Medical Forum / Diseases and Disorders / Prostate BPH / January 2004
PVP at Haywards Heath Jan.13 i.e. PVP+3
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Maurice Batey - 16 Jan 2004 22:15 GMT Had PVP at the Ashdown Nuffield Hospital at Haywards Heath, UK on Tuesday, Jan.13th, under Tim Larner. Herewith summary of events:
Tues.13/1/04:
10.35 Checked in - having already undergone pre-admission tests last month. 14.00 - 15.30**: PVP (general anaesthetic) 16.00 Back in room. Bladder painful (see ** below). 2 CODYDAMOL tablets cooled that down within an hour. Oxygen mask (until 17.50), saline drip (until19.40), catheter until next morning. 17.50 Enjoyed 2 large salmon sandwiches & salad, + banana & hot choc. No pain or even discomfort - not even from catheter, surprisingly. Started reading Ludlum novel 'Treveyne'. 22:45 Hot chocolate, lactulose, + assortment of pills/tablets (incl sleeping pill).
Wed. 14/1 (PVP+1)
07.50 Cup of tea. No pain - not even discomfort (even from catheter). 08.15 Breakfast 09.30 Catheter out after Larner' visit. Hardly a twinge, surprisingly. Hadn't looked forward to catheter, but it wasn't really a problem (except need to avoid rolling over on wrong side!). And it was nice to be able to knock bedtime drinks back without having to get up during the night! 10.15 Hot bath! 11.05 Cranberry juice 11.25 First post-PVP pee (300ml)! Dark pink, but good flow and no hesitation. Little discomfort, surprisingly. 12.15 3-course lunch 12.30 2nd pee (400ml). Still quite pinky. No discomfort. Checked no residual (ultrasound). 13.30 Left hospital. Walked to HH railway station (10 mins) 14.05 Caught train to Southampton. determined not to use train WC! 15.40 Arrived Southampton. Just held on long enough to get to WC. Flow not as good as first 2 pees, though. Disappointing... 17.00 Home. Already peeing clear urine - and has stayed that way, except for the odd drop of blood from penis tip at first.
They started me on 25mg VIOXX (Rofecoxib) anti-inflammatory tablets (1/day), and 500mg Ciprofloxacin (2/day) and sent me home with 7 days' and 14 days' supply respectively.
Overnight at home was up every 1-2 hours, and flow was even worse - almost back to pre-PVP - in fact the first (01.30) I thought I had gone into full retention - scary. I hope this is quite temporary - presumably due to swelling due to traumatisation by instruments.
PVP+2 (Thurs)
In the morning I felt so well - no discomfort even - that I played snooker for 1.5 hours, then had a lazy afternoon. No toilet calls from bladder between 10.30 and 12.45, although when I got home and started thinking about it, all of a sudden there was a strong urge to go and I hardly made it to the WC in time! Felt perfectly normal the rest of the day. No urgent bladder calls... Kept off alcohol, although no one had said I should. Just thought it a good idea pro tem. Was it?! Overnight, up 3 times (not due to urgency, but because something woke me up and there was some feeling of something in there, so went out of habit, I suppose). But flow still pathetic.
PVP+3 (Friday)
Felt entirely normal apart from much discomfort overnight due to bowels still gummed up from the general anaesthetic. (This has been by far the biggest post-op nuisance!) Amazingly, still no discomfort peeing, bearing in mind all the things that had gone on down there during the op, including destruction of that part of the urethra within the prostate., and (see ** below). Also, at last - after downing several dollops of lactulose - Mafeking has finally been relieved... However, flow is still *abysmal*. Has anyone else had this in the first few days? Is it simply some swelling somewhere that will soon go away, or could it be some debris that is partially blocking flow (which was quite good for the first 2 pees on PVP+1)? WC visits during the day have been more than pre-PVP, as drinking water more often; about 2-hourly, but if ignore gentle 'WC visit indicated' signals until the 'Quick, get in there' signal then there isn't much time to spare!
So, to summarise so far, an incredibly fast and painless recovery, but - so far - with a dismal flow rate.
Will post further if anything changes (hopefully improvement in flow...). (Would, welcome others' thoughts on latter.)
