US20080249526A1 - Method and apparatus for surgical dissection - Google Patents

Abstract

An apparatus for dissecting tissue in a substantially uniform plane of dissection includes a housing configured to be advanced under a tissue layer, and control one of a depth of dissection or tissue flap thickness. The housing thermally shields at least a portion of the tissue flap. A roller is coupled to the housing. The roller is configured to smoothly advance housing over tissue. An energy delivery device is coupled to housing. The energy delivery device is configured to be coupled to an energy source. The energy delivery device has a geometry that substantially defines a plane of dissection.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS
• This application is a continuation of U.S. Ser. No. 10/620,311 filed Jul. 14, 2003, which application claims the benefit of U.S. Ser. No. 60/396,038, filed Jul. 14, 2002, U.S. Ser. No. 60/416,206, filed Oct. 3, 2002, and U.S. Ser. No. 60418,089 filed Oct. 13, 2002, all of which applications are fully incorporated herein by reference.
BACKGROUND OF THE INVENTIONField of the Invention
• This invention relates to a method and apparatus for treating tissue. More particularly, the invention relates to a method for treating tissue using the delivery of energy. Still more particularly the invention relates to a method and apparatus for treating tissue using the delivery of energy to perform electro-surgical procedures.
• The human skin is composed of two elements: the epidermis and the underlying dermis. The epidermis with the stratum corneum serves as a biological barrier to the environment. In the basilar layer of the epidermis, pigment-forming cells called melanocytes are present. They are the main determinants of skin color. The dermis is composed mainly of an extra-cellular protein called collagen.
• There are many causes of skin irregularities and deformities including skin laxity, sun damage etc. These irregularities are the result of changes in the structure and properties of the skin and underlying tissue layers. One of the more prominent causes of surface irregularities is cellulite which results in a dimpled, lumpy, or bulging skin surface. Cellulite appears in the subcutaneous level of skin tissue, that is the level below the dermis. Fat cells in the subcutaneous layer are arranged in chambers surrounded by connective tissue called septae. As fat cells increase in size to the deposition of intracellular of fat, the fibrous septae, which encase fat loculations and which connect the deep aspect of the dermis to the subjacent muscle fascia, are placed under increasing tension.
• The growth in size of the fat loculations and the increase in tension of the fibrous septae are combined with a progressive laxity of skin due to age. This multifactorial complex of increasing tension of the fibrous septae, increasing size of fat loculations and progressive age related skin laxity results in a three dimensional dimpling of the skin. This results in areas of the skin being held down while other sections bulge outward, resulting in the lumpy, ‘cottage-cheese’ appearance.
• As described above, the dermis is composed mainly of an extracellular protein called collagen. Collagen is produced by fibroblasts and synthesized as a triple helix with three polypeptide chains that are connected with heat labile and heat stable chemical bonds. When collagen-containing tissue is heated, alterations in the physical properties of this protein matrix occur at a characteristic temperature. The structural transition of collagen contraction occurs at a specific “shrinkage” temperature. The shrinkage and remodeling of the collagen matrix with heat is the basis for the technology.
• Collagen crosslinks are either intramolecular (covalent or hydrogen bond) or intermolecular (covalent or ionic bonds). The thermal cleavage of intramolecular hydrogen crosslinks is a scalar process that is created by the balance between cleavage events and relaxation events (reforming of hydrogen bonds). No external force is required for this process to occur. As a result, intermolecular stress is created by the thermal cleavage of intramolecular hydrogen bonds. Essentially, the contraction of the tertiary structure of the molecule creates the initial intermolecular vector of contraction.
• Collagen fibrils in a matrix exhibit a variety of spatial orientations. The matrix is lengthened if the sum of all vectors acts to distract the fibril. Contraction of the matrix is facilitated if the sum of all extrinsic vectors acts to shorten the fibril. Thermal disruption of intramolecular hydrogen bonds and mechanical cleavage of intermolecular crosslinks is also affected by relaxation events that restore preexisting configurations. However, a permanent change of molecular length will occur if crosslinks are reformed after lengthening or contraction of the collagen fibril. The continuous application of an external mechanical force will increase the probability of crosslinks forming after lengthening or contraction of the fibril.
• Hydrogen bond cleavage is a quantum mechanical event that requires a threshold of energy. The amount of (intramolecular) hydrogen bond cleavage required corresponds to the combined ionic and covalent intermolecular bond strengths within the collagen fibril. Until this threshold is reached, little or no change in the quaternary structure of the collagen fibril will occur. When the intermolecular stress is adequate, cleavage of the ionic and covalent bonds will occur. Typically, the intermolecular cleavage of ionic and covalent bonds will occur with a ratcheting effect from the realignment of polar and non-polar regions in the lengthened or contracted fibril.
• Cleavage of collagen bonds also occurs at lower temperatures but at a lower frequency. Low level thermal cleavage is frequently associated with relaxation phenomena in which bonds are reformed without a net change in molecular length. An external force that mechanically cleaves the fibril can reduce the probability of relaxation phenomena and provides a means to lengthen or contract the collagen matrix at lower temperatures while reducing the potential of surface ablation.
• Soft tissue remodeling is a biophysical phenomenon that occurs at cellular and molecular levels. Molecular contraction or partial denaturization of collagen involves the application of an energy source, which destabilizes the longitudinal axis of the molecule by cleaving the heat labile bonds of the triple helix. As a result, stress is created to break the intermolecular bonds of the matrix. This is essentially an immediate extracellular process, whereas cellular contraction can require a lag period for the migration and multiplication of fibroblasts into the wound as provided by the wound healing sequence. In higher developed animal species, the wound healing response to injury involves an initial inflammatory process that subsequently leads to the deposition of scar tissue.
• The initial inflammatory response consists of the infiltration by white blood cells or leukocytes that dispose of cellular debris. Seventy-two hours later, proliferation of fibroblasts at the injured site occurs. These cells differentiate into contractile myofibroblasts, which are the source of cellular soft tissue contraction. Following cellular contraction, collagen is laid down as a static supporting matrix in the tightened soft tissue structure. The deposition and subsequent remodeling of this nascent scar matrix provides the means to alter the consistency and geometry of soft tissue for aesthetic purposes.
• Dissection is the surgical separation of soft tissue components or the creation of a separation interface within a soft tissue component. The plane of dissection is the surgical plane of soft tissue where different or the same soft tissue components have been separated from or within each other. The plane of dissection implies a horizontal orientation along soft tissue components. Incise implies a vertical orientation of dissection through soft tissue components. The undermined area is the area in a plane of dissection that is separated from the subjacent soft tissue. Referring toFIGS. 1(a)-1(f), the cutaneous flap, shown inFIG. 1(a) is a composite isolate of skin and subcutaneous soft tissue that has been surgically separated along a horizontal plane of dissection from the subjacent soft tissue. The subdermal plexus is the superficial vascular supply of a cutaneous flap. Flap can also mean an isolate of skin and soft tissue that will be advanced or moved to an adjacent recipient site or used to close an adjacent soft tissue defect. A synonymous term is ‘random cutaneous flap’.
• The myocutaneous flap, shown inFIG. 1(b) is a thicker composite isolate of skin, subcutaneous soft tissue and muscle that has been surgically separated from surrounding soft tissue. The myocutaneous perforators (e.g. arteries) are the deeper and more robust vascular supply of a myocutaneous flap. Flap necrosis is a nonviable portion of a flap that has an inadequate vascular supply. Flap necrosis is more likely to occur in cutaneous flaps because of their less robust vascular supply. Other types of flaps will exhibit a less or more robust vascular supply.
• The fasciocutaneous flap shown inFIG. 1(c) that consists of the skin, subcutaneous layer, and fascia is more robust in it's circulation than the cutaneous flap which consists of the skin and a viable thickness of subcutaneous layer. In comparison, the fascio-subcutaneous flap (shown inFIG. 1(d)) which consists of the variable amount in the deep portion of the subcutaneous layer with the subjacent fascia, is less robust than the fasciocutaneous flap but more robust than a subcutaneous flap (shown inFIG. 1(e)) that consists only of the subcutaneous layer. However the most robust flap is the myofascial flap (shown inFIG. 1(f)) with has an axial circulation that runs longitudinally through the length of the flap. Flaps may also be combination flaps (shown inFIG. 1(g)) where the proximal portion of the flap involves a deeper tissue component such as the muscle or fascia but which extend distally with more superficial components such as the subcutaneous layer and/or skin.
• There are a number of surgical, reconstructive, cosmetic, dermatological procedures tissue where it is useful to dissect a selected tissue layer having a uniform thickness while minimizing injury to surrounding tissue. Such procedures include tissue reconstructions, mastectomy and breast reconstruction, mastopexy, face lifts, liposuction, buttocks lifts and the like. There is a need for instruments for such procedures. Further, there are also a number of surgical, cosmetic, dermatological procedures that lend themselves to treatments which in addition to surgical remodeling, thermal energy is delivered to the skin and underlying tissue to cause a contraction of collagen, and/or initiate a wound healing response so as to tighten or rejuvenate the skin and underlying tissue at the tissue site. Such procedures include tissue reconstructions, breast reconstruction, breast repositioning, liposuction, face lift skin remodeling, resurfacing, skin tightening, wrinkle removal and the like.
• There is a need for an improved dissection, cutting device that dissects tissues at a controlled depth.
SUMMARY OF THE INVENTION
• Accordingly, an object of the present invention is to provide an apparatus, and its methods of use, that delivers energy to a tissue site and dissect a tissue plane at a controlled depth.
• Another object of the present invention is to provide an apparatus, and its methods of use, that delivers energy to a tissue site, dissect a tissue plane at a controlled depth, produces a tissue flap with a substantially uniform thickness while protecting or minimizing injury to tissue or structures within the flap
• Still another object of the present invention is to provide an apparatus, and its methods of use, that used RF energy to dissect tissue and create one or more tissue flaps with a substantial uniform thickness.
• A further object of the present invention is to provide an apparatus, and its methods of use, that creates a uniform surgical release and mass shifting of overlying soft tissue structures from subjacent tissue structures by uniformly dissecting the overlying structures from the underlying tissue.
• Yet another object of the present invention is to provide an apparatus, and its methods of use, that creates a uniform surgical release and a shifting of overlying soft tissue structures.
• Another object of the present invention is to provide an apparatus, and its methods of use, that creates a means to surgically shift soft tissue through smaller less visible incisions.
• These and other objects of the present invention are achieved in an apparatus for dissecting tissue in a substantially uniform plane of dissection. A housing is configured to be advanced under a tissue layer and control one of a depth of dissection or tissue flap thickness. The housing thermally shields at least a portion of the tissue flap. A roller is coupled to the housing. The roller is configured to smoothly advance housing over tissue. An energy delivery device is coupled to housing. The energy delivery device is configured to be coupled to an energy source. The energy delivery device has a geometry that substantially defines a plane of dissection.
• In another embodiment, an electro-surgical apparatus includes an electrode with a cutting edge. A housing is coupled to the electrode. The housing includes a top with a top proximal section and a bottom with a bottom proximal section. The top proximal section has a geometry that facilitates creation of a skin flap with a substantially uniform thickness that includes a skin layer and an adjacent layer of subcutaneous tissue. The bottom proximal section has a geometry that preserves a plane of tissue that is positioned adjacent to the adjacent layer of subcutaneous tissue
• In another embodiment, a dissection apparatus includes an energy delivery device with an energy delivery surface. A housing is coupled to the energy delivery device. The housing includes a guide configured to permit the energy delivery surface provide a surgical plane of dissection to free a skin section and an underlying thickness of subcutaneous tissue while preserving an adjacent plane of tissue.
• In another embodiment, a tissue dissection apparatus includes an electrosurgical energy delivery device with an electrosurgical cutting edge. A housing is coupled to the energy delivery device. The housing includes a guard that guides and facilitates a dissection to create a surgical plane of dissection to free a skin section and an underlying thickness of subcutaneous tissue while preserving an adjacent plane of tissue.
• In another embodiment, a method of creating a tissue effect provides an electro-surgical device that includes an energy delivery device with an energy delivery surface. A housing is coupled to the electrode with a guide that provides for cutting a skin layer and an underlying thickness of subcutaneous tissue while preserving an adjacent plane of tissue. The energy delivery surface is positioned at the skin surface. Sufficient energy is delivered from the energy delivery device to cut the skin surface and the underlying thickness of subcutaneous tissue at a selected depth while preserving the adjacent plane of tissue.
• In another embodiment, a method of creating a tissue effect provides an electro-surgical device that includes an electrode with a cutting edge, a housing coupled to the electrode with a guide that provides for cutting a skin layer and an underlying thickness of subcutaneous tissue while preserving an adjacent plane of tissue. The cutting edge is positioned at the skin surface. The skin surface and a layer of an adjacent underlying tissue are cut. A tissue effect is created.
BRIEF DESCRIPTION OF THE FIGURES
• FIGS. 1(a) through1(g) illustrated cross-sectional views of a skin surface, and various underlying structures.
• FIG. 2(a) is a cross-sectional view of one embodiment of an apparatus for dissecting or cutting tissue of the present invention.
• FIG. 2(b) is a cross-sectional view of another embodiment of the an apparatus for dissecting or cutting tissue of the present invention.
• FIG. 2(c) is a top down view of another embodiment of the an apparatus for dissecting or cutting tissue of the present invention that includes a chamber.
• FIG. 3 is a cross-sectional view of an apparatus of the present invention for dissecting or cutting tissue that includes suction capability.
• FIGS. 4 and 5(a) are cross-sectional views of an apparatus of the present invention for dissecting or cutting tissue with a housing that can function as a tissue guide and a tissue guard, or guide-guard to guide the electrode through tissue to produce a uniform plane of dissection.
• FIG. 5(b) is a cross-sectional view of an apparatus of the present invention for dissecting or cutting tissue that includes a buffer section on one or both electrode ends to bound the electrode.
• FIG. 5(c) is a cross-sectional view of an apparatus of the present invention for dissecting or cutting tissue with a housing that includes a sheath.
• FIG. 5(d) is a cross-sectional view of an apparatus of the present invention for dissecting or cutting tissue that can be configured to allow the surgeon to advance the housing through the skin with the housing in a pitched-up fashion.
• FIG. 5(e) is a cross-sectional view of an apparatus of the present invention for dissecting or cutting tissue that with an extender that can include a deflectable section.
• FIGS. 6,7 and8 are cross-sectional views of an apparatus of the present invention for dissecting or cutting tissue that include a roller.
• FIGS. 9 and 10 are cross-sectional views of an apparatus of the present invention for dissecting or cutting tissue that that has a flat rectangular section positioned proximally behind) thehousing14 and provide stabilization.
• FIGS. 11(a) and11(b) are cross-sectional view of an apparatus of the present invention for dissecting or cutting tissue that element with a substantially U-shaped section positioned proximal to housing.
• FIG. 12 is a cross-sectional view of an apparatus of the present invention for dissecting or cutting tissue that with a stabilizing element that can be positioned between a first roller and a second roller.
• FIGS. 13aand13billustrate an apparatus of the present invention for dissecting or cutting tissue with a gap distance between the electrode and the roller configured to control or facilitate control of the thickness of the skin envelope or tissue flap and/or the dissection depth.
• FIGS. 14-18 illustrate an apparatus of the present invention for dissecting or cutting tissue that include trans-cutaneous markers.
• FIGS. 16(a) and16(b) illustrate an apparatus of the present invention for dissecting or cutting tissue with a pattern of bumps which corresponding to different dissection depths, to provide the physician with a real time visual indication of the depth of dissection.
• FIG. 17 illustrates an apparatus of the present invention for dissecting or cutting tissue with different bump shapes
• FIG. 18 illustrates an apparatus of the present invention for dissecting or cutting tissue with marking ridges to provide a visual bracketing or cue of the width of the plane of dissection.
• FIGS. 19(a) through20billustrate an apparatus of the present invention for dissecting or cutting tissue with a detachable section or movable or variable shaped contour.
• FIGS. 21 through 22(b) illustrate an apparatus of the present invention for dissecting or cutting tissue that provides a guarding function of the housing to protect the dermal and sub-dermal vascular and neural plexus or other selected layer of the skin envelope or tissue flap from thermal injury and/or necrosis.FIGS. 23 through 25 illustrate an apparatus of the present invention for dissecting or cutting tissue that includes delivery of a cooling fluid
• FIG. 24 illustrate an apparatus of the present invention for dissecting or cutting tissue with apertures to direct or infuse a cooling solution onto the skin envelope or tissue flap.
• FIG. 25 illustrate an apparatus of the present invention for dissecting or cutting tissue with a porous section coupled to thehousing14 and fluidically coupled to one or more lumens.
• FIGS. 26 through 28 illustrate an apparatus of the present invention for dissecting or cutting tissue that is configured to dissect tissue in deeper planes of dissection than the dermis or superficial fascia.
• FIGS. 29(a) and29(b) illustrate an apparatus of the present invention for dissecting or cutting tissue configured to dissect fascial layers by a variety of different approaches.
• FIGS. 30(a) through30(c) illustrate an apparatus of the present invention for dissecting or cutting tissue that include a port device.
• FIGS. 31(a) through31(c) illustrate an apparatus of the present invention for dissecting or cutting tissue configured to provide a uniform surgical release and mass shifting of overlying soft tissue structures from subjacent tissue structures by uniformly dissecting the overlying structures from the underlying tissue.
• FIGS. 32 through 34 illustrate an apparatus of the present invention for dissecting or cutting tissue with a housing fabricated from any number of medical polymers.
• FIG. 35 illustrate an apparatus of the present invention for dissecting or cutting tissue with a housing configured to vary the amount that the electrode can be advanced or retracted in an out of the housing.
• FIGS. 36(a) through37 illustrate an apparatus of the present invention for dissecting or cutting tissue with a housing that can include one or both of a linear or curved or contoured portions.
• FIG. 37 illustrates an apparatus of the present invention for dissecting or cutting tissue with a plurality of conformable portions having different flexural moduli.
• FIG. 38 illustrates an apparatus of the present invention for dissecting or cutting tissue that is configured to move over a curved tissue surface and still maintain a substantially uniform depth of dissection.
• FIGS. 39(a) through39(c) illustrate an apparatus of the present invention for dissecting or cutting tissue configured to provide advancement of housing on curved surfaces.
• FIGS. 40 through 44 illustrate an apparatus of the present invention for dissecting or cutting tissue with one or more roller devices that can also be a sliding or linear translation device.
• FIGS. 42 and 43 illustrate an apparatus of the present invention for dissecting or cutting tissue with rollers located above and below theelectrode18.
• FIG. 44 illustrate an apparatus of the present invention for dissecting or cutting tissue with a roller that can generate sufficient frictional force with the contacting tissue so as to put all or a portion of the subjacent tissue layers in contact with the housing.
• FIGS. 45(a) through45(b) illustrate an apparatus of the present invention for dissecting or cutting tissue with a housing that provides a force application surface configured to allow the physician to press down on the housing to apply a downward force from the rollers to the underlying tissue layer.
• FIG. 45(c) illustrate an apparatus of the present invention for dissecting or cutting tissue with other means for force application.
• FIGS. 46 through 48 illustrate an apparatus of the present invention for dissecting or cutting tissue with anelectrode18 that is fabricated from a variety of conductive materials
• FIG. 49 illustrate an apparatus of the present invention for dissecting or cutting tissue with an electrode that has a wedge shaped or “cow catcher shaped” that provides a wedge or force concentration affect in cutting through the tissue.
• FIG. 50 illustrate an apparatus of the present invention for dissecting or cutting tissue with one or both ends of the electrode attached to the sides of the housing.
• FIGS. 51(a) through51(b) illustrate an apparatus of the present invention for dissecting or cutting tissue with the electrode coupled to the housing with a strut member.
• FIG. 52 illustrate an apparatus of the present invention for dissecting or cutting tissue with an electrode that is electromagnetically coupled to an energy source.
