Stent insertion device for connecting human digestive organs

Abstract

A stent insertion device for connecting human digestive organs includes a first handle being connected to one side of an outer tube, the first handle including a first inner passage communicating with the outer tube, a second handle being connected to a first side of an inner tube, the second handle including a second inner passage communicating with the inner tube, wherein a mounting space is provided between the outer tube and the inner tube at a second side of the inner tube, a stent for connecting human digestive organs being compressed and mounted to the mounting space, a third handle being connected to a first side of an insulation tube, the third handle including a third inner passage communicating with the insulation tube, and a needle knife being connected to a second side of the insulation tube.

Claims

1. A stent insertion device for connecting human digestive organs, the stent insertion device comprising: a first handle being connected to one side of an outer tube, the first handle including a first inner passage communicating with the outer tube; second handle being connected to a first side of an inner tube moveably inserted into the outer tube and the first inner passage, the second handle including a second inner passage communicating with the inner tube, wherein a mounting space is provided between the outer tube and the inner tube at a second side of the inner tube, a stent for connecting human digestive organs being compressed and mounted to the mounting space; a third handle being connected to a first side of an insulation tube moveably inserted into the inner tube and the second inner passage, the third handle including a third inner passage communicating with the insulation tube; and a needle knife being connected to a second side of the insulation tube, the needle knife including a fourth inner passage communicating with the insulation tube and protruding from the outer and inner tubes during hole forming operations on a stomach and a biliary duct wherein the needle knife is inserted into the inner tube by the third handle moving rearward after the hole forming operation on the stomach and the biliary duct are completed.

2. The stent insertion device of claim 1, wherein a guide wire is provided to be moveably inserted into the third inner passage, the insulation tube, and the fourth inner passage.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The above and other objects, features and other advantages of the present invention will be more clearly understood from the following detailed description when taken in conjunction with the accompanying drawings, in which:

(2) FIG. 1 is a view of a stent insertion device for connecting human digestive organs according to an embodiment of the present invention;

(3) FIGS. 2a and 2b are sectional views of FIG. 1; and

(4) FIGS. 3a, 3b, 4a, 4b, 5a, 5b, 6a, 6b, and 7 are operation state views of the stent insertion device according to the embodiment of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

(5) Hereinbelow, an exemplary embodiment of the present invention will be described in detail with reference to the accompanying drawings.

(6) As shown in FIGS. 1 to 7, a stent insertion device 100 for connecting human digestive organs according to the embodiment of the present invention is used when a stent 1 for connecting human digestive organs is mounted so as to connect the biliary duct 4 and the stomach 5 to each other when a lesion part having stenosis or blockage occurs at a portion of the biliary duct 4 adjacent to the duodenum 3.

(7) That is, the stent insertion device 100 for connecting human digestive organs is used when the stent 1 for connecting human digestive organs is mounted such that digestive enzymes of the liver 6 and the pancreas 7 or abscesses caused due to the lesion part are moved to the stomach 5 by osmotic pressure.

(8) In addition, the stent insertion device 100 for connecting human digestive organs includes an outer tube 10 and a first handle 11 connected to one side of the outer tube 10.

(9) Here, the first handle 11 includes a first inner passage 11a provided therein communicating with the outer tube 10.

(10) Furthermore, the stent insertion device 100 for connecting human digestive organs includes an inner tube 20 moveably inserted into the outer tube 10 and the first inner passage 11a and a second handle 21 being connected to a first side of the inner tube 20.

(11) Here, the second handle 21 includes a second inner passage 21a communicating with the inner tube 20, and a mounting space 20a is provided between the outer tube 10 and the inner tube 20 at a second side of the inner tube 20, the stent 1 for connecting human digestive organs being compressed and mounted to the mounting space.

(12) In addition, the stent insertion device 100 for connecting human digestive organs includes an insulation tube 30 moveably inserted into the inner tube 20 and the second inner passage 21a, and a third handle 31 connected to a first side of the insulation tube 30.

(13) Here, the third handle 31 includes a third inner passage 31a provided therein communicating with the insulation tube 30, and a needle knife 32 is connected to a second side of the insulation tube 30 and protrudes from the outer and inner tubes 10, 20 during hole forming operations on the stomach 5 and the biliary duct 4.

(14) In addition, the needle knife 32 includes a fourth inner passage 32a provided therein communicating with the insulation tube 30 and is connected to an electric wire 2a of a high frequency generator 2 inserted into the third inner passage 31a, the insulation tube 30, and the fourth inner passage 32a.

(15) Furthermore, the stent insertion device 100 for connecting human digestive organs includes a guide wire 40 moveably inserted into the third inner passage 31a, the insulation tube 30, and the fourth inner passage 32a.

(16) In addition, the stent 1 for connecting human digestive organs includes expanded tube parts 1a protruding from opposite sides thereof and coated with medical membranes having affinity with the human body.

