System and method for drug preparation and delivery

Patent metadata

Field	Value
Publication number	US-9408966-B2
Application number	US-201414451904-A
Country	US
Kind code	B2
Filing date	Aug 5, 2014
Priority date	Aug 22, 1997
Publication date	Aug 9, 2016
Grant date	Aug 9, 2016

Abstract

A disposable cassette for mixing a drug in a vial includes a liquid inlet for connection to a liquid supply, a first vial spike, a second vial spike, a chamber and a valve mechanism. The chamber, the first and second vial spikes, and the liquid inlet are in fluid communication with each other. The valve mechanism may be actuated to control flow between the chamber, the vial receptacles and the liquid inlet.

First claim

What is claimed is:

1. A medical fluid delivery device configured to deliver fluid into a patient, comprising:
a pump configured to pump fluid;
a keypad configured to receive a dosage level;
an alarm configured to sound an alarm;
a control unit in operative communication with the pump, the keypad, and the alarm, wherein the control unit is configured to:
receive the dosage level from the keypad;
sound the alarm when the received dosage level is greater than a maximum dosage level;
override the maximum dosage level to deliver the received dosage level; and
control the pump to deliver the received dosage level.

2. The device according to claim 1 , wherein the control unit is configured to determine if a medical provider has sufficient authority to override the maximum dosage prior to the control unit allowing the medical provider to override the maximum dosage level to deliver the received dosage level.

3. The device according to claim 1 , wherein the keypad is configured to receive information regarding a desired drug delivery cycle for a given patient, wherein the information is enterable into the system and a drug is prepared and delivered according to the desired drug delivery cycle.

4. The device according to claim 1 , wherein the control unit stores a safety framework.

5. The device according to claim 4 , wherein the control unit is configured to sound the alarm if a drug delivery cycle entered into the keypad does not fall within the safety framework.

6. The device according to claim 1 , wherein the control unit is configured to download safe dosage levels including the maximum dosage level via a network.

7. The device according to claim 1 , wherein the control unit is configured to download patient information.

8. The device according to claim 7 , wherein the patient information includes at least one drug allergy.

9. The device according to claim 1 , wherein the keypad is configured to receive information regarding a desired drug delivery cycle, and wherein:
the information regarding the desired drug delivery cycle is enterable into the device, and
the control unit is configured to deliver a drug according the desired drug delivery cycle.

10. The device according to claim 1 , wherein the control unit is configured to operatively receive a patient's identification code.

11. The device according to claim 1 , wherein the control unit is further configured to sound the alarm when at least one of a patient's drug allergy and a patient's low weight, as indicated by downloaded patient information, is determined to create an unsafe condition.

12. The system according to claim 11 , wherein the unsafe condition is based on at least one of a drug to be delivered and a drug delivery cycle.

13. The device according to claim 1 , wherein the control unit is configured to receive a list of dangerous drug interactions provided by a network.

14. The device according to claim 13 , wherein the list of dangerous drugs is configured to be updatable by a pharmacy.

15. The device according to claim 13 , wherein the control unit is configured to sound the alarm when an entered drug delivery corresponds to a dangerous drug interaction as indicated by the list of dangerous drug interactions.

16. The device according to claim 13 , wherein the control unit is further configured to sound an alarm in response to a proposed drug delivery which the list of dangerous drug interactions indicates will cause a dangerous interaction if delivered.

17. The device according to claim 1 , wherein the control unit is configured to record all drugs provided to the patient within a network.

18. The device according to claim 1 , wherein the maximum dosage level is configured to be updateable by a pharmacy.

19. The device according to claim 1 , wherein the control unit is configured to receive a safety framework from a network.

20. The device according to claim 19 , wherein the control unit is configured to sound the alarm if a drug delivery cycle programmed into the control unit does not fall within the safety framework.

21. The device according to claim 1 , wherein the control unit is configured to store information regarding a drug delivery to the patient and a time frame corresponding to the drug delivery.

22. The device according to claim 21 , the control unit is configured to communicate the stored information with a network.

23. The device according to claim 22 , wherein the network is configured to provide the stored information for later review by a medical provider and to communicate billing information regarding the stored information.

24. The device according to claim 23 , wherein the billing information is configured for communication to the patient.

25. The device according to claim 23 , wherein the billing information is configured for communication to an insurance company.

26. A medical fluid delivery device configured to deliver fluid into a patient, comprising:
a user interface configured to receive a dosage level;
an alarm configured to sound an alarm; and
a control unit configured to compare the dosage level received from the user interface and sound the alarm when the dosage level is above a predetermined threshold,
wherein:
the user interface is configured to receive an override, and
the control unit is configured to override the predetermined threshold if the override meets a predetermined criterion.

27. The device according to claim 26 , wherein the predetermined criterion is sufficient authority.

Assignees

• Deka Products Lp

Inventors

• Kamen Dean

Classifications

• A61M2205/8206

  battery-operated · CPC title

• A61M39/24

  Check- or non-return valves · CPC title

• A61M2005/1402

  Priming · CPC title

• F16K5/0414

  Plug channel at 90 degrees to the inlet · CPC title

• A61M2205/35

  Communication · CPC title