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  • 专利说明
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    • 专利摘要:
    SURGICAL INSTRUMENT, CAUTERIZATION INSTRUMENT AND METHOD FOR CAUTTERIZING AND SEPARATING TISSUE. A cauterizing instrument (10) intended, in particular, for delicate operations, has two extensions (15, 16) with cauterizing jaws (19, 20, 36, 37), which can be actuated by a cauterizing tension, preferably , between 80 and 120 volts. The tissue receptacles (53, 54), which are separated from each other by a wall-like extension (24) at their lower edge carrying a cutting electrode (31), are defined between the extensions (15, 16). A cutting voltage of 300-500 volts is applied between an extension (16) and the cutting electrode. When the extensions are closed the trapped tissue is simultaneously sealed between the cauterizing jaws (19, 36 and 20, 37) and is cut by the cutting electrode (31). Even if the tissue is completely cut, for example after 0.3 to 0.5 seconds and cauterization requires more time, approximately 1.5 to 3.5 seconds, generally speaking, the ripples of tissue trapped in the receptacles of tissue (53, 54) act as anatomic protection of the edges of the blood vessel in the tool (12).
    公开号:BR102015015264B1
    申请号:R102015015264-7
    申请日:2015-06-24
    公开日:2022-01-25
    发明作者:Volker Mayer；Rolf Weiler；Heiko Schall；Achim Brodbeck；Tobias Amann
    申请人:Erbe Elektromedizin Gmbh；
    IPC主号:
    专利说明:

    [0001] The invention relates to a surgical instrument for cauterizing and separating biological tissue.
    [0002] Cauterization instruments, of the specified type, are used to perform operations on human patients or live animals. They are used to secure and close the fabric under the influence of pressure and current flow and also the resulting heat. Additionally, such instruments can be used to cut clotted or closed tissue.
    [0003] US 2007/0078456 A1 discloses such an instrument, having two movable extensions, which are used to secure empty blood vessels. The two extensions can be energized, so that the trapped and compressed empty blood vessel is heated between the extensions, and the walls of the blood vessel are connected to each other. The blood vessel, which is closed and thus sealed in this aspect, can then be cut at the cauterization zone by means of a displaceable blade.
    [0004] In order to close the blood vessel, the two extensions of the tool have flat contact surfaces, between which the blood vessel is closed. The contact surfaces must have a considerable minimum width in order to reliably close the blood vessel. The miniaturization of such tools is therefore subject to limits.
    [0005] Additionally, US 6 113 598 A discloses an instrument having two extensions, where one extension (the upper one) has a blade-shaped protrusion, which fits into a groove in the lower extension, which is delimited by two halves of resilient extension.
    [0006] With such an instrument it is possible to hold, impermeably, the ends of the blood vessel during coagulation. Here too, however, miniaturization is subject to limits.
    [0007] US 2002/0115997 A1 discloses an instrument which is intended, in particular, for the resection of lung tissue. The instrument has two extensions, which can be moved towards each other and away from each other, with electrode structures on both extensions. The electrode structures are profiled on either side of a cutting slit, through which a separating element can move, such that the retained tissue is held in an anatomical manner and is closed between the extensions. Here, both the upper and lower extensions, on either side of the cutting slit, contain a positive and a negative contact in order to produce the widest possible cautery edge on the tissue.
    [0008] US 8 394 094 discloses a similar electrosurgical instrument, in which the cutting electrode is determined to be a spring-mounted support.
    [0009] The purpose of the invention is to specify a cauterization instrument in which the design allows for a miniaturization of the tool.
    [0010] This objective is achieved with the cauterization instrument, according to claim 1, and with a method, according to claim 15.
    [0011] The cauterization instrument according to the invention for endoscopic, laparoscopic or open surgical application has two extensions. The first extension has at least two cauterizing electrodes, which are preferably electrically interconnected. The second extension also has at least two cauterizing electrodes, which are preferably electrically interconnected. One of the extensions (eg the top one) has a cutting electrode holder with a wall or extension similar to the cutting edge. The other extension has a matching bearing for the cutting electrode. Cauterization electrodes are mounted on the edges of the two extensions to produce cauterization edges on the biological tissue. Tissue receptacles are formed between the cutting electrode and the cauterizing jaws. These receptacles are preferably of such a volume that the density of current occurring is not much less than between the cauterizing jaws. Electrical energy is passed through the tissue retained between the cutting electrode and the cauterizing jaws, i.e. in the tissue located in the tissue receptacles, but during this process said tissue shrinks to a lesser extent compared to the tissue retained between the jaws to form a cautery edge. The tissue forms at least one undulation (“roll”) which, when the extensions are closed, strikes both the first cauterizing jaw and the second cauterizing jaw in approximately an anatomical manner from behind. The tissue receptacle and the tissue held therein thus act as anatomical protection for the tissue retained between the cauterization jaws, even when only a very narrow cauterization edge and a very delicate tissue cord is formed. Tissue cannot slip off the cautery instrument before the tool is opened.
