Prosthesis (i.e. – artificial body members) – parts thereof – or ai – Arterial prosthesis – Stent structure
Reexamination Certificate
2000-10-24
2003-05-20
McDermott, Corrine (Department: 3738)
Prosthesis (i.e., artificial body members), parts thereof, or ai
Arterial prosthesis
Stent structure
Reexamination Certificate
active
06565598
ABSTRACT:
BACKGROUND OF THE ART
Stents of that kind are known from the state of the art in many different forms. Those stents are used inter alia in connection with percutaneous transluminal angioplasty (PCTA, Percutaneous Transluminal Balloon Angioplasty), in vascular surgery of the heart. Stents however can also serve to dilate other openings in the body or to keep such openings in a dilated condition. That medical procedure is initially preceded by determining the location of the constriction in a coronary blood vessel. A so-called angioplasty balloon is then moved in the artery which has the constriction, the so-called stenosis, to the location of the stenosis where it is inflated. Due to the radially outwardly directed force of the inflated balloon the constriction is dilated and in the optimum case the original passage cross-section of the previously constricted artery is restored. Besides successful dilation of the vessel however side-effects can also occur, which include local splits in the artery, disintegration effects and projections of plate portions and flakes into the lumen of the artery so that, in spite of the dilation effect, blockage of the vessel can still occur. In addition it is possible that a stenosis can recur due to the vessel wall elastically springing back and/or due to the growth of the intima of the vessel. Statistically, that occurs within six months in the case of over 30% of the patients who were treated with PCTA.
In order now immediately after dilation of the blood vessel to ensure a relatively smooth inside wall surface for the vessel and to be able to avoid renewed stenosis, the stents set forth in the opening part of this specification were developed. Those small tubes serve inter alia in conjunction with PCTA to maintain the vessel flow cross-section which is produced by balloon angioplasty in order thereby to ensure long-term success with the PCTA procedure.
The success of such so-called stenting also depends inter alia on how uniformly the stent can come to bear against the wall of the vessel. For, the more uniformly the wall of the vessel is supported, the correspondingly more probable it is that vessel constrictions will not recur in the region of the stent. In that respect a regular stent structure produces a relatively smooth inside surface for the vessel and, with a relatively smooth inside vessel surface, blood particles can only be deposited thereon with difficulty. In addition growths of the intima into the interior of the vessel are prevented to a greater degree by a regular stent structure which covers over the inside surface of the vessel in a relatively closed configuration.
Stents of that kind with a so-called closed structure are also known from the state of the art. By way of example reference may be made here to one of the best-known stents of that kind, the so-called wall stent. That is known for example from U.S. Pat. No. 4,655,771. This stent which has a closed structure is formed from two wires which are regularly knitted in a mesh-like structure and which extend in a spiral configuration on the longitudinal axis of the stent.
The advantage of the closed structure of stents of that kind is however only achieved at the cost of the disadvantage that the stents involve relative longitudinal stiffness during insertion. Those stents do not therefore make it possible in the optimum manner for the stent to be guided through possibly very severely curved vessel portions in the coronary arteries upon insertion in a direction towards the stenosis to be treated. In order to avoid those disadvantages of a closed structure, stents have now been developed which are of a so-called modular nature. In the case of those stents of a modular nature, individual portions which are provided with a closed structure are connected together by flexible connections. Stents of that kind are known for example from U.S. Pat. No. 5,104,404.
A disadvantage with those modular or segmented stents however is that the front edges of the individual modules or segments, which lead in the direction of insertion of the stent, can hook in the inside wall of the vessel. That can give rise to serious complications when inserting a stent. That is particularly problematical more especially insofar as the modular stents—as already referred to above—are used in particular when major curvatures have to be negotiated on the way to the location to be treated. For, it is in such a curve that such a leading edge of a segment becomes particularly easily hooked at the inside surface of the vessel, which is on the outside of the curvature, through which the stent is being passed.
Therefore the object of the invention is to avoid the above-mentioned disadvantages and to provide a stent of the kind set forth in the opening part of this specification which both permits the inside surface of the vessel to be covered in a closed configuration at the location of the stenosis to be treated while at the same time it is sufficiently flexible that it can be displaced to that location.
SUMMARY OF THE INVENTION
In the case of the present invention that object is attained by a stent of the kind set forth in the opening part of this specification, in that the openings provided in the stent have a substantially V-shaped opening area.
The advantages of the invention are in particular that the V-shaped openings, that is to say the V-shaped configuration of the area of the openings, in the tubular structure of the stent, provides a structure which is closed overall so as to provide for good covering of the lesion while at the same time by virtue of the V-shaped openings the flexibility in the longitudinal direction of the stent is increased in comparison with the closed stent structures which are known from the state of the art.
The invention involves the realization that, with V-shaped openings which are arranged in the longitudinal direction of the stent in its tubular portion, in the region of the converging tip of the opening area of the V-shaped openings, there is a region of the material delimiting the opening area, which region is movable in the transverse direction of the stent and which, when the stent is pushed through curves for example in coronary blood vessels permits an adequate degree of flexibility of the stent so that it is easily possible to negotiate such curves.
An advantageous embodiment of the invention is distinguished by first openings of a first size and by second openings of a second size, wherein the second openings are larger than the first openings. In that way, the above-mentioned flexibility of the closed structure is further improved as the small openings can move transversely to an even greater degree within the large openings, in particular if they are engaged into the latter in internested relationship, upon curvature of the stent when it is being pushed through curved coronary blood vessels.
A further preferred embodiment of the invention is distinguished in that first and second openings can occur in alternate succession in the longitudinal direction of the tubular portion of the stent. That provides an optimum compromise between the closed structure and enhanced flexibility of the stent in the transverse direction.
A further preferred embodiment of the present invention is distinguished in that the first and second openings occur in alternate succession in the peripheral direction of the tubular portion of the stent according to the invention. In this embodiment accordingly the advantage already mentioned in regard to the alternate arrangement of the openings in the longitudinal direction is achieved by the alternate arrangement of the openings in the peripheral direction. In this case the advantages of both embodiments can also be combined so that first and second opening sizes occur in alternate succession respectively both in the peripheral and also in the longitudinal direction.
A further advantageous development of the stent according to the invention is distinguished in that the second limbs which form the V of the second opening are longer than the first
Biotronik Mess -und Therapiegeraete GmbH & Co. Ingenieurbuero Be
Grant Stephen L.
Hahn Loeser + Parks LLP
Matthews William H
McDermott Corrine
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