The application claims the benefit of Taiwan application serial No. 105127901 filed on Aug. 30, 2016, and the entire contents of which are incorporated herein by reference.
The present invention relates to a medical apparatus and, more particularly, to a vascular puncture sealing device.
Vascular interventional procedures involve accessing a corporeal vessel or other lumen through a percutaneous sheath. The sheath is inserted into vascular lumen so that a medical procedure can be performed through the sheath.
The indwelling sheath must be removed after the medical treatment using the vascular interventional procedures. At this time, the puncture hole in the vessel wall must be sealed and stanched, preventing bleeding at the puncture wound that could cause serious complications.
To fix the above problem, in addition to directly pressing the puncture wound with an external force for several hours, as shown in
After the medical worker has finished the vascular interventional therapy, the sheath I used in the operation is indwelled. Namely, an end of the sheath I is moved into the blood vessel V via an opening O in the vessel wall W. Next, the vascular puncture sealing device 9 is placed into the sheath I, and the first and second sealing members 92 and 93 are moved toward the blood vessel V along the sheath I by using the pressing member 94 until the first sealing member 92 enters the blood vessel V. Then, the medical worker pulls the wire 91 and the sheath I backward to abut the first sealing member 92 against an inner side of the vessel wall Q, accomplishing positioning of the first sealing member 92.
Next, as shown in
By pressing the first sealing member 92 and the second sealing member 93 against the inner side and the outer side of the vessel wall W, respectively, an appropriate pressure can be imparted to the opening O to reliably achieve the stanching purposes. However, in actual operation, it is not easy to accurately position the second sealing member 93 in the desired location outside of the blood vessel W, such that the vascular puncture sealing device 9 provides an unsatisfactory stanching effect. Furthermore, the medical worker has to proceed with positioning of the first sealing member 92 and the second sealing member 93 separately, which is troublesome in use and requires a longer operational period by the medical worker. Thus, improvement to the vascular puncture sealing device 9 is necessary.
To solve the above problem, the present invention provides a vascular puncture sealing device that can effectively seal an opening in a blood vessel.
Another objective of the present invention is to provide a vascular puncture sealing device that can be used simply and easily.
A vascular puncture sealing device according to the present invention includes a tube unit and a sealing unit. The tube unit includes an inner tube and an outer tube. The inner tube includes a first compartment therein. The outer tube includes a second compartment therein. The inner tube is slidably received in the second compartment. The sealing unit is coupled to an end of the inner tube. The sealing unit includes an abutting portion and an expansion portion. The abutting portion includes a first face and a second face opposite to the first face. The abutting portion further includes a through-hole extending from the first face through the second face. The expansion portion includes a chamber therein. The chamber intercommunicates with the through-hole of the abutting portion.
The vascular puncture sealing device according to the present invention uses the abutting portion to abut the inner side of the vessel wall and uses the expansion portion having the chamber filled with blood flow to thereby expand the expansion portion for sealing the opening in the vessel wall and for anchoring the outer side of the vessel wall. Thus, the sealing unit can reliably be positioned to the opening of the vessel wall while simultaneously exerting pressures to the inner side and the outer side of the vessel wall, effectively achieving the stanching purposes.
In an example, the outer tube includes a positioning hole extending through a tubular wall of the outer tube and intercommunicated with the second compartment. Thus, a medical worker can know that the vascular puncture sealing device has been moved in an insertion direction to the predetermined position according to the presence of blood in the second compartment.
In an example, the abutting portion and the expansion portion are integrally connected with each other to increase the structural strength of the sealing unit during use, thereby effectively exerting pressures on the inner side and the outer side of the vessel wall.
In an example, the abutting portion is located in the second compartment, and the expansion portion extends through the end of the inner tube into the first compartment and is located in the first compartment. This reduces interference form the abutting portion when the expansion portion is expanding into the predetermined shape.
In an example, the sealing unit can be made of a biocompatible material, such as polyurethane, polytetrafluoroethylene, titanium, or a titanic alloy. Thus, when the sealing unit is placed into a body of an organism to seal a vessel, the sealing unit will not cause harm to the organism. The sealing unit can be made of a biodegradable material, such as polylactic acid. Thus, the sealing unit can be degraded in the body.
In an example, the inner surface of the expansion portion is coated with thrombogenic agents, such as thrombin or chitosan. Thus, when blood flows through the through-hole into the chamber, the blood can rapidly clot under the action of thrombogenic agents, such that the expansion portion can rapidly expand into the predetermined shape.
In an example, the abutting portion includes a stagnant film located in the through-hole. The stagnant film with a plurality of apertures stagnates blood flow within the chamber of the expansion portion.
In an example, the sealing unit includes a pull string attached to an outer periphery of the expansion portion. Thus, the medical worker can pull the pull string in the retraction direction to fix the expansion portion.
