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Author Topic: 3x4 -> 2x5  (Read 4920 times)
GoingThere
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« on: November 18, 2010, 05:15:16 AM »

Hi!

My D neph put me on 2x5 hrs instead of 3x4 hrs. I will be on this new regime for 14 days and then lab test will be done. If they will be ok, I will be able to stay on that regime. My neph friend doesn't agree with that decision. I must admit that I trust her, so I'm thinking to switch back on 3x4 hrs.

What is your opinion? All blood markers are ok. I'm still peeing superb.

GT
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1995 - kidney biopsy - IgA
2002 - BP 220/140 - hospitilized
2004 - stage 3 of kidney failure
2005 - stagae 4of kidney failure
2009 - on the edge of stage 5
july 2010 - stage 5
14 july 2010 - catheter inserted and first D session
15 july 2010 - AV fistula created
dec. 2012 - tx with major rejection (plasmapheresis, atg, prednisone pulses)
apr 2013 - kidney function stable
Hazmat35
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« Reply #1 on: November 18, 2010, 05:25:06 AM »

I know that my Neph has repeatedly told me that LONGER and SLOWER is BETTER.  I personally have not heard of 2 x 5 but then again, what do I know!!!  I'm no DR. 

I have heard of people only doing Hemo Dialysis 2x per week. 

Good luck.  Let us know how it works!
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Brother Passed away - 1990 - Liver Disease
Diagnosed w/ Polycystic Kidney Disease - 1998
Mother passed away - Feb. 1999 - PKD
Sister passed away - Feb. 2006 - PKD
AV Fistula / Upper Left Arm - September 2009
Father passed away - September 2009
In-Center Hemo Dialysis - April 2010
Broken Knee Cap - January 2015
Diagnosed w/ A-Fib October 2017
Surgery to repair Hiatal Hernia 2018
Multiple Fistula Grams / Angioplasty's since then!


Hating Dialysis since Day 1 and everyday since then!!!!  :)
Zach
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"Still crazy after all these years."

« Reply #2 on: November 18, 2010, 07:20:13 AM »

Hi!

My D neph put me on 2x5 hrs instead of 3x4 hrs. I will be on this new regime for 14 days and then lab test will be done. If they will be ok, I will be able to stay on that regime. My neph friend doesn't agree with that decision. I must admit that I trust her, so I'm thinking to switch back on 3x4 hrs.

What is your opinion? All blood markers are ok. I'm still peeing superb.

GT

Do you still have some kidney function?

8)
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."
Desert Dancer
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« Reply #3 on: November 18, 2010, 07:30:03 AM »

Hi, GT -

Well, if you look at all the available information the one constant you will find is: MORE dialysis is better. Long, slow runs allow you to take off more fluid at a gentler rate, and many of the bigger molecules that cause us problems (such as phosphorus) can ONLY be removed with long, slow dialysis.

If you'd like some reading on adequate dialysis vs. optimal dialysis, here is a really good place to start:
http://www.billpeckham.com/from_the_sharp_end_of_the/optimal_dialysis/

Just my  :twocents; of course, and YMMV.
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August 1980: Diagnosed with Familial Juvenile Hyperurecemic Nephropathy (FJHN)
8.22.10:   Began dialysis through central venous catheter
8.25.10:   AV fistula created
9.28.10:   Began training for Home Nocturnal Hemodialysis on a Fresenius Baby K
10.21.10: Began creating buttonholes with 15ga needles
11.13.10: Our first nocturnal home treatment!

Good health is just the slowest possible rate at which you can die.

The glass is neither half-full nor half-empty. The glass is just twice as large as it needs to be.

The early bird may get the worm but the second mouse gets the cheese.
lorna
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« Reply #4 on: November 18, 2010, 08:33:40 AM »

i was recently switched to 4x per week 4 hours at a time. As much as i hate going i feel better and find it easier to manage fluids. I did pd daily so maybe im just used to it but i dont know that i would trust 2x5. Everyone is different though so if it does work for you go for it, you will have more time to yourself
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Zach
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"Still crazy after all these years."

« Reply #5 on: November 18, 2010, 08:44:55 AM »


Well, if you look at all the available information the one constant you will find is: MORE dialysis is better. Long, slow runs allow you to take off more fluid at a gentler rate, and many of the bigger molecules that cause us problems (such as phosphorus) can ONLY be removed with long, slow dialysis.


Actually, phosphorus is a small molecule solute, but it behaves similar to a middle molecule solute in that its removal is time dependent.

8)
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."
Desert Dancer
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Posts: 961


« Reply #6 on: November 18, 2010, 08:47:53 AM »

Thank you, Zach - I stand corrected!
Logged

August 1980: Diagnosed with Familial Juvenile Hyperurecemic Nephropathy (FJHN)
8.22.10:   Began dialysis through central venous catheter
8.25.10:   AV fistula created
9.28.10:   Began training for Home Nocturnal Hemodialysis on a Fresenius Baby K
10.21.10: Began creating buttonholes with 15ga needles
11.13.10: Our first nocturnal home treatment!

