The present disclosure relates generally to intravenous (IV) catheter assemblies and, more specifically, to IV catheter assemblies with manually-actuable valve mechanisms to stop flow through the catheter adapter and/or any attached extension sets and allow for replacement of various components.
Catheters are commonly used for a variety of infusion therapies. For example, catheters may be used for infusing fluids, such as normal saline solution, various medicaments, and total parenteral nutrition, into a patient. Catheters may also be used for withdrawing blood from the patient.
A common type of intravenous (IV) catheter device includes a catheter that is over-the-needle. As its name implies, the catheter that is over-the-needle may be mounted over an introducer needle having a sharp distal tip. The IV catheter device may include a catheter adapter, the catheter extending distally from the catheter adapter, and the introducer needle extending through the catheter. The catheter and the introducer needle may be assembled so that the distal tip of the introducer needle extends beyond the distal tip of the catheter with the bevel of the needle facing up away from skin of the patient. The catheter and introducer needle are generally inserted at a shallow angle through the skin into vasculature of the patient.
IV catheter devices can include an extension set with a plurality of ports and/or connectors for administering or withdrawing fluids from the patient, and/or flushing the catheter device. One or more of these ports and/or connectors may be replaceable; however, there is currently no way to occlude the extension set during such a replacement procedure. Thus, a need exists in the art for an IV catheter device that allows for simple occlusion of tubing associated therewith.
Provided herein is an intravascular catheter assembly, including a catheter adapter having a distal end, a proximal end, a first lumen arranged between and in fluid communication with the distal end and the proximal end, a catheter arranged at the distal end of the catheter adapter and in fluid communication with the lumen, and a first side port in fluid communication with the lumen, with a first fluid conduit having a distal end and a proximal end. The distal end of the fluid conduit may be coupled to the side port and a connector having a proximal end, a distal end connected to the fluid conduit, and a second lumen therethrough, the connector including a manually-actuable valve.
In certain configurations, the valve is arranged at the proximal end of the connector. Optionally, the valve may be arranged at the distal end of the connector. The valve may include a sliding mechanism configured to displace a portion of the second lumen, such that the portion of the second lumen has a longitudinal axis that is offset from a longitudinal axis of the second lumen. The connecter may be a t-connector. Optionally, the connector may be a y-connector.
In additional configurations, the assembly may also include a second fluid conduit extending from the connector. In further configurations, the assembly also includes a needleless access connector coupled to the connecter, wherein the valve is rotatable between at least a first position in which the valve obstructs fluid flow to the needleless access connector, a second position in which the valve obstructs fluid flow to the second fluid conduit, and a third position in which fluid can flow through the valve to both the needles access connector and the second fluid conduit.
The second lumen of the assembly may have an inner diameter substantially equivalent to an inner diameter of the first fluid conduit and the second fluid conduit. Optionally, the valve may be rotatable around an axis defined by the first fluid conduit. In certain configurations, the valve may include a stopcock. The stopcock may be a one-way stopcock. In other configurations, the stopcock may be a three-way stopcock. Optionally, the stopcock may include one or more arms. The stopcock may be rotatable about an axis normal to a flow of fluid through the second lumen.
In other configurations, the connector of the assembly may also include a second side port in fluid communication with the second lumen. Optionally, the stopcock may be rotatable about an axis defined by the second side port. In still other configurations, the assembly may include a needleless access connector coupled to the connector. The needleless access connector may be releasably coupled to the connector. In still other configurations, the valve may be rotatable between at least a first position in which the valve obstructs fluid flow through the second lumen, and a second position in which fluid can flow through the lumen. The valve, when in the first position, engages with the needleless access connector, thereby preventing removal of the needleless access connector.
In still other configurations, the intravascular catheter assembly includes a catheter adapter having a distal end, a proximal end, a first lumen arranged between and in fluid communication with the distal end and the proximal end, a catheter arranged at the distal end of the catheter adapter and in fluid communication with the lumen, and a first side port in fluid communication with the lumen. The intravascular catheter assembly further includes a first fluid conduit having a distal end and a proximal end, the distal end of the fluid conduit coupled to the side port, a connector comprising a proximal end, a distal end connected to the fluid conduit, and a second lumen therethrough, and a needleless access connector coupled to the connecter. At least one of the connector and the needleless access connector includes a valve that is rotatable between at least a first position in which the valve obstructs fluid flow to the needleless access connector, a second position in which the valve obstructs fluid flow to the second fluid conduit, and a third position in which fluid can flow through the valve to both the needles access connector and the second fluid conduit.
The following description is provided to enable those skilled in the art to make and use the described embodiments contemplated for carrying out the invention. Various modifications, equivalents, variations, and alternatives, however, will remain readily apparent to those skilled in the art. Any and all such modifications, variations, equivalents, and alternatives are intended to fall within the spirit and scope of the present invention.
For purposes of the description hereinafter, the terms “upper”, “lower”, “right”, “left”, “vertical”, “horizontal”, “top”, “bottom”, “lateral”, “longitudinal”, and derivatives thereof shall relate to the invention as it is oriented in the drawing figures. However, it is to be understood that the invention may assume various alternative variations, except where expressly specified to the contrary. It is also to be understood that the specific devices illustrated in the attached drawings, and described in the following specification, are simply exemplary embodiments of the invention. Hence, specific dimensions and other physical characteristics related to the embodiments disclosed herein are not to be considered as limiting.
