CA2590373A1 - Longitudinally flexible stent - Google Patents

Abstract

An expandable stent comprises multiple enclosed flexible spaces. Each includes a first, second, third, fourth, fifth, sixth, seventh, eighth, ninth, and tenth members having first and second ends. The first ends of the first and second members, the third and fourth members, the sixth and seventh members and the eighth and ninth members communicate. The second ends of the second and third members, the fifth and sixth members, the seventh and eighth members and the ninth and tenth members communicate.
The first end of the fifth member communicates with the second end of the first member.
The first end of the tenth member communicates with the second end of the fourth member.
The first and second members, the third and fourth members, the fifth and sixth members, the seventh and eighth members and the ninth and tenth members have curved portions at their ends forming loops.

Description

LONGITUDINALLY FLEXIBLE STENT

This is a division of co-pending Canadian Patent Application No. 2,439,088 filed on May 21, 2002.

FIELD OF THE INVENTION

The present invention relates generally to stents, which are endoprostheses implanted into vessels within the body, such as blood vessels, to support and hold open the vessels, or to secure and support other endoprostheses in the vessels. In particular, the present invention relates to a stent which is longitudinally flexible before and after expansion.
BACKGROUND OF THE INVENTION

Various stents are known in the art. Typically stents are generally tubular in shape, and are expandable from a relatively small, unexpanded diameter to a larger, expanded diameter. For implantation, the stent is typically mounted on the end of a catheter, with the stent being held on the catheter at its relatively small, unexpanded diameter.
By the catheter, the unexpanded stent is directed through the lumen to the intended implantation site. Once the stent is at the intended implantation site, it is expanded, typically either by an internal force, for example by inflating a balloon on the inside of the stent, or by allowing the stent to self-expand, for example by removing a sleeve from around a self-expanding stent, allowing the stent to expand outwardly. In either case, the expanded stent resists the tendency of the vessel to narrow, thereby maintaining the vessel's patency.

U.S. Patent No. 5,733,303 to Israel et al. ("'303"), shows a unique stent formed of a tube having a patterned shape which has first and second meander patterns having axes extending in first and second directions. The second meander patterns are intertwined with the first meander patterns to form flexible cells. Stents such as this one are very flexible in their unexpanded state such that they can be tracked easily down tortuous lumens. Upon expansion, these stents provide excellent radial support, stability, and coverage of the vessel wall. These stents are also conformable, in that they adapt to the shape of the vessel wall during implantation.

One feature of stents with a cellular mesh design such as this one, however, is that they have limited longitudinal flexibility after expansion, which maybe a disadvantage in particular applications. This limited longitudinal flexibility may cause stress points at the end of the stent and along the length of the stent. Conventional mesh stents like that shown in U.S. Patent No. 4,733,665 may simply lack longitudinal flexibility, which is illustrated by Figure 1, a schematic diagram of a conventional stent 202 in a curved vessel 204.

To implant a stent, it may be delivered to a desired site by a balloon catheter when the stent is in an unexpanded state. The balloon catheter is then inflated to expand the stent, affixing the stent into place. Due to the high inflation pressures of the balloon -- up to 20 atm -- the balloon causes the curved vessel 204 and even a longitudinally flexible stent to straighten when it is inflated. If the stent, because of the configuration of its mesh is or becomes relatively rigid after expansion, then the stent remains or tends to remain in the same or substantially the same shape after deflation of the balloon. However, the artery attempts to return to its natural curve (indicated by dashed lines) in Figure 1 with reference to a conventional mesh stent. The mismatch between the natural curve of the artery and the straightened section of the artery with a stent may cause points of stress concentration 206 at the ends of the stent and stress along the entire stent length. The coronary vasculature can impose additional stress on stents because the coronary vasculature moves relatively significant amounts with each heartbeat. For illustration purposes, the difference between the curve of the vessel and the straightened stent has been exaggerated in Figure 1.

