Prostate Artery Embolization (PAE)
Posted , 39 users are following.
Hi All. Wondering if anyone had complications after the PAE procedure. Thank you.
0 likes, 165 replies
Posted , 39 users are following.
Hi All. Wondering if anyone had complications after the PAE procedure. Thank you.
0 likes, 165 replies
We want the community to be a useful resource for our users but it is important to remember that the community are not moderated or reviewed by doctors and so you should not rely on opinions or advice given by other users in respect of any healthcare matters. Always speak to your doctor before acting and in cases of emergency seek appropriate medical assistance immediately. Use of the community is subject to our Terms of Use and Privacy Policy and steps will be taken to remove posts identified as being in breach of those terms.
davidha fiora
Posted
Best Reguards
David H.
jennings21352 davidha
Posted
Also what was the total in $s?
ktmxc-f fiora
Posted
Approx. 100cc measured by Mri. No median lobe.
Increased painful frequency first day urinating every hour or so. Ten times first night. Frequency and pain decreased daily, although it still burns. By day eight urinating twice at night. Voiding every 2 to 3 hours. Feels as if post void residual has diminished. Still taking two flomax per day.
Flow: Increased dramatically after Pae procedure, not sure if the catheter dilation was cause. Flow slowed down to slow but steady stream the next six days. Day eight flow is improving, pain while urinating is minimal (still burns).
One problem I was having prior Pae was first morning void was always a worry. A few times near complete AUR.
Since Pae morning voids are steady.
hank1953 ktmxc-f
Posted
ktmxc-f hank1953
Posted
hank1953 ktmxc-f
Posted
Did you have any other symptoms ?
How did you decide on pae ?
Thanks. Hank
ktmxc-f hank1953
Posted
I had the usual symptoms. Frequency, urgency, watched diet very closely.
I decided to pull the trigger after a serious bout of urine retention.
I have been researching Pae for years, I have contacted many men and Dr.s. My opinion (not a doctor) Pae is the least invasive procedure with 80% positive results. If it doesn't work I will consider focal laser ablation next.
ktmxc-f
Posted
Hello,
I'm on day 10. Last couple of days have been difficult. Frequency every hour most of the day (painful). Last night I did go 7 hours before urinating. This morning flow is decent, pain is near zero. Morning run and things are looking good,
hank1953 ktmxc-f
Posted
ktmxc-f hank1953
Posted
ktmxc-f hank1953
Posted
I am approximately 20 days out. Average time between bathroom breaks is 2 to 4 hours now. I can also hold it now. Before "Gotta go now or wet the pants". Flow is sometimes great other times a little slow, better than before the procedure. No regrets so far.
jennings21352 ktmxc-f
Posted
ktmxc-f jennings21352
Posted
Big_T155 jennings21352
Posted
ktmxc-f Big_T155
Posted
Best improvement is time between and urgency.
hank1953 ktmxc-f
Posted
ktmxc-f hank1953
Posted
Hi Hank,
Every Man is different, I'm not sure.about size of Prostate. Dr. Nutting mentioned larger Prostates (100cc) sometimes fare better. Ive listed a few studies. Dr. Mark Little is a good one. Dr. Isaacson at UNC is very good at responding. message me and I can provide his email. Best to you.
Moderator comment: I have removed the link(s) directing to site(s) unsuitable for inclusion in the forums. If users want this information please use the Private Message service to request the details.
ktmxc-f hank1953
Posted
Hi Hank,
Im not sure about size. Dr. Nutting mentioned larger prostates may have better results.
I tried to send numerous studies to you but the site went into "waiting to be moderated"
If you message me I will send studies to help you.
Kt
hank1953 ktmxc-f
Posted
Thanks kt. 80mg used to be the minimum prostate size for PAE. I am just curious what it is now. This site doesn't like links so you can send me the links via private message (PM). Hank
sam19736 hank1953
Posted
hank1953 sam19736
Posted
hank1953 ktmxc-f
Posted
richp21 hank1953
Posted
No need for foley catheter.
