This invention relates to a valve for use with intravenous containers or circuits.
Air embolism can occur when air enters a patient's circulation via an intravenous catheter. The consequences can be significant and include stroke and death. The use of locking fittings within intravenous, giving sets and associated devices has reduced the incidence of entrainment of air when an intravenous line becomes disconnected and the patients venous pressure becomes sufficiently low (negative) to allow air to enter the circulation. This is a significant risk in the use of central venous catheters.
Up until relatively recently most intravenous fluids were contained in rigid bottles and in order for the fluid within the bottle to flow into the intravenous line by gravity a venting needle was placed in the bottle to allow air to enter the bottle as the fluid emptied. When this system was common-place nursing staff and medical personnel were always aware of the risk of air entering the giving tube once the bottle had emptied, and particular care was taken to prevent this occurrence or to deal with air in the giving set before it entered the patient's circulation. For the last 15 or 20 years most intravenous fluids are now presented in collapsible bags. For this reason there is no need to use a vent needle to allow air to enter the bags as they allow all of their contents to empty by simply collapsing. This has greatly reduced the likelihood of air entering the circuit. Many giving sets also come equipped with a pump. This facilitates the rapid infusion of fluid into the patient.
Recently a very popular intravenously administered analgesic (paracetamol) has been available. This is presented in a small glass bottle and requires the use of a venting needle in the same fashion as the older intravenous fluid bottles mentioned previously. Unfortunately the contents of these small bottles can empty quite quickly and the attendant may not notice the air entering the intravenous line. This poses the risk of air embolism. The air that has entered the line may be flushed into the patient's circulation by simply replacing the empty bottle with new fluids or by using the pump to, administer fluids.
A number of valves have been designed in the past that close when the contents of a container or burette empty these are of a float valve style and are dependent on gravity and tend to be bulky, or stick as a result of the negative pressure developed when the valve closes.
Furthermore, any valve or device that is intended to address this problem would need to be of low cost and single use. Such a device could be incorporated within the giving set or could be an addition to such a system.
According to the present invention there is provided a valve for use with a container having intravenous liquid therein, the valve including:
a valve body including a valve chamber formed therein;
an inlet in fluid communication with the valve chamber;
means for connecting the inlet, in use, to the container so that liquid can flow through the inlet to said valve chamber;
an outlet having means for connection, in use, to a catheter for intravenous delivery of the liquid;
the outlet including an outlet port which opens to said chamber, the port being surrounded by a valve seat;
a diaphragm;
mounting means for mounting the diaphragm to the body so that a peripheral edge or edge region sealingly engages the body and closes said chamber and such that the diaphragm sealingly engages the valve seat;
the arrangement being such that, in use, the head of liquid within the container unseats the diaphragm from the valve seat so that the liquid flows to said outlet but when the level of liquid in the container falls to a predetermined level the diaphragm sealingly engages the valve seat to stop further flow of liquid to the outlet.
The invention also provides an apparatus for delivery of a liquid intravenously to a subject, the apparatus including:
a container having intravenous liquid therein;
a bung, or receptacle for receiving a giving set spike, closing the container;
a valve as defined above, wherein the pointed end penetrates the bung and said inlet ports are in fluid communication with the intravenous liquid in the container, the arrangement being such that when the container is disposed with its bung downwards the head of liquid unseats the diaphragm from the valve seat so that the liquid is intravenously delivered to a subject until the level of liquid in the container falls to a level where the liquid cannot hold the diaphragm away from the valve seat and flow stops.
Preferably, said means for connecting the inlet includes an inlet spigot which is formed with a pointed end which can penetrate a bung in the container.
Preferably, the inlet spigot includes inlet passageways which extend from the valve chamber to said pointed end where they terminate in inlet ports on said pointed end.
Preferably, the diaphragm is moulded from resilient material.
Preferably, the diaphragm is moulded from silicon rubber.
Preferably, the periphery of the diaphragm is relatively thin and the centre thereof is relatively thick so that resilient flexure occurs at the periphery of the diaphragm whereas the centre moves like a solid body or disc.
Preferably, the ratio of the area of the diaphragm exposed to the chamber relative to the area of the outlet port is in the range 50 to 350.
Preferably, the ratio is about 100.
Preferably, the area of the diaphragm exposed to the chamber is about 178 sq mm and the area of the outlet port bounded by said valve seat is about 1.75 sq mm.
Preferably, the silicon rubber has a Shore A hardness in the range 10 to 30.
Preferably, the periphery of the diaphragm includes annular grooves which define an integral flange having a thickness of about 0.5 mm.
Preferably, the centre of the closure of the diaphragm has a thickness greater than about 1.7 mm.
Preferably, the body includes a cylindrical wall and a base wall which define the valve chamber and wherein the mounting means includes a mounting ring snugly received in said cylindrical wall and operable to clamp the periphery of the diaphragm against said base wall.
Preferably, the base wall includes an annular shoulder and the periphery of the diaphragm is clamped against the shoulder by the mounting ring.
Preferably, the shoulder includes a projecting rib which is received within an annular groove formed in the periphery of the diaphragm.
Preferably, the valve consists of three moulded parts: the valve body; the diaphragm; and the mounting means, the inlet, outlet and means for connecting the inlet being integrally moulded with the valve body.
Preferably, the valve body is moulded from transparent plastics material and wherein the valve is disposable.