--------------------- ** Before doing the PVP, Larner did his routine check of the bladder, where he found 3 small 'pre-tumour's, which he removed using 'diathermy', taking samples for biopsy. He said they were the benign kind that grew outwards rather than into the flesh, but that I would need to have regular checks as they tended to grow back (like basal cell carcinomas presumably) - or perhaps he was just saying that to stop me panicking. Is a bit scary... Anyway, that presumably explains why the op took so long (35 mins for the PVP, 55 for the bladder), and why the bladder hurt afterwards. -----------------------
Maurice Batey (Retired in Hampshire, UK) (age = 70, but still quite fit!)
http://www.maurice.eurobell.co.uk
(Change "no.spam" to "." in E-mail address.)
Derry Argue - 16 Jan 2004 22:50 GMT > Enjoyed 2 large salmon sandwiches Good report, Maurice, but I see you live dangerously!<G> Presumably, you have seen the news about salmon since!:(
Sorry about the poor flow. All I can say is that I kept soft drinks handy and kept sipping and had no problems. Flow has slowed from "fire hose" to normal for me since but that is to be expected.
Good luck.
Derry
Sasha Gottfried - 16 Jan 2004 23:33 GMT Hi,
I'm 2 months post PVP and it is 3 PM here in California. My mornings and early afternoons can be quite dysfunctional......minimal, painful stream, and urgency. It is just now that I can sit down and calmly report this as I often spend much of the day in virtual misery. I attribute this to bowel movements inflaming the already sore prostate (they are quite proximate and share the same nerves). As soon as the rectum relaxes (can take 6-8 hours) I get a decent painless flow with less urgency. You might consider this in assessing your problem. A couple of Extra Stregnth Tylenol seem to ease the situation. Occasionally, a perfect, stress-free bowel movement gets the flow up and the urgency down, earlier in the day.
Certainly not the "one or two week" back to normal scenario presented by Laserscope.
Keep us informed.
Good Luck,
Marcus
Had PVP at the Ashdown Nuffield Hospital at Haywards Heath, UK on Tuesday, Jan.13th, under Tim Larner. Herewith summary of events:
Tues.13/1/04:
10.35 Checked in - having already undergone pre-admission tests last month. 14.00 - 15.30**: PVP (general anaesthetic) 16.00 Back in room. Bladder painful (see ** below). 2 CODYDAMOL tablets cooled that down within an hour. Oxygen mask (until 17.50), saline drip (until19.40), catheter until next morning. 17.50 Enjoyed 2 large salmon sandwiches & salad, + banana & hot choc. No pain or even discomfort - not even from catheter, surprisingly. Started reading Ludlum novel 'Treveyne'. 22:45 Hot chocolate, lactulose, + assortment of pills/tablets (incl sleeping pill).
Wed. 14/1 (PVP+1)
07.50 Cup of tea. No pain - not even discomfort (even from catheter). 08.15 Breakfast 09.30 Catheter out after Larner' visit. Hardly a twinge, surprisingly. Hadn't looked forward to catheter, but it wasn't really a problem (except need to avoid rolling over on wrong side!). And it was nice to be able to knock bedtime drinks back without having to get up during the night! 10.15 Hot bath! 11.05 Cranberry juice 11.25 First post-PVP pee (300ml)! Dark pink, but good flow and no hesitation. Little discomfort, surprisingly. 12.15 3-course lunch 12.30 2nd pee (400ml). Still quite pinky. No discomfort. Checked no residual (ultrasound). 13.30 Left hospital. Walked to HH railway station (10 mins) 14.05 Caught train to Southampton. determined not to use train WC! 15.40 Arrived Southampton. Just held on long enough to get to WC. Flow not as good as first 2 pees, though. Disappointing... 17.00 Home. Already peeing clear urine - and has stayed that way, except for the odd drop of blood from penis tip at first.
They started me on 25mg VIOXX (Rofecoxib) anti-inflammatory tablets (1/day), and 500mg Ciprofloxacin (2/day) and sent me home with 7 days' and 14 days' supply respectively.
Overnight at home was up every 1-2 hours, and flow was even worse - almost back to pre-PVP - in fact the first (01.30) I thought I had gone into full retention - scary. I hope this is quite temporary - presumably due to swelling due to traumatisation by instruments.
PVP+2 (Thurs)
In the morning I felt so well - no discomfort even - that I played snooker for 1.5 hours, then had a lazy afternoon. No toilet calls from bladder between 10.30 and 12.45, although when I got home and started thinking about it, all of a sudden there was a strong urge to go and I hardly made it to the WC in time! Felt perfectly normal the rest of the day. No urgent bladder calls... Kept off alcohol, although no one had said I should. Just thought it a good idea pro tem. Was it?! Overnight, up 3 times (not due to urgency, but because something woke me up and there was some feeling of something in there, so went out of habit, I suppose). But flow still pathetic.
