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MS'ers who have had hip replacement surgery?

Posted: Mon Jan 23, 2012 1:20 pm
by reece
Hi, I am a 44 year old male who has been diagnosed by 5 orthpedic surgeons as a patient needing a total hip replacement. I have had RRMS for about 20 years now and was wondering what I should expect, be aware of, etc. if I decide to proceed.

Thanks for any input here!

Re: MS'ers who have had hip replacement surgery?

Posted: Fri Feb 03, 2012 3:18 pm
by drsclafani
so sorry for you difficulties.

why would you need a total hip replacement at age 44. Did you have an injury? Do you have rheumatoid arthritis? Do you have asceptic necrosis of the hip from steroid treatments for MS exacerbations??

Re: MS'ers who have had hip replacement surgery?

Posted: Fri Feb 03, 2012 3:44 pm
by reece
I have a torn labrum, socket bone fragments, FAI, and thin cartiledge. All this has induced osteoathritis near the injury.

Re: MS'ers who have had hip replacement surgery?

Posted: Fri Feb 03, 2012 4:22 pm
by drsclafani
I do not have MS so i cannot answer your questions about preparation as a PwMS.

I do have an interest in osteonecrosis related to steroid treatment causing avascular necrosis. How often have you been treated with steroids?

are there any other patients who have required total hip replacement or been advised to undergo this procedure?

Re: MS'ers who have had hip replacement surgery?

Posted: Tue Feb 07, 2012 9:59 am
by reece
Dr. Sclafani -

I don't believe my hips issues are steroid related. Over the course of 20 years, I have probably only done 3 or 4 flare-up cycles. I more attribute the injuries and related athritis to ms-induced hip muscle weakness combined with being physically active.

Re: MS'ers who have had hip replacement surgery?

Posted: Tue Feb 07, 2012 11:01 am
by drsclafani
drsclafani wrote:I do not have MS so i cannot answer your questions about preparation as a PwMS.

I do have an interest in osteonecrosis related to steroid treatment causing avascular necrosis. How often have you been treated with steroids?

are there any other patients who have required total hip replacement or been advised to undergo this procedure?
Thanks for sharing. Good luck with surgery

Re: MS'ers who have had hip replacement surgery?

Posted: Wed Feb 08, 2012 7:53 am
by KyleW
I'm a 52 year old male. I was dx with SPMS this past October. 3 years ago I was unaware of my MS, but did have my left hip replaced. My problem was bone on bone osteoarthritis. In my case it was the bone conserving hip resurfacing procedure.

There were no complications related to my MS. Even though I was unaware at the time that I had MS, apparently I have had it for at least 20 years.

Based on my experience, short of making sure everyone knows what drugs you are taking, there is no MS related reason not to proceed.

Before my hip surgery I couldn't walk10 yards without pain. Now, given that my my hip is made of chromium, I have no pain :) My advice would be to proceed!

Kyle

Re: MS'ers who have had hip replacement surgery?

Posted: Wed May 09, 2012 11:25 am
by AllyB
To Drs Sclafani
I have had MS since 1999, have had around 10 courses of high dose iv steroids (1000mg of solumedrol per day for 5 days per course), been on Avonex for 6 years and have stage 2 osteo necrosis of the left hip, probably from steroids - I have been offered the surgery where they drill little holes into the head of the femur to encourage revascularization (forget what it is called!), but I am still thinking about it.
Regards

Re: MS'ers who have had hip replacement surgery?

Posted: Mon Dec 10, 2012 1:34 pm
by panda11
Hello
I had a THA left hip (almost 15 months post op). The first couple of months I was doing very well. However, for the last, what feels like eternity, 10 plus months, I have had weight bearing pain- mostly on crutches now...'been shuttled' from test to test... now to get another 3 phase bone scan this month (as the first one suggested 'loosening'), ... be on the safe side, 2nd opinion doc said 'it's a more accurate read 15 months post op...
history: I have M.S, been on Avonex for 10 years. I am 48 year old woman. Normally very active- mural painter/textile/community artist. In 1996 I had AVN/core decompression surgery.
Question: is there any connection between M.S, THA, the polyethylane acet. component in my body and the chance that osteolysis is happening...?? I am doing research to see what might be possibly going on... at this point no specific components in me have been recalled, however what about the polyethylane... does my autoimmune challenge with M.S create a possibility that my body is reacting?!
The initial surgeon wants to go in there and see what's going on; the 2nd opin. doc suggests I wait, as I'm doing...
thoughts?
thanks

Re: MS'ers who have had hip replacement surgery?

