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Has anyone had their shoulder replaced and/or resurfaced or an elbow replacement? If so, I'd like to hear from you. It seems shoulders aren't as long lasting as hips (about 10 years) and I was told by my surgeon yesterday there's a much higher infection risk - 30% as opposed to 1% for THR's! X-rays revealed I have no cartilege left in my shoulder joints and only a small amount in my elbows. Radial head excision was mentioned last year but now he's seen my x-rays it will have to be full elbow replacements. Crikey, get all that done, plus my hips and neck, I could audition for the tin man at Christmas! Carol
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Blimey Carol, that's a lot of surgery isn't it? Lots to think about for you. I'm going to be watching this thread with interest, as I think my right shoulder is also on the way out. That's such an amazingly higher risk of infectoin isn't it? I wonder what the reason is. All the best, Franky
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Hi Franky, Last year, when talking about radial head excision, the same surgeon told me infection risk was high as there's not a lot of flesh covering an elbow, the metal work is only just underneath the skin, unlike a THR, and the slightest knock could open up the wound etc. I assume the same applies to shoulders? Then there's the lack of blood flow (immune system) over a prosthesis, to help zap any nasties. I emailed NRAS as I couldn't find anything on shoulder replacements and they referred me to an ARC booklet and another website, neither of which say much about infection risk. How long have you had shoulder problems? I've had mine for over 20 years and I have to say the pain was worse than a hip initially, but isn't as bad now which could be because I'm no longer working and not using it as much. I've lost quite a bit of movement, especially in the right, which he pointed out was tendon damage. If the infection risk was minimal and they could guarantee improvement in range of movement, I'd have it all done tomorrow. Carol
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>thunk<
that's the sound of me hitting the floor at notion of pins under skin and everything. as that might tell you, i' a lightweight who's only had a problem for a year. It's actually worse since everything deflamed with successful Humira treatment. ThiS and my R hip, I never paid much attention before, as I was always focused on function of hands and level of fatigue, rather than pain in rest of joints, I just ignored it all. Niow I note it.
So, if they can't guarantee those things, what are you hoping for? I'l m going off to try and find you some more info as well ... xfx
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Hi Carol,
You must be feeling a lot stronger after all the THR problems to be contemplating more surgery! I am glad to hear it, though very sorry your shoulders and elbows are so bad.
My surgeons always say surgery is last resort, but on the other hand its best to operate when there is enough healthy bone to attach replacements to!
I had my shoulders replaced 25 years ago, a very long time and I believe the technique has come a long way since then. Neither op was straightforward due to my osteoporosis, but I still have the right shoulder joint in. The left had to be removed because of bone quality problems but I manage without a joint on that side, muscles compensate if you work hard on physio. I had no infection in either replacement.
My elbows were treated to radial head excision and rearrangement of ulnar nerve (20 years ago) and I was on the waiting list for replacements, but was told the movement would be more limited though pain relieved. I couldnt afford to lose more movement for just remaining independent for feeding, washing etc, so have stayed as I am for now. The elbow ops helped a lot. I have heard of infections with elbow replacements more than shoulders and think you are right, there is little around it to protect the elbow joint from friction. Shoulders are more protected.
I hadn't realised that in a bad flare the replacement joints get very flared too, or mine do anyway.
I realise that my surgery was a long time ago, but though I still have very aggressive RA, I am pleased with the results.
I do wish you luck with your decisions and do ask the surgeons loads of questions if you decide to go ahead. As always, the physio after surgery is crucial.
Take care and keep as well as possible, Lizxx
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Dear Carol,
I am amazed at the percentage factor difference in THR and shoulder!
The radical head excision, is this what they call an elbow replacement? I wanted to ask if one could have their elbows replaced....I can't imagine how it would work, do you know?
Would you say the bone erosion is quite severe due to you having the RA for so long? Do you believe that bones can become eroded without any feeling for a number of years?
Apologies for the litany of questions, I have also had RA nearly 30 years and was wondering!
Love,
Amanda
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annamaria wrote:Hi Carol,
You must be feeling a lot stronger after all the THR problems to be contemplating more surgery! I am glad to hear it, though very sorry your shoulders and elbows are so bad.
