WO2023016421A1 - 医用支架操作系统 - Google Patents

医用支架操作系统 Download PDF

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Publication number
WO2023016421A1
WO2023016421A1 PCT/CN2022/110924 CN2022110924W WO2023016421A1 WO 2023016421 A1 WO2023016421 A1 WO 2023016421A1 CN 2022110924 W CN2022110924 W CN 2022110924W WO 2023016421 A1 WO2023016421 A1 WO 2023016421A1
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WO
WIPO (PCT)
Prior art keywords
sheath
operating
operating system
medical
hole
Prior art date
Application number
PCT/CN2022/110924
Other languages
English (en)
French (fr)
Inventor
陈阶晓
Original Assignee
陈阶晓
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 陈阶晓 filed Critical 陈阶晓
Priority to CA3227896A priority Critical patent/CA3227896A1/en
Priority to CN202280054871.4A priority patent/CN117940073A/zh
Priority to JP2024507897A priority patent/JP2024528293A/ja
Priority to KR1020247007770A priority patent/KR20240039196A/ko
Priority to EP22855402.8A priority patent/EP4385425A1/en
Publication of WO2023016421A1 publication Critical patent/WO2023016421A1/zh

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/34Trocars; Puncturing needles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/95Instruments specially adapted for placement or removal of stents or stent-grafts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/95Instruments specially adapted for placement or removal of stents or stent-grafts
    • A61F2/9517Instruments specially adapted for placement or removal of stents or stent-grafts handle assemblies therefor
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/95Instruments specially adapted for placement or removal of stents or stent-grafts
    • A61F2/962Instruments specially adapted for placement or removal of stents or stent-grafts having an outer sleeve
    • A61F2/966Instruments specially adapted for placement or removal of stents or stent-grafts having an outer sleeve with relative longitudinal movement between outer sleeve and prosthesis, e.g. using a push rod
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/95Instruments specially adapted for placement or removal of stents or stent-grafts
    • A61F2/962Instruments specially adapted for placement or removal of stents or stent-grafts having an outer sleeve
    • A61F2/966Instruments specially adapted for placement or removal of stents or stent-grafts having an outer sleeve with relative longitudinal movement between outer sleeve and prosthesis, e.g. using a push rod
    • A61F2002/9665Instruments specially adapted for placement or removal of stents or stent-grafts having an outer sleeve with relative longitudinal movement between outer sleeve and prosthesis, e.g. using a push rod with additional retaining means

Definitions

  • the invention relates to a medical support operating system, in particular to a medical support operating system that can assist in placing the medical support into a human body or assisting in taking the medical support out of the human body.
  • an idea of the present invention is to provide a medical stent operating system that can assist in inserting the medical stent into the human body or assisting in removing the medical stent from the human body.
  • the present invention provides a medical stent operating system, comprising: a sheath portion having a first cavity extending along the length direction of the sheath portion; a gripping portion connected to the sheath part, and has a second cavity; the operating part is connected to the grip part in a movable manner, and the operating part has a first operating end part and a second operating end part, and the first operating end part is arranged on the second operating end part.
  • the second operating end is arranged outside the gripping part; and the bracket moving part is connected to the first operating end and extends in the first cavity and the second cavity, and the bracket moves The end of the part is in contact with the medical support; wherein the operating part moves relative to the holding part, and the medical support is moved by the support moving part.
  • the sheath is a transparent tubular body.
  • the medical support operating system further includes: an optical sensing device having a sensing part and a transmitting part, the sensing part is connected to the transmitting part; wherein the sensing part is arranged on the handle The holding end of the holding part; wherein the sensing part is at least partially disposed in the sheath part, and the sensing part is located at the end of the sheath of the sheath part; wherein the transmission part is at least partly extended in the first cavity Inside.
  • the bracket moving part has a pushing part
  • the pushing part is arranged at the end of the bracket moving part
  • the pushing part is in the shape of a hollow cylinder
  • the pushing part can be relative to the transmission
  • the transmission part fits in the way that the part moves.
  • the sheath portion has a sheath end, and the sheath end has a lateral communication outlet.
  • the bracket moving part has a hooking part, and the hooking part is arranged at the end of the bracket moving part.
  • the sheath part is detachably connected to the handle part.
  • the bracket moving part has a pushing part, and the pushing part is arranged at the end of the bracket moving part.
  • the medical stent has a first expansion section, a second expansion section and a third expansion section, and the third expansion section is arranged between the first expansion section and the second expansion section.
  • the medical support operating system has a staged movement mechanism, and the operating part moves relative to the gripping part in stages through the staged movement mechanism, and makes the first stretching section, the The third stretching section and the second stretching section are sequentially pushed out of the tube sheath by the bracket moving part in stages.
  • the step-type moving mechanism is that the gripping portion has a plurality of engaging holes, and the first operating end of the operating portion has an engaging portion, and the engaging portion is used for the operation During the movement of the part relative to the holding part, it is engaged with one of the plurality of engaging holes.
  • the plurality of engaging holes include a first engaging hole, a second engaging hole and a third engaging hole;
  • first stretching section is pushed out of the tube sheath by the bracket moving part; wherein when the engaging portion is engaged with the second engaging hole, the third stretching section is pushed out by the bracket The moving part is pushed out of the tube sheath; wherein when the engaging part engages with the third engaging hole, the second stretching section is pushed out of the tube sheath by the bracket moving part.
  • the grip part has an elongated through hole, and the elongated through hole is extended along the length direction of the grip part on the grip part, and the second part of the operation part
  • An operating end has a protruding portion protruding outward through the elongated through hole, and the protruding portion can move along the elongated through hole.
  • the medical stent has a first expansion section, a second expansion section and a third expansion section, and the third expansion section is arranged between the first expansion section and the second expansion section.
  • the medical support operating system makes the protrusion contact with the through hole end, so that the operating part cannot be pushed out relative to the The holding part continues to move; wherein when the protruding part contacts the end of the through hole, the medical stent operating system exposes the second stretching section of the medical stent to the outside of the tube sheath through the stent moving part.
