Systems and methods to compensate for compression forces in an intravascular device

Abstract

A system and method for providing vent channel geometries to compensate for compression forces experienced by a septum within an intravascular device.

Claims

1. An intravascular device comprising: a catheter adapter having a cylindrical inner surface, wherein the diameter of the inner surface increases from a first location until a second location, the second location being distal to the first location; and a septum having an outer surface, a proximal end, and a distal end forming a distal surface, the outer surface having one or more vents that each extend from the proximal end to the distal end to thereby allow air or liquid to bypass the septum by passing through the one or more vents, wherein each vent comprises a vent outer surface that is recessed from the outer surface of the septum and a vent distal surface disposed distally and inwardly with respect to the vent outer surface; wherein the septum is positioned within the inner surface of the catheter adapter with the distal end of the septum being located at the second location such that, when the septum is compressed within the inner surface of the catheter adapter, the diameter of the distal end of the septum is greater than the diameter of a portion of the septum located at the first location.

2. The intravascular device of claim 1, wherein the vent outer surface and the vent distal surface form an edge that is not chamfered.

3. The intravascular device of claim 1, wherein the one or more vents comprise a plurality of vents.

4. The intravascular device of claim 3, wherein the plurality of vents are equally spaced around the outer surface of the septum.

5. The intravascular device of claim 1, wherein the inner surface includes a protrusion at the second location against which a portion of the distal end of the septum is positioned.

6. The intravascular device of claim 1, wherein, when the septum is positioned within the inner surface of the catheter adapter, the first location is distal to the proximal end of the septum.

7. The intravascular device of claim 6, wherein the first location is distal to a midpoint of the septum.

8. An intravascular device comprising: a catheter adapter having a cylindrical inner surface, wherein the diameter of the inner surface increases from a first location until a second location, the second location being distal to the first location; and a septum having an outer surface, a proximal end, and a distal end forming a distal surface, the outer surface having one or more vents that each extend from the proximal end to the distal end to thereby allow air or liquid to bypass the septum by passing through the one or more vents, wherein each of the vents extends along an entire length of the septum; wherein the septum is positioned within the inner surface of the catheter adapter with the distal end of the septum being located at the second location such that, when the septum is compressed within the inner surface of the catheter adapter, the diameter of the distal end of the septum is greater than the diameter of a portion of the septum located at the first location.

9. The intravascular device of claim 8, wherein the vent outer surface and the vent distal surface form an edge that is chamfered.

10. The intravascular device of claim 8, wherein the one or more vents comprise a plurality of vents.

11. The intravascular device of claim 10, wherein the plurality of vents are equally spaced around the outer surface of the septum.

12. The intravascular device of claim 8, wherein the inner surface includes a protrusion at the second location against which a portion of the distal end of the septum is positioned.

13. The intravascular device of claim 8, wherein, when the septum is positioned within the inner surface of the catheter adapter, the first location is distal to the proximal end of the septum.

14. The intravascular device of claim 13, wherein the first location is distal to a midpoint of the septum.

Description

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS

(1) In order that the manner in which the above-recited and other features and advantages of the invention are obtained will be readily understood, a more particular description of the invention briefly described above will be rendered by reference to specific embodiments thereof which are illustrated in the appended drawings. These drawings depict only typical embodiments of the invention and are not therefore to be considered to limit the scope of the invention.

(2) FIG. 1 is a perspective view of an intravascular device in accordance with a representative embodiment of the present invention.

(3) FIG. 2 is a perspective view of an intravascular device following removal of an introducer needle in accordance with a representative embodiment of the present invention.

(4) FIG. 3 is an exploded cross-sectioned view of an intravascular device in accordance with a representative embodiment of the present invention.

(5) FIG. 4 is a perspective cross-sectioned view of a compression compensating septum in accordance with a representative embodiment of the present invention.

(6) FIG. 5 is a perspective cross-sectioned view of an assembled intravascular device incorporating compression relief features in accordance with a representative embodiment of the present invention.

(7) FIG. 6 is a detailed perspective cross-sectioned view of FIG. 5 in accordance with a representative embodiment of the present invention.

(8) FIG. 7 is a perspective view of a septum having compression relief features in accordance with a representative embodiment of the present invention.

(9) FIG. 8A is a cross-section view of the septum of FIG. 7 in accordance with a representative embodiment of the present invention.

