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Author Topic: Fistula Care after transplant...  (Read 6881 times)
carol1987
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« on: June 01, 2011, 06:52:07 AM »

I have a 2 year old fistula and rec'd a transplant in january...  Do you ever see your vascular doc to check the fistula after transplant?  Is there anything you need to be careful of or maintain with a fistula after transplant?? 

Do you try and keep the fistula "healthy " and usable just in case???
« Last Edit: June 01, 2011, 07:13:00 AM by carol1987 » Logged

Diagnosed with  PKD July 2002 (no family history)
Fistula placed April 2009
Placed on Transplant list April 2009
Started HD 10/6/10
Transplanted 1/6/11 (Chain Transplant My altruistic donor was  "Becky from Chicago" , and DH Mike donated on my behalf and the chain continued...)
Chris
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« Reply #1 on: June 01, 2011, 08:17:07 AM »

I'm thinking most don't see their vascular surgeon unless there is a problem. After I had my fistual and then graft, I never needed to see him again after post op follow up. My graft is sometimes checked by nurses and doctors to see if they still can hear a thrill, but it's not on their priority list of things to check. My thinking is to exercise your fistula with an exercise ball every now and then to keep it going, but not big enough to notice. I don't think this has been brought up in a topic befoore, so let's see what others have to say.
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Diabetes -  age 7

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willowtreewren
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« Reply #2 on: June 01, 2011, 08:33:06 AM »

During Carl's post-Tx briefing they told him that they would not do anything if his fistula should fail.

Aleta
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C904
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« Reply #3 on: June 05, 2011, 07:45:42 AM »

My fistula closed up during the transplant surgery and it was no big deal to any of the docs.  I think it is safe to say it is pretty much up to you if you want to try and keep it healthy and going.  The only tip I would give is that if the fistula shuts down to still avoid having blood drawn from that main vein higher up your arm where they do blood draws from.  When the fistula shuts down the blood is still raging down that vein it just diverts once it hits the closed fistula.  This might just be common sense to people who have a fistula, but I was thinking it is fine to hit that vein during blood draws because the fistula is closed.  With the blood still raging down that vein I had problems on two different occasions of having the blood pool up where they did the blood draw from.
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bette1
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« Reply #4 on: June 05, 2011, 01:54:15 PM »

I was told to follow the previous instructions;  don't carry over 10 lbs on that arm, don't sleep on that arm, don't let anyone take blood from that arm, etc.  My doc said that it's your insurance in case something happens to your transplant.
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« Reply #5 on: June 05, 2011, 02:35:25 PM »

Jenna's fistula failed on the day of her transplant. They did not attempt to rescue it as they did not want to risk any infection with a new kidney.
If you feel the "thrill" and it seems same as always, I think you can do as mentioned, to protect it.
If the sounds gets weak, or you notice any symptoms of a blockage, I'd see a vascular doctor to evaluate it. Here's more info http://ihatedialysis.com/forum/index.php?topic=4287.0
Have you read about Meinuk's fistula removal? There is good info that you might need later down the road. http://ihatedialysis.com/forum/index.php?topic=18735.0
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lawphi
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« Reply #6 on: June 05, 2011, 04:35:26 PM »

We were told it would eventually fail.  A good friend lost his fistula two years post transplant.

His buttonholes are already gone.
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« Reply #7 on: June 05, 2011, 04:46:32 PM »

don't let anyone take blood from that arm, etc. 

I was told that also, but already knew that from dialysis. They will not take blood from any part of that arm here.
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Diabetes -  age 7

Neuropathy in legs age 10

Eye impairments and blindness in one eye began in 95, major one during visit to the Indy 500 race of that year
   -glaucoma and surgery for that
     -cataract surgery twice on same eye (2000 - 2002). another one growing in good eye
     - vitrectomy in good eye post tx November 2003, totally blind for 4 months due to complications with meds and infection

Diagnosed with ESRD June 29, 1999
1st Dialysis - July 4, 1999
Last Dialysis - December 2, 2000

Kidney and Pancreas Transplant - December 3, 2000

Cataract Surgery on good eye - June 24, 2009
Knee Surgery 2010
2011/2012 in process of getting a guide dog
Guide Dog Training begins July 2, 2012 in NY
Guide Dog by end of July 2012
Next eye surgery late 2012 or 2013 if I feel like it
Home with Guide dog - July 27, 2012
Knee Surgery #2 - Oct 15, 2012
Eye Surgery - Nov 2012
Lifes Adventures -  Priceless

