The present disclosure generally relates to the healthcare field and, more particularly, to a jejunal system and apparatus that provides nutrients, aspiration, and redirects fluids in patients.
Gastrostomy is a surgical procedure that involves inserting a tube directly into a patient's stomach via an artificial opening. One end of the tube remains inside the stomach, and the other end of the tube extends from outside the stomach and the patient's body. Nutrients can be passed through the tube and directly into the stomach for patients who are unable to orally consume an appropriate amount of calories and/or nutrients to promote growth and/or sustain healthy body function. In some cases, there can be slow gastric motility/propulsion which may result in particular foods (e.g., milk) backing up through the artificial opening or refluxing into the patient's esophagus. In such cases, trans pyloric-jejunal feeding tubes (gastro-jejunal tubes) may be used.
A trans pyloric-jejunal feeding tube is typically extended into the patient's duoendum/jejunum where continuous feeds are directly transported to the small intestine. Some trans pyloric-jejunal feeding tubes include a double lumen. One of the lumens is placed in the stomach for feeding, venting, and decompression, while the other lumen is placed in the jejunum for feeding.
Trans pyloric-jejunal feeding tubes are frequently used to provide nutrients to sick infants. In this application, there are commonly complaints of stomach distension, feeding intolerance, feeding residuals, vomiting, and even aspiration, which can lead to death or severe comorbidities. It is believed that these complaints stem from the fact that, despite there being a gastric outlet, the amount of gastric contents is too great to be emptied. This may be due to the fact that one of the lumens partially obstructs the gastric outlet at the narrowest and most muscular part of the pyloric junction.
A jejunal system and methods of operation are disclosed. The jejunal system includes a sheath having a proximal end and a distal end. A plurality of lumens extend through the sheath between the proximal end and the distal end. A first lumen of the plurality of lumens is provided with a first aperture set and a second aperture set. The first aperture set is in fluid communication with the second aperture set via the first lumen. The jejunal system is dimensioned and configured such that, when the jejunal system is inserted into a human body, the first aperture set is located in a stomach of the human body, and the second aperture set is located in a small intestine of the human body.
The jejunal system is formed by advancing a plurality of lumens through a sheath, the plurality of lumens running between a proximal end of the sheath and a distal end of the sheath. A first aperture set and a second aperture set are dimensioned in a first lumen of the plurality of lumens, wherein the first aperture set is in fluid communication with the second aperture set via the first lumen. The jejunal system is dimensioned and configured such that, when the system is inserted into a human body, the first aperture set is located in a small intestine of the human body, and the second aperture set is located in a stomach of the human body.
A jejunal system includes a sheath having a proximal end and a distal end and a plurality of lumens extending through the sheath between the proximal end and the distal end. The plurality of lumens comprises a first lumen being provided with a first aperture set, a second aperture set and a third aperture set. The first lumen comprises a partition fluidly separating the first lumen into a first flow path and a second flow path, wherein the first aperture set and the second aperture set are in fluid communication with the first flow path, and the third aperture set is in fluid communication with the second flow path. A second lumen is provided with a fourth aperture set. Wherein the jejunal system is dimensioned and configured such that, when the system is inserted into a human body, the first aperture set and the fourth aperture set are located in a small intestine of the human body, and the second aperture set and the third aperture set are located in a stomach of the human body.
The foregoing and other features and advantages of the present disclosure will become apparent to one skilled in the art to which the present disclosure relates upon consideration of the following description of the invention with reference to the accompanying drawings, wherein like reference numerals, unless otherwise described refer to like parts throughout the drawings and in which:
Referring now to the figures wherein like numbered features shown therein refer to like elements throughout unless otherwise noted. The present disclosure relates generally to the healthcare field and, more particularly, to a jejunal system and apparatus that provides nutrients, aspiration, and redirects solids and fluids in patients.
