WO2022250191A1 - Medical resection device - Google Patents

Medical resection device Download PDF

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Publication number
WO2022250191A1
WO2022250191A1 PCT/KR2021/007008 KR2021007008W WO2022250191A1 WO 2022250191 A1 WO2022250191 A1 WO 2022250191A1 KR 2021007008 W KR2021007008 W KR 2021007008W WO 2022250191 A1 WO2022250191 A1 WO 2022250191A1
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WO
WIPO (PCT)
Prior art keywords
electrode
insulating
exposed
abrasive cutting
hole
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Application number
PCT/KR2021/007008
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French (fr)
Korean (ko)
Inventor
고영웅
정재혁
신명영
윤섭
문웅진
민병훈
Original Assignee
유앤아이 주식회사
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Publication of WO2022250191A1 publication Critical patent/WO2022250191A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/32Surgical cutting instruments
    • A61B17/320016Endoscopic cutting instruments, e.g. arthroscopes, resectoscopes
    • A61B17/32002Endoscopic cutting instruments, e.g. arthroscopes, resectoscopes with continuously rotating, oscillating or reciprocating cutting instruments
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/32Surgical cutting instruments
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B18/00Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B18/00Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
    • A61B18/04Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
    • A61B18/12Surgical 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
    • A61B18/14Probes or electrodes therefor
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B18/00Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
    • A61B18/04Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
    • A61B18/12Surgical 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
    • A61B18/14Probes or electrodes therefor
    • A61B18/148Probes or electrodes therefor having a short, rigid shaft for accessing the inner body transcutaneously, e.g. for neurosurgery or arthroscopy
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B18/00Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
    • A61B18/04Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
    • A61B18/12Surgical 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
    • A61B18/14Probes or electrodes therefor
    • A61B18/1482Probes or electrodes therefor having a long rigid shaft for accessing the inner body transcutaneously in minimal invasive surgery, e.g. laparoscopy
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B18/00Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
    • A61B18/04Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
    • A61B18/12Surgical 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
    • A61B18/14Probes or electrodes therefor
    • A61B18/149Probes or electrodes therefor bow shaped or with rotatable body at cantilever end, e.g. for resectoscopes, or coagulating rollers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61B17/32Surgical cutting instruments
    • A61B17/320016Endoscopic cutting instruments, e.g. arthroscopes, resectoscopes
    • A61B17/32002Endoscopic cutting instruments, e.g. arthroscopes, resectoscopes with continuously rotating, oscillating or reciprocating cutting instruments
    • A61B2017/320024Morcellators, e.g. having a hollow cutting tube with an annular cutter for morcellating and removing tissue
    • AHUMAN NECESSITIES
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    • A61B17/320068Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic
    • A61B2017/32007Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic with suction or vacuum means
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    • A61B17/320068Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic
    • A61B17/320092Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic with additional movable means for clamping or cutting tissue, e.g. with a pivoting jaw
    • A61B2017/320095Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic with additional movable means for clamping or cutting tissue, e.g. with a pivoting jaw with sealing or cauterizing means
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    • A61B2018/00053Mechanical features of the instrument of device
    • A61B2018/00059Material properties
    • A61B2018/00071Electrical conductivity
    • A61B2018/00083Electrical conductivity low, i.e. electrically insulating
    • AHUMAN NECESSITIES
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    • A61B2018/00571Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body for achieving a particular surgical effect
    • A61B2018/00589Coagulation
    • AHUMAN NECESSITIES
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    • A61B2018/00571Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body for achieving a particular surgical effect
    • A61B2018/0063Sealing
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B18/00Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
    • A61B18/04Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
    • A61B18/12Surgical 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
    • A61B18/14Probes or electrodes therefor
    • A61B2018/1405Electrodes having a specific shape
    • A61B2018/142Electrodes having a specific shape at least partly surrounding the target, e.g. concave, curved or in the form of a cave
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B18/00Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
    • A61B18/04Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by heating
    • A61B18/12Surgical 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
    • A61B18/14Probes or electrodes therefor
    • A61B2018/1475Electrodes retractable in or deployable from a housing
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B2217/00General characteristics of surgical instruments
    • A61B2217/002Auxiliary appliance
    • A61B2217/005Auxiliary appliance with suction drainage system

Definitions

  • the present invention relates to a medical ablation device.
  • Arthroscope treatment is a method of surgery by making 2 to 4 small incisions less than about 1 cm in the joint, inserting a small camera and surgical instruments, and looking inside the joint through the camera. It can be considered in many lesions such as cartilage damage, and as arthroscopy technology develops, the scope of application is increasing for various diseases of the knee joint.
  • laparoscopic surgery is a technology that operates only with a small hole-sized incision without making a large incision in the abdomen, etc. is being applied
  • Medical resection to remove parts of the body, such as tissues and bones in the opening, in the course of treatment through arthroscopy or laparoscopy, which involves making minimal incisions in the body, or through natural openings in the body, such as the nostrils. instrument is being used.
  • a medical cutting device a shaver device is usually used, and the shaver device provides high-speed cutting of tissues and the like.
  • tissue when tissue is resected through the shaver device, bleeding may occur during the surgical procedure, and therefore, hemostasis must be performed.
  • an electric cautery device that cauterizes by applying an electrical signal to the electrode can be used.
  • the shaver device To use the electric cautery device, the shaver device must be removed and the electric cautery device inserted. You have to go through the process of removing the inserted electric cautery device and reinserting the shaver device. In this way, if the operation of repeatedly inserting and removing the electric cautery device and the shaver device is performed, there is a problem that the operation time is prolonged due to tool replacement and there is a risk of infection during the replacement process.
  • the technical problem to be achieved by the technical idea of the present invention is to provide an abrasive cutting function such as a shaver, a burr, and a cautery or coagulation function in one instrument, thereby reducing the operation time, reducing the hassle of replacing tools, It is to provide a medical ablation device that prevents the risk of infection.
  • a medical ablation apparatus includes a first electrode part extending in a first direction, at least a part of which has a hollow shape having a first through hole therein, and at least the first electrode part therein.
  • a second electrode part having a hollow shape, at least a part of which has a second through hole so that a part thereof is located, is positioned between the first electrode part and the second electrode part, and insulates between the first electrode part and the second electrode part.
  • a second insulating part having a first open part, at least a part of which is disposed to cover a part of the first electrode part, a part of which is exposed to the outside, and is open toward a direction different from the first direction;
  • a third insulating portion covering at least a portion of the second electrode portion so that a portion of the second electrode portion is exposed to the outside, and a polishing cutting region located inside the first through hole and adjacent to the second insulating portion, It may include a rotatable abrasive cutting unit.
  • a region of the first electrode part exposed to the outside and not covered by the second insulating part and the third insulating part Tissues are coagulated or ablated by the region of the second electrode part exposed to the outside and not covered by the part, and when the abrasive cutting part is rotated, tissue or bone is ground or cut by the abrasive cutting area. It can be.
  • one side of both sides of the second insulating portion along the first direction may cover the first electrode portion, and a first suction hole may be formed on the other side.
  • the first electrode unit at least a portion of which is located inside the second through-hole, has the first through-hole therein, and is not exposed to the outside by the second insulating portion.
  • a first electrode exposed portion located on the outer surface of the second insulating portion and exposed to the outside, and electrically connecting the first electrode main body and the first electrode exposed portion, wherein at least a portion of the second insulating portion is exposed. It may include a first electrode connection portion that is not exposed to the outside by the.
  • At least a portion of the second insulating portion is positioned on the outer surface of the first electrode body so that the first electrode body is not exposed to the outside, but the first electrode connection portion is on at least a portion of the outer surface.
  • a seat portion is formed to be positioned, and the second insulating body portion on the outer surface of which the first electrode exposed portion is located is coupled to the second insulating body portion so that at least a portion of the first electrode connection portion is not exposed to the outside, and at least a portion thereof Is positioned between the second electrode portion and the first electrode body portion may include a second insulating cover portion to insulate between the second electrode portion and the first electrode body portion.
  • the first insulating part may include a 1-1 insulating part located on at least a part of the outer surface of the first electrode part, and a 1-2 insulating part located on at least a part of the outer surface of the 1-1 insulating part.
  • a portion between the first electrode portion and the second electrode portion includes a first region and a second region, wherein the first region includes the 1-1 insulating portion and the second electrode portion on the 1-1 insulating portion. Insulated by a second insulating cover part, the second region may be insulated by the 1-1 insulating part and the 1-2 insulating part on the 1-1 insulating part.
  • a first blade region is formed in the first open portion of the second insulating portion, and when the abrasive cutting portion is rotated, tissue or bone is polished or polished by the abrasive cutting region and the first blade region. can be cut
  • the abrasive cutting unit includes a second open portion opened in a direction different from the first direction, and the abrasive cutting region is formed in the second open portion to polish or cut the tissue. It may be a second blade region.
  • At least a portion of the abrasive cutting portion may have a hollow shape having a third through hole used as a suction passage for suction therein.
  • a second suction hole is formed in a direction opposite to the first open part of the second insulating part, and a third suction hole is formed in a position corresponding to the second suction hole in the first electrode part.
  • the suction target may be suctioned through the suction passage by sequentially passing through the third suction hole, the second suction hole, and the second open part or a fourth suction hole formed in the opposite direction of the second open part.
  • the abrasive cutting unit may be a burr for grinding or cutting the bone.
  • the first electrode part may have a third open part opened toward the same direction as the first open part.
  • a third blade region is formed in the third open portion, and when the abrasive cutting portion is rotated, tissue or bone may be polished or cut by the abrasive cutting region and the third blade region.
  • the second electrode unit may include an exposed portion located on an outer surface of the second insulating portion and exposed to the outside, and a body portion at least partially covered by the third insulating portion and coupled to the exposed portion.
  • a medical ablation device provides an abrasive cutting function and a cauterization or coagulation function in one device, thereby reducing operation time and reducing the burden of patients and users according to medical practice and device replacement. You can reduce your risk of infection.
  • FIG. 1 is a diagram schematically showing a medical device system including a medical ablation device according to an embodiment of the present invention.
  • FIG. 2 is a perspective view showing the medical ablation apparatus shown in FIG. 1;
  • FIG. 3 is a cross-sectional view showing the medical ablation apparatus shown in FIG. 2 .
  • FIG. 4 is an exploded perspective view showing some components of the medical ablation apparatus shown in FIG. 1 by disassembling them.
  • FIG. 5 is a perspective view showing an abrasive cutting part of the medical ablation apparatus shown in FIG. 1;
  • FIG. 6 and 7 are cross-sectional views for explaining the operation of the abrasive cutting unit of the medical ablation apparatus shown in FIG. 1 .
  • FIG. 8 is a perspective view showing an abrasive cutting part of a medical ablation device according to another embodiment of the present invention.
  • FIG. 9 is a perspective view showing a medical ablation device according to another embodiment of the present invention.
  • FIG. 10 is a cross-sectional view showing the medical ablation apparatus shown in FIG. 9 .
  • FIG. 11 is an exploded perspective view showing some components of the medical ablation apparatus shown in FIG. 9 in an exploded manner.
  • first, second, A, B, (a), and (b) may be used. These terms are only used to distinguish the component from other components, and the nature, order, or order of the corresponding component is not limited by the term.
  • a component when a component is described as “connected”, “coupled” or “connected” to another component, the component may be directly connected or connected to the other component, but each component It should be understood that another component may be “connected”, “coupled” or “connected” between elements. In the case of "connected”, “coupled” or “connected”, it is understood that not only physically “connected”, “coupled” or “connected”, but also electrically “connected”, “coupled” or “connected” as necessary. It can be.
  • each component to be described below may be combined into one component, or one component may be divided into two or more for each more subdivided function.
  • each component to be described below may additionally perform some or all of the functions of other components in addition to its main function, and some of the main functions of each component may be performed by other components. Of course, it may be dedicated and performed by .
  • FIG. 1 is a diagram schematically showing a medical device system including a medical ablation device 100a according to an embodiment of the present invention. With reference to this, a medical device system including the medical ablation device 100a according to the present embodiment will be described.
  • the medical device system may include a medical ablation device 100a, a hand piece 200, a control unit 300, and a suction unit 400.
  • the medical ablation device 100a according to the present embodiment may be mounted at the end of the handpiece 200, and a driving unit such as a motor is mounted on the handpiece 200 to cut the abrasive cutting portion of the medical ablation device 100a ( ; shown in Figure 2) can be rotated. Accordingly, while the abrasive cutting part 180a of the medical resection instrument 100a is rotated, tissues or bones may be ground or cut.
  • the handpiece 200 can be controlled by the control unit 300 and is connected to the suction unit 400 so as to suction blood, tissue or bone through the medical ablation device 100a.
  • the handpiece 200 may be connected through a power source and transmits an electrical signal to the medical ablation device 100a under the control of the control unit 300 so that the medical ablation device 100a coagulates or cauterizes tissue. ) can be made.
  • FIG. 2 is a perspective view showing the medical ablation device 100a shown in FIG. 1
  • FIG. 3 is a cross-sectional view showing the medical ablation device 100a shown in FIG. 2 .
  • the medical ablation device 100a according to the present embodiment will be described.
  • the medical ablation apparatus 100a includes a first electrode portion 110a at least partially hollow, and at least a portion of the first electrode portion 110a therein.
  • the hollow second electrode portion 120a to be positioned, the first insulating portion 130a insulating between the first electrode portion 110a and the second electrode portion 120a, and at least a portion of the first electrode portion 110a.
  • the second insulating portion 140a covering the , the third insulating portion 170a covering at least a portion of the second electrode portion 120a, and at least a portion thereof are located inside the hollow of the first electrode portion 110a and are rotatable. It may include an abrasive cutting part (180a) implemented in such a way.
  • FIG. 4 is an exploded perspective view showing some components of the medical ablation device 100a shown in FIG. 1 in an exploded manner.
  • the first electrode part 110a, the second electrode part 120a, the first insulating part 130a, and the third insulating part of the medical ablation device 100a according to the present embodiment Let's take a look at (170a).
  • the first electrode unit 110a is a member that coagulates or cauterizes tissue when an electric signal is applied together with the second electrode unit 120a, and may extend along a first direction, that is, a longitudinal direction.
  • the first electrode unit 110a may be made of, for example, a metal such as stainless steel, tungsten or a tungsten alloy, molybdenum or a molybdenum alloy, titanium or a titanium alloy, etc. to receive an electrical signal, and at least a part thereof It may be implemented in a hollow shape having a first through hole 111 .
  • the first electrode part 110a may include a first electrode body part 112 , a first electrode exposed part 113 , and a first electrode connection part 114 .
  • the first electrode body portion 112 may be implemented in a hollow shape having a first through hole 111 therein, and at least a portion of the second through hole 121 of the second electrode portion 120a is formed. can be located in
  • at least a portion of the first electrode body portion 112 may be covered by a first insulating portion 130a to be described later, and the remaining portion may be covered by a second insulating portion 140a to be described later. It may be covered by the body part 150 . Accordingly, the first electrode main body 112 may not be exposed to the outside in a finished product state as shown in FIG. 1 .
  • the first electrode exposed portion 113 may be located on the outer surface of the second insulating body portion 150 of the second insulating portion 140a, and is implemented in a plate shape to be exposed to the outside in a finished product state as shown in FIG. can Accordingly, the first electrode exposed portion 113 may be in contact with the tissue and may be used as a part for applying an electrical signal to the tissue.
  • a third suction hole 115 may be formed in the first electrode exposed portion 113 to provide an inlet through which blood, tissue, or bone is suctioned.
  • the first electrode connection unit 114 may have a bent wire shape, for example, in the shape of a letter "a", and may be implemented in two or more to improve electrical stability. Among both ends of the first electrode connection part 114, the first connection end 116 is in contact with the first electrode main body 112 and the second connection end 117 is in contact with the first electrode exposed part 113, It is possible to electrically connect between the first electrode connection part 114 and the first electrode main body part 112 .
  • the first connection end 116 may be in surface contact or line contact with the first electrode body 112, and the second connection end 117 is the other side of the first electrode connection part 114. It may be implemented in a spherical shape having a larger diameter than the part.
  • the other part of the first electrode connection part 114, except for the second connection end 117, is inserted into the connection hole 113a penetrating the first electrode exposed part 113, and has a diameter greater than the diameter of the connection hole 113a.
  • the large second connection end 117 does not pass through and can be electrically connected to the first electrode exposed portion 113 in contact with it.
  • the first electrode connection portion 114 is not exposed to the outside in the finished product state as shown in FIG. 1, which may be because it is covered by the second insulation portion 140a. Specifically, the first connection end 116 part of the first electrode connection part 114 is connected to the first connection end 116 and the second connection end 116 by the second insulating cover part 160 of the second insulation part 140a. The remaining portion except for the end 117 may be covered by the second insulating body portion 150 of the second insulating portion 140a, and thus the remaining portion except for the second connection end 117 will not be exposed to the outside.
  • first electrode connection portion 114 may be connected to the first electrode body portion 112 and the first electrode exposed portion 113 through a combination such as welding, soldering, bonding, or a separate process (welding, etc.)
