Role is to support patient & provider with chronic pain management. To provide education, assist pain, allow patient to express or reiterate experiences, offer feedback and be advocate for patient.
|
They [patients] have our teams to turn to; they get to know they have the support they need.
|
Futile feeling when there is not any options
|
You can only do so much hearing them telling you how much pain their in; you feel helpless
|
Most of the patients come to PCC as walk in and time is limited.
|
We are constantly made aware of Patients chronic pain by telephone, and walk-in to their provider
|
Constant request for increase in dose/quality of pain meds
|
I see a growing trend how some patients come repeatedly as they know pain = medication.
|
Feeling skeptical of whether pt. is “really in pain” or misusing (selling/giving to others)
|
There seems to be a real problem with drug dependence & misuse. We know there are some who genuinely need the med, but some are just taking too many
|
[patients] can be verbally abusive and staff does not always have recourse for this
|
Patients become very angry-They will call patient advocate to complain
|
After issues have been resolved, there is a sense of accomplishment. Reinforcement of my belief that frequent patient contact improves their outcome.
|
Positive to see improvement when the patient can adjust to and live with chronic pain without always having narcotics
|