    [0012] Fabric receptacles preferably have a rectangular cross section. The base face and the tissue support face are each preferably flat and each preferably extends from one cauterizing jaw of an extent to the other cauterizing jaw of the same extent. The base face and the fabric backing face preferably join the respective cauterizing jaws substantially at right angles.
    [0013] This concept also opens up the possibility of working with a cutting electrode that is activated at the same time as the cauterization electrodes, in such a way that they start the coagulation process and the cutting process, therefore, at the same time. Tissue can be cut by the cutting electrode before cauterization between the cauterizing jaws is complete. The simultaneous action of the cutting electrode and the cauterizing jaws on the tissue is not mandatory, but possible. The chronological sequence of cutting and cauterizing is preferably defined by the voltages applied to the cutting electrode and cauterizing jaws. The separation and cauterization time can thus be reduced, the working process can be simplified, and the instrument can be electrically driven. For example, a cautery voltage (e.g. 97V) between the cautery jaws and a cutoff voltage (e.g. 437V) between the cautery jaws and the cutting electrode can be applied simultaneously from a power circuit. Voltages can be supplied from an autotransformer. Power can be supplied initially with a slope-like current profile and then with constant voltage. The treatment may additionally be carried out in a time-controlled manner. A minimum time of 1.4 s and/or a maximum time of, for example, 2.8 s can be set. As a switch-off criterion in the time window thus defined, it can be specified that the power supply will be switched off when, after the first drop in tissue resistance, a further increase in said tissue resistance is determined, whereby a time tolerance of the power supply, for example 0.4 s, is implemented where appropriate. Additionally, the instrument, or apparatus supplying the same, may be provided with a spark and overvoltage detection device. A temporary voltage drop may be provided in order to extinguish identified sparks.
    [0014] Additionally, the specified concept is capable of being miniaturized. Due to the anatomical protection of the blood vessel ends or tissue ends in the tissue receptacles, the cauterization regions can be limited to very narrow, almost line-like strips, without the risk that the unclosed tissue edges will prematurely escape from the cauterization instrument.
    [0015] The tissue receptacles, which are formed on one side of the cutting electrode, have a shape where a particularly good fit can be achieved between the tissue and the closed instrument. Additionally, the width of the tissue receptacles is preferably greater than the width of the extension in the wall form which carries the cutting electrode. Additionally, the width of the tissue receptacles is preferably greater than the width of the cauterizing jaws. This also contributes to a reliable fit and to a sufficient reduction in current density within the tissue located in the receptacle.
    [0016] The cauterizing jaws preferably have a cross-sectional contour with rounded transitions. In particular, the cauterizing jaws are rounded towards the tissue receptacles, through which a build-up of current is avoided. Here, these rounded portions are formed in such a way that, except at the lowest current concentration, a reliable fit between the fabric and the closed extensions is possible. The cauterizing jaws of the two extensions preferably define cauterization distances from each other, which together define an obtuse angle. The rounding of the cauterizing jaws which are arranged closer to the cutting electrode can therefore achieve a large radius of rounding, whereby the current density is precisely limited here. If the cutting electrode is attached to the upper extension, the rounding radii of the lower extension, which are arranged towards the tissue receptacles, may have a different value compared to the rounding radii of the upper extension. These rays however preferably have the same value. The rounding radii of the cauterizing jaws on the outside of the extension have larger values than the rounding radii towards the tissue receptacles. The effect of fabric outside the extensions can thus be better controlled. Due to the slanted position of the cauterization distances, the extensions are automatically centered in relation to each other. Additionally, the cauterizing jaws on the fixing faces thereof, have radii towards the tissue receptacles from, for example, 0.05 mm to 0.1 mm, in order to achieve good anatomy between tissue and instrument. , and having radii on the outside of the extension from, for example, 0.1 mm to 0.3 mm, in order to achieve good etching properties. The fastening faces together define an attachment or cauterization distance of 0 to 0.1 mm, preferably 0 to 0.05 mm, which allows secure attachment of even thin tissue.
    [0017] The cautery jaws may have a main body with insulated regions, e.g. made of epoxy resin with etch electrodes arranged in a row, e.g. made from the main body material of the extension, e.g. high-grade steel quality. The main body of the extensions can be formed from a solid material or a stamped/bent core. The electrodes of the opposing cauterizing jaws are preferably arranged or formed in a manner that does not overlap each other. The insulating regions can be formed by inserts inserted or molded (cast or injected) within the extensions or by a number of cladding locations made of insulating material. Alternatively, an extension may be formed of ceramic, where it is then formed to be conductive, eg, metallized, in the region of the etch electrodes. It is also possible to form the extension from ceramics having different properties. The extension, for example, may be formed exclusively from ceramic, where it then comprises a non-conductive ceramic substance in the insulating regions and a conductive ceramic substance for the electrode region. The insulating regions prevent an electrical short circuit between the cauterizing electrodes of the two cauterizing jaws, even when the extensions touch. The mutual longitudinal spacing between the electrodes of the two extensions is 0.1 mm to 0.3 mm, preferably 0.25 mm. Additionally, a current flow is provided in the biological tissue having a component along the cauterizing jaws, i.e. an extension of the current parts with an improvement of the biological effect of thermal form. Additionally, the cauterizing jaws, on their sides in contact with the tissue receptacles, may be provided with a non-metallic material, for example PTFE, plastic resin or the like. The current flow of the cutting current is thus concentrated, on the one hand to the cutting electrode and, on the other hand, to the tissue region gripped between the cauterizing jaws. The risk of tissue sticking to tissue receptacles is overcome or considered to be minimized.