  • the second insulation body portion 150 of the second insulation portion 140a and the second insulation cover portion 160 may be connected through pressure by coupling without passing through the second insulation portion 140a.
  • the second electrode unit 120a is a member that coagulates or cauterizes tissue when an electric signal is applied together with the first electrode unit 110a, and like the first electrode unit 110a, the second electrode unit 110a moves in the first direction, that is, the longitudinal direction. It may extend along the surface and may be made of, for example, stainless steel, tungsten or a tungsten alloy, molybdenum or a molybdenum alloy, titanium or a titanium alloy, and the like so as to receive or transmit an electrical signal.
  • the first electrode part 110a can function as an active electrode and the second electrode part 120a can function as a passive electrode.
  • the first electrode part 110a can function as a passive electrode.
  • the second electrode unit 120a may function as an active electrode.
  • the first electrode portion 110a and the second electrode portion 120a in order for the first electrode portion 110a and the second electrode portion 120a to coagulate or cauterize human tissue by receiving an electrical signal, at least a portion of the first electrode portion 110a must be exposed to the outside.
  • the second connection end 117 of the first electrode exposed portion 113 and the first electrode connection portion 114 is not covered by the third insulating portion 170a in the case of the second electrode portion 120a.
  • the phosphorus exposure area 122 may be a portion exposed to the outside.
  • the second electrode part 120a may be implemented in a hollow shape having a second through hole 121 therein.
  • the first electrode part 110a In the second through hole 121, at least a part of the first electrode part 110a, more specifically, At least a portion of the first electrode body portion 112 of the first electrode portion 110a may be located.
  • the first insulation part 130a it is necessary to insulate the first electrode part 110a and the second electrode part 120a from each other, and this insulation may be performed by the first insulation part 130a.
  • the first insulating portion 130a may be positioned inside the second through hole 121 of the second electrode portion 120a and implemented in a hollow shape having the first insulating through hole 131 therein.
  • At least a portion of the first electrode portion 110a may be positioned inside the first insulating through hole 131 so that the first insulating portion 130a is positioned between the second electrode portion 120a.
  • the first insulating part 130a may include, for example, a double structure of a 1-1 insulating part 132 and a 1-2 insulating part 133 .
  • the 1-1 insulation part 132 is located on at least a part of the outer surface of the first electrode part 110a
  • the 1-2 insulation part 133 is located on at least a part of the outer surface of the 1-1 insulation part 132. It may have a structure that is positioned.
  • the 1-1 insulation part 132 may be made of PTFE (Polytetrafluoroethylene) and implemented thinly
  • the 1-2 insulation part 133 is made of FEP (Fluorinated Ethylene Propylene copolymer) for more reliable insulation.
  • the first insulating portion 130a is not limited to these materials, and may include PTFE, FEP, PFA (Poly Fluoro Alkoxy), PEEK (Poly Ether Ether Ketone), PVDF (Polyvinylidene fluoride), PET (Poly Ethylene Terephthalate), etc. Any material capable of insulating may be implemented in various ways.
  • the first area 134 is the 1-1 insulating part ( 132) and the second insulating cover part 160 of the second insulating part 140a on the 1-1 insulating part 132
  • the second region 135 is formed by the 1-1 insulating part 132
  • the thickness of the 1-2 insulating part 133 is the second insulating cover part interposed therebetween. It is implemented to be the same as the thickness of (160) to increase structural completeness.
  • the 1-1 insulating portion 132 does not necessarily need to be included.
  • the 1-1 insulation part 132 it is possible to prevent damage to the medical ablation device 100a due to fluid from the human body passing through the space between parts.
  • the second insulating portion 140a is a member that performs an ablation function together with the abrasive cutting portion 180a while performing an insulating role.
  • the second insulating portion 140a may structurally include a second insulating body portion 150 and a second insulating cover portion 160 .
  • the second insulating body 150 may provide an area where the first electrode unit 110a is located, and the area A 151 is the outer surface of the first electrode body 112 of the first electrode unit 110a. It is possible to cover a part of the first electrode body 112 together with the second insulating cover 160 so that it is not exposed to the outside. is formed to allow the first electrode connecting portion 114 of the first electrode portion 110a to be seated on the seating portion 154, and the first electrode exposed portion ( 113) may be provided with a space located on the outer surface. At this time, the seating portion 154 may be extended and formed in the C region 153, and the first electrode connection portion 114, which is relatively weak against external impact, may be safely protected by the seating portion 154.
  • a second suction hole 156 may be formed in region C 153 of the second insulating body 150 at a position corresponding to the third suction hole 115 of the first electrode part 110a, This allows blood, tissue or bone to be suctioned out.
  • a first suction hole 155 may be additionally formed at the end of the C region 153 of the second insulating body 150, and blood, tissue, or bone may be suctioned through the first suction hole 155. This can improve the suction efficiency.
  • a first open portion 157 may be formed in a direction opposite to the second suction hole 156 of the second insulating body portion 150 .
  • the first open portion 157 may have a shape opened toward a direction different from the first direction in which the second electrode portion 120a extends, and more particularly, toward a second direction perpendicular to the first direction.
  • a first blade region 158 may be formed in the first open portion 157, and the first blade region 158 may cut tissue according to interaction with the abrasive cutting portion 180a to be described later. have.
  • the first open portion 157 and the first suction hole 155 may have shapes connected to each other, and blood, some tissues or bones may be suctioned through the first open portion 157 to improve efficiency.
  • the second insulating cover part 160 is a member that covers the first electrode connection part 114 located on the seating part 154 of the second insulating body part 150 so that it is not exposed to the outside. Since the first electrode connection portion 114 may be implemented as a wire, it may be vulnerable to external impact, and when exposed to the outside, electrical signals may flow to the outside through tissue or the like and may be damaged. Therefore, it is necessary to cover the first electrode connection portion 114 so as not to be exposed to the outside. ) can be covered.
  • the second insulating cover part 160 covers the D area 161 that covers the first electrode connection part 114 and the E area 162 that covers a part of the first electrode body part 112.
  • the E region 162 is implemented in a hollow shape and may be positioned so as to be in close contact with a portion of the outer surface of the first electrode body 112 where only the 1-1 insulation part 132 is covered, and thus the 1-1 insulation part
  • the first region 134 of the first electrode portion 110a and the second electrode portion 120a may be insulated from each other through 132 and the E region 162 of the second insulating cover portion 160 .
  • the D region 161 covers the first electrode connection part 114 seated on the seating part 154 and is in close contact with the second insulating body part 150, and is a part of B of the second insulating body part 150.
  • the end of region D 161 adheres to the first stepped portion 159 between region 152 and region C 153, and region B to the second stepped portion 163 formed inside D region 161.
  • the second insulating body 150 and the second insulating cover 160 may be coupled.
  • the second insulating body portion 150 and the second insulating cover portion 160 may be coupled in various ways, such as through mechanical coupling using protrusions, grooves, or the like, or through bonding.
  • the second insulating portion 140a may be made of a ceramic having high mechanical strength, such as alumina (Al 2 O 3 ) or zirconia (ZrO 2 ).
  • the second insulating portion 140a is a portion in direct contact with tissue or bone and should have high mechanical strength, but should cover and insulate the rest except for a part of the first electrode portion 110a, so ceramic may be the most desirable material. .
  • electrical stability can be improved by implementing a part directly contacting tissue in the surgical site with the second insulating part 140a made of an insulating material rather than metal.
  • the portion directly contacting the surgical site is made of metal, electrical signals are not concentrated, so tissue coagulation or cauterization is not smoothly performed, and problems such as undesirable short circuiting may occur.
  • most of the portion directly contacting the surgical site is composed of the second insulating portion 140a, so that the electrical signal is exposed to the first electrode of the first electrode portion 110a.
  • the portion 113 and the exposure area 122 of the second electrode portion 120a may be concentrated so that tissue coagulation or cauterization can be smoothly performed.
  • the third insulating portion 170a covers at least a portion of the second electrode portion 120a to insulate the medical ablation device 100a from the outside.
  • the third insulating portion 170a may be implemented in a hollow shape having a third insulating through hole 171 therein, and the second electrode portion 120a is positioned inside the third insulating through hole 171. As much as possible, the second electrode portion 120a may be covered.
  • the third insulating portion 170a is a portion that becomes the exterior of the medical resection device 100a and may be formed of FEP (Fluorinated ethylene propylene copolymer) to be relatively thick to perform stable insulation.
  • FEP Fluorinated ethylene propylene copolymer
  • the third insulator 170a is not limited to these materials, and may include PTFE, FEP, PFA (Poly Fluoro Alkoxy), PEEK (Poly Ether Ether Ketone), PVDF (Polyvinylidene fluoride), PET (Poly Ethylene Terephthalate), etc. Any material capable of insulating may be implemented in various ways.
  • the exposed area 122 of the second electrode portion 120a is the third insulating portion 170a. ) may not be covered by
  • FIG. 5 is a perspective view showing the abrasive cutting part 180a of the medical ablation instrument 100a shown in FIG. 1
  • FIGS. 6 and 7 are the abrasive cutting part 180a of the medical ablation instrument 100a shown in FIG. It is a cross-sectional view to explain the operation.
  • a polishing cutting part 180a according to the present embodiment will be described with reference to FIGS. 2 to 7 .
  • the abrasive cutting part 180a is a member for grinding or cutting tissue or bone, and is located inside the first through hole 111 of the first electrode part 110a and has the internal configuration of the handpiece 200 described in FIG. It can be connected and rotatably implemented.
  • An abrasive cutting area for grinding or cutting tissue or bone may be formed in the abrasive cutting portion 180a.
  • the abrasive cutting part 180a of the medical cutting instrument 100a is a shaver for cutting tissue, and the abrasive cutting area may be implemented as the second blade area 181.
  • the abrasive cutting part 180a may have a second open part 182 opened in a second direction that is different from the first direction, which is the extension direction of the first electrode part 110a.
  • a second blade region 181 may be formed in the open portion 182 .
  • at least a portion of the polishing cutting part 180a may be implemented in a hollow shape having a third through hole 183 therein, and the third through hole 183 of the polishing cutting part 180a is shown in FIG.
  • the abrasive cutting portion 180a is not necessarily implemented in a hollow shape, and when the abrasive cutting portion 180a is not implemented in a hollow shape, the first through hole 111 of the first electrode portion 110a is a suction passage. can function as
  • a fourth suction hole 184 may be formed in a direction opposite to the second open part 182 of the abrasive cutting part 180a, and the fourth suction hole 184 is rotated according to the rotation of the abrasive cutting part 180a. ) coincides with the positions of the second suction hole 156 and the third suction hole 115, the suction target, such as blood, tissue or bone fragments, sequentially passes through the third suction hole 115 and the second suction hole 156. ) and the fourth suction hole 184 and may be suctioned through the third through hole 183 .
  • the suction target is the third suction hole. 115, the second suction hole 156, and the second open portion 182 may be suctioned through the third through hole 183.
  • the end of the abrasive cutting part 180a is open, tissues, etc., which are suctioned through the first suction hole 155 of the second insulating part 140a, can be naturally suctioned through the third through hole 183. .
  • tissue can be cut by the interaction between the first blade region 158 of the second insulating portion 140a and the second blade region 181 of the abrasive cutting portion 180a.
  • the suction unit 400 operates to make the third through hole.
  • tissue is suctioned (pulled) through the second open portion 182, and as shown in FIG. 7, the abrasive cutting portion 180a rotates inside the first electrode portion 110a.
  • the first open portion 157 and the second open portion 182 face in different directions, and in this process, the first blade region 158 and the second blade region 181 act like scissors to create suction. Tissues (pulled) can be cut. That is, the tissue can be cut while the second blade region 181 rotates inside the first blade region 158 .
  • the first blade region 158 and the second blade region 181 may be implemented in a simple blade shape or may be implemented in a sawtooth shape to improve cutting capability.
  • the medical ablation device 100a can perform not only the function of a shaver but also the function of electrocautery, and the abrasive cutting part 180a can be removed while the medical ablation device 100a is inserted into the surgical site.
  • an electrical signal may be applied to the first electrode unit 110a or the second electrode unit 120a to coagulate or cauterize the tissue, thereby enabling hemostasis.
  • the surgical site can be kept clean by continuously suctioning blood, tissues, bone fragments, and the like.
  • the control unit 300 shown in FIG. 1 includes suction according to the suction unit 400, coagulation or cauterization according to the first electrode part 110a and the second electrode part 120a, and the second insulating part 140a. And it is possible to control the hand piece 200 and the medical cutting device 100a so that the cutting according to the abrasive cutting part 180a is smoothly performed. According to the rotational position or use time of the abrasive cutting part 180a, a suction signal, It is also possible to give different coagulation or cauterization signals, or it may be possible to continuously control rotation, suction, coagulation, or cauterization of the abrasive cutting unit 180a to proceed.
  • FIG. 8 is a perspective view showing an abrasive cutting part 180b of a medical ablation device according to another embodiment of the present invention.
  • the medical ablation apparatus according to the present embodiment will be described.
  • the medical ablation device includes a first electrode part 110a, a second electrode part 120a, a first insulating part 130a, a second insulating part 140a, and a third insulating part as in the previous embodiment. It includes a portion 170a and an abrasive cutting portion 180b, but the abrasive cutting portion 180b has the shape of a burr rather than the shape of a shaver having the second blade region 181 as in the previous embodiment. can be characterized.
  • the medical ablation device may be used for grinding or cutting bone, not for cutting tissue, and the abrasive cutting part 180b grinds or cuts the bone, and the first electrode part 110a and the second electrode unit 120a may perform a coagulation or cauterization function for hemostasis or the like.
  • a separate blade region may not be formed in the second insulating portion 140a.
  • FIG. 9 is a perspective view showing a medical ablation device 100c according to another embodiment of the present invention
  • FIG. 10 is a cross-sectional view showing the medical ablation device 100c shown in FIG. 9 .
  • the medical ablation device 100c according to the present embodiment will be described.
  • the medical ablation device 100c includes a first electrode part 110c, a second electrode part 120c, a first insulating part 130c, and a second insulating part.
  • a portion 140c, a third insulating portion 170c, and a polishing cutting portion 180c may be included.
  • the first electrode part 110c is a member that coagulates or cauterizes tissue together with the second electrode part 120c when an electrical signal is applied, and is made of, for example, stainless steel, tungsten or a tungsten alloy, molybdenum or It may be composed of metals such as molybdenum alloys, titanium or titanium alloys, and the like.
  • the first electrode part 110c may be implemented in a hollow shape extending in a first direction, which is a longitudinal direction, and having at least a portion of the first through hole 111c therein.
  • a third open part 118 opened in the same direction as the first open part 157c at a position corresponding to the first open part 157c of the second insulating part 140c. can be formed.
  • a third blade region 119 may be formed in the third open portion 118, and tissue or bone may be polished or cut by interaction with the abrasive cutting region 181 of the rotatable abrasive cutting portion 180c. .
  • FIG. 11 is an exploded perspective view showing some components of the medical ablation device 100c shown in FIG. 9 in an exploded manner.
  • the second electrode part 120c, the first insulating part 130c, the second insulating part 140c, the third insulating part 170c and the polishing cutting part according to the present embodiment Let's take a look at (180c).
  • the second electrode part 120c is a member that coagulates or cauterizes tissue together with the first electrode part 110c when an electrical signal is applied, and like the first electrode part 110c, the electrical signal is well conducted, for example, stainless steel. It may consist of metals such as steel, tungsten or tungsten alloys, molybdenum or molybdenum alloys, titanium or titanium alloys, and the like.
  • the second electrode unit 120c extends in the first direction, which is the longitudinal direction, and at least a portion thereof may be implemented in a hollow shape having a second through hole 121c therein, and a second electrode unit 120c may have a second through hole 121c therein. At least a part of the first electrode part 110c may be located.
  • the second electrode unit 120c may function as an active electrode
  • the first electrode unit 110c may function as a passive electrode, or vice versa.
  • the second electrode part 120c may include a body part 123 and an exposed part 124 .
  • the exposed part 124 is a part located on the outer surface of the second insulating part 140a and exposed to the outside, and the main body part 123 has most of the area surrounded by the outside of the second electrode part 120c. 3 may not be exposed to the outside by the insulating portion 170c.
  • the exposed portion 124 may be coupled, for example, by welding in an overlapped state with at least a portion of the body portion 123, and a suction hole for suction may be formed in each of the exposed portion 124 and the body portion 123.
  • the exposed part 124 and the main body part 123 may be integrally formed rather than separated.
  • the first insulating portion 130c is a member that insulates at least a portion between the first electrode portion 110c and the second electrode portion 120c.
  • the first insulating part 130c is implemented in a tube shape and may be positioned between the first electrode part 110c and the second electrode part 120c in a form surrounding at least a part of the first electrode part 110c. .
  • the first electrode portion 110c and the second electrode portion 120c are not insulated only by the first insulating portion 130c, and between the first electrode portion 110c and the second electrode portion 120c.
