I hate pain scales, they're patronising and the person asking the question never explains what 0-10 stages actually mean. They don't have a chart that the patient can read and think about and discuss together with the clinician.
A friend of mine who has chronic pain shared
this great pain scale that explains what each level might mean. When I saw pain management in 2019 for my crappy dislocating shoulder which is surgically fucked, I printed that scale out and took it with me to my assessment appointment. The otherwise pretty decent pain physio (who did a better shoulder assessment than her shoulder physio colleagues) refused to read or discuss my printed pain scale, or define her pain scales. I argued that without us having a common metric the question was meaningless and annoying but absolutely no willingness to calibrate a scale. So I answered based on that one and left the print out in the room and asked her to put it in my notes with my summary history notes.
Another issue with pain scales is that I always feel like unless I say 8 or higher that I am not going to be taken seriously by medics. There's almost a badassery attitude (and I even see it in this thread) where people brag (possibly not even intentionally) about the pain they've survived/ignored etc and that having a higher pain threshold is treated like some moral goodness that a person has a choice about.
There also isn't enough conversation or reassurance from clinicians that it's OK to raise lower levels of pain and have those taken seriously especially when that pain is frequent or constant. As it was, my pain clinic did take baseline of 4-5 rising to 6-7 at its worst pretty seriously. Unfortunately pain management's medication, nerve block and denervation options didn't work so pain management clinic didn't do me much use except a few medical letters I might throw at the DWP one day.
The gabapentin discussion is interesting. My pain management service gave me a note to ask GP to try gabapentin and didn't tell me they were discharging me - I found out from the clinic letter... I am even less impressed that they're fobbing people off to GPs for gabapentin after the thread here!
Gabapentin gave me hideous migraines like neurology's attempt to treat my migraines with anti-epileptics. I also get hideous migraines off paracetamol, Cox2 inhibitors, mefenamic acid and flurbiprofen. Cannabis is also one of my major lifelong migraine triggers, hate the stuff, can't smell it distinct from cigs which I also loathe until it's made me ill, evil stuff.
I wish a patient could know in advance which pain clinics are good and which are either not good enough like mine was or evil shitty "everything is psychological and using any meds mean you're an addict and we'll treat you punitively like an addict" like a friend had once. There seems to be such variation.