Syringe pump abstract
A syringe pump adapted to inject a liquid medicine in the syringe
according to a predetermined infusion pattern, comprising a syringe
diameter detecting means for detecting the volume of the syringe,
an infusion pattern input means for inputting an infusion pattern,
an occlusion pressure setting means, a pusher position calculating
means, and a drive control means for drive-controlling a motor on
the basis of an inputted infusion pattern to push the pusher of
the syringe so as to infuse the liquid medicine in the syringe,
and characterized in that the pusher position is calculated on the
basis of the set-inputted infusion pattern and the occlusion detection
level is automatically changed according to the pusher position.
Syringe pump claims
1. A syringe pump which infuses a liquid medicine in a syringe
according to a predetermined infusing pattern comprising: a syringe
diameter detection means which detects the capacity of the syringe,
a liquid infusing pattern input means which inputs a liquid feeding
pattern, an occlusion pressure setting means, a pusher position
calculating means and a drive control means which controls the driving
of a motor on the basis of an input liquid infusing pattern and
injects the liquid medicine in the syringe by pushing the pusher
of the syringe; characterized in that a pusher position is calculated
on the basis of the set and input liquid feeding pattern and that
an occlusion detection level is automatically changed according
to said pusher position.
2. The syringe pump in accordance with claim 1 characterized in
that said pusher position in which a remaining amount of liquid
medicine in the syringe decreases is set as an alarm position, that
said occlusion detection level is set at a low level, and that a
push-finish position until said remaining amount is infused by the
movement of the pusher from said alarm position by use of said drive
control means is calculated from a relational expression of LE=LNE+VNE/A,
in which VNE is the remaining amount, LNE is said alarm position,
LE is said push-finish position and A is a cross-sectional area
of the syringe.
3. The syringe pump in accordance with claim 1 characterized in
that said pusher position in which a remaining amount of liquid
medicine in the syringe decreases is set as an alarm position, that
said occlusion detection level is set at a low level, and that a
push-finish position until said remaining amount is infused by the
movement of the pusher from said alarm position by use of said drive
control means is calculated from a relational expression LE=LNE+R.times.T/A,
in which LNE is said alarm position, LE is said push-finish position,
R is an infusion rate, T is remaining time and A is a cross-sectional
area of the syringe.
4. A method of infusing a liquid medicine in a syringe according
to a predetermined liquid infusing pattern, characterized in that
the method of feeding a liquid medicine by use of a syringe pump
comprising the first step of detecting the capacity of the syringe,
the second step of inputting a liquid infusing pattern, the third
step of controlling the driving of a motor on the basis of an input
liquid infusing pattern and infusing the liquid medicine in the
syringe by pushing the pusher of the syringe, and the fourth step
of calculating a pusher position on the basis of the set and input
liquid infusing pattern and automatically changing an occlusion
detection level according to said pusher position.
5. The method of infusing a liquid medicine according to claim
4 characterized in that in said fourth step, said pusher position
in which a remaining amount of liquid medicine in the syringe decreases
is set as an alarm position, that said occlusion detection level
is set at a low level, and that a push-finish position until said
remaining amount is injected by the movement of the pusher from
said alarm position by use of said drive control means is calculated
from a relational expression LE=LNE+VNE/A, in which VNE is the remaining
amount, LNE is said alarm position and LE is said push-finish position
and A is a cross-sectional area of the syringe.
6. The method of infusing a liquid medicine according to claim
4 characterized in that in said fourth step, said pusher position
in which a remaining amount of liquid medicine in the syringe decreases
is set as an alarm position, that said occlusion detection level
is set at a low level, and that a push-finish position until said
remaining amount is infused by the movement of the pusher from said
alarm position by use of said drive control means is calculated
from a relational expression LE=LNE+R.times.T/A, in which LNE is
said alarm position, LE is said push-finish position, R is an infusion
rate, T is remaining time and A is a cross-sectional sectional area
of the syringe.
Syringe pump description
TECHNICAL FIELD
[0001] The present invention relates to a syringe pump which deliver
(administer) a liquid medicine to a patient on the basis of a predetermined
liquid infusing (administration) pattern and can change a blockage
pressure detection level according to a pusher position and a method
of infusing (administrating) a liquid medicine by use of this syringe
pump.
BACKGROUND ART
[0002] There have been proposed syringe pumps which inject a liquid
medicine on the basis of a set infusing rate by selecting beforehand
a occlusion pressure detection level from a plurality of regions
(for example, Japanese Patent Registration No. 2785114). Furthermore,
there have been proposed fluid infusion devices which raise an alarm
before the completion of injection by detecting a pusher position
(for example, the Japanese publication of examined patent application
No. 62-44505 Japanese publication of examined patent application
No. 1-17380 etc.). However, due to the pusher position detection
accuracy of a syringe pump and variations in the syringe size, with
pusher position detection means alone, it has been difficult to
accurately detect the position in which the infusion (or administration)
of a liquid medicine in the syringe is completed.
DISCLOSURE OF THE INVENTION
[0003] Therefore, the present invention was made in view of the
above-described situation and has as its object the provision of
a syringe pump which can change a occlusion pressure detection level
(a threshold value) according to a detected pusher position and
a method of infusing a liquid medicine by use of the syringe pump.
[0004] To achieve the above-described object, the syringe pump
of the invention is a syringe pump which infuse a liquid medicine
in a syringe according to a predetermined infusion pattern, comprising
syringe diameter detection means which detects the volume of the
syringe, liquid infusing (administrating) pattern input means which
inputs a liquid infusing pattern, occlusion pressure setting means,
pusher position calculating means, and drive control means which
controls the driving of a motor on the basis of an input liquid
infusing pattern and injects the liquid medicine in the syringe
by pushing the pusher of the syringe, characterized in that a pusher
position is calculated on the basis of the set and input liquid
infusing pattern and that the occlusion detection level is automatically
changed according to the pusher position.
[0005] The method of infusing (administrating) a liquid medicine
by use of a syringe pump of the invention is a method of infusing
a liquid medicine in a syringe according to a predetermined liquid
infusing pattern, characterized by comprising the step of detecting
the capacity of the syringe, the step of inputting a liquid infusing
pattern, and the step of controlling the driving of a motor on the
basis of an input liquid infusing pattern and injecting the liquid
medicine in the syringe by administrating the pusher of the syringe,
and further comprising the step of calculating a pusher position
on the basis of the set and input liquid feeding pattern and automatically
changing an occlusion detection level according to the pusher position.
[0006] Incidentally, the present invention is not limited to the
embodiments described below and it is needless to say that the various
constitutions specified in the claims are possible.