(10) FIG. 8B is a cross-section view of FIG. 8A following assembly of an intravascular device in accordance with a representative embodiment of the present invention.

(11) FIG. 9A is a cross-section view of a catheter adapter having compression relief features and a septum in accordance with a representative embodiment of the present invention.

(12) FIG. 9B is a cross-section view of the catheter adapter of FIG. 9A fitted with a septum in accordance with a representative embodiment of the present invention.

(13) FIG. 10A is a perspective view of the distal end of a septum having compression relief features prior to being assembled in accordance with a representative embodiment of the present invention.

(14) FIG. 10B is a perspective view of the distal end of a septum having compression relief features as installed in a catheter adapter of an intravascular device in accordance with a representative embodiment of the present invention.

(15) FIG. 10C is a perspective view of the proximal end of a septum having compression relief features as installed in a catheter adapter of an intravenous device in accordance with a representative embodiment of the present invention.

(16) Embodiment of the present invention will be best understood by reference to the drawings, wherein like reference numbers indicate identical or functionally similar elements. It will be readily understood that the components of the present invention, as generally described and illustrated in the figures herein, could be arranged and designed in a wide variety of different configurations. Thus, the following more detailed description, as represented in the figures, is not intended to limit the scope of the invention as claimed, but is merely representative of presently preferred embodiments of the invention.

DETAILED DESCRIPTION OF THE INVENTION

(17) Referring now to FIG. 1, an intravascular device 10 is illustrated. The intravascular device 10 generally includes a catheter 12 coupled to a distal end 16 of a catheter adapter 14. The catheter 12 and the catheter adapter 14 are integrally coupled such that an inner lumen of the catheter adapter 14 is in fluid communication with an inner lumen of the catheter 12. The catheter 12 generally comprises a biocompatible material having sufficient rigidity to withstand pressures associated with insertion of the catheter into a patient.

(18) In some embodiments, as shown, the catheter 12 is an over-the-needle catheter that is made of a flexible or semi-flexible polymer material and which may be used in combination with a rigid introducer needle 22. The rigid introducer needle 22 enables the insertion of the non-rigid over-the-needle catheter into a patient. The introducer needle 22 can be coupled to a needle hub 26 that is selectively coupled to the proximal end 18 of the catheter adapter 14. The introducer needle 22 is typically inserted through the catheter 12 such that a tip of the needle 22 extends beyond the tapered tip 20 of the catheter 12. Insertion of the introducer needle 22 into the vein of the patient creates an opening in the vein through which the tapered tip 20 of the catheter 12 is inserted. The outer surface of the tapered tip 20 enables gradual insertion of the catheter 12 into the opening.

(19) In other embodiments, the catheter 12 is not an over-the-needle catheter, but comprises a rigid, polymer material, such as vinyl. Rigid catheters can include a beveled cutting surface that is utilized to provide an opening in a patient to permit insertion of the catheter 12 into the vascular system of the patient. Accordingly, in some embodiments, the catheter 12 comprises a metallic material, such as titanium, stainless steel, nickel, molybdenum, surgical steel, and alloys thereof. Still, in other embodiments, surgically implanted catheters may also be used in combination with the present invention.

(20) In some embodiments, catheter 12 is a peripheral-type intravenous catheter that generally comprises a short or truncated catheter for insertion into a small peripheral vein. Such catheters generally comprise a diameter of about a 14-gauge catheter or smaller (on a Stubs scale), and are between about 13 mm to 52 mm in length. Peripheral intravenous catheters are typically designed for temporary placement. The short length of the catheter facilitates convenient placement of the catheter. In other embodiments, catheter 12 is a midline or central catheter, which may be longer and used for more extended periods.

(21) Referring now to FIG. 2, once catheter 12 is inserted into the vein of the patient, the introducer needle 22 is removed proximally from catheter 12 to provide a fluid conduit through the interior lumen 36 of catheter 12, which can be connected to a fluid source. In some embodiments, a portion of catheter 12 and/or catheter adapter 14 is configured to be connected to a section of intravenous tubing 40 to further facilitate delivery of a fluid to, or removal of a fluid from a patient.

