U.S. patent number 3,796,245 [Application Number 05/186,059] was granted by the patent office on 1974-03-12 for drip meters.
Invention is credited to Otto M. Wildensteiner.
United States Patent |
3,796,245 |
Wildensteiner |
March 12, 1974 |
DRIP METERS
Abstract
A drip meter that is an integral part of a flexible parenteral
solution container.
Inventors: |
Wildensteiner; Otto M.
(Rockville, MD) |
Family
ID: |
5898680 |
Appl.
No.: |
05/186,059 |
Filed: |
October 4, 1971 |
Current U.S.
Class: |
604/255; 251/342;
383/67; 383/35; 604/262; 604/408 |
Current CPC
Class: |
A61J
1/05 (20130101); A61M 31/00 (20130101); F16K
3/34 (20130101); A61M 39/22 (20130101) |
Current International
Class: |
A61J
1/00 (20060101); A61M 31/00 (20060101); A61M
39/22 (20060101); A61M 39/00 (20060101); F16K
3/34 (20060101); F16K 3/00 (20060101); B65d
033/36 () |
Field of
Search: |
;128/214C,214D ;251/342
;229/56,62.5 ;137/625.3,625.33 ;150/1,3,9 |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
|
|
|
|
|
|
|
483,580 |
|
Aug 1953 |
|
IT |
|
378,624 |
|
Jul 1964 |
|
CH |
|
Primary Examiner: Norton; Donald F.
Claims
I claim:
1. Parenteral fluid administering equipment comprising: a flexible
walled container having means integral therewithin for setting a
variable predetermined fluid administration rate.
2. Parenteral fluid administering equipment as in claim 1 wherein
said means comprises interdigitated elements, alternate ones of
said elements being associated with the same flexible wall.
3. Parenteral fluid administering equipment as in claim 2 wherein
said interdigitated elements have at least one flow passage in at
least one of said interdigitated elements.
4. Parenteral fluid administering equipment as in claim 3 having
detent means associated with said interdigitated elements for
holding said interdigitated elements in any one of a plurality of
relationships.
5. A flexible walled fluid container comprising: sheets of flexible
material placed in overlying relationship to one another and sealed
at their peripheries to form a fluid reservoir therewithin, said
reservoir being subdivided by adjustable valve means into two
reservoirs, said adjustable valve means controlling the rate of
flow of fluid between said reservoirs.
6. A container as in claim 5 wherein said valve means comprises
interdigitated elements, alternate ones of said interdigitated
elements being associated with the same fluid reservoir wall.
7. A container as in claim 6 wherein said interdigitated elements
have at least one flow passage in at least one of said
elements.
8. A container as in claim 7 having detent means associated with
said interdigitated elements for holding said interdigitated
elements in any one of a plurality of relationships.
Description
Intravenous feeding of solutions other than whole blood or plasma
has become very common. The usual solutions are normal saline, 5
percent glucose, Ringer's lactate, and the like. When any of these
solutions are fed, it is imperative that it be fed in at a
controlled pre-determined rate. For each solution there is a
maximum rate that must not be exceeded. If this maximum rate is
exceeded, the bloodstream at the infusion point will become diluted
due to the over-concentration of solution at that point and serious
damage could result. Likewise, there is a minimum desirable rate,
since damage could result from a too leisurely rate of infusion of
the solution into the patient. Thus, it can be seen that there is a
range of infusion rates for each solution, and that the actual rate
must be kept somewhere in this range.
The method of maintaining the proper infusion rate is to employ the
use of a device called a drip meter. Reduced to its most basic
terms, a drip meter is simply a variable area restriction somewhere
in the flow path from parenteral solution container to patient,
followed immediately by a large chamber where the individual drops
of solution coming through the drip meter can be seen and counted.
The nurse or other person administering the solution adjusts the
variable area restriction to get an approximation of the correct
flow rate, and then obtains the correct flow rate by counting the
number of drops per unit of time and either increasing or
decreasing the amount of restriction in the line to respectively
decrease or increase the flow rate. While this method is
satisfactory, it is time-consuming; it would be preferable to have
a drip meter that could be set to the proper flow rate without
requiring that the nurse go through a tedious trial and error
process.
