Bipolar forceps

Abstract

In various surgical techniques, a bipolar forceps can be used to seal a vessel in two locations such that the vessel can be incised at a location positioned intermediate the two seal locations. The bipolar forceps can include a cutting element which can be configured to incise the vessel. In various embodiments, the cutting element can include a sharp edge which can be moved relative to the vessel. In at least one embodiment, the cutting element can be electrically connected to a source of energy. The bipolar forceps can include first and second electrodes positioned within first and second jaw members, respectively, wherein at least one of the jaw members can include a substantially tapered profile and can be configured to pull the vessel away from the surrounding soft tissue. Such jaw members can include ridges, teeth, and/or a textured outer surface configured to grip the soft tissue and/or vessel.

Description

RELATED APPLICATION

The present application is related to U.S. patent application Ser. No. 11/986,420, entitled BIPOLAR FORCEPS, now U.S. Pat. No. 8,262,655, which is a commonly-owned U.S. patent application filed concurrently herewith, the entire disclosure of which is hereby incorporated by reference herein.

BACKGROUND

1. Field of the Invention

The present invention generally relates to electrical ablation surgical instruments and, more particularly, to bipolar forceps for performing various surgical techniques.

2. Description of the Related Art

Previous bipolar forceps have included a grasping device which is configured to grasp and manipulate soft tissue, for example. In various circumstances, the grasping device has included a first electrode and a second electrode where, when one of the electrodes is brought into close opposition to the other electrode, an electrical current can pass therebetween. More particularly, when soft tissue is captured between the electrodes, current can be supplied to the first electrode and flow to the second electrode through the soft tissue. In such circumstances, the current can cauterize, vaporize, and/or otherwise treat, the soft tissue. Previous bipolar forceps, referring to U.S. Pat. No. 5,944,718, the entire disclosure of which is hereby incorporated be reference herein, have included a first electrode which can be pivoted relative to a stationary second electrode. These forceps have further included a first wire attached to the first electrode where the first wire is configured to supply current to the first electrode from an electrical source. In addition, these forceps have included a second wire which is attached to the second electrode where the second wire is configured to complete the electrical circuit and return the current back to the electrical source. In order for the first wire to remain in electrical communication with the first electrode when the first, or movable, jaw member is pivoted, the first wire must often bend and/or stretch in order to accommodate this movement. In some circumstances, such bending or stretching may cause the wire to break and/or the insulation covering the wire to become chaffed, thereby rendering the surgical instrument inoperative or unreliable. What is needed is an improvement over the foregoing.

SUMMARY

In at least one form of the invention, a bipolar forceps can include a first electrode, a second electrode, and a conductor, or wire, operably connected to an electrical source, for example, wherein the conductor can be selectively placed in electrical communication with the first electrode when the first electrode is moved between open and closed positions. In various embodiments, the wire can include a contact end which is not in contact with the first electrode when the first electrode is in its open position. In such an open position, the first electrode may not be in electrical communication with the electrical source and, as a result, current may not flow through the first electrode. In at least one such embodiment, the first electrode can be moved into its closed position such that the first electrode is in contact with the contact end of the wire. In such a closed position, the first electrode may be in electrical communication with the electrical source allowing current to flow through the first electrode. As a result of the above, the first electrode can move relative to the wire such that the wire does not have to move with the first electrode when the first electrode is moved between its open and closed positions and, as a result, the likelihood that the wire may become damaged or broken can be reduced.

In at least one form of the invention, a bipolar forceps can include two or more electrodes wherein the electrodes can be positioned against, or adjacent to, a vessel, such as a blood vessel, for example, and energy can be supplied to the electrodes. In various circumstances, the energy can be sufficient to at least substantially seal the vessel such that blood does not substantially flow therethrough. In at least one surgical technique, the bipolar forceps can be used to seal the vessel in two locations such that the vessel can be incised, or transected, at a location positioned intermediate the two seal locations. In at least one embodiment, the bipolar forceps can include a cutting element which can be configured to incise the vessel. In various embodiments, the cutting element can include a sharp edge which can be moved relative to the vessel. In at least one embodiment, the cutting element can be electrically connected to a source of energy wherein the energized cutting element can be configured to incise the tissue.

In at least one form of the invention, a bipolar forceps can include first and second electrodes positioned within first and second jaw members, respectively, wherein at least one of the jaw members can include a substantially tapered profile. In various surgical techniques, the jaw members can be positioned in a substantially closed position such that the distal end of the jaw members can be positioned intermediate a vessel, for example, and tissue at least partially surrounding the vessel. Thereafter, in at least one surgical technique, the jaw members can be opened in order to pull the vessel away from the soft tissue. In various techniques, the jaw members can be opened and closed repeatedly to enlarge a hole between the vessel and the tissue and/or otherwise separate the vessel from the tissue. In at least one embodiment, at least one of the jaw members can include ridges, teeth, and/or a textured outer surface configured to grip the soft tissue and/or vessel.

