IP Library Granted Patent US 7,008,413
Granted Patent B2
US 7,008,413 · App. 10/459,672 · Granted Mar 7, 2006

Generic multi-step therapeutic treatment protocol

Assignee: Medtronic, Inc.
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Quick Facts
Patent No.
US 7,008,413
App. No.
10/459,672
Granted
Mar 7, 2006
Kind
B2
Abstract

A generic treatment protocol is disclosed for therapeutically treating a patient via an implantable treatment device. Treatment steps can be defined to start and end at absolute times, or can be programmed via telemetry to start a certain amount of time after termination of a previously executed treatment step. Treatment steps have a treatment rate or dose attribute and a duration attribute. Treatment steps may optionally enable patient-activated bolus overlays. Patient-activated rate or dosage adjustments can also optionally be enabled. Repeated-execution treatment-step groups are also provided. Such treatment-step groups can have start and end times, a group duration, and a group total dose, each defined in a manner similar to that for a treatment step. Treatment-step groups include a repetition count, which could be set to a value that causes the group to repeat forever. Single execution treatment steps can, accordingly, be programmed to execute before and/or after a repeated-execution treatment-step group.

Claims (40)

1. A computer-readable medium containing computer-executable instructions that cause a human-implantable therapeutic treatment device to perform a specific therapeutic treatment protocol by performing steps comprising:

performing at least one treatment step that is defined, at least in part, by generic treatment parameters including a treatment rate or dose and a treatment duration, which have been downlinked to the treatment device;

performing at least one treatment-step group a number of times that is specified by a treatment-step-group repetition count that has been downlinked to the treatment device; and

administering at least one activated bolus in accordance with downlinked generic treatment parameters including:

a start delay or start time,

a treatment rate or dose, and

a treatment duration.

2. The computer-readable medium of claim 1 , wherein the at least one treatment step starts executing after a programmed delay relative to when the generic treatment protocol parameters are downlinked to the implantable device.

3. The computer-readable medium of claim 1 , wherein the at least one treatment step is programmed to start executing after a predetermined amount of time elapses following completion of a preceding treatment step.

4. The computer-readable medium of claim 1 , wherein the at least one treatment step starts executing at a programmed absolute start time.

5. The computer-readable medium of claim 1 , comprising further computer-executable instructions for performing a patient-activated bolus while performing the at least one treatment step.

6. The computer-readable medium of claim 5 , comprising further computer-executable instructions for disallowing an attempted patient-activated rate adjustment that would exceed a programmed maximum rate adjustment for the at least one treatment step.

7. The computer-readable medium of claim 1 , wherein the at least one treatment-step group starts and ends in accordance with an absolute start time and an absolute end time, respectively.

8. The computer-readable medium of claim 1 , wherein the at least one treatment-step group starts in accordance with a programmed delay relative to completion of an earlier executed treatment step.

9. The computer-readable medium of claim 1 , wherein the at least one treatment step group includes providing treatment at a background rate when no treatment step is actively providing treatment.

10. The computer-readable medium of claim 1 , wherein a maximum amount of treatment administered by the at least one treatment-step group is limited by a programmed maximum dosage.

11. The computer-readable medium of claim 1 , wherein the treatment-step-group repetition count specifies that the at least one treatment-step group should repeat forever.

12. The computer-readable medium of claim 1 , wherein the bolus includes a programmed priority that specifies that the bolus has a priority selected from the group consisting of:

a low-priority patient-activated bolus that takes precedence over treatment steps that specifically allow themselves to be overlaid by low-priority boluses, and

a high-priority physician-activated bolus that takes precedence over treatment steps.

13. A system for causing a human-implantable therapeutic treatment device to perform a specific therapeutic treatment protocol, the system comprising:

means for performing at least one treatment step that is defined, at least in part, by generic treatment parameters including a treatment rate or dose and a treatment duration, which have been downlinked to the treatment device;

means for performing at least one treatment-step group a number of times that is specified by a treatment-step-group repetition count that has been downlinked to the treatment device; and

means for administering at least one activated bolus in accordance with downlinked generic treatment parameters including:

a start delay or start time,

a treatment rate or dose, and

a treatment duration.

14. The system of claim 13 , wherein the at least one treatment step starts executing after a programmed delay relative to when the generic treatment protocol parameters are downlinked to the implantable device.

15. The system of claim 13 , wherein the at least one treatment step is programmed to start executing after a predetermined amount of time elapses following completion of a preceding treatment step.

16. The system of claim 13 , wherein the at least one treatment step starts executing at a programmed absolute start time.

17. The system of claim 13 , further comprising: means for performing a patient-activated bolus while performing the at least one treatment step.

18. The system of claim 13 , further comprising: disallowing an attempted patient-activated rate adjustment that would exceed a programmed maximum rate adjustment for the at least one treatment step.

19. The system of claim 13 , wherein the at least one treatment-step group starts and ends in accordance with an absolute start time and an absolute end time, respectively.

20. The system of claim 13 , wherein the at least one treatment-step group starts in accordance with a programmed delay relative to completion of an earlier executed treatment step.

21. The system of claim 13 , wherein the at least one treatment step group includes means for providing treatment at a background treatment while no treatment step is actively providing treatment.

22. The system of claim 13 , wherein a maximum amount of treatment administered by the at least one treatment-step group is limited by a programmed maximum dosage.

23. The system of claim 13 , wherein the treatment-step-group repetition count specifies that the at least one treatment-step group should repeat forever.

24. The system of claim 13 , wherein the bolus includes a programmed priority that specifies that the bolus has a priority selected from the group consisting of:

a low-priority patient-activated bolus that takes precedence over treatment steps that specifically allow themselves to be overlaid by low-priority boluses, and

a high-priority physician-activated bolus that takes precedence over treatment steps.

Continuity (2)
Division 0930261300 · Apr 30, 1999
Related Publication 20030199854A1 · Oct 23, 2003