WO2017047114A1 - 医療用デバイス - Google Patents
医療用デバイス Download PDFInfo
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- WO2017047114A1 WO2017047114A1 PCT/JP2016/053327 JP2016053327W WO2017047114A1 WO 2017047114 A1 WO2017047114 A1 WO 2017047114A1 JP 2016053327 W JP2016053327 W JP 2016053327W WO 2017047114 A1 WO2017047114 A1 WO 2017047114A1
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- state
- insertion portion
- protrusion
- medical device
- light
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
- A61B1/00147—Holding or positioning arrangements
- A61B1/00154—Holding or positioning arrangements using guiding arrangements for insertion
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/30—Devices for illuminating a surgical field, the devices having an interrelation with other surgical devices or with a surgical procedure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
- A61B1/00112—Connection or coupling means
- A61B1/00121—Connectors, fasteners and adapters, e.g. on the endoscope handle
- A61B1/00128—Connectors, fasteners and adapters, e.g. on the endoscope handle mechanical, e.g. for tubes or pipes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
- A61B1/06—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with illuminating arrangements
- A61B1/07—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with illuminating arrangements using light-conductive means, e.g. optical fibres
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/32—Surgical cutting instruments
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/34—Trocars; Puncturing needles
- A61B17/3478—Endoscopic needles, e.g. for infusion
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B18/04—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
- A61B18/12—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating by passing a current through the tissue to be heated, e.g. high-frequency current
- A61B18/14—Probes or electrodes therefor
- A61B18/1442—Probes having pivoting end effectors, e.g. forceps
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B18/04—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
- A61B18/12—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating by passing a current through the tissue to be heated, e.g. high-frequency current
- A61B18/14—Probes or electrodes therefor
- A61B18/1485—Probes or electrodes therefor having a short rigid shaft for accessing the inner body through natural openings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00831—Material properties
- A61B2017/00876—Material properties magnetic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B2018/00571—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body for achieving a particular surgical effect
- A61B2018/00601—Cutting
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
- A61B18/04—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
- A61B18/12—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating by passing a current through the tissue to be heated, e.g. high-frequency current
- A61B18/14—Probes or electrodes therefor
- A61B2018/1405—Electrodes having a specific shape
- A61B2018/1412—Blade
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/30—Devices for illuminating a surgical field, the devices having an interrelation with other surgical devices or with a surgical procedure
- A61B2090/306—Devices for illuminating a surgical field, the devices having an interrelation with other surgical devices or with a surgical procedure using optical fibres
Definitions
- the present invention relates to a medical device, and more particularly to a medical device used for surgery on a test site in a body cavity.
- Japanese Unexamined Patent Application Publication No. 2010-82041 discloses that in an electronic endoscope system, a fluorescent reagent such as ICG (Indocyanine Green) is administered to a subject, and a living tissue in the subject is obtained.
- a fluorescent reagent such as ICG (Indocyanine Green)
- ICG Indocyanine Green
- a configuration is disclosed in which a fluorescence image is acquired by irradiating near-infrared laser light as excitation light and imaging the living tissue emitted in response to the irradiation of the excitation light.
- Japanese Patent Application Laid-Open No. 2010-82041 discloses a predetermined amount of light detected by a photodetector arranged at a position where light emitted from the scope tip of a laparoscope scope or upper gastrointestinal scope does not reach.
- a configuration is disclosed in which the power source of the laser light source is turned off when exceeding the predetermined value, and the power source of the laser light source is turned on when the amount of light detected by the photodetector is equal to or less than the specified value.
- the scope is connected to the subject because the laser light source is turned on when the room where the scope is placed is darkened.
- the laser light emitted from the laser light source is emitted from the distal end of the scope.
- the present invention has been made in view of the above-described circumstances, and provides a medical device capable of sufficiently ensuring safety when performing an operation on a test site in a body cavity while using high-energy light.
- the purpose is to do.
- the medical device of one embodiment of the present invention is supplied from a light source that has an elongated shape that can be inserted into an insertion hole of an insertion assisting tool that assists insertion of a subject into a body cavity, and a light source.
- a light guide member that guides light to the distal end portion of the insertion portion, and provided in the insertion portion, emits light forward from the distal end portion of the insertion portion in conjunction with the insertion state of the insertion portion with respect to the insertion hole.
- An interlock mechanism configured to shift to either a possible state or a state in which light cannot be emitted forward from the distal end portion of the insertion portion.
- the figure for demonstrating the structure of the insertion part of the medical device which concerns on a 2nd Example The figure which shows an example of the state which penetrated the insertion part of the medical device which concerns on a 2nd Example to the trocar.