My surgeons always say surgery is last resort, but on the other hand its best to operate when there is enough healthy bone to attach replacements to!
I had my shoulders replaced 25 years ago, a very long time and I believe the technique has come a long way since then. Neither op was straightforward due to my osteoporosis, but I still have the right shoulder joint in. The left had to be removed because of bone quality problems but I manage without a joint on that side, muscles compensate if you work hard on physio. I had no infection in either replacement.
My elbows were treated to radial head excision and rearrangement of ulnar nerve (20 years ago) and I was on the waiting list for replacements, but was told the movement would be more limited though pain relieved. I couldnt afford to lose more movement for just remaining independent for feeding, washing etc, so have stayed as I am for now. The elbow ops helped a lot. I have heard of infections with elbow replacements more than shoulders and think you are right, there is little around it to protect the elbow joint from friction. Shoulders are more protected.
I hadn't realised that in a bad flare the replacement joints get very flared too, or mine do anyway.
I realise that my surgery was a long time ago, but though I still have very aggressive RA, I am pleased with the results.
I do wish you luck with your decisions and do ask the surgeons loads of questions if you decide to go ahead. As always, the physio after surgery is crucial.
Take care and keep as well as possible, Lizxx
Hi Liz, I'm having my left hip replaced first, within the next 11 weeks and will allow another year to get over that and build up my leg muscles and walking. I agree, surgery is a last resort and for 10 years I didn't really listen to my shoulder surgeon as I was too scared to think about surgery. However, 12 ops later, you do get used to it and I'm no longer frightened about surgery, just the infection risk. I note you've had RA for approx. the same length of time as me so its interesting to hear what surgery someone else has had. As I mentioned above, my right shoulder started seizing up over 20 years ago and the slightest movement (I was typing all day) was excrutiatingly painful but I had to carry on to do my work. How do you manage with no shoulder joint? Are you able to drive? I've read somewhere that a shoulder surgeon probably only does 10 replacements a year, suggesting the technology is a way behind hips and knees? I don't think I will rush into it just yet. Take care Carol
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amanda_lewin wrote:Dear Carol,
I am amazed at the percentage factor difference in THR and shoulder!
The radical head excision, is this what they call an elbow replacement? I wanted to ask if one could have their elbows replaced....I can't imagine how it would work, do you know?
Would you say the bone erosion is quite severe due to you having the RA for so long? Do you believe that bones can become eroded without any feeling for a number of years?
Apologies for the litany of questions, I have also had RA nearly 30 years and was wondering!
Love,
Amanda Hi Amanda, I too was surprised by the increased infection risk. I used to think infections only occurred in elderly, infirm patients - how wrong I was! I now wonder whether my THR infection was caused by something as simple as an infected ingrown toenail. My feet are looked after by a chiropodist! Radial head excision is where they operate on the radius bone at the elbow end, that's all I know! I remember my surgeon saying something about a "floppy hinge" and I think he was referring to RHE. A full elbow replacement is different, a bigger operation and looks similar to a hip replacement on x-rays. It all depends on what your joints look like on x-ray and which movements cause you pain. I suppose bone erosion is inevitable with RA, especially after 39+ years. The drugs just help to slow it down. I don't think you'd know your bones were eroding until you lose cartilege, have crepitis, lose movement and feel pain. Have you had any replacements or other surgery yet? I went 31 years before my neck was fused, but that was after a RTC, so it's possible I could have gone longer. I wasn't anticipating hip replacements just yet either and was surprised at how quickly they deteriorated, within about 6 months. I had no cartilege left there either and I used to take Glucosamine and Chondroitin. Its good to know elbow and shoulder surgery is available, but I'm not sure the benefits would outweigh the risks. Carol
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Hi Carol you really are going through it at the moment I hope things get better for you I have not had any joints replased so I am sorry I cant help with that take care will be thinking about you Mary L
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Wow Carol thats some surgery ! ive only had my knee replaced and that was enough !! Hope every thing goes well for you Sophie x
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Thanks Mary & Sophie. It's not something I'm going to rush into, not until I'm at least one year post new THR. If I do go ahead, I'd only have one joint done at a time, to limit the infection risk. Carol
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Hi Carol
Firstly, sorry I haven't replied to your pm - but NRAS have, in their infinite wisdom, decided to remove that facility from us!