    [0018] The cutting electrode holder can be formed from ceramic, plastic or an insulated coated metal. Additionally, the cutting electrode holder may have a surface that tissue does not adhere to. To this end, the surface of the cutting electrode holder can be formed, for example, coated in an anti-adhesive manner. Additionally, the cutting electrode holder has a high tracking resistance or a high CTI value (comparative tracking index), preferably above 600. The cutting electrode is preferably incorporated as a thin strip, which entails a exposed end face and being anchored by suitable means, in particular a number of feet, in or on the electrode holder. The thermal inertia of the cutting electrode is thus limited to a minimum. The counter support can be resiliently arranged to prevent the fabric from being crushed and to guide the cut by electrical influence. This benefits the cauterization reliability, since in this way a movement, caused by the cut tissue, between the cutting electrode of one extension and the counter bearing of the other extension, does not cause a movement of the extension to the same extent, and therefore, does not causes movement between opposing cauterizing jaws. Alternatively, or additionally, the cutting electrode holder can be spring mounted. In this case, the bearing can be rigidly fixed.
    [0019] If the cutting electrode holder is formed from plastic, the cutting electrode is preferably over-molded with plastic. The cutting electrode may consist, for example, of high-quality sheet steel. The width of the cutting electrode is preferably approximately 0.1 mm. The thickness of the plastic on both sides of the cutting electrode is preferably approximately 0.15 mm. The cutting electrode preferably ends with the two plastic walls covering the sides of said electrode (without the cutting edge protrusion). A thermoset such as plastic is preferably used. Alternatively, the cutting electrode in the unused state may protrude slightly beyond the plastic walls, for example by 0.02 mm to 0.04 mm. The protrusion can change during instrument operation, for example, by burning (“burn-up”) of the cutting electrode holder.
    [0020] If the cutting electrode holder is made of ceramic, preferably ZrO2 ceramic, the cutting electrode holder and the cutting electrode are prefabricated separately and then joined together. The width of the cutting electrode is preferably 0.2 to 0.25 mm. It may consist of a sheet of metal, in particular high-quality sheet steel. The insulating walls on both sides of the cutting electrode are preferably 0.15 mm thick. A protrusion of the cutting edge of 0.02mm to 0.04mm is preferably defined. The cutting electrode can be interconnected with the cutting electrode holder, pressed with it or integrally connected with it. There is normally a distance between the cutting electrode and the thin insulating walls of the cutting electrode holder. This distance can be filled with adhesive, silicone or similar. Alternatively, the cutting electrode may have a side insulation, formed, for example, from a paint or a coating, for example, parylene. The lateral contact face of the cutting electrode is therefore insulated, and the influence of a fluid located in the distance between the cutting electrode and the cutting electrode holder on the cutting effect of the cutting electrode is minimized, preferably prevented.
    [0021] The counter bearing arranged opposite the cutting electrode, can preferably be mounted with a spring. The spring travel can be set to less than 1 mm, preferably 0.5 mm. The counter-bearing is used to maintain the clamping force between the cauterizing jaws. This is achieved through the mechanical decoupling of the tissue fixation in the region of the cauterization jaws, from the tissue fixation between the cutting electrode and the counter bearing. Wrinkling of the tissue during cutting and during cauterization is thus also decoupled from the clamping force between the cauterizing jaws. This effect also occurs in embodiments with the counter-bearing arranged rigidly, and a cutting electrode mounted on springs.
    [0022] The top face or fabric support face of the counter bearing may sit, when the extensions are closed, in another plane compared to the cauterization jaws. The cutting plane of the cutting electrode projects beyond the cauterizing jaws of the cauterizing electrodes arranged over the same length. The cutting process is therefore performed on a different plane compared to the cauterization process.
    [0023] When the extensions are open, the counter bearing may project beyond the cauterization jaws of the same extension. When the extensions are closed the resiliently or resiliently mounted counter-bearing is then compressed and in doing so is pressed into the extension. The spring force working against the cutting element is thus created.
    [0024] The counter-bearing preferably consists of an insulator with a non-stick surface, eg made of PTFE, and similar or identical tracking resistance properties compared to the cutting electrode holder. This spring assembly of the counter bearing results in a behavior with which the cutting distance is adapted to the shrinkage of the fabric during cutting. The elongated counter-bearing can be resilient at the proximal end thereof and independently of the distal end thereof and thus can also define a wedge-shaped distance with the cutting electrode when different tissue thicknesses are present along the electrode. cutting.