U.S. Patent No. 5,807,404 to Richter, shows another stent which is especially suited for implantation into curved arterial portions or osteal regions. This stent can include sections adjacent the end of the stent with greater bending flexibility than the remaining axial length of the stent. While this modification at the end of the stent alleviates the stress at the end points, it does not eliminate the stress along the entire length of the stent.

Various stents are known that retain longitudinal flexibility after expansion.
For example, U.S. Patent Nos. 4,886,062 and 5,133,732 to Wiktor ("the Wiktor '062 and '732 patents") show various stents formed of wire wherein the wire is initially formed into a band of zig-zags forming a serpentine pattern, and then the zig-zag band is coiled into a helical stent. The stents are expanded by an internal force, for example by inflating a balloon.

The coiled zig-zag stents that are illustrated in Figures 1 through 6 of the Wiktor '062 and '732 patents are longitudinally flexible both in the expanded and unexpanded condition such that they can be tracked easily down tortuous lumens and such that they conform relatively closely to the compliance of the vessel after deployment. While these stents are flexible, they also have relatively unstable support after expansion.
Furthermore, these stents leave large portions of the vessel wall uncovered, allowing tissue and plaque prolapse into the lumen of the vessel.

Thus, it is desired to have a stent which exhibits longitudinal flexibility before expansion such that it can easily be tracked down tortuous lumens and longitudinal flexibility after expansion such that it can comply with the vessel's natural flexibility and curvature while still providing continuous, stable coverage of a vessel wall that will minimize tissue sag into the lumen.

SUMMARY OF THE INVENTION

In accordance with one aspect of the present invention there is provided a An expandable stern comprising a plurality of enclosed flexible spaces, each of the plurality of enclosed flexible spaces including: a) a first member having a first end and a second end;
b) a second member having a first end and a second end; c) a third member having a first end and a second end; d) a fourth member having a first end and a second end, the first end of of the first member communicating with the first end of the second member, the second end of the second member communicating with the second end of the third member, and the first end of the third member communicating with the first end of the fourth member;
e) the first member and the second member with the curved portion at their ends forming a first loop;
f) the third member and the fourth member with the curved portion at their ends forming a second loop; g) a fifth member having a first end and a second end; h) a sixth member having a first end and a second end; i) a seventh member having a first end and a second end; j) an eighth member having a first end and a second end; k) a ninth member having a first end and a second end; 1) a tenth member having a first end and a second end, the first end of the fifth member coupled to the second end of the first member, the second end of the fifth member communicating with the second end of the sixth member, the first end of the sixth member communicating with the first end of the seventh member, the second end of the seventh member communicating with the second end of the eighth member, the first end of the eighth member communicating with the first end of the ninth member, the second end of the ninth member communicating with the second end of the tenth member, and the first end of the of the tenth member coupled to the second end of the fourth member; m) the fifth member and the sixth member with the curved portion at their ends forming a third loop;
n) the seventh member and the eighth member with the curved portion at their ends forming a fourth loop; and o) the ninth member and the tenth member with the curved portion at their ends forming a fifth loop.

BRIEF DESCRIPTION OF THE DRAWINGS

Figure 1 shows a schematic diagram of a conventional rigid stent deployed in a curved lumen;

Figure 2 shows a schematic diagram of a stent of the present invention deployed in a curved lumen;

Figure 3 shows a pattern for a stent made in accordance with the present invention;

Figure 4 shows an enlarged view of one cell of the pattern of Figure 3;
Figure 5 shows a pattern for a stent made in accordance with the present invention;

Figure 6 shows an enlarged view of one cell of the pattern of Figure 5;

Figure 7 shows a pattern for a stent constructed according to the principles of the invention which has variable geometry along its length; and Figure 8 shows the expansion of a portion of a horizontal meander pattern built according to the principles of the invention.