BRIEF DESCRIPTION OF DRAWINGS
[0007] FIG. 1 is an external perspective view of a syringe pump
1 of the invention;
[0008] FIG. 2(a) is an external perspective view showing how a
syringe S is set in a syringe pump 1 and FIG. 2(b) is an external
perspective view to explain the operation of a clamp 5 which detachably
holds a syringe S in a syringe pump 1 in an immobile state;
[0009] FIG. 3 is a front view showing a rough construction of a
slider mechanism which drives a slider assembly 50;
[0010] FIG. 4 is a plan view of an operating panel part 2f;
[0011] FIG. 5 is a flow chart showing blockage detection; and
[0012] FIG. 6 is a block diagram of a syringe pump of the invention.
BEST MODE FOR CARRYING OUT THE INVENTION
[0013] Embodiments of the invention will be described below by
referring to the accompanying drawings. FIG. 1 is an external perspective
view of a syringe pump 1. In this figure, an operating panel part
2f is installed forward so that a setting dial 6 for setting flow
rate etc. which is usually operated with the right hand can be seen.
[0014] In this figure, this syringe pump 1 is a small amount liquid
continuously infusing pump aimed at nutritional support, blood transfusion
and infusing (administrating) liquid medicines, such as chemotherapy
drugs and anesthetics in an ICU (intensive care unit), a CCU (coronary
care unit) and an NICU (neonatal intensive care unit), and the operating
panel part 2f for performing flow rate display etc. is provided
in a manner almost concentrated on the top surface as shown in the
figure to ensure good operability.
[0015] This operating panel 2f is basically covered with an embossed
sheet cover and drip-proof design is performed to satisfy the drip-proof
test of JIS 0920. For example, this operating panel enables carelessly
spilled liquid medicines etc. to be easily wiped off and has high
drip-proofness to prevent liquid medicines etc. from entering the
interior. For this reason, an upper cover 2 and a lower cover 3
are integrally molded from a molding resin material having high
chemical resistance and are secured by screws, with a rubber seal
4 made of silicone elastomer, for example, interposed at the mutual
connection surfaces of each of the covers 2 3 thereby preventing
foreign substance such as a liquid from entering the interior.
[0016] Furthermore, in order to attach importance to high accuracy
of liquid infusing and an improvement in operability, the realization
of precise infusion action (operation) control by microcomputer
control is made possible. At the same time, by causing an action
indicator 7 which is provided so as to protrude upward in a position
readily seen from the outside, to light up or blink red or greenly
in multicolor or perform display as a revolving light, it is ensured
that the action status or alarm status can be monitored from a distance,
whereby a carefully thought-out measure is taken for safety. Moreover,
a buzzer is built in and various alarm functions are provided for
safety.
[0017] Furthermore, because the syringe pump is compact and lightweight,
it is easy to carry on and is designed so as to be convenient for
being used even in a case where multiple units are used at a time.
In addition, by turning the setting dial 6 on the right-hand surface
of the apparatus, the numerical setting of fluid infusion flow rate
(ml/h), fluid infusion volume (ml), etc. corresponding to the rotation
speed and rotation angle can be performed in a short time. On the
other hand, by causing set numerical values to be displayed in a
display part 11 of a display panel, the setting of numerical values
of flow rate etc. can be easily changed by one action by operating
the setting dial 6.
[0018] Moreover, this syringe pump has a shape which can permit
multiple use (simultaneous use of multiple units), is easy to use,
and has design which permits buildup. The size is small, for example,
110 mm in height, 322 mm in width and 115 mm in depth. The weight
is about 1.8 kg. The power source is of three systems, i.e., a commercial
power source, a built-in battery and 12V DC.
[0019] The charge time of the built-in battery is 15 H (hours).
In order to facilitate replacement from the outside, the built-in
battery is covered with a cover at the bottom of the lower cover
3 and detachably provided by being connector-connected. Furthermore,
the replacement life is not less than 3 years and charge control
is tricle charge. In addition, the prevention of excessive discharge
and charge is realized by taking measures for cell breakage detection
and cell breakage safety of the charge battery. A heat resistant
nickel-cadmium (Ni--Cd) battery is used and a new battery can work
for not less than 180 minutes until an alarm is raised and for not
less than 210 minutes until a shutdown.
[0020] A display part 10 for the injection of a medicine per body
weight in .mu.g/kg/min, mg/kg/h, etc., the display part 11 for flow
rate, predetermined amount and integrated amount, etc., are provided
on the operating panel 2f. On the other hand, a concavity 6e is
formed so that the setting dial 6 can be easily removed for cleaning,
and the setting dial is so constructed that it can be removed by
being moved outward, with the tiptoe put into this portion and rotated.
[0021] Next, in FIG. 2(a), in mounting the syringe S to the syringe
pump 1 a clamp 5 and a slider assembly 50 are moved beforehand
to the positions shown in the figure, a flange SF of the main body
in which a liquid medicine is housed is moved in the direction of
the arrow and set in a slit 2c, a pusher SP is set in the slider
assembly 50 and after that, the clamp 5 is set in such a condition
that the clamp 5 pushed the main body of the syringe S, whereby
the mounting is completed. In order to set the syringe S in this
manner, in the upper cover 2 there are integrally formed a syringe
stage 2a and the slit part 2c having a shape which permits the setting
of the flange part SF of the syringe main body.
[0022] In order to ensure that various syringes S which are made
by different manufacturers, or which have different outside dimensions
and total lengths and different capacities, or which have a pusher
SP in different positions can be handled at this time of mounting,
the syringe pump is so constructed as to arbitrarily change the
pushing position of the clamp 5 and the position of the slider assembly
50. For this purpose, as shown in FIG. 2 the clamp 5 is fixed onto
a freely rotatable shaft body 2b and constructed so as to bring
the main body of the syringe S into a pressed condition by the action
of a built-in spring (not shown) by being rotated in the direction
of the arrow D2 after being manually drawn up in the direction of
the arrow D1.
[0023] In order to move the slider assembly 50 which holds the
pusher SP in an arbitrary position, the slider assembly 50 can be
brought into a free state by pushing a clutch lever 52. Therefore,
the pressure SP is set by manually moving the slider assembly 50.
By starting the syringe pump after setting the syringe in this manner,
the liquid medicine in the syringe S can be infused (delivered)
via a tube T.
[0024] It is obligatory to provide the function of monitoring the
pressure state during this infusion process. When occlusion occurs
in the interior of the tube T etc. for some unexpected reason, such
as a bend, a red light-emitting diode built in the above-described
action indicator 7 rotates and blinks in order make this occlusion
state known to a nurse and other persons.
[0025] Again, with reference to FIG. 1 the slider assembly 50
driven in the direction of the arrow A4 in this figure reciprocally
moves on a concavity 2d of the case 2 and is fixed by being connected
to a slider feed mechanism at the end portions of a pipe shaft and
an inner clutch shaft, which will be described later. Therefore,
by manually operating the clutch lever 52 of the slider assembly
50 the pusher SP of the syringe can be easily attached or detached.
