Prostate :: Green Light Prostatectomy - Difficulty Passing Urine
May 16, 2012
Hello,I am 61 years old. Six days ago I had a "Green Light" surgery to core out my narrowing prostate. I was catheterization for 24 hours and stayed in hospital. When I tried to urinate the stream was very poor. Initially my bladder was holding over 300mls and it was difficult to pass urine in the day, it was virtually impossible to pass in the night. I went back to the hospital after 3 days and I was then holding 280 mls after urinating. I complained to the consultant (who I trust greatly) and he remeasured the bladder after 5 days an there was 150 mls. The worry is a man will go in urinary retention (very painful) and would need emergency catheterisation. Currently my stream is still very poor. I am upset the treatment has made me worse, but I am hopeful the stream will improve as my Consultant believes it will. I am coping at the moment and will wait. If anyone wishes to follow my progress I am willing to share my experiences.
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Just got Gleason score 4+3
PSA risen from 17.8 to 20
plan for robotic radical prostatectomy in 3 weeks - has anyone else had this surgery?
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Well, I got home this afternoon (Thurs) after the op Tues @ 7 p.m. And things seem to be working OK. No more Tamsulosin needed, so that's one benefit right there. I'll update after a few days as the the other possible effects.
The anesthetist chose a spinal anesthetic, which I was somewhat chary of, preferring to be totally knocked out. Later I remembered that there'd been some research that found that older people who had anesthetics died earlier, so he was right on that score. He also told me that this way I had a smaller number of anesthetics (general meant 14!, this way 1 to 3).
I didn't like the thought of being awake and watching the op, but he assured me I wouldn't feel a thing; I wouldn't see anything; and I'd be able to feed and drink more or less straight afterward rather than many hours later. And so it came to pass. Just numb legs for a while. I really didn't feel anything. All over in about an hour. I even dozed a bit on the op table.
However, that night (Tues) was not good. I had a constant feeling of wanting to sh*t. However, no matter how hard I tried (and I used two laxative suppositories), virtually nothing happened. I later found out this is a side effect of the somewhat larger catheter and balloon that was put in place.
So I found it hard to sleep. But just when I did doze off once, the nurse came in for the fourth time to take my blood pressure (2.00 am?). I was really upset and told her not to do any more (all the previous ones had been OK anyway). But by then I couldn't get back to sleep. So I was wretched all the next day (yesterday).
However, last night I got to sleep about 8:30 pm; and slept right through to breakfast. Bliss.
The surgeon had come in on Weds; told me about the defecation urge origin; said I could go home today if my urine was pretty clear by then and the catheter had come out. I see him again in a couple of weeks, when the result of the biopsy will be with him. He also said only 10% need the op again in 10 years; most are fixed for good. Here's hoping.
I was apprehensive about the removal of the catheter. In the end though, it wasn't too bad. I did most of it myself, easing it and rotating it a bit when it seemed to stick. Whew! Great. Then I pee'd a couple of times to test things; told I was OK to go. I left.
Home by 3 pm today. Then did a good walk (4 miles) and all's well. Still some blood and bits, but most clear. Good flow. Now to see how I am at night.
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I have had great difficulty in passing stool for about the past 2 or 3 months, I have mentioned this to doctors and all I have had back in prescribed stool softeners and soluble laxatives to help me go. But I am still only managing to go once every 10 days at best. In addition it is very sore when I do manage to pass stool and occasionally bloody, though not in the stool itself. I also have a very sore coccyx, or a pain in that area but nothing shows on the x-ray.
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Am a male aged 35 I've been having pains in my penis when passing urine for while but yesterday when I was urinating the pain became Unbearable so I paused a bit when I started again a clot of blood came out there after I couldn't pass urine anymore cause of the pain,as I tried to slowly release the urine blood continued to come out I've since been to the hospital where I was examined but was told it was not because of any std, what I want to know is what could have caused it
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I had unprotected sex before 5 days ago and now I'm having a pain after passing urine near vagina, Am I pregnant?
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there are rumors going around about the implanon, the little rod that goes in your arm that it causes infertilization. I want kids here in the near future and that is like my worst fear. So... I am having it removed. But I was wanting to know if any of you other ladies out there have heard the same.
Also I am having a very light odorless green discharge it will only appear for a little while during the day and then go away and then I will have a brown discharge. I have not seen my ob gyn and plan on it very soon.
I also have bad gas. I am still on the implanon which is making me gain weight as well.