• FIGS. 53(a) and53(b) illustrate an apparatus of the present invention for dissecting or cutting tissue configured to use high frequency, high power RF energy in conjunction with injection or infusion of an electro-conductive or electrolytic solution.
• FIGS. 56 through 57 illustrate an apparatus of the present invention for dissecting or cutting tissue with a hand piece configured to be attached to the electrode housing to provide similar tactile sensation.
• FIGS. 58 through 59 illustrate an apparatus of the present invention for dissecting or cutting tissue with a housing configured to be deployable in situ to allow subcutaneous insertion of all or portion of thehousing14 through a single incision.
• FIG. 60 illustrates an apparatus of the present invention for dissecting or cutting tissue that provides transcutaneous visualization.
• FIG. 61 illustrates an apparatus of the present invention for dissecting or cutting tissue that is configured to be monitor by temperature of tissue adjacent or near the housing.
• FIG. 62 illustrates an apparatus of the present invention for dissecting or cutting tissue with cooling that can be achieved by irrigation of the tissue surface or selected portions of the tissue site with a cooled fluid.
• FIG. 63 illustrate an apparatus of the present invention for dissecting or cutting tissue that provides cooling of the skin and adjacent tissue by suctioning off, capturing or cooling a vapor produced from vaporization of tissue during energy delivery.
• FIGS. 64(a) through64(f) illustrate use of an apparatus of the present invention in the performance of a skin preservation mastectomy in which no breast skin is resected.
• FIG. 65 illustrate use of an apparatus of the present invention for a facelift patient with redundant skin the cheeks, jowls and neck.
• FIGS. 66 and 67 illustrate the use of an apparatus of the present invention for a patient with breast ptosis.
• FIGS. 68 through 71 illustrate the use of an apparatus of the present invention for the aesthetic surgical discipline of ‘closed advancement’ using a closed flap dissection with a uniform flap.
• FIG. 72 illustrates the use of an apparatus of the present invention with an open or closed loop feedback system/resources.
• FIG. 73 illustrates the use of an apparatus of the present invention with a current sensor and voltage sensor.
• FIG. 74 illustrates the use of an apparatus of the present invention with a temperature and impedance feedback system.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
• Embodiments of the invention provide a method and apparatus for use in various surgical procedures such as plastic surgery procedures and minimally invasive surgical procedures. In an embodiment, the apparatus can comprise an electro-surgical instrument configured to use radio-frequency (RF) or other electromagnetic energy to perform various surgical procedures including, but not limited to, cutting, dissection, coagulation and the like. In an embodiment, the apparatus can be configured to be used in surgical dissection procedures to produce one or more tissue flaps having a substantially uniform thickness.
• Referring now toFIGS. 2(a) through7, these figures illustrate embodiments of anapparatus10 that can be configured to dissect tissue or treat tissue at atarget tissue site8 such as a subcutaneous tissue site and create a selected plane ofdissection8pdhaving a selectable and substantially uniform depth ofdissection8ddand a selectable and substantiallyuniform flap thickness8t.
• In various embodiments,apparatus10 can create (i) a uniform plane of flap dissection, including but not limited to electrosurgical, a uniform flap thickness of or a uniform flap of variable thickness, (ii) a reduced surface area in a plane of dissection due to flap uniformity, (iii) a more uniform plane of wound healing with a reduction on volumetric scarring within the plane of dissection, uniform thermal tightening of the dissected skin flap, (iv) a uniform primary tightening, which is a thermal molecular collagen contraction within the plane of dissection, (v) a uniform secondary tightening: delayed secondary wound healing contraction within the plane of dissection, (vi) a reduction in iatrogenic surface contour irregularities of the flap surface, (vii) a uniform release of subjacent soft tissue structures, and the like.
• Apparatus10 can also be utilized to create secondary aesthetic guide effects including but not limited to, (i) 3 dimensional contour enhancement from flap advancement, (ii) 2 dimensional surface area tightening from primary and secondary thermal tightening of the skin flap, (iii) creation of a surgical portal for suction curettment of a liposuction treatment site that can provide a more uniform contour reduction than standard liposuction, (iv) provide a surgical portal for lifting plication of the subjacent soft tissue, (v) create a uniform release of pre-existing tethering fibrous septae which causes cellulite dimpling of the skin surface.
• Apparatus10 can have guard effects, relative to tissue dissection and/or cutting, that can be utilized for a variety of applications and result in, (i) a reduction of electrosurgical complications of flap dissection, (ii) a reduced incidence of full thickness flap lacerations (button holing), (iii) a reduced incidence of deep tissue injuries of the subjacent vital structures such as nerves, vessels and muscle either from transaction or thermal conductive damage, (iv) a reduced incidence of flap necrosis due to interruption of flap blood supply, (v) a reduced incidence of electrosurgical burns of the flap, and the like.
• FIGS. 1 and 2(a) through2(c) illustrate an embodiment ofapparatus10 that can include ahousing14 having proximal anddistal portions14pand14d(here distal refers to the front ofhousing14 that is advanced into tissue and proximal refers to the trailing end of housing14). Ahand piece15 is coupled toproximal portions14pand can be fixedly coupled or pivotally coupled via apivotal coupling14cop.Handpiece15 can include or be coupled to anextension member22. Thedistal portions15dof the hand piece or extension member can be at least partially recessed withinhousing14 to reduce friction or drag from the handpiece. An electrode or otherenergy delivery device18 having anelectrode cutting edge18ceis coupled todistal portions14dofhousing14 directly or via aninsulative coupling14icop.
• Electrode18 can be positioned distally tohousing14 and is configured to cut or dissect through tissue via the use of RF energy (other electromagnetic energy) to produce a selected plane of dissection within or between one or more tissue layers such as the subcutaneous layer of the skin or the muscle fascia.Electrode18 and/orapparatus10 can be configured to be coupled to apower source20 via apower connecting member20cm. In various embodiments, one or more rollers orroller elements17 can be coupled tohousing14.Rollers17 can be positioned at thedistal portions14dofhousing14, can be positioned adjacent, above or belowelectrode18 or can be attached to the bottom14bor the top ofhousing14t.Rollers17 positioned above the electrode, are configured to assist in rolling or advancing the nascently dissected tissue flap overhousing14.Rollers17 positioned below can be configured to allowhousing14 to roll over underlying tissue ashousing14 is advanced in thedissection pocket8dpat thetarget tissue site8 or elsewhere.
• Referring now toFIGS. 2(b) and2(c), in oneembodiment housing14 is configured to be advanced under a tissue layer and control one of a depth of dissection or tissue flap thickness.Housing14 thermally shields at least a portion of the tissue flap.Roller17 can be coupled tohousing14, as more fully explained hereafter.Roller17 is configured to smoothly advancehousing14 over tissue.Electrode18 is coupled tohousing14 and has a geometry that substantially defines a plane of dissection.
• In another embodiment,housing14 includes a top with a topproximal section14′ and a bottom with a bottomproximal section14″. Topproximal section14′ has a geometry that facilitates creation of a skin flap with a substantially uniform thickness that includes a skin layer and an adjacent layer of subcutaneous tissue. Bottomproximal section14″ has a geometry that preserves a plane of tissue that is positioned adjacent to the adjacent layer of subcutaneous tissue
• In one embodiment, illustrated inFIG. 2(b), bottomproximal section14“has a most proximal point at “A”, and the top proximal section has a most proximal point at “B”, wherein A is more proximal than B. Bottomproximal section14″ is defined by point A and a more distal point “C”.Electrode18 extends from point A to pointB. Electrode18 forms the hypoteneus of a triangle defined by points A, B, and a point D which is positioned at a more proximal position than point B. Bottomproximal section14″ forms a hypotenuse of a triangle defined by points A, C and a point E, wherein E is more proximal than point C. In various embodiments, the distance between points D and A can be in the range of 1 mm to 2.5 cm, the distance between points D and B can be in the range of 0 mm to 1.5 cm, the distance between points A and E can be in the range of 0 mm to 1.5 cm, and the distance between points E and C can be in the range of 0 mm to 1.5 cm.
• As illustrated inFIG. 2(c),housing14 can include a chamber that facilitates creation of the skin flap.
• In an embodiment shown inFIGS. 4 and 5(a),housing14 can be substantially hood shaped with a configuration that allowshousing14 to function as a tissue guide and a tissue guard, or guide-guard to guide the electrode through tissue to produce a uniform plane of dissection and protect subjacent and overlying tissue layers from thermal injury as will be discussed more fully herein. Thedistal portion14dofhousing14 orhood14 can include a small recessedarea12 and the proximal portion of the hood can also include a recessedarea13, one or both of which can be substantially vertically centered on thevertical center line14vcof the hood. The two recessedareas12 and13 can be curved or rectangular in profile.
• Electrode18 can be approximately positioned in thevertical center line12vcof the recessed area with the cutting edge of theelectrode18ceprotruding distally in front ofhousing14 and out of recessedarea12 by a selectable distance (e.g. 1 to 40 mms). The electrode can be attached tohousing14 near thesides12sof the recessedarea12. The distal portion of thehand piece15dorextender22dcan be recessed under theproximal portions14pof thehood housing14 and can be attached in recessedarea13. The attachment can be viapivotal couple14copsuch as an axel that allowshand piece15 to pivot up and down with respect to thevertical center14vcof the hood. Alternatively, thehand piece15 orextender22 can be fixedly attached using a screw, nut, adhesive bond or othermechanical attachment14ammeans known in the art.
• In various embodiments,housing14 can also be configured to avoid lacerating the skin envelope including full thickness lacerations. Such lacerations are also known in the surgical arts as “button holing”. Means for avoiding skin lacerations or button holing (e.g. skin laceration avoidance means) can include one or more of the following configurations of housing14: (i) configuringhousing14 such that the distal top portions ofhousing14 are above the electrode (that is that14heheight ofhousing14 is substantially above the electrode as is discussed herein, (ii) coupling the electrode tohousing14 the such that electrode and/or electrode plane is vertically bounded by the top an bottom portions ofhousing14, (iii) positioning the electrode onhousing14 such that electrode plane or cutting plane is substantially aligned with the vertical center ofhousing14, (iv) configuringhousing14 width to be greater than the electrode width (iv) configuring the electrode ends to be bounded on either side byhousing14 and (iv) configuringhousing14 to have a sheath portion on either end of the electrode.
• One or more of these features can also be utilized to havehousing14 protect subjacent tissue from unwanted perforation, or laceration ashousing14 is advanced through tissue. Such subjacent tissue can include, without limitation, muscle, nerve, blood vessels, arteries, veins tendons and the like.
• As shown inFIG. 5(b), in an embodiment for reducing button holing,housing14 width14wcan be greater than the electrode width18wand can be further configured to have abuffer section14bson one or both electrode ends18eto bound the electrode. As shown inFIG. 5(c),housing14 can also includesheath portions14shpon either end of the electrode.Sheath portion14shpcan be configured to reduce button holing by shielding or overlying the electrode ends to keeping the electrode ends from protruding into the skin. This can be further facilitated by fabricatingsheath portions14shpfrom pliable polymers such that the sheath portions will at least partially deform when pressed into the skin envelope so as not to perforate or lacerate the skin envelope and also provide sufficient structural support and/or elastic cushioning to keep the electrode from do so.
• Suitable pliable materials forsheath portions14shpcan include silicone and polyurethane elastomers and other resilient polymers known in the art such as PEBAX. Other means for reducing button holing can include the use of insulated sections18ldisposed near the electrode ends of the electrode as is discussed herein.
• In a related embodiments shown inFIGS. 5dand5e,housing14 can be configured to allow the surgeon to advancehousing14 through the skin withhousing14 in a pitched-up fashion. In use, advancinghousing14 in a pitched-up fashion helps to protect subjacent tissue layers (such as muscle, nerve and blood vessels, etc) as well as providing a tenting of the skin visually indicating to the surgeon whereapparatus10 is at least partially under the skin and that subjacent tissues are not being dissected. In various embodiments,housing14 pitch can be accomplished by manual manipulation of thehandpiece15 and/extender22 by the surgeon such that he or she sees the skin tenting orprotuberance8tentproduced by and indicative ofhousing14 being pitched up.
• Alternatively in an embodiment shown inFIG. 5e,extender22 can include adeflectable section22defwhich the surgeon can manipulate by virtue of a actuatingmember39 ordeflection mechanism25 and an actuator15a′ on the hand piece which can be configured to allow the surgeon to deflect extender selectable amount to pitchhousing14 at a selectable angel ofattack14aawith respect to skin surface ortissue layer81Actuator15a′ can be a slide mechanisms known in the art and can include graduatedmarkings15gmindicting angle ofattack14aa.
• Also in this and related embodiments,electrode18 can be configured to be swivelable through aselectable arc18arcto have selected cuttingangle18aaby virtue of swivel orpivot mechanism18sw. Swivel orpivot mechanism18swcan be any swivel or pivot mechanism known in the art including a bearing mechanism. Also in an embodiment,swivel mechanism18swcan be coupled to an actuator15a″ on hand piece15 (by an actuating member39), whereactuator15a″ is configured to allow the surgeon to swivelelectrode18 to aselectable cutting angle18aa.
• Actuator15a″ can also be a slide mechanisms known in the art and can include graduatedmarkings15gmindicting cuttingangle18aa. In use,swivel mechanism18swcan be configured to allow the surgeon to dissect tissue along a selectedtissue plane8pd(which can be substantially parallel to a select tissue layer81) even whilehousing14 is pitched up or pitched down.
• In an embodiment shown inFIGS. 6 and 7,apparatus10 can comprise aroller17 pivotably coupled to a hand piece15 (or hand piece extender22) via anaxel17a. Thedistal end15dor22dof thehand piece15 orhand piece extender22 can be substantially crescent shaped, with sufficient clearance space15sto allow for movement ofroller17 and/or pivotal movement of thehand piece15 orhand piece extender22.Electrode18 can be attached to theroller axis17a, to thedistal end15dof thehand piece15 or thedistal end22dof thehand piece extender22.
• In either configuration, the electrode and roller are in a fixed vertical relationship with each. The electrode can be positioned distally in front of the roller and preferably is substantially vertically aligned with the center ofroller17cen, but can also be positioned above or below the roller center. The electrode is positioned far enough in front of the roller to allow the developing skin envelope to slide over the roller after dissection by the electrode.
• In various embodiments, this distance known as theelectrode gap distance18gd, can be 1 to 40 mm.Roller17 can be configured to roll or advance subcutaneously over underlying tissue by the application of force fromhand piece15 andadvance electrode18 through tissue (such as subcutaneous tissue) to uniformly dissect a plane ofdissection8pd.
• As described herein, in various embodiments,housing14 can be configured to act as a tissue guide for advancing the electrode through tissue to produce a substantially uniform plane ofdissection8pdand also as guard to protect tissue and tissue layers81 above and below the plane of dissection. In these embodiments,housing14 can thus be a tissue guide-guard for performing uniform depth tissue flap dissection using an energized cutting means such an RF electrode. The above lying protected tissue layers can include the skin envelope including the dermal and sub-dermal plexus. The subjacent protected tissue can include nerves, muscle, tendon, arteries, veins and the like.
• As a tissue guide,housing14 can be configured to guide and stabilize the electrode through tissue to produce a plane ofdissection8pdhaving a uniform depth ofdissection8dd. More specifically it can be configured to function as a guide for generating a uniform depth ofdissection8ddduring a minimally invasive procedure to undermine or dissect selected tissue layers81 such as theskin envelope8seusing an electro-cautery cutting electrode18 or other energy delivery device configured for tissue dissection or cutting.
• The guiding function ofhousing14 is to guide the electrode through tissue and control the dissection depth and thetissue flap thickness8tcan be accomplished by a variety of means including the shape, structure and material and mechanical properties ofhousing14. For example, as described herein, thedistal portion14dofhousing14 can have a curved shape configured to facilitate smooth advancement of the dissectedskin envelope8seover the top ofhousing14. This reduces the frictional and other forces, which may act onhousing14 to push the electrode and thus theelectrode plane18peup or down and out of the selected plane ofdissection8pd.
• In other embodiments the guiding function ofhousing14 can also be accomplished by configuringhousing14 to function to stabilize the plane of theelectrode18pe(which substantially defines the plane of dissection) relative to the selected plane ofdissection8pdsuch thatelectrode plane18pedoes not substantially pitch up or pitch down into tissue ashousing14 is advanced or otherwise moved through tissue. This stabilization function can be accomplished through several means. First the plane of theelectrode18pecan be configured to resist tissue applied forces tending to deform its shape through the use of rigid materials forelectrode18 and/or strut members19 (described herein) coupled to the electrode andhousing14 or aroller axel17adescribed herein.
• Housing14 can be configured to resist or otherwise attenuate tissue applied forces causing the electrode plane to dip down or dip up. Referring now toFIG. 8, this can be accomplished by configuringhousing14 to act as a counterbalancinglever arm14cla(at the point wherehousing14 couples to the electrode such as the roller axel) to counter balance downward or upward tissue applied forces (or other forces) on the electrode. This in turn can be accomplished by configuringhousing14 to have sufficient length14land/or shape such that normal forces from tissue onhousing14 will counteract tissue applied forces on the electrode. In such embodiments the length ofhousing14 can be between ¼ to 4 inches.
• Housing14 can have sufficient mass and/or length relative to the distance the electrode projects in front of housing14 (also calledelectrode gap distance18gddiscussed herein) such that tissue applied forces and resulting torque or moment on the electrode will not be sufficient to overcome the counterbalancing torque/moment forces ofhousing14. In embodiments the mass ofhousing14 can exceed that of the electrode by a range of ratios from 1:10 to 1:100 and the length ofhousing14 can exceed that of the electrode plane by a ratio range of 1:5 to 1:100. Alsohousing14 can be configured to stabilize the electrode by having a center ofmass14cm(that of housing14) located substantially at itsgeometric center14gcor in a selected axis (e.g. x, y or z).
• In other embodiments, stabilization can be achieved by configuringhousing14's center ofmass14 cm to be located below housing14svertical center14vcin a range of about 5 to 99% of half ofhousing14height14htwith specific embodiments of 10, 25 and 75%.
• Referring now toFIGS. 9-12 (showing embodiments of a stabilizing element) in other embodiments, stabilization of theelectrode plane18pecan be achieved by means of a stabilizingelement27 positioned proximally tohousing14 and coupled tohousing14 or theroller axis17a. Similar to the description above, the stabilizing element serves to provide a counter balancing torque or moment arm opposing forces on the electrode orhousing14 causing theelectrode plane18peto pitch up or down.
• In an embodiment, stabilizingelement27 can be substantially planer having athickness27tthinner than thethickness14tofhousing14 orroller diameter17d, and having aplane27pthat this is substantially parallel to theelectrode plane18pe. Stabilizingelement27 can have a variety of shapes including, square, rectangular, rectangular with radiused edges, circular, semicircular, or fin-shaped.
• In an embodiment shown inFIGS. 9 and 10 the stabilizingelement27 can comprise a flat rectangular section positioned proximally (e.g. behind)housing14 orroller17. The element can be coupled to theroller axel17aor theproximal section14pofhousing14. In another embodiment, shown inFIGS. 11aand11belement27 can be a substantially U-shaped section positioned proximal tohousing14 orroller17, with the apex of theU27a, pointing away from the back (proximal direction) ofhousing14.
• In yet another embodiment shown inFIG. 12, the stabilizingelement27 can be positioned between afirst roller17fand asecond roller17s. In a related embodiment, stabilizingelement27 can comprise a connectingsection27csbetween the two rollers. In a related embodiment, the stabilizingelement27 can comprise a stabilizingstrut member27mconnecting the first roller to the second roller.
• In various embodiments, thethickness27tof the stabilizing element can be in the range of 0.05 to 0.5 inches with specific embodiments of 0.1, 0.2 and 0.3 inches. Also the ratio of the thickness of the stabilizing element to the thickness/height ofhousing1414hordiameter17dofroller17 can be in the range of 1:1 to 10:1, with specific embodiments of 2:1, 4:1 and 6:1.