  • the protruding portion is subjected to a first external force to leave the end of the through hole and the elongated through hole, and then the operating portion is subjected to a second external force to move relative to the push-out direction.
  • the holding part moves, and the second stretching section is pushed out of the tube sheath by the bracket moving part.
  • the sheath part has a liquid delivery part, and the liquid delivery part communicates with the first cavity, and the medical stent operating system delivers a liquid into the sheath part through the liquid delivery part .
  • Fig. 1 is a schematic diagram of a specific embodiment of the medical stent operating system of the present invention.
  • Fig. 2A is a schematic diagram of a specific embodiment of the gripping part and the optical sensing device of the medical stent operating system of the present invention.
  • Fig. 2B is a schematic diagram of a specific embodiment of the operating part and the rack moving part of the medical rack operating system of the present invention.
  • Fig. 2C is a schematic diagram of a specific embodiment of the sheath part of the medical stent operating system of the present invention.
  • Fig. 3 is a partial schematic diagram of a specific embodiment of the stent moving part of the medical stent operating system of the present invention.
  • Fig. 4 is a partial schematic view of a specific embodiment of the sheath part, the extension part and the pushing part.
  • Fig. 5 is a partial schematic view of a specific embodiment of the sheath part, the extension part and the engaging part.
  • FIG. 1 illustrates a schematic view of a specific embodiment of a medical stent operating system according to the present invention.
  • the medical support operating system 100 includes an operating part 1100, a grip part 1200, a tube sheath part 1300, a support moving part (not shown in the figure, which will be described in detail later), an optical sensing device ( Not shown in the figure, and will be described in detail later) and the protection part 1600.
  • the sheath part 1300 is a hollow component with a first cavity inside, and the first cavity extends along the length direction 810 of the sheath part 1300 .
  • the sheath end 1320 of the sheath part 1300 may have a lateral communication outlet 1310 (for the arrangement of the lateral communication outlet 1310, please refer to the Taiwan invention patent application number 110103890, whose invention name is "Surgical Use Medical device and its system".
  • the Taiwan invention patent application No. 110103890 is incorporated herein in its entirety by reference.
  • the grip part 1200 is a hollow component with a second cavity inside.
  • the tube sheath part 1300 is detachably connected to the handle part 1200 .
  • the operating part 1100 is movably connected to the grip part 1200, wherein the operating part 1100 has a first operating end and a second operating end, and the first operating end of the operating part 1100 is set on the second end of the grip 1200.
  • the second operating end of the operating part 1100 is disposed outside the grip part 1200 .
  • the connection relationship and actuation relationship between the operation part 1100 and the grip part 1200 are similar to the push rod part and the syringe part of a general medical syringe device.
  • the rack moving part of the medical rack operating system 1000 is connected to the first operating end of the operating part 1100, and the rack moving part extends in the first cavity and the second cavity.
  • the medical stent can be first placed in the tube sheath 1300 (preferably, the medical stent is first placed in the tube sheath 1300, close to the tube sheath position of the tube sheath end 1320 of 1300), and make the medical stent contact the end of the stent moving part.
  • the user can then move the operating part 1100 relative to the grip part 1200 to move the medical support through the support moving part connected to the operating part 1100 , and gradually push the medical support out of the sheath part 1300 .
  • the protection part 1600 is detachably installed (for example plugged in) on the sheath end 1320 of the sheath part 1300 to protect the sheath part 1300 , the stent moving part and the optical sensing device inside the sheath part 1300 .
  • the transmission part 1520 (such as a transmission line) of the optical sensing device can be extended in the first cavity and the second cavity.
  • the protective part 1600 may not be used, and the protective part 1600 may be removed from the sheath end 1320 of the sheath part 1300 .
  • the protection part 1600 may not be required.
  • FIG. 2A illustrates a schematic diagram of a specific embodiment of the gripping portion and the optical sensing device of the medical support operating system according to the present invention.
  • the grip portion 2200 includes a grip body portion 2210 and an extension portion (or may be referred to as a grip extension portion) 2220 , and the grip body portion 2210 is connected to the extension portion 2220 .
  • the grip body portion 2210 has engaging holes (which may be referred to as grip engaging holes) 2232 , 2234 , 2236 , an elongated through hole 2240 and a grip engaging portion 2250 .
  • the engaging hole 2232 is closer to the extension portion 2220 than the through hole 2240 , and the elongated through hole 2240 is extended along the length direction of the grip portion 2200 on the grip body portion 2210 of the grip portion 2200 .
  • the end portion 2242 of the elongated through hole 2240 is disposed between the engaging hole 2234 and the engaging hole 2232 .
  • the optical sensing device of the medical stent operating system includes a sensing unit 2510 and a transmission unit 2520 , and the sensing unit 2510 is connected to the transmission unit 2520 .
  • the sensing part 2510 is disposed (or connected) at the end of the extension part 2220 (may be referred to as the grip end), and the transmission part 2520 is extended and disposed in the second cavity of the grip part 2200 (in detail, the transmission part 2520 extends It is disposed in the extension part 2220 and the main body part 2210, and extends outward from the main body part 2210).
  • the sensing unit 2510 can acquire in-vivo images during the operation of the medical stent operating system, and can transmit the acquired images to the display device through the transmission unit for users to watch the images.
  • the transmission unit 2520 may have a processing unit 2530 , which may assist in processing the images acquired by the sensing unit 2510 .
  • FIG. 2B illustrates a schematic diagram of a specific embodiment of the operating part and the rack moving part of the medical rack operating system according to the present invention.
  • the operating portion 2100 has a first operating end portion 2110 , a second operating end portion 2120 , an engaging portion 2130 and a protruding portion 2140 . Both the engaging portion 2130 and the protruding portion 2140 are disposed on the first operating end portion 2110 .
  • One end of the rack moving part 2400 is connected to the operating part 2100 , and the other end of the rack moving part 2400 (which may be referred to as an end or a rack moving end) has a pushing part 2410 .
