I'm at an EPIC based hospital, and have encountered a couple of safety events relating to patients admitted with an implanted intrathecal pain pump that is managed in the outpatient setting.
- Do you have a policy for implanted pumps (can you share)?
- How does your facility document the implanted pump? Are drug specific orders placed and is it charted upon in the MAR?
- What's your process to adjust the infusion rate or turn off the pump if an adverse drug event occurs?
- What requirements do you have for notifying the outpatient prescriber of the pain pump?
Thanks,
Brian