The present disclosure relates to medical devices. More particularly, the disclosure relates to internal seals within endoscope systems.
The statements in this section merely provide background information related to the present disclosure and may not constitute prior art.
Internal body cavities and body lumens may become blocked, or the walls surrounding them may develop growths. In some cases, removal of these blockages or growths, or other treatment thereof, may be necessary. Endoscopic or other minimally invasive techniques may be used to treat these situations.
One type of treatment includes the use of catheters or other endoscopic devices that are inserted into the body lumen or cavity and toward the area where treatment is desired. Insertion of the endoscope to the target area can allow for visualization of the target area and a determination of the desired procedure and the specific location of the area to be treated.
In general, endoscopes have been designed to be operated with the same fundamental mechanisms, and have not had transformational improvements. Endoscopes generally include a camera and a set of wheels that an operator, such as a physician, operates with a first hand (in some cases, the left hand) to control scope deflection, while the second (generally, right) hand switches between the insertion tube of the endoscope and the accessory channel in order to control scope and device advancement, respectively, through the anatomy of a patient.
Specialized endoscopes, tailored to specific procedures, are becoming more common in the field of endoscopy with the trend from reusable scopes to disposable scopes. Whereas traditional endoscopes include accessory channel(s) that are fixed from axial movement, specialized endoscopes may include a feature in which the accessory channels may move proximally or distally so as to change the camera between forward-viewing and side-viewing configurations. Escape of gas from the proximal end of the insertion tube should be minimized, and the escape of gas has traditionally been minimized by use of static seals. Given the proximal or distal movement of accessory channels in some specialized endoscopes, static sealing methods used in traditional endoscopes are not possible between the accessory channels and the insertion tube. Further, in such specialized endoscopes, deflection wires, coils, or cables used to provide deflection of the distal end of the endoscope must be exposed distally to allow the accessory channels to deflect between the bending section linkages. Accordingly, static sealing around the deflection wires is insufficient. Additionally, in such specialized endoscopes, electrical or fiber optic wires are used to provide power, one-way signaling, two-way signaling, communication for data, or light at the distal end of the endoscope to power LED(s), other sensors, circuits, or light, and static sealing around electrical or fiber optic wires is insufficient.
In an example, the present disclosure provides a medical device. The medical device includes an elongate tube including a lumen extending therethrough, the elongate tube defining a longitudinal axis therethrough. The medical device further includes a movable member extending longitudinally at least partially within the lumen. The medical device further includes a dynamic seal, including a dynamic seal member at a proximal end of the elongate tube, the movable member configured to translate proximally and distally through the dynamic seal member, and a flexible seal through which the movable member extends longitudinally. The dynamic seal member is configured to prevent fluid from flowing proximally to the dynamic seal member. The flexible seal member may be an elastomeric seal. The flexible seal may include an amorphous sealing material. The movable member may be an accessory channel of an endoscope system. The movable member may be a deflection wire of an endoscope system. The movable member may be an electrical wire or a fiber-optic wire of an endoscope system. The medical device may include a plurality of movable members and the dynamic seal may include a plurality of flexible seals, one movable member of the plurality of movable members each extending extend through one flexible seal of the plurality of flexible seals. The medical device may include a second dynamic seal member wherein the dynamic seal member may be within the second dynamic seal member and the second dynamic seal member may be rotationally decoupled from the dynamic seal member. The dynamic seal member may be variably adjustable and configured to increase or decrease friction on the movable member.
In another example, the present disclosure provides a medical device. The medical device includes an elongate tube including a lumen extending therethrough, the elongate tube defining a longitudinal axis therethrough. The medical device further includes a movable member extending longitudinally at least partially within the lumen. The medical device further includes a first dynamic seal member at a proximal end of the elongate tube, the movable member configured to translate proximally and distally through the first dynamic seal member. The medical device further includes a flexible seal through which the movable member extends longitudinally. The medical device further includes a second dynamic seal member rotationally decoupled from the first dynamic seal member. The first dynamic seal member is within the second dynamic seal member. The first dynamic seal member is configured to prevent fluid from flowing proximally to the first dynamic seal member. The flexible seal may be an elastomeric seal. The flexible seal may include an amorphous sealing material. The movable member may be an accessory channel of an endoscope system. The movable member may be a deflection wire of an endoscope system. The movable member may be an electrical wire or a fiber-optic wire of an endoscope system. The medical device may include a plurality of movable members and the first dynamic seal member may include a plurality of flexible seals, one movable member of the plurality of movable members each extending through one flexible seal of the plurality of flexible seals. The medical device may include a catch proximal to the second dynamic seal member, the second dynamic seal member configured to move between a locked configuration and an unlocked configuration, the second dynamic seal member being biased to the locked configuration. When the second dynamic seal member is in the unlocked configuration, the second dynamic seal member may be rotatable about the longitudinal axis relative to the first dynamic seal member. When the second dynamic seal member is in the locked configuration, the second dynamic seal member may engage with the catch and not be rotatable about the longitudinal axis relative to the first dynamic seal member.