A plurality of lumens 42A-42C extend through the sheath 22 between the proximal end 24 and the distal end 26, as illustrated in
The first and second lumen aperture sets 44A, 44B are provided on the first lumen 42A and are in fluid communication with one another via the first lumen 42A. The first and second lumen aperture sets 44A, 44B are located substantially adjacent the first and second sheath aperture sets 34A, 34B so as to be in fluid communication with the first and second sheath aperture sets 34A, 34B, respectively. In one example embodiment, the first sheath aperture set 34A, in conjunction with the first lumen aperture set 44A, forms a first aperture set 35A, as illustrated in
An end cap 54 can be secured to the proximal end 24 of the sheath 22. The end cap 54 can include a plurality of ports 56A-56C. In one example, the end cap 54 can include three ports 56, with a second port 56B being substantially aligned along a longitudinal axis (see
Each of the ports 56 can be provided with attachment features (not shown) that enable a conduit to be retained to the port 56. For example, each of the ports 56 can be provided with a Luer-Lok connection fitting. However, it will be appreciated that any other attachment features can be used (e.g., interference fit). Each of the ports 56 can further be provided with sealing members 59A-59B that close off the ports 56. In one example, the sealing members 59 can be provided with ribs that retain each sealing member 59 within the respective port 56. It is understood that any other appropriate sealing member 59 can be used.
Referring to
As stated above, the primary change in the jejunal tube 120 in
Referring to
The gastro-jejunal system 20 is dimensioned and configured such that, when the retention collar 38 rests against the patient's skin 206, the second and third sheath aperture sets 34B, 34C are located in the stomach 200, and the first and fourth sheath aperture sets 34A, 34D are located in the small intestine 202 with the sheath 22 extending through the pyloric junction 208. In particular, the first and fourth sheath aperture sets 34A, 34D are located in the jejunum 204.
With the retention collar 38 resting against the patient's skin 206, the balloon 58 can be inflated to anchor the position of the gastro-jejunal system 20 within the stomach 200 and small intestine 202 of the patient. Inflation of the balloon 58 is accomplished by, first, attaching an inflation conduit (not shown) to the third port 56C. The inflation conduit can be configured to provide an inflation medium to the gastro-jejunal system 20. In one example, the inflation medium may be a fluid such as water. However, it will be appreciated that any other appropriate inflation medium can be used (e.g., air). The inflation medium, supplied from the inflation conduit, flows into the third port 56C, through the third lumen 42C, through the outlet 57, as illustrated in
The inflation conduit continues to supply the inflation medium until the balloon 58 is inflated such that the parts of the human body located between the balloon 58 and the retention collar 38 are “clamped” therebetween. This clamping anchors the position of the gastro-jejunal system 20 relative to the patient, thereby ensuring that the second and third sheath aperture sets 34B, 34C remain in the stomach 200 and the first and fourth sheath aperture sets 34A, 34D remain in the jejunum 204. The inflation conduit is removed from the third port 56C once inflation of the balloon 58 is complete.
With the gastro-jejunal system 20 and the sheath 22 positions anchored, a feeding conduit (not shown) can be attached to the second port 56B to deliver nutrients directly to the jejunum 204. Nutrients flow from the feeding conduit, into the second post 56B, and through the second lumen 42B to the fourth lumen aperture set 44D. Due to the fluid communication between the fourth sheath aperture set 34D and the fourth lumen aperture set 44D, the nutrients can flow out of the second lumen 42B and then the sheath 22 via the fourth lumen aperture set 44D and the fourth sheath aperture set 34D.
The gastro-jejunal system 20 can also be used to deliver nutrients to the stomach 200 or vent the stomach 200. If it is desired to deliver nutrients to the stomach 200, the feeding conduit can be attached to the first port 56A. Nutrients can flow from the feeding conduit, into the first port 56A, and through the second flow path 52 of the first lumen 42A to the third lumen aperture set 44C. The fluid communication between the third lumen aperture set 44C and the third sheath aperture set 34C enables nutrients to flow out of the first lumen 42A and then the sheath 20 via the third lumen aperture set 44C and the third sheath aperture set 34C. If it is desired to vent the stomach, a venting conduit (not shown) can be attached to the first port 56A. Contents to be vented from the stomach can pass through the sheath 22 and into the second flow path 52 of the first lumen 42A via the third sheath aperture set 34C and the third lumen aperture set 44C. The contents to be vented can then be removed from the stomach via the second flow path 52 of the first lumen 42A, the first port 56A, and the venting conduit.
