Pain/burning on urination 4 weeks post catheter
After RARP my catheter was removed on Nov. 5th. Still have some pain urinating, spraying pee or narrow stream, discomfort when pushing. Anyone had similar issues? Haven been tested yet, waiting for appointments.
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@jeffmarc I can see the confusion. Im on my 9th week post surgery, and the catheter was in for 8 days. When they took catheter out, he wanted to see me 3 weeks later. A few days before i saw him after the 3 weeks, thats when i started to have burning issues. I can say the day i got catheter out leading up to my next visit, no pain at all, but started like 2 days before i saw him..
At six weeks post surgery....I noticed a burning painful sensation when urinating. It was a new sensation and not pleasant. Then, I spotted a couple of short nylon threads in my pad and went aha, the urethral sutures are coming out. In that same week, I even spotted a small nylon thread hanging out from my tip. Yikes-that's weird. The good news...I think I've peed out all the sutures and that burning sensation is gone.
Good luck and hope all goes smooth.
Best wishes that all goes better from here forward.
Regarding incontinence: My RARP was in 2015. After initial recovery, I had persistent stress incontinence, going through 1-2 pads per day. Finally, in 2023, my urologist performed a urethral sling surgery (outpatient). I immediately regained 100% continence. Even after salvage radiation last fall, I am fully continent, except for a drip here and there (I’m 73, so no complaints). Still no need for pads or diapers. The sling surgery was a life changer.
@melvinw
It’s good to hear the sling worked for you, even after radiation. That is unusual, I wonder if it’s because you had it done before the radiation.
At a recent Mayo Clinic monthly meeting. The urologist talked about the three different treatments that were available for incontinence. The sling and ProACT worked quite well as long as you did not have radiation treatment,. He recommended against doing either one of them if you had radiation.
The AUS was the only device recommended if someone had radiation.
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4 ReactionsGoing into salvage radiation, my urologist forewarned me that I would likely lose some continence, even with the sling. To my surprise, his warning has not come true, so far. The best I can come up with is that my previous urologist who performed the sling procedure was very skilled. I also have kept up with core strengthening exercises, so maybe that has had an impact. Seven months now since finishing radiation and I really have no lingering SEs of significance. The urge to go comes on a bit faster perhaps, but that hasn’t caused me any real problems. And I can’t rule out that being something that just comes with being in my 70s, like so many things.
Interesting to hear that the sling ProACT are not recommended for post-radiation incontinence. If I was faced with a primary therapy decision of surgery versus radiation, that is something I would want to factor in.
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