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Author Topic: I Have a Question... PLEASE HELP  (Read 4013 times)
rhaggz
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« on: June 04, 2013, 07:47:17 PM »

Has anyone ever heard of a dialysis machine arbitrarily take fluid off of you? I was told by a center technician that if you have extra fluid the machine will take it even if the UF Filter is turned off. I have been fighting this for a couple of weeks now.

Normally I have a couple of pounds on and they calculate for the settings on the machine. However I have been under all but once in the last two weeks. The day I was not under I had the technician turn the UF Filter off 50 minutes early and I was .8# over. The time before that I had them turn the filter off 30 minutes early and I was 1.4# under. The next time I only had 0.40# on and told them not to take any. My dialyser is new every time  and they have to flush it every 30 minutes so they supposedly only took what they flushed, However when I weighed out I was 2.4 under.

I am lucky in the fact that I can feel in my legs before I start to cramp and I tell them to stop the UF Filter, but my legs hurt for the rest of the day and I have trouble walking. I usually have to nap for 2-4 hours and even though the pain in my legs goes away. The best description I can come up with is that it feels like they are trying to pull the marrow out of my bones. My legs are always weak afterwards, usually until the next day.

I have had the Dr increase my dry weight as I gain weight and I keep a close watch on that... They have taken as much as 11# off me without any side effects when I first started so it is not too much taken off as I have severely curbed my liquid intake.

Please can somebody assist in answering my question or supply some assistance in conquering this problem.
« Last Edit: June 05, 2013, 06:17:41 PM by rhaggz » Logged

They say you are what you eat... I do a lot of fast food so I'm fast, cheap and easy...
Angiepkd
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« Reply #1 on: June 04, 2013, 08:24:09 PM »

Hmmmm....I am not sure about this one.  I use NxStage at home, and my nurse told me that the only fluid my machine pulls is my rinse back and whatever I set the UF to remove.  Technically that means that I do remove fluid, even if the UF is off, but only the amount that I am given back at the end of treatment.  I have never used any other machine, but I am sure someone here will give you a better answer.  It would be a plus if the NxStage cycler would just take off whatever it needed to, but it definitely does not.  Hope you find the answer.  Nothing worse than feeling lousy after treatment, especially if it is from pulling fluid you don't need to!


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PKD diagnosis at 17
Cancer May 2011, surgery and no further treatment but placed on 2 year wait for transplant
October 2011 first fistula in left wrist
April 2012 second fistula in upper arm, disconnect of wrist
January 2013, stage 5 ESRD
March 2013 training with NxStage home hemo
April 2013 at home with NxStage
April 2013 fistula revision to reduce flow
May 2013 advised to have double nephrectomy, liver cyst ablation and hernia repair. Awaiting insurance approval to begin transplant testing. Surgery in June.
June 2013 bilateral nephrectomy.
August 2013 finishing testing for transplant, 4 potential donors being tissue typed.
January 2014 husband approved to donate kidney for me
March 4th 2014 received transplant from awesome hubby. Named the new bean FK (fat kidney) lol!  So far we are doing great!
rhaggz
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« Reply #2 on: June 04, 2013, 09:00:22 PM »

Hmmmm....I am not sure about this one.  I use NxStage at home, and my nurse told me that the only fluid my machine pulls is my rinse back and whatever I set the UF to remove.  Technically that means that I do remove fluid, even if the UF is off, but only the amount that I am given back at the end of treatment.  I have never used any other machine, but I am sure someone here will give you a better answer.  It would be a plus if the NxStage cycler would just take off whatever it needed to, but it definitely does not.  Hope you find the answer.  Nothing worse than feeling lousy after treatment, especially if it is from pulling fluid you don't need to!

I'm on hemodialysis 3 days a week at a treatment center. the machines are Fresenius, but I can't remember the model number...
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They say you are what you eat... I do a lot of fast food so I'm fast, cheap and easy...
Wildrose
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« Reply #3 on: June 04, 2013, 10:30:55 PM »

I still can't figure out how it works, but I can tell you that when they set it to minimum (to NOT pull any fluid off) it still does. I've left the dialysis center as much as 1 kilo (2 lbs) lighter than when I went in, with the machine set to not pull any fluid. I don't get it at all. It drys me out. I come home and sleep all day.

