Background
And aortic distensible diseases including aortic aneurysm, aortic dissection and the like. Clinically, the aortic dilatation disease is a very dangerous vascular disease, and once the aortic dilatation disease is treated, the aortic dilatation disease should be treated correspondingly as soon as possible. At present, the minimally invasive interventional therapy technology utilizing the intracavity isolation principle is widely utilized, and a compressed aorta stent with a tectorial membrane is delivered to the position of a diseased aorta by a set of delivery system with a thinner caliber and then is released accurately. The aorta bracket is covered on the diseased aorta and forms a new blood flow channel; after the diseased aorta loses the blood supply, the residual blood at the diseased aorta gradually organizes and forms thrombus until gradually recovering to be close to the original shape, thereby achieving the aim of treatment. This technique greatly reduces surgical trauma while allowing the patient to recover more quickly.
However, since there are many branch arteries in the aorta, after the covered aortic stent is placed in the aorta, blood supply to the diseased aorta is lost and blood circulation through the branch arteries is prevented, so that clinically, it is necessary to open windows in the corresponding branch arteries of the aortic stent to maintain blood supply in the branch arteries. In the clinical operation process, some doctors can choose to temporarily open windows on the covered stent according to the condition of a patient, the window opening position is inaccurate or the size is difficult to control due to temporary window opening, and the whole covered stent is damaged due to high window opening difficulty when the control is not good; in part, the covered stent with a window is customized according to the condition of a patient, so that the window opening accuracy can be achieved, but the operation time is inevitably prolonged, the inconvenience is brought to a doctor patient, and particularly, the life risk is caused to a critical patient.
Disclosure of Invention
In order to solve the problems, the invention provides a customization-free accurate external windowing aortic stent which does not need to be customized, and medical workers can rapidly and accurately window on the aortic stent according to the condition of a patient in the using process.
In order to achieve the purpose, the invention is realized by the following technical scheme: a subscription-free precision extra-corporeal fenestration aortic stent, comprising:
the metal stent is a tubular body, and the shape and the size of meshes of the metal stent are the same; and
the covering film is formed by sequentially arranging a plurality of covering sheets at the beginning, the covering film covers the metal support and blocks the meshes, and different marks are engraved on each covering sheet.
Further, the covering pieces sequentially cover the meshes, and the covering pieces are arrayed and overlapped end to end.
Further, the cover piece includes the upper strata membrane and pastes the lower floor film on the upper strata membrane, the edge of upper strata membrane surpasss the edge of lower floor film, the lower floor film can inlay and establish in the mesh.
Furthermore, the metal support net is provided with positioning pins extending towards the inside of the metal support net, and the positioning pins sequentially penetrate through the mutually overlapped upper layer films.
Further, the end of the positioning pin is provided with a fixing cap.
Further, the top of the fixing cap is provided with a hook.
Further, the lower surface of the covering piece is provided with waterproof sealant, and the waterproof sealant can seal the two adjacent overlapped covering pieces with a film.
The customization-free precise external windowing aortic stent at least comprises the following advantages:
the customization-free precise external windowing aortic stent comprises a metal stent mesh and a covering film. The covering film is formed by sequentially arranging a plurality of elastic covering sheets in an array from head to tail in a sealing and overlapping manner. When windowing is needed, simulation positioning is carried out through a computer, the covering piece corresponding to the branch artery is found accurately, and the covering piece at the corresponding position is taken down according to the digital mark on the covering piece, so that the accuracy of windowing can be guaranteed. Because the cover film comprises a plurality of single cover pieces, the single cover piece can be quickly taken down, so that the windowing time can be shortened, the windowing quality is improved, the whole operation time is shortened, the operation success rate is finally improved, and meanwhile, the operation on the whole support can be avoided, and the misoperation is reduced.
Detailed Description
Embodiments of the present invention will be described in detail below with reference to the accompanying drawings. The following examples are only for illustrating the technical solutions of the present invention more clearly, and therefore are only examples, and the protection scope of the present invention is not limited thereby.
Referring to fig. 1 to 4, a free-form precise external windowingaortic stent 10 includes ametal stent mesh 100 and acover film 200.
