Patient controlled analgesia device for use with ultrashort acting opioid medication and method for using the same

• US 6,010,483 A
• Filed: 12/19/1997
• Issued: 01/04/2000
• Est. Priority Date: 12/23/1996
• Status: Expired due to Fees

• Current Assignee: Robert F. Spencer
• Original Assignee: Robert F. Spencer
• Inventors: Spencer, Robert F.
• Primary Examiner(s): Smith, Jeffrey A.
• Application Number:
  US08/995,140
• Time in Patent Office: 746 Days
• Field of Search: 604/131, 604/151, 128/DIG. 13, 128/DIG. 12
• US Class Current: 604/151
• CPC Class Codes: A61M 2005/1405 Patient controlled analgesia [PCA]
• CPC Class Codes: A61M 2005/14208 with a programmable infusion control system, characterised by the infusion program
• CPC Class Codes: A61M 5/172 electrical or electronic A61M5/16804, A61M5/16831 take precedence
• CPC Class Codes: A61P 29/00 Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
• CPC Class Codes: G16H 20/17 delivered via infusion or injection

Abstract

A pump or method supplying patient controlled analgesia to a patient. The infusion flow rate of the analgesic is increased in response to a command given by the patient receiving the analgesic, and a lock out interval is provided during which time the actuation of the pump by the patient produces no further incremental increase in the flow rate of the analgesic.

Claims

1. A pump for supplying patient controlled analgesia, said pump comprising means for increasing the infusion flow rate of the analgesic in response to a single command given by the patient receiving the analgesia, and means for providing a lock-out interval during which time actuation of the pump by the patient produces no further incremental increases in the flow rate of the analgesic.

2. A pump as defined in claim 1, further comprising means for setting the infusion rate to a maximum.

3. A pump as defined in claim 1, further comprising means for allowing the patient to decrease the base infusion rate if early symptoms of opioid toxicity occur.

4. A pump as defined in claim 1, further comprising feedback means regarding sedation or respiratory depression that may indicate profound opioid overdose and for triggering discontinuation of the infusion until the patient again commands an increase in the infusion rate.

5. A pump as defined in claim 1, further comprising audible alarm means for arousing the patient in the event of an overdose causing sedation or respiratory depression.

6. A method for supplying analgesia to a patient, comprising the step of increasing the infusion flow rate of the analgesic in response to a single command given by the patient receiving the analgesia, and providing a lock-out interval during which time any further command by the patient produces no further incremental increase in the flow rate of the analgesic.

7. A method as defined in claim 6, wherein the infusion flow rate of the analgesic is increased for a predetermined period of time and is the reduced.

8. A pump for supplying patient controlled analgesia, said pump comprising means for increasing the infusion flow rate of the analgesic in response to a command given by the patient receiving the analgesia;

means for providing a lock-out interval during which time actuation of the pump by the patient produces no further incremental increase in the flow rate of the analgesic; and

means for allowing the patient to decrease the base infusion rate if early symptoms of opioid toxicity occur.