My HoLEP prostatectomy
Posted , 48 users are following.
I thought I'd report whilst things are still fresh in my memory.
Well, I got home this afternoon (Thurs) after the op Tues @ 7 p.m. And things seem to be working OK. No more Tamsulosin needed, so that's one benefit right there. I'll update after a few days as the the other possible effects.
The anaesthetist chose a spinal anaesthetic, which I was somewhat chary of, prefering to be totally knocked out. Later I remembered that there'd been some research that found that older people who had anaesthetics died earlier, so he was right on that score. He also told me that this way I had a smaller number of anaesthetics (general meant 14!, this way 1 to 3).
I didn't like the thought of being awake and watching the op, but he assured me I wouldn't feel a thing; I wouldn't see anything; and I'd be able to feed and drink more or less straight afterward rather than many hours later. And so it came to pass. Just numb legs for a while. I really didn't feel anything. All over in about an hour. I even dozed a bit on the op table.
However, that night (Tues) was not good. I had a constant feeling of wanting to sh*t. However, no matter how hard I tried (and I used two laxative suppositories), virtually nothing happened. I later found out this is a side effect of the somewhat larger catheter and balloon that was put in place.
So I found it hard to sleep. But just when I did doze off once, the nurse came in for the fourth time to take my blood pressure (2.00 am?). I was really upset and told her not to do any more (all the previous ones had been OK anyway). But by then I couldn't get back to sleep. So I was wretched all the next day (yesterday).
However, last night I got to sleep about 8:30 pm; and slept right through to breakfast. Bliss.
The surgeon had come in on Weds; told me about the defecation urge origin; said I could go home today if my urine was pretty clear by then and the catheter had come out. I see him again in a couple of weeks, when the result of the biopsy will be with him. He also said only 10% need the op again in 10 years; most are fixed for good. Here's hoping.
I was apprehensive about the removal of the catheter. In the end though, it wasn't too bad. I did most of it myself, easing it and rotating it a bit when it seemed to stick. Whew! Great. Then I pee'd a couple of times to test things; told I was OK to go. I left.
Home by 3 pm today. Then did a good walk (4 miles) and all's well. Still some blood and bits, but most clear. Good flow. Now to see how I am at night.
2 likes, 171 replies
bill20925 ianC
Posted
I tried pills (I call "FloMax" FloMin!!). I had Greenlight. In my opinion any doctor recommending that is a doctor you should no longer go to because it was a heavily marketed procedure that has proven to be minimally effective. It did nothing for me, however it did put money in some Uroplogists pocket!!
I had TURP next, about 18 months later. It helped for about 12-218 months but things got pretty bad as time went on (I had a catheter in for 3 months).
The doctors office who perfomed TURP was 30-60+ minutes away from my home. When my prostate shut down all urinary flow (frequent), I was in emergency help conditions. I told my doctor I needed to find a doctor close to my home for this reason. He said the most important thing to me: "Whatever you do, be sure to tell the doctors you have a prostate larger than 100 grams". That got me thinking, and I typed that sentence into search on the internet.
I came across a forum talking about HoLEP. Everyone on it raved about the procedure. It mentioned names of doctors who performed it. Many were at Mayo Clinics. The top guy was/is Dr Lingeman out of Indianapolis, Indiana. He has done close to 3000 HoLEP procedures.
I ended up having my HoLEP procedure done by Dr Lingeman and it has been highly successful, 3 years now since it was done. Read on for more input!
Prior to HoLEP, I ended up seeing 6 Urologists. NONE OF THEM, ever mentioned HoLEP. Why? Because Urology is a business. Urologists have full practices, ie there is plenty of demand for their services. None of those doctors were willing to invest the time to learn HoLEP becauee it would cost them a lot of traingin time which is money out of their pockets. When I found out about HoLEP, I asked 2-3 Urologists (I met them at the emergency rooms), and THEY ALL SAID, HoLEP is risky and bad, and why aren't I coming to see them as my primary care doctor? In other words, they wanted my business and they did not want to invest in learning newer, better methods!! So I would walk out on any doctor who does not perform HoLEP because he or she is not investing in modern methods.
