To rant and rant about doctors and Butrans patches (long)(44 Posts)
I have something wrong with my hands. The doctors don't know what (had since mid teens) in that I have little to no grip or strength and pain. It's like a cross between having hands in freezing iced water and the worst writer's cramp ever.
Not lupus, not rheumatoid, raised inflammatory markers sometimes but not at othertimes. Doctors flummoxed, advised to lose weight (4 stone down now and still going) but basically decided to treat with pain relief and stop
draining my blood continually to see if it has changed at all testing.
You name it, I've taken it. Ibuprofen, aspirin, paracetamol, co-codamol, codeine, naproxen, diclofenac, celecoxib (none of them effective even in combination), amitriptyline (worked perfectly, made me obsessed with suicide down to planning methods), gabapentin (made me cry at everything and ineffective), pregablin (made me angry at everything and ineffective) and then, finally, Butrans patches. Which were perfect with no side effects.
BUT my stupid skin now blisters and is covered in open sores where the patch was so doctor wants me to come off immediately and has referred me to the pain clinic. Waiting time for which is 5 - 6 weeks. And can't give me any other pain relief to keep me going until I go and won't let me carry on with patches (run out).
Last time I came off medication cold turkey (pregablin), I was in full drug withdrawal (sickness, cold, shivering, sleeplessness) and am worried about that. Also very worried about doing 6 weeks with no pain relief during cold winter months when hands are bad!!! At worst, I couldn't hold a make up brush, open bottles or jars, peel potatoes, carry things etc. Even with meds, can't handwrite and drop things but have an almost life...
AIBU to have a hissy fit and say that I cannot cope with NOTHING?!
holidays we move the patch every time it is applied so it is in different locations (upper arms, shoulders, upper back, ridge of shoulders etc) and every location at the end of the week has the same redness and sores. It also itches like crazy during the week!
thenames, I think this will probably happen! I can't see them tomorrow as v. full day at uni which will give me a weekend to see how it goes. Then, Monday / Tuesday / Wednesday (quiet days), I can go and have a chat.
SoonToBeSix I don't suffer with chronic pain, but lack of personal experience of symptoms doesn't negate my knowledge of the system and what is available. I have been a doctor for 22 years, have worked in A&E, and have been a GP for many years.
I truly sympathise OP, and I would advise you to try and speak to your GP tomorrow. It is unreasonable to expect you to go several weeks without sufficient pain relief.
Sounds like a nightmare op, I agree that you must insist to be seen, you cannot possibly go that long with no pain relief
I use butrans patches and I've come off them twice cold turkey with no side effects, so fingers crossed it doesn't affect you too badly
Have you tried oramorph? I use it as well as my butrans patches and tramadol and it does take the edge off
Sounds like the undertongue wud be good then if the dosage can be sorted.
Aside from this, I would be pushing to see why this is occuring. A nerve conduction test, referral to neuro if appropriate etc could all be ideas.
Those are industrial strength meds u are on, without much in the line of investigations.
Please, please keep going back to your surgery. See a different GP, get a referral for x-rays and an MRI. Get something short term for six weeks. You cannot continue to suffer. I have chronic pain and it's taken me six months of being fobbed off with painkillers to finally get a referra as of this morning.
I don't normally post in AIBU but have you tried asking for oxycodone slow release tablets in combination with oxycodone liquid for breakthrough pain? I don't have your exact same symptoms but I suffer with an uncommon nerve disease called CRPS (complex regional pain syndrome) which affects my nerves, muscles and bones and I am prescribed the oxycodone tablet/liquid combination along with the highest dose of pregabalin available for prescription. Please push to be seen by a specialist at a pain management clinic asap, as there are a lot of tests and services they can offer you, to try and not only find out what's wrong but also how to manage it so that you have the best quality of life possible. They have a great deal of experience, even with as yet diagnosed conditions and those, like mine, which are uncommon/rare. If you want to ask anything about what to expect from a pain clinic, please feel free to PM me and I will try to answer any questions you have. I hope you aren't waiting too long and can find some relief in the mean time
Need scanning to check nerve roots emerging from cervical spine, sounds like anatomical compression
I would try some alternative therapy, acupuncture comes to mind or naturopathy. My daughter has been cured by acupuncture for a condition that allopathic medicine has no cure for and I have one friend who was cured of lupus and another was cured of arthritis by naturopathy.
You are so not being unreasonable. The doctor is being cruel - to take someone off a strong painkiller like that and give no replacements at all. Is it possible to see another doctor to ask for something else?