- the figure for demonstrating the structure of the insertion part of the medical device which concerns on a 3rd Example The figure which shows an example of the state which penetrated the insertion part of the medical device which concerns on a 3rd Example to the trocar.
- (First embodiment) 1 to 3 relate to a first embodiment of the present invention.
- the medical system 101 includes a medical device 1, a power supply device 3, a main body device 4, and a display device 5.
- FIG. 1 is a diagram illustrating a configuration of a main part of a medical system having a medical device according to an embodiment.
- the medical device 1 is inserted into a body cavity of a subject, for example, and a test site such as a living tissue existing in the body cavity of the subject with energy corresponding to the power supplied from the power supply device 3 It is comprised as a treatment tool which can be applied to and perform treatment.
- the medical device 1 is configured by, for example, a bipolar electric knife or a high-frequency treatment instrument.
- the medical device 1 includes an insertion unit 11 and an operation unit 12 as illustrated in FIG. 1, for example.
- optical fibers 13 for guiding illumination light supplied from the main body device 4 and return light generated in response to irradiation of the illumination light are provided inside the insertion unit 11 and the operation unit 12. It is inserted through.
- the insertion portion 11 is formed to have an elongated shape that can be inserted into the body cavity of the subject via a trocar placed on the body wall of the subject, such as a cylindrical shape. That is, the insertion portion 11 is formed to have an elongated shape that can be inserted into a trocar insertion hole that is an insertion aid for assisting insertion of the medical device 1 into the body cavity of the subject.
- the insertion portion 11 is configured by providing a treatment portion 11 a for applying energy according to the power supplied from the power supply device 3 at the distal end portion.
- a projection portion 11 b is provided so as to protrude in the outer diameter direction that is a direction orthogonal to the longitudinal direction of the insertion portion 11.
- the insertion part 11 is connected to the operation part 12 via the connection connector CC provided in the base end part.
- the insertion portion 11 is linked to the insertion state of the trocar through the insertion hole, and the illumination light can be emitted forward from the distal end portion of the insertion portion 11 or forward from the distal end portion of the insertion portion 11.
- An interlock mechanism is provided that is configured to perform an operation for shifting to any of the unemitted states.
- the interlock mechanism of the insertion portion 11 includes a projection portion 11b, a switch portion including a cylindrical body portion 11d and a pressing switch 11f, and an elastic mechanism 11e.
- the treatment unit 11 a includes a pair of jaws Ja that are opened and closed according to the operation of the operation unit 12, and supplies energy to a living tissue or the like grasped by the pair of jaws Ja. It is comprised so that it can apply.
- the protrusion 11b is formed, for example, so as to come into contact with the entrance-side surface of the trocar when the insertion portion 11 is inserted by a predetermined length into the trocar insertion hole. Further, as shown in FIG. 2, for example, the protruding portion 11 b corresponds to the longitudinal direction on the side surface of the insertion portion 11 according to the external force applied to the action surface AS that is the surface on the tip side of the insertion portion 11. It is comprised so that it can slide along the linear groove part 11c provided in the parallel direction. Further, as shown in FIG. 2, the protruding portion 11 b is formed integrally with the cylindrical portion 11 d inside the insertion portion 11.
- FIG. 2 is a diagram for explaining the configuration of the insertion portion of the medical device according to the first embodiment.
- a cylindrical portion 11d Inside the insertion portion 11, a cylindrical portion 11d, an elastic mechanism 11e, and a push switch 11f are provided.
- the cylindrical portion 11 d is formed to have a hollow cylindrical shape through which the optical fiber 13 can be inserted, and is formed integrally with the protruding portion 11 b inside the insertion portion 11.
- the cylindrical body portion 11d is configured as a cylindrical movable member that moves in a direction parallel to the longitudinal direction of the insertion portion 11 in conjunction with the movement of the projection portion 11b.
- the cylindrical body portion 11d has a distal end portion disposed in the vicinity of the protruding portion 11b and a push switch 11f ( It is formed so that the base end portion is disposed in the vicinity of (described later).
- the elastic mechanism 11e is formed by, for example, a compression coil spring that contracts in response to an external force. Moreover, the elastic mechanism 11e is arrange
- the end surface MS is configured to have a length that can be connected to the end surface MS.
- the elastic mechanism 11 e is configured to generate a biasing force that biases the protrusion 11 b toward the distal end side of the insertion portion 11.
- the elastic mechanism 11e places the protrusion 11b in a state where no external force is applied to the action surface AS at a predetermined position (hereinafter also referred to as an initial position) on the most distal end side of the groove 11c. Is configured to generate a possible biasing force.
- the elastic mechanism 11e is formed in a form other than the form having the compression coil spring as long as it is formed so as to generate a biasing force that biases the protrusion 11b toward the distal end side of the insertion part 11. It may be.