You want to go to a HoLEP doctor who has done at least 30 of these procedures and hopefully much more because there is a learning curve. So ask.
I did have a severe complication not cause by HoLEP but want to mention it to make people aware of a certain risk. I am an active sports person. I had the catheter in for 3 months. I learned how to function fine with it without a foley bag (I just had a valve and pee'd in urinals by opening the value, it worked really well). I started to have mild pain in that eneral area but assumed it was from the catheter poking and that was it. MY MISTAKE!! It turned out to be an infection, it ended up as a severe infection, it destroyed one of my testicals, and it feels like my libido is much lower and I only have retrograde ejaculation as a result. So if you are using a catheter for any length of time and experience any pain, get it checked out asap and probably get on meds to kill any infection.
Lastly, there is a new procedure out that I think looks promising though it is very early days. You probably should know that we humans are suckers for believing that when we go to our primary care doctor for a given ailment, that practice is the only one who can help. Turns out "Interventional Radiologists" (specialists in hospitals who do many wonderful, non-invasive procedures) have a prostate procedure that is very different than others. They do no cutting or laser eblation stuff. They just go through your veing to the prostate and insert some type of slivers that cut off blood flow to the prostate which shrinks it. The challenges with this procedure are 1) it is new, so if you want to consider this anytime soon, you probably need to travel to the top experts in the US (I am tols it was perfected in Europe so you may be better off there!), and 2) the prostate has many veins which are not fully mapped out making it harder for IR's to pinpoint the problem area and get it right the first time. But if I had the problem today, I would travel to the top IR hwo does this work before making any decisions.
I highly recommend HoLEP, and am happy to help you get in contact with a top IR in your area if you want to look into their Prostate Embolization procedure. I also have a research paper on it I can share with you. Please DO NOT assume the uroligist you go to is giving you the proper advice unless he or she performs HoLEP and also discusses the IR procedure. By the way, for those on blood thinners, the IR procedure, if per4fected, probably has the lowest risk of bleeding since it has no cutting.
bob120 bill20925
Posted
Do you know if you had a large median lobe? From what I have read, the prostatic artery embolization doesn't help if you have a large median lobe.
Wonder if you know how the holmium laser (holep) does with that condition?
I had 70g of a 120g.+ prostate removed with the GL laser, followed a year and a half later by a bladder neck resection and removal of stones. But I have a large median lobe pretty much intact that protrudes into the bladder. I think it's just a matter of time before this will caue a problem as my flow is already somewhat restricted just 9 months later.
Not sure how this will be addressed short of a prostatectomy.
RonTexan bob120
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bob120 RonTexan
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Bob
RonTexan bob120
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RonTexan bill20925
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bill20925 RonTexan
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Also, I noticed a very negative note from someone overseas from around 2 years ago on HoLEP. But that person may have gone to a doctor who was just learning how to do it. I also noticed some urologist out of Florida replied to it and gave the guy some names and links which attempted to further discredit HoLEP. So I clicked on the doctor and saw he touted himself as some top urologist but found he had 1 patient who posted a really bad experience from him. Point is, don't let urologists who do not do HoLEP scare you away, but do your homework and only go to guys who have performed MANY HoLEP procedures (I was told 30 or more to open).
derek76 bill20925
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Over the next eight years my prostate re-grew to 125grms and last May I had Thulium Laser surgery at a different hospital. It has been done in the UK for a number of years but only recently in the USA. The surgeon who did it called PVP a commercial procedure and not a cure.
I was still passing blood on day two and was sent home with a catheter in and told to come back in two weeks to have it removed. Wearing the catheter was not to much of a problem and I was able to get out and about. With the catheter in I acquired an infection and had to take antibiotics. During that time my urine was pink and I was passing debris and a few blood clots. When the catheter was removed and my bladder flushed out my urine was clear from that moment. Again my flow was not brilliant but slowly improved.
