Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
  • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
  • A61M5/168—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
  • A61M5/172—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body electrical or electronic
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
  • A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
  • A61M5/168—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
  • A61M5/16804—Flow controllers
  • A61M5/16809—Flow controllers by repeated filling and emptying of an intermediate volume

Definitions

• This invention relates to apparatus.
• this invention relates to apparatus for delivery of solutions to be given intravenously to an animal.
• the present invention provides intravenous administration apparatus comprising a chamber, an inlet to the chamber provided with a first valve, an outlet from the chamber provided with a second valve, a first liquid level sensor disposed to detect a first liquid level in the chamber, a second liquid level sensor disposed to detect a second liquid level in the chamber being a level higher than the first liquid level, and control means operative in use when an intravenous solution is supplied under pressure to the inlet to perform a cycle including opening the first valve to commence filling of the chamber with the solution, closing the first valve on the solution reaching the second level, opening the second valve whereby to allow the solution to pass out of the outlet under gravity, and closing the second valve on the solution falling to the first level.
• the above described apparatus will deliver a constant volume of solution per cycle and if it is supplied at the inlet with the solution at constant pressure it will cycle at a substantially constant rate.
• rate control means for controlling the cycle rate whereby a selected and substantially constant volume of the solution " with respect to time can be fed to a patient.
• rate control Various methods of rate control are possible such as pressurizing the chamber above the second level to a predetermined pressure but in general electronic control of rate is preferred.
• One means of rate control is to use a third valve downstream of the second valve and timing means to open the third valve at selected time intervals and for selected times.
• Another means of rate control involves conditional circuit means in a circuit controlling the second valve which will result in the second valve only opening at preselected time intervals.
• preferred means includes a normally open means in a circuit controlling the second valve and timer means to close that means at preselected time intervals.
• rate control is at least in part governed by computer or micro-computer means which may control the rate of administration in response to signals derived from a patient or from a predetermined programme.
• the inlet may be supplied with the solution by a pump but in general a gravity feed will suffice.
• first level is sufficiently above the outlet to guard against the possibility of air entering the outlet and causing air embolism in a patient.
• the first and second valves may be operated in any convenient way but solenoid control is currently preferred.
• the apparatus of this invention is preferably in at least two separable parts; a first part desirably carries the chamber, the inlet, the outlet and the first and second valves, and a second part desirably carries means such as solenoids for operating the first and second valves and the first and second liquid level sensors.
• the first part may be intended for single use only and if desired may be discarded after a single use.
• the second part may be intended to be reusable.
• the second part preferably has no physical contact with the solution and hence need not necessarily be used in sterile
• the first part will have contact with the solution it is preferable that it be supplied in sterile condition. Since the first part will have contact with the solution it is preferable that it be supplied in sterile condition.
• the second liquid level sensor may be adjustable in position to vary the second liquid level and hence the quantity of the solution dispensed in each cycle. This is not essential but it is desirable as it is preferred that the solution is substantially constantly dispensed rather than substantially intermittently dispensed This last desiderata can alternatively be met by using different first parts of different chamber volumes notwithstanding that the height difference between the first and second liquid levels may be the same.
• first and second valves be metering valves and in general it is preferred that they are merely on-off valves.
• the liquid level sensors are preferably opto ⁇ electronic devices and may operate using transmitted or reflected light.
• the sensors may include a discrete light emitter and a discrete light receptor. However, a range of units combining an emitter and receptor is currently available and these may be used if desired.
• the sensors are preferably adapted to detect the passing of a meniscus.
• a third liquid level sensor may be provided to shut off the apparatus if due to some fault the liquid level in the chamber should rise to a third level above the second level.
• Fig. 1 is a schematic drawing of the apparatus as set up for use
• Fig. 2 is an exploded perspective view of the apparatus
• Fig. 3 is a cross-section on line A-A in Fig. 2
• Fig. 4 is a cross-section on line B-B in Fig. 2
• Fig. 5 is a schematic circuit diagram of part of the apparatus
