Catheter assembly including sealing member

Abstract

A catheter assembly includes a catheter, a hub, and a sealing member. The catheter defines one or more lumens. The hub includes one or more hub extensions dimensioned to be received within the one or more lumens of the catheter. The sealing member is positioned adjacent the interface of the catheter and the hub. The sealing member includes an expandable material which increases in volume upon exposure to moisture.

Claims

1. A catheter assembly, comprising: a catheter defining at least one lumen; a hub including at least one hub extension dimensioned to be received within the at least one lumen of the catheter; and a sealing member being of an expandable material which increases in volume upon exposure to moisture, wherein the at least one hub extension defines a first connector surface and the at least one lumen of the catheter is defined by a second connector surface, wherein when the at least one hub extension is received within the at least one lumen of the catheter, the first connector surface engages the second connector surface to define an interface, wherein the sealing member is positioned adjacent the interface and is configured to expand into the interface between the first connector surface and the second connector surface upon exposure to the moisture such that the expandable material fills in any gaps between the at least one hub extension and the at least one lumen at the interface.

2. The catheter assembly of claim 1, wherein at least a portion of at least one of the catheter or the hub includes a rigid material and wherein at least a portion of at least one of the catheter or the hub includes an elastomeric material.

3. The catheter assembly of claim 1, wherein the expandable material includes a hydrophilic polymer.

4. The catheter assembly of claim 1, wherein the expandable material includes a hydrophilic gel.

5. The catheter assembly of claim 1, wherein the sealing member defines a sleeve, the sleeve being positionable on at least a portion of at least one of the first or second connector surfaces.

6. The catheter assembly of claim 5, wherein the catheter defines at least two lumens, and the sleeve defines at least two lumens, each lumen of the sleeve being dimensioned to accommodate at least one of the at least two lumens of the catheter.

7. The catheter assembly of claim 6, wherein at least one of the at least two lumens of at least one of the catheter or the sleeve are substantially D-shaped.

8. The catheter assembly of claim 1, wherein the sealing member includes a bioactive agent.

9. The catheter assembly of claim 1, wherein the first connector surface of the at least one hub extension does not fully engage the second connector surface defining the at least one lumen of the catheter such that one or more points of poor engagement exist between the first connector surface and the second connector surface, and wherein the sealing member is configured to expand into the one or more points of poor engagement between the first connector surface and the second connector surface.

10. The catheter assembly of claim 1, wherein the sealing member is compressed between the hub and a proximal end of the catheter.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) Various embodiments of the presently disclosed catheter assemblies including improved sealing features are described herein with references to the accompanying drawings, wherein:

(2) FIG. 1 is a perspective view of a catheter assembly in accordance with the present disclosure;

(3) FIG. 2 is an enlarged perspective view of a distal portion of the hub assembly of the catheter assembly shown in FIG. 1 with one embodiment of the presently disclosed sealing member positioned thereon;

(4) FIG. 3 is a perspective view, with parts separated, of a portion of another embodiment of a catheter assembly according to the present disclosure;

(5) FIG. 3A is a front plan view of the sealing member of FIG. 3;

(6) FIG. 4 is a perspective view of the catheter assembly of FIG. 3 after the hub assembly and catheter have been assembled; and

(7) FIG. 5 is an enlarged perspective view of a distal portion of another embodiment of the present disclosure.

DETAILED DESCRIPTION OF THE EMBODIMENTS

(8) In the discussion that follows, the term proximal or trailing will refer to the portion of a structure that is closer to a clinician, while the term distal or leading will refer to the portion of a structure that is farther from the clinician. As used herein, the term subject refers to a human patient or other animal. The term clinician refers to a doctor, nurse or other care provider and may include support personnel.

(9) FIG. 1 illustrates one embodiment of a catheter assembly 10. The catheter assembly 10 includes a catheter 50, a hub assembly 20 and first and second extension tubes 30, 40 extending proximally from the hub assembly 20. The hub assembly 20 includes a hub 26 and one or more hub extensions 22, 24 which extend distally from the hub 26. The hub extensions 22, 24 each define substantially D-shaped lumens 22L, 24L therethrough. In particular, hub extensions 22, 24 each have a proximal end 22P, 24P and a distal end 22D, 24D. At least a portion of the hub assembly 20 may include a substantially rigid material, such as a polymeric material.

(10) The catheter 50 defines one or more lumens. In embodiments, the catheter 50 defines two adjacent substantially D-shaped lumens 52A, 52B. The lumens 52A, 52B of the catheter 50 have complimentary mating surfaces with the D-shaped hub extensions 22, 24. As illustrated, distal ends 22D, 24D of the hub extensions 22, 24 may be positioned within lumens 52A, 52B of catheter 50. The one or more hub extensions 22, 24 are dimensioned to be received within the one or more lumens 52A, 52B of the catheter 50 and define one or more first connector surfaces 26. The catheter 50 defines one or more second connector surfaces 54 that engage first connector surfaces 26 in a close geometric fit when the one or more hub extensions 22, 24 are received within the one or more lumens 52A, 52B of the catheter 50. In this manner, hub assembly 20 fluidly couples first and second extension tubes 30, 40 with catheter 50. Alternately, the catheter lumens and hub extensions may have a variety of different configurations.

(11) With continued reference to FIG. 1, the first extension tube 30 has a proximal end 30P and a distal end 30D. Distal end 30D of first extension tube 30 is attached to hub assembly 20 and proximal end 30P of first extension tube 30 is connected to a first luer adapter 60. Second extension tube 40 has a proximal end 40P and a distal end 40D. Distal end 40D of second extension tube 40 is coupled to hub assembly 20, while proximal end 40P of second extension tube 40 is coupled to a second luer adapter 70. Each extension tube 30, 40 may include a clamp 80 for inhibiting and/or permitting the passage of fluids through extension tubes 30, 40 upon the clamping and/or unclamping thereof.

