INJECTION PORT PROTECTOR

Abstract

A shielded injection port for use in an intravenous (IV) medication delivery system includes a single piece spherical shaped body having a hollow interior. The spherical shaped body is truncated, at a location above a plane that passes through a center of the spherical shaped body and defines a diameter of the spherical shaped body, so as to define a first opening formed at a first end of the spherical shaped body for receiving a fluid delivery member into the hollow interior. The shielded injection port also includes an injection port body that is integrally formed with the spherical shaped body. The injection port body has a first end that is contained within a bottom half of the hollow interior of the spherical shaped body such that the spherical shaped body is configured to surround and extend above the first end of the injection port body.

Claims

1. A shielded injection port for use in an intravenous (IV) medication delivery system, the shielded injection port comprising: a single piece spherical shaped body having a hollow interior, the spherical shaped body being truncated, at a location above a plane that passes through a center of the spherical shaped body and defines a diameter of the spherical shaped body, so as to define a first opening formed at a first end of the spherical shaped body for receiving a fluid delivery member into the hollow interior, the first opening having a diameter that is less than the diameter of the spherical shaped body; and an injection port body that is integrally formed with the spherical shaped body, the injection port body having a first end that is contained within a bottom half of the hollow interior of the spherical shaped body such that the spherical shaped body is configured to surround and extend above the first end of the injection port body, the injection port body extending outward from a second end of the spherical shaped body in a direction that is opposite the first end.

2. The shielded injection port of claim 1, wherein the spherical shaped body and the injection port body are formed of a molded plastic material.

3. The shielded injection port of claim 1, wherein the first end of the injection port body comprises a septum that is configured to allow a fluid from a fluid delivery device to be injected into the injection port body.

4. The shielded injection port of claim 1, wherein the injection port body comprises an elongated main body section with a flange at the first end that has a diameter greater than a diameter of the main body section.

5. The shielded injection port of claim 4, wherein the flange seats against the second end of the spherical shaped body.

6. The shielded injection port of claim 1, wherein the injection port body is configured to attach to a first tubing along a side of the injection port body and attach to a second tubing at a second end of the injection port body that is opposite the first end of the injection port body.

7. The shielded injection port of claim 6, wherein the injection port body and the second tubing are coaxial.

8. The shielded injection port of claim 1, wherein a length of the injection port body that is contained within the hollow interior is less than a length of the injection port body that lies outside the spherical shaped body.

9. The shielded injection port of claim 1, wherein the first opening of the spherical shaped body is located at a top edge of the spherical shaped body and is opposite and coaxial with the injection port body.

10. The shielded injection port of claim 1, wherein a side wall of the spherical shaped body is curved inwardly for positioning above the first end of the injection port body and the first opening is positioned for placement directly above the first end of the injection port body.

11. The shielded injection port of claim 1, wherein the plane that passes through the center of the spherical shaped body is a parallel to a plane that contains the entire first end of the spherical shaped body.

12. An intravenous (IV) medication delivery system comprising: a main line that is configured to be placed in fluid communication with a source of fluid for delivery to a patient and terminates in a distal end that is configured for insertion into the patient; and the shielded injection port of claim 1, wherein the injection port body is in fluid communication with the main line and the first end of the injection port body has an interface that is configured to allow a fluid from a fluid delivery device to be injected into the main line through the injection port body.

13. The system of claim 12, wherein the fluid delivery device comprises a syringe.

14. The system of claim 12, wherein a side wall of the spherical shaped boy is curved inwardly above the first end of the injection port body and the first opening is positioned directly above the first end of the injection port body.

15. The system of claim 12, wherein the spherical shaped body and the injection port body are formed of a molded plastic material.

16. The system of claim 12, wherein the first end of the injection port body comprises a septum that is configured to allow the fluid from the fluid delivery device to be injected into the main line.

17. The system of claim 12, wherein the injection port body comprises an elongated main body section with a flange at the first end that has a diameter greater than a diameter of the main body section.

18. The system of claim 12, wherein a length of the injection port body that is contained within the hollow interior is less than a length of the injection port body that lies outside the spherical shaped body.

19. The system of claim 12, wherein the first opening of the spherical shaped body is located at a top edge of the spherical shaped body and is opposite and coaxial with the injection port body.

