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Medical Forum / Diseases and Disorders / Prostate BPH / May 2004

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Info on post PVP

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news - 20 May 2004 00:05 GMT
I have learned a lot from all you folks on this newsgroup, thank you.
I am a 51 yr old who has just had the PVP done last week.  Large medium lobe
and down the middle zapped.  The procedure went well and the only real
discomfort was the general anthesia caused me a bit of nausea later that
afternoon.  A little burning the next few days and urgency every 2 hours or
so but better flow again.
However, about 5 dyas after, I had started to get a strange sensation that
wasn't really pain but a hard to explain feeling from, I guess, my prostate
area.  This sensation only happens at the end of the urination and  is close
to the feeling you get when you tighten your sphincter but stronger.  Now, a
few days later it has turned to more a pain then not.  When the sensation is
particularly intense, I get a little bit of blood and the end of the
urination.  My Uro said it may be reaction by the prostate (something in
latin which I did not remember) and will probably go away.
What I would ask the group, has anyone experienced this and how long might
it last? Also, does the need to urinate every 2 hours eventually improve as
I am told it will?  I am up every 1.5 to 2 hours every night which is quite
a bit more than the 1 to 2 times before the PVP.
I am glad I had the operation and would certainly recommend the PVP
procedure over all others from what I experienced and researched.
Joe
nambucca - 20 May 2004 06:22 GMT
> I have learned a lot from all you folks on this newsgroup, thank you.
> I am a 51 yr old who has just had the PVP done last week.  Large medium lobe
[quoted text clipped - 17 lines]
> procedure over all others from what I experienced and researched.
> Joe

I had the same kind of effect you describe it slowly faded over the weeks
and was 100% gone by 5 months
I am now 10 months post PVP and absolutely delighted with the results and
again being able to sleep thru the night .......I did have to retrain my
body though ........by staying in bed and ignoring the call .......it took a
few days but it worked

The only downside is the months I spent on Flomax and Proscar have caused a
Hiatus Hernia as a result of the muscle relaxant effect ........so i would
caution people not to take Flomax
Gutbuster - 23 May 2004 12:15 GMT
> I had the same kind of effect you describe it slowly faded over the weeks
> and was 100% gone by 5 months
> I am now 10 months post PVP and absolutely delighted with the results and
> again being able to sleep thru the night .......I did have to retrain my
> body though ........by staying in bed and ignoring the call .......it took a
> few days but it worked

It's interesting you say you had to stay in bed and ignore the call. That
plus the fact that the work I do is normally urgent and thus I cant get to a
toilet as I am driving from one business to another MADE me "train my body"
really. I can go from 8:30AM to 4PM without getting near a toilet. By the
time I get home, I feel like I could fill a river and I pee for a real long
time but that is all I ever did apart from taking Proseren which contains
Saw Palmetto. I have been diagnosed for years and am obviously chronic, get
the pains everyone is aware of etc. I dont have, thankfully, cancer. So it
makes me wonder what can be done with the right motivation. I am not saying
it is the answer nor even an alternative for most people but I guess for
some it is worth trying. I am, however, one of those people who smoked a
packet and a half a day for over 10 years then one day said "I am not going
to smoke any longer" and threw the packet away and didnt smoke again. So,
maybe it is easier for me to say "No peeing" than some.

> The only downside is the months I spent on Flomax and Proscar have caused a
> Hiatus Hernia as a result of the muscle relaxant effect ........so i would
> caution people not to take Flomax

So many damned tablets turn out to be crap these days. Interesting that Saw
Palmetto made me feel very sick for weeks until my body got used to it and
it took a long while to note a difference but it sure is nice to sit in my
recliner of a night evenly instead of ONLY on the right side of my backside!
Samy Elterman - 23 May 2004 14:11 GMT
Why right side of...?

> From: "Gutbuster" <dont-stare@me.dot>
> Newsgroups: sci.med.prostate.bph
> Date: Sun, 23 May 2004 21:15:24 +1000
> Subject: Re: Info on post PVP
> ...sure is nice to sit in my
> recliner of a night evenly instead of ONLY on the right side of my backside!
Gutbuster - 24 May 2004 10:25 GMT
....because pain from the prostate was going - and sometimes still does go -
into the left side of my backside and into the pelvis at the front. Was like
that for many years. Imagine the difficulty when I flew "cattle class" to
Hawaii and then on from there to Vancouver on another plane. Except for the
break at Hawaii, it was 25 hours of sitting on one side of my arse just
about! Luckily I had the forethought to ask for an aisle seat!