BRIEF DESCRIPTION OF THE DRAWINGS

The above-mentioned and other features and advantages of the various embodiments of this invention, and the manner of attaining them, will become more apparent and the invention itself will be better understood by reference to the following description of embodiments of the invention taken in conjunction with the accompanying drawings, wherein:

FIG. 1 is a perspective view of a hand piece and a shaft assembly of a surgical instrument in accordance with an embodiment of the present invention;

FIG. 2 is a schematic of an electrical source and an actuator for use with the surgical instrument of FIG. 1 in accordance with an embodiment of the present invention;

FIG. 3 is an elevational view of an end effector and a shaft assembly of a surgical instrument in accordance with an embodiment of the present invention;

FIG. 4 is a perspective view of the end effector of FIG. 3;

FIG. 5 is an additional perspective view of the end effector of FIG. 3;

FIG. 6 is a left elevational view of the end effector of FIG. 3;

FIG. 7 is a right elevational view of the end effector of FIG. 3;

FIG. 8 is an end view of the end effector of FIG. 3

FIG. 9 is a left elevational view of the end effector of FIG. 3 with a clevis removed;

FIG. 10 is a left elevational view of a coupling between the end effector and the shaft assembly of the surgical instrument of FIG. 3;

FIG. 11 is a left elevational view of the coupling of FIG. 10 with additional components removed;

FIG. 12 is a perspective view of the shaft assembly of the surgical instrument of FIG. 3;

FIG. 13 is a perspective view of a surgical instrument in accordance with an embodiment of the present invention;

FIG. 14 is a cross-sectional view of a hand piece of the surgical instrument of FIG. 13;

FIG. 15 is a perspective view of an end effector of a surgical instrument having a cutting element in accordance with an embodiment of the present invention;

FIG. 16 is a perspective view of an end effector of a surgical instrument having a cutting element in accordance with an alternative embodiment of the present invention;

FIG. 17 is a perspective view of an end effector of a surgical instrument having a cutting element extending from an electrode in accordance with an alternative embodiment of the present invention;

FIG. 18 is a perspective view of an end effector of a surgical instrument having a cutting element configured to be energized in accordance with an alternative embodiment of the present invention;

FIG. 19 is a detail view of an insulator positioned intermediate an electrode and the cutting element of FIG. 18;

FIG. 20 is a perspective view of an end effector of a surgical instrument having a tapered profile in accordance with an alternative embodiment of the present invention;

FIG. 21 is an elevational view of the end effector of FIG. 20;

FIG. 22 is a top view of the end effector of FIG. 20;

FIG. 23 is a perspective view of the end effector of FIG. 20 in an open configuration; and

FIG. 24 is an elevational view of the end effector of FIG. 20 in the configuration of FIG. 23.

Corresponding reference characters indicate corresponding parts throughout the several views. The exemplifications set out herein illustrate preferred embodiments of the invention, in one form, and such exemplifications are not to be construed as limiting the scope of the invention in any manner.

DETAILED DESCRIPTION

Certain exemplary embodiments will now be described to provide an overall understanding of the principles of the structure, function, manufacture, and use of the devices and methods disclosed herein. One or more examples of these embodiments are illustrated in the accompanying drawings. Those of ordinary skill in the art will understand that the devices and methods specifically described herein and illustrated in the accompanying drawings are non-limiting exemplary embodiments and that the scope of the various embodiments of the present invention is defined solely by the claims. The features illustrated or described in connection with one exemplary embodiment may be combined with the features of other embodiments. Such modifications and variations are intended to be included within the scope of the present invention.

The various embodiments described herein are related to electrical therapy ablation devices. Generally, electrical therapy ablation devices can comprise electrodes that can be positioned in, or in proximity to, a tissue treatment region, or target site, within a patient. These devices, and the surgical techniques for using the same, may be employed to treat tissue masses, tissue tumors, and lesions, for example, (all of which are hereinafter referred to as ‘diseased tissue’) at the tissue treatment region. In various embodiments, these devices can be utilized in open surgical procedures as well as external and non-invasive medical procedures. In other various embodiments, these devices may be adapted to provide minimally invasive access to the tissue treatment region or anatomic location, such as lung and liver tissue, for example, in order to diagnose and treat the condition at the tissue treatment region more accurately and effectively. In various embodiments, portions of the electrical therapy ablation devices may be introduced in the tissue treatment region endoscopically (e.g., laparoscopically and/or thoracoscopically), or through a trocar extending through a small incision. Portions of other devices may be introduced into the tissue treatment region by way of a natural orifice through a cannula or catheter. Minimally invasive procedures which introduce medical instruments to a tissue treatment region through a natural opening of the patient are known as Natural Orifice Translumenal Endoscopic Surgery (NOTES)™. In other embodiments, portions of the electrical therapy devices can be introduced percutaneously or in any combination of the methods described above.

Once positioned, the electrical therapy electrodes can deliver electrical current to the treatment region. The electrical current can be generated by a control unit or generator located external to the patient, for example, where the electrical current may be characterized by a particular waveform in terms of frequency, amplitude, and pulse width. Depending on the diagnostic or therapeutic treatment rendered, the diseased tissue can be electrically ablated or destroyed. More particularly, the electrical therapy ablation devices may be employed to deliver sufficient energy to the diseased tissue to ablate or destroy tumors, masses, lesions, and other abnormal tissue growths. In at least one embodiment, the electrical therapy ablation devices and techniques described herein may be employed in the treatment of cancer by quickly creating necrosis and destroying live cancerous tissue in-vivo. Such devices and techniques are further described in a commonly-owned, co-pending U.S. patent application Ser. No. 11/897,676, entitled ELECTRICAL ABLATION SURGICAL INSTRUMENTS, filed on Aug. 31, 2007, the entire disclosure of which is hereby incorporated by reference herein.

