Open-loop control of drug infusion

• US 4,741,732 A
• Filed: 05/09/1985
• Issued: 05/03/1988
• Est. Priority Date: 05/10/1984
• Status: Expired due to Term

• Current Assignee: University of Melbourne The Victoria of Grattan St
• Original Assignee: University of Melbourne
• Inventors: Boyd, Malcolm D., Crankshaw, David P.
• Primary Examiner(s): DAVIS JR, ALBERT
• Application Number:
  US06/732,147
• Time in Patent Office: 1,090 Days
• Field of Search: 604/67, 604/65, 604/50, 604/154, 604/155
• US Class Current: 604/503
• CPC Class Codes: A61M 2202/048 Anaesthetics see also A61M19/00
• CPC Class Codes: A61M 5/1723 using feedback of body parameters, e.g. blood-sugar, pressure measurement of body parameters A61B5/00
• CPC Class Codes: G16H 20/17 delivered via infusion or injection

Abstract

A method of determining a generalised infusion rate profile for the delivery of drugs into the circulation comprising the steps of:

(a) infusing a drug at arbitrary but known rates into a group of patients for each of whom the Lean Body Mass has been determined;

(b) determining the plasma arterial concentration of the drug in each patient at a number of specific time intervals throughout each infusion period;

(c) for each patient, estimating the rates of loss of drug from the circulation at a number of specific time instants by dividing the known infusion rates per Lean Body Mass of these instants by the plasma arterial concentrations of the drug at each of these instants;

(d) calculating the average of the estimated rates of loss of drug from the circulation per Lean Body Mass unit at each specific time interval for the group of patients;

(e) interpolating the successive average points between the specific time intervals to produce an infusion profile;

(f) infusing said drug in accordance with said infusion profile determined from said interpolations into a group of patients for each of whom the Lean Body Mass has been determined, said infusion rate being scaled according to said Lean Body Mass of each patient, and

(g) repeating steps (b) to (f) until a desired steady plasma arterial content of the drug is substantially maintained throughout the infusion period.

Claims

1. A method of infusion of a drug into a patient comprising the steps of:

(i) determining the Lean Body Mass of the patient;

(ii) selecting a predetermined profile for the rate of delivery of drug, which rate reduces with time and is configured to maintain a selected substantially steady plasma arterial content of the drug in the patient throughout an infusion period;

said profile being determined by;

(a) infusing a drug at arbitrary but known rates into a group of patients for each of whom the Lean Body Mass has been determined;

(b) determining the plasma arterial concentration of the drug in each patient at a number of specific time intervals throughout each infusion period;

(c) for each patient, estimating the rates of loss of drug from the circulation at a number of specific time instants by dividing the known infusion rates per Lean Body Mass of these instants by the plasma arterial concentrations of the drug at each of these instants;

(d) calculating the average of the estimated rates of loss of drug from the circulation per Lean Body Mass unit at each specific time interval for the group of patients;

(e) interpolating the successive average points between the specific time intervals to produce an infusion profile;

(f) infusing said drug in accordance with said infusion profile determined from said interpolations into a group of patients for each of whom the Lean Body Mass has been determined, said infusion rate being scaled according to said Lean Body Mass of each patient, and

(g) repeating steps (b) to (f) until a desired steady plasma arterial content of the drug is substantially maintained throughout the infusion period;

(iii) scaling said predetermined infusion profile by the determined Lean Body Mass of the patient and by the desired substantially steady plasma arterial content of the drug to be maintained in the system of the patient, and

(iv) administering the drug to the patient in accordance with said scaled profile by means of an infusion device which is controlled to deliver said drug at said scaled infusion rate profile.

2. The method of claim 1, wherein said predetermined drug delivery rate profile is stored in a storage device which controls said infusion device at a rate which is subjected to said scaling.

3. The method of claim 2, wherein said storage device is a programmable read only memory which co-operates with a micro processor to control said infusion device.

4. An infusion system for regulating the delivery of a drug to a patient, including control means for controlling the operation of an infusion pump, said control means including pre-programmed means for varying the infusion rate with respect to elapsed time, said pre-programmed means varying the infusion rate in accordance with a profile which varies with time and which is adapted to maintain a desired substantially steady plasma arterial content of the drug throughout the infusion period;

said profile being determined by;

(a) infusing a drug at arbitrary but known rates into a group of patients for each of whom the Lean Body Mass has been determined;

(b) determining the plasma arterial concentration of the drug in each patient at a number of specific time intervals throughout each infusion period;

(c) for each patient, estimating the rates of loss of drug from the circulation at a number of specific time instants by dividing the known infusion rates per Lean Body Mass of these instants by the plasma arterial concentrations of the drug at each of these instants;

(d) calculating the average of the estimated rates of loss of drug from the circulation per Lean Body Mass unit at each specific time interval for the group of patients;

(e) interpolating the sucessive average points between the specific time intervals to produce an infusion profile;

(f) infusing said drug in accordance with said infusion profile determined from said interpolations into a group of patients for each of whom the Lean Body Mass has been determined, said infusion rate being scaled according to said Lean Body Mass of each patient, and

(g) repeating steps (b) to (f) until a desired steady plasma arterial content of the drug is substantially maintained throughout the infusion period; and

operator adjustable scaling means for setting the desired concentration of said drug in the patient, for setting the Lean Body Mass of the patient, said scaling means causing modification of the pre-programmed infusion rate by a fixed proportion over each time period of operation of said infusion pump.

