter of the stagnation.

(8) The needle of (4) above, wherein the channel is symmetrically communicated to both sides of the tip of the needle.

(9) The donut of (1) or (2), wherein a groove is formed at the tip of the needle.

(10) The donut of (1) or (2), wherein a hole communicating with the conduit is formed on a side of the stagnant body.

(11) The needle of (10), wherein the distance from the tip of the needle to the hole is 1/3 to 1/2 of the entire length of the needle.

The doorking according to the present invention can simplify the procedure by simultaneously performing the stitching and / or the healing process, and relieve the pain that the patient is burdened in the procedure.

1 is a perspective view of a donut according to the prior art;
2 is a perspective view of a donut according to a first embodiment of the present invention;
3 is a perspective view and an exploded perspective view of a doorknob according to a second embodiment of the present invention;
4 is an enlarged view of the needle aspiration according to the third embodiment of the present invention;
FIG. 5 is an enlarged view of a saliva of a needle according to a fourth embodiment of the present invention; FIG.
FIG. 6 is an enlarged view of a needle of a donut according to a fifth embodiment of the present invention; FIG.
7 is a partially enlarged view of the doorknob according to the sixth embodiment of the present invention;

Hereinafter, the present invention will be described in detail with reference to examples. Prior to this, terms and words used in the present specification and claims should not be construed as limited to ordinary or dictionary terms, and the inventor should appropriately interpret the concepts of the terms appropriately It should be construed as meaning and concept consistent with the technical idea of the present invention. Therefore, the configuration of the embodiment described in the present specification is merely the most preferred embodiment of the present invention, and does not represent all the technical ideas of the present invention, so that various equivalents And variations may be made. On the other hand, in the drawings, the same or similar reference numerals are given to the same or equivalent elements in the drawings, and, in the entire specification, when a component is referred to as being "comprising" But may include other components.

Fig. 2 shows a perspective view of a donut according to a first embodiment of the present invention.

The needle 100 is in the shape of a cylindrical needle and has a needle 100 held by a practitioner, a stump 120 corresponding to a body, and a needle 130 for cutting or cutting a soft tissue, And the needle 130 is tapered and its tip 130a is shaped like a knife or chisel to facilitate cutting or cutting. In this case, the outer diameter of the doorknock 100 is preferably 0.5 to 3.0 mm, and the length of the doorknob 100 is preferably 40 to 150 mm.

The dovetail 100 includes a channel 122 formed in the stagnant 120 to perform a medicine treatment for administering a drug solution or an injection solution to the soft tissue along with the intrinsic treatment, ) Can also be performed simultaneously. In this case, the soldering operation is performed in a state in which a seal or a chamber is inserted into the channel 122.

In the embodiment of FIG. 2, the channel 122 communicates with the tip of the needle 130 and the rear end of the needle 110. The channel 122 is communicated from the side of the needle 130 to the center thereof and the channel 122 exposed by the tapered shape of the needle 130 has a generally elliptic shape.

In this case, the inner diameter of the channel 122 is secured to a sufficient diameter to allow the chamber 200 to be inserted, and is preferably 1/2 to 3/4 of the outer diameter of the cylindrical dent 120. If the inner diameter of the channel 122 is less than 1/2, it is difficult to carry out the injecting operation due to excessive external pressure, and if it is more than 3/4, it is difficult to maintain the chisel shape of the tip 130a of the needle 130, .

A connection member 140 is detachably attached to the needle 110 so as to be coupled to a tool for injecting a medicine solution or an injection solution such as a syringe. The connecting member 140 has a hollow truncated conical shape and is tapered from a rear end 144 coupled to a syringe (not shown) to a front end 142 coupled to the vending bottle 110.

In this case, it is preferable that the front end portion 142 is formed to have a sufficient length so as to have a good fastening force with the vial 110. The material of the connecting member 140 is not particularly limited, but a resin or metal material having sufficient rigidity is preferably used for ensuring gripping force against the doorknock 100 and for good connection.

The connecting member 140 also serves as an element gripped by the practitioner when performing the dovetail operation.