• Element27 can be fabricated from biocompatible polymers known in the art and described herein. In an embodiment,element27 can be fabricated from low friction materials or have alubricous coating27csuch as TEFLON® or other PTFE known in the art. In use the stabilization element, by stabilizing the electrode plane, helps the surgeon maintain a uniform depth of dissection as the electrode andhousing14 are advanced through tissue.
• Referring now toFIGS. 13aand13b, in various embodiments, thegap distance18gdbetween the electrode and the roller and or between electrode and upper distal end ofhousing14udecan be configured to control or facilitate control of thethickness8tof the skin envelope or tissue flap and/or thedissection depth8dd. The distance between the electrode andhousing14 can be in the range of 0.05 to 1 inch with specific embodiments of 0.1, 0.2, 0.25, 0.3. 0.5 and 0.75 inches. Smaller gaps can be employed for procedures utilizing smaller tissue flaps thickness and larger gaps for procedures using large flap thickness. Preferably, but not necessarily,electrode distance18gdheight is less thanheight14he(the height ofhousing14 above the electrode) and forembodiments using rollers18gdis less than theradius17rof17 roller (or less than thediameter17dfor upper roller embodiments). Alsoheight14hecan be configured to have the top ofhousing14 high enough above the electrode to minimize button holing ofapparatus10 through the skin envelope (as discussed herein). In various embodiments this can be accomplished with aheight14hein the range of 0.25 to 2 inches with specific embodiments of 0.3, 0.5, 0.75, and 1.5 inches.
• In related embodiments,flap thickness8tand/or the depth ofdissection8ddcan also be controlled by manipulation of (i) the ratio of thegap distance18gdto distance14he, defined as the gap to height ratio and/or (ii) the ratio ofdistance18gdto theradius17r(or less than thediameter17dfor upper roller embodiments) ofroller17, defined as the gap to radius ratio. In various embodiments, either of these two ratios can be in the range of 1:1 to 1:10 (i.e., the radius of the roller is 10 times greater than the electrode gap distance) with specific embodiment of 1:2, 1:4, 1:5 and 1:7. In addition, control of the depth of dissection and skin flap thickness manipulation of one or both of these ratios, can be used to control or affect (i) the amount of conductive heat transfer to the dissected skin envelope/tissue flap, (ii) temperature of the dissected skin envelope/tissue flap, (iii) the amount of tightening of the skin envelope, (iv) the tension of the nascent skin envelope and (v) the amount of cutting or separation force applied to tissue at the plane of dissection. Large ratios will more readily push the nascent skin envelope away from the electrode after dissection and thus reduce the amount of conductive heat transfer to portions of the envelope (from RF energy delivery) and also provide a thermal shielding to the envelope/tissue flap. Larger ratios may also by used to produce more of a cutting or wedge affect in the tissue.
• Referring now toFIGS. 14-18 (illustrations showing embodiments having trans-cutaneous markers), in another approach for facilitating control of dissection depth and flap thickness in various embodiments,housing14 can have one ormore ridges21r, protuberances or bumps21borpatterns21pbof bumps having a substantially parallel orientation (or other selected orientation) to thelongitudinal axis14laofhousing14 as shown inFIG. 14. The ridges or bumps can be configured as trans-cutaneous markers21 to provide trans-cutaneous visualization of one or more of the following: (i) the depth of dissection, (ii) the width of the dissection plane, and (iii) the path of the plane of dissection. In related an embodiment shown inFIG. 15,roller17 can have one ormore ridges21ror bumps21bconfigured as trans-cutaneous markers to provide similar visualizations.
• As shown inFIGS. 16aand16b, the pattern ofbumps21bpcan include different patterns of bumps (for example afirst bump pattern21bp′ such as a square and asecond bump pattern21bp″ such as a circle) havingdifferent heights21h′ and21h″ corresponding todifferent dissection depths8dd, to provide the physician with a real time visual indication of the depth of dissection, including any variations in the desired depth ashousing14 is advanced over the selected tissue plane. In use, these and related embodiments can be configured to provide the physician with both a qualitative and quantitative indication of the depth of dissection. In related embodiments, the height of the ridges or bumps can be adjustable to allow the physician to have trans-cutaneous visualization of pr at different depths of dissection. This can be accomplished using an adjustment means21aknown in the art including a setscrew, ratchet, swage fitting, locking device, clamp and the like.
• In various embodiments, the shape of the visualization bumps21bscan include round, square, diamond oval triangular and combinations thereof. In an embodiment shown inFIG. 17, different bump shapes can havedifferent heights21h, which correspond todifferent dissection depths8dd. Specifically bumps21 can include afirst bump21b′ having afirst height21h′ andsecond bump21b″ having asecond height21h″. For example, a diamond shape bump could have a height that correspond to a dissection depth of 4 mm and round shaped bump could have a height that corresponds to a dissection depths of 8 mm. In use these and related embodiments ofhousing14 having a pattern-height specific visualization bumps21 allows the surgeon to readily discern the dissection depth as well as changes there to without having to palpitate the skin, endoscopically view the plane of dissection or remove the device from the tissue site. Further these and related embodiments can also allow the surgeon to readily discern the slope ofhousing14 advancement and thus readily make adjustment to maintain the plane of dissection or change it if so desired without having to remove either hand from the hand piece. This in turn provides for a greater degree of control of the dissection procedure.
• Also in an embodiment shown inFIG. 18,housing14 orroller17 can have a pair of markingridges21mr, corresponding approximately todissection width18wdof the electrode to provide a visual bracketing or cue of thewidth8wdof the plane of dissection. In a related embodiment,housing14 or roller can include athird ridge21rcwhose position corresponds to the lateral center18cof the electrode, to provide an indication of thecenter line8clof the plane of dissection. In another embodiment, the guard/guide components ofhousing14 can be configured to mimic the visual impression that a surgical instrument, such as Metzenbaum scissors, make on the skin surface during the dissection process.
• Referring now toFIGS. 19a-19band20a-20b(Figures illustrating an embodiment having a detachable section or movable or variable shaped contour). In various embodiments, the shape, contour or height ofhousing14 can be selectable and can be adjustable using an adjustment mechanism known in the art such as a telescoping mechanism or articulated mechanism or using a variablesize roller device17. Also in various embodiments, the electrode housing can have different widths and different dissection depths. The width14wand/ordissection depth8ddofhousing14 can be pre-selected or adjusted depending on the surgical application (e.g. cutting into dermal, fascia or fat tissue, face lift etc). In various embodiments, thedissection depth8ddcan be in the range of 0 to 2 inches with specific embodiments of 0.1, 0.2, 0.25, 0.5, 0.75 and 1.0 inches.
• An embodiment for adjusting the height or other dimension ofhousing14 can include a detachable section orshim14ds.Detachable section14dscan attach to the bottom14b, top14tor other area ofhousing14 using a snap fit, spring loaded latch or otherreversible detachment mechanism14dmknown in the art.Detachable section14dscan be of varying height, but can otherwise have the same dimensional footprint or profile ashousing14. In various embodiments, all or portions ofhousing14 can bevariable shape portions14vsconfigured to be variable in shape, contour and/or dimension. Means for varying the shape and dimensions ofhousing14 can include configuring portions ofhousing14 to be expandable or include an integralexpandable member14im(such as expandable balloon described herein and also known in the medical device arts) or use of a lifting or force generatingmechanism37 such as a spring, cam or lever that is integral or otherwise disposed withinhousing14.Expandable member14imcan be configured to be operator actuable viadevice15awhich is coupled to aninflation device24idwhich can bepressure source24p.
• Liftingmechanism37 can also be configured to be operator actuable via mean of a control wire, rod or other actuatingmember39 coupled to thehand piece15 via anactuating device15a. Inembodiment actuating device15acan be a slide, thumb switch, rocker arm and the like. In embodimentforce generating mechanism37 can also comprisedeflection mechanism25 described herein.
• In various embodiments, variable shapedportions14vscan be configured to control or alter one more of the following parameters: (i) change theelectrode gap distance18gd, (ii) change the height ofhousing14, (iii) change the height ofhousing14 above the electrode, (iv) change the contour ofhousing14 for example increase or decrease an amount of taper or concavity (v) change the angle at which the skin envelope slides overhousing14, (vi) change the height of the nascent dissected skin envelope abovehousing14, (vi) change the distance between the newly dissected superior and inferior tissue layers, (vii) change the amount of tension in the developing skin envelope, (viii) change the stabilizing function ofhousing14 and (ix) change the wedge or tissue separating qualities ofhousing14. Manipulation of one or more of these parameters can in turn allow the physician to vary the shape ofhousing14 to control one or more of (i) tissue flap thickness, (ii) the angle of the plane of dissection, (iii) the amount of heat transfer to the selected portions of the skin envelop/tissue flap and the associated temperature of those portions, (iv) the amount of thermal conductive tightening of selected portions of the skin envelope/tissue flap and (v) the amount of thermal injury of selected portions of the skin envelope/tissue flap.
• For example, in an embodiment shown inFIGS. 20aand20b(drawing showing use of a variable shapedhousing14 to expand or contract an insulatory pocket between the electrode and the skin envelope) tissue expandablevariable shape portion14vscan be used to vary theheight14hofhousing14 to vary thevertical distance14dsebetween theelectrode18 and where the nascent skin envelope/tissue flap8sefirst contacts the top ofhousing14tso as to create, increase or decrease an insulatory space or pocket81pbetween the electrode and the developing skin envelope/tissue flap. This serves in turn to decrease or increase the amount of conductive heat transfer to the skin envelope which can be used to control the amount of collagen contraction and/or thermal injury of selected portions of the skin envelope.
• Referring now toFIGS. 1-4,13,21,22aand22bin various embodiments, the guarding function ofhousing14 can be configured to protect the dermal and sub-dermal vascular and neural plexus or other selected layer of the skin envelope or tissue flap from thermal injury and/or necrosis directly or indirectly resulting from the delivery of energy from electrode18 (or other energy delivery device) during the dissection procedure. This is accomplished by configuringhousing14 to shield, insulate or otherwise distance portions of the skin envelope or tissue flap from RF current and/or thermal current (e.g. via conduction heat transfer) resulting from RF energy delivery to the target tissue site8 (e.g. the plane of dissection).
• One or more of these functions ofhousing14 can in turn be accomplished through selection of one or more of the shape, dimensions, mechanical and material properties ofhousing14. For example, in an embodiment shown inFIG. 4, the top ofhousing14tcan have a curved or curvedtapered shape14csat or near itsdistal portion14dthat is configured to guide or direct thenascent skin envelope8seoverhousing14 and away from theelectrode17. By directing the skin envelope in the manner, the shape ofhousing14 reduces the amount of heat transfer from the electrode to the skin envelope after dissection.
• This skin envelope/tissue flap directing function can also be facilitated by selection of theelectrode gap distance18gddescribed herein. Theelectrode gap18gddistance can be adjusted (by electrode advancement means described herein) for variations in flap thickness, tissue type and tissue mechanical properties (e.g. bending modulus) to optimize flap/envelope slide over. For example, electrode gap distance can be increased for more rigid tissue (e.g. cartilage or muscle one versus adipose tissue) and similarly, the degree of curvature ofsection14cscan be decreased (e.g. the radius of curvature is increased). In various embodiments, electrode gap distance can be adjusted between 1 and 60 mm.
• In an embodiment shown inFIG. 21 (embodiment ofapparatus10 with a roller positioned at top of housing14), the skin envelope sliding process (and thus the shielding function of housing14) can facilitated by the placement of aroller17 on the distalupper portion14duofhousing14 above and proximal to the electrode. Theroller17 serves to reduce friction betweenhousing14 and the skin envelope. In embodiments shown inFIGS. 4 and 22a, reduced friction betweenhousing surface16 and the skin envelope and thus smooth slide over can also be facilitated by use of alubricous coating14lcover the top14tor other portions ofhousing14, particularly the distal top portions to reduce friction betweenhousing surface16 and theskin envelope8se.
• The shielding function ofhousing14 can also be facilitated by configuring the distal14dandtop portions14tofhousing14 surface to have a thermally and electrically insulative coating14icdescribed herein which can be configured to shield the nascent skin envelope from direct ohmic heating by the electrode as well as conductive heating from one or more of the electrode, tissue vapor and heat of the surrounding tissue (seeFIGS. 4 and 22b).
• Referring now toFIG. 23-25 (Figure showing embodiments ofhousing14 having fluid distribution ports) In various embodiments, the tissue protective or shielding function ofhousing14 can also be accomplished by the delivery of cooling fluid through one or more fluid distributions ports orapertures33 as is shownFIG. 23.Apertures33 can be fluidically coupled to one ormore lumens24′ and can be configured (by virtue of their size and shape) to ooze, infuse or spray a coolingfluid29 to the cool all or selected portions of the overlying skin envelope/tissue flap and/or underlying tissue (e.g. muscle) as well. This and related embodiments can be configured to produce a reverse thermal gradient in the skin envelope or tissue flap. That is subjacent layers/or structures in contact with the cooling solution such as the dermal-subdermal plexus are cooled while the overlying collagen containing layers such as the dermis are at a selected elevated temperature due to conductive heat transfer from RF energy delivery fromelectrode18.
• In this way, embodiments using cooling solution can allow for collagen contraction of the dermis and, hence skin tightening, while preventing or minimizing damage of the dermal and sub-dermal plexus and thus facilitates or helps to maintain the viability of the newly dissected skin envelope or tissue flap both in the short after it is reattached and in the long term. Thus embodiment using cooling solution can be configured to improve the postoperative viability of the tissue flap or skin envelope. Moreover, embodiments ofapparatus10 and methods of the invention that employ cooling of the skin envelope via cooling solution or other cooling means can also be utilized to reduce the incidence of one or more post operative complications such as tissue necrosis, nerve or sensation loss, infection, skin discoloration or un even coloration which can occur due to damage of sub-dermal dermal plexus.
• Apertures33 can be positioned throughout the surface ofhousing14 includingtissue contact surface16, singularly or in selectable patterns such as a substantially circular or linear pattern. In oneembodiment apertures33 can be configured and distributed on the surface ofhousing14 to produce afilm29fof coolingfluid29 that oozes or wicks out of the apertures and cools the skin envelope by combination of convective and conductive cooling.Film29fcan also be configured as a lubricous film that reduces the friction ofhousing14 with overlying and underlying tissue layers and thus facilitates smooth advancement ofhousing14 between tissue layers during dissection process or positioning ofhousing14 within the tissue pocket.
• All or portions ofapertures33 can also be configured asnozzles33nto spray cooling fluid (which can be a liquid or a gas) onto the skin envelope and/or onto portions ofelectrode18. In aparticular embodiment apertures33 ornozzles33ncan be positioned on thedistal portions14dofhousing14 so as to infuse or spray cooling solution onto the electrode to cool the electrode or otherwise prevent the buildup of charred tissue on the electrode. In another embodiment apertures ornozzles33ncan be positioned on the top and/or top distal portions ofhousing14 to infuse or spray cooling solution onto the skin envelope or tissue flap which is in close proximity to the electrode so as to cool the skin envelope/tissue flap immediately or near immediately after it is dissected from underlying tissue layers.
• In a related embodiment shown inFIG. 24,apertures33 can positioned or otherwise directed to infuse or spray cooling solution onto the skin envelope or tissue flap at a selectable distance proximal from the electrode. In use this configuration can allow the skin flap to continue to be heated or otherwise remain at an elevated temperature (e.g. cook) for a selectable time sufficient to cause thermal collagen contraction but stay below a level of thermal injury to damage the subdermal plexus. Inrelated embodiments apertures33 ornozzles33ncan also be configured to provide irrigation within the pocket ofdissection8pdand/or surrounding tissue layers to remove debris and blood and assist in endoscopic visualization.
• In various embodiments,apertures33 can be substantially round, oval or other shape and can be produced by molding, machine drilling, laser drilling and like methods known in the medical device arts.Apertures33 can have adiameter33din the range of 0.0001 to 0.5 inches with specific embodiments of 0.001, 0.005, 0.01, 0.05, 0.1 and 0.25 inches. Larger aperture diameters can used for infusing embodiments and smaller diameters for oozing embodiments. For oozing embodiments,apertures33 can have adiameter33din the range 0.001 to 0.01 inches.Aperture33 can also be configured for the delivery of other fluids as well such as electro-conductivity enhancing solutions (e.g. saline), medicament solutions (e.g. anesthetics), irrigating solutions, and other solutions used in plastic surgery procedures.
• In an embodiments shown inFIG. 25,apertures33 can also comprise a porous section33P coupled to surface ofhousing14 and fluidically coupled to one ormore lumens24′. Porous section33P can be configured (by virtue of their porosity, and wetting characteristics) to ooze orwick fluid29 including afluid film29f. In an embodiment, porous section33P can be made from a porous polymer membranes or polymer foam known in the art such including but not limited to knitted polyester, continuous filament polyester, polyester-cellulose, rayon, polyamide, polyurethane, polyethylene and the like. Suitable commercial products include, (i). OPCELL available from Centinal Products (Corp., Hyannis, Mass.), (ii). ULTRASORB, HC4201 or HT 4644 MD available from Wilshire Contamination Control, (Carlsbad, Calif.) and polyethersulfone membranes (SUPER MEMBRANE) manufactured by the Pall Corporation (Ann Arbor, Mich. or East Hills, N.Y.).
• Referring now toFIGS. 26-28, inother embodiments apparatus10 can be configured to dissect tissue in deeper planes of dissection than the dermis or superficial fascia. In one embodiment,apparatus10 can be configured to produce a plane ofdissection8pdas deep as the muscle facial layer or deeper. In an and related embodiment shown inFIG. 26,housing14 can include tworollers17 or fourwheels17w.Hand piece15 is pivotally coupling either directly tohousing14 atpivotal coupling14pcopor indirectly via the coupling ofextender22 tohousing14 atpivotal coupling14pcop. Thepivotal coupling14pcopcan be configured to allow the hand piece and extender to swing through and arc of 180° or greater whilehousing14 is located within the tissue pocket and under one or more tissue layers. Portions of the extender or hand piece, such asdistal portions15dand22dcan be configured to bedeflectable portions15defor22defvia means of anactuation member15am(e.g. pull wires and the like) orother deflection mechanism25
• In use, deflectable embodiments of the hand piece or extender can be configured to allow the surgeon to gain access to obstructed or difficult to reach target tissue layers by deflecting the extender or hand piece around the obstruction (e.g. bone, blood vessels, cartilage, organs) and still transmit axial force to advancehousing14 through an embodiment of method for doing a deeper tissue dissections is illustrated inFIG. 28 hereapparatus10 can be utilized to produce a deep plane of dissection to dissect the glandular breast tissue from the Pectoralis Fascia. In this embodiment, dissection of the fascia can be initiated at atissue perimeter8tpwhere the skin envelope or tissue flap merges directly merges with the muscle fascia layer. This dissection of the muscle fascia can be done after or before the skin envelope is dissected from the tissue site. Embodiments of this method can be utilized for one or more of a skin sparing mastectomy, lumpectomy or even biopsy procedures. They can be utilized for skin sparing implant procedures of pace makers; cardiac device battery, power packs, energy converters, or control devices; or insulin pumps and the like in the breast, pectorolis or even other regions such as the abdominal regions through the selected tissue plane.
• In related method embodiments shown inFIGS. 29aand29b,apparatus10 can be configured to dissect fascial layers by several different approaches. One method is to start the facial dissection at a tissue perimeter where the fascia and the dermal layer/subcutaneous layers converge such as the perimeter of the breast. Another approach is make an angled dissection or cut down to the deeper layer using the transcutaneous markers to assess thedissection depth8ddand the angle; the third approach is to make an incision down to the fascia or deeper tissue layer and then insert or advancehousing14 through incision to facial layer. In an embodiment,housing14 can be inserted vertically through the incision and then pivoted or reoriented to a horizontal position on the selected tissue layer to be dissected using a pull/push wire or rod15wor other actuatingmember15am(orother deflection mechanism25 known in the art) disposed withinextender22 orhand piece15 and operable byactuator15aon or coupled to the hand piece.
