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Author Topic: Getting sick on hemo  (Read 7419 times)
7piglets
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« on: August 15, 2008, 08:32:55 PM »

HI I throw up 10-15 mins every time after I get hooked up to hemo. They dont take out any fluid on me since I never gain ..I cant take it anymore my whole rest of day is shot because of how sick I feel.. I just dont want to go anymore...Also, I have skipped fridays 3 weeks in a row and my numbers still are good is anyone on just 2 days a week?? Is it possible.???
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Mercurial
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« Reply #1 on: August 15, 2008, 10:09:54 PM »

It's rare.

Is it the treatment itself making you ill, or the blood and needles part of it?

Sounds like you might need some anti-nausea prescribed.

M:>
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7piglets
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« Reply #2 on: August 15, 2008, 10:58:10 PM »

it is the treatment itself.. I have permacath so definatley not the needles and blood doesnt bother me at all.
It happens right after being put on and I get almost foggy headed , hard to breathe , sweats then nauseous
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Bajanne
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« Reply #3 on: August 15, 2008, 11:39:53 PM »

So what is your nephrologist saying about it?  And the nurses/techs?  This sounds like something that needs checking by a professional.
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Gram2Twinz
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« Reply #4 on: August 15, 2008, 11:54:41 PM »

Yes, I agree. It sounds like a reaction to something- perhaps the fluid, perhaps the meds they put in prior to treatment. Have you had any allergy testing done? My husband often mentioned the sensation he gets at the beginning of treatment, but they began at a very slow flow rate and it helped him.
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Husband diagnosed w/ 1 working kidney 1975 Mayo Clinic
A/V Fistula March 2004
Placed on transplant list July 2004
In center dialysis began July 2007
Home Hemo NxStage training began Nov. 2007
Rockford, IL Davita-Roxbury Center
1st patient trained for home hemo by this center
Transplant 6-5-08 Loyola@Chicago
Loretta
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« Reply #5 on: August 16, 2008, 12:27:37 AM »

  :cuddle;
Wow! I am sorry you get so sick.  I hope your Dr. can figure out what is causing it.

Loretta
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« Reply #6 on: August 16, 2008, 01:39:21 AM »

You have my sympathy , there is nothing worse than having to go through everything and be made to feel worse for it . I hope things get better soon  :cuddle;
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OH NO!!! I have Furniture Disease as well ! My chest has dropped into my drawers !
monrein
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« Reply #7 on: August 16, 2008, 03:21:49 AM »

Is your pressure dropping just after you hook up?  That could cause sweats and nausea.  But I agree that you need to really have your neph figure out what's happening because it shouldn't be like that ongoingly.  It could also be anxiety.  Understandable for sure but not pleasant.
Keep us updated on what happens and I'm thinking of you. :cuddle;
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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
stauffenberg
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« Reply #8 on: August 16, 2008, 07:28:54 AM »

As distressing as it may be, you really shouldn't cut back on the amount of time per week you spend on dialysis.  The normal dialysis prescription is geared only to remove 10 to 14% of the toxic waste products from your blood which the kidneys normally remove.  As such, it is really just sufficient to keep you alive, not enough to keep you healthy.  The standard dialysis dose was originally determined financially, not medically, as the amount of treatment time required so that the total cost of dialysis was still less than the cost of having to treat dialysis patients for medical complications secondary to renal failure.  You should really try to spend more time on dialysis than you have been assigned, not less, or your health will suffer over the long-term.

The parts of the dialysis equipment which come into contact with the patient's blood are not perfectly biocompatible, so all patients experience some reaction to this contact of their circulation with foreign matter.  The plastic in the dialysis tubing is made of the same substance which was recently banned from babies' toys as a carcinogen.  Patients experience cytokine release when dialysis starts, which causes a general but usually mild inflammatory state throughout the body.  Perhaps you are hypersensitive to these effects.
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pelagia
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« Reply #9 on: August 16, 2008, 08:03:47 AM »

Okay, but what can she do Stauff?  Would benadryl help if it is some sort of allergic reaction?
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As for me, I'll borrow this thought: "Having never experienced kidney disease, I had no idea how crucial kidney function is to the rest of the body." - KD
G-Ma
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« Reply #10 on: August 16, 2008, 08:15:09 AM »

