The present invention relates generally to the field of medical devices. More specifically, the invention is in the subfield of tubing, channels, drains, catheters, and ports connected to a subject patient.
The percutaneous endoscopic gastrostomy, or the PEG, as it is now most commonly known, was first introduced in 1980 by Gauderer, Ponsky, and Izant. Currently, more than 215,000 PEGs are placed annually [See 1, Gauderer, 2001]. Due to the design of the PEG, a major complication is “premature removal” or accidental dislodgement, from which significant morbidity and mortality may occur [See 4, Shapiro, 1996]. Secondary complications occur with premature removal, as the gastrocutaneous fistula tract has not fully matured, allowing the stomach to separate from the anterior abdominal wall and the open gastrostomy to leak gastric contents. Accidental dislodgement rates are well published and have been reported up to 12.8% when followed longitudinally for the lifetime of the originally placed PEG. [See 9, Chowdhury]
While early dislodgements can be clinically devastating, late dislodgements after gastrocutanous fistula maturation are less detrimental, however, they may require expensive emergency department visits, surgical consultations, replacement tubes, and radiographic confirmation of position [See 10, Rosenberger].
The mechanism that causes disruption of the PEG, may also cause disruption of any channel that is positioned inside a subject. Catheters, drains, and various other tubes are all subject to disruption when tractive force is applied to the portion of those tubes that are external to the subject.
Therefore, there is need in the art for a device which reduces the disruption of channels placed inside a subject.
An aspect of an embodiment of the present invention provides an assembly device for use in a medical environment to be used with a first channel and a second channel, wherein the first channel has an internal portion located at an intended position inside a subject. The device may comprise: a first connector comprising a first interface member and a channel communication section; a second connector comprising a second interface member and a channel communication section; said first interface member of said first connector and said second interface member of said second connector configured to join together to form a coupling configured to allow fluid to flow between the first channel and the second channel, said coupling having a decoupling force; wherein said coupling is joined to the first channel and the second channel at said communication section of said first connector and said communication section of said second connector; and wherein said decoupling force is the force required to separate said first connector and the second connector from one another to allow the internal portion to maintain its intended position in the subject.
An aspect of an embodiment of the present invention provides an assembly device for use in a medical environment to be used with a first channel and a second channel, wherein the first channel has an internal portion located at an intended position inside a subject. The device may comprise: a first connector; a second connector; said first connector and said second connector configured to join together to form a coupling configured to allow fluid to flow between the first channel and the second channel, said coupling having a decoupling force; wherein said coupling is joined between the first channel and the second channel; and wherein said decoupling force is the force required to separate said first connector and the second connector from one another to allow the internal portion to maintain its intended position in the subject.
An aspect of an embodiment of the present invention provides a system for use in a medical environment. The system may comprise: a first channel; a second channel, wherein the first channel has an internal portion located at an intended position inside a subject; and an assembly device. The assembly device may comprise: a first connector comprising a first interface member and a channel communication section; a second connector comprising a second interface member and a channel communication section; said first interface member of said first connector and said second interface member of said second connector configured to join together to form a coupling configured to allow fluid to flow between said first channel and said second channel, said coupling having a decoupling force; wherein said coupling is joined to said first channel and said second channel at said communication section of said first connector and said communication section of said second connector; and wherein said decoupling force is the force required to separate said first connector and the second connector from one another to allow the internal portion to maintain its intended position in the subject.
An aspect of an embodiment of the present invention provides a system for use in a medical environment, wherein said system comprises a first channel; a second channel, wherein the first channel has an internal portion located at an intended position inside a subject; and an assembly device. The assembly device may comprise: a first connector; a second connector; said first connector and said second connector configured to join together to form a coupling configured to allow fluid to flow between said first channel and said second channel, said coupling having a decoupling force; wherein said coupling is joined between said first channel and said second channel; and wherein said decoupling force is the force required to separate said first connector and the second connector from one another to allow the internal portion to maintain its intended position in the subject.