[0026] Next, FIG. 3 is a plan view of a slider feed mechanism of
the slider assembly 50. In this figure, mechanism parts which have
already been described are given like reference characters and their
descriptions are omitted. The slider assembly 50 uses as its mounting
base a base 211 which is fixed to the case 2 in which the slit 2c
is formed in a concave shape to receive a pressure that is a reaction
force generated in the flange SF of the syringe S. And in left and
light wall surface portions 211b, 211a of this base 211 an inner
shaft 214 etc. are rotatably supported.
[0027] Around this inner shaft 214 there is provided a pipe shaft
212 at one end thereof is fixed the above-described slider assembly
50 and at the other end thereof are fixed a half nut holder 215
provided with a half nut 215a and a block 216 in such a manner that
the half nut holder 215 is released from a state of meshing engagement
with a tooth portion of a lead screw 217 by being rotated by the
pressing operation of the above-described clutch lever 52. And the
middle portion of this pipe shaft 212 is rotatably supported in
a freely slidable manner by a sliding bearing 213 indicated with
broken lines in the figure so that the slider assembly 50 is driven
in one direction with the driving of the lead screw 217 whereby
the pusher SP is moved to infuse (deliver) a liquid medicine through
the tube T.
[0028] The left end of the shaft of this lead screw 217 is supported
by a radial bearing which is not shown in the figure. Furthermore,
in the vicinity of the right end of the lead screw 217 a gear 219
which is in meshing engagement with a gear fixed to an output shaft
of a motor 218. The lead screw 217 passes through a hole drilled
through a right wall surface portion 211a and the shaft of the lead
screw 217 is freely rotatably supported by a bearing which is fixed
to a spring plate 220 to which a pressure sensor 221 comprising
a strain gauge which is the occlusion pressure detection means is
fixed.
[0029] In the above-described configuration, it is possible to
bring the half nut 216 into a state of meshing engagement with the
lead screw 217 and a state of release from meshing engagement by
operating the clutch lever 52 and, at the same time, occlusion
detection is carried out by performing the detection of loads generated
in the direction of the arrow by use of the pressure sensor 221
fixed to the end of the lead screw 217.
[0030] Next, FIG. 4 is a plan view of an operating panel part 2f.
In this figure, a power switch 15 an AC/DC lamp 16 and a battery
lamp 17 are arranged in a centralized manner at the left end portion
of the operating panel part 2f. Adjacent to these lamps is provided
the display part of injection of medicines per body weight 10 which
displays the injection of medicines per body weight. However, a
model which is not provided this display part of injection of medicines
per body weight 10 can be sufficiently used, such a model is also
available. This display part of injection of medicines per body
weight 10 is provided with a unit changeover switch (which serves
also as a display on/off switch) 10a and an item changeover switch
10b.
[0031] On the other hand, on top of this display part 10 there
is provided a syringe display lamp (a syringe display part) 18
which performs automatic measurement by use of syringe diameter
detection means 50 which detects the outside diameter (capacity)
of the syringe after converting the vertical moving distance of
the clamp into electrical signals upon setting of the syringe by
use of the clamp 5 and displays the capacity (volume) of the set
syringe in 10 cc (ml), 20 cc (ml), 30 cc (ml) and 50 cc (ml) and
the syringe maker name.
[0032] Also, below the clamp 5 there is provided the action indicator
7 which is molded from a transparent acrylic resin etc. so as to
have a shape protruding upward so that the action indicator can
display the liquid feeding action state by electric light, for example,
by the lighting up or blinking of built-in light-emitting diodes
7a to 7d which appropriately glow red and greenly or by the rotation
in the direction indicated by the arrows in the figure so as to
accomplish the scattering of light inside.
[0033] Adjacent to the clamp 5 are provided display lamps 19a,
19b, 19c, which display in a three-level switchover manner the set
pressure detected by a occlusion detection mechanism provided in
the syringe pump. Adjacent to these lamps, a remaining amount alarm
lamp 20 a battery alarm lamp 22 etc. are arranged in a centralized
manner. There are also provided a blockage pressure monitor display
part 19d, which performs alarm display by lighting up by an LED
etc. when the occlusion pressure becomes not less than a prescribed
ratio (for example, not less than 50%) of a set value (mm Hg), and
a pusher/clutch disengagement display part 19e, which displays the
disengagement of the pusher and clutch.
[0034] Adjacent to these lamps, there is provided the 7-segment
LED display part 11 which is provided with a flow rate lamp 23
a predetermined amount lamp 24 and an integrated amount lamp 25.
In this display part 11 a maker name which is set and input by
maker input means 40 or a maker name read by identification information
reading means (not shown) is indicated by symbols or characters.
[0035] On the right side of this display part 11 there are provided
a display changeover switch 26 and an integrating clearing switch
27. And below the display part 11 are provided a rapid feed switch
30 a start switch 29 and a stop/mute switch 28. There is also provided
selection means (a selector switch) (not shown) which can select
either or both of a remaining amount position alarm and a remaining
time (finish time) alarm. Also, there is provided a manual switch
31 to maintain a medicine-in-blood concentration at a prescribed
value when this concentration has reached the prescribed value.
The medicine-in-blood concentration can be set at a prescribed value
by pressing this manual switch 31 for a prescribed time (1 to 3
seconds).
[0036] To set the flange of the syringe in the slit 2c, the flange
of the syringe is put into the slit 2c. After that, the main body
of the syringe S is set on the syringe stage 2a and then clamping
is performed by use of the clamp.
[0037] A small-diameter circular-arc groove portion is further
integrally formed in the above-described slit 2c and syringe stage
2a so that a small-capacity, small-diameter syringe can be held
in an immobile state. With the foregoing, the setting of the syringe
is completed. By installing reading means which reads identification
information (a bar code etc.) which is attached to the syringe and
identifies the syringe maker and the syringe type including the
syringe capacity at this time, it is possible to specify the syringe
and/or the liquid medicine housed in the syringe.
[0038] Subsequently, the slider assembly 50 is moved by operating
the clutch lever. When the clutch lever 52 of the slider assembly
50 shown in FIG. 3 is pressed for this purpose, it becomes possible
to manually move the slider assembly 50. Then, when the clutch lever
52 is released after the pusher SP of the syringe is brought into
engagement with the slider assembly 50 a hook 231 in a pair of
light and left portions comes to automatically hold the pusher SP
of the syringes. That is, when the clutch lever 52 is released,
the hook 231 comes to sandwich the pusher SP of the syringes. The
foregoing is the basic setting action.