Good health is just the slowest possible rate at which you can die.

The glass is neither half-full nor half-empty. The glass is just twice as large as it needs to be.

The early bird may get the worm but the second mouse gets the cheese.
GoingThere
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Posts: 150


« Reply #7 on: November 18, 2010, 11:27:20 AM »

I have no problems with fluid. I still pee a lot.
Logged

1995 - kidney biopsy - IgA
2002 - BP 220/140 - hospitilized
2004 - stage 3 of kidney failure
2005 - stagae 4of kidney failure
2009 - on the edge of stage 5
july 2010 - stage 5
14 july 2010 - catheter inserted and first D session
15 july 2010 - AV fistula created
dec. 2012 - tx with major rejection (plasmapheresis, atg, prednisone pulses)
apr 2013 - kidney function stable
Zach
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"Still crazy after all these years."

« Reply #8 on: November 18, 2010, 01:05:16 PM »

I have no problems with fluid. I still pee a lot.

How are your phosphorus and PTH levels so far?

8)
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."
Stoday
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« Reply #9 on: November 18, 2010, 01:05:50 PM »

If you still uinate a lot, then presumably you still have a greater residual kidney function than most of us. You might well get away with 2 days a week; only you can tell if it's OK by trying it out. Write down how you feel now just before the M/T session. Give it a month and then review how you feel just before the session after the 4-day interval.

Best of luck!
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Diagnosed stage 3 CKD May 2003
AV fistula placed June 2009
Started hemo July 2010
Heart Attacks June 2005; October 2010; July 2011
KICKSTART
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In da House.

« Reply #10 on: November 18, 2010, 02:20:43 PM »

This is slightly off topic but i couldnt help but notice you mention your 'neph friend'  is this the one you are dating ? because already she is influencing what you should do regarding treatment. Forget what she says and ask yourself what YOU would do. At worst go back to your neph and ask him the advantages of doing these hours.
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OH NO!!! I have Furniture Disease as well ! My chest has dropped into my drawers !
GoingThere
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« Reply #11 on: November 18, 2010, 04:20:12 PM »

@Kickstart - I asked her for opinion as I asked you. I know that I'm responsible for myself and no one else. I feel extremley fine, yesterday I was riding a bike without any problems, today I worked 10 hours at my faculty and now I was dancing salsa and bachata for three hours. Not tired at all  :beer1;

@Zach - my phosporus, calcium and potassium levels are within normal range. i do have a strict diet which I obey with military discipline  :2thumbsup;

I think I will give my new regime some time and then I will reevaluate my decision.

Tnx.

 
Logged

1995 - kidney biopsy - IgA
2002 - BP 220/140 - hospitilized
2004 - stage 3 of kidney failure
2005 - stagae 4of kidney failure
2009 - on the edge of stage 5
july 2010 - stage 5
14 july 2010 - catheter inserted and first D session
15 july 2010 - AV fistula created
dec. 2012 - tx with major rejection (plasmapheresis, atg, prednisone pulses)
apr 2013 - kidney function stable
boswife
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us and fam easter 2013

« Reply #12 on: November 18, 2010, 08:09:39 PM »

I think your wonderfuly lucky to have a Neph friend or like us,  a tech friend!  One of the techs at our unit was so knowledgeable and we trusted him (as a friend) completly! Im not saying be blinded or anything, but i feel that "friends" with knowledge are looking out for your best interest and a lucky find..
« Last Edit: November 18, 2010, 08:14:21 PM by boswife » Logged

im a california wife and cargiver to my hubby
He started dialysis April 09
We thank God for every day we are blessed to have together.
november 2010, patiently (ha!) waiting our turn for NxStage training
January 14,2011 home with NxStage
RichardMEL
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« Reply #13 on: November 19, 2010, 02:01:09 AM »

my only concern would be the length of time between treatments will be increased if you move to 2x5 (you will only really be doing 1/6th less dialysis over the course of a week, which isn't much). I guess if your remaining kidney function is decent that perhaps you will be OK in terms of toxin build up. It sounds like you're doing so wonderfully well right now with all the stuff you are able to do (I'm tired reading it!!!) :) So glad to read - good luck with whatever you wind up doing.
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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!
boswife
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us and fam easter 2013

« Reply #14 on: November 19, 2010, 11:05:37 AM »

and........ btw  :) , i"m  OBVIOUSLY no dr OR neph, so im not promoting any which way, but as much as i would love to have hubby on the 2 day thing, and was actually pushing for it at one time, for as much as i've learned, for *us* it wouldnt be a safe thing i dont think.  We're looking for daily now, but am very anxious to see how you do (if your going through with it)  One thing good is that it sounds like you'll be getting good monitoring so that part should keep ya safe.  Please keep us up on the outcome ok...
Logged

im a california wife and cargiver to my hubby
He started dialysis April 09
We thank God for every day we are blessed to have together.
november 2010, patiently (ha!) waiting our turn for NxStage training
January 14,2011 home with NxStage
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