BACKGROUND
Technical Field
The present disclosure relates to tissue dissectors and, more particularly, to deployable tissue dissectors that include a shaft having an expandable distal end.
Background of Related Art
During an electrosurgical procedure, e.g., a thermal ablation procedure, target tissue is heated to high temperatures, i.e., temperatures high enough to ablate tissue. Under certain surgical environments, it is sometimes necessary to protect critical tissue structures, e.g., organ, bone matter, etc., adjacent the target tissue from the heat associated with the thermal ablation procedure. To protect adjacent or nearby tissue, the adjacent tissue is typically dissected, covered, shielded or otherwise treated. For example, one technique that is commonly utilized for protecting adjacent tissue structure during a thermal ablation procedure includes dissecting adjacent tissue by injecting a fluid, e.g., saline, CO2, D5W, etc., into a space between target tissue and the adjacent tissue. While this technique works well under certain surgical environments, this technique is limited, however, because it is difficult to control the location of the fluid and it is difficult to remove all the fluid from the body. In addition, and in the instance where the fluid is a gas, e.g., CO2, the CO2 often dissolves into the tissue, which requires the CO2 to be replenished (sometimes quite frequently) during a surgical procedure. As can be appreciated, having to replenish the CO2 during a surgical procedure may increase the length of time needed to effectively perform the surgical procedure.
SUMMARY
The present disclosure provides a tissue dissector. The tissue dissector includes an introducer that includes a lumen extending along a length thereof and defines a longitudinal axis therethrough. The introducer configured for placement adjacent to target tissue. A shaft operably coupled to the introducer is deployable from a distal end thereof and includes a proximal end for approximating the distal end of the shaft adjacent target tissue. The distal end of the shaft is movable from a non-expanded configuration to an expanded configuration for separating target tissue from neighboring tissue such that the neighboring tissue is not critically affected during the electrosurgical procedure.
The present disclosure provides a system for electrosurgically treating tissue. The system includes a source of electrosurgical energy, an electrosurgical instrument that is adapted to operably couple to the source of electrosurgical energy and configured to electrosurgically treat tissue of interest and a tissue dissector. The tissue dissector includes an introducer that includes a lumen extending along a length thereof and defines a longitudinal axis therethrough. The introducer configured for placement adjacent to target tissue. A shaft is operably coupled to the introducer and is deployable from a distal end of the introducer. The shaft includes a proximal end for approximating the distal end of the shaft adjacent target tissue. The distal end of the shaft is movable from a non-expanded configuration to an expanded configuration for separating target tissue from neighboring tissue such that the neighboring tissue is not critically affected during the electrosurgical procedure.
The present disclosure also provides a method for electrosurgically treating tissue. A step of the method includes positioning an introducer of a tissue dissector adjacent target tissue. Deploying a shaft from the introducer between the target tissue and neighboring tissue is a step of the method. The method includes expanding a distal end of the shaft such that the neighboring tissue separates from the target tissue. And, electrosurgically treating the target tissue is a step of the method.
BRIEF DESCRIPTION OF THE DRAWINGS
Embodiments of the presently disclosed tissue dissectors are described hereinbelow with reference to the drawings wherein:
FIG. 1 is a schematic view of a system for performing an electrosurgical procedure according to an embodiment of the present disclosure;
FIGS. 2A-2B are schematic views of a tissue dissector associated with the system depicted in FIG. 1;
FIGS. 2C-2D are schematic views illustrating various distal end configurations that may be utilized with the tissue dissector depicted in FIGS. 2A and 2B;
FIGS. 3A-3D are schematic views of a tissue dissector configured for use with the system depicted in FIG. 1 according to another embodiment of the present disclosure;
FIG. 3E is a cross-sectional view taken along the line segment 3E in FIG. 3D;
FIGS. 4A-4B are schematic views of a tissue dissector configured for use with the system depicted in FIG. 1 according to yet another embodiment of the present disclosure; and
FIG. 5 is a top, elevational view of a shaft configured for use with the tissue dissectors depicted in FIGS. 2A, 3A and 4A.
