MEDICAL TUBE
20210031021 ยท 2021-02-04
Inventors
Cpc classification
A61M39/12
HUMAN NECESSITIES
B29L2031/753
PERFORMING OPERATIONS; TRANSPORTING
A61J15/0011
HUMAN NECESSITIES
B29K2075/00
PERFORMING OPERATIONS; TRANSPORTING
B29C45/14311
PERFORMING OPERATIONS; TRANSPORTING
A61J15/0003
HUMAN NECESSITIES
B29C45/14336
PERFORMING OPERATIONS; TRANSPORTING
B29C45/14639
PERFORMING OPERATIONS; TRANSPORTING
A61M39/1011
HUMAN NECESSITIES
B29L2031/7544
PERFORMING OPERATIONS; TRANSPORTING
International classification
Abstract
Aspects of the present invention relate to a medical tube for delivering nutrients or medication to a patient. The tube comprises a flexible tubular body for conveying the nutrients or medication to the patient and a small-bore connector for connecting the medical tube to a syringe or pump. The small-bore connector is secured to the tubular body by an overmoulded component that encapsulates a portion of the tubular body and a portion of the connector thereby securing the connector relative to the tubular body of the medical tube.
Claims
1. A medical tube for delivering fluids to a patient, the tube comprising: a flexible tubular body for conveying the fluids; and a connector for connecting the medical tube to a source of fluids; wherein the connector is secured to the tubular body by an overmould structure that encapsulates a portion of the tubular body and at least a portion of the connector thereby securing the connector to the tubular body.
2. A medical tube as claimed in claim 1, wherein the connector comprises a central bore and a distal end of the tubular body is received within the central bore.
3. A medical tube as claimed in claim 1, wherein the connector comprises a mechanical retention feature for securing the overmould structure to the connector.
4. A medical tube as claimed in claim 3, wherein the mechanical retention feature comprises a distally-facing wall and a proximally-facing wall that are mutually spaced in a longitudinal direction to define an annular recess between them.
5. A medical tube as claimed in claim 4, wherein a portion of the overmould structure extends into and engages within the annular recess.
6. A medical tube as claimed in claim 3, wherein the mechanical retention feature comprises a proximally-tapering barb.
7. A medical tube as claimed in claim 3, wherein the overmould structure encapsulates the mechanical retention feature.
8. A medical tube as claimed in claim 3, wherein the overmould structure tapers from a first diameter at a distal end to a second diameter at a proximal end.
9. A medical tube as claimed in claim 8, wherein the overmould structure extends proximally from the connector to a length that exceeds the first diameter.
10. A medical tube as claimed in claim 6, wherein an outer surface portion of the overmould structure tapers proximally and that tapered portion is longitudinally aligned with the proximally-tapering barb.
11. A medical tube as claimed in claim 1, wherein an outer surface portion of the overmould structure is substantially aligned with a longitudinal axis of the connector.
12. A medical tube as claimed in claim 1, wherein the overmould structure is bonded to the connector and to the tubular body.
13. A medical tube as claimed in claim 12, wherein the bond is a heat-bond and wherein the heat-bond forms a seal between the overmould structure and the connector and/or the tubular body.
14. A medical tube as claimed in claim 1, wherein the connector has a flexural modulus of at least 700 MPa and the tubular body has a flexural modulus of less than or equal to 100 MPa.
15. A medical tube as claimed in claim 1, wherein the overmould structure has a flexural modulus that is equal to or greater than a flexural modulus of the tubular body.
16. A medical tube as claimed in claim 1, wherein the overmould structure has a flexural modulus that is lower than or equal to a flexural modulus of the tubular body.
17. A medical tube as claimed in claim 1, wherein the overmould structure is moulded from an injection-mouldable version of the material of the tubular body.
18. A medical tube as claimed in claim 1, wherein the material of the overmould structure has a melting or softening temperature that is equal to or lower than a melting or softening temperature of the tubular body.
19. A medical tube as claimed in claim 1, wherein the material of the overmould structure has a melting or softening temperature that is equal to or higher than a melting or softening temperature of the tubular body.
20. A feeding tube for enteral feeding, the feeding tube comprising: a flexible tubular body for conveying nutrients to a patient's stomach; and a connector for connecting the flexible tubular body to a source of nutrients; wherein the connector is secured to the tubular body by an overmould structure that encapsulates a portion of the tubular body and at least a portion of the connector thereby securing the connector to the tubular body.
21. A feeding tube as claimed in claim 19, wherein the feeding tube is connected to a syringe or a pump for delivering nutrients to a patient.
22. A method of manufacturing a medical tube for use in a medical application, the medical tube comprising a flexible tubular body and a connector, the method comprising: placing an end portion of the tubular body inside the connector; placing the tubular body and the connector into a mould; and injecting an overmould material into the mould to encapsulate a portion of the tubular body and at least a portion of the connector, forming an overmould structure that secures the connector relative to the tubular body.
