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AU2002323281A1 - Intravenous set flow volumetric measurement device - Google Patents

Intravenous set flow volumetric measurement device

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Publication number
AU2002323281A1
AU2002323281A1 AU2002323281A AU2002323281A AU2002323281A1 AU 2002323281 A1 AU2002323281 A1 AU 2002323281A1 AU 2002323281 A AU2002323281 A AU 2002323281A AU 2002323281 A AU2002323281 A AU 2002323281A AU 2002323281 A1 AU2002323281 A1 AU 2002323281A1
Authority
AU
Australia
Prior art keywords
radiation
drip chamber
drop
passing
volume
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
AU2002323281A
Other versions
AU2002323281B2 (en
Inventor
Zeev Burko
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BURKO SYSTEMS AND DEVELOPMENT Ltd
Original Assignee
BURKO SYSTEMS AND DEVELOPMENT Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US09/945,786 external-priority patent/US6599282B2/en
Application filed by BURKO SYSTEMS AND DEVELOPMENT Ltd filed Critical BURKO SYSTEMS AND DEVELOPMENT Ltd
Publication of AU2002323281A1 publication Critical patent/AU2002323281A1/en
Application granted granted Critical
Publication of AU2002323281B2 publication Critical patent/AU2002323281B2/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Description

INTRAVENOUS SET FLOW VOLUMETRIC MEASUREMENT DEVICE
FIELD AND BACKGROUND OF THE INVENTION
_ The present invention relates to the flow of fluids into a patient's
blood stream and, more particularly, to a system and method for the
volumetric measurement of fluids administered in any standard gravity
intravenous infusion set.
The intravenous infusion of fluids into a patient's bloodstream is a
common medical procedure. Fluids that are typically administered
intravenously include glucose and saline solutions, drugs, and blood.
Intravenous (IV) systems generally comprise a reservoir, a drip chamber, a
feed tube, and an IV needle. The reservoir, also called an IV bag, holds a
quantity of the fluid to be infused. The reservoir is coupled to a dripper by
means of a feed tube. The dripper, in turn, is coupled by the feed tube to the
hollow IV needle, which is injected into a vein of the patient. The fluid in
the reservoir drips through the needle and into the bloodstream, with the
drip rate being controlled by the dripper.
In the past, two major approaches have been used to control the rate
at which fluids are administered intravenously. The first approach is to use a
conventional drip chamber which is manually controlled to adjust the drop
rate through the drip chamber until the drops fall at a predetermined rate.
This approach brings with it the advantage of simplicity in that only gravitational forces are needed to maintain the flow of fluids through the
drip chamber.
However, manually controlled drip chambers are not satisfactory for
all applications, for such drip chambers can permit fluid flow rate
inaccuracies above or below the requested flow rate. These inaccuracies are
due to the fact that the size of individual drops passing through the drip
chamber can vary from set to set, the flow rate with which the fluid passes
through the drip chamber, fluid pressure, and vibrational influences on the
drip chamber. Furthermore, unless the drip chamber is carefully made to
exacting tolerances, the drop volume may vary from one drip chamber to the
next and definitely from one type of set to the next type. This means that a
drop rate appropriate for a preselected fluid flow rate with a first drip
chamber is not necessarily appropriate for a second drip chamber.
Moreover, because of cold flow of tubing used in conjunction with
conventional pinch clamps, a conventional, manually controlled drip
chamber which is operating at a desired drop rate initially may well vary
from this drop rate in time.
In an effort to provide greater accuracy of infusion rates, positive
displacement infusion pumps have come into widespread use. Such pumps
provide the advantage of accurately controlled infusion rates, largely
independently of the pressure or the viscosity of the fluid being infused.
However, such infusion pumps suffer from their own disadvantages. Because they typically operate at pressures of up to 60 psi, the danger of
overpressure infusion is always present. Furthermore, infusion pumps tend
to be relatively expensive, as well as heavy and cumbersome. In large part,
the weight of infusion pumps is related to the size of the back up battery
needed to power the pump in the event of a power failure. Because pumps
operate motors on a regular basis, back up batteries for infusion pumps
require large capacity.
The most basic part of control is to first obtain a precise volumetric
measurement of the fluid administered.
US Pat. No. 4,525,163 to Slavik et al teaches a flow control device
including a sensor for measuring drop sizes. The drop sizes are measured as
a calculation of averages after a certain number of optically detected drops
fall into a burette. This is not a volumetric measurement and an additional
drawback is that the administered fluid has to pass through the device, this
being an invasive device.
US Pat. No. 4,504,263 to Steur et al describes an invasive flow
monitor where the flow of fluid passes through the monitor. The
disadvantage of the invasive devices is that they have to be sterilized
between uses and that becomes the responsibility and a resulting nuisance of
the hospital requiring multiple devices with extras for sterilization. In the
