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Author Topic: Doc reduces dialysate flow, what's yours?  (Read 9653 times)
circleNthedrain
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« on: July 30, 2009, 10:02:38 AM »

I've been going to the same unit for over 2 1/2 years and recently you can really feel all the cutbacks.  i have always run at 400 blood pump speed and 800 dialysate flow.  Yesterday they changed my dialysate flow to 600.  When I asked why, they said it was Doctors orders for all his patients.  WTH?  Anybody else experience this?  What flows do you run at?  Needless to say, I'm not happy and plan to talk to him about it as soon as I SEE him.
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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
dwcrawford
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« Reply #1 on: July 30, 2009, 10:45:55 AM »

Bill, I only run at 250 but then I still have only one needle.  I don't really understand but I'd ask Zach or somebody with as much experience and knowlege as you have.  How will that save them money? 
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Nothing that I post here is intended for fact but rather for exploration into my personal thought processes.  Any slight, use of words with multiple connotations or other percieved insults are totally unintended.  I reserve my insults for private.
BigSky
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« Reply #2 on: July 30, 2009, 01:55:14 PM »

I run at 800 dialysate flow.

Some people I know run as low as 500.  I would ask him to what medical reasoning he did that and if your labs justify such a change.
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circleNthedrain
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« Reply #3 on: July 30, 2009, 03:05:27 PM »

Dan, I think you are talking about blood pump speed but I am talking about dialysate pump speed.  Less dialysate = less money.  With some of the chicken sh** cutbacks I've seen lately, I'm surprised they keep the lights on!

Thanks BigSky, you can bet I'll be asking some questions!
« Last Edit: July 30, 2009, 03:08:32 PM by circleNthedrain » Logged

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
dwcrawford
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Getting the heck out of town.

« Reply #4 on: July 30, 2009, 03:43:23 PM »

oops.  I told you the other night that I know nothing...

actually I'm not really sure what either of them are but don't take any less or more than you need.
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Come to think of it, nothing is funny anymore.

Nothing that I post here is intended for fact but rather for exploration into my personal thought processes.  Any slight, use of words with multiple connotations or other percieved insults are totally unintended.  I reserve my insults for private.
del
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« Reply #5 on: July 30, 2009, 04:24:18 PM »

On a 7 hour nocturnal run hubby has a 250 pump speed and a dialysate flow of 300. 
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Zach
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« Reply #6 on: July 31, 2009, 05:11:30 AM »

I'm at 800 dialysate flow (Qd).  But 700 seems to be the norm at my unit.
This refers to conventional 3 x week hemodialysis (3.5 - 5 hours)

I've been at some units where the dialysate flow was set at 1,000.  It's rarely used, but for higher blood pump speeds (Qb) of 500 or greater, it may be the most efficient for high-flux.

But remember, not all dialyzers are made for those higher blood pump speeds.  And there are many factors that lead to better clearances (time on the machine is perhaps most important).

In high-flux, dialysate flow twice the speed of the blood flow is perhaps considered the most efficient for the removal of urea, etc. Dialysate flow 1.5 x blood pump speed is a little less efficient, but perhaps not significantly.

Here's a look at the newer 2008K2 hemodialysis machine with it's dialysate "AutoFlow."
http://www.2008k2.com/2008k2_AutoFlow.html

Make sure you pay close attention to your monthly chemistries for any significant changes and then meet with your Nephrologist.

8)
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Uninterrupted in-center (self-care) hemodialysis since 1982 -- 34 YEARS on March 3, 2016 !!
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
No transplant.  Not yet, anyway.  Only decided to be listed on 11/9/06. Inactive at the moment.  ;)
I make films.

Just the facts: 70.0 kgs. (about 154 lbs.)
Treatment: Tue-Thur-Sat   5.5 hours, 2x/wk, 6 hours, 1x/wk
Dialysate flow (Qd)=600;  Blood pump speed(Qb)=315
Fresenius Optiflux-180 filter--without reuse
Fresenius 2008T dialysis machine
My KDOQI Nutrition (+/ -):  2,450 Calories, 84 grams Protein/day.