Prior art drip meters have the additional drawback of being a
separate unit. That is, they consist of a unit that is separate and
distinct from both the solution container and the tubing that leads
to the patient. This latter feature means that not only must the
hospital inventory and stock a separate item, it also means that
the nurse who is about to administer a parenteral solution must
pick up and carry to the patient's room the drip meter as well as
the container of solution, tubing, needle, etc. With many separate
items required, it is inevitable that there are occasions when one
of the items is either lost or forgotten, which causes a delay
while the nurse retraces her steps to obtain another. Thus, it can
be seen that a combined container - drip meter will reduce the
burden on the nurse and the administrative staff by reducing the
number of items that each must handle.
Furthermore, the present trend is toward the use of plastic
(generally polyethylene) bags as containers for the parenteral
solutions rather than glass bottles; the plastic bags are disposed
of after use, saving the costs of returning the empty bottle and
sterilizing it before re-use. A drip meter that is capable of being
made an integral part of such a plastic bag, to be disposed of with
the bag, would further enhance the use of such plastic bags.
Accordingly, it is an object of this invention to provide a drip
meter that can be integrally molded into a disposable plastic bag
used to hold parenteral solutions.
A further object is to provide a drip meter that is composed of
only two parts adapted for relative sliding motion.
A further object is to provide a drip meter that includes provision
for setting a desired flow rate without time-consuming adjustment
procedures on the part of the user.
Other objects and advantages will be apparent from the following
specification and drawings.
SUMMARY
Briefly, the drip meter of the present invention comprises two
elements designed for sliding motion relative to each other. Each
element is joined to its adjacent sidewall to prevent leakage past
the drip meter. One element is grooved, the second element is
shaped to slide within this groove. The element having the groove
also has flow passages in it, these flow passages being
perpendicular to the groove. When the second element is slid fully
into the groove, the flow passages are closed off; progressively
withdrawing the second element from the groove exposes increasing
areas of the flow passages to flow therethrough.
The drip meter of the present invention can be thought of as a
modified gate valve with flow passages in the element in which the
gate seats. Gate valves in general are not new, and gate valves
having flow passages in the translating element which must be in
registration with other flow passages before flow can occur are
also not new (see U. S. Pat. No. 3,517,697). However, all prior art
gate valves require actuating mechanisms that are external to the
flow path. Thus, these gate valves are not only complicated and
bulky, they offer leakage paths both into and out of the valve. By
contrast, the modified gate valve of the present invention consists
of only 2 parts, both of which are entirely within the walls of the
parenteral solution bag, thereby precluding the possibility of any
leakage.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a front elevation of the lower half of a flexible
parenteral solution container that is hung vertically in its normal
use position, showing the drip meter in profile;
FIG. 2 is a cross section through the drip meter, taken along the
line 2--2 in FIG. 1;
FIG. 3 is taken along line 3--3 in FIG. 2;
FIG. 4 shows an additional set of flow passages that may be
incorporated;
FIG. 5, taken along line 5--5 of FIG. 3, shows detent means for
setting pre-determined drip rates;
FIG. 6 is a perspective view of the present invention applied to a
conventional glass container.
DESCRIPTION OF THE PREFERRED EMBODIMENT
The parenteral solution bag, generally indicated at 1, includes a
body portion 2 and a neck portion 3, the latter containing the drip
meter 4. Since parenteral solution bags of this type are generally
made of two sheets of plastic joined to each other at their
peripheries, a cross section of the neck portion 3 perpendicular to
the centerline of the bag is approximately oval in shape. As can be
seen in FIG. 1, the drip meter 4 has a curved profile. This curve
assures that all of the solution that goes through the meter will
collect at a common point and fall into collection chamber 5 in a
single series of drops rather than from several points along the
meter.