DETAILED DESCRIPTION OF THE INVENTION

Figure 2 shows a schematic diagram of a longitudinally flexible stent 208 of the present invention. The stent 208 may be delivered to a curved vessel 210 by a balloon catheter, and implanted in the artery by inflating the balloon. As described before, the balloon causes the artery to straighten upon inflation of the balloon.
However, upon deflation of the balloon, the stent 208 assumes the natural curve of the vessel 210 because it is and remains longitudinally flexible after expansion. This reduces any potential stress points at the ends of the stent and along the length of the stent. Furthermore, because the stent is longitudinally flexible after expansion, the stent will flex longitudinally with the vessel during the cycles caused by a heartbeat. This also reduces any cyclic stress at the ends of the stent and along the length of the stent.
Figure 3 shows a pattern of a stent according to the present invention. This pattern may be constructed of known materials, and for example stainless steel, but it is particularly suitable to be constructed from NiTi. The pattern can be formed by etching a flat sheet of NiTi into the pattern shown. The flat sheet is formed into a stent by rolling the etched sheet into a tubular shape, and welding the edges of the sheet together to form a tubular stent. The details of this method of forming the stent, which has certain advantages, are disclosed in U.S. Patent Nos. 5,836,964 and 5,997,973. Other methods known to those of skill in the art such as laser cutting a tube or etching a tube may also be used to construct a stent which uses the present invention. After formation into a tubular shape, a NiTi stent is heat treated, as known by those skilled in the art, to take advantage of the shape memory characteristics of NiTi and its superelasticity.

The pattern 300 is formed from a plurality of each of two orthogonal meander patterns which patterns are intertwined with each other. The term "meander pattern" is taken herein to describe a periodic pattern about a center line and "orthogonal meander patterns"
are patterns whose center lines are orthogonal to each other.

A meander pattern 301 is a vertical sinusoid having a vertical center line 302.
It will be recognized that this is not a perfect sinusoid, but only an approximation thereof.
Thus, as used herein, the term sinusoid refers to a periodic pattern which varies positively and negatively symmetrically about an axis; it need not be an exact sine function.
A meander pattern 301 has two loops 304 and 306 per period wherein loops 304 open to the right while loops 306 open to the left. Loops 304 and 306 share common members 308 and 310, where member 308 joins one loop 304 to its following loop 306 and member 308 joins one loop 306 to its following loop 304. The vertical sinusoid of meander pattern 301 has a first frequency.

A meander pattern 312 (two of which have been shaded for reference) is a horizontal pattern having a horizontal center line 314. A horizontal meander pattem 312 also has loops labeled 316, 318, 320, 322, and between the loops of a period is a section labeled 324.
Looked at another way, these loops are part of a vertical sinusoid 303 which has a higher frequency than that of the meander patterns 301 . Vertical sinusoids 301 alternate with vertical sinusoids 303. Vertical sinusoids 303 have a second frequency higher than the first frequency of the vertical meander patterns, i.e., sinusoids 301.

Vertical meander pattern 301 is provided in odd and even (o and e) versions which are 180N out of phase ivith each other. Thus, each left opening loop 306 of meander pattern 301 o faces a right opening loop 304 of meander pattem 301 e and a right opening loop 304 of meander pattern 301 o faces a lefft opening loop 306 of meander pattem 301 e.