In yet another example, the present disclosure provides a medical device. The medical device includes a lumen extending therethrough, the elongate tube defining a longitudinal axis therethrough. The medical device further includes a movable member extending longitudinally at least partially within the lumen. The medical device further includes a dynamic seal includes a dynamic seal member at a distal end of the elongate tube, the movable member configured to translate proximally and distally through the dynamic seal member and a flexible seal through which the movable member extends longitudinally. The dynamic seal member may be configured to prevent fluid from flowing proximally to the dynamic seal member.
Further areas of applicability will become apparent from the description provided herein. It should be understood that the description and specific examples are intended for purposes of illustration only and are not intended to limit the scope of the present disclosure.
In order that the present disclosure may be well understood, there will not be described various forms thereof, given by way of example, reference being made to the accompanying drawings. The components in the figures are not necessarily to scale. Moreover, in the figures, like-referenced numerals designate corresponding parts through the different views.
The drawings described herein are for illustration purposes only and are not intended to limit the scope of the present disclosure in any way.
The following description is merely exemplary in nature and is not intended to limit the present disclosure, application, or uses. It should be understood that throughout the drawings, corresponding reference numerals indicate like or corresponding parts and features.
In adding reference denotations to elements of each drawing, although the same elements are displayed on a different drawing, it should be noted that the same elements have the same denotations. In addition, in describing one aspect of the present disclosure, if it is determined that a detailed description of related well-known configurations or functions blurs the gist of one aspect of the present disclosure, it will be omitted.
In the following discussion, the terms “proximal” and “distal” will be used to describe the opposing axial ends of the device, as well as the axial ends of various component features. The term “proximal” is used in its conventional sense to refer to the end of the device (or component) that is closest to the medical professional during use of the assembly. The term “distal” is used in its conventional sense to refer to the end of the device (or component) that is initially inserted into the patient, or that is closest to the patient during use. The term “longitudinal” will be used to refer to an axis that aligns with the proximal-distal axis of the device (or component). The terms “radially” and “radial” will be used to refer to elements, surfaces, or assemblies relative to one another that may extend perpendicularly from a longitudinal axis. The terms “circumference,” “circumferentially,” and “circumferential” will be used to refer to elements, surfaces, or assemblies relative to one another encircling a longitudinal axis at a radius. The terms “diameter” and “diametrical” refer to a line passing through a circle that touches two points on the circumference of the circle and the center of the circle. The terms “chord” and “chordal” refer to a line passing through a circle that touches two points on the circumference of the circle but does not touch the center of the circle.
The uses of the terms “a” and “an” and “the” and similar referents in the context of describing the present disclosure (especially in the context of the following claims) are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. The use of the term “plurality of” is defined by the Applicant in the broadest sense, superseding any other implied definitions or limitations hereinbefore or hereinafter unless expressly asserted by the Applicant to the contrary, to mean a quantity of more than one. Recitation of ranges of values herein are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if it were individually recited herein. All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context.
As used herein the terms “comprise(s),” “include(s),” “having,” “has,” “can,” “contain(s),” and variants thereof, are intended to be open-ended transitional phrases, terms, or words that do not preclude the possibility of additional acts or structures. The present description also contemplates other examples “comprising,” “consisting of,” “and consisting essentially of,” the examples or elements presented herein, whether explicitly set forth or not.
In describing elements of the present disclosure, the terms 1st, 2nd, first, second, A, B, (a), (b), and the like may be used herein. These terms are only used to distinguish one element from another element, but do not limit the corresponding elements irrespective of the nature or order of the corresponding elements.
Unless otherwise defined, all terms herein, including technical or scientific terms, have the same meanings as those generally understood by those skilled in the art to which the present disclosure pertains. Such terms as those defined in a generally used dictionary are to be interpreted as having meanings equal to the contextual meanings in the relevant field of art.