20. A method for shielding an injection port that is located along tubing that is part of an intravenous (IV) medication delivery system and is configured to permit injection of a fluid into the tubing, the method comprising the step of: at least partially encapsulating the injection port within a hollow interior of a truncated spherical shaped protective shell such that at least a first end of the injection port is surrounded by the truncated spherical shaped protective shell and a top edge of the truncated spherical shaped protective shell lies above the first end of the injection port which lies within a bottom half of the protective shell with the top edge of the truncated spherical shaped protective shell defining a first opening that has a diameter less than a maximum diameter of the truncated spherical shaped protective shell, wherein the injection port and the truncated spherical shaped protective shell are integrally formed with one another to define a single part.

Description

BRIEF DESCRIPTION OF THE DRAWING FIGURES

[0012] FIG. 1 is a schematic of an exemplary intravenous (IV) medication delivery system having at least one inline injection port and at least one stopcock;

[0013] FIG. 2 is a side perspective view of a device according to a first embodiment for shielding an inline injection port to prevent surface contamination thereof;

[0014] FIG. 3 is a side and bottom perspective view of the device of FIG. 2;

[0015] FIG. 4 is a top and side perspective view of the device of FIG. 2;

[0016] FIG. 5 is a transverse cross-sectional view of the device of FIG. 2;

[0017] FIG. 6 is a top and side perspective view of the device of FIG. 2 with the inline injection port inserted and held therein;

[0018] FIG. 7 is a longitudinal cross-sectional view of the device of FIG. 2 with the inline injection port inserted and held therein;

[0019] FIG. 8 is a side perspective view of a device according to a second embodiment for mating with a stopcock or injection port and providing a shielded interface through which fluid can be injected;

[0020] FIG. 9 is a longitudinal cross-sectional view of the device of FIG. 8;

[0021] FIG. 10 is a transverse cross-sectional view of the device of FIG. 8;

[0022] FIG. 11 is a longitudinal cross-sectional view of the device of FIG. 8 including a movable cover which is shown in a closed position;

[0023] FIG. 12 is a longitudinal cross-sectional view of the device of FIG. 8 with the cover in an open position;

[0024] FIG. 13 is a side perspective view of a luer cap that is configured to cover the interface at which fluid is delivered to the IV system;

[0025] FIG. 14 is a side perspective view of a luer cap with a shield that is configured to cover the interface at which fluid is delivered to the IV system and the body of the device itself;

[0026] FIG. 15 is cross-sectional view showing a stopcock within integral protector; and

[0027] FIG. 16 is a cross-sectional view showing an injection port with integral protector.

DETAILED DESCRIPTION OF CERTAIN EMBODIMENTS

[0028] FIG. 1 shows a general schematic of an exemplary intravenous (IV) medication delivery system 10. The system 10 includes a fluid source 20 (e.g., an IV fluid which is typically mostly formed of water) and typically, the fluid source 20 is in the form of an IV bag. A drip chamber 25 is located just below the IV bag 20. Inside, the drip chamber 25, one can see the fluid drip down from the IV bag 20 into IV tubing 30 (IV conduit in the form of flexible clear plastic tubing). Along the IV tubing 30 includes a roller clamp 35 which is a device that is used to control the rate at which the IV fluid infuses. If the roller clamp 35 is rolled in one direction, the roller clamp 35 squeezes the IV tubing 30 more tightly, making it narrower and therefore making the fluid flow through the IV tubing 30 more slowly. Conversely, if the roller clamp 35 is rolled in the opposite direction, the device 35 loosens its pinching of the IV tubing 30, making the IV tubing 30 less narrow, and allowing the IV fluid to flow through at a faster rate.

[0029] A slide clamp 40 is disposed along the IV tubing 30 and is configured to completely stop the IV from flowing without having to adjust the roller clamp 35. The slide clamp 40 operates by pinching the IV tubing 30 completely shut when the IV tubing 30 is slid into the narrowest part of the slide clamp 40.

[0030] A cannula 50 is a hollow needle, or more often a length of flexible plastic tubing which has been inserted into the vein (arm or hand) using a needle. The IV tubing 30 is typically taped to the patient's arm to prevent the cannula 50 from coming out when the patient moves. There are two different kinds of veins that can be used for the placement of the cannula; namely, a peripheral vein, which is any vein that is not in the torso, or a larger more central vein in the chest. Thus, a peripheral line is an IV that is attached to a peripheral vein (typically inserted to the arm of hand), while a central line is an IV that is attached to a vein in the chest.

