Electrical conduction block implant device

• US 9,398,967 B2
• Filed: 01/17/2006
• Issued: 07/26/2016
• Est. Priority Date: 03/02/2004
• Status: Expired due to Fees

• Current Assignee: Syntach AG
• Original Assignee: Syntach AG
• Inventors: Cornelius, Richard
• Primary Examiner(s): McDermott, Corrine
• Assistant Examiner(s): SIMPSON, SARAH A
• Application Number:
  US11/333,966
• Publication Number:
  US 20060178725A1
• Time in Patent Office: 3,843 Days
• Field of Search: 623/1.15, 623/1.31, 623/1.35
• US Class Current: 1/1
• 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 2002/065 Y-shaped blood vessels
• CPC Class Codes: A61F 2002/821 Ostial stents
• 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 2002/9511 the retaining means being filaments or wires
• CPC Class Codes: A61F 2220/0016 with sharp anchoring protrusions, e.g. barbs, pins, spikes
• CPC Class Codes: A61F 2230/0013 Horseshoe-shaped, e.g. crescent-shaped, C-shaped, U-shaped

Abstract

The present invention provides an electrical block implant sized and shaped for securement at the perimeter of the pulmonary ostium of the left atrium. By utilizing various expandable ring designs and optional anchoring mechanisms, the present invention causes even, circular scarring around the perimeter of the pulmonary ostium, achieving reliable blocking of aberrant electrical signals responsible for atrial fibrillation.

Claims

1. A pulmonary vein implant for treating arrhythmia comprising:

a first ring having a compressed state and an expanded state sized to contact an inner diameter of a pulmonary vein;

said first ring having a first cross section size;

a second ring having a compressed state and an expanded state sized to contact ostial tissue associated with said pulmonary vein;

said second ring having a second cross section size smaller than said first cross section size;

a plurality of connecting members disposed between said first ring and said second ring;

said connecting members having an expanded state urging said second ring into said ostial tissue;

wherein a radial expansion force generated by said first ring is at least partially conveyed to said second ring by said connecting members for increasing a force per area of said second ring on said ostial tissue.

2. The pulmonary vein implant of claim 1, wherein said plurality of connecting members are positioned substantially perpendicular to said first ring and said second ring.

3. The pulmonary vein implant of claim 1, wherein said plurality of connecting members expand radially away from a center of said implant.

4. The pulmonary vein implant of claim 1, wherein said expanded state of said first ring includes a plurality of curved regions.

5. The pulmonary vein implant of claim 4, wherein said curved regions form regularly repeating peaks.

6. The pulmonary vein implant of claim 4, wherein said first ring includes a plurality of barbs positioned towards said second ring.

7. The pulmonary vein implant of claim 1, wherein said expanded state of said second ring is larger than said expanded state of said first ring.

8. The pulmonary vein implant of claim 1, wherein said first ring includes a width greater than said second ring.

9. The pulmonary vein implant of claim 1, wherein said expanded state of said plurality of connecting members produce a radial force on said second ring to generate a scar in said ostial tissue.

10. An implant for treating atrial arrhythmia comprising:

a spatial anchoring portion having an expanded configuration and a serpentine unexpanded configuration;

said spatial anchoring portion having a first thickness;

a scar-generating portion having an expanded configuration and a serpentine unexpanded configuration;

said scar-generating portion having a second thickness smaller than said first thickness;

a plurality of connecting arms connecting said spatial anchoring portion to said scar-generating portion, said plurality of connecting arms biasing said scar-generating portion radially from said implant such that a radial expansion force generated by said spatial anchoring portion is applied to said scar-generating portion for increasing a force per area of said scar-generating portion on ostial tissue;

wherein said expanded configuration of said scar-generating portion has a larger diameter than said anchoring portion.

11. The implant of claim 10, wherein said plurality of connecting arms are positioned substantially perpendicular to said spatial anchoring portion and said scar-generating portion.

12. The implant of claim 10, wherein said spatial anchoring portion includes a plurality of curved regions forming a plurality of regularly repeating peaks.

13. The implant of claim 12, wherein said spatial anchoring portion further comprises a plurality of barbs directed towards said scar-generating portion.

14. The implant of claim 12, wherein said spatial anchoring portion forms a ring.

15. The implant of claim 12, wherein said expanded configuration of said scar-generating portion radially expands in about three-fourths of a circumference of said implant.

16. The implant of claim 10, wherein said unexpanded configuration of said scar-generating portion includes a plurality of curved regions forming a plurality of regularly repeating peaks.

17. The implant of claim 10, wherein said plurality of connecting arms have a radius of curvature of approximately 2 mm when in an expanded state.

18. The implant of claim 10, wherein said plurality of connecting arms are composed of Nitinol and have a thickness of 0.010 inches.

19. The implant of claim 10, wherein said plurality of connecting arms have a length that varies in thickness.

20. The implant of claim 10, wherein said scar-generating portion includes a side prevented from radial expansion in said expanded configuration.

21. The implant of claim 20, further comprising a second implant having a second scar-generating portion including a side prevented from radial expansion in an expanded configuration.

22. The implant of claim 21, wherein said first implant and said second implant are positioned adjacent to each other within a patient to form a continuous scar.