device described by Steuer the individual drops are measured by a infrared sensor. An additional drawback to the in asiveness of Steuer's invention is
that he assumes that the drops are spherical which is not always the case.
There exist prior art describing non-invasive devices for counting
drops such as described in US Pat. No. 6,083,206 to Molko. Molko teaches
a device that can count drops with great precision by sensing infra-red
radiation passing through the drip chamber, but does not account for the
volumetric measurement of each drop and must rely on the drop size
designated by the particular set.
The necessity for volumetric precision becomes critical for tiny
infants who receive even less than two milliliters of fluid administered in an
IV drip per hour.
As infusion pumps and gravity fed intravenous sets have the
abovementioned disadvantages it would be highly advantageous to have a
simple gravity fed intravenous set devoid of the above limitations.
SUMMARY OF THE INVENTION
According to one aspect of the present invention there is provided a
device for the volumetric measurement of a fluid administered in a gravity
infusion set including a drip chamber. The device includes a housing
configured for releasable deployment around a cylindrical surface of the
drip chamber. The housing includes a source of radiation configured to emit
radiation through the drip chamber in a path substantially perpendicular to an axis of the cylindrical surface and an optical receiver deployed to be
adjacent to a portion of the cylindrical surface substantially opposite the
source of radiation. The optical receiver is configured for quantitatively
sensing the radiation and a processor operative to calculate a volume of
each drop passing through the drip chamber as a function of the relative loss
of radiation quantitatively sensed by the receiver during passing of a drop
against a background radiation.
According to another aspect of the present invention there is
provided a method for calculating a volume delivered through an
intravenous set with a drip chamber configured for the flow of the fluid
substantially along the drip chamber's axis. The method includes the steps
of passing radiation from the exterior of the drip chamber through the drip
chamber via a path generally perpendicular to the drip chamber axis to a
sensor positioned on an opposite position on the exterior of the drip
chamber, detecting and quantifying a background radiation value passing
through the drip chamber, detecting and quantifying a radiation value
passing through a drop falling through the drip chamber in order to obtain
data indicative of a radiation loss due to the drop passing though the
radiation path; and calculating a volume of the drop as a function of the
relative loss of radiation detected during passing of the drop against the
background radiation value. According to yet another aspect of the present invention there is
provided a method for calculating a volume delivered through an
intravenous set with a drip chamber configured for the flow of the fluid
substantially along the drip chamber's axis. The method comprises the steps
of passing radiation from the exterior of the drip chamber through the drip
chamber via a path generally perpendicular to the drip chamber axis to a
sensor positioned on an opposite position on the exterior of the drip
chamber, detecting and quantifying a background radiation value passing
through the drip chamber, detecting and quantifying a radiation value
passing through a drop falling through the drip chamber in order to obtain
data indicative of a radiation loss due to the drop passing though the
radiation path; and deriving a volume measurement for the drop using a
lookup table, the lookup table formed by accumulating empirical data.
According to further features in preferred embodiments of the
invention described below, the radiation is configured to function in pulsed
mode.
According to still further features in the described preferred
embodiments the radiation is configured to function in continuous mode.
According to further features in preferred embodiments of the
invention described below, the radiation is light radiation.
According to still further features in the described preferred
embodiments the radiation is infra-red radiation. According to still further features in the described preferred
embodiments a volume calculated is used for controlling the flow of a fluid
administered in a gravity infusion set.
According to still further features in the described preferred
embodiments a relative loss of radiation is converted into a volume with the
aid of a lookup table. The lookup table is created by accumulating empirical
data of drops passing through various infusion sets determining a relative
loss of radiation during the passing of the drop through the radiation and
then weighing the drops and determining the volume of each drop in
proportion to its specific gravity. The device and method is suitable for use
with any IV set and is non-invasive.
The present invention successfully addresses the shortcomings of the
presently known configurations by providing a device and method for
measuring the volume of a drop, which can be used to determine the volume
of a fluid administered in a gravity infusion set.
BRIEF DESCRIPTION OF THE DRAWINGS
The invention is herein described, by way of example only, with
reference to the accompanying drawings. With specific reference now to
the drawings in detail, it is stressed that the particulars shown are by way
of example and for purposes of illustrative discussion of the preferred