[0031] As discussed herein, medicine or fluids other than those in the IV bag 20 are injected into the IV tubing 30 at one or more locations using one or more different techniques. For example, an inline injection port, generally shown at 60 in FIG. 1, is one type of device through which medication (or other fluid) can be delivered directly into the IV tubing 30 for rapid administration. Alternatively, and as shown also in FIG. 1, medication can also be delivered into the IV tubing 30 by use of a stopcock 70 that assists the caretaker in controlling fluid flow through IV delivery system 10. Each of the injection port 60 and stopcock 70 is described in more detail below. It will also be understood that the system 10 can be configured to deliver one more medications to the patient and thus, the system 10 can include one or more injection ports 60 and/or one or more stopcocks 70.

[0032] Moreover, the IV delivery system 10 can also include one or more other injection points at which fluid, such as medication, can be injected. For example, FIG. 1 shows a secondary line 90 that is in fluid communication with the IV tubing 30 (which represents the main IV line) and a proximal end of the secondary line 90 terminates in a secondary injection port 91 that is configured to mate with a fluid delivery member, such as a syringe, for injecting fluid into the secondary line 90 and then into the IV tubing 30 for delivery to the patient. The main line (IV tube 30) and secondary line 90 can join one another at a catheter device 80 or the like that allows the combined fluid to flow to the patient.

[0033] In accordance with the present invention, each access point at which fluid (e.g., medication) is injected into the IV tubing 30 is protected against contamination (e.g., surface and/or airborne) by a device that can be thought of as a protector. As set forth below, depending on the type of access point (e.g., injection port or stopcock type injection port), the construction of the device (protector) will vary.

[0034] FIGS. 1-7 illustrate a first device (first protector) 100 according to a first embodiment and configured to shield an injection port that is associated with intravenous medication delivery as a means for preventing contamination of the injection port. More specifically, the first device 100 is configured to mate and be used with one inline injection port 60. As shown in FIGS. 1, 6 and 7, the injection port 60 can be in the form of a Y-shaped connector that is mounted at a desired location of the flow line (IV tubing 30) close enough to the lower or infusion end of the line to enable the fluid injection through the port 60 to be rapidly administered. The injection port 60 includes a main conduit section 62 that attaches to the IV tubing 30 and an upwardly raised arm 64 that extends radially outward from the main conduit section 62 a sufficient distance to provide ready access to a needle. The distal end of the arm 64 is capped with a needless injection port septum or a needle penetratable membrane 65 which can be formed of rubber or any other suitable material that is known and used in the art. Fluid, such as medication, is thus injected through the arm 64 into the main conduit section 62 where it joins the fluid from the IV bag and is delivered through the IV tubing 30 to the patient.

[0035] As mentioned herein, the illustrated device 100 is configured to be detachably coupled to the injection port 60. The device 100 is generally in the form of a structure that surrounds the injection port 60 and more specifically, surrounds the port septum 65 so as to prevent a foreign article, such as the caretaker's hand or fingers or any other material, from contacting the port septum 65. As discussed herein. The illustrated device 100 has a wall structure that extends above the port septum 65 so as to prevent easy access to the port septum 65 and has only limited access to the center of the device 100 in which the port septum 65 is located.

[0036] The device 100 can be in the form of a hollow structure that has a hollow interior 103 in which the port septum 65 is disposed with a wall of the device 100 surrounding and shielding the port septum 65 from contact with foreign matter. The device 100 also is configured to accommodate the injection port 60 in that the device 100 allows the main conduit section 62 and the arm 64 to pass therethrough. The device 100 can thus be detachably coupled to the injection port 60. In the illustrated embodiment, the device 100 has a generally spherical shaped body 101 with one end 102 being truncated and defining a main entrance into the hollow interior 103. It will be understood that the body 101 can have other shapes, such as a dodecahedron or other non-spherical shape so long as it has a hollow interior 103. Due to the spherical shape of the device 100, the truncation at the one end 102 defines a circular shaped opening (orifice) 105 that provides direct access to the hollow interior 103 and in particular, is sized so as to allow insertion of a syringe. An opposite end 104 of the body 101 also provides access to the hollow interior 103 in that a hole 110 is formed through the body 101. The hole 110 is formed at one end (a closed end) of a first slot 120 that is formed in the body 101. The first slot 120 extends from the hole 110 to the opening 105. As shown, the dimensions of the hole 110 can be enlarged relative to a width of the first slot 120. The hole 110 can be circular shaped and the first slot 120 can be a continuous slot having a uniform width. The first slot 120 receives the efferent limb of the IV tubing 30 and/or a portion of the inline injection port 60 that connects to the efferent limb.