  • a part of the insulation layer 130c may be insulated and the rest may be insulated by the second insulation unit 140c. At this time, as in the previous embodiment, it is also possible to realize more perfect insulation by implementing the first insulation part 130c as two layers.
  • the second insulating part 140c may insulate the first electrode part 110c and the second electrode part 120c from being short-circuited inside while wrapping a part of the first electrode part 110c so as not to be exposed to the outside.
  • a first open portion 157c open in the same direction as the third open portion 118 of the first electrode portion 110c may be formed in the second insulating portion 140c. Therefore, while the third open portion 118 of the first electrode portion 110c is exposed to the outside through the first open portion 157c, the third blade region 119 formed in the third open portion 118 is exposed to the outside. can be exposed.
  • a part of the second electrode unit 120c may function as an exposed electrode by being located on the outer surface of the second insulation unit 140c, and the second insulation unit corresponding to the suction hole of the second electrode unit 120c ( A suction hole is formed at the position 140c) so that blood, tissue or bone can be suctioned.
  • a separate side suction hole 155c may be further formed at an end of the second insulating portion 140c, and suction may be performed through this, so that suction efficiency may be improved.
  • the corresponding positions of the first electrode part 110c and the polishing cutting part 180c may be open so that there is no problem with suction.
  • the abrasive cutting part 180c is rotatably implemented as a member for grinding or cutting tissue or bone, is located inside the first through hole 111c of the first electrode part 110c, and has a second insulating part ( A polishing cutting area 181 may be formed in an area adjacent to 140c).
  • the second open part 182 may be formed in the abrasive cutting part 180c, and the abrasive cutting area implemented as a blade area is formed in the second open part 182. (181) can be formed.
  • tissue is suctioned (pulled) through the second open part 182, and the abrasive cutting part 180c ) is rotated, the abrasive cutting area 181 of the second open portion 182 is rotated inside the third blade area 119 of the third open portion 118, and tissue can be cut.
  • This embodiment is different from the previous embodiment in that the blade region is formed on the first electrode part 110c instead of the second insulating part 140c.
  • the blade region is formed on the first electrode part 110c instead of the second insulating part 140c.
  • the third blade region 119 is formed on the first electrode portion 110c made of metal, mechanical strength may be excellent, and both the second blade region 181 and the third blade region 119 are Since it is made of metal, mutual matching is improved and cutting power can be further improved.
  • the abrasive cutting part 180c is a shaver

Abstract

A medical resection device according to an aspect of the technical idea of the present invention comprises: a first electrode portion extending in a first direction and having a hollow shape in which at least a part thereof has a first through-hole therein; a second electrode portion having a hollow shape in which at least a part thereof has second through-hole such that at least a part of the first electrode portion is positioned therein; a first insulating portion positioned between the first and second electrode portions so as to insulate between the first and second electrode portions; a second insulating portion disposed such that at least a part thereof covers a part of the first electrode portion, a part of the second insulating portion being exposed to the outside, and the second insulating portion having a first open portion that is open towards a direction different from the first direction; a third insulating portion covering at least a part of the second electrode portion such that a part of the second electrode portion is exposed to the outside; and a polishing/cutting portion positioned inside the first-through hole, the polishing/cutting portion having a polishing/cutting area formed in an area adjacent to the second insulating portion, and being rotatable.

Description

의료용 절제기구medical ablation device
본 발명은 의료용 절제기구에 관한 것이다.The present invention relates to a medical ablation device.
관절경 치료는 관절에 약 1cm 미만의 작은 절개 구멍을 2~4개 내고 작은 카메라와 수술용 기구를 삽입하여 카메라를 통해 관절 안을 살펴보면서 수술을 하는 방법으로, 반월상 연골판 손상, 슬관절 인대 손상, 관절 연골 손상 등 많은 병변에서 고려될 수 있으며, 점차 관절경의 기술이 발달함에 따라 그만큼 슬관절의 여러 질환에 관하여 적용 범위가 늘어나고 있다.Arthroscope treatment is a method of surgery by making 2 to 4 small incisions less than about 1 cm in the joint, inserting a small camera and surgical instruments, and looking inside the joint through the camera. It can be considered in many lesions such as cartilage damage, and as arthroscopy technology develops, the scope of application is increasing for various diseases of the knee joint.
또한, 인체 내부에서 일어날 수 있는 다양한 질환에 대한 수술적 치료를 위하여 복부 등을 크게 절개하지 않고 작은 홀 크기의 절개부위만으로도 수술하는 기술로서 카메라가 부착된 복강경을 뱃속으로 넣어 수술을 하는 복강경 수술이 적용되고 있다. In addition, for surgical treatment of various diseases that can occur inside the human body, laparoscopic surgery is a technology that operates only with a small hole-sized incision without making a large incision in the abdomen, etc. is being applied
이러한 관절경 또는 복강경 등과 같이 인체에 최소한의 절개 개구를 내고 진행하는 치료 과정 또는 콧구멍과 같은 인체의 자연스러운 개구를 통한 치료 과정에 있어서, 개구 내 조직, 뼈 등 신체의 일부를 절제하기 위하여 의료용 절제기구가 사용되고 있다. 이러한 의료용 절제기구로서는 통상 쉐이버(Shaver) 기구가 사용되고 있는데, 쉐이버 기구는 조직 등에 대한 고속 절제를 제공한다. Medical resection to remove parts of the body, such as tissues and bones in the opening, in the course of treatment through arthroscopy or laparoscopy, which involves making minimal incisions in the body, or through natural openings in the body, such as the nostrils. instrument is being used. As such a medical cutting device, a shaver device is usually used, and the shaver device provides high-speed cutting of tissues and the like.
이와 같이 쉐이버 기구를 통해 조직을 절제할 경우 수술 과정에서 출혈이 발생될 수 있으며, 이에 지혈 과정을 거쳐야 한다. 지혈을 위해서는 전극에 전기 신호를 인가함으로써 소작 작용을 하는 전기 소작 기구를 사용할 수 있는데, 전기 소작 기구를 사용하기 위해서는 쉐이버 기구를 빼고 전기 소작 기구를 삽입하는 과정을 거쳐야 하며, 지혈 후 다시 절제를 위해서는 삽입했던 전기 소작 기구를 빼고 쉐이버 기구를 재삽입하는 과정을 거쳐야 한다. 이와 같이 전기 소작 기구와 쉐이버 기구를 반복적으로 넣고 빼고 하는 작업을 거칠 경우 툴 교체에 따른 수술 시간이 길어지는 문제와 교체하는 과정에서 감염의 위험이 있다.In this way, when tissue is resected through the shaver device, bleeding may occur during the surgical procedure, and therefore, hemostasis must be performed. For hemostasis, an electric cautery device that cauterizes by applying an electrical signal to the electrode can be used. To use the electric cautery device, the shaver device must be removed and the electric cautery device inserted. You have to go through the process of removing the inserted electric cautery device and reinserting the shaver device. In this way, if the operation of repeatedly inserting and removing the electric cautery device and the shaver device is performed, there is a problem that the operation time is prolonged due to tool replacement and there is a risk of infection during the replacement process.
본 발명의 기술적 사상이 이루고자 하는 기술적 과제는, 쉐이버, 버(Burr) 등 연마절삭 기능과 소작 또는 응고 기능을 하나의 기구에서 제공하여, 수술 시간을 감소시키고, 툴 교체에 따른 번거로움을 감소시키며 감염 위험을 예방하는 의료용 절제기구를 제공하기 위한 것이다.The technical problem to be achieved by the technical idea of the present invention is to provide an abrasive cutting function such as a shaver, a burr, and a cautery or coagulation function in one instrument, thereby reducing the operation time, reducing the hassle of replacing tools, It is to provide a medical ablation device that prevents the risk of infection.
본 발명의 기술적 사상에 의한 일 양태에 따른 의료용 절제기구는, 제1 방향으로 연장되되, 적어도 일부가 내부에 제1 관통홀을 갖는 중공 형상인 제1 전극부, 내부에 상기 제1 전극부의 적어도 일부가 위치되도록 적어도 일부가 제2 관통홀을 갖는 중공 형상인 제2 전극부, 상기 제1 전극부와 상기 제2 전극부 사이에 위치되어 상기 제1 전극부와 상기 제2 전극부 간을 절연하는 제1 절연부, 적어도 일부가 상기 제1 전극부의 일부를 커버하도록 배치되고 일부는 외부로 노출되며, 상기 제1 방향과 상이한 방향을 향해 오픈된 제1 오픈부를 구비하는 제2 절연부, 상기 제2 전극부의 일부가 외부로 노출되도록 상기 제2 전극부의 적어도 일부를 커버하는 제3 절연부, 및 상기 제1 관통홀의 내부에 위치되되 상기 제2 절연부와 인접한 영역에 연마절삭영역이 형성되고 회전 가능한 연마절삭부를 포함할 수 있다.A medical ablation apparatus according to one aspect according to the technical idea of the present invention includes a first electrode part extending in a first direction, at least a part of which has a hollow shape having a first through hole therein, and at least the first electrode part therein. A second electrode part having a hollow shape, at least a part of which has a second through hole so that a part thereof is located, is positioned between the first electrode part and the second electrode part, and insulates between the first electrode part and the second electrode part. A second insulating part having a first open part, at least a part of which is disposed to cover a part of the first electrode part, a part of which is exposed to the outside, and is open toward a direction different from the first direction; A third insulating portion covering at least a portion of the second electrode portion so that a portion of the second electrode portion is exposed to the outside, and a polishing cutting region located inside the first through hole and adjacent to the second insulating portion, It may include a rotatable abrasive cutting unit.
예시적인 실시예에 따르면, 상기 제1 전극부 또는 상기 제2 전극부에 전기 신호가 인가되면, 상기 제2 절연부에 의해 커버되지 않고 외부로 노출된 상기 제1 전극부의 영역과 상기 제3 절연부에 의해 커버되지 않고 외부로 노출된 상기 제2 전극부의 영역에 의해 조직이 응고(coagulation) 또는 소작(ablation)되며, 상기 연마절삭부가 회전되면 상기 연마절삭영역에 의해 조직 또는 뼈가 연마 또는 절삭될 수 있다.According to an exemplary embodiment, when an electric signal is applied to the first electrode part or the second electrode part, a region of the first electrode part exposed to the outside and not covered by the second insulating part and the third insulating part Tissues are coagulated or ablated by the region of the second electrode part exposed to the outside and not covered by the part, and when the abrasive cutting part is rotated, tissue or bone is ground or cut by the abrasive cutting area. It can be.
예시적인 실시예에 따르면, 상기 제2 절연부의 상기 제1 방향에 따른 양측 중 일측은 상기 제1 전극부를 커버하고 타측에는 제1 석션홀이 형성될 수 있다.According to an exemplary embodiment, one side of both sides of the second insulating portion along the first direction may cover the first electrode portion, and a first suction hole may be formed on the other side.
예시적인 실시예에 따르면, 상기 제1 전극부는, 적어도 일부가 상기 제2 관통홀의 내부에 위치되고 내부에 상기 제1 관통홀을 가지며 상기 제2 절연부에 의해 외부로 노출되지 않는 제1 전극본체부, 상기 제2 절연부의 외면에 위치되어 외부로 노출되는 제1 전극노출부, 및 상기 제1 전극본체부와 상기 제1 전극노출부 사이를 전기적으로 연결하되, 적어도 일부가 상기 제2 절연부에 의해 외부로 노출되지 않는 제1 전극연결부를 포함할 수 있다.According to an exemplary embodiment, the first electrode unit, at least a portion of which is located inside the second through-hole, has the first through-hole therein, and is not exposed to the outside by the second insulating portion. A first electrode exposed portion located on the outer surface of the second insulating portion and exposed to the outside, and electrically connecting the first electrode main body and the first electrode exposed portion, wherein at least a portion of the second insulating portion is exposed. It may include a first electrode connection portion that is not exposed to the outside by the.
예시적인 실시예에 따르면, 상기 제2 절연부는, 적어도 일부가 상기 제1 전극본체부의 외면에 위치되어 상기 제1 전극본체부가 외부로 노출되지 않도록 하되, 외면의 적어도 일부에 상기 제1 전극연결부가 위치되도록 안착부가 형성되며, 외면에 상기 제1 전극노출부가 위치된 제2 절연바디부, 및 상기 제1 전극연결부의 적어도 일부가 외부로 노출되지 않도록 상기 제2 절연바디부에 결합되되, 적어도 일부가 상기 제2 전극부와 상기 제1 전극본체부 사이에 위치되어 상기 제2 전극부와 상기 제1 전극본체부 사이를 절연하는 제2 절연커버부를 포함할 수 있다.According to an exemplary embodiment, at least a portion of the second insulating portion is positioned on the outer surface of the first electrode body so that the first electrode body is not exposed to the outside, but the first electrode connection portion is on at least a portion of the outer surface. A seat portion is formed to be positioned, and the second insulating body portion on the outer surface of which the first electrode exposed portion is located is coupled to the second insulating body portion so that at least a portion of the first electrode connection portion is not exposed to the outside, and at least a portion thereof Is positioned between the second electrode portion and the first electrode body portion may include a second insulating cover portion to insulate between the second electrode portion and the first electrode body portion.
예시적인 실시예에 따르면, 상기 제1 절연부는, 상기 제1 전극부의 적어도 일부 외면에 위치되는 제1-1 절연부, 및 상기 제1-1 절연부의 적어도 일부 외면에 위치되는 제1-2 절연부를 포함하고, 상기 제1 전극부와 상기 제2 전극부의 사이는 제1 영역 및 제2 영역을 포함하며, 상기 제1 영역은 상기 제1-1 절연부 및 상기 제1-1 절연부 상의 상기 제2 절연커버부에 의해 절연되고, 상기 제2 영역은 상기 제1-1 절연부 및 상기 제1-1 절연부 상의 상기 제1-2 절연부에 의해 절연될 수 있다.According to an exemplary embodiment, the first insulating part may include a 1-1 insulating part located on at least a part of the outer surface of the first electrode part, and a 1-2 insulating part located on at least a part of the outer surface of the 1-1 insulating part. A portion between the first electrode portion and the second electrode portion includes a first region and a second region, wherein the first region includes the 1-1 insulating portion and the second electrode portion on the 1-1 insulating portion. Insulated by a second insulating cover part, the second region may be insulated by the 1-1 insulating part and the 1-2 insulating part on the 1-1 insulating part.
예시적인 실시예에 따르면, 상기 제2 절연부의 상기 제1 오픈부에는 제1 칼날영역이 형성되고, 상기 연마절삭부가 회전되면 상기 연마절삭영역과 상기 제1 칼날영역에 의해 조직 또는 뼈가 연마 또는 절삭될 수 있다.According to an exemplary embodiment, a first blade region is formed in the first open portion of the second insulating portion, and when the abrasive cutting portion is rotated, tissue or bone is polished or polished by the abrasive cutting region and the first blade region. can be cut
예시적인 실시예에 따르면, 상기 연마절삭부는 상기 제1 방향과 상이한 방향을 향해 오픈된 제2 오픈부를 구비하고, 상기 연마절삭영역은 상기 제2 오픈부에 형성되어 상기 조직을 연마 또는 절삭하기 위한 제2 칼날영역일 수 있다.According to an exemplary embodiment, the abrasive cutting unit includes a second open portion opened in a direction different from the first direction, and the abrasive cutting region is formed in the second open portion to polish or cut the tissue. It may be a second blade region.
예시적인 실시예에 따르면, 상기 연마절삭부의 적어도 일부는 내부에 석션을 위한 석션통로로 활용되는 제3 관통홀을 갖는 중공 형상일 수 있다.According to an exemplary embodiment, at least a portion of the abrasive cutting portion may have a hollow shape having a third through hole used as a suction passage for suction therein.
예시적인 실시예에 따르면, 상기 제2 절연부의 상기 제1 오픈부의 반대 방향에는 제2 석션홀이 형성되고, 상기 제1 전극부에는 상기 제2 석션홀에 대응되는 위치에 제3 석션홀이 형성되며, 석션 대상은 상기 제3 석션홀, 상기 제2 석션홀 및 상기 제2 오픈부 또는 상기 제2 오픈부의 반대 방향에 형성된 제4 석션홀을 차례로 통과하여 상기 석션통로를 통해 석션될 수 있다.According to an exemplary embodiment, a second suction hole is formed in a direction opposite to the first open part of the second insulating part, and a third suction hole is formed in a position corresponding to the second suction hole in the first electrode part. The suction target may be suctioned through the suction passage by sequentially passing through the third suction hole, the second suction hole, and the second open part or a fourth suction hole formed in the opposite direction of the second open part.
예시적인 실시예에 따르면, 상기 연마절삭부는 상기 뼈를 연마 또는 절삭하기 위한 버(Burr)일 수 있다.According to an exemplary embodiment, the abrasive cutting unit may be a burr for grinding or cutting the bone.
예시적인 실시예에 따르면, 상기 제1 전극부는 상기 제1 오픈부와 동일한 방향을 향해 오픈된 제3 오픈부를 구비할 수 있다.According to an exemplary embodiment, the first electrode part may have a third open part opened toward the same direction as the first open part.
