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Author Topic: New technique for PD catheter insertion  (Read 3342 times)
MooseMom
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« on: August 28, 2012, 02:23:03 PM »

I know very little about PD, but I happened across this blog entry over on Renal Fellow Network and thought it might be of some interest to anyone thinking about PD.

http://renalfellow.blogspot.com/2012/08/bury-it.html
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"Eggs are so inadequate, don't you think?  I mean, they ought to be able to become anything, but instead you always get a chicken.  Or a duck.  Or whatever they're programmed to be.  You never get anything interesting, like regret, or the middle of last week."
Annig83
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« Reply #1 on: August 28, 2012, 05:09:04 PM »

How cool is this?!  I think that it's quite the innovation.  Success rate seems fairly similar to having a "normal" procedure being done.   :2thumbsup;
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*~Annie~*
Any change, even a change for the better, is always accompanied by drawbacks and discomforts.
Arnold Bennett
Even though I have gone through so much with ESRD, my son is my inspiration to keep going.  He was delievered at 28 weeks weighing 1 lb 12 oz and today he is a fun-loving 1 year old, whom I love with all my heart!

Diagnosed with Nephrotic Syndrome Age 13- 1996 Unknown Cause. 35% functioning of both kidneys.
Stable until Age 27; complications with pregnancy, loss of 25% function. (Current functioning is between 5-7%).
December 3, 2010- PD Catheter Placed on Left Side
March 2011- PD Catheter Removal (Due to malfunction)
April 2011- PD Catheter Placement on Right Side
April 2011- Surgery to adjust Catheter and "tacking of fatty tissue"
May 2011- CCPD Started
October 2012- Infection of PD catheter.  PD Cath. removal surgery. Perma-Cath. Placed for Hemodialysis.
Hemodialysis started October 12, 2012.
January 16 2013- First Fistula
On Transplant List in Indiana, awaiting 1st Transplant at IU Health in Indianapolis.
Joe
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« Reply #2 on: August 28, 2012, 05:39:17 PM »

When I was getting ready to start dialysis, my Neph and vascular surgeon weren't sure when I would need to actually start. They were going to bury my cath until it was needed. Unfortunately, I degraded faster than we all were planning so wound up leaving it out. I started dialysis 3 weeks a later.
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Rain
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« Reply #3 on: August 29, 2012, 07:33:39 AM »

they do that at the hospitals here for years now.. If only i was able to do PD..
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1988  Diagnosed with reflux and kidney damage
2006-  Diagnosed with Renal Failure and start dialysis in centre with catheter
2007- Fistula created and in centre hemo with fistula
2012- Fistula clotted and central line inserted
May 2014- Received Kidney from deceased donor
kporter85db
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« Reply #4 on: August 30, 2012, 09:10:03 PM »

This is how my catheter was placed. My catheter was put in and left buried in March 2011, and externalized as an outpatient procedure under local anesthetic in the surgery center in July 2011. That same day I went right away to my dialysis clinic and started training/doing dialysis.

I just assumed this was the way they did all pd catheters.

It was really weird feeling the catheter under my skin for those few months.
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May/2010 Sulfa based antibiotics killed my already weakened kidneys, almost
Feb/2011 PD catheter placed
July/2011 Started Peritoneal Dialysis
Nov/2013 Started NxStage 5 days/week

Ken
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« Reply #5 on: September 04, 2012, 02:22:45 PM »

Of course, my "brilliant" hospital, Brigham and Women's in Boston, does not use this technique. I say brilliant sarcastically, as they miserably fail the day-to-day patient, and grab headlines only when they do something like a double hand transplant. I hate to tell you how many mistakes the hospital and their doctors have committed in my case over the years. Serious mistakes with my anticoaculation leading to catastrophic bleeding, mistakes with my phosphorous/PTH management, leading to calciphylaxsis, etc. I have transferred my accrued waiting time for a kidney to Fletcher-Allen Hospital in Burlington VT where the wait time is half that of Brigham's. I am told I am at the top of the list for my blood type. Didn't want Brigham to screw up the transplant. As it is I don't even know who my transplant coordinator or my surgeon is at Brigham, they have such a revolving door. TMD sindrome - Too Many Doctors.
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