PVP+3 (Friday)
Felt entirely normal apart from much discomfort overnight due to bowels still gummed up from the general anaesthetic. (This has been by far the biggest post-op nuisance!) Amazingly, still no discomfort peeing, bearing in mind all the things that had gone on down there during the op, including destruction of that part of the urethra within the prostate., and (see ** below). Also, at last - after downing several dollops of lactulose - Mafeking has finally been relieved... However, flow is still *abysmal*. Has anyone else had this in the first few days? Is it simply some swelling somewhere that will soon go away, or could it be some debris that is partially blocking flow (which was quite good for the first 2 pees on PVP+1)? WC visits during the day have been more than pre-PVP, as drinking water more often; about 2-hourly, but if ignore gentle 'WC visit indicated' signals until the 'Quick, get in there' signal then there isn't much time to spare!
So, to summarise so far, an incredibly fast and painless recovery, but - so far - with a dismal flow rate.
Will post further if anything changes (hopefully improvement in flow...). (Would, welcome others' thoughts on latter.)
--------------------- ** Before doing the PVP, Larner did his routine check of the bladder, where he found 3 small 'pre-tumour's, which he removed using 'diathermy', taking samples for biopsy. He said they were the benign kind that grew outwards rather than into the flesh, but that I would need to have regular checks as they tended to grow back (like basal cell carcinomas presumably) - or perhaps he was just saying that to stop me panicking. Is a bit scary... Anyway, that presumably explains why the op took so long (35 mins for the PVP, 55 for the bladder), and why the bladder hurt afterwards. -----------------------
Maurice Batey (Retired in Hampshire, UK) (age = 70, but still quite fit!)
http://www.maurice.eurobell.co.uk
(Change "no.spam" to "." in E-mail address.)
Chris - 16 Jan 2004 23:43 GMT >Had PVP at the Ashdown Nuffield Hospital at Haywards Heath, UK on >Tuesday, Jan.13th, under Tim Larner. I told you the sandwiches were good there, Maurice!
Same thing happened with my flow.... first pee after catheter was perfect, then it slowed down. I think partly it was because the bladder was used to retaining 200ml or so, but after PVP I got this urgent need to pee with very little in there, and the bladder was too thick-walled to contract easily to push it out. What's the flow like at high volume? Is that more encouraging?
If not, since Mr Larner gives you an anti-inflammatory to take, that suggests something is likely to get inflamed.... it's the urethra that has had most to put up with, considering the size of the laser tubing; maybe that swells up, and narrows the passage.
Anyway, don't be disheartened by that flow rate.... At PVP +3 months I agree with others who've said it takes that long to get the full benefit of the operation.
Derek F - 17 Jan 2004 00:45 GMT Great stuff Maurice, hope that the flow improves with the days. Two questions, did you opt for the general anaesthetic or was it reccommended and why the oxygen mask later? Derek. Had PVP at the Ashdown Nuffield Hospital at Haywards Heath, UK on Tuesday, Jan.13th, under Tim Larner. Herewith summary of events:
Tues.13/1/04:
10.35 Checked in - having already undergone pre-admission tests last month. 14.00 - 15.30**: PVP (general anaesthetic) 16.00 Back in room. Bladder painful (see ** below). 2 CODYDAMOL tablets cooled that down within an hour. Oxygen mask (until 17.50), saline drip (until19.40), catheter until next morning. 17.50 Enjoyed 2 large salmon sandwiches & salad, + banana & hot choc. No pain or even discomfort - not even from catheter, surprisingly. Started reading Ludlum novel 'Treveyne'. 22:45 Hot chocolate, lactulose, + assortment of pills/tablets (incl sleeping pill).
Wed. 14/1 (PVP+1)
07.50 Cup of tea. No pain - not even discomfort (even from catheter). 08.15 Breakfast 09.30 Catheter out after Larner' visit. Hardly a twinge, surprisingly. Hadn't looked forward to catheter, but it wasn't really a problem (except need to avoid rolling over on wrong side!). And it was nice to be able to knock bedtime drinks back without having to get up during the night! 10.15 Hot bath! 11.05 Cranberry juice 11.25 First post-PVP pee (300ml)! Dark pink, but good flow and no hesitation. Little discomfort, surprisingly. 12.15 3-course lunch 12.30 2nd pee (400ml). Still quite pinky. No discomfort. Checked no residual (ultrasound). 13.30 Left hospital. Walked to HH railway station (10 mins) 14.05 Caught train to Southampton. determined not to use train WC! 15.40 Arrived Southampton. Just held on long enough to get to WC. Flow not as good as first 2 pees, though. Disappointing... 17.00 Home. Already peeing clear urine - and has stayed that way, except for the odd drop of blood from penis tip at first.
