Ive been an attending for a bout 3 years. I have seen obvious CRPS, and had patients referred to you for CRPS were they defintely dont have CRPS. Has anybody had patiens with persistent foot or extremity pain with a questionable etiology but there are some components of CRPS, and the patient is adamant they want neuromodulation, but you are on the fence if its really CRPS? Do you continue to follow the patient and try less invasivce things first that is always what I have done.
I had an experience today were records were extremely limited, but patient had a unknown surgery for some mass in calcaneus (again records limited). She has had persistent pain prior workup not coming up with another obvious diagnosis including EMG, MRI ankle, and L spine. She had seen a prior pain group who diagnosed her with CRPS had tried some gabapentin and lum symp block with no benefit. She was going to move forward with Stim trial however per patient history insurance wouldnt allow this so she in some round about way ended up at my office.
On my initial evaluation she had some aspects of CRPS, she didnt fit budapest criteria. In addition she supposedly had a 2nd opinion with a surgeon who per patient said there maybe a surgery that could help her (again per patien hx records really limited but is there another etiology contributing to patietns symptoms). I expressed apprehension about an SCS trial and possible implant, and started to explain is there another etiology and is there less invasive treatment options and she blew up. I'm an idiot and not helping her as I didnt automatically want to put a SCS in her since that's what the other pain docs wanted to do but per patient hx insurance wouldnt let them.
I have been kind of torn in that I never want a patient to push me into a procedure. Maybe I am more conservative with neuromodulation then others. I feel torn as I dont think SCS wouldt at some point be a reasonable thing but I just really reserve it if I feel I have nothing less invasvie that may help patients (ie patient hadn't evn done CRPS related PT, etc,etc. In any event patient thinks I am an idiot and is going to get another opinion.
I had an experience today were records were extremely limited, but patient had a unknown surgery for some mass in calcaneus (again records limited). She has had persistent pain prior workup not coming up with another obvious diagnosis including EMG, MRI ankle, and L spine. She had seen a prior pain group who diagnosed her with CRPS had tried some gabapentin and lum symp block with no benefit. She was going to move forward with Stim trial however per patient history insurance wouldnt allow this so she in some round about way ended up at my office.
On my initial evaluation she had some aspects of CRPS, she didnt fit budapest criteria. In addition she supposedly had a 2nd opinion with a surgeon who per patient said there maybe a surgery that could help her (again per patien hx records really limited but is there another etiology contributing to patietns symptoms). I expressed apprehension about an SCS trial and possible implant, and started to explain is there another etiology and is there less invasive treatment options and she blew up. I'm an idiot and not helping her as I didnt automatically want to put a SCS in her since that's what the other pain docs wanted to do but per patient hx insurance wouldnt let them.
I have been kind of torn in that I never want a patient to push me into a procedure. Maybe I am more conservative with neuromodulation then others. I feel torn as I dont think SCS wouldt at some point be a reasonable thing but I just really reserve it if I feel I have nothing less invasvie that may help patients (ie patient hadn't evn done CRPS related PT, etc,etc. In any event patient thinks I am an idiot and is going to get another opinion.
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