ABLATION INSTRUMENTS WITH A MEMBER HAVING A TRIANGULAR CROSS-SECTION
20170319267 · 2017-11-09
Inventors
Cpc classification
A61B2018/00023
HUMAN NECESSITIES
A61B18/18
HUMAN NECESSITIES
International classification
Abstract
An ablation needle assembly includes an outer member, an inner member, and a feedline. The outer member defines a first lumen that receives the inner member therein. The inner member defines a second lumen that receives the feedline therein. The first and second lumens cooperate to circulate fluid about the feedline. Either the inner or outer member has a triangular cross-section.
Claims
1. An ablation needle assembly comprising: an outer member defining a first lumen; an inner member disposed within the first lumen and defining a second lumen; and a feedline disposed within the second lumen, wherein the first lumen and the second lumen cooperate to circulate fluid about the feedline, wherein one of the outer member or inner member has a triangular cross-section.
2. The ablation needle assembly according to claim 1, wherein the outer member has a triangular cross-section.
3. The ablation needle assembly according to claim 2, wherein the inner member has a circular cross-section and includes an outer surface in continuing contact with internal faces of the outer member.
4. The ablation needle assembly according to claim 3, wherein the continuing contact of the outer surface of the inner member with the internal faces of the outer member divides the first lumen into three separate channels.
5. The ablation needle assembly according to claim 2, wherein the inner member has a circular cross-section and an outer surface having a diameter smaller than a diameter defined by the internal faces of the outer member.
6. The ablation needle assembly according to claim 1, wherein the inner member has a triangular cross-section
7. The ablation needle assembly according to claim 6, wherein the outer member has a circular cross-section and an internal surface, the internal surface in continuing contact with external corners of the inner member.
8. The ablation needle assembly according to claim 7, wherein the continuing contact of the internal surface of outer member with the external corners of the inner member separates the first lumen into three channels.
9. The ablation needle assembly according to claim 6, wherein the feedline is in continuing contact with internal faces of the inner member.
10. The ablation needle assembly according to claim 9, wherein the continuing contact of the feedline with the internal faces of the inner member separates the second channel lumen into three channels.
11. The ablation needle assembly according to claim 6, wherein the feedline has an outer diameter smaller than a diameter defined by the internal faces of the inner member.
12. The ablation needle assembly according to claim 1, wherein the first and second lumens are configured to circulate a cooling fluid about the feedline.
13. The ablation needle assembly according to claim 12, wherein a proximal end of the second lumen is in fluid communication with an inflow tube and a proximal end of the first lumen is in fluid communication with an outflow tube.
14. The ablation needle assembly according to claim 12, wherein a distal end of the first lumen is in fluid communication with a distal end of the second lumen.
15. The ablation needle assembly according to claim 1, wherein the triangular cross-section of one of the outer member or inner member provides longitudinal stiffness to the ablation needle assembly to prevent longitudinal deflection of the ablation needle assembly.
16. An ablation instrument comprising: a needle assembly including: an outer member defining a first lumen; an inner member disposed within the first lumen and defining a second lumen; and a feedline disposed within the second lumen; a cable assembly having a connector at a first end, the cable assembly including a first conductor; a housing coupled to a second end of the cable assembly, the housing electrically coupling the first conductor to the feedline, the housing fluidly coupling an inflow tube with a proximal end of the second lumen and an outflow tube with a proximal end of the first lumen.
17. The ablation instrument according to claim 16, wherein the cable assembly includes a second conductor disposed about the first conductor, the housing electrically coupling the second conductor to the inner member.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0016] Various aspects of the present disclosure are described hereinbelow with reference to the drawings, which are incorporated in and constitute a part of this specification, wherein:
[0017]
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DETAILED DESCRIPTION
[0024] The present disclosure is generally directed to ablation systems having an ablation needle assembly with a member having a triangular cross-sectional area to reduce the overall cross-section of the ablation needle assembly. Hereinafter, embodiments of ablation systems with a fluid-cooled ablation needle assembly including the same of the present disclosure are described with reference to the accompanying drawings. Like reference numerals may refer to similar or identical elements throughout the description of the figures. As shown in the drawings and as used in this description, and as is traditional when referring to relative positioning on an object, the term “proximal” refers to that portion of the apparatus, or component thereof, closer to the user and the term “distal” refers to that portion of the apparatus, or component thereof, farther from the user. As it is used in this description, “ablation procedure” generally refers to any ablation procedure, such as, for example, microwave ablation, radiofrequency (RF) ablation, or microwave or RF ablation-assisted resection.