embodiments of the present invention only, and are presented in the cause of providing what is believed to be the most useful and readily
understood description of the principles and conceptual aspects of the
invention. In this regard, no attempt is made to show structural details of
the invention in more detail than is necessary for a fundamental
understanding of the invention, the description taken with the drawings
making apparent to those skilled in the art how the several forms of the
invention may be embodied in practice.
In the drawings:
FIG. 1 is a device for the volumetric measurement of a fluid
administered in a gravity infusion set;
FIG. 2 is an illustration of the radiation pulses before and after
passing through a drip chamber, before and during the passage of a drop
through the chamber; and
FIG. 3 is a flow chart of a method for calculating the volume of a
drop.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
The present invention is of a device and method for measuring the
volume of a drop, which can be used to determine the volume of a fluid
administered in a gravity infusion set.
Specifically, the present invention can be used to determine the volume of
each drop administered in a gravity infusion set facilitating a most accurate knowledge of a total volume administered which can be used in the control
of the flow of the fluid.
The principles and operation of a device and method for measuring
the volume of a drop according to the present invention may be better
understood with reference to the drawings and accompanying descriptions.
Before explaining at least one embodiment of the invention in detail,
it is to be understood that the invention is not limited in its application to the
details of construction and the arrangement of the components set forth in
the following description or illustrated in the drawings. The invention is
capable of other embodiments or of being practiced or carried out in various
ways. Also, it is to be understood that the phraseology and terminology
employed herein is for the purpose of description and should not be
regarded as limiting.
Referring now to the drawings, Figure 1 illustrates a device 10 for
the volumetric measurement of a fluid administered in a gravity infusion set
12 including a drip chamber. Some of the parts are illustrated out of
proportion in order to get a better understanding of the parts of the invention
involved and how they combine with a gravity infusion set. Gravity infusion
set 12 typically includes a reservoir 16, a drip chamber 14, a feed tube 18,
and an IV needle 20.
Device 10 includes a housing 22 configured for releasable
deployment around a cylindrical surface 24 of drip chamber 14. Housing 22 fits over drip chamber 14 and is attached to any of a number of places
including the tube leading into drip chamber 14 or alternately to the top
portion of drip chamber 14 or to the stand supporting set 12. Housing 22
includes a source of radiation 26. Source of radiation 26 is configured to
emit radiation 28 through drip chamber 14 in a path substantially
perpendicular to an axis 30 of cylindrical surface 24. An optical receiver 32
configured for quantitatively sensing radiation is deployed to be adjacent to
a portion of cylindrical surface 24 substantially opposite source of radiation
26.
Preferably the radiation from a source of radiation 26 emitted is
infrared light. Alternately or additionally other types of radiation could be
used as well. Source of radiation 26 includes an array of infrared light
emitting diodes that generate infrared light. According to the present
invention the infrared radiation is emitted either in a continuous mode or
alternately in a pulsed mode.
Among the advantages of a pulsed mode are improved control in
accounting for background radiation level and in saving energy. A
preferable pulse rate is a rate of thousands of pulses and preferably at
approximately 100,000 pulses per second. Pulsed mode is helpful in
prevention of disturbances in background radiation measurements for
example when light from an external source such as sunlight shines onto the
drip chamber. A pulser in source of radiation 26 periodically energizes the light
emitting diodes to produce a series of energized and non-energized states.
Figure 2 illustrates the difference between pulses of radiation
detected and quantified by optical receiver 32 after having passed through
drip chamber 14 with no drop (figure 2a) in the path of the radiation and
with a drop 40 (figure 2b) in the path of the radiation.
Figure 2a illustrates pulses of radiation 14 represented digitally. An
Analog-to-Digital converter is used to convert radiation pulses into digital
code, a measurable voltage or some other measurable electrical reaction to
the analog signal. Pulses 40 passing through drip chamber 14 when no drop
is in the path of the radiation are measured and there is no significant
variation in height between the pulses measured by optical receiver 32
passing through chamber 14. There is of course a difference between the
radiation going in to chamber 14 and detected by optical receiver 32 on the
other side of chamber 14. This is the background or reference level. Device
preferably 10 calibrates itself before and after each drop passing through
drip chamber 14 which takes into account any changes in the environment
inside or outside. Examples of changes that need to be taken accounted for
are foggy-like droplets formed on the outside of chamber 14 or tiny droplets
splashed on the inside surface of chamber 14. As device 10 is suitable for
any gravity IV set 12, there are inherent differences between various drip
