Multi-region staged inflation balloon

• US 8,728,073 B2
• Filed: 10/10/2006
• Issued: 05/20/2014
• Est. Priority Date: 10/10/2006
• Status: Active Grant

• Current Assignee: Biosense Webster Incorporated (Johnson & Johnson)
• Original Assignee: Biosense Webster Incorporated (Johnson & Johnson)
• Inventors: McDaniel, Benjamin
• Primary Examiner(s): Dvorak, Linda
• Assistant Examiner(s): SCOTT, AMANDA L
• Application Number:
  US11/539,935
• Publication Number:
  US 20080086073A1
• Time in Patent Office: 2,779 Days
• Field of Search: 606/41, 606/197, 600115-116, 60410101-10105, 604/103.06
• US Class Current: 606/41
• CPC Class Codes: A61B 17/2202 the ultrasound transducer being inside patient's body at the distal end of the catheter
• CPC Class Codes: A61B 18/1492 having a flexible, catheter-like structure, e.g. for heart ablation A61B18/1477 takes precedence
• CPC Class Codes: A61B 18/18 by applying electromagnetic radiation, e.g. microwaves radiation therapy A61N5/00
• CPC Class Codes: A61B 18/24 with a catheter A61B18/26, A61B18/28 take precedence
• CPC Class Codes: A61B 2018/00065 porous
• CPC Class Codes: A61B 2018/00214 Expandable means emitting energy, e.g. by elements carried thereon
• CPC Class Codes: A61B 2018/00238 porous

Abstract

The present invention involves a surgical device and method of use, particularly an assembly and method incorporating a shaped expandable member along the distal region of an ablation device to facilitate ablation of a circumferential region of tissue engaged by the expandable member. The ablation device assembly includes an elongate body with a proximal end portion, a distal end portion, and a longitudinal axis. A contact member is located along the distal end portion of the elongate body. The contact member has a circumferential wall and is expandable from a radially collapsed condition to a radially expanded condition. The contact member also includes a single chamber having a single bulbous section. The single bulbous section has a plurality of longitudinally adjacent circumferential regions wherein adjacent regions have dissimilar wall thicknesses. The ablation device also has an ablation element having an ablative energy source that is located along the distal end portion, wherein the ablation element cooperates with the contact member such that the ablative energy source emits a substantially circumferential pattern of energy through the circumferential wall.

Claims

1. An ablation device assembly for ablating a circumferential region of tissue at a location within a body space where a pulmonary vein extends from an atrium, comprising:

an elongate body with a proximal end portion, a distal end portion, and a longitudinal axis;

an elastic contact member located along the distal end portion, the contact member having a circumferential wall and being expandable from a radially collapsed condition to a radially expanded condition, the contact member including a single chamber having a single bulbous section, the single bulbous section having a proximal region, a distal region and an intermediate region there between, a portion of the intermediate region having a thickened section along the circumferential wall, the thickened section configured to constrain a portion of the circumferential wall and prevent the single bulbous section from uniformly expanding and forming a spherical or conical shape when in the radially expanded condition; and

an ablation element having an ablative energy source that is located along the distal end portion, wherein the ablation element cooperates with the contact member such that the ablative energy source emits a substantially circumferential pattern of energy through the circumferential wall.

2. The assembly of claim 1, wherein the contact member comprises an inflatable elastic balloon, the circumferential wall comprises an elastic outer skin of the balloon, and the ablative energy source is adapted to emit the circumferential pattern of energy through the outer skin of the balloon and into the circumferential region of tissue.

3. The assembly of claim 1, wherein the ablation element comprises a thermal ablation element.

4. The assembly of claim 1, wherein the ablation element comprises an ultrasound ablation element.

5. The assembly of claim 1, wherein the ablation element comprises a microwave ablation element.

6. The assembly of claim 1, wherein the ablation element comprises a cryoablation element.

7. The assembly of claim 1, wherein the ablation element comprises a fluid delivery element.

8. The assembly of claim 1, wherein the ablation element comprises a light emitting ablation element.

9. The assembly of claim 1, wherein the ablation element comprises an element that emits ionizing radiation.

10. The assembly of claim 1, further comprising a guidewire lumen along the distal end portion of the elongate body and which is adapted to slideably engage and track over a guidewire positioned within the body space.

11. The assembly of claim 10, wherein the guidewire lumen further comprises a guidewire passageway which extends along the elongate body between a proximal guidewire port located along the proximal end portion and a distal guidewire port located along the distal end portion.

12. The assembly of claim 1 wherein the elongate body is a steerable delivery member with a proximal end portion and a distal end portion that is deflectable and steerable by rotating the proximal end portion.

13. The assembly of claim 1, wherein the contact member further comprises a contoured elastic balloon that includes a balloon skin that forms the chamber and which is inflatable with an inflation medium in order to expand from the radially collapsed condition to the radially expanded condition.

14. The assembly of claim 1, wherein the contact member is constructed from the group of materials consisting of polyurethane, silicone, Mylar, latex, and combinations and blends thereof.

15. The assembly of claim 14, wherein the contact member exhibits at least about a 400% elastic expansion before yield.

16. The assembly of claim 14, wherein the contact member has a profile in the radially collapsed condition that is between about 0.060 and 0.200 inches, inclusive, and the expanded outer diameter is between about 0.25 and 1.5 inches, also inclusive.

17. The assembly of claim 1, wherein the elongate body further comprises:

a fluid passageway extending between a proximal port, which is located along the proximal end portion and is adapted to couple to a pressurizeable fluid source, and a distal port, which is located along the distal end portion and through which the fluid passageway is fluidly coupled to the contact member.

18. The assembly of claim 1, further comprising an expansion actuator that is adapted to expand the expandable member from the radially collapsed condition to the radially expanded condition.

19. The assembly of claim 1 wherein the wall thickness of the distal region is smaller than the wall thickness of the proximal region.

20. The assembly of claim 1 wherein the distal region includes a narrow tubular section and the proximal region includes a large spherical section.

21. The assembly of claim 1 wherein the most distal circumferential region has different mechanical properties than the most proximal circumferential region.

22. An elastic contact member having a circumferential wall and being expandable from a radially collapsed condition to a radially expanded condition, the contact member including a single chamber having a single bulbous section, the single bulbous section having a proximal region, a distal region and an intermediate region there between, wherein the distal region and the proximal region have dissimilar tensile strengths, the intermediate region having a thickened section along the circumferential wall, the thickened section configured to constrain a portion of the circumferential wall and prevent the single bulbous section from uniformly expanding and forming a spherical or conical shape when in the radially expanded condition.