Greenlight versus Acquablation

Posted , 19 users are following.

So I've finally found a doctor I like. I dropped the creepy female uro who wanted really wanted to do a 12-needle biopsy for no damn reason. I got a doctor who came recommended by a friend, He operated on him and got a good result. The guy is a professor of Uro.

Anyway, he wanted to do a Greelight or Acquablation. I asked which one he thought I should have, which one has a better result, etc., and he said the Acqualbation because "it's cooler" cuz it uses a robot. But now my insurance has declined it. My insurance will pay for a Greenlight Lazer. Should I fight the insurance for the acquablation? His office is telling me they are both equal and in fact there's less bleeding with the lazer. Anyone have any thoughts? Thanks.

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  • Posted

    Motto,

    Who was the Dr that was performing the Aquablation or Gl? I am researching Aquablation or Holep, after trying less invasive Itind then FLA in past 5 years. Dr Gomez Sancha was actually the one who did the Itind procedure, but he said i should have had his GL procedure and been done with it.

    Both of the procedures gave me relief, but not long lasting. So I think it is time to have a more permanent solution.

    I have been in contact with Procept 6 months or so ago, no one in Northwest USA does the procedure, but have found it in California.

    • Posted

      I would look into Rezum too. Aquablation brings a long recovery and Holep gives you RE for life. If Rezum doesn't work, you can always do Holep or Aquablation. Also, make sure that your prostate is the main issue - the more failures you have the more that brings something else into play.

    • Posted

      Just to second oldbuzzard on Rezum as the procedure to try first. I would definitely not do HoLEP because it will give you RE for life. With GLEP there is a 50 percent chance of RE. With Rezum it is under 10 percent. I had no RE from my Rezum.

      .

      I can't comment on Aquablation other than very few urologists are doing it.

      .

      Also make sure that you have a urodynamics test and cystoscopy to see if there is bladder damage that might prevent any BPH procedure from being successful. Finally, if you do chose Rezum, find a urologist who has been done over 50 of them.

    • Posted

      I looked into Rezum, but they didn't want to do this because of the work I already had done. Thought it might be too risky and suggested I go to a teaching hospital. I was not a candidate for PAE because of the small prostate size.

      I do have a weak bladder, perhaps caused by BPH. But what is the fix for that? All people I have ever seen have said that removing any obstruction will be the best for me and my weak bladder to overcome. And my personal experience has been just that, two times. The procedures just didn't last. So I have already done two less invasive/less risky procedures.

      I am not a fan of RE, but I have it now because of the FLomax, so having it without the other issues Flomax brings sounds like an improvement.

    • Posted

      "Holep gives you RE for life" Give the stats for that ridiculous statement..

    • Posted

      Motoman,

      .

      You do not want to go to a teaching hospital for Rezum unless the urologist who does the Rezum has been doing them for a while. You absolutely do not want a newbie to be doing your Rezum.

      .

      Removing the obstruction may provide some help for a damaged bladder but it is worth getting a better understanding on the bladder damage. That is what a cystoscopy and urodynamics test will do.

      .

      For the record, I flunked the detrusor part of my urodynamics test and the cystoscopy showed moderate trabeculation so I had a damaged bladder from years of BPH. As me and oldbuzzard have said, bladder recovery is a slow process.

      .

      What I find interesting is that there is a lot in the medical literature on how bladder outlet obstruction (BOO) from BPH causes bladder damage, but there is nothing tracking bladder recovery after a BPH procedure to remove the BOO.

      .

      After my Rezum, my post void residuals (PVR's) measured by self-cathing were just under 150 ml. Now almost 11 months later, my PVR's are under 100 ml which for my age is OK. Bladder recovery is a slow process.

      .

      Also, to make the Rezum last, I am staying on Finasteride to prevent prostate regrowth. I have had no bad side effects from Finasteride and my bald spot has filled in which maybe is a good side effect 👍

      .

      Steve

    • Posted

      I had Gl in 2004 with no retro when I was about 70 as my median lobe was not to bad and they did a bladder neck sparing version. I had thulium/holmiun laser similar to HoLep in 2013 by then I was part way to retro from Tamsulosin and nearing 80.