예시적인 실시예에 따르면, 상기 제3 오픈부에는 제3 칼날영역이 형성되며, 상기 연마절삭부가 회전되면 상기 연마절삭영역과 상기 제3 칼날영역에 의해 조직 또는 뼈가 연마 또는 절삭될 수 있다.According to an exemplary embodiment, a third blade region is formed in the third open portion, and when the abrasive cutting portion is rotated, tissue or bone may be polished or cut by the abrasive cutting region and the third blade region.
예시적인 실시예에 따르면, 상기 제2 전극부는, 제2 절연부의 외면에 위치되어 외부로 노출되는 노출부, 및 적어도 일부가 제3 절연부에 의해 커버되며 상기 노출부와 결합된 본체부를 포함할 수 있다.According to an exemplary embodiment, the second electrode unit may include an exposed portion located on an outer surface of the second insulating portion and exposed to the outside, and a body portion at least partially covered by the third insulating portion and coupled to the exposed portion. can
본 발명의 특징 및 이점들은 첨부도면에 의거한 다음의 상세한 설명으로부터 더욱 명백해질 것이다.Features and advantages of the present invention will become more apparent from the following detailed description taken in conjunction with the accompanying drawings.
이에 앞서, 본 명세서 및 청구범위에 사용된 용어나 단어는 통상적이고 사전적인 의미로 해석되어서는 아니 되며, 발명자가 그 자신의 발명을 가장 최선의 방법으로 설명하기 위해 용어의 개념을 적절하게 정의할 수 있다는 원칙에 입각하여 본 발명의 기술적 사상에 부합되는 의미와 개념으로 해석되어야만 한다.Prior to this, the terms or words used in this specification and claims should not be interpreted in a conventional and dictionary sense, and the inventor should properly define the concept of the term in order to explain his or her invention in the best way. It should be interpreted as a meaning and concept consistent with the technical idea of the present invention based on the principle that it can be.
본 발명의 기술적 사상에 의한 실시예들에 따른 의료용 절제기구는 연마절삭 기능과 소작 또는 응고 기능을 하나의 기구에서 제공하여, 수술 시간을 줄여 의료행위에 따른 환자 및 사용자의 부담, 기기 교체에 따른 감염 위험을 줄일 수 있다.A medical ablation device according to embodiments according to the technical concept of the present invention provides an abrasive cutting function and a cauterization or coagulation function in one device, thereby reducing operation time and reducing the burden of patients and users according to medical practice and device replacement. You can reduce your risk of infection.
본 발명의 상세한 설명에서 인용되는 도면을 보다 충분히 이해하기 위하여 각 도면의 간단한 설명이 제공된다.In order to more fully understand the drawings cited in the detailed description of the present invention, a brief description of each drawing is provided.
도 1은 본 발명의 일 실시예에 따른 의료용 절제기구를 포함하는 의료기기 시스템을 개략적으로 나타낸 도면이다. 1 is a diagram schematically showing a medical device system including a medical ablation device according to an embodiment of the present invention.
도 2는 도 1에 도시한 의료용 절제기구를 나타낸 사시도이다.FIG. 2 is a perspective view showing the medical ablation apparatus shown in FIG. 1;
도 3은 도 2에 도시한 의료용 절제기구를 나타낸 단면도이다. FIG. 3 is a cross-sectional view showing the medical ablation apparatus shown in FIG. 2 .
도 4는 도 1에 도시한 의료용 절제기구의 일부 구성을 분해하여 나타낸 분해사시도이다. FIG. 4 is an exploded perspective view showing some components of the medical ablation apparatus shown in FIG. 1 by disassembling them.
도 5는 도 1에 도시한 의료용 절제기구의 연마절삭부를 나타낸 사시도이다.5 is a perspective view showing an abrasive cutting part of the medical ablation apparatus shown in FIG. 1;
도 6 및 도 7은 도 1에 도시한 의료용 절제기구의 연마절삭부 동작을 설명하기 위한 단면도이다. 6 and 7 are cross-sectional views for explaining the operation of the abrasive cutting unit of the medical ablation apparatus shown in FIG. 1 .
도 8은 본 발명의 다른 실시예에 따른 의료용 절제기구의 연마절삭부를 나타낸 사시도이다. 8 is a perspective view showing an abrasive cutting part of a medical ablation device according to another embodiment of the present invention.
도 9는 본 발명의 또 다른 실시예에 따른 의료용 절제기구를 나타낸 사시도이다.9 is a perspective view showing a medical ablation device according to another embodiment of the present invention.
도 10은 도 9에 도시한 의료용 절제기구를 나타낸 단면도이다. FIG. 10 is a cross-sectional view showing the medical ablation apparatus shown in FIG. 9 .
도 11은 도 9에 도시한 의료용 절제기구의 일부 구성을 분해하여 나타낸 분해사시도이다.FIG. 11 is an exploded perspective view showing some components of the medical ablation apparatus shown in FIG. 9 in an exploded manner.
본 발명의 목적, 특정한 장점들 및 신규한 특징들은 첨부된 도면들과 연관되는 이하의 상세한 설명과 실시예로부터 더욱 명백해질 것이다. 본 명세서에서 각 도면의 구성요소들에 참조번호를 부가함에 있어서, 동일한 구성 요소들에 한해서는 비록 다른 도면상에 표시되더라도 가능한 한 동일한 번호를 가지도록 하고 있음에 유의하여야 한다. 또한, 본 발명을 설명함에 있어서, 관련된 공지 기술에 대한 구체적인 설명이 본 발명의 요지를 불필요하게 흐릴 수 있다고 판단되는 경우 그 상세한 설명은 생략한다.Objects, certain advantages and novel features of the present invention will become more apparent from the following detailed description and examples taken in conjunction with the accompanying drawings. In adding reference numerals to components of each drawing in this specification, it should be noted that the same components have the same numbers as much as possible, even if they are displayed on different drawings. In addition, in describing the present invention, if it is determined that a detailed description of related known technologies may unnecessarily obscure the subject matter of the present invention, the detailed description will be omitted.
본 발명의 구성 요소를 설명하는 데 있어서, 제1, 제2, A, B, (a), (b) 등의 용어를 사용할 수 있다. 이러한 용어는 그 구성 요소를 다른 구성 요소와 구별하기 위한 것일 뿐, 그 용어에 의해 해당 구성 요소의 본질이나 차례 또는 순서 등이 한정되지 않는다. 또한, 본 명세서에서, 어떤 구성 요소가 다른 구성 요소에 "연결", "결합" 또는 "접속"된다고 기재된 경우, 그 구성 요소는 그 다른 구성 요소에 직접적으로 연결되거나 또는 접속될 수 있지만, 각 구성 요소 사이에 또 다른 구성 요소가 "연결", "결합" 또는 "접속"될 수도 있다고 이해되어야 할 것이다. "연결", "결합" 또는 "접속"의 경우, 물리적으로 "연결", "결합" 또는 "접속"되는 것뿐만 아니라 필요에 따라 전기적으로 "연결", "결합" 또는 "접속"되는 것으로 이해될 수 있다. In describing the components of the present invention, terms such as first, second, A, B, (a), and (b) may be used. These terms are only used to distinguish the component from other components, and the nature, order, or order of the corresponding component is not limited by the term. In addition, in this specification, when a component is described as "connected", "coupled" or "connected" to another component, the component may be directly connected or connected to the other component, but each component It should be understood that another component may be “connected”, “coupled” or “connected” between elements. In the case of "connected", "coupled" or "connected", it is understood that not only physically "connected", "coupled" or "connected", but also electrically "connected", "coupled" or "connected" as necessary. It can be.
본 명세서에 기재된 "~부(유닛)", "~기", "~자", "~모듈" 등의 용어는 적어도 하나의 기능이나 동작을 처리하는 단위를 의미하며, 이는 하드웨어나 소프트웨어 또는 하드웨어 및 소프트웨어의 결합으로 구현될 수 있다. 또한, 본 명세서에 기재된 "포함하다", "구성하다" 또는 "가지다" 등의 용어는, 특별히 반대되는 기재가 없는 한 해당 구성 요소가 내재될 수 있음을 의미하는 것이므로, 다른 구성 요소를 제외하는 것이 아니라 다른 구성 요소를 더 포함할 수 있는 것으로 해석되어야 한다.Terms such as "~unit (unit)", "~group", "~character", and "~module" described in this specification mean a unit that processes at least one function or operation, which is hardware, software, or hardware. And it can be implemented as a combination of software. In addition, terms such as "comprise", "comprise" or "having" described in this specification mean that the corresponding component may be inherent unless otherwise stated, excluding other components. It should be construed as being able to further include other components.
그리고 본 명세서에서의 구성부들에 대한 구분은 각 구성부가 담당하는 주기능 별로 구분한 것에 불과함을 명확히 하고자 한다. 즉, 이하에서 설명할 2개 이상의 구성부가 하나의 구성부로 합쳐지거나 또는 하나의 구성부가 보다 세분화된 기능별로 2개 이상으로 분화되어 구비될 수도 있다. 그리고 이하에서 설명할 구성부 각각은 자신이 담당하는 주 기능 이외에도 다른 구성부가 담당하는 기능 중 일부 또는 전부의 기능을 추가적으로 수행할 수도 있으며, 구성부 각각이 담당하는 주기능 중 일부 기능이 다른 구성부에 의해 전담되어 수행될 수도 있음은 물론이다. In addition, it is intended to make it clear that the classification of components in this specification is merely a classification for each main function in charge of each component. That is, two or more components to be described below may be combined into one component, or one component may be divided into two or more for each more subdivided function. In addition, each component to be described below may additionally perform some or all of the functions of other components in addition to its main function, and some of the main functions of each component may be performed by other components. Of course, it may be dedicated and performed by .
이하, 첨부된 도면을 참조하여 본 발명의 실시예를 상세히 설명하기로 한다.Hereinafter, embodiments of the present invention will be described in detail with reference to the accompanying drawings.
도 1은 본 발명의 일 실시예에 따른 의료용 절제기구(100a)를 포함하는 의료기기 시스템을 개략적으로 나타낸 도면이다. 이를 참조하여 본 실시예에 따른 의료용 절제기구(100a)를 포함하는 의료기기 시스템에 대해 살펴보기로 한다.1 is a diagram schematically showing a medical device system including a medical ablation device 100a according to an embodiment of the present invention. With reference to this, a medical device system including the medical ablation device 100a according to the present embodiment will be described.
도 1에 도시한 바와 같이, 본 실시예에 따른 의료기기 시스템은 의료용 절제기구(100a), 핸드피스(200), 제어유닛(300) 및 석션유닛(400)을 포함할 수 있다. 여기서, 핸드피스(200)의 단부에는 본 실시예에 따른 의료용 절제기구(100a)가 장착될 수 있으며, 핸드피스(200)에는 모터 등 구동부가 장착되어 의료용 절제기구(100a)의 연마절삭부(; 도 2에 도시함)를 회전시킬 수 있다. 이에 의료용 절제기구(100a)의 연마절삭부(180a)가 회전되면서 조직 또는 뼈가 연마 또는 절삭될 수 있다. 핸드피스(200)는 제어유닛(300)에 의해 제어될 수 있으며, 석션유닛(400)과 연결되어 있어 의료용 절제기구(100a)를 통해 혈액, 조직 또는 뼈 등을 석션하도록 할 수 있다. 핸드피스(200)는 전원을 통해 연결될 수 있으며 제어유닛(300)의 제어 하에 의료용 절제기구(100a)에 전기 신호를 전달하여, 의료용 절제기구(100a)가 조직을 응고(coagulation) 또는 소작(ablation)하도록 할 수 있다.As shown in FIG. 1 , the medical device system according to the present embodiment may include a medical ablation device 100a, a hand piece 200, a control unit 300, and a suction unit 400. Here, the medical ablation device 100a according to the present embodiment may be mounted at the end of the handpiece 200, and a driving unit such as a motor is mounted on the handpiece 200 to cut the abrasive cutting portion of the medical ablation device 100a ( ; shown in Figure 2) can be rotated. Accordingly, while the abrasive cutting part 180a of the medical resection instrument 100a is rotated, tissues or bones may be ground or cut. The handpiece 200 can be controlled by the control unit 300 and is connected to the suction unit 400 so as to suction blood, tissue or bone through the medical ablation device 100a. The handpiece 200 may be connected through a power source and transmits an electrical signal to the medical ablation device 100a under the control of the control unit 300 so that the medical ablation device 100a coagulates or cauterizes tissue. ) can be made.
도 2는 도 1에 도시한 의료용 절제기구(100a)를 나타낸 사시도이고, 도 3은 도 2에 도시한 의료용 절제기구(100a)를 나타낸 단면도이다. 이하, 이를 참조하여 본 실시예에 따른 의료용 절제기구(100a)에 대해 살펴보기로 한다.FIG. 2 is a perspective view showing the medical ablation device 100a shown in FIG. 1 , and FIG. 3 is a cross-sectional view showing the medical ablation device 100a shown in FIG. 2 . Hereinafter, with reference to this, the medical ablation device 100a according to the present embodiment will be described.
도 2 및 도 3에 도시한 바와 같이, 본 실시예에 따른 의료용 절제기구(100a)는 적어도 일부가 중공 형상인 제1 전극부(110a), 내부에 제1 전극부(110a)의 적어도 일부가 위치되도록 중공 형상인 제2 전극부(120a), 제1 전극부(110a)와 제2 전극부(120a) 사이를 절연하는 제1 절연부(130a), 제1 전극부(110a)의 적어도 일부를 커버하는 제2 절연부(140a), 제2 전극부(120a)의 적어도 일부를 커버하는 제3 절연부(170a) 및 적어도 일부가 제1 전극부(110a)의 중공 내부에 위치되고 회전 가능하게 구현되는 연마절삭부(180a)를 포함할 수 있다.As shown in FIGS. 2 and 3, the medical ablation apparatus 100a according to the present embodiment includes a first electrode portion 110a at least partially hollow, and at least a portion of the first electrode portion 110a therein. The hollow second electrode portion 120a to be positioned, the first insulating portion 130a insulating between the first electrode portion 110a and the second electrode portion 120a, and at least a portion of the first electrode portion 110a. The second insulating portion 140a covering the , the third insulating portion 170a covering at least a portion of the second electrode portion 120a, and at least a portion thereof are located inside the hollow of the first electrode portion 110a and are rotatable. It may include an abrasive cutting part (180a) implemented in such a way.
도 4는 도 1에 도시한 의료용 절제기구(100a)의 일부 구성을 분해하여 나타낸 분해사시도이다. 이하, 도 2 내지 도 4를 참조하여 본 실시예에 따른 의료용 절제기구(100a)의 제1 전극부(110a), 제2 전극부(120a), 제1 절연부(130a) 및 제3 절연부(170a)에 대해 살펴보기로 한다.FIG. 4 is an exploded perspective view showing some components of the medical ablation device 100a shown in FIG. 1 in an exploded manner. Hereinafter, referring to FIGS. 2 to 4 , the first electrode part 110a, the second electrode part 120a, the first insulating part 130a, and the third insulating part of the medical ablation device 100a according to the present embodiment Let's take a look at (170a).
제1 전극부(110a)는 제2 전극부(120a)와 함께 전기 신호를 인가받으면 조직을 응고 또는 소작하는 부재로, 제1 방향, 즉 길이방향을 따라 연장될 수 있다. 여기서, 제1 전극부(110a)는 전기 신호를 인가받을 수 있도록 예를 들어 스테인리스 스틸, 텅스텐 또는 텅스텐 합금, 몰리브덴 또는 몰리브덴 합금, 티타늄 또는 티타늄 합금 등과 같은 금속으로 구성될 수 있으며 적어도 일부가 내부에 제1 관통홀(111)을 갖는 중공 형상으로 구현될 수 있다. The first electrode unit 110a is a member that coagulates or cauterizes tissue when an electric signal is applied together with the second electrode unit 120a, and may extend along a first direction, that is, a longitudinal direction. Here, the first electrode unit 110a may be made of, for example, a metal such as stainless steel, tungsten or a tungsten alloy, molybdenum or a molybdenum alloy, titanium or a titanium alloy, etc. to receive an electrical signal, and at least a part thereof It may be implemented in a hollow shape having a first through hole 111 .
예시적으로, 제1 전극부(110a)는 제1 전극본체부(112), 제1 전극노출부(113) 및 제1 전극연결부(114)를 포함할 수 있다. 여기서, 제1 전극본체부(112)는 내부에 제1 관통홀(111)을 갖는 중공 형상으로 구현될 수 있으며, 적어도 일부가 제2 전극부(120a)의 제2 관통홀(121)의 내부에 위치될 수 있다. 또한, 제1 전극본체부(112)는 이후에 설명되는 제1 절연부(130a)에 의해 적어도 일부가 커버될 수 있고, 나머지 일부는 이후에 설명되는 제2 절연부(140a)의 제2 절연바디부(150)에 의해 커버될 수 있다. 이에 제1 전극본체부(112)는 도 1과 같은 완제품 상태에서 외부로 노출되지 않을 수 있다. Illustratively, the first electrode part 110a may include a first electrode body part 112 , a first electrode exposed part 113 , and a first electrode connection part 114 . Here, the first electrode body portion 112 may be implemented in a hollow shape having a first through hole 111 therein, and at least a portion of the second through hole 121 of the second electrode portion 120a is formed. can be located in In addition, at least a portion of the first electrode body portion 112 may be covered by a first insulating portion 130a to be described later, and the remaining portion may be covered by a second insulating portion 140a to be described later. It may be covered by the body part 150 . Accordingly, the first electrode main body 112 may not be exposed to the outside in a finished product state as shown in FIG. 1 .
