Artificial support for a blood vessel

Claim 2

A stent having a compressed position for deployment in a blood vessel and an expanded position for supporting a blood vessel, comprising: a closed loop of material bent into a plurality of clockwise and counterclockwise arcuate sections, each section having a cusp at which the material reverses directions, said material not crossing itself at any point; said arcuate sections forming a coil with a longitudinal axis about which said arcuate sections are circumferentially disposed; said cusps of said clockwise and counterclockwise arcuate sections overlapping to form at least one region of overlap; and said region of overlap extending helically about the longitudinal axis.

Claim 3

The stent according to claim 1 wherein said region of overlap defines an angle less than 360 degrees when the stent is in its compressed position.

Claim 4

The stent according to claim 1 wherein said region of overlap defines an angle less than 180 degrees when the stent is in its compressed position.

Claim 5

A stent for supporting a blood vessel, comprising: a single length of material having a mid-point and first and second terminal ends; said material being bent to form a coil about a longitudinal axis with alternating arcuate sections extending circumferentially about the longitudinal axis; and said first and second terminal ends being joined to form a continuous loop; said coil being bent such that said material does not cross itself at any point.

Claim 6

A stent for supporting a blood vessel, comprising: a single length of material having a mid-point and first and second terminal ends; said material being bent to form a coil about a longitudinal axis with alternating arcuate sections extending circumferentially about the longitudinal axis; and said first and second terminal ends being joined to form a continuous loop; said coil being bent such that said material does not cross itself at any point.

Claim 7

The stent of claim 4 wherein said mid-point is located on one end of said coil and said joined first and second terminal ends are on another end of said coil;

Claim 8

A double-helix stent, comprising: a single length of material having first and second ends and forming first and-second halves, each half comprising a series of arcuate sections, each section comprising a pair of curved turns, adjacent turns being joined by cusps, said material reversing direction at each cusp and never crossing over itself, said halves being constructed so that the cusps of said first half intermesh with the cusps of said second half, thereby forming two diametrically opposed regions of overlap, each region of overlap being shifted incrementally circumferentially with each turn so that the two regions of overlap describe a double helix around the stent.

Claim 9

A double-helix stent, comprising: a single length of material having first and second ends and forming first and-second halves, each half comprising a series of arcuate sections, each section comprising a pair of curved turns, adjacent turns being joined by cusps, said material reversing direction at each cusp and never crossing over itself, said halves being constructed so that the cusps of said first half intermesh with the cusps of said second half, thereby forming two diametrically opposed regions of overlap, each region of overlap being shifted incrementally circumferentially with each turn so that the two regions of overlap describe a double helix around the stent.

Claim 10

The stent according to claim 6 wherein said first and second ends of said material are joined so as to form a continuous loop.

Claim 11

The stent according to claim 6 wherein the stent is constructed of a malleable plasticly deformable biocompatible substance.

Claim 12

The stent of claim 8 wherein the substance is wire.

Claim 13

The stent of claim 9 wherein the substance is a stainless steel alloy.

Claim 14

The stent of claim 6 wherein the coils are coated with a biocompatible substance.

Claim 15

The stent of claim 11 wherein the coils are coated with a biolized coating comprising a mixture of collagen and gelatin.

Claim 16

A stent according to claim 6 wherein said cusps of said arcuate sections alternate clockwise and counterclockwise directions.

Claim 17

A bifurcated stent for supporting a bifurcated vessel without obstructing fluid flow therethrough, comprising: a major coil; and two minor coils extending from one end of the major coil; said major and minor coils being constructed from a single continuous piece of wire that does not cross itself.

Claim 18

A bifurcated stent for supporting a bifurcated vessel without obstructing fluid flow therethrough, comprising: a major coil; and two minor coils extending from one end of the major coil; said major and minor coils being constructed from a single continuous piece of wire that does not cross itself.

Claim 19

A bifurcated stent for supporting a bifurcated vessel without obstructing fluid flow therethrough, comprising: a major coil; and two minor coils affixed to one end of the major coil; wherein the major and minor coils each comprise first and second halves, each half comprising a series of curved turns, adjacent turns being joined by cusps and said material reversing direction at each turn and never crossing itself, said halves being constructed so that the cusps of said first half intermesh with the cusps of said second half, thereby forming two diametrically opposed regions of overlay, each region of overlap being shifted incrementally circumferentially with each turn that the two regions of overlap define a double helix around the coil, said coils comprising a single continuous loop of material.