"Living a life, not an apology."
Hemodoc
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« Reply #7 on: July 31, 2009, 08:15:31 AM »

My unit did the same.  It is entirely a cost saving issue for water usage. However, since I was on self care in unit, I put mine back up to 800 and it did make over a 10% difference in my clearances.  The squeeky wheel gets the grease.  See what you clearances are at 600 compared to 800.  If it drops, I would insist on returning to 800.  Like I said, since I set up my own machine in unit, not much they were going to do about it anyway in my case.

So, it is all about a lower water bill and America's concept of adequate instead of optimal dialysis.  Just one more example.
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Peter Laird, MD
www.hemodoc.info
Diagnosed with IgA nephropathy 1998
Incenter Dialysis starting 2-1-2007
Self Care in Center from 4-15-2008 to 6-2-2009
Started  Home Care with NxStage 6-2-2009 (Qb 370, FF 45%, 40L)

All clinical and treatment related issues discussed on this forum are for informational purposes only.  You must always secure your own medical teams approval for all treatment options before applying any discussions on this site to your own circumstances.
circleNthedrain
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« Reply #8 on: July 31, 2009, 08:36:00 AM »

Thanks Hemodoc!  This was exactly my feeling on this and I would think it would have to reduce blood clearances...you can bet I will be watching mine very closely.  Lately more than ever, the bottom line seems to be the only concern.  "Adequate instead of optimal" is a very sorry state of affairs.
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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
circleNthedrain
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« Reply #9 on: July 31, 2009, 09:12:49 AM »

Sorry Zach....I lost my reply to you!!  Thanks for all the interesting information, I had hoped you would reply to this.  I am on 3X a week for 3 hours.  Recently we changed from Polyflux 210H dialyzer to Gambro Revaclear high-flux dialyzer.  They say the Polyflux will no longer be available in the US. I really don't like it when they make changes (25% dialysate flow reduction) without any explanation offered.  I will be keeping a very close eye on my labs.  Thanks again Zach!

"
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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
kidneyless_In_PA
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« Reply #10 on: July 31, 2009, 12:35:47 PM »

my blood flow rate was put up to 350 a few months back.. I am on 3 1/2 hours. 3 times a week.
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Busy 3 times a week and the other 4 days so cold and weak etc.
BigSky
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« Reply #11 on: July 31, 2009, 01:23:55 PM »

You might ask them why they didnt do a Kt/V the day they changed your flow rate.  Nothing is worse than having filters or flow rates changed and having to wait weeks to find out at the next regular lab draw if your Kt/V is where its suppose to be at or if you were getting piss poor dialysis during that whole time since they changed something.

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kidneyless_In_PA
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« Reply #12 on: July 31, 2009, 01:28:45 PM »

they don't care about us
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Busy 3 times a week and the other 4 days so cold and weak etc.
Hemodoc
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« Reply #13 on: July 31, 2009, 02:24:02 PM »

kt/v doesn't tell the whole story since they are only looking at the minimal standards, not optimizing all factors for the patients.  This is one for the pocket book of the unit owners, pure and simple.
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Peter Laird, MD
www.hemodoc.info
Diagnosed with IgA nephropathy 1998
Incenter Dialysis starting 2-1-2007
Self Care in Center from 4-15-2008 to 6-2-2009
Started  Home Care with NxStage 6-2-2009 (Qb 370, FF 45%, 40L)

All clinical and treatment related issues discussed on this forum are for informational purposes only.  You must always secure your own medical teams approval for all treatment options before applying any discussions on this site to your own circumstances.
circleNthedrain
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« Reply #14 on: September 10, 2009, 08:58:29 AM »

Well, I'm back to 800 dialysate flow!  Yay!  My kt/v dropped from 1.66 to 1.55 since they reduced the flow to 600 a little over a month ago.  This is lower than it's ever been. Grrr!!  I'm pushing for 4 hours instead of 3, and so far I'm up to 3 1/2.  Gotta take our little victories where we can. 
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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
Zach
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"Still crazy after all these years."

