Apparatus for Attachment of a Light Receiving Device to a Surgical Instrument
20220117649 · 2022-04-21
Inventors
- Markus Reiterer (Loipersbach, AT)
- Achim Brodbeck (Metzingen, DE)
- Klaus Fischer (Nagold, DE)
- Marc Mueller (Tuebingen, DE)
Cpc classification
A61B2017/22074
HUMAN NECESSITIES
A61B5/0075
HUMAN NECESSITIES
A61B2218/001
HUMAN NECESSITIES
A61B90/36
HUMAN NECESSITIES
A61B2018/00982
HUMAN NECESSITIES
A61B2018/00607
HUMAN NECESSITIES
A61B18/1482
HUMAN NECESSITIES
A61B5/0084
HUMAN NECESSITIES
A61B18/1492
HUMAN NECESSITIES
International classification
Abstract
An apparatus (10) serves for attachment of a light receiving device (24) for light analysis on an instrument (11) or an instrument component (12) during surgery by the surgery user of a surgical instrument (11) or their assistant. The apparatus (10) is preferably configured to releasably attach the light receiving device (24) on the instrument (11) or the instrument component (12). The apparatus (10) can comprise a light receiving device (24) and an electrode (15) fixed relative thereto. The electrode (15) can alternatively also be part of the instrument (11). The apparatus (10) can be releasably attachable to the instrument (11) or the instrument component (12) and can form an adapter for attachment of the light receiving device (24) on the instrument (11) or the instrument component (12) or can also be configured as part of the instrument (10).
Claims
1. An apparatus (10) configured for attachment of a light receiving device (24) for light analysis on a surgical instrument (11) or on an instrument component (12) of the surgical instrument (11) by a surgical user of the surgical instrument (11).
2. The apparatus (10) according to claim 1, wherein the apparatus (10) is configured to allow attachment of the light receiving device (24) in one single spatial position or in a plurality of predefined spatial positions relative to the instrument component (12) and/or the instrument (11).
3. The apparatus (10) according to claim 1, wherein the instrument (11) comprises an electrode (15) configured to be supplied with electrical RF energy, wherein the apparatus (10) is configured to allow attachment of the light receiving device (24) in one single spatial position or in a plurality of predefined spatial positions relative to the electrode (15).
4. The apparatus (10) according to claim 1, wherein the apparatus (10) is configured to support an electrode (15) and is configured to allow attachment of the light receiving device (24) in one single spatial position or in a plurality of predefined spatial positions relative to the electrode (15).
5. The apparatus (10) according to claim 1, comprising a mount (25) configured to limit movement of the instrument in the mount (25), except for movement of the instrument in an axial direction (L), wherein the mount (25) is configured to hold the instrument (11) in the axial direction (L) and includes a device (17, 51, 53, 21, 54, 55) for subsequent definition or limitation of the axial position of the instrument (11) in the mount (25).
6. The apparatus (10) according to claim 5, wherein the device (17, 51, 53, 21, 54, 55) for subsequent definition or limitation of the axial position of the instrument (11) comprises a section (21) that is movable transverse to the axial direction (L), wherein the section (21) is configured to engage the instrument (11) by a lateral movement of the section (21) after arrangement of the instrument (11) in the mount (25) in order to define or limit the axial position of the instrument (11) in the mount (25).
7. The apparatus (10) according to claim 6, wherein the section (21) is attached to the mount (25) in a flexible manner.
8. The apparatus (10) according to claim 1, wherein the apparatus (10) comprises a flushing channel (28, 58), wherein the flushing channel (28, 58) is configured to output a flushing medium that laterally passes a light inlet (31) of the light receiving device (24).
9. The apparatus (10) according to claim 1, wherein the apparatus (10) comprises a flushing channel (28, 58), wherein the apparatus defines a spatial position of the flushing channel relative to the light receiving device (24).
10. The apparatus (10) according to claim 8, wherein the light inlet (31) of the light receiving device (24) is arranged inside the apparatus (10) when the light receiving device (24) is attached thereto.
11. The apparatus (10) according to claim 8, wherein the light inlet (31) is arranged inside the flushing channel (58) when the light receiving device (24) is attached to the apparatus (10).
12. The apparatus (10) according to claim 8, wherein the light receiving device (24) extends at least completely or partly inside the flushing channel (28) when the light receiving device (24) is attached to the apparatus (10).
13. The apparatus (10) according to claim 1, further comprising a channel section (58) limited on one side by a wall (45a, 45b, 46) and is configured to be limited on another side by a first longitudinal side (16a) of an electrode (15) wherein the channel section (58) is configured to be flushed with a flushing medium, wherein the channel section 58 is configured such that a second longitudinal side (16b) of electrode (15) opposite the first longitudinal side (16a) is exposed at least in sections along the channel section (58) when the light receiving device (24) is attached to the apparatus (10).
