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Author Topic: PHOSPHORUS!!! HELP!!!  (Read 7257 times)
jshabanian
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« on: April 26, 2012, 02:32:41 PM »

I am on hemo dialysis and recently my phosphorus level has been really high, like 10.7. This has been going on for about 1.5 months now.  I have switched binders several times and upped the doses.  I am now taking 2 Phoslo and 3 Renvela with each meal. I am aware of which foods contain phos. and am avoiding or limiting those foods.  I feel so frustrated because I know I am doing what I need to do and nothing seems to be working.  I was taking a generic phoslo type product and just added Renvela last week.  How long does it take for the levels to come down?

Has anyone of you struggled with Phos?
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Cordelia
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« Reply #1 on: April 26, 2012, 03:03:03 PM »

I completely undertand your frustration!!!!         :grouphug;
Phos is my weakness and I have to watch. Unfortunately, I don't know what to tell/advise you since I'm on Renagel. I've never been on any of the other binders you are on.

I hope it all gets sorted out. Hang in there though. It took me months-a good six months it seemed before my levels really started coming down. I hated having the docs on my case about it montly. It was a thorn in my side.       ::)
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Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
ChrisEtc
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« Reply #2 on: April 26, 2012, 03:38:45 PM »

I've had trouble with that the last few months.  It seems a lot of the drinks I buy have phosphorous and this surprised me.  Things like orange juice, lemonade, etc.  It's really not just what you eat!
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Cordelia
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« Reply #3 on: April 26, 2012, 03:52:32 PM »

You're right. From my understanding, there's a certain amount of phosphorus in pretty much everything         ::)
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Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
Whamo
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« Reply #4 on: April 26, 2012, 11:43:34 PM »

Lemonade?  It's on my list for good drinks for dialysis patients.
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deniferfer
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« Reply #5 on: April 27, 2012, 12:51:30 AM »

My phosphorus is always high!! Its the one thing that is the hardest to keep in check. But I take tums(3 or 4 depending on what I eat) and it works for me along watching what I eat and drink. I hate when I think I'm safe and eat something to find out later that it had phosphorus in it.
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1981-1995: Perfectly fine
1996: November, started feeling sick
1997: April, creatine at 17 and began dialysis    
1997: May Place on PD
2006: Had to replace PD tube
sparklelady
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« Reply #6 on: April 27, 2012, 06:56:39 AM »

From my understanding, canned lemonade and iced tea have quite a bit of phosphorus.
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Cordelia
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« Reply #7 on: April 27, 2012, 07:05:35 AM »

Yup, so does Coca Cola
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Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
mcclane
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« Reply #8 on: April 27, 2012, 08:10:18 AM »

From personal experience, frequent and long dialysis times help in reducing phosphate levels.  I was on home nocturnal hemo, which req'd dialysis 6 days a week/8 hour runs, and my phosphate levels were within range.

The closer I got to my surgery date, I slacked off my dialysis regimen and just did 3 hour runs but high flow rate, and my phosphate levels went through the roof.

As cordelia mentioned, all foods contain phosphorous, it is just a matter of how much. 
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MomoMcSleepy
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My son Roddy McSleepy at 6 months! sry pic sidewz

« Reply #9 on: April 27, 2012, 09:35:04 AM »

 :grouphug;
I've had trouble with that the last few months.  It seems a lot of the drinks I buy have phosphorous and this surprised me.  Things like orange juice, lemonade, etc.  It's really not just what you eat!

Probably depends on the type of drink, overly-processed drinks, or that you make forma powder, probably are worse.  I like to make things from scratch, so i know what's in it. 

Also, o don,t know what your function level is, Chris, but I don't even drink orange juice except for like, a shot glass full, because of the potassium.

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35 years old, first dx w/  chronic renal insufficiency at  28, pre-dialysis

born with persistent cloaca--have you heard of it?  Probably not, that's ok.

lots of surgeries, solitary left kidney (congenital)

chronic uti's/pyelonephritis

AV fistula May 2012
Kidney Transplant from my husband Jan. 16, 2013
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Zach
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« Reply #10 on: April 27, 2012, 10:37:00 AM »

Some more reading on IHD about phosphorus (PO4):

Food labels hide phosphorus content
http://ihatedialysis.com/forum/index.php?topic=12406.msg213156#msg213156

Hidden Phosphorus -- In Jello Mix!
http://ihatedialysis.com/forum/index.php?topic=23235.msg378163#msg378163

Teaching Dialysis Patients About Phosphorus
http://ihatedialysis.com/forum/index.php?topic=18865.msg322661#msg322661

And these oldies but goodies:
High Phosphorus
http://ihatedialysis.com/forum/index.php?topic=1742.msg22626#msg22626

Effect of Phosphorus Binders
http://ihatedialysis.com/forum/index.php?topic=11307.msg192723#msg192723

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.)
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sbmyluv
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« Reply #11 on: April 27, 2012, 01:19:51 PM »

Speak with the Dietician at your center and tell him/her the things you eat or drink on a daily basis.  They will be able to tell you what is driving your levels up.  Almost everything includeds some phosphorus and when consumed in high doses it brings your levels up.  ESPECIALLY PACKAGED FOODS!!!!
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1997-Dx. w/ FSGS & IGA Nephropathy
11/2011-ESRD; Fistula Placed
1/2012-Transplant Waiting List
1/2012-Perma Cath placed
1/2012-Started In Center Dialysis
6/2012-PD Cath Placed
8/2012-PD Started Night Treatments
Arcticat2000
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What. Me worry?