The hospital where I had my original PVP now use the newer Green Light laser but mainly use HoLep laser.
bill20925 derek76
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If I didn't mention it, I believe HoLEP was invented in Europe somewhere, so there should be doctors over there with good experience.
bill20925 derek76
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"The enlarged median lobes fellows do the best. HoLEP is best for this as it combines the most complete removal of the tissue resulting in the best short and long term outcomes. Further, patients can get back to regular activity in one week."
lwhitaker bill20925
Posted
If you would not mind sharing the research paper and suggest some top Docs to perform HoLEP, I would really appreciate it.
I live in Austin, TX.
Thank you
Larry Whitaker
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michael8714 bill20925
Posted
One of the purposes of the discussion with Dr Schneider was to schedule the tests necessary to completely evaluate my condition (BPH).
June 30th was a full day of testing, resulting in the discovery of the prostate size...a little over 100+ and visibly intruding to the bladder. Other than frequency, not emptying and night time attempts to empty, there is a sudden urgency with a burning sensation. There are no infections...at least none were discovered.
While scheduling the "tests" I opted against biopsy because of the risk for infection and the fact that any cancer beneath 6 on the Gleason scale is typically not treated...just further cause for anxiety in my opinion.
Having had two complete shoulder replacements at Steadman Clinic, Vail, CO in 2014...right shoulder, June 2014, Left shoulder November 2014, I'm concerned with possibility of blood infection from the typical transrectal prostate biopsy.
My main concern is to "fix" the going issue with an immediate prostate procedure. After becoming aware of the HoLEP procedure, I'm convinced this is the way I should and will go. As matter of fact, we scheduled the procedure at Mayo Phoenix for Wednesday 16 September. Dr Scneider wants me to arrive Monday for tests and preparation.
This is where I'm finally getting to the point of my post...Dr Schneider is very young. I asked the nurses performing procedures this last visit..who is the HoLEP procedure doc at your clinic? They didn't reply with Dr Schneider's name. I can't recall the urologist they mentioned but Dr Schneider did say the urologist they mentioned would be on the team and available if there were complications. Dr Schneider said he'd completed 58 of the HoLEP procedures and the "other" urologist...the more experienced one, has completed more than 400. Has anyone heard of Dr Schneider, Mayo clinic, Phoenix and what would be your position in selecting the surgeon? I really liked Dr Schmeider but experience is what concerns me. I learn d at Steadman Clinic, during two complete shoulder replacements...the quality of the procedure is not wholly dependent upon the one surgeon but the team he puts together. Maybe I'm answering my own question...I have faith that Mayo would assemble a top notch team for this, self-admitted, complicated procedure. My other area of concern is going under general anesthesia for two hours once again. Each of the two,shoulder procedures was two hours under a general along with a nerve block. Remember, the first was June 2014, the second was November 2014. Does anyone have an opinion or knowledge of the effects of a 64 year old man going under for that length of time again...the third time within 16 months? Dr Schneider did not mention the option of a nerve block with no general and I forgot to ask. I'm not over weight, in good enough shape to do 10-12 mile hikes at 7000' elevation and I'm not taking any meds except Ativan...stressful job and helps take the edge off for sleep. I hope I didn't ramble to much...I appreciate forums such as this and I'm a firm believer in taking responsibility for your own health choices...I'm looking to be as informed as possible. Information helps remove the stress! Thanks a bunch for any and all help/advice
RonTexan michael8714
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Something just occurred to me, I has interviewed by several doctors at the Mayo before surgery, one was a tall, beautiful, young, woman Doctor and I don't recall her name. I know she was part of the Holep staff. Could this have been your Dr Schneider?
michael8714 RonTexan
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RonTexan michael8714
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Best of luck and let us hear from you. Ron
michael8714 lwhitaker
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michael8714 RonTexan
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lester90053 RonTexan
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Need help.
derek76 lester90053
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Lumenis Inc. – Main Office
2033 Gateway Place, Suite 200
San Jose, CA 95110
USA
Tel: 408-764-3000
Fax: 408-764-3999
Lumenis Inc.