> Why right side of...?
>
[quoted text clipped - 4 lines]
> > ...sure is nice to sit in my
> > recliner of a night evenly instead of ONLY on the right side of my backside!
Samy Elterman - 24 May 2004 18:29 GMT
Did you ever ask a neurologist about the exact cause of the sensations? Is
it possible that the original cause of the problem was the spine, which
might even have caused the "prostate problem" ?

> From: "Gutbuster" <dont-stare@me.dot>
> Newsgroups: sci.med.prostate.bph
[quoted text clipped - 17 lines]
>>> recliner of a night evenly instead of ONLY on the right side of my
> backside!
Gutbuster - 25 May 2004 14:16 GMT
No need to because those are classic prostate problems, nothing to do with
the spine.

> Did you ever ask a neurologist about the exact cause of the sensations? Is
> it possible that the original cause of the problem was the spine, which
[quoted text clipped - 21 lines]
> >>> recliner of a night evenly instead of ONLY on the right side of my
> > backside!
Sasha Gottfried - 20 May 2004 15:52 GMT
Joe and group:

This is just another example of why medical advertising needs to be held
accountable to reality.
Prostate surgery (even PVP) is invasive surgery and can take months to
recover from. I had PVP 6 months ago and am now pain free. However, for
several months following the surgery I had similar
pain......and severe urgency, making my life virtually dysfunctional for a
good part of the day. I'm sure your pain and urgency will work itself out,
but it could take a lot longer than the "one or two weeks"
that Laserscope suggests.

Marcus

> I have learned a lot from all you folks on this newsgroup, thank you.
> I am a 51 yr old who has just had the PVP done last week.  Large medium lobe
[quoted text clipped - 17 lines]
> procedure over all others from what I experienced and researched.
> Joe
nambucca - 20 May 2004 18:45 GMT
> Joe and group:
>
[quoted text clipped - 41 lines]
> >
> Marcus you know only too well that you have other health problems that
will exacerbate your bodys capacity to heal after any surgury .........its
unfair to damm PVP in the way that you do

I too had a longer recovery time but the discomfort etc was nothing compared
to the BPH problems i encountered beforehand

Since the Flomax I took for BPH for a mere 6 months has caused a Hiatus
Hernia I am madder than a hornets nest about that discomfort and ensuing
problems with all kinds of food that i experience and will have to endure
now for life .........ops for HH are extremely dangerous and not undertaken
lightly and even then leave one with problems
Sasha Gottfried - 21 May 2004 02:31 GMT
I'm not damning PVP.......however, I am highly critical of their unethical
marketing.
There are several entries on this group referring to recovery time far
beyond that advertised by Laserscope...as a matter of fact, I have pages and
pages of documentationof their less than advertised experience, many of
which have been curiously deleted from the postings here on this newsgroup.I
doubt these patients all had "other health problems." Joe asked what kind of
recovery to expect. I give him my experience and a legitimate critique of
Laserscope's overly optimistic, self-serving picture of what to expect.

Marcus

> > Joe and group:
> >
[quoted text clipped - 56 lines]
> now for life .........ops for HH are extremely dangerous and not undertaken
> lightly and even then leave one with problems
Frederic E Henzi - 22 May 2004 06:39 GMT
I had PVP a year ago and stopped light bleeding in three weeks. Like you, I
continued with a more or less stinging sensation after voiding. Strong urges
to go continued for about three month. All these negative after -effects
faded away with time and "mental re-adjustment". If I responded to every
sensation in the groin area, I could go every  hour  and void around
100-200ml, but when busy and distracted, I could hold it three and four
hours, depending on water, tea and coffee consumption. Eventually I learned
to live with the sensation to go for hours. I believe that if the bladder
isn't full, there is no real need to go. My bladder hold up to 700 ml but I
usually void 300-400 ml every 3-4 hours.

After two or three hours of driving or flying, it need a bit of time to get
the flow started, but then it flows nicely at 25- 30 ml/sec. A bit of
walking after driving  or cramped sitting does wonders to relax the bladder.

Fred Henzi

ws" <emilyrb@cox.net> wrote in message
> I have learned a lot from all you folks on this newsgroup, thank you.
> I am a 51 yr old who has just had the PVP done last week.  Large medium lobe
[quoted text clipped - 17 lines]
> procedure over all others from what I experienced and researched.
> Joe
Lee M. - 23 May 2004 16:07 GMT
Though I have had no surgical treatment yet (my PVP-capable urologist is not
sure it will help), I too have found that when kept busy, I seen to not
notice the urges and void less frequently.  OTOH, in situations where I'm
not mentally or physically preoccupied, travelling by car or plane or
sitting at work for example, I find the urge more difficult to avoid.
Despite my small prostate size (20 ml according to a TRUS), a median lobe
(diagnosed via cystoscope exam) makes voiding difficult if I wait too long
and my volume is typically no more than 4-6 ounces.