In various embodiments, electrical therapy ablation may employ electroporation, or electropermeabilization, techniques where an externally applied electric field (electric potential) significantly increases the electrical conductivity and permeability of a cell plasma membrane. Electroporation is the generation of a destabilizing electric potential across such biological membranes. In electroporation, pores are formed when the voltage across the cell plasma membrane exceeds its dielectric strength. Electroporation destabilizing electric potentials are generally in the range of several hundred volts across a distance of several millimeters. Below certain magnitude thresholds, the electric potentials may be applied across a biological membrane as a way of introducing some substance into a cell, such as loading it with a molecular probe, a drug that can change the function of the cell, a piece of coding DNA, or increasing the uptake of drugs in cells. If the strength of the applied electrical field and/or duration of exposure to it are suitably chosen, the pores formed by the electrical pulse reseal after a short period of time, during such period extra-cellular compounds may enter into the cell. Below a certain field threshold, the process is reversible and the potential does not permanently damage the cell membrane. This process may be referred to as reversible electroporation (RE). On the other hand, excessive exposure of live cells to large electric fields can cause apoptosis and/or necrosis—the processes that result in cell death. Excessive exposure of live cells to large excessive electrical fields or potentials across the cell membranes causes the cells to die and therefore may be referred to as irreversible electroporation (IRE). Electroporation may be performed with devices called electroporators. These appliances can create the electric current and send it through the cell. Electroporators may comprise two or more metallic (e.g., aluminum) electrically conductive electrodes connected to an energy source. The energy source can generate an electric field having a suitable characteristic waveform output in terms of frequency, amplitude, and pulse width.

In various embodiments, an electrical ablation system may be employed in conjunction with a flexible endoscope, such as a GIF-100 model available from Olympus Corporation, for example. In at least one such embodiment, the endoscope, a laparoscope, or a thoracoscope, for example, may be introduced into the patient trans-anally through the colon, the abdomen via an incision or keyhole and a trocar, or trans-orally through the esophagus, for example. These devices can assist the surgeon to guide and position the electrical ablation system near the tissue treatment region to treat diseased tissue on organs such as the liver, for example. In another embodiment, these devices may be positioned to treat diseased tissue near the gastrointestinal (GI) tract, esophagus, and/or lung, for example. In various embodiments, the endoscope may comprise a flexible shaft where the distal end of flexible shaft may comprise a light source, a viewing port, and at least one working channel. In at least one such embodiment, the viewing port can transmit an image within its field of view to an optical device such as a charge coupled device (CCD) camera within the endoscope, for example, so that an operator may view the image on a display monitor (not shown).

In various embodiments, referring to FIG. 1, surgical instrument, or bipolar forceps, 20 can include an end effector, shaft assembly 22, and hand piece 24. In at least one embodiment, shaft assembly 22 can comprise a flexible shaft of an endoscopic surgical instrument wherein at least portions of the end effector and shaft assembly 22 can be configured to be positioned within and/or inserted through a working channel of an endoscope. Hand piece 24 can be configured to be grasped by a surgeon and, in at least one embodiment, hand piece 24 can comprise a pistol grip including stationary member 26 and movable member, or trigger, 28. In use, as described in greater detail below, trigger 28 can be moved toward stationary member 26 as indicated by arrow 27, for example, in order to operate the end effector within a surgical site. Although not illustrated, surgical instrument 20 can include a switch which can place the end effector in electrical communication with an electrical source, or generator, via wires 30 and 32. In at least one embodiment, wires 30 and 32 can terminate in connector 34 where, referring to FIG. 2, connector 34 can be configured to be operably connected to connector 36 of generator 38.

In various embodiments, referring to FIGS. 3-9, an end effector, such as end effector 50, for example, can include a grasping device comprising first jaw member 52 and second jaw member 54, where at least one of jaw members 52 and 54 can be moved relative to the other. In at least one embodiment, jaw members 52 and 54 can be movably coupled to housing, or clevis, 56 such that they can be moved, or pivoted, between open and closed positions about pivot pin 58. In use, jaw members 52 and 54 can be positioned in their closed, or at least partially closed, positions before they are inserted into a surgical site through a trocar, for example. In various embodiments, jaw members 52 and 54 can be configured such that they can be positioned within and/or inserted through a working channel of an endoscope. Once positioned within the surgical site, jaw members 52 and 54 can then be reopened. In their open position, jaw members 52 and 54 can be positioned on, or relative to, the targeted soft tissue within the surgical site. Thereafter, in at least one embodiment, jaw members 52 and 54 can be pivoted into their closed position to hold the soft tissue therebetween. In various embodiments, at least one of jaw members 52 and 54 can include serrations, or teeth, 60 which can be configured to securely hold the soft tissue therebetween.

In order to more easily position end effector 50, the shaft assembly extending between end effector 50 and hand piece 24 can be flexible. In at least one embodiment, referring to FIG. 3, shaft assembly 80 can include a flexible elongate member 82 and a flexible coil spring 84 positioned therearound. In various embodiments, referring to FIGS. 7-11, a surgical instrument can further include adapter assembly 86 for operably connecting end effector 50 to shaft assembly 80. In at least one embodiment, adapter assembly 86 can include ring capture 88 which can include an aperture therein, or any other suitable feature, for receiving and retaining an end of coil spring 84. Adapter assembly 86 can further include bushing coupler 83 which can include projection 85, or any other suitable feature, which can be fixedly connected to housing 56. In addition to the above, adapter assembly 86 can also include inner housing coupler 87 which can be configured to connect ring capture 88 to bushing coupler 83 such that end effector 50 is correspondingly coupled to shaft assembly 80.