또한, 제1 전극노출부(113)는 제2 절연부(140a)의 제2 절연바디부(150) 외면에 위치될 수 있으며, 판 형상으로 구현되어 도 1과 같이 완제품 상태에서 외부에 노출될 수 있다. 이에 제1 전극노출부(113)는 조직과 접촉될 수 있으며 조직에 전기 신호를 인가하는 부분으로 활용될 수 있다. 또한, 제1 전극노출부(113)에는 제3 석션홀(115)이 형성될 수 있으며, 이에 혈액, 조직 또는 뼈 등이 석션되는 입구를 제공할 수 있다.In addition, the first electrode exposed portion 113 may be located on the outer surface of the second insulating body portion 150 of the second insulating portion 140a, and is implemented in a plate shape to be exposed to the outside in a finished product state as shown in FIG. can Accordingly, the first electrode exposed portion 113 may be in contact with the tissue and may be used as a part for applying an electrical signal to the tissue. In addition, a third suction hole 115 may be formed in the first electrode exposed portion 113 to provide an inlet through which blood, tissue, or bone is suctioned.
이와 같이 제1 전극본체부(112)는 외부로 노출되지 않고 제1 전극노출부(113)는 외부로 노출되는바, 제1 전극본체부(112)와 제1 전극노출부(113) 사이를 전기적으로 연결하는 부분이 필요하며, 제1 전극연결부(114)가 이러한 역할을 수행할 수 있다. 제1 전극연결부(114)는 예를 들어 "ㄱ" 자와 같이 절곡된 와이어 형상을 가질 수 있으며, 전기적 안정성 향상을 위해 2개 이상으로 구현될 수도 있다. 제1 전극연결부(114)의 양단 중 제1 연결단(116)은 제1 전극본체부(112)와 접촉되고 제2 연결단(117)은 제1 전극노출부(113)와 접촉되어, 제1 전극연결부(114)와 제1 전극본체부(112) 사이를 전기적으로 접속할 수 있다. 이때, 전기적 안정성 향상을 위해 제1 연결단(116)은 제1 전극본체부(112)와 면접촉 또는 선접촉할 수 있으며, 제2 연결단(117)은 제1 전극연결부(114)의 다른 부분보다 지름이 큰 구(球) 형상으로 구현될 수 있다. 제2 연결단(117)을 제외한 제1 전극연결부(114)의 다른 부분은 제1 전극노출부(113)를 관통하는 연결홀(113a)에 삽입되며, 연결홀(113a)의 지름보다 지름이 큰 제2 연결단(117)은 통과되지 못하고 제1 전극노출부(113)와 접촉되어 전기적으로 연결될 수 있다. As such, the first electrode main body 112 is not exposed to the outside and the first electrode exposed portion 113 is exposed to the outside, so that there is a gap between the first electrode main body 112 and the first electrode exposed portion 113. An electrically connecting part is required, and the first electrode connecting part 114 can perform this role. The first electrode connection unit 114 may have a bent wire shape, for example, in the shape of a letter "a", and may be implemented in two or more to improve electrical stability. Among both ends of the first electrode connection part 114, the first connection end 116 is in contact with the first electrode main body 112 and the second connection end 117 is in contact with the first electrode exposed part 113, It is possible to electrically connect between the first electrode connection part 114 and the first electrode main body part 112 . At this time, in order to improve electrical stability, the first connection end 116 may be in surface contact or line contact with the first electrode body 112, and the second connection end 117 is the other side of the first electrode connection part 114. It may be implemented in a spherical shape having a larger diameter than the part. The other part of the first electrode connection part 114, except for the second connection end 117, is inserted into the connection hole 113a penetrating the first electrode exposed part 113, and has a diameter greater than the diameter of the connection hole 113a. The large second connection end 117 does not pass through and can be electrically connected to the first electrode exposed portion 113 in contact with it.
이러한 제1 전극연결부(114)는 제2 연결단(117)을 제외하고는 도 1과 같은 완제품 상태에서 외부로 노출되지 않는데, 제2 절연부(140a)에 의해 커버되기 때문일 수 있다. 구체적으로, 제1 전극연결부(114)의 제1 연결단(116) 부분은 제2 절연부(140a)의 제2 절연커버부(160)에 의해, 제1 연결단(116)과 제2 연결단(117)을 제외한 나머지 부분은 제2 절연부(140a)의 제2 절연바디부(150)에 의해 커버될 수 있으며, 이에 제2 연결단(117)을 제외한 나머지 부분은 외부로 노출되지 않을 수 있다. 또한, 제1 전극연결부(114)는 제1 전극본체부(112) 및 제1 전극노출부(113)와 용접, 납땜, 본딩 등의 결합을 통해 연결될 수 있으며, 또는 별도의 과정(용접 등)을 거치지 않고 제2 절연부(140a)의 제2 절연바디부(150)와 제2 절연커버부(160)의 결합에 의한 압력을 통해서 연결될 수도 있다.Except for the second connection end 117, the first electrode connection portion 114 is not exposed to the outside in the finished product state as shown in FIG. 1, which may be because it is covered by the second insulation portion 140a. Specifically, the first connection end 116 part of the first electrode connection part 114 is connected to the first connection end 116 and the second connection end 116 by the second insulating cover part 160 of the second insulation part 140a. The remaining portion except for the end 117 may be covered by the second insulating body portion 150 of the second insulating portion 140a, and thus the remaining portion except for the second connection end 117 will not be exposed to the outside. can In addition, the first electrode connection portion 114 may be connected to the first electrode body portion 112 and the first electrode exposed portion 113 through a combination such as welding, soldering, bonding, or a separate process (welding, etc.) The second insulation body portion 150 of the second insulation portion 140a and the second insulation cover portion 160 may be connected through pressure by coupling without passing through the second insulation portion 140a.
한편, 제2 전극부(120a)는 제1 전극부(110a)와 함께 전기 신호를 인가받으면 조직을 응고 또는 소작하는 부재로, 제1 전극부(110a)와 마찬가지로 제1 방향, 즉 길이방향을 따라 연장될 수 있으며, 전기 신호를 인가받거나 전달할 수 있도록 예를 들어 스테인리스 스틸, 텅스텐 또는 텅스텐 합금, 몰리브덴 또는 몰리브덴 합금, 티타늄 또는 티타늄 합금 등과 같은 금속으로 구성될 수 있다. 이때, 제1 전극부(110a)는 능동전극(active electrode)으로, 제2 전극부(120a)는 수동전극(passive electrode)으로 기능할 수 있으며, 반대로 제1 전극부(110a)가 수동전극으로, 제2 전극부(120a)가 능동전극으로 기능하는 것도 가능할 수 있다. 이와 같이 제1 전극부(110a)와 제2 전극부(120a)가 전기 신호를 인가받아 인체의 조직을 응고 또는 소작을 하기 위해서는 적어도 일부가 외부로 노출되어 있어야 하는데, 제1 전극부(110a)의 경우 제1 전극노출부(113)와 제1 전극연결부(114)의 제2 연결단(117)이, 제2 전극부(120a)의 경우 제3 절연부(170a)에 의해 커버되지 않는 부분인 노출영역(122)이 외부로 노출되어 있는 부분일 수 있다.On the other hand, the second electrode unit 120a is a member that coagulates or cauterizes tissue when an electric signal is applied together with the first electrode unit 110a, and like the first electrode unit 110a, the second electrode unit 110a moves in the first direction, that is, the longitudinal direction. It may extend along the surface and may be made of, for example, stainless steel, tungsten or a tungsten alloy, molybdenum or a molybdenum alloy, titanium or a titanium alloy, and the like so as to receive or transmit an electrical signal. At this time, the first electrode part 110a can function as an active electrode and the second electrode part 120a can function as a passive electrode. Conversely, the first electrode part 110a can function as a passive electrode. , it may be possible for the second electrode unit 120a to function as an active electrode. In this way, in order for the first electrode portion 110a and the second electrode portion 120a to coagulate or cauterize human tissue by receiving an electrical signal, at least a portion of the first electrode portion 110a must be exposed to the outside. In the case of , the second connection end 117 of the first electrode exposed portion 113 and the first electrode connection portion 114 is not covered by the third insulating portion 170a in the case of the second electrode portion 120a. The phosphorus exposure area 122 may be a portion exposed to the outside.
이러한 제2 전극부(120a)는 내부에 제2 관통홀(121)을 갖는 중공 형상으로 구현될 수 있는데, 제2 관통홀(121)에는 제1 전극부(110a)의 적어도 일부, 더욱 구체적으로는 제1 전극부(110a)의 제1 전극본체부(112) 적어도 일부가 위치될 수 있다. 이때, 제1 전극부(110a)와 제2 전극부(120a)를 서로 절연시킬 필요가 있는데, 이러한 절연은 제1 절연부(130a)가 수행할 수 있다. 구체적으로 제1 절연부(130a)는 제2 전극부(120a)의 제2 관통홀(121) 내부에 위치되되 내부에 제1 절연관통홀(131)을 갖는 중공 형상으로 구현될 수 있으며, 제1 전극부(110a)는 적어도 일부가 제1 절연관통홀(131)의 내부에 위치되어 제2 전극부(120a)와의 사이에 제1 절연부(130a)가 위치되도록 할 수 있다. The second electrode part 120a may be implemented in a hollow shape having a second through hole 121 therein. In the second through hole 121, at least a part of the first electrode part 110a, more specifically, At least a portion of the first electrode body portion 112 of the first electrode portion 110a may be located. At this time, it is necessary to insulate the first electrode part 110a and the second electrode part 120a from each other, and this insulation may be performed by the first insulation part 130a. Specifically, the first insulating portion 130a may be positioned inside the second through hole 121 of the second electrode portion 120a and implemented in a hollow shape having the first insulating through hole 131 therein. At least a portion of the first electrode portion 110a may be positioned inside the first insulating through hole 131 so that the first insulating portion 130a is positioned between the second electrode portion 120a.
이러한 제1 절연부(130a)는 예를 들어 제1-1 절연부(132)와 제1-2 절연부(133)의 2중 구조를 포함할 수 있다. 구체적으로 제1-1 절연부(132)는 제1 전극부(110a)의 적어도 일부 외면에 위치되고 제1-2 절연부(133)가 제1-1 절연부(132)의 적어도 일부 외면에 위치되는 구조를 가질 수 있다. 이때, 제1-1 절연부(132)는 PTFE(Polytetrafluoroethylene)로 구성되어 얇게 구현될 수 있으며, 제1-2 절연부(133)는 보다 확실한 절연을 위해 FEP(Fluorinated Ethylene Propylene copolymer)로 제1-1 절연부(132)에 비해 두껍게 구현될 수 있다. 다만, 제1 절연부(130a)는 이러한 물질에 국한되는 것은 아니며, PTFE, FEP, PFA(Poly Fluoro Alkoxy), PEEK(Poly Ether Ether Ketone), PVDF(Polyvinylidene fluoride), PET(Poly Ethylene Terephthalate) 등 절연 가능한 물질이라면 다양하게 구현될 수 있다. 이에 제1 전극부(110a)와 제2 전극부(120a) 사이의 영역을 제1 영역(134)과 제2 영역(135)을 나누면, 제1 영역(134)은 제1-1 절연부(132)와 제1-1 절연부(132) 상에 있는 제2 절연부(140a)의 제2 절연커버부(160)에 의해, 제2 영역(135)은 제1-1 절연부(132)와 제1-1 절연부(132) 상에 있는 제1-2 절연부(133)에 의해 절연되는 것으로 볼 수 있으며, 제1-2 절연부(133)의 두께는 개재된 제2 절연커버부(160)의 두께와 동일하게 구현되어 구조적 완성도를 높일 수 있다. 이와 같이 제1 영역(134)은 제1-2 절연부(133)와 제2 절연커버부(160)에 의해 절연될 수 있으므로, 제1-1 절연부(132)는 필수적으로 포함될 필요는 없을 수 있다. 다만, 제1-1 절연부(132)를 두는 경우 부품 간 공간을 통해 인체로부터의 유체 등이 통과되어 의료용 절제기구(100a)가 손상되는 것을 방지할 수 있다.The first insulating part 130a may include, for example, a double structure of a 1-1 insulating part 132 and a 1-2 insulating part 133 . Specifically, the 1-1 insulation part 132 is located on at least a part of the outer surface of the first electrode part 110a, and the 1-2 insulation part 133 is located on at least a part of the outer surface of the 1-1 insulation part 132. It may have a structure that is positioned. At this time, the 1-1 insulation part 132 may be made of PTFE (Polytetrafluoroethylene) and implemented thinly, and the 1-2 insulation part 133 is made of FEP (Fluorinated Ethylene Propylene copolymer) for more reliable insulation. -1 It can be implemented thicker than the insulating part 132 . However, the first insulating portion 130a is not limited to these materials, and may include PTFE, FEP, PFA (Poly Fluoro Alkoxy), PEEK (Poly Ether Ether Ketone), PVDF (Polyvinylidene fluoride), PET (Poly Ethylene Terephthalate), etc. Any material capable of insulating may be implemented in various ways. Accordingly, when the area between the first electrode part 110a and the second electrode part 120a is divided into the first area 134 and the second area 135, the first area 134 is the 1-1 insulating part ( 132) and the second insulating cover part 160 of the second insulating part 140a on the 1-1 insulating part 132, the second region 135 is formed by the 1-1 insulating part 132 It can be seen as being insulated by the 1-2 insulating part 133 on the 1-1 insulating part 132, and the thickness of the 1-2 insulating part 133 is the second insulating cover part interposed therebetween. It is implemented to be the same as the thickness of (160) to increase structural completeness. In this way, since the first region 134 can be insulated by the 1-2 insulating portion 133 and the second insulating cover portion 160, the 1-1 insulating portion 132 does not necessarily need to be included. can However, when the 1-1 insulation part 132 is provided, it is possible to prevent damage to the medical ablation device 100a due to fluid from the human body passing through the space between parts.
제2 절연부(140a)는 절연 역할을 수행하면서도 연마절삭부(180a)와 함께 절제 기능을 함께 수행하는 부재이다. 여기서, 제2 절연부(140a)는 구조적으로 제2 절연바디부(150)와 제2 절연커버부(160)를 포함할 수 있다. The second insulating portion 140a is a member that performs an ablation function together with the abrasive cutting portion 180a while performing an insulating role. Here, the second insulating portion 140a may structurally include a second insulating body portion 150 and a second insulating cover portion 160 .
제2 절연바디부(150)는 제1 전극부(110a)가 위치되는 영역을 제공할 수 있는데, A 영역(151)은 제1 전극부(110a)의 제1 전극본체부(112)의 외면 일부를 커버하여 제2 절연커버부(160)와 함께 제1 전극본체부(112)가 외부로 노출되지 않도록 할 수 있고, A 영역(151)에 인접한 B 영역(152)에는 안착부(154)가 형성되어 안착부(154)에 제1 전극부(110a)의 제1 전극연결부(114)가 안착되도록 할 수 있으며, B 영역(152)에 인접한 C 영역(153)에는 제1 전극노출부(113)가 외면에 위치되는 공간이 제공될 수 있다. 이때, C 영역(153)에도 안착부(154)가 연장되어 형성될 수 있으며, 안착부(154)에 의해 외부 충격에 상대적으로 약한 제1 전극연결부(114)가 안전하게 보호될 수 있다. 또한, 제2 절연바디부(150)의 C 영역(153)에는 제1 전극부(110a)의 제3 석션홀(115)에 대응되는 위치에 제2 석션홀(156)이 형성될 수 있으며, 이를 통해 혈액, 조직 또는 뼈가 석션될 수 있다. 또한, 제2 절연바디부(150)의 C 영역(153) 단부에는 제1 석션홀(155)이 추가적으로 형성될 수 있으며, 제1 석션홀(155)을 통해서도 혈액, 조직 또는 뼈 등을 석션할 수 있어 석션 효율성이 향상될 수 있다.The second insulating body 150 may provide an area where the first electrode unit 110a is located, and the area A 151 is the outer surface of the first electrode body 112 of the first electrode unit 110a. It is possible to cover a part of the first electrode body 112 together with the second insulating cover 160 so that it is not exposed to the outside. is formed to allow the first electrode connecting portion 114 of the first electrode portion 110a to be seated on the seating portion 154, and the first electrode exposed portion ( 113) may be provided with a space located on the outer surface. At this time, the seating portion 154 may be extended and formed in the C region 153, and the first electrode connection portion 114, which is relatively weak against external impact, may be safely protected by the seating portion 154. In addition, a second suction hole 156 may be formed in region C 153 of the second insulating body 150 at a position corresponding to the third suction hole 115 of the first electrode part 110a, This allows blood, tissue or bone to be suctioned out. In addition, a first suction hole 155 may be additionally formed at the end of the C region 153 of the second insulating body 150, and blood, tissue, or bone may be suctioned through the first suction hole 155. This can improve the suction efficiency.