    [0025] Additionally, or alternatively, it is possible to mount the spring on the cutting element. The bearing in this case can be mounted rigidly or similarly resiliently movably. It is also possible to mount one of the elements so as to be pivotable about a transverse geometric axis and to mount the spring on the other element, e.g. with particularly short spring travel, e.g. less than 0.5 mm , in order to achieve a good adaptation of the cutting electrode and the counter-bearing to different tissue resistances along the cutting electrode.
    [0026] The method, according to the invention, for cauterizing and separating the tissue preferably comprises at least the following steps: - the tissue is retained between two extensions in such a way that it is clamped between the jaws of cauterization and also between the cutting electrode and the tissue support face, where tissue receptacles are formed between closed cauterizing jaws and a cutting electrode holder, where the tissue receptacles are filled at least in part, by parts tissue, and energy is fed simultaneously to the cauterizing jaws and cutting electrode.
    [0027] Due to the simultaneous power supply to the cauterization electrodes and the cutting electrode, the processes of cauterization of blood vessels and separation (cutting) of blood vessels, occur simultaneously. Separation of blood vessels can be completed before cauterization of blood vessels is completed. The tissue receptacles, during the blood vessel cauterization process, protect the edges of the tissue within the extensions until the cauterization process is completely finished. According to the invention, due to the design, the extensions together with the type of power supply, according to the invention, the processing, in particular the separation and cauterization of blood vessels, can be formed with the highest quality . The entire process is short, usually due to the simultaneous start of cauterization and cutting, and usually lasts no longer than cauterization alone.
    [0028] Additional details of the advantageous embodiment of the invention will become more apparent from the drawing of the description or claims. In the drawings:
    [0029] Figure 1 shows an illustration, in schematic perspective, of a complete cauterization instrument;
    [0030] Figure 2 shows an illustration of the cauterization instrument tool, according to Figure 1, in partially enlarged perspective in section;
    [0031] Figure 3 shows the tool, according to Figure 2, in the closed state in cross section;
    [0032] Figure 4 shows the tool, according to Figure 3, when closing and separating an empty blood vessel;
    [0033] Figure 5 shows the cutting electrode of the tool, according to figure 2, in a partially cut perspective illustration, in a first embodiment;
    [0034] Figure 6 shows the cutting electrode, according to Figure 5, in cross-section;
    [0035] Figure 7 shows a modified embodiment of a cutting electrode and a cutting electrode holder, in longitudinal section; and
    [0036] Figure 8 shows a perspective illustration of the further modified embodiment of a cutting electrode.
    [0037] Figure 1 shows an instrument 10 with an elongated shaft 11, in which the distal end of the same carries a tool 12. The proximal end of the shaft 11 is connected to a housing 13, in which the driving elements 14 are arranged. for the movement and actuation of the tool 12. The instrument 10 is a cauterization instrument. Consequently, the tool 12 is used to properly close and cut the tissue where the blood vessels and spaces belonging to the tissue are to be closed and therefore sealed at the edge of the created tissue.
    [0038] The tool 12 provided in the instrument 10 is formed in a particular way. It has a first extension 15, in Figure 2, the upper extension, and a second extension 16, in Figure 2, the lower extension, at least one of which is pivotally mounted on an axis of rotation 17. In this case , depending on the application, the first extension 15 or the second extension 16, or both extensions 15, 16, can be mounted so as to be pivotable or otherwise movable around a common axis or on different articulation axes, in such a way that the extensions 15, 16 can be moved towards each other and away from each other.
    [0039] The extensions 15, 16 are again shown separately in cross-section in Figures 3 and 4. The first extension 15 may consist, for example, of metal or other material resistant to bending. It has a main body 18 with a U-profile cross-section. The main body 18 has two first etching jaws 19, 20, which run parallel to each other, are preferably electrically interconnected, and which delimit a groove 21 between one and the other. This groove preferably extends through most of the length of the first extension 15 and is used to receive a support for the cutting electrode 22. This has a base 23 which is matched to the contour of the groove 21 and rests on the in a stationary, immobile manner. From one face of the base 23a, an extension in the form of wall 24 extends away from the base 23, which, for example, is rectangular in cross-section, preferably centered between the two cauterizing jaws 19, 20, so that that said extension protrudes from the groove 21. The groove 21 is delimited by the edges of the cauterizing jaws 19, 20, on which cauterizing electrodes 25, 26 are formed. The face of the base 23a, 23b, starting from the cauterizing jaws 19 and 20, respectively, extends as the extension 24 is adjusted backwards with respect to the cauterizing electrodes 25, 26. The cauterizing electrodes 25, 26 may be electrically conductive connected to the main body 18. The cauterizing electrodes 25, 26, as can be seen, in particular from Figure 2, preferably form a row of individual conductive faces spaced apart, which are spaced apart from each other. by insulating regions 27, 28. Extension 15 may additionally have an electrically insulating coating 29, so that the electric current introduced into extension 15 can be introduced into biological tissue 30 (Figure 4) only at cauterization electrodes 25, 26 Preferably, there is a spacing between the insulating coating 29 and the insulating regions 27, 28 such that the material from the etch electrodes is not insulated in this region. region. Good cauterization quality is thus obtained.