In order to move jaw members 52 and 54 between their open and closed positions as described above, trigger 28 of hand piece 24 can be pivoted relative to stationary member 26 such that trigger 28 can displace actuator, or rod, 44 (FIG. 1) relative to shaft 22. In various embodiments, actuator 44 can be round, or any other suitable shape, and can be either solid or tubular. In either event, referring to FIG. 6, actuator rod 44 can be operably engaged with actuator 46 such that, when trigger 28 is pivoted toward stationary member 26 as described above, actuator rod 44 and actuator 46 can be slid proximally such that actuator 46 pulls on jaw links 53 and 55. It will be appreciated that the terms “proximal” and “distal” are used herein with reference to a clinician gripping hand piece 24 of instrument 20, for example. Thus, end effector 50 is distal with respect to hand piece 24. When jaw links 53 and 55 are pulled proximally, jaw links 53 and 55 can apply a force to jaws 52 and 54, respectively, such that they are pivoted about pivot pin 58 into their closed positions. In order to move jaws 52 and 54 into their open positions, trigger 28 can be moved away from stationary portion 26 and, correspondingly, actuator rod 44 and actuator 46 can be moved distally by trigger 28. Similarly, actuator 46 can move links 53 and 55 distally such that such that links 53 and 55 apply a force to jaws 52 and 54 and rotate them about pivot pin 58 in the opposite, or open, direction. Now referring to another exemplary embodiment illustrated in FIGS. 13 and 14, when trigger 28′ is pivotally moved (e.g., squeezed) in the direction indicated by arrow 29, actuator rod 44 can be moved in the direction indicated by arrow 47, and the first and second jaw members 52 and 54 can close in the direction indicated by arrow 49. When trigger 28′ is pivotally moved (e.g., released) in the direction indicated by arrow 31, actuator 44 can be moved in the direction indicated by arrow 45, and the first and second jaw members can open in the direction indicated by arrow 51.

Further to the above, in various embodiments, at least a portion of the distal end of actuator rod 44 can be fixedly received in shaft collar 66′ (FIG. 14) such that, when collar 66′ is moved by trigger 28′, actuator 44 can be moved proximally and distally as described above. In at least one embodiment, trigger 28′ can be operably engaged with pin 67′ in shaft collar 66′ such that the rotational movement of trigger 28′ can be converted to translational movement of shaft collar 66′. More particularly, although not illustrated, trigger 28′ can include a cam slot which is configured to receive pin 67′ such that, when trigger 28′ is rotated as described above, the sidewalls of the slot can motivate shaft collar 66′, and actuator 44 operably engaged therewith, along a path defined by housing portion 65′. In various embodiments, although not illustrated, hand piece 24′ can further include a biasing member, or spring, which is configured to bias trigger 28′, and jaw members 52 and 54, into one of a closed or open position.

In at least one embodiment, referring to FIG. 14, hand piece 24′ can further include spring holders 68′ and 70′ where the spring can be positioned therebetween. In various embodiments, shaft collar 66′ can be connected to one of spring holders 68′ and 70′ and the other of spring holders 68′ and 70′ can be connected to housing portion 65′. In such embodiments, when shaft collar 66′ is moved relative to housing portion 65′, one of spring holders 68′ and 70′ can be moved relative to the other such that the spring is placed in either tension or compression and can apply a spring force to trigger 28′. In at least one embodiment, when trigger 28′ is released from its closed position as indicated by arrow 31, the spring force can bias trigger 28′ into its open position as indicated by arrow 29. In various other embodiments, although not illustrated, trigger 28′ can be biased into its closed position or any other suitable position. In at least one embodiment, trigger 28′ can further include latch 25′ which can be configured to hold trigger 28′ to stationary portion 26′ against the biasing force of the spring.

In various embodiments, referring to FIG. 2, hand piece 24 can include rotation knob 21 and, similarly, referring to FIG. 13, hand piece 24′ can include rotation knob 21′, where rotation knobs 21 and 21′ can be configured to rotate an end effector of their respective surgical instruments relative to hand pieces 24 and 24′. In various embodiments, referring to FIGS. 13 and 14, a portion of actuator rod 44 can be slidably received within aperture 23′ in rotation knob 21′ wherein at least one of the actuator rod 44 and aperture 23′ can include a non-circular profile. In such embodiments, the non-circular profile can allow actuator rod 44 to be rotated by knob 21′ yet allow actuator rod 44 to slide relative thereto when it is moved proximally and distally by trigger 28′ as described above. In at least one embodiment, when rotation knob 21′ is rotated in the direction indicated by arrow 62, end effector 50 can also rotated in the direction indicated by arrow 62. Similarly, when rotation knob 21′ is rotated in the direction indicated by arrow 64, end effector 50 can be rotated in the direction indicated by arrow 64. As a result of the above, jaw members 52 and 54 can be rotated within the surgical site and can be more accurately positioned by a surgeon.

Once end effector 50 has been positioned in a surgical site and jaw members 52 and 54 have been closed onto the soft tissue, as outlined above, the soft tissue can be treated by an electrical current that passes between jaw members 52 and 54. More particularly, in at least one embodiment, surgical instrument 20 can include an electrical circuit which is configured to receive an electrical current from current generator 38 (FIG. 2) and transmit the current to a first electrode 72 positioned within jaw member 52 via first conductor, or wire, 30. In various embodiments, the current can be conducted through the soft tissue positioned between jaw members 52 and 54 such that the current flows into a second electrode 74 positioned in second jaw member 54. The current can return to electrical generator 38 through second conductor, or wire, 32 to complete the circuit. In at least one such embodiment, generator 38 can include plug 42 which can be configured to provide commercially available current to generator 38 where generator 38 can be configured to transform the current as needed. In at least one embodiment, generator 38 can further include a switch, such as foot pedal 40, for example, which can be configured to place surgical instrument 20 in electrical communication with generator 38. In various embodiments, switch 40 can be utilized in addition to, or in lieu of, a switch on surgical instrument 20.