한편, 제2 절연바디부(150)의 제2 석션홀(156)의 반대 방향에는 제1 오픈부(157)가 형성될 수 있다. 제1 오픈부(157)는 제2 전극부(120a)가 연장된 방향인 제1 방향과 상이한 방향, 더욱 상세하게는 제1 방향과 수직한 제2 방향을 향해 오픈된 형상을 가질 수 있다. 이러한 제1 오픈부(157)에는 제1 칼날영역(158)이 형성될 수 있으며 이러한 제1 칼날영역(158)은 이후에 설명될 연마절삭부(180a)와의 상호 작용에 따라 조직을 절제할 수 있다. 또한, 제1 오픈부(157)와 제1 석션홀(155)은 서로 연결된 형상을 가질 수 있으며, 제1 오픈부(157)를 통해서도 혈액, 일부 조직 또는 뼈가 석션될 수 있어 효율성을 향상시킬 수 있다.Meanwhile, a first open portion 157 may be formed in a direction opposite to the second suction hole 156 of the second insulating body portion 150 . The first open portion 157 may have a shape opened toward a direction different from the first direction in which the second electrode portion 120a extends, and more particularly, toward a second direction perpendicular to the first direction. A first blade region 158 may be formed in the first open portion 157, and the first blade region 158 may cut tissue according to interaction with the abrasive cutting portion 180a to be described later. have. In addition, the first open portion 157 and the first suction hole 155 may have shapes connected to each other, and blood, some tissues or bones may be suctioned through the first open portion 157 to improve efficiency. can
제2 절연커버부(160)는 제2 절연바디부(150)의 안착부(154)에 위치된 제1 전극연결부(114)를 커버하여 외부로 노출되지 않도록 하는 부재이다. 제1 전극연결부(114)는 와이어로 구현될 수 있으므로 외부 충격에 약할 수 있으며, 외부로 노출될 경우 조직 등을 통해 전기 신호가 외부로 흘러 파손될 수 있다. 이에 제1 전극연결부(114)를 외부로 노출되지 않도록 커버할 필요가 있으며, 본 발명의 실시예에 따른 의료용 절제기구(100a)는 제2 절연커버부(160)를 통해 제1 전극연결부(114)를 커버할 수 있다.The second insulating cover part 160 is a member that covers the first electrode connection part 114 located on the seating part 154 of the second insulating body part 150 so that it is not exposed to the outside. Since the first electrode connection portion 114 may be implemented as a wire, it may be vulnerable to external impact, and when exposed to the outside, electrical signals may flow to the outside through tissue or the like and may be damaged. Therefore, it is necessary to cover the first electrode connection portion 114 so as not to be exposed to the outside. ) can be covered.
이때, 제2 절연커버부(160)는 제1 전극연결부(114)를 커버하는 부분인 D 영역(161)과 제1 전극본체부(112)의 일부를 커버하는 부분인 E 영역(162)을 포함할 수 있다. E 영역(162)은 중공 형상으로 구현되어 제1 전극본체부(112)의 외면에 제1-1 절연부(132)만 커버된 부분에 밀착되도록 위치될 수 있으며, 이에 제1-1 절연부(132)와 제2 절연커버부(160)의 E 영역(162)을 통해 제1 전극부(110a)와 제2 전극부(120a)의 제1 영역(134)이 서로 절연될 수 있다. 또한, D 영역(161)은 안착부(154)에 안착된 제1 전극연결부(114)를 커버하면서 제2 절연바디부(150)와 밀착되는 부분으로, 제2 절연바디부(150)의 B 영역(152)과 C 영역(153) 사이의 제1 단차부(159)에 D 영역(161)의 단부가 밀착되고, D 영역(161)의 내부에 형성된 제2 단차부(163)에 B 영역(152)의 단부가 밀착되면서, 제2 절연바디부(150)와 제2 절연커버부(160)가 결합될 수 있다. 이때, 제2 절연바디부(150)와 제2 절연커버부(160)는 돌기, 홈 등을 활용한 기계적 결합을 통해 또는 본딩을 통하는 등 다양한 결합 방식으로 결합될 수 있을 것이다.At this time, the second insulating cover part 160 covers the D area 161 that covers the first electrode connection part 114 and the E area 162 that covers a part of the first electrode body part 112. can include The E region 162 is implemented in a hollow shape and may be positioned so as to be in close contact with a portion of the outer surface of the first electrode body 112 where only the 1-1 insulation part 132 is covered, and thus the 1-1 insulation part The first region 134 of the first electrode portion 110a and the second electrode portion 120a may be insulated from each other through 132 and the E region 162 of the second insulating cover portion 160 . In addition, the D region 161 covers the first electrode connection part 114 seated on the seating part 154 and is in close contact with the second insulating body part 150, and is a part of B of the second insulating body part 150. The end of region D 161 adheres to the first stepped portion 159 between region 152 and region C 153, and region B to the second stepped portion 163 formed inside D region 161. As the ends of the 152 come into close contact, the second insulating body 150 and the second insulating cover 160 may be coupled. At this time, the second insulating body portion 150 and the second insulating cover portion 160 may be coupled in various ways, such as through mechanical coupling using protrusions, grooves, or the like, or through bonding.
한편, 제2 절연부(140a)는 알루미나(Al2O3), 지르코니아(ZrO2)와 같은 기계적 강도가 높은 세라믹으로 구현될 수 있다. 제2 절연부(140a)는 직접 조직이나 뼈와 맞닿는 부분으로 기계적 강도가 높아야 하면서도, 제1 전극부(110a)의 일부를 제외한 나머지를 커버하여 절연시켜야 하므로, 세라믹이 가장 바람직한 물질이 될 수 있다.Meanwhile, the second insulating portion 140a may be made of a ceramic having high mechanical strength, such as alumina (Al 2 O 3 ) or zirconia (ZrO 2 ). The second insulating portion 140a is a portion in direct contact with tissue or bone and should have high mechanical strength, but should cover and insulate the rest except for a part of the first electrode portion 110a, so ceramic may be the most desirable material. .
이와 같이 본 실시예에 따른 의료용 절제기구(100a)는 수술 부위에 있어 조직과 직접 맞닿는 부분을 금속이 아닌 절연물질로 구성된 제2 절연부(140a)로 구현함으로써, 전기적 안정성을 향상시킬 수 있다. 구체적으로, 수술 부위에 직접적으로 닿는 부분의 대부분이 금속으로 구성되는 경우 전기 신호가 집중되지 않아 조직의 응고 또는 소작이 원활하게 이루어지지 않으며, 원치 않게 단락되는 등 문제가 발생될 수 있다. 그러나, 본 실시예에 따른 의료용 절제기구(100a)는 수술 부위에 직접적으로 닿는 부분의 대부분을 제2 절연부(140a)로 구성함으로써, 전기 신호가 제1 전극부(110a)의 제1 전극노출부(113)와 제2 전극부(120a)의 노출영역(122)으로 집중되도록 하여 조직의 응고 또는 소작이 원활하게 이루어지도록 할 수 있다.As described above, in the medical resection device 100a according to the present embodiment, electrical stability can be improved by implementing a part directly contacting tissue in the surgical site with the second insulating part 140a made of an insulating material rather than metal. Specifically, when most of the portion directly contacting the surgical site is made of metal, electrical signals are not concentrated, so tissue coagulation or cauterization is not smoothly performed, and problems such as undesirable short circuiting may occur. However, in the medical ablation apparatus 100a according to the present embodiment, most of the portion directly contacting the surgical site is composed of the second insulating portion 140a, so that the electrical signal is exposed to the first electrode of the first electrode portion 110a. The portion 113 and the exposure area 122 of the second electrode portion 120a may be concentrated so that tissue coagulation or cauterization can be smoothly performed.
한편, 제3 절연부(170a)는 제2 전극부(120a)의 적어도 일부를 커버하여 의료용 절제기구(100a)를 외부에 대해 절연하는 부분이다. 여기서, 제3 절연부(170a)는 내부에 제3 절연관통홀(171)을 갖는 중공 형상으로 구현될 수 있으며, 제3 절연관통홀(171)의 내부에 제2 전극부(120a)가 위치되도록, 제2 전극부(120a)를 커버할 수 있다. 이때, 제3 절연부(170a)는 의료용 절제기구(100a)의 외관이 되는 부분으로 안정적인 절연을 수행할 수 있도록 FEP(Fluorinated ethylene Propylene copolymer)로 비교적 두껍게 형성될 수 있다. 다만, 제3 절연부(170a)는 이러한 물질에 국한되는 것은 아니며, PTFE, FEP, PFA(Poly Fluoro Alkoxy), PEEK(Poly Ether Ether Ketone), PVDF(Polyvinylidene fluoride), PET(Poly Ethylene Terephthalate) 등 절연 가능한 물질이라면 다양하게 구현될 수 있다. 또한, 제2 전극부(120a)의 적어도 일부는 외부로 노출되어야 전기 신호를 통해 조직을 응고 또는 소작할 수 있으므로, 제2 전극부(120a)의 노출영역(122)은 제3 절연부(170a)에 의해 커버되지 않을 수 있다.Meanwhile, the third insulating portion 170a covers at least a portion of the second electrode portion 120a to insulate the medical ablation device 100a from the outside. Here, the third insulating portion 170a may be implemented in a hollow shape having a third insulating through hole 171 therein, and the second electrode portion 120a is positioned inside the third insulating through hole 171. As much as possible, the second electrode portion 120a may be covered. At this time, the third insulating portion 170a is a portion that becomes the exterior of the medical resection device 100a and may be formed of FEP (Fluorinated ethylene propylene copolymer) to be relatively thick to perform stable insulation. However, the third insulator 170a is not limited to these materials, and may include PTFE, FEP, PFA (Poly Fluoro Alkoxy), PEEK (Poly Ether Ether Ketone), PVDF (Polyvinylidene fluoride), PET (Poly Ethylene Terephthalate), etc. Any material capable of insulating may be implemented in various ways. In addition, since at least a portion of the second electrode portion 120a must be exposed to the outside to coagulate or cauterize the tissue through an electrical signal, the exposed area 122 of the second electrode portion 120a is the third insulating portion 170a. ) may not be covered by
도 5는 도 1에 도시한 의료용 절제기구(100a)의 연마절삭부(180a)를 나타낸 사시도이고, 도 6 및 도 7은 도 1에 도시한 의료용 절제기구(100a)의 연마절삭부(180a) 동작을 설명하기 위한 단면도이다. 이하, 도 2 내지 도 7을 참조하여 본 실시예에 따른 연마절삭부(180a)에 대해 살펴보기로 한다.5 is a perspective view showing the abrasive cutting part 180a of the medical ablation instrument 100a shown in FIG. 1, and FIGS. 6 and 7 are the abrasive cutting part 180a of the medical ablation instrument 100a shown in FIG. It is a cross-sectional view to explain the operation. Hereinafter, a polishing cutting part 180a according to the present embodiment will be described with reference to FIGS. 2 to 7 .
연마절삭부(180a)는 조직 또는 뼈를 연마 또는 절삭하는 부재로, 제1 전극부(110a)의 제1 관통홀(111) 내부에 위치되며 도 1에서 설명한 핸드피스(200)의 내부 구성과 연결되어 회전 가능하게 구현될 수 있다. 이러한 연마절삭부(180a)에는 조직 또는 뼈를 연마 또는 절삭하기 위한 연마절삭영역이 형성될 수 있다.The abrasive cutting part 180a is a member for grinding or cutting tissue or bone, and is located inside the first through hole 111 of the first electrode part 110a and has the internal configuration of the handpiece 200 described in FIG. It can be connected and rotatably implemented. An abrasive cutting area for grinding or cutting tissue or bone may be formed in the abrasive cutting portion 180a.
본 실시예에 따른 의료용 절제기구(100a)의 연마절삭부(180a)는 조직을 절삭하기 위한 쉐이버(Shaver)로서 연마절삭영역은 제2 칼날영역(181)으로 구현될 수 있다. 구체적으로, 연마절삭부(180a)는 제1 전극부(110a)의 연장 방향인 제1 방향과 상이한 방향인 제2 방향으로 오픈된 제2 오픈부(182)를 구비할 수 있으며, 이러한 제2 오픈부(182)에 제2 칼날영역(181)이 형성될 수 있다. 또한, 연마절삭부(180a)의 적어도 일부는 내부에 제3 관통홀(183)을 갖는 중공 형상으로 구현될 수 있으며, 연마절삭부(180a)의 제3 관통홀(183)은 도 1에 도시한 핸드피스(200)를 통해 석션유닛(400)과 연결되어 석션통로로 활용될 수 있다. 다만, 연마절삭부(180a)가 반드시 중공 형상으로 구현되는 것은 아니며, 연마절삭부(180a)가 중공 형상으로 구현되지 않는 경우 제1 전극부(110a)의 제1 관통홀(111)이 석션통로로서 기능할 수 있다.The abrasive cutting part 180a of the medical cutting instrument 100a according to the present embodiment is a shaver for cutting tissue, and the abrasive cutting area may be implemented as the second blade area 181. Specifically, the abrasive cutting part 180a may have a second open part 182 opened in a second direction that is different from the first direction, which is the extension direction of the first electrode part 110a. A second blade region 181 may be formed in the open portion 182 . In addition, at least a portion of the polishing cutting part 180a may be implemented in a hollow shape having a third through hole 183 therein, and the third through hole 183 of the polishing cutting part 180a is shown in FIG. It is connected to the suction unit 400 through one handpiece 200 and can be used as a suction passage. However, the abrasive cutting portion 180a is not necessarily implemented in a hollow shape, and when the abrasive cutting portion 180a is not implemented in a hollow shape, the first through hole 111 of the first electrode portion 110a is a suction passage. can function as
이때, 연마절삭부(180a)의 제2 오픈부(182)에 반대되는 방향에는 제4 석션홀(184)이 형성될 수 있으며, 연마절삭부(180a)의 회전에 따라 제4 석션홀(184)의 위치가 제2 석션홀(156) 및 제3 석션홀(115)의 위치와 일치하면, 혈액, 조직 또는 뼈 조각 등 석션 대상은 차례로 제3 석션홀(115), 제2 석션홀(156) 및 제4 석션홀(184)을 통과하여 제3 관통홀(183)을 통해 석션될 수 있다. 또한, 연마절삭부(180a)의 회전에 따라 제4 석션홀(184)의 위치가 제2 석션홀(156) 및 제3 석션홀(115)의 위치와 일치하지 않더라도 석션 대상은 제3 석션홀(115), 제2 석션홀(156) 및 제2 오픈부(182)를 통과하여 제3 관통홀(183)을 통해 석션될 수 있다. 또한, 연마절삭부(180a)의 단부는 오픈되어 있어 제2 절연부(140a)의 제1 석션홀(155)을 통해 석션된 조직 등은 자연스럽게 제3 관통홀(183)을 통해 석션될 수 있다.At this time, a fourth suction hole 184 may be formed in a direction opposite to the second open part 182 of the abrasive cutting part 180a, and the fourth suction hole 184 is rotated according to the rotation of the abrasive cutting part 180a. ) coincides with the positions of the second suction hole 156 and the third suction hole 115, the suction target, such as blood, tissue or bone fragments, sequentially passes through the third suction hole 115 and the second suction hole 156. ) and the fourth suction hole 184 and may be suctioned through the third through hole 183 . In addition, even if the position of the fourth suction hole 184 does not coincide with the position of the second suction hole 156 and the third suction hole 115 according to the rotation of the abrasive cutting part 180a, the suction target is the third suction hole. 115, the second suction hole 156, and the second open portion 182 may be suctioned through the third through hole 183. In addition, since the end of the abrasive cutting part 180a is open, tissues, etc., which are suctioned through the first suction hole 155 of the second insulating part 140a, can be naturally suctioned through the third through hole 183. .