It should be understood that any numerical range recited herein is intended to include all values and sub-ranges subsumed therein. For example, a range of “1 to 10” is intended to include all sub-ranges between (and including) the recited minimum value of 1 and the recited maximum value of 10, that is, having a minimum value equal to or greater than 1 and a maximum value of equal to or less than 10.
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In some non-limiting embodiments or aspects, the first catheter assembly 10 may include a first catheter 22 extending from the distal end 14. In some embodiments, the first catheter 22 may include a peripheral intravenous catheter, a midline catheter, or a peripherally-inserted central catheter. Catheter 22 may be formed of any suitable material and may be of any useful length, as known to those of skill in the art. In some non-limiting embodiments or aspects, the first catheter assembly 10 may include a first fluid conduit 24 extending from the side port 18. First fluid conduit 24 may be formed of any suitable material known to those of skill in the art, and may have a distal end 26 and a proximal end 28, and first fluid conduit 24 may be coupled, at distal end 26 thereof, to side port 18. In some non-limiting embodiments or aspects, a connector 30 may be coupled to a proximal end 28 of first fluid conduit 24. Connector 30 may be a t-connector (e.g., one side port arranged at a 90 degree angle relative to a longitudinal axis of connector 30), a y-connector (e.g., one side port arranged at an angle of about 15 to about 75 degrees, optionally a 25, 60, or 75 degree angle, relative to a longitudinal axis of connector 30), or any other type of connector known in the art, and may include a second lumen 31 (shown in
In some non-limiting embodiments or aspects, catheter assembly 10 may include an extension set including a second fluid conduit 34. In non-limiting embodiments, connector 30 includes a side port to which extension set (e.g., second fluid conduit 34) may be connected. Extension sets are known to those of skill in the art and are commercially available from, for example, Becton, Dickinson and Company under the tradename NEUTRACLEAR. In some non-limiting embodiments or aspects, second fluid conduit 34 may include a luer connection 36 at an end thereof. In some non-limiting embodiments or aspects, the extension set may include a clamp 40, to allow for occlusion of second fluid conduit 34. Clamp 40 and second fluid conduit 34 may be formed of any suitable materials known to those of skill in the art. In non-limiting embodiments, second lumen 31 has an inner diameter that is substantially equivalent to an inner diameter of first fluid conduit 24 and/or second fluid conduit 34.
Catheter assembly 10 may include manually-actuable valve 32 for slowing and/or stopping fluid flow, for example through first fluid conduit 24, between first fluid conduit 24 and connector 30, and/or between connector 30 and a second fluid conduit 34, by occluding flow. As used herein, “occlude” or “occlusion” means at least a slowing of fluid flow through a conduit, such as fluid conduit 24, and includes within its scope complete cessation of flow through an occluded portion of a conduit. While the accompanying drawings may show valve 32 as part of, or separate from, connector 30, those of skill will appreciate that useful valves as described herein can be arranged, relative to connector 30, in any suitable manner to occlude flow to one or both of a needleless access connector 38 and/or a second fluid conduit 34.
Those of skill will appreciate that arrangements of manually-actuable valve 32 along fluid conduit 24 and/or as part of connector 30 can allow for cessation of flow of fluid, such as blood, from first lumen 20 to connector 30 and/or second fluid conduit 34. This can allow a user, such as a healthcare professional, to replace one or more components of catheter assembly 10, such as needleless access connector 38. Needleless access connectors are known to those of skill in the art and are commercially available from, for example, Becton, Dickinson and Company under the tradenames MAXPLUS, MAXZERO, SMARTSITE, and Q-SYTE. Manually-actuable valve 32 can assume any useful configuration, for example those as described and illustrated herein. That is, while certain exemplary figures may depict manually-actuable valve 32 as a stopcock, sliding mechanism, or the like, it is to be appreciated that any manually-actuable valve 32 shown in any accompanying figure may be utilized in any other embodiment shown and described herein.
In non-limiting embodiments, manually-actuable valve 32 is part of connector 30, which may connect first fluid conduit 24 to second fluid conduit 34 and/or to needleless access connector 38. Manually-actuable valve 32 may be arranged at a distal end of connector 30, a proximal end of connector 30, or between a proximal end and distal end of connector 30.
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Although the present disclosure has been described in detail for the purpose of illustration based on what is currently considered to be the most practical and preferred embodiments or aspects, it is to be understood that such detail is solely for that purpose and that the present disclosure is not limited to the disclosed embodiments or aspects, but, on the contrary, is intended to cover modifications and equivalent arrangements that are within the spirit and scope of the appended claims. For example, it is to be understood that the present disclosure contemplates that, to the extent possible, one or more features of any embodiment may be combined with one or more features of any other embodiment.
The present application claims priority to U.S. Provisional Application Ser. No. 63/321,945, entitled “Integrated Catheter with Manually-Actuable Valve Mechanism”, filed Mar. 21, 2022, the entire disclosure of which is hereby incorporated by reference in its entirety.
Number | Date | Country | |
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63321945 | Mar 2022 | US |