WO2015044834A1

WO2015044834A1 - Needle-free connector

Info

Publication number: WO2015044834A1
Application number: PCT/IB2014/064562
Authority: WO
Inventors: Giuseppe Maffei
Original assignee: Giuseppe Maffei
Priority date: 2013-09-25
Filing date: 2014-09-16
Publication date: 2015-04-02
Also published as: ITMO20130263A1

Abstract

The needle-free connector (1) for an infusion line comprises: a containment body (4) which can be coupled to the line, comprising a housing (5) having a base (6) at one end and an entry (7) at the opposite end; a pipe (8, 17) suitable for the fluid-dynamic communication with the line, which pipe (8, 17) comprises a tubular element (8) having an access (9, 10) and protruding from the base (6) in the housing (5), so as to define between the tubular element (8) and the housing (5) a chamber which is closed at the base (6); and a sealing element (14) suitable for moving between an occlusion position where it seals the entry (7) and an opening position where it frees the entry (7), the sealing element (14) being sealingly fitted onto the tubular element (8), obstructing the access (9, 10) thereof in the occlusion position, and comprising an occlusion portion (15) which plugs the chamber, so as to define a pneumatic spring.

Description

NEEDLE-FREE CONNECTOR

Technical Field

The present invention relates to a needle-free connector for infusion lines.

Background Art

Needle-free connectors are known, used as valves for the selective insertion of fluids in infusion lines, e.g., of the type comprising venous catheters.

This type of connector permits the intravenous administration of drugs or other fluids using needle-free syringes or "sets" circuits terminating in a standard needle-free connector.

In detail, the syringes have a connection sleeve which fits into the connector through one of its free ends, moving a sealing element of the connector that seals such end when it is not coupled with syringes.

Such sleeve couples in a removable way to the above-mentioned free end, by means of a Luer connection or the like.

This way, the intravenous infusion of medical fluids can be obtained, avoiding cases of medical personnel being accidentally pricked or of accidental catheter lacerations.

Numerous cases have nevertheless occurred of blood infections related to the use of catheters (or CRBSI), the aetiology of which seems traceable to the use of this type of connector.

These infections are most likely tied to the formation of blood clots inside the catheter, due to a backflow of blood from the patient's vessel to the catheter connected to it, the backflow being caused by a phenomenon known in the technical sector by the name of negative displacement, i.e., the movement of the blood inside the catheter.

In fact, during the injection of the fluid from the syringe to the catheter, the above-mentioned sleeve occupies a certain volume inside the connector, where it is placed in fluid-dynamic communication with the catheter and, therefore, with the blood vessel.

Following the separation of the syringe from the connector itself, the sleeve leaves a space that tends to be filled by the fluid inside the catheter.

This movement of the fluid from the catheter into the connector produces a backflow, or movement, of the patient's blood inside the catheter.

This blood can cause a clot which, in certain conditions, above all if of large size, can lead to the growth of pathogens and/or occlusions inside the catheter which can seriously jeopardize the patient's health.

Risks for the patient's health have also been found in the case of positive displacement.

Description of the Invention

The main aim of the present invention is to provide a needle-free connector for infusion lines which permits avoiding or strongly restricting the above- mentioned negative or positive displacements.

Another object of the present invention is to provide a needle-free connector for infusion lines which can overcome the above mentioned drawbacks of the prior art in the ambit of a simple, rational, easy and effective to use as well as low cost solution.

The above mentioned objects are achieved by the present needle-free connector for infusion lines made according to claim 1.

Brief Description of the Drawings

Other characteristics and advantages of the present invention will become better evident from the description of a preferred, but not exclusive, embodiment of a needle-free connector for infusion lines, illustrated by way of an indicative, but not limitative example in the accompanying drawings in which:

Figure 1 is an axonometric view of the connector according to the invention;

Figure 2 is an axonometric exploded view of the connector according to the invention;

Figure 3 is a longitudinal section view of the connector;

Figure 4 is an axonometric view of the connector and of a syringe before their coupling;

Figure 5 is a longitudinal section view of the connector according to the invention which is moved close to the syringe;

Figure 6 is the view of the previous illustration, wherein the connector is coupled to the syringe.

Embodiments of the Invention With reference to these figures, globally indicated by 1 is the needle-free connector of the invention.