[0025] The ablation instrument of the present disclosure may be used in combination with the i-Logic® target identification, navigation, and marker placement systems developed by superDimension™, Ltd and currently marketed by Medtronic. In particular the present disclosure describes devices and systems for the treatment tissue or organs through microwave ablation of targets identified in the patient for treatment. For example, it is contemplated that the systems and methods of the present disclosure may be used to treat liver tissue, kidney tissue, pancreatic tissue, gastrointestinal tissue, interstitial masses, and other portions of the body known to those of skill in the art to be treatable via microwave ablation.
[0026] The ablation needle assembly includes an outer member that defines a first lumen, an inner member disposed within the first lumen that defines a second lumen, and a feedline disposed within the second lumen. The first and second lumens are in communication with one another at a distal end of the ablation needle assembly such that cooling fluid circulates through the first and second lumens to cool the feedline. One of the inner or outer members has a circular cross-section and the other has a triangular cross-section to reduce the cross-section of the ablation needle assembly and to provide lateral rigidity to the ablation needle assembly.
[0027] Referring now to
[0028] Referring also to
[0029] With reference to
[0030] With particular reference to
[0031] Referring also to
[0032] The inner member 44 includes an inner surface 74 that defines the second lumen 84. The feedline 46 is disposed within the second lumen 84 of the inner member 44. As shown, the feedline 46 floats within the second lumen 84 and may intermittently contact portions of the inner surface 74 of the inner member 44.
[0033] It will be appreciated that the triangular cross-section of the outer member 42 reduces the overall size (i.e., diameter) of the cross-section of the outer member 42 when compared to an outer member having a circular cross-section. In addition, the triangular cross-section of the outer member 42 provides lateral stiffness to the ablation needle assembly 40. It is envisioned that the cross-sectional area of the inner and/or outer lumens 82, 84 may be larger when one of the inner or outer members 42, 44 has a triangular cross-section allowing greater fluid flow. The greater fluid flow may result in increased cooling of the feedline 46 such that the ablation needle assembly 40 may deliver a greater amount energy to tissue when compared to an ablation needle assembly having inner and outer members having a similar cross-section to one another and a similar overall diameter to the ablation needle assembly 40.
[0034] Referring to
[0035] It is envisioned that circulating fluid through the ablation needle assembly 40 may create a uniform dielectric constant about a radiating portion of the feedline 46 which can generate spherical ablations and can improve the efficiency of energy transfer from microwave to thermal, particularly in the near field. Examples of systems and methods for generating spherical ablations are disclosed in U.S. patent application Ser. No. 14/831,467, entitled “Systems and Methods for Spherical Ablations,” filed Aug. 20, 2015 by Joseph D. Brannan, the entire contents of which are hereby incorporated by reference.
[0036] With reference to
[0037] The triangular cross-section of the inner member 244 of the needle assembly 240 reduces the overall cross-sectional area of the outer member 242 required to carry a feedline when compared to a needle assembly having inner and outer members each having a circular cross-section. Specifically, the diameter of the outer member 242 can be reduced while maintaining fluid lumens (e.g., first and second lumens 82, 84) between the feedline 246 and the inner member 244 and between the inner member 244 and the outer member 242. In addition, the triangular cross-section of the inner member 244 may provide longitudinal stiffness to the needle assembly 240.
[0038] Referring to
[0039] Although embodiments have been described in detail with reference to the accompanying drawings for the purpose of illustration and description, it is to be understood that the inventive processes and apparatus are not to be construed as limited thereby. It will be apparent to those of ordinary skill in the art that various modifications to the foregoing embodiments may be made without departing from the scope of the disclosure.