- the press switch 11f is formed, for example, by a push button switch or the like, and is configured to be turned on when pressed and turned off when not pressed. Further, for example, as shown in FIG. 2, the push switch 11 f is provided at a position on the base end face MS facing the base end portion of the cylindrical body portion 11 d and is hollow to allow the optical fiber 13 to be inserted therein. It has a cylindrical shape or a ring shape.
- the protrusion portion 11b extends along the groove portion 11c. While moving from the initial position to the proximal end side of the insertion portion 11 (sliding), the cylindrical portion 11d moves to the proximal end side of the insertion portion 11 in conjunction with the protrusion portion 11b. Further, according to the configuration of the insertion portion 11 as described above, the pressing state of the pressing switch 11f changes according to the position of the proximal end portion of the cylindrical body portion 11d that moves in conjunction with the protruding portion 11b. The state shifts to either an on state where light can be emitted forward from the distal end portion of the insertion portion 11 or an off state where light cannot be emitted forward from the distal end portion of the insertion portion 11. be able to.
- the operation unit 12 is connected to the insertion unit 11 via the connection connector CC. Further, for example, as illustrated in FIG. 1, the operation unit 12 includes a handle portion 12 a capable of performing an operation related to opening and closing of the pair of jaws Ja of the treatment unit 11 a. In addition, a detection circuit 12 b is provided inside the operation unit 12.
- the handle portion 12a has a treatment switch 121 capable of performing an operation for turning on or off the power supply from the power supply device 3, and an operation for turning on or off the supply of illumination light from the main body device 4. And an illumination switch 122 capable of performing the above.
- the detection circuit 12b is configured to detect the on / off state of the push switch 11f and the illumination switch 122, respectively.
- the detection circuit 12b is configured to generate a state detection signal indicating the detection result of the on / off state of the push switch 11f and the illumination switch 122, and to output the generated state detection signal to the main body device 4. ing.
- the base end portion of the optical fiber 13 is provided so as to extend from the base end side of the operation unit 12 and is configured to be detachably connected to the main body device 4. Moreover, the front-end
- the illumination light emitted through the end face is condensed near the end face at the tip of the optical fiber 13 and the return light generated in response to the illumination light is condensed to the end face.
- a condensing lens (not shown) for incidence is provided. That is, the optical fiber 13 is configured as a light guide member that guides illumination light supplied from a laser light source 41 (described later) of the main body device 4 to the distal end portion of the insertion portion 11.
- the power supply device 3 includes, for example, a high frequency power supply. Further, the power supply device 3 is configured to supply power to the medical device 1 to be connected when it is detected that the treatment switch 121 of the handle portion 12a is turned on. Further, the power supply device 3 is configured to stop the power supply to the medical device 1 to be connected when it is detected that the treatment switch 121 of the handle portion 12a is turned off.
- the main unit 4 includes a laser light source 41, a photodetector 42, a signal processing circuit 43, and a control circuit 44.
- the laser light source 41 includes, for example, a laser diode or the like, and is configured to generate laser light as illumination light that irradiates a test site to be treated by the medical device 1.
- the laser light source 41 is configured to supply laser light to the optical fiber 13 connected to the main body device 4 when turned on in accordance with control of the control circuit 44. Further, the laser light source 41 is configured to stop the supply of laser light to the optical fiber 13 connected to the main body device 4 when turned off in accordance with the control of the control circuit 44.
- the light detector 42 includes, for example, an avalanche photodiode and the like, detects return light emitted through the optical fiber 13 connected to the main body device 4, and detects light according to the intensity of the detected return light. A signal is generated and output.
- the signal processing circuit 43 performs predetermined signal processing on the light detection signal output from the light detector 42 to generate an image that visualizes the state of the test site treated by the medical device 1. And output.
- the control circuit 44 is configured to be able to perform control related to the operation of each part of the main device 4. Specifically, for example, the control circuit 44 is based on the state detection signal output from the detection circuit 12b of the medical device 1 connected to the main body device 4, and both the push switch 11f and the illumination switch 122 are in the on state. In this case, control for turning on the laser light source 41 is performed, and control for turning off the laser light source 41 is performed when at least one of the pressing switch 11f and the illumination switch 122 is in the off state. It is configured.
- the display device 5 includes, for example, a liquid crystal display and is configured to display an image output from the main device 4.
- a user such as a surgeon connects each part of the medical system 101 and turns on the power, and then, for example, inflates the abdominal cavity of the subject with pneumoconiosis gas supplied from an insufflation apparatus (not shown).
- the insertion portion 11 is inserted through the opening on the entrance side of the insertion hole of the trocar 61A.