The proposed connector 1 is intended for use with an infusion line, especially of the type comprising an intravenous catheter or of the type made up of or comprising a medical bag or the like.

In practice, the connector is an inlet valve for the administration of medical fluids or saline solution, etc.

In detail, the connector 1 is of the type adapted to receive the outlet sleeve 2 (or taper) of the needle-free syringe 3 containing the above-mentioned fluid.

The proposed connector 1 comprises a containment body 4 which can be coupled, preferably in a releasable way, both to said infusion line and to said syringe.

Preferably, this occurs by using locking systems of the Luer lock type or the like.

In actual fact, at its distal end 20, intended for coupling to the syringe 3, and at its proximal end 19, intended for coupling to the catheter, the connector 1 has threaded coupling means that can be of the Luer lock type or the like.

Herein below, for more convenient exposition but without loss of general information, reference will be made to the case wherein the infusion line is made up of the above-mentioned catheter, connected at one end to a vessel of a patient while at the other end it is coupled to the connector 1.

In practice, as is known, the patient's circulatory system remains connected to the catheter, while the syringe is coupled to the connector 1 only when a substance has to be administered.

At the end of administration, the syringe is separated from the connector 1.

The body 4, preferably made of polycarbonate or other plastic material, comprises a housing 5, preferably of tubular shape, intended to be coupled to the syringe, in the way explained above.

The housing 5 has a base 6, at its own end, and an entry 7 at the opposite end 20, i.e. at the free end.

The connector 1 of the invention comprises a pipe 8, 17 suitable for the fluid- dynamic communication with the catheter, following coupling between this and the connector 1.

In turn, the pipe 8, 17 comprises a tubular element 8, substantially needle shaped, having at least an access 9, 10 and protruding from the base 6 in the housing 5, so as to define between the tubular element 8 and the housing 5 itself a chamber, which is closed at the base 6.

In practice, the tubular element 8 protrudes from the base 6 towards the inside of the housing 5, so that between the external side surface thereof and the internal lateral surface of the housing 5 a chamber is identified which is closed at the base 6.

Furthermore, the pipe preferably comprises an outlet tang 17 which can be coupled to the catheter.

Preferably, the housing 5 and the pipe 8, 17 are axial-symmetric, coaxial and both elongated.

In particular, the tubular element 8 is shorter than the housing 5 and its free end 11 does not protrude from the above-mentioned entry 7 and is in fact separate from this and located inside the housing 5.

Always preferably, the tubular element 8 is tapered towards its free end 11, which can be pointed.

Even more in detail, the tubular element 8 can comprise one or more access through holes 9, 10 obtained on its lateral wall, in order to define a fluid- dynamic path 12 which originates from said hole 9, 10, crosses the pipe 8, 17 mentioned and terminates in an exit 13 arranged at the attachment with the catheter.

Preferably, the body 4 of connector 1 is, in its entirety, axial-symmetric.

The proposed connector 1 comprises a sealing element 14, this too preferably axial-symmetric, contained in the housing 5.

The sealing element 14 is suitable for moving between an occlusion position where it seals the entry 7 of the housing 5, preventing the fluid-dynamic communication between the outside of the connector 1 and the aforementioned fluid-dynamic path 12, and an opening position wherein it frees the entry 7. According to an important aspect of the invention, the sealing element 14 is sealingly fitted onto the tubular element 8. In detail, in its occlusion position, the sealing element 14 obstructs the access 9, 10 of the tubular element 8.

The sealing element 14 comprises an occlusion portion 15 which plugs the above-mentioned chamber, so as to define a pneumatic spring.

In practice, the chamber of the housing 5 comprises air and, since it is closed at the base 6, as explained above, and since it is plugged by the occlusion portion 15 of the sealing element 14, a closed space, or inter-space 21, is created in it, which provides resistance to the compression caused by the shift of the sealing element 14.

To be precise, such occlusion portion 15 completely occupies, instant by instant, a section of the chamber, i.e., one of its longitudinal portions.

In practice, when the sealing element 14 is in the occlusion position, the pneumatic spring in the rest position, or in any case of maximum extension. When, instead, the sealing element 14 is in the opening position, then the spring is loaded.

At the time of describing the operation of the invention, it will be explained how such pneumatic spring helps achieve the proposed objects.

The sealing element 14 is flexible, and preferably made of a yielding and in particular compressible material, e.g., silicone.