14. The apparatus (10) according to claim 1, wherein an optical axis (OA) of the light receiving device (24) is oriented at an acute angle (W) with respect to a longitudinal axis of an electrode (15) of the instrument (11) when the instrument (11) is attached to the apparatus.
15. A method of using the apparatus (10) of claim 1, comprising attaching a light receiving device (24) on a surgical instrument (11) or an instrument component (12) of the surgical instrument (11) during a surgery with the apparatus (10).
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0038] Additional features and advantageous embodiments of the apparatus and the arrangement are derived from the following description as well as the figures. The figures show by way of example:
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DETAILED DESCRIPTION
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[0062] The applicator forming the instrument 11 comprises a handle part 12 having operating elements 13. In the distal end section of the handle part 12 an electrode holding shank 14 having an electrode 15 is mounted. The handle part 12 is connected with an electrical line 68 via which the electrode 15 can be applied with electrical radio frequency power.
[0063] The apparatus 10 comprises a distal section 17 in which the applicator 11 is inserted. The proximal end section 18 of the distal section 17 of apparatus 10 comprises a half shell holding the applicator 11. The half shell 18 is open on one longitudinal side 19 (top side) in order to provide access to the operating elements 13 of the instrument 11 at the top side 20 of the instrument 11.
[0064] The device further comprises a proximal section 21 that has, according to the example, a half shell form. It is open at the longitudinal side 19 of the apparatus 10 at which the proximal end section 18 is open as well. A proximal section 21 is connected with the distal section 17 of the apparatus 10 by means of a flexible transition section 22. The apparatus 10 surrounds the applicator 11 at least partly in a form-fit manner in order to define the relative position of a light conducting device and/or light receiving device 24 relative to the applicator 11. The light conducting device and/or light receiving device can particularly comprise at least one optical fiber.
[0065] The apparatus 10 extends from the proximal end to the distal end substantially in an axial direction R. The distal section 17 and/or the proximal section 21 can have a curved extension around an axis of curvature extending parallel to the longitudinal direction L. According to the example, the transition section 22 is rod-shaped. The transition section 22 is connected with the distal section 17 and/or the proximal section 21 at a central location from which the two shell parts of the distal section 17 or the proximal section 21 curve away in opposite directions in order to form the respective half shell. Particularly the transition section 22 does not form a concave mounting area for the applicator 11, contrary to the distal section 17 and the proximal section 21.
[0066] The distal section 17, the transition section 22 and the proximal section 21 consist preferably of the same plastic. The transition section 22 is preferably seamlessly monolithically connected with the distal section 17 and the proximal section 21. The apparatus 10 can be particularly manufactured by means of an injection molding process. The flexibility of the transition section 22 compared with the distal section 17 and the proximal section 21 is achieved according to the example, in that the transition section 22 is formed slimmer than the distal section 17 and the proximal section 21. It can particularly have a small dimension in each direction transverse to its extension ensuring the flexibility. Preferably the apparatus 10 or at least the distal section 17 is transparent in order to provide an improved view onto the operative site.
[0067] As particularly illustrated in
[0068] The apparatus 10 comprises in addition, as particularly also shown in
[0069] The line 28 extends in a protected manner laterally next to the applicator 11 between the flexible transition section 22 and the applicator 11 through the half shell-shaped proximal section 21 of the distal section 17 of the apparatus 10.
[0070] The second mount 27 for the line 28 is configured to guide it in sections substantially parallel to the applicator 11 in direction toward the distal end 29 of the apparatus 10. As particularly illustrated in
[0071] The optical fiber 24 can be centrally held in the line 28 or can substantially coaxially follow its extension. For example, holding elements (not shown) can serve for this purpose that are arranged inside the line 28 that allow a flushing medium flow through line 28 to the distal end 29 of the apparatus 10 and concurrently keep the optical fiber 28 at a distance to the inner wall surface 37 of line 28. As an alternative, the fiber 24 can be placed loosely in the line hose 28, for example, wherein an end section 34 of the fiber can be rigidly connected with the apparatus 10, as described below. For example, the optical fiber 24 is preferably secured also against twist of the optical fiber 24 around a longitudinal axis of the optical fiber 24. The volume flow of flushing medium is guided in the embodiment substantially concentrically relative to the optical fiber 24. As an alternative, the volume flow can be laterally supplied at the distal end 38 of the optical fiber 24. In both embodiments the flushing flow flowing around the distal end 38 of the optical fiber 24 serves to avoid contamination by spraying tissue liquid droplets or flying particles on the light inlet 31 of the optical fiber 24.