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I am a 16 year old girl who for the most part was healthy prior to the start of my digestive problems. I am 5"3 and have never weighed over 99 lbs but my weight has now dropped to below 94 lbs due to inability to eat without pain and nausea. Around August 2011, I started having moderate-severe nausea and abdominal pain following most/all meals, which over time progressed to be nearly constant pain and nausea that made eating nearly unbearable. Starting in early March, I had multiple blood tests, an ultrasound, a HIDA scan, and an upper endoscopy. The only explanation offered to my mother (a doctor) and myself was that my gallbladder was hyperactive and excreted bile way too quickly, with an ejection fraction of 89%. Normal ejection fractions are considered to be roughly between 30-75%, but high ejection fractions are a gray area in the medical world at the moment, as most bad gallbladders have a low ejection fraction. All the children's surgeons refused to take out my gallbladder for this reason, but with it being our only hope we searched for a surgeon willing to take the chance. We were luckily able to find a surgeon with some knowledge of hyperactive gallbladders who removed my gallbladder in early May. My surgery went well and there were no complications immediately following. I did not have constant diarrhea following my procedure and my pain and nausea were alleviated until approximately early-mid June. I began having moderate nausea and pain again following nearly all foods and some drinks such as slushies or shakes. It increasingly worsened but has not yet reached the constant pain/nausea i was experiencing pre-surgery. I also had approximately 3-5 bouts that lasted about 10-20 minutes of extreme nearly unbearable pain, usually in my left abdomen just below the ribs approximately 20-30 minutes after I had eaten. Each time brought me to the floor and to tears. I visited the GI doctor again July 5 and was told their best explanation was Functional Dyspepsia and that I should begin taking 30g Amitriptyline each night. I was told results should appear approximately 3 weeks after I start regular dosage, which I did on July 5. I have seen some improvement in my pain and nausea as they do not necessarily occur after every single time I eat anymore, but they are still way too frequent and persistent for me to feel normal, much less function normally. Over the past week or so, my stools have been a bright green color and my urine has been clear for the most part. There seems to be no connection between my symptoms and my hormones as they do not worsen or alleviate with my menstrual cycle. I am sick and tired of being so sick and tired as my symptoms have majorly impacted my life and prevented me from participating in many things as they caused me to miss over 40 days of school just since January 2012. Please please please offer any ideas or thoughts you might have, i truly am desperate.
current symptomsgreen stoolclear urinemoderate/severe nausea and pain after eatingoccasional extreme pain during digestioneasily tired
gallbladder removed may 2012currently taking 30g Amitriptyline daily
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I had my TURP operation 8 weeks ago, the bleeding stopped after about 10 days and along with a few scabs. At the moment I find when I go to pass urine, although it comes out fast, there does not seem to be a great amount. Has anyone else come across this.
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Hi, for the past 2 weeks I have been getting these symptoms, dizziness, nausea, lightheaded, weak, headaches, neck pains, and tired. It is getting severe and im worried. I have had urines tests and blood test, they are all negative. Its constant and all day, it never goes away although some hours are worse then others. I have been on a medication called pristiq which is an antidepressant for almost 2 years, I tried increasing the dose in case that was causing it but it didn't work, can anyone help me please? Thank you
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Is it better to take the green tea capsules or drink the green tea.
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tuberculosis..? difficulty swallowing , difficulty breathing, cough out blood, dark-brown phlegm, cough doesn't go and mucus, weight loss,tired always......
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2 Days waking up tired, feeling miserable,slight headache and light cramps above my bladder. little bit of nausea in the mornings.
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My husband had his prostate removed laparoscopically for prostate cancer. The surgery went well. He had a catheter for a week. It was removed and all seemed well. Good control, no leakage. None of the things he feared. But then urine flow slowed then stopped, and we had to go to the ER to have a catheter re-inserted, 16 hours after removal (OF COURSE this could not happen during office hours, so we could just go to the urologist). 2 days later it was removed again. This time he lasted 50 hours before it slowed to a trickle again. He had decided to go to work that day. In the interim I had read about taking hot baths to relax the urethra and bladder and taking ibuprofen to reduce swelling. The flow had already been stopped 5 hours before I knew of it and could suggest them. He tried those, but it was too late; no idea if they would have helped anyway. Doctors office said probably not.
What can he do to keep things open? All along he has been drinking a lot and urinating frequently, as instructed. The only exception has been at night (he usually gets up once, but will set his alarm more often if it will help).
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On a doctor's visit back in December, it was discovered that i had microscopic blood in my urine. This went on for a few months, and increased with every doctor's check up. A urologist did an ultrasound of the kidney/bladder back in February, and all was normal. He also did cystoscopy which was normal too. He also did a test which shows my bladder holds sufficient amount of urine. The problem is, we never really figured out what the cause was, and recently i have had a new symptom (mucus tissue looking things in my urine). I am considering going back to a different urologist, but has anyone experienced something similar, or know what tissue looking bits in urine is?
