The present invention relates generally to endoscope systems.
The following patent publications are believed to represent the current state of the art:
U.S. Pat. Nos. 5,518,501; 5,876,329; and 6,485,409.
There is thus provided in accordance with a preferred embodiment of the present invention an endoscope insertion assembly for performing endoscopy, including an endoscope insertion tube operative for passage through a body cavity, and an optical assembly operative for inspection of the body cavity, the optical assembly being selectably insertable within the endoscope insertion tube.
In accordance with a preferred embodiment of the present invention the optical assembly is selectably detachable from the endoscope insertion tube. Preferably, the endoscope insertion assembly includes a coupling element operative for engaging the optical assembly with the endoscope insertion tube. Additionally, the endoscope insertion tube and the coupling element are operative to isolate the optical assembly from fluids external to the endoscope insertion assembly.
In accordance with another preferred embodiment of the present invention the coupling element includes an optical window adapted for inspection by the optical assembly therethrough. Preferably, the endoscope insertion assembly includes a pulling element operative for selectably inserting the optical assembly within the endoscope insertion tube. Additionally, the pulling element is detachably engaged with the coupling element for selectable detachment therefrom.
In accordance with yet another preferred embodiment of the present invention the endoscope insertion assembly includes a mechanical stopper operative to prevent the optical assembly from being pulled out and frontward of the endoscope insertion tube. Preferably, the endoscope insertion tube further includes an instrument channel. Additionally, the endoscope insertion tube is a flexible endoscope insertion tube.
In accordance with still another preferred embodiment of the present invention the endoscope insertion tube is generally fluid impermeable.
There is thus provided in accordance with another preferred embodiment of the present invention an endoscope insertion assembly for performing endoscopy, including an endoscope insertion tube for passage through a body cavity, and an optical assembly for inspection of the body cavity, the optical assembly being selectably removable from the endoscope insertion tube. Additionally, the optical assembly is selectably insertable within the endoscope insertion tube.
There is thus provided in accordance with yet another preferred embodiment of the present invention a method for preparing an endoscope insertion assembly for performing endoscopy, including providing the endoscope insertion assembly including an endoscope insertion tube operative for passage through a body cavity, and an optical assembly operative for inspection of the body cavity, and selectably inserting the optical assembly within the endoscope insertion tube.
In accordance with a preferred embodiment of the present invention the method includes inspecting the body cavity employing the endoscope insertion assembly. Additionally, the method includes removing the optical assembly from the endoscope insertion tube following the inspection. Preferably, the method includes engaging the optical assembly with the endoscope insertion tube by employing a coupling element.
In accordance with another preferred embodiment of the present invention inspecting the body cavity is performed via an optical window. Preferably, the method includes isolating the optical assembly from fluids external to the endoscope insertion assembly. Additionally, inserting is performed by a pulling element operative for selectably inserting the optical assembly within the endoscope insertion tube.
In accordance with yet another preferred embodiment of the present invention the pulling element is detachably engaged with the coupling element for selectable detachment therefrom. Preferably, the method includes preventing the optical assembly from being pulled out and frontward of the endoscope insertion tube by employing a mechanical stopper.
The present invention will be best understood and appreciated from the following detailed description, taken in conjunction with the drawings in which:
The terms “endoscope” and “endoscopy” are used throughout in a manner somewhat broader than their customary meaning and refer to apparatus and methods which operate within body cavities, passageways and the like, such as, for example, the small intestine, the large intestine, arteries and veins. Although these terms normally refer to visual inspection, as used herein, they are not limited to applications which employ visual inspection and refer as well to apparatus, systems and methods which need not necessarily involve visual inspection.
The term “distal” refers to the remote end of an endoscope, accessory or tool furthest from the operator.
The term “proximal” refers to the end portion of an endoscope, accessory or tool closest to the operator, typically outside an organ or body portion of interest.