  • FIG. 3 illustrates a specific embodiment in which the end of the bracket moving part 2400 has a hooking part. In the embodiment shown in FIG. 3 , the end of the bracket moving part 3400 has a hooking part 3420 .
  • FIG. 2C illustrates a schematic view of a specific embodiment of the tube sheath part of the medical stent operating system according to the present invention.
  • the sheath part 2300 has a sheath body part 2370 , a sheath extension part 2330 , liquid delivery parts 2340 , 2350 and an engaging hole (which may be referred to as a sheath engaging hole) 2360 .
  • the sheath main part 2370 is connected to the sheath extension part 2330
  • the liquid delivery parts 2340 , 2350 are connected to the sheath main part 2370
  • the engaging hole 2360 is disposed on the sheath main part 2370 .
  • the liquid delivery part 2340, 2350 communicates with the first cavity of the tube sheath part 2300, so that the liquid (such as water, physiological saline, etc., but not limited thereto) can be delivered to the tube via the liquid delivery part 2340, 2350.
  • the liquid such as water, physiological saline, etc., but not limited thereto
  • the sheath 2300 Inside the sheath 2300.
  • the stent moving part 2400 can be extended and disposed in the first cavity of the sheath part 2300 and the second cavity of the handle part 2200 .
  • the end of the bracket moving part 2400 can contact the medical bracket.
  • the medical bracket can be gradually pushed out of the sheath part 2300 through the pushing part 2410 of the bracket moving part 2400 .
  • the medical stent can be gradually pulled into the inside of the sheath part 2300 (ie, into the first cavity) through the hooking part of the stent moving part 2400 .
  • the stent moving part 2400 and the extension part 2220 of the handle part 2200 can be extended to the first cavity of the tube sheath part 2300 at the same time.
  • the pushing part 2410 can be in the shape of a hollow cylinder, and the pushing part 2410 can be moved relative to the transmission part 2520 and the extension part 2220.
  • the transmission part 2520 and the extension part 2220 exemplifies a partial schematic view of a specific embodiment of the sheath, the extension and the pusher. In the embodiment shown in FIG.
  • the end of the bracket moving part 4400 has a pushing part 4410 , the pushing part 4410 is in the shape of a hollow cylinder, and the pushing part 4410 is fitted on the holding extension part 4220 in a movable manner relative to the holding extension part 4220 .
  • the pushing part 4410 is also nested in the transmission part in a manner that can move relative to the transmission part.
  • the sheath part is a transparent tubular body, or at least the sheath extension part 4330 of the sheath part is a transparent tubular body, so as to prevent the sheath extension part 4330 from blocking the view of the sensing part 4510.
  • the transmission part is partially extended in the handle extension part 4220 (that is, the transmission part is partially extended in the first cavity of the sheath part), and the transmission part is partially extended in the handle part. in the second cavity.
  • the sensing part 4510 is disposed in the sheath extension part 4330 of the sheath part, and placed (or disposed) at the end of the sheath of the sheath extension part 4330 place.
  • the sensing part 4510 can be completely disposed in the sheath part according to requirements, or slightly exposed outside the end of the sheath. And when the grip extension 4220 moves relative to the sheath extension 4330 (for example, the grip extension 4220 is removed from the sheath extension 4330), the sensing portion 4510 can move relative to the grip extension 4220. Move in the sheath extension 4330 (for example, the sensing part 4510 can be removed from the sheath extension 4330 by grasping the extension 4220 ).
  • FIG. 5 illustrates a partial schematic view of a specific embodiment of the sheath portion, the extension portion and the engaging portion.
  • the grip extension part 5220 and the stent moving part 5400 are disposed in the sheath extension part 5330 , and the end of the stent moving part 5400 has a hooking part 5420 .
  • the sensing part 5510 at the end of the grip extension part 5220 can still continue Capture images without being affected by the hook 5420.
  • the sheath part is a transparent tubular body, or at least the sheath extension part 5330 of the sheath part is a transparent tubular body, so as to prevent the sheath extension part 5330 from blocking the view of the sensing part 5510 .
  • the sensing part 5510 is arranged in the sheath extension part 5330 of the sheath part, and is placed (or arranged) at the end of the sheath of the sheath extension part 5330 place.
  • the sensing part 5510 can be completely disposed in the sheath part according to requirements, or slightly exposed outside the end of the sheath.
  • the sensing portion 5510 can move relative to the grip extension 5220. Move in the sheath extension 5330 (eg, the sensing part 5510 can be removed from the sheath extension 5330 by gripping the extension 5220 ).
  • the medical support operated (or moved) by the medical support operating system of the present invention may have a first expansion section, a second expansion section and a third expansion section, and the third expansion section is arranged between the first expansion section and the second expansion section.
  • the two stretching sections please refer to the aforementioned Taiwan invention patent application No. 110103890.
  • the medical stent operating system of the present invention is not only applicable to this type of medical stent).
  • the medical support operating system of the present invention can have a staged movement mechanism, wherein the operating part can move relative to the holding part in stages through the staged movement mechanism, and then make the first stretching section, the third stretching section and The second stretching section is sequentially pushed out of the tube sheath by the stent moving part in stages.
  • the staged moving mechanism can be, for example, the accommodating device described in FIGS. 7 to 8C in the aforementioned Taiwan Patent Application No. 110103890, but is not limited thereto.
  • the staged moving mechanism of the medical support operating system can be, for example, that the gripping main part 2210 of the gripping part 2200 has engaging holes 2232, 2234, 2236, and the first part of the operating part 2100
  • the operating end portion 2110 has an engaging portion 2130 , and the engaging portion 2130 can engage with one of the engaging holes 2232 , 2234 , 2236 when the operating portion 2100 moves relative to the grip portion 2200 .
  • the engaging portion 2130 engages with the engaging hole 2236 (the engaging hole 2236 may be referred to as the first engaging hole)
  • the first stretching section of the medical stent is pushed out by the pushing portion 2410 of the stent moving portion 2400 outside the sheath end 2320 of the sheath portion 2300 .