    [0040] The cutting electrode support 22 has a cutting electrode 31, which is arranged on the end face of said support. Here, the cutting electrode 31 sits in a groove or recess of the wall-shaped extension 24, where the cutting electrode 31 is exposed through an end face 32. The cutting electrode 31 is received between two walls 33, 34 of the slot. The walls 33, 34 of the groove preferably have a width which is approximately as large as the width of the cutting electrode 31. Reference is made in this connection to Figure 6. The width B of the electrode 31 may be in the range of 0.05-0.25 mm and is preferably 0.1 mm. The walls 33, 34 of the insulating groove preferably have a thickness of the same dimension. For example, they have a thickness of 0.15 mm. They end with each other apart from a small bulge. The protrusion U of the end face 32 of the cutting electrode 31 beyond the end faces of the groove walls 33, 34 is merely a few tens of µm, for example from 0 to 40 µm.
    [0041] The length of the wall-shaped extension 24, measured from the base 23 to the cutting electrode 31 is preferably such that the end face 32 projects beyond the cauterizing jaws 19, 20 to, for example , from 0.5 to 1 mm, preferably 0.9 mm accordingly, the fabric supporting face 44 of the second extension 16 is pressed approximately the same distance to the second extension 16 by the wall-shaped extension 24 of the first extension 15, when the extensions are closed, in which they determine the contact of the cauterizing jaws 19, 36 and 20, 37 or almost contact with each other. This distance is shown in figure 3 on the right side next to tool 12 as the T dimension.
    [0042] Figure 3 also shows the second extension 16 which also has a main body 35, preferably made of electrically conductive material. The main body 35 again has a U-shaped cross-section, in which a groove 38 is formed between two second cauterizing jaws 36, 37. The cauterizing electrodes 39, 40 (Figure 2) are again formed on, preferably interconnected, electrically to the second cauterizing jaws 36, 37 of the second extension 16e, are arranged in a row along the upper edges of the cauterizing jaws 36, 37. The cauterizing electrodes 39, 40 are shorter as measured in the longitudinal direction of the jaw than in the insulating regions 27, 28 of the first extension 15. Similarly, the cauterizing electrodes 25, 26 of the first extension 15 are shorter, as measured in the longitudinal direction of the jaw, than in the insulating regions 61, 62 , that is, the distances between the second cauterization electrodes 39, 40 of the second extension 16. Additionally, the first cauterization electrodes 25, 26 are positioned over the first extension 15, such that they are disposed between the second etch electrodes 39, 40 when the extensions 15, 16 are closed, i.e. contact the insulating regions 61, 62 of the second extension 16. That is, therefore, an electrical short circuit between the first extension 15 and the second extension 16 is prevented.
    [0043] The second extension 16, as shown in Figure 3, may, in turn, be provided with an insulating coating 41. A counter bearing 42 for the cutting electrode 31 is arranged in the groove 38. The counter bearing 42 may be movably mounted parallel to the cauterizing jaws 36, 37, and can be pressed into the groove 38, for example against the force of a spring element 43. For example, the counter bearing 42 is a similar element the blade, consisting of plastic or ceramic, or other electrically non-conductive, preferably with a flat tissue backing face 44 forming a supporting face for the biological tissue 30 and in the rest position is disposed below the cauterizing electrodes 39 , 40, i.e. within the groove 38. The fabric backing face 44 extends starting from the cauterizing jaw 36 to the cauterizing jaw 37. As required, the fabric backing face 44 can also be formed into a structured way, or in the form one curve or a combination thereof.
    [0044] The spring element 43 may be a compression spring, which is supported at one end in the bottom of the groove 38 and at the other is operatively connected to the counter bearing 42. A plurality of such compression springs may also be arranged along of extension 16 in a row. Alternatively, an elastomer element may be seated or secured to the bottom of the groove, like a spring, upon which the elastomer element of the counter bearing 42 is supported. The travel of the counter-bearing spring 42 may be relatively low and, for example, may be limited to less than one millimeter, preferably 0.5 mm. The counter-bearing spring travel is dependent on the spring element 43. With a preloaded spring element 43 this travel is reduced, for example, to 0.5 mm or less, and with a non-preloaded spring element loaded 43 this stroke also includes the path with which the preload is generated, and may be 1 mm or more. Alternatively, the functions of the bearing 42 and spring element 43 can be provided in a single component, for example a component produced from elastomer.
    [0045] The cauterizing jaws 36, 37 are rounded on the upper side thereof. Together with the cauterizing jaws 19, 20 of the first extension 15, which work in pairs to delimit, in each case, a distance 45, 46, in which the orientation is indicated in Figure 3 by dashed and dot lines 47, 48. orientation of distances 45, 46 may be determined by planar facets 49, 50, 51, 52 provided on cauterizing jaws 19, 20, 36, 37. The directions fixed by distances 45, 46 and defined by lines 47, 48 form an obtuse angle with a vertex or point of intersection S, which marks the peak of the angle. This indicates the direction of the cutting electrode 31. The obtuse angle is preferably in a range of 130 to 150°.
