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Claims  |
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We claim:
1. An enteral feeding system, comprising an aseptically packaged container
of a low acid liquid nutritional, a testing and dispensing apparatus
including dispensing means for dispensing the liquid nutritional from the
container, said dispensing means being a tubular element defining a bore
extending axially therethrough, said tubular element including a first end
having a pointed tip to puncture the container in order to gain access to
the interior thereof and a second end having a connector, and indicating
means for indicating the pH of the liquid nutritional and hence whether
the liquid nutritional has spoiled, said indicating means being an
elongate member which is slidably received in said bore of said tubular
element such that said elongate member is removably associated with said
tubular element, whereby said elongate member can be inserted into the
container together with said tubular element and then withdrawn from the
container by removing said elongate member from said tubular member, said
elongate member including a first end having a pH indicator positioned in
said first end of said tubular element, whereby said pH indicator may be
exposed to the contents of the container when said tubular element and
said elongate member are inserted into the container as a unit, and a
second end extending outwardly from said second end of said tubular
element and having a gripping handle to remove said elongate member from
said bore of said tubular element, whereby said pH indicator can be viewed
to provide a visual indication of the pH of the liquid nutritional and
hence whether the liquid nutritional has spoiled, and withdrawing means
connected to said connector of said tubular element for withdrawing the
liquid nutritional from the container through said tubular element after
said elongate member has been removed from said tubular element to provide
a visual indication as to whether the liquid nutritional has spoiled.
2. An enteral feeding system according to claim 1, wherein said tubular
element includes venting means for venting the interior of the container
to the outside atmosphere, whereby the creation of a partial vacuum in the
container is inhibited during the withdrawal of the liquid nutritional
therefrom.
3. An enteral feeding system according to claim 2, wherein said venting
means includes filtering means for filtering air flowing fron the outside
atmosphere to the interior of the container through said venting means,
whereby microbial contamination of the liquid nutritional in the container
is inhibited.
4. An enteral feeding system according to claim 3, wherein said tubular
element includes covering means for covering the puncture formed in the
container by said pointed tip of said tubular element.
5. An enteral feeding system according to claim 4, wherein said covering
means is a flange extending outwardly from said tubular element
intermediate said first and second ends thereof.
6. An enteral feeding system according to claim 5, wherein said withdrawing
means includes a pump connected between said tubular element and a
patient.
7. An enteral feeding system according to claim 5, wherein said venting
means includes a hollow vent tube extending alongside said tubular element
and passing through said flange. |
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Claims  |
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Description  |
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cl FIELD OF THE INVENTION
The present invention relates to a testing and dispensing apparatus and
method, and, more particularly, to such an apparatus and method which are
especially adapted for use in connection with an enteral feeding system.
BACKGROUND OF THE INVENTION
Existing enteral nutritionals are supplied either as powders requiring
mixing or as liquids contained in cans and bottles which require transfer
to a secondary application container. The use of sterile aseptic packaging
would allow these products to be supplied in a "ready to use" form.
Furthermore, if the contents of these containers could be accessed in an
aseptic manner, the contents would have a reduced susceptibility to
spoilage during use and would require no refrigeration.
There are two separate and distinct problems which would normally prevent
such aseptic access. The first problem is that the contents of the
container could not be withdrawn without creating a partial vacuum in the
container, unless the container were vented to the atmosphere. Because
open venting would allow microbial invasion of the container, spoilage
would result.
The other problem is that all low acid food processing is subject to a
failure rate of about eight containers per one hundred thousand for
microbiological reasons. Approximately five of these failures are due to
bacteria which produce carbon dioxide that causes the container to swell
and leak. Such failures are immediately apparent to any end user and would
result in the container being discarded prior to use. However, the other
three failures would be of the "flat sour" type. The bacteria which cause
"flat sour" failures contaminate the contents of the container, but do not
generate carbon dioxide. Thus, the spoilage is not readily apparent. The
three characteristics associated with "flat sour" failures are off odors,
curdling and increased acidity (the pH would be lowered from approximately
6.5 to about 4.8). Because feeding of such a spoiled product to a
compromised patient might have catastrophic effects, all containers would
normally be opened and then examined both visually and aromatically prior
to use. Such inspection would prevent the nutritional from being
transferred to the patient directly from the container.
In the past, pH indicators have been proposed for determining whether
various types of food have spoiled (see, for instance, U.S. Pat. Nos.