      I'm now supporting Hank on the amount of misinformation being repeated as 'fact' on this Forum. It is time to start drawing the Moderators attention to much of it.

      Do you realise that you can look at actual medical information on this site as it is run for British patients and Patient UK provides services for the UK medical system and patients.

      You can search for professional articles on here like this one.

      https://patient.info/doctor/benign-prostatic-hyperplasia

    • Posted

      Derek,

      Very few Uro surgeons offer sphincter (bladder neck) sparing GL or even HoLEP operations in USA. This site is not only of British patients. The majority are from USA and other English speaking countries. The misinformation on this forum is not that rampant as you suggest. It's rather that many patients are poorly educated in the anatomy of the bladder or prostate. In most case with clinical symptoms the median lobe is enlarged and is obstructing the bladder neck. So, sparing the bladder neck, and corresponding sphincters responsible for the RE is practically impossible. Most operating UROs won't even bother. I personally had a serious obstruction of the bladder neck (three full obstructions) over the course of 4 years) and proven moderate trabeculation of the bladder wall on my contrast CT scans and cystoscopy (including a diverticula of the wall just before my PAE in March 2018. It's all gone for the most part of it 6 month after PAE, except for the small volume of my bladder. Technically it could be probably extended to 1L or but usually, I have an urge, when it contains 150--200 cc. Never measured my residual after PAE. It was zero on ultrasound PVR instrument 3 months after PAE. . Probably around 100 cc now. Only one trip per night to the BR after 4 hrs of sleep. Rarely can wait more than 3-4 hours between the voids during the daytime. It's OK for my age 72. Unlikely the wall become more elastic with time. Everything returned to were it was roughly in my early 50th. So traveling back in time 20 year s is not that bad, given the relatively low invasiveness of PAE, of which you are a great critic. Read on what people right here about TURP and GL, when the prostate capsule starts to look like a prune due to the plenty of heat generated during TURP or GL. Some are luckier than others . ..

      It's all about your age and unique skills and knowledge of your Uro performing the surgery.

      I don't think that RE is such a menace at ages 60+, when searing a child is not such a priority for a male, but statistically all invasive BPH treatment results in 90% of RE and around 30% of ED and incontinence. The latter can be transient and improves in 2-3 years.

      RE due to Flomax can be easily avoided in 90% of cases by switching to easily tolerable and inexpensive Alfuzosin, which is the same type, but more targeted alpha-blocker.

    • Posted

      After both my GL and Thulium/Holmium laser procedures my PVR was negligible after having usually been over 300 mls and on one measurement 450 mls.

      My PSA was down from about 9.8 to 5.0 after GL and from 7.8 to 0.74 after Thulium/Holmium.

      My last surgeon suggested I take Avodart to prevent regrowth. I asked if at my age it would have time to. He glanced at his screen and said perhaps not.

    • Posted

      Gene,

      .

      I have wondered how many on this forum are from the U.K. vs. U.S. given the populations of 66 million vs. 327 million. This forum is a great resource and it is unfortunate that in the U.S. we don't have something similar to this website. I am not holding my breath on this happening.

      .

      I agree that the misinformation on this forum is not that extensive but that many patients are poorly educated. During the 10 months of catheters before my Rezum, I had lots of time to educate myself with this forum being one of my resources.

      .

      During my "education period", I was fortunate to have a family member who was an MD for over 40 years and I have known for over 60 years to help me. As a retired research scientist, and under his guidance, I did the Internet research on the various BPH options available today.

      .

      We made a good team. When I comment on this forum, I try to present what we both learned about the various BPH options available today. Unfortunately as I learned, you may not get the information that you need to know from your urologist.

      .

      I agree that peeing like you did 20 years ago is great. If you have catheters, then you can measure your PNR's. It sounds like at age 72 after your BPH procedure you are doing good now.

      .

      Steve

    • Posted

      Obviously the Forum was set up by a UK company for British patients but was discovered by others when searching. Though it does use an American spell checker. It has been often suggested that there should be somewhere to put your nationality in your heading but your version of English is usually apparent to most of us. The differences between our health care systems can cause confusion to many Brits who do not have your wider choice of doctors. also some of your newer procedures have not reached us. Using the old News Groups I knew about GL when it first started and was eagerly awaiting it.