- the action surface AS of the projection portion 11 b of the trocar 61 ⁇ / b> A installed on the abdominal wall AW. Since it is pressed while being in contact with the surface on the inlet side, a pressing force is generated in the direction of the arrow AR1 that is parallel to or substantially parallel to the longitudinal direction of the insertion portion 11.
- FIG. 3 is a diagram illustrating an example of a state where the insertion portion of the medical device according to the first embodiment is inserted through the trocar.
- the cylindrical body portion 11d and the pressing switch 11f of this embodiment maintain the OFF state when the pressing force exceeding the urging force by the elastic mechanism 11e is not applied to the acting surface AS of the protruding portion 11b, and the pressing portion 11f.
- the state is switched from the off state to the on state.
- the user performs an operation for turning on the treatment switch 121 and the illumination switch 122 in a state where the treatment portion 11a is protruded from the opening on the outlet side of the trocar 61A after the insertion portion 11 is inserted and arranged inside the trocar 61A.
- the treatment of the test site in the abdominal cavity of the subject is started.
- the detection circuit 12b detects the on / off state of the push switch 11f and the illumination switch 122, respectively, and generates a state detection signal indicating a detection result that both the push switch 11f and the illumination switch 122 are on. Output to device 4.
- control for turning on the laser light source 41 is performed by the control circuit 44, and supply of laser light from the laser light source 41 to the optical fiber 13 is started.
- the user removes the insertion portion 11 from the trocar 61A after completing the treatment of the examination site in the abdominal cavity of the subject by performing an operation for turning off the treatment switch 121.
- the action surface AS is disposed at a position separated from the entrance-side surface of the trocar 61A.
- the applied pressing force is removed.
- the protrusion 11b and the cylindrical portion 11d move to the distal end side of the insertion portion 11 according to the urging force of the elastic mechanism 11e, and the cylindrical body
- the base end of the portion 11d moves to a position away from the pressing switch 11f, and the pressing switch 11f switches from the on state to the off state.
- the cylindrical body portion 11d and the pressing switch 11f of this embodiment are linked to the contact state between the trocar 61A and the projection portion 11b, and are in an on state in which light can be emitted forward from the distal end portion of the insertion portion 11.
- an operation for shifting to any one of an off state in which light cannot be emitted forward from the distal end portion of the insertion portion 11 is performed.
- the detection circuit 12b detects the on / off state of the push switch 11f and the illumination switch 122, and generates a state detection signal indicating a detection result that the push switch 11f is in the off state and the illumination switch 122 is in the on state. And output to the main unit 4. Then, according to the operation of the detection circuit 12b, control for turning off the laser light source 41 is performed by the control circuit 44, and supply of laser light from the laser light source 41 to the optical fiber 13 is stopped.
- the present embodiment for example, when a situation occurs in which the insertion portion 11 is removed from the trocar 61A and placed outside the body of the subject while the illumination switch 122 is turned on. Even if it exists, supply of the laser beam from the laser light source 41 to the optical fiber 13 can be stopped, that is, emission of the laser beam from the distal end portion of the insertion portion 11 can be prevented in advance. Therefore, according to the present embodiment, it is possible to sufficiently ensure safety when performing an operation on the test site in the body cavity while using high energy light.
- each part of the present embodiment for example, when the acting surface AS comes into contact with a desired object such as the surface on the inlet side of the trocar 61A, the cylindrical body part 11d is inserted into the insertion part 11.
- the pressure switch 11f is turned on by moving to the proximal end side and the working surface AS is not in contact with the desired object, the cylindrical body portion 11d moves to the distal end side of the insertion portion 11 and presses The switch 11f may be turned off.
- control circuit 44 is not limited to the control for switching the on / off state of the laser light source 41 based on the state detection signal output from the detection circuit 12b.
- the detection circuit 12b You may make it perform the operation
- an illumination optical fiber for guiding illumination light supplied from the main body device 4 to the distal end portion of the insertion portion 11 and generated in response to irradiation of the illumination light.
- a light receiving optical fiber for guiding return light from the distal end portion of the insertion portion 11 to the main body device 4 is provided instead of the optical fiber 13
- the light is guided by the illumination optical fiber.
- the interlock mechanism may be configured so that the illumination light can be emitted forward from the distal end portion of the insertion portion 11 or cannot be emitted.
- the medical device 1 according to the present embodiment includes, for example, an insertion portion 11P as shown in FIG. 4 instead of the insertion portion 11 shown in FIG.
- FIG. 4 is a diagram for explaining the configuration of the insertion portion of the medical device according to the second embodiment.
- the insertion part 11P is provided with a cylindrical part 11g instead of the cylindrical part 11d of the insertion part 11, and has substantially the same configuration as that obtained by removing the pressing switch 11f from the insertion part 11.