[0037] The body 101 also includes a second slot 130 for receiving the afferent limb of the IV tubing 30 and/or a portion of the inline injection port 60 that connects to the afferent limb. The second slot 130 is formed in the body 101 at a location that is generally opposite the first slot 120; however, it will be appreciated that it can be formed at other locations as well to accommodate different types of injection ports 60. The second slot 130 is defined by a circular shaped hole 131 at a closed end of the second slot 130 and extends to the opening 105. Thus, each of the first and second slots 120, 130 can be accessed at the opening 105 and this permits, as described herein for insertion of the injection port 60 and the IV tubing 30. As shown, the sizes of the hole 110 and the hole 131 can be different or in some embodiments, the sizes can be the same. The first slot 120 has a longer length compared to the second slot 130.

[0038] Internally within the hollow interior 103 of the body 101 is a retaining structure that assists in holding the injection port 60 in place. For example, the retaining structure can be in the form of first and second supports (rails or brackets) 140, 150 that extend transversely across the body 101 and more particularly, extends transversely along a bottom surface of the body 101. Since the body 101 has a spherical shape, the bottom surface has a concave shape.

[0039] The first and second supports 140, 150 can be in the form of upstanding rails that protrude upwardly from the bottom surface. The first and second supports 140, 150 are spaced apart from one another and portions of the first and second supports 140, 150 are located on opposite sides of the first slot 120. This placement thus locates the first slot 120 centrally between the first and second supports 140, 150.

[0040] Since the hole 110 is preferably located at the center of spherical body 101, the center portions of the first and second supports 140, 150 can be formed to accommodate the hole 110 which has an enlarged shape relative to the first slot 120 as mentioned herein. Thus, the inner surfaces of the first and second supports 140, 150 can have opposing arcuate shaped recessed portions 141, 151, respectively, so as to accommodate the injection port 60 that is received through the hole 110. The end portions of the first and second supports 140, 150 can be parallel to one another. Preferably, the heights of the first and second supports 140, 150 are the same. The first and second supports 140, 150 can be integrally formed with the body 101 as by a common molding process when the device 100 is formed of a moldable material. In FIG. 6, the first and second supports 140, 150 have been removed to allow for clearer illustration of the other components and the injection port 60.

[0041] It will be understood that the injection port 60 can comprise a rigid plastic piece that is integral to the IV tubing which can have a more flexible material characteristic relative to the rigid plastic piece. It will therefore be understood that in one embodiment, the flexible IV tubing that is attached to the rigid plastic piece (injection port 60) can be the structures that pass through the slots 120, 130, while the rigid plastic piece can be contained within the body 101. Alternatively, a portion of the rigid plastic piece may pass through the slot 120. In any event, the slots 120, 130, permit routing of the IV tubing 30 in an inline injection port scheme. The body 101 is then disposed over the injection port 60 so as to surround the injection port 60.

[0042] The use of the device 100 with the injection port (an aseptic inline injection port) 60 will be understood with reference to FIGS. 6 and 7. The injection port 60 is disposed within the hollow interior 103 by inserting the efferent limb of tubing (IV tubing 30) through the first slot 120 and by pulling the injection port 60 down through the opening 105. The injection port 60 is disposed between the first and second supports 140, 150 so that the injection port 60 becomes wedged therebetween. The afferent limb of the IV tubing 30 is inserted through the second slot 130 to hold it in place during use. The injection port 60 is held in place by the first and second supports 140, 150, preventing twisting or dislodgement during use, and is shielded from contact with contaminated surfaces by the body (shell) 101. It will be understood that the construction of the body 101 is such that the side wall of the body 101 extends above the port septum 65 so as to prevent lateral contact with the port septum 65. In the case of sphere shaped body 101, the side wall not only extends above the port septum 65 but it also has inward curvature and therefore, the side wall extends inwardly toward the port septum 65 so as to provide additional protective coverage of the port septum 65.

