Reducing pred: dead slow and nearly stop method
Posted , 122 users are following.
Copied from Eileen's post in another discussion.
A group of us worked out reduction schemes individually that have allowed us to reduce far further than ever before but they are all basically the same - and they were based on a scheme a Swedish gentleman worked out when he simply couldn't get below 3mg without pain. Img at that level is 33%, 1/2mg is 17% - way above the 10% that has been recommended for years. So he used table to see the daily doses and took the new dose on one day, old dose for a few days and then proceeded by repeating that and then reducing the number of days of old dose - until he got to everyday new dose. It worked, he got off pred and has been off pred for at least 3 years (it could be longer). Something similar to mine is being tried by a consultant rheumatologist in the north of England and he too finds it works for every single patient he has given it to. As it did for several ladies beforehand.
My reductions are VERY slow. I use the following pattern to reduce each 1mg:
1 day new dose, 6 days old dose
1 day new dose, 5 days old dose
1 day new dose, 4 days old dose
1 day new dose, 3 days old dose
1 day new dose, 2 days old dose
1 day new dose, 1 day old dose
1 day old dose, 2 days new dose
1 day old dose, 3 days new dose
1 day old dose, 4 days new dose
1 day old dose, 5 days new dose
1 day old dose, 6 days new dose
By that stage if I feel OK I feel safe to go all new dose. I suppose you might be OK starting and stopping at "1 day new, 4 days old" but I was terribly sensitive to steroid withdrawal pain so I err on the safe side. Once you get to the "everyday new dose" - if you feel OK you can start on the next reduction, no real need to spend a month at the new dose.
This avoids steroid withdrawal pain - which is so similar to PMR pain that you often can't tell which is which and some of us suspect that many flares are NOT the PMR returning but problems with steroid withdrawal. Using a scheme like this also means you can stop immediately if you have any problems - you might be fine at one day old dose, 2 days new (lower) dose but not at a 3 day gap - but you have dropped your dose a lot and that is the idea. It also isn't as slow as you would think - you can reduce at a rate of about 1mg/month on a continual basis.
The Bristol group start new patients with PMR with 6 weeks 15mg, 6 weeks at 12.5mg and then a year at 10mg before continuing the reduction and that achieves a far lower rate of flare (20% instead of 60%) and I suspect their flares then come below 10mg as they then do the 1mg at a time reduction. Just below 10mg is a common dose for people to get stuck at - and I (and others) believe it is because even 10% drops are too much for many patients. These patients are then labelled as "steroid resistant" or told they need methotrexate to help them reduce but we have seen this slow reduction work for those patients too. We believe that methotrexate (MTX) works for patients who have late onset rheumatoid arthritis (LORA) or LORA and PMR together. Very few patients get off pred altogether when taking the MTX - those who do are probably the mis-diagnosed LORA patients - or another arthritis that responds to MTX."
Further comment from Eileen in original discussion:
Can I add a codicil to the very slow reduction plan in the above post:
When you are at doses below 5mg it is a good idea to rest at each new dose for a month at least before trying the next reduction. At this point you risk overshooting the dose that is controlling the inflammation so waiting a short time to see if symptoms reappear is helpful. If you just continue there is a possibility that you get to very slightly below the "right dose" and inflammation will start to reappear very slowly. The blood tests will lag even further behind the dose reduction - there must be enough inflammation to increases the proteins being measured for the blood tests to rise.
Someone has asked this question:
"I'm at 7mg going down to 6mg, and I'm at the point where I'm starting to shift from more 6mg than 7mg, but I can tell the pain is returning. So...do I jump up big to say 10mg, or try 7mg or 8mg? I hate the very idea of going up at all, but it is what it is."
My reply was:
No - you go back to the last dose that worked well immediately and stop the reduction. This isn't a "flare", this is your body telling you that you have got to the dose you are looking for: the LOWEST DOSE THAT MANAGES THE SYMPTOMS. It doesn't mean you won't get lower, it just means not yet. However slowly you reduce, whatever scheme you use, you will not get below that dose without a return of symptoms because of left-over inflammation that hasn't been removed by the amount of pred you took. It is if you ignore these warnings that you will allow a build-up of the inflammation to the stage where you will have a flare on your hands.
To comment on something someone else said - you have differentiated between steroid withdrawal and a return of symptoms by using DSNS. If you were going to suffer with steroid withdrawal you will notice it the first day you use the new lower dose. That is the idea of DSNS - you go back to the dose your body is happy at for a few days and then show the new dose to your body again. For me it usually takes about 3 times for my body to accept the new lower dose and stop complaining.