(22) In some embodiments, a proximal end 18 of catheter adapter 14 further includes a flange 32. Flange 32 provides a positive surface which may be configured to enable coupling of an intravenous tubing 40 or patient conduit to the catheter assembly 10. In some embodiments, the flange 32 includes a set of threads 30. The threads 30 are generally provided and configured to compatibly receive a complementary set of threads 44 comprising a portion of a male luer or conduit coupler 42. Conduit coupler 42 is generally coupled to an end portion of the patient conduit 40 in a fluid-tight manner. In some embodiments, an inner portion of conduit coupler 42 is extended outwardly to provide a probe member 46.

(23) In some embodiments, probe member 46 is compatibly inserted within a proximal end 18 of the catheter adapter 14 to activate the septum therein, thus opening a fluid path within catheter adapter 14. In some configurations, following insertion of the probe member 46 into the proximal end 22 of catheter adapter 14, conduit coupler 42 is interlock with the coupler 42 and the flange 28 (via the sets of threads 30 and 44), such as by rotation. In some embodiments, the position of probe 46 within catheter adapter 14 advances a septum activator 80 through a septum 50 of the catheter adapter 14, thereby opening a fluid pathway, as taught in U.S. patent application Ser. No. 12/544,624, which is incorporated herein by reference.

(24) Referring now to FIG. 3, an exploded, cross-sectional view of an intravascular device 10 is shown. In some embodiments, intravascular device 10 comprises a catheter adapter 14 having an inner surface 60 for receiving a septum 50. In some embodiments, inner surface 60 comprises a recessed groove having a length and depth sufficient to accommodate the length and outer diameter of septum 50. Further, inner surface 60 may include one or more vents 70 which provide fluid communication between a distal chamber 62 and proximal chamber 64 of the catheter adapter 14. For example, in some embodiments vents 70 permit passage of air from distal chamber 62 to proximal chamber 64 thereby equilibrating air pressures within the adjacent chambers 62 and 64. This equilibration prevents buildup of air pressure within distal chamber 62 which may prevent a desirable flashback during insertion of catheter 12 into a patient.

(25) In some embodiments, the one or more vents 70 are designed to allow the flow of air and stop the flow of blood. In some embodiments septum 50 comprises a single vent. In other embodiments septum 50 comprises a plurality of vents. For example, in some embodiments septum 50 comprises between two vents and forty vents. Further, in some embodiments septum 50 comprises six vents.

(26) In some embodiments, vents 70 further comprise a proximal opening 74 and a distal opening 76. A cross sectional area of proximal and distal openings 74 and 76 may be selected to permit or exclude passage of air and/or liquid through vents 70. Accordingly, in some embodiments proximal and distal openings 74 and 76 comprise a cross sectional area between about 0.000007 to 0.00004 inches.sup.2. In other embodiments, the openings 74 and 76 have a cross sectional area between about 0.00001 to 0.00003 inches.sup.2. In other embodiments, openings 74 and 76 have a cross sectional area of about 0.00002 inches.sup.2. For instance, in some embodiments openings 74 and 76 have a height of approximately 0.001 to 0.003 inches and a width of approximately 0.010 inches. In other embodiments, openings 74 and 76 have a height of about 0.002 to 0.003 inches and a width of about 0.005 inches.

(27) Similarly, vents 70 between the septum 50 and the inner surface 60 of the catheter adapter 14 can be specifically configured to permit blood and air to pass therethrough at an estimated range of flow rates. For instance, in some embodiments vents 70 permit blood to flow therethrough at a rate between about 10 to 200 ml/hr. In other embodiments, vents 70 permit blood to flow therethrough at a rate between about 15 to 150 ml/hr. In yet other instances, vents 70 permit blood to flow therethrough at a rate between about 50 to 100 ml/hr. At these rates, the rate of blood flow into the proximal chamber 64 can be paced to provide a clinician with adequate time to correctly locate the catheter within a patient's blood vessel. Accordingly, in some embodiments, vents 70 have a cross sectional area greater than 0.00003 inches.sup.2. In other embodiments, the vents 70 have a cross sectional area greater than 0.00004 inches.sup.2. In other embodiments, the vents 70 have a cross sectional area of about 0.0001 inches.sup.2. In other embodiments, the vents 70 have a cross sectional area of about 0.001 inches.sup.2.

