METHODS FOR MANUFACTURING AN ENDOPROSTHESIS

• US 20100299911A1
• Filed: 05/12/2010
• Published: 12/02/2010
• Est. Priority Date: 05/13/2009
• Status: Abandoned Application

• Current Assignee: Abbott Cardiovascular Systems Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Abbott Cardiovascular Systems Incorporated (Abbott Laboratories Incorporated)
• Inventors: Pike, Kelly A., Gianotti, Marc G.
• Application Number:
  US12/778,589
• Publication Number:
  US 20100299911A1
• Time in Patent Office: Days
• US Class Current: 29/592
• CPC Class Codes: A61F 2/86 Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2/915 with bands having a meander structure, adjacent bands being connected to each other
• CPC Class Codes: A61F 2240/002 Designing or making customized prostheses
• CPC Class Codes: Y10T 29/49 Method of mechanical manufacture

Abstract

Method for manufacturing an endoprosthesis are described. The method may include selecting an indication range based on a range of inner diameters of a body lumen. A nominal diameter of the endoprosthesis may be selected. A range of chronic outward force, a range of radial force, a range of safety factors, or combinations thereof may be selected. A design characteristic may be determined based on the indication range, the nominal diameter, and at least one of the range of chronic outward force, the range of radial force, and the range of safety factors. The endoprosthesis may be manufactured based on the determined design characteristic.

Claims

1. A method for manufacturing an endoprosthesis:

selecting an indication range based on a range of inner diameters of a body lumen;

selecting a nominal diameter of the endoprosthesis;

selecting a range of chronic outward force; and

determining a design characteristic based on the indication range, the nominal diameter, and the range of chronic outward force.

2. The method of claim 1, further comprising selecting a nominal chronic outward force.

3. The method of claim 2, wherein the nominal chronic outward force is at least sufficient to maintain vessel patency.

4. The method of claim 1, wherein the range of chronic outward force is between about ON to about 10 N.

5. The method of claim 4, wherein the range of chronic outward force is between about 1 N to about 8 N.

6. The method of claim 5, wherein the range of chronic outward force is between about 3 N to about 6 N.

7. The method of claim 1, wherein the indication range is between about 1 mm to about 5 mm of inner diameters of the vessel.

8. The method of claim 1, wherein the indication range is based on a length of a treatment site.

9. The method of claim 1, wherein the design characteristic is at least one of material type, material processing, web pattern, wall coverage, vessel compliance, and fatigue life.

10. The method of claim 9, wherein the design characteristic is the web pattern and the web pattern comprises a plurality of struts and a plurality of crowns connecting the plurality of struts.

11. The method of claim 10, wherein an aspect of the plurality of struts is determined based on the indication range and the range of chronic outward force.

12. The method of claim 1, wherein the nominal diameter is between about 4 mm and about 12 mm.

13. A method for manufacturing an endoprosthesis:

selecting an indication range based on a range of inner diameters of a body lumen;

selecting a nominal diameter of the endoprosthesis;

selecting a range of safety factors; and

determining a design characteristic based on the indication range, the nominal diameter, and the range of safety factors.

14. The method of claim 13, wherein the indication range is between about 1 mm to about 5 mm of inner diameters of the vessel and the range of safety factors extends from at least about 1.

15. The method of claim 13, wherein the safety factors are based on an endoprosthesis design that does not fracture for about four million pulse cycles at about three percent vessel dilation.

16. The method of claim 15, wherein the nominal diameter of the endoprosthesis is about 6 mm and the indication range extends from about 2 mm of inner diameters of the vessel and the range of safety factors extends from at least about 1 to about 10.

17. The method of claim 15, wherein the nominal diameter of the endoprosthesis is about 8 mm and the indication range extends from about 4.5 mm of inner diameters of the vessel and the range of safety factors extends from at least about 4 to about 14.

18. The method of claim 15, wherein the nominal diameter of the endoprosthesis is about 6 mm and the indication range extends from about 2.5 mm of inner diameters of the vessel and the range of safety factors extends from at least about 9 to about 19.

19. The method of claim 13, wherein the design characteristic is at least one of material type, material processing, web pattern, wall coverage, vessel compliance, and fatigue life.

20. The method of claim 19, wherein the design characteristic is the web pattern and the web pattern comprises a plurality of struts and a plurality of crowns connecting the plurality of struts.

21. The method of claim 20, wherein a length of the plurality of struts is determined based on the indication range and the range of safety factors.

22. A method for manufacturing a self-expanding stent, comprising:

selecting an indication range based on a range of inner vessel diameters, the indication range being between about 3.0 mm to about 5.5 mm;

selecting a range of chronic outward force extending between about 3 N to about 6 N;

determining a design characteristic based on a nominal diameter of about 6.0 mm, the indication range, and the range of chronic outward force; and

manufacturing the self-expanding stent based on the determined design characteristic.

23. The method of claim 22, wherein a nominal chronic outward force is about 15 N.

24. The method of claim 23, wherein the range of chronic outward force extends from about 9 N to about 18 N.