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Author Topic: Feeling Cold, Chills and Sweating after Hemo?  (Read 6227 times)
smcd23
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The patient, the baby and the donor - October 2010

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« on: June 12, 2014, 07:13:32 PM »

My husband does hemo 3x a week. Since they stopped nocturnal at his center, he has been going to the "later" evening shift. He gets home around 11 and then goes to bed shortly after. He will come home and feel okay, maybe a slight chill but it's summer now so that isn't happening as much. We will get in bed and within a short time he is freezing, he gets extra blankets for the bed and will still be very cold. But then on other nights, maybe once a week after the cold and chills a few hours later, in the middle of the night he will wake up hot and sweating. And it's not like sweating from too many blankets, it's drench the blankets, pillow, sheets sweating. I've seriously had to go out to WalMart and buy him a new pillow more than once because his didn't dry out overnight.

Is this something other people have experienced? Or normal? We both get annoyed (I hate having to change the sheets all the time, and buy new pillows) but he doesn't sleep good on the nights it happens.  :(
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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?
jeannea
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« Reply #1 on: June 12, 2014, 07:43:27 PM »

I have experienced that but it was after transplant not after dialysis. I know Prednisone can cause night sweats. Other meds could too. And dialysis affects each of us differently.

BTW, most pillows can be washed in the washer then put in the drier so they're ready again. Check the label.
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Speedy1wrc
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« Reply #2 on: June 12, 2014, 07:53:25 PM »

I have run into that after a significant BP drop. If it goes horribly low I sweat profusely then once it climbs I get then chills. I usually am so frazzled I fall asleep and will wake in an hour or two drenched in sweat.

What is his BP post treatment. Does he take BP meds at bedtime?
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smcd23
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The patient, the baby and the donor - October 2010

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« Reply #3 on: June 12, 2014, 08:27:03 PM »

I have run into that after a significant BP drop. If it goes horribly low I sweat profusely then once it climbs I get then chills. I usually am so frazzled I fall asleep and will wake in an hour or two drenched in sweat.

What is his BP post treatment. Does he take BP meds at bedtime?

He takes his BP meds before dialysis, around 630pm each night. His BP has been really decent, actually, usually in the "normal" range of 130/85 (he was really high for awhile). His dry weight has also been up and down, mostly down, because its summer, he is sweating more and the past few Mondays he has walked in only 1kg over his dry weight, when over the winter he would usually gain about 3-4kg over a weekend. I know he said on more than one occasion in recent weeks his BP has gone low during treatment and they had to give him some saline.

I'll have to try and remember to ask him what his BP was when he leaves dialysis the next few nights. I know for a fact he had left under their threshold a few times because it went to like 90/50 and no matter how much fluid they gave back they couldn't get it up, and he was feeling okay so they let him leave.

Haha I just asked him and he said it is usually low, like around 100/70. Maybe the mystery has been solved?
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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?
Speedy1wrc
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« Reply #4 on: June 13, 2014, 05:56:41 AM »

At least it's something to look into.

If you have a BP monitor at home you could always check it when he gets home.

I am at home so when my BP hits 120 I back off on my UF so I don't crash. The drop and rebound are nasty if it goes too low. In center the patient may not know what their BP trends are. Talk to your nephrologist and let them know about the drops and see if they can write orders to modify his UF goal on the fly if necessary.
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KarenInWA
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« Reply #5 on: June 14, 2014, 12:46:36 PM »

If his BP is low after treatment, maybe he should talk to his dr about taking his meds at a different time of the day.

KarenInWA
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1996 - Diagnosed with Proteinuria
2000 - Started seeing nephrologist on regular basis
Mar 2010 - Started Aranesp shots - well into CKD4
Dec 1, 2010 - Transplant Eval Appt - Listed on Feb 10, 2012
Apr 18, 2011 - Had fistula placed at GFR 8
April 20, 2011 - Had chest cath placed, GFR 6
April 22, 2011 - Started in-center HD. Continued to work FT and still went out and did things: live theater, concerts, spend time with friends, dine out, etc
May 2011 - My Wonderful Donor offered to get tested!
Oct 2011  - My Wonderful Donor was approved for surgery!
November 23, 2011 - Live-Donor Transplant (Lynette the Kidney gets a new home!)
April 3, 2012 - Routine Post-Tx Biopsy (creatinine went up just a little, from 1.4 to 1.7)
April 7, 2012 - ER admit to hospital, emergency surgery to remove large hematoma caused by biopsy
April 8, 2012 - In hospital dialysis with 2 units of blood
Now: On the mend, getting better! New Goal: No more in-patient hospital stays! More travel and life adventures!
smcd23
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The patient, the baby and the donor - October 2010

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« Reply #6 on: August 14, 2014, 07:30:00 PM »

Follow up post because I'm so angry right now...

Hubby is still sweating tons after dialysis. Cut back on one of his bp meds to no avail. Last night he soaked the sheets, the blanket on TOP, of him, soaked through the "waterproof" rubber lined mattress pad and into the mattress to the point it's STILL soaked 12 hours later, thus staining and voiding the warranty on our not even a year old expensive mattress. I'm beyond upset, like we cannot sleep in the bed tonight because it's so wet, and I have to work in the morning. I don't know what to do...
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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?
jeannea
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Posts: 1955

« Reply #7 on: August 15, 2014, 03:05:05 PM »

Wow! Has the doc said anything else or just ignored him? Someone should know why this is happening.
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smcd23
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Posts: 528


The patient, the baby and the donor - October 2010

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« Reply #8 on: August 15, 2014, 04:45:01 PM »

Per usual, complaints fall on deaf ears. He is going to bring it up again when he sees the doctor and he said the social worker was going to call me (about an unrelated issue) and I'm going to mention it to her and add that they can buy me a new mattress.
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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?
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