chambers, such as wall thickness or wall constitution. A processor 34 controls the energizing of the infrared emitting diodes in accordance to the
radiation sensed on the other side of chamber 14 and adjusts the radiation
for each set and continues to calibrate itself many times between each drop.
Figure 2b illustrates a drop 42 passing through chamber 14 and the
resultant decrease in radiation passing through chamber 14. A dip 44 in
radiation sensed by sensor 32 is illustrated, wherein the minimum signal 46
in dip 44 corresponds to the thickest segment diameter of drop 42 passing
through chamber 14. Figure 2b illustrates the significance of preferably
having many tens of thousands of pulses per second, which means that a
few hundred pulses would pass through each drop 42 passing through drip
chamber 14. Accuracy of device 10 in the volumetric measurement of a
drop increases with the amount of pulses passing through a drop. Each pulse
represents a segment of a drop so more pulses passing through a drop give a
more accurate final result which is the volume of the drop. Device 10
calculates the volume of a drop regardless of the shape of the drop or the
type of IV set. A drop may be elongated or alternately a relatively wide and
flat drop. Many factors influence the shape of the drop including pressure,
the width of the entrance into the drip chamber, the fluid viscosity and
whether the entrance to the drip chamber is perfectly round or not.
Processor 34 is operative to calculate a volume of each drop 42
passing through drip chamber 14 as a function of the relative loss of radiation quantitatively sensed by receiver 32 during passing of drop 42
against a background or reference level of radiation.
In order to be able to calculate a volume for each drop, a lookup table
is first formed by accumulating empirical data. Empirical data is obtained
by running device 10 with numerous sets, each set with its own drop types.
Each drop has its own dip in radiation passing through. Each drop is then
weighed on an analytical balance to produce a precise weight. Taking into
account the specific gravity for each type of fluid, a volume for each can be
easily calculated. For example with water 1 kilogram water occupies a
volume of one liter. Various specific gravities of fluids will have
corresponding volumes slightly different than that of water. This procedure
is repeated many times, preferably thousands of times, such that it is
possible to relate a weight and therefore a volume to a dip or an integral
which is the value that is related to the dip.
Infrared light emitted in continuous mode is be more precise than
pulsed mode as the information missing between the pulsed will be
provided, and the drawback of sunshine or other light interfering with the
infrared can be overcome by making housing 22 non transmitting to light
from the outside, much like a black box. A significant drawback is the high
demand for power for a continuous flow of radiation. In many cases where
the preferable power supply to device 10 is a battery powered supply which
enables easy mobility from one patient to another, a continuous mode of radiation supply would deplete the batteries rapidly. Alternatively, in
another embodiment of the present invention, device 10 is powered by AC
current, and preferably has a source of batteries for backup in which case
continuous mode would be the preferred mode. This would be particularly
advantageous for a permanently positioned device 10 or when more
precision is required.
Reference is now made to Figure 3 which is a flow diagram of a
method 60 for calculating a volume delivered through an intravenous set
with a drip chamber configured for the flow of the fluid substantially along
the drip chamber's axis. Method 60 includes the steps of passing radiation
62 from the exterior of the drip chamber through the drip chamber via a
path generally perpendicular to the drip chamber axis to a sensor positioned
on an opposite position on the exterior of the drip chamber and detecting
and quantifying 64 a background radiation value passing through the drip
chamber. If the background radiation value was either too low or too high
65, then the amount of radiation to be passed through chamber 14 is
modified to a higher or lower radiation and is passed through again 62. This
stage is repeated until a predetermined level of radiation is reached. This
could depend on many factors, such as set type and formation of frost on the
chamber. Once a predetermined level of radiation has been reached, it is
possible to calculate the volume of a drop. The next step occurs when a
drop passes through the chamber 68. Radiation preferably in the form of infrared light is passed through a drop falling through the drip chamber 70.
The sensor detects and quantifies the radiation 72 in order to obtain data
indicative of a radiation loss due to the drop passing though the radiation
path. The volume of the drop is then calculated as a function of the relative
loss of radiation detected during passing of the drop against the background
radiation value. The volume calculated for a drop is used in the control of
fluid administered making control more precise.
Although the invention has been described in conjunction with
specific embodiments thereof, it is evident that many alternatives,
modifications and variations will be apparent to those skilled in the art.
Accordingly, it is intended to embrace all such alternatives, modifications
and variations that fall within the spirit and broad scope of the appended
claims.

