Ultrasoft embolism devices and process for using them

• US 5,718,711 A
• Filed: 05/15/1995
• Issued: 02/17/1998
• Est. Priority Date: 11/18/1992
• Status: Expired due to Term

• Current Assignee: Stryker European Operations Holdings, LLC (Stryker Corporation)
• Original Assignee: Target Therapeutics, Inc. (Boston Scientific Corporation)
• Inventors: Zenzen, Wendy J., Chee, Uriel Hiram, Sepetka, Ivan, Berenstein, Alejandro
• Primary Examiner(s): Dawson, Glenn K.
• Application Number:
  US08/436,282
• Time in Patent Office: 1,009 Days
• Field of Search: 606/1, 606/108, 606/151, 606/191-200, 606/213, 128/898
• US Class Current: 606/191
• CPC Class Codes: A61B 17/12022 Occluding by internal devices, e.g. balloons or releasable wires plugging an opening in the wall of an organ A61B17/0057; occluders for the cervical canal A61F6/146; vas deferens occluders A61F6/20
• CPC Class Codes: A61B 17/1204 temporary occlusion
• CPC Class Codes: A61B 17/12109 in a blood vessel
• CPC Class Codes: A61B 17/1214 Coils or wires
• CPC Class Codes: A61B 17/1215 comprising additional materials, e.g. thrombogenic, having filaments, having fibers, being coated
• CPC Class Codes: A61B 17/12163 having a string of elements connected to each other
• CPC Class Codes: A61B 2017/00526 Methods of manufacturing
• CPC Class Codes: A61B 2017/00539 hydraulically
• CPC Class Codes: A61B 2017/12063 electrolytically detachable
• CPC Class Codes: A61B 2017/1209 detachable by electrical current or potential, e.g. electroactive polymer
• CPC Class Codes: A61B 90/39 Markers, e.g. radio-opaque or breast lesions markers

Abstract

An exceptionally flexible, ultrasoft vaso-occlusive or embolism forming device made of a material which may be a braid, coil, or chain which forms a long, thin thread-like device having little rigidity or column strength. The device is sufficiently flexible and small that it may be hydraulically delivered to a site within the vasculature of a human body using an injected drug or fluid flush through a catheter.

Claims

1. A process for the introduction of a flexible, vaso-occlusive device comprising a coil, braid, or chain having an outside diameter less than about 0.010 inches and a flexibility such that a chosen one cm length of the device bends more than about 20°

under its own weight when an end of that one cm length is held in a horizontal position, into a human body comprising the steps of advancing a catheter having a lumen and a distal end into the human vasculature until the distal end reaches a selected site within that vasculature, introducing the flexible, vaso-occlusive device through the catheter lumen and out the catheter distal end.

2. The process of claim 1 additionally comprising the step of hydraulically impelling the device out the catheter distal end.

3. The process of claim 1 additionally includes the step of electrolytically releasing the device from an attached guidewire after passage of the device out the catheter distal end.

4. The process of claim 1 additionally comprising the step of introducing one or more additional vaso-occlusive coils, braids, or chains having a larger diameter to said selected vascular site.

5. The process of claim 1 additionally comprising the step of introducing tissue adhesives or particulate embolization materials comprising microparticles of polyvinyl alcohol foam or chemotherapeutic agents to said selected vascular site.

6. The process of claim 5 where one of the tissue adhesives is a cyanoacrylate resin.

7. The process of claim 6 where the cyanoacrylate resin is n-butylcyanoacrylate.

8. The process of claim 1 where the device comprises a member selected from the group consisting of a coil, a braided tube, a combination braid and coil, and a chain.

9. The process of claim 8 where the device is a regularly wound coil.

10. The process of claim 8 where the device is a coil which is not regularly wound.

11. The process of claim 8 where the device has an outer surface and additionally comprises filamentary material attached to the outer surface.

12. The process of claim 1 where the device outside diameter is between 0.0014 inches and 0.0095 inches.

13. The process of claim 12 where the device outside diameter is between 0.004 and 0.0075 inches.

14. The process of claim 1 where the device comprises a filament having a diameter of less than about 0.0025 inches.

15. The process of claim 14 where the device comprises a filament having a diameter between 0.00045 and less than 0.00225 inches.

16. The process of claim 15 where the device comprises a filament having a diameter of between 0.0005 and 0.002 inches.

17. The process of claim 16 where the device comprises a filament having a diameter of between 0.001 and 0.002 inches.

18. The process of claim 1 where the device comprises a ribbon having a major axis between 0.001 and 0.002 inches and a minor axis is 0.0007 and 0.001 inches.

19. The process of claim 1 where the device bends more than about 35°

under its own weight when one cm of the device is held in a horizontal position.

20. The process of claim 1 where the length of the device is between 2 mm and 120 cm.

21. The process of claim 20 where the length of the device is between 30 cm and 120 cm.