    [0046] The geometry determining the function of the tool 12 additionally includes two fabric receptacles 53, 54. These are formed on both sides of the wall-shaped extension 24, and comprise regions of the grooves 21 and 38. They are delimited. vertically between the base 23 and the fabric support face 44 of the counter bearing 42. This vertical extension V is indicated in Figure 3 and rests, when the extensions are closed without fabric, for example, in the range of 0.7 mm to 2.5 mm, preferably 1.4 mm. The distance 45, 46 is arranged approximately centered with respect to the vertical extent V of the tissue receptacle 53 or 54 or, preferably, is arranged slightly offset towards the face of the base 23a.
    [0047] The two tissue receptacles 53, 54 are preferably of equal size. They have a horizontal extension H, which is determined by the distance between the wall-shaped extension 24 and the respective cauterizing jaws 19, 36 and 20, 37. This horizontal extension H is preferably greater than the thickness of the extension. 24 to be measured in the same direction. The horizontal extent of such a tissue receptacle is preferably approximately 0.2 to 0.6 times the vertical extent. When the extensions 15, 16 are closed, the fabric receptacles 53, 54, which are preferably rectangular in cross section, are formed in the direction of movement B between the fabric bearing face 44 of the counter bearing 42 and the base face. 23a of the base 23, and also transversely to the direction of movement B between the extension 24 and the first cauterizing jaws 19, 36 and also between the extension 24 and the second cauterizing jaws 20, 37.
    [0048] The instrument described in this aspect works as follows:
    [0049] In order to cauterize and separate tissues, in particular empty blood vessels or tissues containing empty blood vessels, this tissue is retained between the extensions 15, 16. Through the appropriate action of the actuating elements 14, the extensions 15, 16 are moved towards each other in such a way that the biological tissue 30 is retained, according to Figure 4. The tissue 30 is subjected during this process to pressure between the cauterizing jaws 19, 36 and 20, 37, despite that said tissue is relatively pressure relieved in tissue receptacles 53, 54. Cutting electrode 31, however, also exerts great pressure on tissue 30.
    [0050] For tissue cauterization an electrical voltage, preferably a high frequency alternating voltage is active between the extensions 15, 16, such that an electrical current flows through the biological tissue 30 between the electrodes 25, 26 of the first extension 15 and the electrodes 39, 40 of the second extension 16, so as to heat said tissue and cause a fusion of the retained tissue. At the same time, the cutting electrode 31 is activated. It is also powered by an electrical voltage, preferably a high-frequency voltage, at which the reference potential lies on one of the extensions 15, 16, preferably on the second extension 16, i.e. on the cauterization electrodes 39. , 40.
    [0051] Due to the small area of the cutting electrode, preferably approximately from about 1 mm2 to 3 mm2, the current density at the end face 32 is high enough that the biological tissue 30 is quickly cut. The fabric retracting under the cutting electrode 31 is supported by the resilient counter bearing 42. Said fabric is pressed by the fabric support face 44 towards the end face 32, in such a way that it remains continuously in contact with the cutting electrode. 31. The current density, however, decreases drastically already a short distance from the end face 32. The cross section available for the flux current changes on the side wall of the extension 24, from the cross section of the narrow distance. wide cross-section of the tissue receptacle 53 or 54. The biological tissue provided therein is therefore only slightly heated and shrinks to a much smaller size compared to the tissue beneath the end face 32. The cauterization edges form thus, between each pair of cauterizing jaws 19, 36 and cauterizing jaws 20, 37, respectively, where all spaces at the cauterizing edges in the tissue 30 are closed and a similar connection before a weld seam is formed in the fabric. At the same time, or in a delayed manner, the tissue below the cutting electrode 31 is cut. From the closed extensions 15, 16, fabric undulations seated in the fabric receptacles 53, 54 prevent the fabric 30 from escaping the tool 12. Only when the tool is opened are the fabric edges released and the treatment process is complete.
    [0052] The fundamental task during tissue treatment 30 is performed by cutting electrode 31 and cutting electrode holder 22. In order to form tissue receptacles 53, 54 so as to be as large as possible with the width minimum total of tool 12, the total width G (Figure 6) of the extension in the form of wall 24, is as small as possible. It is preferably a few tenths of a millimeter in size. This also has the effect that the current density just under the cutting electrode 31 has a value sufficient to cut the tissue and then drastically decreases so as to form ripples seated in the tissue receptacles 53, 54.
    [0053] Figure 5 shows the variant of a cutting electrode 22 made of ceramic. The wall-shaped extension 24 on the end face thereof has a groove 55, in which the blade-shaped cutting electrode 31 sits. This preferably has a series of attachment extensions 56, 57 extending through the openings of the cutting electrode holder 22. The electrode arrangement thus formed can be adhesively joined from a holder of the cutting electrode. cutting electrode 22 formed with ceramic. One or more clamping extensions 56, 57 can be connected at the base 23 to an electrical line 58, which supplies current to the cutting electrode 31.