2,626,855 and 3,067,015). However, none of these indicators is combined
with an insertable dispensing device for dispensing the food after a
determination has been made that the food is suitable for consumption.
Vented dispensing devices have also been proposed in the past (see, for
instance, U.S. Pat. Nos. 1,615,873 and 2,409,343). However, none of these
devices incorporates a spoilage indicator.
SUMMARY OF THE PRESENT INVENTION
The present invention relates to the testing and dispensing of the contents
of a container, such as a low acid liquid nutritional contained in an
aseptically packaged container, using a unique testing and dispensing
apparatus which includes dispensing means for dispensing the contents of
the container and indicating means for indicating the condition of the
contents of the container. The indicating means is removably associated
with the dispensing means so that the indicating means can be inserted
into the container together with the dispensing means and then withdrawn
from the container by removing the indicating means from the dispensing
means. After the indicating means has been removed from the dispensing
means, the indicating means can be visually inspected to determine the
condition of the contents of the container before dispensing the contents
from the container.
If, for instance, the testing and dispensing apparatus is used in
connection with an enteral feeding system, the indicating means can be a
pH indicator which provides a visual indication as to whether the acidity
of a low acid food (i.e., a liquid nutritional) is in a range which would
indicate that the food has spoiled. When the testing and dispensing
apparatus is used in connection with such a system, the dispensing means
is provided with venting means for venting the interior of the container
to the outside atmosphere, whereby the creation of a partial vacuum in the
container is inhibited during the withdrawal of the contents thereof. By
providing the venting means with filtering means for filtering air flowing
from the outside atmosphere to the interior of the container through the
venting means, microbial contamination of the contents of the container
can be inhibited. The dispensing means is also provided with puncturing
means for puncturing the container to gain access to the interior thereof
and covering means for covering the puncture formed in the container by
the puncturing means.
In one embodiment, the dispensing means is a tubular element having a bore
extending axially therethrough and the indicating means is an elongate
member slidably received in the bore of the tubular element. More
particularly, the tubular element includes a first end having a pointed
tip adapted to puncture a container in order to gain access to the
interior thereof and a second end having a connector adapted to connect
the tubular element to a liquid distribution system. The elongate member
includes a first end having a pH indicator positioned in the first end of
the tubular element such that the pH indicator can be exposed to the
contents of the container when the tubular element and the elongate member
are inserted into the container as a unit. A second end of the elongate
member extends outwardly from the second end of the tubular element and
has a gripping handle adapted to be gripped by an individual to remove the
elongate member from the bore of the tubular element. By removing the
elongate member from the tubular element, the pH indicator can be viewed
to provide a visual indication of the pH of the contents of the container.
BRIEF DESCRIPTION OF THE DRAWINGS
For a more complete understanding of the present invention, reference is
made to the following detailed description of an exemplary embodiment
considered in conjunction with the accompanying drawings, in which:
FIG. 1 is an exploded perspective view of a testing and dispensing
apparatus constructed in accordance with the present invention and
including a dispensing member and an indicating member adapted to be
removably received in the dispensing member;
FIG. 2 is a cross-sectional view taken through a portion of an aseptically
packaged container into which the testing and dispensing apparatus of FIG.
1 has been inserted with the indicating member removably received in the
dispensing member;
FIG. 3 is a view similar to FIG. 2, except that the indicating member has
been removed from the dispensing member and the dispensing member has been
connected to a liquid distribution system; and
FIG. 4 is a cross-sectional view, taken along line IV--IV of FIG. 2 and
looking in the direction of the arrows, of the testing and dispensing
apparatus illustrated in FIG. 2.
DESCRIPTION OF THE EXEMPLARY EMBODIMENT
Although the present invention is applicable to many different types of
liquid distribution systems, it is especially suitable for use in
connection with an enteral feeding system. Accordingly, the present
invention will be described in connection with an enteral feeding system.
Referring to FIGS. 1-4, a testing and dispensing apparatus 10 includes a
food tube 12 and an indicating member 14. The food tube 12 is provided
with a bore 16, which extends axially through the food tube 12 from a
lower end 18 to an upper end 20. The lower end 18 of the food tube 12
terminates in a point 22. A connector 24 is provided at the upper end 20
of the food tube 12. A hollow vent tube 26 extends alongside the food tube
12. The vent tube has a pointed lower end 28 and a curved upper end 30,
which receives a bacteriostatic filter cap 32 made from a porous material
which is impervious to bacteria. A flange 34 extends around the food tube
12 and the vent tube 26. Except for the filter cap 32, the entire food
tube is preferably made from plastic, although any other suitable material
or materials may be used.