The horizontal meander pattern 312 is also provided in odd and even forms. The straight sections 324 of the horizontal meander pattern 312e intersect with every third common member 310 of the even vertical meander pattern 301 e. The straight sections 324 of the horizontal meander pattem 312o also intersect with every third common member 310 of the odd vertical meander pattern 301. Viewed as vertical sinusoids 303, altemating sinusoids 303 are intermittently coupled to the meander patterns 301. For example, between points 315 and 317, where vertical pattern 303 is coupled to vertical pattern 301 e, there are two loops 306 and one loop 304 of vertical pattern 301e and three loops 319 and two loops 321 of vertical pattern 303.
This corresponds to two cycles of pattern 301 e and 3 cycles of pattem 303.
Similarly, between two points of coupling between vertieal pattem 301 o and vertical pattern 303 are two loops 304 and one loop 306, again making two cycles. Thcre will be three loops 321 and two loops 319, again equal to three cycles of pattern 303.
, Upon expansion of the stent, the loops of the vertical meander patterns 301 open up in the vertical direction. This causes them to shorten in the horizontal direction. The loops in the horizontal meander pattern 312 open up both in the vertical direction and the horizontal direction, compensating for the shottrning of the loops of the vertical meander patterns.
It should bc noted that the loops of the horizontal meander pattern 312, which ane the loops of the vertical pattern 303 in the present invention avoids foreshortening in a self-expanding stent in a particularly effective manner. A self-expanding stent formed of a shape-memory alloy must be compressed from an expanded position to a compressed position for delivery. As shown in Fig. 7, because of the configuration of the loops 319 and 321 of the horizontal meander pattern 312, when the stent is compressed from an expanded position 602 to a compressed position 604, the length 606 of the horizontal meander pattern (width of the vertical pattern 330) naturally shrinks. Consequently, when the stent expands, the loops 319 and 321 elongate and compensate for the shortening of the vertical meander patteins 301 e and 301 o, as the vertical meander patterns 301e and 301o expand. In contrast, a horizontal meander pattern with such shapes as N-shapes will not naturally shrin~ longitudinally when compressed from an expanded position 608 to a compressed position 610, as illustrated in Fig. 8..

A stent formed from the pattern of Figure 3 and made of NiTi is particularly well suited for use in the carotid artery or other lumens subject to an outside pressure. One reason is that because the stent is formed ofNiTi, it is reboundable, which is a desirable property for stents placed in the carotid artery. The other reason is that the stent of Figure 3 offers excellent scaffolding, which is particularly important in the carotid artery.
Scaffolding is especially important in the carotid artery because dislodged particles in the artery mav embolize and cause a stroke.
Figure 4 is an expanded view of one flexible cell 500 of the pattetn of Figure 3.
Each flexible cell 500 includes: a first member 501 having a first end 502 and a second end 503;
a second member 504 having a first end 505 and a second end 506; a third member 507 having a first end 508 and a second end 509; and a fourth member 510 having a first end 511 and a second end 512. The first cnd 502 of the first member 501 is joined to the first cnd 505 of the second member 504 by a first curved member 535 to form a first loop 550, the second end 506 of the second member 504 is joined to the second end 509 of the third member 508 by a second curved mernber 536, and the first cnd 508 of the third mcmber 507 is joined to the first end 511 of the fourth member 510 by a third curved member 537 to form a second loop 531. The fitst loop 530 defines a first angle 543. The second loop 531 defines a second angle 544.
Each ce11500 also includes a fifth member 513 having a first end 514 and a second end 515; a sixth member 516 having a first end 517 and a second end 51 8; a seventh member 519 having a first end 520 and a second end 521; an eighth member 522 having a first end 523 and a second end 524; a ninth member 525 having a first end 526 and a second end 527; and a tenth member having a first end 529 and a second end 530. The first end 514 of the fifth member 513 is joined to the second end 503 of the first member 501 at second junction point 542, the second end 515 of the fifth member 513 is joined to the second end 518 of the sixth member by a curved member 539 to forn a third loop 532, the first end 517 of the sixth member 516 is joined to the first end 520 of the seventh member 519 by a fifth curved member 548, the second end 521 of the seventh member 519 is joined to the second end 524 of the eighth member 522 at third junction point 540 to form a fourth loop 533, the first end 523 of the eighth member 522 is joined to the first end 526 of the ninth member 525 by a sixth curved member 549, the second end 526 of the ninth member 525 is joined to the second end 530 of the tenth member 528 by a seventh curved member 541 to form a fifth loop 534, and the first end 529 of the tenth member 528 is joined to the second end 512 of the fourth member 510. The third loop 532 defines a third angle 545. The fourth loop 533 defines a fourth angle 546. The fifth loop 534 defines a fifth angle 547.