In various embodiments, a surgical instrument in accordance with the present invention can be configured such that at least one electrode can be selectively placed in electrical communication with a conductor associated therewith. In at least one embodiment, referring to FIGS. 5 and 6, first electrode 72 can be placed in electrical communication with first conductor 30 when jaw member 52 is in a first position and can be placed out of electrical communication with conductor 30 when jaw member 52 is in a second position, for example. In at least one such embodiment, first electrode 72 can be configured to abut, or contact, contact end 33 of conductor 30 when jaw 52 is in its closed, or at least a substantially closed, position such that current can flow between first electrode 72 and first conductor 30. In such embodiments, first electrode 72 can be moved away from contact end 33 when jaw member 52 is moved into its open, or at least a substantially open, position such that current cannot flow between first electrode 72 and first conductor 30. In various embodiments, conductor 30 does not have to be attached to first electrode 72 and, as a result, first electrode 72 can be moved relative to conductor 30.

Further to the above, in at least one embodiment, conductor 30, including contact end 33, can remain stationary, or at least substantially stationary, when first electrode 72 is moved between first and second positions as described above and, as a result, conductor 30 does not have to be bent or stretched to accommodate the movement of first electrode 72. In various circumstances, as a result, the likelihood that conductor 30 may break or become otherwise damaged can be reduced. As illustrated in FIGS. 5 and 6, surgical instrument 20 can include one or more additional electrodes which can be selectively placed in electrical communication with a conductor associated therewith. In at least one embodiment, similar to the above, second electrode 74 can be placed in electrical communication with second conductor 32 when jaw member 54 is in a first position and can be placed out of electrical communication with second conductor 32 when jaw member 54 is in a second position, for example. Although not illustrated, surgical instrument 20 can include one or more stationary jaws and electrodes which do not move relative to a corresponding conductor. In such embodiments, the conductor may be attached to the stationary electrode, for example.

In various embodiments, first electrode 72 and first conductor 30 may be coupled to the positive terminal of generator 38 and second electrode 74 and second conductor 32 may be coupled to the negative terminal. In other various embodiments, this arrangement may be reversed. In either event, the switches described above, including foot pedal 40 (FIG. 2), may be placed intermediate, or in series between, the positive terminal and the electrode coupled thereto. In such embodiments, the switch may prevent current from flowing from the generator to this electrode until the switch is actuated. Absent such a switch, current could flow through the circuit comprising first conductor 30, second conductor 32, first electrode 72, and second electrode 74 when the electrodes are placed in electrical communication with the conductors. In these embodiments, current could be immediately transferred to the electrodes, and the soft tissue positioned therebetween, when jaw members 52 and 54 are moved into their closed, or at least substantially closed, positions. While such embodiments can be useful, various surgical techniques may require that the electrodes be manipulated or repositioned on the soft tissue after the jaw members have been closed thereon. In such embodiments, the jaw members could be closed onto the soft tissue and the current could be delivered to the electrodes when a switch is activated as described above.

In various embodiments, referring to FIGS. 4 and 5, each jaw member 52 and 54 can further include an insulator 75 which can be configured to prevent current from flowing from electrodes 72 and 74, respectively, to the other portions of the jaw members. More particularly, absent an insulator 75 positioned intermediate second electrode 74 and outer portion 76 of jaw 54, for example, the current may flow between electrode 74 to outer portion 76 and then flow into adjacent tissue which is not the targeted tissue. In at least one embodiment, insulator 75 may be at least partially comprised of a ceramic material, for example. In various embodiments, conductors 30 and 32 can be comprised of insulated wires. For example, each conductor can include an inner core comprised, of copper, brass, and/or aluminum, for example, and an outer jacket, or sheath, which can cover the core, wherein the jacket can be comprised of PVC or any other suitable polymer, for example. In various embodiments, electrodes 72 and 74 can be comprised of any suitable conductive material such as gold plated stainless steel, for example. In various embodiments, referring to FIG. 12, elongate member 82 can include at least one aperture, or lumen, 81 extending therethrough which can be configured to receive and protect conductors, or wires, 30 and 32 extending between end effector 50 and hand piece 24 as described above. In various embodiments, a lumen 81 can be configured to receive actuator 44 which, as described above, is operably engaged with hand piece 24 and end effector 50.

In various embodiments, an electrode can be formed having a substantially flat paddle-like shape, and/or any other suitable shape. In such embodiments, as described above, the electrode can include a flat surface which can be configured to abut contact end 33 of a conductor. In at least one embodiment, the inner core of the conductor can be configured to touch a portion of this flat surface and place the electrode and the conductor in electrical communication. In various other embodiments, although not illustrated, the electrode can include an aperture, or receptacle, which can be configured to receive contact end 33 therein, for example. In at least one embodiment, contact end 33 can be configured to abut a sidewall of the receptacle or it can be configured to fit snugly therein. In either event, the engagement between the receptacle and contact 33 can prevent, or at least reduce the possibility of, relative movement between the conductor and the electrode when the jaw member is in its closed position. Such relative movement could cause intermittencies in the current flowing therebetween which could affect the reliability of the surgical instrument. In various embodiments, contact end 33 can comprise an electrical contact which is soldered onto, or otherwise attached to, the end of the inner core of the conductor. Such electrical contacts can be configured such that they fit snugly within the receptacles in the electrodes and may require a force to remove them therefrom.

In various embodiments, a bipolar forceps having two or more electrodes can be utilized to seal a vessel, such as a blood vessel, for example. In at least one embodiment, the electrodes can be positioned against, or adjacent to, the vessel and energy can be supplied to the electrodes. In various circumstances, the energy can be sufficient to at least substantially seal the vessel such that blood does not substantially flow therethrough. In at least one surgical technique, the bipolar forceps can be used to thermally seal the vessel in two locations such that the vessel can be incised, or transected, at a location positioned intermediate the two sealed locations. In various embodiments, the bipolar forceps can include a cutting element which can be configured to incise the vessel. Such bipolar forceps can reduce the complexity of various surgical techniques by allowing a surgeon to seal and transect soft tissue with a single surgical instrument as opposed to using at least two surgical instruments which were previously required.