5. The system of claim 4, wherein said pre-programmed means comprises a read only memory module containing said profile relating to the drug to be administered, said control means including a port for receiving said module.

6. The system of claim 4 or claim 5, including operator adjustable scaling means for setting the concentration of said drug in a fluid containing said drug.

7. The system of claim 5, wherein said read only memory module contains information related to the drug to be delivered, including the usually prescribed concentration of the drug in a fluid containing such drug, an average plasma concentration for achieving an effect in the patient with the drug and an acceptable range of plasma concentrations of the drug.

8. The system of claim 4, wherein said infusion pump comprises means for receiving a syringe containing a drug-containing fluid to be administered, syringe actuator means and means for driving said actuator means to move the plunger of said syringe to deliver fluid therefrom, said drive means including a permanently maintained connection between said drive means and a position sensing device by means of which the position of said actuator means is monitored at all times.

9. The system of claim 8, wherein said drive means comprises a motor and a drive train driven by said motor, said drive train including said permanently maintained connection, and means for disconnecting drive between said motor and said drive train to enable said actuator means to be freely moved whilst maintaining said permanent connection so that the position of said actuator means is monitored.

10. The system of claim 9, wherein said drive train includes a driven wheel, a driving head connected to be driven by said driven wheel, a further driving head spaced from said driving head and a flexible driving connection interconnecting said driving heads so that said further driving head is positively driven by said driving head.

11. The system of claim 10, wherein said flexible driving connection comprises a toothed belt, the teeth of which positively engage teeth formed on said driving heads.

12. The system of claim 11, wherein said permanently maintained connection comprises a plate clamped to said belt and rigidly secured to means for moving said actuator means.

13. The system of claim 12, wherein said position sensing device comprises a rotary potentiometer driven by said further drive head, the output of said potentiometer being connected to control circuitry for said motor whereby the position of said actuator means is sensed.

14. The system of claim 9, wherein said means for disconnecting drive between said motor and said drive train comprises manually actuatable means on said actuator means.

15. The system of claim 14, wherein said means on said actuator means comprises at least one depressible lever which causes actuation of a further lever which disengages said motor from said drive train.

16. The system of claim 15, wherein said motor is mounted on a pivoted arm to which a bell-crank lever is connected by a linkage a said bell-crank lever being actuated by depression of said at least one lever.

17. The system of claim 16, wherein said actuator means supports two manually operable levers which are in turn connected to tubes rotatably mounted in the actuator means and slideably supported by guide rails, said tubes also being rotatably mounted in a slider spaced from said actuator means and to which said permanently maintained connection is attached, said tubes supporting cams which engage a motor releasing lever when said levers carried by said actuator means are manually depressed to disengage said motor from said drive train.

18. The infusion system of claim 8, further comprising a syringe holding and sizing means in the form of a syringe clamp to which a sizing mechanism is connected.

19. The system of claim 18, wherein said sizing mechanism comprises a rotary potentiometer, the output of which is connected to control circuitry for said pump whereby the diameter of the syringe is automatically measured thereby enabling the calculation of the volume of said syringe.

20. The system of claim 8, further comprising control circuitry for said pump which controls the rate of delivery of said drug containing fluid, said control circuitry including a programmable module which is pre-programmed with information concerning each drug to be administered by means of said infusion pump according to a predetermined profile which varies with time and which maintains a desired substantially steady level of the drug in the patient to whom the drug containing fluid is delivered.

21. The system of claim 20, wherein said control circuitry further comprises means for scaling the programmed profile in said module in accordance with the estimated Lean Body Mass of the person, the desired level of drug to be maintained in the person.

22. The system of claim 8, further comprising a switch mounted on said actuator means and positioned to engage the plunger of a syringe supported by said pump, said switch being connected in control circuitry for said pump to indicate that the actuator means has engaged a syringe mounted on said pump.

23. The system of claim 20, wherein means is provided for varying the rate of delivery of said drug containing fluid in accordance with a variation in the concentration of the drug in the fluid.

24. The system of claim 23, wherein means is provided for entering a variation in the concentration of the drug in the fluid.

25. The system of claim 8, comprising means for displaying the quantity of drug infused.

26. The system of claim 8, including means to detect a pressure greater than a predetermined pressure required to deliver fluid.

27. The system of claim 19 or 26, including means to vary said predetermined pressure in relation to variation in syringe size.

28. The system of claim 22 or 24, including means to determine that an overpressure has been released.

29. The system of claim 8, 19 or 22, including means for detecting a syringe replacement, a variation in syringe size and means adapted to store an accumulation of drug dosage consequent on syringe replacement and/or variation of syringe size.