Reference is now made to
The detection means 102 may be one or more of a Charged Coupled Device (CCD), a CMOS detector, array of optical fibers, a light guide or other detection means such as detection means used in standard endoscopy or other optical imaging systems. The illumination means 104 may be one or more of a Light Emitting Diode (LED), fiber optic illumination using one fiber or a bundle of fibers, a laser diode, or other means of optical illumination. Passive optical components that may be included in the optical assembly 100, and in particularly included in the detection means 102 and/or in the illumination means 104, may include any optical component, such as lenses, windows, mirrors, optical stops, and opto-mechanical assemblies with a plurality of optical components.
As seen in
Both the data conduits 106 and the illumination conduits 108 may also include means for electrical noise reduction, temperature management, mechanical and electrical durability and other means generally required for electrical and mechanical components and conduits. The detection means 102 may be a conventional CCD such as a FTF2020M CCD commercially available from Dalsa Corporation, of 605 McMurray Rd., Waterloo, Ontario, Canada. The illumination means 104 may be a conventional LED, such as a L3-W34N-BR LED commercially available from Sloan AG of Basle, Switzerland.
Data conduits 106 and illumination conduits 108 may connect to a conventional endoscopy console (not shown) at respective end portions 110 and 112 thereof, via a console interface or a dedicated interface (not shown), as well known in the art. The endoscopy console may include, for example, a CV-100 video system center, a CLV-U20 light source, a SONY PVM-2030 video monitor, and an OFP flushing pump, all commercially available from Olympus America Inc. of 2 Corporate Center Drive, Melville, N.Y. 11747, USA, or a EPK-1000 video processor and a SONY LMD-2140MD medical grade flat panel LCD monitor, all commercially available from Pentax Europe GmbH, 104 Julius-Vosseler St., 22527 Hamburg, Germany.
It is noted that a single illumination means 104 or multiplicity of illumination means 104 may be employed. Additionally, a multiplicity of detection means 102 may be employed.
Data conduits 106 and illumination conduits 108 may be enclosed within a generally cylindrical housing 120 operative to enclose electrical wires 106 and light guide 108. Housing 120 may be constructed of a thin and flexible material, such as a thin TEFLON®, silicone, or PVC tube, thereby providing flexibility and bendability to optical assembly 100, as will be further described hereinbelow with reference to
A generally cylindrical enclosing element 122 may extend from an end portion 124 of housing 120. Enclosing element 122 is operative to encase detection means 102 and illumination means 104, to protect detection means 102 and illumination means 104 from an environment external to the optical assembly 100 and to allow positioning of the optical assembly 100 within an endoscope insertion tube, as will be further described hereinbelow with reference to
A generally circumferential protrusion 126 protrudes from an external surface 128 of enclosing element 122 and is provided to fit within a coupling element, as will be further described hereinbelow with reference to
It is appreciated that optical assembly 100 may be a single-use disposable optical assembly, or a multiple-use optical assembly.
Reference in now made to
A generally circumferential recess 160 extends along an external surface 164 of ring 152 and may be provided to fit within an endoscope insertion tube as will be further described hereinbelow with reference to
End portion 170 extends from ring 152 and defines a protrusion 172 with a generally triangular cross-section circumferentially extending along an external surface 174 of end portion 170. End portion 170 and protrusion 172 are provided to fit within a pulling element so as to allow tight engagement of coupling element 150 with the pulling element but to an extent that pulling element may be disengaged from coupling element 150 by selective exertion of force thereon, as will be further described hereinbelow with reference to
A wall 176 encloses end portion 170 and may be provided to function as an optical window so as to allow optical communication of detection means 102 and illumination means 104 or any other optical device comprised in optical assembly 100, with an environment external to optical assembly 100 during operation, such as in vivo inspection of the gastro-intestinal tract, or other endoscopic procedures.
Wall 176 may be further provided to insulate optical assembly 100, and in particular, detection means 102 and illumination means 104 or any other optical device comprised in optical assembly 100, from an environment external to optical assembly 100. Wall 176 may be formed of any suitable material, such as a thin optically transparent glass or a plastic disc adhered to end portion 170 of coupling element 150. Alternatively, wall 176 may be formed as an integral part of coupling element 150, such as by forming coupling element 150 and wall 176 by optical injection molding of an optically transparent plastic, such as transparent polycarbonate, for example, or any other suitable material.