DETAILED DESCRIPTION
Detailed embodiments of the present disclosure are disclosed herein; however, the disclosed embodiments are merely examples of the disclosure, which may be embodied in various forms. Therefore, specific structural and functional details disclosed herein are not to be interpreted as limiting, but merely as a basis for the claims and as a representative basis for teaching one skilled in the art to variously employ the present disclosure in virtually any appropriately detailed structure.
In the drawings and in the descriptions that follow, the term “proximal,” as is traditional, will refer to an end of a surgical instrument that is closer to the user, while the term “distal” will refer to an end of a surgical instrument that is farther from the user.
Referring to FIG. 1, a system 100 for electrosurgically treating tissue is illustrated including a source of electrosurgical energy, e.g., an electrosurgical generator 2, an electrosurgical instrument, e.g., a microwave antenna assembly 4, and a tissue dissector 6. The system 100 may be configured to perform one or more electrosurgical procedures for treating tissue including, but not limited to ablating, coagulating, and fulgurating tissue. For purposes herein, the system 100 is described in terms of a use for ablating tissue.
With continued reference to FIG. 1, electrosurgical generator 2 is configured to generate electrosurgical energy suitable for ablating tissue. Microwave antenna assembly 4 is adapted to operably couple to the electrosurgical generator 2 and is configured to electrosurgically treat tissue of interest (hereinafter referred to as target tissue “T”). For a more detailed description of the electrosurgical generator 4 including the microwave antenna assembly 4, reference is made to commonly-owned patent application Ser. No. 12/606,767 to Brannan, filed on Oct. 27, 2009.
Continuing with reference to FIG. 1, and with reference to FIGS. 2A and 2B, an embodiment of the tissue dissector 6 is shown including an introducer (in the form of an introducer or catheter 8) and a shaft 10.
In the illustrated embodiment, catheter 8 is configured to pierce tissue and, subsequently, be positioned adjacent target tissue “T”. To facilitate piercing tissue, the catheter 8 includes a generally sharpened distal tip 14 (FIGS. 1-2B). In certain embodiments, it may prove advantageous to provide the catheter 8 with a distal tip that is relative dull or blunt, such as, for example, in the instance where the catheter 8 is not configured to pierce tissue. Catheter 8 defines a longitudinal axis “A-A” therethrough and includes a lumen 12 defined therein that extends along a length thereof (FIGS. 2A-2B). The lumen 12 is configured to receive a shaft 10 therein (FIG. 2A) such that the shaft 10 or operable component associated therewith, e.g., a distal end 18, is deployable from an open distal end of the catheter 8 adjacent the distal tip 14 (FIG. 2B). Shaft 10 includes a proximal end (not shown) that is maneuverable by a user, e.g., a clinician, such that a user may position the shaft 10 within the lumen 12 of the catheter 8. Distal end 18 is movable from a non-expanded configuration (FIG. 2A) for loading the shaft 10 into, and deploying the distal end 18 from, the catheter 8, to an expanded configuration for separating neighboring tissue “NT” from target tissue “T” (FIG. 2B), described in greater detail below.
Distal end 18 operably couples to the shaft 10 by one or more suitable coupling methods, e.g., soldering, ultrasonic welding, etc.
In the embodiment illustrated in FIGS. 2A and 2B, the distal end 18 of the shaft 10 includes a mesh structure configured from a plurality of wires 20. In some embodiments, the wires 20 are made from a material such as, for example, shape memory alloy, e.g., nitinol, and a compressible elastomeric material that is normally in an expanded configuration. In the expanded configuration, the distal end 18 of the shaft 10 may exhibit one or more suitable shapes. For example, in the expanded configuration the distal end 18 may include a shape including, but not limited to a sphere (FIG. 2C), a rectangle (FIG. 2D), and a helix (FIG. 2B). As can be appreciated, the specific shapes that the distal end 18 may exhibit in the expanded configuration may vary for a different surgical procedure, the type of tissue that is to be electrosurgically treated, the location of the tissue that is to be treated, a manufacturer's preference, etc.
Distal end 18 expands in a radial direction outward. As shown in FIG. 2B, in the expanded configuration, the helix of distal end 18 spans a distance (or includes a width) “x” that corresponds to a distance that the neighboring tissue “NT” is separated from the tissue of interest (FIG. 2B). This distance “x” is sufficient to ensure that the neighboring tissue “NT” is not critically affected during the electrosurgical procedure.