In detail, the sealing element 14 is fitted tightly over the tubular element 8 and, preferably, completely covers it when it is in its occlusion position.

In the preferred embodiment of the invention, the sealing element comprises a sheath 14 which tightly covers the external surface of the tubular element 8.

In this case, the sealing element 14 can comprise a cavity, preferably blind, suitable for housing at least a distal portion of the tubular element 8 comprising its free end 11.

In practice, the sheath 14 can internally shape a cavity, e.g., with a shape complementary to that of the tubular element 8, which cavity, when idle, can have smaller dimensions than those of such element.

This way, once the sealing element 14 has been fitted over the tubular element

8, the flexible characteristics of the former hold it firmly onto the latter.

In particular, the sheath 14 is coupled with interference to the tubular element 8. In the preferred embodiment of the invention, the sheath 14 shapes a thickened head 15 comprising the above-mentioned occlusion portion.

In this case, the sealing element 14 can also comprise a thinner tail 16 than the head 15, shaped like a sleeve, which tail 16 extends between the head 15 and the base 6 of the housing 5.

In practice, the head 15 abuts with interference the internal lateral surface of the housing 5, and therefore of the chamber, and is suitable for sliding along said tubular element 8, without the continuous adhesion between sheath 14 and tubular element 8 ever failing.

In detail, in the preferred embodiment wherein the access 9, 10 or the accesses of the tubular element 8 are placed in distal portion 11 of the tubular element 8, the head 15 of the sealing element 14 closes, at the same time, such accesses and the entry 7 of the housing 5, when the sealing element 14 is in occlusion position.

In an embodiment not shown, the sheath 14, at one or more points along the above-mentioned tail 16, has a number of ribs or grooves to obtain its programmed deformation.

Said ribs or grooves can be obtained at the external surface (facing the interspace 21) or the inner surface (i.e., in the above-mentioned inner cavity) of the sheath itself.

This solution facilitates both the collapse and the elastic return in the initial configuration of the sheath 14.

Herein below, for convenience of exposure and without loss of general information, reference will be made to the preferred case wherein the tubular element 8 is a pointed needle having a number of above-mentioned side holes 9, 10 arranged at its free distal end 11.

In this case, the head 15 of the sheath 14 makes up a distal end of the sealing element 14 through which the needle or better its pointed distal end 11 can penetrate.

Consequently, when the sheath 14 is in the occlusion position, the head 15 surrounds and surmounts the tip of the needle 8, extending above it until it closes the access 9, 10, while it extends laterally between the needle 8 and the housing 5 to plug the chamber (see Figures 4 and 6).

When it moves towards the opening position, according to the procedures shown below, the head 15 moves towards the base 6 of the housing 5, allowing itself to be perforated by the tip of the needle 8 and surpassing the distal portion 11 of the latter, so as to free the entry 7 of the housing 5 and the accesses of the needle 8, while however keeping sealed the above-mentioned inter-space 21 which helps define the pneumatic spring (see Figure 7).

In practice, the elasticity characteristics of the head 15 are such that the needle 8 is able to perforate it through a deformable orifice formed in it, which orifice closes again automatically, sealing itself, when the sealing element 14 returns to the occlusion position and the needle 8 therefore exits from the channel.

While the head 15 is pierced by the needle 8, the lateral walls of the latter are always very adhered onto the orifice, so as to prevent any flow of fluids, including air, through the orifice itself.

It must be noticed that the fact that the needle 8 comprises a tip without openings at its top, which tip penetrates the head 15 of the sheath 14 also when this is in the occlusion position, permits avoiding having empty spaces or discontinuities between the needle 8 and the head 15, wherein air or other fluids could trickle, thus germinating pathogens and in any case potentially compromising the isolation of the fluid-dynamic path 12 from the non-sterilized external environment.

In an embodiment of the invention not shown here, the housing 5 comprises, at its base 6, at least a groove wherein the proximal end of the sheath 14 is interference fitted.

In practice, the edge of the proximal end, which preferably identifies a ring around the needle 8, is fastened within a groove obtained for the purpose in the base 6, so as to assist the tight adhesion of sheath 14 to the external surface of the needle 8.

The operation of the invention is described below.

Initially, the connector 1 is connected to the catheter at one of its proximal ends

19, while its distal end 20 which comprises the entry 7 is free.