23. The method as claimed in claim 22, wherein the method comprises forming the connector prior to injecting the overmould material.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0039] One or more embodiments of the invention will now be described, by way of example only, with reference to the accompanying drawings, in which:
[0040]
[0041]
[0042]
[0043]
[0044]
[0045]
[0046]
[0047]
[0048]
DETAILED DESCRIPTION
[0049] In general terms, embodiments of the invention relate to a method of securing a small-bore connector to a tubular body or line to make a medical tube for conveying fluid such as medication, nutrients, air or oxygen to a patient. In a broad sense, the method comprises securing the connector to the tube by overmoulding a plastics material over at least a portion of the connector and a portion of the tube. The overmoulded component may, at least partially, encapsulate a portion of the connector and a portion of the tube to secure the connector relative to the tube.
[0050] The skilled reader will understand that whilst the invention is described herein in the context of enteral feeding, the inventive concepts described may be applied to other medical applications; for example, but not limited to: breathing systems, urinary collection systems, limb cuff inflation, neuraxial applications and intravenous systems.
[0051] To place embodiments of the invention in a suitable context, reference will firstly be made to
[0052] The connector 22 of
[0053] The connector 22 comprises an interface 28 at its distal end that is unique to the medical application for which the connector 22 is designed. In the context of enteral feeding, the interface 28 comprises a threaded interface for connecting the connector 22 to an enteral syringe or pump (not shown) to deliver liquid food to the patient's stomach. The interface 28 is unique to the medical application to prevent misconnection of the connector 22 to the wrong syringe or pumping device.
[0054] A central bore 24 runs along a central longitudinal axis of the connector 22 such that fluids may be conveyed to the feeding tube 20 from a pump or syringe connected to the connector 22. As shown in
[0055] Turning now to
[0056]
[0057] The connector 22 comprises a connector body 42. A barbed portion 40 extends from a proximal end of the connector body 42 and is rotationally symmetrical about the central longitudinal axis 23. The central bore 24 extends along the central longitudinal axis 23 of the connector body 42 to define a passage that extends longitudinally through the full length of the connector body 42 and also through the barbed portion 40 at the proximal end of the connector body 42. Thus, the central bore 24 penetrates the full length of the connector 22.
[0058] The connector body 42 comprises a planar proximally-facing wall 46 from which the barbed portion 40 extends. The wall 46 lies in a plane that is orthogonal to the central longitudinal axis 23.
[0059] The barbed portion 40 comprises a tubular neck 43 that is integral with and extends longitudinally from the wall 46 in a proximal direction. A hollow frusto-conical barb 44 is positioned at the opposing proximal end of the neck 43 and tapers in a proximal direction away from the neck 43.
[0060] The barb 44 comprises a distally-facing wall 45 that faces the proximally-facing wall 46 of the connector body 42 and is spaced from that wall 46 by the length of the neck 43. In this example, the wall 45 also lies in a plane that is orthogonal to the central longitudinal axis 23 and so is parallel to the wall 46.
[0061] As shown in
[0062] As the overmould structure 30 cures the surface of the connector 22 and tube 20 may melt slightly thereby forming a heat-bond with the overmould structure 30. The heat-bond forms a seal between the overmould structure 30 and the connector 22 and tube 20 which beneficially prevents fluids leaking at the point the tube 20 is connected to the connector 22.
[0063] Additionally, the barbed portion 40 is an example of a mechanical retention feature or engagement formation that further improves the strength of the connection between the overmould structure 30 and the connector 22. Specifically, a portion of the overmould structure 30 extends into and fills the annular recess 47 between the distally-facing wall 45 of the barb 44 and the proximally-facing wall 46 of the connector body 42. This portion of the overmould structure 30 trapped between the barb 44 and the connector body 42 inhibits longitudinal movement of the overmould structure 30 relative to the connector 22. Thus, the barbed portion 40 provides an additional mechanical connection between the overmould structure 30 and the connector 22.
[0064] As shown in
[0065] More specifically, the overmould structure 30 tapers in steps that, moving proximally, are defined by a cylindrical distal end portion, a first frusto-conical step that tapers proximally, a cylindrical intermediate portion and a second frusto-conical step that tapers proximally to the proximal end. The distal end portion and the intermediate portion each have an outer surface that lies parallel to the central longitudinal axis 23.
[0066] The distal end portion of the overmould structure 30 is aligned longitudinally with the neck 43. The first frusto-conical step is aligned with, and extends proximally beyond, the tapering surface of the barb 44. The second frusto-conical step reduces the diameter of the overmould structure 30 to near the outer diameter of the tube 20.
[0067] By virtue of its tapered and preferably stepped outer shape, the overmould structure 30 generally follows the underlying shape of the barb feature 40 and the tube 20. This reduces the volume of material in the overmould structure and so beneficially reduces material consumption and the energy and pressure requirements for its formation by injection moulding. This beneficially minimises the temperature required in the overmoulding process which in turn prevents the soft plastics material of the tube 20 from melting or over-softening and thus deforming. Furthermore, the increased thickness of the distal end portion and the first frusto-conical step of the overmould structure 30 in the region of the barb feature 40 reduces the risk of the barb 44 inducing stress cracks in the overmould structure 30.