« Reply #15 on: September 10, 2009, 12:23:03 PM »

Well, I'm back to 800 dialysate flow!  Yay!  My kt/v dropped from 1.66 to 1.55 since they reduced the flow to 600 a little over a month ago.  This is lower than it's ever been. Grrr!!  I'm pushing for 4 hours instead of 3, and so far I'm up to 3 1/2.  Gotta take our little victories where we can.
:beer1;
Logged

Uninterrupted in-center (self-care) hemodialysis since 1982 -- 34 YEARS on March 3, 2016 !!
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
No transplant.  Not yet, anyway.  Only decided to be listed on 11/9/06. Inactive at the moment.  ;)
I make films.

Just the facts: 70.0 kgs. (about 154 lbs.)
Treatment: Tue-Thur-Sat   5.5 hours, 2x/wk, 6 hours, 1x/wk
Dialysate flow (Qd)=600;  Blood pump speed(Qb)=315
Fresenius Optiflux-180 filter--without reuse
Fresenius 2008T dialysis machine
My KDOQI Nutrition (+/ -):  2,450 Calories, 84 grams Protein/day.

"Living a life, not an apology."
paddbear0000
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« Reply #16 on: September 10, 2009, 03:24:31 PM »

When i first started, they started me out at 800 dialysate flow, but it gave me massive headaches and made me sick. We found that the highest I can tolerate is 600, but i'm a small person, so that may make a difference. My clearances could be better, but I feel less sick at the slower rate than I do at the higher rate!
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I HAVE DESIGNED CKD RELATED PRODUCTS FOR SALE TO BENEFIT THE NKF'S 2009 DAYTON KIDNEY WALK (I'M A TEAM CAPTAIN)! CHECK IT OUT @ www.cafepress.com/RetroDogDesigns!!

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Diagnosed type 1 diabetic at age 6, CKD (stage 3) diagnosed at 28 after hospital error a year before, started dialysis February '09. Listed for kidney/pancreas transplant at Ohio State & Univ. of Cincinnati.
circleNthedrain
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« Reply #17 on: September 10, 2009, 04:15:16 PM »

Hey paddbear...with dialysis you have to experiment to find what works best for you.  Glad you found the slower speed helps!
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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
paddbear0000
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Dogs & IHDer's are always glad to see you!

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« Reply #18 on: September 10, 2009, 07:56:03 PM »

My URR isn't great, but it's the lesser of 2 evils!
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********************************************************
I HAVE DESIGNED CKD RELATED PRODUCTS FOR SALE TO BENEFIT THE NKF'S 2009 DAYTON KIDNEY WALK (I'M A TEAM CAPTAIN)! CHECK IT OUT @ www.cafepress.com/RetroDogDesigns!!

...or sponsor me at http://walk.kidney.org/goto/janetschnittger
********************************************************
Twitter.com/NKFKidneyWalker
www.facebook.com/profile.php?id=1659267443&ref=nf 
www.caringbridge.org/visit/janetschnittger

Diagnosed type 1 diabetic at age 6, CKD (stage 3) diagnosed at 28 after hospital error a year before, started dialysis February '09. Listed for kidney/pancreas transplant at Ohio State & Univ. of Cincinnati.
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« Reply #19 on: November 08, 2009, 08:31:11 PM »

Can i ask why do you only have one needle? How does that work? I never heard of someone only having one needle on dialysis.

Lisa
Bill, I only run at 250 but then I still have only one needle.  I don't really understand but I'd ask Zach or somebody with as much experience and knowlege as you have.  How will that save them money?
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It is my utmost dream and desire to reach out to other kidney patients for them to know that they are not alone in this, also to reach out to those who one day have to go on dialysis though my book i am writing!

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circleNthedrain
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« Reply #20 on: November 26, 2009, 07:05:14 PM »

Hi Lisa...I think Dan was still using one tube from his perma-cath and one needle in his fistula.  This is a common practice while waiting for a fistula to mature.  You could PM him to find out for sure.
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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
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