Re: Health Staff And Relatives Underestimate Chronic Pain Experienced By SNF Residen
something happened last weekend at work that has been on my mind all week...
pt admitted on friday to SNF. had been in/out of hospital since respiratory failure,ARDS,sepsis in july. still getting over all complications involved. came to us for therapy to strengthen her before she goes back home.
pt also has chronic back pain and had been on MS contin for years. one week before the last hospitalization, she was stepped down to percocet 10/325mg with pain specialist. (she had requested to step down).
one day after the med change, she ended up back in hospital. all last week at the hospital, she received the percocet for pain and was well controled with it. she and husband both were happy with the pain control of the new med.
on discharge to my facility, the hospitalist at the hospital that had followed her case checked the box to not continue the percocet at the SNF.
fast forward to saturday morning.....
she's in a lot of pain. she didnt sleep the night before from the pain. all we had to give her was tylenol.
so i call the doc on call and ask for something. he says to continue the percocet and how he cant believe the doc didnt order it on discharge.
i tell him thanks and say "dont forget to fax me a prescription so i can get the med from the pharmacy".
he says "i dont have time for that. just give her tramadol then".
the tramadol was not effective. the night shift nurse reported to me that she had slept very little and said the pain was not gone even after 2 doses of the tramadol WITH tylenol.
the on call doc on sunday wouldnt fax me a prescription either telling me "have the doc do it on rounds tomorrow". i tell him i dont have a doc in facility until tuesday. he tells me "well they can do it then".
all this because of the new DEA rules about having to have hard copies for narcotics. ok...i understand why this is needed in the home setting. but LTC is getting jumbled in to the "home" category because techincally it is the patient's "home".
this is so wrong. now the DEA is dictation who gets meds. so now we have the insurance companies telling docs how they should treat patients and the DEA telling the docs what meds they can have.
i'm just sick about it. i've thought about it all week. i've decided that not one of my patients EVER AGAIN is going to be without pain control. if i have to, i will drive to the hospital to pick up the prescription myself!
i cant live with myself over it. and never again am i going to look a patient in the eye and tell them i cant help them because of the DEA.
i've also decided that i'm going to write a letter to the DEA about it. they probably wont even read it but i'm going to send it anyway. i might even send it weekly.
this has to be changed!
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