The construction of the gastro-jejunal system 20 also allows contents of the stomach 200 to be drained into the small intestine 202. As explained above, the gastro-jejunal system 20 is dimensioned and configured to locate the second sheath aperture set 34B, (and fluidly coupled second lumen aperture set 44B) in the patient's stomach and the first sheath aperture set 34A (and fluidly coupled first lumen aperture set 44A) in the small intestine 202. Additionally, as explained above, the second lumen aperture set 44B is in fluid communication with the first lumen aperture set 44A via the first fluid flow path 50 of the first lumen 42A. Accordingly, the construction of the gastro-jejunal system 20 effectively puts the stomach 200 in fluid communication with the small intestine 202. Stomach contents or pressure can enter into the first fluid flow path 50 via the second sheath aperture set 34B and second lumen aperture set 44B, flow through the first fluid flow path 50, and into the small intestine 202 via the first lumen aperture set 44A and the first sheath aperture set 34A. Thus, the gastro-jejunal system 20 ensures that fluid communication between the stomach 200 and the small intestine 202 is not obstructed.
Referring to
In the foregoing specification, specific embodiments have been described. However, one of ordinary skill in the art appreciates that various modifications and changes can be made without departing from the scope of the disclosure as set forth in the claims below. Accordingly, the specification and figures are to be regarded in an illustrative rather than a restrictive sense, and all such modifications are intended to be included within the scope of present teachings. For example, the apertures 36, 46 of both the sheath 22 and the lumens 44 can be replaced with a wire mesh, fluid permeable membrane, or any other suitable structure that allows fluid flow.
The benefits, advantages, solutions to problems, and any element(s) that may cause any benefit, advantage, or solution to occur or become more pronounced are not to be construed as a critical, required, or essential features or elements of any or all the claims. The disclosure is defined solely by the appended claims including any amendments made during the pendency of this application and all equivalents of those claims as issued.
Moreover in this document, relational terms such as first and second, top and bottom, and the like may be used solely to distinguish one entity or action from another entity or action without necessarily requiring or implying any actual such relationship or order between such entities or actions. The terms “comprises,” “comprising,” “has”, “having,” “includes”, “including,” “contains”, “containing” or any other variation thereof are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises, has, includes, contains a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. An element proceeded by “comprises . . . a”, “has . . . a”, “includes . . . a”, “contains . . . a” does not, without more constraints, preclude the existence of additional identical elements in the process, method, article, or apparatus that comprises, has, includes, contains the element. The terms “a” and “an” are defined as one or more unless explicitly stated otherwise herein. The terms “substantially”, “essentially”, “approximately”, “about” or any other version thereof are defined as being close to as understood by one of ordinary skill in the art. In one non-limiting embodiment the terms are defined to be within for example 10%, in another possible embodiment within 5%, in another possible embodiment within 1%, and in another possible embodiment within 0.5%. The term “coupled” as used herein is defined as connected or in contact either temporarily or permanently, although not necessarily directly and not necessarily mechanically. A device or structure that is “configured” in a certain way is configured in at least that way, but may also be configured in ways that are not listed.
To the extent that the materials for any of the lore going embodiments or components thereof are not specified, it is to be appreciated that suitable materials would be known by one of ordinary skill in the art for the intended purposes.
The Abstract of the Disclosure is provided to allow the reader to quickly ascertain the nature of the technical disclosure. It is submitted with the understanding that it will not be used to interpret or limit the scope or meaning of the claims. In addition, in the foregoing Detailed Description, it can be seen that various features are grouped together in various embodiments for the purpose of stream lining the disclosure. This method of disclosure is not to be interpreted as reflecting an intention that the claimed embodiments require more features than are expressly recited in each claim. Rather, as the following claims reflect, inventive subject matter lies in less than all features of a single disclosed embodiment. Thus the following claims are hereby incorporated into the Detailed Description, with each claim standing on its own as a separately claimed subject matter.
The following application claims priority under 35 U.S.C. § 119(e) to co-pending U.S. Provisional Patent Application Ser. No. 62/160,343 filed May 12, 2015 entitled JEJUNAL SYSTEM AND APPARATUS. The above-identified application is incorporated herein by reference in its entirety for all purposes.
Filing Document | Filing Date | Country | Kind |
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PCT/US2016/032098 | 5/12/2016 | WO | 00 |
Number | Date | Country | |
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62160343 | May 2015 | US |