In certain instances, and in the expanded configuration, the distal end 18 of the shaft 10 may be configured to stop and/or impede the propagation of microwave energy during an ablation procedure. In this instance, it may prove advantageous to tightly weave the wires 20 of the distal end 18 such that the distal end 18 functions as a faraday cage, see FIGS. 2C and 2D for example.
Operation of the system 100 is now described in terms of use of a method for electrosurgically treating tissue. Catheter 8, initially, is utilized to pierce tissue such that the catheter 8 may be positioned adjacent target tissue “T”, e.g., tissue that is to be electrosurgically treated (FIG. 2A). The shaft 10 is positioned within the lumen 12 of the catheter 8 and, subsequently, the distal end 18 is deployed from the catheter 8 such that the distal end 18 is positioned between the target tissue “T” and neighboring tissue “NT” (FIG. 2B). When the distal end 18 is deployed from the catheter 8, the distal end 18 transitions from the non-expanded configuration to an expanded configuration. As the distal end 18 transitions from the non-expanded configuration to the expanded configuration, the distal end 18 separates neighboring tissue “NT” from the target tissue “T”. Thereafter, the target tissue “T” is electrosurgically treated via the microwave antenna assembly 4.
As can be appreciated, the tissue dissector 6 disclosed herein effectively separates and isolates the neighboring tissue “NT” from the target tissue “T” and reduces and/or eliminates the likelihood of the neighboring tissue “NT” being critically affected as the target tissue “T” is electrosurgically treated. This is accomplished without the need of having to introduce any extra fluid to the surgical environment, which, as noted above, may increase the length of time needed to effectively perform the surgical procedure.
With reference to FIGS. 3A-3E, a tissue dissector according to another embodiment of the present disclosure is shown designated tissue dissector 106. Tissue dissector 106 is substantially similar to the tissue dissector 6. Accordingly, only those features that are unique to tissue dissector 106 are described in detail herein.
A cannula 108 is substantially similar to that of cannula 8. However, unlike cannula 8, cannula 108 is configured to receive a shaft 110 that, in the embodiment illustrated in FIGS. 3A-3E, is larger than a diameter of the shaft 10. The larger diameter of the shaft 110 is configured to accommodate an actuator 107, described in greater detail below.
Shaft 110 includes an elongated configuration having a generally circumferential shape when viewed in cross-section (FIG. 3E). Unlike shaft 10, a distal end 118 of shaft 110 includes a plurality of spaced slits or slots 115a-115f (collectively referred to as slits 115), as best seen in FIG. 3E. The slits 115 function to facilitate moving the distal end 118 from a non-expanded configuration (FIG. 3A) to an expanded configuration (FIG. 3C). That is, the slits 115 facilitate expansion and contraction of the distal end 118 of the shaft 110. In particular, the slits 115 allow the distal end 118 of the shaft 110 to “swell” or “bulge” about the slits 115 when the actuator 107 is pulled proximally.
In the embodiment illustrated in FIGS. 3A-3E, the six slits 115a-115f are evenly spaced at approximately 60 degrees apart from each other. However, the number of slits 115 may vary for a different surgical procedure, the type of tissue that is to be electrosurgically treated, the location of the tissue that is to be treated, a manufacturer's preference, etc. For example, in an instance where two (2) slits 115 are utilized, e.g., slits 115a and 115b, they be spaced approximately 180 degrees apart from each other; in an instance where three (3) slits 115 are utilized, e.g., slits 115a, 115b and 115c, they may be spaced approximately 120 degrees apart from each other; in an instance where four (4) slits 115 are utilized, e.g., slits 115a, 115b, 115c and 115d, they may be spaced approximately 90 degrees apart from each other; and in an instance where five (5) slits 115 are utilized, e.g., slits 115a, 115b, 115c, 115d and 115e, they may be spaced approximately 72 degrees apart from each other. One skilled in the art will appreciate that any number of slits may be utilized. Six (6) slits 115a-115f were found to provide an even distribution of an expansion force that is generated when the distal end 118 of the shaft 110 transitions from a non-expanded configuration, to an expanded configuration.