[0072] As illustrated in
[0073] In order to counteract contamination of the optical fiber 24, the optical fiber 24 preferably does not end flush with the apparatus 10 and also does not protrude from the apparatus 10. Rather the optical fiber 24 ends preferably relative to the distal end 29 of apparatus 10 offset backwardly inside a channel-shaped region 44, as illustrated in
[0074] The region 44 of the apparatus 10 is preferably open to one side. For example, if also the proximal end section 18 of the distal section 17 is open, the region 44 can be open to the same side (e.g. toward “the top”, for example in
[0075] The apparatus 10 comprises two side wall sections 45a, 45b in the region 44 that extend laterally past the optical fiber 24 such that the distal end 38 of the optical fiber 24 is offset backwardly relative to the distal end 29 of apparatus 10. In doing so, the light inlet 31 is protected at the face of the optical fiber 24 at least from particles and/or droplets that move from specific angles in direction toward the light inlet 31. The side wall sections 45a, 45b are connected via a bottom wall section 46 such that the region 44 or the apparatus 10 can have a U- or V-shaped cross-section there, for example, as apparent from
[0076] The light acceptance angle 47 is drawn in dashed lines in
[0077] For example, a section of the electrode 15 can be part of the form-fit section 26 of the applicator 11. A section of the electrode holding shank 14 of electrode 15 of the applicator 11 is part of the form-fit section 26 in the illustrated embodiment. The form-fit section 26 comprises a shape that fits a respective complimentary counter-shape of the first mount 25 of apparatus 10. In the illustrated embodiment the electrode holding shank 14 has a cylindrical shape that fits in the cylindrical form (bore) of first mount 25. Alternatively to the cylindrical form of form-fit section 26 and the first mount 25, they can have, e.g. polyhedral shapes fitting one another, e.g. a rectangular shape. By means of the pair of form-fit section 26 and first mount 25 the relative movability of the form-fit section 26 inside the first mount 25 and relative to the first mount 25 is blocked in all directions orthogonal to the center axis MA of the first mount 25 or to the longitudinal axis ELA of the electrode holding shank 14 and thus also relative to the working section 15a of electrode 15. By means of the first mounting channel 25, that can be closed in all radial directions, the position of electrode 15 relative to the end section 34 of the optical fiber 24 is defined radially in all directions.
[0078] A respective first stop 51 (see particularly
[0079] A second stop 54 for axial securing and particularly positioning of applicator 11 is formed on the proximal section 18 of apparatus 10. A second counter stop 55 of instrument 11 is formed by the proximal end of applicator 11 in the embodiment (see
[0080] In order to capture as much light as possible from the RF spark—that forms a divergent light source—the diameter of the light inlet 31 of the optical fiber 24 should be as large as possible and the light inlet 31 should be positioned as close as possible to the location of creation of the light appearance, e.g. an RF spark, at the electrode tip 50a in a manner maintaining the position. In order to counteract a contamination of optical fiber 24, e.g. by fume particles, aerosols or by spraying tissue particles, e.g. fat droplets, the light inlet 31 of optical fiber 24 would have to be located, however, as far as possible away from the location of creation of the light appearance. By means of defining the position of the applicator 11 between first stop 51 and second stop 54 and relative to the apparatus 10, an intensive light reception on one hand and an at most low contamination on the other hand is guaranteed.
[0081] The working section 15a of electrode 15 can be spatula-shaped (as illustrated) or needle-shaped, for example. The electrode 15 projects from the distal end 29 of apparatus 10 or protrudes beyond the distal end 29 of apparatus 10 in distal direction. For example the electrode 15 is orientated such that a flat side 50b (that can also be denoted as spatula side) of electrode 15 obliquely faces the light input 31 of optical fiber 24. Alternatively, the electrode 15 can be orientated such that the light input 31 faces a narrow side 50d, 50e (that can also be denoted as edge) of electrode 15. The rotational orientation of apparatus 10 or optical fiber 24 around the longitudinal axis ELA of electrode 15, e.g. the longitudinal axis of the spatula-formed working section 15a, can be defined by means of an alignment structure 56 and a counter alignment structure 57, as an example, e.g. during connection of the instrument 11 with the apparatus 10.