(12) Referring now to FIG. 2, hub extensions 22, 24 of hub assembly 20 may include a sealing member 100 positioned thereon in order to provide a close geometric compression fit seal at the interface between the hub assembly 20 and the catheter 50. The sealing member 100 is positioned adjacent the interface of the catheter 50 and the hub assembly 20 and is formed of an expandable material which increases in volume upon exposure to moisture, such as blood. The expandable material may expand to a volume sized to improve the seal at the interface of the catheter 50 and the hub 26. In this respect, the expandable material fills any gaps at the interface upon exposure to moisture to prevent the ingression and/or egression of fluids between catheter 50 and hub extensions 22, 24 of hub assembly 20. The expandable material may include a hydrophilic polymer, such as Tecophilic, and/or a hydrophilic gel. During and/or after assembly, the expandable material may be exposed to water to cause the expandable material to expand to help seal the catheter 50 to the hub 26, and lessen or eliminate any potential leaks. The sealing member 100 may also include any suitable bioactive agent to prevent undesirable biological growth.

(13) The sealing member 100 may be coated and/or chemically bonded to the external surface of at least a portion of the hub extensions 22, 24 relative to the one or more first connector surfaces 26. As illustrated in FIG. 2, the sealing member 100 is coated on the proximal ends 22P, 24P of the hub extensions 22, 24. Alternately, the sealing member 100 may be coated and/or chemically bonded to at least a portion of the inner wall of catheter 50 defining the one or more lumens 52A, 52B of the catheter 50. In this respect, the sealing member 100 may improve the securement of the catheter 50 to the hub assembly 20 and may improve the seal between the catheter 50 and hub assembly 20.

(14) With reference to FIGS. 3-4, in another embodiment, a sealing member, generally referred to as 200, is provided which is similar to sealing member 100. However, as best illustrated in FIG. 3A, sealing member 200 defines a sleeve 202. In embodiments, the sleeve 202 may define a gasket (e.g., an o-ring) type seal. The sleeve 202 is positionable relative to at least a portion of one or more of the first and second connection surfaces 26, 54. The sleeve 202 may be produced by a coating applied to a portion of the hub assembly 20 in liquid suspension that dries to form the sleeve 202.

(15) As shown in FIG. 3A, the sleeve 202 defines one or more lumens 204A, 204B dimensioned to accommodate the hub extensions 22, 24 of hub assembly 20. In the illustrated embodiment, the sleeve 202 defines two adjacent substantially D-shaped lumens 204A, 204B that are dimensioned to receive hub extensions 22, 24 of hub assembly 21. When catheter 50 is secured to hub extensions 22, 24 of hub assembly 21, sealing member 200 is compressed between a body 27 of hub assembly 21 and a proximal end of catheter 50 (FIG. 4). As discussed above with respect to sealing member 100, sealing member 200 is formed from an expandable material, such as a hydrophilic polymer, which expands upon exposure to moisture to improve the seal between the catheter 50 and the hub extensions 22, 24 of hub assembly 21. Because the sealing member 200 is compressed between a body 27 of hub assembly 21 and the proximal end of the catheter 50, the sealing member 200 provides a seal within the butt joint, and may expand upon exposure to moisture to compensate for and seal any irregularities in the proximal end of the catheter 50. For example, if the lumens 204A, 204B at the proximal end of the catheter 50 do not fully engage the hub extensions 22, 24, the sealing member 200 may expand into those points of poor engagement to provide a seal.

(16) As illustrated in FIG. 5, another embodiment of a hub assembly, shown generally as 23, includes a hub 29. The hub 29 has a casing 300 and one or more hub extensions 22, 24 which extend distally from the hub 29. The casing 300 defines a cavity 302 dimensioned to accommodate the sealing member 200. When the catheter 50 is secured within the casing 300, a proximal end of the catheter 50 is positioned to abut the sealing member 200 within the casing 300 such that the seal between the hub extensions 22, 24 and the one or more lumens 52 of the catheter 50 is improved. As discussed above, sealing member 200 is formed from an expandable material. In this manner, the casing 300 and the sealing member 200 provide an improved sealed connection between the catheter 50 and the hub 29. In this embodiment, the sealing member 200 provides a seal at the butt joint between the proximal end of the catheter 50 and the casing 300, similar to the seal described above. Because the sealing member 200 is disposed within the cavity 302, the sealing member is constrained in the radially outward direction. This radial constraint directs the sealing member 200 into any irregularities at the proximal end of the catheter 50 as the sealing member 200 expands, thus providing a seal.

(17) In order to prevent undesirable biological growth, the sealing members or an internal surface of the catheter may have medicinal agents or bioactive agents impregnated and/or coated thereon.

(18) Medicinal agents that may be incorporated into or provided on the disclosed sealing members or on an internal surface of the catheter include antimicrobial agents, anti-virals, anti-fungals, and the like. Antimicrobial agents as used herein is defined by an agent which by itself or through assisting the body (immune system) helps the body destroy or resist microorganisms which may be pathogenic (disease causing). The term antimicrobial agent includes antibiotics, quorum sensing blockers, surfactants, metal ions, antimicrobial proteins and peptides, antimicrobial polysaccharides, antiseptics, disinfectants, anti-virals, anti-fungals, and combinations thereof.

(19) While several embodiments of the disclosure have been shown in the drawings and/or discussed herein, it is not intended that the disclosure be limited thereto, as it is intended that the disclosure be as broad in scope as the art will allow and that the specification be read likewise. Therefore, the above description should not be construed as limiting, but merely as exemplifications of particular embodiments. Those skilled in the art will envision other modifications within the scope and spirit of the claims appended hereto.