- the interlock mechanism of the insertion part 11P comprises the protrusion part 11b, the elastic mechanism 11e, and the cylinder part 11g.
- the elastic mechanism 11e of the insertion portion 11P is disposed at a position substantially opposite to the cylindrical portion 11g along the longitudinal direction of the insertion portion 11.
- the cylinder part 11g is formed of a material having low thermal conductivity such as silicone or fluororesin. Further, for example, as shown in FIG. 4, the cylindrical portion 11 g is formed to have a hollow cylindrical shape through which the optical fiber 13 can be inserted, and is integrated with the protruding portion 11 b inside the insertion portion 11. Is formed. In other words, the cylindrical portion 11g is configured as a cylindrical movable member that moves in a direction parallel to the longitudinal direction of the insertion portion 11 in conjunction with the movement of the projection portion 11b. Further, for example, as shown in FIG.
- the cylindrical body portion 11g has a distal end portion disposed between the pair of jaws Ja in a state where no external force is applied to the acting surface AS, and the protruding portion 11b. Is formed so that the base end portion is disposed in the vicinity of.
- the distal end portion of the cylindrical body portion 11 g forms a predetermined shape such as a dome shape and closes the light.
- the closed state in which the laser beam emitted through the end face of the tip end portion of the fiber 13 is shielded is maintained.
- the distal end portion of the cylindrical portion 11g is emitted through the end surface of the distal end portion of the optical fiber 13 by being deformed into a shape that can be accommodated in the insertion portion 11 in response to the application of an external force to the working surface AS. It is comprised so that it may transfer to the open state which lets a laser beam pass.
- An absorbent for absorbing the laser light emitted through the end face of the tip of the optical fiber 13 in a closed state is applied to the inner peripheral surface of the tip of the cylindrical body 11g. Further, a pipe line (not shown) capable of circulating a coolant such as water for removing heat generated in response to the absorption of the laser beam in the closed state is provided on the outer peripheral surface of the cylindrical portion 11g. It has been.
- the protrusion 11b extends along the groove 11c. While moving (sliding) from the initial position to the proximal end side of the insertion portion 11, the cylindrical body portion 11g moves to the proximal end side of the insertion portion 11 in conjunction with the projection portion 11b. Moreover, according to the structure of the insertion part 11P as described above, the light emitted through the optical fiber 13 is changed by changing the shape of the tip part of the cylindrical part 11g that moves in conjunction with the protrusion part 11b. It is possible to shift to either an open state in which the light passes through or a closed state in which light emitted through the optical fiber 13 is blocked.
- the detection circuit 12b of the present embodiment is configured to detect the on / off state of the illumination switch 122.
- the detection circuit 12 b according to the present embodiment is configured to generate a state detection signal indicating a detection result of the on / off state of the illumination switch 122 and output the generated state detection signal to the main body device 4.
- the control circuit 44 of the present embodiment turns on the laser light source 41 when the illumination switch 122 is on based on the state detection signal output from the detection circuit 12b of the medical device 1 connected to the main body device 4. And a control for turning off the laser light source 41 when the illumination switch 122 is in the off state.
- a user such as a surgeon connects each part of the medical system 101 and turns on the power, and then, for example, inflates the abdominal cavity of the subject with pneumoconiosis gas supplied from an insufflation apparatus (not shown).
- the insertion portion 11P is inserted from the opening on the entrance side of the insertion hole of the trocar 61A.
- the action surface AS of the projection portion 11 b is Since it is pressed in a state in contact with the surface on the inlet side, a pressing force is generated in the direction of the arrow AR2 that is a direction parallel to or approximately parallel to the longitudinal direction of the insertion portion 11P.
- FIG. 5 is a diagram illustrating an example of a state where the insertion portion of the medical device according to the second embodiment is inserted through the trocar.
- the cylindrical portion 11g of the present embodiment is closed by forming a predetermined shape and closing when a pressing force exceeding the urging force by the elastic mechanism 11e is not applied to the action surface AS of the protrusion 11b.
- the shape is changed from the predetermined shape to shift from the closed state to the open state.
- the user performs an operation for turning on the treatment switch 121 and the illumination switch 122 in a state where the treatment portion 11a is protruded from the opening on the outlet side of the trocar 61A after the insertion portion 11P is inserted and arranged inside the trocar 61A.
- the treatment of the test site in the abdominal cavity of the subject is started.
- the detection circuit 12b detects the on / off state of the illumination switch 122, generates a state detection signal indicating a detection result that the illumination switch 122 is in the on state, and outputs the state detection signal to the main body device 4.
- control for turning on the laser light source 41 is performed by the control circuit 44, and supply of laser light from the laser light source 41 to the optical fiber 13 is started.