Monrein mentioned BP and that was my first thought.  This sweating, throwup, nausea, light headed....happened to me one time about 3 weeks ago in center, during the 1st hour of 4 hour run.  My BP was 56/20....They put oxygen on me, stopped the pull and monitored.  It was freaky but has not happened again.  Please talk to your Dr.  It's not good to skip and I do believe you can overcome this too.  We are all here for you.
Ann
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Lost vision due to retinopathy 12/2005, 30 Laser Surg 2006
ESRD diagnosed 12/2006
03/2007 Fantastic Eye Surgeon in ND got my sight back and implanted lenses in both eyes, great distance & low reading.
Gortex 4/07.  Started dialysis in ND 5/4/2007
Gortex clotted off Thanksgiving Week of 2007, was unclotted and promptly clotted off 1/2 hour later so Permacath Rt chest.
3/2008 move to NC to be close to children.
2 Step fistula, 05/08-elevated 06/08, using mid August.
Aug 5, 08, trained NxStage and Home on 9/3/2008.
Fistulagram 09/2008. In hospital 10/30/08, Bowel Obstruction.
Back to RAI-Latrobe In Center. No home hemo at this time.
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7piglets
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« Reply #11 on: August 16, 2008, 08:24:29 AM »

It is not b/p as I usually run on low side it actually goes up alitltle ..It is not anxiety as I am fine then all of a sudden the symptoms start. I have mentioned to the tech/nurses (and they are there every time it happens and they said they dont know what is causing it) I called my neph dr on Wed and asked what can be done he called while I was at dialysis so I have to wait now until mon to call him back..
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G-Ma
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« Reply #12 on: August 16, 2008, 08:27:56 AM »

Yes, I always run low too...always under 98 over whatever and generally go up during D.  Correct me if I'm wrong but I think anxiety does act like this...fine and then bump.
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Lost vision due to retinopathy 12/2005, 30 Laser Surg 2006
ESRD diagnosed 12/2006
03/2007 Fantastic Eye Surgeon in ND got my sight back and implanted lenses in both eyes, great distance & low reading.
Gortex 4/07.  Started dialysis in ND 5/4/2007
Gortex clotted off Thanksgiving Week of 2007, was unclotted and promptly clotted off 1/2 hour later so Permacath Rt chest.
3/2008 move to NC to be close to children.
2 Step fistula, 05/08-elevated 06/08, using mid August.
Aug 5, 08, trained NxStage and Home on 9/3/2008.
Fistulagram 09/2008. In hospital 10/30/08, Bowel Obstruction.
Back to RAI-Latrobe In Center. No home hemo at this time.
GOD IS GOOD
RichardMEL
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« Reply #13 on: August 16, 2008, 09:43:47 AM »

7piglets - I'm concerned when you say you "skip" Fridays... is this your choice (ie you just don't go?) or what? If you skip a lot of sessions you might be considered non compliant with your dialysis, which could get in the way of a transplant.... plus as Staufenberg said you really need as much of it as you can get - even if the labs are OK.

I am surprised the staff are not offering anything in terms of you throwing up (which would account for the lack of fluid "gain" if you're throwing up enough of it)... poor thing that is pretty yuky... I hope whatever is causing it can be resolved. I've never thrown up on Hemo... touch wood....

 :cuddle;
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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!
willieandwinnie
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« Reply #14 on: August 16, 2008, 10:01:03 AM »

HEPARIN! Len went through the same thing when he was on dialysis. There are 2 types of heparin, I remember one had something to do with pork, and for the life of me I can't remember the other. Len had the same reaction to the pork type and once they switch him, that seemed to do the trick. Ask the nurse at your clinic. Len also had a reaction to the dialyzer if they did not rinse the machine enough. Hope you get to the bottom of things. 7piglets, When Len first came home from the hospital in 2001, he only went 2 times a week and only ran for 2 hours, he got fluids, never any taken off. He had labs drawn each treatment to keep an eye on things. Keep us posted.  :cuddle;
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Mercurial
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« Reply #15 on: August 16, 2008, 12:02:50 PM »

It is not b/p as I usually run on low side it actually goes up alitltle ..It is not anxiety as I am fine then all of a sudden the symptoms start. I have mentioned to the tech/nurses (and they are there every time it happens and they said they dont know what is causing it) I called my neph dr on Wed and asked what can be done he called while I was at dialysis so I have to wait now until mon to call him back..