Sorry you are having the same problem, wish I had some advice for you but I can't figure it out myself and no one else (at my dialysis center) seems to have an answer.  ???
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1995 - Diagnosed with 'some kind' of kidney disease during first pregnancy at 16 yrs old due to excess protein in urine
1998 - Biopsy diagnosis of IGA Nephropathy at age 18
2007 - Successful second pregnancy, creatnine of 1.8 something
2009 - Successful third pregnancy creatnine of 2 something
2009-November of 2011 - Somehow went from Creatnine of 2 something to 5.43
November 2011 - Diagnosed with End Stage Renal Disease
3/28/12 - Started Peritoneal Dialysis
5/21/12 - Ended up in hospital for 5 days with PD fluid leaking through hole in diaphragm to right lung
5/25/12 - IJ catheter placed, 5/26/12 - First in center hemo treatment
6/15/12 - Back on PD for three weeks and hemo at same time, 7/7/12 - PD fluid leaked again, off PD and still on hemo, 7/15/12 - on PD again and hemo
7/23/12 - chest xray shows fluid leak again, off PD for one month with possible thoracic surgery in future to fix hole in diaphragm. 5.70 creatnine
8/7/12 - 24 hr urine test shows improved kidney function. 3.47 creatnine - Dr reduced hemodialysis from 3x's to 2xs a week.
rocker
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« Reply #4 on: June 05, 2013, 06:40:51 PM »

This also happens with NxStage.  Our current cycler regularly pulls 300-600ml extra.  It seems to be very cycler-dependent - the last cycler didn't pull nearly as much.  I'm not sure if time is also a factor, as he runs for about 8 hours.

I just know that if he has, say, 1L to come off, and he drinks maybe 500ml during treatment, he'll generally come out about even.  If he falls asleep early and doesn't drink much, I'll reduce the UF so he's not overdrawn.
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Rerun
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« Reply #5 on: June 05, 2013, 10:22:12 PM »

This doesn't sound right to me.  Not a liter extra.  I'd talk to another tech or the BioTech about it.
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KatieV
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« Reply #6 on: June 06, 2013, 06:12:00 AM »

This also happens with NxStage.  Our current cycler regularly pulls 300-600ml extra.  It seems to be very cycler-dependent - the last cycler didn't pull nearly as much.  I'm not sure if time is also a factor, as he runs for about 8 hours.

I just know that if he has, say, 1L to come off, and he drinks maybe 500ml during treatment, he'll generally come out about even.  If he falls asleep early and doesn't drink much, I'll reduce the UF so he's not overdrawn.

I just got a replacement cycler as my NxStage machine was pulling extra.  It was within NxStage's tolerances, but was affecting me quite a bit.  I tried adjusting for the extra, but it still had me dizzy, rapid pulse (130 bpm!), and blagh feeling.  It was taking off between 0.8 and 1.7 liters extra.  I, too, run for 8 hours.  My new cycler is much better.       
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~~~~~~~~~~~~
March 2007 - Brother diagnosed with ESRD, started dialysis 3 days later
April 2007 - Myself and sister also diagnosed with Senior-Loken Syndrome (Juvenile Nephronophthisis and Retintis Pigmentosa)

Since then, I've tried PD three times unsuccessfully, done In-Center hemo, NxStage short daily, Nocturnal NxStage, and had two transplants.  Currently doing NxStage short daily while waiting for a third transplant.

