I Hate Dialysis Message Board
Welcome, Guest. Please login or register.
November 23, 2024, 03:33:01 AM

Login with username, password and session length
Search:     Advanced search
532606 Posts in 33561 Topics by 12678 Members
Latest Member: astrobridge
* Home Help Search Login Register
+  I Hate Dialysis Message Board
|-+  Dialysis Discussion
| |-+  Dialysis: Home Dialysis
| | |-+  Has any one had their Pd tube replaced?
0 Members and 1 Guest are viewing this topic. « previous next »
Pages: [1] Go Down Print
Author Topic: Has any one had their Pd tube replaced?  (Read 5686 times)
billybags
Elite Member
*****
Offline Offline

Gender: Female
Posts: 2190


« on: August 12, 2009, 12:05:43 PM »

I know I keep moaning on about my husband having had peritonitis and his pd tube was removed in case it had the e-coli bug.Well he has been given a date in early September to have it replaced, he is on Heamo at the moment.
 My question is: Has any one else had this done, was it ok, did you get a good dialysis with it or has the peritoneal  membrane been weakened by the bug. He does not know what to do, he hates Heamo, he hates sitting for 4 hours, 3 times a week. He was doing fine on CAPD before this crap happened. Like to hear some view on this please.
Logged
Restorer
Sr. Member
****
Offline Offline

Gender: Male
Posts: 786


WWW
« Reply #1 on: August 12, 2009, 04:53:15 PM »

I had a catheter put in last August, and it never worked. We were taking out time letting me heal before putting the catheter to use, but it ended up tangled in omentum and not able to drain. I ended up in the hospital with uremia before I could get it replaced.

Later in September I was finally able to have the catheter replaced. The plan was to just untangle it laparoscopically, but after I was under and they took a look at it, they decided to replace the catheter entirely.

The incision was painful for longer than my first cathether placement (probably because they cut right through the just-healed previous incision), and it took longer to heal. I really needed to be getting dialysis, so I started using the catheter exactly a week after it was replaced, with small volume fills and very low fill speeds - manually regulated by partially closing the clamp. Within a month I was doing better with the fills.

When I had my second, worse case of peritonitis earlier this year, it did affect my membrane. I ultrafiltrate less, and apparently my Kt/V is lower. I used to never have problems with potassium, but now I do. It could also be compounded by continuing loss of kidney function, though.
Logged

- Matt - wasabiflux.org
- Dialysis Calculators

3/2007Kidney failure diagnosed5/2010In-center hemodialysis
8/2008Peritoneal catheter placed1/2012Upper arm fistula created
9/2008Peritoneal catheter replaced3/2012Started using fistula
9/2008Began CAPD4/2012Buttonholes created
3/2009Switched to CCPD w/ Newton IQ cycler            4/2012HD catheter removed
7/2009Switched to Liberty cycler            4/2018Transplanted at UCLA!
mikey07840
Elite Member
*****
Offline Offline

Gender: Male
Posts: 1225


Her royal highness Queen Ruth on her throne, RIP

« Reply #2 on: August 12, 2009, 05:02:32 PM »

I had my PD catheter removed. After too many infections, I have switched back to heamodialysis. I am getting much better dialysis results. I do not know if I will try PD again, but for now I am sticking with heamo.
Logged

06/85 Diagnosed with type 1 Diabetes
10/04 Radical Nephrectomy (Kidney Cancer or renal cell carcinoma)
02/08 Started Hemodialysis
04/08 Started Peritoneal Dialysis (CAPD)
05/08 Started CCPD (my cycler: The little box of alarms)
07/09 AV Fistula and Permacath added, PD catheter removed. PD discontinued and Hemodialysis resumed
08/09 AV Fistula redone higher up on arm, first one did not work
07/11 Mass found on remaining kidney
08/11 Radical Nephrectomy, confirmed that mass was renal cell carcinoma
12/12 Whipple, mass on pancreas confirmed as renal cell carcinoma

• Don't Knock on Death's door; Ring the bell and run away. Death hates that.

• I'm not a complete Idiot -- some parts are missing.
Hanify
Elite Member
*****
Offline Offline

Gender: Female
Posts: 1814


Hadija, Athol, Me and Molly at Havelock North 09

« Reply #3 on: August 12, 2009, 07:21:57 PM »

Early on my catheter twisted and kinked and they had to do the operation again to straighten it.  I hadn't had peritonitis though, so I'm not sure about that side of things.  The op itself was no problem and they made a different incision so I didn't have a lot of pain.
Logged

Diagnosed Nov 2007 with Multiple Myeloma.
By Jan 2008 was in end stage renal failure and on haemodialysis.
Changed to CAPD in April 2008.  Now on PD with a cycler.  Working very part time - teaching music.  Love it.  Husband is Paul (we're both 46), daughter Molly is 13.
sico
Full Member
***
Offline Offline

Gender: Male
Posts: 310


wheres my bike gone?