An aspect of an embodiment of the present invention provides a method used in a medical environment to be used with a first channel and a second channel, wherein said first channel has an internal portion located at an intended position inside the subject. The method may comprise: providing a first connector; providing a second connector; joining said first connector and said second connector to form a coupling to allow fluid to flow between the first channel and the second channel, said coupling having a decoupling force; wherein said coupling is joined to the first channel and the second channel; and wherein said decoupling force is the force required to separate said first connector and said second connector from one another to allow the internal portion to maintain its intended position.
An aspect of an embodiment of the present invention provides a method used in a medical environment. The method may comprise: providing a first channel; providing a second channel, wherein said first channel has an internal portion located at an intended position inside the subject; providing a first connector; providing a second connector; joining said first connector and said second connector to form a coupling to allow fluid to flow between said first channel and said second channel, said coupling having a decoupling force; wherein said coupling is joined to said first channel and said second channel; and wherein said decoupling force is the force required to separate said first connector and said second connector from one another to allow the internal portion to maintain its intended position.
These and other advantages and features of the invention disclosed herein, will be made more apparent from the description, drawings and claims that follow.
The accompanying drawings, which are incorporated into and form a part of the instant specification, illustrate several aspects and embodiments of the present invention and, together with the description herein, serve to explain the principles of the invention. The drawings are provided only for the purpose of illustrating select embodiments of the invention and are not to be construed as limiting the invention.
FIGS. 3(A)-(D) provide sectional views of several specific embodiments of the first connector having different embodiments of the channel communication section. It should be appreciated that these embodiments of the channel communication section are equally applicable to the second connector.
It should be appreciated that the first connector and second connector may be interchanged with one another respective to the first channel and second channel.
Still referring to the assembly device 1 of
For instance, referring to the device of assembly of
Referring to
Again referring to
Still referring to
Still referring to
It should be appreciated that the decoupling force may be increased or decreased so as to comply with operative, structural and anatomical demands associated with design and practice of the various embodiments disclosed herein.
Referring now to
Still referring to
Referring now to FIGS. 3(A)-(D), which provide sectional views of several specific embodiments of the channel communication section 16 typical on the first connector 12. The channel communication section 16 of the first connector 12 (and channel communication section 26 the second connector 22 although not shown in
Referring now to
Referring now to FIGS. 5(A)-(C), which provides assorted views of an embodiment of a first connector 12,
Referring now to FIGS. 6(A)-(C), which provide assorted views of an embodiment of a second connector 22,
Referring now to
Referring now to
Referring now to
FIGS. 9(B)-(C) provide an elevation schematic view of an embodiment of the coupling 40 in a disconnected position and connected position, respectively.
Furthermore, it should be appreciated that various components of this device may be manufactured or formed from a multitude of materials that satisfy the working requirements of the invention. This includes, but is not limited to, plastics, polymers, composites, metals, alloys and any combination thereof. This also includes, but is not limited to, materials molded or otherwise formed in order to have changing properties in any fashion including, but not limited to, along their length or across their section. This change in properties may either be by section or continuous in nature. The materials selected for the device 1 may be selected based on ease of manufacturing, price, material properties such as density, strength, modulus of elasticity, electrical or thermal conductivity, and biological compatibility.
The device 1, any of its components or sub-components, or any portions thereof may be manufactured or formed from a multitude of materials that satisfy the working requirements of the invention. This includes, but is not limited to, plastics, polymers, composites, metals, alloys and any combination thereof. This also includes, but is not limited to, materials molded or otherwise formed in order to have changing properties in any fashion including along their length or across their section. This change in properties may either be sectioned or continuous in nature. The materials selected for the device 1 may be selected based on ease of manufacturing, price, material properties such as density, strength, modulus of elasticity, electrical or thermal conductivity, and biological compatibility.