[0039] This slider feed mechanism is further provided with a blockage
detection mechanism. A liquid medicine housed in the syringe can
be injected by pushing the pusher of the syringe. At this time,
due to the action of the resistance in the syringe and other fluid
infusion passages, a force which acts in the reverse direction indicated
by the arrow in FIG. 3 is generated.
[0040] The force thus generated causes the deflection of the above-described
pressure sensor 221 which uses a strain gauge etc. This mechanical
deflection is converted into an electrical signal. When the value
of this electrical signal reaches a set value (a threshold value)
which is set for each maker and syringe size (syringe outside diameter)
and stored in storage means (E.sup.2PROM, RAM) 100 this condition
is displayed on the action indicator 7 as an alarm to make the abnormal
condition known to the user and an alarm sound (a buzzer) is generated
(sounded) to alert the user.
[0041] The setting of a load thus generated from the resistance
in the syringe and other fluid infusion passages is displayed in
a three-level switchover manner by use of the three display lamps
19a, 19b, 19c provided in the display panel on the upper cover 2.
The set load values are as follows:
[0042] (1) H (high): (800.+-.200 mm Hg)
[0043] (2) M (medium): (500.times.100 mm Hg)
[0044] (3) L (small): (300.+-.100 mm Hg)
[0045] These set load values are presented in a table for each
syringe maker (one or more table makers) in consideration of syringe
outside diameter D(cm), syringe size (syringe capacity) (ml), syringe
sectional area A (cm.sup.2), sliding resistance of syringe Fs (kgf),
etc. and stored in the storage means (memory) 100 as a threshold
value P (kgf/cm.sup.2).
[0046] Furthermore, a comparison is made between a converted value
Fp of one selected threshold value P (kgf/cm.sup.2) [=P (kgf/cm.sup.2).multidot-
.A(cm.sup.2).multidot.+Fs(kgf)] on the basis for a syringe which
is included in a table, set and specified and a value of pressure(load
F (kgf)) which acts through the slider assembly 50 as indicated
by the arrow in FIG. 3 and detected by the above-described pressure
sensor 221.
[0047] Preferably, this load F (kgf) is obtained by taking a predetermined
number of samples, for example, 16 samples at predetermined sampling
intervals, for example, every 0.05 second and obtaining a moving
average thereby to remove noise components due to the backlash,
etc. of the syringe and the drive part. The result thus obtained
is segment displayed on the segment display part 19d, and a warning
(an alarm) to the effect that blockage at not less than a predetermined
threshold value has occurred is generated and displayed by blinking
etc.
[0048] On the other hand, a remaining amount detection/remaining
amount position mechanism provides an important function for the
case where the remaining amount becomes small during operation.
When the pump continues its action and as a result the pusher of
the syringe is moved and reaches an arbitrary position, the pusher
comes into contact with a lever 234 of a potentiometer 233 fixed
to a frame.
[0049] When the movement is further continued from this contact
condition, the value on the potentiometer 233 reaches a predetermined
value which has been stored beforehand (a predicted alarm position
which will be described later in detail). At this time, the threshold
value of blockage detection is automatically set and changed by
threshold value changing means 110. For example, when the above-described
initial setting is H (high) [800.+-.200 mm Hg], this value becomes
300.+-.100 mm Hg; when the initial setting is M (medium) [500.+-.100
mm H], this value becomes (300.+-.100 mm Hg); and when the initial
setting is L (small) [300.+-.100 mm Hg], this value becomes [300.+-.100
mm Hg], preferably, 30 to 100% of the initial setting. Furthermore,
as an alarm to make known the fact that a planned injection is to
be finished after a predetermined time (hour and minute), this is
displayed in a remaining amount alarm lamp 21. And at the same time,
either a remaining time (minute) or a remaining amount (ml) is displayed
in a remaining time/remaining amount display part (not shown) or
a remaining time (minute) and a remaining amount (ml) are alternately
displayed and an alarm sound is generated and displayed.
[0050] When the liquid medicine infusion action of the pump is
completed as described above, the slider assembly 50 is returned
to the initial position by moving in the direction reverse to the
feed direction. Incidentally, the lever 234 of the potentiometer
233 is so constructed as to return to its initial position by the
force of a tension spring (not shown) connected to the lever.
[0051] Incidentally, if during the feed action of the pump the
engagement state of the half nut 216 and lead screw 217 that constitute
the clutch is cut when the user grips the clutch lever 52 by mistake
or a similar phenomenon occurs for some action of load etc., the
syringe pusher/clutch disengagement detection mechanism generates
an alarm sound and causes the pusher/clutch disengagement display
part 19e to blink, thereby making the abnormality known to the user.
[0052] Next, data on the syringe sectional area A (cm.sup.2), push-finish
position (push-finish completion position) LE (cm) and syringe outside
diameter D (cm) is stored for each syringe S maker (one or more
makers) and for each size. Also, data on syringe sectional area
is stored and retained in an exchangeable memory (E.sup.2PROM) within
a CPU. Furthermore, there are provided the display part for the
infusion (gamma infusion) of medicines per body weight and the display
part for the infusion of a predetermined amount, alarms and a drive
state. The alarm display is a three-dimensional display and a place
lighted up by an LED rotates in a drive state.
[0053] The display of the remaining amount of a battery is performed
by the battery lamp 17 as a three-level display. Conventionally,
the detection of the remaining amount of a battery is detected on
the basis of battery voltage. In this syringe pump, however, the
remaining amount of a battery is detected at higher accuracy by
the integration of current.
[0054] When the setting dial 6 is clockwise rotated, various set
values appear in an increasing manner on the setting dial 6 and
are displayed on the display part 11 shown in FIGS. 1 and 2. Similarly
when setting dial 6 is anticlockwise rotated, set values are displayed
on the display part 11 in a decreasing manner.
[0055] Concretely, when the display changeover switch 26 disposed
on the display panel of FIG. 4 is pressed, the flow rate lamp 23
and the prescribed amount lamp 24 light up sequentially and various
kinds of setting can be performed.
[0056] In performing flow rate setting, the flow rate lamp 23 is
brought into a lighting up state by pressing the display changeover
switch 26 and after that, this setting is performed by rotating
the setting dial 6. As a result, the display of set values is performed
in the display part 11. The display range is 0.0 to 1200 ml/h (to
999.9: 0.1 ml/h steps) (1000 to: 1 ml/h steps). The minimum flow
rate is 0.0 and it is possible to set the flow rate in a wide injection
range. Furthermore, flow rate setting is ensured for various types
of syringes of various makers. It is also ensured that when the
flow rate set value is "0" the buzzer makes a one-shot
sound and the action indicator lights up red instantaneously thereby
to prevent a start. Also in a case where a set flow rate value exceeds
a flow rate range which permits driving, the buzzer makes a one-shot
sound and the action indicator lights up red instantaneously thereby
to prevent a start.