Posted: Tue Dec 11, 2012 11:00 am
by broomdancer
Dear Dr Sclafani: My husband's first serious MS flare up occured in 2003. He started falling down at work, I took him to the Emergerency room where our GP happened to be on call. Our Dr first thought that might be Cancer in the spine. Immediately he was given an MRI where MS was discovered. He was put on a 2-4 week steroid regiment. (can't remember exactly the duration). In the past year my husband has discovered that he needs 2 hip replacements (one worse then the other). He has been wall walking since then and very slowly. Our dilema is, the surgeon doesnot want to do the surgery until he can't stand the pain any longer. His fear is that it could ascerbate the MS ( dx'd PPMS). Are you aware of this happening? I have previously posted my concerns and unfortunately know one has replied to me ...He had the liberation treatment June 2010 by Dr Simca in Poland where his walking really improved for about 6 weeks. There have been 2 scans done within the first yr of treatment, in Barrie, On & the technician said his neck was fine. Dr Simca stated that he believed his Azorles (forgot name) was okay although it was mangled ( I believe that was how it was phrased)...My husband (age 61) thinks, there may well be arthritis involved but how would we know this?..I would really appreciate any input or help that you could provide I am at my wit's end on what course of action we need to take.. Thank you...Cheers Diana

Re: MS'ers who have had hip replacement surgery?

Posted: Sat Nov 30, 2013 7:34 am
by cooper08
I am a 53 year old who had hip replacement surgery in May 2013. I had so much pain all over my right leg. Nothing I did would help it (treatment, medication). I am now completely out of pain although it stole my mobility which I had with a rollator before surgery. I have had MS for 18 years. I had no idea that recovery would be so difficult. I was in the hospital 3 weeks. When I got home, I couldn't go 5 minutes without having to go to the bathroom. That has cleared up, but the mobility issue is distressing, as I live alone. I don't know what will happen in the future, if I will walk again. If you can stand the pain, don't do it. No one told me what I was in for. I am trying to do everything I can to walk again, and I won't give up as I used to be very active.

Re: MS'ers who have had hip replacement surgery?

Posted: Sun Oct 19, 2014 6:33 am
by shaanie420
Hiya, i'm going to be having a hip replacement tomorrow. Yep, nervous. It's was having that or suffering for a long time. I also believe that it was the Presdisplone steroid treatment which has worn away my hip structure. I'm 37 years old living in damp old England United kingdom. I would be lying if I said I haven't had any distress from the ex rebating pain, certainly have. To reduce the inflammation was a beer awaiting an operation, I was prescribed naproxen. I have found this to be useful somewhat. My other coping mechanism is to distract best I can. Although it is easier said than done. My other coping mechanisms are staying away from people who are miserable.

Re: MS'ers who have had hip replacement surgery?

Posted: Sun Oct 19, 2014 7:55 am
by Leonard
I will give you my take on things.
I think MS and arthritis are related, are auto immune diseases, caused by the herpes family.
In MS, the herpes virus anchors in permissible cells, that is the OPCs, in time of immune deficiency establishing transgenic cells, without immune memory established. I think inflammation of the sinus cartilage is an collateral issue. Later on, if infected again - may be a chronic EBV infection - immune complexes cross react with transgeneic cells causing autoimmunity i.e the reaction against the self.
In arthritis, the same process takes place. The herpes virus archors in the cartilage between the joints in times of immune deficiency without immune memory established making cells transgenic. Later on, this invokes autoimmunity of the joints in the same way.
The common thing in MS and arthritis is the virus.
See also the last few pages of http://www.thisisms.com/forum/general-d ... 8-585.html
You don't have to believe me, but at least read the pages and think it over.

Re: MS'ers who have had hip replacement surgery?

Posted: Sun Oct 19, 2014 1:42 pm
by Scott1
Hi,

If it was me I would find a physio, or pilates instructor who would focus on building my fitness and muscle tone as much as possible before surgery. If you're going to do it then get as strong as you can beforehand. If it hurts beforehand you want to give yourself the best recovery you can. Starting in a weakened state then doing the surgery doesn't sound like a great strategy for a quick recovery. It may not be comfortable but I would try to prepare for it not just go in cold.

Regards