(17) According to the embodiment of the present invention, the operation and effect of the stent insertion device 100 for connecting human digestive organs, which has above-mentioned configuration, will be described hereinafter.

(18) As shown in FIGS. 1 to 7, when the lesion part having stenosis or blockage occurs at a portion of the biliary duct 4 adjacent to the duodenum 3, a portion of a human body surface is cut, and an endoscope and the outer tube 10 are pushed through the cut part and inserted into the human body.

(19) Here, the needle knife 32 does not protrude from the outer and inner tubes 10, 20, the guide wire 40 is inserted into the third inner passage 31a, the insulation tube 30, and the fourth inner passage 32a, and the stent 1 for connecting human digestive organs is compressed and mounted to the mounting space 20a defined between the outer tube 10 and the inner tube 20.

(20) In addition, when an operation position of the stomach 5 is checked by the endoscope, the outer tube 10 is located at the operation position of the stomach 5.

(21) Next, after the needle knife 32 is exposed from the outer and inner tubes 10, 20 by the third handle 31 moving forward, the high frequency generator 2 is operated such that electric current is supplied to the needle knife 32 via the electric wire 2a.

(22) Accordingly, high-frequency heat is produced in the needle knife 32.

(23) Next, the needle knife 32 pierces the stomach 5 and the biliary duct 4 so as to form holes thereon by the first, second, and third handles 11, 21, 31 and the guide wire 40 moving forward together from the stomach 5 to the biliary duct 4.

(24) Here, while positions of holes to be formed on the stomach 5 and the biliary duct 4 are burned by high-frequency heat produced in the needle knife 32, the holes are formed by a piercing force of the needle knife 32.

(25) Furthermore, since the guide wire 40 supports the outer and inner tubes 10, 20 and the insulation tube 30 during the hole forming operations on the stomach 5 and the biliary duct 4 by the needle knife 32, the outer and inner tubes 10, 20 and the insulation tube 30 moving forward are not bent.

(26) In addition, after the hole forming operations on the stomach 5 and the biliary duct 4 are completed, an operation of the high frequency generator 2 stops while the needle knife 32 positioned in the binary duct 4 is inserted into the inner tube 20 by the third handle 31 moving rearward.

(27) Here, the third handle 31 is moved rearward along the guide wire 40 inserted into the third inner passage 31a, and the insulation tube 30 is also moved rearward along the inserted guide wire 40.

(28) Next, the outer tube 10 is moved rearward until the stent 1 compressed to be mounted to the mounting space 20a of the inner tube 20 is expanded to an initial state by the first handle 11 moving rearward.

(29) Here, the first handle 11 is moved rearward along the inner tube 20 inserted into the first inner passage 11a, and the outer tube 10 is also moved rearward along the inserted inner tube 20.

(30) Accordingly, while the stent 1 for connecting human digestive organs is fitted to holes formed on the stomach 5 and the biliary duct 4, the expanded tube parts 1a of the stent 1 are held on positions neighboring the holes.

(31) That is, the stomach 5 and the biliary duct 4 are connected to each other by the stent 1 for connecting human digestive organs.

(32) Next, the first, second, and third handles 11, 21, 31 are moved rearward such that the outer and inner tubes 10, 20, the insulation tube 30, and the needle knife 32 are escaped from a human body.

(33) Here, since the guide wire 40 inserted into the third inner passage 31a, the insulation tube 30, and the fourth inner passage 32a supports the outer and inner tubes 10, 20 and the insulation tube 30, the outer and inner tubes 10, 20 and the insulation tube 30 moving rearward are not bent.

(34) In addition, a mounting operation of the stent 1 for connecting human digestive organs is completed by the guide wire 40 moving rearward to escape from the human body.

(35) Accordingly, digestive enzymes of the liver 6 and the pancreas 7 do not stagnate in the lesion part having stenosis or blockage occurring at a portion of the biliary duct 4 adjacent to the duodenum 3 and are moved from the biliary duct 4 to the stomach 5 through the stent 1 for connecting human digestive organs by the osmotic pressure.

(36) That is, food digestion performed in the duodenum 3 by digestive enzymes of the liver 6 and the pancreas 7 is performed in the stomach 5.

(37) In addition, abscesses caused due to the lesion part are moved to the stomach 5 by the osmotic pressure and do not stagnate in the lesion part having stenosis or blockage occurring at a portion of the biliary duct 4 adjacent to the duodenum.

(38) Meanwhile, when the stent insertion device 100 does not require high-frequency heat during the hole forming operations on the stomach 5 and the biliary duct 4, that is, during a nonelectric operation, the high frequency generator 2 is not operated such that an electric current is not supplied to the needle knife 32 by the electric wire 2a.

(39) That is, an operation is performed only by a piercing force of the needle knife 32 without the high-frequency heat.

(40) Although a preferred embodiment of the present invention has been described for illustrative purposes, those skilled in the art will appreciate that various modifications, additions and substitutions are possible, without departing from the scope and spirit of the invention as disclosed in the accompanying claims.