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Author Topic: Showering with a catheter  (Read 6604 times)
frankswife
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« on: September 26, 2012, 12:02:41 PM »

Does anyone have any experience with the catheter protection bandages, not sure what they are called, I just know I paid $53 for 12 if them! Anyway, Frank is feeling very grubby and wants desperately to take a shower, so I ordered these things for him. But now he is hesitating to use them, nervous that he'll still get the catheter wet. I don't blame him, that catheter scares me silly. Has anyone used these things and do they work well? And do drugstores carry them? Thanks!
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Lillupie
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« Reply #1 on: September 26, 2012, 12:07:40 PM »

What cathater does he use? THe PD cath you can only shower with.

Lisa
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frankswife
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« Reply #2 on: September 26, 2012, 12:27:02 PM »

He's got the neck catheter
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Sydnee
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« Reply #3 on: September 26, 2012, 12:30:56 PM »

When Ed had the tunnel catheter in we were first at the hospital so I got to see how they bagged it up so he could take a shower. When we got home we used a quart sized ziplock bag and did the same thing they did at the hospital. We cut the bag so it was one big piece of plastic then taped it on the top and both sides (but NOT the bottom) we domed it a little so he could move his arm. It worked well. There is no way that Ed would have let me spend $53 on something he used in the shower.

Hope that helps :flower;
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cause PKD diagnosed age 14

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jeannea
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« Reply #4 on: September 26, 2012, 12:45:37 PM »

I found the best thing is Glad Press n Seal. Cover the catheter and the area around it with the cling wrap. Just lay it on flat. Then use a hand held shower attachment to strategically aim the water. The outside of the cling wrap will get wet but underneath will be dry. Cheap and practical. I did it for 6 months and never got the dressing wet.
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Darthvadar
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« Reply #5 on: September 26, 2012, 01:04:57 PM »

And run the shower for a minute before getting in... Just in case there are a few bugs sitting in the shower head.... I put our shower head into a bucket of hot water with bleach in it every week or so...

Darth...
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« Reply #6 on: September 26, 2012, 01:07:47 PM »

yeah wouldnt trust the shower... He doesnt want to take a bath?
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Check out my Facebook profile for CKD "Help Lisa Spread Awareness for Kidney Disease"

It is my utmost dream and desire to reach out to other kidney patients for them to know that they are not alone in this, also to reach out to those who one day have to go on dialysis though my book i am writing!

dx with lupus nephritis 5/99'
daughter born 11/2005
stage IV CKD 11/2005-6/2007
8/2007- PD cathater inserted
9/2007- revision of PD Cathater
10/2007 started PD
frankswife
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« Reply #7 on: September 26, 2012, 01:28:30 PM »

We remodeled our bathroom right before the catheter and put in a shower stall. We do have the spray attachment. We didn't know he was gonna need a cath, so... Drat! I think we're going to hold off taking a shower for now.
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noahvale
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« Reply #8 on: September 26, 2012, 01:58:06 PM »

^
« Last Edit: September 18, 2015, 08:04:47 PM by noahvale » Logged
dialysis.sucks
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« Reply #9 on: December 30, 2012, 12:43:06 AM »

I found the best thing is Glad Press n Seal. Cover the catheter and the area around it with the cling wrap. Just lay it on flat. Then use a hand held shower attachment to strategically aim the water. The outside of the cling wrap will get wet but underneath will be dry. Cheap and practical. I did it for 6 months and never got the dressing wet.

PRess n seal is great. Cut a piece big enough to cover. Then take the clear tape from Dialysis (ask them first of course) and do up all four sides. No need to hold the cover on. I wouldn't take to many direct blasts. I always do the strategic turn side to side, but everything stays dry! Also you may be inclined to buy the cloth tape they have hanging up at walgreens. DON'T! The steam in the air is enough to get that to pull off. Definitely ask for the clear tape they use at your center. If you dont like asking for tape every other week (the techs are cool like that at mine), look at the type on the box (the name escapes me now) and you can buy a whole large box of it on Amazon. But free is always better  :beer1;
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smcd23
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« Reply #10 on: December 30, 2012, 06:56:08 PM »

Tony gets a weekly shower with his catheter. We have some shower shield things, and have found them to be somewhat useless. We always seem to get the stupid bandage wet. I generally tape a plastic sandwich bag over the thing, use lots of tape and help him shower making sure he keeps that area out of the direct flow of water. We have a 50/50 success rate.