In the embodiment sho'wn in Fig. 4, the first member 501, the third member 507, the sixth member 516, the eighth member 522, and the tenth member 528 have substantially the same angular orientation to the longitudinal axis of the stent and the second member 504, the fourth member 510, the fifth member 513, the seventh member 519, and the ninth member 512 have substantially the same angular orientation to the longitudinal axis of the stent. In the embodiment shown in Figure 4, the lengths of the first, second, third and fourth membcrs 501, 504, 507, 510 are substantially equal. The lengths of the fifth, sixth, seventh, eighth, ninth and tenth members 513, 516, 519, 522, 51-5, 528 are also substantially equal.
Other embodiments where lenr~~*ths'of individual members are tailored for specific.applications, materials of construction or methods of delivery arc also possible, and may be preferable for them. It can be sczn that each cell includes two cycles of the lower frequency vertical pattem and three cycles of the higher frequency vertical pattcrn.

The first, second, third, and fourth members 501, 504, 507, 510 may have a width that is greater than the width of the fifth, sixth, seventh, eighth, ninth, and tenth members 513, 516, 519, 522, 525, 528 in that cell. The differing widths of the first, second, third, and fourth members and the fifth, sixth, seventh, eighth, ninth, and tenth members with respect to each other contribute to the overall flexibility and resistance to radial compression of the cell. The widths of the various members can be tailored for specific applications. For example, the ratio of width may be approximately 50 70%. The fifth, sixth, seventh, eighth, ninth, and tenth members may be optimized predominantly to enable longitudinal flexibility, both before and after expansion, while the first, second, third, and fourth members may be optimized predominantly to enable sufficient resistance to radial compression to hold a vessel open. Although specific members may be optimized to predominantly enable a desired characteristic, all the portions of the cell interactively cooperate and contribute to the characteristics of the stent.

Figures 5 and 6 show a pattem and an expanded view of one cell of an embodiment of the present invention which is specially adapted for a stent made of stainless steel. The pattern is similar to the pattem of Figures 3 and 4, and the same reference numerals are used to indicate the generally corresponding parts.

The embodiments of Figures 3 and 5 can also be viewed as being made up of high frequency and low frequency vertical sinusoidal patterns or vertical loop containing sections which arc arranged gencrally in the circumferential direction and which are periodically interconnected. Thus, there is a first loop containing section with loops occurring at a first frequency extending along line 301 and a second loop containing section with also occurring at said first frequency extending along line 302. A third loop containing section 303 extending along line 305 has loops occurring at a second frequency that is higher than said first frequency.
It is disposed betwcen the first and second loop containing sections and alternately joined to the first and second loop containing sections. In the illustrated embodiment, the high frcquency is in a ratio of 3/:.' to the low frequcncy. As notcd above, the higher frequency loop containing clcmcnts are smallcr in width. The rclativc widths can be sclcctcd so that the high frcqurncy clemcnts arc crimpablc to the same diameter as the lower frequency elements.

A stent according to claim 4, wherein the higher frequency elements provide improved flexibility.
Furthermore the high frequency vertical pattems of smaller width result in elements having a lower maximal strain. Specifically, when the stent is expanded, the lower maximal strain is below the maximum strain without non-elastic deformation for the material of the stent.
In this embodiment where the stent is made of stainless steel the lower maximal strain is below approximately 0.5%, even for a'150B bend, as confinned by finite element analysis. On the other hand, in a'303 type stent, for an equivalent amount of bending, exhibits a maximum strain of 8%. Thus, the increased flexibility of the stent of the present invention means that, in.
addition to confomning better to the curved lumen, it will bend with each beat of the heart. The strain during heartbeat happens 8,000,000 times every year and cannot be much above elastic limit without the stent breal:ing. Since, embodiments of the present invention keep the strain below the limit means that the stent of the present invention can bend with the lumen as the heart beats, for many years without breaking.