« Reply #4 on: August 12, 2009, 07:31:15 PM »

My first PD catheter never really worked well. Even after having the omentum partially removed. Then it flipped and i was about to give up on it and get a fistula made (had my veins mapped) for HD. But i'm glad i persevered with PD and agreed to a new catheter. 2nd time around i had a different surgeon put it in another way and it's all been great since. :)
Logged

Brad      "Got myself a one way ticket, going the wrong way" - Bon Scott

6/11/08 diagnosed with ESRF, dialysis that day

HD and PD

8th of April 2010 Live kidney transplant from my father.
billybags
Elite Member
*****
Offline Offline

Gender: Female
Posts: 2190


« Reply #5 on: August 13, 2009, 02:26:52 AM »

Restorer, Did it take you along time to recover after your bouts of peritonitis. My husband seems to be so tired , can not sleep and having sweats at night. Being on emergency Heamo we thought he would be a lot better, but no. I think he is scared of having the pd pipe in again after all the pain. Looking forward to your answer..
Logged
Restorer
Sr. Member
****
Offline Offline

Gender: Male
Posts: 786


WWW
« Reply #6 on: August 14, 2009, 12:54:51 AM »

billybags, the only problems I had from peritonitis were abdominal pain and fibrin. All of my episodes of peritonitis were caused by the same bug, Staph aureus, so I don't know what it would be like with something nastier. It took me just a day or two to feel better after the first one. The second was a little worse, and it took me a couple days longer to feel better.

The third was by far the worst, the only time I needed IV pain meds in the ER. The pain stuck around for at least a week, and I burned through most of my supply of pain meds (darvocet). I stayed on PD and didn't need to go to emergency hemo.
Logged

- Matt - wasabiflux.org
- Dialysis Calculators

3/2007Kidney failure diagnosed5/2010In-center hemodialysis
8/2008Peritoneal catheter placed1/2012Upper arm fistula created
9/2008Peritoneal catheter replaced3/2012Started using fistula
9/2008Began CAPD4/2012Buttonholes created
3/2009Switched to CCPD w/ Newton IQ cycler            4/2012HD catheter removed
7/2009Switched to Liberty cycler            4/2018Transplanted at UCLA!
billybags
Elite Member
*****
Offline Offline

Gender: Female
Posts: 2190


« Reply #7 on: August 14, 2009, 07:16:34 AM »

Thanks for that Restorer, Husband came home to day after Heamo session and he was told he was not doing very well on it and it would have to be tweaked. He still car'nt make his mind up whether to go back to CAPD. Isn't life a shitt*er. Have to see the neph on Wednesday so will be asking for answers.
Logged
Hanify
Elite Member
*****
Offline Offline

Gender: Female
Posts: 1814


Hadija, Athol, Me and Molly at Havelock North 09

« Reply #8 on: August 14, 2009, 03:46:41 PM »

That's for sure.  It kind of strikes me a funny (not funny ha ha) that you have to make a choice between PD or Haemo!  Who wants to make that damned choice anyway! 
Logged

Diagnosed Nov 2007 with Multiple Myeloma.
By Jan 2008 was in end stage renal failure and on haemodialysis.
Changed to CAPD in April 2008.  Now on PD with a cycler.  Working very part time - teaching music.  Love it.  Husband is Paul (we're both 46), daughter Molly is 13.
peleroja
Elite Member
*****
Offline Offline

Gender: Female
Posts: 1585


I have 16 hats, all the same style!

« Reply #9 on: August 15, 2009, 10:55:19 AM »

I had my first ever peritonitis last November (after being on PD for 5 years), and they had to remove the catheter as I had pseudomonas, a particularly virulent bug.  In April they gave me a new PD catheter which didn't work, so they did revision surgery in May, and it has been working fine ever since.  Unfortunately, they say my Kt/V is too low and they may have to do some tweaking to my prescription.  No one has yet mentioned having to go on hemo again.
Logged
koutsounel
Newbie
*
Offline Offline

Posts: 22

WWW
« Reply #10 on: August 17, 2009, 07:13:28 AM »

My son's first pd catheter didn't work properly, so he had to have it removed. Fortunately he didn't need dialysis at the time - as with his condition, renal failure caused by nephrectomy was the "cure" for nephrotic syndrome. When he had the second catheter put in, the surgeon also did omentectomy, as this caused a problem the first time. 15 months later and it is still working fine!
The only thing I noticed, the pd catheter scar is bigger than the nephrectomy one, and the operation is quite a big one. Of course, if someone needs to have it again, there is not much you can do, but in our son's case we asked for it to be delayed because we felt it was too much for him. I can understand that hemo is not great, but going to theater is far more serious, and having one general anaesthetic after another is not the best thing that can happen to you.
Logged

And no resident will say: “I am sick.”
Isaiah 33:24
koutsounel
Newbie
*
Offline Offline

Posts: 22

WWW
« Reply #11 on: December 22, 2009, 07:51:17 AM »

I had my first ever peritonitis last November (after being on PD for 5 years), and they had to remove the catheter as I had pseudomonas, a particularly virulent bug.  In April they gave me a new PD catheter which didn't work, so they did revision surgery in May, and it has been working fine ever since.  Unfortunately, they say my Kt/V is too low and they may have to do some tweaking to my prescription.  No one has yet mentioned having to go on hemo again.

I noticed you mention Pseudomonas, did it take aprox. 6 months to replace the catheter because this particullar bacteria takes a long time to clear? My son lost his catheter for this reason, and they told us it is a difficult bug to clear, but our understanding was we would wait 2 months
Logged

And no resident will say: “I am sick.”
Isaiah 33:24
Pages: [1] Go Up Print 
« previous next »
 

Powered by MySQL Powered by PHP SMF 2.0.17 | SMF © 2019, Simple Machines | Terms and Policies Valid XHTML 1.0! Valid CSS!