I hope and pray you are now getting over the horror of the shunt and that everyone who was involved is recovering well. I'm sure you hurt in places you didn't even know you had for a few days afterwards and it can't have done the RA any good at all. Driving is still a problem for me - my right leg is 2" shorter than the left and I struggle!!!
As for your elbow and shoulder - can only give you info second hand. Gwenda has had shoulder replacement which was fine, but she had an elbow replacement last year which (like your THR) had to come out because of acute infection. She's now waiting for it to be put back. Sorry this isn't what you wated to hear, but as you know from experience, it can happen.
Still hoping you will be able to make Leicester - and persuadethat old Red dog to join us!
Love Jxx
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Hello Carol,
I had a total elbow replacement a year ago. As I'm on Humira I had to stop it for 2 weeks before the op and for 2 weeks after. The surgeon gave me massive dose of antibiotics and it went well and infection free.
I am not able to straighten the arm but I couldn't before, I can now twist the arm whereas before I couldn't. So I have gained some, lost some. It apparently can still improve for another year according to the surgeon who I saw last week. He seemed pleased with the xrays which really do look strange.....it's a metal and plastic hinge!!!
Physiotherapists were useless as they had never seen anyone with a new elbow before, so it was just letting the arm do what it would and not forcing it straight.
I suspect that I will have to have the other elbow done at some stage, but will wait until it's a lot worse than at the moment.
Regards Sandy
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jeanb wrote:Hi Carol
Firstly, sorry I haven't replied to your pm - but NRAS have, in their infinite wisdom, decided to remove that facility from us!
I hope and pray you are now getting over the horror of the shunt and that everyone who was involved is recovering well. I'm sure you hurt in places you didn't even know you had for a few days afterwards and it can't have done the RA any good at all. Driving is still a problem for me - my right leg is 2" shorter than the left and I struggle!!!
As for your elbow and shoulder - can only give you info second hand. Gwenda has had shoulder replacement which was fine, but she had an elbow replacement last year which (like your THR) had to come out because of acute infection. She's now waiting for it to be put back. Sorry this isn't what you wated to hear, but as you know from experience, it can happen.
Still hoping you will be able to make Leicester - and persuadethat old Red dog to join us!
Love Jxx Hi Jean, Two weeks today since the RTC and we're all ok thanks, although I'm still experiencing numbness and tingling in my left hand and forearm. I know I should see my GP, but you know what its like, over things take over and I keep putting it off. Poor Gwenda, do you know which infection she had? I hope the revision goes well for her. I'm not going to rush into shoulder and elbow surgery just yet. Carol
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sandy wrote:Hello Carol,
I had a total elbow replacement a year ago. As I'm on Humira I had to stop it for 2 weeks before the op and for 2 weeks after. The surgeon gave me massive dose of antibiotics and it went well and infection free.
I am not able to straighten the arm but I couldn't before, I can now twist the arm whereas before I couldn't. So I have gained some, lost some. It apparently can still improve for another year according to the surgeon who I saw last week. He seemed pleased with the xrays which really do look strange.....it's a metal and plastic hinge!!!
Physiotherapists were useless as they had never seen anyone with a new elbow before, so it was just letting the arm do what it would and not forcing it straight.
I suspect that I will have to have the other elbow done at some stage, but will wait until it's a lot worse than at the moment.
Regards Sandy Hi Sandy, I'm pleased your op went well and was infection free. I too think some physios are useless and tend to focus on one area, when with RA, its usually the whole body that needs it. Do you have a "floppy" hinge? I agree, only have surgery as a last resort, when the pain is too much. Carol
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Hello Carol
I'm not sure whether it's floppy or not! It's the Coonrad/Morrey one. Forgot to say that the new one is mostly without pain, and that is why it was done. Certainly not pretty!