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Test show that I have a enlarged kidney, I have protien in my urine, severe back pain to the right side, strong smelly urine, blood pressure very high now on 10mg blood pressure tablets, Doctors have done tests on my kidneys and say the test shows the kidneys are functioning normally so I have not to go back to hospital for six months.
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I'm a 26 yr old male, I've been peeing cloudy for months now, not every time I pee, usually just once a day, and the rest seem normal. Lately it seems like it's more cloudy than before. Also at night i have to get up alot to pee, but its usually just a few drops each time. Just recently two things happened, on two different occasions. First, I was peeing and it seemed to be normal color, but at the last end it turned white/cloudy and right at the last drop or two it looked like white flaky particles in it. Since then I've been noticing the particles more often. Second thing, almost two weeks after noticing the particles I was peeing one night and it seemed to burn quite bad at the last few drops, and when I was done it didn't feel like a finished, felt like I still had more. I went to outpatients the other night, did a urine sample and the test come back negative for UTI, so they sent it to a lab, next morning they did blood work and another urine sample. Waiting for the results now. Dr thinks it could be a prostate infection (prostatitis) caused from chlamydia so he put me on Ciprofloxacin. I dont think its from chlamydia because the two girls I've had unprotected sex with both been tested recently and come back clean. He also said its possible it could be stones.
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Im 29 year old female, i've always thought my painful bladder and urination was from chronic bladder infections for years until my doctor recently sent me to a specialist and sent off for urine culture and came back negative. .have all the symptoms of a bladder infection. Have large amount of blood (4+) ..Urologist sent my for a ct ivp to look for stones or look for something abnormal with ureters or kidney, nothing ..everything came back normal..now the urologist ordered a test to look at the bladder with scope through my urethra and also take a biopsy of bladder wall to look for cancer cells..owww. Any answers on what this can be I have all the symptoms of bladder cancer but im young and no family history of bladder cancer im a non smoker /alcohol drinker.
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I had been diagnosed with prostate cancer in may ,2009. The only real option for me was to have a radical prostatectomy because of age (58 years old and retired) :-( . I had this done in july, 2009 and since then there has been no evidence of cancer return. All PSA's have been less than 0.1. I have noticed over this time period a gradual weight gain of 7 lbs. I've always watch my diet and walk 5.5 miles a day. I'm 6'0" and now weigh 189 lbs. I do have rheumatoid arthritis which has been under control (sed rate=10) for a number of years using 0.5 mg prednisone and 1 or 2 vicodin es to control pain and flareup. Why is this happening with the weight gain? Is there any evidence or articles out there to support weight gain after radical prostatectomy ? Is this related to testosterone levels?
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Does anyone suffer with the same severe low back, thigh and groin pain as I have been for the past seventeen months following my radical prostatectomy. I am fine for the first twenty minutes of walking or general activity before the pains starts and increases in intensity if I don't stop. I have had M.R.I's and scans. The spinal consultant said it is caused by a lymphocele which I have had drained once, but urology don't think this is the cause. Can anyone offer any suggestions please. The nerve pain can get unbearable.
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I am actually writing for my fiance (drew) we are storing here frustrated.. today is his bday and we can't even have intercourse after 15 months..
Anyways, we are curious, does this sound like a venous leak, or is this all still normal after 15 post op?
Viagra does not work, period.
Calais gives him about a 20% erection, but at 40.00 a pill, it's impossible to afford on our tight budget.
Using a pump combined with the tightest ring, only gives him about a 30-40% erection for about 5 minutes.
We did try trimex but the third time we used it we face him to much and he had to to to the e.r. and go thru the absolutely most horrible thing I've ever witnessed in my life. So to say the least we haven't tried it again and its been almost 9 months.
Morning erections are rare and only about 30-40%.
When. We use a penis pump, the base of his penis blows up like a doughnut. A good inch or inch n half is as wide as the pump. Once we slip the ring in, even if we pump his penis up almost as long as the tube, his erection always immediately drops. Without getting to graphic, his head does turn n keep blue, so we know he had decent blood flow.
Other then this he is a fairly healthy man, turned 55 today, he is about 40lbs overweight, but ask his blood work is normal, never high cholesterol, no diabetes, and his heart is fine. Ever since his prostate cancer we are insistent in getting all his blood work done every 90 days.
So i guess what we are asking, is does anyone know if this is still normal?
We know ed problems are can be an issue for a few yrs, but he had one of the best surgeons in the US and was done with a davinci robot and nerve sparing. When this is all brought up to any if his doctors, they just offer scripts for ed medications we can not simply afford.
Is this a leak or still ed problems?
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