Medical Forum / Diseases and Disorders / Prostate Cancer / February 2007
Impotence & Incontinency
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Lon - 10 Feb 2007 00:37 GMT If the reason that some opt for one procedure over another is to prevent impotence or incontinency, I suspect that there is a definite risk of that happening irrespective of the procedure. Shouldn't the main concern be to get rid of the cancer?
John Loomis - 10 Feb 2007 02:09 GMT Hi Lon, The main concern is to rid the body of cancer or minimize its effects on the body. In the process of doing either of these the risk of ED and or incontinence as well as other ailments are present. You can talk with your Dr. and depending on your staging,age, or prostate cancer agressivcness choose a therapy that matches your condition. No Dr. can guarantee either potence or continece although they have a pretty good idea of what they can do. Nerve sparing in radical prostatectomy is a factor with ED. If the Dr. sees the nerves are cancerous he may remove one or both...... If one is spared erectile function is "highly possible" Radiation, (EBRT) Brachy(seeding) also have effects on ED and continence. Hormone therapy can /will effect Libido and effect Erectile Function.... There are many ways to combat these effects, and yes the main concern is to minimize the cancer... John Loomis
> If the reason that some opt for one procedure over another is to > prevent impotence or incontinency, I suspect that there is a definite > risk of that happening irrespective of the procedure. Shouldn't the > main concern be to get rid of the cancer? safire - 10 Feb 2007 09:33 GMT > If one is spared erectile function is "highly possible" CU Medical Guide says that 60 to 90% of patients undergoing RP suffer from ED. It notes that the nerves involved may heal, though very slowly. Recovery may take up to two years and is unusual before 3 months after surgery. CU also cites a British study that says regularly doing Kegel exercises generally helps against ED; that report does not specifically address ED caused by RP.
http://adam.about.com/reports/000033_10.htm
This source says that sexual impairment (i.e. impotency) risk is only 10% better if both nerves are spared and 7% if one nerve is spared (66% if no nerve spared, 59% unilateral, 56% bilateral). Medicine is not supposed to help in case both nerves are not spared for patients over 55.
http://www.henryfordhealth.org/body.cfm?id=46058
Dr. Menon, on the other hand, claims that 82% of his institute's patients 60 years of age had return of sexual function at six months. Not sure whether he is much better at sparing nerves than others, but the Adam numbers suggest that that by itself doesn't make that much of a difference.
The Adam report puzzles me. Are the nerves not essential? Can you, at least in theory, recover even if both nerves are not spared? If so, does doing Kegels (presumambly to stimulate blood flow) speed up recovery? Is Viagra or Cialis potentially helpful if at least one nerve is spared, as in my case?
John Loomis - 10 Feb 2007 19:13 GMT Hello Safire, I had Radical Prostatectomy in 1999. I was also fearful of the effects that may appear after the prostate and cancer was removed. I was greatful that the cancer was taken out and then I needed to try to regain any salvageable functions. I was totally incontinent in about 3 weeks...... I also had problems with erectile function since one nerve was spared. With the help of the "pump", and injection use for a few months, and then slight success with viagra, and after about 1.5 years to 2 years, I am up and running. Now in 2007, a light 1/3 of a 100mgs pill of viagra and 15 minutes later.....I feel 100% erectile function. It takes time, and work at it..... John Loomis
>> If one is spared erectile function is "highly possible" > [quoted text clipped - 25 lines] > recovery? Is Viagra or Cialis potentially helpful if at least one nerve is > spared, as in my case? John Loomis - 11 Feb 2007 01:01 GMT That is (continent) grammar
> Hello Safire, > I had Radical Prostatectomy in 1999. [quoted text clipped - 3 lines] > regain any salvageable functions. > I was totally continent..........
in about 3 weeks......
> I also had problems with erectile function since one nerve was spared. > With the help of the "pump", and injection use for a few months, and then [quoted text clipped - 34 lines] >> recovery? Is Viagra or Cialis potentially helpful if at least one nerve >> is spared, as in my case? callalily - 11 Feb 2007 23:27 GMT Dear Safire,
[Any relation to the writer?]
Welcome to the club. Hope I could be of some use.
CU Medical Guide says that 60 to 90% of patients undergoing RP suffer
> from ED. It notes that the nerves involved may heal, though very slowly. > Recovery may take up to two years and is unusual before 3 months after > surgery. CU also cites a British study that says regularly doing Kegel > exercises generally helps against ED; that report does not specifically > address ED caused by RP. What exactly is the CU Guide? Consumer Reports? Columbia U? Please explain. (BTW, Consumer Reports does rate treatments, medicines and "supplements". It might be worthwhile. Am going to revisit it)
Yes, it takes time, but the nerves do heal. My husband is 15-mos post- op and his erectile function has improved noticeably in the last few mos. And the numbers you cite for men suffering from ED look credible to me. If you have ED after RP, know that you are not alone and you're perfectly normal.
