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Medical Forum / Diseases and Disorders / Prostate BPH / November 2006

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PVP - back again!

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Derry - 17 Nov 2006 05:18 GMT
Hi Everyone,

I had a PVP in December 2003 without problems. Unfortunately, I was
left with retro but everything else was OK.

Well, I am now back to square one and did not expect to be back on
this newsgroup. Recent tests revealed that my prostate is now bigger
than it was before PVP!

The problem I am now having is getting my local surgeon (Inverness,
Scotland) and the surgeon who did the PVP (Gordon Muir, King's
College, London) to communicate with each other. So far, I have been
polite but as my flow decreases my patience also evaporates. I am
still on the NHS (state health service) which probably accounts for
the slow progress.

I've done a search on "Repeat PVP" and I gather having to have a
second one done is not unusual. My local surgeon is trying to talk me
into a TURP which is nothing unusual either.

Derry
Derek F - 17 Nov 2006 10:05 GMT
> Hi Everyone,
>
[quoted text clipped - 17 lines]
>
> Derry
Sorry to hear that, you were the first British success story, mainly due to
your own determination in getting a referral to Gordon Muir. Have you
thought of contacting him directly and telling him of your problem. He will
remember YOU !
Another thought would be to contact Mike Degum of Laserscope for advice of
other NHS hospitals doing the procedure, there must be many more by now. As
You know I referred myself to the NHS hospital in Newcastle. Once they said
that they would see me I asked the consultant in Edinburgh to refer me... he
was very keen to get a troublemaker like me off his books.
Derek.
Derry - 18 Nov 2006 08:45 GMT
>> Hi Everyone,
>>
[quoted text clipped - 15 lines]
>was very keen to get a troublemaker like me off his books.
>Derek.

Derek,

You are right!<g>  I am very patient, up to a point, but started
politely agitating ealrier this week -- Recorded Delivery letters,
emails marked URGENT, phone calls, etc. (Thy don't like it!<g>).

Spoke to someone in the local hospital yesterday and was assured that
things are happening as my medical notes have been recovered from
storage! I have put myself back on Flomax so all is ok in the short
term. Mike was informed a while back that things were going down hill
and he was as helpful as usual. I expect a mention here did not go
unnoticed either.

Derry
blkwhite123@aol.com - 17 Nov 2006 11:02 GMT
> Hi Everyone,
>
[quoted text clipped - 17 lines]
>
> Derry
blkwhite123@aol.com - 17 Nov 2006 11:18 GMT
> Hi Everyone,
>
[quoted text clipped - 17 lines]
>
> Derry

Hi Derry,
I am back to square one as well.  I had a PVP in August 2003 with Tim
Larner at Princess Royal.  I posted about it under the username William
and you did reply to the postings at the time.  My flowrate improved
and I was able to go off Flowmax after the PVP but my frequency stayed
the same.
My flowrate has now decreased to 11 mls/sec and I get up every 2 hours
at night.  I am going for a repeat PVP with Gordon Muir at King's
College on 4 Dec.  He will use the new Greenlight HPS machine.  I am
going privately, the all in cost is ?4560.
I thought that PVP was a permanent fix.  It is surprising that we both
need repeats after 3 years.  Will keep the board posted of the results.
Salmon Egg - 17 Nov 2006 18:24 GMT
On 11/17/06 3:18 AM, in article
1163762326.651085.235750@j44g2000cwa.googlegroups.com, "blkwhite123@aol.com"

> I am back to square one as well.  I had a PVP in August 2003 with Tim
> Larner at Princess Royal.  I posted about it under the username William
[quoted text clipped - 7 lines]
> I thought that PVP was a permanent fix.  It is surprising that we both
> need repeats after 3 years.  Will keep the board posted of the results.

After the glowing reports here on PVP, I thought that I had wasted my time
and pain on TUMT. Off hand, it now seems that TUMT works as well. Three
years after a second treatment my flow rate is about the same as yours.  I
am posting on my recovery from my latest TUMT. This time, I was cooked to a
higher temperature than before.