Although a post-void residual check at the uro's office reported zero, I
know that is not always the case.  The other evening, I waited a little too
long (having drank about 16 oz of water during the previous 2 hours.)  With
difficulty starting and a very weak stream, I produced only 6 oz and didn't
feel empty.  15-20 minutes later, I produced another 5 oz with a much better
stream and felt good.

> I had PVP a year ago and stopped light bleeding in three weeks. Like you, I
> continued with a more or less stinging sensation after voiding. Strong urges
[quoted text clipped - 8 lines]
>
> Fred Henzi
Jim W. - 23 May 2004 23:10 GMT
I have a similar situation but I have PVP scheduled for July if for nothing
else to get off the Flomax.  Are you on medication?  Jim W.

> Though I have had no surgical treatment yet (my PVP-capable urologist is not
> sure it will help), I too have found that when kept busy, I seen to not
[quoted text clipped - 28 lines]
> >
> > Fred Henzi
Lee M. - 23 May 2004 23:58 GMT
I have tried saw palmetto & beta sistosterol without effect.  Also tried
Flowmax and Uroxatrol, also no effect.  Latest thing was Detrol LA.  Took it
for a  month but the effects were minimal.  I may give it one more try after
see my uro next month.  Although subjectively it didn't seem to make a
difference, I recorded my voiding and fluid intake on 3 different Saturdays
and the day while on Detrol showed the best results.

> I have a similar situation but I have PVP scheduled for July if for nothing
> else to get off the Flomax.  Are you on medication?  Jim W.
[quoted text clipped - 39 lines]
> > >
> > > Fred Henzi
Gutbuster - 24 May 2004 10:27 GMT
> I have tried saw palmetto & beta sistosterol without effect.  Also tried

I have read a report saying that there is no clinical evidence that Saw
Palmetto does any good. I also know it did me good.

What I suggest to you is check the dose of it that you are getting in
whatever it is you are taking. The tablet form I take is called Proseren and
I take 2 tablets each morning which is about 1500 grams of the stuff. I was
taking 3 but I couldn't stomach it after about a year and had to cut back. I
have even gone off them to check how things go and within a week am back to
the old pain days. Maybe your dose was too low for you. IMHO the dose varies
per person.
Bill Hale - 24 May 2004 20:02 GMT
> > I have tried saw palmetto & beta sistosterol without effect.  Also tried
>
[quoted text clipped - 8 lines]
> the old pain days. Maybe your dose was too low for you. IMHO the dose varies
> per person.

My experience:  Saw Palmetto, no help.  Beta Sisterol -- helped for about
a year.  Then I did a PVP.  Bill Hale
Frederic E Henzi - 25 May 2004 19:02 GMT
> Despite my small prostate size (20 ml according to a TRUS), a median lobe
> (diagnosed via cystoscope exam) makes voiding difficult if I wait too long
> and my volume is typically no more than 4-6 ounces.

On me, DRE indicated a prostate of 20 ml, a quick ultrasound through the
abdomen 90 ml, and an ultrasound through the rectum, 40 ml. Obviously, size
determination is rather vague.
For 12 years I had progressively worsening voiding. I tried drugs and saw
palmetto but improvements were slight and temporary.

BPH is a mechanical constriction and, in my humble opinion,  only a
mechanical intervention would solve it. As an old mechanical engineer, I'm
likely totally biased towards mechanical fixes. I just can't accept that a
drug can selectively shrink the prostate without affecting other related
organs.

After a long research period, I had PVP done a  year ago. This has solved
all my peeing problems and made my retirement enjoyable again.
I just came back from three weeks in Europe. There was a two ten hour flight
and nine hours of jet lag and a radical change in routine including plenty
of espresso and wine. I had no voiding problems whatsoever. I whish all BPH
had the same results as I have.

Fred Henzi
Liz - 25 May 2004 19:10 GMT
> > Despite my small prostate size (20 ml according to a TRUS), a median lobe
> > (diagnosed via cystoscope exam) makes voiding difficult if I wait too long
[quoted text clipped - 11 lines]
> drug can selectively shrink the prostate without affecting other related
> organs.

I just started proscar 10 days ago and it shrinks other stuff besides the
prostate.

> After a long research period, I had PVP done a  year ago. This has solved
> all my peeing problems and made my retirement enjoyable again.
[quoted text clipped - 4 lines]
>
> Fred Henzi
Samy Elterman - 25 May 2004 22:43 GMT
Liz,
Is it shrinking your breasts? Something else?

