Device forming an endoluminal intracorporeal endoprosthesis, in particular for the abdominal aorta

Claim 2

An endoluminal endoprosthesis device comprising: a first element deployable from a closed, non-deployed position for installation purposes to a deployed, working position and having an upstream end and a downstream end, said first element comprising a first segment having first and second end openings and sized for filling a cross-section of a blood vessel in which said first element is to be incorporated when said first element is in said deployed, working position, said first element further comprising a second segment connected to one of said first and second end openings of said first segment and forming at least two independent trunks, each of said at least two independent trunks having an upstream first opening communicating with said first segment and a downstream second opening, said first element further comprising a third segment connected to and communicating with said downstream second opening of said each of said at least two independent trunks of said second segment, said third segment having a diameter in said deployed state for facilitating access of a second endoprosthesis-forming device through said third segment into engagement in one of said at least two independent trunks for treating a blood vessel downstream therefrom, said first element comprising at least one of a wire and tape, wherein said at least one of said wire and tape is made of a biocompatible alloy having shape memory, and said first, second, and third segments being formed by a continuous one of a single meshworking step and a single knitting step of said at least one of a wire and tape such that there are no gaps between the first segment and the second segment and between said second segment and said third segment; and a second element comprising a leak-proof envelope substantially surrounding said first element including said at least two independent trunks of said second segment, said envelope providing a leak-proof fluid seal about said first element and permitting fluid flow from said upstream end to said downstream end of said first element.

Claim 3

The device of claim 1, wherein said diameter of said third segment is substantially equal to a diameter of said first segment.

Claim 4

The device of claim 1, wherein said third segment is shorter in length than said first segment.

Claim 5

The device of claim 1, wherein said first segment is equal in length to or greater than twice said third segment.

Claim 6

The device of claim 1, wherein each of said at least two independent trunks is sized for receiving said second endoprosthesis-forming device and effecting a leak-free and non-slip connection therebetween.

Claim 7

The device of claim 1, further comprising a radio-opaque marker element mounted at an upstream end of said second segment for facilitating viewing of a position of said second segment.

Claim 8

The device of claim 1, wherein said at least one of said wire and tape comprises a bent wire forming substantially annular units, each of said annular units having a plurality of bends, said first, second, and third segments comprising bonding means for connecting said annular units.

Claim 9

The device of claim 7, wherein a fraction of the plural bends are connected by said bonding means for facilitating a greater flexibility of said annular units.

Claim 10

The device of claim 7, wherein said wire has a non-circular cross-section.

Claim 11

The device of claim 1, wherein each of said at least two independent trunks has a constricted blood flow diameter in the deployed state less than half of a diameter of the first segment in the deployed state for facilitating an accelerated blood flow through said second segment thereby promoting increased downstream bloodflow.

Claim 12

The device of claim 1, further comprising a fixing segment for connection of said first element to a healthy portion of a blood vessel upstream of said first element and separated from said first element by links of a predetermined length.

Claim 13

The device of claim 11, wherein said fixing segment comprises at least another one of a wire and tape, wherein said at least one of another wire and tape is made of a biocompatible alloy having a shape memory.

Claim 14

The device of claim 12, wherein said fixing segment comprises a number of rings, the number being within a range including 1 to 3, each of said rings comprising said one of a wire and tape of a biocompatible material bent into a zigzag form and bonding means for connecting adjacent bends of adjacent ones of said rings.

Claim 15

The device of claim 1, wherein said envelope does not cover said first element at areas proximate said upstream end and said downstream end of said first element, thereby facilitating connection of said device to the blood vessel of the patient.

Claim 16

The device of claim 1, wherein each of said first, second, and third segments is deployable to any overall diameter within a range including 20 to 30 mm.