In cross section (FIG. 2) the drip meter can be seen to consist of
two elements: member 6, which as can be seen has a rather deep
groove 8 running the length of one side, and member 7, which forms
a tongue that is disposed in groove 8 of member 6. Members 6 and 7
may be molded integrally with the respective sidewalls of the neck
portion of the bag; or the drip meter (elements 6 and 7) may be
molded separately, assembled in tongue and groove relationship, and
then each half of the unit bonded to its respective sidewall by any
suitable means. In the center of each member 6 and 7 and projecting
through the sidewall of the bag is a tab 9, which tab is the means
of operating the drip meter. These tabs 9 are not essential to the
operation of the drip meter, since the base of each member can be
grasped through the flexible sidewalls 12. However, the inclusion
of tabs 9 facilitates the opening of the drip meter as will be
explained later. The material which comprises members 6 and 7 can
be any plastic that is compatible with the solutions to be
administered, but it must possess a certain amount of flexibility
and resilience, as will be explained later.
FIG. 3 is a view looking down on the drip meter with the drip meter
closed to flow. As can be seen, member 7 is seated fully in groove
8 of member 6, thereby blocking flow through slots 10 of member
6.
It is imperative that all of the flow into collection chamber 5 be
through slots 10 in member 6 (see FIG. 3). Therefore, it is
necessary that the juncture of the ends of drip meter 4 with the
sides of the neck portion 3 (these juncture points being designated
4') be sealed to prevent leakage at this point. Of course, this
problem is obviated if the two parts of the drip meter are molded
into their respective side-walls.
If desired, additional flow passages 11 could be provided in member
7' as shown in FIG. 4. These passages would be exposed when member
7' is withdrawn from groove 8, thereby providing increased flow
area for a given amount of withdrawal of member 7'.
The operation of the drip meter is as follows: Before the bag is
filled, member 7 is pushed all the way into groove 8 in member 6
thereby closing off the flow passages 10. However, it is not
necessary that these passages be completely blocked since the bag
is sealed around its outer periphery; any solution that gets past
the drip meter merely fills up the collection chamber 5. If
parenteral solution has filled up the collection chamber, all that
is necessary is that the bag be inverted, the meter opened, and the
solution drained back into the main portion of the bag. With the
collection chamber empty and the drip meter closed, the bag is
allowed to hang with the collection chamber at the bottom. The
needle on the infusion tubing is inserted through the wall of the
bag which forms the bottom of the collection chamber. Each tab 9 is
then grasped between the thumb and forefinger of one hand, and the
tabs are gently pulled apart. As the tabs are pulled apart, member
7 is pulled out of the groove in member 6, exposing passages 10 to
the flow of solution therethrough. As the solution flows through
the slots 10, it collects at the low point on the curved surface of
the drip meter and then falls into the collection chamber 5 in
easily seen and counted drops. Member 7 is designed to be held in
groove 8 by a friction fit. That is, while member 7 can be easily
moved in groove 8, it will remain in position when tabs 9 are
released. Thus a given flow rate can be set and it will not vary
due to slippage of member 7 in groove 8.
If desired, detent means can be incorporated into the drip meter to
lock member 7 in relation to member 6 at points corresponding to
the most commonly used drip rates. As shown in FIG. 5, this can
take the form of a series of hemispherical depressions 12 in member
6 and a corresponding projection 13 on member 7. Withdrawing member
7 from groove 8 until projection 13 is felt to "snap" into the
first of depressions 12 will thus set a known flow rate without the
need for any other checking or adjustments. Note that there is also
a depression 14 for locking the drip meter in the closed
position.
It will be noted that since members 6 and 7 are joined at each end,
when tabs 9 are pulled apart, members 6 and 7 must bend along their
length; for this reason members 6 and 7 must be made of a
relatively flexible plastic or other material. However, the slots
in member 6 will increase its flexibility; further, if the slots
are wide, only a limited amount of relative movement will be
necessary to expose the required flow area.
Up to this point the invention has been described with regard to a
flexible bag; however, it can also be used in conjunction with a
glass container, as shown in FIG. 6. In this latter configuration,
the only modification that is required is not to the drip meter per
se but to the sidewalls that enclose it and form the collection
chamber. These sidewalls must be contoured so that they go from the
circular neck of the bottle to the narrow, somewhat rectangular,
section of the bottom of the collection chamber, with the drip
meter disposed in the middle as in the flexible bag. The sidewalls
can be secured to the neck of the bottle by any convenient means,
resulting in a cover for a glass parenteral solution container that
has sealed within it an integral drip meter.
* * * * *