In the valve of the invention, the diaphragm is biased so that it normally is resiliently held against the valve seat so that the valve is closed. When the valve is fitted into a full container of liquid, either in a big or bottle, or fitted in a line from a bag or bottle, it needs only a few centimeters of water pressure to unseat the diaphragm from the valve seat so that fluid can flow through the valve into the outlet where it can be delivered by catheter to the patient. When, however, the level of liquid in the container falls to a few centimeters of water, the pressure of the liquid is insufficient to hold the diaphragm away from the valve seat and the valve closes. This effectively prevents any air passing through the valve because it requires pressure of the intravenous liquid to hold the valve open.
The effect of the negative pressure below the valve that tends to hold float valve designs closed, even when there is fluid above the float, is mitigated in the valve of the invention by the large ratio of the surface area of the diaphragm acted on by the fluid head above the valve to the very small surface area of the inlet surrounded by the valve seat exposed to the negative pressure below.
Preferably further, the diaphragm includes a central projection which is accessible to a user and enables the user to grasp the projection and manually unseat the diaphragm from the valve seat.
In an alternative embodiment, an air channel is integrally formed with the outlet so as to enable air to enter the container to replace the intravenous liquid draining therefrom.
The invention will now be further described with reference to the accompanying drawings, in which:
A vent needle 23 is penetrated through the bung 8 in the normal way to vent air into the container 6 as the liquid 4 flows therefrom in order to prevent build-up of negative pressure within the container.
The pointed end 20 of the inlet spigot 16 enables the pointed end to be pierced through the resilient bung 8, as mentioned above. The inlet spigot 16 includes three longitudinally extending passages 46, 48 and 50 which open to the pointed end 20 as inlet ports and communicate with an inlet manifold 51 formed beneath the base wall 38 of the body 30. The outlet spigot 18 includes an outlet passage 52 which communicates with an outlet port 5.4 formed within a projection 56, the end face constituting an annular valve seat 58. In the illustrated arrangement, the valve seat 58 is raised approximately 0.5 mm with respect to the top surface of the shoulder 40.
The diaphragm 32 is preferably injection moulded from silicon rubber having a predetermined hardness. Typically the hardness will be in the range from 10 to 30 Shore A and preferably about 20. The actual hardness will depend on the thickness of the diaphragm, as will be apparent from the explanation below.
The diaphragm includes a peripheral mounting portion 60 which includes an annular groove 61 which is complementary to the rib 44 of the shoulder 40 so that the rib is received within the groove 61. The mounting ring 34 has a size and shape such that it is snugly received within the inner wall 42 of the sidewall 36. It serves to clamp the peripheral mounting portion 60 of the diaphragm between it and the shoulder 40. The ring has an interference fit within the inner wall 42 so that it securely retains the diaphragm 32 clamped in position.
The space between the base wall 38, lower face. 62 of the diaphragm and the annular inner wall of the shoulder 40 define a valve chamber 64. The valve chamber communicates with the ports formed at the pointed end of the inlet spigot 16 via the inlet manifold 51 and passages 46, 48 and 50. It will be seen from
The diaphragm 32 is formed with a cavity 63 which is somewhat wider at its lower end, as seen in
The diaphragm 32 is illustrated in more detail in
When the pressure within the valve chamber 64 increases to a predetermined level, resilient flexure will occur at the flange 72 and the central portion 70 of the diaphragm will move away from the projection 56 so that the lower face 62 of the flange will no longer sealingly engage the annular valve seat 58. When this occurs, the intravenous liquid 4 flows through the passages 46, 48 and 50 into the manifold 51 into the valve chamber 64 and then through the port 54 and finally into the outlet passage 52 of the outlet spigot 18.
As best seen in
The arrangement of the valve of the invention is such that when the pressure within the valve chamber 64 is greater than 2 or 3 cm of water, the diaphragm 32 will be unseated from the valve seat 58 and fluid flow will occur. Thus, in the arrangement of
The opening and closing of the valve is essentially dependent on the elasticity of the resilient flange 72 as well as the differential forces across the diaphragm. These differential forces depend on the relative areas of the outlet port 54 compared to the surface area of the lower face 62 of the diaphragm which is exposed to the fluid pressure within the chamber 64. Typically, the diameter of the diaphragm is in the range 20 mm to 30 mm and preferably about 25 mm but somewhat less than this is exposed to the pressure of fluid in the chamber 64 because the peripheral mounting portion 60 is not exposed. Typically, the diameter of the outlet port 54 is about 1.2 mm. Accordingly, the ratio of the surface area of the exposed part of the diaphragm relative to the cross-sectional area of the outlet port 54 is large and typically in the range 50 to 350.
As best seen in
In the illustrated arrangement, the components are injection moulded from relatively inexpensive materials and are easily assembled. This makes the valve cheap enough to be disposable or suitable for single use.
It will be appreciated that the valve of the invention can be modified. For instance, the inlet and outlet spigots 16 and 18 could be provided with Luer connectors which are integrally moulded therewith so that the valve can be fitted in a line or catheter which extends from a supply of intravenous liquid to the patient.
The main difference between the valve 100 and the earlier embodiment is that it includes an air channel 102 in the outlet spigot 18 so as to perform the function of the vent needle 23. As best seen in
Many modifications will be apparent to those skilled in the art without departing from the spirit and scope of the invention.
Number | Date | Country | Kind |
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2010905023 | Nov 2010 | AU | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/AU2011/001407 | 11/3/2011 | WO | 00 | 7/29/2013 |