• Pivoting ofhousing14 can be configured to occur atpivotal coupling14copor other point. In a related embodiment using this approach (advancement through an incision), embodiments ofapparatus10 having adeployable housing14 can be utilized wherebyhousing14 is advanced through the incision in a non deployed state and then deployed to the deployed state (using a deployment mechanism described herein or known in the medical device arts such as a pull wire or deployable balloon) once the selected tissue layer is reached. Also in embodiments for doing deep plane dissection all, or portions of electrode(s)18 can be wedge shaped (as described herein) to assist in applying force to initiate can continue the plane of dissection.
• Referring now toFIG. 30a-30cembodiments are illustrated showing use ofapparatus10 with a port device. In various embodiments, for doing deep plane dissection or even skin enveloped dissection,apparatus10 can be configured to be introduced through a surgical port, sheath or other introducingdevice30 known in the art.Port30 can be configured to facilitate access and positioning ofapparatus10 within thetissue pocket8dpat thetarget tissue site8. This can be facilitated by fabricating all or portions ofport30 from lubricous biocompatible materials known in the art such as PTFE.
• Port30 can also be configured via itsshape30sand size to help initiate or define thedissection pocket8dp. The port opening30ocan have a sufficient shape and diameter to allow passage ofextender22 and/orhand piece15 and an endoscope, suction tube or laproscopic or surgical instrument The opening30oofport device30 can configured to have an entry diameter30din the range of 0.25 to 5 inches with specific embodiments of 0.5, 1, 2.5 and 4 inches. Also port opening30ocan have a variety of shapes including circular, semicircular, crescent, oval, square, rectangular and the like. In an embodiment, the port opening can include a openings30oincluding a first port opening30o1 and a second opening30o2. The first opening can be configured for the introduction of a first device such asapparatus10 and the second opening can be configured for the introduction of a second device such as an endoscope.
• Port30 can also be configured to stabilize unwanted movement of the extender or hand piece in one or more axises. This can be accomplished by selecting the entry diameter30dto be slightly larger (e.g. by several mms) than the extender orhand piece diameter22diaand15dia. It can also be accomplished through selection of the shape of the port opening30o. In an embodiment shown inFIG. 30c,port30 can have a substantially rectangular or slot shaped opening30ohaving athickness30tclose to that of the extender orhand piece diameter15diaor22diaso as to substantially limit movement of either (and subsequently housing14) in a direction parallel to the longitudinal axis301aof opening30o.
• In other methods embodiments,apparatus10 can be utilized to perform deep plane dissection for various procedures to create a full thickness subcutaneous flap by dissecting the deep aspect of the subcutaneous tissue (e.g. adipose tissue) from the subjacent muscle fascia. The deeper plane of dissection can be reached using one or more of the three approaches described above. In such embodiments trans-cutaneous markers21 can be configured or adjusted to a selectedheight21hsufficient to indicate theproper dissection depth8ddand/or when the desired plane of dissection has been reached. This depth can be determined by making an incision (at or near the target tissue site) down to the desired tissue layer and then measuring the proper dissection depth. Themarker height21hcan then be adjusted accordingly accounting for the height ofhousing14. In use, this approach compensates for variations in thickness in one or tissue layers including subcutaneous adipose tissue.
• Other surgical method applications for utilizingembodiments apparatus10 for doing deep plane dissection (e.g. to the facial or deep layers) can include, without limitation, abdominoplasty, buttock lift, thigh lift, subglandular breast augmentation with endoscopic visualization (through the axilla or umbilicus).Extender length221, electrode andhousing14 size can be sized to the needs of each procedure. In these andrelated embodiments apparatus10 can be used to generate a plane ofdissection8pdby being configured to advance or mow over the muscle fascia or other desired subjacent tissue layer. Accordingly in these and related embodiments,apparatus10 can include one ormore rollers17 and apivotable hand piece15 orextender22, configured to allowhousing14 or roller to make multiple passes over the selected plane of dissection. Once the surgeon is finished going in one direction he/she can use the hand piece or extender towithdrawal housing14 back over the selected plane in the opposite direction and make additional passes on the same tissue path or start a new tissue path. In use, this configuration allows the surgeon to go back over the dissection plane as many times as he or she desires to do one or more of the following: (i) smooth out the plane of dissection, (ii) widen the width of dissected skin envelope or other tissue flap; (iii) go back over the dissection plane to coagulate any bleeding tissue or vessels, (iv) deliver additional amounts of heat to the skin envelope or selected tissue flap to titrate the amount of collagen contraction and resultant skin tightening.
• Referring now toFIG. 31a-31cother embodiments provide methods and apparatus to provide a uniform surgical release and mass shifting of overlying soft tissue structures from subjacent tissue structures by uniformly dissecting the overlying structures from the underlying tissue. The uniform surgical release of soft tissue creates a separation interface or uniform plane of surgical dissection which allows for mass shifting of soft tissue in a uniform fashion. A related embodiment also provides a means to surgically shift soft tissue through smaller, lessvisible incisions8 is. This skin is then shifted to a more aesthetically pleasing location.
• In related embodiments,apparatus10 can also be configured and used to surgically alter or facilitate the surgical alteration of the subjacent soft tissue or tissue structure underlying the skin or the dissected skin envelope.
• This can be done usingapparatus10 to dissect and release one or more tissue flaps that lie within or include the soft tissue structure to be modified or portions (e.g. layers) thereof using methods described herein. Such tissue flaps can include without limitation, the dissected skin envelope, cutaneous flaps (the skin and subcutaneous tissue), subcutaneous flaps, fasciocutaneous (the fascia, the subcutaneous layer and the skin) myocutaneous flaps, fascial subcutaneous flap (includes subcutaneous fat layer and the fascia, but not the skin) and myofascial-subcutaneous flaps (these include subcutaneous tissue or portions of it, the fascia and the muscle, but not the skin; subcutaneous means below the skin but above the fascia). The subjacent soft tissue structure can be shifted by plication where a flap is not raised but instead the tissue is tightened by stapling or suturing of adjacent tissue together.
• After theflap8fis released it can then be advanced to the desiredattachment site8a, the redundant tissue is excised and the flap is attached using surgical staples, mooring sutures or other surgical attachment means or procedure known in the art. Alternatively the excised skin need not be removed but can be folded or otherwise hidden within the attachment site depending on its size and shape. In an embodiment,apparatus10 can be configured to allow such attachment withapparatus10 in place or it can be removed. For the former case, this can be accomplished by configuringapparatus10 to allow the passage in the dissection pocket of one or more surgical instruments over or through the apparatus. For example, instruments can be advanced through one ormore lumens24′ which can have sufficient diameter for the passage of such instruments including endoscopic or laproscopic surgical instruments known in the art. For deployable embodiments of apparatus/housing10,apparatus10 can be put in the non-deployed state (or at least partially) to allow passage of appropriate surgical instruments.
• In various method embodiments,apparatus10 can be used to dissect a tissue flap using an incision and/orattachment site8 is,8athat is more removed from the target tissue site to be reconstructed than is typical for standard face lift and other flap dissection related surgical procedures. This in turn allows for the incision and/or attachment site to be placed in a location that is hidden or less visible such as the scalp. Further in,apparatus10 can also allow for the incision site to be much smaller and less obtrusive than current facelift and other flap dissection related surgical procedures.
• In various method embodiments,apparatus10 can be configured to dissect a tissue flap or skin envelope than can be re-attached via the use of mooring sutures. More specifically, mooring sutures can be used to moor or secure the dissected skin envelope down to the subjacent soft tissue structure with or without skin excision. Sutures are placed on the deep surface of the dissected skin envelope to secure or moor the advanced skin envelope to the deeper structures. The mooring suture is placed in the deep surface/or deeper aspects of the dissected skin envelope and secured down to the deeper structures. The sutures are placed just proximal to point of redundancy in the dissected skin envelope to hold it down in place at the point. This procedure serves to maintain the level of surgical advancement of the skin envelope or tissue flap and thus the aesthetic correction or new shape of the skin.
• Turning now to a further discussion ofhousing14 and with reference toFIGS. 2-5 and32-33, in various embodiments,housing14 can be fabricated from any number of medical polymers known in the art such as thermoset, or moldable polymers such as ABS, acrylic, polycarbonate and the like and other medical polymers known in the art. Also all or portions ofhousing14 can also be made from materials having high dielectric strength and thermal resistance such as Ultem® 1000, available from the General Electric Corporation. Alsohousing14 can be disposable and can include a tissue contact layer orsurface16 which can include one or morefluid distribution ports33.Surface16 can also be fabricated from material that is both thermally resistant and has a high dielectric strength.Surface16 can also be configured to substantially atraumatic and can be made from biocompatible biomaterials known in the art.
• Also in an embodiment all, or portions, ofhousing14, includingtissue surface16 can have acoating14cwhich can be aninsulative coating14ic, an electricalconductive coating14ec, alubricous coatings14lcor a thermallyreflective coating14trc. These and other coatings can be applied using dip coating, spray coating, electro-deposition, plasma coating, lithographic and other coating methods known in the art.
• For purposes of this application, an insulative coating is defined to be both an electrical and a thermal insulative coating. In an embodiment,housing14 has aninsulative coating14icthat insulates against the transmission of RF energy.Coating14iccan be made from electrically and thermally insulative polymers known in the art including, but not limited to, TEFLON®, PTFE and other fluorocarbons known in the art, polyamide, polyamide and copolymers thereof. Such coatings can range inthickness14ctfrom 0.0001 to 0.1 inches, which in an embodiment can be 0.001 to 0.003 inches
• In a related embodiment, coating14ccan be a non-stick orlubricous coating14lcconfigured to keep surface16 (or other portion of housing14) from sticking to tissue in thedissection plane8por theskin envelope8sebefore during or after, RF energy delivery (e.g. cutting) and/or advancement ofhousing14. Such coatings can include PARALENE, PTFE, TEFLON® and other fluorocarbon polymers, silicones, and other low surface tension non-stick coatings known in the art.
• In still other embodiments coating14ccan be a patternedcoating14pcconfigured to increase the coefficient of friction withtissue layer81 in one or more directions. In particular embodiments patterned coating14pccan be a directionally biased pattern coating configured to increase the coefficient of friction in one direction and serve to stabilize or limit the movement ofhousing14 in that direction. In an embodiment shown inFIG. 32, coating14pccan be a direction pattern coating14dpcconfigured to have an increased coefficient of friction with respect to thelateral axis14lataof housing14 (i.e. a lateral friction bias) but still permit free movement in the longitudinal direction.Coatings14dpcconfigured in this manner provide a lateral stabilization function, that is they serves to stabilize or reduce side to side movement ofhousing14 during movement ofhousing14 over or through tissue. Furthersuch coating14dpccan also be configured onhousing14 to provide a lateral stabilization function to the developingskin envelope8seto facilitate its sliding overhousing14 in a longitudinal direction with reduced or minimal lateral movement of the envelope. This can be accomplished by havingdirectional coating14dpcontop portions14tofhousing14. Coating orpattern14pccan also be configured to be substantially tissue atraumatic. This can be accomplished through the use of biocompatible materials described herein such as PTFE or silicone.
• Suitable patterns for a directional coating can include a pattern ofridges14randchannels14choriented parallel to thelongitudinal axis14laofhousing14 as shown inFIGS. 33aand33b.Ridges14rcan have aheight14rhfrom 0.001 to 0.025 inches with specific embodiments of 0.002, 0.005, 0.01, 0.05 and 0.1 inches. Also the distance between ridges orchannel width14chw, can be 0.0005 to 0.2 inches with specific embodiments of 0.001, 0.002, 0.005, 0.01, 0.05 and 0.1 inches. Suitable pattern coating materials can include polyethylene, HDPE, LDPE, polyurethane, acrylic and silicone.Ridges14rcan be formed using hot stamping or polymer molding methods known in the art.Ridges14rcan be flexible and can be fabricated from elastomeric polymers such as silicone and other resilient polymers known in the art.Ridges14rcan also have acurved tip14rt. Also thechannel width14chw, can be sufficient to allow tissue to press into the channels so as to be able to exert a normal force against thelongitudinal axis14laofridges14rand in turn exert an opposing lateral force in response to lateral movement ofhousing14. This opposing lateral force can configured to stabilizehousing14 in the lateral direction. In an embodiment,channel width14wchcan be 0.0005 to 0.01 inches.
• Housing14 can have a variety of shapes depending upon the medical application or procedure. Referring now toFIGS. 34a-34e, in various embodiments,housing14 can be disc, square, rectangular, spherical, semi-spherical shaped or crescent shaped and combinations thereof. In an embodiment,housing14 can be rectangular shaped having side radiusededges14reand a top raisededge14tewhich can be radiused or not. Alternatively,housing14 can be disc shaped again having a radiusedperimeter edge14reand one or more raisedtop edge14tewhich is substantially straight. In either embodiment, the distance between the two top edges14wcan be configured to be greater than the working or cutting width18wofelectrode18. In anembodiment housing14 width and widths14wand18wcan be configured to be provide a buffer space ofhousing14 on either end of the electrode. This buffer space can be configured to reduces button-holing or lacerations of the skin envelope as is discussed herein. Another configuration for reducing buttonholing is shown inFIG. 34ein which the distal end ofhousing14 is flared back. In another embodiment14wcan substantially equivalent to the working or cutting width18wofelectrode18.
• As discussed herein in various embodiments,housing14 can be adjustable to control a number of dimensional and other parameters relating to the dissection procedure. Referring now toFIG. 35, for example, in an embodiment,housing14 can be configured to vary the amount that theelectrode18 includingcutting edge18cecan be advanced or retracted in an out ofhousing14. This can be accomplished using an advancement/locking mechanism25 known in the art such as a pull wire, cam mechanism, ratchet or gear driven mechanism.
• Referring now toFIGS. 36a,36band37, in various embodiments,housing14 can include one or both of a linear14linportion or curved orcontoured portions14cpas is shown inFIG. 36a. The curvature can be selected to substantially match or conform all or in part to the contour8cof a selectedtissue site8.
• In various embodiments, thecurved portions14cpcan be configured to match one or more of the contours of the following anatomical sites: the face, the breast, the buttocks, the abdomen and the like. In an embodiment shown in36b, thecurved portion14cpcan include only a single radius of curvature,14cr1, a second radius ofcurvature14cr2, or a varying radius ofcurvature14crvand combinations thereof.
• The amount of curvature ofhousing14 can be pre-selected or can shaped by the physician for malleable embodiments ofhousing14 described herein. This can accomplished through the use of an articulatedhousing14, or ahousing14 made from pliable, malleable and/or conformable polymers known in the art such as silicone rubber or polyurethane and copolymers thereof. In alternative embodiments, it can also be achieved through the use of shape memory metals and associated methods known in the art such as nickel titanium alloys.
• Also all or portion ofhousing14 can include aconformable portion14 con made of conformable or malleable materials that are sufficiently flexible to conform to various anatomical contours. Examples of conformable materials include without limitation, silicone rubber, butyl rubber, polyurethane and copolymers thereof. The bending strength or flexural modulus (also known as a bending modulus) of the conformable portion can be selected to conform to the resistive forces offered by one of bone, cartilage, muscle, adipose or a skin layer. Accordingly, in various embodiments, the flexural modulus ofconformable portion14concan be selected to be below the bending or compressive modulus of bone, muscle, cartilage, fat or skin all of which are known in biomechanical arts. In various embodiments, the flexural modulus ofconformable portion14concan be in the range of 0.001 to 10 GPa with specific embodiment of 0.01, 0.05, 0.1, 0.5, 1 and 5 GPa.
• Also in an embodiment shown inFIG. 37,conformable portion14concan a plurality of conformable portions having different flexural moduli include afirst portion14con1 having a firstflexural modulus14fm1 andsecond portion14con2 having a secondflexural modulus14fm2. In use, embodiments ofhousings14 with multipleconformal portions14con, can be configured to allowhousing14 to bend or otherwise conform different amounts for different tissue structures to facilitate movement ofhousing14 over curved or irregular shaped anatomical surfaces such as the face having multiple tissue components (e.g. bone and cartilage) with different mechanical properties. This in turn facilitates maintenance of thedissection depth8ddduring advancement ofhousing14 through or within thedissection pocket8dportissues site8.
• In one embodiment of a method of shaping and using a pliable ormoldable housing14, the physician could shape ahousing14 made out of shapable metal such as spring steel by (i) shapinghousing14 by hand, (ii) shaping by pressinghousing14 against the contour of the desired tissue site, or (iii) shaping using a shaping template or tool or even a surgical tool. In another embodiment the medical practitioner could shapehousing14 by sufficiently heatinghousing14 to make it pliable (e.g. heat above the glass transition temperature for the material selected) to (i) shapehousing14 by hand, (ii) shape by pressinghousing14 against the contour of the desired tissue site, or (iii) shape using a shaping template or tool or even a surgical tool and then after the shaping was completed cool housing14 (below the glass transition temperature) to set the shape by quenching in chilled water, ice water, cryogenic gas or other cooling fluid or medium known in the art. The sequence of these steps is exemplary and need not be done in this order. Insuch embodiments housing14 could be made of variety of resilient polymers or metals known in the art that have glass transition temperatures above room temperature.
• Referring now toFIGS. 2-7,36-38,apparatus10 can also be configured to move over a curved tissue surface8cand still maintain a substantially uniform depth of dissection. In an embodiment, this can be accomplished through the use of a movable or pivotinghand piece15 coupled tohousing14 via apivotal coupling14pcop.Pivotal coupling14pcopcan be any pivoting device or mechanism known in the art including gimbals, ratchet, bearing and cam mechanisms known in the art. In usepivotal coupling14pcopserves to maintain or assist in maintaining the tissue contacting portion ofhousing14 in substantially parallel contact (or other selected orientation) with respect to atissue plane8pdashousing14 is advanced along a contoured or uneven tissue plane usinghand piece15. This can be achieved for longitudinal, lateral or curvilinear translation ofhousing14 along the tissue plane by configuringpivot coupling14pcopto pivot in a longitudinal or lateral axis (or both) with respect to the direction of travel (e.g. advancement)14dtofhousing14. In an shown inembodiments pivot mechanism14pcopcan include andindexing mechanism14pciconfigured to allow the user to select the pivot axis(es)15paofhand piece15 such that hand piece only pivots in the selected axis through anarc15arc. Alternatively the mechanism can be configured to allow movement ofhand piece15 in multiple axes.
• Referring now toFIGS. 39a-39c, other means for advancinghousing14 on curved surfaces can includehousing14 having an articulatedportion14art, a bendableelastic portion14b, or aprecurved portion14prc. The bendable portion can be fabricated from bendable elastomers known in the art such as silicone, polyurethane or butyl rubber and the like. The curved portion can have a factory fabricated amount of curvature selected by the physician for the particular tissue site or can be shaped by the physician using procedures described herein.
• In one method embodiment of usingapparatus10 to dissect tissue along a curved surface, the physician would select or shapehousing14 to have a degree of curvature corresponding to a tissue contour such as the contour of the fascia over the pectorolis muscle for mastectomy and related procedures. For use of abendable housing14 having bendable or articulatedportion14bor14c, the physician could press or form fit the curvature of the bendable or articulated portion to match that of the desired contour.
• Referring now toFIGS. 2-3 and40-44 in various embodiments,housing14 can include on or more roller devices,17 which can also be a sliding orlinear translation device17s. Roller or slidingdevice17 functions to roll or movehousing14 smoothly along a tissue plane to allow the surgeon to advancehousing14 in a smooth lawn mover like fashion over a tissue plane.Roller device17 can be configured to roll or glide in a substantially atraumatic fashion along a tissue plane or tissue surface81ssuch as the sub-dermal, fascia, subfascia or muscle tissue layers. Alsoroller device17 can be configured to substantially maintain the position ofelectrode18 with respect to the plane ofdissection8pdso as to produce a substantially uniform dissection depth8DD as the surgeon advanceshousing14 over a selected tissue surface at atarget tissue site8.