I see you mention codeine - you can get co-dydramol over the counter and is stronger than codeine alone. I also found it didn't cause so many stomach issues.
In terms of coming off the patches cold turkey (which I've done a couple of times by forgetting the change the patch for sometime due to memory issues) I found a marked increase in pain - which obviously makes sense. I found myself quite emotionally unsteady and tearful. Everyone is different though. I've stopped many strong medications cold turkey without an issue.
Please don't let your doctor shrug their shoulders and say you have to cope with the pain for some weeks. You wouldn't be on Butrans in the first place if your pain was minor.
Hi, this is a common reaction to the Butrans patches. It's a reaction to the drug, rather than the patch or adhesive unfortunately. It should clear up with some hydrocortisone cream.
If you can put up with it, it's OK to continue the patches - some people find that putting some hydrocortisone on the area first prevents the reaction being quite so bad but some people just can't manage them at all.
I'd suggest co-codamol regularly would be a good stop gap until you get to pain clinic as you clearly need specialist advice.
I am a doctor and happy to confirm my GMC number in a private message if you want.
I'd ask them to assess you for Thoracic Outlet Syndrome - its where the nerve and blood vessels going into the arms are compressed by the first rib. Causes pain, weakness, blood flow issues
Thanks everyone, particularly Kundry! I did say to the GP I'd rather continue with the patches and just put up with the side effects but I got told no way =(.
It's really helpful to have some ideas of things to suggest to the doctor next time - tonight is patch removal time so we shall see! If I have a bad weekend, I'll be at the doctors Monday morning (can't get there today but hey ho)
I might even print off some of the messages so I can ask about some of the medications / causes etc.
It's good to not feel alone - I've even started doing that whole "maybe my pain is really minor and I'm just over thinking this and that's why they won't give me anything", which isn't true. One of the rheumatologists I saw actually said that it was "my fault" and that I had caused this by being overweight. I'm a student lawyer and he told me that "nobody wants a fat lawyer" and that if my hands still hurt when I'd lost weight, he'd eat his hat as it was totally self inflicted. Oh, and to "let the thin girl out, the fat girl has had far too much time being in charge" and that I needed to buy orlistat "because then I could but myself some motivation". Four stone down, they still bother me so I've said I'm not prepared to see him again (he made me cry for an hour following my consultation). Hopefully the pain clinic will be more helpful!
Wow what a terribly unkind thing to say to someone , that rheumatologists needs redo his bed side manner course . Given that you havent been given a diagnosis , how can he be so sure your weight is the cause ? Muppet !
How the heck can being overweight cause pain in the hands?
That was my argument - I have no issues with hips / knees / ankles etc and it's just my hands / wrists / elbows (although we think that may be due to overcompensating).
The active ingredient in Butrans - buprenorphine - is available in sublingual tablet form too. I think (but am not certain) that it is usually only used for opiate addiction treatment in the tablet form. No idea whether it could be prescribed for you if the substance works fine but the administration method (patches) doesn't? May be worth asking your GP or the pain clinic about.
I imagine if you have been on the patches for a while, you will go into withdrawal after a few days. I think that's really shitty just leaving you to deal with that for six weeks, without the added pain that you will be suffering due to your condition. I would complain very loudly.
Just to say do ask for fentanyl instead. I also had skin irritation with butrans (and likewise had been through all the meds on your list with similar symptoms!).
Fentanyl is much better I find (although one of the brands gave increased irritation, so the pharmacist now has a specific brand noted for me). The patches I use are changed every three days, so much more scope for varying the bit of skin to use!
Try to contact the pain clinic directly and ask for an urgent appointment there. See if you can get a call back from your consultant, they might do a prescription for fentanyl with a phone consultation if they know you.
I came off butrans cold turkey, and it wasn't too bad, but I always have top-up codeine, and dihydracodeine around. Hope you get seen soon, but get on the phone to the pain clinic appointments secretary this afternoon.
24 hrs off patch and joy of joys, withdrawal signs...
Started last night, restless and twitchy, fidgeting, can't get comfy or concentrate (I always have a book in one hand so this is not like me at all), hot and cold, can't sleep - think I got 3 hours in total, and, joy of joys, ridiculously emotional (1 hour crying jag over a pair of Father of the Bride cufflinks).
Luckily, OH is now home and looking after me. First thing Monday at doctors if this doesn't calm down, methinks!!
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