      Most here see an NHS consultant and that's it and find it difficult to get a second opinion far less several. I had quite a fight to be referred from Scotland where I was then living to an English hospital doing initial trials of it. Two other friends did the same and we all ended up having sucessfull GL's at different hospitals although one had his done privately rather than end up in a queue.

      https://patient.info/terms-and-conditions

    • Posted

      Derek,

      You are mistaken again. BPH in UK and USA have the same features and treatments, the tails that everybody is so-o-o different is more of the medical tail. It's rather that the skill of the doctors performing TURP,PAE, HoLEP, etc. are so-o-o different. Secondary, most of us in US, except for those who are older than 65 yo, and not using a truncated version of Medicare (roughly(65%) are bounded to the HMO organizations, which are even worse than UK NHS-analog of our Medicare. HMO almost never will allow you the second opinion and in most cases will offer you the most outdated treatment. The major difference is that out medicine is exclusively for profit (even some hospitals will claim nonprofit status) and profit wind up in the pockets of doctors and clinic administrators.

      For example, in UK NHS will offer you PAE or Resum as a less expensive treatment vs. TURP or HoLEP, while in US these are most likely paid out of pocket procedures or covered by Medicare if you choose the most expensive version of it, which typically will cost $350+ per month. Yes, thsi option allows to travel to any doctor or hospital in USA. Are you ready to pay regularly 4000 pounds per year for your hypothetical medical services?

      REgarding the English> I believe that part of the correspondents on this forum are just not native English speakers. Has much less to do with British vs, American dialect of the language.

      For some reasons we in US know much more about your NHS than you about our outdated and quirky multifaceted medical services that became unaffordable long ago. For instance, to have the PAE in US you have to pay out of pocket ($10000) or be extremely lucky to have doctor in the area who accepts Medicare and be 65 or older.

  • Posted

    What you are telling us that FLA didn't give you lasting results? Who was the Dr. performing FLA? It's only one doctor in TX to the bet of my knowledge, and he guarantees results. I'm not sure that recovery from FLA is so fast as it's claimed sometimes, but it's very expensive and precise if done properly. Treats even some localized forms of P-cancer. iTind is definitely questionable, but works for some. Are you sure your problems are BPH related? FLA should have fixed the problem. It's local but very invasive.

    • Posted

      There is no guarantee with FLA, don't know where you heard that. I had my procedure done over 2.5 years ago, coming up on 3 years in February, I think I have given it enough time.

      The Dr was great, the best I have ever had the pleasure of seeing/working with, and by a long ways. He went above and beyond for me with follow up, etc.

      If you look, you will find others where the FLA wasn't successful. We are in the minority, but out there. Mostly smaller prostates. Mine had cysts fill with fluid where the tissue had been ablated.

      Since I had decent results with both procedures, there is reason to believe a more robust procedure will have more lasting results. I had instant relief with both procedures, but it just didn't last.

      I would not call FLA very invasive. That is what I would call TURP, Holep, Aquablation, etc. It is why I went for the less invasive procedures to begin with, supposedly I could try other procedures after. Which is why I am currently looking again.

  • Posted

    What about trying PAE if your prostate has grown large enough. You need 50-60 cc to see dramatic results with PAE, albeit given what you said about cysts filled with fluid PAE can eliminate them potentially cutting the blood supply. Regarding FLA it is invasive and any laser ablation, it's just more targeted and less traumatic to urethra and bladder neck, From what I understand, recovery after FLA can last up to three months as well. Not typical for less invasive. Of course , details can vary on case by case basis.

    If I were you, I won't look for a permanent solution. Remember, permanent removal of the most part of your prostate can mean permanent interruption or termination of your other functions related to this important male organ. I went through PAE 18 month ago and still am very happy, but not as as happy as at 12 months. Only permanent prostatectomy guarantees permanent solution. Read about some dramatic results of SP on this forum in three months and later.

    Good luck!

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