• Embodiments ofroller device17 can comprise one or more rollers movably or rotably coupled tohousing14. In various embodiments, roller device can comprise between 1-20 roller bearings, with specific embodiments of 2, 4, 6, and 10 roller bearings. In an embodiment, the roller can be located behind the electrode with the center of theroller17cencorresponding to the height of theelectrode18h(with respect to the roller bottom17b) or otherwise located on theelectrode plane18pe. In various embodiments, the gap distance orclearance18gtbetween the electrode and the face of theroller17wcan be between 0.01 and 1 inch with specific embodiments of 0.05, 0.1, 0.25 and 0.5 inches.
• In an embodiment shown inFIG. 42, therollers17 can be located above and below theelectrode18 and the correspondingelectrode plane18pe. Theupper roller17ucan be configured to roll or otherwise guide thenascent skin envelope8se, ortissue flap8fover the roller and away from the electrode (e.g. in a proximal direction) and thus protect the skin envelope from further thermal exposure. In performing this function, the upper roller also facilitates maintenance of the uniformity of thethickness8tof thetissue flap8fby doing one or more of the following: reducing the tendency of the nascent skin flap to bunch up, crimp or otherwise come back in contact with the electrode after the first pass and uniformly guide the skin flap away from the electrode after the first pass. Thelower roller171 is configured to smoothly advancehousing14 over the selected tissue plane.
• Examples of suitable rollers include roller bearings known in the art including needle bearings.Rollers17 can be fabricated from bearing metals known in the art or polymers such as acrylic, polycarbonate, PTFE or other bearing polymers known in the art. Examples of suitable bearing include those manufactured by the SKF Corporation and the Timken Corporation. In a embodiment shown inFIG. 42,rollers17 can be movably coupled tohousing14 using aspring coupling mechanism14scknown in the art.Spring coupling mechanism14sccan be configured to perform a stabilizing or shock absorbing function to allowhousing14 to maintain a substantially horizontal and/or parallel alignment with atissue layer81 despite roughness or unevenness on tissue layer surface81s. In various embodiments,spring coupling mechanism14sccan include a coiled spring, a leaf spring and other springs known in the art.
• Spring mechanism14sccan be configured to have sufficient spring force to compensate for protuberance or unevenness in the tissue plane and allowhousing14 to maintain a substantially parallel orientation with respect to all or portions of the tissue plane ashousing14 is advanced over the tissue plane. In various embodiments,spring mechanism14sccan have between about 0.01 and about 1 lb of spring force or more, with specific embodiments of 0.05, 0.1, 0.2, 0.5 and 0.7 lbs of force.
• In various embodiments, all or portions ofrollers17 or slide17scan be thermally or electrically insulative or both. In a particular embodiment, all or portions ofrollers17 or slide17scan be insulative to RF energy. An example of a suitable thermally and electrically insulative material includes polyetherimide, other materials can include polyimide, polycarbonate and insulative ceramics known in the art.
• In other embodiments,device17 can be include a low friction coating orlayer17cconfigured to allowhousing14 to slide smoothly along a tissue plane.Coating17ccan include low surface tension coatings configured to have both low coefficients of friction and/or minimize or substantially prevent tissue adhesion tohousing14. Examples of low surface energy materials are described above and can include TEFLON® or other PTFE polymer or copolymer known in the art. Also layer17ccan include surface modification coatings known in the art such those produced using, plasma treatment, vacuum sputtering, chemical vapor deposition, and electro deposition methods known in the art to reduce the surface energy of coating17c. Also,layer17ccan also be thermally and/or electrically insulative.
• Also all or portions ofrollers17 can be fabricated from low surface energy materials to minimize or substantially prevent tissue adhesion torollers17 orhousing14. Examples of low surface energy materials or coating include Polytetrafluoroethylene (PTFE) available as TEFLON® from the Dupont Corporation, silicone rubber (including RTV and silica free silicon), polyurethane, polyethylene, HDPE, and copolymers thereof known in the art.Coatings17ccan also include surface modification coatings.
• In use,roller device17 can be configured to allow the surgeon to smoothly andatraumatically advance housing14 over a tissue surface81sorlayer81 within thedissection pocket8dpand useelectrode18 to produce a tissue flap having a substantiallyuniform dissection depth8dd. Embodiments ofapparatus10 havingrollers17 can be adapted for a number of surgical or minimally invasive surgical procedures including without limitation, plastic surgery procedures such as face lifts, breast lifts, liposuction, eyelifts and the like, dermatological procedures such as biopsies, mole or tissue removal and other surgical procedures such as removal of tissue masses such as lipomas, cysts and the like as well as other procedures described herein.
• Thedissection depth8ddcan be selected for each procedure and controlled by physician manipulation ofhousing14 within the dissection pocket, as well as by selection of the configuration ofhousing14,roller device17 or both.
• In various embodiments,different rollers17 or roller mechanisms can employed for different dissection procedures and tissue locations as needed. Also the number and frictional characteristics ofrollers17 orroller bearing17bcan be varied depending on the procedure. For example, more rollers can be employed for rough or uneven tissue surfaces such as dissection through muscular or fibrous tissue. Similarly, lower friction materials (e.g. PTFE) can employed in such settings or other tissue locations to reduce rolling friction and/or reduce tissue adhesion to the rollers orsurface17s. In various embodiments, the surface energy of the materials in rollers can be less about 50, 40, 30, or 20 dynes/cm.
• Referring now toFIG. 44, in other embodiments the frictional or material properties ofroller17 orsurface17scan be configured to generate sufficient frictional force with the contacting tissue so as to put all or a portion of the subjacent tissue layers in contact withhousing14 in tension. This can be accomplished by configuring all or portions ofroller17 orsurface17sto have sufficient friction to grip and pull the contactingtissue8ctin an opposite direction to the direction oftravel14dtofhousing14. This puts the segment ofskin8ssand/or contactinglayer81 betweenroller17 orsurface17sandelectrode18 in tension. Thus,roller17 orsurface17scan be so configured to act astissue tensioning element17tevia atissue gripping portions17tgs.
• Means for tensioning by tensioningelement17teortissue gripping surface17tgscan include one or more the following configurations: (i) use of a textured surface over all or a portion ofroller17 orsurface17s(ii) use of rubberized otherwise compressible gripping layers over all or a portion ofroller17 orsurface17s, (iii) use of a gripping fiber surface over all or a portion ofroller17 orsurface17s, (iv) use of vacuum ports over all or a portion ofroller17 orsurface17sto adhere the tissue againstroller17 orsurface17svia vacuum pressure, wherein the ports are coupled to a vacuum source24vvialumens24′. Examples of texturized surface can include knitted or woven DACRON®, or texturized rubber having a criss-cross, diamond or other pattern known in the art. Also in these and related embodiments higher coefficients of friction ofsurface17tgs, by selection of the material properties ofroller17 or17sincluding use of materials with higher surface energies.
• Higher surface energies can be achieved by vacuum sputtering, CVD, electro-deposition, plasma, chemical etching, shot-peening and other surface modification coating treatments known in the art for plastics or metals. In various embodiments, the surface energy of grippingportion17tgscan be above 50 dynes/cm, above 80 dynes/cm or above 100 dynes/cm
• In various embodiments, tensioningelement17tecan be configured to maintain tissue layers81 (either or super or subjacent) in between 0.01 and 3 lbs of tension with specific embodiments of 0.1, 0.2, 0.5, 1 and 2 lbs of tension. Tissue tensioning can be facilitated by the application of downward force (e.g. a force normal totissue layer81 ordissection plane8pl) onhousing14. Referring now toFIGS. 45a-45b, this can be accomplished by the physician pressing down on thetop portions14tofhousing14, or use of the downward force from the overlying tissue layers81 (which may be in a condition of tension ashousing14 is advanced into the tissue plane) or both.
• Accordingly, in embodiments shown inFIGS. 45a-45b,housing14 can have aforce application surface14fsor fixture configured to allow the physician to press down onhousing14 to apply a downward force fromrollers17 to theunderlying tissue layer81. Force application surface/fixture14fscan be located on the top or other portion ofhousing14 and can also be located on or coupled to hand-piece15 orextender22.
• In an embodiment, all or portions ofhousing14, such as top14tor bottom14b, can be configured as aforce application surface14fs.Surface14fscan be substantially flat, concave, convex and combinations thereof.Force application surface14fscan be configured to apply a downward force over all or portion ofsubjacent tissue layer81 in contact with the bottom ofhousing14. In an embodiment shown inFIG. 45b,surface14fscan be configured to substantially only a apply a downward force totissue gripping surface17tgsand the underlying tissue.
• Referring now toFIG. 45c, other means for force application can include use ofvacuum ports24vplocated on all or portions ofhousing14 as is shown inFIG. 45c.Vacuum ports24vpcan be configured to be coupled to vacuum source24v. The placement and number ofports24vpcan be further configured to apply a vacuum force to a selectedportions8ploflayers81 to at least partially adhere those layers to all or portions ofhousing14 such that whenhousing14 is advanced, layers81 are put in tension.
• In use, the physician can employ thetensioning element17te, orvacuum ports24vpto put selected portions of a tissue layer in tension before, during or after the application of RF energy to the tissue site. In one method embodiment the physician can useapparatus10 to pre-stress the selectedtissue81 before the application of RF energy for cutting or skin tightening. This can be accomplished by advancing the front ofhousing14 into the developingdissection pocket8dporincision site8 is while maintaining a slight downward pressure onhousing14 to keep the roller in contact with subjacent tissue layers and so generate friction between the roller and subjacent tissue.
• Also in use, embodiments having atensioning element17tecan be configured to facilitate the dissection of tissue layers81 attissue site8 by keeping the selected tissues layers81 in tension and preventing them from bunching up or otherwise deforming aselectrode18 is advanced through the plane of dissection. This in turn facilitates maintenance of a substantiallyuniform dissection depth8dd.
• Turning now to a discussion ofelectrode18 and with reference toFIGS. 2-5 and46-48, in various embodiments,electrode18 can be fabricated from a variety of conductive materials known in the art including stainless steel, 304 v stainless steel, shape memory metals and alloys thereof.Electrode18 can also have one or more lumens18lfor passage of fluids and/or gases for cooling, heating, conduction, irrigation or aspiration. In various embodiments,electrode18 can have a variety of shapes and geometries including but not limited to a blade or scalpel configuration, ring-like, ball, hemispherical, cylindrical, conical, needle or needle-like
• In an embodiment shown inFIGS. 46aand46b,electrode18 can be made from conductive wire and can be fabricated to have a curved shaped18csusing wire or metal working methods known in the art.Shape18cscan be semicircular, U-shaped, parabolic, or any curve with a selectable amount ofarc18arc(e.g. degrees). In an embodiment, shape can18cscan also be configured to be substantially contained or bounded in single plane, also calledelectrode plane18pe. In other embodiments shape18cscan be in two or more planes.
• Also in various embodiments,shape18cscan have a single radius of curvature,18rcor multiple radii ofcurvature18rc. Thediameter18dofcurve18cscan be in the range of 0.1 to 5 inches with specific embodiment of 0.25, 0.5. 1, 1.5, 2, 3 and 4 inches. For facelift applications diameter18dcan be about 0.4 to about 1 inch and for abdominal and other large tissue sites, such as theabdomen diameter18dcan be in the range of about 2 to about 4 inches.Electrode18 can also be configured to allow thediameter18dto be adjusted by the physician depending upon the tissue site and procedure. This can be accomplished by electrode adjusting means described herein.
• In these andrelated embodiments electrode18 can be configured to have sufficient strength including bending strength (e.g. bending or flexural modulus) to substantially maintain its curved shape as its through tissue and/or maintain theelectrode plane18pe. In an embodiment, the bending modulus is selected to substantially maintainshape18csas it is advanced through soft tissue such as the skin, adipose tissue, fascia and muscle but to deform upon contact with more rigid tissue such as bone. In other embodiments,electrode18 can be configured to maintain its shape on contact with skin and adipose tissue but deform upon contact with muscle and/or other harder tissue such as bone, cartilages. In use this selectable deformability ofelectrode18 can be configured to provide the physician with tactile feedback of the tissue type that electrode18 is being advanced into. The bending strength ofelectrode18 can be controlled through the selection of one or more of the 18wire diameter18d, material composition (e.g. alloys) and metal treatment (e.g. annealing, work hardening etc.)
• Electrode18 can be spring-loaded or otherwise have shape memory such that if it is deformed due to tissue-applied forces it will substantially reassume its shape upon removal of the force. In these and related embodiments, where the electrode is configured to have a shape memory it fabricated from spring steels or shape memory materials such as nickel titanium alloys using shape memory processing methods known in the art. In these andrelated embodiments electrode18 can have sufficient spring force to substantially maintain its shape as it cuts or dissections through a variety of soft tissues such skin, adipose tissue, fascia and the like. In various embodiments,electrode18 can be configured to have between 0.1 to 5 lbs of spring force with specific embodiments of 0.2, 0.5, 1 and 2.5 lbs of force.
• In an embodiment shown inFIG. 47,shape18cscan consist of three sections, afirst section18s1, attaching to a first side14s1 or front edge ofhousing14, asecond section18s2 and athird section18s3 attaching to the other side or front edge of housing14s2, whereinsections18s1,18s2 and18s3 have radii ofcurvature18rc1,18rc2 and18rc3. In an embodiment,sections18rc1 and18rc3 can be substantially more curved thansection18rc2; in another embodiment this configuration can be reversed. Also radii ofcurvature18s1 and18s3 can be substantially less than18s2. In an embodiment, theelectrode18 can be configured to have camber, which is configured to substantially maintain its shape in response to a selectable amount of normal or other force tending to deform the electrode as the electrode is advanced through tissue.
• Also, in an embodiment shown inFIGS. 48a-48b, all or portions ofelectrode18 can be taperedportions18t. The taper can be produced using wire grinding and drawing methods known in the art. In one embodiment the taperedportion18tcan have a decreasing taper (e.g. decreasing diameter) moving in a direction fromsection18s1 to18s2. In another embodiment, the taper can be increasing. The taper can be configured to control the rigidity of portions of the electrode, for to provide increased strength or rigidity toside sections18rc1 and18rc3 by having making those sections have a larger diameter.
• The taper can also be configured to vary the electro-cautery cutting characteristics of the electrode. A decreasing taper can be used to increase the current density over selected portions of the electrode, forexample section18s2 so as to increase the “cutting current” in that portion. In other embodiments curvedelectrodes18 can be configured to have a cutting or sharpenededge18ceon the leading edge of the electrode. Cuttingedge18cefacilitates dissection through tissue by acting like a knife-edge as well as increasing the cutting current at the edge.
• Referring now toFIG. 49, in an embodiment shown inFIG. 49, the electrode can be wedge shaped or “cow catcher shaped” to have a wedge or force concentration affect in cutting through the tissue. This shape can be configured to simultaneously cut and undermine or separate tissue layers81 by cutting the tissue at the point or apex18aof the electrode wedge and then force the tissue over wedge. This shape can be particularly useful when starting the beginning of the dissection. Also selected portions of the wedge can have an electrical and/or thermally insulative layer18l. In an embodiment, thepoint portion18aof the electrode can be conductive and the remainder insulated, this configuration serves to provide a cutting force concentration affect and thermally shield or otherwise minimize heat transfer to the nascent tissue flap in close proximity to the electrode.
• Referring now toFIG. 50, one or both ends18eofelectrode18 can be attached to the sides14sofhousing14, either directly or via aninsulative coupling14icop. Examples of insulative coupling can ceramics, insulative polymers and other insulators known in the art having a high dielectric strength. In related embodiments insulative coupling can comprise an insulative coating on the electrode portion in proximity tohousing14. Examples of suitable insulative coatings can include, polyimide, polyamide, TEFLON, NYLON PARALENE and other insulative polymers known in the art. In various embodiments, insulative coatings18lcan extend a selected length over the electrode and can be slidably movable over the length of the electrode (e.g. by sliding in and out of the interior of housing14) in order to select a length ofactive electrode18ae. The coating can be configured to be slid or advanced a fixed length and held in place by virtue of friction between the coating and the electrode or lockingdevice18ldpositioned at the juncture between the electrode andhousing14 or insulative coating. Examples of locking devices can include a bolt, screw or clamp known in the art.
• Referring now toFIGS. 51aand51b, in various embodiments,electrode18 can be coupled tohousing14 via astrut member19.Strut member19 can be configured to provide sufficient structural support to electrode18 to substantially maintain the shape of the electrode (e.g. in a U shape) as the electrode is advanced through tissue. In various embodiments, asingle strut member19 can be located at alocus18locof the center curve of the electrode. In another embodiment, two strut members can be coupled toelectrode18 and can be substantially equidistant from each In or embodiments three or more strut member can employed strut members can be of metals such as steel, 304 v steel or tool steel, or rigid polymers such as polycarbonate, acrylic, or Nylon.Member19 can also have sufficient column strength to substantially maintain the shape ofelectrode18 in response to forces applied by tissue (e.g. normal forces) tending to deform the shape of the electrode as the electrode is advanced through issues.
• In an alternative embodiment, the column strength and position of strut member(s)19 can be also configured to provide for some flex in the shape or camber ofelectrode18. The amount of flex can be configured to provide the surgeon with tactile feedback of the resistance encountered by the electrode as it is advanced through tissue. Further this amount of flex can be configured to allow the surgeon to discriminate between softer tissue such as dermal adipose tissue, less soft tissue such as muscle, vascularized, fibrous and cartilage tissue and rigid tissue such as bone.
• In an embodiment,electrode18 and strut member(s)19 can be configured to vary the shape of the cutting surface of theelectrode18cein response to tissue applied forces. In an another embodiment,electrode18 andstrut member19 be configured to haveelectrode18 deform into a pointed or curved arrow head shape in response to a selectable amount of applied tissue force as the electrode is advanced into tissue. These and related embodiments can be configured to facilitate smoother advancement of the electrode and/or a more uniform width ofdissection8wd(also calleddissection swath8wd) particularly for tissue non-uniformities (e.g. scar tissue), uneven tissue, or anatomical deformities.
• This can be accomplished by having the electrode assume a pointed shape when encountering more resistance from tissue, thus concentrating the current density (due to edge effects) and the cutting or tissue shearing force in the tip or point of the electrode. This biases cutting or dissection in the horizontal center of the plane of dissection and in so doing, facilitates a more even horizontal dissection and reduces the likelihood of the electrode veering out of the selected plane of dissection. Once the more resistive tissue is cut through, the electrode is configured to have sufficient spring force to spring back to its original curved shape or degree of camber.
• In these andrelated embodiments electrode18 can be fabricated from flexible wire, spring steel or nickel titanium alloys. This can be accomplished by positioning asingle strut member19 in the center orlocus18locofcurved electrode18 and can configuring the electrode to have sufficient elasticity to deform inwardly in one of a curved, a convex curved, inward parabolic curved, or hyperbolic curved manner in response to a selected amount of force.
• In an another embodiment,member19 can be advancable in and out ofhousing14 in order to change theadvanced length19alof the strut member. This can be accomplished by virtue ofslot14stinhousing14 and alocking device14ld, such as a locking screw, or bolt positioned at the slot opening14stinhousing14. Embodiments having anadvancable strut member19 can be configured to change the shape and overall dimensions of the electrode. More specifically the amount ofcurvature18csof the electrode can be varied as well as thediameter18d, for example from a first curvature anddiameter18cs1,18d1 to a second curvature anddiameter18cs2,18d2.
• Housing14 can also haveslots14sofor advancement and retraction of the electrode as well in and out ofhousing14 as well as an associated locking mechanisms. Other electrode adjusting means can include anactuation member15amsuch as pull wires and the like coupled directly or indirectly to the electrode.