- the user completes the treatment of the site to be examined in the abdominal cavity of the subject by performing an operation for turning off the treatment switch 121, and then removes the insertion portion 11P from the trocar 61A.
- the action surface AS is disposed at a position separated from the entrance-side surface of the trocar 61A as the insertion portion 11P is removed from the trocar 61A.
- the applied pressing force is removed.
- the protrusion 11b and the cylindrical part 11g move to the distal end side of the insertion part 11P according to the urging force of the elastic mechanism 11e, and the cylindrical body
- the tip of the portion 11g shifts from the open state to the closed state.
- the cylindrical portion 11g of the present embodiment is linked to the contact state between the trocar 61A and the protrusion 11b, and is opened through the light emitted through the optical fiber 13 or emitted through the optical fiber 13. It shifts to one of the closed states where the light to be blocked is blocked.
- the present embodiment for example, when a situation occurs in which the insertion portion 11P is removed from the trocar 61A and placed outside the subject's body with the illumination switch 122 turned on. Even if it exists, since the laser beam emitted through the optical fiber 13 is blocked by the closed cylindrical portion 11g, the emission of the laser beam from the distal end portion of the insertion portion 11P can be prevented in advance. Therefore, according to the present embodiment, it is possible to sufficiently ensure safety when performing an operation on the test site in the body cavity while using high energy light.
- the medical device 1 according to the present embodiment includes, for example, an insertion portion 11Q as shown in FIG. 6 instead of the insertion portion 11 shown in FIG.
- FIG. 6 is a diagram for explaining the configuration of the insertion portion of the medical device according to the third embodiment.
- the insertion portion 11Q has substantially the same configuration as that in which the magnetic sensor 11k is provided inside the projection portion 11b of the insertion portion 11 and the pressing switch 11f is removed from the insertion portion 11. Moreover, the interlock mechanism of the insertion part 11Q is comprised including the projection part 11b and the magnetic sensor 11k.
- the magnetic sensor 11k is provided, for example, inside the protrusion 11b, detects a magnetic field in the vicinity of the working surface AS of the protrusion 11b, and outputs a magnetic field detection signal having a signal level corresponding to the detected magnetic field intensity. Configured to generate. That is, the magnetic sensor 11k is configured to move in a direction parallel to the longitudinal direction of the insertion portion 11 in conjunction with the movement of the protrusion 11b. Further, the magnetic sensor 11k is configured to output the magnetic field detection signal generated as described above to the detection circuit 12b via a signal line (not shown) inserted into the protrusion 11b and the cylindrical body 11d, for example. Has been.
- the detection circuit 12b of the present embodiment is configured to detect the signal level of the magnetic field detection signal output from the magnetic sensor 11k and the on / off state of the illumination switch 122, respectively.
- the detection circuit 12b according to the present embodiment generates a state detection signal indicating the detection result of the signal level of the magnetic field detection signal output from the magnetic sensor 11k and the on / off state of the illumination switch 122, and generates the state detection signal.
- a state detection signal is output to the main unit 4.
- the control circuit 44 of the present embodiment has a predetermined signal level of the magnetic field detection signal output from the magnetic sensor 11k based on the state detection signal output from the detection circuit 12b of the medical device 1 connected to the main body device 4.
- the control is performed to turn on the laser light source 41 when the threshold value TH is exceeded and the illumination switch 122 is on.
- the control circuit 44 of the present embodiment has a signal level of the magnetic field detection signal output from the magnetic sensor 11k based on the state detection signal output from the detection circuit 12b of the medical device 1 connected to the main body device 4.
- the control for turning off the laser light source 41 is performed either when it is less than the predetermined threshold TH or when the illumination switch 122 is in the off state.
- a user such as a surgeon connects each part of the medical system 101 and turns on the power, and then, for example, inflates the abdominal cavity of the subject with pneumoconiosis gas supplied from an insufflation apparatus (not shown).
- the insertion portion 11Q is inserted from the opening on the entrance side of the insertion hole of the trocar 61B.
- FIG. 7 is a diagram illustrating an example of a state where the insertion portion of the medical device according to the third embodiment is inserted through the trocar.
- the magnetic sensor 11k generates a magnetic field detection signal having a signal level SG1 equal to or higher than a predetermined threshold TH as a magnetic field detection signal corresponding to the strength of the magnetic field emitted from the magnet 62, and outputs the magnetic field detection signal to the detection circuit 12b.
- the magnetic sensor 11k is linked to the contact state between the trocar 61B and the protrusion 11b, and is arranged at a position where the magnetic field emitted from the magnet 62 can be detected.
