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Author Topic: Advances in Peritoneal Dialysis 2008  (Read 3926 times)
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weKANer
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« on: September 08, 2008, 12:20:06 PM PDT »

From the recent Conference on Peritoneal Dialysis, the following articles on exciting developments in PD.  Some are a bit clinical, but a lot of good info is available...

Advances in Peritoneal Dialysis 2008
25 free, full-text articles in the annual issue (Volume 24) from MultiMed Inc.

http://www.advancesinpd.com/
« Last Edit: November 28, 2008, 10:22:01 PM PST by kidneysp »

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nsoc2008
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« Reply #1 on: October 01, 2008, 05:10:05 PM PDT »

Hi - My name is Allison, and I'm a Nursing student at Ohlone College in Fremont, CA.  I have a school project this semester, and the topic is Peritoneal Dialysis.  We will present on the process, and an interview with a patient and family if possible.  I wondered if anyone would be interested in answering a few of my questions regarding how dialysis works for you, pros and cons, and the life changes you have made (easy and difficult).

Thank you for the welcome to the forums!

Allison

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Marina
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« Reply #2 on: October 02, 2008, 02:31:42 PM PDT »

Hi - My name is Allison, and I'm a Nursing student at Ohlone College in Fremont, CA.  I have a school project this semester, and the topic is Peritoneal Dialysis.  We will present on the process, and an interview with a patient and family if possible.  I wondered if anyone would be interested in answering a few of my questions regarding how dialysis works for you, pros and cons, and the life changes you have made (easy and difficult).

Thank you for the welcome to the forums!

Allison

Hi  Allison,

 I  think  it's  great  that  you're  doing  a  project  on  PD,  I  feel that  so  little  is  known  of  this type  of  dialysis.  When  I  tell people  I'm  on dialysis  they  always  ask,   "oh  they  take  out  your  blood  and  put  it  back  in"    Or  when making  a  Dr's  appt   they  always  aks  "okay  we  can  work  around  your  dialysis  schedule, which  days   do  you dialyze?"          I  then  explain  I  dialyze  at  home  everyday,  and  most  people  are  confused  about  this.  I  always  get you  dialyze  every day  4x/day?   you  must  be  really  sick   LOL

 I'll be  more  than  happy  to  help  out  with  this  project.  Send  me  a  PM  or e-mail me.

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CAPD  since  April 2004
awaiting  a  kidney  and  pancreas  TX
"backup" call on  Jan  21, 2010
Angie
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« Reply #3 on: October 07, 2008, 11:25:33 AM PDT »

I was on Peritoneal Dialysis for 4 1/2 years before switching to Hemo so you can email me as well if you wish Smiley PM me.

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Always check advice you get online!

My Site | My Pix | KK Mall | Dialysis Ethics (new)

PD = 4 1/2 yrs
HD = 2 1/2 hrs
2nd Transplant: 9/30/07
jules17
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« Reply #4 on: October 08, 2008, 07:55:48 AM PDT »

Hi Allison!  I am a transplant recipient, but also did peritoneal dialysis.  I used the PD cycler.  You can feel free to email me with any questions you have. I am so glad you are doing your nursing project on dialysis.

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nsoc2008
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« Reply #5 on: October 08, 2008, 12:28:44 PM PDT »

Thank you!

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peterd196
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« Reply #6 on: October 22, 2008, 06:17:03 AM PDT »

Thank you for this update.  I have been on HD since May08 and I am strongly considering PD.  This will help for sure.  BTW I like the clinical stuff b/c I am a clinical pharmascist (not currently practicing).
Peter

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flosschick
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« Reply #7 on: July 01, 2009, 06:22:59 AM PDT »

I was a PD patient for 10 months.  After my transplant (about one year) I woke up one morning, looked down, and saw I had an incisional hernia.  When I went in for a consult prior to the surgical repair, I was told that this occurred fairly commonly with PD patients.  So, how many of you have experienced the same thing?
Flosschick

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Lillupie
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« Reply #8 on: September 02, 2009, 10:21:49 PM PDT »

i know what you mean. i have had 4 hernias so far. 2 umbicial, 2 groin, so i take time out every year yo go back on hemo to repair my hernias
Lisa
I was a PD patient for 10 months.  After my transplant (about one year) I woke up one morning, looked down, and saw I had an incisional hernia.  When I went in for a consult prior to the surgical repair, I was told that this occurred fairly commonly with PD patients.  So, how many of you have experienced the same thing?
Flosschick

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Angie
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« Reply #9 on: September 05, 2009, 12:44:22 PM PDT »

I was a PD patient for 10 months.  After my transplant (about one year) I woke up one morning, looked down, and saw I had an incisional hernia.  When I went in for a consult prior to the surgical repair, I was told that this occurred fairly commonly with PD patients.  So, how many of you have experienced the same thing?
Flosschick

I have had one Umbilical Hernia directly related to my PD as well. It was pretty easy to repair. They put in a disk behind my belly button for added support as I was still going to be on PD for awhile at that time. Wink

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Always check advice you get online!