The present invention will become clearer in light of the following detailed description of illustrative embodiments of this invention described in connection with the drawings.
The “vascular puncture sealing device” described in the invention can cooperate a sheath I used in vascular interventional technology. As shown in
With reference to
Specifically, the tube unit 1 includes an inner tube 11 and an outer tube 12. The inner tube 11 includes a first end 11a and a second end 11b opposite to the first end 11a. The outer tube 12 includes a first end 12a and a second end 12b opposite to the first end 12a. The inner tube 11 includes a first compartment S1 therein. The outer tube 12 includes a second compartment S2 therein. The inner tube 11 is slidably received in the second compartment S2. An outer diameter of the outer tube 12 matches with an inner diameter of a sheath I. Thus, the outer diameter of the outer tube 12 and the inner diameter of the sheath I can be appropriately fit.
In this embodiment, the outer tube 12 includes a positioning hole 121 extending through a tubular wall of the outer tube 12 and intercommunicated with the second chamber S2. When the first end 12a of the outer tube 12 extends beyond an end of the sheath I to expose the positioning hole 121 outside of the sheath I, the blood in the blood vessel can flow into the second compartment S2, such that a medical worker can know that the outer tube 12 is located in a predetermined position. Alternatively, in a case that the outer tube 12 does not include the positioning hole 121, the medical worker has to adjust the position of the outer tube 12 extending beyond an end of the sheath I to locate the outer tube 12 in the predetermined position.
The sealing unit 2 is coupled to the first end 11a of the inner tube 11. In an example, the sealing unit 2 includes an engaging portion 21 coupled to an inner periphery of the inner tube 11 at a location adjacent to the first end 11a. The sealing unit 2 further includes an abutting portion 22 and an expansion portion 23. The abutting portion 22 and the expansion portion 23 can be integrally connected with each other to increase the structural strength of the sealing unit 2 during use, thereby effectively exerting pressures on the inner side and the outer side of the vessel wall W.
In this embodiment, the abutting portion 22 is in the form of an abutting plate having a first face 22a and a second face 22b opposite to the first face 22a. The second face 22b faces the first end 11a of the inner tube 11. The abutting portion 22 further includes a through-hole 221 extending from the first face 22a through the second face 22b. The abutting portion 22 can be bent to make at least a portion of the second face 22b face an outer periphery of the inner tube 11 and to make at least a portion of the first face 22a face an inner periphery of the outer tube 12, such that a portion of the abutting portion is restrained between the outer periphery of the inner tube 11 and the inner periphery of the outer tube 12. The expansion portion 23 is coupled to the second face 22b of the abutting portion 22 and includes a chamber S3 therein. The chamber S3 intercommunicates with the through-hole 221 of the abutting portion 22. Thus, the abutting portion 22 can be located in the second compartment S2. The expansion portion 23 can extend through the first end 11a of the inner tube 11 into the first compartment S1 and is located in the first compartment S1.
The sealing unit 2 can be made of a biocompatible material, such as polyurethane, polytetrafluoroethylene, titanium, or a titanic alloy. Thus, when the sealing unit 2 is placed into a body of an organism to seal a hole of the vessel wall W, the sealing unit 2 will not cause harm to the organism. The sealing unit 2 can be made of a biodegradable material, such as polylactic acid. Thus, the sealing unit 2 can degrade in the body of organism. Furthermore, the inner surface of the expansion portion 23 can be coated with a thrombogenic material, such as thrombin or chitosan. Thus, when blood flows through the through-hole 221 into the chamber S3, the blood can rapidly clot under the action of the thrombogenic material, such that the expansion portion 23 can rapidly expand into a predetermined shape.
With reference to
With reference to
Next, as shown in
With reference to
In view of the foregoing, the vascular puncture sealing device according to the present invention uses the abutting portion 22 to abut the inner side of the vessel wall W and uses the expansion portion 23 having the chamber S3 into which blood can flow to thereby expand the expansion portion 23 for sealing the opening O in the vessel wall W and for abutting the outer side of the vessel wall W. Thus, the sealing unit 2 can reliably be positioned to the opening O of the vessel wall W while simultaneously exerting pressures to the inner side and the outer side of the vessel wall W, effectively achieving the stanching purposes.
Thus since the invention disclosed herein may be embodied in other specific forms without departing from the spirit or general characteristics thereof, some of which forms have been indicated, the embodiments described herein are to be considered in all respects illustrative and not restrictive. The scope of the invention is to be indicated by the appended claims, rather than by the foregoing description, and all changes which come within the meaning and range of equivalency of the claims are intended to be embraced therein.
Number | Date | Country | Kind |
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105127901 | Aug 2016 | TW | national |