한편, 제2 절연부(140a)의 제1 칼날영역(158)과 연마절삭부(180a)의 제2 칼날영역(181)의 상호 작용에 의해 조직이 절삭될 수 있는데, 도 6과 같이 제2 절연부(140a)의 제1 오픈부(157)와 연마절삭부(180a)의 제2 오픈부(182)가 동일한 방향을 바라보고 있는 상태에서, 석션유닛(400)이 동작하여 제3 관통홀(183) 내에 진공이 인가되면 제2 오픈부(182)를 통해 조직이 석션되며(잡아 당겨지며), 도 7과 같이 연마절삭부(180a)가 제1 전극부(110a)의 내부에서 회전되면서 제1 오픈부(157)와 제2 오픈부(182)가 서로 상이한 방향을 바라보게 되며, 이러한 과정에서 제1 칼날영역(158)과 제2 칼날영역(181)이 가위와 같이 작용하여 석션된(잡아 당겨진) 조직을 절삭할 수 있다. 즉, 제2 칼날영역(181)이 제1 칼날영역(158)의 내측에서 회전되면서 조직을 절삭할 수 있다. 이때, 제1 칼날영역(158)과 제2 칼날영역(181)을 단순한 칼날 형상으로 구현할 수 있고 또는 절삭 능력을 향상시키기 위하여 톱니 형상으로 구현하는 것도 가능하다.Meanwhile, tissue can be cut by the interaction between the first blade region 158 of the second insulating portion 140a and the second blade region 181 of the abrasive cutting portion 180a. With the first open part 157 of the insulating part 140a and the second open part 182 of the abrasive cutting part 180a facing the same direction, the suction unit 400 operates to make the third through hole. When a vacuum is applied within the 183, tissue is suctioned (pulled) through the second open portion 182, and as shown in FIG. 7, the abrasive cutting portion 180a rotates inside the first electrode portion 110a. The first open portion 157 and the second open portion 182 face in different directions, and in this process, the first blade region 158 and the second blade region 181 act like scissors to create suction. Tissues (pulled) can be cut. That is, the tissue can be cut while the second blade region 181 rotates inside the first blade region 158 . At this time, the first blade region 158 and the second blade region 181 may be implemented in a simple blade shape or may be implemented in a sawtooth shape to improve cutting capability.
이와 같이 연마절삭부(180a)와 제2 절연부(140a)의 상호 작용으로 인해 조직을 절삭하면 출혈이 발생될 수 있다. 기존에는 지혈을 위하여 절삭을 수행한 쉐이버 기구를 수술 부위에서 빼고 지혈을 위한 전기 소작 기구를 삽입하는 방식을 활용하였으며, 이에 수술 기구를 넣고 빼는 등 번거롭고 수술 시간이 길어지는 문제와 툴 교체에 따른 감염 위험의 문제가 있었다. 그러나, 본 실시예에 따른 의료용 절제기구(100a)는 쉐이버의 기능뿐만 아니라 전기 소작의 기능까지 함께 수행할 수 있으며, 의료용 절제기구(100a)를 수술 부위에 넣은 상태에서 연마절삭부(180a)의 동작에 따라 조직을 절삭한 후 제1 전극부(110a) 또는 제2 전극부(120a)에 전기 신호를 인가하여 조직을 응고 또는 소작할 수 있고, 이에 지혈이 가능하도록 할 수 있다. 또한, 지속적으로 석션이 이루어지도록 하여 혈액, 조직, 뼈 조각 등이 석션되도록 하여 수술 부위를 깨끗하게 유지할 수 있다.In this way, when tissue is cut due to the interaction between the abrasive cutting portion 180a and the second insulating portion 140a, bleeding may occur. In the past, a method of removing the shaver device that performed the cutting from the surgical site and inserting an electric cautery device for hemostasis was used for hemostasis, and thus, troublesome problems such as inserting and removing the surgical device and prolonged operation time and infection due to tool replacement There was a question of risk. However, the medical ablation device 100a according to the present embodiment can perform not only the function of a shaver but also the function of electrocautery, and the abrasive cutting part 180a can be removed while the medical ablation device 100a is inserted into the surgical site. After the tissue is cut according to the operation, an electrical signal may be applied to the first electrode unit 110a or the second electrode unit 120a to coagulate or cauterize the tissue, thereby enabling hemostasis. In addition, the surgical site can be kept clean by continuously suctioning blood, tissues, bone fragments, and the like.
한편, 도 1에서 도시한 제어유닛(300)은 석션유닛(400)에 따른 석션, 제1 전극부(110a) 및 제2 전극부(120a)에 따른 응고 또는 소작, 제2 절연부(140a) 및 연마절삭부(180a)에 따른 절삭이 원활하게 이루어지도록 핸드피스(200) 및 의료용 절제기구(100a)를 제어할 수 있는데, 연마절삭부(180a)의 회전 위치 또는 사용 시간에 따라 석션 신호, 응고 또는 소작 신호를 달리 주는 것도 가능하며, 또는 지속적으로 연마절삭부(180a)의 회전, 석션, 응고 또는 소작이 모두 진행되도록 제어하는 것도 가능할 수 있다.On the other hand, the control unit 300 shown in FIG. 1 includes suction according to the suction unit 400, coagulation or cauterization according to the first electrode part 110a and the second electrode part 120a, and the second insulating part 140a. And it is possible to control the hand piece 200 and the medical cutting device 100a so that the cutting according to the abrasive cutting part 180a is smoothly performed. According to the rotational position or use time of the abrasive cutting part 180a, a suction signal, It is also possible to give different coagulation or cauterization signals, or it may be possible to continuously control rotation, suction, coagulation, or cauterization of the abrasive cutting unit 180a to proceed.
도 8은 본 발명의 다른 실시예에 따른 의료용 절제기구의 연마절삭부(180b)를 나타낸 사시도이다. 이하, 이를 참조하여 본 실시예에 따른 의료용 절제기구에 대해 살펴보기로 한다.8 is a perspective view showing an abrasive cutting part 180b of a medical ablation device according to another embodiment of the present invention. Hereinafter, with reference to this, the medical ablation apparatus according to the present embodiment will be described.
본 실시예에 따른 의료용 절제기구는 이전 실시예와 동일하게 제1 전극부(110a), 제2 전극부(120a), 제1 절연부(130a), 제2 절연부(140a), 제3 절연부(170a) 및 연마절삭부(180b)를 포함하되, 연마절삭부(180b)가 이전 실시예와 같이 제2 칼날영역(181)을 갖는 쉐이버의 형태가 아니라 버(Burr)의 형태를 갖는 것을 특징으로 할 수 있다.The medical ablation device according to the present embodiment includes a first electrode part 110a, a second electrode part 120a, a first insulating part 130a, a second insulating part 140a, and a third insulating part as in the previous embodiment. It includes a portion 170a and an abrasive cutting portion 180b, but the abrasive cutting portion 180b has the shape of a burr rather than the shape of a shaver having the second blade region 181 as in the previous embodiment. can be characterized.
이에 본 실시예에 따른 의료용 절제기구는 조직을 절삭하는 것이 아닌, 뼈를 연마 또는 절삭하기 위한 용도로 활용될 수 있으며 연마절삭부(180b)가 뼈를 연마 또는 절삭하고 제1 전극부(110a)와 제2 전극부(120a)는 지혈 등을 위해 응고 또는 소작 기능을 수행할 수 있다.Accordingly, the medical ablation device according to the present embodiment may be used for grinding or cutting bone, not for cutting tissue, and the abrasive cutting part 180b grinds or cuts the bone, and the first electrode part 110a and the second electrode unit 120a may perform a coagulation or cauterization function for hemostasis or the like.
이와 같이 연마절삭부(180b)가 버(Burr)로 구현되는 경우 제2 절연부(140a)에는 별도로 칼날영역이 형성되지 않을 수도 있다.In this way, when the abrasive cutting portion 180b is implemented as a burr, a separate blade region may not be formed in the second insulating portion 140a.
도 9는 본 발명의 또 다른 실시예에 따른 의료용 절제기구(100c)를 나타낸 사시도이고, 도 10은 도 9에 도시한 의료용 절제기구(100c)를 나타낸 단면도이다. 이하, 이를 참조하여 본 실시예에 따른 의료용 절제기구(100c)에 대해 살펴보기로 한다.FIG. 9 is a perspective view showing a medical ablation device 100c according to another embodiment of the present invention, and FIG. 10 is a cross-sectional view showing the medical ablation device 100c shown in FIG. 9 . Hereinafter, with reference to this, the medical ablation device 100c according to the present embodiment will be described.
도 9 및 도 10에 도시한 바와 같이, 본 실시예에 따른 의료용 절제기구(100c)는 제1 전극부(110c), 제2 전극부(120c), 제1 절연부(130c), 제2 절연부(140c), 제3 절연부(170c) 및 연마절삭부(180c)를 포함할 수 있다.9 and 10, the medical ablation device 100c according to the present embodiment includes a first electrode part 110c, a second electrode part 120c, a first insulating part 130c, and a second insulating part. A portion 140c, a third insulating portion 170c, and a polishing cutting portion 180c may be included.
제1 전극부(110c)는 전기 신호가 인가되면 제2 전극부(120c)와 함께 조직을 응고 또는 소작하는 부재로, 전기 신호가 잘 통전되도록 예를 들어 스테인리스 스틸, 텅스텐 또는 텅스텐 합금, 몰리브덴 또는 몰리브덴 합금, 티타늄 또는 티타늄 합금 등과 같은 금속으로 구성될 수 있다. 또한, 제1 전극부(110c)는 길이 방향인 제1 방향으로 연장되며 적어도 일부가 내부에 제1 관통홀(111c)을 갖는 중공 형상으로 구현될 수 있다. 여기서, 제1 전극부(110c)에는 제2 절연부(140c)의 제1 오픈부(157c)에 대응되는 위치에 제1 오픈부(157c)와 동일한 방향으로 오픈된 제3 오픈부(118)가 형성될 수 있다. 제3 오픈부(118)에는 제3 칼날영역(119)이 형성될 수 있으며 회전 가능한 연마절삭부(180c)의 연마절삭영역(181)과 상호 작용에 의해 조직 또는 뼈를 연마 또는 절삭할 수 있다.The first electrode part 110c is a member that coagulates or cauterizes tissue together with the second electrode part 120c when an electrical signal is applied, and is made of, for example, stainless steel, tungsten or a tungsten alloy, molybdenum or It may be composed of metals such as molybdenum alloys, titanium or titanium alloys, and the like. In addition, the first electrode part 110c may be implemented in a hollow shape extending in a first direction, which is a longitudinal direction, and having at least a portion of the first through hole 111c therein. Here, in the first electrode part 110c, a third open part 118 opened in the same direction as the first open part 157c at a position corresponding to the first open part 157c of the second insulating part 140c. can be formed. A third blade region 119 may be formed in the third open portion 118, and tissue or bone may be polished or cut by interaction with the abrasive cutting region 181 of the rotatable abrasive cutting portion 180c. .
도 11은 도 9에 도시한 의료용 절제기구(100c)의 일부 구성을 분해하여 나타낸 분해사시도이다. 이하, 도 9 내지 도 11을 참조하여 본 실시예에 따른 제2 전극부(120c), 제1 절연부(130c), 제2 절연부(140c), 제3 절연부(170c) 및 연마절삭부(180c)에 대해 살펴보기로 한다.FIG. 11 is an exploded perspective view showing some components of the medical ablation device 100c shown in FIG. 9 in an exploded manner. Hereinafter, referring to FIGS. 9 to 11 , the second electrode part 120c, the first insulating part 130c, the second insulating part 140c, the third insulating part 170c and the polishing cutting part according to the present embodiment Let's take a look at (180c).
제2 전극부(120c)는 전기 신호가 인가되면 제1 전극부(110c)와 함께 조직을 응고 또는 소작하는 부재로, 제1 전극부(110c)와 마찬가지로 전기 신호가 잘 통전되도록 예를 들어 스테인리스 스틸, 텅스텐 또는 텅스텐 합금, 몰리브덴 또는 몰리브덴 합금, 티타늄 또는 티타늄 합금 등과 같은 금속으로 구성될 수 있다. 제2 전극부(120c)는 길이 방향인 제1 방향으로 연장되며 적어도 일부가 내부에 제2 관통홀(121c)을 갖는 중공 형상으로 구현될 수 있으며, 제2 관통홀(121c)의 내부에 제1 전극부(110c)의 적어도 일부가 위치될 수 있다. 여기서, 제2 전극부(120c)는 능동전극으로, 제1 전극부(110c)는 수동전극으로 기능할 수 있으며, 반대로 기능하는 것도 가능하다 할 것이다.The second electrode part 120c is a member that coagulates or cauterizes tissue together with the first electrode part 110c when an electrical signal is applied, and like the first electrode part 110c, the electrical signal is well conducted, for example, stainless steel. It may consist of metals such as steel, tungsten or tungsten alloys, molybdenum or molybdenum alloys, titanium or titanium alloys, and the like. The second electrode unit 120c extends in the first direction, which is the longitudinal direction, and at least a portion thereof may be implemented in a hollow shape having a second through hole 121c therein, and a second electrode unit 120c may have a second through hole 121c therein. At least a part of the first electrode part 110c may be located. Here, the second electrode unit 120c may function as an active electrode, and the first electrode unit 110c may function as a passive electrode, or vice versa.
한편, 제2 전극부(120c)는 본체부(123)와 노출부(124)를 포함할 수 있다. 여기서, 노출부(124)는 제2 절연부(140a)의 외면에 위치되어 외부로 노출되는 부분이며, 본체부(123)는 대부분의 영역이 제2 전극부(120c)의 외부에 감싸지는 제3 절연부(170c)에 의해 외부로 노출되지 않을 수 있다. 노출부(124)는 본체부(123)의 적어도 일부와 중첩된 상태로 예를 들어 용접에 의해 결합될 수 있고 노출부(124)와 본체부(123) 각각에는 석션을 위한 석션홀이 형성될 수 있다. 또한, 노출부(124)와 본체부(123)는 분리된 부재가 아니라 일체로 형성되는 경우도 가능하다 할 것이다.Meanwhile, the second electrode part 120c may include a body part 123 and an exposed part 124 . Here, the exposed part 124 is a part located on the outer surface of the second insulating part 140a and exposed to the outside, and the main body part 123 has most of the area surrounded by the outside of the second electrode part 120c. 3 may not be exposed to the outside by the insulating portion 170c. The exposed portion 124 may be coupled, for example, by welding in an overlapped state with at least a portion of the body portion 123, and a suction hole for suction may be formed in each of the exposed portion 124 and the body portion 123. can Also, the exposed part 124 and the main body part 123 may be integrally formed rather than separated.
제1 절연부(130c)는 제1 전극부(110c)와 제2 전극부(120c) 사이의 적어도 일부를 절연하는 부재이다. 여기서, 제1 절연부(130c)는 튜브 형태로 구현되어 제1 전극부(110c)의 적어도 일부를 감싸는 형태로 제1 전극부(110c)와 제2 전극부(120c) 사이에 위치될 수 있다. 이때, 제1 전극부(110c)와 제2 전극부(120c) 사이는 제1 절연부(130c)에 의해서만 절연되는 것은 아니며, 제1 전극부(110c)와 제2 전극부(120c) 사이에 있어서 일부는 제1 절연부(130c)에 의해 절연되고 나머지는 제2 절연부(140c)에 의해 절연될 수 있다. 이때, 이전 실시예와 같이 제1 절연부(130c)를 2개의 층으로 구현하여 더욱 완벽한 절연을 구현하는 것도 가능하다.The first insulating portion 130c is a member that insulates at least a portion between the first electrode portion 110c and the second electrode portion 120c. Here, the first insulating part 130c is implemented in a tube shape and may be positioned between the first electrode part 110c and the second electrode part 120c in a form surrounding at least a part of the first electrode part 110c. . At this time, the first electrode portion 110c and the second electrode portion 120c are not insulated only by the first insulating portion 130c, and between the first electrode portion 110c and the second electrode portion 120c. A part of the insulation layer 130c may be insulated and the rest may be insulated by the second insulation unit 140c. At this time, as in the previous embodiment, it is also possible to realize more perfect insulation by implementing the first insulation part 130c as two layers.
제2 절연부(140c)는 제1 전극부(110c)의 일부를 외부로 노출되지 않도록 감싸면서 제1 전극부(110c)와 제2 전극부(120c)가 내부에서 단락되지 않도록 절연할 수 있다. 여기서, 제2 절연부(140c)에는 제1 전극부(110c)의 제3 오픈부(118)와 동일한 방향으로 오픈된 제1 오픈부(157c)가 형성될 수 있다. 따라서, 제1 오픈부(157c)를 통해 제1 전극부(110c)의 제3 오픈부(118)가 외부로 노출되면서 제3 오픈부(118)에 형성된 제3 칼날영역(119)이 외부로 노출되도록 할 수 있다. 이때, 제2 전극부(120c)의 일부는 제2 절연부(140c)의 외면에 위치되어 노출 전극으로서 기능할 수 있으며, 제2 전극부(120c)의 석션홀에 대응되는 제2 절연부(140c) 위치에는 석션홀이 형성되어 혈액, 조직 또는 뼈 등이 석션되도록 할 수 있다. 또한, 제2 절연부(140c)의 단부에는 별도의 측면 석션홀(155c)이 더 형성될 수 있으며 이를 통해서도 석션이 가능하여 석션 효율성을 향상시킬 수 있다. 이때, 석션에 문제가 없도록 제1 전극부(110c)와 연마절삭부(180c)의 대응되는 위치는 오픈되어 있을 수 있다.The second insulating part 140c may insulate the first electrode part 110c and the second electrode part 120c from being short-circuited inside while wrapping a part of the first electrode part 110c so as not to be exposed to the outside. . Here, a first open portion 157c open in the same direction as the third open portion 118 of the first electrode portion 110c may be formed in the second insulating portion 140c. Therefore, while the third open portion 118 of the first electrode portion 110c is exposed to the outside through the first open portion 157c, the third blade region 119 formed in the third open portion 118 is exposed to the outside. can be exposed. At this time, a part of the second electrode unit 120c may function as an exposed electrode by being located on the outer surface of the second insulation unit 140c, and the second insulation unit corresponding to the suction hole of the second electrode unit 120c ( A suction hole is formed at the position 140c) so that blood, tissue or bone can be suctioned. In addition, a separate side suction hole 155c may be further formed at an end of the second insulating portion 140c, and suction may be performed through this, so that suction efficiency may be improved. At this time, the corresponding positions of the first electrode part 110c and the polishing cutting part 180c may be open so that there is no problem with suction.