Optionally, the dovetail 100 may further include a cap 150 to seal the rear end 144 of the connecting member 140. This stopper 150 is provided to block the inside of the connecting member 140 from external contaminants when it is not accompanied by a medicine treatment. In this case, the end of the cap 150 is preferably machined into a shape corresponding to the hollow truncated conical shape of the rear end 144 of the connecting member 140.

Fig. 3 is a perspective view and an exploded perspective view of the doorknob according to the second embodiment of the present invention.

2, a pipeline 122 is formed in the stagnant 120, and a connecting member 140, which can be coupled to the syringe, and a cap (not shown) 150 are provided.

The dovetail 100 according to the embodiment of FIG. 3 further includes a grip member 160 coupled to the needle 110. Most of the vials 110 are inserted into the holding member 160. In some cases, the end side of the vial 110 may be slightly exposed to the end side of the gripping member 160. [

In this case, the connecting member 140 is inserted into the end side of the grip member 160 in which the vial 110 is inserted, and the front end portion 142 of the connecting member 140 is inserted into the inside of the grip member 160, 110).

The grip member 160 is provided to secure gripping force with respect to the dovetail 100 when the doorknob is performed, and is preferably provided in a flat shape so as to have sufficient area elements.

Fig. 4 shows an enlarged view of the needle penetration according to the third embodiment of the present invention.

2, the structure of the channel 122, the connecting member 140, and the stopper 150 according to the embodiment of FIG. 2 may be the same, and the grip member 160 according to the embodiment of FIG. Configuration can be adopted.

The dovetail 100 according to the embodiment of FIG. 4 is different from the embodiment of FIG. 2 in that the conduit 122 communicates in the lateral direction from the end of the needle 130 to form an outlet 122a do. When the donut 100 is inserted into the soft tissues for the purpose of corpuscular surgery or acupuncture treatment, if the outlet of the channel 122 is formed at the center of the end side of the needle 130 as in the embodiment of FIG. 2 Insertion resistance from soft tissues may occur. In the embodiment of FIG. 4, since the outlet of the channel 122 is formed in the end side direction of the needle 130, the resistance in the soft tissue insertion process can be minimized.

4 (a), when the outlet of the channel 122 is formed only in one direction of the tip side of the needle 130, the solution or injected solution is biased toward the general incense of the soft tissue at the time of the treatment, . In order to prevent or mitigate this, as shown in FIG. 4 (b), the channel 122 preferably has symmetrical outlets 122a and 122a 'formed on both sides of the tip of the needle 130 Do.

Fig. 5 shows an enlarged view of the needle penetration according to the fourth embodiment of the present invention.

In the case of this embodiment as well, as in the embodiment of Fig. 4, the constitution of the pipeline 122, the connecting member 140 and the plug 150 according to the embodiment of Fig. 2 may be the same, The configuration of the holding member 160 according to the example can be adopted.

The dovetail 100 according to the embodiment of FIG. 5 is characterized in that a hook 132 is integrally formed on the side surface of the needle 130 in order to easily mount the seal or chamber to the dovetail 100 . The hooks 132 are preferably formed in a losing manner inwardly from the side of the needle 130 so that the outer diameter of the dovetail 100 does not expand.

In this case, it is advantageous in terms of facilitating the mounting of the chambers or chambers, but it should not be so large as to interfere with the formation of the channel 122, and may be excessively larger than the outer diameter of the chambers or chambers, It should not be so difficult as to keep the mounting state for the user. Therefore, it is preferable to determine the amount of weight loss by appropriately considering this point.

It is also preferable that the tip 132a of the hook 132 be formed in a slightly curved shape inward so as not to receive the insertion resistance from the soft tissue during the procedure.

Fig. 6 shows an enlarged view of the needle penetration according to the fifth embodiment of the present invention.

The dovetail 100 according to the embodiment of FIG. 6 is characterized in that a groove 134 is formed at the tip of the needle 130. The grooves 134 can minimize the damage to fine blood vessels and nerves by finely removing the adhered tissues in a state in which fine blood vessels and nerves are inserted and fixed in the procedure of performing the needle surgery. In this case, it is preferable that the groove 134 is formed at a tip intermediate portion, and the inside of the groove 134 is formed in a rounded shape so that the inserted blood vessels and nerves are not damaged.