Claims (19)

WHAT IS CLAIMED IS:
1. A device for the volumetric measurement of a fluid
administered in a gravity infusion set including a drip chamber, device
comprising:
(a) a housing configured for releasable deployment around a
cylindrical surface of the drip chamber, said housing including:
(i) a source of radiation, said source of radiation
configured to emit radiation through the drip chamber in a
path substantially perpendicular to an axis of said cylindrical
surface; and
(ii) an optical receiver deployed to be adjacent to a portion
of said cylindrical surface substantially opposite said source of
radiation, said optical receiver configured for quantitatively
sensing said radiation; and
a processor operative to calculate a volume of each drop passing
through the drip chamber as a function of the relative loss of
radiation quantitatively sensed by said receiver during passing of a
drop against a background radiation.
2. The device of claim 1, wherein said radiation is configured to
function in pulsed mode.
3. The device of claim 1, wherein said radiation is configured to function in continuous mode.
4. The device of claim 1, wherein said radiation is light
radiation.
5. The device of claim 1, wherein said radiation is infra-red
radiation.
6. The device of claim 1, wherein a volume calculated is used for controlling the flow of a fluid administered in a gravity infusion set.
7. A method for calculating a volume delivered through an
intravenous set with a drip chamber configured for the flow of the fluid
substantially along the drip chamber's axis, method comprising the steps of:
(a) passing radiation from the exterior of the drip chamber
through the drip chamber via a path generally perpendicular to the
drip chamber axis to a sensor positioned on an opposite position on
the exterior of the drip chamber;
(b) detecting and quantifying a background radiation value
passing through the drip chamber;
(c) detecting and quantifying a radiation value passing through a
drop falling through the drip chamber in order to obtain data indicative of a radiation loss due to said drop passing though said
radiation path; and
(d) calculating a volume of said drop as a function of the relative
loss of radiation detected during passing of said drop against said
background radiation value.
8. The method of claim 7, wherein said radiation is configured to
function in pulsed mode.
9. The method of claim 7, wherein said radiation is configured to
function in continuous mode.
10. The method of claim 7, wherein said radiation is light
radiation.
11. The method of claim 7, wherein said radiation is infra-red
radiation.
12. The method of claim 7, further comprising the step of
controlling the flow of a fluid administered in a gravity infusion set using
the volume calculated for a drop.
13. A method for calculating a volume delivered through an intravenous
set with a drip chamber configured for the flow of the fluid substantially
along the drip chamber's axis, method comprising the steps of:
(a) passing radiation from the exterior of the drip chamber
through the drip chamber via a path generally perpendicular to the
drip chamber axis to a sensor positioned on an opposite position on
the exterior of the drip chamber;
(b) detecting and quantifying a background radiation value
passing through the drip chamber;
(c) detecting and quantifying a radiation value passing through a
drop falling through the drip chamber in order to obtain data
indicative of a radiation loss due to said drop passing though said
radiation path; and
(d) deriving a volume measurement for said drop using a lookup
table, said lookup table formed by accumulating empirical data.
14. The method of claim 13, wherein said radiation is configured
o function in pulsed mode.
15. The method of claim 13, wherein said radiation is configured
o function in continuous mode.
16. The method of claim 13, wherein said radiation is light
radiation.
17. The method of claim 13, wherein said radiation is infrared
radiation.
18. The method of claim 13, further comprising the step of
controlling the flow of a fluid administered in a gravity infusion set using
the volume calculated for a drop.
19. The method of claim 13, wherein said empirical data is
accumulated by weighing a plurality of drops passed through said radiation
path and determining the volume of each drop in proportion to its specific
gravity.
AU2002323281A 2001-09-05 2002-08-21 Intravenous set flow volumetric measurement device Ceased AU2002323281B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US09/945,786 US6599282B2 (en) 2001-09-05 2001-09-05 Intravenous set flow volumetric measurement device
US09/945,786 2001-09-05
PCT/US2002/026504 WO2003020345A1 (en) 2001-09-05 2002-08-21 Intravenous set flow volumetric measurement device

Publications (2)

Publication Number Publication Date
AU2002323281A1 true AU2002323281A1 (en) 2003-06-05
AU2002323281B2 AU2002323281B2 (en) 2007-10-11

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Country Status (15)

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US (1) US6599282B2 (en)
EP (1) EP1429824A4 (en)
JP (2) JP2005501611A (en)
KR (1) KR100655524B1 (en)
CN (1) CN1262314C (en)
AU (1) AU2002323281B2 (en)
CA (1) CA2459871C (en)
CO (1) CO5570686A2 (en)
EA (1) EA007006B1 (en)
IL (1) IL159946A0 (en)
MX (1) MXPA04002026A (en)
NO (1) NO20040863L (en)
UA (1) UA79239C2 (en)
WO (1) WO2003020345A1 (en)
ZA (1) ZA200401584B (en)

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