The applicant contemplates within the context of this invention that it may be produced in any geometrical form with variable length, width, shape, size, or other dimensional variability to match the requirements of specific applications for use.
It should be appreciated that the device 1 may be manufactured in a variety of ways. Specifically, this includes forming, molding, casting, forging, or otherwise producing components, sub-components, or portions thereof. The device may be produced as an assembly of parts wherein those parts are attached in any manner, including but not limited to fusing, welding, friction fits, threaded connections, snap connections, adhesives, or any other method for connecting one component, sub-component, or any portion thereof to another component, sub-component or portion thereof. The device 1 may also be manufactured so as to combine different functional elements into a single, multi-function component that would take on the function of two otherwise separate components.
It should be appreciated that as discussed herein, a subject may be a human or any animal. It should be appreciated that an animal may be a variety of any applicable type, including, but not limited thereto, mammal, veterinarian animal, livestock animal or pet type animal, etc. As an example, the animal may be a laboratory animal specifically selected to have certain characteristics similar to human (e.g. rat, dog, pig, monkey), etc. It should be appreciated that the subject may be any applicable human patient, for example.
It should be appreciated that various sizes, dimensions, contours, rigidity, shapes, flexibility and materials of any of the components or portions of components in the various embodiments discussed throughout may be varied and utilized as desired or required. Similarly, locations and alignments of the various components may vary as desired or required.
It should be appreciated that any of the components or modules referred to with regards to any of the present invention embodiments discussed herein, may be integrally or separately formed with one another. Further, redundant functions or structures of the components or modules may be implemented.
It should be appreciated that the device 1 and related components discussed herein may take on all shapes along the entire continual geometric spectrum of manipulation of x, y and z planes to provide and meet the anatomical and structural demands and operational requirements. Moreover, locations and alignments of the various components may vary as desired or required.
Practice of an aspect of an embodiment (or embodiments) of the invention will be still more fully understood from the following examples and experimental results, which are presented herein for illustration only and should not be construed as limiting the invention in any way.
Data Acquisition Study:
The Applicants' UVA Institutional Review Board (IRB)-approved trial (UVA-IRB#14526) was conducted on 60 patients to quantify the force required to intentionally remove a PEG from the stomach by gentle external traction. This data was used to determine the ideal force that an embodiment of the present invention device should disconnect. The force to remove the PEG was quantified by using a force measurement gauge (American Weigh® SR-20 Digital Hanging Scale 20×0.01 kg, and Extech Instruments Digital Force Gauge: Model 475044) to remove the PEGs out intentionally in clinic by external traction. This data allowed determination of the force (i.e., decoupling force) at which the device should separate in order to prevent the PEG from accidentally being pulled through the abdominal wall.
Referring to the graph of
Referring to the graph of
Turning to
For example, two standard deviations (0.93 kg) below the mean (2.88 kg) is a value of 1.02 kg. This is the “force” at which the device will separate. If the device disconnects at approximately 1.0 kg of force one can predict it will prevent 97.6% of PEG dislodgements as calculated from the original data.
In summary, an aspect of an embodiment of the present invention PEG coupling device will prevent accidental removal of the PEG feeding tube by being a point of disconnection to prevent the PEG tube's internal bumper from collapsing and dislodging through the abdominal wall. External fraction placed anywhere along the length of the tubing will cause the two-piece device to separate, relieving all pressure from the internal bumper preventing its collapse and dislodgement. This device is applicable for all PEGs with a soft internal bumper and not those with an intragastric balloon.
A great benefit of various embodiments of the present invention device is that it does not require any pre-market modification of the PEG tubes and insertion kits. This can be added to the PEG tubing following placement and does not require a well-healed gastrocutaneous fistula tract (as is required for a replacement balloon gastrostomy tube). It is also designed to fit any 24-French PEG tubing and therefore is applicable regardless of PEG brand. Patient safety organizations have already become concerned with the restraining of patients, and more regulations have been put into place restricting the use of wrist restraints and hand mitts. With increasing regulations such as these, it is anticipated that there will be more frequent PEG dislodgements and an even greater need for a novel safety mechanism.