Sandy
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Hi Carol,
I have had both a right shoulder and right elbow replacement (as well as R ankle and L knee). My shoulder was replaced 12 and a half years ago,- 7 and half years after my RA diagnosis (I have aggressive RA), and my elbow was done 8 and a half yrs ago. Although the range of movement I have is very limited, I have no pain at all from the shoulder and just some minor stiffness pain in the elbow- both joints are still doing as well as when they were first put in. I have had no infection problems after any of my ops, however I do not class either of these replacements as successful as my lower limb replacements, in terms of function. Apparently the elbow is considered one of the trickiest joints to operate on and I did have a minor-ish complication with that op as my medial epicondyle (sp?) fractured and chipped off during the op which meant I had to have plastercast on for several weeks after the op and perhaps as a consequence of this I never did regain the ability to straighten my arm. Mind you, it was stuck bent before the surgery anyway. I did not have any choice but to have the ops as the joints were basically destroyed by the time I had surgery and I am glad I did. The replacements will obviously be better now than they were when I had mine..I know the shoulder I have has a long stem (which also may have complicated the elbow surgery) and now they are much smaller and stemless I think. My elbow also has stem which again I think has improved to a stemless version now? I would try to select an NHS surgeon who specialises only in the joint to be operated on...some claim to be experts in several joints but I feel that a surgeon who only does one joint has deeper knowledge and enhanced competence in that surgery.
Hope I haven't waffled on too much about myself...hard to know how much info to give or not. Good luck with your decision...feel free to ask any questions if you feel I can help.
Diane x
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sandy wrote:Hello Carol
It's the Coonrad/Morrey one. Forgot to say that the new one is mostly without pain, and that is why it was done. Certainly not pretty!
Sandy Thanks Sandy, I'll google and see if I can find piccies. Do you mean the scar is not pretty, or something else? Carol
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hen wrote:Hi Carol,
I have had both a right shoulder and right elbow replacement (as well as R ankle and L knee). My shoulder was replaced 12 and a half years ago,- 7 and half years after my RA diagnosis (I have aggressive RA), and my elbow was done 8 and a half yrs ago. Although the range of movement I have is very limited, I have no pain at all from the shoulder and just some minor stiffness pain in the elbow- both joints are still doing as well as when they were first put in. I have had no infection problems after any of my ops, however I do not class either of these replacements as successful as my lower limb replacements, in terms of function. Apparently the elbow is considered one of the trickiest joints to operate on and I did have a minor-ish complication with that op as my medial epicondyle (sp?) fractured and chipped off during the op which meant I had to have plastercast on for several weeks after the op and perhaps as a consequence of this I never did regain the ability to straighten my arm. Mind you, it was stuck bent before the surgery anyway. I did not have any choice but to have the ops as the joints were basically destroyed by the time I had surgery and I am glad I did. The replacements will obviously be better now than they were when I had mine..I know the shoulder I have has a long stem (which also may have complicated the elbow surgery) and now they are much smaller and stemless I think. My elbow also has stem which again I think has improved to a stemless version now? I would try to select an NHS surgeon who specialises only in the joint to be operated on...some claim to be experts in several joints but I feel that a surgeon who only does one joint has deeper knowledge and enhanced competence in that surgery.
Hope I haven't waffled on too much about myself...hard to know how much info to give or not. Good luck with your decision...feel free to ask any questions if you feel I can help.
Diane x Thanks Diane. Are you able to drive? I'm finding with bent elbows, my arms are shorter and I have to bring the steering wheel forwards. I'd hate to go through surgery and then not be able to drive. My surgeon does specialise in shoulders and elbows and doesn't do hips and knees, although he did a couple of my hip debridements last year. I probably ought to ask him how many shoulder and elbow replacements he's done. Carol
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Hi Carol,
yes I am able to drive short distances. As my right arm is much more bent than my left, I have altered where I have my hands on the steering wheel to where is most comfortable. I had a removable steering ball adaptation put on my latest mobility car but to be honest I don't find it helpful and for me it is easier to manage without it.
Yes do ask your surgeon how many shoulders and/or elbows he's done and how successful they've been, which particular replacement they use and why etc. I always ask loads of questions and a good surgeon shouldn't mind this.
Btw, I was on mtx for all my ops and didn't stop it at all. In fact I took part in a longitudinal study examining whether taking mtx at the time of surgery increases the risk of post op infection...it was concluded that there was no significant difference between infection rates in those continuing with mtx as normal and those interupting mtx for various time lengths. (obviously anti tnf is different and must be stopped pre-op.)
The scars arnt pretty but they do fade a lot with time.
Hope this helps, if I can help with anything else please ask
Diane x
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