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Author Topic: Night sweats and filter/dialyser  (Read 9867 times)
Bruno
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« on: October 11, 2010, 01:22:30 AM »

Has anyone heard of a connection between night sweats and the type of dialyser being used? I get real bad sweats after dialysis and if I'm off dialysis for a day or two they ease off but come back again after a session. I go to bed and get to sleep only to wake up in a lather a few hours later. This is about 12 hours after I finish dialysis.
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KICKSTART
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In da House.

« Reply #1 on: October 11, 2010, 04:27:38 AM »

I dont get sweats a such but always find im very hot (or so im told  :rofl; ) No seriously , i was talking to a guy at dialysis who was the same , turned out its our BP meds. He came off his and the sweats went away, are you on any ?
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OH NO!!! I have Furniture Disease as well ! My chest has dropped into my drawers !
Hazmat35
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« Reply #2 on: October 11, 2010, 04:37:58 AM »

I constantly find myself with HOT FLASHES and NIGHT SWEATS!  It drives me crazy.  I usually take a long cool shower to try to cool off, or sit in front of the fan with a cool rag on my forehead!  It doesn't really help, but it's worth a try. 
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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!!!!  :)
ChickenLittle56
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Chickenlittle and Maria

« Reply #3 on: October 11, 2010, 11:17:41 AM »

I also get night sweats, I get up and the sheets are damp. I am seing my cardiologist in about two weeks I will ask him if there is any side effects on my meds.
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As I was coming out the Nephrologist office, I thought the sky was falling.
Knew I was going on dialysis since November 1999.
Had a fistula put in January 2000.
Been on 4-1/2 hour dialysis since August 28, 2001. (They took out 35Kg that single week)

Maria hasbeen on hemodualysis since January, 2005
Bruno
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« Reply #4 on: October 12, 2010, 02:01:42 AM »

I'm off all of my BP meds because when I went on diallysis it went down and stayed down. The only BP med (at least I think it is) is Avapro which is supposed to be good for my heart (I'm an open heart surgery...triple bypass...survivor).
I was wondering what it might be about dialysis that could be causing it. I saw someone on the site claim that it was his filter.
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greg10
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« Reply #5 on: October 12, 2010, 07:55:29 AM »

There is no good answer to this as far as I have read.  Some think it has to do with infection and you should watch your temperature carefully, others think this may be a natural response to the catabolic process of hemodialysis where glucagon and adrenaline and other catabolic hormones are released.

http://www.medhelp.org/posts/Kidney-Disease--Disorders/Kidney-Patient-Excessive-Sweating/show/615988
« Last Edit: October 12, 2010, 08:32:07 AM by greg10 » Logged

Newbie caretaker, so I may not know what I am talking about :)
Caretaker for my elderly father who has his first and current graft in March, 2010.
Previously in-center hemodialysis in national chain, now doing NxStage home dialysis training.
End of September 2010: after twelve days of training, we were asked to start dialyzing on our own at home, reluctantly, we agreed.
If you are on HD, did you know that Rapid fluid removal (UF = ultrafiltration) during dialysis is associated with cardiovascular morbidity?  http://ihatedialysis.com/forum/index.php?topic=20596
We follow a modified version: UF limit = (weight in kg)  *  10 ml/kg/hr * (130 - age)/100

How do you know you are getting sufficient hemodialysis?  Know your HDP!  Scribner, B. H. and D. G. Oreopoulos (2002). "The Hemodialysis Product (HDP): A Better Index of Dialysis Adequacy than Kt/V." Dialysis & Transplantation 31(1).   http://www.therenalnetwork.org/qi/resources/HDP.pdf
calypso
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« Reply #6 on: October 12, 2010, 08:24:29 AM »

I've been on hemodialysis for almost a year, PD for 6 years. On PD I don't think I've ever gotten night sweats. On HD I have gotten night sweats maybe 4 or 5 times all year. No idea what it was attributed to. I know I was a bit overhydrated when it happened, but I've been overhydrated without it happening as well. So it's not hydration level related.

I have no idea what the cause is but it's happened so infrequently to me that I never looked into it. I don't have diabetes, if that helps. Good luck finding the cause and treating it.
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"The very powerful and the very stupid have one thing in common. Instead of altering their views to fit the facts, they alter the facts to fit their views ... which can be very uncomfortable if you happen to be one of the facts that needs altering.
-Doctor Who, "Face of Evil"

"The trouble with the world is not that people know too little, but that they know so many things that ain't so." - Mark Twain

"Darkness cannot drive out darkness; only light can do that. Hate cannot drive out hate; only love can do that." -Martin Luther King Jr.
carson
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« Reply #7 on: October 15, 2010, 07:17:14 PM »

Am I the only one who FREEZES? I wear: t-shirt, flannel pjs,  socks, electric blanket, cotton sheet, down duvet, light comforter and, of course, my trusty cat (the furnace). I can't take the cold and might even welcome the idea of night sweats for a change.
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2009 infection treated with Vancomycin and had permacath replaced
2009 septic infection that wouldn't go away
2007 began Nocturnal Home Hemo with Permacath
1997 began Peritoneal Dialysis
1982 had cadaver transplant
1981 diagnosed with GN2 and began Peritoneal Dialysis
Bruno
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« Reply #8 on: October 17, 2010, 10:18:46 PM »

My nurse has given me a new filter to try, supposedly it is allergy free. I had sweats immediately after dialysis today and think I smelt like a polecat which was embarrassing. I'll let you know whether The new filter helps.
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Marinterry
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« Reply #9 on: August 11, 2014, 08:19:04 PM »

I started hemo-dialysis one month ago. After two weeks, I began having night sweats after my sessions. Not sure what it's attributed to, but it only happens on dialysis days. Maybe the blood pressure meds in conjunction with the dialysis does it. It is definitely no fun. I think I should not be sleeping in my bed on those nights, but rather on top of it with a blanket. Haven't yet, hope it passes.
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cassandra
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When all else fails run in circles, shout loudly

« Reply #10 on: August 12, 2014, 01:32:34 PM »

What's your BP after treatment? I have terrible nightsweats when my BP is too low. So I increased my dry weight quite a bit (probably cos I (can) eat 6 times as much on home hemo than on in-center), lol
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I started out with nothing and I still have most of it left

1983 high proteinloss in urine, chemo, stroke,coma, dialysis
1984 double nephrectomy
1985 transplant from dad
1998 lost dads kidney, start PD
2003 peritineum burst, back to hemo
2012 start Nxstage home hemo
2020 start Gambro AK96

       still on waitinglist, still ok I think
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