[0082] Exemplary alignment structure 56 and counter alignment structure 57 are shown in
[0083] During assembly of the apparatus 10 and instrument 11 during operation, the user of the device, e.g. a surgeon or an assistant of the surgeon, can proceed for example as follows: The user presses the proximal section 21 of apparatus 10 laterally away from a longitudinal axis of the distal section 17 or the longitudinal axis L of the first mount 25 against a spring force of transition section 22 (see arrow PP in
[0084] If the instrument 11 is arranged in the apparatus 10, the electrode 15 or electrode holding shank 14 largely closes the region 44 of apparatus 10 in which the optical fiber 24 ends relative to the bottom wall section 46 as by way of example illustrated in
[0085] The surgeon can operate with instrument 11 or apparatus 10, e.g. as follows: The applicator is preferably usable also without the apparatus 10. During surgical use of applicator 11 the user guides the applicator 11by holding it with handle part 12 and influences thereby the tissue by means of the applicator 11. For example, the surgeon can open and expose the operative site in an RF surgical manner by means of the applicator 11 without apparatus 10 being connected therewith. In this phase of the medical intervention no light analysis is usually required. An unnecessary contamination of the optical fiber 24 can thus be completely avoided in this phase. If the surgeon has prepared the location at which the preparation intervention shall be executed in the described manner, he/she or a surgery assistant can connect the apparatus 10 and thus the optical fiber 24 quickly and in the correct position with the instrument 11. A reliable light analysis is now possible by means of the optical fiber 24.
[0086] A system comprising the apparatus 10 can be configured such that the flow or flushing medium is automatically switched on prior to supply of applicator 11 with electrical radio frequency (RF) energy, if the apparatus 10 is connected with instrument 11, in order to be able to counteract a contamination from the outset by a flow around the optical fiber 24 at the distal end. For example, a gas can be used as flushing medium. Alternatively, the system can be configured, for example, such that—provided that instrument 11 is connected with apparatus 10—the supply of the electrode 15 with RF energy is only released, if line 28 is supplied with flushing medium. The flushing medium flow slows down droplets and/or flying particles sprayed away from the location of intervention and deflects them as far as possible, such that they do not hit the light inlet 31 of optical fiber 24. The mass or volume flow of flushing medium can be preferably adjusted to a value or limited to a maximum value by the system, at which the target tissue or the target structure on which the intervention shall be carried out is displaced in a manner that does not affect the surgical precision, but reliably slowing down and/or deflecting particles and/or droplets. Also a gas embolism is preferably avoided by means of the adjustment or limitation of the maximum volume flow and pressure by means of the system. In narrow body cavities the volume flow of flushing medium can in addition displace fume and/or liquid media such as blood or molten fat and thus allow an improved view on the operative site.
[0087] The surgeon can grab the assembled group of instrument 11 and apparatus 10 comprising the handle 12 of instrument 11 at the apparatus 10 for operation. Now the apparatus 10 serves at least as a part of a handle piece for handling the assembled group. Now the RF energy supply of electrode 15 is switched on again and the surgeon can continue working on the operative site with the instrument. Light created thereby, e.g. spark light, enters into the light inlet 31 and is analyzed by means of a not illustrated analysis device in order to provide information about the treated tissue to the surgeon, for example.
[0088] While
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[0093] Preferably the suction unit 61 comprises an extension section 61c that is guided in the distal section 61b in a telescopic manner and is displaceable by a forward slideable movement of a slide section 62, if required, in distal direction from a proximal position (shown in
[0094] The suction unit 61 can be transparent at the distal end in order to provide an improved view on the operative site. For example, the suction unit 61 consists or, if provided, at least the extension section 61c of transparent plastic. In prefer embodiments the suction unit 61 as well as the apparatus 10 are transparent at their distal ends.
[0095] As an alternative to the embodiment described above, the suction unit 61 can also be an undetachable part of apparatus 10.
[0096] The suction unit 61 serves to distract fume from the operative site created during RF surgical application by suction. The suction unit 61 comprises suction channel 63 that extends in the illustrated embodiment through the distal section 61b and the extension section 61c up to a suction opening 63a at the distal end of the suction unit 61. The apparatus 10 limiting the flushing channel 58 and containing the optical fiber 24 extends through the suction unit 61 and in the illustrated embodiment through the suction channel 63 and particularly through the suction opening 63a. While the electrical line 68 for supply of RF power (RF supply line), the line for the flushing medium and the suction line 64 are illustrated in
[0097] In this embodiment the suction opening 63a is compared to mouth of flushing channel 58a offset in proximal direction in each position of the extension section 61c. In
[0098] In another embodiment the suction opening 63a can be arranged closer to the distal end of electrode 15 than the mouth 58a of flushing channel 58. Such an embodiment is illustrated in
[0099] All indications in liter for the volume flows refer to the standard volume (standard liter) of the fluid.