Do the Kegels. Never hurt anybody. But I'm pretty sure they are not very helpful in the erectile-function improvement.
> http://adam.about.com/reports/000033_10.htm > > This source says that sexual impairment (i.e. impotency) risk is only > 10% better if both nerves are spared and 7% if one nerve is spared (66% > if no nerve spared, 59% unilateral, 56% bilateral). Medicine is not > supposed to help in case both nerves are not spared for patients over 55. First of all, who is the authority for the ADAM medical encyclopedia? I like "about.com", but they are not a teaching hospital. You have to be careful in whom you trust. About nerve sparing, it is a complicated affair. One doctor who does this told me it depends not only on whether the nerve was spared, but *how* the nerve was spared, whether it was cauterized, etc. My husband had his nerves spared and it didn't seem to help much.
Medicine -- if you mean Viagra & Co., they will not work if the erectile nerves are too badly damaged. This happens in many cases, but there are still ways to have a good sex life and an erection, if that's what you want. And they are working on a gene therapy which has gotten a lot of publicity. It might help men whose nerves are damaged in the sense that they would have to go to the doctor once or twice a year to get a shot. After that, their EF whould be normal. (No further shots needed until the next 6 mos-1 yr.) However, this is still *in progress*, we don't know what will happen!
> The Adam report puzzles me. Are the nerves not essential? Can you, at > least in theory, recover even if both nerves are not spared? > If so, does doing Kegels (presumambly to stimulate blood flow) speed up > recovery? Is Viagra or Cialis potentially helpful if at least one nerve > is spared, as in my case? Of course I am no expert, but I don't think you can have natural erections in you have no nerve function at all in that area. Viagra can help a person who has some erectile nerve function have sex,, i.e., get an erection, but **it does not help "rehabilitate" the person's own natural erectile function. I don't think it's a bad idea to take one of these meds (of course, with your doc's approval). My husband has been on Cialis for a couple of months and I think it might have helped. But we had to ask for it. And, I think the PDE5's work better once the nerves have healed somewhat.
I don't think doing Kegels helps in increasing blood flow to the genitals, which is important. I read that a lot of men use pumps, or vacuum erection devices, to "exercise" their penis. Or, get some injections.
I don't know why you are asking all of us this. Where is your doctor in this picture?
It sounds to me like you are post-op and concerned about your future sex life, naturally.
**The first thing you should do is go to "penile rehab". Find a doctor who specializes in ED! Although there's not a whole lot of evidence out there, penile injections for ED have been shown to boost a man's natural erectile function if started early**. And, you can have a sex life in the meantime.
Run, don't walk.
If you need a referral for an ED doc, try sexhealthmatters.org. They have the best. Or try the Urology Channel, (urohealth.org?) use "doctor finder", but click on "practice details" and find a urologist who's number-one interest is ED.
Good luck to you.
Leah
callalily - 11 Feb 2007 23:35 GMT > Dear Safire, Forgot to tell you the most important thing. If you want up-to-date, reliable information about Pca, go to "endotext.org". This is like an encyclopedia for practicing physicians but it is understandable. And they give you facts, not opinions. I kick myself for not remembering to go there more often.
[If you go to this site, you have to click on male reproductive endocrinology and search pca, I think.]
> Good luck to you. > > Leah RML - 12 Feb 2007 10:13 GMT "Viagra..., but **it does not help "rehabilitate" the person's own natural erectile function. "
Please point us to research which supports the above contention.
Many docs are providing daily or every other day Viagra for 2 week periods after RP, for this exact reason.
RML
callalily - 14 Feb 2007 02:20 GMT Dear RML,
> "Viagra..., but **it does not help "rehabilitate" the > person's own natural erectile function. " [quoted text clipped - 5 lines] > > RML I had done a lot of research on this subject and written a whole lot about "penile rehab" starting last November. (See "Sex After Surgery", (11/11/06) and "Sex After Surgery - Update" (11/13/06). In the latter msg, I presented some evidence in response to a question which was basically the same as yours. I always rely on credible sources, be they hospitals, people, journals, etc.
Apparently, people found the above posts useful, because I got a lot of good feedback about them. So, I would like to provide an update on this subject, very briefly.
