Bifurcation delivery system

• US 8,353,944 B2
• Filed: 03/14/2005
• Issued: 01/15/2013
• Est. Priority Date: 03/14/2005
• Status: Expired due to Fees

• Current Assignee: Boston Scientific Scimed (Boston Scientific Corporation)
• Original Assignee: Boston Scientific Scimed (Boston Scientific Corporation)
• Inventors: Weber, Jan, Jagger, Karl A., Eidenschink, Tracee
• Primary Examiner(s): DOWE, KATHERINE MARIE
• Application Number:
  US11/079,756
• Publication Number:
  US 20060206188A1
• Time in Patent Office: 2,864 Days
• Field of Search: 623/1.11, 604/533, 604/535, 604/530, 285/272, 285/282
• US Class Current: 623/1.11
• CPC Class Codes: A61F 2/856 Single tubular stent with a side portal passage
• 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 2002/30426 Bayonet coupling
• CPC Class Codes: A61F 2220/0025 Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
• CPC Class Codes: A61M 2025/0058 having an electroactive polymer material, e.g. for steering purposes, for control of flexibility, for locking, for opening or closing
• CPC Class Codes: A61M 2025/1045 for treating bifurcations, e.g. balloons in y-configuration, separate balloons or special features of the catheter for treating bifurcations
• CPC Class Codes: A61M 25/0043 characterised by structural features

Abstract

A catheter assembly comprises a catheter shaft having a proximal region a distal region and a rotational seal therebetween. The rotational seal comprises a first component fixedly engaged to the proximal region and a second component fixedly engaged to the distal region. The components engaged in an overlapping arrangement. The rotational seal is actuatable between a non-activated and activated states. In the non-activated state the first component and the second component are separated by a gap which provides for the distal region of the catheter shaft to be rotatable relative to the proximal region. In the activated state at least a portion of the first component and the second component being sealingly engaged together such that distal region is made static relative to the proximal region.

Claims

1. A catheter assembly comprising:

a catheter shaft, the catheter shaft having a proximal region, a distal region, and a rotational seal therebetween,

the rotational seal comprising a first component and a second component, the first component fixedly engaged to the proximal region of the catheter shaft, the second component fixedly engaged to the distal region of the catheter shaft, the first component and the second component being overlappingly engaged, and

the rotational seal having an activated state and a non-activated state, in the non-activated state the first component and the second component being separated by a gap which provides for the distal region of the catheter shaft to be rotatable relative to the proximal region of the catheter shaft, in the activated state the first component and the second component being sealingly engaged together such that the distal region is made static relative to the proximal region;

wherein a portion of the first component of the rotational seal is engaged with a portion of the second component of the rotational seal in both the activated and non-activated states to prevent axial separation of the proximal region of the catheter shaft from the distal region of the catheter shaft.

2. The catheter assembly of claim 1 wherein the rotational seal further comprises a layer of electro-active polymer (EAP) material, in the non-activated state the layer of EAP material being fixedly engaged to one of the first and second components, a portion of the layer of EAP material defining at least a portion of the gap, in the activated state the EAP layer expanding in volume to sealingly engage the other component.

3. The catheter assembly of claim 2 wherein in the activated state the layer of EAP material expands in volume by about 1 to about 30 percent.

4. The catheter assembly of claim 2 wherein the EAP material is selected from at least one material of the group consisting of:

Poly-pyrrole (PPY), Poly-Aniline (PAni), Poly-Thiofene (PTH), Poly-Paraphenylene Vinylene (PPV), Nafion, and any combination thereof.

5. The catheter assembly of claim 1 wherein the first component and the second component are overlappingly arranged in a bayonet lock configuration.

6. The catheter assembly of claim 1 wherein the second component is constructed of a material that is harder than the first component.

7. The catheter assembly of claim 1 wherein the first component comprises a pin, the pin having a plurality of arms, each of the arms separated by a slot, wherein the slot is defined by the adjacent arms, each of the arms having an engagement portion, each of the engagement portions being at least partially positioned within a recess defined by the second component.

8. The catheter assembly of claim 1 wherein the catheter shaft defines a first guidewire lumen for passage of a first guidewire therethrough, the first guidewire lumen extending through the proximal region and the distal region.

9. The catheter assembly of claim 1 wherein the distal region comprises an expandable balloon.

10. The catheter assembly of claim 9 further comprises a secondary guidewire housing, the secondary guidewire housing being engaged to the balloon and defining a secondary guidewire lumen for passage of a secondary guidewire therethrough.