[0043] The body (shell) 101 thus at least partially encapsulates the port septum 65 of the injection port 60. Due to the spherical shape of the shell 101 and the location of the injection port 60 within the hollow interior 103 provides for the partial encapsulation of the injection port 60 and therefore, it is very difficult for a contaminated surface to come into contact with the port septum 65 since the only point of access to the port septum 65 is through the small opening 105 that is located above the port septum 65.

[0044] To use the injection port 60, the body (shell) 101 is grasped in the hand and a syringe is inserted through the opening 105 and medication is injected into the injection port 60 through the port septum 65. Grasping the body 101 positions the hand a distance from the injection port and thus, in the case that there is surface contamination on the hand, the contamination is prevented from contacting the port septum 65.

[0045] In yet another embodiment, the device 100 can be an integral part of the injection port 60 in that the device 100 is permanently coupled to the injection port 60 and is not meant to be separated therefrom. In other words, the shell is permanently connected to the injection port structure such that it forms a single part that is used with an IV line. In this embodiment as in the others, the device 100 at least partially encapsulates the port interface of the injection port that receives the fluid. Any number of suitable manufacturing techniques can be used to form such a structure, including bonding and molding techniques.

[0046] The device 100 can be formed of any number of different materials that are suitable for the intended application described herein. For example, the device 100 can be formed of any number of different plastic materials that can have different degrees of flexibility (e.g., rigid, semi-rigid, etc.). The device 100 is of sufficient rigidity such that when the user grasps the body 101, the body 101 maintains its shape and does not collapse so as to cause the side wall of the body 101 to make contact with the port septum 65.

[0047] Now turning to FIGS. 1 and 8-10 which depict a second device (second protector) 200 in accordance with a second embodiment of the present and intended for use with the stopcock 70. There are many different types of stopcocks 70; however, all are configured such that a pivotable lever 71 controls flow of fluid through the stopcock 70 which is in fluid communication with the IV tubing 30. In the illustrated embodiment, the stopcock 70 has main legs 72, 72 to which the IV tubing 30 is inserted so as to place the stopcock 70 in the fluid circuit. A side leg 75 is the portion of the stopcock 70 through which the medication is delivered. The pivotable lever 71 is manipulated so as to control delivery of fluid from the side leg 75 into the IV tubing 30. The side leg 75 is typically in the form of a luer connector to allow for easy connection to a syringe or the like. In the illustrated embodiment, the side leg 75 comprises a female luer connector.

[0048] The second device 200 can be in the form of a hollow structure that has a hollow interior 203 into which a syringe or the like can be inserted for delivering the medication to the side leg (e.g., female luer connector) 75 of the stopcock 70 in a manner in which the attachment point between the fluid delivery member (e.g., a syringe) and the second device 200 is shielded. The device 200 is configured to be detachably coupled to the stopcock 70.

[0049] In the illustrated embodiment, the second device 200 has a generally spherical shaped body 201 with one end 202 being truncated and defining a main entrance into the hollow interior 203. It will be understood that the body 201 can have other shapes, such as a dodecahedron or other non-spherical shape so long as it has a hollow interior 203. Due to the spherical shape of the device 200, the truncation at the one end 202 defines a circular shaped opening (orifice) 205 that provides direct access to the hollow interior 203 and in particular, is sized so as to allow insertion of a syringe. An opposite end 204 of the body 201 also provides access to the hollow interior 203 in that a hole or channel 210 is formed through which fluid exits the body 201.

[0050] The body 201 includes a connector 220 that is configured to mate with both the stopcock 70 and the fluid delivery member (syringe). The connector 220 is located at the bottom of the body 201 and is securely coupled (attached) to the body 201 using any number of suitable techniques including a sealed snap-fit arrangement, use of a bonding agent, a molding process in which the connector 220 is integral to the body 201, etc. The connector 220 can be integrally formed with the body 201 and has a first end 222 that has a first connector part 230 and at an opposite second end 224, a second connector part 240 is formed. The first connector part 230 is disposed within the hollow interior 203 and is thus configured to mate with the fluid delivery member, while the second connector part 240 is disposed outside of the body (shell) 201 and is thus configured to mate with the side leg 75 of the stopcock 70. For example, the first connector part 230 can be in the form of a female luer connector that is configured to mate with a distal end (e.g., a male luer connector) of the fluid delivery member. The second connector part 240 can be in the form of a male luer connector that is configured to mate with a female luer connector (side leg 75) of the stopcock 70, thereby providing a fluid connection between the fluid delivery member (syringe) and the stopcock 70 to allow controlled delivery of medication or the like into the IV tubing 30.