An aspect of an embodiment of the present invention and related method is intended to prevent the accidental dislodgement of percutaneous endoscopic gastrostomy (PEG) tubes, as shown in
The standard PEG tube provides direct access to the stomach and provides enteral nutrition via the long, flexible feeding tube with a soft internal bumper. Conveniently, the soft inner bumper of the PEG collapses and slides out through the tube tract, allowing the PEG to be removed with relatively minimal external traction. This feature allows easy, intentional removal in an outpatient, clinic setting without the need for an operation or sedation when the patient has recovered from their initial insult.
Consequently, due to this flexible inner bumper, a major complication is premature removal or accidental dislodgement, from which significant morbidity and mortality may occur. Secondary complications occur with premature removal as the gastrocutaneous fistula tract has not fully matured allowing the stomach to separate from the anterior abdominal wall and the open gastrostomy to leak gastric contents. Complications include peritonitis requiring laparotomy, abdominal wall necrotizing fasciitis, candida peritonitis, and hemoperitoneum following gastrostomy tube reinsertion. Accidental dislodgement rates are well published and have been reported as up to 12.8% when followed longitudinally for the lifetime of the originally placed PEG. See Rosenberger L H, Newhook T, Schirmer B, Sawyer R G. Late accidental dislodgement of the percutaneous endoscopic gastrostomy: an underestimated burden on patients and the healthcare system. Surgical Endoscopy. 2011; 25:3307-3311, of which is hereby incorporated by reference herein in its entirety.
While early dislodgements can be clinically devastating, late dislodgements after gastrocutanous fistula maturation are less detrimental, however, they may require expensive emergency department visits, surgical consultations, replacement tubes, and radiographic confirmation of position. See Rosenberger L H, Newhook T, Schirmer B, Sawyer R G., 2011 One aspect of an embodiment of the present invention is a solution to what has become the “Achilles Heel” of the PEG tube; accidental dislodgement.
Applicants conducted a study at the University of Virginia to assess the effectiveness of an embodiment of the present invention in a PEG tube as shown in
Following standard PEG placement, an embodiment of the invention was placed in close proximity to the patient's abdominal wall. Typically, PEG tubing was cut transversely approximately 2 cm above the top of the external bumper and the device was installed. This resulted in relatively short first channel and a longer second channel connected to the feeding apparatus.
A total of 53 patients completed the initial phase of the study, 1 resulting in accidental PEG dislodgement, 37 in intentional removal of the PEG, 0 with exchange of the original PEG for a replacement balloon gastrostomy, and 15 in death with the device in place. A Kaplan-Meier survival analysis was performed comparing the prospective cohort (PEG tubes with an embodiment of the present invention, N=53) with the historic cohort (PEG tubes without an embodiment of the invention, N=563). The analysis shows a clear and significant longer survival of a single PEG tube with an embodiment of the invention in place. The exemplary embodiment of invention is shown to prevent accidental dislodgement and allow any given PEG to remain in place longer than previously shown. Referring to the graph of
The top line represents the prospective cohort with invention in place and the bottom line represents the historical cohort without invention in place
It should be appreciated that as an embodiment of the invention has demonstrated effectiveness in preventing the accidental dislodgment of PEG tubes, further embodiments should be equally able to prevent accidental dislodgment of other tubes and channels that have an internal portion inside a subject. Such other embodiments of tubes or channels, and applications include, but are in no way limited to:
Foley Catheter—where the internal portion of the catheter is positioned in the bladder for gravity drainage. An external force on the tubing can cause disruption of the internal portion of the catheter. An embodiment of the invention could be installed in-line, a short distance from the body and would separate when a tractive force was applied that would typically disrupt the internal portion of the catheter.