Referring to fig. 1 to 3, in particular, the metal stent mesh is a tubular body. Themesh openings 110 of themetal stent netting 100 are identical in shape and size. In this implementation. Themesh 110 may besquare mesh 110 formed by criss-cross of wires, orinclined diamond mesh 110 formed by obliquely crossing of wires. Thecover film 200 is formed by sequentially and hermetically overlapping a plurality ofcover sheets 210 in an array from end to end. Thecover film 200 is covered on the metal holder. The coveringsheet 210 is jammed over themesh 110. Each of the cover sheets is imprinted with a different mark. The mark can be a regularly arranged number, a specific symbol or a coordinate position. During operation, firstly, the computer is used for simulating and positioning the pathological changes and the covered stent, so that the position of the branch artery corresponding to the position needing windowing on the free-customized accurate external windowingaortic stent 10 can be accurately determined; then, according to the marked position, thecovering sheet 210 at the corresponding position is removed, so that the fenestration can be formed, and the exempt precise in-vitro fenestrationaortic stent 10 can be communicated with the branch artery; finally, the non-customized precise external windowingaortic stent 10 is sent to a preset position in the aorta. Through this exempt from to customize accurate external windowingaortic support 10, need not customize in advance, then can be quick, accurate windowing, can reduce the windowing time, improve the windowing quality, and then reduce whole operation time, finally improve the operation success rate, simultaneously, this kind of mode can also avoid operating whole support to reduce the maloperation.
With continued reference to fig. 1, in this embodiment, thecovering sheets 210 are sequentially overlaid on themesh 110, and thecovering sheets 210 are arrayed and stacked end-to-end. When the non-customized precise extra-corporealaortic stent 10 is placed in the aorta, the head end of thecover sheet 210 is located at the blood inlet end of the aorta, and the tail end of thecover sheet 210 is located at the bleeding end of the aorta (the direction of the arrow in fig. 1 is the blood flow direction). When the non-customized accurate extracorporeal windowingaortic stent 10 is positioned in an aorta, under the action of blood pressure, the arrayed end-to-end overlappingcover sheets 210 form fish scales which are mutually attached to form a blood flow channel, and the fish scale type bionic structure is convenient for blood circulation and can prevent blood leakage.
Referring to fig. 1 and 4, in the present embodiment, the coveringsheet 210 includes anupper film 211 and alower film 212 attached to theupper film 211. The edge of theupper film 211 extends beyond the edge of thelower film 212, and thelower film 212 can be embedded in thesquare mesh 110. In this way, thecovering sheets 210 can be pre-fixed, and thecovering sheets 210 are regularly arranged, so that the distance between thecovering sheets 210 is kept unchanged, and thecovering sheets 210 are prevented from being dislocated and leaking, thereby ensuring the sealing performance of the whole coveringfilm 200. In the present embodiment, themetal stent mesh 100 is provided withpositioning pins 120 extending toward the inside of themetal stent mesh 100. Thepositioning pins 120 sequentially pass through theupper films 211 stacked on each other. The end of thepositioning pin 120 is provided with afixing cap 130. The top of thefixing cap 130 is provided with ahook 131. Thepositioning pin 120 is arranged inside themetal support net 100, so that the smoothness of the outer wall of theaorta support 10 with an accurate external windowing is guaranteed, the human tissue is prevented from being scratched by the raisedpositioning pin 120, and the comfort of a human body can be improved. The two pieces of theupper film 211 stacked on each other can be further fixed by thepositioning pins 120 and thefixing caps 130, and knocking and leakage between theupper films 211 can be prevented. Thehook 131 on thefixing cap 130 is convenient to take down thefixing cap 130, when thesingle covering sheet 210 needs to be removed, the straight rod tool with thehook 131 at the end portion can extend into theaorta support 10 free of customization of accurate external windowing, thehook 131 on the straight rod is hung on thehook 131 on thefixing cap 130, the straight rod is pulled, thefixing cap 130 can be taken down, and thecorresponding covering sheets 210 can be taken down in sequence.