[0051] It will also be appreciated that there are other types of luer connectors and the connector 220 can thus be substituted with any of these types of luer connectors.

[0052] Similar to the first device 100, the second device 200 is configured such that the fluid entry point, in this case, the first connector part 230 is shielded by the body 201 from contamination, such as surface contamination. It will be understood that the construction of the body 201 is such that the side wall of the body 201 extends above the first connector part 230 so as to prevent lateral contact with the first connector part 230. In the case of sphere shaped body 201, the side wall not only extends above the first connector part 230 but it also has inward curvature and therefore, the side wall extends inwardly toward the first connector part 230 so as to provide additional protective coverage of the first connector part 230.

[0053] To use the second device 200, the body 201 is grasped in the hand and a syringe is inserted through the opening 205 and is connected to the first connector part 230 (female luer connector). The stopcock 70 is then opened, as by manipulating the lever, to permit inflow from the syringe and the medication is injected into the stopcock 70 (i.e., the side leg 75 thereof).

[0054] In yet another embodiment, the second device 200 is configured to mate to a needless luer-lock injection port that includes a needless septum. This type of injection port includes a luer type connector at one end which is configured to mate to the second connector part 240 of the device 200. Thus, device 200 is not limited to use of stopcock constructions but can be used with any luer type needleless injection port.

[0055] In yet another embodiment shown in FIG. 15, the device 200 can be an integral part of the stopcock 70 in that the device 200 is permanently coupled to the side leg through which medication is injected. In this embodiment, the stopcock and shell form a single part that is then used with the IV line. Any number of techniques can be used to form such structure including suitable bonding and molding operations. In this embodiment, as with the other embodiments, the shell still at least partially encapsulates the interface, such as a luer connector or septum, that receives fluid from the fluid delivery device (e.g., syringe).

[0056] FIG. 16 shows another embodiment in which a device 400 (which can have the same or similar construction as the device 200) is integral to the injection port 60 structure to form a single piece (part). The septum 65 is located within the hollow interior as in the embodiment of FIG. 7; however, since there are no slots, the IV tubing 30 passes and is routed outside the shell. The shell is thus coupled to the septum 65 and surrounds it.

[0057] Each of the first and second devices 100, 200 can be constructed so as to include a cap or cover structure that strategically covers either the main opening through which a syringe is inserted to access the needle penetrable membrane as in the case of device 100 and/or a cap or shield that covers the luer connector of the second device 200 and/or the main opening.

[0058] The device 100, 200 can be constructed such that it includes a cover or cap that can move between an open and closed position relative to the opening 105, 205. FIGS. 11 and 12 show a cover 250 that is part of the device 200; however, it will be readily understood that the cover 250 can be constructed in the same manner with respect to the device 100 and in such case, closes off the opening 105. The cover 250 can be constructed such that it is in the form of the truncated portion of the spherical shell (body) that was removed to form the opening 105, 205. The cover 250 thus completes the sphere and has a concave bottom surface and convex top surface as shown. It can be coupled to the remaining part of the device 100, 200 using any number of techniques, including the use of a hinge 255 as shown in the figures. To open the cover 250, a lip or tab 259 is formed at one edge of the cover 250. The cover can be spring loaded as well to ensure that it remain in a closed position.

[0059] In one embodiment, a cover or cap can be intended to cover at least the port septum 65 and in some embodiments, is intended to cover the opening 105. For example, a cap can be configured to fit over and be secured to the port septum 65 and since the cap is intended to be placed on the port septum 65 without having to touch the port septum 65, the cap can be disposed at a distal end of an elongated handle. A user thus holds the cap by the handle and inserts the cap through the opening 105 and by manipulating the handle, the cap is placed on the port septum 65. A friction fit or luer connection can be formed between the cap and the membrane.