"Penile rehab" is a nascent field -- there's not a whole lot known about it. However, when I did my research back in the fall, I did not come across a single article that said Viagra and other PDE5's worked to restore natural erections. There was one report based on a study done by the mfr which I discounted, and another study which scientists found to be flawed. There was (almost) no positive info relating to Viagra and "penile rehab". (It was shown to help preserve smooth muscle tissue.)
You can't prove a negative, so the burden would be on you and whoever believes Viagra to be effective for restoring EF to present some evidence of this. As a matter of fact, I have posted this msg or variations of it everywhere and invited people to submit contrary info and I haven't gotten anything.
However, things do change quickly in this arena, and so I did an updated search of this topic yesterday and came up with certain promising, and maybe even probative, articles. I still have to digest them. I can't really do any heavy thinking right now because my husband's being in medical limbo is making me tired, depressed and muddled. So for the moment, I will have to think "lite".
But here is a summary from the Johns Hopkins website:
"A relatively new strategy in clinical management after radical prostatectomy has arisen from the idea that *early induced sexual stimulation and blood flow in the penis may facilitate the return of natural erectile function and resumption of medically unassisted sexual activity. **There is an interest in using oral PDE5 inhibitors for this purpose, since this therapy is noninvasive, convenient, and highly tolerable. However, while the early, regular use of PDE5 inhibitors or other currently available, "on-demand" therapies is widely touted after surgery for purposes of erection rehabilitation, such therapy is mainly empiric. Evidence for its success remains limited."
I am not against anybody taking Viagra after surgery. I would do the same. The only point I was really trying to make is that if you end up in the subset of men who have sustained serious nerve damage, I don't think Viagra will do anything for you, either to get you an erection or to restore long-term natural EF. And you don't really know which category you'll end up in, in spite of what the doctor has told you about nerve sparing. That's why some people consider it playing it safe to try early injections or VED, which I think have been found to be somewhat effective (not by everybody).
I am just trying to promote good clinical practice offered by such hospitals as Sloan-Kettering and Columbia Presb. in my area. As Tom R. wrote here, after he had surgery w/Dr. Eastham st MSK, he was immediately scheduled for a 6-week follow-up to examine his sexual function. Both hospitals I mentioned have experts in "sexual medicine" on board who deal w/sexual function and "penile rehab". So I suggest, that if a man does not regain EF after 2 mos, he should see an ED specialist because it's always better to intervene earlier than later.
There's also evidence that a lot of men who do not respond to Viagra at first will respond later when their nerves have had a chance to heal (for example, at 15 mos.) (Dr. Samadi mentions 9 mos. as a ballpark) I suggested to my own husband that we should add Cialis to his regimen of injections for ED about a year post-RP because there wasn't really anything to lose (unless you have a heart problem, I think). We tried it and I don't know if it has worked -- always hard to distinguish a placebo effect. But, as I have told everybody here, my husband seems to have miraculously regained his erectile function at 14 mos-post op (and now I can attest that it was "replicated"). It seems like the wires are starting to function.
Anyway, I already have a stack of updated articles on sexual rehab sitting right by me, so I will try to summarize them quickly to see if anything is new. (This is just a quickie.)
1) There is a study ongoing on JH to test the effectiveness of a nightly dose of Vit. V on men who've had nerve-sparing laparscopic RP.
2) Study by Donatucci, et al, Duke U., 11/06. "Recovery of Sexual Function after PC Treatmnent". Bottom line: they believe "No standard treatment or prophylaxis exists for post-tx ED. **Neuroprotective and regenerative therapies, including the immunophilin ligands, hold promise to reduce morbidity of localized pca therapy". Amen.
3) "Update on EF in PCa Patients", Current Opinion in Urology, 16(3); 186-195, May 'O6. Summary: data shows that pharm. rehab programs provide a higher rate of EF following RP. "Both intracavernosal and intraurethral approaches are thought to provide integral roles for the maintenance of sexual function in men undeergoing PC therapy". Notice the absence of PDE5's. It says that they, injections and VED's have all been reported "in a positive light". That's all.
4) Article from Cleveland Clinic, "Early Combination Therapy: intracavernosal injections and sildenafil following RP increases sexual activity and the return of natural Erections" Int. Journ. of Impotence Research, Feb. '06. Combo of injections and Viagra seemed to work.
5) "Can an erectogenic pharm. regimen after RP improve post-op EF?" (Nature Clinical practice Urology (2006) 3, 72-73, Eardley, I.) Recovery of EF may take 18 mos or even longer, even in men who've had bilateral NS. ** In those men who do develop Ed, a number of factors have been implicated, including "unrecognized nerve injury, arterial injury, and veno-occlusive dysfunction caused by structural alterations in the cavernosal smooth muscle." **These can be discovered by Doppler Ultrasound, done 6 mos. after surgery.
