PAE in the UK
Posted , 11 users are following.
I have been offered a TURP by my urologist, I am on alfuzosin, which isn't working and makes me tired all the time. I can't have a proper pee, and I am getting really fed up with it all. I ready about PAE today and don't know what to do next, is there anywhere in the UK, I think Southampton offer it, but not sure if it is on the NHS or you have to pay. It is the other end of the country, I am in Leicester. Any help apprecited. Does PAE work for BPH?
0 likes, 67 replies
tom86211 philip42830
Posted
oldbuzzard tom86211
Posted
david19922 oldbuzzard
Posted
philip42830
Posted
My PAE jorney started two months ago. I had read about PAE, spoke to various people including the consultant at the Churchill Hospital in Oxford.
I went to Oxford a month ago for a CT and MRI scan to see if was a suitable candidate but also had to have a consulation with a urologist, who asked for me to have a flexible cystoscopy to check if I had a uretheral stricture. The also did a PSA.
The MRI revealed I had a lump on my prostate.
The urologist found I don't have a stricture and the procedure was planned for the 23rd August.
I went into the produre room at 1pm and came out at 4.15pm, the process was painless except for the initial local to number the groin area.
The result was they couldn't inject the beads into ether side of my prostate, as my arteries were not suitable, the prostate arteries are linked to the supply of my bladder, so they decided not to proceed.
The hospital was very professinal, I cannot fault the care I received.
The lump is something the surgeons have said is not a issue.
The team are seing my scans and my case to a local urologist, I am sure I am going to be living with BPH for a long time, as I won't be going for a TURP or HOLEP.
I wish other people good luck with their PAE treatments.
Philip.
scraggs philip42830
Posted
Sorry to hear they couldn't do this.
I am considering using Oxford but am a little concerned about the lack of experience they may have with the proceedure.
philip42830 scraggs
Posted
My advice is, ask a lot of questions, make sure you have all the data and the options and possible success rates etc.
I feel I did everything I could.
My comment about the Oxford Team is they did everything they could, I couldn't fault the professional approach and their post operative care.
Amazing team, you would be in very good hands.
Experience: I think they have done 60 and only 2 of us couldn't have the treatment, I was just unlucky.
At least I have had a MRI and CT and lots of tests, including a flow rate, and before the PAE, the only test I had was a PSA, so it has given me a better understanding of my condition and I am going to look at my options.
I am not going to rush into anything.
Just take your time Scraggs.
philip42830 scraggs
Posted
Just to add: I believe my experience shows how experienced the Oxford Team are in relation to PAE, as they didn't proceed with my insertion of beads, based on their comprehensive understanding of the risks. I am pleased with the outcome, as I am no worse off.
scraggs philip42830
Posted
I thought the scan was to see if you were suitable for the proceedure.
philip42830 scraggs
Posted
philip42830
Posted
I have in the past had a lower back pain issue, but without any issues for 10 years, but as I was laying on the table for 4 hours and in bed for another 4 hours, my back has been in spasm for 2 weeks. Something for potential PAE patients to consider before undertaking the procedure.