[0057] An integrated amount is obtained by the integration of a
pulse count value of an encoder (not shown) fixed to the output
shaft of the motor 218 and also by the addition of a rapidly-fed
amount which is rapidly fed after the pressing of the rapid feed
switch 30.
[0058] An infused amount can be set by body weight in the range
of 0.0 to 300.0 kg (in 0.1 kg steps), by an amount of medicine in
the range of 0.0 to 999.9 mg (in 0.1 mg steps), by an amount of
solution in the range of 0.0 to 999.9 ml (0.1 ml steps) and by a
dose in the range of 0.00 to 99.99 (.mu.g/kg/min or mg/kg/h) (0.01
steps).
[0059] A minimum flow rate is indicated from 0.0 and when body
weight, an amount of medicine, an amount of solution and a dose
are input, the flow rate is automatically calculated and displayed.
The injection is started with the displayed flow rate. When this
calculation result deviates from flow rates capable of being set
(not less than 0.1 ml/h but not more than 1200 ml/h), the flow rate
display of the display part 11 becomes a display other than numerals,
i.e., [ - - - - ], the buzzer makes a one-shot sound before and
after this display change, and the action indicator lights up red
instantaneously thereby to prevent the start of pump action.
[0060] On the other hand, the calculation result is displayed when
the calculation result is within 1200 ml/h, whereas when the calculation
result is not less than 300.1 ml/h and it is automatically detected
that the syringe type is 10 to 30 cc, the buzzer makes a one-shot
sound and the action indicator lights up red instantaneously thereby
to prevent a start even when the start switch 29 is pressed.
[0061] Next, when the rapid feed switch 30 is pressed, the liquid
infusion rate is increased and liquid infusing is performed at a
rate of 1200 ml/h for a 50 cc syringe, at 500 ml/h for a 30 cc syringe,
at 400 ml/h for a 20 cc syringe, and at 300 ml/h for a 10 cc syringe.
[0062] The display range for the setting of a predetermined amount
is 0.0 to 999.9 ml (in 0.1 ml steps), and a minimum predetermined
set value is 0.0. Action selection is made possible by use of an
internal selector switch. In the case of a predetermined amount
of 0.0 when the start switch 29 is pressed, the buzzer makes a
one-shot sound, the action indicator lights up red instantaneously
and, at the same time, the predetermined amount lamp 24 of the predetermined
amount LED blinks thereby to prevent a start.
[0063] In the case of a predetermined amount.ltoreq.an integrated
amount, the predetermined amount lamp 24 of the predetermined amount
LED blinks and the buzzer makes a sound thereby to prevent a continuation.
In the case of a predetermined amount.ltoreq.an integrated amount
during injection, the predetermined amount lamp 24 of the predetermined
amount LED blinks, the buzzer makes a sound and the operation is
automatically switched over to the KOR (keep open rate) run mode.
Because at this time the flow rate is displayed as KOR (0.1 ml/h),
the sound vanishes when the stop/mute switch 28 is pressed once.
An alarm is given again during the continuation of this KOR operation,
and the operation is stopped when the stop switch 28 is pressed
again.
[0064] On the other hand, the initial display which appears when
the power is made on for the syringe pump, is "0" ml except
during the memory mode.
[0065] The order of priority of sounding is basically set so that
priority decreases in the order of (a) occurrence of blockage, syringe
disengagement and clutch disengagement, (b) a decrease in battery
voltage (2 minutes, 4 minutes, 6 minutes, 8 minutes, 10 minutes,
not less than 10 minutes), (c) a push-finish foretelling alarm (remaining
amount foretelling alarm) and (d) a sound to announce a forgotten
start. Furthermore, when multiple alarms have been given, a changeover
is made to an alarm of higher order. Similarly, when multiple alarms
have been given during the mute mode, it is ensured that an alarm
of higher order is given and, at the same time, it is ensured that
a key click sound and a one-shot sound are made in an interrupting
manner while alarms are being intermittently given as with a sound
to announce a forgotten start.
[0066] Again with reference to FIG. 2 the action of the action
indicator 7 is as follows. (a) During normal operation, the built-in
light-emitting diodes 7a to 7d gradually blink greenly clockwise
at four different speeds in response to set flow rates. (b) During
the stop of operation, green lamps go out with the exception of
red color lighting up during an alarm. (c) In the case of a sound
to announce a forgotten start, all light-emitting diodes 7a to 7d
blink red. (d) When communication from the outside is received,
the lamps blink instantaneously.
[0067] How to use the above-described syringe pump will be described
below for the first embodiment by referring to the flow chart of
FIG. 5 and the block diagram of FIG. 6.
[0068] To make preliminary arrangements, tools are first checked
and it is ascertained that the syringe pump 1 and a pole clamp,
an AC power cable, a fluid infusion stand, a syringe containing
a liquid medicine and a lock needle, which are accessories, (all
being not shown) are complete. After that, the pole clamp is fixed
to the fluid infusion stand and the pole clamp is firmly fixed to
the fluid infusion stand. For this purpose, an attaching screw of
the pole clam is put into a screw hole in the bottom of the syringe
pump and fixed. Next, the AC power cable is connected to an AC inlet
8 on the right side surface of the main body and a plug is then
connected to a 100 V AC receptacle provided with a ground terminal.
[0069] When the AC power is connected, the battery lamp 17 lights
up and it is indicated that the built-in battery is being charged.
[0070] When the power is turned on by pressing the power switch
15 for about 1 second in order to put the power supply to work,
all lamps blink three times, the buzzer sounds and self-check is
automatically performed (Step S1). At this time, the AC/DC lamp
16 lights up and each of the display lamps of flow rate, predetermined
amount and integrated amount 23 24 25 lights up. The syringe maker
name which is set beforehand in the display part 11 of flow rate,
predetermined amount and integrated amount is displayed by numerals
for about 3 seconds. It is necessary to ascertain whether the set
syringe corresponds to the syringe maker name (Step S2).
[0071] When the syringe maker name is inappropriate, a right maker
name is input by use of the maker name input part (means) 40 (Step
S3). The set and input maker name is displayed in the display part
11 by letters or symbols.
[0072] After a lapse of a predetermined time, the numerals of the
syringe maker of the display part 11 of flow rate, predetermined
amount and integrated amount disappear and the display part 11 indicates
"0.0." The action indicator 7 is off at this time.
[0073] On the other hand, with all of the four built-in display
lamps 18 of syringe type blinking, the display lamps indicate that
the syringe S has not been mounted, thereby expediting the setting
of the syringe. The setting of the syringe is started when all of
the above-described indications have been ascertained. When the
syringe filled with a liquid medicine is connected to the injection
line (the tube T) in aseptic environment, the main body of the syringe
is set on the stage 2a and engaged to this stage by use of the clamp
5.