11. The catheter assembly of claim 9 wherein the catheter shaft defines an inner shaft and an outer shaft, the inner shaft having an inner shaft rotational seal between a proximal region of the inner shaft and a distal region of the inner shaft, the outer shaft having an outer shaft rotational seal between a proximal region of the outer shaft and the distal region of the outer shaft.

12. The catheter assembly of claim 11 wherein the inner shaft and the outer shaft define an inflation lumen, the inflation lumen in fluid communication with the balloon.

13. A system for delivery of a stent to a vessel bifurcation comprising:

a catheter, the catheter comprising a catheter shaft, the catheter shaft having a proximal region, a distal region, and a rotational seal therebetween, at least a portion of the distal region comprising an expandable balloon,

the rotational seal comprising a first component and a second component, the first component fixedly engaged to the proximal region of the catheter shaft, the second component fixedly engaged to the distal region of the catheter shaft, the first component having a first reduced diameter portion, the second component having a first engagement portion, the first engagement portion being radially aligned with the first reduced diameter portion,

the rotational seal having an activated state and a non-activated state, in the non-activated state the first component and the second component being separated by a gap which provides for the distal region of the catheter shaft to be rotatable relative to the proximal region of the catheter shaft, in the activated state at least a portion of the first component and the second component being sealingly engaged together such that the distal region is made static relative to the proximal region;

wherein the first component has a second engagement portion and the second component has a second reduced diameter portion, the second engagement portion being radially aligned with the second reduced diameter portion to provide engagement of the first and second engagement portions in both the activated and non-activated states of the rotational seal to prevent axial separation of the proximal region of the catheter shaft from the distal region of the catheter shaft; and

a stent, the stent being expandable from a pre-delivery state to a delivery state, wherein in the delivery state the stent has a greater diameter than in the pre-delivery state, in the pre-delivery state the stent being disposed about at least a portion of the balloon.

14. The system of claim 13 wherein the catheter shaft defines a first guidewire lumen for passage of a first guidewire therethrough, the first guidewire lumen extending through the proximal region and the distal region.

15. The system of claim 13 further comprising a secondary guidewire housing, the secondary guidewire housing being engaged to the balloon and defining a secondary guidewire lumen for passage of a secondary guidewire lumen therethrough, the stent being at least partially disposed about the secondary guidewire housing.

16. A method of treating a vessel bifurcation comprising the steps of:

advancing a first guidewire through a first vessel, such that the first guidewire extends proximally beyond a bifurcation of the first vessel and a second vessel;

advancing a second guidewire through the first vessel to the bifurcation and into the second vessel;

providing a stent delivery system, the system comprising;

a catheter, the catheter having a catheter shaft, the catheter shaft having a proximal region, a distal region, and a rotational seal therebetween, at least a portion of the distal region comprising an expandable balloon, the catheter shaft defining a first guidewire lumen for passage of the first guidewire therethrough, the first guidewire lumen extending through the proximal region and the distal region,

a secondary guidewire housing being engaged to the balloon, the secondary guidewire housing defining a secondary guidewire lumen for passage of the secondary guidewire lumen therethrough, the stent being at least partially disposed about the secondary guidewire housing,

the rotational seal comprising a first component and a second component, the first component fixedly engaged to a distal end of the proximal region of the catheter shaft, the second component fixedly engaged to a proximal end of the distal region of the catheter shaft, the first component and the second component being overlappingly engaged,

the rotational seal having an activated state and a non-activated state, in the non-activated state, at least a first portion of the first component and at least a first portion of the second component being separated by a gap which provides for the distal region of the catheter shaft to be rotatable relative to the proximal region of the catheter shaft, in the activated state at least the first portion of the first component and the second component being sealingly engaged together such that the distal region is made static relative to the proximal region;

wherein a second portion of the first component of the rotational seal is engaged with a second portion of the second component of the rotational seal in both the activated and non-activated states to prevent axial separation of the proximal region of the catheter shaft from the distal region of the catheter shaft; and

a stent, the stent being expandable from a pre-delivery state to a delivery state, wherein in the delivery state the stent has a greater diameter than in the pre-delivery state, in the pre-delivery state the stent being disposed about at least a portion of the balloon, the stent defining a secondary opening for passage of the secondary guidewire therethrough;

advancing the stent delivery system along the first guidewire and the second guidewire through the first vessel, wherein the rotational seal is in the non-activated state;

rotationally aligning the distal region of the catheter shaft such that the secondary opening of the stent is in communication with the second vessel;

actuating the rotational seal from the non-activated state to the activated state; and

expanding the balloon to deliver the stent.