No two day's are the same, are they?
staceyand joe92
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« Reply #8 on: June 05, 2011, 05:26:29 PM »

My fistula was HUGE and became very achy after my transplant. At about 6 months post transplant my neph and vascular surg thought it was best to remove it comptletely. I didn't give it a second thought. It was more dangereous to keep it than to  chance I may need it later in life.
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sullidog
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« Reply #9 on: June 05, 2011, 06:15:49 PM »

I've heard that a lot of them do fail after transplant. I know someone also if you grab him by that area it will hurt. This same friend, his fistula, you can't fill a thrill anymore but he still has a bit of bruit.
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May 13, 2009, went to urgent care with shortness of breath
May 19, 2009, went to doctor for severe nausea
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RichardMEL
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« Reply #10 on: June 06, 2011, 01:43:19 AM »

mine is still going strong six months post. Sometimes in clinic the docs feel the thrill, but don't really give it much attention. At one time one of the senior guys did say "maybe after a year we'll think about doing something about that" but he was a bit vague about what exactly that meant.

I think when it's still relatively early days and it's still working it's great to have that "standby" there just in case the very worst happens.

I just treat it as normal like others have said - I don't allow BP's on it, I don't have blood taken from that arm etc and don't lift anything too heavy but basically I ignore it. every other day I feel for the thrill but understand that if it does fail it's not the end of the world and just report it at next clinic rather than rush to ER if I was still needing it for D.

Hoping I won't need to use it anytime soon!!! :)
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3/1993: Diagnosed with Kidney Failure (FSGS)
25/7/2006: Started hemo 3x/week 5 hour sessions :(
27/11/2010: Cadaveric kidney transplant from my wonderful donor!!! "Danny" currently settling in and working better every day!!! :)

BE POSITIVE * BE INFORMED * BE PROACTIVE * BE IN CONTROL * LIVE LIFE!
rsudock
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« Reply #11 on: June 06, 2011, 11:04:59 AM »

The fistula I use now is the same one I had 10 years during my previous transplant. Mine never slowed down, but did get stronger after I started dialysis for the first time. Like others have said no BPs, blood draws, and do not sleep on it. Even after transplant number 2 I will still try and protect it.

xo,
R
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Born with autosomal recessive polycystic kidney disease
1995 - AV Fistula placed
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10 transplant years = spleenectomy, gall bladder removed, liver biopsy, bone marrow aspiration.
July 27, 2010 Started dialysis for the first time ever.
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carol1987
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« Reply #12 on: June 06, 2011, 02:59:14 PM »

Thanks everyone!!!   :waving;
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Diagnosed with  PKD July 2002 (no family history)
Fistula placed April 2009
Placed on Transplant list April 2009
Started HD 10/6/10
Transplanted 1/6/11 (Chain Transplant My altruistic donor was  "Becky from Chicago" , and DH Mike donated on my behalf and the chain continued...)
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« Reply #13 on: June 06, 2011, 04:15:16 PM »

Mine is still going strong more than 2 years post-transplant.  First one clotted off several months after first trx.  I saw my vascular surgeon because I thought it was big and might cause problems but he thought it looked "fantastic" and said not to worry.  No BPs, bloods etc and I'm pretty protective overall.  The worst thing is I never wear shorter than elbow length sleeves...so if that's the worst thing, who cares!
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Pyelonephritis (began at 8 mos old)
Home haemo 1980-1985 (self-cannulated with 15 gauge sharps)
Cadaveric transplant 1985
New upper-arm fistula April 2008
Uldall-Cook catheter inserted May 2008
Haemo-dialysis, self care unit June 2008
(2 1/2 hours X 5 weekly)
Self-cannulated, 15 gauge blunts, buttonholes.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
carol1987
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« Reply #14 on: June 07, 2011, 08:36:35 AM »

Monrein... Mine is on my lower arm   and I have a huge scar also from surgery to raise the fistula..  This will be my first summer with it so we shall see if I get stares or comments...

I have been continuing to follow the no BP or bloods... I went thru a lot to get the fistula so I want to protect it as much as possible..
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Diagnosed with  PKD July 2002 (no family history)
Fistula placed April 2009
Placed on Transplant list April 2009
Started HD 10/6/10
Transplanted 1/6/11 (Chain Transplant My altruistic donor was  "Becky from Chicago" , and DH Mike donated on my behalf and the chain continued...)
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