• Fig. 5a is a schematic representation of part of the apparatus described above,
• Fig. 6 is a block diagram of part of electrical circuitry which may be used
• Fig. 7 is a circuit diagram of other circuitry which may be used
• Fig. 8 is a front perspective view of a first part of another apparatus
• Fig. 9 is a rear perspective view of the first part shown in Fig. 8,
• Fig. 10 is a front perspective view of a second part of said another apparatus
• Fig. 11 is a . schematic representation of portion of said another apparatus
• Fig. 12 is a flow chart illustrating the manner of operation of said another apparatus
• Fig. 13 is a circuit diagram of said another apparatus.
• the apparatus in accordance with this invention shown in Fig. 1 comprises a first part 1 and a second part 2.
• the first part 1 comprises a body 10 having an inlet 41, a valve 16 downstream of the inlet, a chamber or column 50 downstream of the valve 16, an outlet 51, a valve 17 upstream of the outlet and wherein upstream of the valve 17 is connected to the column 50.
• the valves 16 and 17 are both identical in construction and are shown in more detail in Fig. 4.
• the valves 16 and 17 have inlet ports 24 which respectively communicate with the inlet 41 and the column 50, outlet ports 25 which respectively communicate with the column 50 and the outlet 51 and valve closure means comprising an elastomeric body 22 located in a chamber 26 and an operator 23.
• the column 50 has arms 54 for connecting the second part 2 thereto.
• the second part 2 includes a body 55 having lugs 56 for connection to the arms 54.
• the body 55 carries solenoids 14 and 15 having cores 141 and 151, has windows 18 and 19 and carries combined diodephoto- transistor units 181 and 191.
• the second part 2 is assembled to the first part 1 and in the region in which the windows 18 and 19 are located the column 50 has the form shown in Fig. 3.
• the column has a window 61 through which light from the diode at one end of the units 181 and 191 may pass to be reflected by a reflective surface 20 through a passing meniscus to the phototransistor of said one of the units 181 and 191 and a curved wall 21 to scatter light so that light reflected from the wall 21 will not substantially affect the phototransistor of said one of the units 181 and 191.
• an identical apparatus distinguished by the reference letter "a" will usually be connected to a bottle 3 containing an intravenous solution such as blood, dextrose or electrolyte mounted to a stand 7.
• the bottle 3 will be connected to the inlet 41 by a tube 4, the column 50 will be provided with an air breather tube 12 and the outlet 51 will be connected to a patient by a line 5.
• a multicable will pass from the electronics of the apparatus to a control unit 8 and, if desired, a microprocessor 9, a recorder/printer 10 and a remote warning device 11.
• the control unit 8 includes switches 71 and 72 which are normally open, means for closing those switches and timer means.
• Wheri operation is to commence the control unit 8 is operated to signal switch 71 to close.
• the solution in the column will then flow under gravity through the valve 17, through the outlet 51 and the tube 5 to the patient.
• the downward going meniscus of the solution in the column 50 reaches the level of the unit 181 that unit will signal the control unit which will open the switch 72 to close the valve 17.
• control unit will repeat the sequence at controlled rate and since the distance between the units 181 and 191 is constant, constant volumes of the solution will be dispensed at controlled rate.
• the microprocessor 9 might monitor body functions of the patient and vary the rate of dispensation to suit and might output to the recorder/printer 10. If the apparatus should fail the warning device 11 may be arranged to give a signal.
• the first part 1 may be discarded after a single use if this is desired but the second part 2 may be re-used many times.
• S indicates the bottle 3
• X and Y indicate the valves 16 and 17
• a and B indicate opto-electronic devices comprising diode emitters and diode light detectors and P indicates patient.
• the devices A and B are such that their outputs are high when clear fluid is present in front of them.
• the operating cycle begins when fluid fills the column 50, A and B are covered and their outputs are high. X and Y are closed.
• the logic state is
• I I I 0 0 where 0 and I denote respectively high and low voltages on ' the logic and closed and open states on the valves. T denotes a negative going trigger pulse, absent here. The device "waits" in this position.
• a negative going trigger pulse T then arrives from a variable frequency oscillator. It is the frequency of this oscillator that determines the cycling frequency of the device and thus the ultimate intravenous flow rate. This frequency may be operator determined (manually controlled potentiometer) or determined automatically by a microprocessor on the basis of some physiological input. Arrival of the trigger pulse causes the opening of valve Y.
• OMPI The trigger pulse then returns to the high level. Opening of valve Y causes the column 50 fluid to fall into patient P causing the output of B to go low.
• the logic is organised so that this causes no change in valve setting.
• the column 50 fluid level now rises under the influence of the head of the bottle 3.
• the output of A goes high.
• the logic is arranged so that this causes no change in valve setting.
• the logic state is now
• the cycle of operation may thus be summarised LOGIC VALVES
