Mediport placement today: I asked by Dr for a... - CLL Support

CLL Support

23,335 members40,038 posts

Mediport placement today

CLLmoxie profile image
16 Replies

I asked by Dr for a Mediport and had it placed today in interventional radiology. It can stay in almost indefinitely (10 plus years), if desired or be removed anytime in office setting. Very little maintenance or chance of infection. Totally under the skin. Needle for infusion or blood draw still goes through your skin but just into little membrane on line. Can apply EMLA cream to skin first, if needed. Saving my peripheral veins!

Written by
CLLmoxie profile image
CLLmoxie
To view profiles and participate in discussions please or .
16 Replies
GMa27 profile image
GMa27

Loved my port! Had it removed 6 months after chemo (last Feb). It worked great. They had a spray to numb mine.

Good luck! 💕

rcknow profile image
rcknow

It was great to have a port. I needed weekly blood transfusions before and during the first three months of FCR and I like having both hands free during transfusions and infusions. It was removed about a year after finishing FCR. Best wishes to you!!

DaveGH profile image
DaveGH

I was unable to get a mediport because I had Chemo a week earlier so they put a PICC in. It worked great for 6 months then my skin started to break down when they changed the bandage. It was removed last week. It lasted for 6 chemo sessions. Next time I will have a mediport.

Good luck with yours!

Dave

Jemorgen profile image
Jemorgen in reply toDaveGH

Lets hope there’s no next time!

BeckyLUSA profile image
BeckyLUSA

Blood draw people are starting to complain about my veins and have mentioned me getting one just for IVIG. Are the mediports something newer than previous kinds of ports?

BeckyL USA

CLLmoxie profile image
CLLmoxie in reply toBeckyLUSA

Yes, I think so. It it put in at interventional radiology under fluoroscopy. It is completely under the skin. A Huber needle is used to draw or inject into it. Can be used for anything. (chemo, meds, CT contrast, blood transfusions, meds, blood draws etc) Also, called ‘power port’ so rapid infusions can be given, if ever needed. Much different than the old subclavian line that was a random (riskier) stab with an IV access hanging out. Also different than PIC line. There are several brands. Mine happens to be a Bard Mediport (power port) which you could Google. Good luck.

Justasheet1 profile image
Justasheet1

I had mine removed after my chemo was done because they need to be flushed and I wanted to stay out of the hospital.

All blood draws were still done via my veins. You have to be specially trained to access the port.

Jeff

CLLMoxie2 profile image
CLLMoxie2 in reply toJustasheet1

Mine needs flushed once a month which I can do at home with Huber needle and heparin.

Justasheet1 profile image
Justasheet1 in reply toCLLMoxie2

My wife’s a nurse and that never was an option for me. That port goes almost directly to the heart, I thought, and a sterile technique was always done while accessing it. It was kind of a big deal but maybe it was because of the chemo?

Great health to you!

Jeff

CLLMoxie2 profile image
CLLMoxie2 in reply toJustasheet1

Jeff,

I was ‘told’ I could flush it but my first opportunity to get supplies , instructions and verify the validity of that will be Monday. I will let you know for hopefully unneeded future reference.

bigunwill2 profile image
bigunwill2

I’ve had a port for BR 3 years ago and decided to keep it. It is great for all the blood draws I’ve had in 3 1/2 years. Having it flushed every month, I also get a a monthly blood test which helps know right away if something is out of whack.

WinJ3 profile image
WinJ3

I had my Mediport in for a year. The surgeon said mine should last for at least 10 years to life. I might leave it in just in case I’ll need to use it again.

CLLmoxie profile image
CLLmoxie in reply toWinJ3

I will probably leave mine in too - it can be used for CT contrast and so many other things that ‘could’ (but hopefully won’t) come up.

bigunwill2 profile image
bigunwill2

They usually won’t put the contrast in my port and certainly not the radioactive for PET scan.

CLLmoxie profile image
CLLmoxie in reply tobigunwill2

True no radioactive stuff.

noeagaman profile image
noeagaman

I still have my port after getting it for FCR back in 2017. I love having it since like you said it saves your vains. Now I get IVIG's and they use the port for that too.

Chris

Not what you're looking for?

You may also like...

Intense itching upper arms,mostly nights

I get the most intense itch...its embarrassing. My upper arms itch so bad they feel like bugs are...
Torid1361 profile image

Cuts, Bruises & CLL

Good day everyone. I have a question regarding cuts and bruises. Is it common to find that you...

A Patient’s Guide to Shingles - Prompt treatment is crucial to avoid severe neurological complications.

Shingles isn't contagious like chickenpox; you can't directly catch shingles from somebody else who...
Jm954 profile image
Administrator

Post Chemo Effects

Hi. Can somebody out there give me some help? I finished my chemo treatment - Bendamustine &...
jaypax profile image

Constant skin rashes

As some may know I have been fighting constant skin rash since November, antibiotics help clear it...
cartwheels profile image

Moderation team

See all
AussieNeil profile image
AussieNeilAdministrator
Newdawn profile image
NewdawnAdministrator
CLLerinOz profile image
CLLerinOzAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.