[0074] Subsequently, as shown in FIG. 3 the flange SF of the syringe
S is put into the slit 2c in order to set the flange SF in the slit
2c. After that, the main body of the syringe S is set on the syringe
stage 2a and the clamp 5 is then rotated in a predetermined direction.
Then, the lock state is canceled and the clamping of the syringe
is automatically performed and the syringe diameter (syringe capacity:
10 ml, 20 ml, 50 ml, etc.) is automatically detected by use of the
syringe diameter detection means (detection part) 50 in a setting
state (Step S4).
[0075] Subsequently, the slider assembly 50 is moved by pushing
the clutch lever 52 of the slider assembly 50 thereby to release
the clutch. At this time, when the clutch lever of the slider assembly
50 is pressed, the slider assembly 50 comes to be capable of being
manually moved.
[0076] Then, the clutch lever 52 is released after the pusher SP
of the syringe is caused to abut against the slider assembly 50
the pair of right and left hook 231 comes to automatically hold
the pusher. That is, when the clutch lever is released, the pair
of right and left hook comes to sandwich the pusher of the syringe.
[0077] When this syringe setting is finished, priming is performed.
This priming must be performed by all means before the puncture
of the patient. When the rapid feed switch 30 is pressed, the action
indicator 7 rotates and performs indication and the pump action
is started, with the result that the liquid medicine flows out of
the tip of the lock needle. The liquid medicine is fed to the tip
of the lock needle by continuously pushing this rapid feed switch
30. At this time the integrated amount lamp 25 blinks.
[0078] During rapid feed, the integrated amount lamp 25 blinks
in the display part 11 of flow rate, predetermined amount and integrated
amount and a priming amount is displayed in the display part 11
of flow rate, predetermined amount and integrated amount. This priming
amount is added to an integrated amount in 0.1 ml steps. It is also
possible to clear the integrated amount to "0" by pressing
the integrating clearing switch 27.
[0079] This priming is important for ensuring that the working
surface of the slider assembly 50 of the main body comes to engagement
with the pusher SP of the syringe without a clearance by eliminating
the clearance between the syringe and the main body and hence must
be performed by all means.
[0080] When the above priming has been completed, a liquid infusing
pattern (an infusion amount) is set by use of a setting and input
means (the input part) 60 (Step S5). At this time, it is ascertained
first that the flow rate lamp 23 is on. When this flow rate lamp
23 is not on, the flow rate lamp 23 is caused to light up by pressing
the display changeover switch 26.
[0081] After that, a flow rate per hour is set by turning the setting
dial 6 which constitutes part of the input part 60. At this time,
in order to ensure safety by preventing a malfunction in the operation
of the setting dial, a numeric value will not change during half
a turn after the start of turning. When half a turn is exceeded,
the buzzer sounds and the numeric value changes.
[0082] An increase or a decrease in this numeric value is such
that the numeric value decreases when the setting dial 6 is turned
forward, whereas the numeric value increases when the setting dial
6 is turned backward. A high-order numeral of a numeric value changes
when the setting dial 6 is turned, with the stop/mute switch 28
kept pressed.
[0083] For the syringe type and maximum flow (infusion) rate, a
maximum flow rate capable of being set is set depending on the syringe
type and, for example, the maximum flow rate is 300 ml/h in the
case of a 30 ml syringe. Therefore, when a numeric value larger
than a maximum value is set and the star switch 29 is pressed, the
set flow rate value blinks and infusion will not be started. Therefore,
setting is performed again and completed.
[0084] The setting of an occlusion pressure detection level is
performed by first pressing the stop/mute switch 28 and then pressing
the display changeover switch 26. First, in changing the setting
of an occlusion pressure detection level, "P***" appears
in the display part 11 of flow rate, predetermined rate and integrated
amount when the display changeover switch 26 is pressed while the
stop/mute switch 28 is being pressed, with the result that the mode
becomes the setting mode. With the stop/mute switch 28 kept depressed,
the display changeover switch 26 is released and then pressed, the
printed letters "L" (low), "M" (medium) and
"H" (high) in the vicinity of the occlusion pressure set
value lamps 19a, 19b, 19c light up sequentially. Therefore, a desired
level of occlusion pressure is selected, set and input. Incidentally,
the above *** are numerical values corresponding to the above L,
M and H. In this manner, the stop/mute switch 28 and the display
changeover switch 26 fulfill the function as the occlusion pressure
selection means.
[0085] On the basis of data selected and input by the remaining
amount/remaining time selector switch (selector means), a predicted
alarm position LNE (cm) is calculated as follows in a control part
(CPU) 90 (Step S6).
[0086] On the basis of the occlusion pressure level which has been
selected and input and the syringe diameter (capacity) and syringe
maker name, an occlusion pressure threshold value (an upper limit
value and/or a lower limit value) which has been presented in a
table beforehand is automatically selected and the infusing of the
liquid medicine is started (Step S7).
[0087] A predetermined number of samples (for example, 16 samples)
are continuously taken at prescribed cycles (for example, every
0.05 second), the moving average value of the samples is calculated,
and a judgment is made as to whether the occlusion pressure exceeds
the threshold value.
[0088] When the occlusion pressure exceeds the threshold value,
an alarm (a warning) is given and the action indicator 7 lights
up (blinks) red to make this known to the user. The user confirms
this and performs resetting when there is no problem. When it is
necessary to change the liquid infusing pattern during liquid infusion,
the set value is changed and a new value is input (Step S8). Infusion
is continued when the occlusion pressure does not exceed the threshold
value.
[0089] <Setting at a Remaining Amount>
[0090] When setting at a remaining amount VNE (ml) of the syringe
S to be set is performed by referring to FIG. 3 the pus-finish
position LE (cm) is calculated on the basis of the above stored
data presented in a table by using the following equation:
Push-finish position LE(cm)=LNE(cm)+VNE(ml)/A(cm.sup.2),
[0091] where LNE (cm) is the alarm position and A (cm.sup.2) is
the syringe sectional area.
[0092] As a result of the foregoing, the movement of the piston
SK of the syringe S can be accurately controlled.
[0093] <Setting at a Remaining Time>
[0094] Similarly, when setting at a remaining amount VNE (ml) to
be set is performed by referring to FIG. 3 the push-finish position
LE (cm) is calculated on the basis of the above stored data presented
in a table by using the following equation:
Push-finish position LE(cm)=LNE(cm)+R(mL/h).times.T(h)/A(cm.sup.2),
[0095] where LNE (cm) is the alarm position, R (mL/h) is the infusion
rate, T (h) is remaining time and A (cm.sup.2) is the syringe sectional
area. As a result of the foregoing, the movement of the piston SK
of the syringe S can be accurately controlled.