Referring to FIG. 15, surgical instrument 120 can include first jaw member 152 and second jaw member 154 wherein, similar to the above, first jaw member 152 can include first electrode 172 and, in addition, second jaw member 154 can include second electrode 174. In at least one embodiment, surgical instrument 120 can further include cutting element 190, wherein cutting element 190 can be configured to incise soft tissue, for example, positioned intermediate jaw members 152 and 154. In various embodiments, cutting element 190 can be configured to be moved relative to jaw members 152 and 154 and/or electrodes 172 and 174. More particularly, in at least one embodiment, cutting element 190 can be moved between a first, or proximal, position, as illustrated in FIG. 15, to a second, or distal, position, within distal end 192. In various alternative embodiments, the cutting element can be moved from a distal position to a proximal position to incise the soft tissue, for example. In either event, in at least one embodiment, cutting element 190 can include a sharp, or knife, edge configured to incise the soft tissue, for example. In various embodiments, second electrode 174 can include slot 191 which can be configured to slidably receive cutting element 190 and guide it along a predetermined path. In at least one embodiment, as illustrated in FIG. 15, the predetermined path can be linear or at least substantially linear. In other various embodiments, the predetermined path can be curved and/or curvilinear. In any event, in at least one embodiment, first electrode 172 can include a slot therein which can also be configured to slidably receive and guide cutting element 190.

In various embodiments, referring to FIG. 16, surgical instrument 220 can include first jaw member 252 and second jaw member 254 where, similar to the above, jaw members 252 and 254 can be positioned relative to a vessel, for example, such that electrodes within the jaw members can be utilized to cauterize or seal the vessel. In at least one embodiment, surgical instrument 220 can further include cutting element, or cutting barrel, 290 movably attached thereto wherein cutting barrel 290 can be moved between first and second positions similar to the above. In use, jaw members 252 and 254 can be used to at least partially clamp the vessel therebetween such that cutting barrel 290 can be slid over the at least partially closed jaws. In other various embodiments, cutting barrel 290 can be slid against jaw members 252 and 254 in order to push them into an at least partially closed position. In either event, in at least one embodiment, cutting barrel 290 can include aperture 293 extending therethrough which can be configured to receive at least a portion of jaws 252 and 254 as cutting barrel 290 is moved toward distal end 292. In at least one surgical technique, a vessel can be thermally sealed at two locations by electrodes 72 and 74 as described above. Thereafter, jaws 252 and 254 can be positioned intermediate the two sealed locations, jaws 252 and 254 can be at least partially closed onto the vessel, and cutting barrel 290 can be slid distally until cutting edge 294 contacts and incises the vessel.

In various embodiments, referring to FIG. 17, surgical instrument 320 can include first jaw member 352 and second jaw member 354 wherein, similar to the above, first jaw member 352 can include first electrode 372 and, in addition, second jaw member 354 can include second electrode 374. In at least one embodiment, at least one of first electrode 372 and second electrode 374 can include at least one cutting element 390 extending therefrom. In various embodiments, cutting element 390 can comprise a projection, or ‘high point’, having at least one cutting edge 394 configured to incise, or otherwise treat, soft tissue, such as a vessel, for example, when jaw members 352 and 354 are closed onto the soft tissue. In at least one embodiment, cutting edge 394 can be sharp enough to incise the soft tissue when a closing force is applied to jaw members 352 and 354. In various embodiments, energy can be applied to the cutting element via the electrode in order for the cutting element to transect the tissue. In such embodiments, the density of the energy within the electrode can be concentrated at the projection, or high point, of the electrode owing to the reduced surface area of the electrode in contact with the soft tissue. In various embodiments, referring to FIG. 18, surgical instrument 420 can include first jaw member 452 and second jaw member 454 wherein, similar to the above, first jaw member 452 can include first electrode 472 and, in addition, second jaw member 454 can include second electrode 474. In at least one embodiment, surgical instrument 420 can further include cutting element 490, wherein cutting element 490 can be configured to incise soft tissue, for example, positioned intermediate jaw members 452 and 454. In various embodiments, similar to the above, cutting element 490 can be configured to be moved relative to jaw members 452 and 454 and/or electrodes 472 and 474 along a predetermined path. In at least one embodiment, at least one of electrodes 472 and 474 and/or jaw members 452 and 454 can include a slot 491 therein which can be configured to slidably receive cutting element 490.

In various embodiments, cutting element 490 can be energized to incise, or otherwise treat, the soft tissue positioned intermediate jaw members 452 and 454. In at least one embodiment, cutting element 490 can be placed in electrical communication with a monopolar output of an electrosurgical generator such that current can flow from the generator into the soft tissue via cutting element 490. In order to complete the monopolar circuit, a return electrode, or pad, can be placed in contact with the patient's body and can be placed in electrical communication with the generator and/or another suitable ground. In other various embodiments, although not illustrated, surgical instrument 420 can include a return circuit for the electrical current. In either event, referring to FIG. 19, jaw member 454 can further include insulator 495 positioned intermediate cutting element 490 and second electrode 474 to electrically insulate cutting element 490 from electrode 474. In at least one embodiment, insulator 495 can define slot 491 such that cutting element 490 is at least substantially surrounded by insulator 495. Insulator 495 can be comprised of any suitable material such as a ceramic material, for example.

