Has anyone had hip replacement surgery with ET jak 2 , on hydroxy and aspirin? I'm due for this in a few weeks with a pre op assessment in 2 weeks time. Surgeon has been made aware of Et situation. I just wondered if anyone has encountered any problems or issues, or whether the procedure was straight forward. Any thoughts would be very welcome.
Hip replacement surgery: Has anyone had hip... - MPN Voice
Hip replacement surgery
Hello. I had hip replacement surgery in Dec of 23. I’m ET JAK2 and am 78. It went extremely well. Was on blood thinner for 2 weeks after the surgery. Before the surgery my Stanford MPN specialist upped my hydroxy from 5 a week to 7 a week to get my platelets in the 300s. They usually run in low 500s which is fine but wanted them lower for surgery. Other than that nothing out of the ordinary. I’m now pain free-so glad I did it. Just do all your exercises and you’ll be up and about in no time. Good luck!!! Marti
Hi Oscarboy, I have ET (diagnosed in 2003) and have been taking Hydroxycarbamide since 2008, and also a daily aspirin. I had a total hip replacement in May last year, such a difference now, no more pain! I would advise that you ensure that all the hospital teams (your haematologist and orthopaedic surgeon) talk to each other about the operation and your ET and medications, right from my first appointment with the orthopaedic surgeon, my ET and medications and my pre-op and post-op recovery were discussed and then followed up with my haematologist, in fact they had communicated with each other before my first appointment.
Both teams ensured that I had clear instructions pre and post-op regarding my Hydroxycarbamide and aspirin, and other blood thinners I needed to take for a couple of weeks after the op. Your orthopaedic surgeon and your haematologist should liaise with each other to advise you about your meds, pre and post-op, and advise you accordingly as to whether or not you need to make any adjustments, and whether or not you will need any blood thinners post-op. The advice I was given about stopping my Hydroxycarbamide and continuing my aspirin was specific to me, so not necessarily the right thing for someone else.
And also make sure that everyone in the hospital knows about your ET and meds, it was very clear on my notes and all the nurses on the ward, the anaesthetist and the team in the post-op recovery ward were all aware and discussed it with me, which was very reassuring.
Post-op recovery for me was fine and went very well, I was up and out of bed a few hours after the op, and walking on crutches the next morning and back home in the afternoon. Make sure you follow the advice you are given about post-op recovery, and do the exercises, they really do help such a lot. I was amazed after the op that I no longer had any pain in my hip, oh the joy, the relief really is immediate, I did have some pain and tenderness, but that was from the op and was expected, but good pain relief helped with that.
For me it was a very good experience, with a fantastic outcome, no more pain, and I hope that it will be the same for you.
Best wishes, Maz
Hi Maz. Thank you so much for all your helpful advice. I have informed the Orthopaedic Consultant doing the surgery, as he said he knew a little about PV and thought sometimes that and ET crossed over. I have given them my haemo consultants email at Darent Valley whom I am under for medication and follow ups. I did see Professor Harrison last week for a review, the day before I was seeing the Orthopaedic Consultant so I was able to speak to her about it, and she said there should be no problem, again provided all obs are ok. Do you know how far before the surgery for example another blood test should be done? I am having pre op assessment on 29th april and the op is then likely within a 2 week period. Would they need to be done again, as the wait time to get them done at the hospital by appointment needs to be at least a couple of weeks ahead as they get very full up. I do have quite a bit of anxiety over how this is all going to work, and whether they will actually communicate with each other, and how I ensure that happens. I meant to ask also did you have this carried out by spinal block? Thanks so much for you help.
hi Oscarboy, you are welcome. I can understand your anxiety, but they will have your notes which will have details about your PV and MPN medications, and just keep reminding everyone that you have PV, they won't mind.
With regards to the blood tests, I had mine done at the pre-op assessment about 2 weeks before the op and then they were repeated at the hospital on the day once I arrived on the ward, they also did other did my blood pressure, so it may be that they will re-do them on the ward. I did have the spinal anaesthetic and had a very thorough and detailed discussion with the anaesthetist about it on the ward so he was able to reassure me about it, and then once down in theatre ready for him to do it I felt more at ease, it was just him and his assistant in the room and they were both great and talked through each step and made sure I was nice and calm and relaxed.
I hope that all goes well for you. Best wishes, Maz
I had hip replacement surgery in 2016 when I first was diagnosed with ET/PV. Although I was not taking anything at the time, the surgery and recovery were pretty straight foward with no complications with either.My surgeon was aware of my recent diagnosis and didn't seem there was cause for alarm. Again, this was early in my diagnosis and my numbers were fairly low.
Good luck with your surgery. I'm sure all will be well.