The groove 134 may also function as a means by which the chamber or chamber 200 can be easily mounted in a soldering operation, similar to the embodiment of Fig. Needless to say, in the embodiment of FIG. 5, a medicine treatment can be performed through the channel 122.

FIG. 7 is a perspective view of an immersion needle according to a sixth embodiment of the present invention. FIG.

Similarly to the embodiment of FIG. 4, the configuration of the pipeline 122, the connecting member 140, and the cap 150 according to the embodiment of FIG. 2 may be the same as in the embodiment of FIG. The configuration of the holding member 160 according to the embodiment can be adopted.

The dovetail 100 according to the embodiment of FIG. 7 is characterized in that a hole 124 communicating with the conduit 122 is formed on the side of the stagnant body 120. The holes 124 prevent the blood from flowing back to the outside of the skin when bleeding due to damage to the blood vessels in the procedure of performing the opacification. In this case, it is preferable that the distance from the tip of the needle 120 to the hole 124 is 1/3 to 1/2 of the total length of the needle. If the distance to the hole 124 is less than 1/3, if the amount of bleeding is large, the function may not be performed. If the amount of bleeding is more than 1/2, if the needle is inserted thinly, blood flows backward to the outside through the hole 124 It is preferable to be between 1/3 and 1/2. The hole 124 is made to be less than 1/3 from the tip 130a of the needle 130 at the same time in the portion of the needle 130 and the portion of the hole 124. [ In this case, it is possible to prevent backflow by the pressure to put the medicine. More preferably, the direction of the hole is obliquely directed toward the tip of the needle to maximize the purpose of preventing backflow.

As described above, the doorknob 100 according to the present invention can simplify the procedure by simultaneously performing the stabbing therapy and / or the medicinal treatment, and can alleviate the burden on the patient during the procedure.

The foregoing is a description of specific embodiments of the present invention. While the present invention has been particularly shown and described with reference to exemplary embodiments thereof, it is to be understood that the invention is not limited to the disclosed embodiments or constructions. It will be apparent to those skilled in the art that various modifications and variations can be made in the present invention. It should be understood that this is possible.

For example, in the embodiment of FIG. 2, the shape of the connecting member 140 is illustrated as a hollow truncated cone, but the shape of the connecting member 140 is not particularly limited as long as at least the hollow portion therein can be coupled to the end of the syringe And may have a shape in which sufficient area elements are provided on the outer surface thereof so that the surgeon can firmly grip the surgeon during surgeries. In this modification, the holding member 160 provided as a separate member in Fig. 3 may be provided in a structure integrated with the connecting member 140. [

It is therefore to be understood that all such modifications and alterations are intended to fall within the scope of the invention as disclosed in the following claims or their equivalents.

100: Macro 110:
120: stagnation 122: channel
124: hole 130: needle
130a: spit tip
132: hook 132a: hook tip
134: groove 140: connecting member
142: front end portion 144: rear end portion
150: stopper 160: grip member
200: Chamber

Claims

And a connecting member capable of engaging with a syringe is provided on the needle, wherein the needle is provided with a corner of the needle, a needle point, a stagnation, and a needle point, .

[2] The donut according to claim 1, wherein the engaging member is provided with a grip member, and the linking member is inserted into the end of the grip member and is engaged with the recess.

The needle as claimed in claim 1 or 2, further comprising a cap coupled to the connecting member.

3. A needle according to claim 1 or 2, wherein the conduit is in communication with the leading edge of the needle.

The needle according to claim 1 or 2, wherein a hook is formed on a side surface of the needle.

The donut as claimed in claim 5, wherein the hook is curved inward.

3. The needle according to claim 1 or 2, wherein the inner diameter of the channel is 1/2 to 3/4 of the outer diameter of the recess.

The needle as claimed in claim 4, wherein the conduit communicates symmetrically with both tip sides of the needle.

The needle according to claim 1 or 2, wherein a groove is formed at a tip of the needle.

The donut according to claim 1 or 2, wherein a hole communicating with the duct is formed on a side of the stagnant body.

The needle according to claim 10, wherein the distance from the tip of the needle to the hole is 1/3 to 1/2 of the total length of the needle.