    [0054] The cutting electrode holder 22, regardless of its specific design, induces an insulation potential between the cutting electrode 31 and the cauterizing electrodes 25, 26, 39, 40. Although the cauterizing electrodes 39 and 40 used, for example, as neutral electrodes, the cauterizing electrodes 25, 26 can be actuated with a voltage causing cauterization, preferably said voltage being lower than the voltage fed to the cutting electrode 31 and intended to cut the tissue. The cauterizing electrode 25, 26, 39, 40 preferably has a total electrode area that is greater than ten times, preferably greater than twenty times, the area of the end face 32, such that the power supplied cuts tissue only on end face 32, but does not cut tissue with cauterization electrodes 25, 26, 39, 40.
    [0055] Figure 7 illustrates a modified embodiment of the cutting electrode holder 22. The cutting electrode 31 again seats in a groove of the cutting electrode holder and is anchored there with the resilient base 59. The main body of the cutting electrode holder 22 may consist of ceramic or plastic. A thermoset or a silicone which, in particular, is stable under high temperature, being flame retardant and stable against ignition erosion, and also having a CTI greater than 600 is suitable as the plastic. Additionally, it must have sufficiently high mechanical strength and a thermal conductivity greater than one W/mK.
    [0056] Such plastic can be provided, in particular, with a built-in electrode 60, according to Figure 8. The cutting electrode 31, also here as in all other embodiments, can consist of a metallic foil, for example, of high quality steel. An internal connection of the plastic and embedded electrode 60 and also a low heat input to the plastic is achieved through the numerous windows provided in the embedded electrode 60.
    [0057] A surgical instrument 10 is intended, in particular, for delicate procedures having two extensions 15, 16 with cauterizing jaws 19, 20, 36, 37, which can be actuated with a cauterizing voltage, preferably between 80 and 120 volts. The tissue receptacles 53, 54, which are separated from each other by an extension in the form of a wall 24 whose lower end carries a cutting electrode 31, are defined between extensions 15, 16. of 300-500 volts, is applied between an extension 16 and the cutting electrode. When the extensions are closed the retained tissue is simultaneously closed between the cauterizing jaws 19, 36 and 20, 37 and is cut by the cutting electrode 31. Although the tissue is completely cut, for example after 0.3 to 0, 5 seconds and cauterization requires more time, in total approximately 1.5 to 3.5 seconds, blood vessel separation with closed blood vessel ends can be achieved. Here, the tissue receptacles 53, 54 act as anatomic protection of the separated ends of the blood vessel and thus ensuring the formation of the end of the blood vessel closed with the edges of the tissue in the tool 12. The ends of the blood vessels are weaker or are not coagulated compared to the cauterization region, and thus form thick areas like ripples, which prevent the edges of tissue from escaping the instrument when said instrument is closed. Reference sign list: 10 Instrument 11 Shaft 12 Tool 13 Housing 14 Handle elements 15 First extension 16 Second extension 17 Pivot shaft 18 First extension main body 15 19.20 First cauterizing jaw 21 Groove 22 Cutting electrode holder 23 Base of cutting electrode holder 23a Face of base 24 Extension in the form of wall of cutting electrode holder 25.26 Cauterization electrodes of the first extension 27.28 Insulating regions of 15 29 Electrically insulating coating 30 Biological tissue 31 Electrode of cut 32 End face 33.34 Groove walls B Cutting electrode width U Protrusion 35 Main body 36.37 Second cauterizing jaw 38 Groove 39.40 Second extension cauterizing electrodes 41 Insulating coating 42 Counter bearing 43 Spring element 44 Tissue support face 45 Distance between cauterization jaws 19 and 36 46 Distance between cauterization jaws 20 and 37 47 Line of illustration distance guidance action 45 48 Distance guidance illustration line 46 49-52 Faces 53.54 Tissue receptacles V Vertical extent of tissue receptacles 53, 54 H Horizontal extent of tissue receptacles 53, 54 55 Groove 56.57 Clamping Extensions T Cutting electrode protrusion away from the cauterizing electrode 58 Row 59 Base 60 Electrode insert 61.62 Insulating regions of 16
    权利要求:
    Claims (14)
    [0001]
    1. Surgical instrument, characterized in that it comprises: - a first extension (15), which has two first cauterization jaws (19, 20) arranged at a distance from each other, delimiting a first groove (21) between them, - an electrically insulated cutting electrode holder (22), which has a base (23), which is arranged in the first groove (21) and which has a base face (23a), which is situated behind in a direction of movement (B) of the first extension (15) so as to be retracted from the cauterizing electrodes (25, 26) disposed on the first cauterizing jaws (19, 20) and from which a wall-shaped extension ( 24) extends outward at a distance from the first cauterizing jaws (19, 20) of the first extension (15), - a cutting electrode (31), which is incorporated in the cutting electrode holder (22) with a face exposed end (32), - a second extension (16), which has two second cauterizing jaws (36, 37), which s are arranged at a distance from each other and which delimit a second groove (38) from each other, the first and second extensions (15, 16) being movable relative to each other and spaced apart in the direction of movement ( B) so as to be closed and opened, - a counter bearing (42), arranged in the second groove (38), for the cutting electrode (31), the counter bearing (42) having a fabric support face (44), which is situated behind the cauterizing electrodes (39, 40) of the second cauterizing jaws (36, 37) when the extensions (15, 16) are closed, with tissue receptacles (53, 54) are formed in the direction of movement (B) between the fabric support face (44) of the counter bearing (42) and the base face (23a) of the base (23) and transversely to the direction of movement (B) between the extension (24) and each of an opposing pair of the first and second cauterizing jaws (19, 36) and between the extension (24) and each of the other opposing pair of the first and second the cauterizing jaws (20, 37) when the extensions (15, 16) are closed; each tissue receptacle having a width (H) measured transversely to the direction of movement (B) between the extension (24) and the first and second cauterizing jaws (19, 36; 20, 37), and each of the first and second cauterizing jaws having a width between an internal surface facing the tissue receptacle and an externally facing surface opposite it, measured transversely to the direction of movement (B) in the tissue contacting the surfaces of their respective cauterizing electrodes (25, 26, 39, 40), the width of each tissue receptacle being greater than said width of each of the first and second cauterizing jaws.