(28) With continued reference to FIG. 3, in some embodiments septum 50 comprises a membrane 52 which provides a defeatable barrier between distal and proximal chambers 62 and 64. For example, in some embodiments membrane 52 comprises a slit 56 which is biased closed due to axial, compressive forces applied to the outer surface of septum 50 when fit into inner surface 60. In other embodiments, membrane 52 comprises a pierceable surface that may be defeated by a sharpened instrument, such as a needle tip.

(29) Generally, septum 50 comprises a hyperelastic material that, when assembled, interfaces with inner surface 60 through interference fit. In some instances, the compressive forces experience by septum 50 in the assembly intravascular device 10 cause the cross sectional area of vents 70 and openings 74 and 76 to be deformed, wherein a portion of the septum 50 is forced into the adjacent vents 70. Accordingly, in some embodiments intravascular device 10 comprises various compression relief features to compensate for compressive forces experience due to the interference fit.

(30) Referring now to FIGS. 3 and 4, in some embodiments a distal portion of septum 50 is modified to compensate for the aforementioned deformation due to compressive forces. For example, in some embodiments a chamfer 58 is provided on the distal end of the outer surface of septum 50. In some embodiments, chamfer 58 tapers inwardly in a distal direction 72, wherein the length of chamfer 58 corresponds approximately to the thickness 66 of membrane 52. In other words, in some embodiments chamfer 58 tapers inwardly from a proximal surface 68 of membrane 52 to a distal surface 78 of membrane 52. Further, in some embodiments a radial distance of chamfer 58 is approximately equal to the maximum deformation of vents 70 under maximum expected compression when assembled. As such, the vent geometry will experience minimal effect from compression, as shown in FIGS. 5 and 6.

(31) Referring now to FIG. 7, in some embodiments a plurality of channels or vents 100 are provided in outer surface 102 of septum 150. Thus, septum 150 may be positioned or seated within a catheter adapter 140 having a smooth inner surface 120 which does not include channels or vents, as shown in FIGS. 8B and 9A-10C, below. Thus, vent 100 provides fluid communication between distal and proximal chambers 62 and 64, in accordance with the previous discussion. Further, vents 100 comprise distal and proximal openings 172 and 174 having respective surface areas for accommodating passage of fluids, as previously discussed.

(32) In some embodiments, a distal portion of vent 100 is chamfered 158 to compensate for the aforementioned deformation due to compressive forces of the interference fit. As shown in FIG. 8A, prior to assembly chamfer 158 provides an increased distal opening 172 which tapers outwardly in a proximal direction to a final vent depth 178. In some embodiments, compressive forces experienced at the proximal end of septum 150 are less than compressive forces experienced at the distal end of septum 150. Accordingly, in some embodiments proximal opening 174 is configured to have a cross section surface area approximately equal to the cross section surface area of vent 100 at vent depth 178. Thus, desirable final geometries of vent depth 178, distal opening 172 and proximal opening 174 are achieved following assembly of intravascular device 10, as shown in FIG. 8B.

(33) Referring now to FIG. 9A, in some embodiments a distal portion 160 of inner surface 120 is chamfered. As such, catheter adapter 140 may be used with a septum 180 having a non-chamfered distal outer surface 182, as shown. Upon assembly, surface 182 is deformed due to compressive forces, thereby causes outer surface 182 to be displaced into the chamfered portion 160 of inner surface 120, as shown in FIG. 9B. As such, the desirable final geometries of vent depth 178, distal opening 172 and proximal opening 174 are achieved.

(34) In some embodiments, septum 250 comprises vent 200 having a distal opening 272 with an initial cross section area that is greater than the desired final cross section area. Once assembled, compressive forces reduce the cross section area of opening 272, thereby achieving a desired final cross section area, as shown in FIG. 10B. Further, in some embodiments the desired final cross section area of distal opening 272 is equal to, or approximately equal to a desired final cross section area of the proximal opening 274, as shown in FIG. 10C. Accordingly, the compression relief features of the present invention compensate for compression forces thereby preventing occlusion or blockage of flow through the respective openings and vents.

(35) The present invention may be embodied in other specific forms without departing from its structures, methods, or other essential characteristics as broadly described herein and claimed hereinafter. The described embodiments are to be considered in all respects only as illustrative, and not restrictive. The scope of the invention is, therefore, indicated by the appended claims, rather than by the foregoing description. All changes that come within the meaning and range of equivalency of the claims are to be embraced within their scope.