Unlike the shaft 10, shaft 110 includes a pointed or sharpened distal tip 116 (FIGS. 3A-3D) that is configured to pierce or penetrate tissue, e.g., target tissue “T” or neighboring tissue “NT,” such that the distal end 118 may be temporarily anchored into target tissue “T” or neighboring tissue “NT,” i.e., the sharpened distal tip 116 is configured to pierce tissue such that a portion of the distal tip 116 may secure to the tissue. As can be appreciated, temporarily anchoring the distal tip 116 into target tissue “T” or neighboring tissue “NT” may facilitate pulling or “drawing” back the catheter 108 during deployment of the distal end 118 from the distal end of the catheter 8.
The actuator 107 extends through a lumen 113 of the shaft 110 and operably couples to the distal tip 116 adjacent the distal end 118 of the shaft 110, as best seen in FIGS. 3B and 3C. The actuator 107 is configured to move the distal end 118 of the shaft 110 from the non-expanded configuration, to the expanded configuration when the actuator 107 is pulled proximally. To this end, the actuator 107 may be any suitable actuator 107 including but not limited to a wire, cable and string. In the illustrated embodiment, the actuator 107 is in a form of a cable.
In use, catheter 108, initially, is utilized to pierce tissue such that the catheter 108 may be positioned adjacent target tissue “T” (FIG. 3A). The shaft 110 is positioned within the lumen 112 of the catheter 108 and, subsequently, the distal end 118 is deployed from the catheter 108 such that the distal end 118 is positioned between the target tissue “T” and neighboring tissue “NT” (FIG. 3C). When the distal end 118 is deployed from the catheter 108 and positioned between the neighboring tissue “NT” and target tissue “T,” the actuator 107 is actuated, e.g., pulled proximally, which, in turn, causes the slits 115 of the distal end 118 to move or transition from the initial non-expanded configuration, to the expanded configuration. As the distal end 118 transitions from the non-expanded configuration to the expanded configuration, the distal end 118 separates the neighboring tissue “NT” from the target tissue “T”. Thereafter, the target tissue “T” is electrosurgically treated as described above.
With reference to FIGS. 4A and 4B, a tissue dissector according to another embodiment of the present disclosure is shown and designated tissue dissector 206. Tissue dissector 206 is substantially similar to the tissue dissector 106. Accordingly, only those features that are unique to tissue dissector 206 are described in detail herein.
A shaft 210 includes a first ring 209a and second ring 209b that are operably disposed at a distal end 218 of the shaft 210 and are coupled to one another via one or more spaced-apart resilient members 211 (three (3) resilient members 211a-211c are shown in the figures) that extend along the longitudinal axis “A-A.” The first and second rings 209a and 209b are configured to couple the distal end 218 of the shaft 210 to a distal tip 216 thereof. The rings 209a and 209b including the resilient members 211a-211c function similar to that of slits 115. That is, the rings 209a and 209b including the resilient members 211a-211c facilitate moving the distal end 218 of the shaft 210 from the non-expanded configuration to the expanded configuration. The resilient members 211a-211c may be made from any suitable resilient materials including but not limited to a wire, a band, a spring, etc. In the embodiment illustrated in FIGS. 4A and 4B, the resilient members 211a-211c are wire strips that are bent around (or otherwise coupled to) the rings 209a and 209b.
In use, a catheter 208 (FIG. 4B), initially, is utilized to pierce tissue such that the catheter 208 may be positioned adjacent target tissue “T. The shaft 210 is positioned within a lumen (not explicitly shown) of the catheter 208 and, subsequently, the distal end 218 is deployed from the catheter 208 such that the distal end 218 is positioned between the target tissue “T” and neighboring tissue “NT.” When the distal end 218 is deployed from the catheter 208 and positioned between the neighboring tissue “NT” and target tissue “T,” a cable 207, is pulled proximally, which, in turn, causes the resilient members 211a-211c of the distal end 218 to move or transition from a non-expanded configuration, to the expanded configuration. As the distal end 218 transitions from the non-expanded configuration to the expanded configuration, the distal end 218 separates the neighboring tissue “NT” from the target tissue “T”. Thereafter, the target tissue “T” is electrosurgically treated.