As used herein, the term “about,” when used in the context of a numerical value or range set forth means a variation of ±15%, or less, of the numerical value. For example, a value differing by ±15%, ±14%, ±10%, or ±5%, among others, would satisfy the definition of “about,” unless more narrowly defined in particular instances.
Referring to
The endoscope system may further include a movable member 40 running through the elongate tube 30 and/or the handle 20. Movable member 40 may be designed as individual elongated tubes that may be movable within the lumen 38 of the elongate tube 30, thus allowing longitudinal movement of the movable member 40 with respect to the elongate tube 30. Examples of movable member 40 may include accessory channel(s), deflection wire(s), electrical wire(s), and fiber-optic wire(s). Electrical wire(s) or fiber-optic wires may provide power, one-way signaling, two-way signaling, communication for data, or light at the distal end of the endoscope to power light emitting diode(s) (LED(s)), other sensors, circuits, or light. When the elongate tube 30 is in a straight configuration, elongate tube 30 defines a longitudinal axis running centrally therethrough, which represents the axis about which elongate tube 30 may rotate relative to handle 20. In practice, even when elongate tube 30 is not in a straight configuration, the longitudinal axis is still defined at the same position, and the portion of elongate tube 30 that is outside of the body of the patient and that substantially surrounds the longitudinal axis will be rotatable about said axis.
While
As illustrated by
Middle dynamic seal member 112 includes bore(s) 126 extending longitudinally through middle dynamic seal member 112, through which movable member(s) 40 may translate in distal and proximal directions. Middle dynamic seal member 112 may be variably adjustable with respect to the dimensions and shape of bore(s) 126 so as to advantageously increase or decrease friction on movable member(s) 40 translating through one or more bores 126 as is necessary, desirable, or preferable. Middle dynamic seal member 112 may include deflection bore(s) 130 extending longitudinally through middle dynamic seal member 112 through which movable member(s) such as deflection wires 402, 404 may translate in distal and proximal directions. Deflection bore(s) 130 are configured to align longitudinally with seal bore(s) 128 in arcuate seals 114, through which deflection wires 402, 404 may translate in distal and proximal directions. Alternatively, or additionally, though not shown in the example illustrated in
Bore(s) 126 may generally have a larger diameter than deflection bore(s) 130 or seal bore(s) 128. Alternatively, bore(s) 126 may generally have the same diameter as, or even a smaller diameter than, deflection bore(s) 130 or seal bore(s) 128. Deflection bore(s) 130 and seal bore(s) 128 may have approximately the same diameter and general size.
Each of seals 110 and 116 and arcuate seals 114 may be formed of flexible silicone, rubber, plastic, elastomer, amorphous sealing material, or any other material suitable to substantially prevent (or at least impede) fluid from flowing across and/or permeating through it. Each of upper dynamic seal member 106, middle dynamic seal member 112, or lower dynamic seal member 118 may be formed of nitrile (Buna), neoprene, ethylene propylene diene monomer (EPDM) rubber, silicone, fluorocarbon (Viton), polytetrafluoroethylene (PTFE, Teflon), perfluoroelastomers (FFKM), or any elastomer. Additionally, each of upper dynamic seal member 106, middle dynamic seal member 112, or lower dynamic seal member 118 may be encapsulated by an additional material such as fluorinated ethylene propylene (FEP) copolymer.
A handle with a locking mechanism as described herein may be used in a number of medical device systems, particularly endoscopes. In particle, the handle of the present disclosure may be used in conjunction with the scopes, devices, and systems described in U.S. patent application Ser. No. 15/445,318 and U.S. patent application Ser. No. 15/445,518, the entire contents of both of which are hereby incorporated by reference herein in their entireties.
Although the present disclosure has been described with reference to examples and the accompanying drawings, the present disclosure is not limited thereto, but may be variously modified and altered by those skilled in the art to which the present disclosure pertains without departing from the spirit and scope of the present disclosure.
The subject-matter of the disclosure may also relate, among others, to the following aspects:
A first aspect relates to a medical device, comprising: an elongate tube comprising a lumen extending therethrough, the elongate tube defining a longitudinal axis therethrough; a movable member extending longitudinally at least partially within the lumen; and a dynamic seal, comprising: a dynamic seal member at a proximal end of the elongate tube, the movable member configured to translate proximally and distally through the dynamic seal member; and a flexible seal through which the movable member extends longitudinally; and wherein the dynamic seal member is configured to prevent fluid from flowing proximally to the dynamic seal member.