[0096] The comparison operation of a predicted alarm position for
the pusher is performed as described above (Step S9). When the pusher
reaches the predicted alarm position, an alarm (a warning) is given.
When the pusher reaches the push-finish position LE (cm), the threshold
value of occlusion detection is automatically changed by the threshold
value level changing means 110 (Step S10). After that, the action
indicator 7 blinks (lights up) red, thereby giving an alarm (Step
S11) and the liquid infusion (administration) is completed (Step
S12).
[0097] Incidentally, if injection is not started even when about
two minutes pass after the completion of flow rate setting after
the setting of a syringe S in the main body 1 the buzzer sounds
to make a forgotten start known to the user. In this case, the buzzer
stops sounding when the stop/mute switch 28 is pressed. When an
infusion pattern (a flow rate) is to be changed during infusion,
the infusion is stopped by performing temporary stop of infusion
and after that, resetting is performed by use of the setting input
means 60 including the setting dial 6. At this time, the action
indicator 7 goes off when the stop/mute switch 28 is pressed.
[0098] When the infusion of a liquid medicine in a predetermined
amount is completed, the stop condition is ascertained and the syringe
is removed. For this purpose, the clamp 5 is drawn upward and then
held in a condition turned by about 90 degrees. Subsequently, the
clutch lever 52 of the slider assembly 50 is pressed and the syringe
is removed by opening the right and left hook members. After that,
when the syringe pump is not used again, the power switch 15 is
cut off by being continuously pressed for not less than about 2
seconds.
[0099] This syringe pump can also be applied to a case where product
information, such as a syringe maker, a syringe diameter (capacity),
medicine type, contained in a bar code and an IC chip applied to
the syringe is automatically read by use of reading means (not shown).
[0100] Now injection per body weight will be described. First,
the unit changeover switch (serving also as a display on/off switch)
10a is continuously pressed for not less than 2 seconds, the above-described
infusion setting display part 10 lights up and it becomes possible
to perform infusion (gamma infusion) per body weight. Subsequently,
the display screen of the infusion setting display part 10 changes
when the item changeover switch 10b is pressed, and each time the
item changeover switch 10b is pressed, an infusion rate (an injected
amount) per body weight, body weight, an amount of medicine and
an amount of solution are displayed in a blinking manner. Areas
where the display is blinking are items whose settings can be changed.
Therefore, by turning the setting dial 6 with a desired item kept
displayed, numeric values are changed by changing the numeric values
on the screen of the infusion setting display part 10. Furthermore,
it is possible to rapidly change each step value by turning the
setting dial 6 while pressing the stop/mute switch 28. The screen
of this gamma infusion setting display part 10 is constructed in
such a manner that a flow rate (an infusion rate) is automatically
calculated and displayed according to the set infusion amount per
body weight, body weight, amount of medicine and amount of solvent.
[0101] For the setting of special functions, the operation of a
changeover switch built in the interior of the main body enables
the setting of various modes to be changed as required. As these
special functions, predetermined amounts in the display part 11
of a flow rate, predetermined amount and integrated amount can be
changed between a standard mode and a predetermined amount mode.
In the standard mode, each time the display changeover switch 26
is pressed, a flow rate and an integrated amount are displayed in
this order and it is impossible to set a predetermined amount.
[0102] Furthermore, when a changeover switch to the predetermined
mode is made by operating the changeover built in the interior of
the main body, the display of the display part 11 appears in the
order of flow rate, predetermined amount and integrated amount,
and it becomes possible to set a predetermined amount. In this setting
of a predetermined amount, the predetermined amount lamp 24 is first
caused to light up by pressing the display changeover switch 26
and a predetermined amount is then set by turning the setting dial
6. This setting can be changed in 0.1 ml steps. In a case where
a predetermined amount is set and injection is started, the predetermined
amount lamp 24 blinks and the buzzer sounds when an integrated amount
has reached the predetermined amount.
[0103] In a case when the setting of a predetermined amount has
been performed in this way, the injection of a liquid medicine is
continued at a flow rate (an infusion rate) of 0.1 ml/h when the
KOR (keep open rate) function works. When the user wants to perform
confirmation, the action indicator 7 lights up by the pressing of
the stop/mute switch 28 and the buzzer stops sounding. At this time,
the keep vein open function continues. When the stop/mute switch
28 is pressed again, the action indicator 7 goes off, the keep vein
open function is canceled and comes to a stop condition, and injection
in the predetermined amount mode is finished.
[0104] A re-alarm permits a change to the standard mode and the
mute mode. Specifically, it is possible to set the standard mode
with the action indicator 7 blinking red with the buzzer enabled
in which when an alarm condition is not canceled for not less than
2 minutes after the buzzer extinguished, the buzzer is caused to
sound again; and the mute mode in which the re-alarm function does
not to work even when an alarm condition continues for not less
than 2 minutes.
[0105] A forgotten start alarm permits a change to the standard
mode and the mute mode. Specifically, it is possible to set the
standard mode with the action indicator 7 blinking red with the
buzzer enabled in which when a stop condition continues for not
less than 2 minutes in a state permitting a start, the buzzer sounds
thereby to make a forgotten start known to the user; and the mute
mode in which the forgotten start alarm function does not work even
when a stop condition continues for not less than 2 minutes.
[0106] A change of a syringe maker name is made possible by use
of the built-in changeover switch. However, it is ensured that usually,
the setting of this special function cannot be performed, because
a trouble might be caused if this function is carelessly performed.
[0107] In changing the setting of the sound volume of the buzzer,
the stop/mute switch 28 is continuously pressed and the integrating
clearing switch 27 is pressed at the same time. Then, "bEL
*2" appears on the display part 11 of flow rate, predetermined
amount and integrated amount and the setting mode begins. With the
stop/mute switch 28 kept pressed, the integrating clearing switch
27 is released and pressed and the display changes to "bEL
: 1" "bEL : 2" and "bEL : 3" according
to "large," "medium," and "small"
of the volume of the buzzer. Therefore, when a desired sound volume
is obtained, the user's fingers are released from all switches,
whereby the setting of the volume of the buzzer is performed.
[0108] The syringe pump can also be operated by use of a DC power
source in a centralized power source box. In this case, it is ascertained
that an AC power cable is detached from the main body 1 and a DC
cable is then connected to a DC connector 9 on the right side surface
of the main body. Subsequently, the AC/DC lamp 16 lights up and
power is supplied from the DC power source when the power switch
15 is turned on.