• the outputs of electro-optical devices A and B are fed to comparators where each signal is compared to a potentiometer-set reference voltage.
• the reference voltage in each case is set so that the comparator changes state when the fluid meniscus crosses the associated electro-optical device.
• the comparator output goes high when clear fluid covers the device.
• the comparator output is fed through a Schmitt trigger to avoid random transients of the comparator at the switching point.
• the logic sequence may be achieved using a microprocessor under interrupt control.
• the apparatus shown in Figs. 8 - 13 differs from that of Figs. 1 - 7 principally in that it is microcomputer controlled but also in other aspects. Where applicable, like reference numerals are used as were used in respect of Figs. 1 - 7.
• the apparatus of Figs. 8 - 13 includes the first part 1 and the second part 2.
• the first part 1 while differently configured to that of Figs. 1 - 7 differs principally in that the air breather tube 12 is omitted, column 50 is made as an integral part of the first part 1 and is connected at its upper end to a sealed chamber 201 which is also an integral part of the first part 1 and in that it has keying lugs 202 and a hole 203 which can be received in and receive recesses 204 and pin 205 in the rear 206 of the second part 2. Further, the second part 2 has a ball catch 207 which also serves to assist in releasably retaining the first (1) and second (2) parts together.
• the first part 1 differs from that of Figs. 1 - 7 as indicated above a d additionally in that it has manual override buttons 211 and 212 for the solenoids 14 and 15 and contains a battery and all control electronics such that it is a self-contained unit not needing connection to any unit other than the first part 1 unless an external power source is to be used.
• the second part 2 contains the solenoids 14 and 15, the windows 18 and 19 but has separate
• the second part 2 has a front panel provided with control switches 221-226 and a four alphanumeric character display 227.
• the display 227 is provided by an integrated circuit being a NSM1416.
• the second part 2 also contains an alarm buzzer 228, a voltage regulator 229 which is a LM340/05, a four unit operational amplifier which is a LM339 of which only two units are used and a microprocessor which is a 6805.
• the microprocessor is made by Motoralais 8-bit and has 4 of PROM.
• Fig. 11 X and Y indicate the valves 16 and 17
• a and B indicate upper and lower liquid level sensors which are constituted by the diodes 181a and 191a and associated phototransistors 181b and 191b
• S indicates the bottle 3
• P indicates patient.
• the microcomputer operates a programme to perform in accordance with the flow diagram of Fig. 12.
• switches 223 and 224 will cause the rate of infusion to increase or decrease and for the so selected rate to be displayed by the display 227.
• Operating a selected one of the switches 225 and 226 will cause the total volume to be delivered (whereafter which volume is delivered the apparatus will be caused to turn off) - - to increase or decrease and for the so selected volume to be displayed by the display 227.
• Operating switch 222 opens both valves X and Y to allow liquid to enter lines and purge air therefrom prior to those lines being connected to a patient.
• the microcomputer is capable of giving alarms, display and shutting down delivery if occlusions occur in lines or if the supply S is empty.
• the second valve for example, valve 17
• Such pulsing may conveniently be achieved by pulsing the associated solenoid 15.
• timer means may be incorporated into the part of the circuit supplying solenoid 15 so as to cause valve 17 to be open and closed for predetermined intervals cyclically during the appropriate part of the cycle. Indeed, by appropriately adjusting the mark space ratio of the valve 17 being open and being closed flow rates, of below 5 ml./hour can be achieved.
• a third liquid level sensor is interposed between the first and second liquid level sensors at, say 2/3 rds the distance between the first and second liquid level sensors above the first liquid level sensor.
• Appropriate circuitry for example switches, may be provided whereby that third liquid level sensor may not be used or be used in lieu of the first or the second liquid level sensor whereby any one of the full volume of the column 50 between the first and second liquid level sensors, l/3rd that volume (between - -
• volume (between the third and first liquid level sensors) may be dispensed as selected.

Landscapes

• Health & Medical Sciences (AREA)
• Vascular Medicine (AREA)
• Engineering & Computer Science (AREA)
• Anesthesiology (AREA)
• Biomedical Technology (AREA)
• Heart & Thoracic Surgery (AREA)
• Hematology (AREA)
• Life Sciences & Earth Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Infusion, Injection, And Reservoir Apparatuses (AREA)
• Flow Control (AREA)

Applications Claiming Priority (2)

Publications (2)

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ID=3769341

Family Applications (1)

Country Status (4)

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Citations (1)

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• 1983
  • 1983-01-27 JP JP58500477A patent/JPS59500254A/ja active Pending
  • 1983-01-27 WO PCT/AU1983/000012 patent/WO1983002561A1/en not_active Ceased
  • 1983-01-27 EP EP19830900410 patent/EP0101689A4/de not_active Withdrawn
  • 1983-09-27 DK DK441483A patent/DK441483A/da not_active Application Discontinuation

Patent Citations (1)

Non-Patent Citations (1)

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