It is appreciated that coupling element 150 may be a single-use disposable coupling element, or a multi-use coupling element.
Reference is now made to
As seen in
A generally circumferential aperture 220 is defined on a bottom surface 222 of base portion 202 so as to allow pulling element 200 to engage with coupling element 150 and optical assembly 100. An internal surface 224 is defined by aperture 220 within base portion 202.
Base portion 202 may be formed of any suitable material, such as any suitable metal or any suitable hard plastic, which may be injection-molded. Pulling wire 204 may be formed of flexible stainless-steel so as to provide high flexibility and bendability and enhanced pulling strength for pulling optical assembly 100 and coupling element 150 along a passageway in an endoscope insertion tube, as will be further described hereinbelow with reference to
Alternatively, pulling wire 204 may be formed of a rigid material and may be employed with relatively short endoscopes.
Base portion 202 may be attached to pulling wire 204 by any suitable means, such as by being molded together, typically by insert-molding, whereas pulling wire 204 is inserted in a molding dye of base portion 202 prior to injection.
Base portion 202 and pulling wire 204 may be replaced by a tube (not shown) inserted within end portion 170 of coupling element 150 and fixed thereto by tight mounting of tube on protrusion 172 of coupling element 150. It is appreciated that pulling element 200 may be a single-use disposable pulling element, or a multiple-use pulling element.
Reference is now made to
Recess 274 may be provided to allow an O-ring 276 to be seated therein. O-ring 276 is provided to tightly engage endoscope insertion tube 250 with coupling element 150 by being partially seated within recess 274 of endoscope insertion tube 250 and partially seated within corresponding recess 160 of coupling element 150 (
A first throughgoing lumen 282 defined within ring portion 260 and tube portion 252 may operate as an accessory instrument channel 284. Instrument channel 284 may be provided for insertion of endoscopy accessories such as biopsy forceps, injection needles, polyp cutters, and any other endoscopy accessories as well known in the art.
Accessory instrument channel 284 may also be used for suction, as well known in the art A second throughgoing lumen 292 defined within ring portion 260 and tube portion 252 may operate as a channel 294 operative for water rinsing and air inflation, such as for intestinal insufflation forward of the endoscope, as common in endoscopy systems.
It is appreciated that ring portion 260 and tube portion 252 may assume any suitable cross sectional shape, and may comprise a multiplicity of lumens of various cross sections.
It is appreciated that a cross section of endoscope insertion tube 250, and specifically the cross sections of ring portion 260 and tube portion 252, may be of a circular shape or any other appropriate shape.
It is appreciated that endoscope insertion tube 250 may be a single-use disposable endoscope insertion tube, or a multiple-use endoscope insertion tube.
It is appreciated that the outer surface of endoscope insertion tube 250 is generally fluid impermeable, thereby preventing fluid passage therethrough and preventing contamination of bore 272 and optical assembly 100 when located therein, such as during endoscopic operation within a patient body, for example, as will be further describe with reference to
It is appreciated that endoscope insertion tube 250 may include additional components, channels and utilities as needed for performing an endoscopic procedure, such as steering wires or other steering assemblies (not shown) for steering the endoscope insertion tube within a body cavity or bending its distal tip portion, as well known in the art. Endoscope insertion tube 250 may further include an inflatable balloon at its distal portion, for example, to allow anchoring of endoscope insertion tube 250 to the internal walls of an inspected organ, such as the intestines, as described in detail in the above mentioned PCT patent applications PCT/IL2005/000152 and PCT/IL2005/000849 which are hereby incorporated by reference.
It is noted that the body cavity may include any body cavity, such as, for example, a cavity of the large intestine, the small intestine, the stomach, veins, arteries the urinal tract and the bronchi.