Claim 20

A bifurcated stent for supporting a bifurcated vessel without obstructing fluid flow therethrough, comprising: a major coil; and two minor coils affixed to one end of the major coil; wherein the major and minor coils each comprise first and second halves, each half comprising a series of curved turns, adjacent turns being joined by cusps and said material reversing direction at each turn and never crossing itself, said halves being constructed so that the cusps of said first half intermesh with the cusps of said second half, thereby forming two diametrically opposed regions of overlay, each region of overlap being shifted incrementally circumferentially with each turn that the two regions of overlap define a double helix around the coil, said coils comprising a single continuous loop of material.

Claim 21

A bifurcated stent for supporting a bifurcated vessel without obstructing fluid flow therethrough, comprising: a major coil; and two minor coils affixed to one end of the major coil; wherein said major coil comprises a single length of material having first and second ends and forming first and second halves, each half comprising a series of curved turns, adjacent turns being joined by cusps and said material reversing direction at each turn and never crossing over itself, said halves being constructed so that the cusps of said first half intermesh with the cusps of said second half, thereby forming two diametrically opposed regions of overlay, each region of overlap being shifted incrementally circumferentially with each turn such that the two regions of overlap define a double helix around said major coil, and wherein said minor coils each forming an extension of one end of the material forming said first coil and comprise a plurality of curved turns without crossovers, each adjacent pair of curved turns curving in opposite directions and being joined by a cusp, and each adjacent pair of cusps overlapping circumferentially to form a single region of overlap, said region of overlap being shifted incrementally circumferentially on each successive turn, so that the region of overlap defines a spiral around each of said minor coils.

Claim 22

A bifurcated stent for supporting a bifurcated vessel without obstructing fluid flow therethrough, comprising: a major coil; and two minor coils affixed to one end of the major coil; wherein said major coil comprises a single length of material having first and second ends and forming first and second halves, each half comprising a series of curved turns, adjacent turns being joined by cusps and said material reversing direction at each turn and never crossing over itself, said halves being constructed so that the cusps of said first half intermesh with the cusps of said second half, thereby forming two diametrically opposed regions of overlay, each region of overlap being shifted incrementally circumferentially with each turn such that the two regions of overlap define a double helix around said major coil, and wherein said minor coils each forming an extension of one end of the material forming said first coil and comprise a plurality of curved turns without crossovers, each adjacent pair of curved turns curving in opposite directions and being joined by a cusp, and each adjacent pair of cusps overlapping circumferentially to form a single region of overlap, said region of overlap being shifted incrementally circumferentially on each successive turn, so that the region of overlap defines a spiral around each of said minor coils.

Claim 23

A stent having a compressed position for deployment in a blood vessel and an expanded position for supporting the blood vessel, comprising: a wire bent into a plurality of successive arcs, adjacent arcs being joined by cusps, said arcs defining a substantially cylindrical coil; said wire reversing direction at each cusp; each of said arcs describing less than 540° when the stent is in its compressed position; and said wire forming a closed loop without crossing itself at any point.

Claim 24

A stent having a compressed position for deployment in a blood vessel and an expanded position for supporting the blood vessel, comprising: a wire bent into a plurality of successive arcs, adjacent arcs being joined by cusps, said arcs defining a substantially cylindrical coil; said wire reversing direction at each cusp; each of said arcs describing less than 540° when the stent is in its compressed position; and said wire forming a closed loop without crossing itself at any point.

Claim 25

A radially expandable stent for intraluminal implantation, comprising: a single length of wire forming a coil with a plurality of alternating expandable arcuate sections, said coil having first and second coil ends; said single length of wire having wire ends which are attached to form a continuous wire; said single length of wire being folded over to form a bend at said first coil end and said attached wire ends being located at said second coil end; said wire not overlapping itself in the radial direction.

Claim 26

A radially expandable stent for intraluminal implantation, comprising: a single length of wire forming a coil with a plurality of alternating expandable arcuate sections, said coil having first and second coil ends; said single length of wire having wire ends which are attached to form a continuous wire; said single length of wire being folded over to form a bend at said first coil end and said attached wire ends being located at said second coil end; said wire not overlapping itself in the radial direction.

Claim 27

The stent of claim 18 wherein said alternating expandable arcuate sections are juxtaposed to one another.

Claim 28

The stent of claim 18 wherein said coil includes at least one leg.

Claim 29

The stent of claim 18 wherein said wire is coated with a biocompatible gelatin compound.