Stent delivery device with embolic protection

• US 7,708,770 B2
• Filed: 06/18/2003
• Issued: 05/04/2010
• Est. Priority Date: 11/09/2001
• Status: Expired due to Fees

• Current Assignee: Boston Scientific Scimed (Boston Scientific Corporation)
• Original Assignee: Boston Scientific Scimed (Boston Scientific Corporation)
• Inventors: Schlegel, Karri L., Edmiston, Daryl R., Linder, Richard J., Johnson, Steven W.
• Primary Examiner(s): Bui; Vy Q
• Application Number:
  US10/464,725
• Publication Number:
  US 20040064179A1
• Time in Patent Office: 2,512 Days
• Field of Search: 623/1.11, 606/200, 606/108, 606/191, 606/194, 606/195, 606/198
• US Class Current: 623/1.11
• CPC Class Codes: A61F 2/011 Instruments for their placement or removal
• CPC Class Codes: A61F 2/013 Distal protection devices, i.e. devices placed distally in combination with another endovascular procedure, e.g. angioplasty or stenting
• CPC Class Codes: A61F 2/95 Instruments specially adapted for placement or removal of stents or stent-grafts
• CPC Class Codes: A61F 2/9517 handle assemblies therefor
• 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 2002/018 made from tubes or sheets of material, e.g. by etching or laser-cutting
• CPC Class Codes: A61F 2002/9511 the retaining means being filaments or wires
• CPC Class Codes: A61F 2230/0006 circular
• CPC Class Codes: A61F 2230/0067 conical
• CPC Class Codes: A61F 2230/008 paraboloidal
• CPC Class Codes: A61F 2250/0071 breakable or frangible

Abstract

A delivery device adapted to insert and deploy a stent within a body lumen. The delivery device includes a guide member adapted to retain a dilation assembly and a stent within a lumen thereof until the stent is to be deployed into the body lumen. The delivery device is configured to enable simultaneous insertion of the guide member, dilation assembly, stent, and optional guidewire within a body lumen. Following deploying the stent, the delivery device can be removed, while providing the capability of optionally maintaining the guide member or the guidewire to function or act as an exchange wire for additional surgical devices.

Claims

1. A device configured to deliver a stent within a body lumen and provide embolic protection, the delivery device comprising:

a filter device adapted to provide embolic protection during a procedure, said filter device comprising;

a guidewire;

a filter assembly mounted to said guidewire, and

a restraining member adapted to apply a restraining force upon at least a portion of said filter assembly to prevent deployment of a filter of the filter assembly, wherein the restraining member includes a cord extending around the filter; and

a stent delivery device, comprising;

a dilation assembly configured to support a stent and assist with placing said stent within the body lumen, said dilation assembly being configured to receive said filter assembly therein when said dilation assembly and said filter assembly are moved axially relative to one another following deployment of said filter.

2. The device as recited in claim 1, wherein said dilation assembly comprises:

a tubular member;

a dilation balloon mounted to said tubular member, said dilation balloon having an interior portion; and

a dilation tube in fluid communication with said interior portion of said dilation balloon.

3. The device as recited in claim 1, wherein said filter assembly further comprises:

a filter basket; and

a filter attached to said filter basket.

4. The device as recited in claim 3, wherein said restraining member is adapted to apply said force upon at least a portion of said filter basket.

5. The device as recited in claim 4, wherein said restraining member comprises at least one actuating member extending from said restraining member to a proximal end of said guidewire, wherein moving said at least one actuating member in a proximal direction releases said force applied by said restraining member to release said filter basket.

6. The stent delivery device as recited in claim 4, wherein said filter basket comprises one or more struts, wherein at least one of said one or more struts is configured to bias outwardly.

7. The stent delivery device as recited in claim 1, wherein said filter assembly is integrally formed with said guidewire.

8. The stent delivery device as recited in claim 1, wherein said filter assembly further comprises an atraumatic tip.

9. The device as recited in claim 1, wherein said dilation assembly comprises a tubular member having a distal end portion configured to receive said filter assembly therein when said dilation assembly and said filter assembly are moved axially relative to one another following deployment of said filter.

10. The device as recited in claim 9, wherein said distal end portion of said tubular member is configured to receive said filter assembly therein when said filter assembly is moved proximally relative to said dilation assembly following deployment of said filter.

11. The device as recited in claim 9, wherein said distal end portion of said tubular member is configured to receive said filter assembly therein when said dilation assembly is moved distally relative to said filter assembly following deployment of said filter.

12. The device as recited in claim 9, wherein said distal end portion of said tubular member is flared radially outward.

13. The device as recited in claim 9, further comprising a tip attached to said guidewire distal to said tubular member of said dilation assembly.

14. The device as recited in claim 13, wherein said tip provides a transition between said guidewire and said tubular member when said filter assembly is disposed within said tubular member.

15. The device as recited in claim 1, wherein said dilation assembly comprises a dilation balloon mounted to a tubular member, the restraining member being at least partially disposed within the tubular member, and the restraining member being arranged so that axially displacing the restraining member relative to the tubular member releases the restraining force applied by said restraining member upon said filter assembly.