• In use, anadvancable member19 can allow the physician to change the shape so as to in turn vary one or more of the electro-cautery, cutting or dissection characteristics of electrode to meet the needs of the a selected tissue site and tissue type. Forexample member19 can be extended to produce a more oblong shape for tougher more fibrous tissue and retracted to produce a flatter curve for softer tissue. Embodiments ofapparatus10 having an extendable electrode can also be configured to vary the amount of tension inelectrode18 and hence the stiffness of the electrode as well. By extendingmember19, the tension inelectrode19 can be increased making the electrode stiffer (e.g. less deformable) and better able to hold its shape in response to tissue-applied forces. Similarlyelectrode18, the electrode can be made more flexible by the shortening or withdrawal ofmember19 back intohousing14.
• In anotherembodiment member19 can be configured to be reciprocating in and outhousing14 to during the dissection procedure and facilitate cutting or dissection by acting in a jackhammer like fashion. This can be accomplished by couplingmember19 to a reciprocating mechanism known in the art, which can include a pneumatic mechanism coupled to a pneumatic pressure source.
• The column strength ofmember19 can be manipulated by selection of the diameter and material strength (e.g. compressive modulus) formember19. Thediameter19dofmember19 can be in the range of 0.005 to 0.3 inches with specific embodiments of 0.05, 0.1, 0.2 inches. Also the column strength of the strut member can be in the range of 0.1 to 10 lbs, with specific embodiments of 0.5, 1, 2, 5 and 7.5 lbs.Strut members19 can be made from insulative material or can be coating with an electrically insulative coating191 described herein.
• Electrode18 can be made of a variety of conductive materials, both metallic and non-metallic. Suitable materials forelectrode18 include, steel such as 304 stainless steel of hypodermic quality, platinum, gold, silver and alloys and combinations thereof. Also,electrode18 can be made of conductive solid or hollow straight wires of various shapes such as round, flat, triangular, rectangular, hexagonal, elliptical and the like. In a specific embodiment all or portions ofelectrodes18 can be made of a shaped memory metal, such as NiTi, commercially available from Raychem Corporation, Menlo Park, Calif. A radiopaque orechogenic marker18mcan be coated onelectrodes18 for visualization purposes using x-ray, ultrasound and other medical imaging methods known in the art.Marker18mcan be made from radio-opaque and/or echogenic materials known in the art.
• In various embodiments, energy delivery device18 and power source20 can be configured to operate within the following parameters: (i) provide a controlled delivery of electromagnetic energy to the skin surface that does not exceed, 1,000 joules/cm2, or 500 joules/sec/cm2; (ii) provide a controlled delivery of electromagnetic energy to the skin surface not exceeding 2000 joules/cm2 during a single treatment session (during a twenty-four hour period); provides a controlled delivery of electromagnetic energy to the skin surface not exceeding 200 joules/cm2 during a single treatment session, or not exceeding 10 joules/sec/cm2; (iii) operate in an impedance range at the skin surface of, 70 ohms cm2 (measured at a frequency of 88 Hz) to 40 Kohms cm2 (measured at a frequency of 10 KHz); (iv) provides a controlled delivery of electromagnetic energy to operate in a range of skin thermal conductivities (at or near the skin surface) of 0.20 to 1.2 k (where k=1*[W/(m ° C.)]); and (v) operate in a range of compression forces applied to the skin surface and/or the underlying soft tissue anatomical structure not exceeding 400 mmHg, not exceeding 300 mm, not exceeding 200 mmHg or not exceeding 100 mmHg.
• Suitable energy sources20 that may be employed in one or more embodiments of the invention include, but are not limited to, the following: (i) a radio-frequency (RF) source coupled to an RF electrode, (ii) a coherent source of light coupled to an optical fiber, (iii) an incoherent light source coupled to an optical fiber, (iv) a heated fluid coupled to a catheter with a closed channel configured to receive the heated fluid, (v) a heated fluid coupled to a catheter with an open channel configured to receive the heated fluid, (vi) a cooled fluid coupled to a catheter with a closed channel configured to receive the cooled fluid, (vii) a cooled fluid coupled to a catheter with an open channel configured to receive the cooled fluid, (viii) a cryogenic fluid, (ix) a resistive heating source, (x) a microwave source providing energy from 915 MHz to 2.45 GHz and coupled to a microwave antenna, (xi) an ultrasound power source coupled to an ultrasound emitter, wherein the ultrasound power source produces energy in the range of 300 KHZ to 3 GHz, (xii) a microwave source or (xiii) a fluid jet.
• For ease of discussion, theenergy delivery device18 is one ormore RF electrodes18 and the power source utilized is an RF power supply. However, all other energy delivery devices and power sources are equally applicable. Referring now toFIG. 52, electrode(s)18 are electromagnetically coupled toenergy source20. The coupling can be direct fromenergy source20 to eachelectrode18 respectively, or indirectly by usingconnector member20cmsuch as a collet, sleeve, connector, cable, cord40w, and the like whichcouple electrodes18 toenergy source20.Electrodes18 can also be multiplexed topower source20 through a multiplexing device20mand associated multiplexing methods known in the art.
• In various embodiments,RF power source20 andelectrode18 can be configured to deliver RF energy in one of a monopolar mode or a bipolar mode, as is known in the art. Further RF power source can be configured to switch or toggle back and forth between monopolar and bipolar mode on operator command or viacontrol system60. In variousembodiment RF electrode18 andpower source20 can be configured to delivery RF energy to perform one or more surgical procedures including without limitation cutting, coagulation, ablation and combinations thereof. Accordingly,power source20 can be configured to generate RF energy in one or more procedural modes known in the electro-surgical arts including without limitation, cut mode, coagulation mode and blended mode. In each of thesemodes RF generator20 can be configured to generate awaveform2xwA that has specific shape, frequency, voltage and current properties to produce selected tissue effects. Againgenerator20 can be configured to switch back and forth among these or other electro-surgical modes known in the art. This switching can be automatically controlled by logic resources201r, or a control system integral or coupled togenerator20 or manually by the surgeon, (e.g. using afoot switch20fs) or both.
• In the cut mode, energy (current) is delivered continuously delivery with a waveform having an undamped sinusoidal shape. The intracellular fluid in the targeted tissue heats to the vaporization state causing cells in the affected tissue to explode which disrupts/destroys the structure of the affected tissue.
• Coagulation mode is characterized by a discontinuous waveform that consists of a dampened cut wave that is duty cycled (e.g. has an on time then an off time) and has higher voltages than a cut waveform. The off time allows cell to cool between heating which in turn allows for the formation of a coagulum and providing a high degree of hemostasis. The blended mode can have a waveform that combines features of the cut and coagulation waveform allowing for an RF current that cuts with varying degrees of hemostasis. The blended wave has an increased duty (e.g. more on time) and lower voltages than a coagulation wave form but higher voltage than a pure cut waveform. Increased levels of coagulation can be obtained by lowering the duty cycle and vice versa. Example blended wave forms can have duty cycles that include but are not limited to the following on off ratios: 50% on 50% off; 40% on 60% off; and 25% on 75% off.
• Apparatus10 can be configured to operate with numerous conventional, commercially available, electro-surgical energy generators.
• An example of a suitable electro-surgical orRF energy generator20 can include a unitary mono-polar-bipolar RF generator, such as the Valleylab “FORCE 2” RF Generator manufactured by Valleylab, a division of Tyco Healthcare Group LP, 5920 Longbow Drive, Boulder, Colo., 80301-2199, U.S.A.Apparatus10 can be coupled topower source20 using aconventional power cord40, which may be long (for example, over two meters) and connect directly to electro-surgical energy generator20 via standardized, monopolar or bipolar connectors, which are well-known in the art.Power cord40 may also be short (less than one third of a meter, for example) and have a standardized, conventional monopolar or bipolar connection (also well-known in the art) to another, longer power cord, which is normally reusable and available with electro-surgical energy generator20. An operator uses a foot-activated switch of electro-surgical energy generator20 to supply energy throughinstrument20 to theelectrode18 and the tissue being treated. The operator can adjusts one or more power settings onelectrosurgical energy generator20, such as the wave form, maximum power setting to be in a sufficiently effective range (e.g. 10 to 100 watts) depending upon the type of tissue to be dissected (e.g. the skin envelope v.s. the fascial layer), size of the dissection path, and amount of skin tightening desired. The foot switch may also have a multi-pedal design to allow the operator to both initiate the delivery of RF energy as well switch between RF wave forms (e.g. thus for cut, versus coagulation or collagen tightening.
• In another embodiment,apparatus10 can be configured to use high frequency high power RF energy and thus can be configured to be coupled to high power high frequency electro-surgical energy generator. In these andrelated embodiments apparatus10 can be configured to utilize RF energy having a frequency range of about 1 to about 15 MHz with specific embodiments of 2.5, 3.5, 10 and 14 MHz; voltage up to about 700 volts rms, a current up to about 2 amps and a delivered power up to about 500 or up to about 1000 watts. The delivered power can be pulsed or continuous, with peak pulsed power capable of exceeding 1000 watts. Further description of high frequency, high power RF generators and their use in electro-cautery and other RF medical procedures is found in PCT application No. PCT/US01/149207 (Publication No. WO 02/053048) and U.S. patent application Ser. No. 09/752,978 which are fully incorporated by reference herein.
• Referring now toFIGS. 53aand53binrelated embodiments apparatus10 can be configured to use high frequency high power RF energy in conjunction with injection or infusion of an electro-conductive orelectrolytic solution29eat the tissue site to create an enhanced ortumescent electrode18en. Enhanced electrode is created by the delivery of sufficient RF power to increase the current density in the electro-conductive fluid surrounding oradjacent electrode18 to the point where that fluid acts as an electro-cautery electrode or energy delivery device to cut, ablate, vaporize or coagulate tissue in contact with or proximate to the enhanced electrode.
• In various embodiments, electro-conductive solution29ecan include various saline solutions known in the medical arts including, buffered saline solutions, 0.9% saline solutions and carrier saline solutions such as tumescent saline carrier solutions infused as part of a liposuction procedure (containing epinephrine and anesthetic such as lidocaine) or saline carrier solution used for injection of local anesthetics such as lidocaine as part of face lift and other plastic surgery procedures using localized injection of an anesthetic. Additionally, the solutions (saline or non-saline solutions) containing lidocaine and/or its chemical derivatives can also be used as electro-conductive solutions by virtue of the electro-conductivity of lidocaine which is itself electro-conductive in solution.
• In an embodiment of a method of using high power/high frequency RF energy for flap dissection, the surgeon would pre-infuse the target tissue site with tumescent saline solution, a saline-based anesthetic solution or other saline or electro-conductive solution29e. The amount of infused saline can vary depending upon the procedure from 0.001 to 5 liters, with specific embodiment of 0.005, 0.1, 0.5, 1 and 2.5 liters. For liposuction the infused volume can be between 0.5 to 4 liters, for face lift procedures it can be between 0.05 to 0.5 liters.
• An incision would be made and theapparatus10 placed within the incision with subsequent saline infusion or injection as needed.Electrode18 would then be energized by highfrequency power source20hfwith the power levels and frequencies adjusted manually or automatically to produce enhancedelectrode18en. After energizing the electrode and generating the enhanced electrode, the surgeon would then advanceapparatus10 within the tissue pocket and use the enhancedelectrode18ento dissect one or more selected tissue flaps. (Alternatively the surgeon could start the dissection procedure withelectrode18 configured as a normal RF electrode and convert to enhancedelectrode18envia manual command or automatic control ofpower source20 or control system60).
• Additional saline infusion or injection could be made as needed and could be done so responsive to monitored impedance and/or temperature levels at the tissue site using impedance and/or temperature sensors including the electrode. The infusions/injection could be done under manual control using aninfusion pump24ipor could be controlled using a control system described herein. In an embodiment, continuous, duty cycled or intermittent infusion could be done throughout the period of RF energy delivery.
• To facilitate use of the above and related methods using an enhanced electrode for more commonly performed plastic surgery procedures that utilize saline infusion or injection such as liposuction, face lifts and the like, in various embodiments,power source20 can be configured to allow the surgeon to enter the type of infusion/injection solution used including the saline and/or other solute concentration. Thepower source20 could then use a power control algorithm orcomputer program404pcto adjust the RF power levels (e.g. voltage and current) and frequencies based on the electro-conductivity and/or solute concentrations of the infusedsolution29eto produce the desired enhanced electrode or enhanced electrode effect (e.g. increased tissue temperatures, etc.). Program404pccould be resident within processor that is part ofpower source20 or could be resident within a processor that is part ofcontrol system60 that is coupled or integral topower source20.
• Enhanced electrode18encomprises both the original metal orwire electrode18 and charged or electrically energizedfluid29efsurrounding the electrode, known as the fluidic component18f. In various embodiments, enhancedelectrode18encan also be configured to generate higher tissue temperatures than standard RF electrode and thus provide an enhanced electro-cautery cutting and ablation effect. This is due to the fact that: (i) the use of the infusion solution with the enhanced electrode reduces or prevents the buildup of charred matter on a wire ormetal electrode18 which can cause a shut down of the generator due to the development of excessive impedance and (ii) the fluidic component18fof the enhanced electrode is itself not subject to the buildup of charred matter.
• These two factors singularly or combined allow for greater amounts of current and hence power to be delivered to the enhanced electrode resulting in higher temperatures (due to Ohm's law) at the electrode and surrounding tissue.
• In an embodiment, the delivered power levels to create anenhanced electrode18encan be about 500 watts or greater at a frequency of about 1 MHz or greater. The size and/or shape of the enhanced electrode can be controlled or modulated by control of one or more of the frequency, power, voltage or current of the RF signal from RF generator. The size of the enhanced electrode can be increased by increasing the RF power, frequency or both. Increasing of one or both of these parameters also serves to increase the electrodes tissue cutting, dissection and ablation and abilities by producing higher current densities and thus higher electrode/tissue temperatures which vaporize, cut or ablate contacting tissue faster and more thoroughly. In various embodiments, enhancedelectrode18encan have the same basic shape or proportions aselectrode18 only larger depending upon the delivered power. Alternatively the enhanced electrode can be a different shape such as spherical, cylindrical depending upon the distribution of theelectrolytic fluid29eand RF parameters.
• Thus embodiments of the invention utilizing an enhanced electrode can be configured to allow or facilitate faster more uniform tissue flap dissections by virtue of one or more of the increased temperature, size and electro-cautery properties of the enhanced electrode.
• Turning now to a discussion ofextenders22 and referring toFIG. 3, in various embodiments,extenders22 can be attached to theelectrode housing14 and/orhand piece15.Extenders22 can also be of variable length. This can be achieved by configuringextenders22 to be telescoping or otherwise having a slidable extension mechanism known in the art. In an embodiment, this can be accomplished through telescoping sections22twhich are coaxial and/or swaged or are otherwise attached together.Extenders22 can be made from thermoset, thermoplastic or moldable polymers known in the art such as ABS, acrylic, polystyrene, polyetherimide and the like.Extenders22 can also be made from metal such as steel, 304 v steel or tool steel and can be coated with a thermally and/or electricallyinsulative layer221. Alternatively, all or portions ofextenders22 can be fabricated from superelastic metals known in the art
• Referring now toFIGS. 2 and 3, in an embodiment,apparatus10 can be configured to have a suction capability via asuction device24 which can include a suction lumen orport24′ running through all or a portion ofapparatus10. This can include portions ofhousing14 and/or theextender22.Suction device24 can be configured to be coupled to a vacuum source known24vin the art.Suction device24 can also be configured to have sufficient suction to suction off steam, water vapor or gases created during use ofapparatus10 in an electro-surgical procedure. Suction can be configured to minimize thermal damage from steam created in a closed system during use of the device. Also suction can be incorporated into apparatus10 (viasuction device24 other suction means known in the art) as a means of convection cooling of thedissection pocket8dpcreated during use ofapparatus10. In an embodiment,suction device24 can configured to provide between 1 and 760 torr of vacuum. Also all or portions ofsuction device24 can be made from heat resistant polymers known in the art such as polyetherimides, polyethers, polyesters, polyamides, polyimides and polybenzoxazole. An example of suitable heat resistant polymer includes Ultem®, available from the General Electric Corporation.Suction device24 can also be an aspiration device known in the art and in an embodiment, can be the same aspiration device used to perform the liposuction. In an embodiment,suction device24 orports24′ can be coupled to asmoke evacuation device24seknown in the electro-surgical arts.
• In relatedembodiments suction device24 can also be configured as insufflation device24ito allow the surgeon to insufflate all or portions of thetissue site8 including thedissection pocket8dpand theskin envelope8se. In use insufflation can allow the surgeon to observe the developing plane ofdissection8pdand adjacent tissue either directly or using an endoscope or other viewing device known in the art. Insufflation device24ican be configured to be coupled to apressure source24psuch as compressed air source known in the medical arts.
• In various embodiments,apparatus10 can be configured for endoscopic viewing capability or to be used in conjunction with an endoscope. This can be achieved through use of an endoscopic orviewing device24ethat is integral to or movably positionable withinapparatus10 or used as separate adjunct device. In various embodiments, endoscopy can also be performed throughlumen24′ or anotherlumen24″ which can each be configured to allow the passage of an endoscopic device, viewing scope and the like. In an embodiment,apparatus10 and/orendoscopy device24e, or an adjunct endoscopy device can be configured to allow endoscopic visualization of subcutaneous tissue sites in the operating site including the subcutaneous plane of dissection. These and related embodiments can be configured to be utilized during electro-cautery procedures such as electro-cautery hemostasis to allow the surgeon to view all or a portion of the subcutaneous plane of dissection to ascertain hemostasis and other tissue conditions. Alternatively, a suction assisted lipectomy canula orlumen24′lccan also be employed.
• Referring now toFIGS. 56-57, in an embodiment,hand piece15 can be configured to attached to theelectrode housing14 and can be configured to provide similar tactile sensation (e.g. feel and visual appearance) as standard surgical instruments such as a Metzenbaum scissors (seeFIG. 3). This can be accomplished by havinghand piece15 have a similar grip as Metzenbaum scissors and/or similar mechanical properties.Hand piece15 can also be configured to attach to adisposable housing14 and can include a quick detachmechanism14dmdescribed herein or known in the art. In use, detachmechanism14dmcan be configured to allow the physician to rapidly detach and replacehousing14 the same or different housing (e.g. having a different height or electrode shape) depending upon the requirements of the procedure. In one embodiment the physician could detachhousing14 when switching from an dissection procedure to an excision procedure or when switching from performing a procedure on a subcutaneous flap to a myocutaneous flap and vice a versa.
• Referring now toFIGS. 58-59, in various embodiments, electrode-housing14 can be configured as to be deployable in situ to allow subcutaneous insertion of all or portion ofhousing14 orapparatus10 through a single incision can be in the range of 0.25 to four inches in length. After insertion, deployment ofhousing14 or portions thereof creates aninitial dissection pocket8dpfor the deployed dissector. Thus,housing14 can have a non-deployed state shown inFIG. 58 and a deployed state shown inFIG. 59. This can be accomplished having all or portions ofhousing14 pivotally coupled toextender22 using a pivot, hinge or cam mechanism known in the art. Also, all or a portion, ofhousing14 can be articulated to be movable from a non-deployed state to a deployed state. This can be accomplished by means of pull wire/rod or pull mechanism known in the medical device/catheter art. It can also be accomplished pneumatically or hydraulically by configuring all or portions ofhousing14 to be actuable by pneumatic or hydraulic means such as the use of a hydraulic or pneumatic device or force application device (e.g. a hydraulic press).
• In an embodiment, this can this can be accomplished by use of using aninflatable member14imknown in the medical device arts (such as inflatable polyethylene or silastic or latex balloon) which is disposed or otherwise coupled to the interior ofhousing14. In another means for deployment,housing14 can include adeployment spring14ds(either a coil or leaf spring) which can be actuable by an actuatingmember wire39 coupled tohand piece15.