Bill
-- Fermez le Bush
Rich256 - 17 Nov 2006 20:48 GMT
> On 11/17/06 3:18 AM, in article
> 1163762326.651085.235750@j44g2000cwa.googlegroups.com, "blkwhite123@aol.com"
[quoted text clipped - 19 lines]
> Bill
> -- Fermez le Bush

There are a couple of us here that tried TUMT without any success.  It
did absolutely nothing for me.  But I figured it was worth trying.

A URO said he has had about 50% success with it.  I wonder what the
difference is with different patients?
Derek F - 17 Nov 2006 21:16 GMT
> On 11/17/06 3:18 AM, in article
> 1163762326.651085.235750@j44g2000cwa.googlegroups.com,
[quoted text clipped - 21 lines]
> Bill
> -- Fermez le Bush

Personally I would rather have three PVP's than one TUMP :-)
It does not matter which treatment you have the prostate is still going to
grow unless you have the radical prostatectomy.  It would appear that some
prostates are more aggressive than others. I had read some experts who
expected the PVP effect to last for about ten years.
Derek.
fgomsan@gmail.com - 18 Nov 2006 08:32 GMT
Hi again, Dick, thanks for your message inviting me to comment on this
issue.

I see that two group users have to go to a repeat PVP after three
years. I will comment on this.

You must know that there is no BPH operation that guarantees freedom
from reoperations. With TURP, 10% of patients need a reoperation in
five years. PVP does the same as TURP, but with less bleeding and risks
than TURP.

I think, but this is only my opinion, that there is a very good
correlation between removal of tissue and durability of the operation.
I know Tim Larner started doing very fast operations, just carving a
tunnel from the bladder neck to the veru montanum, I watched the videos
he posted in the internet and I did not like that way of performing
PVP. Later on he changed his mind because he was seeing patients coming
back, he recognized this during a European Congress. Gordon Muir was
more agressive than him, but still he did not think that complete
removal of tissue was so important.

I have discussed this with Gordon Muir many times, I have always
thought that the chances of reoperation will be less if you are
agressive with PVP, that means using a lot of energy, spending as long
as it takes (I have operated patients with big glands for up to 4 hours
with the 8 watt laser) and removing as much BHP tissue as possible.

The new HPS makes that task easier for the surgeon, because it
vaporizes much much faster, and halves the surgical time. Mr Muir got
the first HPS laser in Europe, I got it after him and I really think
that this device allows us to perform a better job in a shorter time

If you read my posts some months ago, I was insisting in finding an
aggressive surgeon... I have always been convinced that to reduce the
chances of reoperation the initial operation has to be very aggressive.

I would recommend discussing this with Mr. Muir, there might be another
reasons for this early need for a reoperation, you did not tell us your
original prostate size... it will be very interesting to know what is
his opinion for the need for a reoperation in your cases. After all, he
is the most experienced surgeon in Europe.

Best regards to all,

Fernando Gómez Sancha
http://drgomezsancha2.blogspot.com
Rich256 - 18 Nov 2006 14:18 GMT
> Hi again, Dick, thanks for your message inviting me to comment on this
> issue.
[quoted text clipped - 42 lines]
> Fernando Gómez Sancha
> http://drgomezsancha2.blogspot.com

Thanks for your input.  A number of us who had PVP more recently (May 5,
here) were getting concerned.

Dick
Derry - 18 Nov 2006 08:58 GMT
>Personally I would rather have three PVP's than one TUMP :-)
>It does not matter which treatment you have the prostate is still going to
>grow unless you have the radical prostatectomy.  It would appear that some
>prostates are more aggressive than others. I had read some experts who
>expected the PVP effect to last for about ten years.
>Derek.