It is further appreciated that endoscope insertion tube may be flexible or rigid.
Reference is now made to
As seen in
Reference is now made to
As seen in
Optical assembly 100 is provided to be selectably insertable within passageway 254 of tube portion 252 and bore 272 of ring portion 260 of endoscope insertion tube 250 (
As seen in
It is a particular feature of the present invention that endoscope insertion tube 250 may be provided for one-time use during a single endoscopic operation and may be discarded following the single endoscopic operation. Optical assembly 100 may be employed in a multiplicity of endoscopic operations and therefore may be selectably inserted within endoscope insertion tube 250, prior to the endoscopic operation, and selectably detached, removed or extracted from endoscope insertion tube 250, following the endoscopic operation, so as to be employed in future endoscopic operations. This feature may be employed, for example, for eliminating the cleaning and/or sterilization of endoscope insertion tube 250 after an endoscopic operation, and/or whereas endoscope insertion tube 250 is generally inexpensive in comparison with optical assembly 100, which is generally costly.
Alternatively, optical assembly 100 may be provided for one-time use during a single endoscopic operation and may be discarded following the single endoscopic operation. Endoscope insertion tube 250 may be employed in a multiplicity of endoscopic operations and therefore a new optical assembly 100 may be inserted within endoscope insertion tube 50, prior to the endoscopic operation, and extracted from endoscope insertion tube 250, following the endoscopic operation. It is appreciated that in such a case endoscope insertion tube 250 may be operative to withstand cleaning, disinfecting or sterilization processes.
Single use of endoscope insertion tube 250 may enhance sterility of the endoscopic operation by providing a new, sterile endoscope insertion tube 250 to perform each endoscopic operation, thus obviating the need to reuse the endoscope insertion tube 250, which may come within direct contact with body cavities, passageways and the like during endoscopic operation.
Reference is now made to
In
Reference is now made to
In
Reference is now made to
As seen in
Reference is now made to
As seen in
Extraction of coupling element 150 and optical assembly 100 from ring portion 260 and eventually from endoscope insertion tube 250 (
Reference is now made to
As seen in
Reference is now made to
As seen in
It is appreciated that during an endoscopic operation with endoscope insertion assembly 302, as described hereinabove, the optical assembly 100 may remain isolated and separated from a body organ or a cavity undergoing an endoscopic operation and avoid contact with the body organ, cavity, with other body fluids or with any fluids external to the endoscope insertion assembly. It is further appreciated that by releasing optical assembly 100 from endoscope insertion tube 250 and coupling element 150 as described hereinabove, optical assembly 100 may remain clean and uncontaminated after the endoscopic operation.
It is yet appreciated that even in a case wherein optical assembly 100 is contaminated and unclean, an assembly comprising the endoscope insertion assembly 302 with the coupling element 150, as described hereinabove, prevents optical assembly 100 from contaminating the body organ or cavity undergoing the endoscopic operation, due to the isolation of optical assembly 100 from the body organ or cavity undergoing the endoscopic operation.
It will be appreciated by persons skilled in the art that the present invention is not limited by what has been particularly shown and described herein above. Rather the scope of the present invention includes both combinations and subcombinations of the various features described hereinabove as well as variations and modifications which would occur to persons skilled in the art upon reading the specifications and which are not in the prior art.
This application is a U.S. National Phase Application under 35 U.S.C. 371 of PCT International Application No. PCT/IL2007/000832, which has an international filing date of Jul. 4, 2007, and which claims priority from U.S. Provisional Patent Application No. 60/818,505, filed Jul. 6, 2006, the disclosures of which are incorporated herein by reference in their entirety. Reference is made to applicant's copending PCT Application No. PCT/IL2005/000152, filed Feb. 7, 2005, and PCT Application No. PCT/IL2005/000849, filed Aug. 8, 2005, the disclosures of which are hereby incorporated by reference.
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PCT/IL2007/000832 | 7/4/2007 | WO | 00 | 1/1/2009 |
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WO2008/004228 | 1/10/2008 | WO | A |
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