In at least one surgical technique, bipolar electrodes 472 and 474 can be utilized to at least partially seal a vessel as described above. Thereafter, electrodes 472 and 474 can be positioned intermediate the two seals and cutting element 490 can be slid until it touches the vessel. To incise the vessel, the surgeon can operate a switch, for example, to allow current to flow to cutting member 490. In various circumstances, depending on the frequency and voltage of the current, for example, cutting element 490 configured to cut and/or coagulate the soft tissue. In either event, surgical instrument 420 can include a switch, for example, which can be configured to place surgical instrument 420 in a plurality of operating modes. In at least one embodiment, the switch can place instrument 420 in a first operating mode in which electrical energy is supplied to electrodes 472 and 474, but not to cutting element 490. The switch can also place instrument 420 in a second operating mode in which electrical energy is supplied to cutting element 490, but not electrodes 472 and 474. In such embodiments, the possibility of energy being unintentionally transmitted to the targeted soft tissue, or the surrounding soft tissue, can be reduced. In at least one embodiment, cutting element 490 can further include cutting edge 494 which can be configured to incise, or bluntly dissect, the soft tissue. Such embodiments can provide a surgeon with several options for incising soft tissue.

In various embodiments, referring to FIGS. 20-24, a bipolar forceps can include first and second jaw members wherein at least one of the jaw members can include a substantially tapered profile. More particularly, in at least one embodiment, surgical instrument 520 can include end effector 550 having proximal end 596 and distal end 592 where end effector 550 can be tapered between proximal end 596 and distal end 592. In various embodiments, proximal end 596 can define a first perimeter and distal end 592 can define a second perimeter wherein the first perimeter can be larger than the second perimeter. Similarly, proximal end 596 can include a cross-section defined by a first diameter and distal end 592 can include a cross-section defined by a second diameter wherein the first diameter can be larger than the second diameter. Although embodiments where ends 592 and 596 have circular cross-sections are envisioned, other embodiments having non-circular cross-sections are also possible. In either event, in various embodiments, a ‘tapered’ end effector can include a cross-section which becomes gradually smaller between proximal end 596 and distal end 592. Such a taper can be constant along the length of end effector 550 or the taper can include at least two sections having different tapered profiles. In either event, as described in greater detail below, a bipolar forceps having a tapered end effector can be useful in various surgical techniques.

In at least one surgical technique, distal end 592 can be positioned intermediate a vessel and soft tissue surrounding the vessel in order to separate the vessel from the soft tissue. More particularly, end effector 550 can be positioned intermediate the vessel and the soft tissue in a substantially closed position and can be opened such that jaw members 552 and 554 contact the vessel and soft tissue and push them away from each other. In various circumstances, end effector 550 can be opened and closed several times to enlarge a hole between the vessel and soft tissue such that the vessel and the soft tissue can be further separated. In various embodiments, again referring to FIGS. 20-24, at least one of jaw members 552 and 554 can further include ridges, teeth, and/or a textured outer surface configured to grip the soft tissue and/or vessel. In at least one embodiment, jaw member 552, for example, can include ridges 597 extending therefrom along a line defined between distal end 592 and proximal end 596. In various embodiments, ridges 597 can be configured such that, when the jaw members contact the soft tissue and/or vessel as described above, the jaw members can pull the soft tissue and vessel therewith. In effect, ridges 597, for example, can prevent, or at least inhibit, jaw members 552 and 554 from sliding past the soft tissue and/or vessel when the jaw members are opened.

In various embodiments, referring to FIGS. 21 and 24, jaw member 552, for example, can include tapered portion 598 and bullet nose portion 599. In at least one embodiment, both tapered portion 598 and bullet nose portion 599 can include ridges 597, for example, extending therefrom. In such embodiments, bullet nose portion 599 can be especially configured to be burrowed between the vessel and the surrounding soft tissue, as described above, as ridges 597 extending from bullet nose portion 599 can facilitate the creation of a hole in the connective tissue intermediate the vessel and the soft tissue. In addition to or in lieu of the above, the outer surfaces of jaw members 552 and 554 can include an outer surface having a rough texture which can also be configured to prevent, or at least reduce, slipping between the jaw members and the soft tissue and/or vessel. In at least one embodiment, the outer surface of jaw members 552 and 554 can be abraded. In various embodiments, a rough coating can be sprayed onto the jaw members. In either event, once the vessel has been at least partially separated from the soft tissue, one of jaw members 552 and 554 can be positioned intermediate the vessel and the soft tissue and the other of jaw members 552 and 554 can be positioned on the opposite side of the vessel. Thereafter, the electrodes positioned within jaw members 552 and 554 can be utilized to thermally seal the vessel as described above.

In at least one embodiment, the first and second electrodes can be adapted to receive an irreversible electroporation (IRE) waveform from an IRE generator. In another embodiment, the first and second electrodes can be adapted to receive a radio frequency (RF) waveform from an RF generator. In various embodiments, the electrical waveform generator may be a conventional, bipolar/monopolar electrosurgical IRE generator such as one of many models commercially available, including Model Number ECM 830, available from BTX Molecular Delivery Systems Boston, Mass. The IRE generator can generate electrical waveforms having predetermined frequency, amplitude, and pulse width. In various circumstances, the application of these electrical waveforms to the cell membranes of the diseased tissue causes the diseased cells to die. Thus, the IRE electrical waveforms may be applied to the cell membranes of diseased tissue in the tissue treatment region in order to kill the diseased cells and ablate the diseased tissue. IRE electrical waveforms suitable to destroy the cells of diseased tissues are generally in the form of direct current (DC) electrical pulses delivered at a frequency in the range of 1-20 Hz, amplitude in the range of 100-1000 VDC, and pulse width in the range of 0.01-100 ms. For example, an electrical waveform having amplitude of 500 VDC and pulse duration of 20 ms may be delivered at a pulse repetition rate or frequency of 10 HZ to destroy a reasonably large volume of diseased tissue. Unlike RF ablation systems which require high powers and energy input into the tissue to heat and destroy, IRE requires very little energy input into the tissue, rather the destruction of the tissue is caused by high electric fields. It has been determined that in order to destroy living tissue, the electrical waveforms have to generate an electric field of at least 30,000V/m in the tissue treatment region. The embodiments, however, are not limited in this context.