Claim 17

An endoluminal endoprosthesis device comprising: a first element deployable from a closed or non-deployed position for installation purposes to a deployed, working position and having an upstream end and a downstream end, said first element comprising a first segment having first and second end openings and sized for filling a cross section of a blood vessel in which said first element is to be incorporated when said first element is in said deployed, working position, said first element further comprising a second segment connected to one of said first and second end openings of said first segment and forming at least two independent trunks, each of said at least two independent trunks having an upstream first opening communicating with said first segment and a downstream second opening, said first element further comprising a third segment connected to and communicating with said down stream second opening of said each of said at least two independent trunks of said second segment, said third segment having a diameter in said deployed state for facilitating access of a second endoprosthesis-forming device through said third segment into engagement in one of said at least two independent trunks for treating a blood vessel downstream from said one of said at least two independent trunks, said first element comprising at least one of a wire and tape, wherein said at least one of said wire and tape is made of a biocompatible alloy having a shape memory, and said first, second, and third segments being formed by a continuous one of a single meshworking step and a single knitting step of said at least one of a wire and tape such that there are no gaps between the first segment and the second segment and between said second segment and said third segment; a second element comprising a leak-proof envelope surrounding said first element including said at least two independent trunks of said second segment, said envelope providing a leak-proof fluid seal about said first element and permitting fluid flow from said upstream end to said downstream end of said first element; and a fixing segment for connection to a healthy portion of a blood vessel upstream of said first segment of said first element and separated from said first segment by links of a predetermined length.

Claim 18

An endoluminal endoprosthesis device comprising: a first element deployable from a closed or non-deployed position for installation purposes to a deployed, working position and having an upstream end and a downstream end, said first element comprising a first segment having first and second end openings and sized for filling a cross section of a blood vessel in which said first element is to be incorporated when said first element is in said deployed, working position, said first element further comprising a second segment connected to one of said first and second end openings of said first segment and forming at least two independent trunks, each of said at least two independent trunks having an upstream first opening communicating with said first segment and a downstream second opening, said first element further comprising a third segment connected to and communicating with said down stream second opening of said each of said at least two independent trunks of said second segment, said third segment having a diameter in said deployed state for facilitating access of a second endoprosthesis-forming device through said third segment into engagement in one of said at least two independent trunks for treating a blood vessel downstream from said one of said at least two independent trunks, said first element comprising at least one of a wire and tape, wherein said at least one of said wire and tape is made of a biocompatible alloy having a shape memory, and said first, second, and third segments being formed by a continuous one of a single meshworking step and a single knitting step of said at least one of a wire and tape such that there are no gaps between the first segment and the second segment and between said second segment and said third segment; a second element comprising a leak-proof envelope surrounding said first element including said at least two independent trunks of said second segment, said envelope providing a leak-proof fluid seal about said first element and permitting fluid flow from said upstream end to said downstream end of said first element; and a fixing segment for connection to a healthy portion of a blood vessel upstream of said first segment of said first element and separated from said first segment by links of a predetermined length.

Claim 19

The device of claim 16, wherein said diameter of said third segment is substantially equal to a diameter of said first segment.

Claim 20

The device of claim 17, wherein said third segment is shorter in length than said first segment.

Claim 21

The device of claim 16, wherein said first segment is equal in length to or greater than twice said third segment.

Claim 22

The device of claim 16, wherein each of said at least two independent trunks is sized for receiving said second endoprosthesis-forming device and effecting a leak-free and non-slip connection therebetween.

Claim 23

The device of claim 16, further comprising a radio-opaque marker element mounted at an upstream end of said second segment for facilitating viewing of a position of said second segment.

Claim 24

The device of claim 16, wherein said at least one of said wire and tape comprises a bent wire forming substantially annular units, each of said annular units having a plurality of bends, said first, second, and third segments comprising bonding means for connecting said annular units.

Claim 25

The device of claim 22, wherein a fraction of the plural bends are connected by said bonding means for facilitating a greater flexibility of said annular units.

Claim 26

The device of claim 22, wherein said wire has a non-circular cross-section.

Claim 27

The device of claim 16, wherein said fixing segment comprises at least another one of a wire and tape, wherein said at least another one of said wire and tape is made of a biocompatible alloy having a shape memory.

Claim 28

The device of claim 25, wherein said fixing segment comprises a number of rings, the number being within a range including 1 to 3, each of said rings comprising said at least another one of a wire and tape bent into a zigzag form and bonding means for connecting adjacent bends of adjacent ones of said rings.

Claim 29

The device of claim 16, wherein said envelope does not cover said first element at areas proximate said upstream end and said downstream end of said first element, thereby facilitating connection of said device to the blood vessel of the patient.