  • the engaging hole 2234 may be called the second engaging hole
  • the third stretching segment of the medical stent is pushed out of the tube sheath by the pushing part 2410 of the stent moving part 2400 Out of the sheath end 2320 of the portion 2300.
  • the second stretching segment of the medical stent is pushed out of the tube sheath by the pushing portion 2410 of the stent moving portion 2400 Out of the sheath end 2320 of the portion 2300.
  • the user can place the first stretched section, the third stretched section, and the second stretched section of the medical bracket in the correct position in the human body in stages (the first stretched section and the second stretched section).
  • segment, the third stretching segment and the correct placement of the second stretching segment can refer to the aforementioned application number No. 110103890 Taiwan invention patent).
  • the user can still release the engaging portion 2130 from the corresponding engaging hole by applying a relatively large force. engage, and allow the operation part 2100 to continue to be pushed or pulled relative to the grip part 2200 .
  • the protruding part 2140 of the operating part 2100 can protrude outwards through the elongated through hole 2240 (for the arrangement therebetween, refer to the protruding part 1140 and the elongated through hole 1240 shown in FIG. 1 ), and the protruding part 2140 can be held along the The elongated through hole 2240 of the part 2200 moves. In this way, when the operation part 2100 moves relative to the overhold part 2200, the protruding part 2140 will not affect the movement between the operation part 2100 and the overhold part 2200.
  • the protruding portion 2140 will first contact the elongated through hole 2240. through the end portion 2242 of the hole, and prevent the operation part 2100 from moving further along the pushing direction 820 relative to the grip part 2200 .
  • the second expanded section of the medical stent is partially exposed outside the sheath end 2320 of the sheath part 2300 .
  • This mechanism can prevent the second stretching section from being pushed out of the sheath end 2320 too quickly due to excessive force applied by the user during the operation of the part 2100, thereby causing the second stretching section to be placed in a wrong position. Or cause the medical stent to harm the human body.
  • the user can apply a first external force to the protruding part 2140 (the first external force can be, for example, pressing the protruding part in the direction perpendicular to the extending direction of the operating part 2100). part 214), the protruding part 2140 leaves the through hole end 2242 and leaves the elongated through hole 2240.
  • the user can then apply a second external force to the operation part 2100 (that is, continue to push the operation part 2100 toward the direction 830), so that the operation part 2100 moves relative to the grip part 2200 along the pushing direction 820, and the second brace of the medical bracket