- a magnetic field detection signal having a signal level SG1 indicating a state in which light can be emitted forward is generated and output.
- the user performs an operation for turning on the treatment switch 121 and the illumination switch 122 in a state where the treatment portion 11a is protruded from the opening on the outlet side of the trocar 61B after the insertion portion 11Q is inserted and arranged inside the trocar 61B.
- the treatment of the test site in the abdominal cavity of the subject is started.
- the detection circuit 12b detects the signal level of the magnetic field detection signal output from the magnetic sensor 11k and the on / off state of the illumination switch 122, the signal level of the magnetic field detection signal is SG1, and the illumination switch 122.
- a state detection signal indicating a detection result that is in the on state is generated and output to the main body device 4.
- control for turning on the laser light source 41 is performed by the control circuit 44, and supply of laser light from the laser light source 41 to the optical fiber 13 is started.
- the user removes the insertion portion 11Q from the trocar 61B after completing the treatment of the examination site in the abdominal cavity of the subject by performing an operation for turning off the treatment switch 121.
- the action surface AS is separated from the entrance-side surface of the trocar 61B as the insertion portion 11 is removed from the trocar 61B, and the magnetic field emitted from the magnet 62 cannot be detected.
- the magnetic sensor 11k is disposed at the position, and the signal level of the magnetic field detection signal output from the magnetic sensor 11k is lowered from SG1 to a signal level SG2 less than a predetermined threshold TH.
- the magnetic sensor 11k is interlocked with the contact state between the trocar 61B and the protrusion 11b, and is disposed at a position where the magnetic field emitted from the magnet 62 cannot be detected.
- a magnetic field detection signal having a signal level SG2 indicating that light cannot be emitted further forward is generated and output.
- the detection circuit 12b detects the signal level of the magnetic field detection signal output from the magnetic sensor 11k and the on / off state of the illumination switch 122, and the signal level of the magnetic field detection signal is SG2 and the illumination switch 122. A state detection signal indicating a detection result that is in the on state is generated and output to the main body device 4. Then, according to the operation of the detection circuit 12b, control for turning off the laser light source 41 is performed by the control circuit 44, and supply of laser light from the laser light source 41 to the optical fiber 13 is stopped.
- the insertion portion 11Q is removed from the trocar 61B and placed outside the subject's body with the illumination switch 122 turned on. Even if it exists, supply of the laser beam from the laser light source 41 to the optical fiber 13 can be stopped, that is, emission of the laser beam from the distal end portion of the insertion portion 11Q can be prevented in advance. Therefore, according to the present embodiment, it is possible to sufficiently ensure safety when performing an operation on the test site in the body cavity while using high energy light.
- the magnetic sensor 11k for example, an optical sensor for detecting light emitted from a light emitting element provided on the entrance-side surface of the trocar 61B is used as the working surface AS of the projection 11b.
- the insertion portion 11Q may be configured by providing the insertion portion 11Q. According to such a configuration, for example, when the signal level of the light detection signal output from the light sensor of the protrusion 11b is equal to or higher than a predetermined threshold THA and the illumination switch 122 is in the on state, Control for turning on the laser light source 41 may be performed by the control circuit 44.
- a force sensor for detecting a pressing force generated by contact with a desired object such as the entrance-side surface of the trocar 61A (or 61B) is provided.
- the insertion portion 11Q may be configured by being provided on the working surface AS of the projection portion 11b.
- Control for turning on the laser light source 41 may be performed by the control circuit 44.
- a distance measuring sensor for measuring a distance from a desired object such as the entrance side surface of the trocar 61A (or 61B) is projected.
- the insertion portion 11Q may be configured by being provided on the working surface AS of the portion 11b. According to such a configuration, for example, when the distance measured by the distance measuring sensor of the protrusion 11b is 0 or substantially 0 and the illumination switch 122 is in the on state, the laser light source 41 is turned on. Control for this purpose may be performed by the control circuit 44.
