최소 단어 이상 선택하여야 합니다.
최대 10 단어까지만 선택 가능합니다.
다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
NTIS 바로가기다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
DataON 바로가기다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
Edison 바로가기다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
Kafe 바로가기국가/구분 | United States(US) Patent 등록 |
---|---|
국제특허분류(IPC7판) |
|
출원번호 | US-0218221 (2011-08-25) |
등록번호 | US-8425505 (2013-04-23) |
발명자 / 주소 |
|
출원인 / 주소 |
|
인용정보 | 피인용 횟수 : 28 인용 특허 : 897 |
A surgical instrument, such as an endoscopic or laparoscopic instrument, includes an ablation device. The ablation device includes an elongate member having first and second channels. First and second probes are disposed within the respective first and second channels. The first and second probes ea
A surgical instrument, such as an endoscopic or laparoscopic instrument, includes an ablation device. The ablation device includes an elongate member having first and second channels. First and second probes are disposed within the respective first and second channels. The first and second probes each define a central axis. The first and second probes each have substantially straight distal ends protruding from the distal ends of the respective first and second channels. The substantially straight distal ends define an outer surface. First and second electrodes are attached to a portion of the outer surface of the substantially straight distal ends of the respective first and second probes. The first and second electrodes are positioned in juxtaposed relationship with the central axis of the first and second probes. A distance between the first and second electrodes is adjustable by rotating at least one of the first and second probes about the respective central axis of the at least one of the first and second probes.
1. An ablation device, comprising: an elongate member comprising first and second channels;first and second probes disposed within the respective first and second channels, the first and second probes each defining a central axis, the first and second probes each having substantially straight distal
1. An ablation device, comprising: an elongate member comprising first and second channels;first and second probes disposed within the respective first and second channels, the first and second probes each defining a central axis, the first and second probes each having substantially straight distal ends protruding from the distal ends of the respective first and second channels, the substantially straight distal ends defining an outer surface; andfirst and second electrodes attached to a portion of the outer surface of the substantially straight distal ends of the respective first and second probes;the first and second electrodes positioned in juxtaposed relationship with the central axis of the first and second probes;wherein a distance between the first and second electrodes is adjustable by rotating at least one of the first and second probes about the respective central axis of the at least one of the first and second probes;wherein the substantially straight distal end of the first probe comprises a sharp distal end and an aperture in communication with a bore formed within the first probe to receive a tissue sample therethrough. 2. The ablation device of claim 1, wherein the substantially straight distal end of the second probe comprises a sharp distal end and an aperture in communication with a bore formed within the second probe to receive a tissue sample therethrough. 3. The ablation device of claim 1, comprising: at least one illuminator positioned to illuminate tissue; andan image sensor positioned to image tissue therethrough. 4. The ablation device of claim 1, wherein at least one of the first and second channels is a working channel. 5. The ablation device of claim 1, wherein at least one of the first and second probes is a diagnostic probe. 6. The ablation device of claim 1, wherein the elongate member is flexible. 7. An ablation system, comprising: an elongate member comprising first and second channels;first and second probes disposed within the respective first and second channels, the first and second probes each defining a central axis, the first and second probes each having substantially straight distal ends protruding from the distal ends of the respective first and second channels, the substantially straight distal ends defining an outer surface;first and second electrodes attached to a portion of the outer surface of the substantially straight distal ends of the respective first and second probes;the first and second electrodes positioned in juxtaposed relationship with the central axis of the first and second probes; andan electrical waveform generator electrically coupled to the first and second electrodes to generate an irreversible electroporation electrical (IRE) waveform sufficient to ablate tissue located proximate to the first and second electrodes;wherein a distance between the first and second electrodes is adjustable by rotating at least one of the first and second probes about the respective central axis of the at least one of the first and second probes;wherein the substantially straight distal end of the first probe comprises a sharp distal end and an aperture in communication with a bore formed within the first probe to receive a tissue sample therethrough. 8. The ablation system of claim 7, wherein the substantially straight distal end of the second probe comprises a sharp distal end and an aperture in communication with a bore formed within the second probe to receive a tissue sample therethrough. 9. The ablation system of claim 7, comprising: at least one illuminator positioned to illuminate tissue; andan image sensor positioned to image tissue therethrough. 10. The ablation device of claim 7, wherein at least one of the first and second channels is a working channel. 11. The ablation device of claim 7, wherein at least one of the first and second probes is a diagnostic probe. 12. The ablation device of claim 7, wherein the elongate member is flexible. 13. The ablation system of claim 7, wherein the electrical waveform generator is adapted to receive IRE electrical waveform parameters from an image processing module; and wherein the IRE electrical waveform parameters are determined based on image information of a tissue treatment region in a patient. 14. The ablation system of claim 13, wherein the IRE electrical waveform parameters are determined based on a volume and outline of a necrotic zone required to treat the tissue treatment region based on the image information. 15. The ablation system of claim 14, wherein the volume and outline of the necrotic zone are determined from geometric information extracted from the image information. 16. The ablation system of claim 13, wherein the IRE electrical waveform parameters comprise amplitude, frequency, and pulse width of an electrical waveform suitable to destroy the diseased tissue. 17. A method, comprising: locating an elongate member comprising first and second channels within a body cavity proximate to a tissue treatment region, wherein the first and second probes are disposed within the respective first and second channels, the first and second probes each defining a central axis, the first and second probes each having substantially straight distal ends protruding from the distal ends of the respective first and second channels, the substantially straight distal ends defining an outer surface; wherein the first and second electrodes are attached to a portion of the outer surface of the substantially straight distal ends of the respective first and second probes; the first and second electrodes positioned in juxtaposed relationship with the central axis of the first and second probes;adjusting a distance between the first and second electrodes by rotating at least one of the first and second probes about the central axis of the at least one of the first and second probes; andreceiving a tissue sample through a sharp distal end and an aperture in communication with a bore formed within either one of the first and second probes. 18. The method of claim 17, comprising: illuminating the tissue treatment region with at least one illuminator positioned to illuminate tissue; andimaging the tissue treatment region with an image sensor positioned to image tissue therethrough. 19. The method of claim 17, comprising: applying an irreversible electroporation electrical (IRE) waveform sufficient to ablate tissue located proximate to the first and second electrodes with an electrical waveform generator electrically coupled to the first and second electrodes of the ablation device. 20. The method of claim 19, comprising: determining IRE electrical waveform parameters based on image information of the tissue treatment region; andreceiving by the electrical waveform generator IRE electrical waveform parameters from an image processing module. 21. The method of claim 20, comprising determining the IRE electrical waveform parameters based on a volume and outline of a necrotic zone required to treat the tissue treatment region based on the image information. 22. The method of claim 21, comprising determining the volume and outline of the necrotic zone from geometric information extracted from the image information. 23. The method of claim 17, comprising applying an irreversible electroporation electrical (IRE) waveform suitable to destroy diseased tissue in the tissue treatment region, wherein the IRE electrical waveform parameters comprise amplitude, frequency, and pulse width.
Copyright KISTI. All Rights Reserved.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.