  • the open section is pushed out of the sheath end 2320 of the sheath part 2300 by the pushing part 2410 of the stent moving part 2400 .
  • the holding engaging portion 2250 of the handle portion 2200 can engage with the engaging hole 2360 of the tube sheath portion 2300 to connect the handle portion 2200 to the tube sheath portion 2300 more firmly.
  • the user can also disengage the engaging portion 2250 from the engaging hole 2360 according to requirements, and further separate the grip portion 2200 and the sheath portion 2300 from each other.
  • the user can first hook the medical stent through the hooking part of the stent moving part 2400, and then connect the engaging part 2250 with the locking
  • the engagement hole 2360 is disengaged, and the stent moving part 2400 and/or the extension part 2220 of the grip part 2200 is removed from the sheath extension part 2330 by pulling the operation part 2100 and/or the grip part 2200 .
  • the medical stent will be removed outside the human body along with the engaging portion.

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  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Heart & Thoracic Surgery (AREA)
  • General Health & Medical Sciences (AREA)
  • Surgery (AREA)
  • Vascular Medicine (AREA)
  • Transplantation (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Cardiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Medical Informatics (AREA)
  • Molecular Biology (AREA)
  • Pathology (AREA)
  • Media Introduction/Drainage Providing Device (AREA)
  • Prostheses (AREA)

Abstract

一种医用支架操作系统(100),包含:管鞘部(1300),具有第一空腔,该第一空腔沿着管鞘部(1300)的长度方向(810)延伸;握持部(1200),连接管鞘部(1300),且具有第二空腔;操作部(2100),以可移动的方式连接握持部(1200),操作部(2100)具有第一操作端部(2110)以及第二操作端部(2120),第一操作端部(2110)设置于第二空腔内,第二操作端部(2120)设置于握持部(1200)外;以及支架移动部(2400),连接第一操作端部(2110),并延伸于第一空腔以及第二空腔内,支架移动部(2400)的末端接触医用支架;其中操作部(2100)相对于握持部(1200)移动,并通过支架移动部(2400)使医用支架移动。

Description

医用支架操作系统 技术领域
本发明涉及一种医用支架操作系统,特别涉及一种可协助将医用支架置入人体,或可协助将医用支架自人体取出的医用支架操作系统。
背景技术
目前传统用于前列腺手术或膀胱颈切开手术的医用支架虽可改善前列腺肥大的问题,但如何将医用支架置入人体内正确位置,或是如何将医用支架自人体取出,仍需由医师凭其经验进行,而往往具有一定的风险。有鉴于此,将需要一种可协助将医用支架置入人体,或可协助将医用支架自人体取出的医用支架操作系统。
发明内容
为了解决上述问题,本发明的一构想在于提供一种可协助将医用支架置入人体,或可协助将医用支架自人体取出的医用支架操作系统。
基于前述构想,本发明提供一种医用支架操作系统,包含:管鞘部,具有第一空腔,该第一空腔沿着该管鞘部的长度方向延伸;握持部,连接该管鞘部,且具有第二空腔;操作部,以可移动的方式连接该握持部,该操作部具有第一操作端部以及第二操作端部,该第一操作端部设置于该第二空腔内,该第二操作端部设置于该握持部外;以及支架移动部,连接该第一操作端部,并延伸于该第一空腔以及该第二空腔内,该支架移动部的末端接触医用支架;其中该操作部相对于该握持部移动,并通过该支架移动部使该医用支架移动。
于本发明的一较佳实施例中,该管鞘部呈透明管状体。
于本发明的一较佳实施例中,该医用支架操作系统进一步包含:光学感测装置,具有感测部以及传输部,该感测部连接该传输部;其中该感测部设 置于该握持部的握持末端;其中该感测部至少部分设置于该管鞘部内,且该感测部位于该管鞘部的管鞘末端;其中该传输部至少部分延伸设置于该第一空腔内。
于本发明的一较佳实施例中,该支架移动部具有推动部,该推动部设置于该支架移动部的末端,该推动部呈中空圆筒状,且该推动部以可相对于该传输部移动的方式而套合于该传输部。
于本发明的一较佳实施例中,该管鞘部具有管鞘末端,该管鞘末端具有侧向连通出口。
于本发明的一较佳实施例中,该支架移动部具有勾合部,该勾合部设置于该支架移动部的末端。
于本发明的一较佳实施例中,该管鞘部以可拆卸的方式连接该握持部。
于本发明的一较佳实施例中,该支架移动部具有一推动部,该推动部设置于该支架移动部的末端。
于本发明的一较佳实施例中,该医用支架具有第一撑开段、第二撑开段以及第三撑开段,该第三撑开段设置于该第一撑开段与该第二撑开段之间;其中该医用支架操作系统具有阶段式移动机构,该操作部通过该阶段式移动机构而阶段式地相对于该握持部移动,并使该第一撑开段、该第三撑开段以及该第二撑开段阶段式地被该支架移动部依序推出于该管鞘部外。
于本发明的一较佳实施例中,该阶段式移动机构为该握持部具有多个卡合孔,该操作部的该第一操作端部具有卡合部,该卡合部于该操作部相对于该握持部移动的过程中,与该多个卡合孔的其中一个相卡合。