[0100] Independent from whether apparatus 10 is connectable with a suction unit 61 or whether the suction unit 61 is an undetachable from apparatus 10, the apparatus 10 can in some or all embodiments define a discrete variety of possible positions of the light receiving device 24 relative to the applicator 11. If the applicator 11 defines a discrete variety of possible positions of electrode 15 relative to the handle 12, the apparatus 10 provides by means of handle 12 a discrete number of possible positions of the light receiving device 24 relative to the electrode 15. All positions of the variety are characterized in that it is guaranteed (if apparatus 10, instrument 11 and light receiving device 24 are determined for one another) that a sufficient amount of light of the light appearance created by instrument 11 can be received by the light receiving device 24. The position (0° location) shown in
[0101] For the embodiment illustrated in
[0102] The respective handle 12 is illustrated in
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[0104] An inventive apparatus 10 is provided for attachment by a user of a surgical instrument 11 of a light receiving device 24 for a light analysis on the instrument 11 or an instrument component 12 of instrument 11by the user of the surgical instrument 11. The apparatus 10 is preferably configured to releasably attach the light receiving device 24 on the instrument 11 or the instrument component 12. Preferably the apparatus 10 is configured such that the apparatus 10 can be repeatedly released and can be repeatedly used. In simple cases the instrument can be a handle 12 having an electrode 15. Embodiments of the apparatus 10 comprise a light receiving device 24 as well as an electrode 15 attached relatively thereto, wherein the apparatus 10 can be attached on the handle 12. Embodiments are possible in which the electrode 15 is not supported by apparatus 10, but by the instrument 11. However, embodiments are preferred in which the electrode 15 is a non-destructively releasable part of the apparatus 10 or is immovably installed in the apparatus 10. Embodiments are preferred in which the apparatus 10 is attachable (and preferably releasable again) by the surgical user or his assistant on the instrument 11 or the instrument component 12 and forms an adapter for attachment of a light receiving device 24 to the instrument 11 or the instrument component 12. In other embodiments the apparatus 10 is formed on the instrument 11, e.g. a channel in the instrument 11, in which an optical fiber 24 can be inserted. Preferably a rotational and/or translational movement of the light receiving device 24 relative to the electrode 15 is limited by means of the apparatus 10 such that the distal end of electrode 15 and/or light appearances created by supply of electrode 15 with electrical radio frequency energy during use of the instrument 11, always remain within the light acceptance angle 47 of the light receiving device 24. Preferably the form of a first mount 25 of apparatus 10 is adapted to the form of the instrument 11 in order to define the relative position and orientation of the light receiving device 24 relative to the electrode 15, except for such relative positions and orientations such that the tip or the distal end 50 of electrode 15 and/or the light appearances created by supply of electrode 15 with electrical radio frequency energy during use of the instrument 11 are in any remaining position within the light acceptance angle 47 of the light receiving device 24.
TABLE-US-00001 List of Reference Signs: 10 apparatus 11 instrument/applicator 12 handle 13 operating element 14 electrode holding shank 15 electrode 15a working section 16a bottom side of electrode holding shank 16b top side of electrode holding shank 17 distal section 18 proximal end section/half shell 19 longitudinal side 20 top side 21 proximal section 22 transition section 24 light receiving device/fiber optic 25 first mount/first mounting channel 26 form-fit section 27 second mount 28 line 28a opening (mouth) of line 29 distal end of device 30 wall surface 31 light inlet 32 distal end of line 33 line section 34 end section of optical fiber 35 mounting bore 36 holding elements 37 inner wall surface 38 distal end of optical fiber 39 support section 40 mounting wall 41 bend 42 mounting area 44 region 45a, b side wall section 46 bottom wall section 47 light acceptance angle 50a tip of electrode 50b flat side or spatula side of electrode 50c flat side or spatula side of electrode 50d narrow side or edge of electrode 50e narrow side or edge of electrode 51 first stop 52 wall section 53 first counter stop 54 second stop 55 second counter stop 56 alignment structure 57 counter alignment structure 58 channel section 58a mouth of channel section/flushing channel 59 trocar 60 abdominal cavity 61 suction unit 61a proximal section 61b distal section 61c extension section 62 slide section 63 suction channel 63a suction opening 64 suction line 65 coupling element 66 form-fit structure 67 mount 68 supply line 70 extension element 71 line part B width L longitudinal axis OA optical axis MA center axis MAV center axis of distal section ELA electrode longitudinal axis LK light acceptance angle W1 angle W2 angle between longitudinal axis of optical fiber and first mount/ electrode P arrow PP arrow PF arrow PS arrow R axial direction