They started me on 25mg VIOXX (Rofecoxib) anti-inflammatory tablets (1/day), and 500mg Ciprofloxacin (2/day) and sent me home with 7 days' and 14 days' supply respectively.
Overnight at home was up every 1-2 hours, and flow was even worse - almost back to pre-PVP - in fact the first (01.30) I thought I had gone into full retention - scary. I hope this is quite temporary - presumably due to swelling due to traumatisation by instruments.
PVP+2 (Thurs)
In the morning I felt so well - no discomfort even - that I played snooker for 1.5 hours, then had a lazy afternoon. No toilet calls from bladder between 10.30 and 12.45, although when I got home and started thinking about it, all of a sudden there was a strong urge to go and I hardly made it to the WC in time! Felt perfectly normal the rest of the day. No urgent bladder calls... Kept off alcohol, although no one had said I should. Just thought it a good idea pro tem. Was it?! Overnight, up 3 times (not due to urgency, but because something woke me up and there was some feeling of something in there, so went out of habit, I suppose). But flow still pathetic.
PVP+3 (Friday)
Felt entirely normal apart from much discomfort overnight due to bowels still gummed up from the general anaesthetic. (This has been by far the biggest post-op nuisance!) Amazingly, still no discomfort peeing, bearing in mind all the things that had gone on down there during the op, including destruction of that part of the urethra within the prostate., and (see ** below). Also, at last - after downing several dollops of lactulose - Mafeking has finally been relieved... However, flow is still *abysmal*. Has anyone else had this in the first few days? Is it simply some swelling somewhere that will soon go away, or could it be some debris that is partially blocking flow (which was quite good for the first 2 pees on PVP+1)? WC visits during the day have been more than pre-PVP, as drinking water more often; about 2-hourly, but if ignore gentle 'WC visit indicated' signals until the 'Quick, get in there' signal then there isn't much time to spare!
So, to summarise so far, an incredibly fast and painless recovery, but - so far - with a dismal flow rate.
Will post further if anything changes (hopefully improvement in flow...). (Would, welcome others' thoughts on latter.)
--------------------- ** Before doing the PVP, Larner did his routine check of the bladder, where he found 3 small 'pre-tumour's, which he removed using 'diathermy', taking samples for biopsy. He said they were the benign kind that grew outwards rather than into the flesh, but that I would need to have regular checks as they tended to grow back (like basal cell carcinomas presumably) - or perhaps he was just saying that to stop me panicking. Is a bit scary... Anyway, that presumably explains why the op took so long (35 mins for the PVP, 55 for the bladder), and why the bladder hurt afterwards. -----------------------
Maurice Batey (Retired in Hampshire, UK) (age = 70, but still quite fit!)
http://www.maurice.eurobell.co.uk
(Change "no.spam" to "." in E-mail address.)
Magna - 17 Jan 2004 10:15 GMT Glad things are progressing reasonably well Maurice and thanks for your post.
Great to be getting more and more UK PVP input into this group - from what Derry has said about the new Laserscopes in the UK we should be getting more and more. I believe that Gordon Muir is right - this will take over from TURP.
A few questions...........
What were your symptoms?
Were you private or NHS?
Are the support staff at Tim Larners hospital urology trained and is it a special urology unit?
Did Tim Larner give you full instructions on any complications (such as retention) and precisely what to do where to go if it happened? This would be one of my main concerns for a "day case" surgery - being a long way from the surgeon and his support staff.
Maurice Batey - 17 Jan 2004 22:28 GMT > What were your symptoms? Pathetic flow rate, and getting worse.
> Were you private or NHS? Private (covered by insurance)
> Are the support staff at Tim Larners hospital urology trained and is > it a special urology unit? Well, they've been doing PVP's there for months. Don't know if have had specific training. Don't know if it's a special unit. Good questions!
> Did Tim Larner give you full instructions on any complications (such > as retention) and precisely what to do where to go if it happened? > This would be one of my main concerns for a "day case" surgery - being > a long way from the surgeon and his support staff. No, I didn't get a list. But he did give me his mobile number. Wasn't 'day case'. Stayed overnight after op. Not allowed to go until can pee freely! (If worried, could always stay nearby for a night or two. Thought about that but decided to take a chance and go straight home, as felt so well.)