In this embodiment, the lower surface of thecover sheet 210 is provided with a waterproof sealant. The waterproof sealant can further seal the twocover sheets 210 that are adjacently stacked. By the waterproof sealant, the sealability between thecover sheets 210 is further increased.
The specific use method of the above-mentioned customization-free precise external windowingaortic stent 10 is as follows:
during surgery, the non-customized precise externalwindowing aorta stent 10 is combined with an aorta in a computer, so that the head end of thecover sheet 210 is positioned at the blood inlet end of the aorta, and the tail end of thecover sheet 210 is positioned at the bleeding end of the aorta; subsequently, simulation positioning is carried out on the pathological changes and the scanning of the covered stent by calculation, and the position of the branch artery corresponding to the covered stent and needing windowing can be accurately determined according to the marks; then, a straight rod with ahook 131 at the end is inserted into the non-customized precise external windowingaortic stent 10, thehook 131 on the straight rod is hung on thehook 131 on the fixingcap 130, and the fixingcap 130 can be taken down by lifting the straight rod; then, pressing thesingle cover sheet 210 inwards from the outside of the non-customized precise in-vitro fenestrationaortic stent 10 until thecover sheet 210 falls off, so that a window can be formed, and the covered stent can be communicated with the branch artery; and finally, after the windowed non-customized accurate in-vitro windowingaortic stent 10 is sent to a preset position in the aorta, the subsequent treatment can be carried out.
The non-customized precise external windowingaortic stent 10 comprises ametal stent mesh 100 and acovering film 200. Thecover film 200 is formed from a plurality ofcover sheets 210 in an array and stacked end-to-end. When the window is required to be opened, the window is simulated in advance according to the computer, and thecovering piece 210 at the corresponding position is determined to be taken down according to the mark, so that the window opening accuracy can be ensured. Because thecover film 200 is composed of a plurality ofsingle cover sheets 210, thesingle cover sheets 210 can be quickly taken down, the windowing time can be shortened, the windowing quality is improved, the whole operation time is shortened, the operation success rate is finally improved, and meanwhile, the operation on the whole bracket can be avoided, so that the misoperation is reduced.
The arrangement mode of thecovering sheet 210 adopts a fish scale type bionic structure, when the non-customized accurate extra-corporealfenestration aorta stent 10 is placed in the aorta, the head end of thecovering sheet 210 is positioned at the inlet end of the aorta, and the tail end of thecovering sheet 210 is positioned at the outlet end of the aorta. Blood flows in from the inlet end and out from the outlet end. The structure not only facilitates the circulation of blood, but also can prevent the blood from leaking. Thecover sheet 210 includes anupper film 211 and alower film 212 adhered to theupper film 211. Theunderlayer 212 can be embedded within thesquare mesh 110. In this way, the coveringsheets 210 can be pre-fixed, and the coveringsheets 210 are regularly arranged, so that the distance between the coveringsheets 210 is kept unchanged, and the coveringsheets 210 are prevented from being dislocated and leaking, thereby ensuring the sealing performance of thewhole covering film 200. Thepositioning pin 120 and the fixingcap 130 can further fix the twoupper films 211 stacked on each other, thereby preventing theupper films 211 from being knocked to bend and causing leakage. Thehook 131 of the fixingcap 130 facilitates the removal of the fixingcap 130. The waterproof sealant further increases the sealability between thecover sheets 210.
Finally, it should be noted that: while there have been shown and described what are at present considered the fundamental principles and essential features of the invention and its advantages, it will be apparent to those skilled in the art that the invention is not limited to the details of the foregoing exemplary embodiments, but is capable of other specific forms without departing from the spirit or essential characteristics thereof. The present embodiments are therefore to be considered in all respects as illustrative and not restrictive, the scope of the invention being 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 therefore intended to be embraced therein. Any reference sign in a claim should not be construed as limiting the claim concerned.
Furthermore, it should be understood that although the present description refers to embodiments, not every embodiment may contain only a single embodiment, and such description is for clarity only, and those skilled in the art should integrate the description, and the embodiments may be combined as appropriate to form other embodiments understood by those skilled in the art.