Do they have you on a reuse filter?  If you are, switching it to 'one use' would be the first thing I'd do.  The chemicals they use to clean the reused filters leave a residue that can definitely provoke an allergic reaction.
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pelagia
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« Reply #16 on: August 16, 2008, 05:06:55 PM »

Sounds like you need to make a list of things they should explore and rule out.  If the blood pressure isn't an issue, then everything else that has been suggested relates to allergic reactions:

dialysis tubing
type of heparin (porcine vs. ???)
reuse of filter/chemicals used to clean the filters

I sure hope they can figure this out soon.

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As for me, I'll borrow this thought: "Having never experienced kidney disease, I had no idea how crucial kidney function is to the rest of the body." - KD
Ang
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« Reply #17 on: August 16, 2008, 08:17:51 PM »

7 piglets  very  strange  that  you  do  not  gain  fluid  and  have  none  removed,  i  was  ubder  the  opinion  that  the  machines  will  not  operate  if  fluid  is  not  removed,they  have  to  allow  for  washback etc  any  drinks  ,food  you  consume  during  dialysis,you  must  spend  all  day  on  thetoilet  if  you've  got  no  fluid gains.

its  matter  of  trial  by  deduction.

make  a  list  of  when  you  get  on  the  machine  up  to  the  point  you  start  feeling  bad
1.is  it  the  heparin
2. what  is  the  pump speed  you  start  feeling  bad.
3. etc  etc  etc

please   do  not  miss  any  sessions  as  the  limited  dialysis  only  removes  a  small   %  of  toxins,it  will  just  accumulate  to  a  dangerous  level  then  trouble.
good  luck  hope  you  work  it  all  out.
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7piglets
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« Reply #18 on: August 16, 2008, 11:04:32 PM »

As for fluid gain no I dont gain and I am told they are not removing anything.. I do know when I weight myself getting there and weigh myself leaving I am usually just a little over start( but not much at all)
As for heparin they dont give me heparin until the end of the session so that wouldnt be it since I get the reaction 10-15mins after starting.
I am curious if they are using a reuse filter and will ask...I dont know the rate and will ask that also on Mon
As for skipping Fridays...It is not like i say oh today I am not going so I am going to skip...My 39 yr old brother died and was buried on friday , I have cancer for 3rd time and had surgery and was discharged from hospital after tumor removed from chest wall and was in so much pain from it couldnt drive on another friday and had a couple of more serious situations that caused the miss .(I believe 4 since I started )
As for uncompliant so cant get a kidney doesn't matter because they wont give me one anyway with cancer
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Jess21
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« Reply #19 on: August 16, 2008, 11:53:19 PM »

They dont give heparin til the end? I was under the impression they gave it towards the beginning since its short lasting and only lasts for the dialysis session.  Am I wrong on this?
You use a cath don't you?  Maybe it's a reaction to the stuff they "push" before connecting you to the machine? Just a thought.
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Hospitalized w/ renal failure- Nov. 2007
Diagnosed w/ ESRD w/ unknown cause- Jan 2008
Lower arm AV Fistula created- March 2008
On IL transplant list- Oct. 8th, 2008
On WI transplant list- June 25th, 2009
Pediatric 2 kidney transplant- July 6th, 2009 (3/6 antigen match)
circleNthedrain
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« Reply #20 on: August 17, 2008, 12:46:02 AM »

Heparin is given to me right at the very beginning and then the machine gives it automatically during the treatment.  It is discontinued during the last hour.
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1979 Diagnosed with kidney failure
1979 Right arm fistula
1979 Start hemodialysis
1980 CAPD catheter
1980 Start CAPD
1989 Cadaveric kidney transplant
1995 2nd cadaveric  kidney transplant
2007 Start hemodialysis
2010 Still drawin' wind
monrein
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« Reply #21 on: August 17, 2008, 01:28:56 AM »

exactly the same for me, except that when I used my permacath it wasn't discontinued the last hour.
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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
7piglets
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« Reply #22 on: August 17, 2008, 07:03:41 AM »

I could be wrong however, near end of my treatment they put 2 filled syringes by the machine and when I asked what it was they told me my heparin...
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bowie
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« Reply #23 on: August 17, 2008, 07:13:10 AM »

The 2 syringes filled with heparin are for your catheter ports.  To help prevent blood clots forming between treatments.  It is a more concentrated dose than you get during your treatment.
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monrein
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« Reply #24 on: August 17, 2008, 01:16:29 PM »

They no longer use heparin here in the catheter ports.  They use a citrate flush but I remember back a long time ago that they used to use a heparin flush.
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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
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