« Reply #12 on: April 27, 2012, 02:31:54 PM »

Try Fosrenol :thumbup;
Worked for me!
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ESRD diagnosed June 2003
Dialysis begins July 2003
Nocturnal Dialysis since Aug.2005-present
3 nights per week @ 7hrs per session
Heart bypass surgery Nov.2007 w artificial valve
bleija
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« Reply #13 on: April 27, 2012, 09:06:11 PM »

tea is fine, my clinic told me it was low, and my phos levels are always high so i dnt know about the renvela which is what i take... but mine is only 5.7 to 5.9 they just tell me to be stricter with my renvelas... yeah so stqy away from dairys and beans, and anything that has taste... cordboard is ok... good fiber too i would think ;)
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Restorer
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« Reply #14 on: April 28, 2012, 01:34:20 AM »

Freshly brewed tea is low in phosphorus. "Tea drinks" from a soda fountain or in a can or soda bottle - like Lipton Brisk or Nestea - have a lot of added phosphorus. There's a rule of thumb about tea in plastic bottles being bad, but tea in glass bottles is fine. Tea from a soda fountain is not good, but tea from a separate "freshly brewed" container is okay.

Any tea you make yourself is okay too.
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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!
SteveK87
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« Reply #15 on: April 28, 2012, 06:21:19 AM »

Try Fosrenol :thumbup;
Worked for me!

 :thumbup;

This is the only thing that works for my wife.
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bleija
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« Reply #16 on: April 28, 2012, 09:36:38 PM »

okay because i mostly drink tea, soda makes me bloated and im not big on water unless it is ice cold, i was tols tea good
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Hazmat35
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« Reply #17 on: April 29, 2012, 08:38:52 AM »

My Phos went up around Easter time, up to 6.0 but I think it was the chocolate i ate and the oranges.  Fresh Oranges are my weekness and when they are falling off the trees, here in Florida, it is hard for me not to eat them. 

I would keep a notepad with you and make a list for a week or so of everything you eat/drink and when and how many binders you take.  Sometimes we forget to take binders, or even forget that you ate or drank something. 
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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!!!!  :)
smcd23
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The patient, the baby and the donor - October 2010

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« Reply #18 on: May 04, 2012, 07:22:02 PM »

Try Fosrenol :thumbup;
Worked for me!

 :thumbup;

This is the only thing that works for my wife.

I third the Fosrenol! Only thing that works for my SO (when he remembers to take it)  >:(
The pills are large and chalky and you eat them like a Tums. My SO's only complaint is that they are chalky and have no taste, so his dietician told him to crush them and eat them in some applesauce, which seems to have been doing the trick.
No lie, his phosphorus is high (like double digits) and when he is faithful about his Fosrenol he can drop it into the good range in one months time.
And depending on your prescription drug coverage, the company offers a co-pay assistance card.  :thumbup;
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Caregiver to Husband with ESRD.

1995 - Diagnosed with vesicoureteral reflux and had surgery to repair at age 11. Post surgery left side still had Stage I VUR, right side was okay. Both sides were underdeveloped.
2005 - Discovered renal function was declining, causing HBP. Regular monitoring began.

March 2008 - Started transplant evaluation for preemptive transplant due to declining function.

September 16, 2008 - Transplanted with my kidney.
September 18, 2008 - Kidney was removed due to thrombosis in the vessels in and leading to the kidney.

October 2008 - Listed in Region I

May 2009 - Started in Center Hemo
January 2010 - Started CCPD on Liberty Cycler

June 15, 2012 - Kidney transplant from a 43 year old deceased donor
June 22, 2012 - Major acute rejection episode and hospitalization began
June 27, 2012 - Nephrectomy to remove kidney after complete HLA antibody rejection. Possibly not eligible for another transplant, ever again.

Now what?
pdpatty
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« Reply #19 on: May 05, 2012, 02:39:38 AM »

http://www.nal.usda.gov/fnic/foodcomp/Data/SR17/wtrank/sr17a305.pdf

Check this out By the way,the amount of phosphorus in a can of cola may surprise you.
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Lovebelle
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« Reply #20 on: May 05, 2012, 08:53:51 PM »

I had alot of issues with my phosphorus as well. Then after months of struggling they noticed my PTH and calcium levels were varying (not significantly, but enough to make them wonder). So they decided to put me on Sensipar. I have to say once I started sensipar, I have not had any issues with my phosphorus levels! My phosphorus levels are now usually between 3.5-4 when before they were upwards of 7+. I have not even taken my fosrenol in months now because the sensipar seems to be doing the trick.

Im not sure what your other lab values are, but its something you may be able to talk to your nutritionist about.
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kitkatz
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« Reply #21 on: May 06, 2012, 03:43:32 PM »

Drop all wheat products from your diet and no sodas. Check everything you eat for wheat.  Anything multigrain drop it now.
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RightSide
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« Reply #22 on: May 13, 2012, 05:13:55 PM »

You're right. From my understanding, there's a certain amount of phosphorus in pretty much everything         ::)
True--but different foods vary in bioavailability--how much phosphorus actually gets absorbed into the bloodstream.

While vegetables like broccoli have significant quantities of phosphorus, they also contain phytate, a chemical which binds to phosphorus and prevents about 75% of it from being absorbed by the body.

Bioavailability is highest with liquids containing phosphorus, such as milk and cola drinks.

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