I had my PAE there last March, and did not need a catheter.
ktmxc-f hank1953
Posted
I think many Men wait till they are in serious retention trouble. I wish I would have had procedure done three years ago. Its not perfect but it has helped me considerably.
hank1953 richp21
Posted
hank1953 ktmxc-f
Posted
stebrunner hank1953
Posted
Prior to my PAE I had severe urinary retention. I also have a large median lobe, and was doing CIC before the procedure. After the PAE they did not send me home with a Foley. However, about a week after I got home, I came down with a UTI, and they put in a Foley for 7 days to give my system time for the inflammation to settle down.
Stebrunner
hank1953 stebrunner
Posted
jennings21352 ktmxc-f
Posted
Jennings Reveley
ktmxc-f hank1953
Posted
Dr. Nutting uses a catheter on all of his patients. Catheter is a marker for him. I was with catheter for two hours post procedure. Once I was able to urinate they released me.
sam19736 jennings21352
Posted
hank1953 ktmxc-f
Posted
ktmxc-f hank1953
Posted
I was able to urinate without catheter prior to procedure. My prostate was swelling at night, very difficult first urination in morning. I know it was a matter of time, I decided to go ahead with procedure.
ktmxc-f jennings21352
Posted
I sent a few Doctors that perform the procedure. Dr. Isaacson quickly responds to any questions. If my insurance did not pay I would have went to UNC. Dr. Justin Mcwilliams at UCLA is another good guy if you have questions, Dr. Bagls charges for consult. I nearly went to chicago to visit Riad Salem for a clinical trial. My psa was over 2.5 so they wanted biopsy. Dr. Salem called me directly to discuss procedure. 312/695-5753
NMH/Arkes Family Pavilion Suite 800
676 N Saint Clair
Chicago IL 60611
stebrunner hank1953
Posted
No, my urethra was too inflamed.
Stebrunner
newzev4 sam19736
Posted
hank1953 sam19736
Posted
Re prostate size for PAE, I asked Dr Picel of UCSD:
"40 g is usually the smallest size treated. The procedure may still be effective on smaller prostates but is likely to have less of a beneficial effect.
Sincerely,
Andrew Picel, MD"
bensha newzev4
Posted
Hello,
I have approximately the same size prostate (50cc), but what worries me most is the large median lobe. I'm considering PAE with Dr Pisco.
Did you have already the PAE, if so how was it and how are you doing today?
What do you know about PAE and large Median lobe?
Thanks,
Yoav.
gene97713 bensha
Posted
Had PAE with Dr. Picel from UCSD exactly 30 days ago. Prostate 120 g, bleeding, bladder neck obstruction.Few times in the past Foley catheter placed for 1 week, self-catheterization lately. It was very painful first days after PAE and then slightly better but better after three weeks. Probably the more the pain, the better are results. After 30 days results are beyond any wild expectations. No pain or burning whatsoever. Stream flow like 30 years ago, at age 40, measures as 10-11 mL/sec. Can stay without restroom up to 4 hrs. Mild incontinence gone totally. During the night wake up only one time around 5;30 am. Expect more improvements in next 3-6 month. No feeling of residual urine in the bladder, The stream is strong all the time. A bit small amount of urine i relived every time, around 150-200 mL, but that is probably due to age, many years of BPH and bladder wall thickening. Otherwise pure magic of Dr. Picel. No bleeding, side effects, or other organs involved. Perfect poster case. Probably due to very large prostate and very skillful intervention of Dr. Picel. Have still to measure new volume and PSA. Erections and sex also improved substantially.
Skillful PAE should totally replace te butchering of TURP and other highly invasive treatment of the BPH. Insurances should cover it as the first resource. Don't know yet how long the positive results will last due to self-vascularization and future prostate growth, which is very individual. Will repeat the procedure without any hesitation, particularly with Dr. Picel.
Good luck with your PAE.
sam19736 bensha
Posted
bensha sam19736
Posted
Thanks for your answer.
Do you know if the PAE blocks compleyely the blood supply to the prostate or just limiting it?
Thanks,
Yoav.
ktmxc-f bensha
Posted
hank1953 gene97713
Posted
bensha ktmxc-f
Posted
Thanks, this is what I heard, I wonder if there is a specific vessel that feeds the median lobe or is the shrinkage of the lobe proportional with the overall shrinkage of the prostate?
Thanks again,
Yoav.