연마절삭부(180c)는 조직 또는 뼈를 연마 또는 절삭하기 위한 부재로 회전 가능하게 구현되며, 제1 전극부(110c)의 제1 관통홀(111c)의 내부에 위치되고, 제2 절연부(140c)와 인접한 영역에 연마절삭영역(181)이 형성될 수 있다. 여기서, 연마절삭부(180c)가 쉐이버로 구현되는 경우, 연마절삭부(180c)에는 제2 오픈부(182)가 형성될 수 있고 제2 오픈부(182)에는 칼날영역으로 구현된 연마절삭영역(181)이 형성될 수 있다. 이때, 석션유닛이 동작하여 연마절삭부(180c)의 제3 관통홀(183) 내에 진공이 인가되면 제2 오픈부(182)를 통해 조직이 석션되며(잡아 당겨지며), 연마절삭부(180c)가 회전되면서 제2 오픈부(182)의 연마절삭영역(181)이 제3 오픈부(118)의 제3 칼날영역(119) 내측에서 회전되면서 조직을 절삭할 수 있다. 또한, 절삭 능력을 향상시키기 위하여 제2 칼날영역(181)과 제3 칼날영역(119)을 톱니 형상으로 구현하는 것도 가능하다. The abrasive cutting part 180c is rotatably implemented as a member for grinding or cutting tissue or bone, is located inside the first through hole 111c of the first electrode part 110c, and has a second insulating part ( A polishing cutting area 181 may be formed in an area adjacent to 140c). Here, when the abrasive cutting part 180c is implemented as a shaver, the second open part 182 may be formed in the abrasive cutting part 180c, and the abrasive cutting area implemented as a blade area is formed in the second open part 182. (181) can be formed. At this time, when vacuum is applied to the third through hole 183 of the abrasive cutting part 180c by operating the suction unit, tissue is suctioned (pulled) through the second open part 182, and the abrasive cutting part 180c ) is rotated, the abrasive cutting area 181 of the second open portion 182 is rotated inside the third blade area 119 of the third open portion 118, and tissue can be cut. In addition, it is also possible to implement the second blade region 181 and the third blade region 119 in a sawtooth shape in order to improve cutting performance.
본 실시예에서는 칼날영역이 제2 절연부(140c)가 아닌 제1 전극부(110c)에 형성되는 점에 있어서 이전 실시예와 차이가 있다. 본 실시예에서는 금속으로 구성된 제1 전극부(110c)에 제3 칼날영역(119)이 형성되므로 기계적 강도가 우수할 수 있으며, 제2 칼날영역(181)과 제3 칼날영역(119)이 모두 금속으로 구성되므로 상호 매칭성이 향상되어 절삭력이 더욱 우수할 수 있다.This embodiment is different from the previous embodiment in that the blade region is formed on the first electrode part 110c instead of the second insulating part 140c. In this embodiment, since the third blade region 119 is formed on the first electrode portion 110c made of metal, mechanical strength may be excellent, and both the second blade region 181 and the third blade region 119 are Since it is made of metal, mutual matching is improved and cutting power can be further improved.
한편, 본 실시예에서는 연마절삭부(180c)가 쉐이버인 경우를 설명하였으나 이전 실시예와 같이 버(Burr)로 구성되는 것도 가능하다 할 것이다.Meanwhile, in this embodiment, the case where the abrasive cutting part 180c is a shaver has been described, but it will also be possible to be composed of a burr like the previous embodiment.
이상 본 발명을 구체적인 실시예를 통하여 상세히 설명하였으나, 이는 본 발명을 구체적으로 설명하기 위한 것으로, 본 발명에 따른 의료용 절제기구는 이에 한정되지 않으며, 본 발명의 기술적 사상 내에서 당해 분야의 통상의 지식을 가진 자에 의해 그 변형이나 개량이 가능함은 명백하다고 할 것이다.Although the present invention has been described in detail through specific examples, this is for explaining the present invention in detail, and the medical ablation apparatus according to the present invention is not limited thereto, and within the technical spirit of the present invention, common knowledge in the art It will be said that it is clear that the modification or improvement is possible by those who have the .
본 발명의 단순한 변형 내지 변경은 모두 본 발명의 영역에 속하는 것으로 본 발명의 구체적인 보호 범위는 첨부된 특허청구범위에 의하여 명확해질 것이다.All simple modifications or changes of the present invention fall within the scope of the present invention, and the specific protection scope of the present invention will be clarified by the appended claims.

Claims (14)

  1. 제1 방향으로 연장되되, 적어도 일부가 내부에 제1 관통홀을 갖는 중공 형상인 제1 전극부;Doedoe extending in a first direction, at least a portion of the hollow first electrode portion having a first through hole therein;
    내부에 상기 제1 전극부의 적어도 일부가 위치되도록 적어도 일부가 제2 관통홀을 갖는 중공 형상인 제2 전극부;a hollow second electrode portion having at least a portion of the second through hole so that at least a portion of the first electrode portion is positioned therein;
    상기 제1 전극부와 상기 제2 전극부 사이에 위치되어 상기 제1 전극부와 상기 제2 전극부 간을 절연하는 제1 절연부;a first insulating part positioned between the first electrode part and the second electrode part to insulate between the first electrode part and the second electrode part;
    적어도 일부가 상기 제1 전극부의 일부를 커버하도록 배치되고 일부는 외부로 노출되며, 상기 제1 방향과 상이한 방향을 향해 오픈된 제1 오픈부를 구비하는 제2 절연부;a second insulator having a first open portion, at least a portion of which is disposed to cover a portion of the first electrode portion, a portion of which is exposed to the outside, and which is open toward a direction different from the first direction;
    상기 제2 전극부의 일부가 외부로 노출되도록 상기 제2 전극부의 적어도 일부를 커버하는 제3 절연부; 및a third insulator covering at least a portion of the second electrode portion so that a portion of the second electrode portion is exposed to the outside; and
    상기 제1 관통홀의 내부에 위치되되 상기 제2 절연부와 인접한 영역에 연마절삭영역이 형성되고 회전 가능한 연마절삭부;an abrasive cutting part located inside the first through hole and having an abrasive cutting area formed in an area adjacent to the second insulating part and being rotatable;
    를 포함하는 의료용 절제기구.A medical resection device comprising a.
  2. 제1항에 있어서,According to claim 1,
    상기 제1 전극부 또는 상기 제2 전극부에 전기 신호가 인가되면, 상기 제2 절연부에 의해 커버되지 않고 외부로 노출된 상기 제1 전극부의 영역과 상기 제3 절연부에 의해 커버되지 않고 외부로 노출된 상기 제2 전극부의 영역에 의해 조직이 응고(coagulation) 또는 소작(ablation)되며,When an electric signal is applied to the first electrode part or the second electrode part, an area of the first electrode part exposed to the outside and not covered by the second insulating part and not covered by the third insulating part are exposed to the outside. The tissue is coagulated or ablated by the area of the second electrode part exposed to
    상기 연마절삭부가 회전되면 상기 연마절삭영역에 의해 조직 또는 뼈가 연마 또는 절삭되는 의료용 절제기구.When the abrasive cutting part is rotated, tissue or bone is abraded or cut by the abrasive cutting region.
  3. 제1항에 있어서,According to claim 1,
    상기 제2 절연부의 상기 제1 방향에 따른 양측 중 일측은 상기 제1 전극부를 커버하고 타측에는 제1 석션홀이 형성된 것을 특징으로 하는 의료용 절제기구.A medical ablation apparatus, characterized in that one side of both sides of the second insulating portion along the first direction covers the first electrode portion and a first suction hole is formed on the other side.
  4. 제1항에 있어서,According to claim 1,
    상기 제1 전극부는,The first electrode part,
    적어도 일부가 상기 제2 관통홀의 내부에 위치되고 내부에 상기 제1 관통홀을 가지며 상기 제2 절연부에 의해 외부로 노출되지 않는 제1 전극본체부;a first electrode main body at least a part of which is located inside the second through hole, has the first through hole therein, and is not exposed to the outside by the second insulating part;
    상기 제2 절연부의 외면에 위치되어 외부로 노출되는 제1 전극노출부; 및a first electrode exposed portion positioned on an outer surface of the second insulating portion and exposed to the outside; and
    상기 제1 전극본체부와 상기 제1 전극노출부 사이를 전기적으로 연결하되, 적어도 일부가 상기 제2 절연부에 의해 외부로 노출되지 않는 제1 전극연결부;a first electrode connecting portion electrically connected between the first electrode body portion and the first electrode exposed portion, at least a portion of which is not exposed to the outside by the second insulating portion;
    를 포함하는 것을 특징으로 하는 의료용 절제기구.A medical ablation apparatus comprising a.
  5. 제4항에 있어서,According to claim 4,
    상기 제2 절연부는,The second insulator,
    적어도 일부가 상기 제1 전극본체부의 외면에 위치되어 상기 제1 전극본체부가 외부로 노출되지 않도록 하되, 외면의 적어도 일부에 상기 제1 전극연결부가 위치되도록 안착부가 형성되며, 외면에 상기 제1 전극노출부가 위치된 제2 절연바디부; 및At least a portion is located on an outer surface of the first electrode body so that the first electrode body is not exposed to the outside, but a seating portion is formed so that the first electrode connection portion is located on at least a portion of the outer surface, and the first electrode is formed on the outer surface. a second insulating body portion in which the exposed portion is located; and
    상기 제1 전극연결부의 적어도 일부가 외부로 노출되지 않도록 상기 제2 절연바디부에 결합되되, 적어도 일부가 상기 제2 전극부와 상기 제1 전극본체부 사이에 위치되어 상기 제2 전극부와 상기 제1 전극본체부 사이를 절연하는 제2 절연커버부;At least a portion of the first electrode connection portion is coupled to the second insulating body portion so as not to be exposed to the outside, and at least a portion is positioned between the second electrode portion and the first electrode body portion so that the second electrode portion and the first electrode body portion are connected to each other. a second insulating cover portion that insulates between the first electrode main body portions;
    를 포함하는 것을 특징으로 하는 의료용 절제기구.A medical ablation apparatus comprising a.
  6. 제5항에 있어서,According to claim 5,
    상기 제1 절연부는,The first insulator,
    상기 제1 전극부의 적어도 일부 외면에 위치되는 제1-1 절연부; 및a 1-1 insulating part located on at least a part of the outer surface of the first electrode part; and
    상기 제1-1 절연부의 적어도 일부 외면에 위치되는 제1-2 절연부;a 1-2 insulating part positioned on at least a part of an outer surface of the 1-1 insulating part;
    를 포함하고,including,
    상기 제1 전극부와 상기 제2 전극부의 사이는 제1 영역 및 제2 영역을 포함하며, 상기 제1 영역은 상기 제1-1 절연부 및 상기 제1-1 절연부 상의 상기 제2 절연커버부에 의해 절연되고, 상기 제2 영역은 상기 제1-1 절연부 및 상기 제1-1 절연부 상의 상기 제1-2 절연부에 의해 절연되는 것을 특징으로 하는 의료용 절제기구.A space between the first electrode part and the second electrode part includes a first region and a second region, and the first region comprises the 1-1 insulating part and the second insulating cover on the 1-1 insulating part. and the second region is insulated by the 1-1 insulating part and the 1-2 insulating part on the 1-1 insulating part.
  7. 제1항에 있어서,According to claim 1,
    상기 제2 절연부의 상기 제1 오픈부에는 제1 칼날영역이 형성되고, 상기 연마절삭부가 회전되면 상기 연마절삭영역과 상기 제1 칼날영역에 의해 조직 또는 뼈가 연마 또는 절삭되는 것을 특징으로 하는 의료용 절제기구.A first blade region is formed in the first open portion of the second insulating portion, and when the abrasive cutting portion is rotated, tissue or bone is polished or cut by the abrasive cutting region and the first blade region. ablation apparatus.
  8. 제7항에 있어서,According to claim 7,
    상기 연마절삭부는 상기 제1 방향과 상이한 방향을 향해 오픈된 제2 오픈부를 구비하고, 상기 연마절삭영역은 상기 제2 오픈부에 형성되어 상기 조직을 연마 또는 절삭하기 위한 제2 칼날영역인 것을 특징으로 하는 의료용 절제기구.The abrasive cutting part has a second open part opened in a direction different from the first direction, and the abrasive cutting area is formed in the second open part and is a second blade area for polishing or cutting the tissue. A medical ablation device made of.
  9. 제8항에 있어서,According to claim 8,
    상기 연마절삭부의 적어도 일부는 내부에 석션을 위한 석션통로로 활용되는 제3 관통홀을 갖는 중공 형상인 것을 특징으로 하는 의료용 절제기구.Medical ablation apparatus, characterized in that at least a portion of the abrasive cutting portion has a hollow shape having a third through-hole used as a suction passage for suction therein.
  10. 제9항에 있어서,According to claim 9,
    상기 제2 절연부의 상기 제1 오픈부의 반대 방향에는 제2 석션홀이 형성되고,A second suction hole is formed in a direction opposite to the first open part of the second insulating part,
    상기 제1 전극부에는 상기 제2 석션홀에 대응되는 위치에 제3 석션홀이 형성되며,A third suction hole is formed in the first electrode part at a position corresponding to the second suction hole,
    석션 대상은 상기 제3 석션홀, 상기 제2 석션홀 및 상기 제2 오픈부 또는 상기 제2 오픈부의 반대 방향에 형성된 제4 석션홀을 차례로 통과하여 상기 석션통로를 통해 석션되는 것을 특징으로 하는 의료용 절제기구.The suction target is medical, characterized in that the suction through the suction passage passes through the third suction hole, the second suction hole, and the second open portion or a fourth suction hole formed in the opposite direction of the second open portion in order. ablation apparatus.
  11. 제1항에 있어서,According to claim 1,
    상기 연마절삭부는 상기 뼈를 연마 또는 절삭하기 위한 버(Burr)인 것을 특징으로 하는 의료용 절제기구.The medical ablation apparatus, characterized in that the abrasive cutting part is a burr for grinding or cutting the bone.
  12. 제1항에 있어서,According to claim 1,
    상기 제1 전극부는 상기 제1 오픈부와 동일한 방향을 향해 오픈된 제3 오픈부를 구비하는 것을 특징으로 하는 의료용 절제기구.The medical ablation apparatus of claim 1 , wherein the first electrode portion includes a third open portion opened toward the same direction as the first open portion.
  13. 제12항에 있어서,According to claim 12,
    상기 제3 오픈부에는 제3 칼날영역이 형성되며, 상기 연마절삭부가 회전되면 상기 연마절삭영역과 상기 제3 칼날영역에 의해 조직 또는 뼈가 연마 또는 절삭되는 것을 특징으로 하는 의료용 절제기구.A third blade region is formed in the third open portion, and when the abrasive cutting portion is rotated, tissue or bone is polished or cut by the abrasive cutting region and the third blade region.
  14. 제12항에 있어서,According to claim 12,
    상기 제2 전극부는,The second electrode part,
    제2 절연부의 외면에 위치되어 외부로 노출되는 노출부; 및an exposed portion located on an outer surface of the second insulating portion and exposed to the outside; and
    적어도 일부가 제3 절연부에 의해 커버되며 상기 노출부와 결합된 본체부;a body portion at least partially covered by a third insulating portion and coupled to the exposed portion;
    를 포함하는 것을 특징으로 하는 의료용 절제기구.A medical ablation apparatus comprising a.
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US20100121321A1 (en) * 2005-03-04 2010-05-13 Gyrus Ent, L.L.C. Surgical instrument and method
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JP2020531201A (en) * 2017-08-28 2020-11-05 リライン コーポレーション Arthroscopy equipment and arthroscopy method

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Publication number Priority date Publication date Assignee Title
US5364395A (en) * 1993-05-14 1994-11-15 West Jr Hugh S Arthroscopic surgical instrument with cauterizing capability
JP2001511043A (en) * 1997-02-10 2001-08-07 ウェスト,ヒュー,エス.,ジュニア. Mechanical and electrical endoscopic surgical instruments
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WO2017136414A1 (en) * 2016-02-04 2017-08-10 RELIGN Corporation Arthroscopic devices and methods
JP2020531201A (en) * 2017-08-28 2020-11-05 リライン コーポレーション Arthroscopy equipment and arthroscopy method

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