In at least one embodiment, the electrical waveform generator may comprise a radio frequency (RF) waveform generator. The RF generator may be a conventional, bipolar/monopolar electrosurgical generator such as one of many models commercially available, including Model Number ICC 350, available from Erbe, GmbH. Either a bipolar mode or monopolar mode may be used. When using the bipolar mode with two electrodes, one electrode can be electrically connected to one bipolar polarity, and the other electrode can be electrically connected to the opposite bipolar polarity. If more than two electrodes are used, the polarity of the electrodes may be alternated so that any two adjacent electrodes have opposite polarities.

The devices disclosed herein can be designed to be disposed of after a single use, or they can be designed to be used multiple times. In either case, however, the device can be reconditioned for reuse after at least one use. Reconditioning can include any combination of the steps of disassembly of the device, followed by cleaning or replacement of particular pieces, and subsequent reassembly. In particular, the device can be disassembled, and any number of the particular pieces or parts of the device can be selectively replaced or removed in any combination. Upon cleaning and/or replacement of particular parts, the device can be reassembled for subsequent use either at a reconditioning facility, or by a surgical team immediately prior to a surgical procedure. Those skilled in the art will appreciate that reconditioning of a device can utilize a variety of techniques for disassembly, cleaning/replacement, and reassembly. Use of such techniques, and the resulting reconditioned device, are all within the scope of the present application.

Preferably, various embodiments of the invention described herein will be processed before surgery. First, a new or used instrument is obtained and if necessary cleaned. The instrument can then be sterilized. In one sterilization technique, the instrument is placed in a closed and sealed container, such as a plastic or TYVEK bag. The container and instrument are then placed in a field of radiation that can penetrate the container, such as gamma radiation, x-rays, or high-energy electrons. The radiation kills bacteria on the instrument and in the container. The sterilized instrument can then be stored in the sterile container. The sealed container keeps the instrument sterile until it is opened in the medical facility. It is preferred that the instrument is sterilized. This can be done by any number of ways known to those skilled in the art including beta or gamma radiation, ethylene oxide, steam.

While this invention has been described as having exemplary designs, the present invention may be further modified within the spirit and scope of the disclosure. This application is therefore intended to cover any variations, uses, or adaptations of the invention using its general principles. Further, this application is intended to cover such departures from the present disclosure as come within known or customary practice in the art to which this invention pertains. Any patent, publication, or other disclosure material, in whole or in part, that is said to be incorporated by reference herein is incorporated herein only to the extent that the incorporated materials does not conflict with existing definitions, statements, or other disclosure material set forth in this disclosure. As such, and to the extent necessary, the disclosure as explicitly set forth herein supersedes any conflicting material incorporated herein by reference. Any material, or portion thereof, that is said to be incorporated by reference herein, but which conflicts with existing definitions, statements, or other disclosure material set forth herein will only be incorporated to the extent that no conflict arises between that incorporated material and the existing disclosure material.

Claims

1. A surgical instrument for treating soft tissue, comprising: a flexible shaft;a housing extending from said flexible shaft;a conductor in electrical communication with an energy source, said conductor having a contact portion; anda jaw rotatably connected to said housing, wherein said jaw is configured to be inserted through a working channel of an endoscope, wherein said jaw is selectively rotatable between a first position, an intermediate position, and a second position, wherein said intermediate position is between said first position and said second position, and wherein said jaw includes: an electrode, wherein said electrode is not in contact with said contact portion when said jaw is in said first position and when said jaw is in said intermediate position, and wherein said electrode is configured to contact said contact portion when said jaw is in said second position such that said electrode is in electrical communication with said conductor to transmit energy to the soft tissue.

2. The surgical instrument of claim 1, wherein said electrode comprises a first electrode, and wherein said surgical instrument further comprises: a second conductor comprising a second contact portion; anda second jaw comprising a second electrode, wherein said second electrode is operably configured to contact said second contact portion such that said second electrode is in electrical communication with said second conductor to transmit energy to said first electrode via the soft tissue.

3. A method for processing an instrument for surgery, the method comprising: obtaining the surgical instrument of claim 1;sterilizing the surgical instrument; andstoring the surgical instrument in a sterile container.

4. A surgical instrument for treating soft tissue, comprising: a flexible shaft;a first jaw;a second jaw rotatably coupled to said first jaw, wherein said first and second jaws are configured to be inserted through a working channel of an endoscope, wherein said second jaw is selectively rotatable between a first position, an intermediate position, and a second position, and wherein said intermediate position is between said first position and said second position;a conductor in electrical communication with an energy source, said conductor having a contact portion; andan electrode, wherein said electrode is not in contact with said contact portion when said second jaw is in said first position and when said second jaw is in said intermediate position, and wherein said electrode is configured to contact said contact portion when said second jaw is in said second position such that said electrode is in electrical communication with said conductor to transmit energy to the soft tissue.

5. The surgical instrument of claim 4, wherein said electrode comprises a second electrode, and wherein said surgical instrument further comprises: a first conductor comprising a first contact portion; anda first electrode on said first jaw, wherein said first electrode is configured to operably contact said first contact portion such that said first electrode is in electrical communication with said first conductor to transmit energy to said second electrode via the soft tissue.

6. A method for processing an instrument for surgery, the method comprising: obtaining the surgical instrument of claim 4;sterilizing the surgical instrument; andstoring the surgical instrument in a sterile container.