Married Sept. 2011 to my wonderful husband, James, who jumped into NxStage training only 51 days after our wedding!
~~~~~~~~~~~~
Riki
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« Reply #7 on: June 06, 2013, 08:06:51 AM »

Do you use the same machine every time?  If you do, I'd demand to have the machine looked at.  You shouldn't have so much taken off while in minimum, and if I were you, until it was fixed, I'd be asking to be taken off whenever you start to feel the cramping come on
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Dialysis - Feb 1991-Oct 1992
transplant - Oct 1, 1992- Apr 2001
dialysis - April 2001-May 2001
transplant - May 22, 2001- May 2004
dialysis - May 2004-present
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HD - Dec 2008-present
rhaggz
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« Reply #8 on: June 06, 2013, 11:43:50 AM »

Do you use the same machine every time?  If you do, I'd demand to have the machine looked at.  You shouldn't have so much taken off while in minimum, and if I were you, until it was fixed, I'd be asking to be taken off whenever you start to feel the cramping come on

I do use the same machine... It least it is in the same place every time... I have them turn off the UF filter when I feel the first tinge of a cramp coming on... I have also contacted the manufacturer to try to get an explanation for the variance... But have not yet heard back from them...
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They say you are what you eat... I do a lot of fast food so I'm fast, cheap and easy...
ianch
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« Reply #9 on: June 06, 2013, 11:52:01 AM »

Cant say I've had that problem, or at least noticed it.  The timing of treatment and meals is a big contributor for me.  I usually weigh exactly what I expect post treatment every time. But then I'm not aggressive with the target as I was told not to be for HomeD.     Never had cramps or hardly any complications since leaving the center.
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Ian Chitty
ESRD suffer, IT specialist, and business owner
(<2yrs) 1Y in-center, 9 months HomeD, 4 weeks tourism dialysis (Philippines/Singapore)

https://kiwimedtec.com
The aim of KiwiMedTec is to develop online solutions and partnered networks for dialysis patients, to make coping with kidney disease a little bit easier.
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« Reply #10 on: June 06, 2013, 02:45:25 PM »

Unless you wear the same clothes/shoes each time you go in, your weight will fluctuate.  The last few weeks have been warmer weather, maybe you aren't wearing as heavy clothing.  It makes a difference since you are still trying to take off the same amount of fluid.

Plus, dialysis machines need to be periodically re-calibrated.  Check to see when the maintenance was last done on the machine in your station.  Also, each machine should be numbered, so it doesn't necessarily mean you have the exact same one each treatment.  Sometimes they are removed from the floor for maintenance.  At my center, each machine has a stenciled number on the lower right front.   Your clinic probably has Fresenius 2008K2 machines.
« Last Edit: June 06, 2013, 03:07:50 PM by PatDowns » Logged

Frank Moiger aka (previously) NoahVale and now PatDowns, the name originally chosen by a good dialysis mate who died in 12/2013.  I started in center hemodialysis as a 22 y.o. in 1978.  Cadaver transplant in 1990 and then back to in center hemodialysis in 2004 (nocturnal shift since 2011) after losing my transplant.  Former Associate  Director/Communications Director of the NKF of Georgia, President of the Atlanta Area AAKP Chapter, and consumer representative to ESRD Network 6.  Self-employed since 1993.

Dialysis prescription:
Sun-Tue-Thur - 6 hours per treatment
Dialysate flow (Qd) - 600 
Blood pump speed(Qb) - 315
Fresenius Optiflux200 NR filter - NO REUSE
Fresenius 2008 K2 dialysis machine
jbeany
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« Reply #11 on: June 06, 2013, 06:58:30 PM »

They all do it so some extent - it's part of the mechanical process involved in cleaning your blood.  In theory, they return the extra back to you with the saline they use to pump the blood back out of the lines at the end.

My only suggestion - take daily notes and start tracking which machine you are on.  (I know my center rotated machines, but not chair spots, so see if you can find some identifying number.)  Then figure out what you want taken off and demand to be allowed to chose your own fluid removal amounts each treatment.  You should be able to do this no matter what, but some centers will fight you on it until you can prove to them that you know why you are choosing particular goals.
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rocker
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« Reply #12 on: June 06, 2013, 07:06:46 PM »

Another suggestion is to bring a bottle of your own beverage with you. Many people find relief by sipping water at the first sign of cramping.
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