6) Dr. Mulhall (of MSK and NY Hosp.) wrote a summary for the Sexual Med. Soc. of N.A., 2005 Fall meeting. He concludes that "there is accumulating evidence that the presence of blood flow abnormalities in the penis after RP is a predictor of long-term ED after RP".
Also from above: animal studies have shown that certain compounds can help in *"erection nerve protection". A group of rats who had undergone "nerve crush Injury" were given a combination of sildenafil and FK506 (an immunosuppressant) after cavernosal nerve injury had the "maximum protective effect on erectile function recovery."
And Eureka!
"Sildenafil alone also appeared to exert a protective effect on EF". (In rats, of course.)
Hope this helps.
Leah
safire - 14 Feb 2007 13:32 GMT > Apparently, people found the above posts useful, because I got a lot > of good feedback about them. And this will continue, Leah. Your contribution is extremely helpful. Thank you.
Leonard Evens - 10 Feb 2007 02:12 GMT > If the reason that some opt for one procedure over another is to > prevent impotence or incontinency, I suspect that there is a definite > risk of that happening irrespective of the procedure. Shouldn't the > main concern be to get rid of the cancer? You are certainly right about what the main concern should be. You are also right that all methods of treating early prostate cancer in an attempt to cure it have similar side effects. But they do differ in how likely a given side effect may be. But other things are also important. Age, in particular plays an important role. For example, for relatively young men, a skilled surgeon can do about as well at preserving erections as can a radiation oncologist, but for men over 70, the risk of impotence after radiation is much less than the corresponding risk after surgery. The important thing to know is what the risks are for you specifically under different treatments. Generalities about all men may not be relevant to your case.
I.P. Freely - 10 Feb 2007 03:21 GMT > If the reason that some opt for one procedure over another is to > prevent impotence or incontinency, I suspect that there is a definite > risk of that happening irrespective of the procedure. Shouldn't the > main concern be to get rid of the cancer? You'd think so, wouldn't you? For most people that's true, but there really are some men who won't risk their erections for anything.
For the rest of us, treatment choice is mainly about optimizing the dizzying array of benefits and side effects and their likelihoods according to our personal priorities. In fact, some leading oncologists consider some treatments so close in benefits that they advise us to choose between them based on their side effects or deliberately postpone treatment until we have symptoms. There are few easy choices in this field, and the easiest choices often occur in the worst cases.
I.P.
Paul - 10 Feb 2007 19:15 GMT >> If the reason that some opt for one procedure over another is to >> prevent impotence or incontinency, I suspect that there is a definite [quoted text clipped - 13 lines] > >I.P. Ah symptoms. In all of my fervor to read here, I have failed to asked just what are the symptoms? My only discomfort is a post ejaculation tightness (sorry, only way to describe it) that doesn't feel normal.
I.P. Freely - 10 Feb 2007 22:04 GMT >> treatment choice is mainly about optimizing the >> dizzying array of benefits and side effects and their likelihoods [quoted text clipped - 6 lines] > just what are the symptoms? My only discomfort is a post ejaculation > tightness (sorry, only way to describe it) that doesn't feel normal. I was referring to symptoms across the board -- all the lists and likelihoods of symptoms and side effects that may occur with all the various treatments and lack thereof. They fill books, and it's unclear to us what you're asking about. At its most specific, my comment above referred to one's timing of and selection from the long ADT (hormone therapy) menu when one's first attempt at curing his cancer has failed, i.e., it's bAAaaack. What ADT protocol do we want, and do we accept it right after RP or RT just in case, when a PSA increase indicates biological failure, when physical symptoms of metastases become noticeable, or when they get bad enough to demand further treatment? More generally, some physicians equate RP and RT prognoses closely enough that they often advise choosing between them based on the patient's side effect priorities, which include symptoms.
Confused even more? Good; I'd be worried if you thought I had actually answered anything specific with that necessarily philosophical response.
I.P.
Paul - 11 Feb 2007 17:52 GMT >>> treatment choice is mainly about optimizing the >>> dizzying array of benefits and side effects and their likelihoods [quoted text clipped - 25 lines] > >I.P. Cofused? Very, and easily done at this point. I've got a lot to learn and maybe in a very short period of time....
I.P. Freely - 11 Feb 2007 23:55 GMT > I've got a lot to learn and maybe in a very short period of time.... Even way late in this sorry game, there's always time to read a PC book or 6. The PC learning curve is much like some contrarian roller coaster that starts with the downhill part and climbs the big, clackety hill *after* the rush. You'll learn *so* much in that first intense week of full-time reading that you'll almost feel like you actually *know* something about PC when you finish, and your PC isn't going anywhere in a week.