于本发明的一较佳实施例中,该多个卡合孔包含第一卡合孔、第二卡合孔以及第三卡合孔;其中当该卡合部与该第一卡合孔相卡合时,该第一撑开段被该支架移动部推出于该管鞘部外;其中当该卡合部与该第二卡合孔相卡合时,该第三撑开段被该支架移动部推出于该管鞘部外;其中当该卡合部与该第三卡合孔相卡合时,该第二撑开段被该支架移动部推出于该管鞘部外。
于本发明的一较佳实施例中,该握持部具有长型通孔,该长型通孔沿着 该握持部的长度方向延伸设置于该握持部上,该操作部的该第一操作端部具有突出部,该突出部经由该长型通孔向外突出,且该突出部可沿着该长型通孔移动。
于本发明的一较佳实施例中,该医用支架具有第一撑开段、第二撑开段以及第三撑开段,该第三撑开段设置于该第一撑开段与该第二撑开段之间;其中该长型通孔具有通孔端部,该医用支架操作系统通过使该突出部接触于该通孔端部,而令该操作部无法沿着推出方向相对于该握持部继续移动;其中当该突出部接触于该通孔端部时,该医用支架操作系统通过该支架移动部使该医用支架的该第二撑开段部分露出于该管鞘部外。
于本发明的一较佳实施例中,该突出部受到第一外力而离开该通孔端部并离开该长型通孔,该操作部接着受到第二外力而沿着该推出方向相对于该握持部移动,并使该第二撑开段被该支架移动部推出于该管鞘部外。
于本发明的一较佳实施例中,该管鞘部具有液体输送部,该液体输送部连通该第一空腔,该医用支架操作系统经由该液体输送部将一液体输送至该管鞘部内。
本发明前述各方面及其它方面依据下述的非限制性具体实施例详细说明以及参照附随的附图将更趋于明了。
附图说明
图1为本发明医用支架操作系统一具体实施例的示意图。
图2A为本发明医用支架操作系统的握持部以及光学感测装置一具体实施例的示意图。
图2B为本发明医用支架操作系统的操作部以及支架移动部一具体实施例的示意图。
图2C为本发明医用支架操作系统的管鞘部一具体实施例的示意图。
图3为本发明医用支架操作系统的支架移动部一具体实施例的局部示意图。
图4为管鞘部、延伸部以及推动部一具体实施例的局部示意图。
图5为管鞘部、延伸部以及勾合部一具体实施例的局部示意图。
附图说明如下:
810     长度方向
820     推出方向
830     方向
1000    医学内视镜系统
1100    操作部
1140    突出部
1200    握持部
1240    长型通孔
1300    管鞘部
1310    侧向连通出口
1320    管鞘末端
1520    传输部
1600    保护部
2100    操作部
2110    第一操作端部
2120    第二操作端部
2130    卡合部
2140    突出部
2200    握持部
2210    握持主体部
2220    延伸部
2232、2234、2236    卡合孔
2240    长型通孔
2250    握持卡合部
2300    管鞘部
2320    管鞘末端
2330    管鞘延伸部
2340、2350    液体输送部
2360    卡合孔
2370    管鞘主体部
2400    支架移动部
2410    推动部
2510    感测部
2520    传输部
2530    处理部
3400    支架移动部
3420    勾合部
4220    握持延伸部
4330    管鞘延伸部
4400    支架移动部
4410    推动部
4510    感测部
5220    握持延伸部
5330    管鞘延伸部
5400    支架移动部
5420    勾合部
5510    感测部
具体实施方式
请参阅图1,其例示说明了根据本发明医用支架操作系统一具体实施例的示意图。如图1所示实施例,医用支架操作系统100包含操作部1100、握 持部1200、管鞘部1300、支架移动部(图中未示出,于后将详细说明)、光学感测装置(图中未示出,于后将详细说明)以及保护部1600。管鞘部1300为中空组件,其内具有第一空腔,该第一空腔沿着管鞘部1300的长度方向810延伸。较佳地,管鞘部1300的管鞘末端1320处可具有侧向连通出口1310(侧向连通出口1310的设置方式可参考申请号第110103890号的台湾地区发明专利,其发明名称为“手术用医疗装置及其系统”。在此并以引用记载方式将申请号第110103890号的台湾地区发明专利全文并入本文中)。握持部1200为中空组件,其内具有第二空腔。管鞘部1300以可拆卸的方式连接握持部1200。操作部1100以可移动的方式连接握持部1200,其中,操作部1100具有第一操作端部以及第二操作端部,操作部1100的第一操作端部设置于握持部1200的第二空腔内,而操作部1100的第二操作端部设置于握持部1200外。较佳地,操作部1100与握持部1200之间的连接关系以及作动关系类似于一般医用针筒装置的推杆部与针筒部。
医用支架操作系统1000的支架移动部连接于操作部1100的第一操作端部,且支架移动部延伸于第一空腔以及第二空腔内。在通过医用支架操作系统100以操作(或移动)医用支架的过程中,医用支架可先放置于管鞘部1300内(较佳地,医用支架先放置于管鞘部1300内,靠近管鞘部1300的管鞘末端1320的位置),并使医用支架接触支架移动部的末端。使用者可接着通过将操作部1100相对于握持部1200移动,而通过连接于操作部1100的支架移动部使医用支架移动,并逐渐将医用支架推出于管鞘部1300外。保护部1600以可拆卸的方式装设(例如塞设于)于管鞘部1300的管鞘末端1320,藉以保护管鞘部1300以及位于管鞘部1300内的支架移动部及光学感测装置。其中,光学感测装置的传输部1520(例如传输线)可延伸设置于第一空腔以及第二空腔内。应了解,在使用医用支架操作系统100的过程中,即可无需使用保护部1600,而可将保护部1600自管鞘部1300的管鞘末端1320移除。在一具体实施例中,也可无需具有保护部1600。
请参阅图2A,其例示说明了根据本发明医用支架操作系统的握持部以及 光学感测装置一具体实施例的示意图。如图2A所示实施例,握持部2200包含握持主体部2210以及延伸部(或可称为握持延伸部)2220,握持主体部2210连接延伸部2220。握持主体部2210具有卡合孔(可称为握持卡合孔)2232、2234、2236、长型通孔2240以及握持卡合部2250。其中,卡合孔2232较长型通孔2240更靠近延伸部2220,长型通孔2240沿着握持部2200的长度方向延伸设置于握持部2200的握持主体部2210上。较佳地,长型通孔2240的通孔端部2242设置于卡合孔2234与卡合孔2232之间。医用支架操作系统的光学感测装置包含感测部2510以及传输部2520,感测部2510连接传输部2520。感测部2510设置(或连接)于延伸部2220的末端(可称为握持末端)处,传输部2520延伸设置于握持部2200的第二空腔内(详细而言,传输部2520延伸设置于延伸部2220内以及主体部2210内,并自主体部2210向外延伸)。感测部2510可在医用支架操作系统的操作过程中获取体内影像,并可通过传输部将所获取到的影像传送至显示设备以供用户观看影像。在一具体实施例中,传输部2520可具有处理部2530,其可协助处理感测部2510所获取到的影像。