    [0002]
    2. Instrument, as defined in claim 1, characterized in that the width (H) of the fabric receptacles (53, 54) is smaller than the height measured in the direction of movement (B) between the counter bearing (42) and the base (23).
    [0003]
    3. Instrument according to claim 1, characterized in that the width (H) of the tissue receptacles (53, 54) is greater than the thickness of the extension (24) measured in the same direction (24) as the width.
    [0004]
    4. Instrument according to claim 1, characterized in that the first and second cauterization jaws (19, 36; 20, 37) end in the tissue contacting surfaces that each have a cross-sectional contour with transitions rounded.
    [0005]
    5. Instrument according to claim 1, characterized in that the opposing pairs of the first and second cauterization jaws (19, 36; 20, 37) each define a cauterization distance (45, 46) from each other when the extensions are closed without the presence of tissue between opposing pairs of the first and second cauterizing jaws.
    [0006]
    6. Instrument according to claim 5, characterized in that both cauterization distances (45, 46) define an obtuse angle (β) with each other.
    [0007]
    7. Instrument according to claim 6, characterized in that the angle (β) has a vertex (S) that points towards the cutting electrode.
    [0008]
    8. Instrument according to claim 1, characterized in that each cauterization mordant (19, 36; 20, 37) has at least one insulating region (27, 28, 61, 62), which is located between the electrodes (25, 26, 39, 40) of each respective cautery jaw arranged in a row.
    [0009]
    9. Instrument according to claim 8, characterized in that the cauterization electrodes (25, 26; 39, 40) of each of the cauterization jaws (19, 20; 36, 37) are electrically interconnected.
    [0010]
    10. Instrument according to claim 8, characterized in that the cauterization electrodes (25, 26; 39, 40) of the opposite pairs of the first and second cauterization jaws (19, 36; 20, 37) are arranged in such a way that one does not overlap the other.
    [0011]
    11. Instrument, according to claim 1, characterized in that the cutting electrode support (22) comprises ceramic or plastic.
    [0012]
    12. Instrument according to claim 1, characterized in that the cutting electrode (31) comprises a continuous blade supporting the exposed end face (32), and the blade is anchored to the electrode support (22) through a plurality of attachment extensions (56, 57).
    [0013]
    13. Instrument according to claim 1, characterized in that the cutting electrode (31) comprises a continuous blade supporting the exposed end face (32), and the blade is anchored to the electrode support (22) through a plurality of resilient feet (59).
    [0014]
    14. Instrument according to claim 1, characterized in that the cutting electrode support (22) is rigidly arranged in the first groove (21) and the counter bearing (42) is movably arranged in the second groove (38), or where the cutting electrode holder (22) is movably arranged in the first groove (21) and the counter-bearing (42) is arranged, rigidly or movably, in the second groove (38).
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    同族专利:
    公开号 | 公开日
    KR20170021817A|2017-02-28|
    PL2959854T3|2018-07-31|
    KR102003099B1|2019-07-23|
    RU2015124783A|2017-01-10|
    JP2016007542A|2016-01-18|
    EP2959854A1|2015-12-30|
    CN105310769B|2018-04-24|
    KR20160000874A|2016-01-05|
    CN105310769A|2016-02-10|
    RU2618186C2|2017-05-02|
    EP2959854B1|2018-03-21|
    BR102015015264A2|2017-12-19|
    US20150374430A1|2015-12-31|
    JP6216741B2|2017-10-18|
    US10130414B2|2018-11-20|
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    法律状态:
    2017-12-19| B03A| Publication of a patent application or of a certificate of addition of invention [chapter 3.1 patent gazette]|
    2018-10-30| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|
    2020-07-07| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]|
    2021-12-28| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|
    2022-01-25| B16A| Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 24/06/2015, OBSERVADAS AS CONDICOES LEGAIS. |
    优先权:
    申请号 | 申请日 | 专利标题
    EP14173954.0A|EP2959854B1|2014-06-25|2014-06-25|Surgical instrument|
    EP14173954.0|2014-06-25|
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