1870 South Milestone Drive
Salt Lake City, Utah. 84104
USA
Tel: 801-656-2300
Fax: 801-972-4884
derek76 lester90053
Posted
Some hospitals here do both procedures.
michael8714 lester90053
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lester90053 derek76
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Thanks for your concern.
derek76 lester90053
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at North Shore Medical Group.
My prostate was 75 grams when I had PVP in 2005 and had grown to 130 gram by 2013 when I had holmium laser. It is now 50grams but problem free.
lester90053 derek76
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derek76 lester90053
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sam2851 lester90053
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derek76 sam2851
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Good luck with the rest of your recovery
bob120 sam2851
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stebrunner michael8714
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Curious as to if you had the PAE done--and where you went. Are you pleased with the results? I, too, checked into having a HoLEP done by Dr. Humphrys at the Mayo Clinic in Phoenix. Their facility and staff are impressive, and I thought it could be a backup option.
Currently I'm checking into having PAE done in Denver by Dr. Charles Nutting. They have my medical records and will let me know soon if I'm a candidate. Might check into having it done on the East Coast, too.
My prostate is quite large with a median lobe pressing into my bladder. At the first of the year I was hospitalized with acute urninary retention. I was told my bladder function probably won't return. Currently I'm learning to self cath--it's not for the faint hearted when you have a huge prostate. But it's taking the pressure off of having to make a hurried decision. My hope is that PAE will make self cathing easier. If it helps my bladder function again, that would be fantastic.
Stebrunner
John-T bill20925
Posted
Great story and thank God you recommend HOLEP,
As for me well I have been wearing a catheter for about 6 weeks and also installed a valve in the past 2 weeks so this way my bladder get to do some work while I wait for the HOLEP operation. I seen 3 different urologist and each proposed a different method, the first one proposed the old TURP, the second one proposed Green Light surgey and the 3rd one HOLEP, I seeked his advise after doing a lot of research and found that urologist the only one in Montreal, Canada doing HOLEP. I just hope that after the operation I will be able to pee normally. I all started when I felt sick and nauseated and went to the ER, they checked me out and found high level of my creatinine 230 and didn't know why but found out that I had 750ml of urine in my bladder after void. I never had problems urinating but could not empty completely my bladder and apparently it went back in my system and increased my creatine, they installed a catheter for 5 days and then I had a systoscopy and following that they ask me to try to pee and I could not which I couldn't understand since I was urinating fine before they put the cath and systoscopy, in any case they put back a cath that I have now for about 6 weeks, of course I had to change it about 2 weeks ago to a new one, they also told me that my prostate was huge and needed to be operated, just hoping that all the retention I had for God knows how long did not damage my bladder, so for the 1st month I gave my bladder a rest by wearing the cath and bags and now I have the valve so hopefully my bladder will get back to normal once I get the HOLEP.
Thanks
John
reg52510 John-T
Posted
Hi John:
Did you have your Holep done in Montreal? If so, could you provide details about your experience? Apparently, it's the only place in Canada where the procedure is done.
Reg
gus64708 bill20925
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Hi Bill , I just saw your comments on this site & I registered in order to be able to communicate with you .
Regarding Holep , which I have been told by Dr.Hermendra Shah to go for it & he has done over 2000 procedures. My questions :
How accurate are they on ED as a non issue
& incontinence....I'm 67 years in good health as per my blood tests & my prostate is 85 gr. & choking my urine flow .Bladder function is very good .
Also you mentioned IR ! WHAT IS IT ? WHERE CAN I GO FOR IT ?
YOUR ADVICE IS GREATLY APPRECIATED.
GUS
mike03369 bill20925
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laura00828 bill20925
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Can you tell me if you think Holep is safe for a high risk senior? My dad is not voiding and we have to decide on something asap. Thanks for any advice.