• Deployable embodiments ofapparatus10 can be configured to have a non-deployed profile or footprint to allow access through small incision sites directly or through surgical sheaths and introducing devices known in the art. Thus in use, deployable embodiments ofapparatus10 can also allow for reduction of the size of theincision site8 is to access thetarget tissue site8 versus standard plastic surgery procedures such as face lift. This reduced incision size can also allow the incision site to less visible upon healing as well as placed in less visible locations such as the scalp
• Apparatus10 can be used by the surgeon to dissect and separate selected tissue layers81 in a selected plane ofdissection8pd. This can be done in one pass to dissect askin envelope8seortissue flap8fcorresponding in width to the width of18wofelectrode18 or can be done in multiple passes for larger tissue flaps.
• The larger the advancement flap, the greater the number of passes that can be done. Although multiple passes may be needed, the overall thickness of the flap will be uniform. This allows the surgeon to preserve or substantially preserve the subdermal vascular plexus of the advancement flap and also avoid or substantially avoid damage to vital subjacent structures such as muscles, nerves and blood vessels.
• After the surgeon has dissected a desired area of a selectedtissue layer81 such as theskin envelope8se, the surgeon can then make further passes at substantially the same site to dissect subjacent or deeper tissue layers such as the adipose layers, breast tissue, or scar layers or transect the fibrous septae to correct cellulite or other selected such as a keloid scar, or cyst or lipoma. Also multiple passes can be done over the same area to sculpt or contour a selected layer, such as an adipose layer to produce a desired contour such as the contour in the buttocks or breast area. In use these and related embodiments can allow the surgeon to produce a desired skin contour by controlling one or more of (i) the depth of dissection and (ii) the number of layers dissected. Further such embodiments can also allow the surgeon to produce a varying contour such as that in the buttocks area by varying the thickness of dissected adipose or tissue layers. This can be done by doing one pass in one location and/or multiple passes in another adjacent or other location.
• Referring back toFIGS. 14-18, in various embodiments,apparatus10 can be configured to allow a surgical dissection to be performed in a closed or ‘blind’ fashion without the surgeon needing to directly visualize the plane of dissection. Instead, the prominence of the superficial guide in situ can be visualized through the skin by the surgeon. As discussed herein this can be facilitated by configuringhousing14 to have a raisedside contour21rscorridges21rwhich can function astranscutaneous markers21 discussed. Raisedside contour21rcsorridges21rcan be curved, u-shaped, triangular, square and combinations thereof.
• Referring now toFIG. 60, in another embodiment, transcutaneous visualization can be accomplished by use of an LED or otherlight source34 integral or attached tohousing14.Light source34 can configured to have a wavelength and intensity sufficient to illuminate through the skin.Suitable lights sources34 include LEDs used for pulse oximeters as known in the art. In a related embodiment,light source34 can also be configured as a thickness measurement device34tto provide a measurement of thethickness8tof theskin envelope8seor selected tissue flap. This can be accomplished using optical range/thickness finding technology known in the art. In an embodiment, this can be accomplished using alight source34 such as a LED (which can be in the red or infrared range) and photo-detector34pdto measure the amount of light absorbed by the skin.
• A correlation can be established between the amount of light absorbance and skin thickness using one or more numerical or curve fitting methods known in the art such as cubic spline, least squares and polynomial curve fitting methods. In various embodiments, photo-detector34pdcan be configured to be placed on top of the skin or substantially adjacentlight source34 where it is configured to measures reflected/scattered light from skin envelope, where the amount of reflected light is proportional (inversely or otherwise) to skin envelope thickness.
• Measurement device34tcan be configured to provide the physician with a real time indication of the skin envelope ortissue flap thickness8tand thus thedissection depth8ddas well. Measurement device34tcan be coupled to a display instrument which34dcan include associated logic resource341rand an optical power source. Optical measurement device34tcan be pre calibrated or can be configured to be calibrated using the patient's skin to account for variations in skin composition (e.g. pigmentation, vascularity, etc.).
• By providing feedback of skin envelop thickness, measurement device34tcan be configured to allow the physician to one or more of the following: (i) have finer control over the dissection procedure including the skin envelope/flap thickness, (ii) make adjustment ofapparatus10 as needed to maintain the selected thickness (iii) obtain a more uniform or precise thickness of the skin envelope or tissue flap over a selected length of dissected tissue; (iv) controllably vary the envelope/flap thickness over a selected length of tissue.
• In a related embodiment,light source34 or measurement device34tcan be configured to detect for the preservation or damage of the dermal or sub-dermal vascular plexus. This can be accomplished by using LEDs or laser diode in the a red (660 nm) and/or an infrared (940 μm) range to detect the presence of blood in the plexus. Should the should the oxygenated signal drop or decrease in slope the surgeon is provided with an indication of thermal affects to the plexus before significant damage occurs and can thus stop the dissection procedure, decrease the power levels from the RF or other energy source, increase the level of cooling to tissue site, or a combination thereof.
• In various embodiments,apparatus10 can be configured to treat one or more of the following anatomical or dermatological deformities, including without limitation, Facial Cervical Rhytids, Breast Ptosis, Brachial Skin Redundancy, Post Partum Laxity of the Abdomen with Lipodystrophy, Lipodystrophy of the Hips and Thighs With Skin Laxity, Buttock Ptosis and Knee Ptosis with Lipodystrophy. Accordingly, in related method embodiments of the invention,apparatus10 can used to perform one or more of the following surgical or medical procedures including, without limitation, Liposuction (Suction Assisted Lipectomy), Face lift (Rhytidectomy), Breast Reduction (Reduction Mammoplasty), Tummy Tuck (Abdominoplasty), Buttock Lift and combinations thereof. Liposuction (Suction Assisted Lipectomy), Face lift (Rhytidectomy), Mastectomy, Breast Reduction (Reduction Mammoplasty), Tummy Tuck (Abdominoplasty), Buttock Lift and combinations thereof.
• Referring back toFIGS. 2-7,apparatus10 can be configured to produce a substantially uniform depth of dissection for one or more of theses procedures. This can be achieved by selection of the size and shape of housing14 (e.g. height),electrode18 andextenders22. For example, theheight14hofhousing14 can be adjusted (increased or decreased using embodiments described herein) to produce different depths of dissection for a breast reduction vs. a tummy tuck procedure. Also asmaller housing14 can be used for procedures with smaller tissue flaps and/or dissection pockets and requiring more precise control of the area or plane of dissection such as face lift procedure.Further housing14 can be narrow for target tissue areas having tight or narrow access.
• In various method embodiments,apparatus10 can be used to perform one or more surgical techniques that can be useful for producing a desired aesthetic tissue affect. For example, in an embodiment,apparatus10 can be used to correct buttock ptosis with reduced or minimal scarring as well as produce diminishment of cellulite in the plane of dissection. This can be accomplished by usingapparatus10 to transect eliminating or reducing dimpling of the skin in the dissected area.
• In another embodiment,apparatus10 can be used as an adjunct to aesthetic procedures such as liposuction where contour reduction from liposuction can be accompanied with smoothing and tightening of the overlying skin envelope. In these andrelated procedures apparatus10 can be configured to be used to produce tightening of the undermined skin envelope. This can be accomplished from one or more effects of closed electro-surgical dissection including but not limited to: (i) closed advancement and (ii) thermal tightening of the tissue flap. Thermal conductive tightening of the skin envelope occurs from primary collagen contraction of the released fibrous septae of the subcutaneous tissue and from primary collagen contraction of the dermis due to heating of the these tissues at or above the temperature of collagen contraction.
• Energy can also be delivered to produce a delayed wound healing tightening of the skin envelope that will occur during subsequent months. Also the combined procedure can function as a portal for closed application contouring of the subcutaneous tissue with endoscopic staples. In these and related embodiments,apparatus10 can be configured for the use of an endoscope as well as introduction of endoscopic staples. This can be accomplished by configuring one ormore lumens24′ to have sufficient diameter to allow the passage of an endoscope. In such embodiments lumens can be 5-20 french in diameter.
• In an embodiment, the RF energy delivered to the tissue site to dissect the tissue plane can also be configured to heat the developing tissue flap immediately overlying the electrodes. This in turn, heats the skin envelope directly or indirectly through conduction, convection or both. This heating in turn will result in contraction, causing tightening of the skin envelope because of tightening of the dermis and fibrous septa. Subjacent tissue can be electro-surgically dissected and contoured and during this process the overlying skin envelope/tissue flap can be tightened by thermal conduction to selected portions of the skin envelope.
• The delivery of energy can be titrated to on the one hand, raise collagen components of the flap to a temperature sufficient to cause shrinkage collegenous matrix of the overlying dermis with a subsequent wound healing response, but on the other stay below a temperature and/or total heat delivery that would cause damage or necrosis of the subdermal plexus.
• In various embodiments, configuration of RF energy for skin tightening can be accomplished by manipulation of the RF energy waveform (e.g. frequency, amplitude, duty cycle etc). In an embodiment, the RF generator can be configured to have two modes of power delivery, one configured for cutting and the second configured for heating of the skin envelope to collagen contraction for skin tightening. The heating waveform can have lower power levels and lower frequencies than the cut waveform. In various embodiments, the power level and frequency of the heating waveform can be in the range of about 5 to about 30 watts and about 250 to about 750 kHz respectively.
• Power source20 or a coupled control system60 (described herein) can be configured to alternate between two wave forms in selected duty cycle or alternatively the physician can manually toggle back and forth between the two via means of a foot switch or other manual control means. Further description of methods and techniques of tissue tightening and remodeling the skin through heating of collagen containing tissue (e.g. the skin) by RF energy and other means is found in U.S. Pat. Nos. 5,919,219, 6,241,753, 6,311,090 and 6,350,276, which are all fully incorporated by reference herein.
• Referring back toFIGS. 23-25, reduction or prevention of thermal injury or necrosis of the subdermal plexus and/or dermal layers can be further facilitated by use of coolingfluid29 that can be delivered to tissue layers and structures above and below the plane of dissection such as sub-dermal plexus or even to the skin surface to prevent excessive thermal injury (e.g. erythemia, blistering, burns etc.) to the dermal layer or skin surface. In various embodiments, coolingfluid29 can be delivered throughlumens24′ or via one or more fluid distributions ports orapertures33 position onhousing14. Further description of methods and techniques of tissue tightening and remodeling through heating of collagen containing tissue (e.g. the skin) by RF energy and other sources and mechanisms is found in U.S. Pat. Nos. 5,919,219, 6,241,753, 6,311,090 and 6,350,276, which are all fully incorporated by reference herein.
• Referring now toFIG. 61, in various embodiments,apparatus10 can be configured to monitor the temperature of tissue adjacent or nearhousing14. This can be accomplished by the use of one ormore temperature sensors23 coupled, integral or disposed on withinhousing14.Temperature sensors23 can the be coupled to a feedback control system described herein or logic resources201rcoupled to thepower source20 to regulated the delivery of energy to electrode18 andtissue site8.
• In use, temperature monitoring can be configured to titrate or otherwise control the delivery of energy to thetarget tissue site8.
• Further, in various method embodiments temperature monitoring can be used to control energy delivery to the tissue site to perform or facilitate of one or more of the following: (i) tightening of the skin envelope via collagen contraction, (ii) tightening of the skin envelop via a wound healing response, (iii) produce a substantially uniform plane of tissue dissection using electro-cautery or other EM cutting energy; and (iv) prevent or minimize thermal injury or necrosis to selected tissue layers such as the subdermal plexus, musculocutaneous and perforator arteries.
• In a particular embodiment, temperature monitoring can be used to titrate the delivery of energy to tighten the skin from thermal collagen contraction and wound healing while minimizing or preventing thermal injury to the dermal-subdermal plexuses.
• Suitable temperatures sensors23 that can be employed include thermisters, thermocouples and other solid state or optical temperature sensors known in the art. In various embodiments,sensors23 can be positioned on the top14t, bottom14bor sides14sofhousing14 as well as on ornear suction device24.
• In aparticular embodiment sensors23 can be positioned on both the top and bottom ofhousing14 so as to provide simultaneous temperature monitoring capability of both superior tissue layers (e.g., the skin envelope) and subjacent or inferior tissue layers. These and related configuration can be used to control delivery of energy to the tissue site to dissect out a selected tissueplane using electrode18 and deliver energy to the skin envelope to tighten the envelope (via thermal contraction of collagen) while minimizing injury to the subdermal plexus and/or other subjacent tissue structures.
• In related embodiments,sensors23 can be distributed along alongitudinal axis14laand/orlateral axis14lataofhousing14 with the distribution configured to generate a lateral or a longitudinal temperature profile23pof superior or subjacent contacting tissue layers. The temperature profile can used to monitor, control or perform one or more of the following functions: (i) delivery of energy to the tissue site, (ii) delivery of cooling to the tissue site, (iii) rate of advancement ofhousing14 by the physician, (iv) direction of advancement of housing14 (iv) positioning ofhousing14 by the physician.
• Inother embodiments sensors23 can be positioned to measure one or more temperature gradients23gsuch as temperature gradient between tissue in contact with the electrode and tissue in the nascent skin envelope or tissue flap. Accordingly insuch embodiments sensors23 can be positioned on ornear electrode18 and also on thetop portions14tofhousing14 or the roller. Such temperature gradients can be utilized by the physician and/or a control system to monitor the delivery of energy for one or more of the following: (i) assure sufficient temperature at or near the electrode for electro-surgical cutting, (ii) assure proper temperature for collagen contraction of selected portions of the skin envelope/tissue flap or (iii) assure temperatures stay below a threshold that would cause thermal damage or severe thermal damage to flap layers containing the sub-dermal plexus or other tissue structures.
• In related method embodiment, the delivered RF power levels can be controlled (by a control system, by the physician, or combination of both) to maintain a selected temperature gradient, such as the gradient between the tissue proximate the electrode and superior tissue in the developing skin envelope. This type of control and associated control systems and algorithms can be employed independently or in conjunction with control systems and/or algorithm that utilize absolute temperature as an input. In another method embodiment, temperature a gradient across the horizontal surface of the electrode can be monitored to assure a substantially uniform (or other selected temperature profile) cutting temperature across the electrode. If a portion of the electrode becomes too hot or too cool, the control system can figured to dynamically respond by changing one or more of the following (i) the delivered RF power level, (ii) the RF wave form or shape, (iii) the power duty cycle, (iv) the shape of the electrode (viastrut member19 or other mechanical means) to alter the current density at that portion of the electrode; or (v) the rate of cooling fluid delivered to selected portions of the electrode (e.g. the hot portions) via cooling apertures or other directed cooling or cooling means.
• In other embodiments,sensors23 can also be positioned adjacent or nearelectrode18 such as on or in thesuction device24 to monitor the temperature of the vapor being generated at the tissue site. This temperature can be utilized to control avapor cooling element29eand/or the delivery of coolingfluid29 to portions ofapparatus10 and the tissue site.
• Tissues temperatures that can be monitored include without limitation that of superior layers such as the skin envelope including dermal-sub-dermal plexus and subjacent layers such as subcutaneous layer, fascial and muscular layers. Suitable temperature sensors can include thermisters, thermocouples, fiber optic, solid state or other temperature sensors known in the art.
• In various embodiments, adjacent tissue and superjacent skin can be cooled by one or more methods to prevent or minimize thermal injury, damage or tissue necrosis to selected tissue layers in the tissue flap and/or subjacent layers. Cooling can be accomplished by the use of a coolingmedia29 to cool non-target tissue by convection, conduction or a combination of both. The coolingmedia29 can be a fluid29 which can be a liquid or a gas, or a combination of both. Examples of suitable cooling fluids include, water, saline solution and ethanol and combinations thereof. Other embodiments can utilize a cooling fluid or gas which serves to cool adjacent tissue by ebullient cooling or Joule Thomson Effect cooling as well as the mechanisms described above. Embodiments utilizing Joule-Thomson Effect cooling can have a nozzle-shapedaperture33nto provide for expansion of a coolingfluid29. Examples of coolingfluid29 include, but are not limited to, Freon, CO₂, and liquid nitrogen. The amount of cooling can be controlled by control of one or more of the following parameters (i) temperature of the cooling solution (ii) flow rates of the cooling solution (iii) heat capacity (e.g. specific heat) of the cooling solution.
• Referring now toFIG. 62, in another embodiment, cooling can be achieved by irrigation of the tissue surface or selected portions of the tissue site with a cooledfluid29 as is used during lavage and related surgical procedures known in the art. Accordingly in these and related embodiments,apparatus10 can include be configured to be used in conjunction with an irrigation device24i, orsuction device24 can also be configured as an irrigation or lavage device24i. In an embodiment, the lavage device can be a pulsatile lavage irrigator known in the art. Examples of suitable pulsed lavage irrigators include, but are not limited to, the Davol® Simpulse® Solo (Manufactured by the Davol Corporation), the Stryker Surgilav® Plus® (Manufactured by the Stryker Corporation) and the Zimmer Pulsavac® III (Manufactured by the Zimmer Corporation).
• Referring now toFIG. 63, in an embodiment, cooling of the skin and adjacent tissue can be achieved by suctioning off, capturing or cooling the vapor (steam etc) produced from vaporization of tissue during energy delivery (e.g. via electro-cautery) to the tissue site fromelectrode18 or other energy delivery device described herein. Suctioning of steam can be accomplished usingsuction device24 or a separate suction or device coupled to a vacuum source. In an embodiment, suction can be performed by the same aspiration device used to perform liposuction. Alternatively, acooling element29ecan utilized to condense or otherwise cool vapor produced during energy delivery fromenergy delivery device18 to the tissue site such as during cutting or coagulation from electro-cautery procedures. Coolingelement29ecan be coupled to or positioned sufficiently proximate toenergy delivery device18 to condense and cool the generated vapor. In an embodiment, coolingelement29ecan itself be cooled by a coolingfluid source29s, such as a cryogenic gas29g, coupled toelement29e. Coolingelement29ecan have a variety of shapes including a coiled shape, spiraled helical shape, or a fin-shape, one or more configured to maximize surface area for conductive and/or convective heat transfer.
• Apparatus10 can also be configured to provide cooling ofelectrodes18 vialumens24′ to prevent tissue from the development of excessive impedance atelectrode18 from the deposition of charred tissue on the surface ofelectrode18. Further description of tissue and skin cooling methods are found in U.S. Pat. Nos. 6,350,276 and 6,377,854 which are fully incorporated by reference herein.
• As discussed herein, in various method embodiments,apparatus10 can be used to perform one or more surgical techniques that can be useful for producing a desired aesthetic tissue affect. Further, by maintaining a substantially uniform skin envelope thickness during dissection,apparatus10 facilitates the removal or reduction of contour irregularities for example, the dimpled skin appearance resulting from cellulite. This can be accomplished by configuringapparatus10 to produce a uniform skin envelope, transect the fibrous septae that are attached to the skin and muscle fascia and deliver thermal energy from the electrode to substantially uniformly tighten the released skin envelope by thermal collagen contraction and a subsequent wound healing response discussed herein. By applying RF energy to a skin envelope having a substantially uniform thickness, as opposed to a non-uniform thickness, the resulting tightening of the skin by RF energy application is itself made more uniform. More simply put, starting with a more uniform tissue layer to be tightened results in a more uniformly tightened layer.Apparatus10 can be configured to facilitate this process by providing the physician qualitative and/or a quantitative assessment of the uniformity of skin envelope thickness pre and/or post tightening through either the use of trans-cutaneous visualization of the developing skin envelope and/or use of skin thickness measurement methods both described herein.
• Skin deformities can be further improved by usingapparatus10 to uniformly transect the fibrous septae at the tissue site with each pass ofapparatus10 through the selected plane of dissection. Accordingly,apparatus10 can be specifically configured to transect the fibrous septae by configuration of one or more of the electrode dimensions (e.g. diameter), shape, stiffness, edge and electro-cautery properties. For example, the electrode stiffness can be increased and/or the electrode can have a sharpened edge. By providing a means for uniformly transecting the fibrous septae,apparatus10 facilitates more uniform tightening because the skin is no longer being pulled down or constrained at intermittent locations to the underlying facia.