I.P.
Alan Meyer - 10 Feb 2007 06:23 GMT > If the reason that some opt for one procedure over another is to > prevent impotence or incontinency, I suspect that there is a definite > risk of that happening irrespective of the procedure. Shouldn't the > main concern be to get rid of the cancer? That's my view. You can love your wife and even have some kind of sex with no erectile function - but only if you're still alive.
Alan
Steve Kramer - 10 Feb 2007 11:50 GMT > If the reason that some opt for one procedure over another is to > prevent impotence or incontinency, I suspect that there is a definite > risk of that happening irrespective of the procedure. Shouldn't the > main concern be to get rid of the cancer? To you, apparently. To me, yes. And, of the several hundred who have passed by here in the last few years, almost to a man, their priorities were 1) Death, 2) Incontinence, and 3) Impotence or 1) Death and the other two reversed.
However, there has been the occasional man who preferred sex over life or dreaded incontinence more than death. These have been manifested in statements such as, "I do not want to live another six years if it means..."
I feel sorry for these men. It means, IMO, that they have made decisions in their lives that have left them with little "life" left to counteract the terrible effects of losing one's 'manhood'. I think if I started subtracting some things from my life; my job, my wife, my friends, my children, my grandchildren, my truck, ..... I could start thinking in those terms.
 Signature PSA 16 10/17/2000 @ 46 Biopsy 11/01/2000 G7 (3+4), T2c RRP 12/15/2000 G7 (3+4), T3cN0M0 Neg margins PSA .1 .1 .1 .27 .37 .75 EBRT 05-07/2002 @ 47 PSA .34 .22 .15 .21 .32 Lupron 07/03 (1 mo) 8/03 (4 mo), 12/03, 4/04, 09/04, 01/05, 5/05, 10/05, 2/06, 6/06 PSA .07 .05 .06 .09 .08 .132 .145 Casodex added daily 07/06 PSA <0.04 Non Illegitimi Carborundum
Ron B - 10 Feb 2007 19:26 GMT I agree with the guys who gave you great advice...
the cancer, for me, was the primary concern.
The other things will work themselves out.
All the very best,
Ron B.
Chicago
RRP in 3/05
Doug Taylor - 12 Feb 2007 14:20 GMT >I feel sorry for these men. It means, IMO, that they have made decisions in >their lives that have left them with little "life" left to counteract the >terrible effects of losing one's 'manhood'. I think if I started >subtracting some things from my life; my job, my wife, my friends, my >children, my grandchildren, my truck, ..... I could start thinking in those >terms. I'm one of those guys, and I feel sorry for people who can't accept their mortality. Everybody dies. If you haven't figured that out yet, best you get moving on it, because it will bite you in the a.s, just around the corner.
I have my own thoughts about people who choose life at any cost over quality of life. For once I'll be circumspect and hold my tongue, inasmuch as that is THE most personal decision any human has, and to each, his or her own.
I will point out, having lived through the spectre of grandparent who spent that last 10 years of his life in constant pain (not from PCa), addicted to painkillers, and a misery to himself AND his loved ones, there are worse things in life than going when it is your time, at peace with yourself, with a decent quality of life. Such as prolonging the inevitable at any cost, including your own comfort and those whom you love.
Tough choice. Always personal. So keep your value judgments to yourself, or you'll just start ANOTEHR flame war. And we all are, or should be, sick of them by now.
3Putt from South Carolina - 12 Feb 2007 23:04 GMT > I'm one of those guys, and I feel sorry for people who can't accept > their mortality. Everybody dies. If you haven't figured that out yet, [quoted text clipped - 17 lines] > yourself, or you'll just start ANOTEHR flame war. And we all are, or > should be, sick of them by now. Well put. My wife and I are both cancer survivors. We also have our one and only 2 1/2 year old grandson that bring new joy to our lives.
alva36@gmail.com - 10 Feb 2007 21:42 GMT > If the reason that some opt for one procedure over another is to > prevent impotence or incontinency, I suspect that there is a definite > risk of that happening irrespective of the procedure. Shouldn't the > main concern be to get rid of the cancer? I was Dx'd at age 61, put on HDT immediately, 6 months later had 5 weeks of external beam and then HDR brachy. SEs played a large part in my choice. Was never incontinent and never suffered ED (no ejaculate, of course, but everything else happened in the normal sequence). Libido is another story - it's very strange: I wasn't interested in sex at all, but didn't care that I wasn't interested. Every great once in a while I'd think about engaging in it just to see if I could. Very strange.
-Gordy
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