My Site | My Pix | KK Mall | Dialysis Ethics (new)

PD = 4 1/2 yrs
HD = 2 1/2 hrs
2nd Transplant: 9/30/07
flosschick
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« Reply #10 on: September 15, 2009, 01:49:55 PM PDT »

Great Allison!  I was a PD patient for 10 months - but transplanted 10 years ago.  I'm sure things have changed considerably since then.  What a wonderful thing you're doing!
Flosschick

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old_fool
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« Reply #11 on: November 27, 2009, 06:36:53 PM PST »

I was a PD patient for 10 months.  After my transplant (about one year) I woke up one morning, looked down, and saw I had an incisional hernia.  When I went in for a consult prior to the surgical repair, I was told that this occurred fairly commonly with PD patients.  So, how many of you have experienced the same thing?
Flosschick

I have had one Umbilical Hernia directly related to my PD as well. It was pretty easy to repair. They put in a disk behind my belly button for added support as I was still going to be on PD for awhile at that time. Wink

OK ladies... I am not sure how I should react to these items.  If there was some way to know what caused these hernias, I would sleep better.  My PD nurse tells me not to lift anything from the ground.  I listen and go my way.  Later in the day I pick up my big 3 year old  Wink who is 65 lbs like I did before my surgery.  My catheter site has always done well and I am not obese.  So I wonder if my PD nurse is "just doing her job" when she tells me of older patients who developed hernias.

Oi.  It's tough not knowing how my body will respond.

So any ideas why some people have such challenges and others don't?

cheers,
~fool

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getlife
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« Reply #12 on: December 01, 2009, 04:50:20 PM PST »

Old Fool, I don't qualify for PD, so I don't know that answer to that one....but if I were you...I would sit down and put my 3 year old on my lap.  No, j/k.  I wouldn't want a hernia either.  Marina, you lift heavy things at work, how do you feel about it?

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CKD 36 years.
2 previous transplants, latter lasting 18 years.
Returned to hemodialysis 1999. 
Presently on In-center Nocturnal Hemodialysis.
Awaiting another transplant.
Angie
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« Reply #13 on: December 02, 2009, 04:23:07 PM PST »

I was a PD patient for 10 months.  After my transplant (about one year) I woke up one morning, looked down, and saw I had an incisional hernia.  When I went in for a consult prior to the surgical repair, I was told that this occurred fairly commonly with PD patients.  So, how many of you have experienced the same thing?
Flosschick

I have had one Umbilical Hernia directly related to my PD as well. It was pretty easy to repair. They put in a disk behind my belly button for added support as I was still going to be on PD for awhile at that time. Wink

OK ladies... I am not sure how I should react to these items.  If there was some way to know what caused these hernias, I would sleep better.  My PD nurse tells me not to lift anything from the ground.  I listen and go my way.  Later in the day I pick up my big 3 year old  Wink who is 65 lbs like I did before my surgery.  My catheter site has always done well and I am not obese.  So I wonder if my PD nurse is "just doing her job" when she tells me of older patients who developed hernias.

Oi.  It's tough not knowing how my body will respond.

So any ideas why some people have such challenges and others don't?

cheers,
~fool

I was only picking up 20 - 45 lb boxes at work when I got Hernia. The thing is, the pressure  of the fluid on the inside of the Peritoneal Cavity is one thing but then lifting something heavy you are adding extra strain on that your stomach muscles. I don't exactly understand but for some reason when you lift something heavy and already have your abdominal area maxed and not able to take much more, it doesn't matter if you are an averagely in shape person, you can still get hernia.

I am not a professional and am only speaking from what I understand of my experience. So because of this I am not sure I am explaining it right but I realized after it happened to me, just how easily it happens. It is not like POOF! Hernia shows up! No .. it is slow and gets larger. I couldn't just quit my job. I was at it too long. But then I needed surgery so I was forced to take time off. The funny thing is my department manager got hernia at the same time (no he is not on dialysis but was just lifting stuff that was too heavy) so he ended up being more understanding about my hernia even though he was the same one who was against me using a cart for the boxes of Idaho Potatoes and Chicken.

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Always check advice you get online!

My Site | My Pix | KK Mall | Dialysis Ethics (new)

PD = 4 1/2 yrs
HD = 2 1/2 hrs
2nd Transplant: 9/30/07
old_fool
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« Reply #14 on: December 04, 2009, 01:50:04 PM PST »

Weird. I had a dream about hernias last night.  Huh?

Thanks for your input Angie.  I'll try to do better with Jeremy.  As I told my new neph Wednesday, if all I had to worry about was CKD, my life would be easy.

If I don' t see your smiling imoticons or chat with you b4 the holidays, have a very merry and anything else that applies.

~fool

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