Prosthesis for placement at a luminal OS

• US 8,926,685 B2
• Filed: 04/27/2010
• Issued: 01/06/2015
• Est. Priority Date: 10/13/2004
• Status: Expired due to Fees

• Current Assignee: Poseidon Medical Inc.
• Original Assignee: Tryton Medical, Inc.
• Inventors: Kaplan, Aaron V., Vargas, Jaime
• Primary Examiner(s): DOWE, KATHERINE MARIE
• Application Number:
  US12/768,562
• Publication Number:
  US 20100211160A1
• Time in Patent Office: 1,715 Days
• Field of Search: 623/1.11, 623/1.12, 623/1.35
• US Class Current: 623/1.12
• CPC Class Codes: A61F 2/856 Single tubular stent with a side portal passage
• CPC Class Codes: A61F 2/91 made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes
• CPC Class Codes: A61F 2/915 with bands having a meander structure, adjacent bands being connected to each other
• CPC Class Codes: A61F 2/954 for placing stents or stent-grafts in a bifurcation
• CPC Class Codes: A61F 2/958 Inflatable balloons for placing stents or stent-grafts
• CPC Class Codes: A61F 2/97 the outer sleeve being splittable
• CPC Class Codes: A61F 2002/821 Ostial stents
• CPC Class Codes: A61F 2002/91508 the meander having a difference in amplitude along the band
• CPC Class Codes: A61F 2002/91516 the meander having a change in frequency along the band
• CPC Class Codes: A61F 2002/91525 within the whole structure different bands showing different meander characteristics, e.g. frequency or amplitude
• CPC Class Codes: A61F 2002/91533 characterised by the phase between adjacent bands
• CPC Class Codes: A61F 2002/9155 Adjacent bands being connected to each other
• CPC Class Codes: A61F 2002/91558 connected peak to peak
• CPC Class Codes: A61F 2002/91575 connected peak to trough
• CPC Class Codes: A61F 2002/9583 Means for holding the stent on the balloon, e.g. using protrusions, adhesives or an outer sleeve
• CPC Class Codes: A61F 2250/0039 differing in diameter
• CPC Class Codes: A61M 25/1002 characterised by balloon shape A61M25/1006, A61M25/1009 take precedence

Abstract

An embodiment of the invention provides a prosthesis delivery system comprising a delivery catheter having an expandable member and a prosthesis carried over the expandable member. The prosthesis includes a radially expandable scaffold section and at least two anchors extending axially from an end thereof; and means for capturing at least the anchors to prevent the anchors from divaricating from the expandable member as the catheter is advanced through a patient'"'"'s vasculature.

Claims

1. A prosthesis capable of being carried through a patient'"'"'s vasculature over a delivery catheter and of being deployed at an Os, the prosthesis comprising:

a radially expandable scaffold section; and

at least two elongate members extending axially from a proximal end of the radially expandable scaffold section;

a restraining device comprising a first circumferential span coupled with two of the elongate members and a second circumferential span coupled with two of the elongate members, the first and second circumferential spans each being spaced from the radially expandable scaffold section, the restraining device having a first configuration for maintaining the at least two elongate members in a collapsed configuration for advancement through the patient'"'"'s vasculature, the restraining device also having a second configuration for permitting the at least two elongate members to expand to an expanded configuration, the restraining device having a proximal end located at or distal of a proximal end of the at least two elongate members, the restraining device having a distal end located on a proximal portion of the at least two elongate members,

wherein at least a majority of expansion of the at least two elongate members from the collapsed configuration to the expanded configuration is provided by an outward pressure from the delivery catheter,

wherein the scaffold section is configured to be not radially constrained by a structure that is separable from the delivery catheter when being carried through the patient'"'"'s vasculature.

2. A prosthesis as in claim 1, wherein the restraining device is expandable by the outward pressure from the delivery catheter to permit the at least two elongate members to be spaced farther apart from each other than when carried over the delivery catheter.

3. A prosthesis as in claim 1, wherein the restraining device is configured to be detached from the at least two elongate members prior to expansion of the at least two elongate members.

4. A prosthesis as in claim 1, wherein the restraining device is plastically deformable to release the at least two elongate members.

5. A prosthesis as in claim 1, wherein the restraining device comprises a band disposed about the at least two elongate members.

6. A prosthesis as in claim 1, wherein the restraining device comprises a radiopaque material.

7. A vascular device, comprising:

the prosthesis of claim 1; and

a second prosthesis configured to be deployed in the vasculature, such that the at least two elongate members are disposed between the second prosthesis and a wall of the vasculature.

8. A vascular device as in claim 7, wherein the second prosthesis is configured to be deployed between the at least two elongate members.

9. A prosthesis as in claim 1, wherein the at least two elongate members are arranged to bend and rotate relative to an axis parallel to a central longitudinal axis of the radially expandable scaffold section such that the at least two elongate members can circumscribe a main vessel lumen to conform to a wall opposite the Os.

10. A prosthesis as in claim 1, wherein the at least two elongate members comprise at least three elongate members extending from the radially expandable scaffold section.

11. A prosthesis as in claim 1, wherein at least one of the elongate members has an axial length that is at least 1.5 times the width of the scaffold section prior to radial expansion.

12. A prosthesis as in claim 1, wherein at least one of the elongate members has an axial length of at least about 2 mm.

13. A prosthesis as in claim 1, wherein the radially expandable scaffold section has a first wall pattern and wherein the prosthesis has a region with a second wall pattern that is different from the first wall pattern, said second wall pattern permitting the at least two elongate members to both bend and rotate.

14. A prosthesis as in claim 1, wherein at least one of the elongate members extends helically from the radially expandable scaffold section.

15. A prosthesis as in claim 1, wherein at least one of the elongate members extends spirally from the radially expandable scaffold section.

16. A prosthesis as in claim 1, wherein at least one of the elongate members extends in a serpentine pattern from the radially expandable scaffold section.

17. A prosthesis capable of being carried through a patient'"'"'s vasculature over a delivery catheter and of being deployed at an Os, the prosthesis comprising:

a radially expandable scaffold section; and

at least two elongate members extending axially from an end of the radially expandable scaffold section, the at least two elongate members having a low profile configuration and a higher profile configuration, the at least two elongate members transitioning from the low profile configuration to the higher profile configuration primarily under outward pressure from the delivery catheter;

a capturing structure configured to prevent the at least two elongate members from divaricating from the low profile configuration as the prosthesis is advanced through the patient'"'"'s vasculature, a proximal end of the capturing structure located at or distal of a proximal end of the at least two elongate members, a distal end of the capturing structure located on a proximal portion of the at least two elongate members,

wherein the scaffold section is configured to be not radially constrained by a structure that is separable from the delivery catheter when being carried through the patient'"'"'s vasculature.

18. A prosthesis as in claim 17, wherein the capturing structure comprises a tether which circumscribes a proximal portion of the prosthesis.

19. A prosthesis as in claim 18, wherein the tether is configured to be detachably attached to the at least two elongate members prior to expansion of the prosthesis.

20. A prosthesis as in claim 17, wherein the capturing structure is configured to break upon expansion of the prosthesis.