Also in this embodiment of the invention, for example, the second loops 531 are made stronger by shortening the third and fourth members 507, 510. This helps assure that the second loops do not "flare out" during delivery of the stent through tortuous anatomy. This "flaring out" is not a concern with NiTi stents which are covered by a sheath during delivery.

Furthermore, the length of the members in this embodiment may be shorter than the length of the corresponding members in the embodiment illustrated in Figures 3 and 4.
Typically, the amount of strain allowed in a self-expanding NiTi stent may be around 10%. In a stainless steel stent, the amount of strain allowed during the plastic deformation which take place, for example, during expansion, typically may be 20% or greater.
Therefore, to facilitate stcnts made of NiTi and stents made of stainless steel expanding to comparable diameters, the mcmbers of the NiTi stent may be longer than the mcmbers of a stainlcss steel stent.

ln the particular embodimcnts described above, the stent is substantially uniform ovcr its entirc length. However, othca applications where portions of the stent are adapted to provide different characteristics are also possible. For example, as shown in Figure 7, a band of cells 850 may be designed to provide different flexibility characteristics or different radial compression characteristics than the remaining bands of cells by altering the widths and lengths of the members malcing up that band. Or, the stent may be adapted to provide increased access to a side branch lumen by providing at least one cell 852 which is larger in size then the remaining cells, or by providing an entire band of cells 854 which are larger in size than the other bands of cells. Note that the cells 854 are formea by a first loop containing section 856, which arranged generally in the circumferential direction, with the loops in first loop containing section 856 occurring at a first frequency; a second loop containing section 858, which is also arranged generally in the circumferential direction, with the loops in the second loop containing section 858 also occurring at the first frequency; and third loop containing sections 860, which are arranged generally in the circumferential direction. The loops in said third loop containing sections 860 occur at a second frequency that is higher than said first frequency and are disposed between and first and second loop containing sections and altemately joined to said first and second loop containing sections.

Or, the stent may be designed to expand to different diameters along the length of the stent. The stent may also be treated after formation of the stent by coating the stent with a medicine, plating the stent with a protective material, plating the stent with a radiopaque material, or covering the stent with a material.

Thus, what is describcd is a longitudinally flexible stent that utilizes a closed cell structure to provide excellent coverage of the vessel wall. The general concepts described herein can be utilized to form stents with diffrrent configurations than the particular embodiments described hercin. For examplc, the general concepts can be used to form bifurcated stents. It will be appreciated by persons skilled in the art that the prescnt invention is not limited to what has been particularly shown and described above. Rathcr, the scope of the present invention is defined by the claims which follow.

Claims (20)

1. An expandable stent comprising a plurality of enclosed flexible spaces, each of the plurality of enclosed flexible spaces including:
a) a first member having a first end and a second end;
b) a second member having a first end and a second end;
c) a third member having a first end and a second end;
d) a fourth member having a first end and a second end, the first end of the first member communicating with the first end of the second member, the second end of the second member communicating with the second end of the third member, and the first end of the third member communicating with the first end of the fourth member;
e) the first member and the second member with the curved portion at their ends forming a first loop;
f) the third member and the fourth member with the curved portion at their ends forming a second loop;
g) a fifth member having a first end and a second end;
h) a sixth member having a first end and a second end;
i) a seventh member having a first end and a second end;
j) an eighth member having a first end and a second end;
k) a ninth member having a first end and a second end;
l) a tenth member having a first end and a second end, the first end of the fifth member coupled to the second end of the first member, the second end of the fifth member communicating with the second end of the sixth member, the first end of the sixth member communicating with the first end of the seventh member, the second end of the seventh member communicating with the second end of the eighth member, the first end of the eighth member communicating with the first end of the ninth member, the second end of the ninth member communicating with the second end of the tenth member, and the first end of the tenth member coupled to the second end of the fourth member;
m) the fifth member and the sixth member with the curved portion at their ends forming a third loop;
n) the seventh member and the eighth member with the curved portion at their ends forming a fourth loop; and o) the ninth member and the tenth member with the curved portion at their ends forming a fifth loop.