37 likes, 145 replies
gbeez Emis_Moderator
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Mousemum Emis_Moderator
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Ive been on prednisolone for 4 years now Im down to 5mg but struggling to get lower. Am I right in thinking the theory is to do the slow method to 41/2 mg then stay on this a month and then start again if ok. Could do with some advice.
BettyE Mousemum
Posted
When you say you are struggling does that mean you are in pain? If so, has that been just recently? Did it follow your latest reduction?
You are down to a low dose and a stage that has given many of us trouble. I stayed there for three months as directed by GP and only tried to get lower if I was completely comfortable.
Also it is often recommended that you do not reduce by more than 10% so that means cutting your pills ( as long as they are not the coated ones ). Alternatively you can reduce in tiny steps by perhaps reducing to the next level on alternate days or spacing the reductions even less frequently.... as one day a week then the lower dose twice a week and so on.
You may not find this necessary but what is essential is not to reduce while in pain because you'll only find yourself back on a higher dose.
It took me five years but I did get there and have been symptom free for more than three years. Good luck!
elizabeth40672 Emis_Moderator
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judy68207 elizabeth40672
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February 2017 I will take 9MG, March 2017 I will take 8MG. Doc prescribes 5MG pills and 1MG pills. So February I take one 5MG and four 2MG tablets daily. So far no flares. I am just waiting for the other shoe to drop though.
RD212 Emis_Moderator
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Oregonjohn-UK RD212
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You would be extremely lucky if you are off within a year? Ten months from 15 mg to zero is very fast! I'm male and started, as a very active 74 year old some 2.5 years ago, at 30 mg and have only just reached zero. I'm considered a fortunate one.
daniel08939 Emis_Moderator
Posted
PMR Key Dates
07/9/11 – Severe pain in hamstrings, shoulders and hips
11/8/11 - Diagnosed with PMR - Prednisone
01/29/11 - After 3 weeks on 7.5 MG pain started returning
03/01/11 - Went to 10 MG
05/20/11 - Went to 9 MG
06.20.11 - Went to 8 MG
07/10/11 - Went to 7 MG
08/04/11 - Went to 6 MG
09/24/11 - Went to 5 MG
10/24/11 - Went to 4 MG
01/24/12 - Went to 3 MG
3/18/12 - Went to 2.5 MG
9/12/12 - Went to 2.0 MG
2/26/13 - Went to 1.5 MG
3/23/13 - Went to 1.0 MG
5/2/13 - Went to .5 MG
5/18/13- Went to Zero
I was free of PMR symptons until 11/2016. It has returned as bad as it was in 2010.
I am back on Presdnisone
iellen32 Emis_Moderator
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Nurse_Nana Emis_Moderator
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Jan20533 Emis_Moderator
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Really useful reading Eileen. Many thanks, I'll take your advice and suggest/discuss with my doctor. It's clear that there are many experienced PMR patients out there who know and understand more than the doctors.
paula21528 Emis_Moderator
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elizabeth40672 Emis_Moderator
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iellen32 Emis_Moderator
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I have experienced exactly what you say.
What looks like a flare up it is not,
Thank you Emis Moderator for the advice!
iellen
Guest Emis_Moderator
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BettyE Guest
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If you were comfortable on 3mgs. I think I'd stay there or even, if necessary, increase up to 5 to have decent quality of life. Lots of us have found 5 a bit of a sticking point and several are happy to stay there for life if necessary.. Ten years may feel like a life sentence especially if, like me, you are not keen on drugs but so is the pain of PMR a life sentence, isn't it?
Perhaps your GP may have his/her reasons for wanting you to continue reducing but you are already on a low dose so they'd have to be convincing.
You'll get plenty more input from others, I'm sure.
Please let us know how you get on and best of luck.
Guest BettyE
Posted
Thank you for your reply. I am fortunate I have a sympathetic GP who has already said I may need to remain on a low dose of steride. The main concern comes from the female doctors concerned about osteoperosis and kidney damage. However I am now taking the Adcal tbs which should be beneficial to the bones. Appart from the stiffness I feel OK and at 77yrs that cant be bad.
BettyE Guest
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I've only just read your reply, must have slipped throught the net.
Glad you're happy with your GP as I was with mine. They do worry about the bone thinning with age and steroids, I know. I was not able to take the bisphosphonate Alendronic Acid and just had calceos but when I had a total hip replacement four years ago aged 81 the surgeon said that I had "amazing bone density for my age" so obviously bone problems are not inevitable.
Also, I have a cyst on one kidney which is monitored twice a year. This is of at least four years standing and all normal so far. Hope that is encouraging and that all goes well for you.
Guest BettyE
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Good to hear that at 81 your bone density is good. I am alternating 3mg and 4mg Predisone daily. I still have stiffness in upper arm and back of my legs first thing in the morning, but carry on regardless and it usually eases up by late morning. Best regards David