> From: "Liz" <Liz@nospam.com>
> Organization: Comcast Online
> Newsgroups: sci.med.prostate.bph
> Date: Tue, 25 May 2004 18:10:30 GMT
> Subject: Re: Info on post PVP

> I just started proscar 10 days ago and it shrinks other stuff besides the
> prostate.
Liz - 25 May 2004 23:02 GMT
something else

> Liz,
> Is it shrinking your breasts? Something else?
[quoted text clipped - 7 lines]
> > I just started proscar 10 days ago and it shrinks other stuff besides the
> > prostate.
Frederic E Henzi - 26 May 2004 00:57 GMT
The suspense is killing me. Are there two of them?

Fred Henzi

> something else
>
[quoted text clipped - 10 lines]
> the
> > > prostate.
Liz - 26 May 2004 04:38 GMT
No, let me clear up some possible confusion
I am not using my real login name.

> The suspense is killing me. Are there two of them?
>
[quoted text clipped - 14 lines]
> > the
> > > > prostate.
Samy Elterman - 26 May 2004 22:02 GMT
But we still don't know what else besides the prostate, that proscar shrunk.
Is there a reason that you won't say?

> From: "Liz" <Liz@nospam.com>
> Organization: Comcast Online
[quoted text clipped - 26 lines]
>>> the
>>>>> prostate.
Liz - 26 May 2004 22:40 GMT
Just embarrassment, the two round things and the long thing.
Perhaps it is my imagination though.

> But we still don't know what else besides the prostate, that proscar shrunk.
> Is there a reason that you won't say?
[quoted text clipped - 29 lines]
> >>> the
> >>>>> prostate.
Samy Elterman - 27 May 2004 03:32 GMT
It didn't happen with me or anyone that I've heard of, so it's probably
imagination.

> From: "Liz" <Liz@nospam.com>
> Organization: Comcast Online
[quoted text clipped - 39 lines]
>>>>> the
>>>>>>> prostate.
Ron - 27 May 2004 03:42 GMT
I just read this in the NY Post - will probably be in tomorrow's paper.

> May 26, 10:13 PM EDT
>
[quoted text clipped - 114 lines]
>
> ---
Jack - 29 May 2004 16:51 GMT
Ron

Saw a similar newspaper article in the Washington Post yesterday.

I remember Gen. Norman Shwarzkoff (sp?) having a PSA < 2 but had a
suspicious DRE that led to a biopsy that was positive.  He then had a
prostatectomy.  I believe he was in his 50's when he had it done.

My personal belief is that the PSA numbers is most valuable when you
look at year over differences.  Any increase >1 from last year's
number should be considered as a warning.  Of course prostatitis could
cause a jump much greater than one, so if the increase is greater than
one, without any DRE change then the PSA should be done again in 6 to
8 weeks.  If the increase stays >1 then a biopsy should be done.  Also
if the increase is <1, but the DRE indicates a change in the texture
of the prostate a biopsy should be done.

In my case, and in a number of others that I know, as we get older the
PSA value increases.  Many doctors think increase is caused by the
growth of the prostate as we get older.  Again in my case before my
PVP last year my PSA was 4.7, growing slowly from 2.3 over 12 years.
After the PVP it dropped to 3.1 and was 3.4 last month.

The PSA test is just one indicator of the possibility of prostate
cancer.  We are all different in our make up.  Some, like Schwarzkoff,
can have prostate cancer with a low PSA and others in this group have
said they have had PSA values of 10 with the prostate biopsy being
negative.  Also the prostate cancers can go from being very slow
growers to being aggressive.  Only a biopsy can tell the difference.

Jack

> I just read this in the NY Post - will probably be in tomorrow's paper.
> >
[quoted text clipped - 114 lines]
> >
> > ---
Ron - 29 May 2004 21:57 GMT
Jack,
My PSA also lowered from each of my 2 PVPs. I've heard that scientists are
now studying how to test for the 15% types that get past the test as well as
separate out the aggressive types from the very slow growing types of
cancer.
Ron

> From: "Jack" <jrcomer@erols.com>
> Newsgroups: sci.med.prostate.bph
[quoted text clipped - 200 lines]
>>>
>>> ---
george - 27 May 2004 20:05 GMT
Had PVP seven months ago and my results are pretty much the same as
Frederic's including the fading urgency feeling over the first couple of
months.  Urgency problem is now gone completely.
I also agree with his point on prostate obstruction being a mechanical fault
best cured by mechanical means (removal).  Went the flomax route and got
only short term temporary relief.
By the way I believe Frederic and I used the same doc (Dr Laube), this guy
is super.  I am now finally enjoying retirement, something I could not do
with the BPH monkey on my back.

best of health to all,
george

> I had PVP a year ago and stopped light bleeding in three weeks. Like you, I
> continued with a more or less stinging sensation after voiding. Strong urges
[quoted text clipped - 43 lines]
> > procedure over all others from what I experienced and researched.
> > Joe
 
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