Intraventricular drain—where the internal portion of the drain channel is positioned inside the ventricles of the brain and where an external force on the external portion of the channel can cause disruption of the internal portion of the channel. An embodiment of the invention could be installed in-line, a short distance from the body and would separate when a tractive force was applied that would typically disrupt the internal portion of the channel.
Chest tube—where the internal portion of the chest tube sits inside the thoracic cavity between the lungs and the chest wall. The chest tube is designed to drain air, fluid, or blood from the thoracic cavity and external force on the tube may cause disruption of the internal position of the tube. An embodiment of the invention could be installed in-line, a short distance from the body and would separate when a tractive force was applied that would typically disrupt the internal portion of the tube.
Nephrostomy tubes—where an internal “pigtail end” of the catheter sits in the renal pelvis to drain urine from the kidney. This pigtail end may be disrupted when an external force is applied to the external portion of the catheter. An embodiment of the invention could be installed in-line, a short distance from the body and would separate when a tractive force was applied that would typically disrupt the pigtail end of the catheter.
Percutaneous transhepatic cholangiography (“PTC”) tube—where an internal channel is placed into the biliary tree to allow bile drainage. Such channel can be disrupted when a force is applied to the external portion of the channel. An embodiment of the invention could be installed in-line, a short distance from the body and would separate when a tractive force was applied that would typically disrupt the internal portion of the channel.
Pigtail catheters for abscess drainage—where an internal “pigtail end” of the catheter sits in any number of intra-abdominal locations to drain fluid from an abscess. This pigtail end may be disrupted when an external force is applied to the external portion of the catheter. An embodiment of the invention could be installed in-line, a short distance from the body and would separate when a tractive force was applied that would typically disrupt the pigtail end of the catheter.
Generally, any channel that has an internal portion inside a subject is subject to disruption when a force is applied to the external portion of the channel. An embodiment of this invention may be placed in-line with the channel to prevent the disruption of the internal portion of the channel when an applicable force is applied beyond the invented device. Similarly, an embodiment of the invention may be implemented with an optimal or desired decoupling force according to the teachings, techniques, structures, components and principles set forth in this disclosure regarding the various embodiments or aspects of the present invention.
An assembly device for use in a medical environment to be used with a first channel and a second channel, wherein the first channel has an internal portion located at an intended position inside a subject. The device may comprise: a first connector comprising a first interface member and a channel communication section; a second connector comprising a second interface member and a channel communication section; the first interface member of the first connector and the second interface member of the second connector configured to join together to form a coupling configured to allow fluid to flow between the first channel and the second channel, the coupling having a decoupling force; wherein the coupling is joined to the first channel and the second channel at the communication section of the first connector and the communication section of the second connector; and wherein the decoupling force is the force required to separate the first connector and the second connector from one another to allow the internal portion to maintain its intended position in the subject.
The device of example 1, wherein the first connector comprises a male connector and the first interface member comprises an insert section.
The device of example 2, wherein the second connector comprises a female connector and the second interface member comprises a receiving section, whereby the coupling is provided by the receiving section receiving the insert section to provide the joining together.
The device of example 1 (as well as subject matter of one or more of any combination of examples 2-3), wherein the first channel and/or second channel comprises: a tube, a conduit, a port or any combination thereof.
The device of example 4 (as well as subject matter of one or more of any combination of examples 2-3), wherein the tube comprises a percutaneous endoscopic gastrostomy (PEG).
The device of example 1 (as well as subject matter of one or more of any combination of examples 2-5), wherein the decoupling force is between 0.5 kilogram-force and 2.5 kilograms-force.
The device of example 1 (as well as subject matter of one or more of any combination of examples 2-6), wherein the decoupling force is between 1.1 kilograms-force and 1.3 kilograms-force.