I think a lot depends on how much prostate tissue is removed. I was
insistent that I didn't want retro so I would guess a minimal amount
of tissue was removed. My local urologist (a confirmed TURP advocate)
remarked that Muir had not removed much, but I do not know how he knew
that although I did go for a thorough checkup after some bleeding.
Anyway, it seems logical that if not much tissue is removed and the
prostate is still growing, the problem will re-occur.

A few years ago I had a good friend who was professor of urology at
Prague University. He assured me that none of these treatments "work"
(presumably meaning that they do not have a 100% success rate) and he
recommended surgical removal of the prostate. He even arranged for me
to go over there and he would do the operation, but I was not keen for
obvious reasons.  He sent me a copy of an article he had written for
an international medical magazine (I forget which now) which roundly
condemned everything except surgical removal. But I understand that is
quite a tricky operation as the surgeon is working in a confined
space.

Anyway, PVP was such a dawdle, I am quite happy to have another and
take my chances. Muir said he would do it, but things then went
silent, hence my current stirrings!<g>

Derry
fgomsan@gmail.com - 18 Nov 2006 09:26 GMT
Derry

If you did not want retro that might explain the short duration of the
benefit. I never try to preserve ejaculation, it can compromise urinary
results... still about 40-50% of patients preserve ejaculation.

Fernando G?mez Sancha
http://drgomezsancha2.blogspot.com

Derry ha escrito:

> >Personally I would rather have three PVP's than one TUMP :-)
> >It does not matter which treatment you have the prostate is still going to
[quoted text clipped - 27 lines]
>
> Derry
Jesse - 20 Nov 2006 01:50 GMT
These fascinating and informative exchanges can be read in precisely
the opposite way: tell your urologist that you want a less aggressive
PVP, avoid retro, and gamble that you won't have to be reoperated on
too soon. This route would preserve sexual function: bringing on retro
is not to be taken that easily, especially if, as some argue, "retro"
is a misnomer, and that, at least in the case of Flomax, what you get
is in fact anejaculation.

I offer this as a friendly comment and wonder what those who argue for
an aggressive approach make of this alternate interpretatiion.

Jesse

> Hi Everyone,
>
[quoted text clipped - 17 lines]
>
> Derry
Jackie Bates - 20 Nov 2006 04:14 GMT
Jesse,

Well said.  I was thinking the same thing.  If I had to go back a few years
later, but spent that time with full sexual function, I wouldn't complain.

Jackie

> These fascinating and informative exchanges can be read in precisely
> the opposite way: tell your urologist that you want a less aggressive
[quoted text clipped - 8 lines]
>
> Jesse
Rich256 - 20 Nov 2006 05:03 GMT
> These fascinating and informative exchanges can be read in precisely
> the opposite way: tell your urologist that you want a less aggressive
[quoted text clipped - 8 lines]
>
> Jesse

You are fortunate that Flowmax worked for you.  Didn't do a thing for me
except make me dizzy and sick.

With the prostate continuing to grow eventually something more
aggressive may have to be done.  But at least you can hope that
something even better comes along.
Unknown@InvalidISP.gov - 20 Nov 2006 07:06 GMT
>These fascinating and informative exchanges can be read in precisely
>the opposite way: tell your urologist that you want a less aggressive
[quoted text clipped - 3 lines]
>is a misnomer, and that, at least in the case of Flomax, what you get
>is in fact anejaculation.

I very much doubt that the retrograde ejaculation resulting from PVP
has anything to do with the anejaculation caused by Flomax. As I
understand it the retro caused by PVP is because of damage to the
bladder neck. On emission the prostatic urethra remains open at the
bladder end allowing the ejaculate to flow backwards into the bladder.

The Flomax problem is because the drug interferes with the D2
(dopaminergic type 2) receptors which are responsible for triggering
ejaculation. The reports of this problem don't say exactly what it
does to the D2 receptors (probably a competitive antagonist--my guess)
nor where these receptors are located. Since they're also involved in
parkinsonism, my guess is that they're in the brain and not local to
the prostate at all.

I agree with you as to the seriousness of each though.
 
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