2. The stent of claim 1, wherein the first member, the third member, the sixth member, the eighth member, and the tenth member have substantially the same angular orientation to the longitudinal axis of the stent and the second member, the fourth member, the fifth member, the seventh member, and the ninth member have substantially the same angular orientation to the longitudinal axis of the stent.

3. The stent of claim 1, wherein the first, second, third, and fourth members in at least one of the plurality of spaces have a width that is greater than the width of the fifth, sixth, seventh, eighth, ninth, and tenth members in that space.

4. The stent of claim 3, wherein the relative widths of the fifth, sixth, seventh, eighth, ninth, and tenth members with respect to said first, second, third, and fourth members is such that when said stent is crimped for insertion into a lumen of a blood vessel, the fifth, sixth, seventh, eighth, ninth, and tenth members are crimpable to essentially the same size as said first, second, third, and fourth members.

5. The stent of claim 4, wherein the fifth, sixth, seventh, eighth, ninth, and tenth members provide improved flexibility.

6. The stent of claim 5, wherein, while flexing, the fifth, sixth, seventh, eighth, ninth, and tenth members have lower maximal strain.

7. The stent of claim 6, wherein, said lower maximal strain is below the maximum strain without non-elastic deformation for the material of the stent.

8. The stent of claim 7, wherein, said stent is made of stainless steel and said lower maximal strain is below approximately 0.5%.

9. The stent of claim 1, wherein a substantial portion of each of the members is substantially straight.

10. The stent of claim 1, wherein the members are comprised of metal.

11. The stent of claim 10, wherein the metal is selected from the group consisting of stainless steel and nitinol.

12. The stent of claim 1, wherein the first, second, third, and fourth members and the fifth, sixth, seventh, eighth, ninth, and tenth members are provided with different flexibilities with respect to each other.

13. The stent of claim 12, wherein the fifth, sixth, seventh, eighth, ninth, and tenth members patterns are more flexible than the first, second, third, and fourth members.

14. The stent of claim 12, wherein at least one portion of at least one of the fifth, sixth, seventh, eighth, ninth, and tenth members is provided with at least one portion that is more flexible than at least one portion of at least one of the first, second, third, and fourth members.

15. The stent of claim 1, wherein the first, second, third, and fourth members and the fifth, sixth, seventh, eighth, ninth, and tenth members are provided with different resistances to radial compression with respect to each other.

16. The stent of claim 15, wherein the first, second, third, and fourth members have a greater resistance to radial compression than the fifth, sixth, seventh, eighth, ninth, and tenth members.

17. The stent of claim 15, wherein the fifth, sixth, seventh, eighth, ninth, and tenth members have a greater resistance to radial compression than the first, second, third, and fourth members.

18. The stent of claim 1, wherein at least one portion of at least one of the first, second, third, and fourth members and at least one portion of at least one of the fifth, sixth, seventh, eighth, ninth, and tenth members are provided with different resistances to radial compression with respect to each other.

19. The stent of claim 18, wherein at least one portion of at least one of the plurality of the first, second, third, and fourth members is provided with at least one portion that has a greater resistance to radial compression than at least one portion of at least one of the fifth, sixth, seventh, eighth, ninth, and tenth members.

20. The stent of claim 18, wherein at least one portion of at least one of the fifth, sixth, seventh, eighth, ninth, and tenth members is provided with at least one portion that has a greater resistance to radial compression than at least one portion of at least one of the first, second, third, and fourth members.