The indicating member 14 includes an elongate body 36, which is made from
wood, plastic, rolled paper or any other suitable material and has a lower
end 38 and an upper end 40. The lower end 38 of the body 36 terminates in
a pH indicator 42 made from an absorbent material, such as paper or
cotton, which has been chemically treated with a pH indicating substance
adapted to change color depending upon the acidity of a liquid to which
the pH indicator 42 is exposed. The upper end 40 of the body 36 is
attached to a handle 44, which is made from any suitable material and has
a size and shape selected so as to permit the handle 44 to be easily
gripped by the fingers of an individual.
The body 36 of the indicating member 14 has a circular cross-sectional
shape (see FIG. 4) which substantially matches the circular
cross-sectional shape of the bore 16 of the food tube 12 (see FIG. 4).
Moreover, the diameter of the body 36 of the indicating member 14 is
slightly less than the diameter of the bore 16 of the food tube 12 so that
the body 36 of the indicating member 14 can be slidably and removably
received within the bore 16 of the food tube 12. When the body 36 of the
indicating member 14 is completely inserted into the bore 16 of the food
tube 12, the pH indicator 42 is positioned in the lower end 18 of the food
tube 12, while the gripping handle 44 of the indicating member 14 is
positioned above the upper end 20 of the food tube 12.
In use in connection with an enteral feeding system, the testing and
dispensing apparatus 10 would be removed from a suitable sterilized
package and then inserted into an aseptically packaged container 46 whose
interior 48 contains a low acid liquid nutritional 50. More particularly
and with reference to FIG. 2, the food tube 12 and the indicating member
14 are inserted as a unit through a top wall 52 of the container 46 or
through a metallic foil seal (not shown) in the top wall 52, the point 22
of the food tube 12 functioning to puncture the top wall 52 or the seal
(not shown) as the testing and dispensing apparatus 10 is inserted into
the container 46. The flange 34 limits the extent to which the testing and
dispensing apparatus 10 is inserted into the container 46 and covers a
puncture 54 formed in the top wall 52 of the container 46 by the point 22
of the food tube 12. When the flange 34 engages the top wall 52 of the
container 46, the lower end 18 of the food tube 12 is in close proximity
to a bottom wall 56 of the container 46. With the testing and dispensing
apparatus 10 so positioned, the pH indicator 42 of the indicating member
14 is exposed to the liquid nutritional 50 contained in the interior 48 of
the container 46.
In order to test the condition of the liquid nutritional 50, the indicating
member 14 is removed from the food tube 12 by gripping the handle 44 of
the indicating member 14 and sliding the body 36 of the indicating member
14 out of the bore 16 in the food tube 12. The pH indicator 42 of the
indicating member 14 can then be visually examined to determine whether
the acidity of the liquid nutritional 50 is in a range which would
indicate that the liquid nutritional 50 has spoiled. For instance, if the
pH indicator 42 has been treated with propyl red, a yellow color would
indicate a pH of about 6.6 and hence that the liquid nutritional 50 has
not spoiled and therefore is safe for consumption, while a red color would
indicate a pH of about 4.8 and hence that the liquid nutritional 50 has
spoiled and therefore is not safe for consumption.
If the liquid nutritional 50 is safe for consumption, the food tube 12 can
be connected to a suitable liquid distribution system. More particularly
and with reference to FIG. 3, a plastic conduit 58 is attached to the
connector 24 on the upper end 20 of the food tube 12. The conduit 58 is
also connected to an inlet (not shown) of a pump 60 (shown schematically).
The pump 60 has an outlet (not shown), which is connected by a conduit 62
to a patient (not shown) to be supplied with the liquid nutritional 50
from the container 46.
As the liquid nutritional 50 is pumped from the container 46 to the patient
(not shown), air from the outside atmosphere flows into the interior 48 of
the container 46 through the vent tube 26 of the food tube 12, thereby
inhibiting the creation of a partial vacuum in the container 46. The air
flowing from the outside atmosphere to the interior 48 of the container 46
through the vent tube 26 passes through the filter cap 32 to thereby
inhibit microbial contamination of the liquid nutritional 50 in the
container 46.
It will be understood that the embodiment described herein is merely
exemplary and that a person skilled in the art may make many variations
and modifications without departing from the spirit and scope of the
invention. All such modifications and variations are intended to be
included within the scope of the invention as defined in the appended
claims.
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Description  |
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