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Author Topic: Are you on a cycler?  (Read 6647 times)
KICKSTART
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« on: July 04, 2009, 08:57:16 AM »

Can i just ask those of you on cyclers what total UF's you are getting on average ?
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OH NO!!! I have Furniture Disease as well ! My chest has dropped into my drawers !
peleroja
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« Reply #1 on: July 04, 2009, 10:06:44 AM »

It depends on how much I drink during the day.  Most days, with all green, I get between 500 and 900.  The more I drink, the more I get out.  The nurses told me that if you're drinking "normally," you should be getting back 500 or more.  If I use a red I may get out as much as 1200.  Hope that helps. 
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« Reply #2 on: July 04, 2009, 11:57:44 AM »

My usual two bags of 2.5% (green) usually gets me between 700 and 1200 out. If a use one 2.5% and one 4.25%, I can get up to 1900 out. When I first started on the cycler, I was terribly fluid-overloaded, and a 2.5% + 4.25% took off 2100-2500 ml each of the first few nights.
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- 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!
KICKSTART
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« Reply #3 on: July 04, 2009, 12:01:02 PM »

Peleroja,       Yes thanks , i just wanted a comparison of other peoples UF  Im really suprised i get an average of 14-1800 per night , sometimes up to 2300 ! Yes i still pass urine as well !  Wow mine seems a lot doesnt it ? and thats with green and orange bags. Also are you not on fluid restrictions ?
« Last Edit: July 04, 2009, 12:02:22 PM by KICKSTART » Logged

OH NO!!! I have Furniture Disease as well ! My chest has dropped into my drawers !
Hanify
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Hadija, Athol, Me and Molly at Havelock North 09

« Reply #4 on: July 04, 2009, 05:48:26 PM »

If I use two greens it varies between 700 - 1200, if I use a yellow and a green it varies between 500 - 700.  I've never quite worked out why it changes so much.  I am pretty careful about my fluid intake.  I guess my body does different things with the fluid on different days. 
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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
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« Reply #5 on: July 05, 2009, 11:42:58 AM »

If I use two greens it varies between 700 - 1200, if I use a yellow and a green it varies between 500 - 700.  I've never quite worked out why it changes so much. 

The lowest number (1.5%) contains the least amount of dextrose, which is what removes the fluid.  Less dextrose means less fluid removed.  As for me, I've never restricted my fluid while on PD, but then I don't drink all that much to begin with.  I just never seem to get thirsty.
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george40
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« Reply #6 on: July 05, 2009, 12:48:18 PM »

Since being back on the cycler I have averaged 600. Thats using 1 green (2.5% bag, 4 cycles, 1000ml fills) I will be going back to the full 2 bag treatment soon, so Ill report back.  BUt even when I was doing the full 2 bags, the total UF still only averaged 650 - 700. I do not restrict my fluids.
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8/2000 - Diagnosed ESRD / Hemo begins with perm cath
1/2002 - Transplant No. 1
4/2006 - Transplant failed due to CMV virus/ Back to Hemo
11/2008 - Moved to PD Modality
9/2012 - Transplanted!
Hanify
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Hadija, Athol, Me and Molly at Havelock North 09

« Reply #7 on: July 05, 2009, 07:13:47 PM »

Thanks Peleroja - I meant I wasn't sure why the uf varies when I use the same bags - i.e two nights in a row I'll use two greens, one night will pull off 700, the next night 1200.  That's the bit I don't quite understand.  I think I must just have drunk more without being aware of it.  Kind of like when I used to diet and not realise how much I'd eaten in a day.  Ha ha.
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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.
prospector
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« Reply #8 on: July 05, 2009, 09:09:45 PM »

I use the Liberty cycler. When using two (2) green bags I get from 1500-1900 UF with a few into the 2000 range. I usually use a 1.5 in conjunction with a 2.5 and consistently get 1100-1300 UF. I ran out of green solution (2.5%) last week and used 2 yellows (1.5%). I was shocked to only get 325 UF return. Dialysis center couldn't offer a good explanation either. Everything went back to normal when the 2.5% solution was back in use.
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« Reply #9 on: July 05, 2009, 09:43:03 PM »

I was ultrafiltrating more my first month on the cycler. After my second episode of peritonitis, I think the way my peritoneum ultrafiltrates changed, and I started ultrafiltrating less. Whereas I was usually on one 1.5% bag and one 2.5%, I've had to go up to two 2.5% bags most nights. The last time I used two 1.5% bags, I got negative UF. I just had my first PET test and 24 hour collection since that change, so I'll have those results and know for sure in a couple days.
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- 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!
Red from Canada
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« Reply #10 on: July 06, 2009, 07:56:40 AM »