A second aspect relates to the medical device of aspect 1, wherein the flexible seal is an elastomeric seal.
A third aspect relates to the medical device of any preceding aspect, wherein the flexible seal comprises an amorphous sealing material.
A fourth aspect relates to the medical device of any preceding aspect, wherein the movable member is an accessory channel of an endoscope system.
A fifth aspect relates to the medical device of any one of aspects 1 to 3, wherein the movable member is a deflection wire of an endoscope system.
A sixth aspect relates to the medical device of any one of aspects 1 to 3, wherein the movable member is an electrical wire or a fiber-optic wire of an endoscope system.
A seventh aspect relates to the medical device of any preceding aspect, comprising a plurality of movable members, wherein the dynamic seal comprises a plurality of flexible seals; and wherein one movable member of the plurality of movable members each extends through one flexible seal of the plurality of flexible seals.
An eighth aspect relates to the medical device of any preceding aspect, further comprising a second dynamic seal member; wherein the dynamic seal member is within the second dynamic seal member; and wherein the second dynamic seal member is rotationally decoupled from the dynamic seal member.
A ninth aspect relates to the medical device of any preceding aspect, wherein the dynamic seal member is variably adjustable and configured to increase or decrease friction on the movable member.
A tenth aspect relates to a medical device, comprising: an elongate tube comprising a lumen extending therethrough, the elongate tube defining a longitudinal axis therethrough; a movable member extending longitudinally at least partially within the lumen; a first dynamic seal member at a proximal end of the elongate tube, the movable member configured to translate proximally and distally through the first dynamic seal member; a flexible seal through which the movable member extends longitudinally; and a second dynamic seal member rotationally decoupled from the first dynamic seal member; wherein the first dynamic seal member is within the second dynamic seal member; and wherein the first dynamic seal member is configured to prevent fluid from flowing proximally to the first dynamic seal member.
An eleventh aspect relates to the medical device of aspect 10, wherein the flexible seal is an elastomeric seal.
A twelfth aspect relates to the medical device of any one of aspects 10 or 11 wherein the flexible seal comprises an amorphous sealing material.
A thirteenth aspect relates to the medical device of any one of aspects 10 to 12, wherein the movable member is an accessory channel of an endoscope system.
A fourteenth aspect relates to the medical device of any one of aspects 10 to 12, wherein the movable member is a deflection wire of an endoscope system.
A fifteenth aspect relates to the medical device of any one of aspects 10 to 12, wherein the movable member is an electrical wire or a fiber-optic wire of an endoscope system.
A sixteenth aspect relates to the medical device of any one of aspects 10 to 15, comprising a plurality of movable members; wherein the first dynamic seal member comprises a plurality of flexible seals; and wherein one movable member of the plurality of movable members each extends through one flexible seal of the plurality of flexible seals.
A seventeenth aspect relates to the medical device of any one of aspects 10 to 16, further comprising a catch proximal to the second dynamic seal member; and wherein the second dynamic seal member is configured to move between a locked configuration and an unlocked configuration, the second dynamic seal member being biased to the locked configuration.
An eighteenth aspect relates to the medical device of aspect 17, wherein, when the second dynamic seal member is in the unlocked configuration, the second dynamic seal member is rotatable about the longitudinal axis relative to the first dynamic seal member.
A nineteenth aspect relates to the medical device of aspect 17, wherein, when the second dynamic seal member is in the locked configuration, the second dynamic seal member engages with the catch and is not rotatable about the longitudinal axis relative to the first dynamic seal member.
A twentieth aspect relates to a medical device, comprising: an elongate tube comprising a lumen extending therethrough, the elongate tube defining a longitudinal axis therethrough; a movable member extending longitudinally at least partially within the lumen; and a dynamic seal, comprising: a dynamic seal member at a distal end of the elongate tube, the movable member configured to translate proximally and distally through the dynamic seal member; and a flexible seal through which the movable member extends longitudinally; and wherein the dynamic seal member is configured to prevent fluid from flowing proximally to the dynamic seal member.
In addition to the features mentioned in each of the independent aspects enumerated above, some examples may show, alone or in combination, the optional features mentioned in the dependent aspects and/or as disclosed in the description above and shown in the figures.
This application claims the benefit of U.S. Patent Application Ser. No. 63/280,700, filed Nov. 18, 2021, the entirety of which is incorporated herein by reference for all purposes.
Number | Date | Country | |
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63280700 | Nov 2021 | US |