From the foregoing, and with reference to the various figure drawings, those skilled in the art will appreciate that certain modifications can also be made to the present disclosure without departing from the scope of the same. For example, it is contemplated that one or more guide wires 380 may operably couple by one or more suitable coupling methods to a shaft 310 that is configured for use with any of the aforementioned tissue dissectors (FIG. 5). The guide wires 380 function as a steering mechanism and are configured to move or steer the shaft 310. More specifically, two independently controllable guide wires 381a and 381b may be operably coupled to the shaft 310 and spaced 180 degrees apart from each other. Separating the guide wires 381a and 381 180 degrees apart from one another provides an even distribution of a pull force across the shaft 310. In the embodiment illustrated in FIG. 5, the guide wires 381a and 381b are operably-disposed within corresponding grooves (not explicitly shown) along an outer periphery of the shaft 310. The guide wires 381a and 381b couple adjacent to the distal end 318 of the shaft 310 by one or more suitable coupling methods, e.g., soldering. For illustrative purposes, distal end 318 includes two slots 315a and 315b spaced approximately 180 degrees apart from each other.
The guide wires 381a and 381b are configured such that actuating, e.g., pulling, a respective one of the guide wires 381a and 381b causes the shaft 310 including a distal end 318 to move laterally or transversely across the longitudinal axis “A-A” in a respective direction, e.g., left or right. Utilizing the guide wires 381a and 381b facilitates positioning the distal end 318 of the shaft 310 adjacent the target tissue “T” and/or neighboring tissue “NT”. For illustrative purposes, when the guide wire 381a is pulled, the shaft 310 including the distal end 318 moves to the left and when the guide wire 381b is pulled, the shaft 310 including the distal end 318 moves to the right.
A portion 305 of the shaft 310 is configured to articulate when either of the guide wires 381a and 381b is pulled. To this end, the portion 305 may include one or more links that are configured to facilitate articulation. The portion 305 of the shaft 310 (or the shaft 310 itself) may be substantially resilient to facilitate bending in one or more directions or the portion 305 of the shaft 310 (or the shaft 310 itself) may be malleable. In the embodiment illustrated in FIG. 5, portion 305 is made from a material that is malleable, e.g., a relatively pliable or compliant plastic, and configured such that when either of the guide wires 381a and 381b is pulled, the shaft 310 bends or moves about the portion 305, which, in turn, steers or moves the distal end 318 in a corresponding direction. The malleable portion 305 is configured to maintain the distal end 318 in the corresponding direction until either one of the guide wires 381 or 381b is actuated. Thus, inadvertent contact between target tissue “T”, neighboring tissue “NT” or other tissue structure and the distal end 318 does not cause the distal end 318 to move.
As can be appreciated, the number of guide wires (and or the location of them along the periphery of the shaft 310) may vary for a different surgical procedure, the type of tissue that is to be electrosurgically treated, the location of the tissue that is to be treated, a manufacturer's preference, etc. For example, in one particular embodiment, four (4) guide wires may be operably disposed along the periphery of the shaft 310. In this instance, the four (4) guide wires may be spaced-apart at 90 degree intervals from each other and configured to move the shaft 310 in a corresponding direction, e.g., left and right of the longitudinal axis “A-A” and above and below the longitudinal axis “A-A.”
Use of any of the aforementioned tissue dissectors, e.g., tissue dissector 206, with a shaft 310 including guide wires 381a and 381b is substantially similar as that described above. One difference being, the guide wires 381a and 381b may be utilized to move or “steer” shaft 310 including the distal end 318, prior to or after the distal end 318 is moved to the expanded condition. As can be appreciated, having the capability of “steering” the distal end 318 may provide an end user with a significant mechanical advantage, especially in the instance where target tissue is in a compromised or hard to reach location.
While several embodiments of the disclosure have been shown in the drawings, it is not intended that the disclosure be limited thereto, as it is intended that the disclosure be as broad in scope as the art will allow and that the specification be read likewise. Therefore, the above description should not be construed as limiting, but merely as exemplifications of particular embodiments. Those skilled in the art will envision other modifications within the scope and spirit of the claims appended hereto.
Patent Application
20170325797