The device of example 1 (as well as subject matter of one or more of any combination of examples 2-7), wherein the channel communication section 16 on the first connector is configured to have an attachment means for attaching to the first channel and/or the second channel.
The device of example 1 (as well as subject matter of one or more of any combination of examples 2-8), wherein the channel communication section 26 on the second connector is configured to have an attachment means for attaching to the first channel and/or the second channel.
The assembly of example 1 (as well as subject matter of one or more of any combination of examples 2-9), wherein the joining of the first interface member of the first connector and the second interface member of the second connector provides faying surfaces, wherein the faying surfaces forms a leak inhibiting seal.
The device of example 1 (as well as subject matter of one or more of any combination of examples 2-10), wherein the first interface member of the first connector includes one or more circumferentially oriented protrusions.
The device of example 7 (as well as subject matter of one or more of any combination of examples 1-6 or 8-11), wherein the one or more circumferentially oriented protrusions are a continuous segment.
The device of example 7 (as well as subject matter of one or more of any combination of examples 1-6 or 8-12), where the one or more circumferentially oriented protrusions are discontinuous segments.
The device of example 7 (as well as subject matter of one or more of any combination of examples 1-6 or 8-13), wherein the second interface member of second connector includes one or more protrusion retention recesses.
The device of example 1 (as well as subject matter of one or more of any combination of examples 2-14), wherein the decoupling force is the force required to separate the first connector and the second connector from one another to allow the internal portion to maintain its intended position in the subject and to allow the separated the first connector and the second connector to remain joined to their the respective channels.
An assembly device for use in a medical environment to be used with a first channel and a second channel, wherein the first channel has an internal portion located at an intended position inside a subject. The device may comprise: a first connector; a second connector; the first connector and the second connector configured to join together to form a coupling configured to allow fluid to flow between the first channel and the second channel, the coupling having a decoupling force; wherein the coupling is joined between the first channel and the second channel; and wherein the decoupling force is the force required to separate the first connector and the second connector from one another to allow the internal portion to maintain its intended position in the subject. Moreover, the system may include subject matter of one or more of any combination of examples 1-15.
The device of example 16 (as well as subject matter of one or more of any combination of examples 1-15), wherein the first channel and/or second channel comprises: a tube, a conduit, a port or any combination thereof.
The device of example 17 (as well as subject matter of one or more of any combination of examples 1-15), wherein the tube comprises a percutaneous endoscopic gastrostomy (PEG).
The device of example 16 (as well as subject matter of one or more of any combination of examples 1-15 or 17-18), wherein the decoupling force is between 0.5 kilogram-force and 2.5 kilograms-force.
The device of example 16 (as well as subject matter of one or more of any combination of examples 1-15 or 17-19), wherein the decoupling force is between 1.1 kilograms-force and 1.3 kilograms-force.
The device of example 16 (as well as subject matter of one or more of any combination of examples 1-15 or 17-20), wherein the first connector is attached to the first channel using an attachment means.
The device of example 16 (as well as subject matter of one or more of any combination of examples 1-15 or 17-21), wherein the first connector is attached to the first channel by way of at least one of the following connectors: male to female friction connector, magnetic connector, connector that uses adhesive, friction connection, ridge/valley connection, snap/click connection, O-ring connection, and screw/twist type mechanism connection.
The device of example 16 (as well as subject matter of one or more of any combination of examples 1-15 or 17-22), wherein the second connector is attached to the second channel using an attachment means.
The device of example 16 (as well as subject matter of one or more of any combination of examples 1-15 or 17-23), wherein the second connector is attached to the second channel by way of at least one of the following connectors: male to female friction connector, magnetic connector, connector that uses adhesive, friction connection, ridge/valley connection, snap/click connection, O-ring connection, and screw/twist type mechanism connection.
The device of example 16 (as well as subject matter of one or more of any combination of examples 1-15 or 17-24), wherein the first connector is joined to the second connector forming the coupling, wherein the coupling comprises at least one of the following: male to female friction connector, magnetic connector, connector that use adhesive, friction connection, ridge/valley connection, snap/click connection, O-ring connection, and screw/twist type mechanisms connection.