The entry 7 is closed by the sealing element 14 which, in this step, is in the occlusion position, where it isolates and seals the above fluid-dynamic path 12 (see Figure 6).

Every time the medical staff members have to administer a substance, they couple the syringe 3 to the housing 5 causing its dispensing sleeve 2 to penetrate through the entry 7 (see Figures 6 and 7).

This way, the sleeve 2, or taper, of the syringe 3 presses against the head 15 of the sealing element 14, moving it along the needle 8 in the direction of the several times mentioned base 6.

In this step, the distal portion of the needle 8 is uncovered, and the sleeve 2 of the syringe 3 receives it internally.

When the sealing element 14 reaches the opening position, the sleeve 2 of the needle 8 also internally comprises the accesses 9, 10 of the needle 8.

The dimensions and the shape of needle 8 and sleeve 2 are selected in such a way that the former fits sealed into the latter.

In this step, the pneumatic spring is loaded, by effect of both the compression of the air contained in the above inter-space 21, and of the elasticity of the sealing element 14 itself.

In sliding along the needle 8, the sheath 14 always remains substantially strongly adhered to it, including thanks to the increase in pressure inside the inter-space 21 which compresses the sheath 14 against the external surface of the needle 8.

This way, no empty space is created between sealing element 14 and needle 8 or between needle 8 and sleeve 2.

It should be noticed that the increase and the decrease in pressure is always and only on the outside of the sheath 14, namely in the inter-space 21 defined around it.

In this step, the fluid-dynamic path 12 defined within the connector 1 places the inside of the syringe 3 in communication with the catheter.

Consequently, the health worker injects the envisaged dose of fluid from the syringe 3 to the catheter passing through the connector 1.

At this point, the operator extracts the sleeve 2 from the housing 5 of the connector 1. Advantageously, the sealing element 14 climbs back up along the needle 8, as the sleeve 2 is gradually removed from the latter, without delay and without therefore allowing an empty space to form between sleeve 2, needle 8 and sealing element 14.

This way, when the sleeve 2 passes by the accesses, the fluid included in the fluid-dynamic path 12 does not undergo any appreciable aspiration in the direction of the accesses of the needle 8 and, consequently, no negative displacement is produced of the blood within the catheter, except to a negligible extent.

What is more, the invention completely prevents the occurrence of positive displacements.

Claims

1) Needle-free connector (1) for an infusion line, comprising:

at least a containment body (4) which can be coupled to said line, comprising a housing (5) having a base (6) at one end and an entry (7) at the opposite end;

at least a pipe (8, 17) suitable for the fluid-dynamic communication with said line, which pipe (8, 17) comprises a tubular element (8) having at least an access (9, 10) and protruding from said base (6) in the housing (5), so as to define between said tubular element (8) and said housing (5) a chamber which is closed at said base (6); and

at least a sealing element (14) suitable for moving between an occlusion position where it seals said entry (7) and an opening position where it frees said entry (7);

characterized by the fact that said sealing element (14) is sealingly fitted onto said tubular element (8), obstructing the access (9, 10) thereof in said occlusion position, and comprises at least an occlusion portion (15) which plugs said chamber, so as to define a pneumatic spring.

2) Connector (1) according to claim 1, characterized by the fact that said sealing element (14) is flexible.

3) Connector (1) according to claim 2, characterized by the fact that said sealing element comprises a sheath (14) which tightly covers the external surface of said tubular element (8).

4) Connector (1) according to claim 3, characterized by the fact that said sheath (14) shapes a thickened head (15) which comprises said occlusion portion (15), which abuts the internal lateral surface of said housing (5) and is suitable for sliding along said tubular element (8).

5) Connector (1) according to one or more of the preceding claims, characterized by the fact that said sealing element (14) comprises a cavity suitable for housing at least a distal portion of said tubular element (8) comprising its free end (11).

6) Connector (1) according to claim 5, characterized by the fact that said sealing element (14) comprises a distal end (15) that can be crossed by said distal portion of the tubular element (8).

7) Connector (1) according to one or more of the preceding claims, characterized by the fact that said tubular element (8) comprises at least a through hole (9, 10) on its own lateral wall, which is said access.

8) Connector (1) according to one or more of the preceding claims, characterized by the fact that said body (4) is axial- symmetric.