请参阅图2B,其例示说明了根据本发明医用支架操作系统的操作部以及支架移动部一具体实施例的示意图。如图2B所示实施例,操作部2100具有第一操作端部2110、第二操作端部2120、卡合部2130以及突出部2140。卡合部2130以及突出部2140均设置于第一操作端部2110上。支架移动部2400的一端连接操作部2100,支架移动部2400的另一端(可称为末端或支架移动末端)具有推动部2410。如此,当使用者移动(或操作)操作部2100时,支架移动部2400即会随着操作部2100移动,并可通过推动部2410以推动医用支架。在一具体实施例中,支架移动部2400的末端不具有推动部,而是具有勾合部。如此,使用者即可通过勾合部以勾住医用支架,并可接着通过移动(或操作)操作部2100以拉动医用支架。图3即例示说明了支架移动部2400的末端具有勾合部的一具体实施例,如图3所示实施例,支架移动部3400的末端具有勾合部3420。
请参阅图2C,其例示说明了根据本发明医用支架操作系统的管鞘部一具体实施例的示意图。如图2C所示实施例,管鞘部2300具有管鞘主体部2370、管鞘延伸部2330、液体输送部2340、2350以及卡合孔(可称为管鞘卡合孔)2360。管鞘主体部2370连接管鞘延伸部2330,液体输送部2340、2350连接管鞘主体部2370,卡合孔2360设置于管鞘主体部2370上。液体输送部2340、2350连通管鞘部2300的第一空腔,如此,即可经由液体输送部2340、2350将液体(例如水、生理食盐水等,但不以此为限)输送至该管鞘部2300内。
请同时参阅图2A、图2B以及图2C。支架移动部2400可延伸设置于管鞘部2300的第一空腔以及握持部2200的第二空腔内。支架移动部2400的末端可接触医用支架。例如当支架移动部2400的末端具有推动部2410时,则可通过支架移动部2400的推动部2410以将医用支架逐渐推出于管鞘部2300的外部。而当支架移动部2400的末端具有勾合部时,则可通过支架移动部2400的勾合部以将医用支架逐渐拉进管鞘部2300的内部(即第一空腔内)。
支架移动部2400以及握持部2200的延伸部2220可同时延伸设置于管鞘部2300的第一空腔。较佳地,当支架移动部2400的末端具有推动部2410时,推动部2410可呈中空圆筒状,且推动部2410以可相对于传输部2520以及延伸部2220移动的方式而套合于该传输部2520以及延伸部2220。图4即例示说明了管鞘部、延伸部以及推动部一具体实施例的局部示意图,如图4所示实施例,握持延伸部4220以及支架移动部4400设置于管鞘延伸部4330内。支架移动部4400的末端具有推动部4410,推动部4410呈中空圆筒状,且推动部4410以可相对于握持延伸部4220移动的方式而套合于握持延伸部4220。其中,由于光学感测装置的传输部延伸设置于握持延伸部4220内,因此,推动部4410也是以可相对于传输部移动的方式而套合于传输部。通过此种配置方式,当用户通过使操作部相对于握持部移动,而使推动部4410相对于握持延伸部4220以及传输部移动时,位于握持延伸部4220的末端处的感测部4510仍可继续获取影像,而不受到推动部4410的影响。较佳地,管鞘部呈透明管状体,或至少管鞘部的管鞘延伸部4330呈透明管状体,如此可避 免管鞘部的管鞘延伸部4330遮挡到感测部4510的视野。在一具体实施例中,传输部部分延伸设置于握持延伸部4220内(也即传输部部分延伸设置于管鞘部的第一空腔内),且传输部部分延伸设置于握持部的第二空腔内。较佳地,在感测部4510获取影像的过程中,感测部4510设置于管鞘部的管鞘延伸部4330内,且被放置于(或设置于)管鞘延伸部4330的管鞘末端处。其中,感测部4510可视需求而完全设置于管鞘部内,或略为露出于管鞘末端外。而当握持延伸部4220相对于管鞘延伸部4330移动时(例如握持延伸部4220自管鞘延伸部4330内被移除),感测部4510即可随着握持延伸部4220而相对于管鞘延伸部4330移动(例如感测部4510可随着握持延伸部4220而自管鞘延伸部4330内被移除)。
请参阅图5,其例示说明了管鞘部、延伸部以及勾合部一具体实施例的局部示意图。如图5所示实施例,握持延伸部5220以及支架移动部5400设置于管鞘延伸部5330内,支架移动部5400的末端具有勾合部5420。当使用者通过使操作部相对于握持部移动,而使勾合部5420相对于握持延伸部5220以及传输部移动时,位于握持延伸部5220的末端处的感测部5510仍可继续获取影像,而不受到勾合部5420的影响。较佳地,管鞘部呈透明管状体,或至少管鞘部的管鞘延伸部5330呈透明管状体,如此可避免管鞘部的管鞘延伸部5330遮挡到感测部5510的视野。较佳地,在感测部5510获取影像的过程中,感测部5510设置于管鞘部的管鞘延伸部5330内,且被放置于(或设置于)管鞘延伸部5330的管鞘末端处。其中,感测部5510可视需求而完全设置于管鞘部内,或略为露出于管鞘末端外。而当握持延伸部5220相对于管鞘延伸部5330移动时(例如握持延伸部5220自管鞘延伸部5330内被移除),感测部5510即可随着握持延伸部5220而相对于管鞘延伸部5330移动(例如感测部5510可随着握持延伸部5220而自管鞘延伸部5330内被移除)。
本发明的医用支架操作系统所操作(或移动)的医用支架可具有第一撑开段、第二撑开段以及第三撑开段,第三撑开段设置于第一撑开段与第二撑开段之间(此类医用支架可参考前述申请号第110103890号的台湾地区发明 专利。然而,应了解,本发明的医用支架操作系统并非仅可用于此类的医用支架)。本发明的医用支架操作系统可具有阶段式移动机构,其中,操作部可通过阶段式移动机构而阶段式地相对于握持部移动,并进而使第一撑开段、第三撑开段以及第二撑开段阶段式地被支架移动部依序推出于管鞘部外。阶段式移动机构可例如为前述申请号第110103890号的台湾地区发明专利中,图7至图8C所述的容纳装置,但不以此为限。
请回参图2A、图2B以及图2C,医用支架操作系统的阶段式移动机构可例如为握持部2200的握持主体部2210具有卡合孔2232、2234、2236,操作部2100的第一操作端部2110具有卡合部2130,卡合部2130在操作部2100相对于握持部2200移动的过程中,可与卡合孔2232、2234、2236其中一者相卡合。其中,当卡合部2130与卡合孔2236(卡合孔2236可称为第一卡合孔)相卡合时,医用支架的第一撑开段被支架移动部2400的推动部2410推出于管鞘部2300的管鞘末端2320外。当卡合部2130与卡合孔2234(卡合孔2234可称为第二卡合孔)相卡合时,医用支架的第三撑开段被支架移动部2400的推动部2410推出于管鞘部2300的管鞘末端2320外。当卡合部2130与卡合孔2232(卡合孔2232可称为第三卡合孔)相卡合时,医用支架的第二撑开段被支架移动部2400的推动部2410推出于管鞘部2300的管鞘末端2320外。通过上述的阶段式移动机构,使用者即可阶段式地将医用支架的第一撑开段、第三撑开段以及第二撑开段分别置放于人体内的正确位置(第一撑开段、第三撑开段以及第二撑开段各自的正确放置位置可参见前述申请号第110103890号的台湾地区发明专利)。较佳地,当卡合部2130与卡合孔2232、2234、2236其中任一者卡合时,使用者仍可通过施加较大的力,以使卡合部2130与对应的卡合孔解除卡合,并让操作部2100可相对于握持部2200而继续被推或拉动。