The device of example 16 (as well as subject matter of one or more of any combination of examples 1-15 or 17-25), wherein the decoupling force is the force required to separate the first connector and the second connector from one another to allow the internal portion to maintain its intended position in the subject and to allow the first connector to remain joined to the first channel and the second connector to remain connected to the second channel.
A system for use in a medical environment, wherein the system comprises: a first channel; a second channel, wherein the first channel has an internal portion located at an intended position inside a subject; and an assembly device. The assembly device may comprise: a first connector comprising a first interface member and a channel communication section; a second connector comprising a second interface member and a channel communication section; the first interface member of the first connector and the second interface member of the second connector configured to join together to form a coupling configured to allow fluid to flow between the first channel and the second channel, the coupling having a decoupling force; wherein the coupling is joined to the first channel and the second channel at the communication section of the first connector and the communication section of the second connector; and wherein the decoupling force is the force required to separate the first connector and the second connector from one another to allow the internal portion to maintain its intended position in the subject. Moreover, the system may include subject matter of one or more of any combination of examples 1-26.
A system for use in a medical environment, wherein the system comprises: a first channel; a second channel, wherein the first channel has an internal portion located at an intended position inside a subject; and an assembly device. The assembly device may comprise: a first connector; a second connector; the first connector and the second connector configured to join together to form a coupling configured to allow fluid to flow between the first channel and the second channel, the coupling having a decoupling force; wherein the coupling is joined between the first channel and the second channel; and wherein the decoupling force is the force required to separate the first connector and the second connector from one another to allow the internal portion to maintain its intended position in the subject. Moreover, the system may include subject matter of one or more of any combination of examples 1-27.
A method used in a medical environment to be used with a first channel and a second channel, wherein the first channel has an internal portion located at an intended position inside the subject. The method may comprise: providing a first connector; providing a second connector; joining the first connector and the second connector to form a coupling to allow fluid to flow between the first channel and the second channel, the coupling having a decoupling force; wherein the coupling is joined to the first channel and the second channel; and wherein the decoupling force is the force required to separate the first connector and the second connector from one another to allow the internal portion to maintain its intended position. Moreover, the system may include subject matter of one or more of any combination of examples 1-28.
The device of example 29 (as well as subject matter of one or more of any combination of examples 1-28), wherein the first connector comprises a male connector and the first interface member comprises an insert section.
The device of example 30 (as well as subject matter of one or more of any combination of examples 1-28), wherein the second connector comprises a female connector and the second interface member comprises a receiving section, whereby the coupling is provided by the receiving section receiving the insert section to provide the joining together.
The method of example 29 (as well as subject matter of one or more of any combination of examples 1-28 or 30-31), wherein the first channel and/or second channel comprises: a tube, a conduit, a port or any combination thereof.
The method of example 32 (as well as subject matter of one or more of any combination of examples 1-28 or 30-31), wherein the tube comprises a percutaneous endoscopic gastrostomy (PEG).
The method of example 29 (as well as subject matter of one or more of any combination of examples 1-28 or 30-33), wherein the decoupling force is between 0.5 kilogram-force and 2.5 kilograms-force.
The method of example 29 (as well as subject matter of one or more of any combination of examples 1-28 or 30-34), wherein the decoupling force is between 1.1 kilograms-force and 1.3 kilograms-force.
The method of example 29 (as well as subject matter of one or more of any combination of examples 1-28 or 30-35), wherein joining of the first interface member of the first connector and the second interface member of the second connector provides faying surfaces, wherein the faying surfaces forms a leak inhibiting seal.
The method of example 29 (as well as subject matter of one or more of any combination of examples 1-28 or 30-36), wherein the decoupling force is the force required to separate the first connector and the second connector from one another to allow the internal portion to maintain its intended position in the subject and to allow the first connector to remain joined to the first channel and the second connector to remain connected to the second channel.
