Elongate member providing a variation in radiopacity

• US 9,216,053 B2
• Filed: 04/10/2007
• Issued: 12/22/2015
• Est. Priority Date: 03/05/2002
• Status: Active Grant

• Current Assignee: Avent Incorporated (Avanos Medical, Inc.)
• Original Assignee: Avent Incorporated (Avanos Medical, Inc.)
• Inventors: Godara, Neil, Shah, Krishan, Lefler, Amy, Harrison, Robert
• Primary Examiner(s): ROANE, AARON F
• Application Number:
  US11/733,515
• Publication Number:
  US 20070203402A1
• Time in Patent Office: 3,178 Days
• Field of Search: 606 41- 52, 607 88- 94
• US Class Current: 1/1
• CPC Class Codes: A61B 18/1477 Needle-like probes
• CPC Class Codes: A61B 90/39 Markers, e.g. radio-opaque or breast lesions markers

Abstract

An elongate member for inserting into a cannula is disclosed. The cannula comprises an electrically insulated region and an electrically exposed conductive region for delivering energy to form a lesion within a patient'"'"'s body at an intended location relative to the electrically exposed conductive region. The elongate member is structured to cooperatively engage with the cannula at a pre-determined insertion depth and to provide a variation in radiopacity, at a pre-determined position relative to the electrically exposed conductive region, when inserted to the pre-determined insertion depth. The variation in radiopacity provides a visual reference for distinguishing, using fluoroscopic imaging, the intended location of the lesion.

Claims

1. An elongate member and cannula assembly, comprising:

a cannula comprising a lumen, an electrically insulated region, and an electrically-exposed conductive region, the lumen extending through the electrically insulated region and the electrically-exposed conductive region, the electrically-exposed conductive region configured for delivering energy to form a lesion within a patient'"'"'s body at an intended location; and

an elongate member configured within the cannula, the elongate member comprising a proximal region, a distal region, and a pre-determined length, the elongate member engaged with the cannula via a structure at the proximal region such that the pre-determined length extends a pre-determined insertion depth within the cannula and remains fixed therein, the elongate member comprising a non-conductive radiopaque marker at a pre-determined position on an outer surface of the distal region of the of the elongate member,

wherein the radiopaque marker provides a variation in radiopacity at the pre-determined position when the elongate member is engaged with the cannula via the structure and inserted to the pre-determined insertion depth, the pre-determined length of the elongate member being sized such that, when the elongate member is cooperatively engaged with the cannula via the structure and inserted to the pre-determined insertion depth, a distal end of the elongate member extends beyond a distal end of the electrically insulated region of the cannula and aligns with a distal end of the electrically-exposed region of the cannula such that the radiopaque marker aligns with the distal end of the electrically insulated region to indicate the intended location of the lesion, the cannula connectable to an energy source for forming the lesion.

2. The assembly of claim 1, further comprising a second radiopaque marker positioned to align with a distal end of the electrically-exposed conductive region of the cannula when the elongate member is inserted to the pre-determined insertion depth so as to provide a frame for the electrically-exposed conductive region and a visual reference for distinguishing the intended location of the lesion.

3. The assembly of claim 1, wherein the radiopaque marker comprises a platinum band.

4. The assembly of claim 1, wherein the radiopaque marker comprises an indentation in the elongate member, the indentation positioned to align with the distal end of the electrically insulated region when the elongate member is inserted to the pre-determined insertion depth.

5. The assembly of claim 1, wherein the proximal region and the distal region are of differing radiopacity, and the proximal region and the distal region are sized such that a boundary between the proximal region and the distal region aligns with a distal end of the electrically insulated region when the elongate member is inserted to the pre-determined insertion depth for providing the variation in radiopacity.

6. The assembly of claim 1, wherein extension of the distal end of the elongate member beyond a distal end of the cannula provides variation in radiopacity.

7. The assembly of claim 1, wherein the proximal region has a smaller diameter than the distal region, and the proximal region and the distal region are sized such that a boundary between the proximal region and the distal region aligns with a distal end of the electrically insulated region when the elongate member is inserted to the pre-determined insertion depth for providing the variation in radiopacity.

8. The assembly of claim 1, wherein a depth stopper on the elongate member provides the cooperative engagement.

9. The assembly of claim 1, wherein the elongate member further comprises a hub at a proximal end thereof, and the hub provides the cooperative engagement.

10. The assembly of claim 1, wherein the elongate member is manufactured from a material selected from the group consisting of stainless steel, titanium, nitinol, alloys thereof, and any combination thereof.

11. A kit comprising:

a cannula comprising a lumen, an electrically insulated region, and an electrically-exposed conductive region, the lumen extending through the electrically insulated region and the electrically-exposed conductive region, the electrically conductive region configured for delivering energy to form a lesion within a patient'"'"'s body at an intended location;

an elongate member inserted within cannula, the elongate member having a proximal region, a distal region, and a pre-determined length, the elongate member engaged with the cannula via a structure at the proximal region such that the pre-determined length extends a pre-determined insertion depth within the cannula and remains fixed therein, the elongate member comprising a non-conductive radiopaque marker at a pre-determined position on an outer surface of the distal region of the of the elongate member, wherein the radiopaque marker provides a variation in radiopacity at the pre-determined position when the elongate member is engaged with the cannula via the structure and inserted to the pre-determined insertion depth;

the pre-determined length of the elongate member being sized such that, when the elongate member is cooperatively engaged with the cannula via the structure and inserted to the pre-determined insertion depth, a distal end of the elongate member extends beyond a distal end of the electrically insulated region of the cannula and aligns with a distal end of the electrically-exposed region of the cannula such that the radiopaque marker aligns with the distal end of the electrically insulated region to indicate the intended location of the lesion, the cannula being connectable to an energy source for forming the lesion.