I use 3-2.5 bags with 5 fills of 2500 each night and get between 1500 and 2000 UF.  I am on the Baxter cycler and have never restricted my fluid.
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KICKSTART
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« Reply #11 on: July 06, 2009, 10:50:28 AM »

I am really amazed that none of you seem to be on fluid restrictions ! I am sick of hearing  about watching my intake (limited to 1500) despite being dehydrated several times!
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OH NO!!! I have Furniture Disease as well ! My chest has dropped into my drawers !
paul.karen
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« Reply #12 on: July 06, 2009, 10:56:30 AM »

Do you pee alot kickstart?
I think that has alot to do with it.
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Curiosity killed the cat
Satisfaction brought it back

Operation for PD placement 7-14-09
Training for cycler 7-28-09

Started home dialysis using Baxter homechoice
8-7-09
Red from Canada
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« Reply #13 on: July 06, 2009, 11:14:01 AM »

I was told that PD wasn't nearly as restrictive as hemo on either fluid or diet, and have never limited fluid.  I seem to take off whatever i take in during the day, even though I no longer pee.  I probably have 50 or 60 oz during the day, mostly ice water or black coffee.
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Hanify
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Hadija, Athol, Me and Molly at Havelock North 09

« Reply #14 on: July 06, 2009, 03:18:01 PM »

I'm like you Kickstart and am really careful with my fluid.  Maybe we need to experiment a bit and loosen up with it?  I will if you will.  It's never occurred to me that the machine will take off more if I drink more...I thought I just had to do as I was told ha ha.  Thanks IHD people.
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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.
djgaryb11
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« Reply #15 on: July 06, 2009, 06:20:33 PM »

I use the Baxter Homechoice Cycler....Typically I use 2 - 6000 ml 2.5 % bags each night....and my UF is around 1000-1400 ....Sometimes I use one 2.5 %  6000 ml bag and one  6000 ml 4.25 % ...and when i do I usually get a UF around 2000-2300 ....Gary
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7/2001 Diagnosed with Hypertension and Chronic Kidney Disease
2/2008 Diagnosed with End Stage Renal Disease
4/2008 Surgery to Create Backup A/V Fistula in Left Arm
7/2008 Placed on "UNOS" list for a Kidney Transplant
10/2008 Surgery to place PD Catheter
10/2008 Started CAPD
11/2008 Started on Baxter HomeChoice PD Cycler ( CCPD)
KICKSTART
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« Reply #16 on: July 07, 2009, 03:36:20 AM »

Before i went on the cycler i had a build up of fluid that wasnt visible and it was round my heart , which led to me having a heart attack, i was on fluid restrictions then ( i always have been) .They put me on the cycler at that time , hence my deciding to try it at home, but no one ever said i could increase my fluid intake. Im not sure about the more i drink the more the cycler will pull off, some mornings i get up feeling quite bloated to start with, as though im fluid overloaded. Im also suprised at how many different regimes we are all on.
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OH NO!!! I have Furniture Disease as well ! My chest has dropped into my drawers !
Ken Shelmerdine
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« Reply #17 on: July 07, 2009, 05:33:41 AM »

For the two years I was on the cycler I used the weakest bags over an 8 hour period  and got an average of 275mls. This doesn't seem a lot but I still pass a lot of fluid and my adequacy was 2.7 which the capd clinic said was way above adequate.

 Now I'm on haemo I don't allow them to take off any UF. If my kidneys are eventually going to stop producing urine I'd rather it start naturally than let the haemo accellerate it.
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Ken
Hanify
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Hadija, Athol, Me and Molly at Havelock North 09

« Reply #18 on: July 07, 2009, 11:39:47 PM »

Before i went on the cycler i had a build up of fluid that wasnt visible and it was round my heart , which led to me having a heart attack, i was on fluid restrictions then ( i always have been) .They put me on the cycler at that time , hence my deciding to try it at home, but no one ever said i could increase my fluid intake. Im not sure about the more i drink the more the cycler will pull off, some mornings i get up feeling quite bloated to start with, as though im fluid overloaded. Im also suprised at how many different regimes we are all on.

That's really frustrating Kickstart.  I only feel a bit bloated at the end of the day after having the extraneal in all day. That usually goes when I drain - usually about 2500. You almost sound like I felt when they tried doing 2.5l bags in me (because I'm tallish).  Any chance they could allow you to have less fluid in during the day?  Just a thought.  I'm also surprised about the different amounts/rules etc.  Strange.
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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.
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