Claim 30

An endoluminal endoprosthesis device comprising: a first element deployable from a closed or non-deployed position for installation purposes to a deployed working position and having an upstream end and a downstream end, said first element comprising a first segment having first and second end openings and sized for filling a cross-section of a blood vessel in which said first element is to be incorporated when said first element is in said deployed, working position, said first element further comprising a second segment connected to one of said first and second end openings of said first segment and forming at least two independent trunks, each of said at least two independent trunks having an upstream first opening communicating with said first segment and a downstream second opening, each of said at least two independent trunks having a constricted blood flow diameter in the deployed state that is less than half of a diameter of the first segment in the deployed state for facilitating accelerated blood flow through said second segment thereby promoting increased downstream bloodflow, said first element further comprising a third segment connected to and communicating with said down stream second opening of said each of said at least two independent trunks of said second segment, said third segment having a diameter in said deployed state for facilitating access of a second endoprosthesis-forming device through said third segment into engagement in one of said at least two independent trunks for treating a blood vessel downstream from said one of said at least two independent trunks, said first element comprising at least one of a wire and a tape, wherein said at least one of said wire and tape is made of a biocompatible alloy having a shape memory, said first, second, and third segments being formed by means of a continuous one of a single meshworking step and a single knitting step of said at least one of said wire and tape such that there are no gaps between said first and second segments and said second and third segments; and a second element comprising a leak-proof envelope surrounding said first element and said at least two independent trunks of said second segment, said envelope providing a leak-proof fluid seal about said first element and permitting fluid flow from said upstream end to said downstream end of said first element.

Claim 31

An endoluminal endoprosthesis device comprising: a first element deployable from a closed or non-deployed position for installation purposes to a deployed working position and having an upstream end and a downstream end, said first element comprising a first segment having first and second end openings and sized for filling a cross-section of a blood vessel in which said first element is to be incorporated when said first element is in said deployed, working position, said first element further comprising a second segment connected to one of said first and second end openings of said first segment and forming at least two independent trunks, each of said at least two independent trunks having an upstream first opening communicating with said first segment and a downstream second opening, each of said at least two independent trunks having a constricted blood flow diameter in the deployed state that is less than half of a diameter of the first segment in the deployed state for facilitating accelerated blood flow through said second segment thereby promoting increased downstream bloodflow, said first element further comprising a third segment connected to and communicating with said down stream second opening of said each of said at least two independent trunks of said second segment, said third segment having a diameter in said deployed state for facilitating access of a second endoprosthesis-forming device through said third segment into engagement in one of said at least two independent trunks for treating a blood vessel downstream from said one of said at least two independent trunks, said first element comprising at least one of a wire and a tape, wherein said at least one of said wire and tape is made of a biocompatible alloy having a shape memory, said first, second, and third segments being formed by means of a continuous one of a single meshworking step and a single knitting step of said at least one of said wire and tape such that there are no gaps between said first and second segments and said second and third segments; and a second element comprising a leak-proof envelope surrounding said first element and said at least two independent trunks of said second segment, said envelope providing a leak-proof fluid seal about said first element and permitting fluid flow from said upstream end to said downstream end of said first element.

Claim 32

The device of claim 28, wherein said at least one of said wire and said tape comprises a bent wire forming substantially annular units, each of said annular units having a plurality of bends, and said first, second, and third segments comprising bonding means for connecting adjacent ones of said annular units.

Claim 33

The device of claim 29, wherein a fraction of the plural bends are connected by said bonding means for facilitating a greater flexibility of said annular units.

Claim 34

The device of claim 29, wherein said wire has a non-circular cross-section.

Claim 35

The device of claim 28, further comprising a fixing segment for connection of said first element to a healthy portion of a blood vessel upstream of said first element and separated from said first element by links of a predetermined length.

Claim 36

The device of claim 32, wherein said fixing segment comprises at least another one of a wire and tape, wherein said at least one of another wire and tape is made of a biocompatible alloy having a shape memory.

Claim 37

The device of claim 33, wherein said fixing segment comprises a number of rings, the number being within a range including 1 to 3, each of said rings comprising said one of a wire and tape of a biocompatible material bent into a zigzag form and bonding means for connecting adjacent bends of adjacent ones of said rings.

Claim 38

The device of claim 28, wherein said envelope does not cover said first element at areas proximate said upstream end and said downstream end of said first element, thereby facilitating connection of said device to the blood vessel of the patient.

Claim 39

The device of claim 16, wherein each of said first, second, and third segments is deployable to any overall diameter within a range including 20 to 30 mm.

Claim 40

The device of claim 28, wherein each of said first, second, and third segments is deployable to any overall diameter within a range including 20 to 30 mm.