操作部2100的突出部2140可经由长型通孔2240向外突出(其间的配置方式可参考图1所绘示的突出部1140以及长型通孔1240),且突出部2140可沿着握持部2200的长型通孔2240移动。如此,操作部2100相对于过持部 2200移动时,突出部2140将不会影响操作部2100与过持部2200之间的作动。但是,在卡合部2130自卡合孔2234向卡合孔2232移动的过程中,于卡合部2130与卡合孔2232相卡合之前,突出部2140会先接触到长型通孔2240的通孔端部2242,并使操作部2100无法沿着推出方向820相对于握持部2200继续移动。此时,医用支架的第二撑开段部分露出于管鞘部2300的管鞘末端2320外。此机制可避免使用者在操作部2100的过程中,因施力过度而令第二撑开段太快被完全推出于管鞘末端2320外,进而导致第二撑开段被放置于错误位置,或导致医用支架伤害到人体的情况发生。
当突出部2140接触到长型通孔2240的通孔端部2242时,使用者可对突出部2140施加第一外力(第一外力可例如为在垂直于操作部2100的延伸方向上,按压突出部214的力),使突出部2140离开通孔端部2242并离开该长型通孔2240。使用者可接着对操作部2100施加第二外力(即继续朝方向830推动操作部2100),以使操作部2100沿着推出方向820相对于握持部2200移动,并使医用支架的第二撑开段被支架移动部2400的推动部2410推出于管鞘部2300的管鞘末端2320外。
握持部2200的握持卡合部2250可与管鞘部2300的卡合孔2360相卡合,以将握持部2200较稳固地连接于管鞘部2300。使用者并可依需求而使卡合部2250与卡合孔2360解除卡合,并进一步将握持部2200与管鞘部2300彼此分开。例如在用户通过医用支架操作系统以将医用支架自患者体内向外移除的过程中,即可先通过支架移动部2400的勾合部以勾住医用支架,接着在将卡合部2250与卡合孔2360解除卡合,并通过拉动操作部2100及/或握持部2200,以将支架移动部2400及/或握持部2200的延伸部2220自管鞘延伸部2330内向外移除。如此,医用支架即会随着勾合部被移除于人体外。
至此,本发明的医用支架操作系统已经由上述说明及附图加以说明。然而,应了解,本发明的各个具体实施例仅是作为说明的目的,在不脱离本申请的保护范围与精神下可进行各种改变,且均应包含于本发明的专利范围中。因此,本说明书所描述的各具体实施例并非用以限制本发明,本发明的真实 范围与精神揭示于以下权利要求书。

Claims (15)

  1. 一种医用支架操作系统,包含:
    管鞘部,具有第一空腔,所述第一空腔沿着所述管鞘部的长度方向延伸;
    握持部,连接所述管鞘部,且具有第二空腔;
    操作部,以可移动的方式连接所述握持部,所述操作部具有第一操作端部以及第二操作端部,所述第一操作端部设置于所述第二空腔内,所述第二操作端部设置于所述握持部外;以及
    支架移动部,连接所述第一操作端部,并延伸于所述第一空腔以及所述第二空腔内,所述支架移动部的末端接触医用支架;
    其中所述操作部相对于所述握持部移动,并通过所述支架移动部使所述医用支架移动。
  2. 如权利要求1所述的医用支架操作系统,其中所述管鞘部呈透明管状体。
  3. 如权利要求1所述的医用支架操作系统,进一步包含:
    光学感测装置,具有感测部以及传输部,所述感测部连接所述传输部;
    其中所述感测部设置于所述握持部的握持末端;
    其中所述感测部至少部分设置于所述管鞘部内,且所述感测部位于所述管鞘部的管鞘末端;
    其中所述传输部至少部分延伸设置于所述第一空腔内。
  4. 如权利要求3所述的医用支架操作系统,其中所述支架移动部具有推动部,所述推动部设置于所述支架移动部的末端,所述推动部呈中空圆筒状,且所述推动部以可相对于所述传输部移动的方式而套合于所述传输部。
  5. 如权利要求1所述的医用支架操作系统,其中所述管鞘部具有管鞘末端,所述管鞘末端具有侧向连通出口。
  6. 如权利要求1所述的医用支架操作系统,其中所述支架移动部具有勾 合部,所述勾合部设置于所述支架移动部的末端。
  7. 如权利要求1所述的医用支架操作系统,其中所述管鞘部以可拆卸的方式连接所述握持部。
  8. 如权利要求1所述的医用支架操作系统,其中所述支架移动部具有推动部,所述推动部设置于所述支架移动部的末端。
  9. 如权利要求1所述的医用支架操作系统,其中所述医用支架具有第一撑开段、第二撑开段以及第三撑开段,所述第三撑开段设置于所述第一撑开段与所述第二撑开段之间;
    其中所述医用支架操作系统具有阶段式移动机构,所述操作部通过所述阶段式移动机构而阶段式地相对于所述握持部移动,并使所述第一撑开段、所述第三撑开段以及所述第二撑开段阶段式地被所述支架移动部依序推出于所述管鞘部外。
  10. 如权利要求9所述的医用支架操作系统,其中所述阶段式移动机构为所述握持部具有多个卡合孔,所述操作部的所述第一操作端部具有卡合部,所述卡合部于所述操作部相对于所述握持部移动的过程中,与所述多个卡合孔的其中一个相卡合。
  11. 如权利要求10所述的医用支架操作系统,其中所述多个卡合孔包含第一卡合孔、第二卡合孔以及第三卡合孔;
    其中当所述卡合部与所述第一卡合孔相卡合时,所述第一撑开段被所述支架移动部推出于所述管鞘部外;
    其中当所述卡合部与所述第二卡合孔相卡合时,所述第三撑开段被所述支架移动部推出于所述管鞘部外;
    其中当所述卡合部与所述第三卡合孔相卡合时,所述第二撑开段被所述支架移动部推出于所述管鞘部外。
  12. 如权利要求1所述的医用支架操作系统,其中所述握持部具有长型通孔,所述长型通孔沿着所述握持部的长度方向延伸设置于所述握持部上, 所述操作部的所述第一操作端部具有突出部,所述突出部经由所述长型通孔向外突出,且所述突出部可沿着所述长型通孔移动。
  13. 如权利要求12所述的医用支架操作系统,其中所述医用支架具有第一撑开段、第二撑开段以及第三撑开段,所述第三撑开段设置于所述第一撑开段与所述第二撑开段之间;
    其中所述长型通孔具有通孔端部,所述医用支架操作系统通过使所述突出部接触于所述通孔端部,而令所述操作部无法沿着推出方向相对于所述握持部继续移动;
    其中当所述突出部接触于所述通孔端部时,所述医用支架操作系统通过所述支架移动部使所述医用支架的所述第二撑开段部分露出于所述管鞘部外。
  14. 如权利要求13所述的医用支架操作系统,其中所述突出部受到第一外力而离开所述通孔端部并离开所述长型通孔,所述操作部接着受到第二外力而沿着所述推出方向相对于所述握持部移动,并使所述第二撑开段被所述支架移动部推出于所述管鞘部外。
  15. 如权利要求1所述的医用支架操作系统,其中所述管鞘部具有液体输送部,所述液体输送部连通所述第一空腔,所述医用支架操作系统经由所述液体输送部将液体输送至所述管鞘部内。
PCT/CN2022/110924 2021-08-08 2022-08-08 医用支架操作系统 WO2023016421A1 (zh)

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