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Abstract
Description
図1から図3は、本発明の第1の実施例に係るものである。
図4及び図5は、本発明の第2の実施例に係るものである。
図6及び図7は、本発明の第3の実施例に係るものである。
Claims (6)
- 被検体の体腔内への挿入を補助する挿入補助具の挿通孔に挿通可能な細長形状を具備して形成された挿入部と、
光源から供給される光を前記挿入部の先端部へ導光する導光部材と、
前記挿入部に設けられ、前記挿通孔に対する前記挿入部の挿通状態に連動し、前記挿入部の先端部より前方へ光を出射可能な状態、または、前記挿入部の先端部より前方へ光を出射不可能な状態のいずれかに移行するように構成されたインターロック機構と、
を有することを特徴とする医療用デバイス。 - 前記インターロック機構は、前記挿入部の側面に設けられ、前記挿入部が前記挿通孔に対して所定の長さだけ挿通された際に前記挿入補助具の表面に接触するように形成された突起部と、前記挿入補助具と前記突起部との接触状態に連動し、前記挿入部の先端部より前方へ光を出射可能な状態であるオン状態、または、前記挿入部の先端部より前方へ光を出射不可能な状態であるオフ状態のいずれかに移行するための動作を行うように構成されたスイッチ部と、を有する
ことを特徴とする請求項1に記載の医療用デバイス。 - 前記インターロック機構は、前記挿入補助具と接触していない状態の前記突起部を前記挿入部の所定の位置に配置させることが可能な付勢力を発生する弾性機構をさらに有し、
前記突起部は、前記付勢力を超える外力が前記挿入補助具との接触に応じて印加された際に、前記所定の位置から前記挿入部の基端側へ移動するように形成されており、
前記スイッチ部は、前記外力が前記突起部に印加されていない場合に前記オフ状態を維持するとともに、前記外力が前記突起部に印加されている場合に前記オフ状態から前記オン状態へ切り替わるように構成されている
ことを特徴とする請求項2に記載の医療用デバイス。 - 前記インターロック機構は、前記挿入部の側面に設けられ、前記挿入部が前記挿通孔に対して所定の長さだけ挿通された際に前記挿入補助具の表面に接触するように形成された突起部と、前記挿入補助具と前記突起部との接触状態に連動し、前記導光部材を経て出射される光を通過させる開状態、または、前記導光部材を経て出射される光を遮光する閉状態のいずれかに移行するように形成された筒体部と、を有する
ことを特徴とする請求項1に記載の医療用デバイス。 - 前記インターロック機構は、前記挿入補助具と接触していない状態の前記突起部を前記挿入部の所定の位置に配置させることが可能な付勢力を発生する弾性機構をさらに有し、
前記突起部は、前記付勢力を超える外力が前記挿入補助具との接触に応じて印加された際に、前記所定の位置から前記挿入部の基端側へ移動するように形成されており、
前記筒体部は、前記外力が前記突起部に印加されていない場合に所定の形状を形成して閉塞することにより前記閉状態を維持するとともに、前記外力が前記突起部に印加されている場合に前記所定の形状から変形することにより前記閉状態から前記開状態へ移行するように形成されている
ことを特徴とする請求項4に記載の医療用デバイス。 - 前記インターロック機構は、前記挿入部の側面に設けられ、前記挿入部が前記挿通孔に対して所定の長さだけ挿通された際に前記挿入補助具の表面に接触するように形成された突起部と、前記突起部の近傍の磁界を検知するように構成された磁気センサと、を有し、
前記磁気センサは、前記挿入補助具に設けられた磁石から発せられる磁界を検知可能な位置に配置された際に、前記挿入部の先端部より前方へ光を出射可能な状態を示す磁界検知信号を出力する
ことを特徴とする請求項1に記載の医療用デバイス。
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JP2016547640A JP6033517B1 (ja) | 2015-09-16 | 2016-02-04 | 医療用デバイス |
EP16840325.1A EP3184059A4 (en) | 2015-09-16 | 2016-02-04 | Medical device |
CN201680002882.2A CN106714713A (zh) | 2015-09-16 | 2016-02-04 | 医疗用设备 |
US15/450,397 US20170172390A1 (en) | 2015-09-16 | 2017-03-06 | Medical device |
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US10959800B2 (en) * | 2016-11-08 | 2021-03-30 | Covidien Lp | Force sensors for surgical devices to prevent ingress of fluids |
CN108784635A (zh) * | 2018-07-17 | 2018-11-13 | 重庆金山医疗器械有限公司 | 一种自动关闭光源的内窥镜***及方法 |
US20210015512A1 (en) * | 2019-07-16 | 2021-01-21 | Covidien Lp | Sensor encapsulating assembly |
DE102020207365A1 (de) * | 2020-06-15 | 2021-12-16 | Siemens Healthcare Gmbh | Einfädelunterstützungseinrichtung zum Einfädeln eines Objektes in eine Führungsvorrichtung |
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US6984203B2 (en) * | 2000-04-03 | 2006-01-10 | Neoguide Systems, Inc. | Endoscope with adjacently positioned guiding apparatus |
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JP2004024618A (ja) * | 2002-06-26 | 2004-01-29 | Olympus Corp | 蛍光観察内視鏡用処置具 |
JP2005118421A (ja) * | 2003-10-20 | 2005-05-12 | Olympus Corp | 修復歯の識別装置 |
JP2010082041A (ja) | 2008-09-30 | 2010-04-15 | Fujifilm Corp | 電子内視鏡システム |
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