[0060] As with the first device 100, the second device 200 can include a cap or cover to shield the first connector part 230 from contaminants, such as airborne contaminants As shown in FIG. 13, a luer cap 300 can be configured to mate with the first connector part 230 so as to cover and shield the first connector part 230. Since the user is not to insert a finger(s) through the opening 205, the luer cap 300 includes an elongated handle 305 that attaches as its distal end to the luer cap 300 and is of a length that permits the user to insert the luer cap 300 through the opening 205 and mate with the first connector part 230. For example, if the first connector part 230 has threads, the handle 305 can be rotated to cause rotation of the luer cap 300 to mate the luer cap 300 to the first connector part 230. It will be appreciated that the luer cap 300 can be a plastic cap and/or can contain an anti-microbial substance (e.g., Curos™ available from 3M).

[0061] In yet another embodiment shown in FIG. 14, the proximal end of the handle 305 is connected to a cover 325 which is sized and shaped to fit and close the opening 205. For example, the cover 325 can have a disk (circular) shape. The cover 325 can have a handle 330 in the form of an upstanding protrusion that can be grasped by the user.

[0062] When the cover is designed to cover the opening 105, 205, a recessed landing can be formed about the opening for receiving the cover. The length of the handle is such that when the luer cap is coupled to the first connector part 230, the cover 325 covers the opening 205.

[0063] It will also be understood that the second device 200 can be used with other types of needleless injection ports that have a luer connector. For example, the system 10 can include a secondary branch defined by a segment of IV tubing. One end of the secondary branch terminates in a connector or the like (e.g., central catheter) in which the main IV line is also fluidly connected. The other end of the secondary branch terminates in a needless port which has an exposed luer connector that is configured to mate with the second device 200. For example, the exposed luer connector can be a female luer connector that mates with the male luer connector 240 of the second device 200. In this way, the second device 200 is fluidly connected to the exposed luer connector of the secondary branch.

[0064] In at least one embodiment of the present invention, the body of the device 100, 200 is formed so as to have an at least substantially spherically shape with the connector being contained in a bottom half of the body and the first opening is formed in a top 20% of the body which is truncated so as to define the first opening. For example, the body can be at least 70% spherical in one embodiment, at least 75% in another, at least 80% in another and at least 90% in yet another embodiment. However, it is possible to truncate the sphere at other locations that are at or above the equator of the sphere depending in part upon the overall size of the sphere, etc.

[0065] The injection interface to which the fluid delivery member mates for delivery fluid to the IV line is preferably located in a bottom one half of the body of the device (protector) and can be located in a bottom one third of the body of the device (protector) and further can be located in a bottom one fourth of the body of the device (protector). In general, the lower the injection interface is located in the hollow interior of the body (shell), the more difficult it is for contamination to occur since this injection interface is well shielded from surface contamination and the like. The above values are calculated based on the height of the body as measured from the open top edge of the shell to the bottom of the shell.

[0066] Notably, the figures and examples above are not meant to limit the scope of the present invention to a single embodiment, as other embodiments are possible by way of interchange of some or all of the described or illustrated elements. Moreover, where certain elements of the present invention can be partially or fully implemented using known components, only those portions of such known components that are necessary for an understanding of the present invention are described, and detailed descriptions of other portions of such known components are omitted so as not to obscure the invention. In the present specification, an embodiment showing a singular component should not necessarily be limited to other embodiments including a plurality of the same component, and vice-versa, unless explicitly stated otherwise herein. Moreover, applicants do not intend for any term in the specification or claims to be ascribed an uncommon or special meaning unless explicitly set forth as such. Further, the present invention encompasses present and future known equivalents to the known components referred to herein by way of illustration.

[0067] The foregoing description of the specific embodiments will so fully reveal the general nature of the invention that others can, by applying knowledge within the skill of the relevant art(s) (including the contents of the documents cited and incorporated by reference herein), readily modify and/or adapt for various applications such specific embodiments, without undue experimentation, without departing from the general concept of the present invention. Such adaptations and modifications are therefore intended to be within the meaning and range of equivalents of the disclosed embodiments, based on the teaching and guidance presented herein. It is to be understood that the phraseology or terminology herein is for the purpose of description and not of limitation, such that the terminology or phraseology of the present specification is to be interpreted by the skilled artisan in light of the teachings and guidance presented herein, in combination with the knowledge of one skilled in the relevant art(s).

[0068] While various embodiments of the present invention have been described above, it should be understood that they have been presented by way of example, and not limitation. It would be apparent to one skilled in the relevant art(s) that various changes in form and detail could be made therein without departing from the spirit and scope of the invention. Thus, the present invention should not be limited by any of the above-described exemplary embodiments, but should be defined only in accordance with the following claims and their equivalents.