A method used in a medical environment, whereby the method comprises: providing a first channel; providing a second channel, wherein the first channel has an internal portion located at an intended position inside the subject; providing a first connector; providing a second connector; joining the first connector and the second connector to form a coupling to allow fluid to flow between the first channel and the second channel, the coupling having a decoupling force; wherein the coupling is joined to the first channel and the second channel; and wherein the decoupling force is the force required to separate the first connector and the second connector from one another to allow the internal portion to maintain its intended position. Moreover, the system may include subject matter of one or more of any combination of examples 1-37.
A method of manufacturing any of the devices or systems (or portions thereof) provided in one or more of any combination of examples 1-28; by implementing, but not limited thereto, fabrication techniques and material selection known to one skilled in art.
The devices, systems, compositions, and methods of various embodiments of the invention disclosed herein may utilize aspects disclosed in the following references, applications, publications and patents and which are hereby incorporated by reference herein in their entirety (and which are not admitted to be prior art with respect to the present invention by inclusion in this section):
In summary, while the present invention has been described with respect to specific embodiments, many modifications, variations, alterations, substitutions, and equivalents will be apparent to those skilled in the art. The present invention is not to be limited in scope by the specific embodiment described herein. Indeed, various modifications of the present invention, in addition to those described herein, will be apparent to those of skill in the art from the foregoing description and accompanying drawings. Accordingly, the invention is to be considered as limited only by the spirit and scope of the following claims, including all modifications and equivalents.
Still other embodiments will become readily apparent to those skilled in this art from reading the above-recited detailed description and drawings of certain exemplary embodiments. It should be understood that numerous variations, modifications, and additional embodiments are possible, and accordingly, all such variations, modifications, and embodiments are to be regarded as being within the spirit and scope of this application. For example, regardless of the content of any portion (e.g., title, field, background, summary, abstract, drawing figure, etc.) of this application, unless clearly specified to the contrary, there is no requirement for the inclusion in any claim herein or of any application claiming priority hereto of any particular described or illustrated activity or element, any particular sequence of such activities, or any particular interrelationship of such elements. Moreover, any activity can be repeated, any activity can be performed by multiple entities, and/or any element can be duplicated. Further, any activity or element can be excluded, the sequence of activities can vary, and/or the interrelationship of elements can vary. Unless clearly specified to the contrary, there is no requirement for any particular described or illustrated activity or element, any particular sequence or such activities, any particular size, speed, material, dimension or frequency, or any particularly interrelationship of such elements. Accordingly, the descriptions and drawings are to be regarded as illustrative in nature, and not as restrictive. Moreover, when any number or range is described herein, unless clearly stated otherwise, that number or range is approximate. When any range is described herein, unless clearly stated otherwise, that range includes all values therein and all sub ranges therein. Any information in any material (e.g., a United States/foreign patent, United States/foreign patent application, book, article, etc.) that has been incorporated by reference herein, is only incorporated by reference to the extent that no conflict exists between such information and the other statements and drawings set forth herein. In the event of such conflict, including a conflict that would render invalid any claim herein or seeking priority hereto, then any such conflicting information in such incorporated by reference material is specifically not incorporated by reference herein.
The present application claims priority under 35 U.S.C. §119(e) from U.S. Provisional Application Ser. No. 61/576,775, filed Dec. 16, 2011, entitled “Coupling Device and Related Method” and Ser. No. 61/587,580, filed Jan. 17, 2012, entitled “Coupling Device and Related Method;” the disclosures of which are hereby incorporated by reference herein in their entirety.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US2012/069793 | 12/14/2012 | WO | 00 | 6/13/2014 |
Number | Date | Country | |
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61576775 | Dec 2011 | US | |
61587580 | Jan 2012 | US |