So we just keep gloves, masks, sterile gauze, iodine and tape on hand and if the bandage gets wet, I remove the old dressing, apply the iodine and recover with the gauze and tape. Next time he sees his neph he is going to ask if we can remove the old bandage/tape, and recover with a new gauze and tegaderm since those stick in the shower but I can't find any big enough to put over his site because the unit uses so much tape. As the nurses on his unit said, we have "medical training" since he did PD for so long, so they trust that we can change a dressing safely.
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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
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Cordelia
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« Reply #11 on: December 30, 2012, 07:54:47 PM »

Never bothered to use  anything like that. I only ever used Glad Saran wrap with an elastic. Never, ever in the 1.5 years I had my cath, never had an infection.

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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
smcd23
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« Reply #12 on: December 30, 2012, 08:34:40 PM »

The key to preventing infection is doing what you can to keep it dry, and in the event it does get wet, change the wet bandage ASAP. We usually unwrap Tony while he is in the bathroom while he is drying off so I can run into the other room and get everything together if the bandage did get wet.

Never bothered to use  anything like that. I only ever used Glad Saran wrap with an elastic. Never, ever in the 1.5 years I had my cath, never had an infection.



Where did you put the elastic?? I am confused. I mean I can see putting it over the lumens but what about the exit site??
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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?
CebuShan
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« Reply #13 on: December 31, 2012, 07:03:18 AM »

I had a hand held shower head that we bought. I, too used Tegaderm and just changed it if it got too wet. When the catheter came out, after it had healed, I went and stood under the shower until the hot water ran out! It felt so good not to have to worry about the site getting wet!
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Cordelia
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« Reply #14 on: January 01, 2013, 07:23:20 AM »

The key to preventing infection is doing what you can to keep it dry, and in the event it does get wet, change the wet bandage ASAP. We usually unwrap Tony while he is in the bathroom while he is drying off so I can run into the other room and get everything together if the bandage did get wet.

Never bothered to use  anything like that. I only ever used Glad Saran wrap with an elastic. Never, ever in the 1.5 years I had my cath, never had an infection.



Where did you put the elastic?? I am confused. I mean I can see putting it over the lumens but what about the exit site??

Yes, over the lumens, just to keep from water seeping in.  I had saran over the whole entire thing.
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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
Joe
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« Reply #15 on: January 01, 2013, 08:13:34 AM »

Ok gang, this has tickled my interest for some time now. As you know, I do PD. And I have a catheter, albeit it comes out of my abdomen and not somewhere else. I don't have any showering restrictions on my catheter, other than I have to do exit site care any time I get it wet. But that's not a big deal, clean it thoroughly when I'm done and bandage it back up (in my case, I tuck it back in my PD belt). So, what is the difference between how I have to care for my catheter and yours with a Hemo Cath? Thanks for helping me understand.
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jeannea
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« Reply #16 on: January 01, 2013, 08:27:25 AM »

The difference is in how the surgery installs the catheter. I had both types at different times. The permacath leaves the incision more exposed and makes it easier to get infection in there. With you PD cath, there is still some risk of infection but a lot less based on the way they close things up. The permacath has to stay bandaged and yours does not. Wet bandages are a real problem. Sorry but I don't know surgery technicalities. I just remember that under my permacath bandage things looked a lot more open.
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Cordelia
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« Reply #17 on: January 01, 2013, 09:37:53 AM »

I had a chest cath and never kept mine bandaged, never had an infection. But, I was given permission to not wear one. You  have to ask your doctor first, I wouldn't do it without approval. I had so much itching and constantly had allergic reactions to the bandage so that was why I got permission to do without.
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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
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