• In an embodiment of a method for usingapparatus10 to correct a skin deformity, the surgeon makes an incision at or adjacent the tissue site. The surgeon then selects the desired tissue plane to dissect for example, the skin envelope from the underlying subcutaneous layers such as facia. The surgeon can visually acquire the desired dissection plane through direct visualization of the tissue within the incision site or through use of endoscopic visualization. If needed the surgeon can pre-adjustapparatus10 to produce the desire depth of dissection by manipulation of one or more of the electrode,housing14 or the roller.
• If desired, the surgeon can manually start the plane of dissection and isolate or separate the respective tissue layers using his/her hands or via means of a surgical instrument such as scalpel, scissors or bovie and the like. The surgeon then insertsapparatus10 through the incision and into the tissue pocket. For deployable embodiments, the surgeon insertsapparatus10 in a non-deployed state and then deploysapparatus10 within tissue pocket. The surgeon can adjustapparatus10 in situ to produce the desired depth of dissection by manipulation of one or more of the electrode,housing14 or the roller. Alternatively, the surgeon can removeapparatus10tomake such adjustments. After connection to an RF power source (via the hand piece), the surgeon then energizes the electrode (using a footswitch or other activating means) to deliver RF energy and advancesapparatus10 through the selected dissection plane to dissect and separate the skin envelope (or other tissue layer) and transect the fiber septae. Advancement can be done by gripping the hand piece or the extender.
• As discussed above, the surgeon can pre-isolate and start the plane of dissection manually or he/she can do so usingapparatus10. As the skin envelope is dissected by the RF electrode, delivery of thermal energy from the electrode cause thermal contraction of collagen within the skin envelope causing immediate tightening of the skin and subsequent tightening from a wound healing response. As the skin envelope is dissected and separated by the electrode it is guided (by the shape ofhousing14 or roller) to slide overhousing14 or roller and is shielded from further heating; thus, protecting the dermal and subdermal plexes from thermal injury and necrosis.
• This shielding can be further facilitated by the use of a cooling fluid delivered to the skin envelope from an irrigation means (e.g. apertures33,nozzles33n,lumens24′, etc.) coupled to housing14 (e.g. via irrigation ports on the surface of housing14) or an external irrigation means. The surgeon can continuously ascertain one or more of the path and depth of the developing dissection plane as well as the amount of skin tightening by transcutaneous visualization of marker ridges or bumps onhousing14 or roller or by using tissue thickness monitor.
• This information is used by the surgeon can make adjustments as need to either the path of dissection or the depth of dissection by manipulation of one or more of the hand piece, extender or RF energy level. There is no need stop advancement or otherwise remove a hand from the hand piece to palpitate the skin to determine the path or depth of dissection (although the surgeon can do this if he/she desires. This results in one or more of (i) a more uniform dissection and uniform tissue flap/skin envelope, (ii) a better aesthetic outcome with smaller incisions and (iii) well as faster procedure times then procedures where it is necessary to stop advancement to palpitate the skin or otherwise remove one or both hands from a dissection instrument to do so.
• The surgeon can advanceapparatus10 to stop at a selected end point within the tissue site. Then using the hand piece, the surgeon can withdrawhousing14 back to the incision site or some selected point in between. The surgeon can then observe the dissection plane either transcutaneously or through endoscopic visualization. Observation can be facilitated by usingapparatus10 or adjunct device(s) to irrigate and/or aspirate the newly dissected tissue plane as well insufflate the dissected area of tissue. If desired, the surgeon can then make multiple passes over the same area of the dissection plane to do one or more of the following: (i) smooth out the plane of dissection, (ii) widen the width of dissected skin envelope or other tissue flap; (iii) go back over the dissection plane to coagulate any bleeding tissue or vessels, (iv) deliver additional amounts of heat to the skin envelope or selected tissue flap to titrate the amount of collagen contraction and resultant skin tightening, or (v) dissect out a deeper tissue plane. For the last step, the surgeon can, if desired, readjustapparatus10 to change the depth of dissection.
• After completion of dissection within a given tissue area or path, the surgeon can then repositionhousing14 either at the existing incision to start a new path or swath of dissection or make a new incision and repositionhousing14 within the new incisions and then repeat one or more of the preceding steps to dissect a new area of tissue to create a continuous skin envelope (either in width lengths or both) or separate skin envelopes. One or more dissected skin envelopes or flaps can be advanced and surgically reattached (e.g. by suturing, stapling etc.) to a different tissue site, or alternatively separate envelopes can themselves by surgically reattached. Prior to attachment a selected area (e.g. length) of the skin envelope can be removed in order to create a selected contour or tightening affect at the target tissue site.
• Accordingly, in various embodiments,housing14 or roller can be configured to facilitate the attachment by serving as an underlying support for suturing, stapling or otherwise attaching the skin envelope or tissue flap to the edge of another incision or another tissue flap. In an embodiment, that incision can be in a concealed site such as the temporal scalp above the ear or occipital scalp behind the ear.Housing14 or roller can also be configured to actually cut or transect sections of theskin envelope8seeither usingelectrode18 or again serving as a support or guide for another surgical instrument such as a scalpel or surgical scissors.
• Once the surgeon has completed the desired procedure, he/she can removeapparatus10 through the original incision site or through another incision. In the latter case the surgeon advanceshousing14 or roller to the second incision and then pulls it out directly or using forceps or other surgical tool. In these embodiments the hand piece or extender can be configured to be sufficiently flexible and atraumatic to be advanced under the skin through the dissection plane and then pulled out the second incision site. This can be accomplished by (i) fabricating the hand piece from flexible polymers and/or metals described herein otherwise known in the art such as superelastic metals (e.g. nitinol) and/or (ii) configuring the diameter of the hand piece or extender to fit through a small incision site (e.g. less 1, 0.5 or 0.25 inches). Once the surgeon has removedhousing14 andapparatus10 he or she can then suture the incision site(s). The order of the above steps is exemplary and other order are equally applicable.
• The following examples illustrate embodiments of methods of use of the invention using one more embodiments ofapparatus10.
EXAMPLE 1
• Referring now toFIGS. 64a-64f, an application of an embodiment ofapparatus10 can be the performance of a skin preservation mastectomy in which no breast skin is resected . . . only the nipple areolar complex is resected with the subjacent breast tissue. With a uniform flap dissecting embodiment ofapparatus10, a subcutaneous flap of the preserved breast skin is ‘closed dissected’ without direct visualization of the plane of dissection. Due to the superficial guide component of the electrode housing, a uniform flap thickness if created with the dissection of the breast skin envelope. The predetermined flap thickness will preserve the subdermal vascular plexus and thereby limit breast skin envelope necrosis. The correct flap thickness will also enhance the oncological effectiveness of the procedure by not leaving breast tissue on the breast skin flap. In other words, an uneven dissection with the side effects of a too thin or a too thick plane of dissection will be avoided. Lastly, scarring is reduced; the entire procedure is performed through a small periareolar incision instead of a larger standard mastectomy incision that extends across the chest.
EXAMPLE 2
• Referring now toFIG. 65, for a facelift patient with redundant skin the cheeks, jowls and neck, a large continuous incision is made that starts in the temporal scalp, extends around the ear and ends in the occipital scalp. With a uniform flap dissecting embodiment ofapparatus10, only 3 small (2 cm) incisions are made as insertion portals for the device. A continuous uniform flap of the scalp, face and neck is developed. With a process termed ‘closed advancement’, the uniform subcutaneous flap is then advanced upwards (superiorly) on the face and temporal scalp and the flap is advanced backwards (posteriorly) on the neck and occipital scalp.
• Without resection of skin, the flap is secured in an advanced position with subdermal sutures at the incision portals. With this technique, a more youthful appearance of the face and neck can be achieved without the unsightly scars of the atypical facelift incision. Because the advancement is maintained with a series of subdermal fixation sutures in the temporal and scalp, any skin redundancy will be hidden in those areas. To provide additional postoperative support and compression, an elastic garment can be worn by the patient until the flap has adhered in an elevated position. As a surgical adjunct, the procedure can use liposuction to jowls and neck through the same incisions.
EXAMPLE 3
• Referring now toFIGS. 66 and 67, for a patient with breast ptosis, large mastopexy (breast uplift incisions that are anchor shaped) incisions can be avoided with closed dissection of the breast skin envelope. Leaving the nipple-areolar complex attached to the underlying breast tissue, the entire breast skin envelope is closed dissected with a uniform flap dissecting embodiment ofapparatus10. For more severe cases of breast ptosis, the entire breast skin envelope including the nipple areolar complex is dissected as a uniform breast skin flap. The uniform breast skin envelope is then advanced superiorly to provide an uplifted contour of the breast. A specifically designed supportive bra can be worn by the patient for 24 hours a day for 3 weeks until adherence of the breast skin flap occurs.
EXAMPLE 4
• Referring now toFIGS. 68-71, the aesthetic surgical discipline of ‘closed advancement’ using a closed flap dissection with a uniform flap dissecting embodiment ofapparatus10 can create new aesthetic procedures in areas that are currently off limits to standard skin resection procedures because the trade off between an unsightly scar is poor in comparison to the Aesthetic benefit. For a patient with buttock ptosis, a uniform subcutaneous flap is raised with closed dissection over the buttocks and the superior aspect of the posterior lateral thigh. The flap is then advanced superiorly, securing the flap in an elevated position with subdermal mooring sutures in the infragluteal fold. Additional support is provided with a specifically designed girdle that is worn by the patient 24 hours a day for 3 weeks.
EXAMPLES 5
• In this example the patient is an elderly woman who required a mastectomy for extensive in situ ductal carcinoma of the right breast. During the reconstruction of the right breast, the patient also requires a mastopexy/repositioning of the left breast to achieve symmetry with the reconstructed right breast. A closed electro-surgical dissection with upward advancement and thermal conductive tightening of the dissected breast envelope could provide necessary repositioning of the left breast for symmetry with the reconstructed right breast. The typical inverted “T” shaped scar was avoided on the repositioned breast.
EXAMPLES 6
• In this example the patient is a middle-aged man with transaction of the left facial nerve from a motor vehicular accident. Surgical repair of the nerve was performed initially but the patient was left with a residual paresis that produced a severe facial deformity with ptosis of the left face and hyperactivity of the non-injured right face. To correct the post traumatic deformity, a facial reconstruction could be performed on the left face that involved a closed electro-surgical dissection with upward advancement and thermal conductive tightening of the dissected skin envelope of the left. Visible preauricular incisions were avoided and the post surgical scars were hidden in the temporal and occipital scalp.
EXAMPLES 7
• In this example the patient is a young woman who sustained a severe contusion to the left lateral thigh from a bicycle accident. As result, a contusion lipolysis occurred that resulted in a traumatic contour depression of the left lateral thigh. To correct the contour depression, a thigh reconstruction could be performed that involved liposuction of the adjacent subcutaneous tissue surrounding the contour depression with closed electro-surgical dissection with redistribution and thermal conductive tightening of the dissected skin envelope of the thigh. The reconstruction could be performed through small incisions that are typically used for liposuction.
(1) OTHER EXAMPLES
• Various embodiments ofapparatus10 can be configured to assist the surgeon in generating a variety of types of tissue flaps and flap patterns known in the surgical arts depending upon the tissue site and/or tissue condition.Apparatus10 can be configured to facilitate dissection without limitation of a myocutaneous flap, a random patter skin flap, an omental flap, an axial flap and the like all known in the surgical arts. Alsoapparatus10 can be configured to allow the surgeon to substantially preserve all portions or the vasculature in the flap such as a musculocutaneous artery, a perforator artery, a segmental artery, or a sub-dermal plexus. This can be accomplished by embodiments ofapparatus10 having endoscopic viewing capability (described herein) as the use of sensors (such as thermal, ultrasound or optical sensor) coupled to the front or other portion ofhousing14 to detect the presence of an artery. In a specific embodiment an ultrasound sensor can be coupled tohousing14 and configured to detect the presence of the flowing blood in artery by virtue of a Doppler ultrasound signal using gated ultrasound technology known in the art. In another embodiment aninfrared sensor23 can be used to detect the higher concentrations of oxygenated blood within the artery (versus other tissue) using pulse oximetry technology known in the art.
• Referring now toFIG. 72, in an embodiment,apparatus10 can be coupled to an open or closed loop feedback system/resources60. As shown inFIG. 72,feedback system60couples sensor346 topower source392. For purposes of illustration,energy delivery device314 is one ormore RF electrodes314 andpower source392 is an RF generator, however all other energy delivery devices and power sources discussed herein are equally applicable.
• The temperature of the tissue, or ofRF electrode314 is monitored, and the output power ofenergy source392 adjusted accordingly. The physician can, if desired, override the closed or open loop system. Acontroller394 ormicroprocessor394 can be included and incorporated in the closed oropen loop system60 to switch power on and off, as well as modulate the power between one or more modes or waveforms (e.g. monopolar, bipolar; cut and coagulate etc). The closed loop system utilizesmicroprocessor394 to serve as a controller to monitor the temperature, adjust the RF power, analyze the result, refeed the result, and then modulate the power. More specifically,controller394 governs the power levels, cycles, and duration that the radio frequency energy is distributed to theindividual electrodes314 to achieve and maintain power levels appropriate to achieve the desired treatment objectives and clinical endpoints such as tissue dissection and conductive heating skin tightening.Controller394 can also in tandem, govern the delivery of cooling fluid.Controller394 can be integral to or otherwise coupled topower source392 and can also be coupled to a fluid delivery apparatus. In oneembodiment controller394 is an Intel® Pentium® microprocessor, however it will be appreciated that any suitable microprocessor or general purpose digital or analog computer can be used to perform one or more of the functions ofcontroller394 stated herein.
• With the use ofsensor346 andfeedback control system60 tissues layers (adipose tissue, fascia etc.) adjacent toRF electrode314 can be maintained at a desired temperature for a selected period of time without causing a shut down of the power circuit to electrode314 due to the development of excessive electrical impedance atelectrode314 or adjacent tissue. EachRF electrode314 is connected to resources which generate an independent output. The output maintains a selected energy atRF electrode314 for a selected length of time.
• Current delivered throughRF electrode314 is measured bycurrent sensor396. Voltage is measured byvoltage sensor398. Impedance and power are then calculated at power andimpedance calculation device400. These values can then be displayed at user interface anddisplay402. Signals representative of power and impedance values are received by acontroller404.
• A control signal is generated bycontroller404 that is proportional to the difference between an actual measured value, and a desired value. The control signal is used bypower circuits406 to adjust the power output in an appropriate amount in order to maintain the desired power delivered atrespective RF electrodes314.
• In a similar manner, temperatures detected atsensor346 provide feedback for maintaining a selected power. Temperature atsensor346 is used as a safety means to interrupt the delivery of energy when maximum pre-set temperatures are exceeded. The actual temperatures are measured attemperature measurement device408, and the temperatures are displayed at user interface anddisplay402. A control signal is generated bycontroller404 that is proportional to the difference between an actual measured temperature and a desired temperature. The control signal is used bypower circuits406 to adjust the power output in an appropriate amount in order to maintain the desired temperature delivered at thesensor346. A multiplexer can be included to measure current, voltage and temperature atsensor346. Energy can be delivered toRF electrode314 in monopolar or bipolar fashion.
• Controller404 can be an analog or digital controller, or a computer with driven by control software. Whencontroller404 is a computer it can include a CPU coupled through a system bus. On the system can be a keyboard, disk drive, or other non-volatile memory systems, a display, and other peripherals,
• as are well known in the art. Also coupled to the bus are a program memory and a data memory. Also,controller404 can be coupled to imaging systems including, but not limited to, ultrasound, thermal and impedance monitors.
• The output ofcurrent sensor396 andvoltage sensor398 are used bycontroller404 to maintain a selected power level atRF electrode314. The amount of RF energy delivered controls the amount of power. A profile of the power delivered toelectrode314 can be incorporated incontroller404 and a preset amount of energy to be delivered may also be profiled.
• Circuitry, software and feedback tocontroller404 result in process control, the maintenance of the selected power setting which is independent of changes in voltage or current, and is used to change the following process variables: (i) the selected power setting, (ii) the duty cycle (e.g., on-off time), (iii) bipolar or monopolar energy delivery; and, (iv) fluid delivery, including flow rate and pressure. These process variables are controlled and varied, while maintaining the desired delivery of power independent of changes in voltage or current, based on temperatures monitored atsensor346.
• Referring now toFIG. 73,current sensor396 andvoltage sensor398 are connected to the input of ananalog amplifier410.Analog amplifier410 can be a conventional differential amplifier circuit for use withsensor346. The output ofanalog amplifier410 is sequentially connected by ananalog multiplexer412 to the input of A/D converter414. The output ofanalog amplifier410 is a voltage which represents the respective sensed temperatures. Digitized amplifier output voltages are supplied by A/D converter414 tomicroprocessor394.
• Microprocessor394 sequentially receives and stores digital representations of impedance and temperature. Each digital value received bymicroprocessor394 corresponds to different temperatures and impedances. Calculated power and impedance values can be indicated on user interface anddisplay402. Alternatively, or in addition to the numerical indication of power or impedance, calculated impedance and power values can be compared bymicroprocessor394 to power and impedance limits. When the values exceed predetermined power or impedance values, a warning can be given on user interface anddisplay402, and additionally, the delivery of RF energy can be reduced, modified or interrupted. A control signal frommicroprocessor394 can modify the power level supplied byenergy source392.
• FIG. 74 illustrates a block diagram of a temperature and impedance feedback system that can be used to control the delivery of energy to tissue site416 byenergy source392 and the delivery ofcooling solution29 or gas29gtoelectrode314 and/or tissue site416 byflow regulator418. Energy is delivered toRF electrode314 byenergy source392, and applied to tissue site416. Amonitor420 ascertains tissue impedance, based on the energy delivered to tissue, and compares the measured impedance value to a set value. If the measured impedance exceeds the set value, a disablingsignal422 is transmitted toenergy source392, ceasing further delivery of energy toRF electrode314. If the measured impedance is within acceptable limits, energy continues to be applied to the tissue.
• The control of the flow of coolingsolution29 toelectrode314 and/or tissue site416 is done in the following manner. During the application of energy,temperature measurement device408 measures the temperature of tissue site416 and/orRF electrode314. Acomparator424 receives a signal representative of the measured temperature and compares this value to a pre-set signal representative of the desired temperature. If the tissue temperature is too high,comparator424 sends a signal to a flow regulator418 (which can be integral to a pump418) representing a need for an increased cooling solution flow rate. If the measured temperature has not exceeded the desired temperature,comparator424 sends a signal to flowregulator418 to maintain the cooling solution flow rate at its existing level.
• The foregoing description of various embodiments of the invention has been presented for purposes of illustration and description. Various methods of the invention are applicable to variety of medical, dermatological and surgical methods including reconstructive and plastic surgery procedures and minimally invasive procedures. It is not intended to limit the invention to the precise forms disclosed. Many modifications, variations and different combinations of embodiments will be apparent to practitioners skilled in this art. Further, elements from one embodiment can be readily recombined with one or more elements from other embodiments.

Claims (1)

1. A method of creating a tissue effect, comprising:

providing an electro-surgical device that includes an energy delivery device with an energy delivery surface, a housing coupled to the electrode with a guide that provides for cutting a skin layer and an underlying thickness of subcutaneous tissue while preserving an adjacent plane of tissue;

positioning the energy delivery surface at the skin surface;

delivering sufficient energy from the energy delivery device to cut the skin surface, create a plane of dissection at a controlled depth with a substantially uniform thickness while minimizing injury to tissue or structures within the flap, wherein the plane of dissection is a surgical plane of soft tissue where different or the same soft tissue components have been separated from or within each other.

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