[0109] When power is supplied neither from the AC power source
nor from the DC power source, power supply is automatically changed
over to the built-in battery, the AC/DC lamp 16 goes off and the
syringe pump can be continuously used for about 3 hours using the
built-in battery. Regardless of the on/off state of the power source,
the built-in battery can be charged when the AC power source or
the DC power source is connected. During this charging the battery
lamp 17 lights up and displays the remaining amount of the battery
at three levels. A rough standard for the remaining amount of the
battery is such that use for not less than about 160 minutes is
possible when all the three lamps are on, the action time is for
not less than 80 minutes when two lamps are on, and use for not
less than 30 minutes is possible when only one lamp is on. A case
where all the three lamps blink and a case where two lamps or only
one lamp lights up indicate that the battery has deteriorated.
[0110] When the remaining amount of the battery decreases further,
the battery alarm lamp 22 blinks and the buzzer sounds. Accordingly,
the syringe pump is rapidly connected to the AC or DC power source
and used.
[0111] For an electrostatic noise margin, to prevent a malfunction
by contact discharge at .+-.8 kV and aerial discharge at .+-.15
kV, this syringe pump is constructed so as to conform to the overseas
standards: FCC Prat. 18 CISPR 11 IEC 60601-1-2 IEC 60601-2-24
and VDEDIN57871. The electric shockproof type for TYPE CY (ground
leakage current: not more than 0.5 mA) in CLASS I (not less than
3 kV) conforms to the domestic standard JIS T1001 and T1002 and
the overseas standard IEC 60601-1.
[0112] For chemical resistance, wiping off with alcohol is prohibited
by operating instructions. However, in order to give the syringe
pump chemical resistance to alcohol and similar substances, the
outer layer is given ABS grade V0 and measures are taken by performing
under printing, for example, so that a nameplate, printed characters,
indications, etc. do not disappear.
[0113] The driving thrust (the force which pushes the pusher) is
about 15 kg.multidot.f maximum and the syringe pump is constructed
so as to withstand about 20 kg.multidot.f. The mechanical (feed)
accuracy can be maintained at high accuracies of within .+-.1% by
actual measurement and ensured for each syringe type of various
syringe makers.
[0114] Concretely, by measuring the moving distance of the slider
assembly 50 the mechanical (feed) accuracy was set as follows:
[0115] (A) Flow (infusion) rate<1.0 ml/h
[0116] 60 minutes (long-term): Not more than .+-.5%
[0117] (B) 1.0 ml/h.ltoreq.flow rate<5.0 ml/h
[0118] 2-minute observation from the observation window: Not more
than .+-.2%
[0119] and at the same time
[0120] 60 minutes (long-term): Not more than .+-.1%
[0121] (C) 5.0 ml/h.ltoreq.flow rate
[0122] 2-minute observation from the observation window: Not more
than .+-.1%
[0123] Discharge rates were measured so that high flow (infusion)
rate accuracies of within .+-.3% can be ensured for each syringe
type of various syringe makers.
[0124] (A) 1.0 ml/h.ltoreq.flow rate<5.0 ml/h
[0125] 2-minute observation from the observation window: Not more
than .+-.5%
[0126] (B) 1.0 ml/h.ltoreq.flow rate 60 minutes (long-term): Not
more than .+-.3%
[0127] (C) It was ascertained that not less than 95% is ensured
for the 10 minutes after the start of infusion.
[0128] The display part 10 of an injected amount per body weight
is a liquid crystal provided with a back light (yellow or green).
This is a numeral indicator composed of seven segments. This display
part can display weight in kg, an amount of medicine in mg, an amount
of solution in ml, a dose in .mu.g/kg/min or mg/kg/h, etc.; body
weight is indicated in 4 digits by the seven segments+a decimal
point by one segment; an amount of medicine is indicated in 4 digits
by the seven segments+a decimal point by one segment; an amount
of solution is indicated in 4 digits by the seven segments+a decimal
point by one segment; and a dose is indicated in 4 digits by the
seven segments+a decimal point by one segment. Usually, when the
ordinary infusion mode is selected, the back light goes off for
the whole screen.
[0129] The display part 11 of flow rate, integrated amount and
predetermined amount is a readily seen LED display, which performs
display in 4 digits by seven segments+a decimal point by one segment,
changes over automatically to a flow rate display during the setting
of the .gamma. mode. Furthermore, during the setting of the mode
for injection per weight body (in .mu.g/kg/min or mg/kg/h, etc.)
this display part whose flow rate indication changes sequentially
in response to a set value is indicated, changes over automatically
to a flow rate display if the display part is left as it is for
about 15 seconds when an integrated amount or a predetermined amount.
[0130] Alarms are given in the case of Er*, an out-of-control CPU,
a switch operation and self-check. These alarms are generated in
a readily perceived sound free from unpleasant feeling and conform
to overseas standards and a changeover at three levels of sound
volume (panel operation) is possible. Set sound volume can be stored
and the levels of sound volume can be displayed during setting.
The maximum sound volume is not less than 65 dB at a distance of
1 m. Furthermore, the alarm system is of the self-excitation type
(which gives an alarm in the case of an out-of-control CPU).
[0131] The tone quality of the alarms is 3 frequencies (2 to 4
kHz or so). PWM output from the CPU is possible and the following
is ensured: alarm.fwdarw.PWM output, watch dog.fwdarw.hardware oscillation.
The procedure for sound volume changeover is as follows. (1) In
the case of an alarm state (excepting a voltage drop and a remaining
amount), a changeover is impossible and the integrating clearing
switch is pushed. (2) Each time the integrating clearing switch
is pushed, with the stop switch kept pressed, a change occurs from
medium.fwdarw.large.fwdarw.smal- l.fwdarw.medium . . . (the buzzer
makes a sound for 1.5 seconds). (3) In synchronization with the
buzzer, the following appears in the flow rate display part in 7
segments: medium="b-2" large="b-3" and small="b-1."
(4) The result is written in E2PROM.
[0132] As described above, in a syringe pump and a liquid infusing
method according to the invention, by utilizing the characteristic
that a detected occlusion value transmitted to the pusher increases
beyond a position at which the infusing of a liquid medicine in
the syringe is completed, it becomes easy to accurately detect a
position at which the infusing of a liquid medicine in the syringe
is completed by combining pusher position detection means and occlusion
detection means. That is, when a remaining amount decreases beyond
a position at which the infusion of a liquid medicine in the syringe
is completed, a detected occlusion value transmitted to the pusher
increases and this position at which the infusion of a liquid medicine
in the syringe is completed may not sometimes be accurately detected.
Therefore, a push-finish position until the remaining amount in
the syringe is injected can be accurately found by finding the push-finish
position from an arithmetic expression by setting a position in
which a remaining amount is small as an alarm position, setting
an occlusion detection level at a low level and ensuring that the
pusher is moved by a slider from the alarm position. |