Maurice Batey (Retired in Hampshire, UK)
http://www.maurice.eurobell.co.uk
(Change "no.spam" to "." in E-mail address.)
Maurice Batey - 17 Jan 2004 22:28 GMT On Sun, 17 Jan 3904 00:45:09, "Derek F" <lordpilrig@NOX.btinternet.com> wrote:
> Two > questions, did you opt for the general anaesthetic or was it reccommended > and why the oxygen mask later? I opted for gen.an. to give me the chance of not having a catheter afterwards. (If have spinal tap/epidural, *must* have catheter.) Lost the bet (possibly because of the extra work in the bladder).
Got the impression it was normal there for this op. Never had one before... Will ask Larner at the review.
Maurice Batey (Retired in Hampshire, UK)
http://www.maurice.eurobell.co.uk
(Change "no.spam" to "." in E-mail address.)
Maurice Batey - 17 Jan 2004 22:28 GMT No change today. feel perfectly normal, no aches or pains - apart from slight ache at penis tip (which was probably pulled about a bit by the catheter).
Sadly, flow is still pathetic. Perhaps I should try drinking much more water and try to build up a good head of steam... Will try to have a word with Larner on Monday, as this problem seems unusual.
ADVICE re ROOMS at the Ashdown Nuffield, Haywards Heath (if overnight on a Tuesday): Try to get a room at the FRONT, as a mobile MRI unit seems to be scheduled to arrive at the REAR just after midnight on Tuesdays, and kicks up a hell of a din as the heavy diesel motor unit shunts it around, after which the unit's generator is started up... If you do have a rear room, keep the window shut!
Maurice Batey (Retired in Hampshire, UK)
http://www.maurice.eurobell.co.uk
(Change "no.spam" to "." in E-mail address.)
dohlund - 18 Jan 2004 16:15 GMT I too will confirm that setbacks can occur. I'm now 16 days post PVP. I felt really good so I started to return to normal activity. Also took some Alleve (naproxen) and had a drink of bourbon. Blood in urine returned and now have a strong burning sensation at the end of the stream. Alcohol and naproxen also created problems after my biopsy. Went out last night with friends but took no pills.
Dennis
No change today. feel perfectly normal, no aches or pains - apart from slight ache at penis tip (which was probably pulled about a bit by the catheter).
Sadly, flow is still pathetic. Perhaps I should try drinking much more water and try to build up a good head of steam... Will try to have a word with Larner on Monday, as this problem seems unusual.
ADVICE re ROOMS at the Ashdown Nuffield, Haywards Heath (if overnight on a Tuesday): Try to get a room at the FRONT, as a mobile MRI unit seems to be scheduled to arrive at the REAR just after midnight on Tuesdays, and kicks up a hell of a din as the heavy diesel motor unit shunts it around, after which the unit's generator is started up... If you do have a rear room, keep the window shut!
Maurice Batey (Retired in Hampshire, UK)
http://www.maurice.eurobell.co.uk
(Change "no.spam" to "." in E-mail address.)
dohlund - 18 Jan 2004 16:20 GMT Oops - I meant to post this in another thread.
Dennis
> I too will confirm that setbacks can occur. I'm now 16 days post PVP. I > felt really good so I started to return to normal activity. Also took some [quoted text clipped - 27 lines] > > (Change "no.spam" to "." in E-mail address.) Maurice Batey - 20 Jan 2004 22:23 GMT On Sun, 17 Jan 3904 22:27:26, I wrote:
> Will try to have a word with Larner on Monday, Had a chat. "Just hang in there another week or two" was the message. "With all that energy the PVP applies to the prostate area there is bound to be significant swelling. Keep drinking plenty of water."
Slight improvement after a day of increased water. Still no discomfort even, though still up 3-4 times overnight.
(Biggest problem has been a second attack of gummed-up bowels! Had helluva job yesterday evening and first thing today after dosing up with lactulose). Every 5-10 minutes an acute feeling of "Get to the WC quick", followed by no action"! Had to stay at home until Mafeking (for the 2nd time since PVP)was relieved, at 11am... PVP itself (even with additional work on bladder) was a breeze compared to this!
Maurice Batey (Retired in Hampshire, UK)
http://www.maurice.eurobell.co.uk
(Change "no.spam" to "." in E-mail address.)
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