[0068] The smooth outer finish provided by the overmould structure is aesthetically pleasing, easy to handle and minimises dirt traps.
[0069] The overmould structure 30 is a plastics material with a melting or softening temperature below the melting or softening temperature of the tube 20. Beneficially, this prevents the tube 20 from melting or over-softening during the overmoulding process. The overmould structure 30 may be an injection-mouldable form of the material from which the tube 20 is made. For example, the overmould structure 30 could be moulded from an injection-mouldable form of polyurethane. or the overmould structure 30 could be moulded from another plastics material that is suitable for injection moulding.
[0070] The overmould structure 30 is typically harder and more rigid than the flexible tubular body of the tube 20. As such, the overmould structure 30 provides strain-relief support to the tube 20 thereby reducing the effect of lateral loads on the tube 20. This is beneficial as cyclical loading may cause the connection between the connector 22 and the tube 20 to fatigue over time. Furthermore, the relative strength and rigidity of the overmould structure 30 prevents the overmould structure deforming and losing its shape over time. This beneficially ensures that the connection between the connector 22 and the tube 20 is not weakened or compromised over time.
[0071] Conversely, the overmould structure 30 is not as rigid as the connector 22 and as such the overmould structure 30 may flex slightly if it is subject to lateral loading. In this sense, the overmould structure 30 can absorb lateral loads. This is beneficial as it reduces the loading that the soft flexible tube 20 is subject to thereby improving the quality of the connection between the connector 22 and the tube 20.
[0072] Method steps for securing the connector 22 to the tube 20 with the overmould structure 30 are outlined in the flow chart of
[0073] Typically, between about 2 mm and 20 mm of the tube 20 is inserted into the central bore 24 of the connector 22 prior to overmoulding the overmould structure 30. This is beneficial as it provides strain relief that prevents the tube 20 inadvertently being disconnected from the connector 22 in the event that the tube 20 is pulled either longitudinally or laterally.
[0074] The connector 22 and the tube 20 may be assembled on a core pin or a mandrel (not shown) prior to being positioned in the mould 60. This is beneficial as it helps to stabilise and secure the connector 22 relative to the tube 20 prior to forming the overmould structure 30.
[0075] Next, in step 502, the tube 20 and connector 22 are placed within a mould 60 as shown in
[0076] In step 503, when the mould 60 has been closed as shown in
[0077] The melt temperature of the overmould material is typically between about 110 C. and 130 C. The overmould material may be injected into the mould 60 at a temperature of between about 160 C. and 180 C. In an example moulding process, injection takes less than 0.5 seconds and the mould 60 is held together for around 4 or 5 seconds to allow the overmould structure 30 to begin to cool and cure. The mould 60 is then opened and the overmould structure 30 is allowed to cool for about 15 seconds in the mould 60 to allow the overmould structure 30 to cure and harden sufficiently to be removed from the mould. The skilled reader will appreciate that the aforementioned parameters are by way of example only and the parameters will vary depending on the application.
[0078] In step 504, after the overmould structure 30 is allowed to cool and at least partially cure, the connector 22 and tube 20 are removed from the mould 60 with the overmould structure 30 securing the connector 22 to the tube 20.
[0079] Many variations are possible within the inventive concept. For example, whilst the barb 44 has been exemplified as a circumferentially-extending retention feature in the figures, the barb 44 could instead comprise one or more radially extending tabs or a radially extending flange to define an engagement zone between the barb 44 and the proximal wall 46. Furthermore, the mechanical retention feature may comprise a proximally extending neck portion 43 without a barb 44. The neck 43 may comprise a series of ridges, ribs or indents that the overmould structure 30 may flow into thereby acting as a mechanical retention feature. Such features advantageously increase the surface area of the connector 22 to which the overmould 30 may bond to.
[0080] The skilled reader will appreciate that the barb 40 could be omitted if the heat-bond between the connector 22 and the overmould structure 30 is sufficient to secure the connector 22 to the tube 20 in certain medical applications. Alternatively, another shape of anchor formation could extend proximally from the connector body 42 around the tube 20 to extend the surface area of the interface between the overmould structure 30 and the connector 22. For example, such an anchor formation could comprise a plain or circumferentially-ridged sleeve around the tube 20.
[0081] As shown in
[0082] The skilled reader will appreciate that whilst the overmould structure 30 has been described in the context of overmoulding it may equally be formed from another manufacturing process, for example, via vacuum casting, compression moulding or through injecting a two-part resin that may encapsulate a portion of the tube 20 and the connector 22 to form the overmould structure 30.
[0083] It will be appreciated that various changes and modifications can be made to the present invention without departing from the scope of the claims.